Features of main POCTs for UTI diagnosis.
\\n\\n
IntechOpen was founded by scientists, for scientists, in order to make book publishing accessible around the globe. Over the last two decades, this has driven Open Access (OA) book publishing whilst levelling the playing field for global academics. Through our innovative publishing model and the support of the research community, we have now published over 5,700 Open Access books and are visited online by over three million academics every month. These researchers are increasingly working in broad technology-based subjects, driving multidisciplinary academic endeavours into human health, environment, and technology.
\\n\\nBy listening to our community, and in order to serve these rapidly growing areas which lie at the core of IntechOpen's expertise, we are launching a portfolio of Open Science journals:
\\n\\nAll three journals will publish under an Open Access model and embrace Open Science policies to help support the changing needs of academics in these fast-moving research areas. There will be direct links to preprint servers and data repositories, allowing full reproducibility and rapid dissemination of published papers to help accelerate the pace of research. Each journal has renowned Editors in Chief who will work alongside a global Editorial Board, delivering robust single-blind peer review. Supported by our internal editorial teams, this will ensure our authors will receive a quick, user-friendly, and personalised publishing experience.
\\n\\n"By launching our journals portfolio we are introducing new, dedicated homes for interdisciplinary technology-focused researchers to publish their work, whilst embracing Open Science and creating a unique global home for academics to disseminate their work. We are taking a leap toward Open Science continuing and expanding our fundamental commitment to openly sharing scientific research across the world, making it available for the benefit of all." Dr. Sara Uhac, IntechOpen CEO
\\n\\n"Our aim is to promote and create better science for a better world by increasing access to information and the latest scientific developments to all scientists, innovators, entrepreneurs and students and give them the opportunity to learn, observe and contribute to knowledge creation. Open Science promotes a swifter path from research to innovation to produce new products and services." Alex Lazinica, IntechOpen founder
\\n\\nIn conclusion, Natalia Reinic Babic, Head of Journal Publishing and Open Science at IntechOpen adds:
\\n\\n“On behalf of the journal team I’d like to thank all our Editors in Chief, Editorial Boards, internal supporting teams, and our scientific community for their continuous support in making this portfolio a reality - we couldn’t have done it without you! With your support in place, we are confident these journals will become as impactful and successful as our book publishing program and bring us closer to a more open (science) future.”
\\n\\nWe invite you to visit the journals homepage and learn more about the journal’s Editorial Boards, scope and vision as all three journals are now open for submissions.
\\n\\nFeel free to share this news on social media and help us mark this memorable moment!
\\n\\n\\n"}]',published:!0,mainMedia:{caption:"",originalUrl:"/media/original/237"}},components:[{type:"htmlEditorComponent",content:'
After years of being acknowledged as the world's leading publisher of Open Access books, today, we are proud to announce we’ve successfully launched a portfolio of Open Science journals covering rapidly expanding areas of interdisciplinary research.
\n\n\n\nIntechOpen was founded by scientists, for scientists, in order to make book publishing accessible around the globe. Over the last two decades, this has driven Open Access (OA) book publishing whilst levelling the playing field for global academics. Through our innovative publishing model and the support of the research community, we have now published over 5,700 Open Access books and are visited online by over three million academics every month. These researchers are increasingly working in broad technology-based subjects, driving multidisciplinary academic endeavours into human health, environment, and technology.
\n\nBy listening to our community, and in order to serve these rapidly growing areas which lie at the core of IntechOpen's expertise, we are launching a portfolio of Open Science journals:
\n\nAll three journals will publish under an Open Access model and embrace Open Science policies to help support the changing needs of academics in these fast-moving research areas. There will be direct links to preprint servers and data repositories, allowing full reproducibility and rapid dissemination of published papers to help accelerate the pace of research. Each journal has renowned Editors in Chief who will work alongside a global Editorial Board, delivering robust single-blind peer review. Supported by our internal editorial teams, this will ensure our authors will receive a quick, user-friendly, and personalised publishing experience.
\n\n"By launching our journals portfolio we are introducing new, dedicated homes for interdisciplinary technology-focused researchers to publish their work, whilst embracing Open Science and creating a unique global home for academics to disseminate their work. We are taking a leap toward Open Science continuing and expanding our fundamental commitment to openly sharing scientific research across the world, making it available for the benefit of all." Dr. Sara Uhac, IntechOpen CEO
\n\n"Our aim is to promote and create better science for a better world by increasing access to information and the latest scientific developments to all scientists, innovators, entrepreneurs and students and give them the opportunity to learn, observe and contribute to knowledge creation. Open Science promotes a swifter path from research to innovation to produce new products and services." Alex Lazinica, IntechOpen founder
\n\nIn conclusion, Natalia Reinic Babic, Head of Journal Publishing and Open Science at IntechOpen adds:
\n\n“On behalf of the journal team I’d like to thank all our Editors in Chief, Editorial Boards, internal supporting teams, and our scientific community for their continuous support in making this portfolio a reality - we couldn’t have done it without you! With your support in place, we are confident these journals will become as impactful and successful as our book publishing program and bring us closer to a more open (science) future.”
\n\nWe invite you to visit the journals homepage and learn more about the journal’s Editorial Boards, scope and vision as all three journals are now open for submissions.
\n\nFeel free to share this news on social media and help us mark this memorable moment!
\n\n\n'}],latestNews:[{slug:"step-in-the-right-direction-intechopen-launches-a-portfolio-of-open-science-journals-20220414",title:"Step in the Right Direction: IntechOpen Launches a Portfolio of Open Science Journals"},{slug:"let-s-meet-at-london-book-fair-5-7-april-2022-olympia-london-20220321",title:"Let’s meet at London Book Fair, 5-7 April 2022, Olympia London"},{slug:"50-books-published-as-part-of-intechopen-and-knowledge-unlatched-ku-collaboration-20220316",title:"50 Books published as part of IntechOpen and Knowledge Unlatched (KU) Collaboration"},{slug:"intechopen-joins-the-united-nations-sustainable-development-goals-publishers-compact-20221702",title:"IntechOpen joins the United Nations Sustainable Development Goals Publishers Compact"},{slug:"intechopen-signs-exclusive-representation-agreement-with-lsr-libros-servicios-y-representaciones-s-a-de-c-v-20211123",title:"IntechOpen Signs Exclusive Representation Agreement with LSR Libros Servicios y Representaciones S.A. de C.V"},{slug:"intechopen-expands-partnership-with-research4life-20211110",title:"IntechOpen Expands Partnership with Research4Life"},{slug:"introducing-intechopen-book-series-a-new-publishing-format-for-oa-books-20210915",title:"Introducing IntechOpen Book Series - A New Publishing Format for OA Books"},{slug:"intechopen-identified-as-one-of-the-most-significant-contributor-to-oa-book-growth-in-doab-20210809",title:"IntechOpen Identified as One of the Most Significant Contributors to OA Book Growth in DOAB"}]},book:{item:{type:"book",id:"65",leadTitle:null,fullTitle:"Advances in Grid Computing",title:"Advances in Grid Computing",subtitle:null,reviewType:"peer-reviewed",abstract:"This book approaches the grid computing with a perspective on the latest achievements in the field, providing an insight into the current research trends and advances, and presenting a large range of innovative research papers. The topics covered in this book include resource and data management, grid architectures and development, and grid-enabled applications. New ideas employing heuristic methods from swarm intelligence or genetic algorithm and quantum encryption are considered in order to explain two main aspects of grid computing: resource management and data management. The book addresses also some aspects of grid computing that regard architecture and development, and includes a diverse range of applications for grid computing, including possible human grid computing system, simulation of the fusion reaction, ubiquitous healthcare service provisioning and complex water systems.",isbn:null,printIsbn:"978-953-307-301-9",pdfIsbn:"978-953-51-5509-6",doi:"10.5772/596",price:119,priceEur:129,priceUsd:155,slug:"advances-in-grid-computing",numberOfPages:286,isOpenForSubmission:!1,isInWos:1,isInBkci:!1,hash:null,bookSignature:"Zoran Constantinescu",publishedDate:"February 28th 2011",coverURL:"https://cdn.intechopen.com/books/images_new/65.jpg",numberOfDownloads:31521,numberOfWosCitations:22,numberOfCrossrefCitations:14,numberOfCrossrefCitationsByBook:1,numberOfDimensionsCitations:23,numberOfDimensionsCitationsByBook:3,hasAltmetrics:0,numberOfTotalCitations:59,isAvailableForWebshopOrdering:!0,dateEndFirstStepPublish:"May 12th 2010",dateEndSecondStepPublish:"June 9th 2010",dateEndThirdStepPublish:"September 14th 2010",dateEndFourthStepPublish:"November 13th 2010",dateEndFifthStepPublish:"January 27th 2011",currentStepOfPublishingProcess:5,indexedIn:"1,2,3,4,5,6,7",editedByType:"Edited by",kuFlag:!1,featuredMarkup:null,editors:[{id:"17194",title:"Dr.",name:"Zoran",middleName:null,surname:"Constantinescu",slug:"zoran-constantinescu",fullName:"Zoran Constantinescu",profilePictureURL:"https://mts.intechopen.com/storage/users/17194/images/1558_n.jpg",biography:"Zoran Constantinescu got his MSc (1997) at the Department of Computer Science from the Politehnica University of Bucharest, Romania. He has been working since, both in the Software Engineering industry and in Higher Education. He got his doctoral degree in Computer Science (2008) from The Norwegian University of Science and Technology, Trondheim, Norway, with a thesis on a desktop grid computing approach to scientific computing and visualization. In fact, he has developed from scratch a new open source desktop grid computing system, named QADPZ, and has proved its viability by testing it on some scientific computing and visualization experiments. Since QADPZ became openly available in 2003, thousands of users around the world have been using it for their computationally intensive tasks and contributed with their feedback to the system’s improvement. Broadly, his research interests include parallel and distributed computing, desktop grid computing, GPS systems, and embedded systems, and he has published 25 research papers dealing with these topics. He is very committed to the open source world and actively participates in this endeavor.",institutionString:null,position:null,outsideEditionCount:0,totalCites:0,totalAuthoredChapters:"1",totalChapterViews:"0",totalEditedBooks:"1",institution:null}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,coeditorOne:null,coeditorTwo:null,coeditorThree:null,coeditorFour:null,coeditorFive:null,topics:[{id:"615",title:"Grid Computing",slug:"grid-computing"}],chapters:[{id:"13940",title:"Application of Discrete Particle Swarm Optimization for Grid Task Scheduling Problem",doi:"10.5772/13950",slug:"application-of-discrete-particle-swarm-optimization-for-grid-task-scheduling-problem",totalDownloads:2777,totalCrossrefCites:2,totalDimensionsCites:2,hasAltmetrics:0,abstract:null,signatures:"Ruey-Maw Chen",downloadPdfUrl:"/chapter/pdf-download/13940",previewPdfUrl:"/chapter/pdf-preview/13940",authors:[{id:"16362",title:"Dr.",name:"Ruey-Maw",surname:"Chen",slug:"ruey-maw-chen",fullName:"Ruey-Maw Chen"}],corrections:null},{id:"13941",title:"A Framework for Problem-Specific QoS Based Scheduling in Grids",doi:"10.5772/14819",slug:"a-framework-for-problem-specific-qos-based-scheduling-in-grids",totalDownloads:1883,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:null,signatures:"Mohamed Wahib, Asim Munawar, Masaharu Munetomo and Kiyoshi Akama",downloadPdfUrl:"/chapter/pdf-download/13941",previewPdfUrl:"/chapter/pdf-preview/13941",authors:[{id:"16278",title:"PhD.",name:"Mohamed",surname:"Wahib",slug:"mohamed-wahib",fullName:"Mohamed Wahib"},{id:"20413",title:"Mr",name:"Asim",surname:"Munawar",slug:"asim-munawar",fullName:"Asim Munawar"},{id:"20414",title:"Dr.",name:"Masaharu",surname:"Munetomo",slug:"masaharu-munetomo",fullName:"Masaharu Munetomo"},{id:"20415",title:"Dr.",name:"Kiyoshi",surname:"Akama",slug:"kiyoshi-akama",fullName:"Kiyoshi Akama"}],corrections:null},{id:"13942",title:"Grid-JQA: A QoS Guided Scheduling Algorithm for Grid Computing",doi:"10.5772/14028",slug:"grid-jqa-a-qos-guided-scheduling-algorithm-for-grid-computing",totalDownloads:2490,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:null,signatures:"Leyli Mohammad Khanli and Saeed Kargar",downloadPdfUrl:"/chapter/pdf-download/13942",previewPdfUrl:"/chapter/pdf-preview/13942",authors:[{id:"16562",title:"Prof.",name:"Leyli",surname:"Mohammad Khanli",slug:"leyli-mohammad-khanli",fullName:"Leyli Mohammad Khanli"}],corrections:null},{id:"13943",title:"Autonomic Network-Aware Metascheduling for Grids: A Comprehensive Evaluation",doi:"10.5772/14087",slug:"autonomic-network-aware-metascheduling-for-grids-a-comprehensive-evaluation",totalDownloads:2106,totalCrossrefCites:0,totalDimensionsCites:1,hasAltmetrics:0,abstract:null,signatures:"Agustín C. 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Urinary tract infections (UTIs) are caused by the presence and multiplication of microorganisms in the urinary tract, sometimes spreading to the bloodstream and possibly resulting in several clinical syndromes (e.g., pyelonephritis, cystitis, urethritis, epididymitis and prostatitis) [1].
\nMost UTIs are caused by bacteria, and when they occur in the urine without causing symptoms, this condition is called asymptomatic bacteriuria; when growth of bacteria leads to a panel of symptoms, this condition is referred to as symptomatic bacteriuria [1]. Urinary tract infections can manifest as bacteriuria with limited clinical symptoms and sepsis, depending on localized or systemic extension [2].
\nThe onset of UTIs is mostly due to the ascent of microorganisms from the urethra, especially organisms of enteric origin, e.g.,
UTIs are among the most prevailing infectious diseases with a substantial financial burden on society [3]. The incidence of community-acquired UTIs is highest in young women [1]: almost half of all women will experience at least one episode of UTI during their lifetime, and nearly 1 in 3 women will have had at least one episode of UTI by the age of 24 years [2]. Urinary tract infection incidence increases with age for both sexes. It is estimated that 10% of men and 20% of women over the age of 65 years have asymptomatic bacteriuria [1].
\nReports from European countries and the USA show that ca. 15% of all community-prescribed antibiotics are dispensed for UTIs [3]. UTIs account for many annual hospital admissions, especially among the elderly: in the UK, the number of emergency admissions of older people with a primary diagnosis of UTI showed a 200% increase from 2001/2002 to 2012/2013, parallel to a related increase in bed days, which both are the second highest increase (in absolute terms) among groups of conditions [4]. Nevertheless, UTIs are believed to have been greatly overcoded in recent years: part of the increase may be due to changes in coding practice, part to increased emergence of antibiotic resistance [4]. Moreover, UTIs represent at least 40% of all hospital acquired infections and most of them occur following catheterization, which is considered one of the main risk factors associated to onset of UTIs [3].
\nThe clinical evidence of UTI is based on a number of basic criteria, including clinical symptoms, and laboratory data which should provide evidence of the presence of microorganisms by culturing of urine samples, or other specific tests [2]. However, the diagnosis of UTIs is primarily based on symptoms and signs. Tests that suggest or prove the presence of bacteria or white cells in the urine may contribute additional information to inform management but rarely have important implications for diagnosis, also considering the long time often required for obtaining results with traditional methods [5].
\nThe gold standard for diagnosis of bacteriuria is culture of appropriate urine sample [6, 7]. Sampling by needle aspiration minimizes the risk of contamination, while catheter and midstream sampling show a higher risk of contamination and therefore yield more false positive results [5]. However, needle aspiration is invasive and midstream sampling is preferred in clinical practice [8]. Routine culture is generally carried out streaking 10 μl of urine sample on agar plates containing selective or differential media and reading results after at least 24–48hours of incubation, considering characteristic colony morphologies and average quantitation. If there is the need for more accurate quantitative results, 100 μl plating following serial dilutions of urine sample must be performed [9]. The main value of urine culture is to identify microorganisms, most often bacteria; indirect indicators of the presence of bacteria (for example, urinary nitrites) are much less valuable than urine culture [5].
\nThe number of bacteria in urine has been considered relevant for the diagnosis of UTIs since the Sixties, when Kass developed the concept of significant bacteriuria (105 CFU/ml) opening up to quantitative microbiology for the diagnosis of infectious diseases; his notion is still generally used to help diagnosis. Nevertheless, it has recently become clear that no fixed bacterial count can be applied to all kinds of UTIs and all circumstances, and even low bacterial concentrations are considered clinically relevant considering specific clinical pictures, sampling protocols and patient’s sex. The problem of counting low numbers must then be considered [2].
\nAlong with pathogen identification, outlining its antimicrobial susceptibility profile is considered to be crucial to ensure an appropriate treatment [10]. Antimicrobial susceptibility testing is routinely performed using the Kirby-Bauer disk diffusion technique according to Clinical and Laboratory Standards Institute (CLSI) guidelines, meaning culturing bacteria from urine samples on agar plates in presence of disks containing selected antibiotics; interpretation of results requires the measurement of halos of inhibition around disks according to reference tables [11].
\nAs with most bacterial infections, diagnosis of UTI depends on culturing the clinical sample in the clinical laboratory, and results are typically delayed of two to three days from sample acquisition [10]. This is due to the need for sample transport to the laboratory and the time required for bacteria to grow on culture media [10]. Thus, the standard method for UTI diagnosis is time consuming and logistically difficult [6].
\nSince the patient cannot remain untreated during this rather prolonged period before definitive diagnosis is obtained, physicians usually prescribe broad spectrum antibiotics prior to antibiogram results. This practice has many undesirable consequences in the short and long terms, such as treatment failure leading to spread or chronicization of infection, increased health care costs, and increased antibiotic resistance by a growing number of bacterial strains. Given these drawbacks, it is obvious that a rapid and accurate method of UTI diagnosis and bacterial antibiotic susceptibility assessment would offer significant health benefits [12].
\nThe introduction of partial and complete automation in clinical diagnostic in the 2000s has allowed the management of large-scale sample volumes and workflows optimization still providing reliable results for both pathogen identification and antibiotic susceptibility testing [10, 13].
\nLarge-scale systems, anyway, are expensive and require more dedicate space, equipment and more personnel competence, which makes them applicable to a large hospital setting, but are difficult to establish in a small hospital, or in a limited-resource setting (e.g., developing countries). These high-throughput culture-based instruments, moreover, remain relatively slow and are not amenable for point-of-care use [10].
\nThe introduction of matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF) technology in microbiology has allowed rapid and reliable bacterial identification, featuring both high sensitivity and specificity, improving efficiency and saving consumables and labor [14, 15]. MALDI-TOF technique is usually coupled with culture of urine samples, to allow isolation of bacteria and therefore obtain pure cultures, which will undergo MALDI-TOF analysis after some sample treatment. Recently, extensive databases have been developed that include protein profiles of main microorganisms involved in infections; some studies have therefore investigated the possibility to apply MALDI-TOF analysis directly to urine samples, yielding promising results also when coupling such analysis with screening methods, such as automated microscopic urine sediment analysis [16, 17]. It must be considered, however, that such high-throughput technology has high installation and maintenance costs, and requires dedicated spaces, limiting its use in routine analyses to centralized laboratories. Moreover, the technique cannot currently identify two species of bacteria when present simultaneously, and cannot determine antibiotic susceptibility; thus, traditional culture of urine samples is still necessary [18].
\nNevertheless, the occurrence of more than one bacterial strain in urine samples participating in the infection should not be overlooked. Polymicrobic infections are more often associated with catheterization and aging, reaching 10% incidence rates in the community and 30% in hospital setting among elderly people [19]. Bacterial strains recovered from polymicrobic infection show metabolic alterations and altered virulence traits, such as antibiotic resistance [19]. However, relationships between coinfecting strains are not yet fully understood [20], although some studies are exploiting such infections’ mechanisms [21, 22]. As clinical laboratories tend to report cultures showing single or clearly predominant bacteria and will not routinely report occurrence of polymicrobic associations, unless significant numbers of each species are detected, quite a large portion of UTIs are not correctly diagnosed nor treated, threatening patient’s safety [19, 23, 24, 25]. Therefore, an improvement of diagnosis and clinical pathways is needed in order to enhance not only detection of pathogens in urine, but also profiling the whole microflora and determining the antimicrobial susceptibility of individual components.
\nEven though the incidence of UTIs is higher in women [6], also related pathologies in men, such as epididymitis and prostatitis, may be caused by migration of pathogens from the urethra or bladder, the most common pathogens isolated being
Urine culture is recommended to determine the presence or absence of clinically significant bacteriuria in patients prior to urological interventions (e.g., surgery) and the presence of bacteriuria is controlled by directed pre-operative treatment of the detected pathogen [2, 6].
\nUrine culture is considered a valuable tool during patients’ follow-up: in women whose symptoms do not resolve or recur within 2–4 weeks after the completion of treatment, urine culture and antimicrobial susceptibility test should be performed and a new antibiotic regimen should be considered. Afterward, in patients who underwent antibiotic treatment, a follow-up with subsequent urine culture should verify the treatment efficacy [2]. Urine culture is also recommended in women who present with atypical symptoms, pregnant women and males with suspected UTI [2].
\nIn case of complicated UTIs, a broader range of bacteria is expected to be involved (often within the Enterobacteriaceae family), and these are more likely to show antibiotic resistance. Moreover, patients with a complicated UTI are more prone to have recurrent infections (more than 3 episodes/year) [2, 8, 27, 28]. Therefore, the choice of a therapy for these conditions must be supported by urine culture and antimicrobial susceptibility testing to avoid ineffective antibiotics administration.
\nUrine culture is also required in pediatric settings, where UTIs are the most common infections in children and infants, together with upper respiratory and gastrointestinal ones, with 30% recurrence rate reported within a year after initial UTI [2, 29]. Diagnosing pediatric UTIs may be difficult, because of communication difficulties in describing symptoms and vagueness of signs in small children; therefore, the definitive diagnosis of infection in children requires a positive urine culture [2].
\nIn febrile patients with negative results on dipstick, microscopic, or automated urinalysis, urine culture is unnecessary if there is an alternative cause of the fever or inflammatory signs. However, if the dipstick and/or urinalysis are positive, confirmation of UTI by urine culture is mandatory [29]. In febrile children with signs of UTI (clinical signs, positive dipstick and/or positive microscopy, better if urine culture is available), antibiotic treatment should be initiated as soon as possible to eradicate the infection, prevent bacteremia, improve clinical outcome, diminish the likelihood of renal involvement during the acute phase of infection, and reduce the risk of immediate and long-term complications, including renal scarring and renal failure [29, 30].
\nThe gold standard for diagnosis and successful management of UTIs is to obtain identification and quantification of the infecting agents, along with antibiotic susceptibility assessment to direct a specific therapy [31]. The use of microbiological culture method is well established in the diagnosis of infectious diseases [32]; however, such reference method is time-consuming, requiring on average 24–48hours, thus laboratory results are not immediately available, especially at patient’s presentation in the Emergency Department [32, 33]. For this reason, in order to avoid even serious complications (e.g., sepsis) and mitigate patients’ discomfort, the initial treatment specified by international guidelines as first step in UTIs management is most often empirical [32]. Nevertheless, this empirical approach contributes to mis- and over-use of antibiotics [10], resulting from unnecessary or inappropriate antimicrobial therapy, participating in recent arise in bacterial resistance. In fact, for people with symptoms of UTI and bacteriuria the main aim of treatment is relief of symptoms, but in case of unsuccessful treatment it could cause some alteration of urinary tract microflora, leading to an increased risk of clinical adverse events, including infections with multi-drug-resistant organisms and the development of antibiotic-resistant UTIs [1]. Infections caused by multi-drug-resistant pathogens, such as extended-spectrum beta-lactamase (ESBL) and carbapenemase producing Gram-negative bacteria, methicillin-resistant
The spread of antibiotic resistance is a threat to patients undergoing urological surgery in general [2], and multi-drug-resistant bacterial infections can limit the availability of effective treatment options, especially in low-income countries, rendering some UTIs difficult to treat and increasing healthcare costs [30].
\nThis situation is generally promoted by several factors, including the overuse and misuse of antimicrobials in human and veterinary medicine and, indirectly, in agriculture. Measures to prevent and control the increase of antimicrobial resistance as well as the dissemination of resistance genes are crucial [35]. Prudent prescribing and rational use of antibiotics is a key component of action plans for reducing antimicrobial resistance [1, 2, 35, 36]. Antimicrobial stewardship programs have become a priority to optimize the outcome of prevention and treatment of infection while limiting overuse and misuse of antimicrobial agents [6], also following a systematic audit approach [37, 38]. In addition, non-antibiotic strategies are being explored [6]. There are many non-antimicrobial measures recommended, especially for recurrent UTIs [2, 28, 39, 40], but only a few results from well-designed studies are available for evidence-based recommendations [2, 41].
\nIn general, the choice of antibiotics should be based, among other factors, upon identification and susceptibility pattern of the organism causing the UTI and the ecological collateral effects including selection of resistant bacteria by the chosen antimicrobial [2].
\nIt must be considered, though, that the in vitro susceptibility of community-acquired uropathogens varies according to age and geographic region, and, as magnitude and variability of antimicrobial resistance patterns in the community grow, so does the need for continuous large-scale surveillance systems, in order to create databases linking epidemiological, clinical and laboratory data [42].
\nTherefore, the development and implementation of new clinical tools in routine medical practice could help optimizing antibiotic administration, leading to a more prudent and rational use of antibiotics. A rapid screen may be a more practical approach to yield benefits for the patient, the physician, and the laboratory [43].
\nThe advent of new innovative diagnostic devices for UTI management, complementary to the reference culture-based methods, may lead to a new deal improving routine practice. Immunocompromised patients (e.g., diabetes mellitus, chronic kidney disease, and kidney transplant) with UTIs could particularly benefit from such diagnostic improvements. Clinical diagnosis of UTIs in this category of patients is challenging, because causative pathogens may be slightly different to those in the general population, and because of patients’ clinical picture complexity. Early diagnosis is imperative in this group, and treatment of UTIs should be tailored according to individual patient characteristics [44].
\nBecause of the clinical importance of early UTI diagnosis, alternative rapid near-patient urine tests have been developed, such as urine dipsticks, which are widely used [31] in spite of their uncertain diagnostic accuracy [6]. The urine dipsticks test is commonly used for presumptive diagnosis of UTIs: it detects the presence of biochemical markers in urine samples which may be useful to establish the diagnosis of UTI [2]. Although many urine biomarkers for UTIs have recently been considered [45], markers that showed best results in diagnostic accuracy are nitrite and leukocyte esterase [6]. Although being cost-effective [46], such test shows low sensitivity that limits its clinical usefulness, [6] and analysis may be biased since a number of bacterial species are unreactive in these tests (e.g., no reduction of nitrates) [47, 48]. Furthermore, urine dipstick test does not detect bacteria, nor their concentration, which is essential to diagnose UTIs according to guidelines, and provides no information about antimicrobial susceptibility. Urine dipsticks are, anyway, cheap, easy to use, can be performed at doctor’s office, in pharmacies or at home (even though urine dipstick test is not intended for self-diagnosis purposes [49], are available without prescription and provide results of easy interpretation within minutes.
\nAmong hospital tests routinely used for urine analysis, microscopy examination of urine sediment has since long time been used, also undergoing automation to improve results. Although sensitivity is high, specificity is too low for exclusive use in clinical settings. Moreover, such technique requires sample centrifugation, and experienced personnel is needed to avoid errors in microscopic examination [6].
\nFlow cytometry found applications in many fields, also including medical disciplines [50]. Automated platforms of urinary flow cytometry have been widely adopted by centralized laboratories [10]. Flow cytometry allows of rapid detection of bacteria, white blood cells, red blood cells, epithelial cells, casts, crystals, yeasts and spermatozoa. They offer the benefit of standardize urine sediment analysis and reduce the error associated with subjective interpretation of results [51]. Nevertheless, the poor quality of available studies was confirmed in a recent meta-analysis, which also showed current low accuracy and specificity of such method that should not be used as the sole screening tool for UTIs ([51], and references therein).
\nDipslide technology has been proposed to simplify traditional culture-based methods: the test allows the detection of bacteria in liquid matrices by observing growth on different agar media (e.g., CLED agar and MacConkey agar) after immersion into sample and following 24-hour incubation. Overall, despite being simple to use and cost-effective, dipslide technology can only be considered as a guide to support further analyses: such test shows low accuracy when compared to the reference culture method [6], and no reliable detection of <104 CFU/ml can be obtained [7]. For this reason, dipslides are currently unsuited to routine use in clinical setting with further studies required to determine the best combination of culture media [6].
\nFor the short term, molecular biology techniques such as real-time PCR could be used to complement conventional culture-based methods for pathogens identification, especially with regard to shortening the time to obtain results, shortening the time to decision of antibiotic therapy [32]. However, this method is limited by the broadness of the panel of pathogens included in the test, and both sensibility and specificity are low when compared to urine culture. Moreover, such technology requires many steps for sample preparation and does not allow a viable count, also considering that up to now the clearance of bacterial DNA from urine is unclear. The need for quantification in UTI diagnosis should drive future developments of commercial real-time PCR pathogen detection tools to include a quantification option [32].
\nIn addition, possible new routes have been explored aiming to develop new clinical tools to help rapidly identify uropathogens, such as: the detection of volatile organic compounds in urine by gas chromatography and mass spectrometry and following comparison between profiles using compounds databases [52]; the use of Raman and Surface Enhanced Raman Spectroscopy, which can provide quantification and identification of bacteria populations and possibly assessment of antibiotic susceptibility, although results are still preliminary and must be significantly expanded [12]; the use of impedance spectroscopy to detect ultra-low concentrations of
Although rapid, these technologies do not provide microbiological diagnosis nor susceptibility information, which remain the cornerstone of diagnosis, particularly in settings of complicated UTI [10].
\nIn summary, laboratory urine culture remains the gold standard investigation for UTI diagnosis [6].
\nSome tests have been developed aiming to provide rapid and accurate diagnostic information to direct treatment decisions at the patient’s bedside, which seem to have yielded good consent among practitioners [54].
\nRapid and definitive near-the-patient diagnosis of UTI would have a favorable impact on its management [10]: a rapid turnaround of results could influence clinical decisions such as triage, referral, and decision to discharge the patient. Prompt clinical interventions could be provided by caregivers, meaning timely antibiotic treatment could be initiated and imprecise empirical treatment avoided [10, 55]. This would improve health outcome also providing diagnostics tools for limited-resource settings [55]. Point-of-care tests (POCTs) can provide considerable savings in health care costs by reducing the number of patients visiting health centers simultaneously improving the quality of life for patients by reducing their number of visits to health care facilities [55]. An early diagnosis based on POCTs can also enable clinicians to start antibiotic administration earlier and thereby increase chances of successfully treating the disease. In future, innovation through rapid and reliable POCTs is advisable, updating technologies to ensure efficient data management and simplify use by healthcare professionals, eventually lowering medical costs [55]. POCTs could allow a better screening and follow-up of patients not only by hospitals, but also by pharmacies and general practitioners, helping decentralize diagnosis and therefore reduce the workload of laboratories, with consequent reduction of costs related to urine analysis and management of UTIs and reduction of human errors leading to mix-ups of patient samples sent to off-site laboratories [55].
\nSeveral POCT for UTIs have been developed and are currently commercially available. They can be distinguished in: (
Biosensors offer a promising approach for improving molecular diagnostic in POC settings [10]. Biosensors are binary systems composed of a recognition and a transducer element that can generate a measurable proportional signal following binding of the target analyte to the recognition element (e.g., antibody, enzyme), which allows quantitative detection of a biological entity [10]. Even though biosensors technology has been applied successfully to the field of clinical diagnostic (e.g., blood glucose and pregnancy tests), no such tests have been implemented to date to improve routine diagnosis of UTIs [55]. Indeed, key features of biosensors, such as portability, rapidity, and cost-effectiveness in comparison with their macro-scale counterparts, could be crucial for the development of a POCT for UTI pathogens identification and antimicrobial susceptibility assessment. Nevertheless, considering the urine matrix, such biosensors would require multistep sample preparation with amplification/enrichment steps to improve target detection, and such biological matrix could impair sensor performance with its variations in biochemical parameters (e.g., inhibitors, non-specific binding). Moreover, such tests should have a multiplex approach to ensure identification of a broad panel of pathogens in different clinical scenarios, and should provide antimicrobial susceptibility testing to drive treatment, but genetic non-culture based approaches are limited by the fast evolution rate of defense mechanisms among bacteria. Biosensors POCTs could anyway complement reference methods helping saving resources in terms of materials, money and time, because rapid, simple and cost-effective tests could optimize further analyses therefore reducing the burden on laboratories [10].
\nThe Micro Biological Survey (MBS) POCT “UTI CHECK” appears to hold good promise for early detection and antimicrobial susceptibility profiling of uropathogens. The MBS method allows rapid and accurate bacterial quantification through an automated colorimetric culture-based test; urine samples are inoculated into disposable ready-to-use reaction vials, which color will change thanks to redox indicators following bacterial growth after incubation (see Figure 1). Results of preliminary
Such findings encouraged further research in hospital settings, and clinical trials have been carried out [31] in which the efficacy of the MBS POCT was compared to the reference method, used in hospital routine, and other methods, such as urine dipsticks: the MBS POCT showed high accuracy, sensitivity and specificity, comparable to the reference method’s and higher than urine dipsticks’ [31]. Although not providing bacterial identification, MBS “UTI CHECK” allows bacteria detection and quantification in urine samples. Preliminary results showed that this POCT can provide uropathogens’ susceptibility pattern to a panel of antibiotics. The analytical time required for UTI diagnosis is usually less than 3 hours (up to 5–6 hours when the bacterial load is equal or less than 1 × 105 CFU/ml) and antimicrobial susceptibility assessment is obtained in less than 10 hours, which could guide downstream medical decisions with crucial information within few hours. Notably, this method features cost-effectiveness, user-friendliness, portability, easy interpretation of results, which all can lead to successful use at the patient’s bedside [31]. The MBS point-of-care testing device could be developed into a valuable aid for the management of UTIs, possibly addressing more precise diagnosis and appropriate therapy also proving useful in treatment outcome evaluation. Features of main POCTs available on market, including MBS “UTI CHECK,” are summarized in Table 1.
\nProduct | \nManufacturer/location | \nDescription of device | \nAnalysis time | \nAdditional equipment required | \nPositive result outcomes | \nMethod principle | \nNumber of samples tested; Test population | \nThreshold for significant growth | \nAccuracy | \nSensitivity (%) (95% CI) | \nSpecificity (%) (95% CI) | \nRef | \n
---|---|---|---|---|---|---|---|---|---|---|---|---|
FLEXICULT™ | \nStatens Serum Institut Diagnostica/Denmark | \nChromogenic agar plate with 6 segments – 5 evaluating anti-biotic sensitivities and 1 control segment | \n24 hours | \nIncubator | \nSemi-quantification of bacterial growth, evaluation of the species present, and assessment of sensitivity to the antibiotics in each of the plate segments | \nMicrobial culture and susceptibility testing | \nN = 200/124 (outpatient setting)/76 (secondary care setting) | \n≥105 CFU/ml | \n— | \n87.0% (67.9–95.5) | \n83.2% (74.7–89.2) | \n[23] | \n
Uricult Trio | \nOrion Diagnostics/Finland | \nPlastic slide with two opposing agar media | \n16–24 hours when incubated at 36.8 °C or 1–3 days at room temperature | \nIncubator | \nSemi-quantification of bacterial growth, evaluation of the species present | \nMicrobial culture | \n198 (pediatric patients aged 0–7) | \n≥104 CFU/ml | \n— | \n68% | \n82% | \n[26] | \n
\n | \n | \n | \n | \n | \n | \n | 434 (primary health care setting) | \n≥103 to ≥105 CFU/ml for doubtful uropathogens | \n88% | \n88% | \n90% | \n[27] | \n
DipStreak (Chromostreak) | \nNovamed/Israel | \nPlastic paddle with two opposing agar media, housed in a closed transparent plastic tube | \n18–24 hours | \nIncubator | \nSemi-quantification of bacterial growth, evaluation of the species present | \nMicrobial culture | \nN = 1070 (251 hospitalized patients and 819 outpatients) | \n>105 CFU/ml (single organism + mixed culture) | \n98% | \n95.7% | \n99.2% | \n[28] | \n
DiaSlide | \nNovamed/Israel | \nHinged plastic case containing two opposing agar media | \n24 hours | \nIncubator | \nSemi-quantification of bacterial growth | \nMicrobial culture | \n473 (prescreened hospital urine specimens using UriScreen) | \n≥104 CFU/ml | \n— | \n98.3% | \n97.5% | \n[29] | \n
onSite | \nTrek Diagnostics System/USA | \nHinged plastic case containing two opposing agar media | \nNot specified | \nIncubator | \nSemi-quantification of bacterial growth, evaluation of the species present | \nMicrobial culture | \n\n | \n | \n | \n | \n | \n |
MBS UTI CHECK | \nMBS srl/Italy | \nMono-use disposable vials for chromogenic analysis | \n3–5 hours | \nMBS Multireader | \nSemi-quantification of bacterial load, assessment of sensitivity to selected antibiotics | \nMeasure of the catalytic activity of redox enzymes of bacteria | \nN = 223 (emergency department) | \n≥105 CFU/ml (single organism + mixed culture) | \n99% | \n92.6% (75.7–99.1) | \n100% (94.9–100) | \n[17] | \n
Features of main POCTs for UTI diagnosis.
To date, hospital settings rely mainly on laboratory analysis following urine culture reference method; this approach requires a considerable effort in terms of workload and up to 3 days to achieve results. Furthermore, it can lead to unnecessary antimicrobial overuse which ultimately promotes the emergence of resistance [31].
\nThe unnecessary use of antibiotic treatment may be minimized following two roads: on one hand by the establishment of antibiotic stewardship programs which require healthcare staff involvement in regular training in best use of antimicrobial agents for an improved adherence to local, national or international guidelines and regular consultation with infectious diseases physicians, with audit [6]; on the other hand by improving diagnostic pathways [1], possibly relying on use of POCTs that feature incorporation of pathogen identification with antimicrobial susceptibility testing, sufficiently versatile to be adaptable for different pathogen profiles in different clinical scenarios [10]. The advent of accurate and robust POCTs could allow a more rational screening before treatment or admission and to improve follow-up of patients for treatment outcome evaluation and for monitoring of antimicrobial prescribing performance and local pathogen resistance profiles [6].
\nSuch approach could ultimately lead to treatment customization according to individual patients’ characteristics through fast antibiotic susceptibility testing results [44], with the ultimate aim of improving patients’ welfare and reduce healthcare costs.
\nProf. Vincenzo Ziparo (Istituto Dermopatico dell’Immacolata – IRCCS, Rome, Italy) is gratefully acknowledged for helpful discussions.
\nAnterior segment ocular trauma is the one of most common ocular condition seen in accident and emergency. The ocular trauma may vary from minor injury such as a corneal abrasion to a grievous sight threatening one such as a corneo-scleral tear or a chemical injury. It has been said to be the most underdiagnosed trauma. In US the prevalence of ocular trauma is 1400 per 100,000US persons with an annual incidence of 8.1 per 100,000. This number is variable depending on the geographic location and more importantly on the occupational safety standards enforced in each country as it is said that 90% of the ocular trauma could have been prevented with protective eyewear.
The most crucial element in the management of ocular injuries is a thorough examination to identify all possible injuries to the eye and institute the appropriate treatment. The initial management plays a very important role in determining the prognosis of the vision, the need for further surgeries and also provide us with realistic goals of visual rehabilitation. In this chapter we aim to enumerate the common modes of ocular injury, manifestations of ocular trauma, the diagnostic features and provide the reader with a comprehensive overview of the treatment instituted. We will also include the accepted international trauma scoring systems and their utility in prognosticating the visual outcome.
Most of the injuries involving the eye, have a bearing on the anterior segment as it is considered to be the most vulnerable part. This is because the structures are usually unable to outlast the impact an injury can have, due to lack of stretchability, presence of highly specialised structures that have poor healing and hence leads to a permanent non-functioning scar tissue [1].
Starting from the anterior-most structure, the possible types of injuries that might be inflicted onto the anterior segment structures are as follows: eyelid edema, eyelid tear, corneal abrasion, focal or total epithelial defects, corneal laceration, corneal perforation, foreign body implantation, scleral tear, iridodialysis, hyphaema/microhyphaema, traumatic iritis, angle recession, traumatic cataract, lens dislocation [2]. Based on the mode of injury they can be broadly classified as mechanical, thermal and chemical injury. There are many classifications of the ocular trauma and the most widely used one is the Birmingham’s eye trauma terminology system (BETTS) which is listed in Figure 1. This was developed by the ocular trauma classification group in 2002 [3]. This classification mainly concentrates on the mechanical injuries. The classification system helps in standardising the terminology used in ocular trauma for prognostic staging as well as for research purposes to quantify the injuries and to study the outcomes of each and every type of insult.
BETTS ocular trauma classification.
The system broadly classifies mechanical injuries into open and closed globe injuries. Open and closed globe injury is further classified based on the type and grade of injury (based on visual acuity at the time of presentation), presence of relative afferent pupillary defect, position of injury (posterior-most part affected in closed globe injury and the location of injury in case of open-globe injury). The definitions of the injuries are as follows.
Kuhn et al. introduced a system of prognosticating the visual outcome based on presenting visual acuity and pupillary reaction and the zones of eye ball involved but it was not commonly used. Further in 2002, a new ocular trauma score (OTS) (Figure 2) was developed to help primary physicians to prognosticate the eye injuries and help them in communicating to the families [5]. Its usefulness has been established in some patients undergoing the three port pars plana vitrectomy for Intra-ocular foreign bodies and it was found that the post operative visual outcome was similar to the OTS prognostication [6]. However there are limitations to the OTS as it does not take into account any other type of injury other than mechanical injury such as thermal and chemical injury nor does it include significant facial and adnexal injuries that might have an impact on the visual outcome.
Table of ocular trauma score.
Addressing these issues Shukla et al. have proposed a new classification system which is a more comprehensive classification and includes injury to adjacent structures and associated injuries such as face and head injuries [7].
Eyelid injuries can occur due to blunt trauma, cutting injuries or road traffic accidents. The most common injuries are eyelid edema and echymoses (Figure 3). These are cosmetically more significant and worrisome for the patients. They usually resolve spontaneously but require a detailed evaluation so as to not overlook any underlying serious pathology to the eye.
A female patient with RTA presented with lid echymosis and edema with abrasions over the eye lid.
The eyelid lacerations can be classified as the following types [4]:
Simple and superficial or deep not involving the lid margin.
Lacerations involving the lid margin
Lacerations involving the canaliculi
Lid lacerations more than 2 mm in linear length require suturing. The contaminated wounds would require debridement of necrotic tissue and suturing. If the wound is infected and necrotic then delayed suturing is planned or else all lid lacerations require primary repair.
Deep laceration involving the superior aspect of upper lid which was subsequently sutured in layers.
Deep laceration involving the lateral aspect of both lids. If these sutures are nor sutured correctly it can lead to a disfiguring scar.
A 56 year old female patient who came with history of blouse hook injury of the lower lid which was sutured using the step-wise approach.
Simple superficial injuries require approximation with interrupted sutures with 6-0 silk or 6-0 plain gut suture. Care must be taken to evert the skin while taking bites and tight sutures should not be applied. They usually do well with minimal scar
Deep lacerations require suturing of different levels (Figure 4). Muscle has to be sutured with 6-0 vicryl and skin with 6-0 silk (Figure 5).
Marginal lid tears repair involves a step-wise approach
The step wise approach can be summarised as follows:
Step 1: The edges of the eyelid margin have to be approximated using 6-0 Silk suture by placing a simple interrupted suture at the grey line. It should be made sure that the sutures are not tied.
Step 2: The tarsal plate has to be identified and partial thickness interrupted sutures using 6-0 absorbable suture will have to be placed to close it. This is the most critical step to maintain the structural integrity of the lid.
Step 3: Place a 6-0 silk suture closer to the lash line and the suture at the grey line can be removed.
Step 4: Suture skin using 6-0 silk with interrupted sutures.
It is very important to suture the marginal lid tears carefully as a well done repair avoids many complications such as trichiasis, ectropion, entropion and cosmetically unacceptable notch. These can be avoided by a meticulous primary repair (Figures 6 and 7).
Eyelid laceration with canalicular tear: These tears require a ministent/Crawford stent/aurostent to be placed during the primary repair to ensure patency of the canaliculus. Once the stent is placed and anchored, skin over it is sutured with interrupted sutures.
A patient with both upper and lower lid laceration involving eyelid margins shows a healed scar with well apposed lid margin.
Conjunctival insults are invariably associated with mechanical trauma to the eye. Conjunctival chemosis and subconjunctival haemorrhage are the most common manifestation of any ocular injury. Conjunctiva can be affected with orbital fractures and even trivial trauma such as finger nail injury.
Presence of a bullous sub conjunctival haemorrhage (Figure 8)
Conjunctival tear along with subconjunctival tear
Associated shallow anterior chamber
Associated hyphaema.
Presence of any of the above associations warrants a detailed examination to rule out underlying scleral tear. A dilated fundus examination has to be done to rule out posterior segment injury.
Bullous subconjunctival haemorrhage which subsequently was attributed to an extensive scleral tear after thorough examination. This patient presented with eye injury following a self-fall at home. Patient underwent primary repair but the visual prognosis was guarded and eventually resulted with phthisis bulbi.
Subconjunctival haemorrhage does not require any treatment. Reassuring the patient is all that is required.
Conjunctival tears can be left unsutured unless they are very large tears or tears extending to the fornix which require suturing with 8-0 absorbable suture such as vicryl.
Being the anterior-most structure of the eye, it bears the brunt of all injuries. The corneal epithelium may have defects, and can range from superficial corneal abrasions to total epithelial defects. As the cornea is highly innervated, abrasions are very painful. It usually takes around 24–48 h for the corneal epithelium to heal [2]. Sometimes it is possible to examine and diagnose the cornea directly under torchlight, however, staining with fluorescein will be required in most cases to diagnose. Any defect will be readily demonstrated by fluorescein staining (Figure 9) [8]. Such defects get healed by “sliding” over of limbal epithelial cells and adhesion of these cells may take up to 6 weeks. Deeper defects will create transformation of keratocytes to myofibroblasts and thus creates scarring of the cornea [9].
A traumatic corneal abrasion as seen after fluorescein staining and observation under the cobalt blue light.
Once an epithelial defect is noted, careful examination has to be done to rule out any foreign body in the superior palpebral conjunctiva and it may be required to do a double eversion of the upper palpebral conjunctiva to examine the fornix and rule out foreign bodies. If no foreign body is detected then the next concern will be to identify is there are any infiltrates along the margin of the epithelial defect. If there are no infiltrates then the eye can be patched with an antibiotic ointment (e.g., chloramphenicol) and lubricating gel and the patient has to be reviewed after 24 h. If there is any discharge or a small defect and patching is not advised and antibiotic eye drops and prophylactic antibiotics are prescribed. The management protocol for corneal abrasion has been shown in Figure 10.
Management of corneal abrasion.
Ocular surface foreign bodies are the second most common type of ocular trauma. The most common aetiology is fall of foreign body into the eye during works such as welding, grinding, hammering or driving without protective eye wear. The patients give a positive history and they usually seek medical help earlier because of the discomfort.
Though the history of fall of foreign body is important but the patients description of the location should not be the guiding point for examination as most often this can be misguiding and foreign bodies may be found elsewhere [10].
When a patient presents with fall of foreign body one needs to a systematic examination to rule out foreign body.
Step 1: Examine the ocular surface for the presence of foreign body (Figure 11)
A superficial corneal foreign body.
Step 2: Retract the lower lid to examine the lower palpebral conjunctiva and evert the upper lid and examine the superior palpebral conjunctiva as the subtarsal sulcus is a common location for lodgement of foreign bodies (Figure 12).
Staining of cornea on eversion of the upper lid was found to have a metallic foreign body in the sub tarsal sulcus.
Step 3: If no foreign body is found then stain the surface with fluorescein dye and examine the ocular surface under cobalt blue filter. This usually reveals any abrasion of the cornea and will likely indicate the position of the foreign body (Figure 13)
Corneal abrasion, evident on fluorescein staining.
Step 4: If no foreign body is found in all the above steps but there is a strong suspicion of foreign body then double eversion of the upper lid has to be done. This is usually rare but some foreign bodies can get lodged there (Figure 14).
Double eversion of the eyelid is done using the Desmarre’s lid retractor to look at the superior fornix.
Once the foreign body (FB) is found it has to be removed as early as possible. The foreign bodies can be superficial or deep. Superficial foreign bodies in adults can be removed under topical anaesthesia under slit lamp. After applying local anaesthetic like proparacaine, the FB can be removed with a cotton tip applicator if it is less than 24 h old. If it is >24 h, it has to be removed with a bevelled 26 G needle. In case of a metallic FB, care should be taken to remove the rust ring completely as the rust ring can cause increased inflammation of the surrounding cornea and leave a scar. If this is in the central cornea it can affect vision.
If it is a deep foreign body, it may be difficult to remove the rust ring completely. These patients have to be called after 24 h and complete removal of the rust ring has to be done.
Deep foreign bodies revealing a full thickness lodgement in the cornea have to be removed only in the operating theatre as these cases may require suturing of the cornea after removal of the foreign body.
In children examination can be very difficult. These patients require examination under anaesthesia and removal.
Blunt or penetrating injuries can lead to traumatic iritis. Usually patients with iritis report late. Following injury, they develop iritis over a few days and may seek help only after few days once the symptoms of pain, watering and photophobia set in. On examination fine keratic precipitates and flare and cells in the anterior chamber will be found and the pupil will be miotic or may show some sphincter tears and mydriasis. IOP may be normal, low or high.
They have to be started on steroids with a careful follow up of IOP to rule out steroid responders. And cycloplegics have to be started.
Once the iritis resolves all these patients have to undergo gonioscopy to rule out angle recession.
Blood in the anterior chamber is called hyphaema. Trauma is the most common cause. Compressive forces can cause damage to the iris, ciliary body, trabecular meshwork and thus disrupt the vasculature and thus cause bleeding. Very rarely it can be because of bleeding dyscrasias. Blunt trauma especially ball injuries, sports injuries and firework injuries can cause hyphaema.
Hyphaema can be graded as follows:
GRADE I: no visible layering of blood but only red blood cells in the anterior chamber (AC) seen only under the slit lamp—called as micro-hyphema
GRADE II: blood that occupies less than one third of the AC
Grade III: blood that occupies one third to half of the AC
Grade IV: blood that occupies the whole AC.
Bright red blood in the AC is called as “total hyphema” and dark red blood in the AC is called as an “8-ball hyphema” or a “blackball” hyphema. It is important to distinguish between the two as the latter suggests longstanding blood in the AC possibly due to pupillary block which could be alarming as it can lead to secondary angle closure [11].
If the grade of hyphema is less than 2 then they can be treated on OPD basis. But a grade 3 and above require inpatient admission as prompt management of complications that can arise will help in saving vision.
Hyphema that are uncomplicated are usually managed conservatively by asking the patients to have limited head movements along with covering the eye with an eye-shield.
It is particularly useful to ask the patients to have head-end elevation at around 30–45° so that the hyphema settles inferiorly. This allows patients by not obstructing the visual axis and also in limiting contact between the red blood cells and the corneal/trabecular meshwork in other areas [12].
Intraocular pressure should be frequently monitored. If found elevated, topical medication should be started (antiglaucoma medication such as B blockers (timolol 0.5%) and alpha agonists like brimonidine tartrate 0.2% thrice daily can be used but best avoided in paediatric age due to the risk of apnea) or carbonic anhydrase inhibitors (dorzolamide 2%) drops can be used. Prostaglandin analogues have to be avoided. Systemic carbonic anhydrase inhibitors are also effective for e.g., acetazolamide and/or methazolamide are some options that can be used in paediatric and adults alike. The former may be given orally or intravenously (IV) at a dose of 5 mg/kg four times a day in children and 250 mg four times in adults. The latter however, is given orally at a dose of 3 mg/kg four times a day in children or 100 mg three times per day in adults.
Topical steroids like prednisolone acetate 1% in tapering dose based on the amount of hyphema to limit inflammation. Started as 8 times a day and tapered according to the response. If the grade of hyphema is 3 or more then oral Prednisolone has to be started at 0.5–1 mg/kg body weight.
Topical cycloplegic agents like homatropine 2% twice daily to relieve pain due to ciliary spasm/photophobia.
Aminocaproic acid and tranexamic acid are two novel lysine analogues that prevent plasmin from attaching to the formed fibrin clot and thereby preventing dissolution of the clot. It also prevents the conversion of plasminogen to plasmin, and thus further reduces clot dissolution. Aminocaproic acid can be administered at a dose of 50 mg/kg orally every 4 h (total cumulative dose not exceeding 30 g/day) and tranexamic acid can be administered at a dose of 25 mg/kg orally three times daily (total dose not exceeding 1.5 g/day).
Immediately following injury there can be traumatic miosis however traumatic mydriasis is more common. Tears of pupillary margins were found to be the most common manifestations. Small sphincteric tears are known to cause notches whereas more severe cuts (like those extending from the margins to the root) cause severe compromise of the function of the iris. This can lead to traumatic mydriasis of the eye.
Apart from tears, other injuries sustained by iris are—iridodialysis which is the separation of the iris root from its attachment at the ciliary body which is visible on gonioscopy.
Lenticular damage that can be inflicted can be either due to lens opacification with or without dislocation. According to Canavan et al. [1], localised anterior cortical lens opacities and posterior cortical lens opacities can be present. These opacities were found to be punctate or also known ‘cobweb’ type and in some instances the typical rosettes can be seen. Vossius ring is the imprint of the pupillary margin against the anterior capsule during the time of injury and this gives an indication of the severity of the injury. Focal lens opacities due to posterior synechiae and acute ocular hypertension (glaucomflecken) are also reported following trauma.
Cataract can be seen as anterior or posterior cortical opacities. The cataract can be due to increase in permeability of the capsule or due to tear in the anterior capsule. If the anterior capsule is not torn then the cataract can be removed in a second surgery once the inflammation reduces and the corneal curvature stabilises as the Intra ocular lens calculation will be more accurate. But however, if the anterior capsule is breached then the cataract extraction has to be done as a primary procedure.
Corneal tears: Corneal tears can be infected or non-infected. Non infected wound requires a different management. First, we will look into management of clean corneal lacerations.
Any sclero-corneal tear warrants to rule out any other injuries which could be life threatening. Only once this is confirmed and other injuries ruled out the corneoscleral tear is managed.
The corneal tear has to be examined to rule out presence of incarcerated intraocular tissue or a intra-ocular foreign body. Most of the times it may not be possible to do a complete examination in the OPD or emergency and a complete examination is possible only during the surgery. Hence the history of the mode of injury is very critical to anticipate what needs to be kept ready during surgery. If an intra-ocular FB is suspected one needs to have the vitrectomy machine ready and possibly a posterior segment surgeon has to be informed. If a break in the anterior capsule is seen then cataract surgery instruments have to be ready and the OT staff have to be informed about these as it is important to have all the instruments ready and a complete surgery is possible only if these are anticipated and the primary surgery has to be performed with utmost precision as this will have an impact on future surgeries.
Timing of the surgery: The cornea-scleral tears have to be repaired as early as possible but however it has been shown that within 36 h of injury the occurrence of endophthalmitis does not significantly increase.
The management protocol has been shown in Figure 15.
Schematic diagram showing management of corneal tear.
The goals of repair are:\t\t
Watertight wound
Prevent infection
Minimise scarring and astigmatism
Lamellar tears: Undisplaced lamellar tears (Figure 16) in the cornea can be treated with a bandage contact lens and antibiotics. These also have to be seen after 24 h and confirmed that there is no increase in the displacement or any infiltrates have to be ruled out and the same treatment can be continued.
An undisplaced lamellar tcornea tear with mucus accumulation.
A child with a pencil injury presented with undisplaced lamellar corneal tear which was sutured.
Small tears <2 mm but Seidel’s test positive can be treated with glue and bandage contact lens. But this should not be tried in patients who cannot be followed up regularly and in children (Figure 17).
Small self-sealed tears <2 mm with a well formed anterior chamber and negative Seidel’s test can be left untreated and prescribed antibiotic drops for 1 week. These patients have to be seen the next day and Seidel’s test has to be treated and if there is no further change they can be left untreated.
However in children and non-compliant patients or patients who are not able to come for regular follow up it is better to suture these wounds too.
Large tears (>2 mm) with or without iris prolapse needs to be repaired as early as possible. Once any life threatening injuries are ruled out patient can be taken up for surgery.
Anaesthesia: The anaesthesia depends on the surgeon’s and patient’s preference. In a cooperative patient and a simple corneal tear without any iris prolapse suturing can be done under topical anaesthesia. In a large corneoscleral where exploration is required then general anaesthesia is preferred. But if general anaesthesia cannot be given due to systemic reasons then suturing can be done under local anaesthesia. But care must be taken that the patient does not squeeze his eyes during local anaesthesia injection. To prevent inadvertent pressure on the globe facial block can be given to paralyse the orbicularis muscle followed by peribulbar which can be given in instalments of 2–3 ml initially followed by a few corneoscleral sutures and repeat infiltration can be done as per the need.
Surgical procedure:
The corneal tear has to be inspected and cleaned and any foreign particle have to be removed.
If iris tissue is prolapsed into the wound it has to be pulled down. It is better to pull down than push the iris tissue from the wound as the iris tends to prolapse into the wound if it is pushed through the wound. A side port incision has to be made adjacent to the wound and the iris tissue has to be swept away from the wound. Viscoelastic can be used to keep the iris away from the wound. Excessive viscoelastic may result in iris prolapse hence one has to be judicious in its use. (Figure 18)
Once the wound is cleared of all the foreign bodies and iris pigments it is important to identify the lamellar and perpendicular tears in the wound. The perpendicular/straight cuts have to sutured first as they are the leaky parts. 10-0 or 9-0 nylon suture is preferred with a 3-1-1 tie or a 2-1-1 tie respectively. Once the straight cuts are sutured the lamellar cuts fall in place and the wound remains well apposed and it becomes easy to suture.
The landmarks such as limbus, and pigment lines or apices of the tear have to be aligned and sutured first.
One should make sure that adequate number of sutures are placed to ensure a watertight seal. One should not be too enthusiastic in applying sutures as these sutures are potential source of scar and astigmatism on the cornea and only as many as necessary have to be applied. (Figures 19–22)
It is very important to bury the knots at the end of the surgery as an unburied knot can cause irritation and can be a source of mucus accumulation and infection of the wound.
If the lens capsule is breached one should not attempt to extract it out from the corneal wound. The corneal tear has to be sutured and the cataract removal has to be performed from a limbal wound. Placement of IOL is arguable as the correct calculation of IOL power is impossible. It is better to place IOL as a secondary procedure.
In case of stellate tears there are many procedures described such as Eisen’s method and Atkins method but however if one is not able use these methods, a simple cross stitch across the stellate tears would be sufficient.
In case of tissue loss sometimes a patch graft might be required to form the anterior chamber. If suturing is not possible then one may have to use a combination of suturing and glue but tight pulling of the tissue which causes distortion of the anterior chamber and angle architecture is not advisable.
The injection of intravitreal antibiotics is also arguable. If the posterior capsule is not breached in the primary injury, it is advisable not to inject any intravitreal antibiotics but if there is a PC rupture of there is evidence of endophthalmitis then intravitreal antibiotics can be injected during the primary procedure.
Iris prolapse and its subsequent repositioning.
A small corneal tear involving the superior half of the pupil requires only two sutures.
An inferior corneal tear sutured.
A corneal tear repair 1 year follow-up had best corrected visual acuity of 6/9.
An 18 year old boy who underwent corneal tear repair and cataract removal and IOL implantation in the primary procedure presented with BCVA of 6/12 at 12 months follow up.
Topical antibiotics and cycloplegic agents along with systemic antibiotics.
Topical steroids: Each case has to be assessed and if there is no evidence of infection on post operative day one, then topical steroids can be started and prescribed for a month in a tapering dose.
The corneal sutures are removed after 6–8 weeks and visual rehabilitation attempted. In paediatric cases the sutures have to be removed much earlier due to faster healing and earlier initiation of visual rehabilitation has to be done.
Considered as one of the true ocular emergencies which requires timely assessment, diagnosis and initiation of treatment.
Aetiologies for chemical burns includes: exposure occurring at home or at work place, during incidents with intent of malice such as criminal assaults.
Nature of chemical could be either acidic or alkali—of which, the latter occurs more commonly [13]. Injuries of such nature are known to produce substantial damage to the anterior segment structures like the ocular surface involving the corneal epithelium and limbal stem cells subsequently leading to a permanent visual impairment in one or both eyes depending on the exposure.
The main goal of management is to protect the cornea and to reconstruct the ocular surface to near-normal.
Alkalis are known to cause extensive damage as they are lipophilic in nature and thus penetrate the cell membrane easily and cause saponification of fatty acids and thus damages the proteoglycans and collagen bundles present in the cornea. Due to further release of proteolytic enzymes, there occurs a progression of the tissue damage. Therefore, alkalis are considered to be more corrosive.
Unlike alkalis, acids act by denaturation and precipitation of proteins of the cornea. This acts by forming a barrier on the corneal surface and thus further damage is intercepted. However, hydrofluoric acid is an exception wherein the fluoride ion has the ability to penetrate the cornea and thereby cause significant anterior segment destruction [14].
The severity of the injury depends on the toxicity of the chemical, period for which the chemical was in contact with the eye, penetration depth, and the areas that are involved. It is crucial therefore to take proper history. If possible, details of the chemical can be checked if patient presents with the packaging-details like composition can be recorded. Nonetheless, all of this should not preclude immediate care to the patient which includes irrigation and removal of any visible retained particulate matter.
After administering required first aid as mentioned above, cursory examination should be done and the depth and severity of injury should be assessed. One should specifically look for conjunctival, corneal and limbal status and the prognosis should be graded accordingly. One of the main goals of stratifying the injuries is to grade the prognosis and to thus choose the most appropriate treatment strategy.
The most commonly used standardised classification is that of Ballen modified by Roper-Hall which has IV grades [15, 16]. Dua later suggested the use of an ‘analogue scale’ which describes the injury in terms of clock-hours of conjunctival and limbal involvement [17]. He also suggested that this scale be used on a daily basis to assess improvement. It becomes important to assess conjunctival status more than limbus involvement because even if the limbus is entirely sabotaged and if sufficient area of conjunctiva remains, it will still be able to re-epithelialize the entire corneal surface and thus prevent perforation of the stroma and can be used as an anchor for limbal stem cell transplantation (LSCT) at a later date if required (Figure 23) [18].
Analogue scale for classification of ocular surface burns. Adapted from [
As a dictum, prevention of exposure to chemicals should always be a priority. If occupational exposure is anticipated, adequate protective measures should be practiced, like wearing protective goggles and shield.
Patients usually present to the Emergency Department the first time with severe pain, excessive watering, spasm of the eyelids and reduced visual acuity.
Before attempting a complete ophthalmic examination, a pH check is mandatory after which thorough irrigation of the eyes should be performed to bring the pH to a physiologic range around 7.11 ± 1.5 [19]. Copious and prolonged irrigation may be performed with sterile water, Ringer’s lactate, balanced salt solution or any fluid with near neutral pH (for example diphoterine in alkali burns has been recommended) [18]. The amount of fluid required for irrigation is decided by the attainment of near-neutral pH. Irrigation of up to 1–2 l is usually done but sometimes, 20 l or more may be required to combat extremes of pH and to bring it to normal [20]. It is prudent to recheck pH after waiting for at least 5 min after irrigation. One should also be aware of various topical medications—such as topical anaesthesia, mydriatics, antibiotics if administered and its bearing on the pH. For instance tropicamide and cyclopentolate hydrochloride 1.0% are often used for cycloplegia as topical ophthalmic solutions and may have a pH of around 4.5 and 4.0–5.8 respectively. Similarly, proparacaine hydrochloride has a pH of approximately 3.5–6.0 is often instilled as topical anaesthetic drops prior to irrigation to remove any visible foreign body. Certain formulations of antibiotic eye drops also contain HCl to adjust pH like for example, ofloxacin drops is unbuffered and formulated with a pH of 6.4–6.8. More importantly, fluorescein dyes that are sometimes used to assess corneal damage after the initial irrigation is basic in nature and may alter the pH status. Therefore, due to the non-neutral pH of these solutions, the reassessed pH value of the eye might not reflect the true pH [18].
Injuries of Dua’s Grades I and II will receive a topical treatment consisting of non-preserved tear substitutes that help in re-epithelialisation and also help with the tear film stability, cycloplegic agents like tropicamide or atropine 1% under a topical antibiotic cover, that will help relieve pain and minimise the occurrence of synechiae. It should be kept in mind that the usage of vasoconstrictive agents like phenylephrine should be avoided at all costs to mitigate the risk of limbal ischaemia.
Injuries of grade III through VI should be admitted and along with the abovementioned treatment, patients should receive analgesics (due to excessive pain caused due to corneal nerve inflammation).
Topical steroids (prednisolone acetate 1% or loteprednol etabonate 0.5%) is indicated every hour. They act by stabilising the lysosomal and the cellular membranes of neutrophils and thus prevents secondary destruction of tissues around. However, they also slow down epithelialization after a week, therefore it should be used only in the acute phase and should be discontinued thereafter and be reincorporated after 5–6 weeks to minimise chronic ocular surface inflammation [21].
In patients with excruciating pain, Amniotic Membrane Transplantation (AMT) can be attempted [21, 22]. As Amniotic Membrane (AM) is rich in transforming growth factor β1 and β2 (TGF β), hepatocyte growth factor (HGF) and epithelial growth factor (EGF) and helps in hindering fibrosis formation and promotes epithelialization. For maximum utilisation of these epitheliotropic properties, AM should be used as a patch of appropriate size with the epithelial side down covering the defective area and also in touch with the limbus. Another advantage is that AM acts as an anchor for LSCT if needed in future.
Injuries of grades V and VI with necrosis of conjunctiva and limbal ischaemia, the necrotic area of conjunctiva is denuded and the underlying tenon’s is advanced in order to cover the defect and to prevent a scleral perforation. In cases with limbal stem cell defect (LSCD), simple limbal epithelial transplantation (SLET), also called in-vivo expansion and cultivated limbal epithelial transplantation (CLET), also called as ex-vivo expansion, can be performed. In-vivo expansion can be obtained from three sites namely: from the innermost area adjacent to the cornea, middle limbus, and from the area located outermost and adjacent to the conjunctiva. Similarly, ex-vivo expansion is obtained from the oral mucosa [23, 24, 25].
The last resort being possibly keratoplasty and keratoprosthesis can be employed to help restore vision.
Ocular burn injuries are a relatively uncommon presentation in the emergency department (ED). Ocular thermal injuries constitute only 7% of all the ocular trauma. 15% of the facial burns patients have associated ocular burns and usually thermal injuries are not severe and very rarely do they cause vision loss [26].
Ocular thermal inuries have been reported to occur due to vegetable oil, fireworks, electric arc, e-cigarette explosion and flash burns. Chemical injuries are usually associated with thermal injury too [12].
Ocular thermal injuries are usually less severe due to the blinking reflex and Bell’s phenomenon (palpebral oculogyric reflex). Cornea may show some charred epihtleium which requires to be removed with a cotton bud after instillation of paracaine drops. Once the charred tissue is removed usually an underlying stromal edema is seen. Epithelial defect can be assessed with fluorescein staining. The corneal stromal edema usually resolves within a few weeks and the cornea clears.
Topical steroids have to be instilled for the first 7–10 days like in chemical injuries as it is important to control inflammation in the initial period. Lubricating drops have to be prescribed.
Acute management of anterior segment injury requires a detailed examination and a meticulous repair as the primary surgery has a lasting impact on visual rehabilitation. Systematic examination and preparedness to handle all possible injuries and a surgeon trained in handling all anterior segment injuries is of paramount importance to achieve good vision in these trauma patients.
None.
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On September, 29th 2006 he has won a post PhD fellowship from the university of Bologna (from October 2006 to October 2008), at the competitive examination he was ranked first in the industrial engineering area. He extensively served as referee for several international journals. He is author/coauthor of more than 100 research papers. He has been involved in some projects supported by MURST and European Community. 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Clinical Practice, Particular Techniques and Special Issues"},signatures:"Thomas Schockert",authors:[{id:"51993",title:"Dr.",name:"Thomas",middleName:null,surname:"Schockert",slug:"thomas-schockert",fullName:"Thomas Schockert"}]},{id:"43328",title:"New Technology: Femtosecond Laser May be Used for Future Acupuncture Therapy",slug:"new-technology-femtosecond-laser-may-be-used-for-future-acupuncture-therapy",totalDownloads:2108,totalCrossrefCites:0,totalDimensionsCites:1,abstract:null,book:{id:"3304",slug:"acupuncture-in-modern-medicine",title:"Acupuncture in Modern Medicine",fullTitle:"Acupuncture in Modern Medicine"},signatures:"Yutaka Takaoka, Mika Ohta, Aki Sugano, Akihiko Ito and Yoichiroh Hosokawa",authors:[{id:"52084",title:"Associate Prof.",name:"Yutaka",middleName:null,surname:"Takaoka",slug:"yutaka-takaoka",fullName:"Yutaka Takaoka"},{id:"60776",title:"Dr.",name:"Mika",middleName:null,surname:"Ohta",slug:"mika-ohta",fullName:"Mika Ohta"},{id:"60777",title:"Dr.",name:"Aki",middleName:null,surname:"Sugano",slug:"aki-sugano",fullName:"Aki Sugano"},{id:"75298",title:"Prof.",name:"Akihiko",middleName:null,surname:"Ito",slug:"akihiko-ito",fullName:"Akihiko Ito"},{id:"157119",title:"Prof.",name:"Yoichiroh",middleName:null,surname:"Hosokawa",slug:"yoichiroh-hosokawa",fullName:"Yoichiroh Hosokawa"}]},{id:"73786",title:"Some Igbo Indigenous Plants with Anti-COVID-19 Properties",slug:"some-igbo-indigenous-plants-with-anti-covid-19-properties",totalDownloads:654,totalCrossrefCites:3,totalDimensionsCites:3,abstract:"Coronavirus (COVID-19) has shaken the world not minding the strength of the global health system leading to over 824, 000 deaths amidst the search of a cure and total prevention. The Igbo states in Nigeria has the average prevalence of 711 cases of COVID-19 with the highest 1096 (Enugu) and least 207 (Anambra) as at 26th August, 2020. This chapter studied some Igbo indigenous plants in use since the outbreak and presents Bitter kola, Garlic, Giloy, Ginger, Lime, and Turmeric which are having anti-COVID-19 properties. The authors suggest that these plants have the properties that alter the PH on the interface between the virus spike proteins and the human respiratory surfaces causing a brake on the interaction with human ACE-2 and where interaction has taken place, the replication and translation stages are disrupted. The plants thus are potential modifiers of this milieu and inhibitor of the main protease and endoribonuclease via epigenetics and homeostasis. These plants consumption should be encouraged as prophylactic or curative measures pending the discovery of a definitive cure. The chapter recommends that the search for COVID-19 cure should not be limited to conventional medicines, rather should be extended to some indigenous plants in Igbo land.",book:{id:"9445",slug:"alternative-medicine-update",title:"Alternative Medicine",fullTitle:"Alternative Medicine - Update"},signatures:"Obeta M. Uchejeso, Ikeagwulonu R. Chinaza, Ohanube A.K. Goodluck and Jwanse I. Rinpan",authors:[{id:"329113",title:"Dr.",name:"Obeta",middleName:"Mark",surname:"M. Uchejeso",slug:"obeta-m.-uchejeso",fullName:"Obeta M. Uchejeso"},{id:"331227",title:"MSc.",name:"Ohanube",middleName:null,surname:"A.K. Goodluck",slug:"ohanube-a.k.-goodluck",fullName:"Ohanube A.K. Goodluck"},{id:"331228",title:"MSc.",name:"Ikeagwulonu",middleName:null,surname:"R. Chinaza",slug:"ikeagwulonu-r.-chinaza",fullName:"Ikeagwulonu R. Chinaza"},{id:"331230",title:"MSc.",name:"Jwanse",middleName:null,surname:"I. Rinpan",slug:"jwanse-i.-rinpan",fullName:"Jwanse I. Rinpan"}]},{id:"21305",title:"Is Acupuncture Meridians a Novel System for Superoxide Disposition",slug:"is-acupuncture-meridians-a-novel-system-for-superoxide-disposition",totalDownloads:2823,totalCrossrefCites:0,totalDimensionsCites:0,abstract:null,book:{id:"386",slug:"acupuncture-concepts-and-physiology",title:"Acupuncture",fullTitle:"Acupuncture - Concepts and Physiology"},signatures:"Jingke Guo and Pingfan Rao",authors:[{id:"58124",title:"Prof.",name:"Pingfan",middleName:null,surname:"Rao",slug:"pingfan-rao",fullName:"Pingfan Rao"},{id:"61129",title:"Mr",name:"Jingke",middleName:null,surname:"Guo",slug:"jingke-guo",fullName:"Jingke Guo"}]},{id:"73945",title:"Impact of Shodhana on Semecarpus anacardium Nuts",slug:"impact-of-shodhana-on-em-semecarpus-anacardium-em-nuts",totalDownloads:365,totalCrossrefCites:0,totalDimensionsCites:0,abstract:"Semecarpus anacardium is classified in Ayurveda under the category of toxic plants. However, this toxic plant is reported to possess anti-inflammatory activity, anti-arthritic effect, antioxidant activity, antimicrobial activity, anti- carcinogenic activity, hypoglycemic activity, cardioprotective, hepatoprotective, neuroprotective, and hypolipidemic activity etc. All these activities are attributed to its various constituents like phenolic compounds, flavonoids, carbohydrates, alkaloids, steroids, etc. In Ayurveda, a series of pharmaceutical procedures which converts a poisonous drug into a safe and therapeutically effective medicine is termed as Shodhana. Shodhana improves the yield, decreases the phenolic and flavonoid content; and converts toxic urushiol into nontoxic anacardol derivative thereby reducing toxicity of nuts of Semecarpus anacardium. There are reports of alteration in pharmacology and phytochemistry of nuts of Semecarpus anacardium due to Shodhana.",book:{id:"9445",slug:"alternative-medicine-update",title:"Alternative Medicine",fullTitle:"Alternative Medicine - Update"},signatures:"Pratap Kumar Sahu and Prashant Tiwari",authors:[{id:"287499",title:"Dr.",name:"Pratap Kumar",middleName:null,surname:"Sahu",slug:"pratap-kumar-sahu",fullName:"Pratap Kumar Sahu"},{id:"326333",title:"Assistant Prof.",name:"Prashant",middleName:null,surname:"Tiwari",slug:"prashant-tiwari",fullName:"Prashant Tiwari"}]}],onlineFirstChaptersFilter:{topicId:"1127",limit:6,offset:0},onlineFirstChaptersCollection:[],onlineFirstChaptersTotal:0},preDownload:{success:null,errors:{}},subscriptionForm:{success:null,errors:{}},aboutIntechopen:{},privacyPolicy:{},peerReviewing:{},howOpenAccessPublishingWithIntechopenWorks:{},sponsorshipBooks:{sponsorshipBooks:[],offset:8,limit:8,total:0},allSeries:{pteSeriesList:[{id:"14",title:"Artificial Intelligence",numberOfPublishedBooks:8,numberOfPublishedChapters:87,numberOfOpenTopics:6,numberOfUpcomingTopics:0,issn:"2633-1403",doi:"10.5772/intechopen.79920",isOpenForSubmission:!0},{id:"7",title:"Biomedical Engineering",numberOfPublishedBooks:12,numberOfPublishedChapters:98,numberOfOpenTopics:3,numberOfUpcomingTopics:0,issn:"2631-5343",doi:"10.5772/intechopen.71985",isOpenForSubmission:!0}],lsSeriesList:[{id:"11",title:"Biochemistry",numberOfPublishedBooks:27,numberOfPublishedChapters:286,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2632-0983",doi:"10.5772/intechopen.72877",isOpenForSubmission:!0},{id:"25",title:"Environmental Sciences",numberOfPublishedBooks:1,numberOfPublishedChapters:9,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2754-6713",doi:"10.5772/intechopen.100362",isOpenForSubmission:!0},{id:"10",title:"Physiology",numberOfPublishedBooks:11,numberOfPublishedChapters:139,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2631-8261",doi:"10.5772/intechopen.72796",isOpenForSubmission:!0}],hsSeriesList:[{id:"3",title:"Dentistry",numberOfPublishedBooks:8,numberOfPublishedChapters:129,numberOfOpenTopics:0,numberOfUpcomingTopics:2,issn:"2631-6218",doi:"10.5772/intechopen.71199",isOpenForSubmission:!1},{id:"6",title:"Infectious Diseases",numberOfPublishedBooks:13,numberOfPublishedChapters:105,numberOfOpenTopics:3,numberOfUpcomingTopics:1,issn:"2631-6188",doi:"10.5772/intechopen.71852",isOpenForSubmission:!0},{id:"13",title:"Veterinary Medicine and Science",numberOfPublishedBooks:9,numberOfPublishedChapters:101,numberOfOpenTopics:3,numberOfUpcomingTopics:0,issn:"2632-0517",doi:"10.5772/intechopen.73681",isOpenForSubmission:!0}],sshSeriesList:[{id:"22",title:"Business, Management and Economics",numberOfPublishedBooks:1,numberOfPublishedChapters:11,numberOfOpenTopics:2,numberOfUpcomingTopics:1,issn:null,doi:"10.5772/intechopen.100359",isOpenForSubmission:!0},{id:"23",title:"Education and Human Development",numberOfPublishedBooks:0,numberOfPublishedChapters:0,numberOfOpenTopics:2,numberOfUpcomingTopics:0,issn:null,doi:"10.5772/intechopen.100360",isOpenForSubmission:!1},{id:"24",title:"Sustainable Development",numberOfPublishedBooks:0,numberOfPublishedChapters:9,numberOfOpenTopics:4,numberOfUpcomingTopics:1,issn:null,doi:"10.5772/intechopen.100361",isOpenForSubmission:!0}],testimonialsList:[{id:"6",text:"It is great to work with the IntechOpen to produce a worthwhile collection of research that also becomes a great educational resource and guide for future research endeavors.",author:{id:"259298",name:"Edward",surname:"Narayan",institutionString:null,profilePictureURL:"https://mts.intechopen.com/storage/users/259298/images/system/259298.jpeg",slug:"edward-narayan",institution:{id:"3",name:"University of Queensland",country:{id:null,name:"Australia"}}}},{id:"13",text:"The collaboration with and support of the technical staff of IntechOpen is fantastic. 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Radiotherapy and Nuclear Medicine Technology has always been my aspiration and my life. As years passed I accumulated a tremendous amount of skills and knowledge in Radiotherapy and Nuclear Medicine, Conventional Radiology, Radiation Protection, Bioinformatics Technology, PACS, Image processing, clinically and lecturing that will enable me to provide a valuable service to the community as a Researcher and Consultant in this field. 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He has been reviewer for several publications of the Optical Society of America\\'s including Photonics Technology Letters and Applied Optics.\n\nPersonal Interests\nThese include motor cycling in a very relaxed manner and performing martial arts.",institutionString:null,institution:{name:"Charité",country:{name:"Germany"}}},{id:"341622",title:"Ph.D.",name:"Eduardo",middleName:null,surname:"Rojas Alvarez",slug:"eduardo-rojas-alvarez",fullName:"Eduardo Rojas Alvarez",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/341622/images/15892_n.jpg",biography:null,institutionString:null,institution:{name:"University of Cuenca",country:{name:"Ecuador"}}},{id:"215610",title:"Prof.",name:"Muhammad",middleName:null,surname:"Sarfraz",slug:"muhammad-sarfraz",fullName:"Muhammad Sarfraz",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/215610/images/system/215610.jpeg",biography:"Muhammad Sarfraz is a professor in the Department of Information Science, Kuwait University, Kuwait. 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After positions as a lecturer at the University of Port Elizabeth, he accepted a position as Associate Professor at the University of Pretoria, South Africa.\r\n\r\nIn 1992, he motivates the concept of 'television and computer-based education” as means to reach large student numbers with only the best of teaching expertise and publishes an article on the concept in the SA Journal of Higher Education of 1993 (and later in 2003). The University of Pretoria subsequently approved a series of test projects on the concept with outreach to Mamelodi and Eerste Rust in 1993. In 1994, the University established a 'Unit for Telematic Education ' as a support section for multiple faculties at the University of Pretoria. In subsequent years, the concept of 'telematic education” subsequently becomes well established in academic circles in South Africa, grew in popularity, and is adopted by many universities and colleges throughout South Africa as a medium of enhancing education and training, as a method to reaching out to far out communities, and as a means to enhance study from the home environment.\r\n\r\nProfessor Snyman in subsequent years pursued research in semiconductor physics, semiconductor devices, microelectronics, and optoelectronics.\r\n\r\nIn 2000 he joined the TUT as a full professor. Here served for a period as head of the Department of Electronic Engineering. Here he makes contributions to solar energy development, microwave and optoelectronic device development, silicon photonics, as well as contributions to new mobile telecommunication systems and network planning in SA.\r\n\r\nCurrently, he teaches electronics and telecommunications at the TUT to audiences ranging from first-year students to Ph.D. level.\r\n\r\nFor his research in the field of 'Silicon Photonics” since 1990, he has published (as author and co-author) about thirty internationally reviewed articles in scientific journals, contributed to more than forty international conferences, about 25 South African provisional patents (as inventor and co-inventor), 8 PCT international patent applications until now. Of these, two USA patents applications, two European Patents, two Korean patents, and ten SA patents have been granted. A further 4 USA patents, 5 European patents, 3 Korean patents, 3 Chinese patents, and 3 Japanese patents are currently under consideration.\r\n\r\nRecently he has also published an extensive scholarly chapter in an internet open access book on 'Integrating Microphotonic Systems and MOEMS into standard Silicon CMOS Integrated circuitry”.\r\n\r\nFurthermore, Professor Snyman recently steered a new initiative at the TUT by introducing a 'Laboratory for Innovative Electronic Systems ' at the Department of Electrical Engineering. The model of this laboratory or center is to primarily combine outputs as achieved by high-level research with lower-level system development and entrepreneurship in a technical university environment. Students are allocated to projects at different levels with PhDs and Master students allocated to the generation of new knowledge and new technologies, while students at the diploma and Baccalaureus level are allocated to electronic systems development with a direct and a near application for application in industry or the commercial and public sectors in South Africa.\r\n\r\nProfessor Snyman received the WIRSAM Award of 1983 and the WIRSAM Award in 1985 in South Africa for best research papers by a young scientist at two international conferences on electron microscopy in South Africa. He subsequently received the SA Microelectronics Award for the best dissertation emanating from studies executed at a South African university in the field of Physics and Microelectronics in South Africa in 1987. In October of 2011, Professor Snyman received the prestigious Institutional Award for 'Innovator of the Year” for 2010 at the Tshwane University of Technology, South Africa. This award was based on the number of patents recognized and granted by local and international institutions as well as for his contributions concerning innovation at the TUT.",institutionString:null,institution:{name:"University of South Africa",country:{name:"South Africa"}}},{id:"317279",title:"Mr.",name:"Ali",middleName:"Usama",surname:"Syed",slug:"ali-syed",fullName:"Ali Syed",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/317279/images/16024_n.png",biography:"A creative, talented, and innovative young professional who is dedicated, well organized, and capable research fellow with two years of experience in graduate-level research, published in engineering journals and book, with related expertise in Bio-robotics, equally passionate about the aesthetics of the mechanical and electronic system, obtained expertise in the use of MS Office, MATLAB, SolidWorks, LabVIEW, Proteus, Fusion 360, having a grasp on python, C++ and assembly language, possess proven ability in acquiring research grants, previous appointments with social and educational societies with experience in administration, current affiliations with IEEE and Web of Science, a confident presenter at conferences and teacher in classrooms, able to explain complex information to audiences of all levels.",institutionString:null,institution:{name:"Air University",country:{name:"Pakistan"}}},{id:"75526",title:"Ph.D.",name:"Zihni Onur",middleName:null,surname:"Uygun",slug:"zihni-onur-uygun",fullName:"Zihni Onur Uygun",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/75526/images/12_n.jpg",biography:"My undergraduate education and my Master of Science educations at Ege University and at Çanakkale Onsekiz Mart University have given me a firm foundation in Biochemistry, Analytical Chemistry, Biosensors, Bioelectronics, Physical Chemistry and Medicine. After obtaining my degree as a MSc in analytical chemistry, I started working as a research assistant in Ege University Medical Faculty in 2014. In parallel, I enrolled to the MSc program at the Department of Medical Biochemistry at Ege University to gain deeper knowledge on medical and biochemical sciences as well as clinical chemistry in 2014. In my PhD I deeply researched on biosensors and bioelectronics and finished in 2020. Now I have eleven SCI-Expanded Index published papers, 6 international book chapters, referee assignments for different SCIE journals, one international patent pending, several international awards, projects and bursaries. In parallel to my research assistant position at Ege University Medical Faculty, Department of Medical Biochemistry, in April 2016, I also founded a Start-Up Company (Denosens Biotechnology LTD) by the support of The Scientific and Technological Research Council of Turkey. Currently, I am also working as a CEO in Denosens Biotechnology. The main purposes of the company, which carries out R&D as a research center, are to develop new generation biosensors and sensors for both point-of-care diagnostics; such as glucose, lactate, cholesterol and cancer biomarker detections. My specific experimental and instrumental skills are Biochemistry, Biosensor, Analytical Chemistry, Electrochemistry, Mobile phone based point-of-care diagnostic device, POCTs and Patient interface designs, HPLC, Tandem Mass Spectrometry, Spectrophotometry, ELISA.",institutionString:null,institution:{name:"Ege University",country:{name:"Turkey"}}},{id:"246502",title:"Dr.",name:"Jaya T.",middleName:"T",surname:"Varkey",slug:"jaya-t.-varkey",fullName:"Jaya T. Varkey",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/246502/images/11160_n.jpg",biography:"Jaya T. Varkey, PhD, graduated with a degree in Chemistry from Cochin University of Science and Technology, Kerala, India. She obtained a PhD in Chemistry from the School of Chemical Sciences, Mahatma Gandhi University, Kerala, India, and completed a post-doctoral fellowship at the University of Minnesota, USA. She is a research guide at Mahatma Gandhi University and Associate Professor in Chemistry, St. Teresa’s College, Kochi, Kerala, India.\nDr. Varkey received a National Young Scientist award from the Indian Science Congress (1995), a UGC Research award (2016–2018), an Indian National Science Academy (INSA) Visiting Scientist award (2018–2019), and a Best Innovative Faculty award from the All India Association for Christian Higher Education (AIACHE) (2019). She Hashas received the Sr. Mary Cecil prize for best research paper three times. She was also awarded a start-up to develop a tea bag water filter. \nDr. Varkey has published two international books and twenty-seven international journal publications. She is an editorial board member for five international journals.",institutionString:"St. Teresa’s College",institution:null},{id:"250668",title:"Dr.",name:"Ali",middleName:null,surname:"Nabipour Chakoli",slug:"ali-nabipour-chakoli",fullName:"Ali Nabipour Chakoli",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/250668/images/system/250668.jpg",biography:"Academic Qualification:\r\n•\tPhD in Materials Physics and Chemistry, From: Sep. 2006, to: Sep. 2010, School of Materials Science and Engineering, Harbin Institute of Technology, Thesis: Structure and Shape Memory Effect of Functionalized MWCNTs/poly (L-lactide-co-ε-caprolactone) Nanocomposites. Supervisor: Prof. Wei Cai,\r\n•\tM.Sc in Applied Physics, From: 1996, to: 1998, Faculty of Physics & Nuclear Science, Amirkabir Uni. of Technology, Tehran, Iran, Thesis: Determination of Boron in Micro alloy Steels with solid state nuclear track detectors by neutron induced auto radiography, Supervisors: Dr. M. Hosseini Ashrafi and Dr. A. Hosseini.\r\n•\tB.Sc. in Applied Physics, From: 1991, to: 1996, Faculty of Physics & Nuclear Science, Amirkabir Uni. of Technology, Tehran, Iran, Thesis: Design of shielding for Am-Be neutron sources for In Vivo neutron activation analysis, Supervisor: Dr. M. Hosseini Ashrafi.\r\n\r\nResearch Experiences:\r\n1.\tNanomaterials, Carbon Nanotubes, Graphene: Synthesis, Functionalization and Characterization,\r\n2.\tMWCNTs/Polymer Composites: Fabrication and Characterization, \r\n3.\tShape Memory Polymers, Biodegradable Polymers, ORC, Collagen,\r\n4.\tMaterials Analysis and Characterizations: TEM, SEM, XPS, FT-IR, Raman, DSC, DMA, TGA, XRD, GPC, Fluoroscopy, \r\n5.\tInteraction of Radiation with Mater, Nuclear Safety and Security, NDT(RT),\r\n6.\tRadiation Detectors, Calibration (SSDL),\r\n7.\tCompleted IAEA e-learning Courses:\r\nNuclear Security (15 Modules),\r\nNuclear Safety:\r\nTSA 2: Regulatory Protection in Occupational Exposure,\r\nTips & Tricks: Radiation Protection in Radiography,\r\nSafety and Quality in Radiotherapy,\r\nCourse on Sealed Radioactive Sources,\r\nCourse on Fundamentals of Environmental Remediation,\r\nCourse on Planning for Environmental Remediation,\r\nKnowledge Management Orientation Course,\r\nFood Irradiation - Technology, Applications and Good Practices,\r\nEmployment:\r\nFrom 2010 to now: Academic staff, Nuclear Science and Technology Research Institute, Kargar Shomali, Tehran, Iran, P.O. Box: 14395-836.\r\nFrom 1997 to 2006: Expert of Materials Analysis and Characterization. Research Center of Agriculture and Medicine. Rajaeeshahr, Karaj, Iran, P. O. Box: 31585-498.",institutionString:"Atomic Energy Organization of Iran",institution:{name:"Atomic Energy Organization of Iran",country:{name:"Iran"}}},{id:"248279",title:"Dr.",name:"Monika",middleName:"Elzbieta",surname:"Machoy",slug:"monika-machoy",fullName:"Monika Machoy",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/248279/images/system/248279.jpeg",biography:"Monika Elżbieta Machoy, MD, graduated with distinction from the Faculty of Medicine and Dentistry at the Pomeranian Medical University in 2009, defended her PhD thesis with summa cum laude in 2016 and is currently employed as a researcher at the Department of Orthodontics of the Pomeranian Medical University. She expanded her professional knowledge during a one-year scholarship program at the Ernst Moritz Arndt University in Greifswald, Germany and during a three-year internship at the Technical University in Dresden, Germany. She has been a speaker at numerous orthodontic conferences, among others, American Association of Orthodontics, European Orthodontic Symposium and numerous conferences of the Polish Orthodontic Society. She conducts research focusing on the effect of orthodontic treatment on dental and periodontal tissues and the causes of pain in orthodontic patients.",institutionString:"Pomeranian Medical University",institution:{name:"Pomeranian Medical University",country:{name:"Poland"}}},{id:"252743",title:"Prof.",name:"Aswini",middleName:"Kumar",surname:"Kar",slug:"aswini-kar",fullName:"Aswini Kar",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/252743/images/10381_n.jpg",biography:"uploaded in cv",institutionString:null,institution:{name:"KIIT University",country:{name:"India"}}},{id:"204256",title:"Dr.",name:"Anil",middleName:"Kumar",surname:"Kumar Sahu",slug:"anil-kumar-sahu",fullName:"Anil Kumar Sahu",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/204256/images/14201_n.jpg",biography:"I have nearly 11 years of research and teaching experience. I have done my master degree from University Institute of Pharmacy, Pt. Ravi Shankar Shukla University, Raipur, Chhattisgarh India. I have published 16 review and research articles in international and national journals and published 4 chapters in IntechOpen, the world’s leading publisher of Open access books. I have presented many papers at national and international conferences. I have received research award from Indian Drug Manufacturers Association in year 2015. My research interest extends from novel lymphatic drug delivery systems, oral delivery system for herbal bioactive to formulation optimization.",institutionString:null,institution:{name:"Chhattisgarh Swami Vivekanand Technical University",country:{name:"India"}}},{id:"253468",title:"Dr.",name:"Mariusz",middleName:null,surname:"Marzec",slug:"mariusz-marzec",fullName:"Mariusz Marzec",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/253468/images/system/253468.png",biography:"An assistant professor at Department of Biomedical Computer Systems, at Institute of Computer Science, Silesian University in Katowice. Scientific interests: computer analysis and processing of images, biomedical images, databases and programming languages. He is an author and co-author of scientific publications covering analysis and processing of biomedical images and development of database systems.",institutionString:"University of Silesia",institution:null},{id:"212432",title:"Prof.",name:"Hadi",middleName:null,surname:"Mohammadi",slug:"hadi-mohammadi",fullName:"Hadi Mohammadi",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/212432/images/system/212432.jpeg",biography:"Dr. Hadi Mohammadi is a biomedical engineer with hands-on experience in the design and development of many engineering structures and medical devices through various projects that he has been involved in over the past twenty years. Dr. Mohammadi received his BSc. and MSc. degrees in Mechanical Engineering from Sharif University of Technology, Tehran, Iran, and his PhD. degree in Biomedical Engineering (biomaterials) from the University of Western Ontario. He was a postdoctoral trainee for almost four years at University of Calgary and Harvard Medical School. He is an industry innovator having created the technology to produce lifelike synthetic platforms that can be used for the simulation of almost all cardiovascular reconstructive surgeries. He’s been heavily involved in the design and development of cardiovascular devices and technology for the past 10 years. He is currently an Assistant Professor with the University of British Colombia, Canada.",institutionString:"University of British Columbia",institution:{name:"University of British Columbia",country:{name:"Canada"}}},{id:"254463",title:"Prof.",name:"Haisheng",middleName:null,surname:"Yang",slug:"haisheng-yang",fullName:"Haisheng Yang",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/254463/images/system/254463.jpeg",biography:"Haisheng Yang, Ph.D., Professor and Director of the Department of Biomedical Engineering, College of Life Science and Bioengineering, Beijing University of Technology. He received his Ph.D. degree in Mechanics/Biomechanics from Harbin Institute of Technology (jointly with University of California, Berkeley). Afterwards, he worked as a Postdoctoral Research Associate in the Purdue Musculoskeletal Biology and Mechanics Lab at the Department of Basic Medical Sciences, Purdue University, USA. He also conducted research in the Research Centre of Shriners Hospitals for Children-Canada at McGill University, Canada. Dr. Yang has over 10 years research experience in orthopaedic biomechanics and mechanobiology of bone adaptation and regeneration. He earned an award from Beijing Overseas Talents Aggregation program in 2017 and serves as Beijing Distinguished Professor.",institutionString:"Beijing University of Technology",institution:null},{id:"255757",title:"Dr.",name:"Igor",middleName:"Victorovich",surname:"Lakhno",slug:"igor-lakhno",fullName:"Igor Lakhno",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/255757/images/system/255757.jpg",biography:"Lakhno Igor Victorovich was born in 1971 in Kharkiv (Ukraine). \nMD – 1994, Kharkiv National Medical Univesity.\nOb&Gyn; – 1997, master courses in Kharkiv Medical Academy of Postgraduate Education.\nPhD – 1999, Kharkiv National Medical Univesity.\nDSc – 2019, PL Shupik National Academy of Postgraduate Education \nLakhno Igor has been graduated from an international training courses on reproductive medicine and family planning held in Debrecen University (Hungary) in 1997. Since 1998 Lakhno Igor has worked as an associate professor of the department of obstetrics and gynecology of VN Karazin National University and an associate professor of the perinatology, obstetrics and gynecology department of Kharkiv Medical Academy of Postgraduate Education. Since June 2019 he’s a professor of the department of obstetrics and gynecology of VN Karazin National University and a professor of the perinatology, obstetrics and gynecology department of Kharkiv Medical Academy of Postgraduate Education . He’s an author of about 200 printed works and there are 17 of them in Scopus or Web of Science databases. Lakhno Igor is a rewiever of Journal of Obstetrics and Gynaecology (Taylor and Francis), Informatics in Medicine Unlocked (Elsevier), The Journal of Obstetrics and Gynecology Research (Wiley), Endocrine, Metabolic & Immune Disorders-Drug Targets (Bentham Open), The Open Biomedical Engineering Journal (Bentham Open), etc. He’s defended a dissertation for DSc degree \\'Pre-eclampsia: prediction, prevention and treatment”. Lakhno Igor has participated as a speaker in several international conferences and congresses (International Conference on Biological Oscillations April 10th-14th 2016, Lancaster, UK, The 9th conference of the European Study Group on Cardiovascular Oscillations). His main scientific interests: obstetrics, women’s health, fetal medicine, cardiovascular medicine.",institutionString:"V.N. Karazin Kharkiv National University",institution:{name:"Kharkiv Medical Academy of Postgraduate Education",country:{name:"Ukraine"}}},{id:"89721",title:"Dr.",name:"Mehmet",middleName:"Cuneyt",surname:"Ozmen",slug:"mehmet-ozmen",fullName:"Mehmet Ozmen",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/89721/images/7289_n.jpg",biography:null,institutionString:null,institution:{name:"Gazi University",country:{name:"Turkey"}}},{id:"243698",title:"M.D.",name:"Xiaogang",middleName:null,surname:"Wang",slug:"xiaogang-wang",fullName:"Xiaogang Wang",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/243698/images/system/243698.png",biography:"Dr. Xiaogang Wang, a faculty member of Shanxi Eye Hospital specializing in the treatment of cataract and retinal disease and a tutor for postgraduate students of Shanxi Medical University, worked in the COOL Lab as an international visiting scholar under the supervision of Dr. David Huang and Yali Jia from October 2012 through November 2013. Dr. Wang earned an MD from Shanxi Medical University and a Ph.D. from Shanghai Jiao Tong University. Dr. Wang was awarded two research project grants focused on multimodal optical coherence tomography imaging and deep learning in cataract and retinal disease, from the National Natural Science Foundation of China. He has published around 30 peer-reviewed journal papers and four book chapters and co-edited one book.",institutionString:"Shanxi Eye Hospital",institution:{name:"Shanxi Eye Hospital",country:{name:"China"}}},{id:"242893",title:"Ph.D. Student",name:"Joaquim",middleName:null,surname:"De Moura",slug:"joaquim-de-moura",fullName:"Joaquim De Moura",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/242893/images/7133_n.jpg",biography:"Joaquim de Moura received his degree in Computer Engineering in 2014 from the University of A Coruña (Spain). In 2016, he received his M.Sc degree in Computer Engineering from the same university. He is currently pursuing his Ph.D degree in Computer Science in a collaborative project between ophthalmology centers in Galicia and the University of A Coruña. His research interests include computer vision, machine learning algorithms and analysis and medical imaging processing of various kinds.",institutionString:null,institution:{name:"University of A Coruña",country:{name:"Spain"}}},{id:"267434",title:"Dr.",name:"Rohit",middleName:null,surname:"Raja",slug:"rohit-raja",fullName:"Rohit Raja",position:null,profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRZkkQAG/Profile_Picture_2022-05-09T12:55:18.jpg",biography:null,institutionString:null,institution:null},{id:"294334",title:"B.Sc.",name:"Marc",middleName:null,surname:"Bruggeman",slug:"marc-bruggeman",fullName:"Marc Bruggeman",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/294334/images/8242_n.jpg",biography:"Chemical engineer graduate, with a passion for material science and specific interest in polymers - their near infinite applications intrigue me. \n\nI plan to continue my scientific career in the field of polymeric biomaterials as I am fascinated by intelligent, bioactive and biomimetic materials for use in both consumer and medical applications.",institutionString:null,institution:null},{id:"244950",title:"Dr.",name:"Salvatore",middleName:null,surname:"Di Lauro",slug:"salvatore-di-lauro",fullName:"Salvatore Di Lauro",position:null,profilePictureURL:"https://intech-files.s3.amazonaws.com/0030O00002bSF1HQAW/ProfilePicture%202021-12-20%2014%3A54%3A14.482",biography:"Name:\n\tSALVATORE DI LAURO\nAddress:\n\tHospital Clínico Universitario Valladolid\nAvda Ramón y Cajal 3\n47005, Valladolid\nSpain\nPhone number: \nFax\nE-mail:\n\t+34 983420000 ext 292\n+34 983420084\nsadilauro@live.it\nDate and place of Birth:\nID Number\nMedical Licence \nLanguages\t09-05-1985. Villaricca (Italy)\n\nY1281863H\n474707061\nItalian (native language)\nSpanish (read, written, spoken)\nEnglish (read, written, spoken)\nPortuguese (read, spoken)\nFrench (read)\n\t\t\nCurrent position (title and company)\tDate (Year)\nVitreo-Retinal consultant in ophthalmology. Hospital Clinico Universitario Valladolid. Sacyl. National Health System.\nVitreo-Retinal consultant in ophthalmology. Instituto Oftalmologico Recoletas. Red Hospitalaria Recoletas. Private practise.\t2017-today\n\n2019-today\n\t\n\t\nEducation (High school, university and postgraduate training > 3 months)\tDate (Year)\nDegree in Medicine and Surgery. University of Neaples 'Federico II”\nResident in Opthalmology. Hospital Clinico Universitario Valladolid\nMaster in Vitreo-Retina. IOBA. University of Valladolid\nFellow of the European Board of Ophthalmology. Paris\nMaster in Research in Ophthalmology. University of Valladolid\t2003-2009\n2012-2016\n2016-2017\n2016\n2012-2013\n\t\nEmployments (company and positions)\tDate (Year)\nResident in Ophthalmology. Hospital Clinico Universitario Valladolid. Sacyl.\nFellow in Vitreo-Retina. IOBA. University of Valladolid\nVitreo-Retinal consultant in ophthalmology. Hospital Clinico Universitario Valladolid. Sacyl. National Health System.\nVitreo-Retinal consultant in ophthalmology. Instituto Oftalmologico Recoletas. Red Hospitalaria Recoletas. \n\t2012-2016\n2016-2017\n2017-today\n\n2019-Today\n\n\n\t\nClinical Research Experience (tasks and role)\tDate (Year)\nAssociated investigator\n\n' FIS PI20/00740: DESARROLLO DE UNA CALCULADORA DE RIESGO DE\nAPARICION DE RETINOPATIA DIABETICA BASADA EN TECNICAS DE IMAGEN MULTIMODAL EN PACIENTES DIABETICOS TIPO 1. Grant by: Ministerio de Ciencia e Innovacion \n\n' (BIO/VA23/14) Estudio clínico multicéntrico y prospectivo para validar dos\nbiomarcadores ubicados en los genes p53 y MDM2 en la predicción de los resultados funcionales de la cirugía del desprendimiento de retina regmatógeno. Grant by: Gerencia Regional de Salud de la Junta de Castilla y León.\n' Estudio multicéntrico, aleatorizado, con enmascaramiento doble, en 2 grupos\nparalelos y de 52 semanas de duración para comparar la eficacia, seguridad e inmunogenicidad de SOK583A1 respecto a Eylea® en pacientes con degeneración macular neovascular asociada a la edad' (CSOK583A12301; N.EUDRA: 2019-004838-41; FASE III). Grant by Hexal AG\n\n' Estudio de fase III, aleatorizado, doble ciego, con grupos paralelos, multicéntrico para comparar la eficacia y la seguridad de QL1205 frente a Lucentis® en pacientes con degeneración macular neovascular asociada a la edad. (EUDRACT: 2018-004486-13). Grant by Qilu Pharmaceutical Co\n\n' Estudio NEUTON: Ensayo clinico en fase IV para evaluar la eficacia de aflibercept en pacientes Naive con Edema MacUlar secundario a Oclusion de Vena CenTral de la Retina (OVCR) en regimen de tratamientO iNdividualizado Treat and Extend (TAE)”, (2014-000975-21). Grant by Fundacion Retinaplus\n\n' Evaluación de la seguridad y bioactividad de anillos de tensión capsular en conejo. Proyecto Procusens. Grant by AJL, S.A.\n\n'Estudio epidemiológico, prospectivo, multicéntrico y abierto\\npara valorar la frecuencia de la conjuntivitis adenovírica diagnosticada mediante el test AdenoPlus®\\nTest en pacientes enfermos de conjuntivitis aguda”\\n. National, multicenter study. Grant by: NICOX.\n\nEuropean multicentric trial: 'Evaluation of clinical outcomes following the use of Systane Hydration in patients with dry eye”. Study Phase 4. Grant by: Alcon Labs'\n\nVLPs Injection and Activation in a Rabbit Model of Uveal Melanoma. Grant by Aura Bioscience\n\nUpdating and characterization of a rabbit model of uveal melanoma. Grant by Aura Bioscience\n\nEnsayo clínico en fase IV para evaluar las variantes genéticas de la vía del VEGF como biomarcadores de eficacia del tratamiento con aflibercept en pacientes con degeneración macular asociada a la edad (DMAE) neovascular. Estudio BIOIMAGE. IMO-AFLI-2013-01\n\nEstudio In-Eye:Ensayo clínico en fase IV, abierto, aleatorizado, de 2 brazos,\nmulticçentrico y de 12 meses de duración, para evaluar la eficacia y seguridad de un régimen de PRN flexible individualizado de 'esperar y extender' versus un régimen PRN según criterios de estabilización mediante evaluaciones mensuales de inyecciones intravítreas de ranibizumab 0,5 mg en pacientes naive con neovascularización coriodea secunaria a la degeneración macular relacionada con la edad. CP: CRFB002AES03T\n\nTREND: Estudio Fase IIIb multicéntrico, randomizado, de 12 meses de\nseguimiento con evaluador de la agudeza visual enmascarado, para evaluar la eficacia y la seguridad de ranibizumab 0.5mg en un régimen de tratar y extender comparado con un régimen mensual, en pacientes con degeneración macular neovascular asociada a la edad. CP: CRFB002A2411 Código Eudra CT:\n2013-002626-23\n\n\n\nPublications\t\n\n2021\n\n\n\n\n2015\n\n\n\n\n2021\n\n\n\n\n\n2021\n\n\n\n\n2015\n\n\n\n\n2015\n\n\n2014\n\n\n\n\n2015-16\n\n\n\n2015\n\n\n2014\n\n\n2014\n\n\n\n\n2014\n\n\n\n\n\n\n\n2014\n\nJose Carlos Pastor; Jimena Rojas; Salvador Pastor-Idoate; Salvatore Di Lauro; Lucia Gonzalez-Buendia; Santiago Delgado-Tirado. Proliferative vitreoretinopathy: A new concept of disease pathogenesis and practical\nconsequences. Progress in Retinal and Eye Research. 51, pp. 125 - 155. 03/2016. DOI: 10.1016/j.preteyeres.2015.07.005\n\n\nLabrador-Velandia S; Alonso-Alonso ML; Di Lauro S; García-Gutierrez MT; Srivastava GK; Pastor JC; Fernandez-Bueno I. Mesenchymal stem cells provide paracrine neuroprotective resources that delay degeneration of co-cultured organotypic neuroretinal cultures.Experimental Eye Research. 185, 17/05/2019. DOI: 10.1016/j.exer.2019.05.011\n\nSalvatore Di Lauro; Maria Teresa Garcia Gutierrez; Ivan Fernandez Bueno. Quantification of pigment epithelium-derived factor (PEDF) in an ex vivo coculture of retinal pigment epithelium cells and neuroretina.\nJournal of Allbiosolution. 2019. ISSN 2605-3535\n\nSonia Labrador Velandia; Salvatore Di Lauro; Alonso-Alonso ML; Tabera Bartolomé S; Srivastava GK; Pastor JC; Fernandez-Bueno I. Biocompatibility of intravitreal injection of human mesenchymal stem cells in immunocompetent rabbits. Graefe's archive for clinical and experimental ophthalmology. 256 - 1, pp. 125 - 134. 01/2018. DOI: 10.1007/s00417-017-3842-3\n\n\nSalvatore Di Lauro, David Rodriguez-Crespo, Manuel J Gayoso, Maria T Garcia-Gutierrez, J Carlos Pastor, Girish K Srivastava, Ivan Fernandez-Bueno. A novel coculture model of porcine central neuroretina explants and retinal pigment epithelium cells. Molecular Vision. 2016 - 22, pp. 243 - 253. 01/2016.\n\nSalvatore Di Lauro. Classifications for Proliferative Vitreoretinopathy ({PVR}): An Analysis of Their Use in Publications over the Last 15 Years. Journal of Ophthalmology. 2016, pp. 1 - 6. 01/2016. DOI: 10.1155/2016/7807596\n\nSalvatore Di Lauro; Rosa Maria Coco; Rosa Maria Sanabria; Enrique Rodriguez de la Rua; Jose Carlos Pastor. Loss of Visual Acuity after Successful Surgery for Macula-On Rhegmatogenous Retinal Detachment in a Prospective Multicentre Study. Journal of Ophthalmology. 2015:821864, 2015. DOI: 10.1155/2015/821864\n\nIvan Fernandez-Bueno; Salvatore Di Lauro; Ivan Alvarez; Jose Carlos Lopez; Maria Teresa Garcia-Gutierrez; Itziar Fernandez; Eva Larra; Jose Carlos Pastor. Safety and Biocompatibility of a New High-Density Polyethylene-Based\nSpherical Integrated Porous Orbital Implant: An Experimental Study in Rabbits. Journal of Ophthalmology. 2015:904096, 2015. DOI: 10.1155/2015/904096\n\nPastor JC; Pastor-Idoate S; Rodríguez-Hernandez I; Rojas J; Fernandez I; Gonzalez-Buendia L; Di Lauro S; Gonzalez-Sarmiento R. Genetics of PVR and RD. Ophthalmologica. 232 - Suppl 1, pp. 28 - 29. 2014\n\nRodriguez-Crespo D; Di Lauro S; Singh AK; Garcia-Gutierrez MT; Garrosa M; Pastor JC; Fernandez-Bueno I; Srivastava GK. Triple-layered mixed co-culture model of RPE cells with neuroretina for evaluating the neuroprotective effects of adipose-MSCs. Cell Tissue Res. 358 - 3, pp. 705 - 716. 2014.\nDOI: 10.1007/s00441-014-1987-5\n\nCarlo De Werra; Salvatore Condurro; Salvatore Tramontano; Mario Perone; Ivana Donzelli; Salvatore Di Lauro; Massimo Di Giuseppe; Rosa Di Micco; Annalisa Pascariello; Antonio Pastore; Giorgio Diamantis; Giuseppe Galloro. Hydatid disease of the liver: thirty years of surgical experience.Chirurgia italiana. 59 - 5, pp. 611 - 636.\n(Italia): 2007. ISSN 0009-4773\n\nChapters in books\n\t\n' Salvador Pastor Idoate; Salvatore Di Lauro; Jose Carlos Pastor Jimeno. PVR: Pathogenesis, Histopathology and Classification. Proliferative Vitreoretinopathy with Small Gauge Vitrectomy. Springer, 2018. ISBN 978-3-319-78445-8\nDOI: 10.1007/978-3-319-78446-5_2. \n\n' Salvatore Di Lauro; Maria Isabel Lopez Galvez. Quistes vítreos en una mujer joven. Problemas diagnósticos en patología retinocoroidea. Sociedad Española de Retina-Vitreo. 2018.\n\n' Salvatore Di Lauro; Salvador Pastor Idoate; Jose Carlos Pastor Jimeno. iOCT in PVR management. OCT Applications in Opthalmology. pp. 1 - 8. INTECH, 2018. DOI: 10.5772/intechopen.78774.\n\n' Rosa Coco Martin; Salvatore Di Lauro; Salvador Pastor Idoate; Jose Carlos Pastor. amponadores, manipuladores y tinciones en la cirugía del traumatismo ocular.Trauma Ocular. Ponencia de la SEO 2018..\n\n' LOPEZ GALVEZ; DI LAURO; CRESPO. OCT angiografia y complicaciones retinianas de la diabetes. PONENCIA SEO 2021, CAPITULO 20. (España): 2021.\n\n' Múltiples desprendimientos neurosensoriales bilaterales en paciente joven. Enfermedades Degenerativas De Retina Y Coroides. SERV 04/2016. \n' González-Buendía L; Di Lauro S; Pastor-Idoate S; Pastor Jimeno JC. Vitreorretinopatía proliferante (VRP) e inflamación: LA INFLAMACIÓN in «INMUNOMODULADORES Y ANTIINFLAMATORIOS: MÁS ALLÁ DE LOS CORTICOIDES. 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Biochemistry examines macromolecules - proteins, nucleic acids, carbohydrates, and lipids – and their building blocks, structures, functions, and interactions. Much of biochemistry is devoted to enzymes, proteins that catalyze chemical reactions, enzyme structures, mechanisms of action and their roles within cells. Biochemistry also studies small signaling molecules, coenzymes, inhibitors, vitamins, and hormones, which play roles in life processes. Biochemical experimentation, besides coopting classical chemistry methods, e.g., chromatography, adopted new techniques, e.g., X-ray diffraction, electron microscopy, NMR, radioisotopes, and developed sophisticated microbial genetic tools, e.g., auxotroph mutants and their revertants, fermentation, etc. More recently, biochemistry embraced the ‘big data’ omics systems. Initial biochemical studies have been exclusively analytic: dissecting, purifying, and examining individual components of a biological system; in the apt words of Efraim Racker (1913 –1991), “Don’t waste clean thinking on dirty enzymes.” Today, however, biochemistry is becoming more agglomerative and comprehensive, setting out to integrate and describe entirely particular biological systems. The ‘big data’ metabolomics can define the complement of small molecules, e.g., in a soil or biofilm sample; proteomics can distinguish all the comprising proteins, e.g., serum; metagenomics can identify all the genes in a complex environment, e.g., the bovine rumen. This Biochemistry Series will address the current research on biomolecules and the emerging trends with great promise.",coverUrl:"https://cdn.intechopen.com/series/covers/11.jpg",latestPublicationDate:"May 15th, 2022",hasOnlineFirst:!0,numberOfOpenTopics:4,numberOfPublishedChapters:286,numberOfPublishedBooks:27,editor:{id:"31610",title:"Dr.",name:"Miroslav",middleName:null,surname:"Blumenberg",fullName:"Miroslav Blumenberg",profilePictureURL:"https://mts.intechopen.com/storage/users/31610/images/system/31610.jpg",biography:"Miroslav Blumenberg, Ph.D., was born in Subotica and received his BSc in Belgrade, Yugoslavia. He completed his Ph.D. at MIT in Organic Chemistry; he followed up his Ph.D. with two postdoctoral study periods at Stanford University. Since 1983, he has been a faculty member of the RO Perelman Department of Dermatology, NYU School of Medicine, where he is codirector of a training grant in cutaneous biology. Dr. Blumenberg’s research is focused on the epidermis, expression of keratin genes, transcription profiling, keratinocyte differentiation, inflammatory diseases and cancers, and most recently the effects of the microbiome on the skin. He has published more than 100 peer-reviewed research articles and graduated numerous Ph.D. and postdoctoral students.",institutionString:null,institution:{name:"New York University Langone Medical Center",institutionURL:null,country:{name:"United States of America"}}},subseries:[{id:"14",title:"Cell and Molecular Biology",keywords:"Omics (Transcriptomics; Proteomics; Metabolomics), Molecular Biology, Cell Biology, Signal Transduction and Regulation, Cell Growth and Differentiation, Apoptosis, Necroptosis, Ferroptosis, Autophagy, Cell Cycle, Macromolecules and Complexes, Gene Expression",scope:"The Cell and Molecular Biology topic within the IntechOpen Biochemistry Series aims to rapidly publish contributions on all aspects of cell and molecular biology, including aspects related to biochemical and genetic research (not only in humans but all living beings). We encourage the submission of manuscripts that provide novel and mechanistic insights that report significant advances in the fields. Topics include, but are not limited to: Advanced techniques of cellular and molecular biology (Molecular methodologies, imaging techniques, and bioinformatics); Biological activities at the molecular level; Biological processes of cell functions, cell division, senescence, maintenance, and cell death; Biomolecules interactions; Cancer; Cell biology; Chemical biology; Computational biology; Cytochemistry; Developmental biology; Disease mechanisms and therapeutics; DNA, and RNA metabolism; Gene functions, genetics, and genomics; Genetics; Immunology; Medical microbiology; Molecular biology; Molecular genetics; Molecular processes of cell and organelle dynamics; Neuroscience; Protein biosynthesis, degradation, and functions; Regulation of molecular interactions in a cell; Signalling networks and system biology; Structural biology; Virology and microbiology.",annualVolume:11410,isOpenForSubmission:!0,coverUrl:"https://cdn.intechopen.com/series_topics/covers/14.jpg",editor:{id:"165627",title:"Dr.",name:"Rosa María",middleName:null,surname:"Martínez-Espinosa",fullName:"Rosa María Martínez-Espinosa",profilePictureURL:"https://mts.intechopen.com/storage/users/165627/images/system/165627.jpeg",institutionString:null,institution:{name:"University of Alicante",institutionURL:null,country:{name:"Spain"}}},editorTwo:null,editorThree:null,editorialBoard:[{id:"79367",title:"Dr.",name:"Ana Isabel",middleName:null,surname:"Flores",fullName:"Ana Isabel Flores",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRpIOQA0/Profile_Picture_1632418099564",institutionString:null,institution:{name:"Hospital Universitario 12 De Octubre",institutionURL:null,country:{name:"Spain"}}},{id:"328234",title:"Ph.D.",name:"Christian",middleName:null,surname:"Palavecino",fullName:"Christian Palavecino",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0033Y000030DhEhQAK/Profile_Picture_1628835318625",institutionString:null,institution:{name:"Central University of Chile",institutionURL:null,country:{name:"Chile"}}},{id:"186585",title:"Dr.",name:"Francisco Javier",middleName:null,surname:"Martin-Romero",fullName:"Francisco Javier Martin-Romero",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bSB3HQAW/Profile_Picture_1631258137641",institutionString:null,institution:{name:"University of Extremadura",institutionURL:null,country:{name:"Spain"}}}]},{id:"15",title:"Chemical Biology",keywords:"Phenolic Compounds, Essential Oils, Modification of Biomolecules, Glycobiology, Combinatorial Chemistry, Therapeutic peptides, Enzyme Inhibitors",scope:"Chemical biology spans the fields of chemistry and biology involving the application of biological and chemical molecules and techniques. In recent years, the application of chemistry to biological molecules has gained significant interest in medicinal and pharmacological studies. This topic will be devoted to understanding the interplay between biomolecules and chemical compounds, their structure and function, and their potential applications in related fields. Being a part of the biochemistry discipline, the ideas and concepts that have emerged from Chemical Biology have affected other related areas. This topic will closely deal with all emerging trends in this discipline.",annualVolume:11411,isOpenForSubmission:!0,coverUrl:"https://cdn.intechopen.com/series_topics/covers/15.jpg",editor:{id:"441442",title:"Dr.",name:"Şükrü",middleName:null,surname:"Beydemir",fullName:"Şükrü Beydemir",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0033Y00003GsUoIQAV/Profile_Picture_1634557147521",institutionString:null,institution:{name:"Anadolu University",institutionURL:null,country:{name:"Turkey"}}},editorTwo:{id:"13652",title:"Prof.",name:"Deniz",middleName:null,surname:"Ekinci",fullName:"Deniz Ekinci",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002aYLT1QAO/Profile_Picture_1634557223079",institutionString:null,institution:{name:"Ondokuz Mayıs University",institutionURL:null,country:{name:"Turkey"}}},editorThree:null,editorialBoard:[{id:"241413",title:"Dr.",name:"Azhar",middleName:null,surname:"Rasul",fullName:"Azhar Rasul",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRT1oQAG/Profile_Picture_1635251978933",institutionString:null,institution:{name:"Government College University, Faisalabad",institutionURL:null,country:{name:"Pakistan"}}},{id:"178316",title:"Ph.D.",name:"Sergey",middleName:null,surname:"Sedykh",fullName:"Sergey Sedykh",profilePictureURL:"https://mts.intechopen.com/storage/users/178316/images/system/178316.jfif",institutionString:null,institution:{name:"Novosibirsk State University",institutionURL:null,country:{name:"Russia"}}}]},{id:"17",title:"Metabolism",keywords:"Biomolecules Metabolism, Energy Metabolism, Metabolic Pathways, Key Metabolic Enzymes, Metabolic Adaptation",scope:"Metabolism is frequently defined in biochemistry textbooks as the overall process that allows living systems to acquire and use the free energy they need for their vital functions or the chemical processes that occur within a living organism to maintain life. Behind these definitions are hidden all the aspects of normal and pathological functioning of all processes that the topic ‘Metabolism’ will cover within the Biochemistry Series. Thus all studies on metabolism will be considered for publication.",annualVolume:11413,isOpenForSubmission:!0,coverUrl:"https://cdn.intechopen.com/series_topics/covers/17.jpg",editor:{id:"138626",title:"Dr.",name:"Yannis",middleName:null,surname:"Karamanos",fullName:"Yannis Karamanos",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002g6Jv2QAE/Profile_Picture_1629356660984",institutionString:null,institution:{name:"Artois University",institutionURL:null,country:{name:"France"}}},editorTwo:null,editorThree:null,editorialBoard:[{id:"243049",title:"Dr.",name:"Anca",middleName:null,surname:"Pantea Stoian",fullName:"Anca Pantea Stoian",profilePictureURL:"https://mts.intechopen.com/storage/users/243049/images/system/243049.jpg",institutionString:null,institution:{name:"Carol Davila University of Medicine and Pharmacy",institutionURL:null,country:{name:"Romania"}}},{id:"203824",title:"Dr.",name:"Attilio",middleName:null,surname:"Rigotti",fullName:"Attilio Rigotti",profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",institutionString:null,institution:{name:"Pontifical Catholic University of Chile",institutionURL:null,country:{name:"Chile"}}},{id:"300470",title:"Dr.",name:"Yanfei (Jacob)",middleName:null,surname:"Qi",fullName:"Yanfei (Jacob) Qi",profilePictureURL:"https://mts.intechopen.com/storage/users/300470/images/system/300470.jpg",institutionString:null,institution:{name:"Centenary Institute of Cancer Medicine and Cell Biology",institutionURL:null,country:{name:"Australia"}}}]},{id:"18",title:"Proteomics",keywords:"Mono- and Two-Dimensional Gel Electrophoresis (1-and 2-DE), Liquid Chromatography (LC), Mass Spectrometry/Tandem Mass Spectrometry (MS; MS/MS), Proteins",scope:"With the recognition that the human genome cannot provide answers to the etiology of a disorder, changes in the proteins expressed by a genome became a focus in research. Thus proteomics, an area of research that detects all protein forms expressed in an organism, including splice isoforms and post-translational modifications, is more suitable than genomics for a comprehensive understanding of the biochemical processes that govern life. The most common proteomics applications are currently in the clinical field for the identification, in a variety of biological matrices, of biomarkers for diagnosis and therapeutic intervention of disorders. From the comparison of proteomic profiles of control and disease or different physiological states, which may emerge, changes in protein expression can provide new insights into the roles played by some proteins in human pathologies. Understanding how proteins function and interact with each other is another goal of proteomics that makes this approach even more intriguing. Specialized technology and expertise are required to assess the proteome of any biological sample. Currently, proteomics relies mainly on mass spectrometry (MS) combined with electrophoretic (1 or 2-DE-MS) and/or chromatographic techniques (LC-MS/MS). MS is an excellent tool that has gained popularity in proteomics because of its ability to gather a complex body of information such as cataloging protein expression, identifying protein modification sites, and defining protein interactions. The Proteomics topic aims to attract contributions on all aspects of MS-based proteomics that, by pushing the boundaries of MS capabilities, may address biological problems that have not been resolved yet.",annualVolume:11414,isOpenForSubmission:!0,coverUrl:"https://cdn.intechopen.com/series_topics/covers/18.jpg",editor:{id:"200689",title:"Prof.",name:"Paolo",middleName:null,surname:"Iadarola",fullName:"Paolo Iadarola",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bSCl8QAG/Profile_Picture_1623568118342",institutionString:null,institution:{name:"University of Pavia",institutionURL:null,country:{name:"Italy"}}},editorTwo:{id:"201414",title:"Dr.",name:"Simona",middleName:null,surname:"Viglio",fullName:"Simona Viglio",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRKDHQA4/Profile_Picture_1630402531487",institutionString:null,institution:{name:"University of Pavia",institutionURL:null,country:{name:"Italy"}}},editorThree:null,editorialBoard:[{id:"72288",title:"Dr.",name:"Arli Aditya",middleName:null,surname:"Parikesit",fullName:"Arli Aditya Parikesit",profilePictureURL:"https://mts.intechopen.com/storage/users/72288/images/system/72288.jpg",institutionString:null,institution:{name:"Indonesia International Institute for Life Sciences",institutionURL:null,country:{name:"Indonesia"}}},{id:"40928",title:"Dr.",name:"Cesar",middleName:null,surname:"Lopez-Camarillo",fullName:"Cesar Lopez-Camarillo",profilePictureURL:"https://mts.intechopen.com/storage/users/40928/images/3884_n.png",institutionString:null,institution:{name:"Universidad Autónoma de la Ciudad de México",institutionURL:null,country:{name:"Mexico"}}},{id:"81926",title:"Dr.",name:"Shymaa",middleName:null,surname:"Enany",fullName:"Shymaa Enany",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRqB9QAK/Profile_Picture_1626163237970",institutionString:null,institution:{name:"Suez Canal University",institutionURL:null,country:{name:"Egypt"}}}]}]}},libraryRecommendation:{success:null,errors:{},institutions:[]},route:{name:"onlineFirst.detail",path:"/online-first/80389",hash:"",query:{},params:{id:"80389"},fullPath:"/online-first/80389",meta:{},from:{name:null,path:"/",hash:"",query:{},params:{},fullPath:"/",meta:{}}}},function(){var e;(e=document.currentScript||document.scripts[document.scripts.length-1]).parentNode.removeChild(e)}()