Key points in diagnosing cesarean scar pregnancy.
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These books synthesize perspectives of renowned scientists from the world’s most prestigious institutions - from Fukushima Renewable Energy Institute in Japan to Stanford University in the United States, including Columbia University (US), University of Sidney (AU), University of Miami (USA), Cardiff University (UK), and many others.
\\n\\nThis collaboration embodied the true essence of Open Access by simplifying the approach to OA publishing for Academic editors and authors who contributed their research and allowed the new research to be made available free and open to anyone anywhere in the world.
\\n\\nTo celebrate the 50 books published, we have gathered them at one location - just one click away, so that you can easily browse the subjects of your interest, download the content directly, share it or read online.
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IntechOpen and Knowledge Unlatched formed a partnership to support researchers working in engineering sciences by enabling an easier approach to publishing Open Access content. Using the Knowledge Unlatched crowdfunding model to raise the publishing costs through libraries around the world, Open Access Publishing Fee (OAPF) was not required from the authors.
\n\nInitially, the partnership supported engineering research, but it soon grew to include physical and life sciences, attracting more researchers to the advantages of Open Access publishing.
\n\n\n\nThese books synthesize perspectives of renowned scientists from the world’s most prestigious institutions - from Fukushima Renewable Energy Institute in Japan to Stanford University in the United States, including Columbia University (US), University of Sidney (AU), University of Miami (USA), Cardiff University (UK), and many others.
\n\nThis collaboration embodied the true essence of Open Access by simplifying the approach to OA publishing for Academic editors and authors who contributed their research and allowed the new research to be made available free and open to anyone anywhere in the world.
\n\nTo celebrate the 50 books published, we have gathered them at one location - just one click away, so that you can easily browse the subjects of your interest, download the content directly, share it or read online.
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These are among the most common complaints in medical offices, and knowledge of the major diseases affecting this system is of fundamental importance to the specialist in otolaryngology. In recent years, great advances have been made in otoneurology, which, coupled with increasing knowledge in the field of neurosciences, have substantially modified the approach of the patient with balance complaints. This book studies the most polemic of these vestibular diseases, Ménière’s disease.",isbn:"978-1-78923-940-9",printIsbn:"978-1-78923-939-3",pdfIsbn:"978-1-83880-551-7",doi:"10.5772/intechopen.77710",price:119,priceEur:129,priceUsd:155,slug:"meniere-s-disease",numberOfPages:144,isOpenForSubmission:!1,isInWos:null,isInBkci:!1,hash:"dda64b6335a1f85313b965777842c80a",bookSignature:"Fayez Bahmad Jr.",publishedDate:"May 27th 2020",coverURL:"https://cdn.intechopen.com/books/images_new/7891.jpg",numberOfDownloads:5403,numberOfWosCitations:0,numberOfCrossrefCitations:1,numberOfCrossrefCitationsByBook:0,numberOfDimensionsCitations:1,numberOfDimensionsCitationsByBook:0,hasAltmetrics:1,numberOfTotalCitations:2,isAvailableForWebshopOrdering:!0,dateEndFirstStepPublish:"September 5th 2018",dateEndSecondStepPublish:"October 22nd 2018",dateEndThirdStepPublish:"December 21st 2018",dateEndFourthStepPublish:"March 11th 2019",dateEndFifthStepPublish:"May 10th 2019",currentStepOfPublishingProcess:5,indexedIn:"1,2,3,4,5,6",editedByType:"Edited by",kuFlag:!1,featuredMarkup:null,editors:[{id:"77351",title:"Prof.",name:"Fayez",middleName:null,surname:"Bahmad Jr",slug:"fayez-bahmad-jr",fullName:"Fayez Bahmad Jr",profilePictureURL:"https://mts.intechopen.com/storage/users/77351/images/system/77351.jpg",biography:"Professor Dr. Fayez Bahmad Jr. is Livre-docente Professor, Department of Ophthalmology and Otorhinolaryngology, School of Medicine, University of São Paulo - FMUSP, São Paulo, SP, Brazil; Professor of the Stricto Sensu Graduate Program of the Faculty of Health Sciences of the University of Brasilia - PPG FCS UnB, Brasilia, DF, Brazil; PhD from the Graduate Program of the Faculty of Medical Sciences of the University of Brasilia - PPG FM UnB; Ad Hoc Consultant and Head of the DRI Special Advisory Group (GAE) of the Higher Education Personnel Improvement Coordination - CAPES; Otology Editor, Brazilian Journal of Otorhinolaryngology - BJORL; Founder and Director of the Brasiliense Institute of Otorhinolaryngology - IBORL, Brasilia, DF, Brazil; President Elected of The International Otopathology Society, which is also known as the “Schuknecht Society,” Harvard Medical School, MA, EUA; Editor in Chief of The International Tinnitus Journal and Editor of the Brazilian Journal of Otorhinolaryngology - BJORL. He completed the ENT Residency Program at the University of Brasilia Hospital (Otolaryngology) and received his PhD at the University of Brasilia Medical School under the orientation of Prof. Carlos A. Oliveira, MD, PhD. Professor Oliveira is well known for establishing one of the most successful research groups in Otology in Brazil and South America. Professor Dr. Fayez Bahmad Jr. was awarded the prestigious Schuknecht Prize at The International Otopathology Society Meeting held in Boston in 2003. He was a Fellow in Otology and Neurotology at the Massachusetts Eye and Ear Infirmary and Fellow in Human Genetics at Seidman Laboratory, Department of Genetics, both at Harvard Medical School when he was engaged in projects under the mentorship of Prof. Saumil N. Merchant, MD, PhD, one of the foremost professors and researchers in otology and otopathology in the Harvard Medical School. Has experience in Medicine, focusing on Otorhinolaryngological Surgery, acting on Surgical Otology;",institutionString:"University of Brasilia",position:null,outsideEditionCount:0,totalCites:0,totalAuthoredChapters:"3",totalChapterViews:"0",totalEditedBooks:"3",institution:{name:"University of Brasília",institutionURL:null,country:{name:"Brazil"}}}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,coeditorOne:null,coeditorTwo:null,coeditorThree:null,coeditorFour:null,coeditorFive:null,topics:[{id:"1099",title:"Otology",slug:"otology"}],chapters:[{id:"71735",title:"Introductory Chapter: Ménière’s Disease (MD)",doi:"10.5772/intechopen.91924",slug:"introductory-chapter-m-ni-re-s-disease-md-",totalDownloads:385,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:null,signatures:"Fayez Bahmad Jr",downloadPdfUrl:"/chapter/pdf-download/71735",previewPdfUrl:"/chapter/pdf-preview/71735",authors:[{id:"77351",title:"Prof.",name:"Fayez",surname:"Bahmad Jr",slug:"fayez-bahmad-jr",fullName:"Fayez Bahmad Jr"}],corrections:null},{id:"69409",title:"Menière’s Disease: Etiopathogenesis",doi:"10.5772/intechopen.84698",slug:"meni-re-s-disease-etiopathogenesis",totalDownloads:813,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:"This chapter will discuss idiopathic Menière’s syndrome. That is to say—Menière’s disease. We will start with a brief recall on the History of Menière’s disease beginning with the description of the syndrome by Prosper Menière in 1861, the description of endolymphatic hydrops in temporal bone studies by Hallpike and Cairns in 1938 and by Yamakaua in the same year. Endolymphatic hydrops became a pathologic correlate for Menière’s syndrome. Theories that considered endolymphatic hydrops as the cause of the syndrome will be discussed. More recent studies questioning the old theories and thinking of endolymphatic hydrops as an epiphenomenon in the course of the syndrome rather than the cause of the symptoms will be discussed. Temporal bone studies were the basis of these new theories too. Familial Menière’s disease will be discussed and several families will be described in detail. Because the phenotype of siblings on each family studied was variable and migraine was present in many affected members of these families a spectrum was postulated going from migraine alone to full blown Menière’s disease. Some siblings had what has been described recently as vertiginous migraine and a detailed description of this syndrome will be provided and the differences between this syndrome and Menière’s disease will be made clear. About 20% of Menière’s disease patients have a familial history. Sporadic Meniere’s disease might have a genetic predisposition and other environmental and behavioral factors contribute for the surfacing of the disease (multifactorial etiology). Because migraine is a central phenomenon and the vertiginous episodes and auditory symptoms are peripheral a hypothesis is presented for the pathophysiology of Menière’s disease. Recent research comparing vestibular migraine and Manière’s disease reinforcing the concept of these syndromes representing a continuum process with similar etiology are discussed at the end.",signatures:"Carlos A. Oliveira",downloadPdfUrl:"/chapter/pdf-download/69409",previewPdfUrl:"/chapter/pdf-preview/69409",authors:[{id:"68849",title:"Prof.",name:"Carlos Augusto C. P.",surname:"Oliveira",slug:"carlos-augusto-c.-p.-oliveira",fullName:"Carlos Augusto C. P. Oliveira"}],corrections:null},{id:"69749",title:"Meniere’s Disease: Nonsurgical Treatment",doi:"10.5772/intechopen.85573",slug:"meniere-s-disease-nonsurgical-treatment",totalDownloads:914,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:1,abstract:"Meniere’s disease or syndrome is one of the most common inner ear diseases. Meniere’s disease is characterized by episodic vertigo, sensorineural hearing loss that fluctuates during episodes, tinnitus, and ear fullness. Ideal treatment should stop vertigo attacks, restore hearing, get rid of tinnitus and ear fullness. Treatment options are decided upon the remaining hearing, severity, and intensity of vertigo attacks. Meniere’s disease is progressive on hearing levels of the patient; some of them develop profound hearing loss that also could affect the other ear. In order to plan a treatment scheme for patient, these conditions should be assessed. It has a destructive and progressive nature, so the first step of treatment should contain more conservative treatment options. If symptom control could not be obtained, destructive treatment options should be considered.",signatures:"Yetkin Zeki Yilmaz, Begum Bahar Yilmaz and Aysegul Batioglu-Karaaltın",downloadPdfUrl:"/chapter/pdf-download/69749",previewPdfUrl:"/chapter/pdf-preview/69749",authors:[{id:"214271",title:"M.D.",name:"Yetkin",surname:"Yilmaz",slug:"yetkin-yilmaz",fullName:"Yetkin Yilmaz"},{id:"275608",title:"Dr.",name:"Begüm Bahar",surname:"Yilmaz",slug:"begum-bahar-yilmaz",fullName:"Begüm Bahar Yilmaz"},{id:"275610",title:"Dr.",name:"Aysegul",surname:"Batioglu-Karaaltin",slug:"aysegul-batioglu-karaaltin",fullName:"Aysegul Batioglu-Karaaltin"}],corrections:null},{id:"65883",title:"The Treatment of Meniere’s Disease by the Intratympanic Therapy",doi:"10.5772/intechopen.84752",slug:"the-treatment-of-meniere-s-disease-by-the-intratympanic-therapy",totalDownloads:754,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:"Meniere’s disease represents one of the most frequent vestibulopathy, with prevalence of 46–200 cases per 100,000, without difference between genders and manifests in fourth decade of life. Features include dizziness/vertigo, hearing loss, tinnitus, and ear fullness. Individuals with Meniere’s disease have poor quality of life due to dizziness, regarding physical, functional, and emotional aspects. The therapeutic measures are proposed, depending on the stage of the disease. About 95% of the patients are well controlled with conservative clinical treatment. The remaining 5% have incapacitating symptoms. These patients are candidates for surgical treatments classics, decompression of the endolymphatic sac, vestibular neurectomy, or labyrinthectomy. Intratympanic gentamicin injections emerged as an alternative to surgical treatments, whose risk and benefit ratio has been shown to be much more satisfactory. Aminoglycosides, such as gentamicin have been used since the decade of 1950 for the vestibular chemical ablation in cases of intractable vertigo. The drawback is that gentamicin causes irreversible destruction to cochlear hair cells with hearing loss. The selective vestibulotoxicity in the treatment of Meniere’s disease can be used in the treatment of the vertigo promoting a chemical labyrinthectomy.",signatures:"Maria Stella A. Amaral, Henrique F. Pauna, Ana Claudia M.B. Reis and Miguel A. Hyppolito",downloadPdfUrl:"/chapter/pdf-download/65883",previewPdfUrl:"/chapter/pdf-preview/65883",authors:[{id:"88917",title:"Prof.",name:"Miguel",surname:"Hyppolito",slug:"miguel-hyppolito",fullName:"Miguel Hyppolito"},{id:"247573",title:"Dr.",name:"Henrique Furlan",surname:"Pauna",slug:"henrique-furlan-pauna",fullName:"Henrique Furlan Pauna"},{id:"273744",title:"M.D.",name:"Maria Stella",surname:"Arantes Do Amaral",slug:"maria-stella-arantes-do-amaral",fullName:"Maria Stella Arantes Do Amaral"},{id:"274348",title:"Prof.",name:"Ana Cláudia M.B.",surname:"Reis",slug:"ana-claudia-m.b.-reis",fullName:"Ana Cláudia M.B. Reis"}],corrections:null},{id:"67598",title:"Intratympanic Gentamicin Treatment for Ménière’s Disease",doi:"10.5772/intechopen.86790",slug:"intratympanic-gentamicin-treatment-for-m-ni-re-s-disease",totalDownloads:1158,totalCrossrefCites:1,totalDimensionsCites:1,hasAltmetrics:0,abstract:"Ménière’s disease (MD) is an inner-ear disease mostly characterized by frequent spontaneous vertigo and fluctuating sensorineural hearing loss. The main purpose of treatment for MD is to reduce or control the vertigo while maximizing the preservation of hearing. Among the various treatments, one that is effective for refractory MD, intratympanic gentamicin (ITG), relies on its ototoxic property to effectively control the vertigo symptoms of most patients. ITG treatment has relatively few side effects compared with surgically destructive treatments, but it also carries a nonnegligible risk of sensorineural hearing loss. So far, there is no consensus on the dosage and treatment duration of ITG. Most researchers recommend that intratympanic injection of gentamicin is more suitable for patients with unilateral onset and impaired hearing function, who are younger than 65 years old, as well as with frequent and severe vertigo attacks, and ineffective prior conservative treatment. Before an ITG treatment, patients should be adequately informed about the risk of hearing loss, and in order to reduce the risk of deafness, low drug dose and long intervals between injections are recommended. In short, to administer an ITG injection, multiple factors should be comprehensively considered including patient selection, pharmacological mechanism, drug dose, the interval of administration, complications, indications, and contraindications.",signatures:"Yongchuan Chai and Hongzhe Li",downloadPdfUrl:"/chapter/pdf-download/67598",previewPdfUrl:"/chapter/pdf-preview/67598",authors:[{id:"277753",title:"Dr.",name:"Hongzhe",surname:"Li",slug:"hongzhe-li",fullName:"Hongzhe Li"},{id:"277754",title:"Dr.",name:"Yongchuan",surname:"Chai",slug:"yongchuan-chai",fullName:"Yongchuan Chai"}],corrections:null},{id:"68573",title:"Surgical Procedures for Ménière’s Disease",doi:"10.5772/intechopen.88014",slug:"surgical-procedures-for-m-ni-re-s-disease",totalDownloads:898,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:1,abstract:"The aim of this chapter is to present a literature review on some of the main articles describing different interventions for the treatment in patients with progressive intractable Ménière disease symptoms. Even though each paper presents good results in defending its techniques, there have been few well-designed clinical studies, that is, studies involving control groups or long-term observation, in the efficacy of surgery with respect to vertigo control and hearing preservation. Focusing on presenting the different techniques established in the literature, we discuss the main indications and results obtained regarding the control of vertigo and the audiological outcomes after the procedure. Physicians should offer additional treatment strategies for Meniere’s disease patients with a long history of limiting symptoms or associated hearing loss. The surgical options for such patients should be considered carefully because surgery can damage the ipsilateral ear and the hearing function of the contralateral ear is often suboptimal. Its importance is that alternatives for treatment can only be offered to a patient when doctor knows them.",signatures:"Ricardo Ferreira Bento and Paula Tardim Lopes",downloadPdfUrl:"/chapter/pdf-download/68573",previewPdfUrl:"/chapter/pdf-preview/68573",authors:[{id:"284068",title:"M.D.",name:"Paula",surname:"Lopes",slug:"paula-lopes",fullName:"Paula Lopes"},{id:"284070",title:"Dr.",name:"Ricardo",surname:"Bento",slug:"ricardo-bento",fullName:"Ricardo Bento"}],corrections:null},{id:"69727",title:"Meniere’s Disease: Surgical Treatment",doi:"10.5772/intechopen.85818",slug:"meniere-s-disease-surgical-treatment",totalDownloads:481,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:"When Meniere’s disease’s vertigo attacks are too frequent and medical treatment options fail, surgical treatment options should be considered. Meniere’s disease is progressive, and there is not a known cure, and all treatment options are symptomatic. Also the possibility of bilateral involvement is another well-known characteristic of this condition as well as its effect on hearing. Some of the patients have progressive hearing loss with vertigo attacks. In order to decide a surgical procedure for these patients, clinicians must be aware of the natural course of Meniere’s disease. In order to their effects on vestibular system, there are two types of surgical procedures. Nondestructive surgeries aim to alter the course of disease, and destructive surgeries aim to control symptoms while eliminating all vestibular functions of the effected ear.",signatures:"Yetkin Zeki Yilmaz, Begum Bahar Yilmaz and Mehmet Yilmaz",downloadPdfUrl:"/chapter/pdf-download/69727",previewPdfUrl:"/chapter/pdf-preview/69727",authors:[{id:"214271",title:"M.D.",name:"Yetkin",surname:"Yilmaz",slug:"yetkin-yilmaz",fullName:"Yetkin Yilmaz"},{id:"275608",title:"Dr.",name:"Begüm Bahar",surname:"Yilmaz",slug:"begum-bahar-yilmaz",fullName:"Begüm Bahar Yilmaz"},{id:"118944",title:"Dr.",name:"Mehmet",surname:"Yilmaz",slug:"mehmet-yilmaz",fullName:"Mehmet Yilmaz"}],corrections:null}],productType:{id:"1",title:"Edited Volume",chapterContentType:"chapter",authoredCaption:"Edited by"},subseries:null,tags:null},relatedBooks:[{type:"book",id:"4654",title:"Update On Hearing 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Cesarean scar pregnancy (CSP) and cervical pregnancy are categorized as non-tubal ectopic pregnancy and may cause massive hemorrhage, uterine rupture, and hysterectomy. In CSP and cervical pregnancy cases, it is possible that the location of the gestational sac (GS) may lead to a misdiagnosis of abortion. Another possibility is a failure to detect CSP until massive hemorrhage occurs following curettage. Therefore, diagnosis and treatment strategies in early pregnancy are important. Delay in the diagnosis and management may lead to massive hemorrhage, which is difficult to control. This complication can be treated with life-saving hysterectomy or uterine arterial embolization, which requires massive blood transfusion [1]. Management based on the pathophysiology of the implantation site that has a rich blood supply is essential. Although management methods vary according to the week of gestation, typical strategies include surgical treatment, administration of drugs such as methotrexate (MTX), and combinations of these treatments. In addition, hemostatic procedures vary and include balloon tamponade, transcatheter arterial embolization (TAE), and surgical treatments such as curettage, evacuation, wedge resection, and hystero-resectoscopy, for control and prevention of hemorrhage.
In the field of obstetrics, TAE is known to be highly effective in controlling uterine hemorrhage and hematoma. This procedure reportedly achieves a high hemostasis rate, and thus, the frequency of hysterectomy has sharply decreased [2, 3]. However, complications such as subsequent endometrial hypoplasia, menstruation disorder, infertility, pregnancy loss, placenta accreta, and uterine rupture have been reported, even in cases that have undergone successful hemostasis with TAE using an absorbable embolus [4, 5, 6]. Recently, a minimally invasive hemostatic strategy in obstetrics, which aims to preserve uterine function and enhance the safety of subsequent pregnancies, has been developed [2, 7]. Therefore, we should reconsider uterus-preserving hemostatic strategies for critical hemorrhage and management of non-tubal ectopic pregnancy under these circumstances by using safe and minimally invasive treatment modalities. We herein discuss how to select the optimal hemostatic strategy and its management based on literatures and our experiences of non-tubal ectopic pregnancy.
When the uterus is observed by ultrasonography more than 3 months after cesarean section (by transverse incision in the lower uterine segment), endometrial defect and defect or thinning of the myometrium at the site of the uterine incision are recognized as a triangular echo-free space at a frequency of approximately 50% [8].
Implantation at this site is considered to be the origin of CSP [9]. Delay in the diagnosis and treatment of CSP may cause uterine rupture and massive hemorrhage, resulting in hysterectomy or massive blood transfusion in serious cases. In the case of CSP, the site of villous anchoring is the isthmus of the uterus or the cervical canal where the endometrium and cervical mucosa are thinner than in the uterine body. Therefore, chorionic villi are likely to penetrate into the myometrium, inducing conditions similar to placenta increta and placenta percreta. The clinical picture and course vary according to the site of villous anchoring [1].
It has been reported that the frequency of CSP is 0.04–0.19% among all pregnancies, 0.15% among those with prior cesarean section, and 6.1% among ectopic pregnancies associated with prior cesarean section [10]. Recently, a national cohort study showed that the estimated incidence of CSP was 0.015% in the UK [11]. It is speculated that the incidence of CSP may increase in the future as the rate of cesarean section rises.
Chorionic villi are smaller and penetrate less deeply into the myometrium in the early stages of pregnancy. Therefore, they are considered to be easier to remove, and it is also believed that the uterus is more likely to be preserved, in early pregnancy. After 9 or 10 weeks of gestation, the placenta invades the myometrium more deeply, and there is abundant blood flow into the placental bed, increasing the risk of massive hemorrhage. The risk of uterine rupture and placental invasion into the bladder is also increased. When accurately diagnosing CSP, it is important to observe the boundary area between the uterine body and the cervix in early pregnancy. The decisive factors in making a diagnosis of CSP are the presence of a gestational sac (GS) in that area and villous adhesion to the anterior wall (Table 1) [1, 8, 12, 13, 14]. Transvaginal ultrasonography is useful for identifying the implantation of chorion frondosum in the scar area (Table 2, Figure 1); the reported sensitivity of this modality is 84.6% [14]. The combined use of color Doppler ultrasonography allows clinicians to estimate the viability of gestational tissue [10, 13], providing useful information for selection of the most appropriate treatment method. The descending GS in the event of an inevitable abortion and GS in CSP can be distinguished by the presence/absence of blood flow in the villous area [1]. Magnetic resonance imaging (MRI) is also useful for determining the thickness of the myometrium in the wound site and the depth of villous invasion into the bladder, as well as for identifying nutrient vessels (Figure 2) [1]. When invasion into the bladder is suspected in the middle stages of pregnancy or thereafter, confirmation by cystoscopy is required.
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Key points in diagnosing cesarean scar pregnancy.
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Ultrasonographic findings of cesarean scar pregnancy.
Findings of transvaginal color Doppler ultrasonography (produced with permission from [
Findings of T2-weighted magnetic resonance imaging (produced with permission from [
Although expectant management of CSP with positive fetal heart activity may still be a choice [11, 15], termination of CSP and cervical pregnancy should be offered to these women and families as one of the therapeutic options. The basic policy for the management of CSP and cervical pregnancy is termination of pregnancy and preservation of the uterus, because these are associated with a high burden of maternal and fetal morbidity including complicated miscarriage, early uterine rupture, prevalence of placenta previa accreta spectrum, massive hemorrhage, hysterectomy, maternal and fetal death, etc. The method of treatment should be selected according to the gestational week, presence/absence of fetal heart beats, the blood hCG level, and abundance of the blood supply adjacent to villi or the gestational sac.
Chemotherapeutic drugs such as methotrexate (MTX) are administered systemically or locally, with or without potassium chloride (KCl), to avoid surgical treatment for CSP [16, 17, 18, 19]. However, achieving the desired healing with drug treatment alone can be time-consuming, and hemorrhage or infection may occur concomitantly during the process of treatment. MTX treatment alone as the first-line therapy showed low success rate. In addition, adverse reactions to drugs, such as stomatitis and leucocytopenia, may also occur. Recent reviews and reports support an interventional or a combination of surgical and medical approaches rather than medical approach alone [20, 21, 22, 23, 24]. In a national cohort study, surgical management appears to be associated with a high success rate, low complication rate, and short posttreatment follow-up [11].
If there is a CSP mass protruded toward outside of the uterus (exogenic type) (Figure 3), or a mass attached to defect or thinning (<2 mm) of lower uterine myometrium, the lesion may be removed laparoscopically or by laparotomy and then sutured [25, 26, 27], because these types of CSPs could be complicated with uterine rupture and bleeding early in pregnancy. But evidence-based treatment still remains unclear in these cases.
Protrusion of the cesarean scar pregnancy lesion toward the bladder (produced with permission from [
Curettage or evacuation allows preservation of fertility, can be performed under intravenous or spinal anesthesia, and is minimally invasive [1, 18, 20, 22, 23, 24, 25, 27, 28]. Curettage or evacuation may be performed under ultrasound guide after administration of MTX and/or KCl. In addition, it requires only a short period of hospitalization in successful cases. On the other hand, there is the risk of massive hemorrhage or uterine perforation during surgery as well as complications such as uterine rupture and residual tissue. Additional treatment such as balloon compression hemostasis or TAE may be required to deal with bleeding [27].
It has been reported that massive hemorrhage, difficult to control, occurred after curettage in patients who had a low hCG level but had abundant blood flows in the lesion, prompting caution in the management of such patients [1]. This is because neovascularity may persist even when the hCG level is decreased after villi have been devitalized by chemotherapy or dilation and curettage (D&C).
In patients with massive hemorrhage after D&C or with CSP diagnosed after massive hemorrhage, priority is given to hemostasis. Therefore, CSP is removed by transvaginal resection [26] or laparotomic resection [29], and uterine artery ligation [30], cervical suture [31], or TAE is performed. When deep villous invasion is predicted in view of the gestational week, the fertilized ovum should be removed by abdominal resection and suture in cases with wound rupture or dehiscence or subserous protrusion of the lesion.
Along with recent advancements in laparoscopic techniques, cases undergoing less invasive laparoscopic or hysteroscopic resection of the lesion have been reported [14, 18, 20, 22, 23]. Surgical resection of the lesion and wound repair (wedge resection and repair) is reportedly less likely to require additional treatment and is highly effective for the prevention of recurrence. However, at present, data on the scientific basis of treatment and recurrence of CSP are lacking.
Several case reports and literatures support surgical therapy alone or in combination with MTX and/or mifepristone rather than medical therapy alone for treatment of cervical pregnancy as the same as those of CSP [21, 32, 33, 34, 35]. Uterine artery embolization for treatment and prevention of hemorrhage during curettage or evacuation is also effective to preserve the uterus [36, 37, 38, 39].
To control bleeding during curettage and evacuation, hemostatic techniques such as hemostatic clamps or cervical cerclage to block cervical blood supply and balloon tamponade by Foley catheter or a cervical ripening balloon were reported [40, 41, 42, 43, 44]. Recently, more minimally invasive total hysteroscopic treatment for cervical pregnancy and also conservative treatment, using a cervical ripening double-balloon catheter alone, were reported [44, 45]. These seem to be an effective, safe, and minimally invasive and single promising treatment without any medical and surgical treatment. These individual managements have to be validated on a large patient population.
Massive hemorrhage reportedly occurs in some cases after evacuation of the uterus D&C has on occasion been performed without an accurate diagnosis. In such cases, balloon tamponade, TAE, and surgical treatment are effective management strategies. If balloon tamponade or TAE is successful in controlling hemorrhage, conservative treatment is also a feasible option. If bleeding is under control, there are several possible treatment options for preservation of the uterus. These options have their own advantages and disadvantages, and selection of the most appropriate treatment varies according to the facility and the time of day. Therefore, the treatments should be tailored to individual patients based on the situation and their wishes regarding fertility.
In cases experiencing massive hemorrhage, pressure hemostasis using balloon tamponade should first be performed. If such hemostasis proves to be ineffective, surgical excision or TAE should be selected next. When performing cesarean scar resection, the right and left uterine arteries are to be clamped.
This is a hemostatic technique used for overall uterine hemorrhage in the puerperal period including atonic bleeding, incomplete cervical laceration, crush syndrome, and bleeding from the separation surface of placenta previa. Balloon tamponade is also effective and useful for uterine hemorrhage from CSP and cervical pregnancy (Figure 4) [46]. In an emergency, insertion and placement of the balloon are technically easy and can be performed expeditiously; this technique is simple and minimally invasive. It is also possible to determine within a short period of time whether hemostasis can be achieved by tamponade alone (tamponade test) [47]. Even when switching to TAE is necessary, the radiology department does not need to be consulted, and the amount of bleeding during preparation for TAE can be decreased. This technique is also useful for temporary hemostasis when a patient must be transferred to an advanced medical facility.
Compression hemostasis by balloon tamponade (produced with permission from [
The balloon should be gently pulled to confirm that it would not easily prolapse into the vaginal cavity and that bleeding from the cervical os has been halted. Long gauze should be retained in the vaginal cavity to prevent prolapse of the balloon. A urethral catheter should be placed in the bladder to prevent urinary retention. If there is no massive hemorrhage that would surpass the absorption capacity of the retained gauze, the balloon is to be removed in 24–48 h. The presence of uncontrollable bleeding immediately after the insertion should be deemed a negative result of the tamponade test, and the procedure is then switched to TAE or laparotomic hemostasis without hesitation.
If bleeding is not controllable by the procedures described above, arterial embolization should be performed without hesitation. TAE is advantageous in that it allows embolization of not only the artery in question but also anastomotic branches while confirming the bleeding point. The rates of hemostasis achievement are reportedly in the range of 89–97% [1, 3].
It is known that, in CSP cases, abnormal growth and anastomosis of inflow vessels occur when the shaggy chorion grows not in the uterine body but in the vicinity of the site of entry into the uterine artery; this causes pathological features different from those associated with the uterine blood flow distribution in normal pregnancy. Therefore, unlike the conventional uterine arterial blood flow, vascular anastomoses are not restricted to those derived from the internal iliac artery. Various anastomoses involving the external iliac artery, lumbar artery, inferior mesenteric artery, sacral artery, superior gluteal artery upstream of the internal iliac artery system, and the external iliac artery system are observed.
Rebleeding may occur due to recanalization or insufficient embolization, and it is difficult to control bleeding when there is abundant blood flow from the external iliac artery region. Therefore, attention should be paid to the patient’s general condition after implementation of TAE. In most cases, bleeding can be controlled by TAE. If TAE is ineffective, or if bleeding persists, it is recommended that the aforementioned balloon tamponade be added to the management. Gelatin sponge is usually used as a temporary solid embolic substance lasting for several days to about 2 weeks. In addition, metal coils as permanent solid embolic substances and N-butyl-2-cyanoacrylate as a permanent liquid embolic substance are also available. The incidence rate of adverse reactions is 6–7.8%. Fever is the most frequent untoward effect. Other adverse reactions include endometrial necrosis, adhesion, myometrial necrosis, ovarian insufficiency, bladder necrosis, gluteal muscle necrosis, and pelvic suppuration [1, 3]. Pregnancy after TAE for postpartum hemorrhage may be associated with increased risk of obstetric hemorrhage due to placenta accreta spectrum. Therefore, precautions in perinatal management are required in managing the subsequent pregnancy.
If bleeding is uncontrollable employing the procedures described above, laparotomic hemostasis should be selected as the last resort. Since TAE became available, application of this technique has mostly been limited to cases of uterine rupture in the affected area. Hysterectomy, ligation of the uterine artery, or wedge resection and repair of the lesion in the scar should be performed. Prompt selection of the optimal procedure, taking into consideration the amount of bleeding, size of the lesion, whether the patient desires fertility preservation, etc., is necessary. Patients with indications for these procedures often have concomitant obstetric coagulopathy. Therefore, sufficient supplementation of coagulation factors is also essential prior to surgery [2, 7].
In cases of massive hemorrhage, patients must be kept in good systemic condition, and local hemostasis must be achieved while paying attention to the possible occurrence of coagulopathy under monitoring of fibrinogen levels as point-of-care testing in order to perform early diagnosis and treatment of coagulopathy [7]. When coagulopathy is present, local hemostasis, such as balloon tamponade, surgical sutures, and TAE, is difficult to achieve because of hemorrhagic tendency. In these cases of coagulopathy, the blood fibrinogen level is often <100 mg/dL. Therefore, the treatment of coagulopathy should be performed by combined administration of concentrated coagulation factors (fibrinogen concentrate and cryoprecipitate) and fresh-frozen plasma promptly to obtain a blood fibrinogen level of at least 150–200 mg/dL [7, 48]. If coagulopathy is eliminated, the conventional hemostatic procedures become effective.
Curettage alone is reportedly not a suitable first-choice procedure because using curettage only may lead to serious complications such as massive hemorrhage or uterine rupture, necessitating additional treatment in 76.2% (16/21) of patients [1]. On the other hand, the methotrexate (MTX) monotherapy is time-consuming in terms of achieving cure and may be accompanied by hemorrhage or infection. Reduction of the chorionic tissue by MTX therapy to decrease blood flow, followed by curettage or laparotomy, rather than MTX or curettage alone, achieves a higher cure rate and is associated with fewer complications such as hemorrhage, infection, and sepsis.
For the management of CSP and cervical pregnancy in the first trimester, we first perform ultrasonography to confirm the implantation site of the gestational sac, observe the status and thickness of the myometrium in surrounding areas and the presence/absence of fetal heart beats, and determine the gestational week. At the same time, we measure the blood hCG level and evaluate blood flow around the gestational sac by Doppler ultrasonography. Changes in the blood hCG levels and the status of blood flow are useful for judging the viability of chorionic villi and the efficacy of estimating chemotherapy. If there is abundant blood flow in the myometrium as well as in the tissues surrounding the gestational sac, villous invasion site on the myometrium is suspected. In such cases, implementation of D&C alone is expected to cause massive hemorrhage.
When there are fetal heart beats, potassium chloride (KCl) is administered directly to the fetus to cause cessation of the heart beating. MTX is administered systemically (1 mg/kg body weight) or by local injection to the villous area at the same time. Subsequently, MTX is administered systemically every 7–10 days. In patients with high blood levels of hCG, MTX therapy used to be performed to decrease the hCG level to a target of 20,000 mIU/mL, or even lower, followed by TAE and curettage. The rates of blood transfusion and/or blood loss of >2500 mL in these combined treatment (MTX + TAE + D&C) were significantly decreased, compared with those in D&C alone, 9.5 and 83.3% respectively.
The rate of additional surgical treatment, such as wedge resection or hysterectomy, in combined treatment, was none, compared with D&C alone, 0 and 50.0%, respectively. There were no complications such as uterine rupture, postoperative infections, menstrual abnormalities, and ovarian dysfunction in D&C alone and combined treatment. These combined treatments yielded satisfactory results with a decreased volume of blood loss, no additional surgical treatment, and a high cure rate, compared with D&C alone (Figure 5, Tables 3 and 4).
Treatment results of cesarean scar pregnancy with fetal heart beats under uterus-preserving management. Thirty patients diagnosed with cesarean scar pregnancy with positive fetal heartbeat in the first trimester were treated at Saitama Medical Center and Juntendo University Hospital from 1998 to 2010. The average maternal age was 33.3 ± 5.8 years (mean ± SD), and average gestational age on admission was 6.6 ± 1.5 weeks of gestation. The average hCG level on admission was 29,534 ± 26,284 mIU/mL, and its level on dilation and curettage was 19,995 ± 24,765 mIU/mL. Twenty-one patients were treated under our uterus-preserving management policy and six patients were transferred to our hospital due to uncontrollable hemorrhage after dilation and curettage. This management strategy yielded satisfactory results with a decreased volume of blood loss and a high cure rate.
Characteristic | D&C alone (n:6) | MTX + TAE + D&C (n:21) | |
---|---|---|---|
Age (years) | 34.5 + 3.0 | 34.0 + 5.8 | 0.84 |
(32–39) | (23–42) | ||
Number of previous CS (n) | 1.5 + 0.8 | 1.3 + 0.6 | 0.47 |
(1–3) | (1–3) | ||
Gestational age at diagnosis (weeks) | 7.8 + 2.4 | 6.3 + 1.1 | 0.19 |
(6–12) | (5–8) | ||
Blood hCG levels at diagnosis (mIU/mL) | 17,551.3+ | 37,876.1+ | 0.18 |
20,483.0 | 33,816.3 | ||
Blood hCG levels at D&C (mIU/mL) | 15,360.8+ | 17,840.5+ | 0.78 |
20,344.9 | 19,111.9 |
Comparison of background between cases with dilation and curettage (D&C) alone and those with methotrexate + transcatheter arterial embolization + D&C.
There are no significant differences in characteristics between D&C alone and combined treatment.
D&C alone (n:6) | MTX + TAE + D&C (n:21) | ||
---|---|---|---|
Blood transfusion/>2500 mL blood loss | 83.3% | 9.5% | 0.001 |
(5/6) | (2/21) | ||
Wedge resection/hysterectomy | 50.0% | 0% | 0.007 |
(3/6) | (0/21) | ||
Hospital stay (days) | 15.5 + 10.4 | 9.6 + 8.4 | 0.163 |
Comparison of outcome and additional treatment between D&C alone and methotrexate + transcatheter arterial embolization + dilation and curettage (D&C).
Combined procedures (MTX + TAE + D&C) yielded satisfactory results with a decreased volume of blood loss, no additional surgical treatment, and a high cure rate, compared with D&C alone.
Currently, prophylactic TAE before D&C is avoided whenever possible, with the aim of preventing short-term complications and uterine rupture in the subsequent pregnancy, and also shortening hospital stay. A target blood hCG levels after MTX is also changed to <40,000 mIU/mL for adverse effects of MTX. Then, ultrasound-guided D&C to evacuate the gestational sac is performed a week later after MTX therapy. Bleeding point during D&C could be found by contrast-enhanced ultrasonography, and a cervical ripening miniballoon (Minimetro®) could be inserted at the bleeding point and inflated until bleeding stops [46, 49]. If bleeding continues, TAE or laparoscopic wedge resection would be performed as soon as possible. Nine patients with CSP (6–12 weeks gestation) and one (7 weeks gestation) with cervical pregnancy were treated under new management. Seven cases were successfully treated with D&C and balloon tamponade after MTX. Additional treatments were needed in three cases for bleeding. This combined therapy resulted in all complete cure and no additional surgical therapy without complications.
Moreover, if early detection of CSP is possible, more minimally invasive treatments might be another option of treatment such as double balloon conservative therapy or hysteroscopic resection without MTX therapy. We also experienced one case with CSP to be successfully treated after cessation of fetal heart beats by local injection of KCl. She selected conservative therapy without chemotherapy and surgical therapy and then was just followed up in outpatient clinic. It took 6 months to be cured completely, but there were no complications and no bleeding. Even in cases with placenta previa on cesarean delivery scar, who were managed to leave the placenta in situ for placenta accreta spectrum disorders after cesarean section near term (median 36 weeks gestation; range 28–38 weeks gestation) in order to preserve the uterus without hysterectomy, the conservative therapy was successful in 25 (69.4%) cases without any additional surgery [50]. Placental resorption occurred postpartum (median 89 days; range 6–510 days). Hysterectomy was performed for the other 11 cases, primarily owing to hemorrhage and/or infection. Considering smaller uterine blood supply and amount of gestational tissues in the first trimester than those in near term, conservative management after cessation of fetal heart beats in cesarean scar pregnancy may have higher success rate, if possible, with close postpartum follow-up for at least several months.
The basic policy for the management of non-tubal ectopic pregnancy, such as CSP and cervical pregnancy, is termination of pregnancy and preservation of the uterus, and the method of treatment should be selected according to the gestational week, presence/absence of fetal heart beats, the blood hCG level, and abundance of the blood supply adjacent to villi or the gestational sac. Recent reviews and reports support an interventional or a combination of surgical and medical approaches for treatment of unruptured CSP and cervical pregnancy rather than medical approach alone. In a national cohort study, surgical management appears to be associated with a high success rate, low complication rate, and short posttreatment follow-up.
Massive hemorrhage reportedly occurs in some cases with spontaneous rupture or after evacuation of the uterus without an accurate diagnosis. In cases experiencing massive hemorrhage, pressure hemostasis using balloon tamponade should first be performed. If such hemostasis proves to be ineffective, surgical excision or TAE should be selected next. If balloon tamponade or TAE is successful in controlling hemorrhage, conservative treatment is also a feasible option. In cases with coagulopathy, the blood fibrinogen level is often <100 mg/dL. Therefore, the treatment of coagulopathy should be performed by combined administration of concentrated coagulation factors (fibrinogen concentrate and cryoprecipitate) and fresh-frozen plasma promptly to obtain a blood fibrinogen level of at least 150–200 mg/dL.
Recently, a minimally invasive hemostatic strategy in obstetrics, which aims to preserve uterine function and enhance the safety of subsequent pregnancies, has been developed. Therefore, we should reconsider uterus-preserving hemostatic strategies for critical hemorrhage and management of non-tubal ectopic pregnancy under these circumstances by using safe and minimally invasive treatment modalities. Moreover, if early detection of CSP is possible, more minimally invasive treatment might be another option of treatment such as double balloon conservative therapy or hysteroscopic resection without chemotherapy. Conservative therapy without chemotherapy and surgical therapy may be the other option. They were just followed up closely in outpatient clinic after cessation of fetal heart beats by local injection of KCl.
The optimal treatment of CSP and cervical pregnancy is still unclear at present. Further evaluation of several therapies and hemostatic techniques by treating a large number of patients is necessary.
None.
Breastfeeding is a birthright of every baby, and also it is the right of every mother to breastfeed her baby. Breastfeeding is a complete nutrition for the baby and has several advantages to the baby and the mother. Breastfeeding (colostrum) has so much benefit for the baby especially immunologically that it is called the first vaccine for the baby. Breastfeeding is hypoallergenic and safe to the baby. It is sterile, hygienic and also economical. Breastfeeding is the saviour of the infant from respiratory and diarrhoeal morbidity and mortality especially in the developing and underdeveloped countries. It relieves a lot of economic burden for the poor countries [1]. In low-income and middle-income countries, only 37% of the babies less than 6 months are exclusively breastfed [2]. Breastfeeding helps in brain growth and improves the intelligence quotient (IQ) of the children and thus benefits the country as a whole [3]. Breastfeeding reduces mortality and morbidity of children under 5 years of age especially in developing and underdeveloped countries. Breastfeeding enhances the bond between the mother and the child, provides tender loving care to the child and keeps the mother happy.
\nDuring the last trimester of antenatal care, the mother’s nipples should be checked. In case of flat nipple or retracted nipple, oil massage and manipulation to make the nipples conducive to breastfeeding should be done. The mother should be given healthy diet, green leafy vegetables, fruits, eggs, fish (omega 3 fatty acid) and plenty of fluids. She should take extra 300 cal and 15 g of protein during the antenatal period and extra 500 cal and 25 g of protein during the lactation period [5].
\nBreastfeeding should be initiated as early as possible after delivery preferably within 1 h after normal delivery and 4 h after Caesarean section [5]. The baby is biologically active immediately after delivery after which the baby goes into sleep and there is difficulty in establishment of breastfeeding; hence breastfeeding should be initiated early. Immediately after delivery, he/she should be put on the mother’s abdomen, crawl to the breast and suckle at the breast; this method helps in early initiation of breastfeeding. Early skin-to-skin contact, putting the baby in mother’s abdomen helps in early initiation of breastfeeding [6]. Keeping the baby with the mother in the same room is called ‘rooming in’, keeping him/her in the same bed with his/her mother is called ‘bedding in’ and keeping him/her in his/her mother’s abdomen is called ‘mothering in’ [5].
\nIn the first 2 days, colostrum is secreted which is rich in lymphocytes, IgA and antibodies; the colostrum secreted is 10–40 ml/day which is sufficient for a term baby and does not require any supplementation. No prelacteal feeds should be given because these can cause infection and delay in establishment of breastfeeding. The baby should be well supported while breastfeeding, and the mother may require help in the first few days. Both the mother and the baby should be comfortable while breastfeeding. A healthy baby will empty the breast within 20 min, and alternating the breasts used for each feed is advised. The baby should completely empty the breast on the one side in order to get adequate hindmilk. Foremilk is the initial milk which is rich in vitamins, proteins, sugar, mineral and fluid, while hindmilk contains fat. Hence foremilk only satisfies the thirst, and the baby needs to get adequate hindmilk to get adequate calories and to satisfy hunger. If a baby does not empty the breast each feed, he/she does not get hindmilk and hence does not get nutritional requirement and feels hungry very fast and does not gain adequate weight. Transitional milk is secreted in the first 10 days followed by mature milk. Milk production increases for the first 6 months and then plateaus off. Average milk secreted is 500–800 ml/day [5].
\nThe correct technique should be followed for successful breastfeeding. The mother should touch the angle of the baby’s mouth with the nipple; rooting reflex causes the baby to open the mouth and take in the nipple and the areola into the mouth.
\nCorrect technique of breastfeeding (cradle hold).
Various positions of breastfeeding (taken from
Positions | \nElements positive | \nElements negative | \n
---|---|---|
Cradle hold | \nClassic position | \nHead tends to wobble | \n
Cross cradle hold | \nProvides good head control | \nLeast familiar | \n
Football or clutch hold | \nFor LBW, minimum head control, avoids Caesarean incision | \nTeaching required | \n
Side lying | \nMinimises fatigue | \nChances of smothering | \n
Various positions for breastfeeding.
How to know if breastmilk is sufficient or not? In the first week of life, there will be weight loss; in an exclusively breastfed term baby, about 5–7% of birthweight is lost in the first week especially by 48–72 h of birth [9]. A term baby usually regains birthweight, on average, by 8.3 days of life [9] and starts gaining minimum ½ ounce/day for the first 3 months [10]. Hence after the first week of life, we know that breastmilk is adequate by observing adequate weight gain, five to six times, pale-coloured urine per day and golden yellow colour stools, and then baby should sleep after each feed. Also when the mother is breastfeeding from one breast, if milk drips from the other breast, it is suggestive of adequacy of milk, and the milk that drips from the other breast is called drip milk. Drip milk is low in energy and fat content. If the baby is not gaining adequate weight and urine output is less after the third day of life, it is suggestive of inadequate breastmilk; the baby needs to attend a paediatrician to prevent complications like hypernatraemic dehydration [10]. However it should be remembered that in the first 2 days of life, only colostrum is secreted which is less in amount; hence urine output may be very less so much so that we can wait for 48 h for the first passage of urine. There is no need to give any complementary feeds to the baby in the first 2–3 days when colostrum is less because whatever colostrum is there, it is enough to meet the nutritional needs of a term baby, and a term baby also contains enough stores of glycogen. In case of early discharge from the hospital exclusively, breastfed babies should be seen by a paediatrician on the third to fifth day of life to check the adequacy of breastmilk and establishment of lactation [10].
\n\n
It is a complete nutrition for the baby till 6 months of age. It is easily digestible due to the presence of lipase and whey proteins.
Breastmilk contains anti-infective properties, antibodies, IgA and lactobacilli which protect the baby from diarrhoea, respiratory tract infection, otitis media and necrotizing enterocolitis.
Breastmilk is hypoallergenic and reduces disorders like asthma and eczema in breastfed babies.
Breastfed babies have less risk of developing diabetes mellitus, high blood pressure, obesity, heart attack and certain cancers in adult life [5, 11, 12, 13].
\n
Breastfeeding releases oxytocin which helps in involution of the uterus which leads to less chance of postpartum haemorrhage.
Mothers who breastfeed have lactational amenorrhoea and have less chance of conception during that period. Night feeds especially help in preventing conception during lactational amenorrhea.
Breastfeeding is convenient, economical and readily available at the desired temperature.
Mothers develop a close bond with the baby; they feel relaxed and happy to take care of their baby.
Mothers regain their prepregnancy weight earlier than in those mothers who formula feed their babies because the energy stored during pregnancy is lost during lactation.
Mothers who breastfeed their babies have less chance of developing breast cancer and ovarian cancer [5, 11, 12, 13].
Breastmilk contains arachidonic acid (AHA), docosahexaenoic acid (DHA), high contents of amino acids like cysteine and taurine, choline, iodine, zinc, lactose and oligosaccharides which promotes maturation, myelination and synaptogenesis of the human brain [3].
\nBreastmilk contains less protein and solute load which are suitable for the baby and their immature kidneys. Cow’s milk protein is predominantly casein, whereas breastmilk contains whey protein which is easily digestible. It is mainly lactalbumin and lactoferrin. Casein to whey protein ratio is 40:60 in human milk and 80:20 in cow’s milk. Cow’s milk contains lactoglobulin which is the cause of intolerance to cow’s milk. Lactobacilli and lactic acid are probiotics which help in digestion in human milk. Nonprotein nitrogen in human milk like urea, amino acids, choline, creatinine, uric acid, ammonia and N-acetylglutamine are bioactive factors which are not present in cow’s milk. Breastmilk is rich in long-chain polyunsaturated fatty acid (PUFA) like eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA). Cow’s milk is rich in saturated fats. The polyunsaturated/saturated fat ratio is 1.2:1 in breastmilk compared to 1:2 in cow’s milk. Carbohydrate in breastmilk is lactose which is double in content in breastmilk than in cow’s milk and is suitable for brain growth and for the development of normal GI flora in babies. Vitamins like K and D are deficient in breastmilk. Especially in vitamin D-deficient mothers, breastmilk contains less vitamin D, and hence vitamin D supplementation in normal newborn exclusively breastfed babies is essential. Vitamin K is given to all babies after birth to prevent haemorrhagic disease of newborn. Minerals are less in breastmilk, but bioavailability is better in breastmilk than in cow’s milk. Cow’s milk contains high levels of electrolytes and hence high solute load and is not suitable for immature kidneys of babies [5, 12] (Table 2).
\nNutrition | \nHuman milk | \nCow’s milk | \n
---|---|---|
Calories | \n65 | \n67 | \n
Protein | \n1.1 g | \n3.5 g | \n
Lactose | \n7.4 g | \n4.5 g | \n
Fat | \n3.5 g | \n3.5 g | \n
Calcium | \n35 mg | \n140 mg | \n
Phosphorus | \n15 mg | \n90 mg | \n
Magnesium | \n4 mg | \n12 mg | \n
Electrolytes (meq/L) | \n||
Sodium | \n6.5 | \n25 | \n
Chloride | \n12 | \n29 | \n
Potassium | \n14 | \n35 | \n
Osmolality (mosm/L) | \n290 | \n350 | \n
Vitamins | \n||
Vitamin A (μg) | \n53 | \n34 | \n
Vitamin D (IU) | \n0.4–10 | \n0.3–4 | \n
Vitamin E (mg) | \n0.2 | \n\n |
Vitamin K1 (μg) | \n0.3 | \n0.7 | \n
Vitamin C (mg) | \n4.3 | \n1.8 | \n
Thiamine (B1) (μg) | \n16 | \n42 | \n
Riboflavin (B2) (μg) | \n43 | \n157 | \n
Niacin (μg) | \n172 | \n85 | \n
Vitamin B6 (μg) | \n11 | \n58 | \n
Folic acid (μg) | \n0.18 | \n0.23 | \n
Vitamin B12 (μg) | \n0.18 | \n0.4 | \n
Biotin (μg) | \n2 | \n22 | \n
Choline (mg) | \n1.3 | \n1.2 | \n
Taurine (mg) | \n5 | \n0.5 | \n
Carnitine (mg) | \n0.8 | \n1 | \n
Iron (mg) | \n0.05–0.2 | \n0.1–0.3 | \n
Iodine (mg) | \n7 | \n21 | \n
Copper (mg) | \n0.04 | \n0.03 | \n
Zinc (mg) | \n0.53 | \n0.38 | \n
In a normal term baby, breastfeeding should be done as and when baby demands. Usually after every 2–3 h, the baby will wake up and cry for feeds; this is called demand feeding. Some babies might sleep for a long duration usually in the first few days after birth; these babies should be awakened and fed if the gap exceeds more than 3 h. Some babies sleep off after few minutes of suckling; they should be aroused by tickling at the ears and flicking the sole, or the mother should try to withdraw the nipple and then the baby starts suckling again [12]. Usually a normal term baby requires 15–20 min to empty one breast; he/she should be allowed to completely empty one breast so that he/she gets both foremilk and the hindmilk, which is required for the satiety of hunger and weight gain. If the baby sleeps off after a few mins, he/she should be aroused and then start suckling again and complete the feed [12]. Breastfeeding should be continued till 2 years of age because the maximum growth and myelination of the brain take place in the first 2 years of life [5]. After 6 months of age, weaning should be started which is done by introducing semisolids or complementary feeds to the diet along with breastfeeding. After 6 months of life, the baby becomes interested in his/her surroundings and shows interest when adults take food; breastmilk output of the mother is not sufficient to meet the needs of the baby, and hence semisolid diet according to the regional availability may be introduced. If weaning is not started by 6 months of age, it might lead to malnutrition. An exclusively breastfed term baby does not require multivitamin supplementation; however the baby may be given vitamin D supplementation for a period of 6 months [10].
\nColostrum is very rich in secretory IgA (sIgA) which protects the mucosal lining of GI tract and respiratory tract and contains lymphocytes and macrophages. After 2–3 days, colostrum is replaced by transitional breastmilk which contains less amount of sIgA than colostrum. SIgA are produced in the mammary gland by the plasma cells that are derived from gut-associated lymphoid tissue (GALT) and bronchus-associated lymphoid tissue (BALT) [5]. Breastmilk contains sIgA and also IgM antibodies. IgM antibodies are transmitted from the mother to the baby by breastmilk; IgM antibodies usually do not cross the placenta and are not transferred from the mother to the baby via the placenta [12]. Breastmilk also contains IgG antibodies, lymphocytes, polymorph, macrophages and plasma cells and nonspecific humoral factors like lysozyme, oligosaccharides, lactoferrin and lactoperoxidase. Probiotics in breastmilk protects the gut from enteric pathogens. It also contains antiviral and anti-staphylococcal factors [12].
\nIf the nipple is flat, the areola and the nipple should be brought out to form the teat; otherwise the baby cannot latch a flat nipple. Occasionally while trying to pull out the nipple, it goes deeper into the breast and this is called inverted nipple; in this case the baby finds difficulty in latching. Nipple protractility test (nipple should be capable of being pulled out) should be done in the last trimester of pregnancy [14]. The nipple might get corrected as the baby sucks. In case of problem, syringe technique should be tried (Figure 3). Supple cups or silicone nipple can be used over flat or inverted nipple to form a teat so that the baby can suckle.
\nSyringe technique for flat and inverted nipple (taken from
Usually by days 2–3, milk production increases, and if the baby is not put for suckling, the breasts get engorged. If the breasts get engorged, then the nipple and areola becomes hard and baby does not suck at the breast. To relieve breast engorgement, breasts have to be emptied; this can be done by putting the baby for frequent suckling at the breast or by emptying the breast using breast pump. Warm packs applied to breasts or a warm shower before feeding combined with massage helps to relieve the congestion [8].
\nThis may occur from strong sucking action of the baby if his/her position is not correct, i.e. if he/she sucks at the nipple instead of the areola; correct breastfeeding technique can prevent sore nipples. The baby should not be forcefully removed from sucking at the breast, but instead a finger can be introduced to break the suction and then remove him/her; he/she should not be allowed to suck for a long time after the breast is emptied; the nipple should not be allowed to remain wet from leaking milk. The mother can keep the nipple exposed to air for 10–15 min after breastfeeding or apply vitamin E lotion, coconut oil and lanolin to prevent soreness. While cleaning the nipples, she should avoid using soap and use only warm water. In case of sore nipple or cracked nipple, nipple shells or nipple shields can be used to allow the baby to suckle and to prevent the mother from pain [7].
\nSometimes a segment of the breast becomes hard due to blocked ducts; in this case proper massage and warm packs with emptying of the breast helps, and if blocked ducts are not treated, it leads to mastitis [5]. Sometimes due to incorrect technique and engorgement of breasts if not treated, the mother may develop mastitis (non-infective); in this condition mothers should be given analgesia (paracetamol) prior to feeds, and the baby should be put for suckling; if baby cannot be put for suckling at the breast due to pain, breasts must be emptied by using breast pump; the mother should take bed rest and plenty of fluids orally. In case the mother develops breast abscess, antibiotics should be given for 10–14 days. Breastfeeding can be continued from the affected breast if there is no pus discharge from the nipple [15]. Breast abscess might require drainage. Candidal infection: sometimes mothers may experience excruciating pain while feeding the baby; if the baby has oral thrush, 1% gentian violet clotrimazole mouth paint may be applied over the nipple and inside the baby’s mouth. Mothers may require systemic antifungal like fluconazole in severe cases [16]. Psychological counselling for the mother is necessary in these cases of feeding problems. A mother needs constant support and guidance in these cases [5].
\nA mother can breastfeed her baby in case of fever, rhinitis, respiratory tract infection, diarrheal diseases and asthma provided she is not very sick and unable to breastfeed. In case of respiratory tract infections, she should wear mask while breastfeeding. If the mother is unable to breastfeed, expressed breastmilk (EBM) can be given through cup and spoon. Breastmilk can be expressed using manual or electric breast pump. Bottle feeds should not be used because it creates nipple confusion in the baby and the baby will refuse to take breastfeeding. Bottle feeding is easier and needs less energy, and henceforth the baby becomes lazy and refuses breastfeeding [12]. If the mother has mastitis, she can breastfeed from the unaffected breast and also from the affected breast if there is no pus discharge from the nipple of affected site [15]. In case of UTI and tuberculosis (if sputum is negative), breastfeeding can be given. In case of hepatitis B-positive mother, the baby should be given hepatitis B immunoglobulin and hepatitis B vaccine after birth, and breastfeeding can be continued [5]. In case of HIV-positive mother, the
Galactosemia, congenital lactose intolerance, chemotherapy, antithyroid drugs except propylthiouracil and antipsychotic drugs like lithium are contraindications for breastfeeding [5].
\nSome babies regurgitate some curdy milk precipitates (fermented milk from the stomach) after each feed; the mother should be advised to burp the baby properly to eructate the swallowed air and to make the baby lie in right lateral position with slight elevation of the head.
\nSome breastfed babies may pass stool after each feed; this is not diarrhoea, and if urine output is good, then there is no dehydration and no treatment required; it is a phenomenon due to gastrocolic reflex. If the urine output is good then it is normal.
\nSome breastfed babies cry during the evening hours due to aerophagia. These babies can be put prone, and burping can be done which will help the air to come out and relieve the colic [12].
\nUsually working mothers get 6 months of maternity leave. In the first 6 months, exclusive breastfeeding can be given and then complementary feeds should be started along with breastfeeding.
\nIdeally there should be a crèche near the working place for the mother to go and feed in between. There should be a private place in the working area for the mother to express her milk and give to her baby in the crèche. Expressed breastmilk can be given to the baby if the mother is away by cup and spoon [5].
\nExpressed breastmilk (EBM) should be stored in a stainless steel, food grade hard plastic or glass container having a tight fitting lid. EBM can be stored at room temperature for 6 h and in the refrigerator for 24 h and in the freezer compartment of the refrigerator for 2 weeks. EBM should be thawed before feeding by running tap or lukewarm water over the container; never use boiling or hot water to thaw the milk. EBM should never be heated or microwaved because the antibodies get destroyed [18].
\nAll drugs taken by the mother will be excreted in the milk, but the concentration of drugs in the breastmilk is less, usually less than 1%. Propylthiouracil and warfarin are safe and can be taken during breastfeeding. Antibiotics taken by the mother may cause increased stooling of the baby. Laxatives taken by the mother can cause diarrhoea in the baby; however milk of magnesia, liquid paraffin and glycerine suppositories are safe. Oral contraceptives, pyridoxine, nicotine and bromocriptine suppress lactation [5].
\nSome mothers with obesity, diabetes mellitus, stress, polycystic ovarian disease, postpartum haemorrhage and retained placenta may have delayed lactation. In these cases galactogogues can be given like domperidone and metoclopramide tablets. However it should be kept in mind that these drugs can cause extra pyramidal symptoms (EPS) in the mother. Domperidone has less chance of EPS and is well tolerated and can be given for 7–10 days at length [5].
\nThe Baby-friendly Hospital Initiative (BFHI) was started in the year 1992 organised by the UNICEF and WHO. The World Alliance for Breastfeeding Action (WABA) is the global agency for the promotion of breastfeeding. The 10 steps of BFHI are as follows [5]:
Every hospital should have a written breastfeeding policy that is routinely communicated to all healthcare staff.
Train all healthcare staff in skills necessary to implement this policy.
Inform all pregnant women about the benefits and management of breastfeeding.
Help mothers to initiate breastfeeding within an hour of birth.
Show mothers how to breastfeed and how to maintain lactation even if they are separated from their infants.
Give newborn infants no food or drink other than breastmilk, unless medically indicated.
Practise rooming-in and allow mothers and infants to remain together 24 h a day.
Encourage breastfeeding on demand.
Give no artificial teats or pacifiers (also called dummies or soothers) to breastfeeding infants.
Foster the establishment of breastfeeding support groups, and refer mothers to them on discharge from the hospital or clinic.
Every year breastfeeding week is celebrated from August 1 to August 7. It commemorates the Innocenti Declaration in August 1990 when the WHO, UNICEF and several other organisations came together to protect, promote and support breastfeeding. Every year there is a theme based on which it is celebrated. Breastfeeding week celebrations are organised by the WABA, UNICEF, WHO and several government and non-government organisations [19].
\nAll mothers should be antenatally motivated for breastfeeding. Breastfeeding should be initiated within 1 h of birth. Early skin-to-skin contact helps in early initiation of breastfeeding. Correct technique of breastfeeding should be taught to the mother. Exclusive breastfeeding should be given for 6 months of age and then complementary feeds should be introduced. In low- and middle-income countries, breastfeeding not only benefits the mother and the baby but also reduces economic burden of the country. Hence we should protect, promote and support breastfeeding not only in low- and middle-income countries but also in developed countries.
\nI would like to acknowledge Dr. Sneha Andrade and Veronica sister for helping me take the picture of the mother while breastfeeding. I would also like to acknowledge the mother for allowing me to take the picture.
\nThe author declares no conflict of interest.
This is a brief overview of the main steps involved in publishing with IntechOpen Compacts, Monographs and Edited Books. Once you submit your proposal you will be appointed a Author Service Manager who will be your single point of contact and lead you through all the described steps below.
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\n\nAfter approval, you will proceed in submitting your full-length manuscript. 50-130 pages for compacts, 130-500 for Monographs & Edited Books.Your full-length manuscript must follow IntechOpen's Author Guidelines and comply with our publishing rules. Once the manuscript is submitted, but before it is forwarded for peer review, it will be screened for plagiarism.
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Aalborg University has Two Satellite Campuses, one in Copenhagen (Aalborg University Copenhagen) and the other in Esbjerg (Aalborg University Esbjerg).\n· He is a member of prestigious IEEE (Institute of Electrical and Electronics Engineers), and IAENG (International Association of Engineers) organizations. \n· He is the chief Editor of the Journal of Software Engineering.\n· He is the member of the Editorial Board of International Journal of Computer Science and Software Technology (IJCSST) and International Journal of Computer Engineering and Information Technology. \n· He is also the Editor of Communication in Computer and Information Science CCIS-20 by Springer.\n· Reviewer For Many Conferences\nHe is the lead person in making collaboration agreements between Aalborg University and many universities of Pakistan, for which the MOU’s (Memorandum of Understanding) have been signed.\nProfessor Akbar is working in Academia since 1990, he started his career as a Lab demonstrator/TA at the University of Sussex. After finishing his P. hD degree in 1992, he served in the Industry as a Scientific Officer and continued his academic career as a visiting scholar for a number of educational institutions. In 1996 he joined National University of Science & Technology Pakistan (NUST) as an Associate Professor; NUST is one of the top few universities in Pakistan. In 1999 he joined an International Company Lineo Inc, Canada as Manager Compiler Group, where he headed the group for developing Compiler Tool Chain and Porting of Operating Systems for the BLACKfin processor. The processor development was a joint venture by Intel and Analog Devices. In 2002 Lineo Inc., was taken over by another company, so he joined Aalborg University Denmark as an Assistant Professor.\nProfessor Akbar has truly a multi-disciplined career and he continued his legacy and making progress in many areas of his interests both in teaching and research. He has contributed in stochastic estimation of control area especially, in the Multiple Target Tracking and Interactive Multiple Model (IMM) research, Ball & Beam Control Problem, Robotics, Levitation Control. He has contributed in developing Algorithms for Fingerprint Matching, Computer Vision and Face Recognition. He has been supervising Pattern Recognition, Formal Languages and Distributed Processing projects for several years. He has reviewed many books on Management, Computer Science. Currently, he is an active and permanent reviewer for many international conferences and symposia and the program committee member for many international conferences.\nIn teaching he has taught the core computer science subjects like, Digital Design, Real Time Embedded System Programming, Operating Systems, Software Engineering, Data Structures, Databases, Compiler Construction. 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Nutrition",value:20,count:2},{group:"subseries",caption:"Animal Reproductive Biology and Technology",value:28,count:4},{group:"subseries",caption:"Animal Science",value:19,count:5}],publicationYearFilters:[{group:"publicationYear",caption:"2022",value:2022,count:3},{group:"publicationYear",caption:"2021",value:2021,count:3},{group:"publicationYear",caption:"2020",value:2020,count:3},{group:"publicationYear",caption:"2019",value:2019,count:1},{group:"publicationYear",caption:"2018",value:2018,count:1}],authors:{paginationCount:229,paginationItems:[{id:"318170",title:"Dr.",name:"Aneesa",middleName:null,surname:"Moolla",slug:"aneesa-moolla",fullName:"Aneesa Moolla",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/318170/images/system/318170.png",biography:"Dr. Aneesa Moolla has extensive experience in the diverse fields of health care having previously worked in dental private practice, at the Red Cross Flying Doctors association, and in healthcare corporate settings. She is now a lecturer at the University of Witwatersrand, South Africa, and a principal researcher at the Health Economics and Epidemiology Research Office (HE2RO), South Africa. Dr. Moolla holds a Ph.D. in Psychology with her research being focused on mental health and resilience. In her professional work capacity, her research has further expanded into the fields of early childhood development, mental health, the HIV and TB care cascades, as well as COVID. She is also a UNESCO-trained International Bioethics Facilitator.",institutionString:"University of the Witwatersrand",institution:{name:"University of the Witwatersrand",country:{name:"South Africa"}}},{id:"419588",title:"Ph.D.",name:"Sergio",middleName:"Alexandre",surname:"Gehrke",slug:"sergio-gehrke",fullName:"Sergio Gehrke",position:null,profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0033Y000038WgMKQA0/Profile_Picture_2022-06-02T11:44:20.jpg",biography:"Dr. Sergio Alexandre Gehrke is a doctorate holder in two fields. The first is a Ph.D. in Cellular and Molecular Biology from the Pontificia Catholic University, Porto Alegre, Brazil, in 2010 and the other is an International Ph.D. in Bioengineering from the Universidad Miguel Hernandez, Elche/Alicante, Spain, obtained in 2020. In 2018, he completed a postdoctoral fellowship in Materials Engineering in the NUCLEMAT of the Pontificia Catholic University, Porto Alegre, Brazil. He is currently the Director of the Postgraduate Program in Implantology of the Bioface/UCAM/PgO (Montevideo, Uruguay), Director of the Cathedra of Biotechnology of the Catholic University of Murcia (Murcia, Spain), an Extraordinary Full Professor of the Catholic University of Murcia (Murcia, Spain) as well as the Director of the private center of research Biotecnos – Technology and Science (Montevideo, Uruguay). Applied biomaterials, cellular and molecular biology, and dental implants are among his research interests. He has published several original papers in renowned journals. In addition, he is also a Collaborating Professor in several Postgraduate programs at different universities all over the world.",institutionString:null,institution:{name:"Universidad Católica San Antonio de Murcia",country:{name:"Spain"}}},{id:"342152",title:"Dr.",name:"Santo",middleName:null,surname:"Grace Umesh",slug:"santo-grace-umesh",fullName:"Santo Grace Umesh",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/342152/images/16311_n.jpg",biography:null,institutionString:null,institution:{name:"SRM Dental College",country:{name:"India"}}},{id:"333647",title:"Dr.",name:"Shreya",middleName:null,surname:"Kishore",slug:"shreya-kishore",fullName:"Shreya Kishore",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/333647/images/14701_n.jpg",biography:"Dr. Shreya Kishore completed her Bachelor in Dental Surgery in Chettinad Dental College and Research Institute, Chennai, and her Master of Dental Surgery (Orthodontics) in Saveetha Dental College, Chennai. She is also Invisalign certified. She’s working as a Senior Lecturer in the Department of Orthodontics, SRM Dental College since November 2019. She is actively involved in teaching orthodontics to the undergraduates and the postgraduates. Her clinical research topics include new orthodontic brackets, fixed appliances and TADs. She’s published 4 articles in well renowned indexed journals and has a published patency of her own. Her private practice is currently limited to orthodontics and works as a consultant in various clinics.",institutionString:null,institution:{name:"SRM Dental College",country:{name:"India"}}},{id:"323731",title:"Prof.",name:"Deepak M.",middleName:"Macchindra",surname:"Vikhe",slug:"deepak-m.-vikhe",fullName:"Deepak M. Vikhe",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/323731/images/13613_n.jpg",biography:"Dr Deepak M.Vikhe .\n\n\t\n\tDr Deepak M.Vikhe , completed his Masters & PhD in Prosthodontics from Rural Dental College, Loni securing third rank in the Pravara Institute of Medical Sciences Deemed University. He was awarded Dr.G.C.DAS Memorial Award for Research on Implants at 39th IPS conference Dubai (U A E).He has two patents under his name. He has received Dr.Saraswati medal award for best research for implant study in 2017.He has received Fully funded scholarship to Spain ,university of Santiago de Compostela. He has completed fellowship in Implantlogy from Noble Biocare. \nHe has attended various conferences and CDE programmes and has national publications to his credit. His field of interest is in Implant supported prosthesis. Presently he is working as a associate professor in the Dept of Prosthodontics, Rural Dental College, Loni and maintains a successful private practice specialising in Implantology at Rahata.\n\nEmail: drdeepak_mvikhe@yahoo.com..................",institutionString:null,institution:{name:"Pravara Institute of Medical Sciences",country:{name:"India"}}},{id:"204110",title:"Dr.",name:"Ahmed A.",middleName:null,surname:"Madfa",slug:"ahmed-a.-madfa",fullName:"Ahmed A. Madfa",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/204110/images/system/204110.jpg",biography:"Dr. Madfa is currently Associate Professor of Endodontics at Thamar University and a visiting lecturer at Sana'a University and University of Sciences and Technology. He has more than 6 years of experience in teaching. His research interests include root canal morphology, functionally graded concept, dental biomaterials, epidemiology and dental education, biomimetic restoration, finite element analysis and endodontic regeneration. Dr. Madfa has numerous international publications, full articles, two patents, a book and a book chapter. Furthermore, he won 14 international scientific awards. Furthermore, he is involved in many academic activities ranging from editorial board member, reviewer for many international journals and postgraduate students' supervisor. Besides, I deliver many courses and training workshops at various scientific events. Dr. Madfa also regularly attends international conferences and holds administrative positions (Deputy Dean of the Faculty for Students’ & Academic Affairs and Deputy Head of Research Unit).",institutionString:"Thamar University",institution:null},{id:"210472",title:"Dr.",name:"Nermin",middleName:"Mohammed Ahmed",surname:"Yussif",slug:"nermin-yussif",fullName:"Nermin Yussif",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/210472/images/system/210472.jpg",biography:"Dr. Nermin Mohammed Ahmed Yussif is working at the Faculty of dentistry, University for October university for modern sciences and arts (MSA). Her areas of expertise include: periodontology, dental laserology, oral implantology, periodontal plastic surgeries, oral mesotherapy, nutrition, dental pharmacology. She is an editor and reviewer in numerous international journals.",institutionString:"MSA University",institution:null},{id:"204606",title:"Dr.",name:"Serdar",middleName:null,surname:"Gözler",slug:"serdar-gozler",fullName:"Serdar Gözler",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/204606/images/system/204606.jpeg",biography:"Dr. Serdar Gözler has completed his undergraduate studies at the Marmara University Faculty of Dentistry in 1978, followed by an assistantship in the Prosthesis Department of Dicle University Faculty of Dentistry. Starting his PhD work on non-resilient overdentures with Assoc. Prof. Hüsnü Yavuzyılmaz, he continued his studies with Prof. Dr. Gürbüz Öztürk of Istanbul University Faculty of Dentistry Department of Prosthodontics, this time on Gnatology. He attended training programs on occlusion, neurology, neurophysiology, EMG, radiology and biostatistics. In 1982, he presented his PhD thesis \\Gerber and Lauritzen Occlusion Analysis Techniques: Diagnosis Values,\\ at Istanbul University School of Dentistry, Department of Prosthodontics. As he was also working with Prof. Senih Çalıkkocaoğlu on The Physiology of Chewing at the same time, Gözler has written a chapter in Çalıkkocaoğlu\\'s book \\Complete Prostheses\\ entitled \\The Place of Neuromuscular Mechanism in Prosthetic Dentistry.\\ The book was published five times since by the Istanbul University Publications. Having presented in various conferences about occlusion analysis until 1998, Dr. Gözler has also decided to use the T-Scan II occlusion analysis method. Having been personally trained by Dr. Robert Kerstein on this method, Dr. Gözler has been lecturing on the T-Scan Occlusion Analysis Method in conferences both in Turkey and abroad. Dr. Gözler has various articles and presentations on Digital Occlusion Analysis methods. He is now Head of the TMD Clinic at Prosthodontic Department of Faculty of Dentistry , Istanbul Aydın University , Turkey.",institutionString:"Istanbul Aydin University",institution:{name:"Istanbul Aydın University",country:{name:"Turkey"}}},{id:"240870",title:"Ph.D.",name:"Alaa Eddin Omar",middleName:null,surname:"Al Ostwani",slug:"alaa-eddin-omar-al-ostwani",fullName:"Alaa Eddin Omar Al Ostwani",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/240870/images/system/240870.jpeg",biography:"Dr. Al Ostwani Alaa Eddin Omar received his Master in dentistry from Damascus University in 2010, and his Ph.D. in Pediatric Dentistry from Damascus University in 2014. Dr. Al Ostwani is an assistant professor and faculty member at IUST University since 2014. \nDuring his academic experience, he has received several awards including the scientific research award from the Union of Arab Universities, the Syrian gold medal and the international gold medal for invention and creativity. Dr. Al Ostwani is a Member of the International Association of Dental Traumatology and the Syrian Society for Research and Preventive Dentistry since 2017. He is also a Member of the Reviewer Board of International Journal of Dental Medicine (IJDM), and the Indian Journal of Conservative and Endodontics since 2016.",institutionString:"International University for Science and Technology.",institution:{name:"Islamic University of Science and Technology",country:{name:"India"}}},{id:"42847",title:"Dr.",name:"Belma",middleName:null,surname:"Işik Aslan",slug:"belma-isik-aslan",fullName:"Belma Işik Aslan",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/42847/images/system/42847.jpg",biography:"Dr. Belma IşIk Aslan was born in 1976 in Ankara-TURKEY. After graduating from TED Ankara College in 1994, she attended to Gazi University, Faculty of Dentistry in Ankara. She completed her PhD in orthodontic education at Gazi University between 1999-2005. Dr. Işık Aslan stayed at the Providence Hospital Craniofacial Institude and Reconstructive Surgery in Michigan, USA for three months as an observer. She worked as a specialist doctor at Gazi University, Dentistry Faculty, Department of Orthodontics between 2005-2014. She was appointed as associate professor in January, 2014 and as professor in 2021. Dr. Işık Aslan still works as an instructor at the same faculty. She has published a total of 35 articles, 10 book chapters, 39 conference proceedings both internationally and nationally. Also she was the academic editor of the international book 'Current Advances in Orthodontics'. She is a member of the Turkish Orthodontic Society and Turkish Cleft Lip and Palate Society. She is married and has 2 children. Her knowledge of English is at an advanced level.",institutionString:"Gazi University Dentistry Faculty Department of Orthodontics",institution:null},{id:"178412",title:"Associate Prof.",name:"Guhan",middleName:null,surname:"Dergin",slug:"guhan-dergin",fullName:"Guhan Dergin",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/178412/images/6954_n.jpg",biography:"Assoc. Prof. Dr. Gühan Dergin was born in 1973 in Izmit. He graduated from Marmara University Faculty of Dentistry in 1999. He completed his specialty of OMFS surgery in Marmara University Faculty of Dentistry and obtained his PhD degree in 2006. In 2005, he was invited as a visiting doctor in the Oral and Maxillofacial Surgery Department of the University of North Carolina, USA, where he went on a scholarship. Dr. Dergin still continues his academic career as an associate professor in Marmara University Faculty of Dentistry. He has many articles in international and national scientific journals and chapters in books.",institutionString:null,institution:{name:"Marmara University",country:{name:"Turkey"}}},{id:"178414",title:"Prof.",name:"Yusuf",middleName:null,surname:"Emes",slug:"yusuf-emes",fullName:"Yusuf Emes",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/178414/images/6953_n.jpg",biography:"Born in Istanbul in 1974, Dr. Emes graduated from Istanbul University Faculty of Dentistry in 1997 and completed his PhD degree in Istanbul University faculty of Dentistry Department of Oral and Maxillofacial Surgery in 2005. He has papers published in international and national scientific journals, including research articles on implantology, oroantral fistulas, odontogenic cysts, and temporomandibular disorders. Dr. Emes is currently working as a full-time academic staff in Istanbul University faculty of Dentistry Department of Oral and Maxillofacial Surgery.",institutionString:null,institution:{name:"Istanbul University",country:{name:"Turkey"}}},{id:"192229",title:"Ph.D.",name:"Ana Luiza",middleName:null,surname:"De Carvalho Felippini",slug:"ana-luiza-de-carvalho-felippini",fullName:"Ana Luiza De Carvalho Felippini",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/192229/images/system/192229.jpg",biography:null,institutionString:"University of São Paulo",institution:{name:"University of Sao Paulo",country:{name:"Brazil"}}},{id:"256851",title:"Prof.",name:"Ayşe",middleName:null,surname:"Gülşen",slug:"ayse-gulsen",fullName:"Ayşe Gülşen",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/256851/images/9696_n.jpg",biography:"Dr. Ayşe Gülşen graduated in 1990 from Faculty of Dentistry, University of Ankara and did a postgraduate program at University of Gazi. \nShe worked as an observer and research assistant in Craniofacial Surgery Departments in New York, Providence Hospital in Michigan and Chang Gung Memorial Hospital in Taiwan. \nShe works as Craniofacial Orthodontist in Department of Aesthetic, Plastic and Reconstructive Surgery, Faculty of Medicine, University of Gazi, Ankara Turkey since 2004.",institutionString:"Univeristy of Gazi",institution:null},{id:"255366",title:"Prof.",name:"Tosun",middleName:null,surname:"Tosun",slug:"tosun-tosun",fullName:"Tosun Tosun",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/255366/images/7347_n.jpg",biography:"Graduated at the Faculty of Dentistry, University of Istanbul, Turkey in 1989;\nVisitor Assistant at the University of Padua, Italy and Branemark Osseointegration Center of Treviso, Italy between 1993-94;\nPhD thesis on oral implantology in University of Istanbul and was awarded the academic title “Dr.med.dent.”, 1997;\nHe was awarded the academic title “Doç.Dr.” (Associated Professor) in 2003;\nProficiency in Botulinum Toxin Applications, Reading-UK in 2009;\nMastership, RWTH Certificate in Laser Therapy in Dentistry, AALZ-Aachen University, Germany 2009-11;\nMaster of Science (MSc) in Laser Dentistry, University of Genoa, Italy 2013-14.\n\nDr.Tosun worked as Research Assistant in the Department of Oral Implantology, Faculty of Dentistry, University of Istanbul between 1990-2002. \nHe worked part-time as Consultant surgeon in Harvard Medical International Hospitals and John Hopkins Medicine, Istanbul between years 2007-09.\u2028He was contract Professor in the Department of Surgical and Diagnostic Sciences (DI.S.C.), Medical School, University of Genova, Italy between years 2011-16. \nSince 2015 he is visiting Professor at Medical School, University of Plovdiv, Bulgaria. \nCurrently he is Associated Prof.Dr. at the Dental School, Oral Surgery Dept., Istanbul Aydin University and since 2003 he works in his own private clinic in Istanbul, Turkey.\u2028\nDr.Tosun is reviewer in journal ‘Laser in Medical Sciences’, reviewer in journal ‘Folia Medica\\', a Fellow of the International Team for Implantology, Clinical Lecturer of DGZI German Association of Oral Implantology, Expert Lecturer of Laser&Health Academy, Country Representative of World Federation for Laser Dentistry, member of European Federation of Periodontology, member of Academy of Laser Dentistry. Dr.Tosun presents papers in international and national congresses and has scientific publications in international and national journals. He speaks english, spanish, italian and french.",institutionString:null,institution:{name:"Istanbul Aydın University",country:{name:"Turkey"}}},{id:"171887",title:"Prof.",name:"Zühre",middleName:null,surname:"Akarslan",slug:"zuhre-akarslan",fullName:"Zühre Akarslan",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/171887/images/system/171887.jpg",biography:"Zühre Akarslan was born in 1977 in Cyprus. She graduated from Gazi University Faculty of Dentistry, Ankara, Turkey in 2000. \r\nLater she received her Ph.D. degree from the Oral Diagnosis and Radiology Department; which was recently renamed as Oral and Dentomaxillofacial Radiology, from the same university. \r\nShe is working as a full-time Associate Professor and is a lecturer and an academic researcher. \r\nHer expertise areas are dental caries, cancer, dental fear and anxiety, gag reflex in dentistry, oral medicine, and dentomaxillofacial radiology.",institutionString:"Gazi University",institution:{name:"Gazi University",country:{name:"Turkey"}}},{id:"256417",title:"Associate Prof.",name:"Sanaz",middleName:null,surname:"Sadry",slug:"sanaz-sadry",fullName:"Sanaz Sadry",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/256417/images/8106_n.jpg",biography:null,institutionString:null,institution:null},{id:"272237",title:"Dr.",name:"Pinar",middleName:"Kiymet",surname:"Karataban",slug:"pinar-karataban",fullName:"Pinar Karataban",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/272237/images/8911_n.png",biography:"Assist.Prof.Dr.Pınar Kıymet Karataban, DDS PhD \n\nDr.Pınar Kıymet Karataban was born in Istanbul in 1975. After her graduation from Marmara University Faculty of Dentistry in 1998 she started her PhD in Paediatric Dentistry focused on children with special needs; mainly children with Cerebral Palsy. She finished her pHD thesis entitled \\'Investigation of occlusion via cast analysis and evaluation of dental caries prevalance, periodontal status and muscle dysfunctions in children with cerebral palsy” in 2008. She got her Assist. Proffessor degree in Istanbul Aydın University Paediatric Dentistry Department in 2015-2018. ın 2019 she started her new career in Bahcesehir University, Istanbul as Head of Department of Pediatric Dentistry. In 2020 she was accepted to BAU International University, Batumi as Professor of Pediatric Dentistry. She’s a lecturer in the same university meanwhile working part-time in private practice in Ege Dental Studio (https://www.egedisklinigi.com/) a multidisciplinary dental clinic in Istanbul. Her main interests are paleodontology, ancient and contemporary dentistry, oral microbiology, cerebral palsy and special care dentistry. She has national and international publications, scientific reports and is a member of IAPO (International Association for Paleodontology), IADH (International Association of Disability and Oral Health) and EAPD (European Association of Pediatric Dentistry).",institutionString:null,institution:null},{id:"202198",title:"Dr.",name:"Buket",middleName:null,surname:"Aybar",slug:"buket-aybar",fullName:"Buket Aybar",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/202198/images/6955_n.jpg",biography:"Buket Aybar, DDS, PhD, was born in 1971. She graduated from Istanbul University, Faculty of Dentistry, in 1992 and completed her PhD degree on Oral and Maxillofacial Surgery in Istanbul University in 1997.\nDr. Aybar is currently a full-time professor in Istanbul University, Faculty of Dentistry Department of Oral and Maxillofacial Surgery. She has teaching responsibilities in graduate and postgraduate programs. Her clinical practice includes mainly dentoalveolar surgery.\nHer topics of interest are biomaterials science and cell culture studies. She has many articles in international and national scientific journals and chapters in books; she also has participated in several scientific projects supported by Istanbul University Research fund.",institutionString:null,institution:null},{id:"260116",title:"Dr.",name:"Mehmet",middleName:null,surname:"Yaltirik",slug:"mehmet-yaltirik",fullName:"Mehmet Yaltirik",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/260116/images/7413_n.jpg",biography:"Birth Date 25.09.1965\r\nBirth Place Adana- Turkey\r\nSex Male\r\nMarrial Status Bachelor\r\nDriving License Acquired\r\nMother Tongue Turkish\r\n\r\nAddress:\r\nWork:University of Istanbul,Faculty of Dentistry, Department of Oral Surgery and Oral Medicine 34093 Capa,Istanbul- TURKIYE",institutionString:null,institution:null},{id:"172009",title:"Dr.",name:"Fatma Deniz",middleName:null,surname:"Uzuner",slug:"fatma-deniz-uzuner",fullName:"Fatma Deniz Uzuner",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/172009/images/7122_n.jpg",biography:"Dr. Deniz Uzuner was born in 1969 in Kocaeli-TURKEY. After graduating from TED Ankara College in 1986, she attended the Hacettepe University, Faculty of Dentistry in Ankara. \nIn 1993 she attended the Gazi University, Faculty of Dentistry, Department of Orthodontics for her PhD education. After finishing the PhD education, she worked as orthodontist in Ankara Dental Hospital under the Turkish Government, Ministry of Health and in a special Orthodontic Clinic till 2011. Between 2011 and 2016, Dr. Deniz Uzuner worked as a specialist in the Department of Orthodontics, Faculty of Dentistry, Gazi University in Ankara/Turkey. In 2016, she was appointed associate professor. Dr. Deniz Uzuner has authored 23 Journal Papers, 3 Book Chapters and has had 39 oral/poster presentations. She is a member of the Turkish Orthodontic Society. 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Dr. Rahman was also adjunctly attached with Kanazawa University, Japan (Visiting Research Professor, Dec 2014 to Mar 2015; JSPS Postdoctoral Research Fellow, Apr 2012 to Mar 2014), and Tokyo Institute of Technology, Japan (TokyoTech-UNESCO Research Fellow, Oct 2004–Sep 2005). \nHe received his Ph.D. degree in Environmental Analytical Chemistry from Kanazawa University, Japan (2011). He also achieved a Diploma in Environment from the Tokyo Institute of Technology, Japan (2005). 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Dr. Şentürk currently works as an professor of Biochemistry in the Department of Basic Pharmacy Sciences, Faculty of Pharmacy, Ağri Ibrahim Cecen University, Turkey. \nDr. Şentürk published over 120 scientific papers, reviews, and book chapters and presented several conferences to scientists. \nHis research interests span enzyme inhibitor or activator, protein expression, purification and characterization, drug design and synthesis, toxicology, and pharmacology. \nHis research work has focused on neurodegenerative diseases and cancer treatment. Dr. Şentürk serves as the editorial board member of several international journals.",institutionString:"Ağrı İbrahim Çeçen University",position:null,outsideEditionCount:0,totalCites:0,totalAuthoredChapters:"2",totalChapterViews:"0",totalEditedBooks:"1",institution:{name:"Ağrı İbrahim Çeçen University",institutionURL:null,country:{name:"Turkey"}}}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null}],selectedSeries:{id:"11",title:"Biochemistry"},selectedSubseries:{id:"18",title:"Proteomics",coverUrl:"https://cdn.intechopen.com/series_topics/covers/18.jpg",editor:{id:"200689",title:"Prof.",name:"Paolo",middleName:null,surname:"Iadarola",slug:"paolo-iadarola",fullName:"Paolo Iadarola",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bSCl8QAG/Profile_Picture_1623568118342",biography:"Paolo Iadarola graduated with a degree in Chemistry from the University of Pavia (Italy) in July 1972. He then worked as an Assistant Professor at the Faculty of Science of the same University until 1984. In 1985, Prof. Iadarola became Associate Professor at the Department of Biology and Biotechnologies of the University of Pavia and retired in October 2017. Since then, he has been working as an Adjunct Professor in the same Department at the University of Pavia. His research activity during the first years was primarily focused on the purification and structural characterization of enzymes from animal and plant sources. During this period, Prof. Iadarola familiarized himself with the conventional techniques used in column chromatography, spectrophotometry, manual Edman degradation, and electrophoresis). Since 1995, he has been working on: i) the determination in biological fluids (serum, urine, bronchoalveolar lavage, sputum) of proteolytic activities involved in the degradation processes of connective tissue matrix, and ii) on the identification of biological markers of lung diseases. In this context, he has developed and validated new methodologies (e.g., Capillary Electrophoresis coupled to Laser-Induced Fluorescence, CE-LIF) whose application enabled him to determine both the amounts of biochemical markers (Desmosines) in urine/serum of patients affected by Chronic Obstructive Pulmonary Disease (COPD) and the activity of proteolytic enzymes (Human Neutrophil Elastase, Cathepsin G, Pseudomonas aeruginosa elastase) in sputa of these patients. More recently, Prof. Iadarola was involved in developing techniques such as two-dimensional electrophoresis coupled to liquid chromatography/mass spectrometry (2DE-LC/MS) for the proteomic analysis of biological fluids aimed at the identification of potential biomarkers of different lung diseases. He is the author of about 150 publications (According to Scopus: H-Index: 23; Total citations: 1568- According to WOS: H-Index: 20; Total Citations: 1296) of peer-reviewed international journals. He is a Consultant Reviewer for several journals, including the Journal of Chromatography A, Journal of Chromatography B, Plos ONE, Proteomes, International Journal of Molecular Science, Biotech, Electrophoresis, and others. He is also Associate Editor of Biotech.",institutionString:null,position:null,outsideEditionCount:0,totalCites:0,totalAuthoredChapters:"2",totalChapterViews:"0",totalEditedBooks:"0",institution:{name:"University of Pavia",institutionURL:null,country:{name:"Italy"}}},editorTwo:{id:"201414",title:"Dr.",name:"Simona",middleName:null,surname:"Viglio",slug:"simona-viglio",fullName:"Simona Viglio",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRKDHQA4/Profile_Picture_1630402531487",biography:"Simona Viglio is an Associate Professor of Biochemistry at the Department of Molecular Medicine at the University of Pavia. She has been working since 1995 on the determination of proteolytic enzymes involved in the degradation process of connective tissue matrix and on the identification of biological markers of lung diseases. She gained considerable experience in developing and validating new methodologies whose applications allowed her to determine both the amount of biomarkers (Desmosine and Isodesmosine) in the urine of patients affected by COPD, and the activity of proteolytic enzymes (HNE, Cathepsin G, Pseudomonas aeruginosa elastase) in the sputa of these patients. Simona Viglio was also involved in research dealing with the supplementation of amino acids in patients with brain injury and chronic heart failure. She is presently engaged in the development of 2-DE and LC-MS techniques for the study of proteomics in biological fluids. The aim of this research is the identification of potential biomarkers of lung diseases. She is an author of about 90 publications (According to Scopus: H-Index: 23; According to WOS: H-Index: 20) on peer-reviewed journals, a member of the “Società Italiana di Biochimica e Biologia Molecolare,“ and a Consultant Reviewer for International Journal of Molecular Science, Journal of Chromatography A, COPD, Plos ONE and Nutritional Neuroscience.",institutionString:null,position:null,outsideEditionCount:0,totalCites:0,totalAuthoredChapters:"2",totalChapterViews:"0",totalEditedBooks:"0",institution:{name:"University of Pavia",institutionURL:null,country:{name:"Italy"}}},editorThree:null,series:{id:"11",title:"Biochemistry"}}},seriesLanding:{item:{id:"11",title:"Biochemistry",doi:"10.5772/intechopen.72877",issn:"2632-0983",scope:"Biochemistry, the study of chemical transformations occurring within living organisms, impacts all areas of life sciences, from molecular crystallography and genetics to ecology, medicine, and population biology. 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:"June 29th, 2022",hasOnlineFirst:!0,numberOfOpenTopics:4,numberOfPublishedChapters:318,numberOfPublishedBooks:32,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:"219081",title:"Dr.",name:"Abdulsamed",middleName:null,surname:"Kükürt",fullName:"Abdulsamed Kükürt",profilePictureURL:"https://mts.intechopen.com/storage/users/219081/images/system/219081.png",institutionString:null,institution:{name:"Kafkas University",institutionURL:null,country:{name:"Turkey"}}},{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://mts.intechopen.com/storage/users/81926/images/system/81926.png",institutionString:"Suez Canal University",institution:{name:"Suez Canal University",institutionURL:null,country:{name:"Egypt"}}}]}]}},libraryRecommendation:{success:null,errors:{},institutions:[]},route:{name:"chapter.detail",path:"/chapters/69449",hash:"",query:{},params:{id:"69449"},fullPath:"/chapters/69449",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)}()