Proportion of health system-related factors.
\\n\\n
Released this past November, the list is based on data collected from the Web of Science and highlights some of the world’s most influential scientific minds by naming the researchers whose publications over the previous decade have included a high number of Highly Cited Papers placing them among the top 1% most-cited.
\\n\\nWe wish to congratulate all of the researchers named and especially our authors on this amazing accomplishment! We are happy and proud to share in their success!
Note: Edited in March 2021
\\n"}]',published:!0,mainMedia:{caption:"Highly Cited",originalUrl:"/media/original/117"}},components:[{type:"htmlEditorComponent",content:'IntechOpen is proud to announce that 191 of our authors have made the Clarivate™ Highly Cited Researchers List for 2020, ranking them among the top 1% most-cited.
\n\nThroughout the years, the list has named a total of 261 IntechOpen authors as Highly Cited. Of those researchers, 69 have been featured on the list multiple times.
\n\n\n\nReleased this past November, the list is based on data collected from the Web of Science and highlights some of the world’s most influential scientific minds by naming the researchers whose publications over the previous decade have included a high number of Highly Cited Papers placing them among the top 1% most-cited.
\n\nWe wish to congratulate all of the researchers named and especially our authors on this amazing accomplishment! We are happy and proud to share in their success!
Note: Edited in March 2021
\n'}],latestNews:[{slug:"intechopen-supports-asapbio-s-new-initiative-publish-your-reviews-20220729",title:"IntechOpen Supports ASAPbio’s New Initiative Publish Your Reviews"},{slug:"webinar-introduction-to-open-science-wednesday-18-may-1-pm-cest-20220518",title:"Webinar: Introduction to Open Science | Wednesday 18 May, 1 PM CEST"},{slug:"step-in-the-right-direction-intechopen-launches-a-portfolio-of-open-science-journals-20220414",title:"Step in the Right Direction: IntechOpen Launches a Portfolio of Open Science Journals"},{slug:"let-s-meet-at-london-book-fair-5-7-april-2022-olympia-london-20220321",title:"Let’s meet at London Book Fair, 5-7 April 2022, Olympia London"},{slug:"50-books-published-as-part-of-intechopen-and-knowledge-unlatched-ku-collaboration-20220316",title:"50 Books published as part of IntechOpen and Knowledge Unlatched (KU) Collaboration"},{slug:"intechopen-joins-the-united-nations-sustainable-development-goals-publishers-compact-20221702",title:"IntechOpen joins the United Nations Sustainable Development Goals Publishers Compact"},{slug:"intechopen-signs-exclusive-representation-agreement-with-lsr-libros-servicios-y-representaciones-s-a-de-c-v-20211123",title:"IntechOpen Signs Exclusive Representation Agreement with LSR Libros Servicios y Representaciones S.A. de C.V"},{slug:"intechopen-expands-partnership-with-research4life-20211110",title:"IntechOpen Expands Partnership with Research4Life"}]},book:{item:{type:"book",id:"5450",leadTitle:null,fullTitle:"Polymerase Chain Reaction for Biomedical Applications",title:"Polymerase Chain Reaction for Biomedical Applications",subtitle:null,reviewType:"peer-reviewed",abstract:"Do you want to know the details that should be taken into consideration in order to have accurate conventional and real-time PCR results? If so, this book is for you. Polymerase Chain Reaction for Biomedical Applications is a collection of chapters for both novice and experienced scientists and technologists aiming to address obtaining an optimized real-time PCR result, simultaneous processing of a large number of samples and assays, performing PCR and RT-PCR on cell lysate without extraction of DNA or RNA, detecting false-positive PCR results, detecting organisms in viral and microbial diseases and hospital environment, following safety assessments of food products, and using PCR for introduction of mutations. This is a must-have book for any PCR laboratory.",isbn:"978-953-51-2796-3",printIsbn:"978-953-51-2795-6",pdfIsbn:"978-953-51-4133-4",doi:"10.5772/62968",price:119,priceEur:129,priceUsd:155,slug:"polymerase-chain-reaction-for-biomedical-applications",numberOfPages:184,isOpenForSubmission:!1,isInWos:1,isInBkci:!0,hash:"fcc7a13834f2748241be560e9c512a76",bookSignature:"Ali Samadikuchaksaraei",publishedDate:"December 14th 2016",coverURL:"https://cdn.intechopen.com/books/images_new/5450.jpg",numberOfDownloads:26258,numberOfWosCitations:41,numberOfCrossrefCitations:28,numberOfCrossrefCitationsByBook:0,numberOfDimensionsCitations:62,numberOfDimensionsCitationsByBook:0,hasAltmetrics:1,numberOfTotalCitations:131,isAvailableForWebshopOrdering:!0,dateEndFirstStepPublish:"April 12th 2016",dateEndSecondStepPublish:"May 3rd 2016",dateEndThirdStepPublish:"August 7th 2016",dateEndFourthStepPublish:"November 5th 2016",dateEndFifthStepPublish:"December 5th 2016",currentStepOfPublishingProcess:5,indexedIn:"1,2,3,4,5,6,8,9",editedByType:"Edited by",kuFlag:!1,featuredMarkup:null,editors:[{id:"187501",title:"Prof.",name:"Ali",middleName:null,surname:"Samadikuchaksaraei",slug:"ali-samadikuchaksaraei",fullName:"Ali Samadikuchaksaraei",profilePictureURL:"https://mts.intechopen.com/storage/users/187501/images/system/187501.jpeg",biography:"Professor Samadikuchaksaraei has received his MD degree from Iran University of Medical Sciences in 1998 and his Ph.D. degree from Imperial College London in 2005. His expertise is mainly focused on regenerative niche engineering for skeletal, integumentary and respiratory systems using stem cells and biomimetic materials. His publications, including book chapters, editorials, abstracts and original articles are published in collaboration with more than 300 scientists from more than 60 institutes in 10 different countries around the world. Some of his research outputs have been patented for commercial purposes. Prof. Samadikuchaksaraei serves on the editorial boards of several journals and regularly reviews for many high-profile publishers. Additionally, he reviews for granting bodies and patent and intellectual properties state organizations.",institutionString:"Iran University of Medical Sciences",position:null,outsideEditionCount:0,totalCites:0,totalAuthoredChapters:"0",totalChapterViews:"0",totalEditedBooks:"2",institution:{name:"Iran University of Medical Sciences",institutionURL:null,country:{name:"Iran"}}}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,coeditorOne:null,coeditorTwo:null,coeditorThree:null,coeditorFour:null,coeditorFive:null,topics:[{id:"384",title:"Chemical Biology",slug:"chemical-biology"}],chapters:[{id:"53176",title:"Guidelines for Successful Quantitative Gene Expression in Real- Time qPCR Assays",doi:"10.5772/65850",slug:"guidelines-for-successful-quantitative-gene-expression-in-real-time-qpcr-assays",totalDownloads:3609,totalCrossrefCites:3,totalDimensionsCites:4,hasAltmetrics:0,abstract:"This chapter was developed to provide some important guidelines for studies with quantitative PCR (qPCR) using either dyes or probes, citing several essential components necessary for a good PCR assay. The efficiency and specificity of quantitative PCR (qPCR) depend on several parameters related to mRNA quantification that must be controlled to avoid mistakes in data interpretation. Avoiding contamination with proteins, carbohydrate and phenolic compounds during RNA extraction and purification processes will improve RNA quality and provide reliable results. Specific primers and sensible probes are also crucial to intensify efficiency, specificity and fluorescence. Other parameters such as the optimization of primer concentrations and efficiency primer curves must be done. During gene-expression profile quantification, qPCR assays using reference genes are required to normalize the target gene expression data. These reference genes are checked for stability to identify the most stable genes among a group of candidate genes that will be used to normalize the qPCR data, using programs such as geNorm, BestKeeper and NormFinder. Additionally, the choice of appropriate reference genes for a specific experimental condition is fundamental. The main aim of this chapter is to provide guidelines and highlight precautions to obtain a successful qPCR assays.",signatures:"Antônio José Rocha, Rafael de Souza Miranda, Antônio Juscelino\nSudário Sousa and André Luis Coelho da Silva",downloadPdfUrl:"/chapter/pdf-download/53176",previewPdfUrl:"/chapter/pdf-preview/53176",authors:[{id:"188806",title:"Dr.",name:"Antônio",surname:"Rocha",slug:"antonio-rocha",fullName:"Antônio Rocha"}],corrections:null},{id:"52927",title:"High-Throughput Platforms in Real-Time PCR and Applications",doi:"10.5772/65760",slug:"high-throughput-platforms-in-real-time-pcr-and-applications",totalDownloads:2302,totalCrossrefCites:8,totalDimensionsCites:19,hasAltmetrics:0,abstract:"The miniaturization of reactions by designing nanoliter-scale PCR platforms, as Taqman® OpenArray®, Dynamic Array™, or SmartChip, has been a big step forward in real-time PCR. Each platform has some particular characteristics that differentiate them. These nanoliter-scale PCR platforms enable substantial savings in the amount of reagents and sample because the reaction volumes are at nanoliter levels. In addition, it is possible to perform thousands of reactions in a few hours. Therefore, high-throughput real-time PCR platforms result in promising systems that are capable of processing a large number of samples simultaneously and also to perform a large number of assays per sample. All of this can be translated in the amazing applicability of this technology in all kinds of analytical fields, such as medical research, animal science, and food safety, among others.",signatures:"Alexandre Lamas, Carlos Manuel Franco, Patricia Regal, José\nManuel Miranda, Beatriz Vázquez and Alberto Cepeda",downloadPdfUrl:"/chapter/pdf-download/52927",previewPdfUrl:"/chapter/pdf-preview/52927",authors:[{id:"127648",title:"Ms.",name:"Patricia",surname:"Regal",slug:"patricia-regal",fullName:"Patricia Regal"},{id:"171990",title:"Dr.",name:"José Manuel",surname:"Miranda",slug:"jose-manuel-miranda",fullName:"José Manuel Miranda"},{id:"189907",title:"Dr.",name:"Carlos",surname:"Franco",slug:"carlos-franco",fullName:"Carlos Franco"},{id:"194841",title:"Dr.",name:"Alexandre",surname:"Lamas",slug:"alexandre-lamas",fullName:"Alexandre Lamas"},{id:"194842",title:"Dr.",name:"Beatriz",surname:"Vázquez",slug:"beatriz-vazquez",fullName:"Beatriz Vázquez"},{id:"194843",title:"Dr.",name:"Aberto",surname:"Cepeda",slug:"aberto-cepeda",fullName:"Aberto Cepeda"}],corrections:null},{id:"52692",title:"Hot Cell-Direct PCR Aimed at Specific Cell Detection",doi:"10.5772/65806",slug:"hot-cell-direct-pcr-aimed-at-specific-cell-detection",totalDownloads:1594,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:1,abstract:"Since the polymerase chain reaction (PCR) was proposed, it has become an essential method in the field of biological gene analysis, providing a method to amplify DNA sequences of interest. To detect and/or analyze genes in cells, the gene or expressed gene must first be extracted before PCR. This procedure takes time and may result in the loss of samples. In order to avoid such drawbacks, two methods, hot cell-direct PCR and reverse transcription-PCR (RT-PCR), were invented, to detect genes in cells. Using hot cell-direct PCR, specific genes in microbial cells such as invA in Salmonella enterica have been easily detected and applied to discriminate Archaea from bacteria. As hot cell-direct PCR and RT-PCR are fairly simple processes, they can be applied to detect genes in single cells. We developed an original compact disc (CD)-shaped microfluidic device with microchambers for single-cell isolation and a detection system for expressed genes in isolated single cells in a microchamber on the device. We succeeded in the detection of PCR and RT-PCR products in individual cells and successfully detected S. enterica cells by hot cell-direct PCR. Expressed genes in Jurkat cells—human leukemia T cells—were analyzed by this method.",signatures:"Izumi Kubo, Yuko H. Itoh and Shunsuke Furutani",downloadPdfUrl:"/chapter/pdf-download/52692",previewPdfUrl:"/chapter/pdf-preview/52692",authors:[{id:"190351",title:"Prof.",name:"Izumi",surname:"Kubo",slug:"izumi-kubo",fullName:"Izumi Kubo"}],corrections:null},{id:"52932",title:"Regulatory Concern of Polymerase Chain Reaction (PCR) Carryover Contamination",doi:"10.5772/66294",slug:"regulatory-concern-of-polymerase-chain-reaction-pcr-carryover-contamination",totalDownloads:3317,totalCrossrefCites:4,totalDimensionsCites:13,hasAltmetrics:1,abstract:"Currently, DNA amplification techniques have become important detection tools. However, the extreme sensitivity of such techniques can easily result in contamination. This is a major problem in using these techniques routinely in a regulatory agency such as the Food and Drug Administration (FDA) because false-positive polymerase chain reaction (PCR) results will fail our mission. Preventing PCR carryover contamination and a capacity to rapidly determine false PCR positives are crucial. In the past, several methods have been used to prevent amplicon carryover contamination. In this chapter, we provide practical suggestions for PCR carryover contamination detection and prevention that work well with most PCR applications in our laboratory.",signatures:"Yuan Hu",downloadPdfUrl:"/chapter/pdf-download/52932",previewPdfUrl:"/chapter/pdf-preview/52932",authors:[{id:"189420",title:"Dr.",name:"Yuan",surname:"Hu",slug:"yuan-hu",fullName:"Yuan Hu"}],corrections:null},{id:"52768",title:"Multiplex Polymerase Chain Reaction Assay for Early Diagnosis of Viral Infection",doi:"10.5772/65771",slug:"multiplex-polymerase-chain-reaction-assay-for-early-diagnosis-of-viral-infection",totalDownloads:1938,totalCrossrefCites:3,totalDimensionsCites:6,hasAltmetrics:0,abstract:"Viral reactivation is one of the most serious complications for immunocompromised patients. Under immunosuppressive conditions, some viruses can be reactivated solely or simultaneously and may thus cause life-threatening infection. Therefore, the prompt and proper diagnosis of viral reactivation is important for the initiation of preemptive therapy. For this purpose, we recently developed a multiplex-virus polymerase chain reaction (PCR) assay. The multiplex PCR assay is designed to qualitatively measure the genomic DNA of 12 viruses at once: cytomegalovirus (CMV), human herpesvirus type 6 (HHV-6), HHV-7, HHV-8, Epstein-Barr virus (EBV), varicella-zoster virus (VZV), BK virus (BKV), JC virus (JCV), parvovirus B19 (ParvoB19), herpes simplex virus type 1 (HSV-1), HSV-2, and hepatitis B virus (HBV). When a specific PCR signal is obtained, the viral load is determined by a quantitative real-time PCR. The qualitative multiplex and quantitative real-time PCR procedures take only 3 hours to complete. With this assay system, we can identify viremia at the early stage and thereby prevent it from progressing to overt and symptomatic viral infection in immunocompromised patients, such as those receiving hematopoietic stem cell transplantation.",signatures:"Hiroko Tsunemine, Yuriko Yoshioka, Miho Nagao, Yasuhiro\nTomaru, Toshiharu Saitoh, Souichi Adachi, Norio Shimizu and\nTakayuki Takahashi",downloadPdfUrl:"/chapter/pdf-download/52768",previewPdfUrl:"/chapter/pdf-preview/52768",authors:[{id:"175658",title:"Dr.",name:"Hiroko",surname:"Tsunemine",slug:"hiroko-tsunemine",fullName:"Hiroko Tsunemine"}],corrections:null},{id:"52716",title:"The Advantages of Using Multiplex PCR for the Simultaneous Detection of Six Sexually Transmitted Diseases",doi:"10.5772/65901",slug:"the-advantages-of-using-multiplex-pcr-for-the-simultaneous-detection-of-six-sexually-transmitted-dis",totalDownloads:2466,totalCrossrefCites:2,totalDimensionsCites:2,hasAltmetrics:1,abstract:"Sexually transmitted diseases (STDs) are among the most common infections. Their clinical identification is difficult because STDs are often asymptomatic. Untreated infections with these pathogens can in time lead to serious consequences. It is documented that isolation of some of these bacteria from cultures is very difficult. Because there is a large number of STD pathogens which can generate coinfections, their simultaneous detection in a unique sample is very important. Multiplex polymerase chain reaction (PCR) is an advanced method of molecular biology which allows for simultaneous detection of multiple pathogens in the same sample. The advantages of the multiplex PCR method were assessed by various researchers by comparing the diagnosis results obtained with different other conventional methods. The sensitivity and specificity of these methods were analyzed on different specimens in comparison to traditional methods, such as culture media or direct microscopic examination. These studies demonstrated beyond any doubt that the multiplex PCR system is highly effective in the detection of each of multiple STD pathogens depicted from a single specimen and argued for multiplex PCR superiority in terms of sensitivity and rapidity.",signatures:"Mihaela L. Vică, Horea V. Matei and Costel V. Siserman",downloadPdfUrl:"/chapter/pdf-download/52716",previewPdfUrl:"/chapter/pdf-preview/52716",authors:[{id:"189561",title:"Dr.",name:"Mihaela Laura",surname:"Vica",slug:"mihaela-laura-vica",fullName:"Mihaela Laura Vica"},{id:"192251",title:"Dr.",name:"Horea Vladi",surname:"Matei",slug:"horea-vladi-matei",fullName:"Horea Vladi Matei"},{id:"192252",title:"Dr.",name:"Costel Vasile",surname:"Siserman",slug:"costel-vasile-siserman",fullName:"Costel Vasile Siserman"}],corrections:null},{id:"52654",title:"A Real-Time PCR-Based Diagnostic Test for Organisms in Respiratory Tract Infection",doi:"10.5772/65740",slug:"a-real-time-pcr-based-diagnostic-test-for-organisms-in-respiratory-tract-infection",totalDownloads:2037,totalCrossrefCites:3,totalDimensionsCites:7,hasAltmetrics:0,abstract:"Respiratory tract infection, especially pneumonia, is a significant cause of morbidity and mortality worldwide. Although rapid and accurate identification of the pathogens and the corresponding treatment, which is based on the microbiological results, is required in the healthcare setting, the current clinical tests lack high sensitivity and flexibility. As of yet, a comprehensive approach has not been able to work these issues out. Meanwhile, the development of molecular techniques enables the detection of organisms from respiratory specimens speedily as well as precisely and aids the settlement of such issues. With our novel approach that employs relative quantification, we successfully set the cutoff value to discriminate the causative pathogen from colonizing commensal organisms by real-time PCR. In this way, a diagnostic system for respiratory pathogens was devised and validated through clinical sample testing. In this chapter, a real-time PCR-based test capable of differentiating causative pathogens in respiratory specimens is described, and also its principle and the utility of this approach are illustrated.",signatures:"Takashi Hirama",downloadPdfUrl:"/chapter/pdf-download/52654",previewPdfUrl:"/chapter/pdf-preview/52654",authors:[{id:"189067",title:"Dr.",name:"Takashi",surname:"Hirama",slug:"takashi-hirama",fullName:"Takashi Hirama"}],corrections:null},{id:"52868",title:"PCR Technique for the Microbial Analysis of Inanimate Hospital Environment",doi:"10.5772/65742",slug:"pcr-technique-for-the-microbial-analysis-of-inanimate-hospital-environment",totalDownloads:1970,totalCrossrefCites:4,totalDimensionsCites:7,hasAltmetrics:0,abstract:"Discipline of molecular ecology and molecular techniques such as polymerase chain reaction (PCR) offers a possibility to study and reveal the microbial diversity in environmental settings with complicated mixed communities, non-culturable organisms, interfering contaminants and low levels of target DNA. Hospital environment represents a new ecological niche for clinically important nosocomial pathogens and antibiotic-resistant microorganisms, which have been commonly found on various hospital surfaces. Accurate characterization of microbial communities depends on several factors, starting with sample collection and conditional enrichment step. In the step of nucleic acid isolation and purification, the DNA, as a dominant signature molecule, is extracted followed by removing co-extracted impurities. PCR target sequences are often 16S rDNA gene, functional gene probes or species-specific probes, depending on the objective of the study. Furthermore, properly prepared PCR amplicons can serve as a basis for characterizing microbial community. The PCR technique is a powerful tool for the analysis of microbial diversity of environmental ecosystems. In a hospital environment, advantages of detecting pathogens and antibiotic-resistant bacteria need to be pointed out.",signatures:"Urška Rozman and Sonja Šostar Turk",downloadPdfUrl:"/chapter/pdf-download/52868",previewPdfUrl:"/chapter/pdf-preview/52868",authors:[{id:"189776",title:"Ph.D.",name:"Urška",surname:"Rozman",slug:"urska-rozman",fullName:"Urška Rozman"}],corrections:null},{id:"52972",title:"PCR: A Powerful Method in Food Safety Field",doi:"10.5772/65738",slug:"pcr-a-powerful-method-in-food-safety-field",totalDownloads:2418,totalCrossrefCites:1,totalDimensionsCites:4,hasAltmetrics:1,abstract:"In this chapter, application of the polymerase chain reaction (PCR) technique in food safety, considering all the branches of this concept, is presented. The area of interest contains important analysis for both human health and the identification of food adulteration. PCR techniques used for detection of genetically modified organisms (GMO) in different matrices, identification of different animal species in meat and dairy products, as well as the detection of food infection with food-borne pathogens and toxicogenic fungi are described. The working methods and result analysis are exemplified, starting with DNA isolation adjusted to different matrices, detection of target genes, and validation for all of these methods. Techniques of simplex PCR, primer multiplexing, primer design, validation of the laboratory methods, optimization of the PCR results, and result interpretation through the analysis of the electrophoresis gels and sequencing data are studied. At the same time, the obtained results, the obstacles encountered, and how they were overcome could be an example for specific analysis developed with less resources and also for adapting the existent validated methods to the new laboratory conditions. The practical applicability and the consumer’s demands are of great importance and always must be considered in developing and validating those methods.",signatures:"Oana-Maria Boldura and Sorina Popescu",downloadPdfUrl:"/chapter/pdf-download/52972",previewPdfUrl:"/chapter/pdf-preview/52972",authors:[{id:"189429",title:"Prof.",name:"Oana-Maria",surname:"Boldura",slug:"oana-maria-boldura",fullName:"Oana-Maria Boldura"},{id:"189451",title:"Prof.",name:"Sorina",surname:"Popescu",slug:"sorina-popescu",fullName:"Sorina Popescu"}],corrections:null},{id:"52975",title:"Site‐Directed Mutagenesis by Polymerase Chain Reaction",doi:"10.5772/66429",slug:"site-directed-mutagenesis-by-polymerase-chain-reaction",totalDownloads:4608,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:"Since genomic data are widely available, many strategies have been implemented to reveal the function of specific nucleotides or amino acids in promoter regions or proteins, respectively. One of the methods most commonly used to determine the impact of mutations is the site‐directed mutagenesis using the polymerase chain reaction (PCR). There are different published protocols to develop single or multiple site‐directed mutagenesis. In this chapter, we reviewed the enzymes commonly used in site‐directed mutagenesis, the methods for simple and multiple site‐directed mutagenesis in large constructs, mediated by insertion of restriction sites. Other methods reviewed include high‐throughput site‐directed mutagenesis using oligonucleotides synthesized on DNA chips, and those based on multi‐site‐directed mutagenesis, based on recombination. Software tools to design site‐directed mutagenesis primers are also presented.",signatures:"Fabiola Castorena‐Torres, Katia Peñuelas‐Urquides and Mario\nBermúdez de León",downloadPdfUrl:"/chapter/pdf-download/52975",previewPdfUrl:"/chapter/pdf-preview/52975",authors:[{id:"188810",title:"Dr.",name:"Mario",surname:"Bermúdez De León",slug:"mario-bermudez-de-leon",fullName:"Mario Bermúdez De León"},{id:"188821",title:"Dr.",name:"Fabiola",surname:"Castorena Torres",slug:"fabiola-castorena-torres",fullName:"Fabiola Castorena Torres"},{id:"198351",title:"Dr.",name:"Katia",surname:"Peñuelas Urquides",slug:"katia-penuelas-urquides",fullName:"Katia Peñuelas Urquides"}],corrections:null}],productType:{id:"1",title:"Edited Volume",chapterContentType:"chapter",authoredCaption:"Edited by"},subseries:null,tags:null},relatedBooks:[{type:"book",id:"7639",title:"Bioinformatics Tools for Detection and Clinical Interpretation of Genomic Variations",subtitle:null,isOpenForSubmission:!1,hash:"94f9f01b510ca80812f0eee467f9428b",slug:"bioinformatics-tools-for-detection-and-clinical-interpretation-of-genomic-variations",bookSignature:"Ali Samadikuchaksaraei and Morteza Seifi",coverURL:"https://cdn.intechopen.com/books/images_new/7639.jpg",editedByType:"Edited by",editors:[{id:"187501",title:"Prof.",name:"Ali",surname:"Samadikuchaksaraei",slug:"ali-samadikuchaksaraei",fullName:"Ali Samadikuchaksaraei"}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}},{type:"book",id:"2553",title:"Lipid Peroxidation",subtitle:null,isOpenForSubmission:!1,hash:"b39734aa940b2d63ae5e8773d3dd5280",slug:"lipid-peroxidation",bookSignature:"Angel Catala",coverURL:"https://cdn.intechopen.com/books/images_new/2553.jpg",editedByType:"Edited by",editors:[{id:"196544",title:"Prof.",name:"Angel",surname:"Catala",slug:"angel-catala",fullName:"Angel Catala"}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}},{type:"book",id:"2323",title:"Carbohydrates",subtitle:"Comprehensive Studies on Glycobiology and Glycotechnology",isOpenForSubmission:!1,hash:"f7c2e6a3566eee14c9884ad0820a6416",slug:"carbohydrates-comprehensive-studies-on-glycobiology-and-glycotechnology",bookSignature:"Chuan-Fa Chang",coverURL:"https://cdn.intechopen.com/books/images_new/2323.jpg",editedByType:"Edited by",editors:[{id:"145728",title:"Prof.",name:"Chuan-Fa",surname:"Chang",slug:"chuan-fa-chang",fullName:"Chuan-Fa Chang"}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}},{type:"book",id:"372",title:"Aflatoxins",subtitle:"Biochemistry and Molecular Biology",isOpenForSubmission:!1,hash:"b7f7359995dc5ee04e12df282495f77e",slug:"aflatoxins-biochemistry-and-molecular-biology",bookSignature:"Ramón Gerardo Guevara-González",coverURL:"https://cdn.intechopen.com/books/images_new/372.jpg",editedByType:"Edited by",editors:[{id:"62559",title:"Dr.",name:"Ramon G.",surname:"Guevara-Gonzalez",slug:"ramon-g.-guevara-gonzalez",fullName:"Ramon G. 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People have always migrated and have moved, but, specifically looking at the last three hundred years, involuntary migration is on the rise. Involuntary migration does not only affect Europe; Asia, Africa, and North as well as South America, have had their fair share of natural catastrophes, invasions, and wars.
\r\n\tThis book will intend to look at different migrant patterns, voluntary and involuntary migration, over the last three centuries. What influenced people to leave their home countries, family, and friends and settle somewhere else? The book may include histories of the 19th century, consider tragedies and movements activated by political events in the 20th century, and/or look at recent events of the 21st century. Push and pull factors are important points. While most of us may be influenced in a negative way by the current happenings in Eastern Europe, the Russian invasion and resulting tragedies also demonstrate some very positive human traits – the preparedness of Ukraine’s surrounding countries to help those in need and to provide a safe place for the present.
\r\n\tWhether one looks at voluntary or involuntary migration into any country, after a period of adjustment, migrants do play a positive role. The research found that migrants contribute to the economy (food, shelter, employment, tax) and enrich a country’s cultural norms. Prerequisites for successful settlements are that the host society adopts a tolerant approach and that the migrants recognize the law and the language of the host country. Nothing is ever easy or without controversy, but I am a migrant (German Australian), and life in Australia has been relatively harmonious. Issues that could be considered in the book are multicultural societies (do monocultural societies still exist?) and theories of acculturation versus integration (settlement processes).
\r\n\tTwo further issues are very important in relation to human migration. There is climate change, global warming, and the environment, which clearly affect people’s movement. Small island populations are very concerned about rising sea levels. 2021 has also seen floods costing human lives: Turkey (August 2021), Brazil (December 2021), Chile (January 2021), and South India (November 2021), to name but a few. In Australia (March 2022), farms and whole townships in New South Wales and Queensland have been flooded for the second time in five years, and plans to resettle these towns are considered. Official and social media provide ample coverage of the events, which leads me to the next issue. There is today’s very important role of the media, of the official and social media. We are constantly bombarded with images of human war tragedies and flood victims. People in industrialized, western countries must be the best-informed populace. How far do the images and up-to-date TV news influence us, make us change our behavior, and perhaps even consider us more generous than we have been?
\r\n\tClimate change and the media are relatively new to the human migration debate, but both issues play important parts, and some interesting discussions are appreciated.
\r\n\t
Tuberculosis (TB) is a chronic infectious disease affecting any part of the body but more commonly the lungs [1]. It is one of the most prevalent human infections and is the second leading cause of deaths from infectious diseases worldwide [2]. In 2013, 80% of TB cases occurred in 22 high-burden countries leading to 1.5 million deaths. Nigeria is the fourth among these 22 countries, wherein the World Health Organization (WHO) estimates an incidence rate for all forms of tuberculosis to be ‘311 per 100,000 populations, incidence of smear positive annually 131 per 100,000 population and prevalence of 546 per 100,000 populations [3, 4]’. Also, TB services are provided mostly as part of the primary health services followed by secondary and tertiary healthcare provided by public and private institutions. Within the public sector, TB consultations, diagnostic, drugs and hospitalization services are provided free of charge [4]. At the private facilities, TB diagnostic and treatment services are provided free of charge; however, all patients irrespective of their health problem visiting the facility pay administrative fees. Following diagnosis, TB patients admitted at the private hospitals are required to pay additional fees for accommodation and feeding. If in any way the care provided in these facilities is found to be substandard, then this will result in poor treatment outcomes, persistent infectiousness as well as possible emergence and spread of drug-resistant strains [2].
The facilities at which TB care is provided are called directly observed therapy (DOTS); their scope of service includes diagnosis of TB (where microscopy services are available), supervised TB treatment, health education and adherence counseling, as well as HIV counseling and testing [4]. While the DOTS approach has been in place and seems to have lessened the burden of care on patients, access and adherence to TB treatment still face multiple challenges at different levels including individual and those that are a result of the system [5, 6, 7].
Individual-level barriers involve physical (distance to TB services and access to transport), financial (the direct and indirect costs of seeking TB services), stigma (stigma surrounding TB and its association with HIV), health literacy (TB-related knowledge and education) and sociocultural (gender roles and status in the family) factors, whereas provider-/system-level barriers include provider’s degree of suspicion for TB, the number and types of providers seen before TB diagnosis, provider adherence to national TB program guidelines and patient satisfaction with TB services [2, 6, 7]. Due to these challenges, a comprehensive understanding of barriers is needed in order to provide insight into TB service programs, research and policy. It is against this background that this study was designed to determine individual and provider’s barriers and delays that limit access and adherence to TB services.
This study was an exploratory cross-sectional design. The study was conducted from June 2016 until November 2016 in 16 randomly selected DOTS facilities in Ibadan, Oyo State, Nigeria.
Nigeria lies on the west coast of Africa between latitudes 4°16′ and 13°53′ north and longitudes 2°40′ and 14°41′ east. It occupies approximately 923,768 square kilometers of land stretching from the Gulf of Guinea on the Atlantic coast in the south to the fringes of the Sahara Desert in the north. The territorial boundaries are defined by the Republics of Niger and Chad in the north, the Republic of Cameroon on the east and the Republic of Benin on the west. Nigeria is the most populous country in Africa and the 14th largest in land mass. The country’s last census conducted in 2006 placed the country’s population at 140,431,790 with a national growth rate estimated at 3.2% per annum [8].
Ibadan is the largest indigenous city south of the Sahara and is located at an altitude generally ranging from 152 m to 213 m with isolated ridges and peaks rising to 274 m. It is the state capital of Oyo State (see Figure 1 above) which is near the forest grassland boundary of south-west of Nigeria on longitude 3° east of the Greenwich meridian and latitude 7° north of the equator. It is at a distance of about 145 km north-east of Lagos. Oyo State is divided into 33 local government area. It comprises largely the Yoruba-speaking tribe and other ethnic groups. Ibadan is dominantly a civil service city with some level of industrial activity, private businesses and other forms of trade and peasant jobs. The estimated population is 2.6 million people. Religious groups in the city are the Christians, Muslims and traditionalists. The study sites include those that are randomly selected from the under listed DOTS centers in Ibadan within the LGAs (strata): (i) Moniya Primary Health Care, (ii) Ojoo Primary Health Care, (iii) Odogbo Military Hospital, (iv) SDP Primary Health Care, (v) Iwo Road Primary Health Care, (vi) Alafia Hospital, (vii) Medical Outpatients-University College Hospital, (viii) Adeoyo Maternity Hospital, (ix) Jaja Health Services-University of Ibadan, (x) Alafara Primary Health Care, (xi) Agodi Prisons, (xii) OLA Catholic Hospital, (xiii) Sabo Primary Health Care, (xiv) Oniyanrin Primary Health Care, (xv) Atolu Primary Health Care, (xvi) Iyana Church, (xvii) Ejiku Primary Health Care, (xviii) Agbongbon Primary Health Care, (xix) SMG Catholic Hospital, (xx) Molete Primary Health Care, (xxi) Adifase Primary Health Care, (xxii) Chest Hospital Jericho, (xxiii) Olomi Primary Health Care, (xxiv) Ring Road State Hospital and (xxv) Apete Primary Health Care.
Nigeria (Ibadan, south-west of Nigeria). (Source: Nigeria Demographic and Health Survey, 2013).
The sampling technique was a multistage stratified random sampling technique. The first stage was to identify all the LGAs in Ibadan, classify the LGAs into strata and make a random selection of LGAs. The second stage was a random selection of the DOTS facility within the selected LGAs from which simple random selection of consenting TB patients attending DOTS facility at the hospitals/health facilities will be was attained. This multistage stratified random sampling technique was employed with the aim of precluding investigator bias and ensuring that the study population selected for the study is representative of TB patients in the study location.
Using the logic for calculating the analysis of variance (ANOVA) that is a collection of statistical models for the analysis of differences among group (DOTS centers) means (includes variations within and without/between groups). The assumption is that the groups are independent (unrelated). ANOVA has the advantage of assessing the importance of one or more factors by comparing the response variable means at the different factor levels:
Effect size: 0.5
Type 1 error: 0.05
Type 2 error: 0.2
Power: 0.80
Number of groups: 2 (representing DOTS centers within each LGA)
Critical F value: 4.15 (value which F should be over to get a significant result)
34 Participants × 16 DOTS facilities = 544 participants.
Assuming nonresponding rate of 20%.
Adjusted sample size (N1) = N/1 − q.
where q = 0.2; N1 = 544/1–0.2 = 680 participants (a
Ethical approval for the study was obtained from the University of KwaZulu-Natal (South Africa), Biomedical Research Ethics Committee’s approval number (BE233/16). Additional approval was given by the Oyo State’s Ministry of Health Ethics Committee (AD 13/479/1045). A full consenting process was applied in respect of all participants.
A descriptive analysis assessing the association between individuals’ sociodemographic and clinical characteristics (independent variable) and system-related barriers (dependent variables) was conducted. The individuals’ sociodemographic characteristics were age, distance from facility, marital status, family type, education, religion, ethnic group and wealth index. The individuals’ clinical characteristics were treatment status, where individuals access healthcare, how often individual access healthcare and HIV status. The system-related barriers were the quality of access to care, the healthcare worker attitude, the healthcare center’s appearance, the number of people seeking treatment and the waiting time at the healthcare center. Chi-square tests were used to determine the associations between sociodemographic and clinical characteristic associations with the individual and system-related barriers. Logistic regression models reporting odds ratios (OR) and 95% confidence intervals were used to determine the relationship between sociodemographic and clinical characteristics with the individual and system-related barriers.
The results show that 59.25% (410) of individuals believed that the quality of access to care was excellent, 89.33% (611) of individuals believed that the attitude of healthcare workers was positive, 78.44% (542) of individuals believed that the appearance of the healthcare facility they attended was excellent, 75.40% (518) of individuals believed that there were many people accessing healthcare facilities and 82.33% (559) reported that they waited less than 30 minutes at a healthcare facility (see Table 1).
Access to care | Frequency (%) |
---|---|
Excellent | 410 (59.25) |
Not excellent | 282 (40.75) |
Positive | 611 (89.33) |
Not positive | 73 (10.67) |
Excellent | 542 (78.44) |
Not excellent | 149 (21.56) |
Many | 518 (75.40) |
Few | 169 (24.60) |
0–30 minutes | 559 (82.33) |
More than 30 minutes | 120 (17.67) |
Proportion of health system-related factors.
The sociodemographic descriptive statistics show that the distance from facility, family type and wealth index were significantly associated with the quality of access to care. Education was partially associated. Education was significantly associated with healthcare worker attitude. Family type was partially significant. The distance from the healthcare facility was associated with the appearance of the facility. Education, religion, ethnic group and wealth index were significantly associated with education which was significantly associated with the waiting time at the healthcare center. Family type was partially associated (see Table 2).
Access to care | Total | Excellent | Not excellent | p-Value |
---|---|---|---|---|
0.847 | ||||
Less than 20 | 55 | 56.3631 | 43.64 (24) | |
21–30 | 183 | 56.28 (103) | 43.72 (80) | |
31–40 | 200 | 59.00 (118) | 41.00 (82) | |
41–50 | 112 | 62.50 (70) | 37.50 (42) | |
51–60 | 66 | 59.09 (39) | 40.91 (27) | |
60+ | 46 | 65.22 (30) | 34.78 (16) | |
<0.001 | ||||
< 5 km | 252 | 69.44 (175) | 30.56 (77) | |
5–10 km | 255 | 47.84 (122) | 52.16 (133) | |
> 10 | 185 | 61.08 (113) | 38.92 (72) | |
0.972 | ||||
Never married | 212 | 59.43 (126) | 40.57 (86) | |
Married | 479 | 59.29 (284) | 40.71 (195) | |
0.049 | ||||
Monogamous | 440 | 61.82 (272) | 38.18 (168) | |
Polygamous | 237 | 54.01 (128) | 45.99 (109) | |
0.088 | ||||
Pre-high school | 233 | 54.08 (126) | 45.92 (107) | |
High school | 282 | 60.64 (171) | 39.36 (111) | |
College/higher education | 175 | 64.57 (113) | 35.43 (62) | |
0.337 | ||||
Christian | 330 | 59.70 (197) | 40.30 (133) | |
Islam | 359 | 58.50 (210) | 41.50 (149) | |
Traditional | 3 | 100.00 (3) | 0.00 (0) | |
0.622 | ||||
Yoruba | 652 | 58.90 (384) | 41.10 (268) | |
Igbo | 26 | 61.54 (16) | 38.46 (10) | |
Hausa | 14 | 71.43 (10) | 28.57 (4) | |
0.003 | ||||
Lower class | 226 | 65.04 (147) | 34.96 (79) | |
Lower middle class | 146 | 65.07 (95) | 34.93 (51) | |
Upper middle class | 262 | 50.38 (132) | 49.62 (130) | |
Upper class | 58 | 62.07 (36) | 37.93 (22) |
Sociodemographic characteristics stratified by access to care.
The clinical descriptive statistics show that where individuals access healthcare and how often individual access healthcare and HIV status were significantly associated with access to care. HIV status was significantly associated with healthcare worker attitude. Where individuals access healthcare and how often individuals access healthcare were significantly associated with perceptions about healthcare center’s appearance. Where individuals access healthcare was significantly associated with the number of people seeking care. HIV status was partially associated. Where individuals access healthcare and HIV status was significantly associated with waiting time at the healthcare center (see Table 3).
Access to care | Total | Excellent | Not excellent | p-Value |
---|---|---|---|---|
0.781 | ||||
Retreatment | 47 | 61.70 (29) | 38.30 (18) | |
Relapse | 44 | 54.55 (24) | 45.45 (20) | |
New treatment | 552 | 58.88 (325) | 41.12 (227) | |
<0.001 | ||||
Private clinic | 179 | 44.13 (79) | 55.87 (100) | |
Non-private clinic | 508 | 64.57 (328) | 35.43 (180) | |
0.001 | ||||
More than once a year | 443 | 52.60 (233) | 47.40 (210) | |
Not more than once a year | 169 | 67.46 (114) | 32.54 (55) | |
0.029 | ||||
Reactive | 49 | 63.27 (31) | 36.73 (18) | |
Non-reactive | 567 | 59.44 (337) | 40.56 (230) | |
Do not know | 41 | 39.02 (16) | 60.98 (25) | |
<0.001 | ||||
Positive | 611 | 62 (279) | 38 (232) | |
Not positive | 73 | 34.2 (25) | 65.8 (48) | |
<0.001 | ||||
Excellent | 611 | 62 (279) | 38 (232) | |
Not excellent | 73 | 34.2 (25) | 65.8 (48) | |
0.270 | ||||
Many | 518 | 60.4 (313) | 39.6 (205) | |
Few | 169 | 55.6 (94) | 45.4 (75) | |
0.003 | ||||
0–30 minutes | 558 | 60.4 (342) | 39.6 (216) | |
More than 30 minutes | 120 | 55.6 (56) | 44.4 (64) |
Participants’ clinical and care-related characteristics.
Access to care | OR | 95% Conf. interval | p-Value |
---|---|---|---|
<5 km (ref) | |||
5–10 km | 2.48 | 1.72–3.56 | <0.001 |
>10 km | 1.45 | 0.97–2.16 | 0.069 |
Monogamous (ref) | |||
Polygamous | 1.38 | 1.00–1.90 | 0.049 |
OR | 95% Conf. interval | p-Value | |
Monogamous (ref) | |||
Polygamous | 1.58 | 0.96–2.61 | 0.069 |
Pre-high school (ref) | |||
High school | 0.44 | 0.24–0.81 | 0.009 |
College/higher education | 1.02 | 0.57–1.80 | 0.959 |
OR | 95% Conf. interval | p-Value | |
<5 km (ref) | |||
5–10 km | 0.41 | 1.25–2.91 | 0.003 |
>10 km | 0.99 | 0.60–1.63 | 0.965 |
OR | 95% Conf. interval | p-Value | |
Pre-high school (ref) | |||
High school | 2.54 | 1.66–3.88 | <0.001 |
College/higher education | 1.26 | 0.76–2.08 | 0.379 |
Christian (ref) | |||
Islam | 1.18 | 0.83–1.67 | 0.361 |
Traditional | Null (too few observations in sample) | ||
Yoruba (ref) | |||
Igbo | 1.74 | 0.76–3.98 | 0.190 |
Hausa | 5.91 | 1.95–17.91 | 0.002 |
Lower class (ref) | |||
Lower middle class | 0.91 | 0.55–1.50 | 0.720 |
Upper middle class | 1.30 | 0.87–1.95 | 0.204 |
Upper class | 0.43 | 0.19–1.01 | 0.054 |
OR | 95% Conf. interval | p-Value | |
Pre-high school (ref) | |||
High school | 0.48 | 0.30–0.78 | 0.003 |
College/higher education | 0.98 | 0.6–1.59 | 0.944 |
Sociodemographic characteristic regression models.
Access to care | OR | 95% Conf. interval | p-Value |
---|---|---|---|
Private clinic (ref) | |||
Non-private clinic | 0.43 | 0.31–0.61 | < 0.001 |
More than once a year (ref) | |||
Not more than once a year | 0.54 | 0.37–0.78 | 0.001 |
Reactive (ref) | |||
Non-reactive | 1.18 | 0.64–2.15 | 0.600 |
Do not know | 2.69 | 1.14–6.33 | 0.023 |
OR | 95% Conf. interval | p-Value | |
Reactive (ref) | |||
Non-reactive | 2.81 | 0.6–11.86 | 0.160 |
Do not know | 6.61 | 1.34–32.63 | 0.020 |
OR | 95% Conf. interval | p-Value | |
Private clinic (ref) | |||
Non-private clinic | 0.45 | 0.31–0.65 | < 0.001 |
More than once a year (ref) | |||
Not more than once a year | 0.57 | 0.40–0.81 | 0.002 |
OR | 95% Conf. interval | p-Value | |
Private clinic (ref) | |||
Non-private clinic | 0.48 | 0.33–0.70 | < 0.001 |
Reactive (ref) | |||
Non-reactive | 0.57 | 0.31–1.04 | 0.068 |
Do not know | 0.35 | 0.13–0.96 | 0.042 |
OR | 95% Conf. interval | p-Value | |
Private clinic (ref) | |||
Non-private clinic | 1.98 | 1.19–3.32 | 0.009 |
Clinical characteristic regression models.
The regression models show that those who lived 5 km–10 km from the healthcare facility were significantly more likely to believe that the quality of access to care was not excellent compared to those who lived within 5 km (OR, 2.48; CI, 1.72–3.56; p < 0.001). Those from polygamous families were more likely to believe that the quality of access to care was not excellent compared to those from monogamous families (OR, 1.38; CI, 1.00–1.90; p = 0.049) (see Table 4). Those individuals who did not usually get care at private clinics were significantly less likely to believe that the quality of access to care was not excellent (OR, 0.43; CI, 0.31–0.61; p < 0.001). Those individuals who accessed care not more than once a year were significantly less likely to believe that the quality of access to care was not excellent compared to those who accessed care more than once a year (OR, 0.54; CI, 0.37–0.78; p = 0.001). Those who did not know their HIV status were significantly more likely to believe that the quality of access to care was not excellent compared to those who were reactive (OR, 2.69; CI, 1.14–6.33; p = 0.023) (see Table 5).
Those individuals who had a high school education were significantly less likely to believe that the attitude of the healthcare workers was not positive compared to those who only had a pre-high school education (OR, 0.44; CI, 0.24–0.81; p = 0.009) (see Table 4). Those individuals who did not know their HIV status were significantly more likely to believe that the attitude of the healthcare workers was not positive compared to those who were reactive (OR, 6.61; 1.34–32.63; p = 0.020) (see Table 5).
Those individuals who lived 5 km to 10 km were significantly less likely to believe that the appearance of the healthcare facility was not excellent compared to those who lived within 5 km of the healthcare facility (OR, 0.41; CI, 1.25–2.91; p = 0.003) (see Table 4). Those individuals who did not access care at private clinics were significantly less likely to believe that the appearance of the healthcare facility was not excellent (OR, 0.45; CI, 0.31–0.65; p < 0.001). Those individuals who did not access healthcare more than once a year were significantly less likely to believe that the appearance of the healthcare facility was not excellent compared to those who accessed healthcare more than once a year (OR, 0.57; CI, 0.40–0.81; p = 0.002) (see Table 5).
Those with a high school education were significantly more likely to believe that there were few people accessing healthcare facilities compared to those with pre-high school education (OR, 2.54; CI, 1.66–3.88; p < 0.001). Those of the Hausa ethnic group were significantly more likely to believe that there were few people accessing healthcare facilities (OR, 5.91; CI, 1.95–17.91; p = 0.002). Those who did not access care at private clinics were significantly less likely to believe that there were few people accessing healthcare (OR, 0.48; CI, 0.33–0.70; p < 0.001). Those individuals who did not know their HIV status were significantly less likely to believe that there were few people accessing care compared to those who were reactive (OR, 0.35; CI, 0.13–0.96; p = 0.042) (Table 5).
Those individuals who had a high school education were significantly less likely to report waiting more than 30 minutes at the healthcare facility compared to those who had a pre-high school education (OR, 0.48; CI, 0.30–0.78; p = 0.003) (see Table 4). Those individuals who did not access healthcare at private hospital were significantly more likely to report waiting more than 30 minutes at a healthcare facility compared to those who accessed healthcare at private clinics (OR, 1.98; CI, 1.19–3.32; p = 0.009) (see Table 5).
In this study, we determined individual and provider’s barriers and delays that limited access and adherence to TB services in 16 hospitals based in one state of Nigeria. We determined this through assessing the association between sociodemographic and quality of access to care, healthcare worker attitude, healthcare facility appearance, number of people accessing healthcare, as well as waiting time at healthcare facility. Our findings supported those reported in previous studies; for example, we report that living outside 5 km from the health facility was associated with poor perception of access to quality care [9, 10, 11]. This finding could be linked to the cost of time and transport incurred in traveling to the healthcare facility and the time taken to receive service upon arrival to the facility especially with treatment such as TB which requires continued contact with healthcare providers [12, 13]. We found that coming from a polygamous marriage or family was linked to significantly associating with not linking healthcare with good quality.
Also, individuals who were never exposed to private healthcare were likely to view public healthcare as providing excellent service. This finding might be due to their inability to compare the services they receive with those provided in private healthcare services. Private healthcare systems are associated with advanced resources, less waiting time and better treatment outcomes; it is therefore not surprising that in our study those who had a pre-exposure to private healthcare were likely to view the current healthcare service as not excellent [13, 14].
Those who knew their HIV status were likely to believe that the quality of care was excellent. This finding is significant because previous findings have shown that co-infection of HIV/TB can lead to negative side effects, high drug burden and poor treatment outcome [14, 15, 16]. The perception by TB-/HIV-co-infected patients that healthcare service was excellent might mean that despite experiencing a double burden of the diseases, access to treatment may be less strenuous as they access treatment at the same facility and are more familiar with the operation of the facility as well as healthcare providers.
Our second aim was to understand the attitudes of participants toward healthcare workers; we found that those who were HIV positive and with high school education, respectively, were likely to perceive healthcare worker’s attitude positively. The finding that having high school education was associated with positive attitude toward healthcare providers could be linked with patient’s ability to understand the instructions with minimal dependence or assistance from healthcare workers. Also, the difference in satisfaction and sociodemographic factor such as education can be explained through the different expectations which patients may have toward how health providers should care for them. Although this may be the case, it is important that patients have a positive perception of healthcare workers in order to comply to treatment and hospital visits [6, 17]. A positive relationship between healthcare providers and patient was found to be linked to patients playing an active role in the management of their disease and adherence until the end of the treatment [18, 19].
The following limitations in this study are acknowledged: the study was cross-sectional, collecting data at one point. The views of the participants may have changed after our first contact with them. Although our findings cannot be generalized because they were conducted in 16 health facilities in one country, the self-reported perception of participants was similar across the different facilities.
Providing good quality care to patients is an ongoing practice, which requires continued consultation with everybody involved including patients who are at the receiving end of the service in order to evaluate and improve on the services rendered. Such practices will motivate compliance to treatment and a collaborative relationship between patients and healthcare providers in TB management. Despite several challenges affecting treatment and patient care, this study reports that healthcare provision was generally satisfactory. Findings from this study are significant in guiding policy and interventions for resource-limited settings.
The authors wish to thank the Dean of Research, College of Health Sciences (Professor Moses Chimbari) for his support and encouragement. We also extend our profound gratitude to the Country Representative of Damien Foundation Belgium (Nigeria Project) (Dr. Osman Eltayeb) and the entire team from the Oyo State Tuberculosis Control Program for their inestimable supports. Dr. Oladimeji is an African Research Fellow hosted by Human Sciences Research Council (HSRC), South Africa, and also has honorary affiliation with Walter Sisulu University (WSU), South Africa. He is indeed grateful for the conducive research environments (HSRC and WSU) provided for him.
The authors declared no competing interests.
OO and JMT conceptualized the idea and designed the study. Data collection, cleaning and processing were conducted by OO. Data analysis and interpretation were conducted by OO, LM and LM OA and supervised by JMT. All authors wrote the initial manuscript and read and approved the final manuscript.
A 3-year postgraduate research scholarship support from the College of Health Sciences and support from Damien Foundation Belgium (Nigeria project).
In 2014 recreational, adult-use of cannabis (interchangeably referred to as marijuana) was established in the state of Colorado. At this time the Colorado Department of Public Health and Environment (CDPHE) was given statutory responsibility in Colorado Revised Statute (C.R.S.) 25-1.5-110, to; “monitor changes … in the emerging science and medical information relevant to the health effects associated with marijuana use.” and “appoint a panel of health care professionals with expertise in, but not limited to, neuroscience, epidemiology, toxicology, cannabis physiology, and cannabis quality control to further direct policy.” Based on this charge, CDPHE appointed a 14-member committee titled the Retail Marijuana Public Health Advisory Committee (RMPHAC) to review scientific literature on the health effects of marijuana.
Under the same statute mentioned previously, the RMPHAC is directed to “…establish criteria for studies to be reviewed, reviewing studies and other data, and making recommendations, as appropriate, for policies intended to protect consumers of marijuana or marijuana products and the general public.” To implement this charge, the RMPHAC meets four or five times a year to review the scientific literature currently available on health effects of marijuana use, evaluate findings without bias, openly discuss the science and apply expert opinion, come to consensus on the science, translate the science into public health messages, make policy-related recommendations, recommend surveillance activities, and identify and address gaps in the science important to public health. All this information is compiled and detailed in a report every two years for the Colorado State Board of Health, the Colorado Department of Revenue, and the Colorado General Assembly, titled “Monitoring Health Concerns Related to Marijuana in Colorado” [1].
Since 2014, and prior to this publication, the RMPHAC has come together on a quarterly basis, held discussions concerning hundreds of articles, and developed over one hundred evidence statements within eleven health topics. As more scientific evidence regarding cannabis health effects are published, this committee continues to build upon existing evidence statements or will construct new statements when appropriate. This chapter will detail the review methods used by the RMPHAC to develop evidence statements about the health effects associated with marijuana use, describe the findings from all eleven health topics, and report the public health statements, recommendations, and research gaps used to inform public health policy in the State of Colorado.
The first step in the process of investigating the health effects from marijuana use was to develop and implement an unbiased, transparent, and complete process for evaluating scientific literature and data on marijuana use and health outcomes. To ensure this, the RMPHAC and CDPHE technical staff developed a twelve step review process guided by the established preferred reporting items for systematic reviews and meta-analyses (PRISMA) framework [2]. These twelve steps are followed for each review and are as follows:
Conduct a broad search of current peer-reviewed publications quarterly. Relevant articles cited in reviews or other primary studies are also included.
Review relevant full-text articles identified in the search.
Rate the findings: each finding in the articles is rated as a high-, medium-, or low-quality finding based on strengths and limitations of the methods. Evaluation of the strengths and limitations was based on criteria in the grading of recommendations assessment, development and evaluation (GRADE) system, a well-accepted method for evaluating the quality of scientific evidence [3].
Group related findings: each finding is categorized based on population, exposure, and outcome (health effect), to answer specific questions.
Weigh the evidence: draft evidence statements that summarize the quantity and quality of evidence answering a specific question.
Translate the evidence: draft public health statement that translate the evidence statement into language at an 11th grade reading level.
Synthesize the evidence: draft public health recommendations (e.g., for education or monitoring) based on important information identified through the review process.
Identify research gaps: draft statements to articulate the research gaps identified during the review process.
Present to committee: findings, evidence statements, public health statements, public health recommendations, and research gaps are publicly presented to the RMPHAC for review and revision during open public meetings.
Public comment: during the open public meetings, interested stakeholders and members of the public are invited to provide comments relevant to the topics presented.
Reach consensus: committee members come to consensus on findings, evidence statement, public health statement, public health recommendations, and research gaps.
Adopt summary statements: committee votes to officially accept findings, evidence statements, public health statements, public health recommendations, and research gaps.
All review methods were approved by the RMPHAC, including the terms used to conduct the ongoing broad search of peer-reviewed publications for relevant literature. Medline is the priority research database used to obtain articles for review. Embase, the biomedical database, and gray literature were secondarily reviewed when references in included articles were not included in Medline searches. Studies of marijuana use in humans were the primary focus of the review, with animal studies included for only specific topics with limited human research. All identified peer-reviewed literature on a given topic was reviewed, regardless of positive or negative findings or quality of the methods utilized. For the ongoing broad Medline search, medical subject heading (MeSH) terms were used and is as follows; “Cannabis”[Mesh] OR Marijuana “Smoking”[Mesh] OR “Marijuana Abuse”[Mesh] OR cannabis OR marijuana OR marihuana OR hash oil OR hashish. In 2014, when this review was established, specific searches were conducted using the appropriate MeSH terms for each topic area.
Once relevant literature is obtained, each finding is rated high, medium, or low quality based on the strengths and limitations of the methods which is determined by criteria in the GRADE system. The GRADE system is a well-established method for systematic literature review and has been used by the Cochrane Collaboration, British Medical Journal, American College of Physicians, World Health Organization, and many others [3]. Findings rated high quality are defined as “We are very confident that the true effect lies close to that of the estimate of the effect outlined in the study.” These are well-designed and well-controlled studies with few limitations. Due to the fact that most studies included in our review are observational epidemiology studies, receiving a high quality rating does not necessarily imply causation. It simply implies that an observed association persists between an exposure and effect in an appropriately-sized study population after adjusting for appropriate confounders. Medium quality findings are defined as “we are moderately confident in the effect estimate outlined in the study. The true effect is likely to be close to the estimate of the effect, but there is a possibility that it is substantially different.” For observational epidemiology studies this implies the finding of an observed association may be limited by a small study population or insufficient adjustment for important confounders. Low quality findings are defined as “our confidence in the effect estimate outlined in the study is limited. The true effect may be substantially different from the estimate of the effect.” For observational epidemiology studies this implies the finding of an observed association with an interpretation that is significantly restricted by study limitations.
Findings from relevant literature are usually grouped based on outcome or the health effect in question. However, in some situations findings are further subdivided based on factors such as: age range of the exposed population, special subject circumstances such as pregnancy or breastfeeding, level or method of marijuana use, time period since last use of marijuana, amount of marijuana used, and THC concentration. Standardized definitions of level of marijuana use (daily, weekly, etc.) and age groups (child, adolescent, young adult, etc.) were established to help facilitate grouping of findings. Once findings are grouped appropriately, the evidence is drafted into evidence statements that summarize the quality and quantity of scientific evidence supporting an association between marijuana use and a health outcome.
In order to make our review findings easily interpretable we used a standardized rating system to classify evidence statements. These statements are also constructed to accurately portray the quality and quantity of all findings used to support the particular health outcome. Evidence statements all use standardized language from one of the following six classifications:
Substantial evidence—indicates robust scientific findings that support an association between marijuana use and the outcome.
Moderate evidence—indicates scientific findings that support an association, but these findings have some limitations.
Limited evidence—indicates modest scientific findings that support an association, but these findings have significant limitations.
Mixed evidence—indicates both supporting and opposing scientific findings for an association, with neither direction dominating.
Insufficient evidence—indicates the outcome has not been sufficiently studied to conclude whether or not there is an association between marijuana use and the outcome.
Body of research failing to show an association—indicates the topic has been researched without evidence of an association; is further classified as a limited, moderate, or substantial body of research.
In the following sections evidence statements will be discussed according to health topic and statements with enough findings to receive a substantial or moderate rating are displayed in tables. All statements, regardless of evidence level, are drafted by CDPHE technical staff, revised based on committee review and feedback from technical advisors and public stakeholders. Statements in their final form are approved by a vote of the committee.
The RMPHAC has reviewed the relationships between adolescent and young adult marijuana use on various areas of concern; including cognitive abilities, academic performance, mental health, and future substance use, displayed in Table 1. Specifically regarding cognitive and academic abilities, weekly marijuana use by adolescents is associated with deficits for at least twenty-eight days after last use. Weekly use among adolescents is also associated with failure to graduate from high school or complete a college degree. Information on how marijuana use affects short-term and long-term IQ is currently insufficient and limited, respectively. As with many of our statements that reflect long-term marijuana use, the paucity of long-term studies is a research gap that will hopefully improve due to the changing legal landscape of cannabis throughout the United States.
Substantial evidence | Moderate evidence | |
---|---|---|
Benefits of quitting | Treatment for cannabis use disorder can reduce use and dependence [4, 5, 6, 7, 8, 9, 10] | Quitting or decreasing marijuana use lowers the risk of adverse mental health outcomes [11, 12, 13, 14] |
Cognitive and academic effects | Weekly, or more frequent, use is associated with a lower rate of graduating high school [15, 16, 17, 18, 19, 20, 21, 22, 23] | Weekly, or more frequent, use is associated with a lower rate of attaining a college degree (among those who start a degree program) [19, 24, 25, 26, 27, 28, 29] |
Weekly, or more frequent, use is associated with ongoing cognitive and academic impairment for at least 28 days after last use [30, 31, 32, 33, 34, 35] | ||
Mental health | Daily or near daily use is associated with future psychotic disorders like schizophrenia [36, 37, 38, 39, 40, 41, 42, 43] | Marijuana use is associated with suicidal thoughts or attempting suicide [22, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63] |
Use is associated with future psychotic symptoms (likelihood increases with more frequent use) [14, 40, 42, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80] | ||
Substance use, abuse, and addiction | Those who use marijuana can develop cannabis use disorder (addiction) [81, 82, 83, 84, 85, 86, 87] | Marijuana use is associated with future use and use disorder for alcohol [15, 20, 88, 89, 90, 91, 92] |
Marijuana use is associated with future use and use disorder for marijuana, tobacco and other drugs [13, 15, 20, 22, 25, 28, 79, 84, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, 100, 101, 102, 103, 104, 105] | ||
High THC (%) concentration | Using marijuana with higher THC concentration (>10% THC) is associated with continued use [38, 106, 107, 108] | |
Use of marijuana with higher THC concentration (>10% THC) is associated with future mental health symptoms and disorders [38, 78, 107] |
Marijuana use among adolescents and young adults.
Adolescents and young adults who use marijuana are more likely to experience psychotic symptoms in adulthood (such as hallucinations, paranoia, and delusional beliefs), future psychotic disorders (such as schizophrenia), and suicidal thoughts or attempting suicide, when compared to adolescents and young adults who do not use marijuana. Additionally, those using marijuana with higher tetrahydrocannabinol (THC) concentration (>10% THC) are more likely than non-users to continue using and to develop future mental health symptoms and disorders. How marijuana use during adolescence affects symptoms or a diagnosis of anxiety in adulthood currently stands at a mixed evidence level, with fourteen articles contributing to this rating. Only one of which received a high quality rating and also reported mixed findings relevant to this evidence statement on anxiety [64]. Results from their main analysis did show an association with adolescent cannabis use and adulthood anxiety, however, results from a monozygotic-only co-twin control analysis reported no association [64].
Evidence shows that adolescents who use marijuana can develop cannabis use disorder, along with marijuana use being associated with developing use disorder for tobacco, alcohol, and other drugs. On a more positive note, evidence shows that adolescents who receive treatment for cannabis use disorder can decrease their use and dependence. Additionally, those who quit using marijuana have lower risks of adverse cognitive and mental health outcomes than those who continue to use.
To assess how marijuana use may or may not be associated with cancer, the RMPHAC reviewed health effects of the chemicals released in marijuana smoke and vapor and evaluated how different rates of marijuana use relate to cancer. Strong evidence shows marijuana smoke contains many of the same cancer-causing chemicals found in tobacco smoke [109]. There is also substantial evidence that daily or near-daily marijuana smoking is associated with pre-malignant lesions in the airway. However, there is conflicting research for whether or not marijuana smoking is associated with lung cancer. As shown by the moderate evidence statement in Table 2, the body of research reviewed has failed to show an association between smoking less than the equivalent of one joint per day for 10 years and lung cancer.
Substantial evidence | Moderate evidence | |
---|---|---|
Cancer and precancerous lesions | Daily or near daily use is associated with pre-cancerous lesions in airway [110, 111, 112] | Smoking less than the equivalent of one joint per day for 10 years is not associated with lung cancer [113, 114, 115, 116, 117, 118] |
Chemicals in MJ smoke or vapor | Marijuana smoke contains many of the same cancer causing chemicals as tobacco smoke [109, 119, 120, 121, 122] | |
Genitourinary Cancer | Use among adult males is associated with increased risk of nonseminoma testicular cancer [123, 124, 125, 126, 127] |
Marijuana use and cancer.
Apart from the respiratory system, most of our statements are not in Table 2 due to the limited evidence available concerning cancers of the bladder, prostate, head and neck. These limited statements all suggest these forms of cancer might not have any association with marijuana use. However, there is evidence that marijuana use among adult males may be associated with nonseminoma testicular cancer. High quality research on non-respiratory tract cancers related to marijuana use remains a research gap identified by the RMPHAC.
Related to cardiovascular health effects, how marijuana use associates with myocardial infarction, stroke, and death from cardiovascular causes were reviewed. Evidence shows that marijuana use or consumption in those under the age of fifty-five years are at an increased risk of ischemic stoke, as shown in Table 3. However, currently there is only limited scientific evidence to support our statements on myocardial infarction and death related to a cardiovascular event.
An important metric to understand is how THC blood levels compare from various marijuana methods of use and the numerous concentrations of THC in available products on the retail marijuana market. For example, there is substantial evidence that smoking more than 10 mg THC (or 10–20% of a 1 g marijuana joint) produces a blood THC level near or above 5 ng/mL within 10 min. As we see the THC concentration of marijuana products increase, we can expect this association to remain strong. One important finding in Table 4 is that it can take up to four hours after consuming an edible marijuana product to reach the peak THC blood concentration and feel the full effects. Another method of use, vaporized THC, shows moderate evidence of producing a similar blood THC level to smoking the same amount.
Substantial evidence | Moderate evidence | |
---|---|---|
THC blood levels resulting from different exposures | It takes up to four hours after ingesting marijuana (edible products) to reach peak blood THC levels [146, 147, 148, 149, 150, 151] | Ingesting (edible products) more than 15 mg THC may produce a blood THC level above 5 ng/mL [148, 152, 153, 154] |
Smoking more than 10 mg THC produces a blood THC level near or above 5 ng/mL within 10 min [152, 155, 156, 157, 158, 159] | Inhaling vaporized THC produces a blood THC level similar to smoking the same dose [149, 159, 160] | |
Secondhand exposure | Typical secondhand marijuana smoke exposure is unlikely to cause a positive drug screen by urine or blood [161, 162, 163, 164, 165, 166, 167, 168, 169] |
Marijuana dose and drug interactions.
Within this topic the RMPHAC reviewed effects of secondhand marijuana smoke, drug-drug interactions involving marijuana, and relationships between marijuana and opioid use. There is credible evidence of clinically important drug-drug interactions between marijuana and multiple medications, including some anti-seizure medications and a common blood-thinner, warfarin. Data about potential interactions are lacking for many drugs at this time and are likely to evolve substantially in the coming years. Other than our statement about secondhand marijuana smoke exposure being unlikely to cause a positive drug screen, our statements in this topic area are all based on limited evidence. Health effects resulting from secondhand marijuana smoke exposure is an area lacking in research. There is also conflicting evidence for whether or not marijuana use is associated with a decrease in opioid use among chronic pain patients or individuals with a history of problem drug use.
As with any psychoactive substance it is imperative to know how marijuana affects a person’s ability to drive and the crash risks associated with use. To fully comprehend how marijuana causes driving impairment we must also understand the pharmacokinetics of THC in the human body to know how long these affects will persist after last use. Table 5 displays all driving related statements that have evidence to provide a substantial or moderate rated statement. Current research shows substantial evidence that recent marijuana use by a driver increases the risk of a motor vehicle crash. In addition, using alcohol and marijuana together increases impairment and the risk of a motor vehicle crash more than using either substance alone.
Substantial evidence | Moderate evidence | |
---|---|---|
Combined marijuana and alcohol use | Combined use of marijuana and alcohol increases crash risk more than either substance alone [170, 171, 172, 173, 174, 175, 176, 177, 178, 179, 180, 181] | |
Impairment and crash risk | Recent marijuana use/consumption by a driver increases the risk of a motor vehicle crash [170, 171, 172, 174, 182, 183, 184, 185, 186, 187, 188] | Higher THC blood level increases the risk of a motor vehicle crash [173, 178, 180, 189] |
Smoking more than 10 mg THC can lead to driving impairment [147, 155, 157, 177, 190, 191, 192, 193, 194, 195, 196, 197, 198, 199, 200] | Blood THC levels of impaired drivers are higher now than they were in the past [201] | |
Orally ingesting more than 10 mg THC can lead driving impairment [146, 147, 153, 155] | ||
Increased risk of driving impairment at blood THC as low as 2–5 ng/mL [155, 185, 190, 202, 203, 204, 205, 206] | ||
Time to wait before driving | Waiting at least 6 after smoking less than 18 mg allows driving impairment to resolve or nearly resolve [155, 190, 207] | Waiting at least 6 h after smoking about 35 mg allows driving impairment to resolve or nearly resolve [157, 192, 196] |
Waiting at least 8 h after orally ingesting less than 18 mg allows driving impairment to resolve or nearly resolve [147, 153, 155, 208] |
Marijuana use and driving.
The RMPHAC also set out to determine how various patterns of marijuana use affect driving. People that consume marijuana less-than-weekly are likely to experience impaired driving after using marijuana containing ten milligrams or more of THC. This statement holds true for smoking or consuming edible marijuana products. Research on driving impairment for those that consume more frequently than weekly is currently lacking in scientific literature. Due to this our evidence statement on crash risk for different levels of use (less-than-weekly compared to more frequent use) has received an insufficient rating at this time.
Articles measuring THC blood levels were also assessed to evaluate for any correlation to driving impairment, crash risk, and to develop statements informing consumers the amount of time to wait prior to driving. There is substantial evidence, including a randomized clinical trial [202], which has displayed meaningful driving impairment with a whole blood THC of 2–5 ng/mL. Additionally, moderate evidence points to a positive relationship between THC blood level and motor vehicle crash risk. In order for marijuana consumers to allow impairment to resolve, less-than-weekly consumers should wait at least six hours after smoking or eight hours after eating or drinking marijuana products. When consuming larger amounts of THC or for people that consume more frequently, evidence is currently insufficient to determine the safe amount of time for impairment to wear off. Evidence is also showing that blood THC levels of marijuana-impaired drivers are higher now than in the past, likely resulting from the increasing THC concentration of available marijuana products.
The RMPHAC reviewed how marijuana use may affect gastrointestinal disease, particularly cyclic vomiting, and infertility or abnormal reproductive function. Displayed in Table 6, evidence shows that long-time, daily or near daily marijuana use is associated with cyclic vomiting, also called cannabinoid hyperemesis syndrome (CHS). A majority of evidence supporting this statement is from case reports or case series of identified CHS patients, however, many review articles detail diagnostic criteria, treatment options, and the physiology behind marijuana use and CHS presentation [220]. Regarding reproductive function, there is limited research showing marijuana use is associated with male infertility or abnormal function, however, the research is conflicting for women.
The RMPHAC reviewed workplace, recreational and other non-driving injuries, burns from hash-oil extraction or failed electronic smoking devices, and physical dating violence. Evidence shows mixed results for marijuana use affecting the risk of workplace injury, recreational injury, and other types of non-driving-related injury. There have been many reports of severe burns resulting from home-extraction of butane hash oil leading to explosions, and cases of electronic smoking devices exploding, leading to trauma and burns.
Concerning dating violence, Table 7 shows our only statement reaching moderate or substantial levels of evidence is that young adult women who use marijuana are unlikely to perpetrate physical dating violence against their dating partners. Otherwise, evidence does show that young adults who use marijuana are unlikely to commit or be victims of physical dating violence, however evidence is limited at this time. Evidence for adolescent boys that use marijuana has mixed findings for physical dating violence perpetration and limited evidence for victimization, with evidence for adolescent girls being the opposite (Table 7).
Similar to statements in our adolescent and young adult section, it is imperative to understand how marijuana could impact neurological, cognitive, and mental health in adult marijuana consumers. This section also explores how marijuana consumption relates to marijuana abuse and addiction among adult consumers. While our review on cognitive effects includes decision making, executive function, memory impairment, and lasting cognitive effects, strong evidence has been found only for memory impairment, as shown in Table 8. We have found substantial evidence that daily or near daily adult marijuana consumers are more likely than non-users to have memory impairments for at least seven days after last use. Evidence is mixed for whether or not these memory impairments or other cognitive effects last for at least twenty-eight days after last use, among the same population of adult consumers.
Substantial evidence | Moderate evidence | |
---|---|---|
Cognitive effects | Daily or near daily use is associated with impaired memory for at least 7 days [30, 227, 228, 229, 230, 231, 232, 233, 234, 235] | |
Mental health effects | Use is associated with acute psychotic symptoms during intoxication, which are worse with higher doses [236, 237, 238, 239, 240, 241, 242, 243] | |
Daily or near daily use is associated with future psychotic disorders like schizophrenia [38, 42, 107, 244, 245, 246] | Use of marijuana with THC concentration > 10% is associated with future psychotic disorders like schizophrenia [38, 107, 247] | |
Substance use, abuse and addiction | Those who use marijuana can develop cannabis use disorder (addiction) [82, 85, 86, 93, 248, 249, 250, 251, 252] | |
Treatment for cannabis use disorder can reduce use and dependence [4, 6, 8, 9, 253, 254, 255, 256, 257] | ||
Those using daily or near daily can experience withdrawal symptoms when abstaining [11, 258, 259, 260, 261, 262, 263, 264, 265, 266, 267, 268, 269, 270] |
Marijuana use and neurological, cognitive, mental health effects.
As with all psychoactive substances, mental health effects in adult marijuana consumers must be examined. An important acute effect of THC with substantial evidence is psychotic symptoms, such as hallucinations, paranoia, and delusional beliefs during intoxication, and these symptoms are worse with higher doses. Additionally, daily or near daily marijuana use is associated with developing a psychotic disorder such as schizophrenia. As detailed in our report focusing on the increasing concentration of THC in products available, there is increased public health concern as these products may lead to higher potential for adverse health effects in consumers [1]. This concern is substantiated by available research enabling us to provide a moderate rated statement showing association between higher concentration THC products and future psychotic disorders in adult marijuana consumers.
Finally, evidence shows marijuana consumers can experience withdrawal symptoms when abstaining and become addicted to marijuana or develop cannabis use disorder. However, as with adolescents, treatment for cannabis use disorder can reduce use and dependence in adult consumers. Many associations within this section lack high quality evidence or research currently exhibits mixed findings, such as marijuana use being associated with anxiety, depression, or bipolar disorder (Table 8).
Table 9 details our evidence concerning marijuana use during pregnancy and breastfeeding. Biological evidence shows THC passes through the placenta to the fetus and is present in the breast milk of women who use marijuana. Scientific evidence shows the fetus absorbs and metabolizes THC passed through the placenta and THC metabolites are found in the meconium or first stool passed by the newborn after birth. Additionally, infants who drink breast milk containing THC absorb and metabolize the THC. These statements show how important it is to understand how marijuana use during pregnancy and/or breastfeeding can affect the offspring or impact delivery of the offspring.
Substantial evidence | Moderate evidence | |
---|---|---|
Effects on exposed offspring | Prenatal marijuana exposure is associated with reduced cognitive function, academic ability, and IQ scores in childhood [271, 272, 273, 274, 275, 276, 277, 278, 279, 280] | |
Prenatal marijuana exposure is associated with attention problems in childhood [273, 281, 282, 283, 284, 285] | ||
Birth defects | Prenatal marijuana use is not associated with birth defects [286, 287, 288, 289, 290, 291, 292] | |
Preterm delivery or abnormal birth weight | Maternal use during pregnancy is associated with infants being born small for gestational age (birth weight less than 10th percentile for gestational age) [286, 287, 289, 292, 293, 294, 295, 296, 297, 298, 299, 300, 301, 302, 303, 304, 305] | |
THC is passed through the placenta of women who use marijuana, the fetus absorbs and metabolizes the THC, and THC metabolites are found in the meconium [306, 307, 308, 309, 310]. | ||
THC is present in the breast milk of women who use marijuana. Infants who drink breast milk containing THC absorb and metabolize the THC [311, 312, 313, 314, 315, 316]. |
Marijuana use during pregnancy and/or breastfeeding.
Specifically regarding exposed offspring, the RMPHAC reviews potential effects starting at birth and later in childhood or adolescence. Marijuana use during pregnancy has shown to not be associated with birth defects in general, but limited evidence of an association with an increased risk of heart defects, stillbirth, and decreased growth in offspring. Stronger evidence was found for effects that are seen in offspring years after birth if a child’s mother used marijuana while pregnant. These include impaired cognitive function and academic ability, lower IQ scores, and attention problems in childhood.
While consumers have a variety of marijuana products to choose from, smoking marijuana flower remains the most common method of use and thus respiratory effects must be evaluated [317]. The RMPHAC reviews respiratory diseases such as chronic obstructive pulmonary disorder (COPD), chronic bronchitis and asthma, respiratory infections, lung function relative to smoked marijuana. The committee has also reviewed potential health effects of vaporized marijuana as those products have emerged on the legal market. Displayed in Table 10, strong evidence shows an association between daily or near-daily marijuana use and chronic bronchitis, including chronic cough, sputum production, and wheezing. Weaker evidence shows daily or near-daily marijuana use may be associated with bullous lung disease leading to pneumothorax in individuals younger than forty years of age. Additionally, limited evidence does show frequent smokers who switch from marijuana smoking to marijuana vaporizing may have fewer respiratory symptoms and improved pulmonary function. Finally, a notable effect of acute marijuana smoking is a short-term improvement in lung airflow, though evidence contributing to this statement is dated (Table 10).
Substantial evidence | Moderate evidence | |
---|---|---|
Smoked marijuana | Use is associated with chronic bronchitis with cough, wheezing and mucus [318, 319, 320, 321, 322, 323, 324, 325, 326, 327] | |
Acute use is associated with short-term lung airflow improvement [328, 329, 330] |
Marijuana use and respiratory effects.
As marijuana becomes more accessible to the public, we must consider unintentional exposures in homes with children and how packaging can affect these. Strong evidence was found, shown in Table 11, that more unintentional exposures of children occur in states with increased legal access to marijuana, and exposures can lead to significant clinical effects requiring medical attention and even hospitalization. However, evidence does show that child-resistant packaging reduces unintentional pediatric marijuana poisonings (Table 11).
Substantial evidence | Moderate evidence | |
---|---|---|
Legal marijuana access increases unintentional marijuana exposures in children [331, 332, 333, 334, 335, 336, 337, 338, 339, 340, 341] | Child-resistant packaging reduces unintentional pediatric poisonings [342, 343, 344] |
Unintentional marijuana exposure in children.
Once evidence statements have been drafted and approved by the RMPHAC, the next step (number 6 from our systematic review process) is to translate the evidence into public health statements. These are designed to accurately reflect the evidence statements using language the public can understand. The committee also wanted to ensure these statements conveyed the volume and quality of research related to the outcome and allowed the statement to stand on its own without context. Similar to our evidence statements, these use standardized language to represent the strength of relationship and use the phrase “associated with” to represent epidemiologic associations that do not imply causation. As of the date of this book’s publication CDPHE has seventy-four public health statements corresponding to all our evidence statements rated moderate or substantial.
In a similar manner, public health statements are subsequently drafted into public health recommendations. These are synthesized in order to inform the development of evidence-based prevention and education campaigns performed by CDPHE. Furthermore, recommendations are separated by data quality issues, surveillance, and education. Our recommendations share common themes to those put forth by the National Academies of Sciences, Engineering, and Medicine’s review of health effects associated with cannabis and cannabinoids [345].
Data quality issues are defined as recommendations to improve current data collection deficiencies at the clinical or governmental level that prevent full analysis of public health outcomes related to marijuana use. It is especially important to improve data quality by systematically collecting information on the frequency, amount, THC content, and method of marijuana use in both public health surveillance and medical care settings. Clinicians should routinely screen for marijuana use during hospitalizations, especially among pregnant or adolescent patients.
Public health surveillance recommendations are based on improving capacity to detect an acute public health danger (e.g., real time emergency department surveillance to detect poisonings from contaminated product); the ability to characterize chronic public health dangers to support policy and other intervention decisions; or the ability to generate epidemiologic data to contribute to planning and evaluating population level interventions. Questions regarding marijuana use should be continued on population-based surveys such as the Behavioral Risk Factor Surveillance System, the Healthy Kids Colorado Survey, and Pregnancy Risk Assessment Monitoring System. Additionally, methods should be expanded to collect more detailed information, such as quantity and methods of use, THC content of products used, and adverse effects experienced.
Education recommendations are included to ensure evidence-based information on potential health effects of marijuana use is provided to the appropriate target audiences. Public education is especially important related to the effects of use during pregnancy, adolescent use, driving after use, increasing THC concentration of products, and unsafe storage around children. Education for health care providers should also be emphasized on the need for marijuana use screening, the known health effects of use, and encouraging more open dialog between providers and patients.
In addition to public health recommendations, important research gaps related to the population-based health effects of marijuana use were identified during the literature review process. These research gaps are based on common limitations of existing research or issues important to public education or policymaking. Research gaps particularly important to public health and safety include the need for: (1) research on the effects of marijuana use on pregnant women and their offspring, including while breastfeeding; (2) research on marijuana and marijuana products that contain THC concentrations consistent with products currently available in legalized markets; (3) research on health effects among individuals who have used marijuana frequently for a long period of time; (4) research on driving impairment among people who use marijuana more than weekly and may have developed tolerance; (5) research to better characterize the pharmacokinetics/pharmacodynamics, potential drug interactions, health effects, and impairment related to non-smoking methods of marijuana use such as edible products and vaporizing; and (6) research to better describe the risk of adverse health effects due to contamination of the marijuana product by fungi, mold, solvents, additives, heavy metals, and pesticides.
Other research gaps identify areas that need improvement in new research moving forward. Such as studies using better and more standardized indicators of marijuana use, including frequency, THC content, and route of exposure, including populations that use marijuana daily or near daily, and stratifying groups by age and gender. Finally one step to provide strong evidence would be research data on a community based cohort to study both beneficial and adverse health effects of marijuana consumption. Identifying these research gaps provides researchers and funding sources with an important framework to prioritize areas of research related to marijuana use and public health.
Since 2014, when CDPHE was designated to monitor the emerging science and medical information relevant to the health effects associated with marijuana use, the RMPHAC and CDPHE technical staff have conducted an ongoing systematic review of scientific literature to establish over one hundred evidence statements with eleven health topics. Our mission is to translate the science into meaningful public health statements and recommendations to inform and educate the general public, healthcare providers, and everyone in-between on the health effects associated with marijuana use.
First, the committee established a strict process to ensure a thorough and unbiased review, set up quarterly meetings to enable open discussions on a continuous basis, and come to consensus on the science and how to present this information to the public. After establishing our process, evidence from scientific research is constantly reviewed and added when appropriate to form a comprehensive review of marijuana health effects across eleven health topic. Strong evidence statements from all health topics were displayed in tables and key findings were detailed in subsections to provide an overview of effects associated with marijuana use across many different populations and health topics. Additional details were described on how these evidence statements are used to inform public health policy in the State of Colorado through public health recommendations and research gaps.
Elyse Contreras, DeLayna Goulding, Daniel I. Vigil, Katelyn E. Hall, Michael Van Dyke, Shireen Banerji, Russell Bowler, Ashley Brooks-Russell, Christopher Domen, Heather Krug, David J Kroll, Sharon Langendoerfer, Andrew Monte, Kenneth Novoa, Judith Shlay, Elizabeth Stuyt, George Sam Wang, Bernadette Albanese, Lisa Barker, Laura Borgelt, Alvin C. Bronstein, Todd Carlson, Rowena Crow, Teresa Foo, Ken Gershman, Tista Ghosh, Heath Harmon, Rebecca Helfand, Renee M. Johnson, Bruce Mendelson, Madeline Morris, Kristina T. Phillips, Allison Rosenthal, Kim Siegal, Scott Simpson, Christian Thurstone.
“The authors declare no conflict of interest.”
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Miller, Hayley Wright, Josie Hough and Francesco P.\nCappuccio",authors:[{id:"77507",title:"Dr.",name:"Michelle A",middleName:null,surname:"Miller",slug:"michelle-a-miller",fullName:"Michelle A Miller"}]},{id:"32269",doi:"10.5772/32991",title:"Epidemiology of Insomnia: Prevalence and Risk Factors",slug:"epidemiology-of-insomnia-prevalence-and-risk-factors",totalDownloads:4726,totalCrossrefCites:5,totalDimensionsCites:12,abstract:null,book:{id:"711",slug:"can-t-sleep-issues-of-being-an-insomniac",title:"Can't Sleep? Issues of Being an Insomniac",fullTitle:"Can't Sleep? Issues of Being an Insomniac"},signatures:"Claudia de Souza Lopes, Jaqueline Rodrigues Robaina and Lúcia Rotenberg",authors:[{id:"93493",title:"Prof.",name:"Claudia",middleName:null,surname:"Lopes",slug:"claudia-lopes",fullName:"Claudia Lopes"},{id:"95778",title:"Dr.",name:"Jaqueline",middleName:null,surname:"Robaina",slug:"jaqueline-robaina",fullName:"Jaqueline Robaina"},{id:"95790",title:"Dr.",name:"Lúcia",middleName:null,surname:"Rotenberg",slug:"lucia-rotenberg",fullName:"Lúcia Rotenberg"}]},{id:"32149",doi:"10.5772/29364",title:"Sleep and Pregnancy: Sleep Deprivation, Sleep Disturbed Breathing and Sleep Disorders in Pregnancy",slug:"sleep-and-pregnancy-sleep-deprivation-sleep-disturbed-breathing-and-sleep-disorders-in-pregnancy",totalDownloads:4026,totalCrossrefCites:1,totalDimensionsCites:5,abstract:null,book:{id:"993",slug:"sleep-disorders",title:"Sleep Disorders",fullTitle:"Sleep Disorders"},signatures:"Michelle A. Miller, Manisha Ahuja and Francesco P. Cappuccio",authors:[{id:"77507",title:"Dr.",name:"Michelle A",middleName:null,surname:"Miller",slug:"michelle-a-miller",fullName:"Michelle A Miller"},{id:"119883",title:"Ms.",name:"Manisha",middleName:null,surname:"Ahuja",slug:"manisha-ahuja",fullName:"Manisha Ahuja"},{id:"119885",title:"Prof.",name:"Francesco P",middleName:null,surname:"Cappuccio",slug:"francesco-p-cappuccio",fullName:"Francesco P Cappuccio"}]},{id:"65707",doi:"10.5772/intechopen.82754",title:"Sleep Physiology and Polysomnogram, Physiopathology and Symptomatology in Sleep Medicine",slug:"sleep-physiology-and-polysomnogram-physiopathology-and-symptomatology-in-sleep-medicine",totalDownloads:1252,totalCrossrefCites:3,totalDimensionsCites:5,abstract:"Over recent years, the importance of sleep physiology and pathology has been better understood in terms of correct diagnosis, treatment, prognosis and innovative research of diseases. Sleep disorders are often confused with clinical symptoms of adult and pediatric medical conditions. In medicine, electrophysiological signal recording methods are very important for establishing a correct diagnosis especially in neurological sciences. Polysomnography (PSG) is a golden standard diagnostic method that records electrophysiological signals used for sleep physiology and diseases. When the medical disciplines and diseases that make use of this diagnostic method are considered, its significance becomes clearer. For example, medical disciplines benefiting from PSG are as follows: “Clinical Physiology, Neurology, Ear Nose and Throat, Dentistry, Psychiatry, Pulmonology, Cardiology, Pediatric Neurology, Pediatric Cardiology, Internal Medicine, Neurosurgery, Endocrinology, etc.” The patient groups diagnosed with PSG are as follows: “Sleep Disordered Breathing (Central Sleep Apnea Syndrome, Obstructive Sleep Apnea Syndrome), Obesity, Morbid Obesity, REM Behavior Disorder, Restless Leg Syndrome, Rhythm Disorders, Epileptic Disorders, Insomnia, Insomnia and Headache, Hypersomnia, Narcolepsy, Secondary Hypertension, etc.” Interpretation and understanding electrophysiological signals correctly show us interactions of body systems with sleep physiology and integrated therapeutic approaches to sleep disorders. In conclusion; new approaches to sleep pathophysiology depend on a better understanding and further advancement of polysomnography.",book:{id:"7076",slug:"updates-in-sleep-neurology-and-obstructive-sleep-apnea",title:"Updates in Sleep Neurology and Obstructive Sleep Apnea",fullTitle:"Updates in Sleep Neurology and Obstructive Sleep Apnea"},signatures:"Murat Kayabekir",authors:[{id:"265598",title:"Associate Prof.",name:"Murat",middleName:null,surname:"Kayabekir",slug:"murat-kayabekir",fullName:"Murat Kayabekir"}]},{id:"32154",doi:"10.5772/33523",title:"Upper Airway Resistance Syndrome - A Twenty-Five Years Experience",slug:"upper-airway-resistance-syndrome-a-twenty-five-years-experience",totalDownloads:5062,totalCrossrefCites:2,totalDimensionsCites:3,abstract:null,book:{id:"993",slug:"sleep-disorders",title:"Sleep Disorders",fullTitle:"Sleep Disorders"},signatures:"Felix del Campo Matías, Tomas Ruiz Albi and Carlos Zamarrón Sanz",authors:[{id:"94382",title:"Prof.",name:"Felix",middleName:null,surname:"Del Campo",slug:"felix-del-campo",fullName:"Felix Del Campo"},{id:"95981",title:"Prof.",name:"Carlos",middleName:null,surname:"Zamarrón Sanz",slug:"carlos-zamarron-sanz",fullName:"Carlos Zamarrón Sanz"},{id:"95982",title:"Dr.",name:"Tomas",middleName:null,surname:"Ruiz Albi",slug:"tomas-ruiz-albi",fullName:"Tomas Ruiz Albi"}]}],mostDownloadedChaptersLast30Days:[{id:"65707",title:"Sleep Physiology and Polysomnogram, Physiopathology and Symptomatology in Sleep Medicine",slug:"sleep-physiology-and-polysomnogram-physiopathology-and-symptomatology-in-sleep-medicine",totalDownloads:1252,totalCrossrefCites:3,totalDimensionsCites:5,abstract:"Over recent years, the importance of sleep physiology and pathology has been better understood in terms of correct diagnosis, treatment, prognosis and innovative research of diseases. Sleep disorders are often confused with clinical symptoms of adult and pediatric medical conditions. In medicine, electrophysiological signal recording methods are very important for establishing a correct diagnosis especially in neurological sciences. Polysomnography (PSG) is a golden standard diagnostic method that records electrophysiological signals used for sleep physiology and diseases. When the medical disciplines and diseases that make use of this diagnostic method are considered, its significance becomes clearer. For example, medical disciplines benefiting from PSG are as follows: “Clinical Physiology, Neurology, Ear Nose and Throat, Dentistry, Psychiatry, Pulmonology, Cardiology, Pediatric Neurology, Pediatric Cardiology, Internal Medicine, Neurosurgery, Endocrinology, etc.” The patient groups diagnosed with PSG are as follows: “Sleep Disordered Breathing (Central Sleep Apnea Syndrome, Obstructive Sleep Apnea Syndrome), Obesity, Morbid Obesity, REM Behavior Disorder, Restless Leg Syndrome, Rhythm Disorders, Epileptic Disorders, Insomnia, Insomnia and Headache, Hypersomnia, Narcolepsy, Secondary Hypertension, etc.” Interpretation and understanding electrophysiological signals correctly show us interactions of body systems with sleep physiology and integrated therapeutic approaches to sleep disorders. In conclusion; new approaches to sleep pathophysiology depend on a better understanding and further advancement of polysomnography.",book:{id:"7076",slug:"updates-in-sleep-neurology-and-obstructive-sleep-apnea",title:"Updates in Sleep Neurology and Obstructive Sleep Apnea",fullTitle:"Updates in Sleep Neurology and Obstructive Sleep Apnea"},signatures:"Murat Kayabekir",authors:[{id:"265598",title:"Associate Prof.",name:"Murat",middleName:null,surname:"Kayabekir",slug:"murat-kayabekir",fullName:"Murat Kayabekir"}]},{id:"67469",title:"Sleep Disorder at High Altitude",slug:"sleep-disorder-at-high-altitude",totalDownloads:836,totalCrossrefCites:2,totalDimensionsCites:2,abstract:"In this chapter, we discuss the occurrence, mechanism, clinical manifestations, outcomes, and managements of a commonly encountered sleep disorder of someone traveling in high altitude for working and sight-seeing. Humans ascending to altitudes above 2500 m usually suffer from substantial disturbances in sleep quality as difficulty in sleep onset, frequent awakenings, respiratory disturbance, and a feeling of drowsiness on the next day. Data obtained from polysomnographic studies demonstrated several variations of sleep architecture in those healthy subjects ascending to high altitude during sleep, including periodic breathing and decreased non-rapid eye movement deep sleep stage 3 and 4 (in new nomenclature N3), which were usually accompanied by and the lowered arterial O2 and restricted ventilation. Hypoxia is most severe during sleep and in correspondence to periodic breathing and sleep disturbance at high altitude. Poor sleep quality impairs cognition and executive abilities at high altitude though it may largely be improved after full time of acclimatization. Evidence-based choices for clinicians to treat sleep disorder at high altitude are relatively scarce at present. Supplemental oxygen and dietary nitrate are effective in alleviating nocturnal hypoxia. There is strong evidence supporting the efficacy and safety of acetazolamide and nonbenzodiazepines in minimizing periodic breathing and improving sleep quality at high altitude.",book:{id:"7076",slug:"updates-in-sleep-neurology-and-obstructive-sleep-apnea",title:"Updates in Sleep Neurology and Obstructive Sleep Apnea",fullTitle:"Updates in Sleep Neurology and Obstructive Sleep Apnea"},signatures:"Fanyi Kong",authors:[{id:"285948",title:"Dr.",name:"Fanyi",middleName:null,surname:"Kong",slug:"fanyi-kong",fullName:"Fanyi Kong"}]},{id:"64983",title:"Cognitive Impairment and Obstructive Sleep Apnea",slug:"cognitive-impairment-and-obstructive-sleep-apnea",totalDownloads:1375,totalCrossrefCites:1,totalDimensionsCites:2,abstract:"Obstructive sleep apnea (OSA) is a frequent sleep disorder characterized by repetitive interruption of ventilation caused by partial or complete collapse of the upper airway during sleep. OSA is highly prevalent in the world and it has been associated with cardiovascular disease and cognitive impairment in children and adults. The cognitive impairment in individuals with OSA includes deficiencies in attention and constructional abilities, delayed long-term visual and verbal memory, and executive functions. Although, the pathogenesis of cognitive impairment in patients with OSA is complex and remains incompletely understood, several mechanisms, such as hypoxia, inflammation and sleep fragmentation have been proposed. The aim of this chapter is to describe some findings reported in the literature to explain the association between OSA and cognitive impairment.",book:{id:"7076",slug:"updates-in-sleep-neurology-and-obstructive-sleep-apnea",title:"Updates in Sleep Neurology and Obstructive Sleep Apnea",fullTitle:"Updates in Sleep Neurology and Obstructive Sleep Apnea"},signatures:"Liliana Otero, María del Carmen Figueredo, Alain Riveros-Rivera and Patricia Hidalgo",authors:[{id:"273415",title:"Ph.D.",name:"Liliana",middleName:null,surname:"Otero",slug:"liliana-otero",fullName:"Liliana Otero"},{id:"280824",title:"Dr.",name:"Carmen",middleName:null,surname:"Figueredo",slug:"carmen-figueredo",fullName:"Carmen Figueredo"},{id:"283338",title:"Dr.",name:"Alain",middleName:null,surname:"Riveros",slug:"alain-riveros",fullName:"Alain Riveros"},{id:"283339",title:"Dr.",name:"Patricia",middleName:null,surname:"Hidalgo-Martinez",slug:"patricia-hidalgo-martinez",fullName:"Patricia Hidalgo-Martinez"}]},{id:"71574",title:"Surgical Treatment Options for Obstructive Sleep Apnea",slug:"surgical-treatment-options-for-obstructive-sleep-apnea",totalDownloads:774,totalCrossrefCites:0,totalDimensionsCites:0,abstract:"Given the increased prevalence of obstructive sleep apnea (OSA) multiple treatment modalities including medical and surgical have been developed. First-line therapy for most of the people with obstructive sleep apnea (OSA) consists of behavioral modification, including weight loss if appropriate, and positive airway pressure (PAP) therapy. Patients who fail or do not tolerate PAP therapy, treatment options include oral appliances and surgical therapy. Surgical therapies have variable efficacy and are very important tool on OSA management in selected patients. This chapter will review the current surgical approaches sleep specialists use when other treatment options fail to accomplish the valuable outcome.",book:{id:"7076",slug:"updates-in-sleep-neurology-and-obstructive-sleep-apnea",title:"Updates in Sleep Neurology and Obstructive Sleep Apnea",fullTitle:"Updates in Sleep Neurology and Obstructive Sleep Apnea"},signatures:"Jimmy Hanna and Anthony Izzo",authors:[{id:"266405",title:"Dr.",name:"Anthony",middleName:null,surname:"Izzo",slug:"anthony-izzo",fullName:"Anthony Izzo"},{id:"312960",title:"Dr.",name:"Jimmy",middleName:null,surname:"Hanna",slug:"jimmy-hanna",fullName:"Jimmy Hanna"}]},{id:"46441",title:"Swallowing, Gastroesophageal Reflux and Sleep Apnea",slug:"swallowing-gastroesophageal-reflux-and-sleep-apnea",totalDownloads:2399,totalCrossrefCites:0,totalDimensionsCites:0,abstract:null,book:{id:"3798",slug:"sleep-and-its-disorders-affect-society",title:"Sleep and its Disorders Affect Society",fullTitle:"Sleep and its Disorders Affect Society"},signatures:"Shinji Teramoto",authors:[{id:"94615",title:"Dr.",name:"Shinji",middleName:null,surname:"Teramoto",slug:"shinji-teramoto",fullName:"Shinji Teramoto"}]}],onlineFirstChaptersFilter:{topicId:"201",limit:6,offset:0},onlineFirstChaptersCollection:[],onlineFirstChaptersTotal:0},preDownload:{success:null,errors:{}},subscriptionForm:{success:null,errors:{}},aboutIntechopen:{},privacyPolicy:{},peerReviewing:{},howOpenAccessPublishingWithIntechopenWorks:{},sponsorshipBooks:{sponsorshipBooks:[],offset:0,limit:8,total:null},allSeries:{pteSeriesList:[{id:"14",title:"Artificial Intelligence",numberOfPublishedBooks:9,numberOfPublishedChapters:90,numberOfOpenTopics:6,numberOfUpcomingTopics:0,issn:"2633-1403",doi:"10.5772/intechopen.79920",isOpenForSubmission:!0},{id:"7",title:"Biomedical Engineering",numberOfPublishedBooks:12,numberOfPublishedChapters:108,numberOfOpenTopics:3,numberOfUpcomingTopics:0,issn:"2631-5343",doi:"10.5772/intechopen.71985",isOpenForSubmission:!0}],lsSeriesList:[{id:"11",title:"Biochemistry",numberOfPublishedBooks:33,numberOfPublishedChapters:330,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2632-0983",doi:"10.5772/intechopen.72877",isOpenForSubmission:!0},{id:"25",title:"Environmental Sciences",numberOfPublishedBooks:1,numberOfPublishedChapters:19,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2754-6713",doi:"10.5772/intechopen.100362",isOpenForSubmission:!0},{id:"10",title:"Physiology",numberOfPublishedBooks:14,numberOfPublishedChapters:145,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2631-8261",doi:"10.5772/intechopen.72796",isOpenForSubmission:!0}],hsSeriesList:[{id:"3",title:"Dentistry",numberOfPublishedBooks:9,numberOfPublishedChapters:141,numberOfOpenTopics:2,numberOfUpcomingTopics:0,issn:"2631-6218",doi:"10.5772/intechopen.71199",isOpenForSubmission:!0},{id:"6",title:"Infectious Diseases",numberOfPublishedBooks:13,numberOfPublishedChapters:123,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2631-6188",doi:"10.5772/intechopen.71852",isOpenForSubmission:!0},{id:"13",title:"Veterinary Medicine and Science",numberOfPublishedBooks:11,numberOfPublishedChapters:112,numberOfOpenTopics:3,numberOfUpcomingTopics:0,issn:"2632-0517",doi:"10.5772/intechopen.73681",isOpenForSubmission:!0}],sshSeriesList:[{id:"22",title:"Business, Management and Economics",numberOfPublishedBooks:1,numberOfPublishedChapters:22,numberOfOpenTopics:3,numberOfUpcomingTopics:0,issn:"2753-894X",doi:"10.5772/intechopen.100359",isOpenForSubmission:!0},{id:"23",title:"Education and Human Development",numberOfPublishedBooks:0,numberOfPublishedChapters:11,numberOfOpenTopics:1,numberOfUpcomingTopics:1,issn:null,doi:"10.5772/intechopen.100360",isOpenForSubmission:!0},{id:"24",title:"Sustainable Development",numberOfPublishedBooks:1,numberOfPublishedChapters:19,numberOfOpenTopics:5,numberOfUpcomingTopics:0,issn:"2753-6580",doi:"10.5772/intechopen.100361",isOpenForSubmission:!0}],testimonialsList:[{id:"13",text:"The collaboration with and support of the technical staff of IntechOpen is fantastic. 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