dc.date.accessioned2022-01-18T19:34:38Z
dc.date.available2022-01-18T19:34:38Z
dc.date.created2022-01-18T19:34:38Z
dc.date.issued2011
dc.identifierhttps://hdl.handle.net/20.500.12866/11085
dc.identifierhttps://doi.org/10.1371/journal.pone.0016705
dc.description.abstractAims: To present a new approach for estimating the "true prevalence" of malaria and apply it to datasets from Peru, Vietnam, and Cambodia. Methods: Bayesian models were developed for estimating both the malaria prevalence using different diagnostic tests (microscopy, PCR & ELISA), without the need of a gold standard, and the tests' characteristics. Several sources of information, i.e. data, expert opinions and other sources of knowledge can be integrated into the model. This approach resulting in an optimal and harmonized estimate of malaria infection prevalence, with no conflict between the different sources of information, was tested on data from Peru, Vietnam and Cambodia. Results: Malaria sero-prevalence was relatively low in all sites, with ELISA showing the highest estimates. The sensitivity of microscopy and ELISA were statistically lower in Vietnam than in the other sites. Similarly, the specificities of microscopy, ELISA and PCR were significantly lower in Vietnam than in the other sites. In Vietnam and Peru, microscopy was closer to the "true" estimate than the other 2 tests while as expected ELISA, with its lower specificity, usually overestimated the prevalence. Conclusions: Bayesian methods are useful for analyzing prevalence results when no gold standard diagnostic test is available. Though some results are expected, e.g. PCR more sensitive than microscopy, a standardized and context-independent quantification of the diagnostic tests' characteristics (sensitivity and specificity) and the underlying malaria prevalence may be useful for comparing different sites. Indeed, the use of a single diagnostic technique could strongly bias the prevalence estimation. This limitation can be circumvented by using a Bayesian framework taking into account the imperfect characteristics of the currently available diagnostic tests. As discussed in the paper, this approach may further support global malaria burden estimation initiatives.
dc.languageeng
dc.publisherPublic Library of Science
dc.relationPLoS ONE
dc.relation1932-6203
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/4.0/deed.es
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectHumans
dc.subjectPeru
dc.subjectstatistical model
dc.subjectcontrolled study
dc.subjectpolymerase chain reaction
dc.subjectdiagnostic test
dc.subjectgeographic distribution
dc.subjectMalaria
dc.subjectPrevalence
dc.subjectstatistics
dc.subjectevaluation
dc.subjectquantitative analysis
dc.subjectSensitivity and Specificity
dc.subjectstandard
dc.subjectDiagnosis, Differential
dc.subjectenzyme linked immunosorbent assay
dc.subjectDiagnostic Tests, Routine
dc.subjectintermethod comparison
dc.subjectBayes Theorem
dc.subjectVietnam
dc.subjectseroprevalence
dc.subjectmathematical computing
dc.subjectCambodia
dc.subjectprocess optimization
dc.subjectbiomicroscopy
dc.titleTrue versus apparent Malaria infection prevalence: The contribution of a Bayesian approach
dc.typeinfo:eu-repo/semantics/article


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