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Comparison of real-time PCR and the Kato-Katz method for the diagnosis of soil-transmitted helminthiasis and assessment of cure in a randomized controlled trial
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 4616800
Author(s) Barda, Beatrice; Schindler, Christian; Wampfler, Rahel; Ame, Shaali; Ali, Said M.; Keiser, Jennifer
Author(s) at UniBasel Barda, Beatrice
Schindler, Christian
Wampfler, Rahel
Keiser, Jennifer
Year 2020
Title Comparison of real-time PCR and the Kato-Katz method for the diagnosis of soil-transmitted helminthiasis and assessment of cure in a randomized controlled trial
Journal BMC microbiology
Volume 20
Number 1
Pages / Article-Number 298
Keywords Diagnosis; Kato-Katz; PCR; Soil-transmitted helminthiasis
Mesh terms Adolescent; Albendazole, pharmacology; Ancylostomatoidea, genetics; Animals; Anthelmintics, pharmacology; Ascariasis, parasitology; Ascaris lumbricoides, genetics; Child; DNA, Helminth, genetics; Diagnostic Tests, Routine; Feces, parasitology; Female; Hookworm Infections, parasitology; Humans; Macrolides, pharmacology; Male; Phenylenediamines, pharmacology; Pyrantel Pamoate, pharmacology; Real-Time Polymerase Chain Reaction, methods; Sensitivity and Specificity; Soil, parasitology; Trichuriasis, parasitology; Trichuris, genetics; Young Adult
Abstract Diagnosis of soil-transmitted helminths (STHs) in developing countries is commonly based on microscopic detection of eggs in stool samples, using the Kato-Katz (KK) method, which has a poor sensitivity for detecting light intensity infections. We compared the performance of the KK method and real-time PCR in the framework of a randomized trial, which evaluated four novel treatments against Trichuris trichiura and concomitant STH infections.; Two stool samples obtained from 320 participants were examined at baseline and follow-up with quadruplicate KK and PCR analyses of one of the two samples using "bead-beating" for DNA extraction. At follow-up, 80 samples were negative according to both PCR and KK and 173 were positive with both methods for any of the STHs. Relative to PCR, the calculated sensitivity of KK at follow-up was 83.6%, 43.0% and 53.8% for T. trichiura, for hookworm and for Ascaris lumbricoides, respectively. The sensitivity of PCR compared with KK at this time point was 89.1% for T. trichiura, 72.7% for hookworm and 87.5% for A. lumbricoides. Cure rates (CRs) for T. trichiura and A. lumbricoides were slightly lower with the PCR method. For hookworm CRs with KK were mostly significantly lower, namely 36.7%, 91.1%, 72.2% and 77.8% for moxidectin, moxidectin in combination with tribendimidine, moxidectin in combination with albendazole and albendazole in combination with oxantel pamoate, respectively, whereas with PCR the CRs were 8.3%, 82.6%, 37.1% and 57.1%, respectively.; In conclusion, a single real-time PCR is as sensitive as quadruplicate KK for T. trichiura and A. lumbricoides detection but more sensitive for hookworm, which has an influence on the estimated treatment efficacy. PCR method with DNA extraction using the "bead-beating protocol" should be further promoted in endemic areas and laboratories that can afford the needed equipment. The study is registered at ISRCTN (no. 20398469).
ISSN/ISBN 1471-2180
edoc-URL https://edoc.unibas.ch/82048/
Full Text on edoc Available
Digital Object Identifier DOI 10.1186/s12866-020-01963-9
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/33008301
ISI-Number WOS:000576990900002
Document type (ISI) Journal Article, Randomized Controlled Trial
 
   

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