Albendazole is effective treatment for chronic strongylodiasis

A total of 301 British ex-Far East prisoners of war, many of whom worked on the Thai-Burma Railway during World War II, consecutively attended The Liverpool School of Tropical Medicine for clinical review between January 1987 and August 1990. Fifty-two (17%) were found to have chronic strongyloidias...

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Bibliographic Details
Published inQJM : An International Journal of Medicine Vol. 86; no. 3; pp. 191 - 193
Main Authors ARCHIBALD, L.K., BEECHING, N.J., GILL, G.V., BAILEY, J.W., BELL, D.R.
Format Journal Article
LanguageEnglish
Published Oxford University Press 01.03.1993
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Summary:A total of 301 British ex-Far East prisoners of war, many of whom worked on the Thai-Burma Railway during World War II, consecutively attended The Liverpool School of Tropical Medicine for clinical review between January 1987 and August 1990. Fifty-two (17%) were found to have chronic strongyloidiasis. Diagnostic criteria included any of the following: characteristic larva currens rash, positive Strongyloides serology, and positive stool examination. Forty-seven were evaluable 6 months, after therapy with albendazole 400 mg twice daily for 3 days, which resulted in a 75% cure rate. Cure was defined as disappearance of the rash, if present, negative serology and negative stool examination. Patients who had more than one positive diagnostic feature were only considered cured if both or all had disappeared or become negative. All 12 of the patients in whom initial treatment failed were given a second course of albendazole: three further cures were obtained in eight evaluable patients. The overall cure rate was 81%. The only side-effects recorded were mild nausea and diarrhoea in one patient. We suggest that albendazole should be the treatment of choice for chronic strongyloidiasis.
Bibliography:ark:/67375/HXZ-TC1BG0WC-Z
istex:1029CD13E2D5467E1087A20A63BB31A7E3DBB881
Address correspondence to Dr NJ Beeching, Liverpool school of Tropical Medicine, Pembroke Place, Liverpool L3 SQA
ArticleID:86.3.191
ISSN:1460-2725
1460-2393
1460-2393
DOI:10.1093/oxfordjournals.qjmed.a068790