AJTMH Tropical Medicine and Hygiene News
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am. J. Trop. Med. Hyg., 42(6), 1990, pp. 587-595
Copyright © 1990 by The American Society of Tropical Medicine and Hygiene

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by King, C. H.
Right arrow Articles by Mahmoud, A. A. F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by King, C. H.
Right arrow Articles by Mahmoud, A. A. F.
Right arrowPubmed/NCBI databases
*Compound via MeSH
*Substance via MeSH
Hazardous Substances DB
*TRICHLORFON

Chemotherapy-Based Control of Schistosomiasis Haematobia

II. Metrifonate vs. Praziquantel in Control of Infection-Associated Morbidity

Charles H. King, George Lombardi, Cheryl Lombardi, Ruth Greenblatt, Sally Hodder, Henry Kinyanjui, John Ouma, Omondi Odiambo, Patrick J. Bryan, Jagon Muruka, Phillip Magak, Dana Weinert, David Ransohoff, Harold Houser, Davy Koech, Timothy K. Arap Siongok AND Adel A. F. Mahmoud
Case Western Reserve University and University Hospitals of Cleveland, Cleveland, Ohio; Kenyatta Hospital, Nairobi, Kenya; Kenya Medical Research Institute, Nairobi, Kenya; Ministry of Health, Nairobi, Kenya

To determine the relative efficacy of metrifonate and praziquantel in controlling urinary tract morbidity due to Schistosoma haematobium infection, a random allocation treatment trial was performed among 1,813 school age S. haematobium-infected children from the Msambweni area of Coast Province, Kenya. Following baseline examination for infection, hematuria, proteinuria, and ultrasonographic urinary tract abnormalities, oral treatment with either metrifonate (10 mg/kg, repeated at 4 month intervals) or praziquantel (1 dose of 40 mg/kg) was given to infected subjects. Prevalence of morbidity was reassessed 12 months later for each treatment group. Results indicated equivalent patient improvement in response to either regimen: prevalence of hematiuria fell from 75% to 17% after either praziquantel or metrifonate therapy. Similarly, prevalence of proteinuria was significantly reduced from 73% to 29% (metrifonate) or 27% (praziquantel) after therapy. Metrifonate and praziquantel caused similar reductions in bladder granulomata and bladder thickening; however, no reduction in hydronephrosis was noted with either drug. Analysis of outcomes in population subgroups defined by age, sex, pretreatment intensity of infection, or severity of pretreatment morbidity showed no consistent advantage for either drug. In this endemic area, both agents provide effective control of morbidity due to urinary schistosomiasis.




This article has been cited by other articles:


Home page
Am J Trop Med HygHome page
S. A. SATAYATHUM, E. M. MUCHIRI, J. H. OUMA, C. C. WHALEN, and C. H. KING
FACTORS AFFECTING INFECTION OR REINFECTION WITH SCHISTOSOMA HAEMATOBIUM IN COASTAL KENYA: SURVIVAL ANALYSIS DURING A NINE-YEAR, SCHOOL-BASED TREATMENT PROGRAM.
Am J Trop Med Hyg, July 1, 2006; 75(1): 83 - 92.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1990 by the American Society of Tropical Medicine and Hygiene.