A 14-year follow-up of ultrasound-detected urinary tract pathology associated with urogenital schistosomiasis in women living in the Msambweni region of coastal Kenya

Author:

Joekes Elizabeth12,McMonnies Kate3,Blanshard Andrew3,Mutuku Francis M4,Ireri Edmund5,Mungai Peter6,Stothard J Russell3,Bustinduy Amaya L7,King Charles H6

Affiliation:

1. Department of Radiology, Liverpool University Hospitals NHS Foundation Trust , Liverpool L7 8XP , UK

2. Department of Clinical Sciences, Liverpool School of Tropical Medicine , Liverpool L3 5QA , UK

3. Department of Tropical Disease Biology, Liverpool School of Tropical Medicine , Liverpool L3 5QA , UK

4. Department of Environment and Health Science, Technical University of Mombasa , Mombasa , Kenya

5. Kenya Medical Research Institute, CCR Radiology Unit , Nairobi , Kenya

6. Center for Global Health and Diseases, Case Western Reserve University, Cleveland , OH 44106 , USA

7. Department of Clinical Research, London School of Hygiene and Tropical Medicine , London WC1E 7HT , UK

Abstract

ABSTRACT Background Complications of urogenital schistosomiasis include acute inflammatory and chronic fibrotic changes within the urogenital tract. Disease burden of this neglected tropical disease is often underestimated, as only active, urine egg-patent Schistosoma infection is formally considered. Previous studies have focussed on short-term effects of praziquantel treatment on urinary tract pathology, demonstrating that acute inflammation is reversible. However, the reversibility of chronic changes is less well studied. Methods Our study compared, at two time points 14 y apart, urine egg-patent infection and urinary tract pathology in a cohort of women living in a highly endemic area having intermittent praziquantel treatment(s). In 2014 we matched 93 women to their findings in a previous study in 2000. Results Between 2000 and 2014 the rate of egg-patent infection decreased from 34% (95% confidence interval [CI] 25 to 44) to 9% (95% CI 3 to 14). However, urinary tract pathology increased from 15% (95% CI 8 to 22) to 19% (95% CI 11 to 27), with the greatest increase seen in bladder thickening and shape abnormality. Conclusions Despite praziquantel treatment, fibrosis from chronic schistosomiasis outlasts the presence of active infection, continuing to cause lasting morbidity. We suggest that future efforts to eliminate persistent morbidity attributable to schistosomiasis should include intensified disease management.

Funder

National Institutes of Health

Fogarty International Center

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Public Health, Environmental and Occupational Health,General Medicine,Parasitology

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