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      The Accuracy of Praziquantel Dose Poles for Mass Treatment of Schistosomiasis in School Girls in KwaZulu-Natal, South Africa

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          Abstract

          Background

          More than 260 million people live with schistosomiasis and regular mass-treatment should be implemented to prevent morbidity. Praziquantel, dosed at 40 milligrams per kilogram bodyweight, is the drug of choice. During the last decades the WHO Tablet Pole–which estimates tablet need by height as representing weight–has been used as a practical and cheap tool in mass treatment. In South Africa this method could be inaccurate given the prevalence of overweight and obesity. In this study in female pupils in KwaZulu-Natal, South Africa, we explored the accuracy of the WHO Tablet Pole and the recently developed Modified Dose Pole for adults with two additional intervals and correction for body mass index (BMI).

          Methodology

          In randomly selected primary and secondary schools of schistosomiasis-endemic areas, height and weight of female pupils were measured. The WHO Tablet Pole and Modified Dose Pole were used to indicate the amount of praziquantel according to height and the dose in milligrams per kilogram bodyweight was calculated. The BMI correction was performed by adding 600 milligrams (1 tablet) to the indicated dose if a person was overweight/obese.

          Principal Findings

          3157 female students were investigated and 35% were found to be overweight/obese. Using the WHO Tablet Pole, 73% would have received an adequate dose (range 30–60 mg/kg). When correcting for BMI, this would have been 94%. Using the Modified Dose Pole with BMI correction, 97% would have been adequately treated.

          Conclusions

          This study shows that the WHO Tablet Pole will be inaccurate in estimating the dose of praziquantel in South African girls due to high prevalence of overweight/obesity. Under-dosing of individuals who appear overweight/obese could be largely prevented by adding an extra praziquantel tablet to the recommended dose. Further research must be done to explore if subjective weight estimates are reliable.

          Author Summary

          Schistosomiasis is an acute and chronic parasitic disease caused by Schistosoma worms, contributing to morbidity and mortality in 261 million people, mainly in poor, rural communities. In an effort to control schistosomiasis, the World Health Organization advocates for regular mass treatment to at-risk populations, administering free praziquantel (40mg/kg). The WHO Tablet Pole, which estimates the number of tablets for each individual by height, is recommended for the dosing of praziquantel. A Modified Dose Pole with two additional height intervals has been developed for adults. In addition, the developers of the Modified Dose Pole suggest to add an extra tablet to the indicated dose if the person appears to be overweight/obese (“correction for body mass index (BMI)”). This study explored the accuracy of these dose pole programmes in 3157 school-girls in schistosomiasis-endemic KwaZulu-Natal, South Africa. Overweight or obesity was found in 35% of the study population. With the WHO Tablet Pole, only 73% would have received an acceptable dose (30-60mg/kg), whereas when correcting for overweight/obesity almost all the girls would have been adequately treated. We suggest adding one tablet to the dose recommended by the WHO Tablet Pole if a person appears to be overweight/obese to prevent under-dosing of these individuals.

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          Most cited references17

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          Use of the Danish Adoption Register for the study of obesity and thinness.

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            Association between genital schistosomiasis and HIV in rural Zimbabwean women.

            To determine the association between female genital Schistosoma haematobium infection and HIV. A cross-sectional study with a 1-year follow-up. Gynecological and laboratory investigations were performed for S. haematobium and HIV. Sexually transmitted infections, demographic and urogenital history were analysed as confounders. The participants were 527 sexually active, non-pregnant, non-menopausal women between the ages of 20 and 49 years. The setting was a rural Zimbabwean community where S. haematobium related lesions were found in 46% of the women, HIV in 29% and herpes simplex type- 2 (HSV-2) in 65%. In permanent residents (>3 years residency), HIV was found in 41% (29/70) of women with laboratory proven genital schistosomiasis as opposed to 26% HIV positive (96/375) in the schistosomal ova negative group [odds ratio (OR), 2.1; 95% confidence interval (CI), 1.2-3.5; P = 0.008. In multivariate analysis S. haematobium infection of the genital mucosa was significantly associated with HIV seropositivity (adjusted OR, 2.9; 95% CI, 1.11-7.5; P = 0.030). All seven women who became HIV positive during the study period (seroincidence 3.1%) had signs of S. haematobium at baseline. In accordance with other studies HIV was significantly associated with HSV-2 (OR, 3.0; 95% CI, 1.7-5.3; P < 0.001), syphilis and human papillomavirus. The highest HIV prevalence (45%) was found in the 25-29 years age group. Women with genital schistosomiasis had an almost three-fold risk of having HIV in this rural Zimbabwean community. Prospective studies are needed to confirm the association.
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              Urogenital schistosomiasis in women of reproductive age in Tanzania's Lake Victoria region.

              We conducted a community-based study of 457 women aged 18-50 years living in eight rural villages in northwest Tanzania. The prevalence of female urogenital schistosomiasis (FUS) was 5% overall but ranged from 0% to 11%. FUS was associated with human immunodeficiency virus (HIV) infection (odds ratio [OR] = 4.0, 95% confidence interval [CI] = 1.2-13.5) and younger age (OR = 5.5 and 95% CI = 1.2-26.3 for ages 35 years). Overall HIV prevalence was 5.9% but was 17% among women with FUS. We observed significant geographical clustering of schistosomiasis: northern villages near Lake Victoria had more Schistosoma mansoni infections (P < 0.0001), and southern villages farther from the lake had more S. haematobium (P = 0.002). Our data support the postulate that FUS may be a risk factor for HIV infection and may contribute to the extremely high rates of HIV among young women in sub-Saharan Africa.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS Negl Trop Dis
                PLoS Negl Trop Dis
                plos
                plosntds
                PLoS Neglected Tropical Diseases
                Public Library of Science (San Francisco, CA USA )
                1935-2727
                1935-2735
                3 May 2016
                May 2016
                : 10
                : 5
                : e0004623
                Affiliations
                [1 ]Department of Parasitology, Leiden University Medical Centre, Leiden, The Netherlands
                [2 ]Faculty of Health, Medicine and Life Science, Maastricht University, Maastricht, The Netherlands
                [3 ]Norwegian Centre for Imported and Tropical Diseases, Department of Infectious Diseases, Oslo University Hospital, Oslo, Norway
                [4 ]Faculty of Medicine, University of Oslo, Oslo, Norway
                [5 ]Discipline of Public Health Medicine, Nelson R Mandela School of Medicine, College of Health Sciences, University of KwaZulu-Natal, Durban, South Africa
                [6 ]Section for Parasitology and Aquatic Diseases, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark
                Children's National Medical Center, UNITED STATES
                Author notes

                The authors have declared that no competing interests exist.

                Conceived and designed the experiments: MB HNGA SG BJV MT LvL EFK. Performed the experiments: MB HNGA SG BJV MT LvL EFK. Analyzed the data: MB HNGA SG BJV MT LvL EFK. Contributed reagents/materials/analysis tools: MB HNGA SG BJV MT LvL EFK. Wrote the paper: MB HNGA SG CGA BJV MT LvL EFK.

                Article
                PNTD-D-15-01269
                10.1371/journal.pntd.0004623
                4854411
                27139497
                8dbe520b-b749-445e-96c7-f1b644da04ac
                © 2016 Baan et al

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 12 October 2015
                : 21 March 2016
                Page count
                Figures: 3, Tables: 2, Pages: 13
                Funding
                Funded by: South-Eastern Regional Health Authority
                Award ID: Norway project no. 2014065
                Award Recipient :
                Funded by: Norwegian Research Council
                Award ID: ref 213702/H10
                Funded by: Prof. Dr. P.C. Flu Foundation
                Funded by: European Research Council under the European Union's Seventh Framework Programme (FP7/2007-2013)
                Award ID: Grant agreement no. PIRSES-GA-2010-269245
                The research leading to these results has received funding from the European Research Council under the European Union's Seventh Framework Programme (FP7/2007-2013) /European Research Commission Grant agreement no. PIRSES-GA-2010-269245 (MB HNGA SG BJV MT LvL EFK), URL; http://ec.europa.eu/research/fp7/index_en.cfm, South-Eastern Regional Health Authority, Norway project no. 2014065 (HNGA), URL; http://www.helse-sorost.no/fag/forskning-og-innovasjon, Prof. Dr. P.C. Flu Foundation (MB, LvL) and the Norwegian Research Council ref 213702/H10 (EFK, HNGA, MT, SG, LvL, BJV). URL; http://www.forskningsradet.no/en/Home_page/1177315753906 The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Social Sciences
                Sociology
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                Physiology
                Physiological Parameters
                Body Weight
                Obesity
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                Physiology
                Physiological Parameters
                Body Weight
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                Parasitic Diseases
                Helminth Infections
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                Schistosomiasis
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                All relevant data are within the paper and its Supporting Information files.

                Infectious disease & Microbiology
                Infectious disease & Microbiology

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