A 5-Year intervention study on elimination of urogenital schistosomiasis in Zanzibar: Parasitological results of annual cross-sectional surveys.
Adolescent
Adult
Animals
Anthelmintics
/ administration & dosage
Child
Cross-Sectional Studies
Disease Eradication
Female
Humans
Indian Ocean Islands
/ epidemiology
Islands
/ epidemiology
Male
Middle Aged
Praziquantel
/ administration & dosage
Prevalence
Schistosoma haematobium
/ drug effects
Schistosomiasis haematobia
/ epidemiology
Snails
/ parasitology
Urine
/ parasitology
Young Adult
Journal
PLoS neglected tropical diseases
ISSN: 1935-2735
Titre abrégé: PLoS Negl Trop Dis
Pays: United States
ID NLM: 101291488
Informations de publication
Date de publication:
05 2019
05 2019
Historique:
received:
05
01
2019
accepted:
26
02
2019
entrez:
7
5
2019
pubmed:
7
5
2019
medline:
24
10
2019
Statut:
epublish
Résumé
The Zanzibar Elimination of Schistosomiasis Transmission (ZEST) project aimed to eliminate urogenital schistosomiasis as a public health problem from Pemba and to interrupt Schistosoma haematobium transmission from Unguja in 5 years. A repeated cross-sectional cluster-randomized trial was implemented from 2011/12 till 2017. On each island, 45 shehias were randomly assigned to receive one of three interventions: biannual mass drug administration (MDA) with praziquantel alone, or in combination with snail control or behavior change measures. In cross-sectional surveys, a single urine sample was collected from ~9,000 students aged 9- to 12-years and from ~4,500 adults aged 20- to 55-years annually, and from ~9,000 1st year students at baseline and the final survey. Each sample was examined for S. haematobium eggs by a single urine filtration. Prevalence and infection intensity were determined. Odds of infection were compared between the intervention arms. Prevalence was reduced from 6.1% (95% confidence interval (CI): 4.5%-7.6%) to 1.7% (95% CI: 1.2%-2.2%) in 9- to 12-year old students, from 3.9% (95% CI: 2.8%-5.0%) to 1.5% (95% CI: 1.0%-2.0%) in adults, and from 8.8% (95% CI: 6.5%-11.2%) to 2.6% (95% CI: 1.7%-3.5%) in 1st year students from 2011/12 to 2017. In 2017, heavy infection intensities occurred in 0.4% of 9- to 12-year old students, 0.1% of adults, and 0.8% of 1st year students. Considering 1st year students in 2017, 13/45 schools in Pemba and 4/45 schools in Unguja had heavy infection intensities >1%. There was no significant difference in prevalence between the intervention arms in any study group and year. Urogenital schistosomiasis was eliminated as public health problem from most sites in Pemba and Unguja. Prevalence was significantly reduced, but transmission was not interrupted. Continued interventions that are adaptive and tailored to the micro-epidemiology of S. haematobium in Zanzibar are needed to sustain and advance the gains made by ZEST.
Sections du résumé
BACKGROUND
The Zanzibar Elimination of Schistosomiasis Transmission (ZEST) project aimed to eliminate urogenital schistosomiasis as a public health problem from Pemba and to interrupt Schistosoma haematobium transmission from Unguja in 5 years.
METHODOLOGY
A repeated cross-sectional cluster-randomized trial was implemented from 2011/12 till 2017. On each island, 45 shehias were randomly assigned to receive one of three interventions: biannual mass drug administration (MDA) with praziquantel alone, or in combination with snail control or behavior change measures. In cross-sectional surveys, a single urine sample was collected from ~9,000 students aged 9- to 12-years and from ~4,500 adults aged 20- to 55-years annually, and from ~9,000 1st year students at baseline and the final survey. Each sample was examined for S. haematobium eggs by a single urine filtration. Prevalence and infection intensity were determined. Odds of infection were compared between the intervention arms.
PRINCIPAL FINDINGS
Prevalence was reduced from 6.1% (95% confidence interval (CI): 4.5%-7.6%) to 1.7% (95% CI: 1.2%-2.2%) in 9- to 12-year old students, from 3.9% (95% CI: 2.8%-5.0%) to 1.5% (95% CI: 1.0%-2.0%) in adults, and from 8.8% (95% CI: 6.5%-11.2%) to 2.6% (95% CI: 1.7%-3.5%) in 1st year students from 2011/12 to 2017. In 2017, heavy infection intensities occurred in 0.4% of 9- to 12-year old students, 0.1% of adults, and 0.8% of 1st year students. Considering 1st year students in 2017, 13/45 schools in Pemba and 4/45 schools in Unguja had heavy infection intensities >1%. There was no significant difference in prevalence between the intervention arms in any study group and year.
CONCLUSIONS/SIGNIFICANCE
Urogenital schistosomiasis was eliminated as public health problem from most sites in Pemba and Unguja. Prevalence was significantly reduced, but transmission was not interrupted. Continued interventions that are adaptive and tailored to the micro-epidemiology of S. haematobium in Zanzibar are needed to sustain and advance the gains made by ZEST.
Identifiants
pubmed: 31059495
doi: 10.1371/journal.pntd.0007268
pii: PNTD-D-18-02043
pmc: PMC6502312
doi:
Substances chimiques
Anthelmintics
0
Praziquantel
6490C9U457
Types de publication
Journal Article
Randomized Controlled Trial
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e0007268Déclaration de conflit d'intérêts
The World Health Organization donated praziquantel to cover biannual mass drug administration conducted by the Neglected Diseases Program of the Zanzibar Ministry of Health, the Schistosomiasis Control Initiative funded the treatment implementation across Zanzibar, and Bayer S.A.S. donated 3 MT Bayluscide for snail control for use in the project.
Références
Acta Trop. 2008 Jan;105(1):45-54
pubmed: 17996207
Trans R Soc Trop Med Hyg. 2002 May-Jun;96(3):323-4
pubmed: 12174788
Wkly Epidemiol Rec. 2017 Dec 08;92(49):749-60
pubmed: 29218962
Infect Dis Poverty. 2017 Mar 22;6(1):63
pubmed: 28327187
PLoS Negl Trop Dis. 2016 Jul 21;10(7):e0004794
pubmed: 27441556
Acta Trop. 2016 Nov;163:142-8
pubmed: 27498244
Trans R Soc Trop Med Hyg. 2009 Oct;103(10):1031-44
pubmed: 19409588
Parasit Vectors. 2016 Jan 04;9:5
pubmed: 26727915
Parasit Vectors. 2018 Oct 23;11(1):552
pubmed: 30352631
PLoS Negl Trop Dis. 2015 Dec 28;9(12):e0004290
pubmed: 26709922
Lancet. 2018 Nov 10;392(10159):1859-1922
pubmed: 30415748
Acta Trop. 2015 Jan;141(Pt B):229-34
pubmed: 25301340
Trop Med Parasitol. 1989 Jun;40(2):189-94
pubmed: 2505381
Pathog Glob Health. 2014 Jul;108(5):246-54
pubmed: 25175875
Lancet Glob Health. 2019 Aug;7(8):e1118-e1129
pubmed: 31255591
Trop Med Int Health. 2010 May;15(5):614-8
pubmed: 20214757
Ann Trop Med Parasitol. 2008 Dec;102(8):679-92
pubmed: 19000385
BMC Public Health. 2012 Oct 30;12:930
pubmed: 23110494
J Biosoc Sci. 2016 Sep;48 Suppl 1:S56-73
pubmed: 27428066
Trans R Soc Trop Med Hyg. 1989 Nov-Dec;83(6):805-10
pubmed: 2515637
Bull World Health Organ. 1990;68(6):721-30
pubmed: 2127381
Acta Trop. 2013 Nov;128(2):423-40
pubmed: 22580511
PLoS Negl Trop Dis. 2013 Oct 17;7(10):e2474
pubmed: 24147165
Parasit Vectors. 2016 Dec 16;9(1):646
pubmed: 27986092
Int J Infect Dis. 2017 Jan;54:130-137
pubmed: 27939558