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1.
Lancet Glob Health ; 5(1): e40-e50, 2017 01.
Artículo en Inglés | MEDLINE | ID: mdl-27955788

RESUMEN

BACKGROUND: Soil-transmitted helminthiasis and schistosomiasis, considered among the neglected tropical diseases by WHO, affect more than a third of the world's population, with varying intensity of infection. We aimed to evaluate the effects of mass deworming for soil-transmitted helminths (with or without deworming for schistosomiasis or co-interventions) on growth, educational achievement, cognition, school attendance, quality of life, and adverse effects in children in endemic helminth areas. METHODS: We searched 11 databases up to Jan 14, 2016, websites and trial registers, contacted authors, and reviewed reference lists. We included studies published in any language of children aged 6 months to 16 years, with mass deworming for soil-transmitted helminths or schistosomiasis (alone or in combination with other interventions) for 4 months or longer, that reported the primary outcomes of interest. We included randomised and quasi-randomised trials, controlled before-after studies, interrupted time series, and quasi-experimental studies. We screened in duplicate, then extracted data and appraised risk of bias in duplicate with a pre-tested form. We conducted random-effects meta-analysis and Bayesian network meta-analysis. FINDINGS: We included 52 studies of duration 5 years or less with 1 108 541 children, and four long-term studies 8-10 years after mass deworming programmes with more than 160 000 children. Overall risk of bias was moderate. Mass deworming for soil-transmitted helminths compared with controls led to little to no improvement in weight over a period of about 12 months (0·99 kg, 95% credible interval [CrI] -0·09 to 0·28; moderate certainty evidence) or height (0·07 cm, 95% CrI -0·10 to 0·24; moderate certainty evidence), little to no difference in proportion stunted (eight fewer per 1000 children, 95% CrI -48 to 32; high certainty evidence), cognition measured by short-term attention (-0·23 points on a 100 point scale, 95% CI -0·56 to 0·14; high certainty evidence), school attendance (1% higher, 95% CI -1 to 3; high certainty evidence), or mortality (one fewer per 1000 children, 95% CI -3 to 1; high certainty evidence). We found no data on quality of life and little evidence of adverse effects. Mass deworming for schistosomiasis might slightly increase weight (0·41 kg, 95% CrI -0·20 to 0·91) and has little to no effect on height (low certainty evidence) and cognition (moderate certainty evidence). Our analyses do not suggest indirect benefits for untreated children from being exposed to treated children in the community. We are uncertain about effects on long-term economic productivity (hours worked), cognition, literacy, and school enrolment owing to very low certainty evidence. Results were consistent across sensitivity and subgroup analyses by age, worm prevalence, baseline nutritional status, infection status, impact on worms, infection intensity, types of worms (ascaris, hookworm, or trichuris), risk of bias, cluster versus individual trials, compliance, and attrition. INTERPRETATION: Mass deworming for soil-transmitted helminths with or without deworming for schistosomiasis had little effect. For schistosomiasis, mass deworming might be effective for weight but is probably ineffective for height, cognition, and attendance. Future research should assess which subset of children do benefit from mass deworming, if any, using individual participant data meta-analysis. FUNDING: Canadian Institutes of Health Research and WHO.


Asunto(s)
Antihelmínticos/uso terapéutico , Crecimiento , Helmintiasis/tratamiento farmacológico , Parasitosis Intestinales , Cognición , Humanos , Metaanálisis en Red , Suelo , Aumento de Peso
2.
J Clin Epidemiol ; 68(9): 1095-8, 2015 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-25797838

RESUMEN

OBJECTIVES: To describe some contextual and methodological challenges to conduct systematic reviews (SR) in developing countries using experiences from Jamaica. STUDY DESIGN AND SETTING: We identified four overarching challenges to conducting SRs in our setting, and present approaches used to overcome them. Challenges were evaluated using experiences in primary research and examples from SRs being conducted by the team. The applicability of global networking to increase capacity for SRs in Jamaica was described. RESULTS: Challenges were: 1) accessibility to the literature, 2) human resources in research, 3) local funding and 4) knowledge translation (KT). We found access to published literature was incomplete. There were limited human resources to conduct SRs, especially information scientists, knowledge brokers and expert SR methodologists as well as limited research funding. The approaches to overcome these challenges were; establishing membership within research networks, implementing training fellowship for SR authors, conducting sensitization and training workshops with specialized groups, and collaborating with developed country researchers for wider access to both funding and human resources. CONCLUSION: Challenges in conducting SR in developing countries can be overcome. Approaches to strengthen KT should be prioritized in order to generate and promote a robust, generalizable evidence base for healthcare and policy.


Asunto(s)
Países en Desarrollo , Literatura de Revisión como Asunto , Humanos , Jamaica , Proyectos de Investigación , Investigación Biomédica Traslacional
3.
Int J Endocrinol ; 2011: 716214, 2011.
Artículo en Inglés | MEDLINE | ID: mdl-22164161

RESUMEN

Background. There are limited data on sleep duration and diabetes from developing countries. We therefore examined the relationship between reported hours of sleep, diabetes prevalence and glucose control in Jamaican adults. Methods. Data on reported hours of sleep and diabetes (based on glucose measurement and medication use) from a national survey of 15-74-year-old Jamaicans were analyzed. Results. The 2,432 participants (31% M, Age 42 ± 16 years, BMI 27.6 ± 6.6 kg/m(2), diabetes prevalence 12%) reported sleeping 8.2 ± 1.8 hours. In men, sleeping less than 6 hours (OR (95% CI) = 2.65 (1.09-6.48)) or more than 10 hours (OR (95% CI) = 4.36 (1.56-12.19)) was associated with diabetes when adjusted for age, BMI, and family history of diabetes. In women sleeping less than 6 hours was associated with a reduced likelihood of diabetes after adjusting for the same confounders ((OR (95% CI) = 0.43 (0.23-0.78)). There was no significant association between sleep and glucose control. Conclusion. Insufficient and excessive sleep was associated with increased diabetes prevalence in Jamaican men but not women.

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