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Linking quantitative microbial risk assessment and epidemiological data: informing safe drinking water trials in developing countries. | LitMetric

Linking quantitative microbial risk assessment and epidemiological data: informing safe drinking water trials in developing countries.

Environ Sci Technol

Department of Fisheries and Wildlife, 13 Natural Resources Building, Michigan State University, East Lansing, Michigan 48824, USA.

Published: May 2012

AI Article Synopsis

  • Intervention trials assess the effectiveness of household water treatment (HWT) devices against diarrheal diseases, but their findings may not always be applicable to other settings due to issues like generalizability and systematic bias.
  • A study analyzing the LifeStraw Family Filter in the Congo used quantitative microbial risk assessment (QMRA) to address biases related to compliance and disease recall, leading to modified effectiveness estimates for the device.
  • The findings underscored the significance of compliance for HWT efficacy, emphasized the need for pathogen data from water sources, and illustrated how biases can affect epidemiological conclusions, aiding in the generalization of trial results to different contexts.

Article Abstract

Intervention trials are used extensively to assess household water treatment (HWT) device efficacy against diarrheal disease in developing countries. Using these data for policy, however, requires addressing issues of generalizability (relevance of one trial in other contexts) and systematic bias associated with design and conduct of a study. To illustrate how quantitative microbial risk assessment (QMRA) can address water safety and health issues, we analyzed a published randomized controlled trial (RCT) of the LifeStraw Family Filter in the Congo. The model accounted for bias due to (1) incomplete compliance with filtration, (2) unexpected antimicrobial activity by the placebo device, and (3) incomplete recall of diarrheal disease. Effectiveness was measured using the longitudinal prevalence ratio (LPR) of reported diarrhea. The Congo RCT observed an LPR of 0.84 (95% CI: 0.61, 1.14). Our model predicted LPRs, assuming a perfect placebo, ranging from 0.50 (2.5-97.5 percentile: 0.33, 0.77) to 0.86 (2.5-97.5 percentile: 0.68, 1.09) for high (but not perfect) and low (but not zero) compliance, respectively. The calibration step provided estimates of the concentrations of three pathogen types (modeled as diarrheagenic E. coli, Giardia, and rotavirus) in drinking water, consistent with the longitudinal prevalence of reported diarrhea measured in the trial, and constrained by epidemiological data from the trial. Use of a QMRA model demonstrated the importance of compliance in HWT efficacy, the need for pathogen data from source waters, the effect of quantifying biases associated with epidemiological data, and the usefulness of generalizing the effectiveness of HWT trials to other contexts.

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Source
http://dx.doi.org/10.1021/es204381eDOI Listing

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