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RESEARCH |
Paul Ogutu, Peter Barasa, Sam Ombeki, and Alex Mwaki are with CARE Kenya, Homa Bay, Kenya, Africa. Valerie Garrett and Robert E. Quick are with the Foodborne and Diarrheal Diseases Branch, Division of Bacterial and Mycotic Diseases, Centers for Disease Control and Prevention, Atlanta, Ga.
Correspondence: Requests for reprints should be sent to Robert E. Quick, MD, MPH, Foodborne and Diarrheal Diseases Branch, Mail Stop A38, Centers for Disease Control and Prevention, Atlanta, GA 30333 (e-mail: rxq1{at}cdc.gov).
| INTRODUCTION |
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We evaluated 3 vessel types: (1) wide-mouthed, 20-L clay vessels; (2) narrow-mouthed, 20-L clay vessels with lids and spigots (modified clay vessel); and (3) narrowmouthed, 20-L plastic jerry cans with lids (Figure 1
). We treated water with 1% sodium hypochlorite and measured free chlorine levels with colorimetric comparators. We assessed the microbiological quality of treated and untreated water with the membrane filtration technique and culture media selective for Escherichia coli.4
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In the village evaluation, 10 of 20 volunteer households were randomly selected to receive new, modified clay vessels. The remaining 10 used their own freshly cleaned traditional clay vessels. Within each group, 5 households also were selected to receive plastic jerry cans. We then filled each vessel with 20 L of river water, treated it with 16 mL of 1% sodium hypochlorite (8 mg/L), and measured free chlorine levels and cultured water after 0.5 and 24 hours.
In the laboratory evaluation, untreated river water had a baseline E coli count of 100 colony-forming units (CFUs) per 100 mL. After treatment, the free chlorine decay rate was 4% per hour in the plastic jerry can, 8% per hour in the modified clay vessel, and 9% per hour in the traditional clay vessel (Figure 2
). After 24 hours, the free chlorine level was highest in the jerry can; however, all vessels had a free chlorine level greater than 0.2 mg/L. E coli (range = 521 CFU/100 mL) was recovered from water from each vessel 0.5 hours after treatment. E coli was not recovered from water from any vessel 24 hours after treatment.
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For more complete data, please refer to http://www.cdc.gov/safewater.
| Acknowledgments |
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This project was supported by a grant from the CARECDC Health Initiative (CCHI).
We thank Patricia Riley, Luke Nkinsi, Reema Jossy, and Lori Buhi of CCHI and Dr Adam Koons and George Kidenda of CARE Kenya for their support of this project. We thank Gwen Ingraham for her editorial assistance. We are especially grateful for the cooperation and enthusiasm of the community members of Ariri village.
| Footnotes |
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Accepted for publication June 5, 2001.
| References |
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2. Quick RE, Venczel LV, Gonzalez O, et al. Narrow-mouthed water storage vessels and in situ chlorination in a Bolivian community: a simple method to improve drinking water quality. Am J Trop Med Hyg.1996;54:511516.
3.
Makutsa P, Nzaku K, Ogutu P, et al. Challenges in implementing a point-of-use water quality intervention in rural Kenya. Am J Public Health.2001;91:15711573.
4. Mates A, Shaffer M. Membrane filtration differentiation of E coli from coliforms in the examination of water. J Appl Bacteriol. 1989;67:343346.[Medline]
5. Deb BC, Sircar BK, Sengupta PG, Sen SP, Saha MR, Pal SC. Intra-familial transmission of Vibrio cholerae biotype El Tor in Calcutta slums. Indian J Med Res.1982;76:814819.[Medline]
6. Swerdlow DL, Malenga G, Begkoyian G, et al. Epidemic cholera among refugees in Malawi, Africa: treatment and transmission. Epidemiol Infect. 1997;118:207214.[Medline]
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