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dc.contributor.authorKotloff, Karen L.en_US
dc.contributor.authorNasrin, Dilrubaen_US
dc.contributor.authorBlackwelder, William C.en_US
dc.contributor.authorWu, Yukunen_US
dc.contributor.authorFarag, Tamer H.en_US
dc.contributor.authorPanchalingham, Sandraen_US
dc.contributor.authorSow, Samba O.en_US
dc.contributor.authorSur, Dipikaen_US
dc.contributor.authorZaidi, Anita K.M.en_US
dc.contributor.authorFaruque, Abu Syed Golamen_US
dc.contributor.authorSaha, Debasishen_US
dc.contributor.authorAlonso, Pedro L.en_US
dc.contributor.authorTamboura, Boubouen_US
dc.contributor.authorSanogo, Dohen_US
dc.contributor.authorOnwuchekwa, Umaen_US
dc.contributor.authorManna, Byomkeshen_US
dc.contributor.authorRamamurthy, Thandavarayanen_US
dc.contributor.authorKanungo, Sumanen_US
dc.contributor.authorAhmed, Shahnawazen_US
dc.contributor.authorQureshi, Shahidaen_US
dc.contributor.authorQuadri, Farheenen_US
dc.contributor.authorHossain, Anowaren_US
dc.contributor.authorDas, Sumon K.en_US
dc.contributor.authorAntonio, Martinen_US
dc.contributor.authorHossain, Mohammad Jahangiren_US
dc.contributor.authorMandomando, Inacioen_US
dc.contributor.authorAcácio, Sozinhoen_US
dc.contributor.authorBiswas, Kousicken_US
dc.contributor.authorTennant, Sharon M.en_US
dc.contributor.authorVerweij, Jaco J.en_US
dc.contributor.authorSommerfelt, Halvoren_US
dc.contributor.authorNataro, James Paulen_US
dc.contributor.authorRobins-Browne, Roy M.en_US
dc.contributor.authorLevine, Myron M.en_US
dc.PublishedKotloff KL, Nasrin D, Blackwelder WC, Wu Y, Farag TH, Panchalingham, Sow SO, Sur D, Zaidi AK, Faruque ASG, Saha D, Alonso PL, Tamboura B, Sanogo D, Onwuchekwa U, Manna B, Ramamurthy T, Kanungo S, Ahmed S, Qureshi S, Quadri F, Hossain A, Das SK, Antonio M, Hossain MJ, Mandomando I, Acácio S, Biswas K, Tennant SM, Verweij JJ, Sommerfelt H, Nataro JP, Robins-Browne RM, Levine MM. The incidence, aetiology, and adverse clinical consequences of less severe diarrhoeal episodes among infants and children residing in low-income and middle-income countries: a 12-month case-control study as a follow-on to the Global Enteric Multicenter Study (GEMS). The Lancet Global Health. 2019;7(5):e568-e584eng
dc.description.abstractBackground Diarrheal diseases remain a leading cause of illness and death among children younger than 5 years in low-income and middle-income countries. The Global Enteric Multicenter Study (GEMS) has described the incidence, aetiology, and sequelae of medically attended moderate-to-severe diarrhoea (MSD) among children aged 0–59 months residing in censused populations in sub-Saharan Africa and south Asia, where most child deaths occur. To further characterise this disease burden and guide interventions, we extended this study to include children with episodes of less-severe diarrhoea (LSD) seeking care at health centres serving six GEMS sites. Methods We report a 1-year, multisite, age-stratified, matched case-control study following on to the GEMS study. Six sites (Bamako, Mali; Manhiça, Mozambique; Basse, The Gambia; Mirzapur, Bangladesh; Kolkata, India; and Bin Qasim Town, Karachi, Pakistan) participated in this study. Children aged 0–59 months at each site who sought care at a sentinel hospital or health centre during a 12-month period were screened for diarrhoea. New (onset after ≥7 diarrhoea-free days) and acute (onset within the previous 7 days) episodes of diarrhoea in children who had sunken eyes, whose skin lost turgor, who received intravenous hydration, who had dysentery, or who were hospitalised were eligible for inclusion as MSD. The remaining new and acute diarrhoea episodes among children who sought care at the same health centres were considered LSD. We aimed to enrol the first eight or nine eligible children with MSD and LSD at each site during each fortnight in three age strata: infants (aged 0–11 months), toddlers (aged 12–23 months), and young children (aged 24–59 months). For each included case of MSD or LSD, we enrolled one to three community control children without diarrhoea during the previous 7 days. From patients and controls we collected clinical and epidemiological data, anthropometric measurements, and faecal samples to identify enteropathogens at enrolment, and we performed a follow-up home visit about 60 days later to ascertain vital status, clinical outcome, and interval growth. Primary outcomes were to characterise, for MSD and LSD, the pathogen-specific attributable risk and population-based incidence values, and to assess the frequency of adverse clinical consequences associated with these two diarrhoeal syndromes. Findings From Oct 31, 2011, to Nov 14, 2012, we recruited 2368 children with MSD, 3174 with LSD, and one to three randomly selected community control children without diarrhoea matched to cases with MSD (n=3597) or LSD (n=4236). Weighted adjusted population attributable fractions showed that most attributable cases of MSD and LSD were due to rotavirus, Cryptosporidium spp, enterotoxigenic Escherichia coli encoding heat-stable toxin (with or without genes encoding heat-labile enterotoxin), and Shigella spp. The attributable incidence per 100 child-years for LSD versus MSD, by age stratum, for rotavirus was 22·3 versus 5·5 (0–11 months), 9·8 versus 2·9 (12–23 months), and 0·5 versus 0·2 (24–59 months); for Cryptosporidium spp was 3·6 versus 2·3 (0–11 months), 4·3 versus 0·6 (12–23 months), and 0·3 versus 0·1 (24–59 months); for enterotoxigenic E coli encoding heat-stable toxin was 4·2 versus 0·1 (0–11 months), 5·2 versus 0·0 (12–23 months), and 1·1 versus 0·2 (24–59 months); and for Shigella spp was 1·0 versus 1·3 (0–11 months), 3·1 versus 2·4 (12–23 months), and 0·8 versus 0·7 (24–59 months). Participants with both MSD and LSD had significantly more linear growth faltering than controls at follow-up. Interpretation Inclusion of participants with LSD markedly expands the population of children who experience adverse clinical and nutritional outcomes from acute diarrhoeal diseases. Since MSD and LSD have similar aetiologies, interventions targeting rotavirus, Shigella spp, enterotoxigenic E coli producing heat-stable toxin, and Cryptosporidium spp might substantially reduce the diarrhoeal disease burden and its associated nutritional faltering. Funding Bill & Melinda Gates Foundation.en_US
dc.rightsCC BY-NC-NDeng
dc.titleThe incidence, aetiology, and adverse clinical consequences of less severe diarrhoeal episodes among infants and children residing in low-income and middle-income countries: a 12-month case-control study as a follow-on to the Global Enteric Multicenter Study (GEMS)en_US
dc.typePeer reviewed
dc.typeJournal article
dc.rights.holderCopyright The Author(s) 2019
dc.source.journalThe Lancet Global Health

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