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Childhood growth during recovery from acute illness in Africa and South Asia: a secondary analysis of the childhood acute illness and nutrition (CHAIN) prospective cohort.
Bourdon, Celine; Diallo, Abdoulaye Hama; Mohammad Sayeem Bin Shahid, Abu Sadat; Khan, Md Alfazal; Saleem, Ali Faisal; Singa, Benson O; Gnoumou, Blaise Siézanga; Tigoi, Caroline; Otieno, Catherine Achieng; Oduol, Chrisantus Odhiambo; Lancioni, Christina L; Manyasi, Christine; McGrath, Christine J; Maronga, Christopher; Lwanga, Christopher; Brals, Daniella; Ahmed, Dilruba; Mondal, Dinesh; Denno, Donna M; Mangale, Dorothy I; Chimwezi, Emmanuel; Mbale, Emmie; Mupere, Ezekiel; Salauddin Mamun, Gazi Md; Ouédraogo, Issaka; Berkley, James A; Njunge, James M; Njirammadzi, Jenala; Mukisa, John; Thitiri, Johnstone; Walson, Judd L; Jemutai, Julie; Tickell, Kirkby D; Shahrin, Lubaba; Mallewa, Macpherson; Hossain, Md Iqbal; Chisti, Mohammod Jobayer; Timbwa, Molline; Mburu, Moses; Ngari, Moses M; Ngao, Narshion; Aber, Peace; Harawa, Philliness Prisca; Sukhtankar, Priya; Bandsma, Robert H J; Bamouni, Roseline Maïmouna; Molyneux, Sassy; Mwaringa, Shalton; Shaima, Shamsun Nahar; Ali, Syed Asad.
Affiliation
  • Bourdon C; Translational Medicine, Hospital for Sick Children, Toronto, ON, Canada.
  • Diallo AH; Department of Public Health, University Joseph Ki-Zerbo, Ouagadougou, Burkina Faso.
  • Mohammad Sayeem Bin Shahid AS; Department of Public Health, Centre Muraz Research Institute, Bobo-Dioulasso, Burkina Faso.
  • Khan MA; Nutrition Research Division, International Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b), Dhaka, Bangladesh.
  • Saleem AF; Health System and Population Studies Division, International Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b), Dhaka, Bangladesh.
  • Singa BO; Department of Pediatrics and Child Health, Aga Khan University, Karachi, Pakistan.
  • Gnoumou BS; Kenya Medical Research Institute, Nairobi, Kenya.
  • Tigoi C; Department of Public Health, University Joseph Ki-Zerbo, Ouagadougou, Burkina Faso.
  • Otieno CA; Clinical Research Department, KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
  • Oduol CO; Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.
  • Lancioni CL; Clinical Research Department, KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
  • Manyasi C; Clinical Research Department, KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
  • McGrath CJ; Department of Pediatrics, Oregon Health and Science University, Portland, OR, USA.
  • Maronga C; Department of Paediatrics, Mbagathi Hospital, Nairobi, Kenya.
  • Lwanga C; Department of Global Health, University of Washington, Seattle, WA, USA.
  • Brals D; Department of Epidemiology, University of Washington, Seattle, WA, USA.
  • Ahmed D; Clinical Research Department, KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
  • Mondal D; Uganda-Case Western Reserve University Research Collaboration, Kampala, Uganda.
  • Denno DM; Department of Global Health, Amsterdam UMC, University of Amsterdam, Amsterdam, Netherlands.
  • Mangale DI; Clinical Microbiology and Immunology Laboratory, Office of Executive Director, International Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b), Dhaka, Bangladesh.
  • Chimwezi E; Nutrition Research Division, International Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b), Dhaka, Bangladesh.
  • Mbale E; Department of Global Health, University of Washington, Seattle, WA, USA.
  • Mupere E; Department of Pediatrics, University of Washington, Seattle, WA, USA.
  • Salauddin Mamun GM; Department of Global Health, University of Washington, Seattle, WA, USA.
  • Ouédraogo I; Department of Paediatrics and Child Health, Kamuzu University of Health Sciences, Blantyre, Malawi.
  • Berkley JA; Department of Paediatrics and Child Health, Kamuzu University of Health Sciences, Blantyre, Malawi.
  • Njunge JM; Department of Paediatrics and Child Health, Makerere University College of Health Sciences, Kampala, Uganda.
  • Njirammadzi J; Infectious Diseases Division, International Centre for Diarrhoeal Disease Research Bangladesh (icddr,b), Dhaka, Bangladesh.
  • Mukisa J; Department of Pediatrics, Banfora Referral Regional Hospital, Banfora, Burkina Faso.
  • Thitiri J; Clinical Research Department, KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
  • Walson JL; Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.
  • Jemutai J; Clinical Research Department, KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
  • Tickell KD; Department of Paediatrics and Child Health, Kamuzu University of Health Sciences, Blantyre, Malawi.
  • Shahrin L; Department of Immunology and Department of Molecular Biology Makerere University College of Health Sciences, Kampala, Uganda.
  • Mallewa M; Clinical Research Department, KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
  • Hossain MI; Departments of International Health and Medicine, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD, USA.
  • Chisti MJ; Clinical Research Department, KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
  • Timbwa M; Department of Global Health, University of Washington, Seattle, WA, USA.
  • Mburu M; Hospitals, Office of Executive Director, International Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b), Dhaka, Bangladesh.
  • Ngari MM; Department of Paediatrics and Child Health, Kamuzu University of Health Sciences, Blantyre, Malawi.
  • Ngao N; Nutrition Research Division, International Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b), Dhaka, Bangladesh.
  • Aber P; Nutrition Research Division, International Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b), Dhaka, Bangladesh.
  • Harawa PP; Clinical Research Department, KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
  • Sukhtankar P; Clinical Research Department, KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
  • Bandsma RHJ; Clinical Research Department, KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
  • Bamouni RM; Clinical Research Department, KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
  • Molyneux S; Uganda-Case Western Reserve University Research Collaboration, Kampala, Uganda.
  • Mwaringa S; Department of Paediatrics and Child Health, Kamuzu University of Health Sciences, Blantyre, Malawi.
  • Shaima SN; Clinical Research Department, KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
  • Ali SA; Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.
EClinicalMedicine ; 70: 102530, 2024 Apr.
Article in En | MEDLINE | ID: mdl-38510373
ABSTRACT

Background:

Growth faltering is well-recognized during acute childhood illness and growth acceleration during convalescence, with or without nutritional therapy, may occur. However, there are limited recent data on growth after hospitalization in low- and middle-income countries.

Methods:

We evaluated growth following hospitalization among children aged 2-23 months in sub-Saharan Africa and South Asia. Between November 2016 and January 2019, children were recruited at hospital admission and classified as not-wasted (NW), moderately-wasted (MW), severely-wasted (SW), or having nutritional oedema (NO). We describe earlier (discharge to 45-days) and later (45- to 180-days) changes in length-for-age [LAZ], weight-for-age [WAZ], mid-upper arm circumference [MUACZ], weight-for-length [WLZ] z-scores, and clinical, nutritional, and socioeconomic correlates.

Findings:

We included 2472 children who survived to 180-days post-discharge NW, 960 (39%); MW, 572 (23%); SW, 682 (28%); and NO, 258 (10%). During 180-days, LAZ decreased in NW (-0.27 [-0.36, -0.19]) and MW (-0.23 [-0.34, -0.11]). However, all groups increased WAZ (NW, 0.21 [95% CI 0.11, 0.32]; MW, 0.57 [0.44, 0.71]; SW, 1.0 [0.88, 1.1] and NO, 1.3 [1.1, 1.5]) with greatest gains in the first 45-days. Of children underweight (<-2 WAZ) at discharge, 66% remained underweight at 180-days. Lower WAZ post-discharge was associated with age-inappropriate nutrition, adverse caregiver characteristics, small size at birth, severe or moderate anaemia, and chronic conditions, while lower LAZ was additionally associated with household-level exposures but not with chronic medical conditions.

Interpretation:

Underweight and poor linear growth mostly persisted after an acute illness. Beyond short-term nutritional supplementation, improving linear growth post-discharge may require broader individual and family support.

Funding:

Bill & Melinda Gates FoundationOPP1131320; National Institute for Health ResearchNIHR201813.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: EClinicalMedicine Year: 2024 Type: Article Affiliation country: Canada

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: EClinicalMedicine Year: 2024 Type: Article Affiliation country: Canada