CHANGE Cohort 2: Chronic disease outcomes after Severe Acute Malnutrition (ChroSAM). Malawi

Kerac, M, Anujuo, K, Lelijveld, N, Kanjala, C, Chimwezi, E and Nyirenda, M. 2022. CHANGE Cohort 2: Chronic disease outcomes after Severe Acute Malnutrition (ChroSAM). Malawi. [Online]. London School of Hygiene & Tropical Medicine, London, United Kingdom. Available from: https://doi.org/10.17037/DATA.00002657.

Kerac, M, Anujuo, K, Lelijveld, N, Kanjala, C, Chimwezi, E and Nyirenda, M. CHANGE Cohort 2: Chronic disease outcomes after Severe Acute Malnutrition (ChroSAM). Malawi [Internet]. London School of Hygiene & Tropical Medicine; 2022. Available from: https://doi.org/10.17037/DATA.00002657.

Kerac, M, Anujuo, K, Lelijveld, N, Kanjala, C, Chimwezi, E and Nyirenda, M (2022). CHANGE Cohort 2: Chronic disease outcomes after Severe Acute Malnutrition (ChroSAM). Malawi. [Data Collection]. London School of Hygiene & Tropical Medicine, London, United Kingdom. https://doi.org/10.17037/DATA.00002657.

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Description of data capture The data comes from a prospective cohort of children, recruited during a randomised controlled trial with null findings, while they were being treated for severe malnutrition (PRONUT study). They were then followed up at 1 year post-discharge (FuSAM). This was a secondary analysis of data collected from children treated for severe wasting and/or nutritional oedema in 2006/7 in Malawi, and followed up seven years later to assess risk of NCD. The objectives of the current analysis were to: (1) Explore rates of Post-malnutrition growth (PMGr) based on a variety of weight- and height-related definitions; (2) Explore different ways of categorising these PMGr definitions into fast and slow; and (3) Explore associations and patterns between the different definitions and categorisations of PMGr with indicators of NCD risk. The original data comes from a prospective cohort of children, recruited during a randomised controlled trial with null findings, while they were being treated for severe malnutrition (PRONUT study). They were then followed up at 1 year post-discharge (FuSAM study) and again at 7-years post-discharge (ChroSAM study), where the focus was more on indicators of NCD risk. Interviews were conducted face-to-face by trained nurses and data collectors, on the ward and then at the households of each participant, in the local language. Details of the data collection methods including anthropometry methods, lab tests, and questionnaires can be found in a number of publications (Kerac et al., 2009, Kerac et al., 2014, Lelijveld et al., 2016). Key features include: All children admitted for treatment during the recruitment period were eligible for inclusion. Admission criteria for treatment were weight-for-length z-score <70% median (using NCHS reference) and/or MUAC<110 mm and/or bilateral oedema. All patients were admitted for initial inpatient treatment, following the WHO 3-stage protocol at that time: stabilisation with F75 therapeutic milk, transition phase where RUTF was introduced to the diet alongside F75, and then rehabilitation phase where children were discharged with a 2-week ration of RUTF to continue their recovery at home and return to the ward for monitoring and to collect another ration every 2 weeks until recovery. Children were discharged from outpatient therapeutic care following 2 consecutive fortnightly visits at or above target weight of 80% median weight-for-height. Minimum time in outpatient care was therefore 4 weeks. Maximum time was 10 weeks. This analysis was coordinated with similar analyses of cohort data for children treated for severe malnutrition in Jamaica and Ethiopia – this had some bearing on the methodology.
Data capture method Measurements and tests
Data Collection Period
FromTo
12 July 20061 January 2014
Date (Date submitted to LSHTM repository) 2 March 2022
Geographical area covered (offline during plugin upgrade)
North LatitudeEast LongitudeSouth LatitudeWest Longitude
-15.468335.408-15.967334.8147
Language(s) of written materials English
Data Creators Kerac, M, Anujuo, K, Lelijveld, N, Kanjala, C, Chimwezi, E and Nyirenda, M
Associated roles Kerac, M (Principal Investigator), Anujuo, K (Project Manager), Lelijveld, N (Co-Investigator), Kanjala, C (Co-Investigator), Chimwezi, E (Other) and Nyirenda, M (Co-Investigator)
LSHTM Faculty/Department Faculty of Epidemiology and Population Health > Dept of Population Health (2012- )
Research Centre Maternal and Child Health Intervention Research Group
Research Group Nutrition
Participating Institutions London School of Hygiene & Tropical Medicine, London, United Kingdom, Malawi-Liverpool-Wellcome Trust Clinical Research Programme, Blantyre, Malawi, College of Medicine, University of Malawi, Blantyre, Malawi
Funders
ProjectFunderGrant NumberFunder URI
Chronic Disease Outcome following Severe Acute Malnutrition (ChroSAM study)Wellcome Trust101113/Z/13/A)https://doi.org/10.13039/100010269
CHild malnutrition & Adult NCDs: Generating new Evidence on mechanistic links to inform future policy and practice (CHANGE project)Medical Research CouncilMR/V000802/1https://doi.org/10.13039/501100000265
Date Deposited 03 Mar 2022 17:31
Last Modified 21 Mar 2022 16:26
Publisher London School of Hygiene & Tropical Medicine

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Filename: ChroSAM_CHANGE_dataset.txt

Description: Access arrangements for the ChroSAM CHANGE dataset are handled in-country by the study investigators, in accordance with study ethics approvals. Please consult the data codebook for information

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Description: CHANGE Cohort 2: Chronic disease outcomes after Severe Acute Malnutrition (ChroSAM). Malawi – User Guide and Codebook

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