Co-trimoxazole or multivitamin multimineral supplement for post-discharge outcomes after severe anaemia in African children: a randomised controlled trial
| dc.contributor.author | Maitland, Kathryn | |
| dc.contributor.author | Olupot-Olupot, Peter | |
| dc.contributor.author | Kiguli, Sarah | |
| dc.contributor.author | Chagaluka, George | |
| dc.contributor.author | Alaroker, Florence | |
| dc.contributor.author | Opoka, Robert O | |
| dc.contributor.author | Mpoya, Ayub | |
| dc.contributor.author | Walsh, Kevin | |
| dc.contributor.author | Engoru, Charles | |
| dc.contributor.author | Nteziyaremye, Julius | |
| dc.contributor.author | Mallewa, Machpherson | |
| dc.contributor.author | Kennedy, Neil | |
| dc.contributor.author | Nakuya, Margaret | |
| dc.contributor.author | Namayanja, Cate | |
| dc.contributor.author | Kayaga, Julianne | |
| dc.contributor.author | Nabawanuka, Eva | |
| dc.contributor.author | Sennyondo, Tonny | |
| dc.contributor.author | Aromut, Denis | |
| dc.contributor.author | Kumwenda, Felistas | |
| dc.contributor.author | Bates, Imelda | |
| dc.contributor.author | von Hensbroek, Michael Boele | |
| dc.contributor.author | Evans, Jennifer A | |
| dc.contributor.author | Uyoga, Sophie | |
| dc.contributor.author | Williams, Thomas N | |
| dc.contributor.author | Frost, Gary | |
| dc.contributor.author | George, Elizabeth C. | |
| dc.contributor.author | Gibb, Diana M. | |
| dc.contributor.author | Walker, A Sarah | |
| dc.date.accessioned | 2019-10-14T11:30:29Z | |
| dc.date.available | 2019-10-14T11:30:29Z | |
| dc.date.issued | 2019 | |
| dc.description.abstract | Background Severe anaemia is a leading cause of paediatric admission to hospital in Africa; post-discharge outcomes remain poor, with high 6-month mortality (8%) and re-admission (17%). We aimed to investigate post-discharge interventions that might improve outcomes. Methods Within the two-stratum, open-label, multicentre, factorial randomised TRACT trial, children aged 2 months to 12 years with severe anaemia, defined as haemoglobin of less than 6 g/dL, at admission to hospital (three in Uganda, one in Malawi) were randomly assigned, using sequentially numbered envelopes linked to a second nonsequentially numbered set of allocations stratified by centre and severity, to enhanced nutritional supplementation with iron and folate-containing multivitamin multimineral supplements versus iron and folate alone at treatment doses (usual care), and to co-trimoxazole versus no co-trimoxazole. All interventions were administered orally and were given for 3 months after discharge from hospital. Separately reported randomisations investigated transfusion management. The primary outcome was 180-day mortality. All analyses were done in the intention-to-treat population; follow-up was 180 days. This trial is registered with the International Standard Randomised Controlled Trial registry, ISRCTN84086586, and follow-up is complete. Findings From Sept 17, 2014, to May 15, 2017, 3983 eligible children were randomly assigned to treatment, and followed up for 180 days. 164 (4%) were lost to follow-up. 1901 (95%) of 1997 assigned multivitamin multimineral supplement, 1911 (96%) of 1986 assigned iron and folate, and 1922 (96%) of 1994 assigned co-trimoxazole started treatment. By day 180, 166 (8%) children in the multivitamin multimineral supplement group versus 169 (9%) children in the iron and folate group had died (hazard ratio [HR] 0·97, 95% CI 0·79–1·21; p=0·81) and 172 (9%) who received co-trimoxazole versus 163 (8%) who did not receive co-trimoxazole had died (HR 1·07, 95% CI 0·86–1·32; p=0·56). We found no evidence of interactions between these randomisations or with transfusion randomisations (p>0·2). By day 180, 489 (24%) children in the multivitamin multimineral supplement group versus 509 (26%) children in the iron and folate group (HR 0·95, 95% CI 0·84–1·07; p=0·40), and 500 (25%) children in the co-trimoxazole group versus 498 (25%) children in the no co-trimoxazole group (1·01, 0·89–1·15; p=0·85) had had one or more serious adverse events. Most serious adverse events were re-admissions, occurring in 692 (17%) children (175 [4%] with at least two re-admissions). Interpretation Neither enhanced supplementation with multivitamin multimineral supplement versus iron and folate treatment or co-trimoxazole prophylaxis improved 6-month survival. High rates of hospital re-admission suggest that novel interventions are urgently required for severe anaemia, given the burden it places on overstretched health services in Africa. | en_US |
| dc.description.sponsorship | Medical Research Council and Department for International Development | en_US |
| dc.identifier.issn | 2214-109X | |
| dc.identifier.uri | https://doi.org/10.60682/t4j3-s984 | |
| dc.language.iso | en | en_US |
| dc.publisher | Elsevier | en_US |
| dc.title | Co-trimoxazole or multivitamin multimineral supplement for post-discharge outcomes after severe anaemia in African children: a randomised controlled trial | en_US |
| dc.type | Article | en_US |