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Co-trimoxazole or multivitamin multimineral supplement for post-discharge outcomes after severe anaemia in African children: a randomised controlled trial.
Maitland, Kathryn; Olupot-Olupot, Peter; Kiguli, Sarah; Chagaluka, George; Alaroker, Florence; Opoka, Robert O; Mpoya, Ayub; Walsh, Kevin; Engoru, Charles; Nteziyaremye, Julius; Mallewa, Machpherson; Kennedy, Neil; Nakuya, Margaret; Namayanja, Cate; Kayaga, Julianne; Nabawanuka, Eva; Sennyondo, Tonny; Aromut, Denis; Kumwenda, Felistas; Musika, Cynthia Williams; Thomason, Margaret J; Bates, Imelda; von Hensbroek, Michael Boele; Evans, Jennifer A; Uyoga, Sophie; Williams, Thomas N; Frost, Gary; George, Elizabeth C; Gibb, Diana M; Walker, A Sarah.
Afiliação
  • Maitland K; Department of Medicine, Imperial College London, London, UK; Kenya Medical Research Institute-Wellcome Trust Research Programme, Kilifi, Kenya. Electronic address: k.maitland@imperial.ac.uk.
  • Olupot-Olupot P; Busitema University Faculty of Health Sciences, Mbale Campus and Mbale Regional Referral Hospital Mbale, Mbale, Uganda.
  • Kiguli S; Department of Paediatrics, Makerere University and Mulago Hospital, Kampala, Uganda.
  • Chagaluka G; College of Medicine, and Malawi-Liverpool-Wellcome Trust Clinical Research Programme, Blantyre, Malawi.
  • Alaroker F; Soroti Regional Referral Hospital, Soroti, Uganda.
  • Opoka RO; Department of Paediatrics, Makerere University and Mulago Hospital, Kampala, Uganda.
  • Mpoya A; Kenya Medical Research Institute-Wellcome Trust Research Programme, Kilifi, Kenya.
  • Walsh K; Nutrition Research Section, Imperial College London, London, UK.
  • Engoru C; Soroti Regional Referral Hospital, Soroti, Uganda.
  • Nteziyaremye J; Busitema University Faculty of Health Sciences, Mbale Campus and Mbale Regional Referral Hospital Mbale, Mbale, Uganda.
  • Mallewa M; College of Medicine, and Malawi-Liverpool-Wellcome Trust Clinical Research Programme, Blantyre, Malawi.
  • Kennedy N; College of Medicine, and Malawi-Liverpool-Wellcome Trust Clinical Research Programme, Blantyre, Malawi; School of Medicine, Dentistry and Biomedical Science, Queen's University, Belfast, UK.
  • Nakuya M; Soroti Regional Referral Hospital, Soroti, Uganda.
  • Namayanja C; Busitema University Faculty of Health Sciences, Mbale Campus and Mbale Regional Referral Hospital Mbale, Mbale, Uganda.
  • Kayaga J; Department of Paediatrics, Makerere University and Mulago Hospital, Kampala, Uganda.
  • Nabawanuka E; Department of Paediatrics, Makerere University and Mulago Hospital, Kampala, Uganda.
  • Sennyondo T; Busitema University Faculty of Health Sciences, Mbale Campus and Mbale Regional Referral Hospital Mbale, Mbale, Uganda.
  • Aromut D; Soroti Regional Referral Hospital, Soroti, Uganda.
  • Kumwenda F; College of Medicine, and Malawi-Liverpool-Wellcome Trust Clinical Research Programme, Blantyre, Malawi.
  • Musika CW; Department of Paediatrics, Makerere University and Mulago Hospital, Kampala, Uganda.
  • Thomason MJ; Medical Research Council Clinical Trials Unit at University College London.
  • Bates I; Liverpool School of Tropical Medicine and Hygiene, Liverpool, UK.
  • von Hensbroek MB; Emma Children's Hospital, Academic Medical Center, Amsterdam, The Netherlands.
  • Evans JA; Department of Paediatrics, University Hospital of Wales, Cardiff, UK.
  • Uyoga S; Kenya Medical Research Institute-Wellcome Trust Research Programme, Kilifi, Kenya.
  • Williams TN; Department of Medicine, Imperial College London, London, UK; Kenya Medical Research Institute-Wellcome Trust Research Programme, Kilifi, Kenya.
  • Frost G; Nutrition Research Section, Imperial College London, London, UK.
  • George EC; Medical Research Council Clinical Trials Unit at University College London.
  • Gibb DM; Medical Research Council Clinical Trials Unit at University College London.
  • Walker AS; Medical Research Council Clinical Trials Unit at University College London.
Lancet Glob Health ; 7(10): e1435-e1447, 2019 10.
Article em En | MEDLINE | ID: mdl-31537373
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 non-sequentially 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. FUNDING: Medical Research Council and Department for International Development.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Combinação Trimetoprima e Sulfametoxazol / Anemia Tipo de estudo: Clinical_trials Limite: Child / Humans / Infant País/Região como assunto: Africa Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Combinação Trimetoprima e Sulfametoxazol / Anemia Tipo de estudo: Clinical_trials Limite: Child / Humans / Infant País/Região como assunto: Africa Idioma: En Ano de publicação: 2019 Tipo de documento: Article