Evidence map›Paper›PMID 31537373›Full record

ArticleThe Lancet. Global health2019

Co-trimoxazole or multivitamin multimineral supplement for post-discharge outcomes after severe anaemia in African children: a randomised controlled trial.

Kathryn Maitland, Peter Olupot-Olupot, Sarah Kiguli, George Chagaluka, Florence Alaroker, Robert O Opoka, Ayub Mpoya, Kevin Walsh, Charles Engoru, Julius Nteziyaremye and 21 more

Open access · goldAbstract read
In one paragraph

Article in The Lancet. Global health, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 4 pooled it
2.5field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

24 citing papers in PubMed, 4 syntheses or guidelines pooled it, 32 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

31 authors at 13 institutions in 5 countries.

Kathryn MaitlandDepartment of Medicine, Imperial College London, London, UK; Kenya Medical Research Institute-Wellcome Trust Research Programme, Kilifi, Kenya. Electronic address: k.maitland@imperial.ac.uk.
Peter Olupot-OlupotBusitema University Faculty of Health Sciences, Mbale Campus and Mbale Regional Referral Hospital Mbale, Mbale, Uganda.
Sarah KiguliDepartment of Paediatrics, Makerere University and Mulago Hospital, Kampala, Uganda.
George ChagalukaCollege of Medicine, and Malawi-Liverpool-Wellcome Trust Clinical Research Programme, Blantyre, Malawi.
Florence AlarokerSoroti Regional Referral Hospital, Soroti, Uganda.
Robert O OpokaDepartment of Paediatrics, Makerere University and Mulago Hospital, Kampala, Uganda.
Ayub MpoyaKenya Medical Research Institute-Wellcome Trust Research Programme, Kilifi, Kenya.
Kevin WalshNutrition Research Section, Imperial College London, London, UK.
Charles EngoruSoroti Regional Referral Hospital, Soroti, Uganda.
Julius NteziyaremyeBusitema University Faculty of Health Sciences, Mbale Campus and Mbale Regional Referral Hospital Mbale, Mbale, Uganda.
Machpherson MallewaCollege of Medicine, and Malawi-Liverpool-Wellcome Trust Clinical Research Programme, Blantyre, Malawi.
Neil KennedyCollege of Medicine, and Malawi-Liverpool-Wellcome Trust Clinical Research Programme, Blantyre, Malawi; School of Medicine, Dentistry and Biomedical Science, Queen's University, Belfast, UK.
Margaret NakuyaSoroti Regional Referral Hospital, Soroti, Uganda.
Cate NamayanjaBusitema University Faculty of Health Sciences, Mbale Campus and Mbale Regional Referral Hospital Mbale, Mbale, Uganda.
Julianne KayagaDepartment of Paediatrics, Makerere University and Mulago Hospital, Kampala, Uganda.
Eva NabawanukaDepartment of Paediatrics, Makerere University and Mulago Hospital, Kampala, Uganda.
Tonny SennyondoBusitema University Faculty of Health Sciences, Mbale Campus and Mbale Regional Referral Hospital Mbale, Mbale, Uganda.
Denis AromutSoroti Regional Referral Hospital, Soroti, Uganda.
Felistas KumwendaCollege of Medicine, and Malawi-Liverpool-Wellcome Trust Clinical Research Programme, Blantyre, Malawi.
Cynthia Williams MusikaDepartment of Paediatrics, Makerere University and Mulago Hospital, Kampala, Uganda.
Margaret J ThomasonMedical Research Council Clinical Trials Unit at University College London.
Imelda BatesLiverpool School of Tropical Medicine and Hygiene, Liverpool, UK.
Michael Boele von HensbroekEmma Children's Hospital, Academic Medical Center, Amsterdam, The Netherlands.
Jennifer A EvansDepartment of Paediatrics, University Hospital of Wales, Cardiff, UK.
Sophie UyogaKenya Medical Research Institute-Wellcome Trust Research Programme, Kilifi, Kenya.
Thomas N WilliamsDepartment of Medicine, Imperial College London, London, UK; Kenya Medical Research Institute-Wellcome Trust Research Programme, Kilifi, Kenya.
Gary FrostNutrition Research Section, Imperial College London, London, UK.
Elizabeth C GeorgeMedical Research Council Clinical Trials Unit at University College London.
Diana M GibbMedical Research Council Clinical Trials Unit at University College London.
A Sarah WalkerMedical Research Council Clinical Trials Unit at University College London.
TRACT trial group
Makerere University · UGImperial College London · GBSoroti Hospital · UGMalawi-Liverpool-Wellcome Trust Clinical Research Programme · MWMbale Hospital · UGKenya Medical Research Institute · KEMedical Research Council · GBUniversity College London · GBAcademic Medical Center · NLBusitema University · UGLiverpool School of Tropical Medicine · GBQueen's University Belfast · GBUniversity Hospital of Wales · GB

Funding

Medical Research Council MC_PC_MR/R019258/1Medical Research Council MC_U122886353Medical Research Council MC_UU_12023/17Medical Research Council MC_UU_12023/26Medical Research Council MR/J012483/1
6 · The paper itself

Abstract

backgroundSevere 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.

methodsWithin 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.

findingsFrom 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).

interpretationNeither 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.

fundingMedical Research Council and Department for International Development.

Indexed as

AnemiaTrimethoprim, Sulfamethoxazole Drug CombinationChildDietary SupplementsHumansInfantMalawiPatient DischargeUgandaTrimethoprim, Sulfamethoxazole Drug Combination

Identifiers

PMID31537373
PMCPMC7024999
OpenAlexW2974572134

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.