Evidence map›Paper›PMID 35147242›Full record

ArticleAmerican journal of hematology2022

A predictive algorithm for identifying children with sickle cell anemia among children admitted to hospital with severe anemia in Africa.

Peter Olupot-Olupot, Roisin Connon, Sarah Kiguli, Robert O Opoka, Florence Alaroker, Sophie Uyoga, Margret Nakuya, William Okiror, Julius Nteziyaremye, Tonny Ssenyondo and 13 more

Open access · hybridAbstract read
In one paragraph

Article in American journal of hematology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Trial
  2. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

23 authors at 6 institutions in 3 countries.

Peter Olupot-OlupotBusitema University Faculty of Health Sciences, Mbale Regional Referral Hospital, Mbale, Uganda.
Roisin ConnonMedical Research Council Clinical Trials Unit (MRC CTU), University College London, London, UK.
Sarah KiguliDepartment of Paediatrics and Child Health, School of Medicine, Makerere University, Kampala, Uganda.
Robert O OpokaDepartment of Paediatrics and Child Health, School of Medicine, Makerere University, Kampala, Uganda.
Florence AlarokerSoroti Regional Referral Hospital, Soroti, Uganda.
Sophie UyogaKenya Medical Research Institute (KEMRI)-Wellcome Trust Research Programme, Kilifi, Kenya.
Margret NakuyaMbale Clinical Research Institute, Mbale, Uganda.
William OkirorMbale Clinical Research Institute, Mbale, Uganda.
Julius NteziyaremyeBusitema University Faculty of Health Sciences, Mbale Regional Referral Hospital, Mbale, Uganda.
Tonny SsenyondoMbale Clinical Research Institute, Mbale, Uganda.
Eva NabawanukaDepartment of Paediatrics and Child Health, School of Medicine, Makerere University, Kampala, Uganda.
Juliana KayagaDepartment of Paediatrics and Child Health, School of Medicine, Makerere University, Kampala, Uganda.
Cynthia Williams MukisaDepartment of Paediatrics and Child Health, School of Medicine, Makerere University, Kampala, Uganda.
Denis AmorutSoroti Regional Referral Hospital, Soroti, Uganda.
Rita MuhindoMbale Clinical Research Institute, Mbale, Uganda.
Gary FrostSection for Nutrition Research, Department of Metabolism, Digestion and Reproduction, Imperial College, London, UK.
Kevin WalshSection for Nutrition Research, Department of Metabolism, Digestion and Reproduction, Imperial College, London, UK.
Alexander W MachariaKenya Medical Research Institute (KEMRI)-Wellcome Trust Research Programme, Kilifi, Kenya.
Diana M GibbMedical Research Council Clinical Trials Unit (MRC CTU), University College London, London, UK.
A Sarah WalkerMedical Research Council Clinical Trials Unit (MRC CTU), University College London, London, UK.
Elizabeth C GeorgeMedical Research Council Clinical Trials Unit (MRC CTU), University College London, London, UK.
Kathryn MaitlandKenya Medical Research Institute (KEMRI)-Wellcome Trust Research Programme, Kilifi, Kenya.
Thomas N WilliamsKenya Medical Research Institute (KEMRI)-Wellcome Trust Research Programme, Kilifi, Kenya.ORCID 0000-0003-4456-2382
Mbale Hospital · UGMakerere University · UGKenya Medical Research Institute · KEMRC Clinical Trials Unit at UCL · GBImperial College London · GBSoroti Hospital · UG

Funding

Medical Research Council MC_UU_00004/05Medical Research Council MC_UU_12023/26Medical Research Council MR/J012483/1Wellcome Trust 202800Wellcome Trust 202800/Z/16/Z
6 · The paper itself

Abstract

Sickle cell anemia (SCA) is common in sub-Saharan Africa where approximately 1% of births are affected. Severe anemia is a common cause for hospital admission within the region yet few studies have investigated the contribution made by SCA. The Transfusion and Treatment of severe anemia in African Children Trial (ISRCTN84086586) investigated various treatment strategies in 3983 children admitted with severe anemia (hemoglobin < 6.0 g/dl) based on two severity strata to four hospitals in Africa (three Uganda and one Malawi). Children with known-SCA were excluded from the uncomplicated stratum and capped at 25% in the complicated stratum. All participants were genotyped for SCA at trial completion. SCA was rare in Malawi (six patients overall), so here we focus on the participants recruited in Uganda. We present baseline characteristics by SCA status and propose an algorithm for identifying children with unknown-SCA. Overall, 430 (12%) and 608 (17%) of the 3483 Ugandan participants had known- or unknown-SCA, respectively. Children with SCA were less likely to be malaria-positive and more likely to have an affected sibling, have gross splenomegaly, or to have received a previous blood transfusion. Most outcomes, including mortality and readmission, were better in children with either known or unknown-SCA than non-SCA children. A simple algorithm based on seven admission criteria detected 73% of all children with unknown-SCA with a number needed to test to identify one new SCA case of only two. Our proposed algorithm offers an efficient and cost-effective approach to identifying children with unknown-SCA among all children admitted with severe anemia to African hospitals where screening is not widely available.

Indexed as

Anemia, Sickle CellAlgorithmsChildHospitalsHumansMalawiUganda

Identifiers

PMID35147242
PMCPMC7612591
OpenAlexW4211256599

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.