Evidence map›Paper›PMID 25345798›Full record

Trial reportAmerican journal of hematology2015

Health-related quality of life in children with sickle cell anemia: impact of blood transfusion therapy.

Lauren M Beverung, John J Strouse, Monica L Hulbert, Kathleen Neville, Robert I Liem, Baba Inusa, Beng Fuh, Allison King, Emily Riehm Meier, James Casella and 3 more

Open access · greenAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in American journal of hematology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 8 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 8 pooled it
3.3field-weighted citation impact, top 7% 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

39 citing papers in PubMed, 8 syntheses or guidelines pooled it, 68 citations in OpenAlex.

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  20. Evaluation of Sickle Cell Module for Quality of Life in Egyptian Children and Adolescents Patients: Impact of Psychiatric and Disease Specific Variables.Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion · 2021
    Article
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

13 authors at 10 institutions in 2 countries.

Lauren M BeverungMedical College of Wisconsin/Children's Research Institute of the Children's Hospital of Wisconsin, Milwaukee, Wisconsin.
John J Strouse
Monica L Hulbert
Kathleen Neville
Robert I Liem
Baba Inusa
Beng Fuh
Allison King
Emily Riehm Meier
James Casella
Michael R DeBaun
Julie A Panepinto
SIT trial investigators
Children's Hospital of Wisconsin · USWashington University in St. Louis · USChildren's Mercy Hospital · USChildren's National · USEast Carolina University · USGuy's and St Thomas' NHS Foundation Trust · GBJohns Hopkins Medicine · USJohns Hopkins University · USMonroe Carell Jr. Children's Hospital · USNorthwestern University · US

Funding

Silent Cerebral Infarct Multi-Center Clinical TrialU01NS042804 · NINDS · WASHINGTON UNIVERSITY · PI DEBAUN, MICHAEL R. · 2003 to 2010
$20.7M
Quality of Life Children With Sickle Cell DiseaseK23HL080092 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI PANEPINTO, JULIE A · 2005 to 2009
$638k
NHLBI NIH HHS K23 HL080092NHLBI NIH HHS K23 HL80092NINDS NIH HHS 3U01NS042804-06S1NINDS NIH HHS 5U01-NS042804NINDS NIH HHS U01 NS042804
6 · The paper itself

Abstract

The completion of the Multicenter Silent Infarct Transfusion Trial demonstrated that children with pre-existing silent cerebral infarct and sickle cell anemia (SCA) who received regular blood transfusion therapy had a 58% relative risk reduction of infarct recurrence when compared to observation. However, the total benefit of blood transfusion therapy, as assessed by the parents, was not measured against the burden of monthly blood transfusion therapy. In this planned ancillary study, we tested the hypothesis that a patient centered outcome, health-related quality of life (HRQL), would be greater in participants randomly assigned to the blood transfusion therapy group than the observation group. A total of 89% (175 of 196) of the randomly allocated participants had evaluable entry and exit HRQL evaluations. The increase in Change in Health, measured as the child's health being better, was significantly greater for the transfusion group than the observation group (difference estimate = -0.54, P ≤ 0.001). This study provides the first evidence that children with SCA who received regular blood transfusion therapy felt better and had better overall HRQL than those who did not receive transfusion therapy.

Indexed as

Blood TransfusionQuality of LifeAdolescentAnemia, Sickle CellCerebral InfarctionChildChild, PreschoolFemaleHumansMalePatient-Centered CareSeverity of Illness IndexSurveys and QuestionnairesTreatment Outcome

Identifiers

PMID25345798
PMCPMC4304929
OpenAlexW2096251237

What OpenQuestion holds

Textmetadata
LicenceTDM
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.