Evidence map›Paper›PMID 25559691›Full record

Trial reportBiology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation2015

Health-related quality of life after allogeneic hematopoietic stem cell transplantation for sickle cell disease.

Monica Bhatia, Elissa Kolva, Laura Cimini, Zhezhen Jin, Prakash Satwani, Mirko Savone, Diane George, James Garvin, Mary Llenell Paz, Courtney Briamonte and 2 more

Open access · greenAbstract readClinical Trial
In one paragraph

Trial report in Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 5 pooled it
5.0field-weighted citation impact, top 4% 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

38 citing papers in PubMed, 5 syntheses or guidelines pooled it, 79 citations in OpenAlex.

  1. Pooled it
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  6. Trial
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  13. 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

12 authors at 3 institutions in 1 country.

Monica BhatiaDivision of Pediatric Hematology, Oncology and Stem Cell Transplantation, Columbia University Medical Center, New York, New York.
Elissa KolvaDepartment of Psychology, Fordham University, New York, New York.
Laura CiminiDepartment of School Psychology, Teachers College, Columbia University, New York, New York.
Zhezhen JinDepartment of Biostatistics, Columbia University, New York, New York.
Prakash SatwaniDivision of Pediatric Hematology, Oncology and Stem Cell Transplantation, Columbia University Medical Center, New York, New York.
Mirko SavoneDivision of Pediatric Hematology, Oncology and Stem Cell Transplantation, Columbia University Medical Center, New York, New York.
Diane GeorgeDivision of Pediatric Hematology, Oncology and Stem Cell Transplantation, Columbia University Medical Center, New York, New York.
James GarvinDivision of Pediatric Hematology, Oncology and Stem Cell Transplantation, Columbia University Medical Center, New York, New York.
Mary Llenell PazDepartment of Biobehavioral Sciences, Teachers College, Columbia University, New York, New York.
Courtney BriamonteDivision of Pediatric Hematology, Oncology and Stem Cell Transplantation, Columbia University Medical Center, New York, New York.
Eduvigis Cruz-ArrietaDivision of Pediatric Hematology, Oncology and Stem Cell Transplantation, Columbia University Medical Center, New York, New York.
Stephen SandsDivision of Pediatric Hematology, Oncology and Stem Cell Transplantation, Columbia University Medical Center, New York, New York. Electronic address: ss2341@columbia.edu.
Columbia University Irving Medical Center · USColumbia University · USFordham University · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Sickle cell disease (SCD) is a hereditary hemoglobinopathy that affects over 100,000 people in the United States. Patients with SCD are known to experience suboptimal health-related quality of life (HRQoL). In addition to the physical manifestations of SCD, psychological and social stress, along with academic difficulties, secondary to the chronicity of the disease and its complications often affect patients with SCD. Although medical therapy of SCD has improved, allogeneic hematopoietic cell transplantation (allo-HCT) remains the only curative therapy. The objective of this study was to measure HRQoL before and after allo-HCT by assessing physical, psychological, and social functioning in patients with SCD who have undergone reduced-toxicity conditioning (busulfan/fludarabine/alemtuzumab) followed by allo-HCT. Patients < 21 years of age undergoing allo-HCT (matched siblings and unrelated donors) for SCD and their primary caregiver were enrolled using either the English or Spanish version of the PedsQoL 4.0. Data were collected at 3 time points: before allo-HCT and on days 180 and 365 after allo-HCT. The change in HRQoL from baseline was assessed with unadjusted and adjusted mixed-effects models in which subjects were treated as random effects, and variance component structure was used. Seventeen patients and 23 primary caregivers were enrolled and reported a mean overall HRQoL of 66.05 (SD, 15.62) and 72.20 (SD, 15.50) at baseline, respectively. In the patient-reported analysis with adjusted mixed-effects models, the estimated improvements in overall HRQoL were 4.45 (SE, 4.98; P = .380) and 16.58 (SE, 5.06; P = .003) at 180 and 365 days, respectively, after allo-HCT. For parent-reported overall HRQoL, the estimated improvements were 1.57 (SE, 4.82; P = .747) and 9.28 (SE, 4.62; P = .053) at 180 and 365 days, respectively, after allo-HCT. Similar results were found across the physical, social, and emotional HRQoL domains with mixed-effects models after adjustment of demographic and medical variables. In addition to the alleviation of clinical manifestations of SCD, these patients demonstrated significant improvement in most aspects of HRQoL by 1 year after allo-HCT. These data represent the trajectory of HRQoL during the initial year of follow-up within this population and should be integrated into the decision-making process when considering allo-HCT in patients with SCD.

Indexed as

Hematopoietic Stem Cell TransplantationQuality of LifeAdolescentAdultAllograftsAnemia, Sickle CellChildChild, PreschoolFemaleFollow-Up StudiesHumansMaleHealth-related quality of lifeQuality of lifeSickle cell diseaseStem cell transplantation

Identifiers

PMID25559691
PMCPMC5580933
OpenAlexW2167764120

What OpenQuestion holds

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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.