Evidence map›Paper›PMID 39691452›Full record

ArticleHemaSphere2024

Definitions matter: Multicenter investigation of incidence and outcome of poor graft function after hematopoietic cell transplantation.

Konradin F Müskens, Winny N R Collot-d'Escury, Rana Dandis, Saskia Haitjema, Jürgen Kuball, Moniek A de Witte, Marc Bierings, Caroline A Lindemans, Stefan Nierkens, Mirjam E Belderbos

Abstract read
In one paragraph

Article in HemaSphere, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

1 citing paper in PubMed, 1 synthesis or guideline pooled it.

  1. Guideline
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

10 authors.

Konradin F MüskensPrincess Máxima Center for Pediatric Oncology Utrecht The Netherlands.
Winny N R Collot-d'EscuryPrincess Máxima Center for Pediatric Oncology Utrecht The Netherlands.
Rana DandisPrincess Máxima Center for Pediatric Oncology Utrecht The Netherlands.
Saskia HaitjemaCentral Diagnostic Laboratory, University Medical Center Utrecht Utrecht University Utrecht The Netherlands.
Jürgen KuballDepartment of Hematology, University Medical Center Utrecht Utrecht University Utrecht The Netherlands.
Moniek A de WitteDepartment of Hematology, University Medical Center Utrecht Utrecht University Utrecht The Netherlands.
Marc BieringsPrincess Máxima Center for Pediatric Oncology Utrecht The Netherlands.
Caroline A LindemansPrincess Máxima Center for Pediatric Oncology Utrecht The Netherlands.
Stefan NierkensPrincess Máxima Center for Pediatric Oncology Utrecht The Netherlands.
Mirjam E BelderbosPrincess Máxima Center for Pediatric Oncology Utrecht The Netherlands.ORCID 0000-0002-6164-2918

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite advances in allogeneic hematopoietic cell transplantation (HCT), poor graft function (PGF) remains an important complication with substantial morbidity and mortality. The investigation of preventive and therapeutic PGF treatments is hindered by inconsistencies in reported incidence and outcomes across studies, which may be explained by heterogeneity in PGF definition. To assess the impact of definition heterogeneity, we conducted a multicenter study, analyzing over 35.000 longitudinal blood counts from 427 pediatric and 405 adult HCT recipients. We compared the incidence, risk factors, and outcome of PGF, based on the three most common definitions. We identified 97 pediatric and 75 adult HCT recipients fulfilling at least one PGF definition. The 2-year cumulative incidence of PGF varied significantly depending on the definition used, ranging from 6.8% to 20% in children and 4.9% to 18% in adults. Two-year mortality for PGF patients ranged from 33% to 40% in children and 46% to 65% in adults. Notably, PGF patients identified solely by lenient definitions had similar mortality to HCT recipients with good graft function. Risk factors for PGF also varied by definition in both cohorts, and included older recipient age and cord blood transplantation. In conclusion, our study demonstrates that differences in PGF definition significantly impact the reported incidence, risk factors, and outcome. This underscores the need to harmonize PGF definitions across scientific studies, clinical practice, and transplant registries. Future studies, using standardized, quantitative thresholds for PGF, are required to determine optimal treatment strategies for both mild and severe forms of PGF.

Identifiers

PMID39691452
PMCPMC11650888

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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.