Evidence map›Paper›PMID 36051041›Full record

ArticleEJHaem2022

Interest of the preventive and curative use of defibrotide on the occurrence and severity of sinusoidal obstruction syndrome after hematopoietic stem cell transplant in children.

Carl J Rudebeck, Cécile Renard, Carine Halfon-Domenech, Marie Ouachée-Chardin, Michael Philippe, Frederic V Valla, Yves Bertrand, Mathilde Penel-Page

Open access · diamondAbstract read
In one paragraph

Article in EJHaem, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 51% 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

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. Review
  2. 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

8 authors at 3 institutions in 1 country.

Carl J RudebeckInstitut d'Hématologie et d'Oncologie Pédiatrique Hospices Civils de Lyon Lyon France.ORCID https://orcid.org/0000-0002-7303-1962
Cécile RenardInstitut d'Hématologie et d'Oncologie Pédiatrique Hospices Civils de Lyon Lyon France.
Carine Halfon-DomenechInstitut d'Hématologie et d'Oncologie Pédiatrique Hospices Civils de Lyon Lyon France.
Marie Ouachée-ChardinInstitut d'Hématologie et d'Oncologie Pédiatrique Hospices Civils de Lyon Lyon France.
Michael PhilippeInstitut d'Hématologie et d'Oncologie Pédiatrique Hospices Civils de Lyon Lyon France.
Frederic V VallaService de Réanimation et Soins Intensifs Pédiatriques - Hôpital Femme Mère Enfant Hospices Civils de Lyon Lyon France.
Yves BertrandInstitut d'Hématologie et d'Oncologie Pédiatrique Hospices Civils de Lyon Lyon France.
Mathilde Penel-PageInstitut d'Hématologie et d'Oncologie Pédiatrique Hospices Civils de Lyon Lyon France.
Institut d’Hématologie et d’Oncologie Pédiatrique · FRUniversité Claude Bernard Lyon 1 · FRHôpital Femme Mère Enfant · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Defibrotide (DF) is indicated for the treatment of severe sinusoidal obstruction syndrome (SOS) following hematopoietic stem cell transplantation (HSCT), but its prophylactic use against SOS is not recommended yet. This study describes the impact of the preventive and curative use of DF on reducing the incidence and severity of SOS in children. Patients aged 0-19 years, who received allogenic HSCT after myeloablative conditioning regimen with busulfan or total body irradiation in our comprehensive cancer center, between 2013 and 2017, were included. The Baltimore or modified Seattle criteria were used for SOS diagnosis. SOS was graded using the 2017 European Society for Blood and Marrow Transplantation classification defining severity criteria of SOS in children. SOS occurrence tended to decrease with prophylactic DF, but no significant difference was observed in terms of severity. When not treated with preventive DF, 50% (19/38) of the patients with SOS were graded severe to very severe, but only 37% (7/19) had organ dysfunction. Curative DF was administered at a median of 2 days post-HSCT, for a median of 6.5 days. The absence of fatal SOS supports the use of early curative DF with acceptable toxicities and questions the optimal duration of DF treatment.

Indexed as

childrendefibrotidegrading classificationhematopoietic cell transplantationpreventiveveno‐occlusive disease/sinusoidal obstruction syndrome

Identifiers

PMID36051041
PMCPMC9421979
OpenAlexW4281750181

What OpenQuestion holds

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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.