Evidence map›Paper›PMID 26619832›Full record

ArticleInternational journal of hematology2016

Hemophagocytic syndrome following haploidentical peripheral blood stem cell transplantation with post-transplant cyclophosphamide.

Sarita Rani Jaiswal, Aditi Chakrabarti, Sumita Chatterjee, Sneh Bhargava, Kunal Ray, Suparno Chakrabarti

Abstract read
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In one paragraph

Article in International journal of hematology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

9 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Post-transplant Hemophagocytic Lymphohistiocytosis in Benign Hematological Disorders: Experience of 4 Cases with Review of Literature.Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion · 2020
    Article
  6. Article
  7. Review
  8. Article
  9. Review
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

6 authors at 3 institutions in 1 country.

Sarita Rani JaiswalDepartment of Blood and Marrow Transplantation and Hematology, Dharamshila Hospital and Research Centre, Vasundhara Enclave, New Delhi, 110096, India. drsaritaranij@gmail.com.ORCID http://orcid.org/0000-0002-9988-3514
Aditi ChakrabartiManashi Chakrabarti Foundation, Kolkata, India.
Sumita ChatterjeeManashi Chakrabarti Foundation, Kolkata, India.
Sneh BhargavaDepartment of Blood and Marrow Transplantation and Hematology, Dharamshila Hospital and Research Centre, Vasundhara Enclave, New Delhi, 110096, India.
Kunal RayCSIR-Indian Institute of Chemical Biology, Kolkata, India.
Suparno ChakrabartiDepartment of Blood and Marrow Transplantation and Hematology, Dharamshila Hospital and Research Centre, Vasundhara Enclave, New Delhi, 110096, India.
Apollo Gleneagles Hospitals · INCentre for Sight · INIndian Institute of Chemical Biology · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hemophagocytic syndrome (HPS) is a rare but serious complication after allogeneic transplantation which has been reported to be particularly high after unrelated cord blood transplantation. We report on the incidence, risk factors and outcome of HPS in 51 patients (age 2-64 years) after haploidentical peripheral blood stem cell (PBSC) transplantation with post-transplantation cyclophosphamide (PTCY). The incidence of HPS was 12.2 %, occurring at a median of 18 days. The non-relapse mortality in patients with HPS was 83.3 % compared to 11.6 % in patients without HPS. Complete donor chimerism was documented in all patients with HPS. Definite infective etiology was identified in two patients only. The others were refractory to multiple lines of treatment and 3 patients underwent a second transplant. Even though the symptoms and biochemical markers of HPS showed prompt response in 2/3 patients undergoing a second allograft, they succumbed to infections before haematological recovery. The others succumbed to multi-organ failure or infections. Age < 10 years, transplantation for non-malignant disease and high CD34 content of the graft were identified as risk factors for HPS. Considering the fact that post-transplant HPS is usually a refractory and fatal condition, we discuss further attempts at deciphering the pathogenesis, developing modalities to prevent this complication and improve the outcome.

Indexed as

HaploidyPostoperative CareAdolescentAdultAllograftsAntigens, CD34ChildChild, PreschoolCyclophosphamideFemaleHumansImmunosuppressive AgentsIncidenceLymphohistiocytosis, HemophagocyticMaleMiddle AgedAntigens, CD34CyclophosphamideImmunosuppressive AgentsHaploidenticalHemophagocytic syndromePBSCPost-transplantation cyclophosphamide

Identifiers

PMID26619832
OpenAlexW2283610026

What OpenQuestion holds

Textmetadata
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.