Evidence map›Paper›PMID 35838917›Full record

ArticleInternational journal of hematology2022

Incidence and predictors of idiopathic pneumonia syndrome in hematopoietic stem cell transplant patients: a nationwide registry study.

Michael A Liu, Chien-Chang Lee, Quan Phung, Quynh-Lan Dao, Babak Tehrani, Ming Yao, Chi-Cheng Li, Kang-Hsi Wu, Tsung-Chih Chen, Jyh-Pyng Gau and 14 more

Abstract read
PubMed Publisher
In one paragraph

Article in International journal of hematology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 40% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

24 authors at 18 institutions in 2 countries.

Michael A Liu *Department of Medicine, Warren Alpert Medical School of Brown University, Providence, RI, USA.
Chien-Chang Lee *Department of Emergency Medicine, National Taiwan University Hospital, National Taiwan University College of Medicine, Taipei, Taiwan.
Quan PhungDepartment of Medicine, Warren Alpert Medical School of Brown University, Providence, RI, USA.
Quynh-Lan DaoDepartment of Medicine, Warren Alpert Medical School of Brown University, Providence, RI, USA.
Babak TehraniDepartment of Medicine, Warren Alpert Medical School of Brown University, Providence, RI, USA.
Ming YaoDepartment of Internal Medicine, National Taiwan University Hospital, National Taiwan University College of Medicine, Taipei, Taiwan.
Chi-Cheng LiDepartment of Internal Medicine, National Taiwan University Hospital, National Taiwan University College of Medicine, Taipei, Taiwan.
Kang-Hsi WuDepartment of Pediatrics, China Medical University Children's Hospital, Taichung, Taiwan.
Tsung-Chih ChenDepartment of Internal Medicine, Taichung Veterans General Hospital, Taichung, Taiwan.
Jyh-Pyng GauDepartment of Internal Medicine, Taipei Veterans General Hospital, Taipei, Taiwan.
Sin-Syue LiDepartment of Internal Medicine, National Cheng Kung University Hospital, Tainan, Taiwan.
Po-Nan WangDepartment of Internal Medicine, Linkou Branch, Chang Gung Memorial Hospital, Taoyun, Taiwan.
Yi-Chang LiuDepartment of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan.
Tso-Fu WangDepartment of Hematology and Oncology, Buddhist Tzu-Chi General Hospital, Hualien, Taiwan.
Lun-Wei ChiouKoo Foundation Sun Yat-Sen Cancer Center, Taipei, Taiwan.
Ming-Yang LeeDepartment of Internal Medicine, Ditmanson Medical Foundation Chiayi Christian Hospital, Chiayi, Taiwan.
Ming-Sun YuDepartment of Internal Medicine, Kaohsiung Veterans General Hospital, Kaohsiung, Taiwan.
Chuan-Cheng WangDepartment of Internal Medicine, Changhua Christian Hospital, Changhua, Taiwan.
Shih-Chiang LinDepartment of Internal Medicine, Far Eastern Memorial Hospital, New Taipei City, Taiwan.
Yeu-Chin ChenDepartment of Medicine, Tri-Service General Hospital, Taipei, Taiwan.
Tsu-Yi ChaoDepartment of Medicine, Taipei Medical University-Shuang Ho Hospital, New Taipei City, Taiwan.
Ming-Chun MaDepartment of Internal Medicine, Kaohsiung Chang-Gung Memorial Hospital, Kaohsiung, Taiwan.
Chih-Cheng ChenDepartment of Internal Medicine, Chang Gung Memorial Hospital, Chiayi, Taiwan.
Hsiu-Hao ChangDepartment of Pediatrics, National Taiwan University Hospital, National Taiwan University College of Medicine, No. 8 Chung-Shan South Road, Taipei, 10041, Taiwan. changhh2001@ntu.edu.tw.ORCID http://orcid.org/0000-0003-1832-8509
Brown University · USNational Taiwan University Hospital · TWBuddhist Tzu Chi General Hospital · TWChanghua Christian Hospital · TWChiayi Chang Gung Memorial Hospital · TWChia-Yi Christian Hospital · TWChina Medical University · TWFar Eastern Memorial Hospital · TWKaohsiung Chang Gung Memorial Hospital · TWKaohsiung Medical University · TWKaohsiung Veterans General Hospital · TWKoo Foundation Sun Yat-Sen Cancer Center · TWLinkou Chang Gung Memorial Hospital · TWNational Cheng Kung University Hospital · TWTaichung Veterans General Hospital · TWTaipei Medical University-Shuang Ho Hospital · TWTaipei Veterans General Hospital · TWTri-Service General Hospital · TW

Funding

Ministry of Science and Technology, Taiwan 109-2314-B-002-129Ministry of Science and Technology, Taiwan 110-2314-B-002-088-MY3National Taiwan University Hospital 110-T05National Taiwan University Hospital 111-S0028
6 · The paper itself

Abstract

Idiopathic pneumonia syndrome (IPS) is a rare but deadly complication of hematopoietic stem cell transplantation (HSCT). This study characterized the incidence and risk factors for IPS after HSCT in Taiwan. Data from January 2009 to February 2019 was collected from the Taiwan Society of BMT national registry. Forty-three (1.1%) of 3924 HSCT patients who developed IPS were identified. Incidence of IPS was lower in patients who received autologous HSCT than patients who received allogeneic HSCT (0.68% vs 1.44%, P = 0.022). Multivariate analysis showed that use of TBI and intravenous busulfan in the conditioning regimen were each independent predictor of IPS after HSCT. In addition, development of IPS was significantly associated with increased risk of death in the first 120 days post-HSCT (HR, 2.09; 95% CI, 1.08 to 4.05, P = 0.029) and 2 years post-HSCT (HR, 1.65; 95% CI, 1.07 to 2.542, P = 0.023), but not beyond 2 years post-HSCT. However, survival outcomes did not differ significantly between patients with IPS who received autologous versus allogeneic HSCT (P = 0.52). In conclusion, despite the relatively low incidence of post-HSCT IPS in Taiwan, mortality remains high. The results of this study will help to identify high-risk patients for early intervention and guide future therapeutic research.

Indexed as

Hematopoietic Stem Cell TransplantationPneumoniaBusulfanHumansIncidenceRegistriesRetrospective StudiesTransplantation ConditioningBusulfanHematopoietic stem cell transplantIdiopathic pneumonia syndromeIncidencePredictors

Identifiers

PMID35838917
OpenAlexW4285592903

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.