TitleHeart failure after allogeneic hematopoietic stem cell transplantation
AuthorsMo, Xiao-Dong
Xu, Lan-Ping
Liu, Dai-Hong
Zhang, Xiao-Hui
Chen, Huan
Chen, Yu-Hong
Han, Wei
Wang, Yu
Wang, Feng-Rong
Wang, Jing-Zhi
Zhao, Ting
Yan, Chen-Hua
Sun, Yu-Qian
Liu, Kai-Yan
Huang, Xiao-Jun
AffiliationPeking Univ, Peoples Hosp, Beijing Key Lab Hematopoit Stem Cell Transplantat, Beijing 100044, Peoples R China.
Inst Hematol, Beijing Key Lab Hematopoit Stem Cell Transplantat, Beijing 100044, Peoples R China.
KeywordsHeart failure
Allogeneic hematopoietic stem
Transplant-related complication
BONE-MARROW-TRANSPLANTATION
HIGH-DOSE CYCLOPHOSPHAMIDE
VERSUS-HOST-DISEASE
CARDIAC COMPLICATIONS
CHILDHOOD-CANCER
PREDICTIVE-VALUE
ONCOLOGY-GROUP
ACUTE GVHD
CARDIOTOXICITY
THERAPY
Issue Date2013
Publisherinternational journal of cardiology
CitationINTERNATIONAL JOURNAL OF CARDIOLOGY.2013,167,(6),2502-2506.
AbstractBackground: Heart failure (HF) occurring after allogeneic hematopoietic stem cell transplantation (allo-HSCT) is rare but severe. We examine the role of pre-HSCT therapeutic exposures, conditioning regimens, pre-HSCT comorbidities, severe transplant-related complications, and post-HSCT cardiovascular risk factors in the development of heart failure after allo-HSCT. Methods: A nested case-control study was designed. Cases with HF and controls matched for age, year of allo-HSCT, and length of follow-up were identified from a cohort of 2455 patients who underwent allo-HSCT between 2000 and 2011 for hematologic malignancies. Results: Forty-two patients suffered from HF; mean age at presentation was 35 years (+/- 14 years) and mean time to presentation was 5 months (+/- 9 months) post-HSCT. The number of pre-HSCT cycles of chemotherapy was significantly greater (7 vs. 5 courses, P=0.023). Cases were significantly more likely to have severe acute GVHD (>= grade III), hemorrhagic cystitis (>= grade 2), and multiple severe transplant-related complications compared with controls (42.9% vs. 20.4%, P=0.008). Multivariate analysis revealed that pre-HSCT cycles of chemotherapy of >= 5 courses (OR=3.5, P=0.003) and two or more severe transplant-related complications (OR=3.6, P=0.003) were independently associated with HF. Conclusions: These results identify the individuals who are at higher risk of developing HF after allo-HSCT. We should pay more attention to these patients and more active management would be reasonable. (C) 2012 Elsevier Ireland Ltd. All rights reserved.
URIhttp://hdl.handle.net/20.500.11897/191204
ISSN0167-5273
DOI10.1016/j.ijcard.2012.06.021
IndexedSCI(E)
PubMed
Appears in Collections:人民医院

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