Cardiogenic shock in patients with active onco-hematological malignancies: A multicenter retrospective study
- PMID: 39848115
- DOI: 10.1016/j.jcrc.2025.155028
Cardiogenic shock in patients with active onco-hematological malignancies: A multicenter retrospective study
Abstract
Purpose: Onco-hematological (OH) patients face significant cardiovascular risks due to malignancy and drug toxicity. Data are limited on the characteristics and outcomes of OH patients with cardiogenic shock (CS) in intensive care units (ICUs).
Methods: This multicenter retrospective study included 214 OH patients with CS across 22 ICUs (2010-2021). The objectives were to (i) identify risk factors for 30-day mortality, (ii) describe early and long-term outcomes, and (iii) assess the prognostic impact of malignancy by comparing OH patients to a control group of CS patients.
Results: The 30-day survival rate was 44.8 %. Multivariate analysis identified previous cardiomyopathy (OR = 1.61), acute kidney injury (OR = 1.62), lactate levels (OR = 1.08 per 1 mmol/L), pulmonary embolism (OR = 3.04), invasive mechanical ventilation (OR = 3.48), and epinephrine use (OR = 2.09) as factors associated with 30-day mortality. Among ICU survivors, 54 % were alive at 1 year with a median left ventricular ejection fraction of 52 %. OH malignancy was significantly associated with 30-day mortality (HR 2.54).
Conclusion: The prognosis for OH patients with CS in the ICU is poor, with epinephrine use associated with worse outcomes. Further research is needed to refine risk stratification and improve treatments for this population.
Keywords: Cardiogenic shock; Onco-hematological malignancy - intensive care.
Copyright © 2025 Elsevier Inc. All rights reserved.
Conflict of interest statement
Declaration of competing interest LZ reports receiving fees for lectures for MSD and Sanofi, outside of the submitted work. EC has received lecturer and conference-speaker fees, as well as reimbursements of travel and accommodation expenses related to attending scientific meetings, from Gilead, Shionogi, and Sanofi-Genzyme. SP received a mobility research grant from Institut Servier, outside of the submitted work. Other authors declare no conflict of interest (ML, HK, OI, JHR, FB, NI, MD, ASM, FT, BM, LC, NM, GL, FW, HW, HM, LA, AK, GD).
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical
