Background: While left ventricular (LV) venting reduces LV distension in cardiogenic shock patients on venoarterial extracorporeal membrane oxygenation (VA-ECMO), it may also amplify risk of acute brain injury (ABI). We investigated the hypothesis that LV venting is associated with increased risk of ABI. We also compared ABI risk of the two most common LV venting strategies, percutaneous microaxial flow pump (mAFP) and intra-aortic balloon pump (IABP). Methods: The Extracorporeal Life Support Organization registry was queried for patients on peripheral VA-ECMO for cardiogenic shock (2013-2024). ABI was defined as hypoxic-ischemic brain injury, ischemic stroke, or intracranial hemorrhage. Secondary outcome was hospital mortality. We compared no LV venting with 1) LV venting, 2) mAFP, and 3) IABP using multivariable logistic regression. To compare ABI risk of mAFP vs. IABP, propensity score matching was performed. Results: Of 13,276 patients (median age=58.2, 69.9% male), 1,456 (11.0%) received LV venting (65.5% mAFP and 29.9% IABP), and 525 (4.0%) had ABI. After multivariable regression, LV-vented patients had increased odds of ABI (adjusted odds ratio (aOR)=1.76, 95% CI=1.29, 2.37, p<0.001) but no difference in mortality (aOR=1.08, 95% CI=0.91-1.28, p=0.39) compared to non-LV-vented patients. In the propensity-matched cohort of IABP (n=231) vs. mAFP (n=231) patients, there was no significant difference in odds of ABI (aOR=1.35, 95%CI=0.69-2.71, p=0.39) or mortality (aOR=0.88, 95%CI=0.58-1.31, p=0.52). Conclusions: LV venting was associated with increased odds of ABI but not mortality in patients receiving peripheral VA-ECMO for cardiogenic shock. There was no difference in odds of ABI or mortality for IABP vs. mAFP patients.
Competing Interest StatementDB reports consulting for LivaNova. He has been on the medical advisory boards for Medtronic, Inspira, Cellenkos and HBOX Therapies. He is the President-elect of the Extracorporeal Life Support Organization (ELSO) and the Chair of the Board of the International ECMO Network (ECMONet), and he writes for UpToDate. The other authors have no conflicts of interest to disclose.
Funding StatementDr. Keller is funded by NIH (5K08HL14332) and DARPA (HR001124S0024). Dr. Cho is supported by NIH (1K23HL157610; 1R21NS135045) and DARPA (HR001124S0024).
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The details of the IRB/oversight body that provided approval or exemption for the research described are given below:
This retrospective observational cohort study was approved by the Johns Hopkins Hospital Institutional Review Board with a waiver of informed consent (IRB00216321).
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Data AvailabilityThe data used in this study were obtained from the Extracorporeal Life Support Organization (ELSO) registry, a comprehensive international database of patients receiving extracorporeal life support. Access to the ELSO registry data is available upon request and subject to approval by the ELSO Scientific Oversight Committee. For more information on accessing the registry data, including submission guidelines and requirements, please visit the ELSO website at www.elso.org.
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