The Effectiveness of Levosimendan on Veno-Arterial Extracorporeal Membrane Oxygenation Management and Outcome: A Systematic Review and Meta-Analysis

Rasha Kaddoura*, Amr S. Omar, Mohamed Izham Mohamed Ibrahim, Abdulaziz Alkhulaifi, Roberto Lorusso, Hagar Elsherbini, Osama Soliman, Kadir Caliskan

*Corresponding author for this work

Research output: Contribution to journalReview articleProfessionalpeer-review

26 Citations (Scopus)
53 Downloads (Pure)

Abstract

Objectives: Veno-arterial extracorporeal membrane oxygenation (VA-ECMO) provides a temporary support system for patients with cardiogenic shock refractory to conventional medical therapies. It has been reported that levosimendan may facilitate VA-ECMO weaning and improve survival. The primary objective of this review was to examine the effect of levosimendan use on VA-ECMO weaning and mortality in critically ill patients on VA-ECMO. Design: MEDLINE, EMBASE, and CENTRAL were searched. A pair of reviewers identified eligible clinical trials. Two reviewers extracted data and independently assessed the risk of bias. A random-effect model was used to combine data. The primary outcome was the success of weaning from VA-ECMO. Measurements and Main Results: Seven studies of observational design, including a total of 630 patients, were selected in the final analysis. The sample size ranged from ten-to-240 patients, with a mean age between 53 and 65 years, and more than half of them underwent cardiac surgeries. The VA-ECMO durations varied between four and 11.6 days. Overall, levosimendan use was significantly associated with successful weaning compared with control (odds ratio [OR] 2.89, 95% CI, 1.53-5.46; poverall effect = 0.001); I2 = 49%). For survival, six studies (n = 617) were included in the meta-analysis involving 326 patients in the levosimendan group and 291 in the comparator group. Pooled results showed a significantly higher survival rate in the levosimendan group (OR 0.46, 95% CI, 0.30-0.71; poverall effect = 0.0004; I2 = 20%). Conclusions: Levosimendan therapy was significantly associated with successful weaning and survival benefit in patients with cardiogenic or postcardiotomy shock needing VA-ECMO support for severe cardiocirculatory compromise. To date, there is limited literature and absence of evidence from randomized trials addressing the use of levosimendan in VA-ECMO weaning. This study may be considered a hypothesis-generating research for randomized controlled trials to confirm its findings.

Original languageEnglish
Pages (from-to)2483-2495
Number of pages13
JournalJournal of Cardiothoracic and Vascular Anesthesia
Volume35
Issue number8
Early online date16 Jan 2021
DOIs
Publication statusPublished - 1 Aug 2021

Bibliographical note

Funding Information:
The authors thank Dr Klaus Distelmaier and Dr Georg Goliasch for their support in providing additional data of their published study. All the authors declare that they have no competing interests. The study was approved by Hamad Medical Corporation through the Medical Research Center. Kindly, to the following to the acknowledgement section: Open Access funding provided by the Qatar National Library

Publisher Copyright:
© 2021 The Authors

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