TY - JOUR
T1 - Outcomes after extracorporeal membrane oxygenation for the treatment of high-risk pulmonary embolism
T2 - A multicentre series of 52 cases
AU - Meneveau, Nicolas
AU - Guillon, Benoit
AU - Planquette, Benjamin
AU - Piton, Gaël
AU - Kimmoun, Antoine
AU - Gaide-Chevronnay, Lucie
AU - Aissaoui, Nadia
AU - Neuschwander, Arthur
AU - Zogheib, Elie
AU - Dupont, Hervé
AU - Pili-Floury, Sebastien
AU - Ecarnot, Fiona
AU - Schiele, François
AU - Deye, Nicolas
AU - De Prost, Nicolas
AU - Favory, Raphaël
AU - Girard, Philippe
AU - Cristinar, Mircea
AU - Ferré, Alexis
AU - Meyer, Guy
AU - Capellier, Gilles
AU - Sanchez, Olivier
N1 - Funding Information:
Conflict of interest: N.M. reports personal fees from Bayer Healthcare, BMS-Pfizer, Sanofi aventis, Boehringer Ingelheim, Abbott, Terumo, and Edwards Lifesciences, outside the submitted work. F.S. reports grants from Glaxo Smith Kline, St Jude Medical, Sanofi aven-tis, Servier, and Daiichi Sankyo—Lilly, personal fees from Boehringer Ingelheim, Novartis, The medicines company, Servier, Astra Zeneca, Amgen, MSD, and Sanofi aventis, outside the submitted work. O.S. reports grants, personal fees and non-financial support from BAYER, grants, personal fees and non-financial support from BMS-PFIZER, grants from PORTOLA, DAIICHI SANKYO, grants, personal fees and non-financial support from MSD, ACTELION, BOEHRINGER INGELHEIM, and personal fees from CHIESI, outside the submitted work. G.M. reports grants from Bayer, non-financial support from Leo Pharma, BMS-Pfizer, and Daiichi Sankyo, outside the submitted work. A.N. reports conference fees from Fresenius Medical Care, outside the submitted work. N.D. reports lecture fees from Bard, speaker and travel fees from Zoll, outside the submitted work. N.A. reports personal fees from Medtronic and Astra-Zeneca, outside the submitted work. A.K. reports non-financial support from Maquet, outside the submitted work. All other authors declared no conflict of interest.
Publisher Copyright:
© 2018 The Author(s).
PY - 2018/12/14
Y1 - 2018/12/14
N2 - Aims The role of extracorporeal membrane oxygenation (ECMO) remains ill defined in pulmonary embolism (PE). We investigated outcomes in patients with high-risk PE undergoing ECMO according to initial therapeutic strategy. Methods and results From 01 January 2014 to 31 December 2015, 180 patients from 13 Departments in nine centres with high-risk PE were retrospectively included. Among those undergoing ECMO, we compared characteristics and outcomes according to adjunctive treatment strategy (systemic thrombolysis, surgical embolectomy, or no reperfusion therapy). Primary outcome was all-cause 30-day mortality. Secondary outcome was 90-day major bleeding. One hundred and twentyeight patients were treated without ECMO; 52 (mean age 47.6 years) underwent ECMO. Overall 30-day mortality was 48.3% [95% confidence interval (CI) 41'56] (87/180); 43% (95% CI 34'52) (55/128) in those treated without ECMO vs. 61.5% (95% CI 52'78) (32/52) in those with ECMO (P = 0.008). In patients undergoing ECMO, 30-day mortality was 76.5% (95% CI 57'97) (13/17) for ECMO ' fibrinolysis, 29.4% (95% CI 51'89) (5/17) for ECMO' surgical embolectomy, and 77.7% (95% CI 59'97) (14/18) for ECMO alone (P = 0.004). Among patients with ECMO, 20 (38.5%, 95% CI 25'52) had a major bleeding event in-hospital; without significant difference across groups. Conclusion In patients with high-risk PE, those with ECMO have a more severe presentation and worse prognosis. Extracorporeal membrane oxygenation in patients with failed fibrinolysis and in those with no reperfusion seems to be associated with particularly unfavourable prognosis compared with ECMO performed in addition to surgical embolectomy. Our findings suggest that ECMO does not appear justified as a stand-alone treatment strategy in PE patients, but shows promise as a complement to surgical embolectomy.
AB - Aims The role of extracorporeal membrane oxygenation (ECMO) remains ill defined in pulmonary embolism (PE). We investigated outcomes in patients with high-risk PE undergoing ECMO according to initial therapeutic strategy. Methods and results From 01 January 2014 to 31 December 2015, 180 patients from 13 Departments in nine centres with high-risk PE were retrospectively included. Among those undergoing ECMO, we compared characteristics and outcomes according to adjunctive treatment strategy (systemic thrombolysis, surgical embolectomy, or no reperfusion therapy). Primary outcome was all-cause 30-day mortality. Secondary outcome was 90-day major bleeding. One hundred and twentyeight patients were treated without ECMO; 52 (mean age 47.6 years) underwent ECMO. Overall 30-day mortality was 48.3% [95% confidence interval (CI) 41'56] (87/180); 43% (95% CI 34'52) (55/128) in those treated without ECMO vs. 61.5% (95% CI 52'78) (32/52) in those with ECMO (P = 0.008). In patients undergoing ECMO, 30-day mortality was 76.5% (95% CI 57'97) (13/17) for ECMO ' fibrinolysis, 29.4% (95% CI 51'89) (5/17) for ECMO' surgical embolectomy, and 77.7% (95% CI 59'97) (14/18) for ECMO alone (P = 0.004). Among patients with ECMO, 20 (38.5%, 95% CI 25'52) had a major bleeding event in-hospital; without significant difference across groups. Conclusion In patients with high-risk PE, those with ECMO have a more severe presentation and worse prognosis. Extracorporeal membrane oxygenation in patients with failed fibrinolysis and in those with no reperfusion seems to be associated with particularly unfavourable prognosis compared with ECMO performed in addition to surgical embolectomy. Our findings suggest that ECMO does not appear justified as a stand-alone treatment strategy in PE patients, but shows promise as a complement to surgical embolectomy.
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U2 - 10.1093/eurheartj/ehy464
DO - 10.1093/eurheartj/ehy464
M3 - Article
C2 - 30137303
AN - SCOPUS:85053008173
SN - 0195-668X
VL - 39
SP - 4196
EP - 4204
JO - European Heart Journal
JF - European Heart Journal
IS - 47
ER -