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DOI 10.1016/j.jtcvs.2023.08.048

Медицинская библиотека · The Journal of thoracic and cardiovascular surgery · 2023

Outcome of patients supported with the HeartMate 3 after extracorporeal life support: On behalf of the Durable Mechanical Circulatory Support After Extracorporeal Life Support Study Group.

Saeed Diyar, Stark Christoffer, Otto Wolfgang, Loforte Antonio, Zimpfer Daniel, Bernhardt Alexander M, Potapov Evgenij, Morshius Michiel, Schibilsky David, Albert Alexander, Raweh Ayman, Riebandt Julia, Pappalardo Federico, Attisani Matteo, Rinaldi Mauro, Haneya Assad, Huenges Katharina, Ramjankhan Faiz, Jorde Ulrich P, Lewin Daniel, Jawad Khalil, Aubin Hug, Ayala Rafael, Reichenspurner Hermann, Lichtenberg Artur, Borger Michael, Gummert Jan

СтатьяМногоцентровое исследованиеПеревод в очереди

Аннотация

OBJECTIVES

The Durable Mechanical Circulatory Support System After Extracorporeal Life Support registry is a multicenter registry of patients who were bridged from extracorporeal life support to a durable mechanical circulatory support system. Although numerous studies have highlighted the favorable outcomes after implantation of the HeartMate 3 (Abbott), the objective of our study is to examine the outcomes of patients who received HeartMate 3 support after extracorporeal life support.

METHODS

Data of patients undergoing HeartMate 3 implantation from January 2016 to April 2022 at 14 centers were collected and evaluated. Inclusion criteria were patients with extracorporeal life support before HeartMate 3 implantation. The outcome was reported and compared with patients receiving other types of pumps.

RESULTS

A total of 337 patients were bridged to durable mechanical circulatory support system after extracorporeal life support in the study period. Of those patients, 140 were supported with the HeartMate 3. The other types of pumps included 170 HeartWare HVADs (Medtronic) (86%), 14 HeartMate II devices (7%), and 13 (7%) other pumps (7%). Major postoperative complications included right heart failure requiring temporary right ventricular assist device in 60 patients (47%). Significantly lower postoperative stroke (16% vs 28%, P = .01) and pump thrombosis (3% vs 8%, P = .02) rates were observed in the patients receiving the HeartMate 3. The 30-day, 1-year, and 3-year survivals in patients receiving the HeartMate 3 were 87%, 73%, and 65%, respectively.

CONCLUSIONS

In this critically ill patient population, the survivals of patients who were transitioned to the HeartMate 3 are deemed acceptable and superior to those observed when extracorporeal life support was bridged to other types of durable mechanical circulatory support systems.

Для цитирования: Saeed Diyar, Stark Christoffer, Otto Wolfgang, Loforte Antonio, Zimpfer Daniel, Bernhardt Alexander M, Potapov Evgenij, Morshius Michiel, Schibilsky David, Albert Alexander, Raweh Ayman, Riebandt Julia, Pappalardo Federico, Attisani Matteo, Rinaldi Mauro, Haneya Assad, Huenges Katharina, Ramjankhan Faiz, Jorde Ulrich P, Lewin Daniel, Jawad Khalil, Aubin Hug, Ayala Rafael, Reichenspurner Hermann, Lichtenberg Artur, Borger Michael, Gummert Jan. Outcome of patients supported with the HeartMate 3 after extracorporeal life support: On behalf of the Durable Mechanical Circulatory Support After Extracorporeal Life Support Study Group.. The Journal of thoracic and cardiovascular surgery. 2023. DOI: 10.1016/j.jtcvs.2023.08.048.

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