STATE OF ARTStructured review of post-cardiotomy extracorporeal membrane oxygenation: part 1—Adult patients
Section snippets
Trends in use
The incidence of ECMO implementation in patients after open-heart surgery has been reported between 0.4% and 3.7% (Table 1). PC-ECMO has increased considerably over the past 2 decades.2 Indeed, from 2007 to 2011, non-percutaneous ECMO cannulation increased 2-fold, while the use of percutaneous ECMO increased by more than 15-fold.2 Maxwell and colleagues, evaluating more than 9,000 ECMO patients from the Nationwide Inpatient Sample database in the United States from 1998 to 2009, identified
Cannulation
The location of ECMO cannulation is influenced by the timing and indication, urgency of deployment, cardio-circulatory versus respiratory support required, and institutional factors including staff familiarity and availability of ECMO circuits. PC-ECMO is most often utilized for failure to wean from CPB, so operating room cannulation occurs most frequently, followed by the ICU, and rarely on the ward (Table 2). While PC-ECMO can be initiated any time in the postoperative course, the majority of
Weaning from PC-ECMO and survival to hospital discharge
As expected, successful weaning from PC-ECMO varies greatly within published series, ranging from 31% to 76%, with almost half of the published experiences showing a weaning rate at or slightly above 50% (Table 4). Survival to hospital discharge rates are far less, ranging from 16% to 52%, with fewer than 30% of the centers reporting survival-to-discharge above 40% (Table 4). Of note, even in the face of considerably improved technology and increased experience in managing ECMO care, survival
Post-cardiotomy veno-venous ECMO for respiratory dysfunction
Respiratory insufficiency is a common complication after cardiac surgery and an independent predictor of in-hospital mortality.97, 98 Despite respiratory complications in 7% to 30% of patients,97, 98 there is a paucity of published reports on ECMO therapy when this complication is severe, treated either with VA- or veno-venous ECMO (VV-ECMO). VV-ECMO has been increasingly employed as therapy for primary, refractory respiratory failure as a result of the outcomes seen in conventional ventilatory
Controversial issues and future perspectives on PC-ECMO
ECMO technology has undergone remarkable progress in the last 20 years. More advanced, user-friendly, miniaturized technology has rendered the wider application of this temporary support possible, in many instances for conditions once viewed as contraindications.12, 101 Obvious targets to improve effectiveness include biocompatible circuitry (e.g., the pump, oxygenator, and tubing design), more reliable anticoagulation, rational vasoactive or inotropic support, a better understanding of the
Limitations of the review
This review has some limitations, as it encompasses different patient conditions and different ECMO approaches in its attempt to be comprehensive. However, underlying cardiopulmonary insufficiency and a lack of response to conservative, conventional treatments after cardiac surgery are common to all the studies included. The scenarios for PC-ECMO include conditions ranging from failure to wean from CPB, to cardiogenic shock hours to days after cardiac surgery, to cardiac arrest in the ICU or on
Conclusions
PC-ECMO represents the most frequent indication for temporary mechanical circulatory support with increasing use expected in the future. Considerable variability regarding surgical access and cannula placement still exists, apparently without major differences in outcomes regardless of the technique used. Although PC-ECMO can be life-saving and is only employed when there are few alternatives, mortality and morbidity remain high, reflecting underlying disease severity and an imperfect solution.
Disclosure statement
R.L. is a consultant and conducts clinical trial for LivaNova (London, UK), is a consultant for Medtronic (Minneapolis, MN), and an advisory board member of PulseCath (Arnhem, The Netherlands). D.B. is on the medical advisory board for Baxter, a past medical advisory board member for ALung Technologies, and an anticipated future medical advisory board member for BREETHE. D.B. is on the Trial Steering Committee for the VENT-AVOID trial sponsored by ALung Technologies. The other authors have no
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These authors contributed equally to this work.