Stamou Sotiris C, Lopez Cassandra, Novello Courtney, Nores Marcos A
Department of Thoracic and Cardiovascular Surgery, JFK Medical Center, Atlantis, Florida.
J Card Surg. 2019 Mar;34(3):118-123. doi: 10.1111/jocs.13993. Epub 2019 Feb 14.
Numerous studies have documented the safety of whole blood cardioplegia on clinical outcomes after cardiac surgery. However, there is a paucity of studies investigating the outcomes of whole blood microplegia after cardiac surgery. Our protocol of whole blood microplegia includes removal of the crystalloid portion and utilizing the Quest Myocardial Protection System, for delivery of del Nido cardioplegia additives in whole blood. This study sought to evaluate the effects of whole blood microplegia on clinical outcomes, following cardiac surgery, in high-risk cardiac surgery patients.
Between February 2016 and December 2017, 131 high-risk patients underwent cardiac surgery operations, utilizing whole blood microplegia and were compared with a contemporaneous control group of 236 low-risk patients. High-risk patients included those who underwent combined coronary artery bypass grafting (CABG) and valve repair or replacement, double-valve surgery, triple-valve repair or replacement, and patients with ejection fraction < 40%. Multivariable logistic regression analysis was performed to identify independent risk factors of mortality after cardiac surgery.
Operative mortality was 7% for high-risk and 0% for low-risk patients (P < 0.001). Of those patients, five had isolated CABG (two had emergent CABG), two had double-valve surgery, two had combined valve/CABG. In multivariate analysis, high-risk classification (odds ratio = 3.66, 95% confidence intervals = 1.04-12.9, P = 0.04), emerged as an independent predictor of operative mortality.
Whole blood microplegia, is a novel myocardial protection strategy that can be applied in high-risk cardiac surgery patients and prolonged operations, requiring cardioplegic arrest with acceptable early clinical outcomes.
众多研究记录了全血心脏停搏液对心脏手术后临床结局的安全性。然而,对心脏手术后全血微停搏液结局进行研究的却很少。我们的全血微停搏液方案包括去除晶体部分,并使用Quest心肌保护系统,以便在全血中输送德尔尼多心脏停搏液添加剂。本研究旨在评估全血微停搏液对高危心脏手术患者心脏手术后临床结局的影响。
2016年2月至2017年12月期间,131例高危患者接受了使用全血微停搏液的心脏手术,并与同期236例低危患者的对照组进行比较。高危患者包括接受冠状动脉旁路移植术(CABG)联合瓣膜修复或置换、双瓣膜手术、三瓣膜修复或置换的患者,以及射血分数<40%的患者。进行多变量逻辑回归分析以确定心脏手术后死亡的独立危险因素。
高危患者手术死亡率为7%,低危患者为0%(P<0.001)。在这些患者中,5例接受单纯CABG(2例为急诊CABG),2例接受双瓣膜手术,2例接受瓣膜/CABG联合手术。在多变量分析中,高危分类(比值比=3.66,95%置信区间=1.04-12.9,P=0.04)成为手术死亡率的独立预测因素。
全血微停搏液是一种新型的心肌保护策略,可应用于高危心脏手术患者和需要心脏停搏的长时间手术,早期临床结局可接受。