Augoustides John G T, Szeto Wilson, Ochroch E Andrew, Cowie Doreen, Weiner Justin, Gambone Andrew J, Pinchasik Dawn, Bavaria Joseph E
Department of Anesthesiology and Critical Care, Hospital of University of Pennsylvania, Philadelphia, PA 19104-4283, USA.
J Cardiothorac Vasc Anesth. 2007 Jun;21(3):388-92. doi: 10.1053/j.jvca.2006.11.024. Epub 2007 Feb 20.
To delineate the incidence, outcome impact, and clinical predictors of atrial fibrillation (AF) after adult aortic arch repair requiring deep hypothermic circulatory arrest (AAR-DHCA) AIMS: To determine the incidence of AF after AAR-DHCA, to determine whether AF after AAR-DHCA affects mortality or stay in the intensive care unit (ICU), to determine multivariate predictors for AF after AAR-DHCA, and to determine whether aprotinin protects against AF after AAR-DHCA.
Retrospective and observational.
Single large university hospital.
All adults undergoing AAR-DHCA in 2000 and 2001.
The cohort size was 144. Antifibrinolytic exposure was 100%, aprotinin 66% and aminocaproic acid 34%. The incidence of AF was 34.0%. AF was not significantly associated with increased mortality or prolonged ICU stay. Advanced age was a multivariate risk factor for AF. Lower temperature nadir during DHCA was protective against postoperative AF. Aprotinin had no demonstrable effect on AF after AAR-DHCA.
AF after AAR-DHCA is common but does not independently increase mortality or ICU stay. The risk of AF after AAR-DHCA increases with age but decreases with the degree of hypothermia during DHCA. Aprotinin does not appear to affect the risk of AF after AAR-DHCA.
明确需要深低温停循环的成人主动脉弓修复术(AAR - DHCA)后房颤(AF)的发生率、对预后的影响及临床预测因素。
确定AAR - DHCA后AF的发生率,确定AAR - DHCA后AF是否影响死亡率或在重症监护病房(ICU)的住院时间,确定AAR - DHCA后AF的多变量预测因素,以及确定抑肽酶是否能预防AAR - DHCA后AF的发生。
回顾性观察研究。
大型单中心大学医院。
2000年和2001年所有接受AAR - DHCA的成人。
队列规模为144例。抗纤溶药物的使用比例为100%,其中抑肽酶66%,氨基己酸34%。AF的发生率为34.0%。AF与死亡率增加或ICU住院时间延长无显著相关性。高龄是AF的多变量风险因素。DHCA期间最低体温较低可预防术后AF。抑肽酶对AAR - DHCA后AF无明显影响。
AAR - DHCA后AF很常见,但不会独立增加死亡率或ICU住院时间。AAR - DHCA后AF的风险随年龄增加而增加,但随DHCA期间低温程度的增加而降低。抑肽酶似乎不影响AAR - DHCA后AF的风险。