首页> 外文期刊>Circulation. Heart failure >Clinical Implications of Respiratory Failure in Patients Receiving Durable Left Ventricular Assist Devices for End-Stage Heart Failure
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Clinical Implications of Respiratory Failure in Patients Receiving Durable Left Ventricular Assist Devices for End-Stage Heart Failure

机译:呼吸衰竭患者接受持续左心室辅助装置的临床影响终级心力衰竭

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Background: The impact of respiratory failure on patients undergoing left ventricular assist device (LVAD) implantation is not well understood, especially since these patients were excluded from landmark clinical trials. We sought to evaluate the associations between immediate preimplant and postimplant respiratory failure on outcomes in advanced heart failure patients undergoing LVAD implantation. Methods and Results: We included all patients in the Interagency Registry for Mechanically Assisted Circulatory Support who were implanted with continuous-flow LVADs from 2008 to 2016. Of the 16 362 patients who underwent continuous-flow LVAD placement, 906 (5.5%) required preimplant intubation within 48 hours before implantation, and 1001 (6.1%) patients developed respiratory failure within 1 week after implantation. A higher proportion of patients requiring preimplant intubation were Interagency Registry for Mechanically Assisted Circulatory Support profile 1, required mechanical circulatory support, and presented with cardiac arrest or myocardial infarction (P<0.001, all). At 1 year, 54.3% of patients intubated preimplant were alive without transplant, 20.1% had been transplanted, and 24.2% died before transplant. Patients requiring preimplant intubation had higher rates of postimplant complications, including bleeding, stroke, and right ventricular assist device implantation (P<0.01 for all). Among Interagency Registry for Mechanically Assisted Circulatory Support profile 1 patients, preimplant intubation incurred additional risk of death at 1 year compared with Interagency Registry for Mechanically Assisted Circulatory Support profile 1 patients not intubated (hazard ratio, 1.37 [95% CI, 1.13-1.65]; P=0.001). After multivariable analysis, both preimplant intubation (hazard ratio, 1.20 [95% CI, 1.03-1.41]; P=0.021) and respiratory failure within 1 week (hazard ratio, 2.54 [95% CI, 2.26-2.85]; P<0.001) were associated with higher all-cause 1-year mortality. Conclusions: Respiratory failure both before and after LVAD implantation identifies an advanced heart failure population with significantly worse 1-year mortality. This data might be helpful in counseling patients and their families about expectations about life with an LVAD.
机译:背景:呼吸衰竭对接受左心室辅助装置(LVAD)植入的患者的影响尚不清楚,特别是由于这些患者被排除在地标临床试验之外。我们试图评估先进心力衰竭患者的直接预体和后期呼吸失败的联想,患者植入的晚期心力衰竭患者。方法和结果:我们将所有患者介绍了从2008年至2016年植入的机械辅助循环支援的机械辅助循环支持。在接受连续流动LVAD放置的1662名362名患者中,906(5.5%)所需的预处理在植入前48小时内插管,1001例(6.1%)患者在植入后1周内发育了呼吸衰竭。需要预致剂插管的患者的较高比例是机械辅助循环支持轮廓1的间歇性登记,所需的机械循环支持,并呈现心脏骤停或心肌梗死(P <0.001,全部)。在1年后,54.3%的患者插管预处理在没有移植的情况下活着,移植了20.1%,移植前24.2%死亡。需要预致剂插管的患者具有更高的后后并发症率,包括出血,中风和右心室辅助装置植入(所有P <0.01)。在机械辅助循环支持概况1患者中,与机械辅助循环支持型材的机械辅助循环支持型材的间歇性登记处,预致病人的预致病性插管在1年内发生了额外的死亡风险1未提包(危险比,1.37 [95%CI,1.13-1.65] ; p = 0.001)。多变量分析后,预致剂插管(危险比,1.20 [95%CI,1.03-1.41]; P = 0.021)和1周内呼吸衰竭(危险比,2.54 [95%CI,2.26-2.85]; P <0.001 )与较高的全部导致1年死亡率有关。结论:LVAD植入前后呼吸衰竭均识别晚期心力衰竭人口,其死亡率明显更差。这种数据可能有助于咨询患者及其家庭关于使用LVAD的生活的期望。

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