Department of Cardiac Surgery, Heidelberg University Hospital, Im Neuenheimer Feld 110, Heidelberg, 69120, Germany.
Department of Anesthesiology, Heidelberg University Hospital, Heidelberg, Germany.
ESC Heart Fail. 2020 Oct;7(5):2853-2861. doi: 10.1002/ehf2.12888. Epub 2020 Aug 5.
Acute right heart failure (RHF) is a severe complication of right ventricular infarction. The management of acute RHF poses a number of challenges, such as providing haemodynamic support. Temporary circulatory support (TCS) may be required upon failing medical therapy. The ProtekDuo® dual lumen cannula provides a minimally invasive option for (TCS) through a groin-free internal jugular vein approach. We present the largest patient series to date using the ProtekDuo® cannula as temporary right ventricular assist device (t-RVAD) in RHF after acute myocardial infarction (MI).
From July 2016 to November 2019, 10 patients underwent t-RVAD implantation for RHF following acute MI. Transthoracic and transoesophageal echocardiography were performed in all patients to assess cardiac function, with a particular focus on RV function. Cumulative 30-day survival was 60%. Mean TAPSE was 6.4 ± 3.1 mm, mean fractional area change was 12.1 ± 4.2%, and mean right ventricular end diastolic area was 19.8 ± 2.7 cm . Mean implantation time was 32.8 ± 8.3 min. Mean interval after first cardiac intervention was 4.6 ± 5.8 days. Mean t-RVAD time was 10.0 ± 7.4 days with a significant reduction in central venous pressure 19.3 ± 2.7 vs. 8.2 ± 2.6 mmHg, P < 0.001 and a significant increase in central venous saturation 52.8 ± 15.6 vs. 80.0 ± 6.0%, P < 0.001. Mean intensive care unit stay was 18.6 ± 12.2 days. Four patients were weaned from TCS. Two patients were bridged to a long-term paracorporeal RVAD. There were no t-RVAD associated complications. Causes of death (n = 4) were multiorgan failure, electromechanical dissociation, and haemorrhagic stroke. Mean follow-up time was 96.0 ± 107.6 days. No independent predictors of mortality were identified in univariate analysis.
We show that groin-free, percutaneous implantation of the ProtekDuo® cannula is a feasible and safe tool for TCS in acute RHF post-MI. This approach provides the advantages of percutaneous implantation including complete mobilization and non-surgical bedside explantation, as well as the option for adding an oxygenator to the t-RVAD circuit.
急性右心衰竭(RHF)是右心室梗死的严重并发症。急性 RHF 的治疗存在许多挑战,例如提供血流动力学支持。在药物治疗失败时可能需要临时循环支持(TCS)。ProtekDuo®双腔管通过股静脉-free 颈内静脉入路为(TCS)提供了一种微创选择。我们报告了迄今为止最大的患者系列,使用 ProtekDuo®套管作为急性心肌梗死后 RHF 的临时右心室辅助装置(t-RVAD)。
从 2016 年 7 月至 2019 年 11 月,10 例患者因急性 MI 后 RHF 接受 t-RVAD 植入。所有患者均进行经胸和经食管超声心动图检查,以评估心功能,特别关注 RV 功能。30 天累积生存率为 60%。平均 TAPSE 为 6.4±3.1mm,平均分数面积变化为 12.1±4.2%,平均右心室舒张末期面积为 19.8±2.7cm。平均植入时间为 32.8±8.3 分钟。首次心脏介入治疗后平均间隔时间为 4.6±5.8 天。平均 t-RVAD 时间为 10.0±7.4 天,中心静脉压显著降低 19.3±2.7mmHg 对 8.2±2.6mmHg,P<0.001,中心静脉饱和度显著增加 52.8±15.6%对 80.0±6.0%,P<0.001。平均 ICU 住院时间为 18.6±12.2 天。4 例患者成功脱机 TCS。2 例患者桥接到长期体外 RVAD。无 t-RVAD 相关并发症。死亡原因(n=4)为多器官衰竭、电机械分离和出血性卒中。平均随访时间为 96.0±107.6 天。单因素分析未发现死亡的独立预测因素。
我们表明,股静脉-free 经皮植入 ProtekDuo®套管是 MI 后急性 RHF 中 TCS 的一种可行且安全的工具。这种方法提供了经皮植入的优点,包括完全活动和非手术床边拔出,以及在 t-RVAD 回路中添加氧合器的选择。