Department of Medicine, Creighton University School of Medicine, Omaha, Nebraska.
Division of Cardiovascular Medicine, Department of Medicine, University of Arkansas School of Medicine, Little Rock, Arkansas.
Am J Cardiol. 2023 Oct 15;205:249-258. doi: 10.1016/j.amjcard.2023.07.170. Epub 2023 Aug 22.
There are limited and conflicting data on the initial management of intermediate-risk (or submassive) pulmonary embolism (PE). This study sought to compare the outcomes of catheter-directed thrombolysis (CDT) in combination with systemic anticoagulation (SA) to SA alone. A systematic search was conducted in MEDLINE, EMBASE, PubMed, and the Cochrane databases from inception to March 1, 2023 for studies comparing the outcomes of CDT + SA versus SA alone in intermediate-risk PE. The outcomes were in-hospital, 30-day, 90-day, and 1-year mortality; bleeding; blood transfusion; right ventricular recovery; and length of stay. Random-effects models was used to calculate the pooled incidence and risk ratios (RRs) with 95% confidence intervals (CIs). A total of 15 (2 randomized and 13 observational) studies with 10,549 (2,310 CDT + SA and 8,239 SA alone) patients were included. Compared with SA, CDT + SA was associated with significantly lower in-hospital mortality (RR 0.41, 95% CI 0.30 to 0.56, p <0.001), 30-day mortality (RR 0.34, 95% CI 0.18 to 0.67, p = 0.002), 90-day mortality (RR 0.34, 95% CI 0.17 to 0.67, p = 0.002), and 1-year mortality (RR 0.58, 95% CI 0.34 to 0.97, p = 0.04). There were no significant differences between the 2 cohorts in the rates of major bleeding (RR 1.39, 95% CI 0.72 to 2.68, p = 0.56), minor bleeding (RR 1.83, 95% CI 0.97 to 3.46, p = 0.06), and blood transfusion (RR 0.34, 95% CI 0.10 to 1.15, p = 0.08). In conclusion, CDT + SA is associated with significantly lower short-term and long-term all-cause mortality, without any differences in major/minor bleeding, in patients with intermediate-risk PE.
在中危(或亚大块)肺栓塞(PE)的初始治疗方面,数据有限且相互矛盾。本研究旨在比较导管溶栓(CDT)联合全身抗凝(SA)与单独 SA 的治疗效果。从研究开始到 2023 年 3 月 1 日,我们在 MEDLINE、EMBASE、PubMed 和 Cochrane 数据库中进行了系统检索,以比较 CDT+SA 与单独 SA 在中危 PE 中的治疗效果。主要结局为院内、30 天、90 天和 1 年死亡率;出血;输血;右心室恢复;以及住院时间。使用随机效应模型计算合并发生率和风险比(RR)及其 95%置信区间(CI)。共纳入 15 项研究(2 项随机对照研究和 13 项观察性研究),共纳入 10549 例患者(2310 例 CDT+SA 和 8239 例 SA 组)。与 SA 相比,CDT+SA 可显著降低院内死亡率(RR 0.41,95%CI 0.30 至 0.56,p<0.001)、30 天死亡率(RR 0.34,95%CI 0.18 至 0.67,p=0.002)、90 天死亡率(RR 0.34,95%CI 0.17 至 0.67,p=0.002)和 1 年死亡率(RR 0.58,95%CI 0.34 至 0.97,p=0.04)。两组之间大出血发生率(RR 1.39,95%CI 0.72 至 2.68,p=0.56)、小出血发生率(RR 1.83,95%CI 0.97 至 3.46,p=0.06)和输血率(RR 0.34,95%CI 0.10 至 1.15,p=0.08)均无显著差异。总之,在中危 PE 患者中,CDT+SA 可显著降低短期和长期全因死亡率,且大出血、小出血和输血发生率无差异。