Comparative Outcomes of Catheter-Directed Thrombolysis Plus Systemic Anticoagulation Versus Systemic Anticoagulation Alone in the Management of Intermediate-Risk Pulmonary Embolism in a Systematic Review and Meta-Analysis

被引:5
|
作者
Balakrishna, Akshay Machanahalli [1 ]
Kalathil, Ruth Ann Mathew [1 ]
Pusapati, Suma [1 ]
Atreya, Auras [2 ]
Mehta, Aryan [3 ]
Bansal, Mridul [4 ]
Aggarwal, Vikas [5 ]
Basir, Mir B. [6 ]
Kochar, Ajar [7 ]
Truesdell, Alexander G. [8 ]
Vallabhajosyula, Saraschandra [9 ]
机构
[1] Creighton Univ, Sch Med, Dept Med, Omaha, NE USA
[2] Univ Arkansas, Sch Med, Dept Med, Div Cardiovasc Med, Little Rock, AR USA
[3] Univ Connecticut, Sch Med, Dept Med, Farmington, CT USA
[4] East Carolina Brody Sch Med, Dept Med, Greenville, NC USA
[5] Univ Michigan, Sch Med, Dept Med, Sect Cardiovasc Med, Ann Arbor, MI USA
[6] Henry Ford Hosp, Dept Med, Sect Cardiovasc Med, Detroit, MI USA
[7] Harvard Med Sch, Brigham & Womens Hosp, Dept Med, Sect Cardiovasc Med, Boston, MA USA
[8] Inova Heart & Vasc Inst, Virginia Heart, Falls Church, VA USA
[9] Wake Forest Univ, Dept Med, Sch Med, Sect Cardiovasc Med, Winston Salem, NC 27109 USA
来源
关键词
catheter-directed thrombolysis; anticoagulation; intermediate-risk pulmonary embolism; submassive pulmonary embolism; meta-analysis; RANDOMIZED-TRIAL; RESPONSE TEAM; INTERVENTIONS; EXPERIENCE; THERAPY; CARE; FIBRINOLYSIS; MORTALITY; ALTEPLASE; STANDARD;
D O I
10.1016/j.amjcard.2023.07.170
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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. (C) 2023 Elsevier Inc. All rights reserved.
引用
收藏
页码:249 / 258
页数:10
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