Department of Radiology, Duke University Medical Center, Durham, North Carolina.
Division of Biostatistics, Washington University in St. Louis, St. Louis, Missouri.
J Vasc Interv Radiol. 2022 Oct;33(10):1161-1170.e11. doi: 10.1016/j.jvir.2022.05.030. Epub 2022 Jul 5.
To identify the baseline patient characteristics that predict who will benefit from pharmacomechanical catheter-directed thrombolysis (PCDT) of acute iliofemoral deep vein thrombosis (DVT).
In the Acute Venous Thrombosis: Thrombus Removal with Adjunctive Catheter-Directed Thrombolysis (ATTRACT) multicenter randomized trial, 381 patients with acute iliofemoral DVT underwent PCDT and anticoagulation or anticoagulation alone. The correlations between baseline factors and venous clinical outcomes were evaluated over 24 months using post hoc regression analyses. Interaction terms were examined to evaluate for differential effects by treatment arm.
Patients with clinically severe DVT (higher baseline Villalta score) experienced greater effects of PCDT in improving 24-month venous outcomes, including moderate or severe postthrombotic syndrome (PTS) (odds ratios [ORs] and 95% confidence intervals [CIs] per unit increase in the baseline Villalta scores were as follows: for PCDT, OR, 1.08 [95% CI, 1.01-1.15]; for control, OR, 1.20 [95% CI, 1.12-1.29]; P = .03), PTS severity (between-arm differences in the Villalta [P = .004] and Venous Clinical Severity Scale [VCSS] [P = .002)] scores), and quality of life (between-arm difference in the Venous Insufficiency Epidemiological and Economic Study Quality of Life score; P = .025). Patients with previous DVT had greater effects of PCDT on 24-month PTS severity than those in patients without previous DVT (mean [95% CI] between-arm difference in the Villalta score, 4.2 [1.56-6.84] vs 0.9 [-0.44 to 2.26], P = .03; mean [95% CI] between-arm difference in the VCSS score, 2.6 [0.94-4.21] vs 0.3 [-0.58 to 1.14], P = .02). The effects of PCDT on some but not all outcomes were greater in patients presenting with left-sided DVT (Villalta PTS severity, P = .04; venous ulcer, P = .0499) or a noncompressible popliteal vein (PTS, P = .02). The effects of PCDT did not vary by sex, race, ethnicity, body mass index, symptom duration, hypertension, diabetes, or hypercholesterolemia.
In patients with acute iliofemoral DVT, greater presenting clinical severity (higher baseline Villalta score) and a history of previous DVT predict enhanced benefits from PCDT.
确定预测哪些患者将从急性髂股深静脉血栓形成(DVT)的药物机械性导管溶栓(PCDT)中获益的基线患者特征。
在急性静脉血栓形成:血栓切除术联合辅助导管溶栓(ATTRACT)多中心随机试验中,381 例急性髂股 DVT 患者接受了 PCDT 和抗凝治疗或单独抗凝治疗。使用事后回归分析评估基线因素与 24 个月静脉临床结局之间的相关性。检查交互项以评估治疗臂的差异效应。
临床严重 DVT(更高的基线 Villalta 评分)的患者接受 PCDT 治疗后,改善 24 个月静脉结局的效果更大,包括中度或重度 PTS(比值比[ORs]和 95%置信区间[CIs]每增加单位基线 Villalta 评分如下:PCDT,OR,1.08 [95%CI,1.01-1.15];对照组,OR,1.20 [95%CI,1.12-1.29];P=0.03)、PTS 严重程度(Villalta 之间的臂间差异[P=0.004]和静脉临床严重程度量表[VCSS] [P=0.002])和生活质量(静脉功能不全流行病学和经济研究质量生活评分的臂间差异;P=0.025)。有 DVT 病史的患者接受 PCDT 治疗后 24 个月 PTS 严重程度的效果大于无 DVT 病史的患者(Villalta 评分的臂间平均[95%CI]差异,4.2 [1.56-6.84] vs 0.9 [-0.44 至 2.26],P=0.03;VCSS 评分的臂间平均[95%CI]差异,2.6 [0.94-4.21] vs 0.3 [-0.58 至 1.14],P=0.02)。PCDT 对某些但不是所有结局的影响在左侧 DVT(Villalta PTS 严重程度,P=0.04;静脉溃疡,P=0.0499)或非可压缩的腘静脉(PTS,P=0.02)患者中更大。PCDT 的影响不因性别、种族、民族、体重指数、症状持续时间、高血压、糖尿病或高胆固醇血症而有所不同。
在急性髂股 DVT 患者中,较高的基线临床严重程度(更高的基线 Villalta 评分)和 DVT 病史可预测 PCDT 的获益增加。