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Endovascular Thrombus Removal for Acute Iliofemoral Deep Vein Thrombosis.
Comerota, Anthony J; Kearon, Clive; Gu, Chu-Shu; Julian, Jim A; Goldhaber, Samuel Z; Kahn, Susan R; Jaff, Michael R; Razavi, Mahmood K; Kindzelski, Andrei L; Bashir, Riyaz; Patel, Parag; Sharafuddin, Mel; Sichlau, Michael J; Saad, Wael E; Assi, Zakaria; Hofmann, Lawrence V; Kennedy, Margaret; Vedantham, Suresh.
Affiliation
  • Comerota AJ; Inova Heart and Vascular Institute, Inova Alexandria Hospital, VA (A.J.C.).
  • Kearon C; Thrombosis and Atherosclerosis Research Institute (C.K.), McMaster University, Hamilton, ON, Canada.
  • Gu CS; Juravinski Hospital and Cancer Centre, Hamilton, ON, Canada (C.K., C.-S.G., J.A.J.).
  • Julian JA; Department of Oncology (C.-S.G., J.A.J.), McMaster University, Hamilton, ON, Canada.
  • Goldhaber SZ; Juravinski Hospital and Cancer Centre, Hamilton, ON, Canada (C.K., C.-S.G., J.A.J.).
  • Kahn SR; Department of Oncology (C.-S.G., J.A.J.), McMaster University, Hamilton, ON, Canada.
  • Jaff MR; Juravinski Hospital and Cancer Centre, Hamilton, ON, Canada (C.K., C.-S.G., J.A.J.).
  • Razavi MK; Division of Cardiovascular Medicine, Brigham and Women's Hospital, and Harvard Medical School, Boston, MA (S.Z.G.).
  • Kindzelski AL; Jewish General Hospital, Lady Davis Institute, Center for Clinical Epidemiology, Montreal, QC, Canada (S.R.K.).
  • Bashir R; Newton-Wellesley Hospital, and Harvard Medical School, Boston, MA (M.R.J.).
  • Patel P; St. Joseph's Hospital, Orange, CA (M.K.R.).
  • Sharafuddin M; National Heart Lung and Blood Institute, National Institutes of Health, Bethesda, MD (A.L.K.).
  • Sichlau MJ; Department of Medicine, Temple University Hospital, Philadelphia, PA (R.B.).
  • Saad WE; Department of Radiology, Medical College of Wisconsin, Milwaukee (P.P.).
  • Assi Z; Division of Vascular Surgery, University of Iowa, Iowa City (M.S.).
  • Hofmann LV; Vascular and Interventional Professionals LLC, Hinsdale, IL (M.J.S.).
  • Kennedy M; Department of Radiology, University of Michigan, Ann Arbor (W.E.S.).
  • Vedantham S; Toledo Radiological Associates, Vascular & Interventional Radiology, OH (Z.A.).
Circulation ; 139(9): 1162-1173, 2019 02 26.
Article in En | MEDLINE | ID: mdl-30586751
ABSTRACT

BACKGROUND:

The ATTRACT trial (Acute Venous Thrombosis Thrombus Removal with Adjunctive Catheter-Directed Thrombolysis) previously reported that pharmacomechanical catheter-directed thrombolysis (PCDT) did not prevent postthrombotic syndrome (PTS) in patients with acute proximal deep vein thrombosis. In the current analysis, we examine the effect of PCDT in ATTRACT patients with iliofemoral deep vein thrombosis.

METHODS:

Within a large multicenter randomized trial, 391 patients with acute deep vein thrombosis involving the iliac or common femoral veins were randomized to PCDT with anticoagulation versus anticoagulation alone (No-PCDT) and were followed for 24 months to compare short-term and long-term outcomes.

RESULTS:

Between 6 and 24 months, there was no difference in the occurrence of PTS (Villalta scale ≥5 or ulcer 49% PCDT versus 51% No-PCDT; risk ratio, 0.95; 95% CI, 0.78-1.15; P=0.59). PCDT led to reduced PTS severity as shown by lower mean Villalta and Venous Clinical Severity Scores ( P<0.01 for comparisons at 6, 12, 18, and 24 months), and fewer patients with moderate-or-severe PTS (Villalta scale ≥10 or ulcer 18% versus 28%; risk ratio, 0.65; 95% CI, 0.45-0.94; P=0.021) or severe PTS (Villalta scale ≥15 or ulcer 8.7% versus 15%; risk ratio, 0.57; 95% CI, 0.32-1.01; P=0.048; and Venous Clinical Severity Score ≥8 6.6% versus 14%; risk ratio, 0.46; 95% CI, 0.24-0.87; P=0.013). From baseline, PCDT led to greater reduction in leg pain and swelling ( P<0.01 for comparisons at 10 and 30 days) and greater improvement in venous disease-specific quality of life (Venous Insufficiency Epidemiological and Economic Study Quality of Life unit difference 5.6 through 24 months, P=0.029), but no difference in generic quality of life ( P>0.2 for comparisons of SF-36 mental and physical component summary scores through 24 months). In patients having PCDT versus No-PCDT, major bleeding within 10 days occurred in 1.5% versus 0.5% ( P=0.32), and recurrent venous thromboembolism over 24 months was observed in 13% versus 9.2% ( P=0.21).

CONCLUSIONS:

In patients with acute iliofemoral deep vein thrombosis, PCDT did not influence the occurrence of PTS or recurrent venous thromboembolism. However, PCDT significantly reduced early leg symptoms and, over 24 months, reduced PTS severity scores, reduced the proportion of patients who developed moderate-or-severe PTS, and resulted in greater improvement in venous disease-specific quality of life. CLINICAL TRIAL REGISTRATION URL https//www.clinicaltrials.gov . Unique identifier NCT00790335.
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Key words

Full text: 1 Database: MEDLINE Main subject: Postthrombotic Syndrome / Femoral Vein / Endovascular Procedures / Mechanical Thrombolysis / Iliac Vein / Anticoagulants Type of study: Clinical_trials / Etiology_studies / Prognostic_studies Limits: Adult / Female / Humans / Male / Middle aged Language: En Year: 2019 Type: Article

Full text: 1 Database: MEDLINE Main subject: Postthrombotic Syndrome / Femoral Vein / Endovascular Procedures / Mechanical Thrombolysis / Iliac Vein / Anticoagulants Type of study: Clinical_trials / Etiology_studies / Prognostic_studies Limits: Adult / Female / Humans / Male / Middle aged Language: En Year: 2019 Type: Article