Endovascular Thrombus Removal for Acute Iliofemoral Deep Vein Thrombosis.


Journal

Circulation
ISSN: 1524-4539
Titre abrégé: Circulation
Pays: United States
ID NLM: 0147763

Informations de publication

Date de publication:
26 02 2019
Historique:
pubmed: 28 12 2018
medline: 4 12 2019
entrez: 28 12 2018
Statut: ppublish

Résumé

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. 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. 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). 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. URL: https://www.clinicaltrials.gov . Unique identifier: NCT00790335.

Sections du résumé

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.

Identifiants

pubmed: 30586751
doi: 10.1161/CIRCULATIONAHA.118.037425
pmc: PMC6389417
mid: NIHMS1518657
doi:

Substances chimiques

Anticoagulants 0

Banques de données

ClinicalTrials.gov
['NCT00790335']

Types de publication

Clinical Trial, Phase III Journal Article Multicenter Study Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1162-1173

Subventions

Organisme : NHLBI NIH HHS
ID : U01 HL088118
Pays : United States
Organisme : NHLBI NIH HHS
ID : U01 HL088476
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR000448
Pays : United States
Organisme : NHLBI NIH HHS
ID : U54 HL112303
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR002345
Pays : United States
Organisme : CIHR
Pays : Canada

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : CommentIn

Références

Eur J Vasc Surg. 1990 Oct;4(5):483-9
pubmed: 2226879
J Lab Clin Med. 1977 May;89(5):1018-29
pubmed: 323387
Ann Surg. 2004 Jan;239(1):118-26
pubmed: 14685109
Circulation. 2011 Apr 26;123(16):1788-830
pubmed: 21422387
Arch Surg. 1997 Jan;132(1):46-51
pubmed: 9006552
J Surg Res. 1977 May;22(5):483-8
pubmed: 140274
Vasc Med. 2016 Aug;21(4):400-7
pubmed: 27247235
Circ Cardiovasc Interv. 2015 Jan;8(1):
pubmed: 25593121
J Vasc Interv Radiol. 2006 Mar;17(3):435-47; quiz 448
pubmed: 16567668
N Engl J Med. 2017 Dec 7;377(23):2240-2252
pubmed: 29211671
J Vasc Surg. 2000 Jul;32(1):130-7
pubmed: 10876214
J Vasc Surg. 2012 Mar;55(3):768-73
pubmed: 22277690
J Thromb Haemost. 2009 May;7(5):879-83
pubmed: 19175497
Radiology. 1999 Apr;211(1):39-49
pubmed: 10189452
Chest. 2016 Feb;149(2):315-352
pubmed: 26867832
J Vasc Interv Radiol. 2013 Jan;24(1):17-24; quiz 26
pubmed: 23176966
Ann Intern Med. 2008 Nov 18;149(10):698-707
pubmed: 19017588
Lancet. 2012 Jan 7;379(9810):31-8
pubmed: 22172244
J Vasc Surg. 2003 Feb;37(2):410-9
pubmed: 12563215
Am Heart J. 2013 Apr;165(4):523-530.e3
pubmed: 23537968
J Thromb Haemost. 2009 May;7(5):884-8
pubmed: 19320818
Am J Med. 1984 Mar;76(3):393-7
pubmed: 6367454
J Vasc Surg. 2010 Nov;52(5):1387-96
pubmed: 20875713
BMJ. 2012 Mar 15;344:e1553
pubmed: 22422832
Eur J Vasc Endovasc Surg. 2012 Aug;44(2):210-3
pubmed: 22658610
Am J Med. 2001 May;110(7):515-9
pubmed: 11343664
J Vasc Interv Radiol. 2006 Mar;17(3):417-34
pubmed: 16567667
Ann Surg. 2001 Jun;233(6):752-60
pubmed: 11371733
J Vasc Interv Radiol. 2014 Sep;25(9):1317-25
pubmed: 25000825
Chest. 2012 Feb;141(2 Suppl):e419S-e496S
pubmed: 22315268
J Vasc Surg. 2007 Nov;46(5):1065-76
pubmed: 17980295
J Thromb Haemost. 2017 Jul;15(7):1351-1360
pubmed: 28440041
JAMA Intern Med. 2017 Apr 1;177(4):554-560
pubmed: 28192563
J Vasc Surg. 1993 Oct;18(4):596-605; discussion 606-8
pubmed: 8411467
J Thromb Haemost. 2005 Apr;3(4):692-4
pubmed: 15842354
J Vasc Surg. 2002 Nov;36(5):889-95
pubmed: 12422097
Eur J Vasc Endovasc Surg. 2002 Sep;24(3):209-14
pubmed: 12217281

Auteurs

Anthony J Comerota (AJ)

Inova Heart and Vascular Institute, Inova Alexandria Hospital, VA (A.J.C.).

Clive Kearon (C)

Thrombosis and Atherosclerosis Research Institute (C.K.), McMaster University, Hamilton, ON, Canada.
Juravinski Hospital and Cancer Centre, Hamilton, ON, Canada (C.K., C.-S.G., J.A.J.).

Chu-Shu Gu (CS)

Department of Oncology (C.-S.G., J.A.J.), McMaster University, Hamilton, ON, Canada.
Juravinski Hospital and Cancer Centre, Hamilton, ON, Canada (C.K., C.-S.G., J.A.J.).

Jim A Julian (JA)

Department of Oncology (C.-S.G., J.A.J.), McMaster University, Hamilton, ON, Canada.
Juravinski Hospital and Cancer Centre, Hamilton, ON, Canada (C.K., C.-S.G., J.A.J.).

Samuel Z Goldhaber (SZ)

Division of Cardiovascular Medicine, Brigham and Women's Hospital, and Harvard Medical School, Boston, MA (S.Z.G.).

Susan R Kahn (SR)

Jewish General Hospital, Lady Davis Institute, Center for Clinical Epidemiology, Montreal, QC, Canada (S.R.K.).

Michael R Jaff (MR)

Newton-Wellesley Hospital, and Harvard Medical School, Boston, MA (M.R.J.).

Mahmood K Razavi (MK)

St. Joseph's Hospital, Orange, CA (M.K.R.).

Andrei L Kindzelski (AL)

National Heart Lung and Blood Institute, National Institutes of Health, Bethesda, MD (A.L.K.).

Riyaz Bashir (R)

Department of Medicine, Temple University Hospital, Philadelphia, PA (R.B.).

Parag Patel (P)

Department of Radiology, Medical College of Wisconsin, Milwaukee (P.P.).

Mel Sharafuddin (M)

Division of Vascular Surgery, University of Iowa, Iowa City (M.S.).

Michael J Sichlau (MJ)

Vascular and Interventional Professionals LLC, Hinsdale, IL (M.J.S.).

Wael E Saad (WE)

Department of Radiology, University of Michigan, Ann Arbor (W.E.S.).

Zakaria Assi (Z)

Toledo Radiological Associates, Vascular & Interventional Radiology, OH (Z.A.).

Lawrence V Hofmann (LV)

Department of Radiology, Stanford University, CA (L.V.H.).

Margaret Kennedy (M)

Department of Medicine, Duke University, Durham, NC (M.K.).

Suresh Vedantham (S)

Mallinckrodt Institute of Radiology, Washington University in St. Louis, MO (S.V.).

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