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Compression stockings to prevent post-thrombotic syndrome: a randomised placebo-controlled trial.
Kahn, Susan R; Shapiro, Stan; Wells, Philip S; Rodger, Marc A; Kovacs, Michael J; Anderson, David R; Tagalakis, Vicky; Houweling, Adrielle H; Ducruet, Thierry; Holcroft, Christina; Johri, Mira; Solymoss, Susan; Miron, Marie-José; Yeo, Erik; Smith, Reginald; Schulman, Sam; Kassis, Jeannine; Kearon, Clive; Chagnon, Isabelle; Wong, Turnly; Demers, Christine; Hanmiah, Rajendar; Kaatz, Scott; Selby, Rita; Rathbun, Suman; Desmarais, Sylvie; Opatrny, Lucie; Ortel, Thomas L; Ginsberg, Jeffrey S.
Afiliación
  • Kahn SR; Centre for Clinical Epidemiology, Jewish General Hospital, Montreal, QC, Canada. Electronic address: susan.kahn@mcgill.ca.
  • Shapiro S; Centre for Clinical Epidemiology, Jewish General Hospital, Montreal, QC, Canada; Department of Epidemiology and Biostatistics, McGill University, Montreal, QC, Canada.
  • Wells PS; Department of Medicine, University of Ottawa/Ottawa Hospital, Ottawa, ON, Canada; Ottawa Hospital Research Institute, Ottawa, ON, Canada.
  • Rodger MA; Ottawa Hospital Research Institute, Ottawa, ON, Canada; Thrombosis Program, Division of Hematology, Department of Medicine, University of Ottawa, Ottawa, ON, Canada.
  • Kovacs MJ; Division of Hematology, London Health Sciences Centre, London, ON, Canada.
  • Anderson DR; Department of Medicine, Dalhousie University, Halifax, NS, Canada; Capital Health, Halifax, NS, Canada.
  • Tagalakis V; Centre for Clinical Epidemiology, Jewish General Hospital, Montreal, QC, Canada.
  • Houweling AH; Centre for Clinical Epidemiology, Jewish General Hospital, Montreal, QC, Canada.
  • Ducruet T; Centre for Clinical Epidemiology, Jewish General Hospital, Montreal, QC, Canada.
  • Holcroft C; The Institute for Clinical Research and Health Policy Studies, Tufts Medical Center, Boston, MA, USA; Tufts Clinical and Translational Science Institute, Tufts University, Boston, MA, USA.
  • Johri M; International Health Unit, University of Montreal Hospital Research Centre, Montreal, QC, Canada; Department of Health Administration, Faculty of Medicine, University of Montreal, Montreal, QC, Canada.
  • Solymoss S; Division of Hematology, Montreal General Hospital, Montreal, QC, Canada; St Mary's Hospital, Montreal, QC, Canada.
  • Miron MJ; Department of Medicine, Hôpital Notre-Dame, Montreal, QC, Canada.
  • Yeo E; Division of Hematology, University Health Network, Toronto, ON, Canada.
  • Smith R; Divisions of Cardiology and Thrombosis, Victoria Heart Institute Foundation, Victoria, BC, Canada.
  • Schulman S; Department of Medicine, McMaster University, Hamilton, ON, Canada; Thrombosis and Atherosclerosis Research Institute, Hamilton, ON, Canada; Karolinska Institute, Stockholm, Sweden.
  • Kassis J; Division of Hematology, Hôpital Maisonneuve-Rosemont, QC, Canada.
  • Kearon C; Department of Medicine, McMaster University, Hamilton, ON, Canada.
  • Chagnon I; Department of Medicine, Hôpital du Sacré-Coeur, University of Montreal, Montreal, QC, Canada.
  • Wong T; Department of Medicine, St Boniface General Hospital, University of Manitoba, Winnipeg, Manitoba, Canada.
  • Demers C; Division of Hematology, CHU de Quebec, Quebec, QC, Canada.
  • Hanmiah R; Division of General Internal Medicine, St Joseph's Hospital, Hamilton, ON, Canada.
  • Kaatz S; Academic Hospital Medicine, Hurley Medical Center, Flint, MI, USA.
  • Selby R; Department of Medicine and Department of Clinical Pathology, Sunnybrook Health Sciences Centre and University Health Network, University of Toronto, Toronto, ON, Canada.
  • Rathbun S; Department of Medicine, Oklahoma University Health Sciences Center, Oklahoma City, OK, USA.
  • Desmarais S; Department of Medicine, Hôpital Pierre-Boucher, Longueuil, QC, Canada.
  • Opatrny L; Professional Services, St Mary's Hospital Center, Montreal, QC, Canada.
  • Ortel TL; Division of Hematology, Duke University Medical Center, Durham, NC, USA.
  • Ginsberg JS; Department of Medicine, McMaster University, Hamilton, ON, Canada.
Lancet ; 383(9920): 880-8, 2014 Mar 08.
Article en En | MEDLINE | ID: mdl-24315521
ABSTRACT

BACKGROUND:

Post-thrombotic syndrome (PTS) is a common and burdensome complication of deep venous thrombosis (DVT). Previous trials suggesting benefit of elastic compression stockings (ECS) to prevent PTS were small, single-centre studies without placebo control. We aimed to assess the efficacy of ECS, compared with placebo stockings, for the prevention of PTS.

METHODS:

We did a multicentre randomised placebo-controlled trial of active versus placebo ECS used for 2 years to prevent PTS after a first proximal DVT in centres in Canada and the USA. Patients were randomly assigned to study groups with a web-based randomisation system. Patients presenting with a first symptomatic, proximal DVT were potentially eligible to participate. They were excluded if the use of compression stockings was contraindicated, they had an expected lifespan of less than 6 months, geographical inaccessibility precluded return for follow-up visits, they were unable to apply stockings, or they received thrombolytic therapy for the initial treatment of acute DVT. The primary outcome was PTS diagnosed at 6 months or later using Ginsberg's criteria (leg pain and swelling of ≥1 month duration). We used a modified intention to treat Cox regression analysis, supplemented by a prespecified per-protocol analysis of patients who reported frequent use of their allocated treatment. This study is registered with ClinicalTrials.gov, number NCT00143598, and Current Controlled Trials, number ISRCTN71334751.

FINDINGS:

From 2004 to 2010, 410 patients were randomly assigned to receive active ECS and 396 placebo ECS. The cumulative incidence of PTS was 14·2% in active ECS versus 12·7% in placebo ECS (hazard ratio adjusted for centre 1·13, 95% CI 0·73-1·76; p=0·58). Results were similar in a prespecified per-protocol analysis of patients who reported frequent use of stockings.

INTERPRETATION:

ECS did not prevent PTS after a first proximal DVT, hence our findings do not support routine wearing of ECS after DVT.

FUNDING:

Canadian Institutes of Health Research.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Medias de Compresión / Síndrome Postrombótico Tipo de estudio: Clinical_trials / Etiology_studies / Guideline / Incidence_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged País/Región como asunto: America do norte Idioma: En Revista: Lancet Año: 2014 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Medias de Compresión / Síndrome Postrombótico Tipo de estudio: Clinical_trials / Etiology_studies / Guideline / Incidence_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged País/Región como asunto: America do norte Idioma: En Revista: Lancet Año: 2014 Tipo del documento: Article