@article{63d0358edb8547818080e25d6a84c523,
title = "Guidance for the treatment of deep vein thrombosis and pulmonary embolism",
abstract = "This guidance document focuses on the diagnosis and treatment of venous thromboembolism (VTE). Efficient, cost effective diagnosis of VTE is facilitated by combining medical history and physical examination with pre-test probability models, D dimer testing and selective use of confirmatory imaging. Clinical prediction rules, biomarkers and imaging can be used to tailor therapy to disease severity. Anticoagulation options for acute VTE include unfractionated heparin, low molecular weight heparin, fondaparinux and the direct oral anticoagulants (DOACs). DOACs are as effective as conventional therapy with LMWH and vitamin K antagonists. Thrombolytic therapy is reserved for massive pulmonary embolism (PE) or extensive deep vein thrombosis (DVT). Inferior vena cava filters are reserved for patients with acute VTE and contraindications to anticoagulation. Retrievable filters are strongly preferred. The possibility of thoracic outlet syndrome and May-Thurner syndrome should be considered in patients with subclavian/axillary and left common iliac vein DVT, respectively in absence of identifiable triggers. The optimal duration of therapy is dictated by the presence of modifiable thrombotic risk factors. Long term anticoagulation should be considered in patients with unprovoked VTE as well as persistent prothrombotic risk factors such as cancer. Short-term therapy is sufficient for most patients with VTE associated with transient situational triggers such as major surgery. Biomarkers such as D dimer and risk assessment models such the Vienna risk prediction model offer the potential to customize VTE therapy for the individual patient. Insufficient data exist to support the integration of bleeding risk models into duration of therapy planning.",
keywords = "Anticoagulant therapy, DOACs, Deep vein thrombosis, NOACs, Pulmonary embolism, Venous thromboembolism",
author = "Streiff, {Michael B.} and Giancarlo Agnelli and Connors, {Jean M.} and Mark Crowther and Sabine Eichinger and Renato Lopes and McBane, {Robert D.} and Stephan Moll and Jack Ansell",
note = "Funding Information: M Streiff: consulted for BiO Medical, Boehringer Ingelheim, CSL Behring, Daiichi-Sankyo, Janssen Healthcare and Pfizer. He has received research grant support from Daiichi-Sankyo, Janssen Healthcare, PCORI and Portola. G Agnelli: none. J Connors: Scientific Advisory Boards: Boehringer Ingelheim, Bristol Myers Squibb. M Crowther: Advisory boards for Octapharma, Bayer, Boehringer Ingelheim, Janssen, Pfizer, Leo Pharma and Portola. Study Steering committees, or other research related activities for projects involving AKP America, Daichii, Bayer and Leo Pharma. Holds a Career Investigator award from the Heart and Stroke Foundation of Ontario, and the Leo Pharma Chair in Thromboembolism Research at McMaster University (income from which is used to support the salary of research employees); his institutions (McMaster University and/or St Joseph{\textquoteright}s Healthcare) have received funding for research projects from the Heart and Stroke Foundation of Canada, Leo Pharma and Bayer for work in which Dr Crowther is involved; received funding for preparation of educational materials and/or presentations from Alexion, Ortho Clinical Diagnostics, BMS-Pfizer alliance, Leo Pharma, Abbvie, Bayer, Celgene, Shire and CSL Behring; participated in various medicolegal activities relating to thrombosis, anticoagulant drugs, or other aspects of hematological practice, and that these activities are bound by confidentiality arrangements. Further this declaration is made to the best of Dr Crowther{\textquoteright}s ability, but may be incomplete or contain material errors due to the foibles of human memory. S Eichinger: Honoraria, consultancies: Bayer, Boehringer Ingelheim, Daiichi-Sankyo, Bristol Myers Squibb, Pfizer. R Lopes: Research Grant from Bristol Myers Squibb and Glaxo SmithKline. Consultant for Bayer, Boehringer Ingelheim, Daiichi-Sankyo, Bristol Myers Squibb, Pfizer, Merck, Portola. R McBane: none. S Moll: Consultant for Portola. J Ansell: Consulting activities and/or honoraria from the following companies: Bristol Myers Squibb; Pfizer; Boehringer Ingelheim; Daiichi Sankyo; Janssen; Perosphere; Roche Diagnostics; Alere, Inc; Instrumentation Laboratories. Equity interest in the following companies: Perosphere, Inc. 2 Funding Information: We wish to acknowledge the support provided by Myelin and Associates with the preparation of this manuscript for submission. The work contained in this manuscript was partially funded by support from the following companies: Boehringer Ingelheim, Daiichi Sankyo and Janssen Pharmaceuticals. This guidance document is endorsed by the Anticoagulation Forum{\textquoteright}s Board of Directors: Mark Crowther, MD, MSc, FRCPC, Jack E. Ansell, MD, Allison Burnett, PharmD, Nathan Clark, PharmD, Adam Cuker, MD, David Garcia, MD, Scott Kaatz, DO, MSc, FACP, Renato D. Lopes, MD, PhD, Tracy Minichiello, MD, Edith Nutescu, PharmD, FCCP, Lynn Oertel, MS, ANP, CACP, Eva Kline-Rogers, MS, RN, NP,Terri Schnurr, RN, CCRC, Michael Streiff, MD, Diane Wirth, ANP, CACP, BCPS, CACP, Daniel Witt, Pharm D, Ann Wittkowsky, PharmD, CACP, FASHP, FCCP. Publisher Copyright: {\textcopyright} 2016, The Author(s).",
year = "2016",
month = jan,
day = "1",
doi = "10.1007/s11239-015-1317-0",
language = "English (US)",
volume = "41",
pages = "32--67",
journal = "Journal of Thrombosis and Thrombolysis",
issn = "0929-5305",
publisher = "Springer Netherlands",
number = "1",
}