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Management of Deep Vein Thrombos in Total Joint Arthroplasty

Management of Deep Vein Thrombos in Total Joint Arthroplasty. Total Hip and Knee Symposium Los Cabos, Mexico. Frank R. Ebert, MD Assistant Chief Department of Orthopædics. The Union Memorial Hospital Baltimore, Maryland. Number of Orthopedic Replacement Procedures/Year.

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Management of Deep Vein Thrombos in Total Joint Arthroplasty

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  1. Management of Deep Vein Thrombos in Total Joint Arthroplasty Total Hip and Knee Symposium Los Cabos, Mexico

  2. Frank R. Ebert, MDAssistant Chief DepartmentofOrthopædics The Union Memorial Hospital Baltimore, Maryland

  3. Number of Orthopedic Replacement Procedures/Year • Total knee replacements: 267,000/year in the US • Total hip replacements: more than 168,000/year in the US AAOS Website availiable at: http://orthoinfo.aaos.org/booklet/bookviacfm?Thread_ID=2&topcategory=knee http://orthoinfo.aaos.org/booklet/bookview.cfm?Thread_ID=2&topcategory=hip

  4. The Cost of DVT • Risk persists for a long time following surgery. • 90% of medical re-admissions following TJR are due to DVT; substantial direct inpatient costs related to DVT

  5. Venous Thromboembolism:Pathogenesis • Venousthrombi • Usually form in regions of sluggish or altered flow in large venous sinuses • May break off, travel to lung – PE • Pathogenic factors • Activation of blood coagulation • Venous stasis • Vascular injury

  6. Venous Thromboembolism:Natural History • Hip Procedures • Have a higher frequency of proximal clots • Knee Procedures • Deep calf veins • Usually asymptomatic • Thrombi tend to be small • Propagation is an issue

  7. Venous Thromboembolism:Natural History (cont’d) • Proximal vein thrombi • Popliteal • Superficial femoral • Common femoral • Iliac veins • Spontaneous lysis of large thrombi uncommon • Strong association between DVT and PE

  8. Venous Thromboembolism:Diagnosis • Clinical Exam 50/50 • Venous duplex ultrasound • Venography

  9. Venous Thromboembolism:Diagnosis (cont’d) • Venous duplex ultrasound • Noninvasive • Assesses vein compressibility • Very sensitive in proximal thrombi • Less sensitive in distal

  10. Venous Thromboembolism:Diagnosis (cont’d) • Venography • FDA standard for DVT • Clinically outmoded

  11. Pulmonary Embolism:Diagnosis • Screening • V/Q scan • Effective non-invasive technique • Probability of PE based on degree of mismatch between ventilation and perfusion

  12. Pulmonary Embolism:Diagnosis (cont’d) • Definitive test • Pulmonary angiogram • Spiral CT

  13. Venous Thromboembolism:Prognosis • Proximal DVT: postoperative, good, if treated for 3 months with anticoagulant therapy • Recurrent events: 5% • After discontinuation of anticoagulant therapy: • 5% to 10% after 1 year • Approximately 30% after 8 years Hirsh J, Hoak J. Circulation. 1996;93:2213.

  14. Clinical Risk Factors for DVT • Major surgery (eg, total joint arthroplasty) • History of DVT • Age ≥40 • Obesity • Prolonged immobility • Genetic predisposition to hematologic abnormalities • Trauma • Other: malignancy, coronary syndromes (eg, unstable angina) Anderson FA Jr, Wheeler HB. Clin Chest Med. 1995;16:236.

  15. Hip Fracture, Hip Arthroplasty, Knee Arthroplasty, and VTERisk (Upper Limits) in Patients without Anticoagulative Prophylaxis 100 Hip arthroplasty 90 84% 80 Knee arthroplasty 70 60% Hip fracture surgery 57% 60 % of patients*† 50 40 36% 36% 30 20% 20 12.9% 0.7% 10 0.4% 0 All DVT Proximal DVT Fatal PE * DVT prevalence statistics obtained by use of mandatory postoperative venography. † Represents the upper limit of prevalence statistics for each procedure. Geerts WH, et al. Chest. 2001;119(suppl):140S.

  16. Patients Not Receiving Anticoagulation Prophylaxis: Summary • Orthopedic surgery creates the ideal conditions for the development of DVT • Vascular damage • Venous stasis • Hypercoagulability • ≥50% of patients undergoing orthopedic surgery will develop DVT • Most frequently utilized agents all demonstrate superiority compared with placebo

  17. Current Strategies for DVT Prophylaxis • Mechanical prophylaxis • Pharmacologic anticoagulant therapy • Combination therapy • Regional anesthesia

  18. Current Strategies:Mechanical Prophylaxis • Intermittent pneumatic compression (IPC) • Pneumatic plantar compression (foot pump) • Literature supports use – Sarmiento JBJS 1999 • Ineffective when BMI > 25 kg/m2

  19. Current Strategies:Mechanical Prophylaxis (cont’d) • Advantages • Local antistasis effects • Systemic humeral effects • No increase in bleeding risk • Disadvantages • Patient intolerance • Compliance difficulties • Impractical post-hospital discharge application • Less effective when BMI >25

  20. Current Strategies:Anticoagulant Therapy and Indications • Oral agents • Warfarin (dose-adjusted to INR 2.0–3.0) • Prophylaxis of venous thrombosis and its extension, and pulmonary embolism • Aspirin • May be effective when combined with mechanical agents – Sarmiento JBJS 1999

  21. Current Strategies:Anticoagulant Therapy and Indications • Injectable/parenteral • Dose-adjusted unfractionated heparin (UFH) • Prophylaxis of venous thrombosis and its extension • Low-molecular-weight heparins (LMWH) • Dalteparin: total hip replacement • Enoxaparin: total hip replacement, total knee replacement

  22. Current Strategies:Oral Anticoagulant Therapy • Warfarin • Reduces DVT and symptomatic PE rate • Lieberman, et al. JBJS 1997 • In combination with mechanical agents, has a reduction in total DVT rate • Freedman, et al. JBJS 2000

  23. Current Strategies:Oral Anticoagulant Therapy • LMWHs • Fractionated Heparin 1/3 molecular weight of standard Heparin – inhibits Clotting Factor 10 • Binds less to plasma protein, increases bioavailability of the LMWHs

  24. Current Strategies:Oral Anticoagulant Therapy • LMWHs • Enoxaparin • Dosage - 30mg SC twice daily • Treatment begun within 24hrs after THA • Significant lowering DVT/PE rate comparable to Warfarin • Colwell, et al. JBJS 1994

  25. Current Strategies:Oral Anticoagulant Therapy • LMWHs • Enoxaparin • In TKA may be superior to Warfarin in reducing DVT rate. • Heit, et al. Thromb Haemost. 1997

  26. Current Strategies:Oral Anticoagulant Therapy • LMWHs • Dalteparin • Dosage – 2500 IU SC 4hrs post surgery followed by 5000 IU SC daily • Dalteparin proved effective in the reduction of total DVT and symptomatic PE when compared to Heparin • Hull, et al. Arch Intern Med. 2000

  27. ANTI-COAGULANT THERAPY LMWH’s • Organon-Highly selective inhibitor for factor X • FDA approved for Hip Fracture, THA, TKA

  28. Disadvantages LMWH SQ route Bleeding risks Must initiate at least 12 hrs post surgery Contraindicated in regional anesthesia - FDA Current Strategies:Parenteral Anticoagulant Therapy • Advantages • Rapid onset • No monitoring (LMWH) • Superior efficacy (LMWH) Hirsh J, Hoak J. Circulation. 1996;93:2212-2245.

  29. Current Strategies:Anticoagulant Therapy • Duration of Prophylactic Treatment • Clinical trials supports usage of prophylaxis • Period of hospitalization – 4-15 days • Post-hospitalization – (meta-analysis review) 19-28 days • Hull, et al. Ann Intern Med. 2001

  30. Current Strategies:Anticoagulant Therapy • Indications for Greenfield Filter Placement • Recurrent history of pulmonary emboli • Unable to use anticoagulant therapy in the presence of a DVT • Presence of pulmonary emboli despite anticoagulation therapy

  31. ACCP 2001 Recommendations: Based on 7 to 10 Days’ Treatment Hip Knee Hip Replacement Replacement Fracture Stockings Adjuvant – – Intermittent Adjuvant Yes Adjuvant pneumatic Grade 2C Grade 1B compression Aspirin – – – Adjusted-dose Yes unfractionated Grade 2A – – heparin Warfarin Yes Yes Yes INR 2-3 INR 2-3 INR 2-3 Grade 1A Grade 1A Grade 1B LMWH Yes Yes Yes Grade 1A Grade 1A Grade 1B Geerts WH, et al. Chest. 2001;119(suppl):157S.

  32. SUMMARY • Treatment of DVT is required following THA, TKA,and Hip Fracture • Aspirin has literature support clearly for THA • Warfarin and LMWH clearly show effectivenss for THA,TKA,and Hip Fracture • Post discharge usage should be for up to 35 days post op

  33. Summary • TJA places patients at risk for VTE • Thromboprophylaxis: the standard of care following TJA due to high rates of VTE without prophylaxis • Significant variation in prescribing practices • There are no data for efficacy of combined mechanical/pharmacologic treatments • Novel thromboprophylactic agents potentially may improve risk/benefit ratio

  34. THANK-YOU

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