DVT Prophylaxis in Orthopedic Patients

DVT Prophylaxis in Orthopedic Patients

Rogers Kyle11/27/12

Key Messages• The new ACCP guidelines for prevention of VTE in orthopedic

surgery patients were published in 2012 and contain many new options

• ASA is now included as one of the acceptable pharmacologic agents for initial prophylaxis (1B) as are SCD’s (1C)

• LMWH is still the preferred alternative (2C/2B)• SCD’s should be used in combination with all pharmacologic

therapies (2C)• Prophylaxis should be extended to 35 days (2B)• With increased bleeding risk used SCD’s or no prophylaxis (2C)• If patient refuses injection use apixaban or dabigatran

Key Messages

Key Messages

Key Messages

ACCP 9 (2012)

• Symptomatic DVT/PE vs. increased major bleeding– “the trade-off”– Patient Values and Preferences

Historical Points

• Trials before 2000 used asymptomatic DVT on screening as primary end point.

• No general agreement on “bleeding”– ‘major and minor’ in older studies– ‘clinically relevant non-major’ in recent studies –

NOT included in current update

Major Bleeding

• Definitions– any fatal bleeding– bleeding into a critical organ (eg, retroperitoneal,

intracranial, intraocular, or intraspinal)– clinically overt (eg, GI) bleeding associated with a

2 g/dL drop in hemoglobin level or requiring 2 units of blood transfused

– bleeding leading to reoperation

Bleeding Risk

Baseline Risk of DVT/PE

• Changes over time– LOS for HFS in 60’s – 35 days. Now 3.2 days.– Pre-1980 – 15 to 30% without prophylaxis– Many changes in the interim• Surgical technique• Early ambulation• Earlier discharge

– Post prophylaxis dropped to 1-2% by 2001

Baseline Risk of DVT/PE

• A Randomized Controlled Trial of a Low-Molecular-Weight Heparin (Enoxaparin) to Prevent Deep-Vein Thrombosis in Patients Undergoing Elective Hip Surgery (NEJM 1986)– LMWH vs. placebo– 100 pts., elective THA– Venography (impedance pleth/fibrinogen) in 76– 10.8% in LMWH vs. 51.3% in placebo– asymptomatic

Baseline Risk of DVT/PE

• Since 2003 rate of symptomatic DVT/PE on LMWH prophylaxis is 1.15% (0.8% DVT, 0.35% for PE)

• Symptomatic VTE rate off prophylaxis – 1.8% DVT, 1% PE.

• Assume that the risk reduction for DVT and PE on LMWH for symptomatic and asymptomatic– 50-60% DVT, 2/3’s PE

• Cumulative – 7, 14, 35 days– Includes TKA, THA, HFS

Baseline Risk of DVT/PE

Baseline Risk of DVT/PE

Baseline Risk of Bleeding

• ‘difficult to estimate’– Better op techniques

• Mostly from placebo (or GCS) arm of LMWH trials and the PEP trial

PEP Trial

• Prevention of pulmonary embolism and deep vein thrombosis with low dose aspirin: Pulmonary Embolism Prevention (PEP) trial (Lancet 2000)– Not in US– 17,000+ pts – THA or HFS

• 160 mg ASA + “any other thromboprophylaxis thought necessary vs. placebo– reductions in pulmonary embolism of 43% (95% CI 18–60;

p=0·002) and in symptomatic deep-vein thrombosis of 29% (3–48; p=0·03) - including patients receiving subcutaneous heparin

Baseline Risk of Bleeding

• ‘difficult to estimate’– Better op techniques

• Mostly from placebo (or GCS) arm of LMWH trials and the PEP trial

• Median rate – 1.5%• Can we estimate the bleeding risk pre-op?

Baseline Risk of Bleeding

• ‘difficult to estimate’– Better op techniques

• Mostly from placebo (or GCS) arm of LMWH trials and the PEP trial

• Median rate – 1.5%• Can we estimate the bleeding risk pre-op?– “did not find any bleeding risk assessments that

have been sufficiently validated in the orthopedic surgery population”

Recommendations

• THA, TKA, HFS– 10-14 days

• Low molecular weight heparin (LMWH) • Fondaparinux• Apixaban• Dabigatran• Rivaroxaban• Low dose heparin (LDUH)• Adjusted dose coumadin• ASA (“One panel member believed strongly that aspirin alone

should not be included as an option”)• Intermittent pneumatic compression devices (IPCD)

Lovenox

• THA– 30 mg SQ Q12H starting 12-24 hrs post-op OR– 40 mg SQ QD starting 12 ± 3 hrs post-op– 7-14 days; up to 35 days (40 mg QD)

• TKA– 30 mg SQ BID– 7-14 days

Lovenox

• Benefit• 13 fewer VTE/1000 with 7-14 days• No increased major bleeding• Symptomatic DVT reduced by ½ with extended

treatment (9 fewer VTE/1000)• No mortality benefit

Fondaparinux

• Fondaparinux vs. enoxaparin; THA (Lancet 2002)– 10 days 2.5 mg fondaparinux vs. 30 mg BID

enoxaparin– Non-inferior

• Fondaparinux 6-8 days followed by placebo vs. fondaparinux for total 19-23 days; HFS (Arch Int Med 2003)– 12 fewer VTE/1000– 12 more major bleeds/1000

Coumadin

• Few trials (8 RCT’s/700 pts); few events– 55% reduction DVT; 80% reduction PE

• INR 2-3• Begin post-op day of surgery– 18 fewer VTE/1000– 7 more major bleeds/1000

Low Dose Unfractionated Heparin

• 5,000 Units SQ BID vs. TID– Chest 2011 – no difference in medical pts (vs.

Chest 2007)– AHRQ Guidelines – “Not recommended”• 13 fewer VTE/1000• 4 more major bleeds/1000

ASA

• Pulmonary Embolism Prevention (PEP) trial– 160 mg, 35 days– HFS (13,000+ pts), THA (4,000+ pts)• 7 fewer VTE/1000• 3 more major bleeds/1000• 2 more non-fatal MI’s

Intermittent Pneumatic Compression Devices (IPCD)

• Not GCS (CLOTS trial Lancet 2009)• Number of IPCD studies , one venous foot

pump study (TKA; 60 pts, less extensive clot; 1992)– 16 fewer VTE/1000– Compliance is problematic; newer battery

powered might be better

Apixaban

• Approved in Europe, Canada• ADVANCE 1, 2, and 3 trials– ADVANCE 1 (NEJM 2009)• TKA• 2.5 mg BID apixaban vs. 30 mg BID enoxaparin x 10-14 days• Symptomatic and asymptomatic DVT, PE, death – ‘Total

venous thromboembolism and all-cause mortality’• No difference but did not meet prespecified criteria for

non-inferiority; less ‘clinically relevant’ bleeding but not major

Apixaban

– ADVANCE 2 (Lancet 2010)• TKA• 2.5 mg BID apixaban vs. 40 mg QD enoxaparin x 10-14

days• Also a non-inferiority trial but demonstrated superiority

in preventing DVT (mostly asymptomatic); not PE, mortality• Same bleeding• ?? difference in enoxaparin (30 mg BID vs. 40 md QD)

Apixaban

– ADVANCE 3 (NEJM 2010)• THA• Apixaban 2.5 mg BID vs. enoxaparin 40 mg QD x 35 days• Also a non-inferiority trial but demonstrated superiority

in preventing DVT (mostly asymptomatic); not PE, mortality• Same bleeding

Dabigatran

• In Europe and Canada• RENOVATE (Lancet 2007)– THA– Dabigatran 220 mg or 150 mg QD vs. enoxaparin

40 mg QD– 30 days– ‘Total venous thromboembolism and all-cause

mortality’– Non-inferior

Dabigatran

• RE-NOVATE II (Thrombosis Haemostasis 2010)– THA– Dabigatran 220 mg QD vs. enoxaparin 40 mg QD– 28-35 days– Primary endpoint - DVT (sym and asym)/PE, mortality –

‘Total venous thromboembolism and all-cause mortality’– Non-inferiority

• Non-inferior for primary endpoint (mostly asym)• Superior for major VTE/VTE related death but only because of

asym proximal DVT

Rivaroxaban

• FDA approved for DVT prophylaxis in THA, TKA• RECORD 1 (NEJM 2008), and 2 (THA); 3 and 4 (TKA)– 10 mg rivaroxaban QD vs 40 mg enoxaparin QD –

extended prophylaxis - 35 days– THA– Primary endpoint - any DVT, nonfatal pulmonary

embolism, or death from any cause.– Non-inferiority/superiority– Rivaroxaban superior efficacy; similar bleeding risk

Rivaroxaban

Rivaroxaban

LMWH vs. LDUH

• ACCP9 – – 20% relative risk reduction of primarily

asymptomatic DVT in favor of LMWH (RR, 0.80; 95% CI, 0.73-0.88), with similar effects seen in the subgroups of THA, TKA, and HFS

– LMWH may reduce symptomatic VTE from 16 per 1,000 with LDUH to 13 per 1,000 without an increase in major bleeding

– Q8H vs Q12H LDUH?

LMWH vs. Coumadin – initial vs. extended prophylaxis

• ACCP9– Initial - LMWH → less asymptomatic DVT, no diff

PE; increased bleeding (initial prophylaxis)– Extended – Coumadin → less PE, same DVT, more

more bleeds

LMWH vs. ASA - initial vs. extended prophylaxis

• ACCP 9– 2 small trials (one is an abstract). One trial was

SCD’s + LMWH vs. SCD’s + ASA– Initial and extended – ASA more asymptomatic

DVT, few PE’s, no bleeding difference• ‘evidence from a head-to head comparison of LMWH

compared with aspirin is sparse and of low quality’

LMWH vs. Fondaparinux - initial vs. extended prophylaxis

• ACCP 9– pooled results failed to demonstrate or exclude a

beneficial or detrimental effect of fondaparinux on symptomatic DVT and PE despite a substantial reduction in asymptomatic DVT

– may increase major bleeding events by nine per 1,000 (fondaparinux)

LMWH vs. Rivaroxaban - initial vs. extended prophylaxis

• ACCP 9– Rivaroxaban reduced symptomatic DVT by > 50%– There may be more bleeds– Therefore – LMWH more appealing than

rivaroxaban for initial prophylaxis; extended unknown

LMWH vs. Dabigatran - initial vs. extended prophylaxis

• ACCP 9– Dabigatran similar to enoxaparin (note – many of

the studies used a 150 mg dose of dabigatran)

LMWH vs Apixaban - initial vs. extended prophylaxis

• ACCP 9– Apixaban reduced symptomatic DVT 60% vs.

LMWH (very small numbers)– No major differences in bleeding– Still favor LMWH (longer experience)

IPCD + ASA vs LMWH

• ACCP 9• There are 2 articles that are interesting and make the

choice of prophylaxis in THA/TKA difficult• These articles are both reviewed in ACCP 9. They are

considered ‘low-quality evidence’ with ‘significant methodologic limitations’• However, these studies either demonstrated a similar

or reduced rate of DVT/PE along with a reduced risk of bleeding (remember definition of bleeding)

IPCD + ASA vs LMWH• Deep Vein Thrombosis Prevention in Joint Arthroplasties

(Journal of Arthroplasty 2006)– 136 patients (no fractures)– SCD’s (mobile) + 100 mg ASA vs. enoxaparin 40 mg– Venograms 5-8 days and clinical evaluation at 30 days– Primary – DVT; secondary – bleeding– Results

• DVT 28.3% LMWH, 6.6% SCD’s/ASA; more prox DVT and contralateral DVT in LMWH

• Very few bleeds in either group (no difference)• Cost - $2600+/pt less with SCD/ASA

– Total savings/1000 pts - $2,628,557

IPCD + ASA vs LMWH

• Thrombosis Prevention After Total Hip Arthroplasty (J Bone Joint Surg 2010)– 400+ pts– SCD’s (mobile) +/- ASA 81 mg vs enoxaparin 30 mg BID

→ 40 mg QD at discharge– U/S– Primary – bleeding; secondary – DVT/PE– Results

• Less bleeding (esp major) 0% vs 6%• No difference in DVT/PE

Summary

• TKA, THA, HFS– LMWH, fondaparinux, apixaban, dabigatran,

rivaroxaban, LDUH, adjusted-dose VKA, aspirin or an IPCD - all are recommended vs no prophylaxis

– LMWH recommended over all alternatives– LMWH 12 hr before or after surgery (not 4 hrs post

op)– Extended duration up to 35 days recommended– Dual prophylaxis recommended – IPCD +

‘antithrombotic agent’

Summary

• If not LMWH (HIT)– Apixaban, dabigatran, rivaroxaban, VKA,

fondaparinux, IPCD, IPCD + ASA• More bleeding with fondaparinux, rivaroxaban, VKA• Compliance – mechanicals, VKA, injection as outpt• Apixaban 2.5 mg BID, Dabigatran 220 mg QD

Summary

• Increased bleeding risk– TKA, THA, HFS – IPCD or no prophylaxis– Remember that ACCP 9 defines bleeding risk as

“major”. Surgeons do not.

Summary

• Increased bleeding risk– TKA, THA, HFS – IPCD or no prophylaxis– If the risk factor is an antiplatelet agent consider

pharmacologic prophylaxis– Don’t use IVC filter as primary prevention– Don’t use IVC filter even if increased bleeding

risk/contraindication to pharmacologic and mechanical prophylaxis