journal club general surgery rotation
DESCRIPTION
Regulation of Coagulation in Orthopedic Surgery to Prevent Deep Venous Thrombosis and Pulmonary Embolism 1 (RECORD 1 ). Journal Club General Surgery Rotation. Background. Prophylactic anticoagulation: standard practice after total hip arthroplasty (THA) Minimum recommended duration = 10 days - PowerPoint PPT PresentationTRANSCRIPT
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Regulation of Coagulation in Orthopedic Surgery to Prevent Deep Venous Thrombosis and Pulmonary Embolism 1 (RECORD 1 )
Journal ClubGeneral Surgery Rotation
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Background
Prophylactic anticoagulation: standard practice after total hip arthroplasty (THA)
Minimum recommended duration = 10 days
Extended prophylaxis x 5 wks (↓ symptomatic & asymptomatic VTE) > short-term prophylaxis
DVT incidence without primary thromboprophylaxis: ~50% of patients undergoing THR
If DVT present, fatal PE incidence: 0.1-2.0%
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Background
Rivaroxaban(R): Oral direct inhibitor of factor Xa
F=80%
Peak: 2.5-4 hours
Dose finding studies: 10 mg OD suitable for phase 3 trials
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Inclusion Criteria
> 18 years
Scheduled to undergo elective total hip arthroplasty
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Exclusion Criteria
Scheduled to undergo staged, bilateral hip arthroplasty
Pregnant or breastfeeding
Active bleeding
At high risk of bleeding
CI for prophylaxis with enoxaparin or a condition that might require an adjusted dose of enoxaparin
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Exclusion Criteria
Conditions preventing bilateral venography
Substantial liver disease
Severe renal impairment (CrCl < 30 ml/min)
Concomitant use of protease inhibitors
Planned intermittent pneumatic compression
Requirement for anticoagulation that could not be stopped
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Baseline Characteristics
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Baseline Characteristics
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Study Design
Randomized, multinational, double-blind
R started 6-8 hrs after wound closure
Enoxaparin (E) 12 hrs before surgery, restarted 6-8 hrs after wound closure
Mandatory bilateral venography the day after the last dose of the study drug (day 36)
Follow-up visit 30-35 days after the last dose of the study drug
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Study Design Sample calculation based on:
Assumed rate of 8% for 1° efficacy outcome
Noninferiority threshold of 3.5%
1562 patients/ group sufficient to show noninferiority with a power of 95% and type 1 error = 2.5%
Per-protocol population of R for 1° efficacy outcomeR = 1537, E = 1492
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Outcome Measures
1° Efficacy Outcome: Composite of any DVT, non-fatal PE or death from any cause up at 36 days
2 ° Efficacy Outcome: Major VTE Composite of proximal DVT, nonfatal PE or
death from VTE
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Safety Outcome Measures
Major bleeding after first dose & up to 2 days after the last dose
Major bleeding
Fatal bleeding, occurred in a critical organ (e.g. retroperitoneal, intracranial, intraocular, intraspinal)
Required reoperation
Clinically overt extrasurgical-site bleeding & associated with a fall in Hgb of at least 2 g/dL or requiring blood transfusion of >2 units of PRBC or whole blood
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Hypothesis
Null hypothesis: R inferior to E in per-protocol population
If non-inferiority: Superiority analysis (mITT) Absolute margin = 3.5% for 1° efficacy outcome 1.5% for major VTE
mITT= Planned surgery done, study drug taken, adequate assessment for thromboembolism
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Results: Per-protocol Population
Outcome Rivaroxaban Enoxaparin ARR
1 efficacy outcome
13/15370.8%
50/14923.4%
2.5% (1.5-3.6)
Major VTE 2/1622 0.1%
29/16041.8%
1.7%(1.0-2.4)
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Results: Incidence of efficacy events (Modified ITT)
Outcome Rivaroxaban Enoxaparin ARR P Value
1 efficacy outcome
18/15951.1%(0.7-1.8)
58/15583.7(2.8-4.8)
-2.6 (-3.7 to -1.5)
<0.001
Major VTE 4/1686 0.2%(0.1-0.6)
33/1678 2.0(1.4-2.8)
-1.7(-2.5 to -1.0)
<0.001
Death during on-tx
4/1595 0.3%(0.1-0.6)
4/1558 0.3(0.1-0.7)
0.0 (-0.4 to 0.4) 1.00
Nonfatal PE 4/1595 0.3%(0.1-0.6)
1/1558 0.1(<0.1 to 0.4)
0.2(-0.1 to 06.) 0.37
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Results: Symptomatic VTE Incidence
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Results: Safety Outcome
Event Rivaroxaban (N=2209)
Enoxaparin (N=2224)
P Value
Any on-treatment bleeding
133 (6.0) 131 (5.9) 0.94
Major bleeding 6 (0.3) 2(0.1) 0.18
Non-major bleeding 128 (5.8) 129(5.8)
Study withdrawal due to adverse effect
85 (3.8) 100 (4.5)
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Results: Safety
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Investigators’ Conclusion
Rivaroxaban 10 mg OD > for extended thromboprophylaxis than SC Enoxaparin 40 mg OD
Similar number of adverse events
Similar safety profiles
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CASP RCT Checklist
Did the study ask a clearly focused question? Yes
Was this a randomized controlled trial (RCT) and was it appropriately so? Yes
Were participants appropriately allocated to intervention and control groups? Yes
Were participants, staff and study personnel ‘blind’ to participants’ study group? Yes
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CASP RCT Checklist
Were all of the participants who entered the trial accounted for at its conclusion? Yes
Were the participants in all groups followed up and data collected in the same way? Yes
Did the study have enough participants to minimize the play of chance? Yes
How are the results presented and what is the main result? Extended thromboprophylaxis with R: very low incidence of thrombosis vs. E with a safety profile similar to that of E
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CASP RCT Checklist
How precise are these results? Definitions of bleed are different amongst
different trials 8% outcome expected; found: 3.7% and
1.1%
Were all important outcomes considered so the results can be applied? Yes except surgical site bleeding not considered as major bleeding
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Limitations
No details regarding allocation concealment
Generalizability of results limited, low # of patients with a previous hx of VTE >than 75 y at extremities of weight
Planned THR patients included but not fracture or trauma patients
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Limitations
Patients with severe renal, hepatic failure or at high risk of bleeding excluded
Clinically important outcomes not assessed: Post-DVT complications (post thrombotic
syndrome) length of hospital stay health related QoL surgical outcomes (infection, wound healing,
drainage, range of motion, chronic pain)
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Limitations Surgical site bleeding excluded from major bleeding
events
Clinical importance of asymptomatic DVTs as a surrogate measure of symptomatic events not fully elucidated
Low incidence of symptomatic VTE, death & major bleeding events: interpret with caution Not powered to investigate differences for these
low-frequency events
Timing of dose
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Implications to Practice
Rivaroxaban approved and in use
No antidote for rivaroxaban
More safety data required
Needs to be tested in other populations (e.g. fracture, trauma patients)
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Terminology mITT: any dvt, non-fatal PE, or all cause mortality
patients who were considered valid for mITT analysis if they had undergone the appropriate surgery, had taken the study drug, and had an adequate assessment for thromboembolism
mITT (major VTE): patients valid for mITT analysis for major VTE if they had undergone the appropriate surgery, had taken the study drug, and had an adequate assessment for thromboembolism in proximal veins
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Terminology
Per-protocol population: Patients who were valid for mITT analysis and had an adequate assessment of thromboembolism with no major protocol deviations
Safety population: took at least 1 dose of study drug
Symptomatic VTE: safety population of patients who underwent surgery (independent of obtaining evaluable venograms).