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P OSTER<br />

A BSTRACTS<br />

Aggressive treatment of many cancers includes surgical interventions,<br />

with accompanying risks of morbidity and mortality. There is<br />

substantial heterogeneity in older adults’ functional reserve and ability<br />

to tolerate and recover from major physiological stressors. Geriatric<br />

assessment has developed in the gerontology literature as an important<br />

prognostic tool to risk-stratify community-dwelling older<br />

adults. These principles have been explored with the goal of identifying<br />

patient-level risk factors for adverse surgical outcomes. In this review,<br />

we examined the utility of components of a Comprehensive<br />

Geriatric Assessment (CGA) as predictors of adverse outcomes<br />

among older patients undergoing major surgery.<br />

Methods: Medline, EMBASE, and the Cochrane Library were<br />

searched for prospective studies examining components of CGA<br />

among geriatric patients undergoing elective surgery. Outcome parameters<br />

included 30 day postoperative complications and mortality,<br />

and discharge to a non-home care institution. Within and across the<br />

studies, we evaluated which CGA components were associated with<br />

the outcome(s) of interest.<br />

Results: The initial search identified 125 potentially relevant articles,<br />

of which ten articles based on seven studies met criteria for<br />

evaluation. Across the studies, chronological age was consistently<br />

found not to be an independent predictor of poor outcomes. Dependencies<br />

in ADLs and cognitive impairment were associated with increased<br />

incidence of complications and mortality. Impairment in<br />

IADLs was also associated with discharge to non-home care institutions<br />

in two studies.<br />

Conclusions: Across a diversity of surgical settings and patient<br />

populations, the results of these studies support an association between<br />

poor functional status and adverse geriatric surgical outcomes.<br />

These consistent results argue for inclusion of focused geriatric assessment<br />

as part of routine presurgical care in older adults. In addition,<br />

the development of targeted interventions for vulnerable individuals<br />

so identified may provide innovative means of mitigating the<br />

risk of major surgical interventions for this increasing proportion of<br />

the population.<br />

D164 Encore Presentation<br />

A Pooled Analysis of Surgical Complications: Results from the<br />

RECORD Program.<br />

M. R. Lassen, 1 M. Gent, 2 A. K. Kakkar, 3,4 B. I. Eriksson, 5<br />

S. D. Berkowitz, 6 A. Turpie. 2 1. Glostrup Hospital, Glostrup,<br />

Denmark; 2. McMaster University, Hamilton, ON, Canada; 3.<br />

Thrombosis Research Institute, London, United Kingdom; 4.<br />

University College London, London, United Kingdom; 5. Sahlgrenska<br />

University Hospital, Mölndal, Sweden; 6. Bayer HealthCare<br />

Pharmaceuticals, Montville, NJ.<br />

Supported By: This research was funded by Bayer HealthCare<br />

Pharmaceuticals Inc. and Janssen Research and Development, LLC.<br />

Background: Surgical complications after total hip or total knee<br />

arthroplasty (THA or TKA) are a primary concern for surgeons and<br />

can increase the cost and length of hospitalization, re-admission rates,<br />

and incur additional surgeries. Such complications include a wide<br />

range of conditions including bleeding, infection, and hemarthrosis.<br />

The phase III RECORD program investigated the oral, direct Factor<br />

Xa inhibitor rivaroxaban for the prevention of venous thromboembolism<br />

after THA (RECORD1, 2) or TKA (RECORD3, 4). The<br />

focus of this analysis from the pooled data from the four RECORD<br />

studies was to investigate whether rivaroxaban regimens are similar<br />

to enoxaparin regimens in the incidence of surgical complications<br />

after THA and TKA.<br />

Methods: Patients (N=12,729) were randomized to receive rivaroxaban<br />

10 mg once daily for 35±4 days or enoxaparin 40 mg once<br />

daily for 35±4 days (RECORD1) or 12±2 days followed by placebo<br />

(RECORD2). In RECORD3 and 4 patients received prophylaxis for<br />

12±2 days with rivaroxaban 10 mg once daily or enoxaparin 40 mg<br />

once daily (RECORD3) or enoxaparin 30 mg twice daily<br />

(RECORD4). Surgical safety outcomes were analyzed in the safety<br />

population over the total treatment duration pool.<br />

Results: The incidence of serious adverse events related to surgery,<br />

such as post-procedural infection, operative hemorrhage, wound<br />

dehiscence, postoperative wound infection, incision site hemorrhage,<br />

and hemarthrosis, was similar in the rivaroxaban (30/6,183: 0.49%)<br />

and enoxaparin (35/6,200: 0.56%) groups.<br />

Conclusions: These data suggest that surgical safety outcomes<br />

are unlikely to differ between rivaroxaban and enoxaparin<br />

regimens.<br />

S242<br />

AGS 2012 ANNUAL MEETING

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