Abstract
Abstract 1386
Poster Board I-408
Medical patients with chronic medical illnesses are often at risk of VTE both in-hospital and post-discharge. However, although injectable prophylaxis options are available and suitable for providing in-hospital and post-discharge prophylaxis, there is often a lack of continuity in VTE post-discharge prophylaxis. This analysis evaluated in-hospital and post-discharge VTE prophylaxis patterns for US medical patients.
Premier's Perspective™ inpatient data were cross-matched at the individual patient level with Ingenix LabRx® outpatient data from the I3 database (January 2005-December 2007) to assess VTE prophylaxis patterns in medical patients (cancer without surgery, heart failure, severe lung disease, infectious disease) at risk of VTE (according to the American College of Chest Physicians 2004 guidelines) and with no contraindications for anticoagulation. Inpatients were assessed for any anticoagulation received in-hospital and were followed post-discharge to assess their outpatient prophylaxis use. Drug utilization and clinical practice patterns during and within 30 days after hospitalization were collected and compared descriptively between groups.
Of the 9,675 medical discharges at risk of VTE and included in this analysis, 6,185 (63.9%) did not receive any anticoagulation at all. Of the remaining 3,490 (36.1%) discharges that did receive anticoagulation, 2,045 (58.6%) received enoxaparin and 1,044 (29.9%) received unfractionated heparin (UFH) (Table). After discharge, 98.2% of all patients did not receive any prophylaxis within the following 30 days. Only 174 (1.8%) discharges received outpatient prophylaxis, with 67.8% receiving warfarin alone and 18.4% receiving enoxaparin and warfarin (Table).
This analysis presents both inpatient and outpatient VTE prophylaxis patterns in real-world medical patients that are at risk of VTE. Nearly 64% of patients received no inpatient VTE prophylaxis, and less than 2% received outpatient prophylaxis. Further efforts to improve VTE prevention in hospitalized patients are required, with particular emphasis needed on the transition to outpatient prophylaxis.
Prophylaxis patterns . | Discharges (%) N=9,675 . | . |
---|---|---|
Anticoagulants during hospitalization | None | 6,185 (63.9) |
Any | 3,490 (36.1) | |
UFH only | 1,044 (29.9) | |
Enoxaparin only | 2,045 (58.6) | |
Other (fondaparinux, dalteparin, warfarin, combination) | 401 (11.5) | |
Anticoagulants within 30 days of discharge | None | 9,501 (98.2) |
Any | 174 (1.8) | |
Warfarin only | 118 (67.8) | |
Enoxaparin + warfarin | 32 (18.4) | |
Other (enoxaparin, fondaparinux, dalteparin ± warfarin or combination) | 24 (13.8) |
Prophylaxis patterns . | Discharges (%) N=9,675 . | . |
---|---|---|
Anticoagulants during hospitalization | None | 6,185 (63.9) |
Any | 3,490 (36.1) | |
UFH only | 1,044 (29.9) | |
Enoxaparin only | 2,045 (58.6) | |
Other (fondaparinux, dalteparin, warfarin, combination) | 401 (11.5) | |
Anticoagulants within 30 days of discharge | None | 9,501 (98.2) |
Any | 174 (1.8) | |
Warfarin only | 118 (67.8) | |
Enoxaparin + warfarin | 32 (18.4) | |
Other (enoxaparin, fondaparinux, dalteparin ± warfarin or combination) | 24 (13.8) |
Amin: sanofi-aventis: Research Funding, Speakers Bureau, The authors received editorial/writing support in the preparation of this abstract funded by sanofi-aventis U.S., Inc.. Lin: sanofi-aventis: Employment. Ryan: sanofi-aventis: Research Funding.
Author notes
Asterisk with author names denotes non-ASH members.