Jason M. Lappé, MS; Joseph B. Muhlestein, MD; Donald L. Lappé, MD; Rodney S. Badger, MD; Tami L. Bair, BS; Ruth Brockman, RN, MBA; Thomas K. French, MStat; Linda C. Hofmann, MS, BSN; Benjamin D. Horne, MStat, MPH; Susan Kralick-Goldberg, RN, MSN; Nan Nicponski, RN, MBA; Janette A. Orton, RN, MS; Robert R. Pearson, BS; Dale G. Renlund, MD; Holly Rimmasch, RN, MSN; Colleen Roberts, RN, MS; Jeffrey L. Anderson, MD
Acknowledgments: The authors thank Julie Burchell, RN, BSN; Michael Carnley; Dal C. Coleman, RPh; Kim Henrichsen, RN, MS, CCRN; Diane Marshall, MAM; Mikelle D. Moore, MBA, MHSA; Lynn R. Nimer, MD; Katey Roundy; Shane R. Stevenson, BS; Diane S. Wallace, RN, MSN, ANP-C; Sharon L. Watson, RHIT; Marie M. Wright, RN; Scott Yardley, RPh; Michelle LeBaron, RN; Susan E. Pollock, BS; Jeanette Wheeler, RN; and the administrative, cardiovascular nursing, and physician staff of Intermountain Health Care for valuable contributions and assistance.
Potential Financial Conflicts of Interest: None disclosed.
Requests for Single Reprints: Joseph B. Muhlestein, MD, LDS Hospital Cardiovascular Department, 8th Avenue and C Street, Salt Lake City, UT 84143.
Current Author Addresses: Mr. Lappé; Drs. Muhlestein, Lappé, Badger, Renlund, and Anderson; Ms. Bair; Ms. Brockman; Mr. French; Ms. Hofmann; Mr. Horne; Ms. Kralick-Goldberg; Ms. Nicponski; Ms. Orton; Mr. Pearson; Ms. Rimmasch; and Ms. Roberts: LDS Hospital Cardiovascular Department, 8th Avenue and C Street, Salt Lake City, UT 84143.
Despite recent advances in the treatment and prevention of cardiovascular disease, a treatment gap for secondary prevention medications still exists.
To develop and implement a program ensuring appropriate prescription of aspirin, statins, β-blockers, angiotensin-converting enzyme inhibitors, and warfarin at hospital discharge.
A nonrandomized before–after study comparing patients hospitalized before (1996–1998) and after (1999–2002) implementation of a discharge medication program (DMP). Patients were followed for up to 1 year.
The 10 largest hospitals in the Utah-based Intermountain Health Care system.
In the pre-DMP and DMP time periods, 26 000 and 31 465 patients, respectively, were admitted to cardiovascular services (n = 57 465).
Prescription of indicated medications at hospital discharge; postdischarge death or readmission.
By 1 year, the rate of prescription of each medication increased significantly to more than 90% (P < 0.001); this rate was sustained. At 1 year, unadjusted absolute event rates for readmission and death, respectively, were 210 per 1000 person-years and 96 per 1000 person-years before DMP implementation and 191 per 1000 person-years and 70 per 1000 person-years afterward. Relative risk for death and readmission at 30 days decreased after DMP implementation; hazard ratios (HRs) for death and readmission were 0.81 (95% CI, 0.73 to 0.89) and 0.92 (CI, 0.87 to 0.99) (P < 0.001 and P = 0.017, respectively). At 1 year, risk for death continued to decrease (hazard ratio, 0.79 [CI, 0.75 to 0.84]; P < 0.001) while risk for readmission stabilized (hazard ratio, 0.94 [CI, 0.90 to 0.98]; P = 0.002), probably because survivors had more opportunities to be readmitted.
The study design was observational and nonrandomized, and the authors could not control for potential confounders or determine the extent to which secular trends accounted for the observed improvements.
A relatively simple quality improvement program aimed at enhancing the prescription of appropriate discharge medications among cardiovascular patients is feasible and can be sustained within an integrated multihospital system. Such a program may be associated with improvements in cardiovascular readmission rates and mortality.
Lappé JM, Muhlestein JB, Lappé DL, et al. Improvements in 1-Year Cardiovascular Clinical Outcomes Associated with a Hospital-Based Discharge Medication Program. Ann Intern Med. 2004;141:446–453. doi: 10.7326/0003-4819-141-6-200409210-00010
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Published: Ann Intern Med. 2004;141(6):446-453.
Cardiology, Hospital Medicine.
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