Arch Phys Med Rehabil. 2018 Jan;99(1):107-115. doi: 10.1016/j.apmr.2017.07.012. Epub 2017 Aug 30.
Association Between Therapy Intensity and Discharge Outcomes in Aged Medicare Skilled Nursing Facilities Admissions.
Abstract
OBJECTIVES:
To determine the association between therapy intensity and discharge outcomes for aged Medicare skilled nursing facilities (SNFs) fee-for-service beneficiaries and to determine the association between therapy intensity and time to community discharge.
DESIGN:
Retrospective observational design.
SETTING:
SNFs.
PARTICIPANTS:
Aged Medicare fee-for-service beneficiaries (N=311,338) in 3605 SNFs.
INTERVENTIONS:
The total minutes of physical therapy, occupational therapy, and speech therapy per day were divided into intensity groups: high (≥60min); medium-high (45-<60min); medium-low (30-<45min); and low (<30min).
MAIN OUTCOME MEASURES:
Four discharge outcomes-community, hospitalization, permanent placement, and death-were examined using a multivariate competing hazards model. For those associated with community discharge, a Poisson multivariate model was used to determine whether length of stay differed by intensity.
RESULTS:
High intensity therapy was associated with more community discharges in comparison to the remaining intensity groups (hazard ratio, .84, .68, and .433 for medium-high, medium-low, and low intensity groups, respectively). More hospitalizations and deaths were found as therapy intensity decreased. Only high intensity therapy was associated with a 2-day shorter length of stay (incident rate ratio, .95).
CONCLUSIONS:
High intensity therapy was associated with desirable discharge outcomes and may shorten SNF length of stay. Despite growing reimbursements to SNFs for rehabilitation services, there may be desirable benefits to beneficiaries who receive high intensity therapy.
Copyright © 2017 American Congress of Rehabilitation Medicine. Published by Elsevier Inc. All rights reserved.
KEYWORDS:
Length of stay; Outcomes, research; Rehabilitation; Skilled nursing facility
- PMID:
- 28860096
- PMCID:
- PMC5748253
- DOI:
- 10.1016/j.apmr.2017.07.012
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