Prospective evaluation of a clinical guideline recommending hospital length of stay in upper gastrointestinal tract hemorrhage
J. A. Hay, L. Maldonado, S. R. Weingarten and A. G. Ellrodt
HealthCare Partners Medical Group, Pasadena, CA 91105, USA.
CONTEXT: Upper gastrointestinal tract hemorrhage (UGIH) is a common and
potentially life-threatening disorder. Resource utilization can vary
without adverse effect on patient outcome. Clinical practice guidelines are
a potential solution to reduce variation in practice while improving
patient outcomes. OBJECTIVE: To validate prospectively the safety,
acceptability, and impact of a clinical practice guideline defining the
medically appropriate length of stay (LOS) for patients hospitalized with
UGIH. DESIGN: Prospective, controlled time-series study with an
alternate-month design. Outcome surveyors and patients were blinded to
study group allocation. GUIDELINE: A retrospectively validated scoring
system using 4 independent variables: hemodynamics, time from bleeding,
comorbidity, and esophagogastroduodenoscopy (EGD) findings to predict risk
of adverse events. The quantitative risk for the low-risk subset was 0.6%
(95% confidence interval [CI], 0.0%-2.0%) for subsequent complications and
0% (95% CI, 0.0%-0.9%) for life-threatening complications from this
retrospective evaluation. SETTING: A 1000-bed, not-for-profit,
university-affiliated teaching hospital. PATIENTS: Consecutive adult
patients hospitalized for acute UGIH. INTERVENTION: Concurrent feedback of
guideline recommendation (same-day hospital discharge) to physicians caring
for patients at low risk for complication. No risk information was provided
during control months. RESULTS: Seventy percent (209/299) of UGIH patients
achieved low-risk status according to the guideline and were therefore
potentially suitable for early discharge from the hospital. Providing
real-time quantitative risk information (intervention group only) was
associated with an increase in guideline compliance from 30% to 70%
(P<.001) and a decrease in mean (SD) LOS from 4.6 (3.5) days to 2.9
(1.3) days (mean reduction of 1.7 days per patient; P<.001). No
differences in complications, patient health status, or patient
satisfaction were found when measured 1 month after discharge. An
independent variable predicting decreased hospital LOS for low-risk UGIH
patients was early EGD. CONCLUSIONS: Implementation of the clinical
practice guideline safely reduced hospital LOS for selected low-risk
patients with acute UGIH. Further prospective validation in other settings
is warranted.
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