Recognising clinical instability in hospital patients before cardiac arrest or unplanned admission to intensive care - A pilot study in a tertiary-care hospital

Citation
Md. Buist et al., Recognising clinical instability in hospital patients before cardiac arrest or unplanned admission to intensive care - A pilot study in a tertiary-care hospital, MED J AUST, 171(1), 1999, pp. 22-25
Citations number
12
Categorie Soggetti
General & Internal Medicine","Medical Research General Topics
Journal title
MEDICAL JOURNAL OF AUSTRALIA
ISSN journal
0025729X → ACNP
Volume
171
Issue
1
Year of publication
1999
Pages
22 - 25
Database
ISI
SICI code
0025-729X(19990705)171:1<22:RCIIHP>2.0.ZU;2-H
Abstract
Objective: To investigate the nature and duration of clinical instability t ie, abnormalities in simple physical observations or laboratory test result s) in hospital patients before a "critical event" (ie, a cardiac arrest or an unplanned admission to intensive care). Design: Retrospective survey of medical records of all patients having crit ical events (CEs) over 12 months. Data on hospital and Intensive Care Unit (ICU) patients were obtained for comparison with the study population. Setting: A 300-bed metropolitan teaching hospital with a seven-bed ICU. Patients: All patients having CEs over a 12-month period (January to Decemb er 1997). Main outcome measures: Number of patients with clinical instability before a CE; duration of clinical instability before a CE; number of medical revie ws of each patient before a CE; mortality rate and length of hospital stay for all patients. Results: There were 122 CEs in 112 patients (median, 1; range, 1-4). Of the CEs, 79 were unplanned ICU admissions (14 subsequent to cardiac arrest cal ls), and 43 were cardiac arrest calls not resulting in ICU admission. Each CE was preceded by a median of two (range, 0-9) criteria for clinical insta bility. The median duration of instability before a CE was 6.5 hours (range , 0-432 hours), and in that time a median of two (range, 0-13) medical revi ews took place. The incidence of CEs in the total hospital population (122 CEs/19 853 admissions) and in ICU patients (79 unplanned admissions/515 adm issions) was 0.6% and 15%, respectively. There were 70 deaths (62%) among t he 112 patients, compared with a total of 392 deaths (2% of admissions) in the hospital, of which 107 were in ICU. Conclusions: Very few patients suffer a CE while in hospital. However, thos e who do frequently manifest abnormalities in simple physical observations and laboratory test results before the CE. More rapid intervention in respo nse to warning signs might provide a better outcome for these patients.