TY - JOUR
T1 - Detection of adverse events in a Scottish hospital using a consensus-based methodology
AU - Williams, D. J.
AU - Olsen, S.
AU - Crichton, W.
AU - Witte, K.
AU - Flin, R.
AU - Ingram, J.
AU - Campbell, M. K.
AU - Watson, M.
AU - Hopf, Y.
AU - Cuthbertson, B. H.
PY - 2008/12
Y1 - 2008/12
N2 - Objective: To determine, using a consensus based methodology, the rate and nature of adverse events (AEs) among patients admitted to acute medicine, acute surgery and obstetrics in a large teaching hospital in Scotland. Methods: Retrospective case-note review of 450 medical, nursing and medication records to identify and classify adverse events. Results: For 354 patients whose length of stay was greater than 24 hours, the overall adverse event rate was 7.9% which ranged from 0% in obstetrics, 7.2% in acute medicine to 13% in acute surgery. Among all AEs, 43% were deemed preventable by a consensus group and 59% of the AEs contributed to a proportion of the patients' hospital stay or led to hospital readmission. Whilst nurse identification of adverse events was highly specific (94%), its sensitivity was poor (43%). Only 10% of the identified AEs were identified by the hospital's voluntary reporting system for adverse events. The estimated additional cost of adverse events in terms of bed days was £69,189 which if extrapolated Scotland-wide could cost £297 million per annum. Conclusions: This study supports the need to continue the traditional retrospective record review to identify adverse events. The current hospital-based reporting of adverse events does not provide a complete measure of adverse events and needs to be complemented by other measures.
AB - Objective: To determine, using a consensus based methodology, the rate and nature of adverse events (AEs) among patients admitted to acute medicine, acute surgery and obstetrics in a large teaching hospital in Scotland. Methods: Retrospective case-note review of 450 medical, nursing and medication records to identify and classify adverse events. Results: For 354 patients whose length of stay was greater than 24 hours, the overall adverse event rate was 7.9% which ranged from 0% in obstetrics, 7.2% in acute medicine to 13% in acute surgery. Among all AEs, 43% were deemed preventable by a consensus group and 59% of the AEs contributed to a proportion of the patients' hospital stay or led to hospital readmission. Whilst nurse identification of adverse events was highly specific (94%), its sensitivity was poor (43%). Only 10% of the identified AEs were identified by the hospital's voluntary reporting system for adverse events. The estimated additional cost of adverse events in terms of bed days was £69,189 which if extrapolated Scotland-wide could cost £297 million per annum. Conclusions: This study supports the need to continue the traditional retrospective record review to identify adverse events. The current hospital-based reporting of adverse events does not provide a complete measure of adverse events and needs to be complemented by other measures.
UR - http://www.scopus.com/inward/record.url?scp=58849135786&partnerID=8YFLogxK
UR - http://dx.doi.org/10.1258/rsmsmj.53.4.26
U2 - 10.1258/rsmsmj.53.4.26
DO - 10.1258/rsmsmj.53.4.26
M3 - Article
C2 - 19051661
AN - SCOPUS:58849135786
SN - 0036-9330
VL - 53
SP - 26
EP - 30
JO - Scottish Medical Journal
JF - Scottish Medical Journal
IS - 4
ER -