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Randomized Controlled Trial
. 2010 Jan;14(1):57-61.
doi: 10.1007/s12603-010-0010-4.

Identifying and preventing adverse drug events in elderly hospitalised patients: a randomised trial of a program to reduce adverse drug effects

C Trivalle  1 , T Cartier, C Verny, A-M Mathieu, P Davrinche, H Agostini, L Becquemont, P Demolis; IMEPAG GROUP
Collaborators, Affiliations
Randomized Controlled Trial

Identifying and preventing adverse drug events in elderly hospitalised patients: a randomised trial of a program to reduce adverse drug effects

C Trivalle et al. J Nutr Health Aging. 2010 Jan.

Abstract

Objectives: Evaluate the impact of educational intervention in decreasing ADEs in elderly patients in a hospital setting.

Design: Randomised prospective study.

Setting: The study was performed in France in the Paris area, in 16 rehabilitation geriatric centres of APHP (Assistance Publique - Hôpitaux de Paris). Patient capacity per centre varied from 15 to 57 with a total of 526.

Participants: All the patients > or = 65 years hospitalized during the 4 week study period were included.

Measurements: During a first 2 week phase without intervention ADE's were recorded in all centres. Then units were then randomised for an educational intervention or not. The educational phase lasted 1 week, without ADE tracking. Then, both types of units (I+ and I-) recorded ADEs for 2 weeks. Possible drug-related incidents were detected using a standardized check list (nurses) and a weekly review of all charts by investigators. Possible drug-related incidents were analysed by a group of reviewers selected from the authors to classify them as ADE or not.

Results: 576 patients (mean age: 83.6 +/- 7.9 years) were consecutively included. The mean number of drugs at inclusion was 9.4 +/- 4.24 drugs per patient. 223 out of 755 events were considered "probable" ADEs (29.5%). Among the 223 ADEs, 62 (28%) could have been prevented. The main outcome of this trial was the change in the proportion of ADEs in elderly patients in the intervention-units, compared to the control group. The main errors were: to high a dose (26%), double therapy (21%), under dose (13%), inappropriate drug (13%), drug-drug interaction (6%), previous same adverse drug reaction (3%) and miscellaneous (11.18%). After a specific educational intervention program, there were fewer ADEs in the intervention group (n = 38, 22%) than in the control group (n = 63, 36%; p = 0.004).

Conclusion: Educational programs could help reduce the prevalence of ADEs by 14% and encourage physicians to change outdated prescription habits.

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Figures

Figure 1
Figure 1
The protocol
See this image and copyright information in PMC

References

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Uncited references

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