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Pierre Pouyanne a Centre de Pharmacovigilance, Département de
Pharmacologie, Université Victor Segalen, CHU, F-33076 Bordeaux,
France, b Centre Régional de Pharmacovigilance Alsace, Service de
Pharmacologie Clinique, Hôpitaux Universitaires, F-67091 Strasbourg,
France
Correspondence to: F Haramburu francoise.haramburu{at}pharmaco.u-bordeaux2.fr
The incidence of adverse reactions to drugs has been
assessed with prospective epidemiological studies conducted within
single units, departments, or hospitals.1-3 Because of
the variability of the results and a lack of representativeness, it is
difficult to confidently extrapolate these results to a national level. To calculate the incidence of admissions caused by adverse drug reactions we conducted a prospective cross sectional study of a
representative nationwide sample of medical wards in public hospitals.
Between 2 March and 20 April 1998, the study was
conducted for 14 days in each of a representative sample of medical
departments in French teaching hospitals and general hospitals. The
sample size required was calculated from the results of a pilot
study.4 All patients admitted to the departments sampled
were included in the study. Each patient was assessed by a team of
local clinicians and pharmacologists to determine whether the admission
was the result of an adverse drug event.
A case was defined as a patient admitted because of an adverse drug
reaction.5 Information collected for each case included the patient's drug treatment, characteristics and evolution of the
adverse reaction, and the duration of the hospital stay. All cases were
later validated by an independent committee.
The 95% confidence interval was calculated for the normal distribution
of complex sampling when requirements for using such a method were
fulfilled In all, 3137 patients were admitted to the 62 medical departments
of the 33 hospitals in the study. Altogether 100 (3.19%) patients had
been admitted to hospital because of an adverse drug reaction (95%
confidence interval 2.37% to 4.01%) (table). These patients tended to
be older than those admitted for other reasons (60.5 v 52.9 years, P=0.009) and were more likely to be female (57/100(57%)
v 1457/3137 (46%), P=0.03). The incidence of admission for
an adverse reaction increased with age (P=0.005). Gastrointestinal complications were the most frequent cause of admission for an adverse
reaction (27/100). Nine of the 100 admissions resulted from
gastrointestinal bleeding caused by non-steroidal anti-inflammatory drugs (incidence 0.29%, 0.13% to 0.55%); 13 patients were admitted with a haemorrhage caused by anticoagulant drugs (data not shown). Of
the 193 drugs identified as being associated with admission, cardiac
stimulants and antiarrhythmic drugs were the most common, accounting
for 18 (9%) of the drugs; they were followed by antineoplastic drugs
(16/193; 8%), antithrombotic drugs (15/193; 8%), and antihypertensive drugs (15/193; 8%).
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Methods and results
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Methods and results
Comment
References
that is when n >20. The Poisson distribution was used when
the design effect was negligible (<1.5). The
2
test and tests of analysis of variance were also used.
Seventy eight of the patients recovered completely, nine had
irreversible lesions, and nine died. Among those who died, the adverse
effect was the direct cause of death in four cases (0.12%, 0.034% to
0.33%). Three patients were lost to follow up. The average stay in
hospital was 9.7 days. Using national statistics we estimated that each
year in France 134 159 (97 382 to 170 777) admissions were caused by
adverse drug reactions (1 285 256 (920 486 to 1 641 263) days
spent in hospital).
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Comment |
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This is the first prospective, national study conducted to determine the incidence of hospital admissions related to adverse drug reactions. Our findings are similar to results obtained by two meta-analyses. In Australia an incidence of between 2.4% and 3.6% was found3 and in the United States an incidence of between 3.1% and 6.2% was found.1 The mortality found in our study is the same as that found in the United States (0.13%, 0.04% to 0.21%). Older age and female sex are considered to be risk factors for hospital admissions caused by adverse drug reactions; this was confirmed by our results.
Admissions caused by adverse reactions are only one aspect of drug
related morbidity and account for about 10% of the adverse effects
observed in hospitals.4 A larger proportion of adverse effects probably occurs in the community and never leads to admission.
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Acknowledgments |
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We thank the physicians who participated in this study as well as the members of the expert committee: Joel Ankri, G Birry, Anne Castot, Dominique Costagliola, Jean Claude Evreux, M Imler, Claudine Soubrié, and Marie Welsch. We also thank Elsa Diarte, Didier Ekouevi, Françoise Ferval, Betty Laborde, Sandy Maumus, Ghada Miremont, Madeleine Mimiague, Eric Pohier, Caroline Roussillon, and Hélène Théophile for their help with randomisation and coding data, and Simone Mathoulin-Pelissier for suggestions about the analysis.
Contributors: PP, FH, JLI and BB jointly analysed and wrote up the study and will act as guarantors.
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Footnotes |
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Funding: Agence française du médicament.
Competing interests: None declared.
A list of investigators from
the participating centres appears on the BMJ's website
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References |
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| 1. |
Lazarou J, Pomeranz BH, Corey PN.
Incidence of adverse drug reactions in hospitalized patients.
JAMA
1998;
279:
1200-1205 |
| 2. | Einarson TR. Drug-related hospital admissions. Ann Pharmacother 1993; 27: 832-838[Abstract]. |
| 3. | Roughead EE, Gilbert AL, Primrose JG, Sansom LN. Drug-related hospital admissions: a review of Australian studies published 1988-1996. Med J Aust 1998; 165: 405-408. |
| 4. | Imbs JL, Pouyanne P, Haramburu F, Welsch M, Decker N, Blayac JP, et al. Iatrogénie médicamenteuse: estimation de sa prévalence dans les hôpitaux publics français. Therapie 1999; 54: 21-27[Medline]. |
| 5. | World Health Organization. International drug monitoring: the role of the hospital. Geneva: World Health Organization, 1996. (Technical report series: No 425.) |
(Accepted 13 January 2000)