R. Buchbinder et al., Clinical features of tiaprofenic acid (surgam) associated cystitis and a study of risk factors for its development, J CLIN EPID, 53(10), 2000, pp. 1013-1019
Citations number
17
Categorie Soggetti
Envirnomentale Medicine & Public Health","Medical Research General Topics
A case-control study was performed to describe the clinical course and iden
tify risk factors predisposing to the development of tiaprofenic acid assoc
iated cystitis. Cases were identified from reports to the Australian Advers
e Drug Reactions Advisory Committee and a two-year (1995-1996) national sur
veillance programme. Definition of a case was onset of symptoms of cystitis
while taking tiaprofenic acid with pyuria (>10 WBC/mu l) and/or hematuria
(>10 RBC/mu l), and no evidence of urinary tract infection. Definitions of
"prescriber-matched" and "unmatched" controls were those who had been presc
ribed tiaprofenic acid by the same prescriber within 12 months of the case
without developing cystitis or were identified from the databases of local
pharmacies of the cases respectively. 81 of 109 identified cases and 109 of
184 potential controls completed a standardised interviewer-administered q
uestionnaire. Median time between the commencement of tiaprofenic acid and
symptom onset was 6.3 months (range 0.1-47.1 months). Median interval betwe
en presentation to doctor and drug cessation was 3.0 months (range 0-24.5 m
onths). In half the patients, symptoms resolved within 14 days of ceasing t
herapy. Increasing age was a risk factor for the development of tiaprofenic
-acid associated cystitis, age >70 years-odds ratio 3.2 (95% confidence int
erval 1.3-7.9) compared with age <55 years. Patients taking aspirin had a r
educed risk (odds ratio 0.3, 95% confidence interval 0.1-0.9). Dose and amo
unt of fluid consumed per day were not related to the risk of cystitis. Ear
lier recognition of tiaprofenic acid associated cystitis can potentially re
duce the morbidity related to this condition. Apart from an increased risk
among older patients, it is likely that this condition represents a drug re
action that cannot be predicted from clinical variables. (C) 2000 Elsevier
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