Key result
Current exposure to modified-release doxasozin was not associated with an increased risk of hip/femur, humerus, or wrist fractures (adjusted OR 0.90; 95% CI 0.68-1.19).
Why the study?
Does modified-release doxazosin exposure increase the risk of fractures in elderly patients?
Case-Control (n=33,035)
Yes
Does modified-release doxazosin exposure increase the risk of fractures in elderly patients?
Odds Ratio: 0.9 (95% CI 0.68–1.19)
Modified-release doxazosin does not appear to increase the risk of fall-related fractures in elderly patients without a history of falls or trauma.
Supports safety of modified-release doxazosin in elderly; leaves open need for prospective confirmation.
PURPOSE: Standard formulation alpha-blocker use has been associated with an increased risk of hypotension-related adverse events, particularly with cardiovascular indications and on treatment initiation. We investigated the association between those fractures that are commonly due to falls and modified-release doxasozin exposure. METHODS: A case-control study using UK primary care records (the THIN database) showed that 6540 cases aged 50 years or older had a record of first fracture of the hip/femur, humerus or wrist after May 2001; 26 495 controls had no fracture and were matched on practice, year of birth and sex. Exclusions for the primary analysis were previous benign prostatic hypertrophy (BPH), lower urinary tract symptoms (LUTS) or prostate cancer, major trauma at the time of the case's fracture, or a history of falls. Conditional logistic regression estimated the association between modified-release doxasozin treatment and the occurrence of fractures. RESULTS: No increased risk of fractures was associated with current use of modified-release doxasozin, adjusted odds ratios (ORs) 0.90 (95%CI 0.68, 1.19); previous use, adjusted OR 0.92 (95%CI 0.73, 1.16) or the start of a treatment episode (</=28 days), crude OR 0.57 (0.17, 1.92). Including those with a history of BPH, LUTS and prostatic carcinoma had little effect, adjusted OR for current use was 0.95 (95%CI 0.74, 1.21). No significant increased risk of fractures was associated with the start of standard preparation alpha-blockers, crude OR 1.42 (95%CI 0.65, 3.07). CONCLUSIONS: We found no association between modified-release doxasozin use and fractured hip/femur, humerus or wrist in those without a recent history of falls, or trauma.
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Hall et al. (2007) conducted a case-control in Fractures of the hip/femur, humerus or wrist (n=33,035). Modified-release doxasozin vs. Unexposed / no current use was evaluated on Occurrence of fractures (hip/femur, humerus or wrist) (OR 0.90, 95% CI 0.68-1.19). Current exposure to modified-release doxasozin was not associated with an increased risk of hip/femur, humerus, or wrist fractures (adjusted OR 0.90; 95% CI 0.68-1.19).
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