1. Systemic Alpha1-Adrenoceptor Antagonists and Increased Risk of Open-Angle Glaucoma: A Nationwide Population-Based Cohort Study
- Author
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Tsung-Cheng Hsieh, Ming-Shan He, Yuan-Chieh Lee, Jung-Lun Wu, and Hong-Zin Lin
- Subjects
Adult ,Male ,medicine.medical_specialty ,hypertension ,National Health Programs ,030232 urology & nephrology ,ocular perfusion pressure ,Taiwan ,open-angle glaucoma ,Hyperlipidemias ,alpha-adrenoceptor antagonists ,Cohort Studies ,03 medical and health sciences ,0302 clinical medicine ,Lower urinary tract symptoms ,Risk Factors ,Internal medicine ,medicine ,Diabetes Mellitus ,Humans ,lower urinary tract symptoms ,Aged ,Proportional Hazards Models ,Retrospective Studies ,business.industry ,Incidence (epidemiology) ,Incidence ,Hazard ratio ,Retrospective cohort study ,Glaucoma ,Middle Aged ,medicine.disease ,Ambulatory ,Propensity score matching ,Urinary Tract Infections ,030221 ophthalmology & optometry ,Adrenergic alpha-1 Receptor Antagonists ,Female ,Diagnosis code ,business ,Glaucoma, Open-Angle ,Cohort study - Abstract
Purpose To examine the risk of open-angle glaucoma (OAG) among patients receiving alpha1-adrenoceptor (α1-AR) antagonists for lower urinary tract symptoms (LUTS). Methods This was a nationwide, population-based, retrospective cohort study from Asia/Taiwan. One million beneficiaries were randomly sampled from among 27.38 million individuals enrolled in the National Health Insurance program, and subjects with a diagnosis of LUTS from 2001 to 2012 were identified (N = 105,341). After 1:1 propensity score matching by gender, age, comorbid medical diseases, number of all medical visits during the observational period, and index date, 4081 patients were enrolled in the study group, comprised of patients who had taken α1-AR antagonists, and 4081 patients were enrolled in the control group, comprised of patients who had never taken α1-AR antagonists. The incidence and risk of OAG (defined as two ambulatory visits with a ICD-9 diagnosis code 365, excluding ICD-9 diagnosis codes 365.2-365.6, 365.02, 365.03, 365.13, 365.14, and 365.8) were calculated. Results Patients taking α1-AR antagonists had a higher incidence ratio of 1.86 (95% confidence interval [CI], 1.30-2.65) for developing OAG. After adjusting for age, gender, and comorbidities, the hazard ratio (HR) for OAG for patients taking α1-AR antagonists was 1.66 (95% CI, 1.16-2.39; P = 0.006). Among patients with hypertension, the hazard ratio for OAG associated with taking α1-AR antagonists increased to 1.79 (95% CI, 1.07-2.99; P = 0.003). On the other hand, the association of α1-AR antagonists with OAG was not significant among patients with diabetes mellitus, hyperlipidemia, or older age. Conclusions The findings of our study suggest an increased risk for OAG among patients taking α1-AR antagonists for LUTS, especially in patients with hypertension.
- Published
- 2020