Chia Nan University of Pharmacy & Science Institutional Repository:Item 310902800/34107
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    標題: Clinical burden of autosomal dominant polycystic kidney disease
    作者: Hung, Peir-Haur
    Lin, Chien-Hung
    Hung, Kuan-Yu
    Muo, Chih-Hsin
    Chung, Mu-Chi
    Chang, Chao-Hsiang
    Chung, Chi-Jung
    貢獻者: Ditmanson Med Fdn, Dept Internal Med, Chiayi Christian Hosp
    Chia Nan Univ Pharm & Sci, Dept Appl Life Sci & Hlth
    Taipei Vet Gen Hosp, Dept Pediat, Div Pediat Immunol & Nephrol
    Natl Yang Ming Univ, Inst Clin Med
    Taipei City Hosp, Dept Pediat, Zhongxing Branch
    Fu Jen Catholic Univ, Coll Sci & Engn
    Natl Taiwan Univ Hosp, Dept Internal Med
    China Med Univ Hosp, Management Off Hlth Data
    Taichung Vet Gen Hosp, Dept Med, Div Nephrol
    China Med Univ Hosp, Dept Urol
    China Med Univ Hosp, Dept Med Res
    China Med Univ, Dept Publ Hlth
    關鍵字: autosomal dominant polycystic kidney disease
    hemorrhagic stroke
    end-stage renal disease
    all-cause mortality
    time-dependent Cox proportional hazard regression
    日期: 2020
    上傳時間: 2022-11-18 11:24:12 (UTC+8)
    出版者: Impact Journals Llc
    摘要: There are no specific therapies for autosomal dominant polycystic kidney disease (ADPKD), and clinical data evaluating the effects of non-specific therapies on ADPKD patients are scarce. We therefore evaluated those effects using data from a longitudinal health insurance database collected from 2000-2010. We individually selected patients with and without ADPKD from inpatient data files as well as from the catastrophic illness registry in Taiwan based on 1:5 frequency matching for sex, age, and index year. The hazard ratios (HR) of all-cause mortality, ischemic stroke, hemorrhagic stroke and end-stage renal disease (ESRD) in ADPKD inpatients were elevated as compared to the controls. Similarly, ADPKD patients from the catastrophic illness registry had an increased risk of hemorrhagic stroke and ESRD. Allopurinol users also had an increased risk of all-cause mortality. The HR for developing ESRD after medication exposure was 0.47-fold for statin and 1.93-fold for pentoxifylline. These results reveal that patients with ADPKD (either inpatient or from the catastrophic illness registry) are at elevated risk for hemorrhagic stroke and ESRD, and suggest that allopurinol and pentoxifylline should not be prescribed to ADPKD patients due to possible adverse effects.
    關聯: Aging-Us, v.12, n.4, pp.12
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