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  4. Association of Permanent Vascular Access Dysfunction with Subsequent Risk of Cardiovascular Disease
 
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Association of Permanent Vascular Access Dysfunction with Subsequent Risk of Cardiovascular Disease

Other Title
A Population-Based Cohort Study
Journal
Journal of Personalized Medicine
Date Issued
2022-04-01
Author(s)
TUNG-WEI HUNG  
SHENG-WEN WU  
JENG-YUAN CHIOU  
DOI
10.3390/jpm12040598
URI
https://www.scopus.com/pages/publications/85128815194
https://scholars.csmu.edu.tw/handle/123456789/29516
Abstract
A functional permanent vascular access (VA) is required to perform a successful hemodialy-sis procedure. Hemodialysis VA dysfunction is a major cause of morbidity and hospitalization in the hemodialysis population. Cardiovascular disease (CVD) is the leading cause of death in patients re-ceiving chronic hemodialysis. Information about CVD associated with hemodialysis VA dysfunction is unclear. We analyzed the association between dialysis VA dysfunction and the risk of developing CVD in hemodialysis patients. This nationwide population-based cohort study was conducted using data from the National Health Insurance Research Database in Taiwan. One million subjects were sampled from 23 million beneficiaries and data was collected from 2000 to 2013. Patients with end-stage renal disease who had received permanent VA construction and hemodialysis and were aged at least 20 years old from 2000 to 2007 were included in the study population. The primary outcome was CVD, as defined by ICD-9-CM codes 410–414 and 430–437. A total of 197 individuals with permanent VA dysfunction were selected as the test group, and 100 individuals with non-permanent VA dysfunction were selected as the control group. Compared with the control group, the adjusted hazard ratio of CVD for the VA dysfunction group was 3.05 (95% CI: 1.14–8.20). A Kaplan–Meier analysis revealed that the cumulative incidence of CVD was higher in the permanent VA dysfunction group than in the comparison group. Permanent VA dysfunction is significantly associated with an increased risk of subsequent CVD.
Type
journal article
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