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12 June 2024 : Database Analysis  

Comparative Cardiovascular Risks of Febuxostat and Allopurinol in Patients with Diabetes Mellitus and Chronic Kidney Disease

Hsin Hsiang Huang1DE, Yun-Yi Chen23BCD, Yu-Wei Fang14ADG, Hung-Hsiang Liou5AD, Jing-Tong Wang1B, Ming-Hsein Tsai14ADE*

DOI: 10.12659/MSM.944314

Med Sci Monit 2024; 30:e944314

Table 5 Comparative stepwise multivariable analysis of febuxostat versus allopurinol.

OutcomesModel 1Model 2Model 3
HR (95% CI)p valueHR (95% CI)p valueHR (95% CI)p value
All-cause hospitalization1.33 (1.24–1.41)<0.0011.33 (1.25–1.41)<0.0011.33 (1.25–1.42)<0.001
Hospitalization for heart failure1.60 (1.42–1.81)<0.0011.59 (1.41–1.80)<0.0011.62 (1.43–1.83)<0.001
Hospitalization for cardiovascular intervention1.52 (1.32–1.74)<0.0011.51 (1.32–1.73)<0.0011.51 (1.32–1.74)<0.001
Model 1 represents a basic analysis following propensity score matching (sex, age, and Charlson comorbidity index) that pairs the febuxostat group and the allopurinol group in a 1: 1 ratio. Multivariable model 2 comprises model l as well as adjustments for comorbidities, including hypertension, ischemic heart disease, congestive heart failure, atrial fibrillation, peripheral vascular disease, stroke, hyperlipidemia, calculus of kidney, and cirrhosis. Multivariable model 3 comprises model 2 as well as adjustments for medications of angiotensin-converting enzyme inhibitors/angiotensin receptor blockers, beta-blocker, calcium channel blockers, antithrombotic agents, non-steroidal anti-inflammatory drug, fenofibrate, statin, and diuretic. HR – hazard ratio; CI – confidence interval.

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Medical Science Monitor eISSN: 1643-3750
Medical Science Monitor eISSN: 1643-3750