“…Although a recent randomized controlled trial in Japanese hemodialysis patients suggested that oral VDRA did not reduce the risk of cardiovascular events, including sudden death 44) , the proportion of sudden death among all cardiovascular events is small (18 of 188), and the effect of VDRA on different genders is death were not evaluated. In particular, serum potassium levels, which could be a strong contributor of sudden death, other dialysis parameters, except for dialysis session length and Kt/V (e.g., blood flow rate and ultrafiltration rate), nutritional parameters, except albumin and body mass index, echocardiographic, and electrocardiographic data (e.g., ejection fraction, left ventricular hypertrophy, and QT interval), cardiac biomarker data, (e.g., troponins and atrial/brain natriuretic peptides), and data of commodity such as sleep apnea syndrome, which is one of the important causes of sudden death 51) , and medical treatment (e.g., antiplatelet agents and -blockers) were missing. Finally, the detailed timing of sudden death (i.e., if deaths occurred in the hours before or after dialysis) is unclear.…”