Cinacalcet and gastrointestinal bleeding risk in patients receiving hemodialysis

• Published in: Pharmacoepidemiology and drug safety 2022-02, Vol.31 (2), p.141-148
• Main Authors: Liu, Jiannong, Guo, Haifeng, Lin, Tzu‐Chieh, Wetmore, James B., Bradbury, Brian D., Gilbertson, David T., Nieman, Kimberly, Peng, Yi, Sprafka, J. Michael, Dluzniewski, Paul J.
• Format: Article
• Language: English
• Subjects: Adolescent; Adult; Aged; Bleeding; Calcimimetic Agents - adverse effects; Calcium; Case-Control Studies; cinacalcet; Cinacalcet - adverse effects; gastrointestinal bleeding; Gastrointestinal Hemorrhage - chemically induced; Gastrointestinal Hemorrhage - epidemiology; Hemodialysis; Humans; Hyperparathyroidism; Hyperparathyroidism, Secondary - drug therapy; Hyperparathyroidism, Secondary - epidemiology; Medicare; Parathyroid; Parathyroid Hormone; Patients; pharmacoepidemiology; Renal Dialysis - adverse effects; secondary hyperparathyroidism; United States - epidemiology
• ISSN: 1053-8569; 1099-1557
• DOI: 10.1002/pds.5337

Purpose Secondary hyperparathyroidism (SHPT) is common among dialysis patients, and calcimimetics are a mainstay of treatment. This study assessed whether cinacalcet use is associated with gastrointestinal bleeding in a large hemodialysis cohort. Methods A linked database of clinical records and medical claims for patients receiving hemodialysis in a large dialysis organization, 2007–2010, was used. A nested case–control study was performed among patients aged ≥18 years who had received hemodialysis for ≥90 days, had Medicare Parts A, B, and D coverage for ≥1 year, and had clinical evidence of SHPT (parathyroid hormone >300 pg/mL). Cases were those who experienced death or hospitalization caused by gastrointestinal bleeding. Each case was matched to up to four controls. Exposure was measured by any cinacalcet use, current use, past use, cumulative exposure days, and cumulative dosage. Conditional logistic models were used to assess the association. Results Of 48 437 patients included, 2570 experienced gastrointestinal bleeding events (2498 non‐fatal, 72 fatal), and 2465 (2397 non‐fatal, 68 fatal) were matched to 9500 controls; 17.2% of cases and 15.8% of controls had cinacalcet exposure and 11.1% of both cases and controls had current use. The adjusted odds ratios (95% CI) of gastrointestinal bleeding for any use, current use, and past use of cinacalcet were 1.04 (0.91–1.19), 0.97 (0.83–1.13), and 1.22 (0.99–1.50), respectively, with no use as the reference. Conclusion The results do not suggest an elevated risk of gastrointestinal bleeding resulting in hospitalization or death for hemodialysis patients exposed to cinacalcet.