A prospective, claims-based assessment of the risk of pancreatitis and pancreatic cancer with liraglutide compared to other antidiabetic drugs

被引:79
作者
Funch, D. [1 ]
Gydesen, H. [2 ]
Tornoe, K. [3 ]
Major-Pedersen, A. [4 ]
Chan, K. A. [5 ,6 ]
机构
[1] Optum, Epidemiol, Waltham, MA USA
[2] Novo Nordisk AS, Epidemiol, Soborg, Denmark
[3] Novo Nordisk AS, Med & Sci, GLP 1, Soborg, Denmark
[4] Novo Nordisk AS, Global Safety, Bagsvaerd, Denmark
[5] Natl Taiwan Univ Hosp, Dept Med Res, Taipei, Taiwan
[6] Natl Taiwan Univ, Coll Med, Grad Inst Oncol, Taipei 10764, Taiwan
关键词
GLP-1; pharmaco-epidemiology; observational study; EXENATIDE; HOSPITALIZATION; THERAPY;
D O I
10.1111/dom.12230
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
AimWe evaluated the relationship between liraglutide and acute pancreatitis or pancreatic cancer in an ongoing post-marketing safety assessment programme. MethodsInitiators of liraglutide, exenatide, metformin, pioglitazone or groups containing initiators of dipeptidyl peptidase-4 inhibitors or sulfonylureas were identified in a US commercial health insurance claims database (1 February 2010 to 31 March 2013) and followed for a median of 15months. We estimated incidence rates (IR/100 000 person-years), rate ratio (RR) and 95% confidence intervals (CI) of new insurance claims with diagnoses of primary inpatient acute pancreatitis or pancreatic cancer from Poisson regression models. ResultsThe IR for acute pancreatitis for liraglutide was 187.5 compared with 154.4 for all non-glucagon-like peptide-1 (GLP-1)-based therapies (adjusted RR 1.10; CI 0.81-1.49). The IR for pancreatic cancer was 19.9 for liraglutide compared with 33.0 for all non-GLP-1-based therapies (adjusted RR 0.65; 95% CI 0.26-1.60). ConclusionWe did not observe excess risk of either outcome associated with liraglutide relative to individual or pooled comparator drugs.
引用
收藏
页码:273 / 275
页数:3
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