Severe hypertriglyceridemia and factors associated with acute pancreatitis in an integrated health care system

被引:44
|
作者
Rashid, Nazia [1 ]
Sharma, Puza P. [2 ]
Scott, Ronald D. [3 ]
Lin, Kathy J. [1 ]
Toth, Peter P. [4 ,5 ]
机构
[1] Kaiser Permanente, Southern Calif Reg, Drug Informat Serv, 12254 Bellflower Blvd, Downey, CA 90242 USA
[2] US Hlth Econ & Outcomes Res, Novartis Pharmaceut Corp, E Hanover, NJ USA
[3] Southern Calif Permanente Med Grp, West Los Angeles, CA USA
[4] CGH Med Ctr, Sterling, IL USA
[5] Johns Hopkins Univ, Sch Med, Ciccarone Ctr Prevent Cardiovasc Dis, Baltimore, MD USA
关键词
Hypertriglyceridemia; Acute pancreatitis; Dyslipidemia; Adherence; Treatment patterns; Integrated health care system;
D O I
10.1016/j.jacl.2016.02.019
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
OBJECTIVE: To evaluate patient characteristics, treatment patterns, comorbidities, and risk factors associated with the development of acute pancreatitis (AP) in patients with severe hypertriglyceridemia (HTG) in an integrated health care delivery system. METHODS: We identified a retrospective cohort of severe HTG patients with a fasting triglyceride level 1000 >= mg/dL during January 1, 2007 to June 30, 2013 (index date) in an integrated health care delivery system. Patients were aged >= 18 years on index date and had 12 months of continuous membership and drug eligibility before the index date and during postindex including index date. Baseline patient characteristics, comorbidities, and risk factors were evaluated during 12-month preindex. Outcomes such as development of AP, treatment patterns, adherence to index therapy, and change in triglyceride (TG) laboratory levels were evaluated during postindex. Descriptive statistics were used to identify differences between patients developing AP vs no development of AIR A stepwise multivariate logistic regression and backward elimination method were used to assess statistically significant predictive factors associated with development of AP vs no AP. RESULTS: We identified 5550 patients with severe HTG, and 5.4% of these patients developed AP during postindex. Patients were mostly male (>= 70%) in both groups; however, younger in the AP group (45 years 10.6) vs no AP group (50 years 11.4) with P value < .0001. The AP group had higher baseline Charslon Comorbidity Index score, alcohol abuse history (42.2%), any pancreatitis history (51.5%), diabetes (47%), and hypertension (55%), vs the no AP group (P values < .05). Patients in the AP group had higher baseline mean TO levels (2148, SD 1578) vs the no AP group (1559, SD 861), P value < .0001. Over 50% of the patients were prescribed their index therapy by a primary care provider. Predictive factors associated with the development of AP included younger age, alcohol use, and prior history of any pancreatitis, hypertension, renal disease stage 4, and other prescriber specialty. From parameters estimates, for each 100 mg/dL unit of increase in the TG level above 1000 mg/dL, there was a 3 percent increase in risk of developing AP. CONCLUSIONS: Patients with severe HTG are at a higher risk of developing AP. A number of co-morbidities, risk factors, and baseline TG levels are associated with an increased incidence of AP. Patients with severe HTG are underdiagnosed, undertreated and are nonadherent to their index lipid therapy. There is a need to better define optimal approaches to treating severe HTG so as to reduce the incidence of AP. Economic studies are also needed to evaluate the burden of AP on various health care systems. (C) 2016 National Lipid Association. All rights reserved.
引用
收藏
页码:880 / 890
页数:11
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