Assessment of potential drug-drug interactions with a prescription claims database

被引:89
作者
Malone, DC
Hutchins, DS
Haupert, H
Hansten, P
Duncan, B
Van Bergen, RC
Solomon, SL
Lipton, RB
机构
[1] Univ Arizona, Coll Pharm, Tucson, AZ 85721 USA
[2] Univ Washington, Sch Pharm, Seattle, WA 98195 USA
[3] Ctr Medicare & Medicaid Serv, Div Finance & Operat, Reisterstown, MD USA
[4] Ctr Healthier Aging, Elkridge, MD USA
[5] Ctr Dis Control & Prevent, Hlth Syst, Atlanta, GA USA
[6] Albert Einstein Coll Med, Dept Neurol, Bronx, NY 10467 USA
关键词
age; anticoagulants; antifungals; antiinflammatory agents; antipsychotic agents; cyclosporine; drug interactions; immunosuppressive agents; interventions; pharmacy benefit management companies; pimozide; prescriptions; rifamycins; toxicity; warfarin;
D O I
10.2146/ajhp040567
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Purpose. The prevalence of 25 clinically important potential drug-drug interactions (DDIs) in a population represented by the drug claims database of a pharmacy benefit management company (PBM) was studied. Methods. A retrospective cross-sectional analysis of pharmaceutical claims for almost 46 million participants in a PBM was conducted to determine the frequency of 25 DDIs previously identified as clinically important. A DDI was counted when drugs in potentially interacting combinations were dispensed within 30 days of each other during a 25-month period between April 2000 and June 2002. Result's. The number of DDIs ranged from 37 for pimozide and an azole antifungal to 127,684 for warfarin and a nonsteroidal antiinflammatory drug (NSAID). The highest prevalence (278.56 per 100,000 persons) and highest case-exposure rate (242.7 per 1,000 warfarin recipients) occurred with the warfarin-NSAID combination. The combination with the lowest overall, prevalence (cyclosporine and a rifamycin, 0.10/100,000) differed from the combination with the lowest case-exposure rate (pimozide and an azole antifungal, 0.028 per 1,000 azole antifungal recipients). Number of cases, prevalence, and case-exposure rates for both sexes generally increased with age. An estimated 374,000 plan participants were exposed to a clinically important DDI during a 25-month period. Between 20% and 46% of prescription drug claims were reversed (canceled) for a medication with a drug interaction when a warning about the interaction was sent to the pharmacy. Conclusion. Analysis of prescription claims data from a major PBM found that 374,000 of 46 million plan participants had been exposed to a potential DDI of clinical importance.
引用
收藏
页码:1983 / 1991
页数:9
相关论文
共 46 条
[31]   Community pharmacists' responses to drug - drug interaction alerts [J].
Murphy, JE ;
Forrey, RA ;
DeSiraju, U .
AMERICAN JOURNAL OF HEALTH-SYSTEM PHARMACY, 2004, 61 (14) :1484-1487
[32]   Digoxin toxicity secondary to clarithromycin therapy [J].
Nawarskas, JJ ;
McCarthy, DM ;
Spinler, SA .
ANNALS OF PHARMACOTHERAPY, 1997, 31 (7-8) :864-866
[33]  
Peng Catherine C, 2003, J Manag Care Pharm, V9, P513
[34]  
PHILLIPS CR, 1998, J MANAG CARE PHARM, V4, P183
[35]   EPIDEMIOLOGICAL STUDY OF CLINICAL SIGNIFICANCE OF DRUG-DRUG INTERACTIONS IN A PRIVATE COMMUNITY HOSPITAL [J].
PUCKETT, WH ;
VISCONTI, JA .
AMERICAN JOURNAL OF HOSPITAL PHARMACY, 1971, 28 (04) :247-&
[36]   Oral erythromycin and the risk of sudden death from cardiac causes [J].
Ray, WA ;
Murray, KT ;
Meredith, S ;
Narasimhulu, SS ;
Hall, K ;
Stein, CM .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 351 (11) :1089-1096
[37]   Establishing realistic performance standards for community pharmacists' drug-use-review activities in managed care contracts [J].
Rupp, MT .
AMERICAN JOURNAL OF HEALTH-SYSTEM PHARMACY, 1999, 56 (06) :566-567
[38]   Medication misadventures resulting in emergency department visits at an HMO medical center [J].
SchneitmanMcIntire, O ;
Farnen, TA ;
Gordon, N ;
Chan, J ;
Toy, WA .
AMERICAN JOURNAL OF HEALTH-SYSTEM PHARMACY, 1996, 53 (12) :1416-1422
[39]   Agreement between the pharmacy medication history and patient interview for cardiovascular drugs: the Rotterdam elderly study [J].
Sjahid, SI ;
van der Linden, PD ;
Stricker, BHC .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1998, 45 (06) :591-595
[40]  
Solberg LI, 2004, AM J MANAG CARE, V10, P753