Simon L S, Zhao S Z, Arguelles L M, Lefkowith J B, Dedhiya S D, Fort J G, Johnson K E
Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.
Clin Ther. 1998 Nov-Dec;20(6):1218-35; discussion 1192-3. doi: 10.1016/s0149-2918(98)80117-3.
This study was conducted to compare the effect of etodolac, nabumetone, and oxaprozin use on gastrointestinal (GI) safety and associated costs based on insurance claims information from practice settings. Data were obtained from a national claims database (MarketScan) for the years 1992 to 1994. The claims data of interest were for patients with arthritis who had used etodolac, nabumetone, or oxaprozin exclusively during a 9-month follow-up period (ONLY groups), or these drugs plus (PLUS groups) the other nonsteroidal anti-inflammatory drugs (NSAIDs) ibuprofen, naproxen, diclofenac, sulindac, piroxicam, ketoprofen, or indomethacin. For each group, we obtained information on the use of inpatient and outpatient services for GI-related events and the associated costs. All GI admissions were classified as NSAID-induced or possibly NSAID-induced events based on International Classification of Diseases, Ninth Revision, Clinical Modification (ICD-9 CM) codes. All outpatient upper GI ulcers or bleeding episodes were also identified by specific ICD-9 CM code. There were no significant between-group demographic differences. The proportions of patients with NSAID-induced and possibly NSAID-induced GI admissions were 0.1% and 0.4% for the etodolac-ONLY, 0.3% and 1.0% for the nabumetone-ONLY, and 0.1% and 0.5% for the oxaprozin-ONLY groups, respectively (P > 0.05), and a similar pattern was observed among the PLUS groups. In outpatient settings, 3.9%, 4.2%, and 4.9% of the etodolac-, nabumetone-, and oxaprozin-ONLY patients, respectively (P > 0.05), and 6.0%, 5.3%, and 4.7% of the etodolac-, nabumetone-, and oxaprozin-PLUS patients, respectively, had at least one upper GI ulcer/bleeding claim (P > 0.05). The total health care costs for 9 months were approximately $3000 each for the etodolac-, nabumetone-, and oxaprozin-ONLY groups. Oxaprozin, nabumetone, and etodolac had similar GI-safety and associated-costs profiles based on information from practice settings. Also, in patients who used multiple NSAIDs, the groups did not differ in their GI-safety and cost profiles.
本研究旨在根据来自实际诊疗机构的保险理赔信息,比较依托度酸、萘丁美酮和奥沙普秦的使用对胃肠道(GI)安全性及相关费用的影响。数据取自1992年至1994年的全国理赔数据库(MarketScan)。感兴趣的理赔数据来自关节炎患者,这些患者在9个月的随访期内仅使用依托度酸、萘丁美酮或奥沙普秦(仅用组),或使用这些药物加(加用组)其他非甾体抗炎药(NSAIDs)布洛芬、萘普生、双氯芬酸、舒林酸、吡罗昔康、酮洛芬或吲哚美辛。对于每组,我们获取了与胃肠道相关事件的住院和门诊服务使用情况及相关费用的信息。所有胃肠道住院病例均根据《国际疾病分类,第九次修订本,临床修订版》(ICD - 9 CM)编码分类为NSAID诱导或可能由NSAID诱导的事件。所有门诊上消化道溃疡或出血发作也通过特定的ICD - 9 CM编码进行识别。组间人口统计学差异无统计学意义。依托度酸仅用组、萘丁美酮仅用组和奥沙普秦仅用组中,NSAID诱导和可能由NSAID诱导的胃肠道住院患者比例分别为0.1%和0.4%、0.3%和1.0%、0.1%和0.5%(P>0.05),加用组中也观察到类似模式。在门诊环境中,依托度酸、萘丁美酮和奥沙普秦仅用组分别有3.9%、4.2%和4.9%的患者(P>0.05),加用组分别有6.0%、5.3%和4.7%的患者至少有一次上消化道溃疡/出血理赔(P>0.05)。依托度酸、萘丁美酮和奥沙普秦仅用组9个月的总医疗费用均约为3000美元。根据实际诊疗机构的信息,奥沙普秦、萘丁美酮和依托度酸具有相似的胃肠道安全性和相关费用情况。此外,在使用多种NSAIDs的患者中,各组在胃肠道安全性和费用情况方面无差异。