Center for Clinical Epidemiology and Biostatistics, University of Pennsylvania, Philadelphia, PA, USA.
Pharmacoepidemiol Drug Saf. 2012 Apr;21(4):366-74. doi: 10.1002/pds.2350. Epub 2012 Jan 25.
Proton pump inhibitors (PPIs) and corticosteroids are commonly prescribed drugs; however, each has been associated with fracture and community-acquired pneumonia. How physicians select patients for co-therapy may have implications for potential additive or synergistic toxicities.
We conducted a retrospective cohort study of 13 749 incident corticosteroid users with no prior PPI exposure using the HealthCore Integrated Research Database(SM) . We used logistic regression to evaluate the association between PPI initiation in the first 30 days of steroid therapy and corticosteroid dose, clinical risk factors including comorbid diseases, and medication use including prescription nonsteroidal anti-inflammatory drugs (NSAIDs).
A new PPI prescription within 30 days of starting corticosteroids was filled by 1050 patients (7.6%). PPI use was associated with the number of baseline comorbid conditions (OR = 1.21 for each additional condition, 95%CI = 1.13-1.28), recent hospitalization (OR = 4.71, 95%CI = 4.02-5.52), prednisone dose higher than 40 mg/day (OR = 1.87, 95%CI = 1.45-2.41), history of gastroesophageal reflux or gastric ulcer disease (OR = 1.54, 95%CI = 1.24-1.91), renal insufficiency (OR = 2.06, 95%CI = 1.73-2.46), and liver disease (OR = 1.82, 95%CI = 1.45-2.28). The concomitant use of prescription NSAIDs was also associated with PPI use (OR = 1.89, 95%CI = 1.32-2.70); however, the total use of PPIs in this group was low (6.3%, 95%CI = 4.4-8.2%).
Overall, PPI therapy among corticosteroid users was uncommon, even among those with risk factors for gastrointestinal toxicity. PPI use was significantly more common among patients who had recently been hospitalized, had a greater burden of comorbid illness, or were receiving high daily doses of corticosteroids.
质子泵抑制剂(PPIs)和皮质类固醇是常用的药物;然而,每种药物都与骨折和社区获得性肺炎有关。医生为患者选择联合治疗的方式可能会对潜在的附加或协同毒性产生影响。
我们使用 HealthCore Integrated Research Database(SM)进行了一项回顾性队列研究,纳入了 13749 名首诊时无质子泵抑制剂(PPI)暴露的皮质类固醇使用者。我们使用逻辑回归评估了在开始皮质类固醇治疗的 30 天内开始使用 PPI 与皮质类固醇剂量、包括合并症在内的临床危险因素以及药物使用(包括处方非甾体抗炎药(NSAIDs))之间的关联。
在开始皮质类固醇治疗的 30 天内,有 1050 名患者(7.6%)开具了新的 PPI 处方。PPI 的使用与基线合并症的数量相关(每增加一种疾病,比值比(OR)为 1.21,95%置信区间(CI)为 1.13-1.28),近期住院(OR 为 4.71,95%CI 为 4.02-5.52),泼尼松剂量高于 40mg/天(OR 为 1.87,95%CI 为 1.45-2.41),胃食管反流或胃溃疡病史(OR 为 1.54,95%CI 为 1.24-1.91),肾功能不全(OR 为 2.06,95%CI 为 1.73-2.46)和肝病(OR 为 1.82,95%CI 为 1.45-2.28)。同时使用处方 NSAIDs 也与 PPI 的使用相关(OR 为 1.89,95%CI 为 1.32-2.70);然而,该组中 PPI 的总使用率较低(6.3%,95%CI 为 4.4-8.2%)。
总体而言,皮质类固醇使用者中 PPI 治疗并不常见,即使是那些有胃肠道毒性风险的患者。PPI 的使用在近期住院、合并症负担较大或接受高剂量皮质类固醇治疗的患者中更为常见。