Section of Digestive Diseases, Division of Gastroenterology and Hepatology, Michael E. DeBakey Veterans Affairs Medical Center, Baylor College of Medicine, Houston, Texas; Houston VA Health Services Research and Development Center of Excellence, Michael E. DeBakey Veterans Affairs Medical Center, Baylor College of Medicine, Houston, Texas.
Clin Gastroenterol Hepatol. 2013 Oct;11(10):1281-7. doi: 10.1016/j.cgh.2013.06.004. Epub 2013 Jun 19.
BACKGROUND & AIMS: Effectiveness of early treatment with biologics and immunomodulator therapy on healthcare utilization remains poorly defined. We assessed rates of hospitalization and surgery within 1 year after initiation of infliximab and/or immunomodulator therapy in a United States cohort of patients with inflammatory bowel disease.
We conducted a retrospective, observational cohort study of veterans with Crohn's disease or ulcerative colitis by using administrative data from 176 Department of Veteran Affairs facilities (October 1, 2001 through September 30, 2009). Inpatient, outpatient, and death records were linked longitudinally with prescription fill data. Each person-day of follow-up was assessed for treatment with infliximab, immunomodulators, both (dual therapy), or neither. We calculated drug exposure time and used Poisson and logistic regression analyses to assess outcomes.
The cohort of 20,474 patients included 8042 patients with Crohn's disease and 12,432 with ulcerative colitis (93.9% male; 72.5% white; mean age, 60.9 ± 14.5 years) prescribed infliximab (0.17%), immunomodulator (1.3%), or dual therapy (1.5%). Adjusted models revealed 50% relative reductions in hospitalization among patients who received 9.2 months of immunomodulator monotherapy, 8 months of infliximab, or 7.7 months of dual therapy. A 50% relative reduction in surgery was observed among patients receiving 7 months of infliximab or 5 months of dual therapy. Analysis of dose-response data revealed 73.1% and 92% reductions in risk of hospitalization and surgery, respectively, after 9 months of dual therapy.
On the basis of a retrospective cohort study, dual therapy with infliximab and an immunomodulator for <8 months is associated with significant reductions in hospitalization and surgery within 1 year of the start of therapy. These findings indicate that patients with IBD are more likely to benefit if dual therapy is initiated earlier in their first year of therapy.
早期使用生物制剂和免疫调节剂治疗对医疗保健利用的效果仍定义不明确。我们评估了在接受英夫利昔单抗和/或免疫调节剂治疗的美国炎症性肠病患者队列中,1 年内住院和手术的发生率。
我们使用来自 176 个退伍军人事务部设施的行政数据(2001 年 10 月 1 日至 2009 年 9 月 30 日)进行了一项回顾性、观察性队列研究,纳入了克罗恩病或溃疡性结肠炎患者。将住院、门诊和死亡记录与处方配药数据进行纵向链接。每随访 1 人/天评估英夫利昔单抗、免疫调节剂、两者(双重治疗)或两者均无的治疗情况。我们计算了药物暴露时间,并使用泊松和逻辑回归分析评估结果。
该队列共纳入 20474 例患者,包括 8042 例克罗恩病患者和 12432 例溃疡性结肠炎患者(93.9%为男性;72.5%为白人;平均年龄 60.9±14.5 岁),分别处方了英夫利昔单抗(0.17%)、免疫调节剂(1.3%)或双重治疗(1.5%)。调整模型显示,接受免疫调节剂单药治疗 9.2 个月、英夫利昔单抗治疗 8 个月或双重治疗 7.7 个月的患者,住院率相对降低 50%。接受英夫利昔单抗治疗 7 个月或双重治疗 5 个月的患者,手术率相对降低 50%。剂量反应数据分析显示,双重治疗 9 个月后,住院和手术的风险分别降低 73.1%和 92%。
基于回顾性队列研究,英夫利昔单抗联合免疫调节剂治疗<8 个月与治疗开始后 1 年内住院和手术的显著减少相关。这些发现表明,如果在炎症性肠病患者治疗的第一年尽早开始双重治疗,患者获益的可能性更大。