Veterans Affairs Center for Clinical Management Research, Ann Arbor, MI 48105, USA.
Clin Gastroenterol Hepatol. 2012 Oct;10(10):1143-51. doi: 10.1016/j.cgh.2012.05.003. Epub 2012 May 18.
BACKGROUND & AIMS: Oral mesalamine drugs are frequently used to treat patients with mild-to-moderate ulcerative colitis (UC). However, these drugs are costly, and long-term adherence is poor. We compared the cost utility of inflammation-targeted, intermittent therapy with that of universal, continuous maintenance therapy with mesalamine agents for patients with mild-to-moderate UC.
We developed a Markov cohort model that simulated a population of adult patients with newly diagnosed, quiescent UC after induction of remission with mesalamine agents. We obtained model inputs from the literature. The perspective taken was that of a short-term payer (health insurance provider) during a 5-year time period. We modeled 3 treatment strategies: symptom-targeted treatment (treatment for symptomatic disease flares only, SYMPT), continuous mesalamine maintenance for all patients (CONT, the current standard of care), and inflammation-targeted treatment (mesalamine therapy for only patients with a stool sample positive for an inflammatory marker, INFLAM). We measured disease flares, quality-adjusted life years (QALYs), costs (2009 U.S. dollars), and incremental cost-effectiveness ratios.
INFLAM was the least costly strategy (cumulative per-patient cost of $22,798), compared with $24,378 for the SYMPT and $25,621 for the CONT strategies. Despite the lower cost, INFLAM was comparable to SYMPT and CONT in effectiveness (4.4986 vs 4.5014 QALYs, respectively), making INFLAM the optimal strategy. Several variables were found to be important in sensitivity analysis; the CONT strategy was optimal only if the cost of mesalamine drugs was markedly reduced.
Inflammation-targeted treatment of patients with UC is effective and costs less than continuous treatment of all patients with mesalamine, the current standard of care. Prospective trials of inflammation-targeted treatment are warranted.
口服美沙拉嗪类药物常用于治疗轻中度溃疡性结肠炎(UC)患者。但这些药物费用高,长期依从性差。我们比较了靶向炎症的间歇性治疗与美沙拉嗪类药物通用持续维持治疗对轻中度 UC 患者的成本效用。
我们开发了一个马尔可夫队列模型,模拟了接受美沙拉嗪诱导缓解后新诊断为静止性 UC 的成年患者人群。我们从文献中获取模型输入。采用短期支付者(健康保险公司)视角,研究时间为 5 年。我们构建了 3 种治疗策略:症状靶向治疗(仅治疗有症状的疾病发作,SYMPT)、所有患者持续美沙拉嗪维持治疗(CONT,当前标准治疗)和靶向炎症治疗(仅对粪便炎症标志物阳性的患者进行美沙拉嗪治疗,INFLAM)。我们测量疾病发作、质量调整生命年(QALY)、成本(2009 年美元)和增量成本效果比。
与 SYMPT(每位患者累积成本为 24378 美元)和 CONT(每位患者累积成本为 25621 美元)策略相比,INFLAM 策略成本最低(每位患者累积成本为 22798 美元)。尽管成本较低,但 INFLAM 与 SYMPT 和 CONT 在疗效方面相当(分别为 4.4986 和 4.5014 QALY),使得 INFLAM 成为最佳策略。敏感性分析发现几个变量很重要;只有当美沙拉嗪药物的成本显著降低时,CONT 策略才是最佳策略。
针对 UC 患者的靶向炎症治疗是有效且成本低于当前的美沙拉嗪类药物通用持续治疗。有必要开展针对靶向炎症治疗的前瞻性试验。