Turvill James, Rook Lisa, Rawle Maxine, Robins Gerry, Smale Simon, Kant Prashant, Phillips Anne
Department of Gastroenterology, York Hospital, York Teaching Hospital NHS Foundation Trust, York, UK.
Frontline Gastroenterol. 2017 Jul;8(3):183-188. doi: 10.1136/flgastro-2016-100780. Epub 2017 Jan 30.
We have previously published an evidence-based care pathway for the use of faecal calprotectin (FC) to monitor patients with Crohn's disease established on therapy. Patients are treated as low, intermediate or high risk of continuing Crohn's disease activity based on their FC, whatever their phenotype and surgical status are. Low-risk patients (FC <100 µg/g) are offered 12 monthly follow-ups or step down of therapy if asymptomatic or initial expectant symptomatic treatment. Intermediate-risk patients (FC 100-250 µg/g) are reviewed at 6 months with a repeat FC. High-risk patients (two consecutive FCs >250 µg/g) are flagged up to the responsible clinician as likely having an active Crohn's disease.
To validate this care pathway over a 2-year period, by determining its negative predictive value (NPV) and positive predictive value (PPV).
123 patients were managed by means of the care pathway for a mean of 24.4 months. The NPV and PPV were 0.97 (CI 0.93 to 0.98) and 0.85 (CI 0.80 to 0.94), respectively (sensitivity: 0.92 (0.83 to 0.96) and specificity: 0.95 (0.92 to 0.98)). Importantly 69% of patients with FC >250 µg/g were in clinical remission, the care pathway identifying patients who would benefit from presymptomatic disease modification.
This validation of a pragmatic clinical care pathway demonstrates a safe and effective mechanism by which to use FC to monitor risk of disease activity in patients with Crohn's disease established on therapy. It provides a framework for prioritising follow-up and for identifying patients at risk of continuing disease activity or those in whom therapy could be stepped down.
我们之前已经发表了一份基于循证医学的护理路径,用于使用粪便钙卫蛋白(FC)监测接受治疗的克罗恩病患者。无论患者的表型和手术状态如何,根据其FC水平将患者分为持续克罗恩病活动的低、中、高风险。低风险患者(FC<100μg/g)如果无症状或初始采用预期的对症治疗,则进行每月12次随访或减少治疗。中风险患者(FC 100 - 250μg/g)在6个月时进行复查并重复检测FC。高风险患者(连续两次FC>250μg/g)被标记给负责的临床医生,提示可能患有活动性克罗恩病。
为了在2年时间内验证这条护理路径,通过确定其阴性预测值(NPV)和阳性预测值(PPV)。
123例患者通过该护理路径进行管理,平均管理时间为24.4个月。NPV和PPV分别为0.97(95%CI 0.93至0.98)和0.85(95%CI 0.80至0.94)(敏感性:0.92(0.83至0.96),特异性:0.95(0.92至0.98))。重要的是,69%的FC>250μg/g的患者处于临床缓解期,该护理路径能够识别出可从症状前疾病改善中获益的患者。
这条实用临床护理路径的验证表明,FC是一种安全有效的机制,可用于监测接受治疗的克罗恩病患者的疾病活动风险。它为确定随访优先级以及识别有持续疾病活动风险的患者或可减少治疗的患者提供了一个框架。