A Treat to Target Strategy Using Panenteric Capsule Endoscopy in Pediatric Patients With Crohn's Disease

被引:43
作者
Oliva, Salvatore [1 ]
Aloi, Marina [1 ]
Viola, Franca [1 ]
Mallardo, Saverio [1 ]
Civitelli, Fortunata [1 ]
Maccioni, Francesca [1 ]
Hassan, Cesare [2 ]
Papoff, Paola [3 ]
Cucchiara, Salvatore [1 ]
Cohen, Stanley A. [4 ]
机构
[1] Sapienza Univ Rome, Pediat Gastroenterol & Liver Unit, Rome, Italy
[2] Nuovo Regina Margherita Hosp, Digest Endoscopy Unit, Rome, Italy
[3] Sapienza Univ Rome, Dept Pediat PICU, Rome, Italy
[4] Childrens Ctr Digest Hlth Care, Atlanta, GA USA
关键词
Pediatric Endoscopy; Mucosal Healing; Deep Remission; Colon Capsule Endoscopy; INFLAMMATORY-BOWEL-DISEASE; INTESTINE CONTRAST ULTRASONOGRAPHY; MUCOSAL HEALING ASSESSMENT; PILLCAM COLON CAPSULE; DEEP REMISSION; MANAGEMENT; VALIDATION; GUIDELINES; INCREASE; EVALUATE;
D O I
10.1016/j.cgh.2018.10.015
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
BACKGROUND & AIMS: Pan-enteric capsule endoscopy (PCE) is effective for assessment of small intestinal and colonic Crohn's disease (CD) in pediatric patients. We aimed to determine whether PCE can be used to monitor mucosal healing and deep remission, in a treat to target strategy for pediatric patients with CD. METHODS: We performed a prospective study of 48 children with a diagnosis of CD at a tertiary care pediatric gastroenterology unit; 46 patients were included in the final analysis. Biomarker, imaging, and PCE analyses were performed at baseline and after 24 and 52 weeks. Small bowel and colonic mucosal healing were defined by Lewis scores <135 and simple endoscopic score for CD <= 1, respectively. Clinical remission was defined as defined as a pediatric CD activity index score <10 and biomarker-based remission based on normal levels of biomarkers; deep remission was defined as a combination of clinical remission, biomarker-based remission, and mucosal healing. Treatments were adjusted based on findings from PCE (imaging was considered only for patients with negative findings from PCE). Therapies were introduced, optimized, switched, or combined at the discretion of treating clinicians. The primary outcome was the ability of PCE to assess mucosal healing and deep remission at 3 timepoints and to guide a treat to target strategy. RESULTS: PCE detected inflammation in 34 patients (71%) at baseline, 22 patients (46%) at week 24, and 18 patients (39%) at week 52 (P for comparison among timepoints <.05). Findings from PCE led to a change in therapy for 34 patients (71%) at baseline and 11 patients (23%) at 24 weeks, whereas only 2 patients with negative results from PCE (4%) changed therapies based on findings from imaging. When the treat to target strategy was applied, proportions of patients with mucosal healing and deep remission increased from 21% at baseline, to 54% at week 24, to 58% at week 52 (P for comparison among timepoints <.05); 2 patients (4%) did not respond to treatment. CONCLUSION: In a prospective study of 48 children with CD, we found a treat to target strategy, based on findings from PCE, to significantly increase the proportions of patients with mucosal healing and deep remission.
引用
收藏
页码:2060 / +
页数:9
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