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A virtual clinic increases anti‐TNF dose intensification success via a treat‐to‐target approach compared with standard outpatient care in Crohn’s disease
Author(s) -
Srinivasan Ashish,
van Langenberg Daniel R.,
Little Robert D.,
Sparrow Miles P.,
De Cruz Peter,
Ward Mark G.
Publication year - 2020
Publication title -
alimentary pharmacology and therapeutics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.308
H-Index - 177
eISSN - 1365-2036
pISSN - 0269-2813
DOI - 10.1111/apt.15742
Subject(s) - medicine , faecal calprotectin , cohort , outpatient clinic , clinical endpoint , observational study , disease , retrospective cohort study , crohn's disease , cohort study , inflammatory bowel disease , physical therapy , calprotectin , randomized controlled trial
Summary Background Virtual clinics represent a novel model of care in inflammatory bowel disease. Their effectiveness in promoting high quality use of biologic therapy and facilitating a treat‐to‐target approach is unknown. Aim To evaluate clinical and process‐driven outcomes in a virtual clinic compared to standard outpatient care amongst patients receiving intensified anti‐TNF therapy for secondary loss of response. Methods We performed a retrospective multi‐centre, parallel, observational cohort study of Crohn's disease patients receiving intensified anti‐TNF therapy for secondary loss of response. Objective assessments of disease activity and anti‐TNF trough levels at secondary loss of response and during subsequent 6‐month semesters, were compared longitudinally between virtual clinic and standard outpatient care cohorts. The primary endpoint was treatment success, with appropriateness of dose intensification, tight disease monitoring and treatment de‐escalation representing secondary outcomes. Results Of 149 patients with similar baseline characteristics, 69 were managed via a virtual clinic and 80 via standard outpatient care. There were higher rates of treatment success in the virtual clinic cohort (60.9 vs 35.0%, P < 0.002). Rates of appropriate dose intensification (82.6% vs 40.0%, P < 0.001), biomarker remission (faecal calprotectin P = 0.002), tight‐disease monitoring (84.1% vs 28.8%, P < 0.001) and treatment de‐escalation (21.3% vs 10.0%, P = 0.027) also favoured the virtual clinic cohort. Conclusion This study favoured a virtual clinic‐led model‐of‐care over standard outpatient care in facilitating treatment success as part of an effective treat‐to‐target approach in Crohn's disease. A virtual clinic model‐of‐care also improved treatment outcomes and quality of use of intensified anti‐TNF therapy through processes that promoted appropriate dose intensification and tight‐disease monitoring, while encouraging more frequent dose de‐escalation.