Volume 46, Issue 2 pp. 423-432
ORIGINAL COMMUNICATION

Exclusive enteral nutrition with oral polymeric diet helps in inducing clinical and biochemical remission in adults with active Crohn's disease

Pradeep Kakkadasam Ramaswamy DNB

Corresponding Author

Pradeep Kakkadasam Ramaswamy DNB

Department of Digestive Health, Gold Coast University Hospital, Gold Coast, Queensland, Australia

Correspondence

Pradeep Kakkadasam Ramaswamy, Department of Digestive Health, Gold Coast University Hospital, 1 Hospital Boulevard, Southport 4215, Queensland, Australia.

Email: [email protected]

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Gold Coast Inflammatory Bowel Diseases Research Group

Gold Coast Inflammatory Bowel Diseases Research Group

Department of Digestive Health, Gold Coast University Hospital, Gold Coast, Queensland, Australia

Department of Nutrition and Food Services, Gold Coast University Hospital, Gold Coast, Queensland, Australia

Faculty of Health Sciences and Medicine, Bond University, Gold Coast, Queensland, Australia

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First published: 07 October 2021
Citations: 2
This is a continuing education article. Please see https://aspen.digitellinc.com/aspen/publications/8/view

Abstract

Background and Aims

Exclusive enteral nutrition (EEN) is not routinely used as induction therapy for adults with active Crohn's disease (CD). The aim of this study was to assess the effectiveness of EEN with oral polymeric formula as an adjunct for inducing clinical and biochemical remission in adults with active CD.

Methods

We performed a retrospective analysis of data from January 2018 to September 2019 on all patients with active CD who commenced EEN. The primary end point (PE) was clinical remission (Crohn's Disease Activity Index [CDAI] ≤150) or response (100-point decrease in CDAI) at 8 weeks. The secondary end point (SE) was biochemical remission (C-reactive protein level ≤5 mg/L or feces calprotectin level ≤150 mcg/g) at 8 weeks in those whose baseline values were elevated. We also aimed to identify predictors of response to EEN therapy.

Results

Sixty-six patients commenced EEN; 53 (of 66; 80.3%) completed the prescribed EEN course. At 8 weeks, 42 (of 66; 63.6%) patients achieved the PE, and 30 (of 53; 56.6%) patients achieved the SE. Patients receiving EEN for ≥6 weeks achieved the PE (72% vs 47.8%; odds ratio [OR], 2.8; P = 0.047; CI, 0.97–8.16) and SE (67.6% vs 36.8%; OR, 3.58; P = 0.035; CI, 1.1–11.63) more frequently compared with patients who received EEN for <6 weeks. Nine patients reported adverse effects.

Conclusion

Polymeric EEN is well tolerated, safe, and effective in inducing clinical and biochemical remission in adults with active CD. EEN duration of ≥6 weeks has better outcomes.

CONFLICT OF INTEREST

None declared.

FUNDING INFORMATION

None declared.

DATA AVAILABILITY STATEMENT

The data underlying this article cannot be shared publicly because of our institutional policies. However, further information can be obtained from the corresponding author.