Abstract

ObjectivesTo compare the distention quality and patient experience of oral mannitol and polyethylene glycol (PEG) for MRE.MethodsThis study is a retrospective, observational study of a subset of patients enrolled in a multicentre, prospective trial evaluating the diagnostic accuracy of MRE for small bowel Crohn’s. Overall and segmental MRE small bowel distention, from 105 patients (64 F, mean age 37) was scored from 0 = poor to 4 = excellent by two experienced observers (68 [65%] mannitol and 37 [35%] PEG). Additionally, 130 patients (77 F, mean age 34) completed a questionnaire rating tolerability of various symptoms immediately and 2 days after MRE (85 [65%] receiving mannitol 45 [35%] receiving PEG). Distension was compared between agents and between those ingesting ≤ 1 L or > 1 L of mannitol using the test of proportions. Tolerability grades were collapsed into “very tolerable,” “moderately tolerable,” and “not tolerable.”ResultsPer patient distension quality was similar between agents (“excellent” or “good” in 54% [37/68] versus 46% [17/37]) with mannitol and PEG respectively. Jejunal distension was significantly better with mannitol compared to PEG (40% [27/68] versus 14% [5/37] rated as excellent or good respectively). There was no significant difference according to the volume of mannitol ingested. Symptom tolerability was comparable between agents, although fullness following MRE was graded as “very tolerable” in 27% (12/45) of patients ingesting PEG, verses 44% (37/84) ingesting mannitol, difference 17% (95% CI 0.6 to 34%).ConclusionMannitol-based solutions and PEG generally achieve comparable distension quality and side effect profiles, although jejunal distension is better quality with mannitol. Neither distension quality nor side-effect profile is altered by ingestion of more than 1 L of mannitol.Key Points• Mannitol-based and PEG-based oral preparation agents generally achieve comparable distension quality for MRE with the exception of the jejunum which is better distended with mannitol.• Mannitol-based and PEG-based oral preparation agents used for MRE have similar side effect profiles.• Neither distension quality nor side-effect profile is altered by ingestion of more than 1 L of mannitol.

Highlights

  • Cross-sectional imaging is sensitive and specific for diagnosing and staging small bowel Crohn’s disease (CD)

  • This study was conducted as a pre-specified sub-study of a larger multi-centre, prospective cohort trial investigating the sensitivity of Magnetic resonance enterography (MRE) and small bowel ultrasound (SBU) (METRIC Trial)

  • We conducted a large multi-centre, prospective diagnostic accuracy trial investigating the sensitivity of MRE and SBU (METRIC trial) [1]

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Summary

Introduction

Cross-sectional imaging is sensitive and specific for diagnosing and staging small bowel Crohn’s disease (CD). Magnetic resonance enterography (MRE) has the advantage of not exposing patients to ionising radiation [1]. It relies upon the combination of good small bowel distension and multi-parametric sequences to accurately identify disease and phenotype as either predominantly inflammatory or fibrostenotic [2, 3]. Distension is influenced by the type and volume of oral preparation agent ingested and a variety of protocols are used clinically [4–7]. A recent literature review by the European Society of Gastrointestinal and Abdominal Radiology (ESGAR) found no evidence for the superiority of one oral preparation over another and made no specific recommendation on either the optimal agent nor ingested volume [8]

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