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1 Department of Gastrointestinal Science, University of Manchester, Manchester, United Kingdom
2 Gastrointestinal Research Unit, University Medical Centre, Utrecht, Netherlands
* To whom correspondence should be addressed. E-mail: lou.harris{at}manchester.ac.uk.
Patients with functional gastrointestinal disorders often demonstrate abnormal visceral sensation. Currently, rectal sensation is assessed by manual balloon distension or barostat. However, neither test is adaptable for use in neurophysiological characterisation of visceral afferent pathways by sensory evoked potentials. The aim of this study was to assess reproducibility and quality of sensation evoked by electrical stimulation (ES) and rapid balloon distension (RBD) in anorectum and to apply the optimum stimulus to examine the visceral afferent pathway with rectal evoked potentials (REP). Healthy subjects (n=8, median age 33 years) were studied on three separate occasions. Variability, tolerance and stimulus characteristics were assessed with each technique. Overall ES consistently invoked pain and was chosen for measuring REP whereas RBD in all cases induced the strong urge to defecate. Rectal intra-class correlation coefficient (ICC) for ES and RBD (0.82 and 0.72 respectively) demonstrated good reproducibility at pain/maximum tolerated volume but not sensory threshold. Only sphincter ICC for ES at pain showed acceptable between study reproducibility (ICC 0.79). Within studies ICC was good (>0.6) for anorectal ES and RBD at both levels of sensation. All subjects reported significantly more unpleasantness during RBD than ES (P<0.01). This study demonstrates that ES and RBD are similarly reproducible. However, the sensations experienced with each technique differed markedly, probably reflecting differences in peripheral and/or central processing of the sensory input. This is of relevance in interpreting findings of neuroimaging studies of anorectal sensation and may provide insight into physiological characteristics of visceral afferent pathways in health and disease.
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