Evaluation of the anti-peristaltic effect of glucagon and hyoscine on the small bowel: comparison of intravenous and intramuscular drug administration

European Radiology - Tập 22 - Trang 1186-1194 - 2012
Andreas Gutzeit1,2, Christoph A. Binkert1, Dow-Mu Koh3, Klaus Hergan2, Constantin von Weymarn1, Nicole Graf4, Michael A. Patak5, Justus E. Roos1, Marcus Horstmann6, Sebastian Kos7, Simone Hungerbühler8, Johannes M. Froehlich1
1Department of Radiology, Cantonal Hospital Winterthur, Winterthur, Switzerland
2Department of Radiology, Paracelsus Medical University Salzburg, Salzburg, Austria
3Department of Radiology, Royal Marsden Hospital, Sutton, UK
4Clinical Trials Center, Center for Clinical Research, University Hospital Zurich, Zurich, Switzerland
5Department of Radiology, University Hospital Zürich, Zurich, Switzerland
6Department of Urology, Cantonal Hospital Winterthur, Winterthur, Switzerland
7Division of Interventional Radiology, Institute of Radiology and Nuclear Medicine, University Hospital Basel, Basel, Switzerland
8Department of Pharmacy, Cantonal Hospital Winterthur, Winterthur, Switzerland

Tóm tắt

To evaluate prospectively duration and effectiveness of aperistalsis achieved by glucagon(GLU) or hyoscine N-butylbromide(HBB) following various administration routes. Six volunteers underwent Magnetic Resonance Imaging (MRI) after standardized oral preparation in random order five separate MR examinations with both spasmolytic agents (HBB intravenous(i.v.) or intramuscular(i.m.), GLU i.v. or i.m., and a combined scheme). The MR protocol included a sagittal 2D cross-section of the small bowel with a temporal resolution of 0.55 s acquired over 60 to 90 min. To quantify bowel motility, small bowel cross-sectional areas were summated over time. The anti-peristaltic i.v. effects of HBB and glucagon started on average after 85 s/65 s and ended after 21 min/23.3 min, respectively. By comparison, the anti-peristaltic effects of i.m. HBB and glucagon started significantly later 5.1/11.6 min (P = 0.001; Wilcoxon signed ranks test) and lasted for 17.7/28.2 min with greater inter-individual differences (P = 0.012; Brown-Forsythe test). The combined scheme resulted in a rapid onset after 65 s with effect duration of 31 min. Anti-peristaltic effects on the small bowel are drug dependant, i.e., their onset is faster and more reliable when administering i.v. than i.m.. Combining i.v. GLU with i.m. HBB provides an early onset of effect, sustained spasmolysis and the highest degree of motility impairment. • Anti-persitaltic agents are widely used before various diagnostic procedures of the abdomen. • The combination of iv-glucagon with im-hyoscine provides reliable spasmolysis with early onset. • Intravenous spasmolysis is more reliable compared to intramuscular administration. • Intravenous glucagon has a prolonged spasmolytic effect compared to intravenous hyoscine.

Tài liệu tham khảo

Husebye E (1999) The patterns of small bowel motility: physiology and implications in organic disease and functional disorders. Neurogastroenterol Motil 11:141–161 Kozak RI, Bennett JD, Brown TC, Lee TY (1994) Reduction of bowel motion artifact during digital subtraction angiography: a comparison of hyoscine butylbromide and glucagon. Can Assoc Radiol J 45:209–211 Laniado M, Grönewäller E, Kopp AF et al (1997) The value of hyoscine butylbromide in abdominal MR imaging with and without oral magnetic particles. Abdom Imaging 22:381–388 Johnson W, Taylor MB, Carrington BM, Bonington SC, Swindell R (2007) The value of hyoscine butylbromide in pelvic MRI. Clin Radiol 62:1087–1093 Martí-Bonmatí L, Graells M, Ronchera-Oms CL (1996) Reduction of peristaltic artifacts on magnetic resonance imaging of the abdomen: a comparative evaluation of three drugs. Abdom Imaging 2:309–313 Wagner M, Klessen C, Rief M et al (2008) High-resolution T2-weighted abdominal magnetic resonance imaging using respiratory triggering: impact of butylscopolamine on image quality. Acta Radiol 49:376–382 Mayo KE, Miller LJ, Bataille D et al (2003) International Union of Pharmacology. XXXV. The glucagon receptor family. Pharmacol Rev 55:167–194 Dubé PE, Brubaker PL (2007) Frontiers in glucagon-like peptide-2: multiple actions, multiple mediators. Am J Physiol Endocrinol Metab 293:E460–E465 Tytgat GN (2008) Hyoscine butylbromide—a review on its parenteral use in acute abdominal spasm and as an aid in abdominal diagnostic and therapeutic procedures. Curr Med Res Opin 24:3159–3173 Huizinga JD, McKay CM, White EJ (2006) The many facets of intestinal peristalsis. Am J Physiol Gastrointest Liver Physiol 290:G1347–G1349 Stone AJ, Browne JE, Lennon B, Meaney JF, Fagan AJ (2011) Stone Quantification of accuracy of ADC measurements from Whole-body DWIBS. Proc Intl Soc Mag Reson Med 19:836 Rowland-Hill CA, Loveday EJ, Thomas ML (1989) A comparison of the value of hyoscine butylbromide and glucagon on aorto iliac intravenous digital subtraction. Vasa 18:301–303 Rogalla P, Lembcke A, Rückert JC et al (2005) Spasmolysis at CT colonography: butyl scopolamine versus glucagon. Radiology 236:184–188 Gutzeit A, Patak MA, von Weymarn C et al (2010) Feasibility of small bowel flow rate measurement with MRI. J Magn Reson Imaging 32:345–351 Froehlich JM, Daenzer M, von Weymarn C et al (2009) Aperistaltic effect of hyoscine N-butylbromide versus glucagon on the small bowel assessed by magnetic resonance imaging. Eur Radiol 19:1387–1393 Froehlich JM, Patak MA, von Weymarn C, Juli CF, Zollikofer CL, Wentz KU (2005) Small bowel motility assessment with magnetic resonance imaging. J Magn Reson Imaging 21:370–375 Wakamiya M, Furukawa A, Kanasaki S, Murata K (2011) Assessment of small bowel motility function with cine-MRI using balanced steady-state free precession sequence. J Magn Reson Imaging 33:1235–1240