Near-fatal outcome after administration of hyoscine-N-butylbromide (Buscopan®)

dc.contributor.authorMilner, A.
dc.date.accessioned2010-10-27T13:58:45Z
dc.date.available2010-10-27T13:58:45Z
dc.date.issued2010-08
dc.description.abstractWhile undergoing conscious sedation for a gastroscopy, an 18-year-old female developed severe hypotension and loss of consciousness. This occurred shortly after an intravenous dose of hyoscine-N-butylbromide (Buscopan®). Resuscitation was performed over a period of 10 minutes and was successful. Once conscious, the patient complained of severe lower abdominal pain. Except for a signi cant metabolic acidosis (BE = -10), initial investigations were negative. She was transferred to the Intensive Care Unit (ICU) where the abdominal pain continued and the urine output was scanty for the rst 12 hours. Investigations were done to exclude: anaphylaxis, mesenteric ischaemia, angioneurotic oedema, pregnancy, porphyria, autoimmune disease and myocardial ischaemia. Finally it was postulated that the drug had either caused an anaphylactoid reaction or grossly augmented cardiovagal nervous inhibition. This resulted in hypotension which caused mesenteric ischaemia that in turn resulted in severe abdominal pain and a degree of renal shutdown.en_US
dc.identifier.citationMilner, A 2010, 'Near-fatal outcome after administration of hyoscine-N-butylbromide (Buscopan®)', Southern African Journal of Anaesthesia and Analgesia, vol. 16, no. 4, pp. 38-41. [http://www.sajaa.co.za/index.php/sajaa]en_US
dc.identifier.issn1027-9148
dc.identifier.urihttp://hdl.handle.net/2263/15100
dc.language.isoenen_US
dc.publisherOpenJournals Publishingen_US
dc.rightsThis work is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 2.5 South Africa License.en_US
dc.subjectAnaphylaxisen_US
dc.subjectAngioneurotic oedemaen_US
dc.subjectHyoscine-N-butylbromideen_US
dc.subjectPorphyriaen_US
dc.titleNear-fatal outcome after administration of hyoscine-N-butylbromide (Buscopan®)en_US
dc.typeArticleen_US

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