| Literature DB >> 1599064 |
Abstract
A patient received a massive overdose of papaveretum intravenously (estimated to be 180 mg) when the glass syringe of a patient-controlled analgesia machine disengaged from the drive mechanism. She was successfully resuscitated. The pump, on loan from the supplier, had passed a brief evaluation by the infusion pump test house designated by the Medical Devices Directorate of the Department of Health; it has since been withdrawn. It is recommended that patient-controlled analgesia equipment should be placed at or below patient heart level. The Department of Health is called on to institute a full, independent evaluation scheme for patient-controlled analgesia equipment.Entities:
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Year: 1992 PMID: 1599064 DOI: 10.1111/j.1365-2044.1992.tb02221.x
Source DB: PubMed Journal: Anaesthesia ISSN: 0003-2409 Impact factor: 6.955