Literature DB >> 8737758

Adverse events with continuous doxapram infusion against late postoperative hypoxaemia.

J Rosenberg1, P A Kristensen, M H Pedersen, H Overgaard.   

Abstract

OBJECTIVE: A randomized double-blind controlled trial of doxapram versus placebo against late postoperative hypoxaemia was planned to include 40 patients (2 x 20).
RESULTS: After inclusion of 18 patients a serious adverse event was encountered with development of a brain stem infarction in a 90-year-old woman receiving doxapram. At this point the randomization code was broken and we decided to terminate the trial. Three of nine patients receiving doxapram had had an adverse event whereas none of the patients receiving placebo had adverse events (P = 0.2). In the 18 patients studied, there was an insignificant trend towards higher mean oxygen saturation in the doxapram group, and a significantly higher minimum oxygen saturation and reduced number of hypoxaemic events on the first postoperative night.
CONCLUSION: Although these preliminary data on the effect of doxapram on postoperative hypoxaemia seem promising, further studies on the effect of continuous nocturnal postoperative doxapram infusion on levels of arterial oxygen saturation should be postponed until more knowledge about the pharmacokinetics of doxapram in this particular clinical situation has been gathered.

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Year:  1996        PMID: 8737758     DOI: 10.1007/s002280050091

Source DB:  PubMed          Journal:  Eur J Clin Pharmacol        ISSN: 0031-6970            Impact factor:   2.953


  1 in total

1.  Doxapram hastens the recovery following total intravenous anesthesia with dexmedetomidine, propofol and remifentanil.

Authors:  Huan-Liang Wang; Shu-Hai Tang; Xue-Qin Wang; Wen-Hua Gong; Xiao-Mei Liu; Wei-Fu Lei
Journal:  Exp Ther Med       Date:  2015-02-02       Impact factor: 2.447

  1 in total

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