bupivacaine

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Reactions 455 - 12 Jun 1993 Bupivacaine First report of cholestasis after interpleural administration: 3 case reports Elevation of liver enzyme levels occurred in 3 women, aged 32, 55 and 44 years, after they received bupivacaine via a right- sided interpleural catheter for the treatment of chronic arm pain. All patients received 6 or 7 doses of 0.5% bupivacaine 30ml over a 2-week period. In two of the women, jaundice and fever were present. Leucopenia and eosinophilia were also present, respectively. Liver aspiration cytology revealed toxic cholestasis in both women. Liver enzyme levels returned to normal within 1 and 2 months, respectively. Liver enzyme elevation was asymptomatic in the third woman. Author comment: Although other published reports of cholestasis with bupivacaine could not be found, there have been anecdotal reports of hepatic adverse effects with the drug, and a single case of jaundice after interpleural bupivacaine. The manufacturer claims that there were no reports of liver damage with bupivacaine in animal studies. ‘The scarcity of reports is puzzling in view of our experience, with cholestasis occurring in 3 of 10 treated cases (of arm pain) .. We recommend prudent monitoring of liver enzymes when repeated doses of interpleural bupivacaine are given for pain relief, especially when the right pleural cavity is used.’ Billstr¨ om R, et al. Cholestasis after interpleural bupivacaine for chronic upper limb pain. Anesthesia and Analgesia 76: 1158-1159, May 1993 - Sweden 800200163 1 Reactions 12 Jun 1993 No. 455 0114-9954/10/0455-0001/$14.95 Adis © 2010 Springer International Publishing AG. All rights reserved

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Page 1: Bupivacaine

Reactions 455 - 12 Jun 1993

★Bupivacaine

First report of cholestasis after interpleuraladministration: 3 case reports

Elevation of liver enzyme levels occurred in 3 women, aged32, 55 and 44 years, after they received bupivacaine via a right-sided interpleural catheter for the treatment of chronic armpain. All patients received 6 or 7 doses of 0.5% bupivacaine30ml over a 2-week period. In two of the women, jaundice andfever were present. Leucopenia and eosinophilia were alsopresent, respectively. Liver aspiration cytology revealed toxiccholestasis in both women. Liver enzyme levels returned tonormal within 1 and 2 months, respectively. Liver enzymeelevation was asymptomatic in the third woman.

Author comment: Although other published reports ofcholestasis with bupivacaine could not be found, there havebeen anecdotal reports of hepatic adverse effects with thedrug, and a single case of jaundice after interpleuralbupivacaine. The manufacturer claims that there were noreports of liver damage with bupivacaine in animal studies.‘The scarcity of reports is puzzling in view of our experience,with cholestasis occurring in 3 of 10 treated cases (of arm pain).. We recommend prudent monitoring of liver enzymes whenrepeated doses of interpleural bupivacaine are given for painrelief, especially when the right pleural cavity is used.’Billstrom R, et al. Cholestasis after interpleural bupivacaine for chronic upper limbpain. Anesthesia and Analgesia 76: 1158-1159, May 1993 - Sweden 800200163

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Reactions 12 Jun 1993 No. 4550114-9954/10/0455-0001/$14.95 Adis © 2010 Springer International Publishing AG. All rights reserved