Skip Navigation

This Article
Right arrow Full Text (PDF)
Right arrow E-Letters: Submit a response to the article
Right arrow Alert me when this article is cited
Right arrow Alert me when E-letters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (20)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by MOGENSEN, T.
Right arrow Articles by KEHLET, H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by MOGENSEN, T.
Right arrow Articles by KEHLET, H.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

British Journal of Anaesthesia, 1988, Vol. 60, No. 5 515-519
© 1988 The Board of Management and Trustees of the British Journal of Anaesthesia


research-article

UNPREDICTABILITY OF REGRESSION OF ANALGESIA DURING THE CONTINUOUS POSTOPERATIVE EXTRADURAL INFUSION OF BUPIVACAINE

T. MOGENSEN, M.D., N.-C. HJORTSØ, M.D., D. BIGLER, M.D., C. LUND, M.D. and H. KEHLET, M.D., PH.D.

Department of Anaesthesia, Hvidovre Hospital Copenhagen, Denmark
Department of Surgical Gastroenterology, Hvidovre Hospital Copenhagen, Denmark

Address for correspondence: Department of Anaesthesia, Hvidovre Hospital, DK-2650 Hvidovre, Denmark

Twenty-four otherwise healthy patients scheduled for elective major abdominal surgery received general anaesthesia plus lumbar extradural analgesia. A loading dose of 0.5% plain bupivacaine was given to produce sensory analgesia (pin prick) from T4 to S5 and followed by a continuous infusion of 0.5% plain bupivacaine 8 ml h–1. Pain, scored on a 5-point scale, and sensory analgesia were assessed hourly for 16 h after skin incision. If sensory analgesia decreased by more than 5 segments from its preoperative level, or if the pain score reached 2 (moderate pain), the patients were removed from the study, and pain was treated otherwise. Only three patients maintained their initial levels of sensory analgesia and a pain score of less than 2. In the remaining patients sensory analgesia decreased at least 5 segments or pain score reached 2 between 4 and 16h after skin incision. We found a weak correlation between increasing age and the duration of sensory analgesia (r=0.46, P<0.05), but no significant correlations between duration of sensory analgesia and sex, weight, height, body surface area, serum albumin concentration, duration or site of operation.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Br J AnaesthHome page
P. D. W. Fettes, C. S. Moore, J. B. Whiteside, G. A. Mcleod, and J. A. W. Wildsmith
Intermittent vs continuous administration of epidural ropivacaine with fentanyl for analgesia during labour
Br. J. Anaesth., September 1, 2006; 97(3): 359 - 364.
[Abstract] [Full Text] [PDF]


Home page
Br J AnaesthHome page
R. G. Wheatley, S. A. Schug, and D. Watson
Safety and efficacy of postoperative epidural analgesia
Br. J. Anaesth., July 1, 2001; 87(1): 47 - 61.
[Abstract] [Full Text] [PDF]


Home page
Anesth. Analg.Home page
D. J. Kopacz, N. E. Sharrock, and H. W. Allen
A Comparison of Levobupivacaine 0.125%, Fentanyl 4 {micro}g/mL, or Their Combination for Patient-Controlled Epidural Analgesia After Major Orthopedic Surgery
Anesth. Analg., December 1, 1999; 89(6): 1497 - 1497.
[Abstract] [Full Text] [PDF]


Home page
Arch OphthalmolHome page
J. P. Fezza, K. A. Klippenstein, and R. E. Wesley
Use of an Orbital Epidural Catheter to Control Pain After Orbital Implant Surgery
Arch Ophthalmol, June 1, 1999; 117(6): 784 - 788.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.