To assess the efficacy and safety of postoperative analgesia with continuous epidural sufentanil and bupivacaine, we performed a prospective study in 614 patients undergoing major surgery. Before surgical incision, all patients received an initial dose of 50 mu g sufentanil in 6-10 mL bupivacaine 0.125% via a lumbar or thoracic catheter. After 1 h, a continuous infusion was started with 50 mu g sufentanil in 50 mL bupivacaine 0.125% at a rate of 6-10 mL/h. The infusion was continued postoperatively for 1-5 days or longer, depending on the type of operation and the patient's analgesic need. In the majority of patients, adequate pain relief was obtained at rest and during movement. Late respiratory depression was observed in three patients; i...
The difference in analgesic activity following lumbar (group I) or thoracic (group II) epidural admi...
Thirty patients undergoing abdominal surgery were randomly assigned postoperatively into two groups ...
One hundred and twenty women undergoing gynaecological abdominal operations were randomized to recei...
To assess the efficacy and safety of postoperative analgesia with continuous epidural sufentanil and...
To assess the efficacy and safety of postoperative analgesia with continuous epidural sufentanil and...
We assessed the efficacy and side effects of postoperative analgesia with three different pain regim...
A prospective, randomised, double-blind study was conducted to compare the efficacy of two doses of ...
In the last decade, studies of quality of postoperative analgesia have yielded disturbing data: the ...
A double-blind randomised clinical trial was undertaken in 40 patients undergoing major abdominal su...
Few studies compare complications of continuous and bolus epidural analgesia. Ninety-eight postopera...
assess the efficacy of epidural sufentanil in providing per- and postoperative analgesia, 40 patient...
This study contrasts the efficacy and side effects of epidural clonidine and sufentanil in the perio...
Background. Ample evidence is now available showing the analgesic efficacy of a local anaestheric-op...
Background and aims: Postoperative pain is one of the most common problems after surgery, especially...
SummaryBackground and objectivesContinuous wound infusion has been investigated as a method of posto...
The difference in analgesic activity following lumbar (group I) or thoracic (group II) epidural admi...
Thirty patients undergoing abdominal surgery were randomly assigned postoperatively into two groups ...
One hundred and twenty women undergoing gynaecological abdominal operations were randomized to recei...
To assess the efficacy and safety of postoperative analgesia with continuous epidural sufentanil and...
To assess the efficacy and safety of postoperative analgesia with continuous epidural sufentanil and...
We assessed the efficacy and side effects of postoperative analgesia with three different pain regim...
A prospective, randomised, double-blind study was conducted to compare the efficacy of two doses of ...
In the last decade, studies of quality of postoperative analgesia have yielded disturbing data: the ...
A double-blind randomised clinical trial was undertaken in 40 patients undergoing major abdominal su...
Few studies compare complications of continuous and bolus epidural analgesia. Ninety-eight postopera...
assess the efficacy of epidural sufentanil in providing per- and postoperative analgesia, 40 patient...
This study contrasts the efficacy and side effects of epidural clonidine and sufentanil in the perio...
Background. Ample evidence is now available showing the analgesic efficacy of a local anaestheric-op...
Background and aims: Postoperative pain is one of the most common problems after surgery, especially...
SummaryBackground and objectivesContinuous wound infusion has been investigated as a method of posto...
The difference in analgesic activity following lumbar (group I) or thoracic (group II) epidural admi...
Thirty patients undergoing abdominal surgery were randomly assigned postoperatively into two groups ...
One hundred and twenty women undergoing gynaecological abdominal operations were randomized to recei...