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Departments of *Anesthesia and
General Practice Medicine, Ullevaal University Hospital, Oslo, Norway
Address correspondence to Johan C. Ræder, MD, PhD, Department of Anaesthesia, Ullevaal University Hospital, N-0407 Oslo. Address e-mail to johan.rader{at}ioks.uio.no
| Introduction |
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The aim of this study was to compare ibuprofen with codeine/acetaminophen for pain control during the first 72 h after ambulatory surgery.
| Methods |
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After IV premedication with 12 mg midazolam, anesthesia was induced with fentanyl 1.5 µg/kg IV and a propofol target control infusion of 4 µg/mL IV. Anesthesia was maintained with a propofol target control infusion of 2.02.5 µg/mL, 66% nitrous oxide in oxygen, and alfentanil 10 µg/kg IV as needed. The patients had spontaneous or assisted ventilation with a laryngeal mask airway with standard intraoperative monitoring. Before the end of the anesthesia, all patients received ketorolac 30 mg IV in addition to local anesthesia with 1020 mL of lidocaine 10 mg/mL at the incision site and paracetamol 1 g rectally. On the recovery ward, the patients received fentanyl 0.5 µg/kg IV for pain control and metoclopramide 10 mg for nausea. According to a double-blinded, randomized study design, the patients received identical-appearing tablets for analgesia at home; these tablets contained either ibuprofen 800 mg or paracetamol 800 mg and codeine 60 mg and were to be taken three times a day for 3 days.
The patients received a written questionnaire, which was to be completed 24 and 72 h after surgery, about their pain experience, general functioning, and side effects. The patients were asked to grade their pain experience from 1 (no pain) to 10 (worst pain possible); average pain and worst pain experienced; and pain during defecating, sitting, coughing, and moving. The patients were asked about their general functioning at home (1 = all their time in bed to 5 = full normal activity) and whether the global experience of the postoperative period was worse, similar, or better compared with what they had expected. The patients were also asked specifically about side effects such as nausea, vomiting, dizziness, constipation (i.e., absence of defecation), nightmares, or anxiety.
The two groups were compared with Students t-test for parametric variables and the Mann-Whitney U-test or
2 test for nonparametric variables, with P values < 0.05 considered statistically significant.
| Results |
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There was no statistically significant difference between the two groups with respect to pain control during the 3-day postoperative observation period (Table 1). There were no significant differences between the groups in postoperative side effects except for significantly more constipation (i.e., absence of defecation) in the Paracetamol plus Codeine patients, both at Day 1 and Day 3 (Table 2). At 72 h after surgery, significantly more patients in the Ibuprofen group rated the global postoperative experience as better than expected (Table 2).
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| Discussion |
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An important issue is whether the results are applicable to a wider population of outpatients with postoperative pain. In our study, 6.4% of the patients declined to participate in the study because they had had a previous bad experience (i.e., side effects) with paracetamol plus codeine medication. It is interesting to note that more patients in the Ibuprofen group experienced nausea in the recovery ward before receiving any study medication. It would seem that short-term treatment with NSAID is relatively free of side effects unless there is a preexisting contraindication to using these nonopioid analgesic drugs (5,6). The most significant side effect in this study was constipation resulting from codeine. This complication may add to the patients feeling of discomfort and explain why the total experience was significantly better in the ibuprofen-treated patients.
In conclusion, oral ibuprofen 800 mg is equianalgesic to paracetamol 800 mg plus codeine 60 mg when given every eight hours for three days after ambulatory surgery. Use of ibuprofen also results in better global satisfaction and significantly less constipation.
| Acknowledgments |
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| References |
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