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Department of Anesthesiology, Baystate Medical Center, Springfield, Massachussetts; and *New England Orthopedic Surgeons, P.C., Baystate Medical Center, Springfield, Massachussetts
Address correspondence and reprint requests to Scott S. Reuben, MD, Department of Anesthesiology, Baystate Medical Center, 759 Chestnut Street, Springfield, MA 01199. Address e-mail to scott.reuben{at}bhs.org
| Abstract |
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IMPLICATIONS: The administration of rofecoxib 50 mg before arthroscopic knee surgery provides a longer duration of analgesia, less 24-h opioid use, and lower pain scores than administering the drug after the completion of surgery.
| Introduction |
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Clinical evidence suggests that surgical trauma may induce prolonged changes in both the peripheral and central nervous systems that together amplify postoperative pain (10). Surgical trauma results in the induction of cyclooxygenase-2 (COX-2), leading to the release of prostaglandins, which sensitize peripheral nociceptors and produce localized hyperalgesia (primary hyperalgesia) (11). In addition, the resultant increase in the excitability of spinal neurons (central sensitization) may produce pain hypersensitivity in the surrounding uninjured tissue (secondary hyperalgesia) (10). Therefore, administering NSAIDs before surgical trauma may be more effective in preventing the development of both peripheral and central sensitization after arthroscopic knee surgery. Although NSAIDs have been administered in either the pre- or postoperative period, no study has examined a NSAID regimen given preoperatively compared with the same dose administered postoperatively to patients undergoing ambulatory knee arthroscopy.
Rofecoxib, an oral COX-2 inhibitor, is effective when administered before major orthopedic surgery (12). The goal of our study was to evaluate the analgesic efficacy of administering rofecoxib either pre- or postoperatively to patients undergoing ambulatory arthroscopic meniscectomy.
| Materials and Methods |
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Postoperative pain was assessed using an 11-point verbal analog pain score, with 0 corresponding to "no pain" and 10 to "the worst imaginable pain." Pain scores were recorded both at rest and with movement at 1, 2, and 24 h after the completion of surgery. Pain scores with movement were recorded immediately after the patient actively flexed the operative knee to 90°. Patients were instructed to take 12 acetaminophen 325 mg/oxycodone 5 mg tablets every 3 h as needed for a verbal analog pain score
3 while at home. When contacted by telephone at 24 h, patients were asked about their time to first analgesic use as well as their 24-h total requirement. Analgesic duration was defined as the time from completion of surgery until the first request for acetaminophen/oxycodone. Patients were discharged from the hospital when they were oriented to time and place, were able to void, had stable vital signs, and could ambulate with the assistance of crutches. Discharge time was classified as the time from the end of surgery until the patients were able to meet the discharge criteria.
Demographic data and times (duration of procedure, time to discharge, and analgesic duration) were assessed by analysis of the variance. Pain scores and amount of postoperative analgesics were analyzed by the Kruskal-Wallis test. If a significant result was obtained, the Mann-Whitney U-test was performed to determine between which groups there was significance; a Bonferroni adjustment was made for multiple comparisons. Significance was determined at the P < 0.05 level. Initial sample size estimation showed that 20 patients should be included in each group to ensure a power of 0.90 to detect a clinically relevant minimal 33% increase in analgesic duration. Using pooled data from our previous arthroscopic meniscectomy studies (12), yielding a mean analgesic duration of 300 min with a standard deviation of 90 min, an
error of 0.05 was used for this study. Data are presented as mean ± SD.
| Results |
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The 24-h consumption of acetaminophen/oxycodone tablets was also significantly different among the three groups (P < 0.001). Patients in the Preincisional rofecoxib group required fewer acetaminophen/oxycodone tablets (1.5 ± 0.6) compared with the Postincisional rofecoxib (3.3 ± 1.3) or the Control (5.5 ± 1.6) groups. In addition, more patients in the Preincisional rofecoxib group (7/20, 35%) reported not using opioid analgesics in the 24-h postoperative period compared with either the Postincisional rofecoxib (2/20, 10%) or Control (0/20, 0%) groups (P < 0.05).
| Discussion |
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The postoperative administration of NSAIDs can significantly decrease synovitis and effusion resulting in diminished pain and improved rate of recovery after arthroscopic knee surgery (13). In a randomized, double-blinded study of 139 patients undergoing arthroscopic meniscectomy, Ogilvie-Harris et al. (1) reported more rapid return of movement and quadriceps function with less time to return to work and sport when a NSAID was administered after surgery. In contrast to the administration of NSAIDs after surgery, the administration of NSAIDs before surgery may be more effective. Operative procedures produce an initial afferent barrage of pain signals and generate a secondary inflammatory response, both of which contribute substantially to postoperative pain. The signals have the capacity to initiate prolonged changes in both the peripheral and the central nervous system that will lead to the amplification and prolongation of postoperative pain (10). Peripheral sensitization, a reduction in the threshold of nociceptor afferent peripheral terminals, is a result of inflammation at the site of surgical trauma (19). Central sensitization, an activity-dependent increase in the excitability of spinal neurons, is a result of persistent exposure to nociceptive afferent input from the peripheral neurons (20). Taken together, these two processes contribute to the postoperative hypersensitivity state ("spinal wind-up") that is responsible for a decrease in the pain threshold, both at the site of injury (primary hyperalgesia) and in the surrounding uninjured tissue (secondary hyperalgesia) (10). Therefore, by administering an analgesic before surgical stimulus, the development of pain hypersensitivity may be reduced or abolished, resulting in less postoperative pain.
The preemptive analgesic effect of NSAIDs has been previously studied after a wide variety of surgical procedures demonstrating equivocal results (10,21). Unfortunately, many methodological problems have been encountered in these studies. Many clinical investigations have compared a NSAID regimen administered before surgery with no intervention at all. This merely represents an enhanced analgesic effect in the treatment group. This methodological flaw was evident in the only three clinical studies (68) that examined a preemptive analgesic effect of NSAIDs after arthroscopic knee surgery. In contrast, our study is the first clinical investigation to examine the analgesic effects of administering the same dose of a NSAID either before or after arthroscopic knee surgery.
The results of our study demonstrate that a single dose of 50 mg rofecoxib is more effective in reducing postoperative pain and analgesic use after arthroscopic meniscectomy in the pre- rather than the postoperative period. This was evidenced by a longer analgesic duration as well as a smaller consumption of acetaminophen/oxycodone tablets during the first 24 h after surgery in the Preincisional group. In addition, pain scores with movement were significantly lower at 1, 2, and 24 h postoperatively in those patients receiving preemptive rofecoxib.
The results of our study contribute to the debate over the analgesic efficacy of preemptive NSAID administration. Many studies that have failed to demonstrate a preemptive analgesic effect may be attributed to either insufficient perioperative nociceptive afferent blockade or the development of central sensitization once the pharmacological action of the preemptive analgesic has worn off (22). For these reasons it may be more important to administer analgesics whose duration of action extends well into the postoperative period (23). Perhaps the combination of rofecoxib, a long-acting NSAID, with bupivacaine, a long-acting local anesthetic, more effectively prevented the development of central sensitization by reducing the afferent barrage of pain signals from reaching the spinal cord for a prolonged period of time. This may have been the reason for the improved analgesic effects observed in our study, in contrast to the lack of clinically significant effects found in other studies using preemptive NSAIDs. A recent review (21) of 18 randomized, single- or double-blinded studies that used a NSAID as the target intervention revealed that only six studies (33%) demonstrated a preemptive analgesic effect. Furthermore, the beneficial effects of preemptive NSAIDs observed in most studies were minimal. Interestingly, two studies (24,25) that demon-strated a significant preemptive analgesic effect used tenoxicam, a long-acting NSAID, with bupivacaine for wound infiltration in patients undergoing a procedure of short duration (breast biopsy) involving primarily somatic afferent pain transmission. The similarities in study design may explain the impressive preemptive analgesic effects observed in both our study and those involving breast biopsy (24,25).
The administration of rofecoxib possesses a more favorable pharmacokinetic profile than other NSAIDs administered orally during the preoperative period. Unlike conventional NSAIDs, rofecoxib may be administered without food to the fasting preoperative patient (26). This NSAID provides onset of clinical analgesia within 27 minutes (27), and with an elimination half-life of 17.5 hours, rofecoxib needs to be dosed only once daily (26). Although the preoperative administration of nonspecific NSAIDs may provide effective analgesia, their ability to decrease platelet aggregation and increase bleeding time (28) may increase the risk of perioperative bleeding (29,30). We have observed increased perioperative bleeding with the preemptive administration of ibuprofen for ambulatory arthroscopic anterior cruciate ligament reconstruction and have since discontinued its use (31). Because rofecoxib has no effect on platelet aggregation or bleeding time, even in doses of 1000 mg per day (32), it may be a safer preemptive analgesic. We have previously demonstrated that the perioperative administration of rofecoxib resulted in no significant increase in the incidence of perioperative bleeding when administered either before spinal fusion surgery (12) or total joint arthroplasty (33).
In conclusion, rofecoxib provides effective postoperative analgesia for arthroscopic meniscectomy. Further, the administration of rofecoxib 50 mg before surgery provides a longer duration of postoperative analgesia, less 24-h opioid use, and lower incidental pain scores compared with administering the drug after the completion of surgery.
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