Opioid-sparing PCA non-inferior to opioid PCA for pain after total knee arthroplasty
This randomized controlled trial compared two patient-controlled analgesia (PCA) regimens for postoperative pain in 98 patients undergoing total knee arthroplasty under spinal anesthesia. The intervention was an opioid-sparing PCA (continuous infusion of 150 mg ketorolac tromethamine and 100 mg nefopam hydrochloride, plus patient-controlled boluses of 300 μg fentanyl). The comparator was an opioid-based PCA (continuous infusion of 1200 μg fentanyl, plus patient-controlled boluses of 300 μg fentanyl).
The primary outcome was the visual analog scale (VAS) pain score at rest on postoperative day (POD) 1. The mean VAS score was 5.45 ± 2.48 in the opioid-based group and 5.90 ± 2.31 in the opioid-sparing group, a mean difference of 0.45 points (95% CI, -0.36 to 1.25). This met the prespecified non-inferiority margin of 1.5 points. A key secondary outcome was rescue analgesic requirements on POD 2, which were significantly reduced in the opioid-sparing group (P = 0.006).
Regarding safety, nausea and vomiting on POD 1 occurred in 34.7% of the opioid-based group versus 12.2% of the opioid-sparing group. The study did not report on serious adverse events, discontinuations, or long-term tolerability. Key limitations include the short follow-up (PODs 1 and 2), lack of reporting on specific mobility results or serious adverse events, and the non-inferiority margin of 1.5 points on the VAS scale. The findings suggest this specific opioid-sparing PCA regimen may be a viable short-term option for managing acute postoperative pain with a potentially better gastrointestinal side effect profile, but its practice relevance is limited by the short observation period and lack of data on critical outcomes like serious adverse events.