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Morphine after anterior cruciate ligament reconstruction: pain reduction did not exceed the MCID
What it means for practice
When considering morphine as an addition to multimodal analgesia, note that lower pain scores were statistically significant, but the mean difference did not exceed the minimal clinically important difference.
Summary
A retrospective analysis of prospectively collected data at a sports surgery center compared two analgesic protocols after primary isolated anterior cruciate ligament reconstruction. Each matched group included 556 patients. The opioid group received oral morphine sulfate as needed in addition to multimodal analgesia; the non-opioid group received multimodal analgesia alone. Listed components of multimodal analgesia included paracetamol, nefopam, and ketoprofen.
Key findings
Adding morphine was associated with lower pain scores during the first 3 postoperative days. On day 0, visual analogue scale (VAS) scores were 5.6 ± 2.7 in the non-opioid group (n = 536/556) versus 5.3 ± 2.7 in the opioid group (n = 522/556; p = 0.0339). On day 1, the corresponding values were 5.2 ± 2.4 (n = 545/556) and 4.8 ± 2.4 (n = 543/556; p = 0.0014).
Dizziness on day 0 was more frequent without morphine: 100/536 patients (18.7%) versus 70/522 (13.4%; p = 0.0236). There was a trend toward more complications in the non-opioid group: 11/556 (2.0%) versus 3/556 (0.5%; p = 0.0558), mainly due to Cyclops syndrome and knee stiffness. Reoperation rates were similar (p > 0.05).
Clinical relevance
Despite statistical significance, the mean difference in VAS scores did not exceed the minimal clinically important difference (MCID). Lower pain scores therefore should not be equated with an established clinically important benefit from adding morphine.
Source
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Moussa MK, Mrabet F, Valentin E, et al. Impact of Morphine on Early Recovery After Anterior Cruciate Ligament Reconstruction: A Case-Control Study. Cureus. 2026;18(9):e117127. doi:10.7759/cureus.117127
PubMed 42959591 DOI 10.7759/cureus.117127 Original: pubmed.ncbi.nlm.nih.gov
Reviewed by: DrugCard editorial team ·
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