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JBJS - 2026-04-21 - Journal Article

Effectiveness of Intraosseous Morphine for Pain Control in Total Knee Arthroplasty: A Double-Blinded, Randomized Trial.

Pekas DR, Adrados M, Lee MM, Lee Y, Burks WG, Martino JM, Coobs BR, Moskal JT

RCTLOE In = 88 (enrolled 100, analyzed 88)14 days postoperative

Topics

arthroplasty
PMID: 42013190DOI: 10.2106/JBJS.25.01037View on PubMed ->

Key Takeaway

Intraoperative intraosseous morphine (10 mg) added to a multimodal protocol including spinal anesthesia and adductor canal block produced no reduction in pain scores or MME consumption at any point over 14 days post-TKA (p=0.969 for pain, p=0.377 for MME).

Summary Depth

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Summary

This double-blinded RCT tested whether adding 10 mg IO morphine to a standardized multimodal protocol (spinal anesthesia, IV sedation, adductor canal block) reduced pain or opioid consumption after primary TKA. Eighty-eight patients were randomized to IO morphine plus vancomycin versus vancomycin alone, with outcomes collected via twice-daily text surveys over 14 days. Linear mixed-effects modeling showed no between-group differences in daily pain scores (p=0.969), daily MME (p=0.377), or total/weekly MME (p≥0.878) at any postoperative time point.

Key Limitation

The study was conducted at a single institution with a highly standardized background protocol (spinal + adductor canal block), limiting generalizability to centers using general anesthesia or without routine regional nerve blocks where IO morphine's marginal effect might differ.

Original Abstract

BACKGROUND

Effective pain management following total knee arthroplasty (TKA) is crucial to optimizing patient outcomes and experiences. Multimodal pain management protocols vary between institutions, with some recently proposing the addition of an intraosseous (IO) injection of morphine intraoperatively. The purpose of this study was to investigate whether the addition of an intraoperative, IO injection of morphine during elective primary TKA would lead to improved pain control and decreased narcotic consumption during the postoperative period.

METHODS

In this double-blinded, randomized controlled trial, 100 patients undergoing elective primary TKA were prospectively enrolled. All patients received spinal anesthesia and intravenous sedation combined with an intraoperative, surgeon-administered adductor canal block. The experimental group received an intraoperative, IO injection containing 10 mg of morphine and 500 mg of vancomycin in 110 mL of normal saline solution. The control group received the same injection but without morphine. All patients received 6 daily text-message surveys (3 in the morning and 3 in the evening) for 14 days postoperatively to collect pain scores, morphine milligram equivalent (MME) consumption, and nausea and vomiting events. Data on demographics, operative factors, post-anesthesia care unit (PACU) pain scores, PACU MME consumption, and patient-reported outcomes were also collected. Linear mixed-effects (LME) models were utilized.

RESULTS

A total of 88 patients (52.3% [n = 46] female; mean age, 69.1 ± 9.0 years [range, 46 to 89 years]; 89.8% [n = 79] White) were included in the analysis. The LME model demonstrated no differences between the groups with respect to daily pain scores at any time point within 14 days postoperatively (p = 0.969). There were no differences between the groups with respect to daily MME consumption at any time point within 14 days postoperatively (p = 0.377). There were also no differences in total MME consumption or weekly MME consumption postoperatively (p ≥ 0.878).

CONCLUSIONS

IO morphine did not significantly improve postoperative pain control or decrease narcotic consumption up to 2 weeks postoperatively among patients undergoing elective primary TKA.

LEVEL OF EVIDENCE

Therapeutic Level I. See Instructions for Authors for a complete description of levels of evidence.