Intrathecal Morphine for Analgesia in Minimally Invasive Cardiac Surgery: A Randomized, Placebo-controlled, Double-blinded Clinical Trial

被引:25
作者
Dhawan, Richa [1 ]
Daubenspeck, Danisa [1 ]
Wroblewski, Kristen E. [3 ]
Harrison, John-Henry [4 ]
McCrorey, Mackenzie [2 ]
Balkhy, Husam H. [2 ]
Chaney, Mark A. [1 ]
机构
[1] Univ Chicago Med, Dept Anesthesia & Crit Care, 5841 South Maryland Ave,MC 4028, Chicago, IL 60637 USA
[2] Univ Chicago Med, Dept Cardiothorac Surg, Chicago, IL USA
[3] Univ Chicago, Dept Publ Hlth Sci, Chicago, IL USA
[4] Univ Wisconsin, Dept Anesthesiol, Sch Med & Publ Hlth, Madison, WI USA
关键词
POSTOPERATIVE PAIN; ENHANCED RECOVERY; ANESTHESIA; BLOCK; MANAGEMENT; METAANALYSIS; EFFICACY; NERVE;
D O I
10.1097/ALN.0000000000003963
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Background: Intrathecal morphine decreases postoperative pain in standard cardiac surgery. Its safety and effectiveness have not been adequately evaluated in minimally invasive cardiac surgery. The authors hypothesized that intrathecal morphine would decrease postoperative morphine consumption after minimally invasive cardiac surgery. Methods: In this randomized, placebo-controlled, double-blinded clinical trial, patients undergoing robotic totally endoscopic coronary artery bypass received either intrathecal morphine (5 mcg/kg) or intrathecal saline before surgery. The primary outcome was postoperative morphine equivalent consumption in the first 24 h after surgery; secondary outcomes included pain scores, side effects, and patient satisfaction. Pain was assessed via visual analog scale at 1, 2, 6, 12, 24, and 48 h after intensive care unit arrival. Opioid-related side effects (nausea/vomiting, pruritus, urinary retention, respiratory depression) were assessed daily. Patient satisfaction was evaluated with the Revised American Pain Society Outcome Questionnaire. Results: Seventy-nine patients were randomized to receive intrathecal morphine (n = 37) or intrathecal placebo (n = 42), with 70 analyzed (morphine 33, placebo 37). Intrathecal morphine patients required significantly less median (25th to 75th percentile) morphine equivalents compared to placebo during first postoperative 24 h (28 [16 to 46] mg vs. 59 [41 to 79] mg; difference, -28 [95% CI, -40 to -18]; P < 0.001) and second postoperative 24 h (0 [0 to 2] mg vs. 5 [0 to 6] mg; difference, -3.3 [95% CI, -5 to 0]; P < 0.001), exhibited significantly lower visual analog scale pain scores at rest and cough at all postoperative timepoints (overall treatment effect, -4.1 [95% CI, -4.9 to -3.3] and -4.7 [95% CI, -5.5 to -3.9], respectively; P < 0.001), and percent time in severe pain (10 [0 to 40] vs. 40 [20 to 70]; P = 0.003) during the postoperative period. Mild nausea was more common in the intrathecal morphine group (36% vs. 8%; P = 0.004). Conclusions: When given before induction of anesthesia for totally endoscopic coronary artery bypass, intrathecal morphine decreases use of postoperative opioids and produces significant postoperative analgesia for 48 h.
引用
收藏
页码:864 / 876
页数:13
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