Continuous Erector Spinae Plane Blocks to Treat Pain after Percutaneous Nephrolithotomy: A Randomized, Triple-masked, Placebo-controlled Clinical Trial

医学 麻醉 布比卡因 局部麻醉剂 安慰剂 羟考酮 导管 外科 丸(消化) 生理盐水 临床试验 类阿片 经皮 芬太尼 局部麻醉 罗哌卡因 神经阻滞 利多卡因 不利影响 麻醉剂 止痛药
作者
John J. Finneran,Seth K. Bechis,Roger L. Sur,Manoj Monga,Kenneth S. Miller,Brenton S. Alexander,Baharin Abdullah,Michael Donohue,Adam N Schaar,Brian M. Ilfeld
出处
期刊:Anesthesiology [Lippincott Williams & Wilkins]
卷期号:145 (3): 569-579 被引量:1
标识
DOI:10.1097/aln.0000000000006129
摘要

BACKGROUND: Single-injection erector spinae plane blocks (ESPB) provide analgesia after percutaneous nephrolithotomy (PCNL) but are limited in their duration. A continuous ESPB involving local anesthetic administered via a perineural catheter may extend analgesia duration. This study hypothesized that adding a continuous ESPB to a single-injection ESPB after outpatient PCNL would decrease pain severity and/or opioid consumption over the first 2 postoperative days (dual primary outcomes). METHODS: Preoperatively, adults undergoing PCNL had an ultrasound-guided perineural catheter inserted at the eighth transverse process after saline injection. Bupivacaine 0.25% with epinephrine (20 ml) was manually injected via the catheter for all participants who were subsequently randomly allocated to one of two postoperative treatments: active with bupivacaine 0.25% or placebo with normal saline. An automatic intermittent bolus of 21 ml was delivered every 4 h using a portable infusion pump for approximately 57 h. RESULTS: During the first 2 postoperative days, the median [interquartile range] average daily pain intensity as measured with the numeric rating scale for active (n = 25) was 3.5 [2.0, 4.5] compared with 3.0 [1.3, 4.5] for placebo (n = 25; estimated difference, 0.25; 95% CI, -1.0 to 1.5; P = 0.538). Cumulative oxycodone consumption during this same period was 10 [0, 25] mg for active versus 15 [0, 30] mg for placebo (estimated difference, 0; 95% CI, -15 to 5; P = 0.358). During this period, the maximum daily pain for active was 7.0 [4.3, 8.0] compared with 6.5 [5.5, 8.0] for placebo ( P = 0.754). Sleep disturbances the second night were 0 [0, 1] for both groups ( P = 0.423). During the day after surgery, pain interference with physical and emotional functioning was 10 [0, 33] for active and 8 [23, 48] for placebo as measured with the Brief Pain Inventory ( P = 0.587). CONCLUSIONS: This investigation failed to identify benefits of adding a continuous ESPB to a single-injection ESPB after PCNL.
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