Kanna Dr Rishi, Jakkepally Dr Sridhar, Shetty Dr Ajoy P, Rajasekaran Dr Shanmuganathan
Department of Orthopaedics and Spine Surgery, Ganga Medical Centre and Hospitals, Coimbatore, India.
Global Spine J. 2023 Sep;13(7):1926-1931. doi: 10.1177/21925682211060043. Epub 2022 Feb 7.
Randomised control study.
Different parenteral analgesics are used to alleviate post-operative pain after transforaminal lumbar interbody fusion (TLIF) but limited by their efficacy and side effects. We performed a RCT to evaluate the safety and efficacy of epidural Morphine-Bupivacaine on post-operative pain management after TLIF.
Consecutive patients (n=100) of TLIF were divided randomly into study (SG) and control groups (CG). At the end of procedure, SG (n=50) received epidural instillation of morphine 5 mg and bupivacaine .25% - 2 mL, along with 6 mL of .25% bupivacaine infiltration in the deep fascia before wound closure. The functional outcomes were assessed at regular intervals (4, 8, 12, 24, 36, 48, 72, 96 hours) with VAS, nausea and vomiting scale, Ramsay sedation scale and breakthrough analgesia needed, time to ambulation and other complications.
The mean VAS score at 4 hours in SG was significantly less (1.16 ± .88) than the CG (3.32 ± 1.0) ( = .000). This significant difference was maintained at each time point during the first 48 hours ( < .004). Similarly, the mean NRS score in SG at 4 hours was 1.02 ± .89, and in CG 3.3 ± .69 ( = .0000) which was maintained at all intervals of assessment till 48 hours ( = .0137). The mean time to first ambulation was significantly less in the SG (4.46 ± 1.04 hours) than CG (11.64 ± 2.3 hours) ( < .001). There were no drug-related complications.
Epidural instillation of bupivacaine and morphine is safe and enables better pain relief in the initial 48 hours which helps in early mobilisation, and enhanced functional recovery.
随机对照研究。
不同的胃肠外镇痛药用于缓解经椎间孔腰椎椎体间融合术(TLIF)后的术后疼痛,但受其疗效和副作用限制。我们进行了一项随机对照试验,以评估硬膜外吗啡-布比卡因用于TLIF术后疼痛管理的安全性和有效性。
连续的TLIF患者(n = 100)被随机分为研究组(SG)和对照组(CG)。手术结束时,SG组(n = 50)接受硬膜外注入5毫克吗啡和2毫升0.25%布比卡因,同时在伤口缝合前于深筋膜处注入6毫升0.25%布比卡因。定期(4、8、12、24、36、48、72、96小时)用视觉模拟评分法(VAS)、恶心呕吐量表、拉姆齐镇静量表评估功能结果,并记录所需的解救镇痛、下地行走时间及其他并发症。
SG组4小时时的平均VAS评分(1.16±0.88)显著低于CG组(3.32±1.0)(P = 0.000)。在最初48小时的每个时间点,这种显著差异均保持(P < 0.004)。同样,SG组4小时时的平均数字评定量表(NRS)评分是1.02±0.89,CG组为3.3±0.69(P = 0.0000),在直至48小时的所有评估间隔中均保持(P = 0.0137)。SG组首次下地行走的平均时间(4.46±1.04小时)显著短于CG组(11.6,4±2.3小时)(P < 0.001)。未出现与药物相关的并发症。
硬膜外注入布比卡因和吗啡是安全的,能在最初48小时内更好地缓解疼痛,有助于早期活动及促进功能恢复。