Dexmedetomidine and Dexamethasone as Adjuvants to the Local Anesthetic Mixture in Rhomboid Intercostal and Sub-Serratus Block for Video-Assisted Thoracoscopic Surgery: A Randomized, Double-Blind, Controlled Trial.

IF 4.7 2区 医学 Q1 CHEMISTRY, MEDICINAL Drug Design, Development and Therapy Pub Date : 2024-10-07 eCollection Date: 2024-01-01 DOI:10.2147/DDDT.S476929
Quan-Fang Liu, Cui-Na Shi, Jian-Hua Tong, Kun-Peng Li, Jian-Jun Yang, Mu-Huo Ji, Qing-Ren Liu
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Abstract

Background: The utilization of adjuvants such as dexamethasone and dexmedetomidine in combination with local anesthetics has proven effective in extending analgesia duration. We aimed to investigate the potential efficacy of combining dexmedetomidine and dexamethasone in rhomboid intercostal and sub-serratus (RISS) block for prolonging postoperative analgesia in patients undergoing video-assisted thoracoscopic surgery (VATS).

Methods: We did this randomized, double-blind, controlled trial in two tertiary-care hospitals. A total of eighty-eight patients undergoing VATS under general anesthesia were enrolled in this study. They were randomly assigned into four groups: ropivacaine (R) group, ropivacaine + dexmedetomidine (RM) group, ropivacaine + dexamethasone (RS) group, or ropivacaine + dexmedetomidine + dexamethasone (RSM) group. The primary outcome measure was the duration of analgesia. Secondary outcomes included Numeric Rating Scale (NRS) scores, cumulative oxycodone consumption, and adverse effects.

Results: The RSM group exhibited a significantly prolonged duration of analgesia at 1073.5 min (932.0-1283.3) compared to the R group with a duration of 154.5 min (80.5-199.3) and the RS group with a duration of 282.0 min (195.3-350.0, P < 0 0.001). The cumulative oxycodone consumption during the 0-12 hours and 0-24-hours period was significantly reduced in the RSM group compared to the R group (P < 0.05). There was also a lower incidence of nausea at 48 hours postoperatively in the RSM group compared to the RM group. However, there were no significant differences between the four groups regarding NRS pain scores.

Conclusion: The combination of ropivacaine, dexmedetomidine, and dexamethasone in RISS block significantly prolongs the duration of postoperative analgesia following VATS.

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右美托咪定和地塞米松作为视频辅助胸腔镜手术中横纹肌肋间和剑突下阻滞的局麻药混合物的辅助剂:随机、双盲、对照试验。
背景:事实证明,地塞米松和右美托咪定等辅助剂与局麻药联合使用可有效延长镇痛时间。我们旨在研究将右美托咪定和地塞米松联合应用于斜方肌肋间和锯齿下(RISS)阻滞以延长视频辅助胸腔镜手术(VATS)患者术后镇痛的潜在疗效:我们在两家三级医院进行了这项随机、双盲、对照试验。共有 88 名在全身麻醉下接受 VATS 手术的患者参与了这项研究。他们被随机分为四组:罗哌卡因(R)组、罗哌卡因+右美托咪定(RM)组、罗哌卡因+地塞米松(RS)组或罗哌卡因+右美托咪定+地塞米松(RSM)组。主要结果是镇痛持续时间。次要结果包括数值评定量表(NRS)评分、累计羟考酮用量和不良反应:结果:RSM 组的镇痛持续时间为 1073.5 分钟(932.0-1283.3),明显长于 R 组的 154.5 分钟(80.5-199.3)和 RS 组的 282.0 分钟(195.3-350.0,P < 0.001)。与 R 组相比,RSM 组在 0-12 小时和 0-24 小时期间的累计羟考酮用量明显减少(P < 0.05)。此外,RSM 组术后 48 小时的恶心发生率也低于 RM 组。然而,四组患者的 NRS 疼痛评分无明显差异:结论:在 RISS 阻滞中联合使用罗哌卡因、右美托咪定和地塞米松可显著延长 VATS 术后镇痛的持续时间。
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来源期刊
Drug Design, Development and Therapy
Drug Design, Development and Therapy CHEMISTRY, MEDICINAL-PHARMACOLOGY & PHARMACY
CiteScore
9.00
自引率
0.00%
发文量
382
审稿时长
>12 weeks
期刊介绍: Drug Design, Development and Therapy is an international, peer-reviewed, open access journal that spans the spectrum of drug design, discovery and development through to clinical applications. The journal is characterized by the rapid reporting of high-quality original research, reviews, expert opinions, commentary and clinical studies in all therapeutic areas. Specific topics covered by the journal include: Drug target identification and validation Phenotypic screening and target deconvolution Biochemical analyses of drug targets and their pathways New methods or relevant applications in molecular/drug design and computer-aided drug discovery* Design, synthesis, and biological evaluation of novel biologically active compounds (including diagnostics or chemical probes) Structural or molecular biological studies elucidating molecular recognition processes Fragment-based drug discovery Pharmaceutical/red biotechnology Isolation, structural characterization, (bio)synthesis, bioengineering and pharmacological evaluation of natural products** Distribution, pharmacokinetics and metabolic transformations of drugs or biologically active compounds in drug development Drug delivery and formulation (design and characterization of dosage forms, release mechanisms and in vivo testing) Preclinical development studies Translational animal models Mechanisms of action and signalling pathways Toxicology Gene therapy, cell therapy and immunotherapy Personalized medicine and pharmacogenomics Clinical drug evaluation Patient safety and sustained use of medicines.
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