舒芬太尼和艾氯胺酮联合静脉注射对心脏手术后疼痛管理和抑郁的有效性:一项随机对照试验。

IF 2.1 3区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS
Cardiovascular diagnosis and therapy Pub Date : 2025-04-30 Epub Date: 2025-04-23 DOI:10.21037/cdt-24-312
Sen Xu, Tianyu Liang, Weicai Xu
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引用次数: 0

摘要

背景:心脏手术通常会导致明显的术后疼痛,这可能导致并发症和延长恢复期。疼痛和抑郁密切相关,有效的疼痛管理可能会降低患抑郁症的风险。阿片类药物舒芬太尼与具有镇痛和抗抑郁作用的药物艾氯胺酮联合使用,可能改善术后患者的疼痛控制和情绪。虽然它们在其他手术中很有前景,但在心脏手术中的效果仍不清楚。这项研究探讨了舒芬太尼和艾氯胺酮如何共同作用来控制心脏手术后的疼痛和减少抑郁。方法:于2021年1月至2023年12月进行随机对照临床试验,纳入104例心脏手术患者。患者年龄61 ~ 64岁,体重指数(BMI) 2,美国麻醉医师学会(ASA) I-II,打鼾、疲倦、观察到的呼吸暂停、高血压、体重指数、年龄、颈围、男性(STOP-Bang)评分结果:实验组PCIA泵按钮按下次数(2.41±0.72)明显少于对照组(6.20±1.31)(p < 12.64±3.25,p < 0.05)(术后T1 =4 h, T2 =8 h, T3 =24 h, T4 =48 h)。各组血氧饱和度差异无统计学意义(P < 0.05)。不良反应发生率实验组为13.46%,对照组为19.23%,差异无统计学意义(P < 0.05)。患者和外科医生的满意度得分在五分制中一致较高(两组的中位数均为5)。结论:舒芬太尼联合艾氯胺酮可有效控制心脏手术后患者的疼痛并显著减轻抑郁症状。实验组PCIA使用减少,临床指标改善。这些发现为加强术后恢复和解决疼痛管理和心理健康提供了有价值的见解。试验注册:Chinese Clinical Trial Registry;标识符:ChiCTR2400092428。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effectiveness of intravenous administration of a combination of sufentanil and esketamine on post-cardiac surgery pain management and depression: a randomized controlled trial.

Background: Cardiac surgery often results in significant postoperative pain, which can lead to complications and prolonged recovery. Pain and depression are closely linked, with effective pain management potentially reducing the risk of depression. Combining sufentanil, an opioid, with esketamine, a medication with both analgesic and antidepressant effects, may improve pain control and mood in postoperative patients. While promising in other surgeries, their effects in cardiac surgery remain unclear. This study explores how sufentanil and esketamine work together to manage pain and reduce depression after cardiac surgery.

Methods: A randomized controlled clinical trial was conducted from January 2021 to December 2023, involving 104 patients who underwent cardiac surgery. Patients [aged 61-64 years, body mass index (BMI) <30 kg/m2, American Society of Anesthesiologists (ASA) I-II, the snoring, tiredness, observed apnea, high blood pressure, body mass index, age, neck circumference, and male gender (STOP-Bang) score <3] were randomly assigned to a control group (n=52) receiving 2.5 µg/kg sufentanil or an experimental group (n=52) receiving 2.0 µg/kg sufentanil with 2 mg/kg esketamine via a central venous catheter for 48 h postoperatively. Exclusion criteria included allergies to fentanyl or etomidate, central nervous system diseases, recent opioid use, liver/kidney failure, or severe respiratory conditions. Outcome measures included patient-controlled intravenous analgesia (PCIA) pump usage, pain scores, clinical indicators, depressive symptoms, adverse events, and satisfaction levels.

Results: The experimental group had significantly fewer PCIA pump button presses (2.41±0.72) than the control group (6.20±1.31) (P<0.001). Visual analog pain scores were lower in the experimental group at multiple postoperative time points (P<0.05). Hamilton Depression Rating Scale (HAMD) scores were significantly lower in the experimental group (7.52±4.24) compared to the control group (13.84±2.76) (P<0.05), as were Hamilton Anxiety Rating Scale (HAMA) scores (8.84±2.13 vs. 12.64±3.25, P<0.05). Heart rate and mean arterial pressure were higher at postoperative time points T2, T3, and T4 in the experimental group (P<0.05), but no difference was observed at T1 (P>0.05) (T1 =4 h, T2 =8 h, T3 =24 h, T4 =48 h post-surgery). Oxygen saturation showed no significant difference between groups (P>0.05). Adverse reactions occurred in 13.46% of the experimental group and 19.23% of the control group, with no statistically significant difference (P>0.05). Patient and surgeon satisfaction scores were uniformly high on a five-point scale (both groups had median =5).

Conclusions: The combined administration of sufentanil and esketamine effectively managed pain and significantly reduced depressive symptoms in post-cardiac surgery patients. The experimental group demonstrated reduced PCIA usage and improved clinical indicators. These findings provide valuable insights for enhancing postoperative recovery and addressing both pain management and psychological well-being.

Trial registration: Chinese Clinical Trial Registry; identifier: ChiCTR2400092428.

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来源期刊
Cardiovascular diagnosis and therapy
Cardiovascular diagnosis and therapy Medicine-Cardiology and Cardiovascular Medicine
CiteScore
4.90
自引率
4.20%
发文量
45
期刊介绍: The journal ''Cardiovascular Diagnosis and Therapy'' (Print ISSN: 2223-3652; Online ISSN: 2223-3660) accepts basic and clinical science submissions related to Cardiovascular Medicine and Surgery. The mission of the journal is the rapid exchange of scientific information between clinicians and scientists worldwide. To reach this goal, the journal will focus on novel media, using a web-based, digital format in addition to traditional print-version. This includes on-line submission, review, publication, and distribution. The digital format will also allow submission of extensive supporting visual material, both images and video. The website www.thecdt.org will serve as the central hub and also allow posting of comments and on-line discussion. The web-site of the journal will be linked to a number of international web-sites (e.g. www.dxy.cn), which will significantly expand the distribution of its contents.
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