The Effect of Low-Dose Dexmedetomidine on Perioperative Neurocognitive Dysfunction in Elderly Patients Undergoing Endoscopic Retrograde Cholangiopancreatography (ERCP): A Randomized, Controlled, Double-Blind Trial.

IF 4.7 2区 医学 Q1 CHEMISTRY, MEDICINAL
Drug Design, Development and Therapy Pub Date : 2024-08-23 eCollection Date: 2024-01-01 DOI:10.2147/DDDT.S470514
Zhangnan Sun, Ji Shi, Chaolei Liu, Jingjing Zhang, Yue Liu, Yini Wu, Xin Han, Hong Dai, Jimin Wu, Lijun Bo, Faxing Wang
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引用次数: 0

Abstract

Objective: This study investigates the effect of low-dose dexmedetomidine infusion on perioperative neurocognitive function in elderly patients undergoing endoscopic retrograde cholangiopancreatography (ERCP).

Patients and methods: This double-blind trial enrolled 80 elderly ERCP patients randomized to receive dexmedetomidine (Group D) or placebo (Group S). Group D received dexmedetomidine at 0.4 μg·kg-1·h-1 starting 15 minutes before surgery until completion, along with propofol at 1.5 mg/kg for anesthesia. Group S received saline and propofol in a similar manner. Anesthesia was maintained with dexmedetomidine at 0.4 μg·kg-1·h-1 and propofol at 1-2 mg/kg during surgery. Cognitive function was assessed using the Mini-Mental State Examination (MMSE) preoperatively and on postoperative days 1, 3, and 5. Primary outcome was perioperative neurocognitive disorder (PND) incidence on day 5; secondary outcomes included changes in perioperative IL-6, cortisol, S100-β, hemodynamics, anesthesia parameters, postoperative pain, agitation scores, and adverse events.

Results: All 80 patients completed the trial. On postoperative day 5, the cumulative probability of PND incidence was significantly lower in Group D than in Group S (12.5% vs 35%, P=0.018). Group D also had lower levels of IL-6 (F=199.472, P<0.001), S100-β (F=2681.964, P<0.001), and cortisol (F=137.637, P<0.001). Propofol doses were lower in Group D (706.1 ± 202.4 vs 1003.3 ± 203.7, P<0.001), and bradycardia rates were higher (45% vs 15%, P=0.003), though atropine use did not significantly differ between groups. Group D showed greater stability in mean arterial pressure. Postoperative complications and adverse reactions were similar across groups.

Conclusion: Perioperative low-dose dexmedetomidine infusion with propofol in elderly ERCP patients ensures safe and effective monitored anesthesia care (MAC), reducing PND incidence by mitigating peripheral inflammation and stress responses. Long-term follow-up is needed to fully evaluate PND incidence.

小剂量右美托咪定对接受内镜逆行胰胆管造影术 (ERCP) 的老年患者围手术期神经认知功能障碍的影响:一项随机、对照、双盲试验。
研究目的本研究探讨了低剂量右美托咪定输注对接受内镜逆行胰胆管造影术(ERCP)的老年患者围手术期神经认知功能的影响:这项双盲试验共招募了80名老年ERCP患者,随机分为右美托咪定(D组)和安慰剂(S组)两组。D 组从手术前 15 分钟开始,以 0.4 μg-kg-1-h-1 的剂量服用右美托咪定,直至手术结束,同时使用 1.5 mg/kg 的丙泊酚进行麻醉。S 组以类似的方式接受生理盐水和异丙酚。手术过程中使用 0.4 μg-kg-1-h-1 的右美托咪定和 1-2 mg/kg 的异丙酚维持麻醉。术前和术后第 1、3 和 5 天使用迷你精神状态检查(MMSE)评估认知功能。主要结果是第5天围手术期神经认知障碍(PND)的发生率;次要结果包括围手术期IL-6、皮质醇、S100-β、血液动力学、麻醉参数、术后疼痛、躁动评分和不良事件的变化:所有80名患者均完成了试验。术后第 5 天,D 组的 PND 累计发生概率显著低于 S 组(12.5% vs 35%,P=0.018)。D 组的 IL-6 水平也较低(F=199.472,P=0.018):在老年 ERCP 患者围术期低剂量右美托咪定与丙泊酚联合输注可确保安全有效的麻醉监测护理 (MAC),通过减轻外周炎症和应激反应降低 PND 的发生率。需要进行长期随访以全面评估PND的发生率。
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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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