丙泊酚二钠和丙泊酚对老年全髋关节置换术患者术后恢复的影响:回顾性研究。

IF 4.7 2区 医学 Q1 CHEMISTRY, MEDICINAL
Drug Design, Development and Therapy Pub Date : 2025-04-11 eCollection Date: 2025-01-01 DOI:10.2147/DDDT.S501222
Sheng Ding, Zaibao Wang, Chunliu Li, Guizhi Wang, Juan Li, Hongrui Zhu, Keqiang He
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引用次数: 0

摘要

目的:异丙酚广泛用于老年患者全身麻醉。丙泊酚二钠是异丙酚的前体,可减少术后恶心和呕吐(PONV)的发生率。然而,这两种药物对患者术后恢复质量的影响尚不清楚。本研究旨在评价两种药物对老年全髋关节置换术患者术后恢复质量的影响。患者和方法:回顾性分析2022年10月至2024年6月在中国科学技术大学第一附属医院就诊的168例患者。根据患者麻醉诱导和维持用药情况,将患者分为丙泊酚二钠组(F)和丙泊酚组(P)。主要观察指标为PONV的发生率。次要结果包括拔管时间、麻醉后护理病房(PACU)住院时间、住院时间、围手术期血流动力学数据和患者肝肾功能。结果:F组PONV发生率低于P组(15.94% vs 33.33%, P < 0.05)。P组拔管时间(25.71 vs 33.36 min, P < 0.05)和PACU住院时间(62.61 vs 65.65 min, P < 0.05)较短,但住院时间较长(6.24 vs 5.8 d, P < 0.05)。两组患者肝肾功能指标及血流动力学指标比较,差异无统计学意义(P < 0.05)。药物种类是影响拔管时间的一个因素。药物类型和患者性别是影响PONV发生的因素。结论:氟丙酚二钠可降低患者PONV的发生率。在老年全髋关节置换术患者中,磷异酚二钠对术后恢复质量的影响与丙泊酚相似。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of Fospropofol Disodium and Propofol on the Postoperative Recovery of Elderly Patients Who Underwent Total Hip Arthroplasty: A Retrospective Study.

Purpose: Propofol is widely used for general anesthesia in elderly patients. Fospropofol disodium, a precursor of propofol, may reduce the incidence of postoperative nausea and vomiting (PONV). However, the effects of these two drugs on patients' postoperative recovery quality are unclear. The present study aimed to evaluate the effects of the two drugs on postoperative recovery quality in elderly patients who underwent total hip arthroplasty.

Patients and methods: We retrospectively analyzed 168 patients from the First Affiliated Hospital of USTC from October 2022 to June 2024. These individuals were assigned to fospropofol disodium group (F) or propofol group (P) according to the patients' anesthesia induction and maintenance medication. The primary outcome was the rate of occurrence of PONV. The secondary outcomes included the time of extubation and the time of stay in post-anesthesia care unit (PACU), hospital length of stay, perioperative hemodynamic data and patients' liver and renal functions.

Results: PONV occurred to be lesser in group F than in group P (15.94% vs 33.33%, P < 0.05). Group P spent less in the extubation time (25.71 vs 33.36 min, P < 0.05) and PACU stay length (62.61 vs 65.65 min, P > 0.05), but hospital length of stay is longer (6.24 vs 5.8 days, P > 0.05). Liver and renal functions indexes and hemodynamic data between the 2 groups were similar (P > 0.05). The type of drug was a factor affecting the time of extubation. The type of drug and the patient's gender were influential factors in the incidence of PONV.

Conclusion: Fospropofol disodium reduces the incidence of PONV in patients. And the effects of fospropofol disodium on postoperative recovery quality are similar to that of propofol in older patients who underwent total hip arthroplasty.

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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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