The Effects of Different Ciprofol Doses on Hemodynamics During Anesthesia Induction in Patients Undergoing Cardiac Surgery: A Randomized, Double-Blind, Controlled Study.

IF 4.7 2区 医学 Q1 CHEMISTRY, MEDICINAL Drug Design, Development and Therapy Pub Date : 2025-03-11 eCollection Date: 2025-01-01 DOI:10.2147/DDDT.S505772
Yingting Zhou, ZiYou Liu, QianQian Li, PengFei Ni, ZuoHui Li, BeiJia Yu, Min Zhang, Jia Yang, YanHu Xie
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Abstract

Objective: To evaluate the effects of different ciprofol doses on hemodynamics in patients undergoing cardiac surgery.

Methods: 209 patients were randomly divided into four groups: 0.2 mg/kg etomidate group (group E, n = 50), 0.2 mg/kg, 0.3mg/kg, 0.4mg/kg ciprofol group (group A, n = 53, group B, n = 51, group C, n = 54). Mean arterial pressure (MAP), heart rate (HR), cardiac output (CO), stroke volume (SV), systemic vascular resistance (SVR), and bispectral index were recorded at the following time points: 5 minutes after entering the operating room (T0); before anesthesia induction (T1); immediately after induction (T2); 1 minute and 2 minutes after induction (T3~T4); at intubation (T5); 1 minute, 3 minutes, 5 minutes and 10 minutes after intubation (T6~T9); at skin incision (T10). The incidence of hypotension and bradycardia and the doses of vasoactive drugs were recorded.

Results: Compared with T0, HR, MAP, SV, CO all decreased to varying degrees after administration, and the decrease time in Group B and Group C were earlier than that in other two groups (P < 0.05). SVR increased slowly after T4 in all groups, but there was no significant differences (P > 0.05). Compared with group E, the norepinephrine dose was significantly lower in groups A and B (both P < 0.05). Group C showed a greater decline in CO and SV than the other three groups from T7 to T10 (P < 0.05), while there was no significant difference between groups A and E in CO and groups A, B, and E in SV (P > 0.05). No significant differences were observed in MAP, SVR, and the incidences of hypotension and bradycardia among the four groups (P > 0.05).

Conclusion: 0.2 mg/kg ciprofol has the least impact on hemodynamics in patients undergoing cardiac surgery, and reduced norepinephrine use.

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目的:评估不同剂量的环丙氟哌酸对心脏手术患者血液动力学的影响:方法:将 209 例患者随机分为四组:0.2 毫克/千克依托咪酯组(E 组,n = 50),0.2 毫克/千克、0.3 毫克/千克、0.4 毫克/千克环丙酚组(A 组,n = 53,B 组,n = 51,C 组,n = 54)。在以下时间点记录平均动脉压(MAP)、心率(HR)、心输出量(CO)、每搏量(SV)、全身血管阻力(SVR)和双谱指数:进入手术室后 5 分钟(T0);麻醉诱导前(T1);诱导后立即(T2);诱导后 1 分钟和 2 分钟(T3~T4);插管时(T5);插管后 1 分钟、3 分钟、5 分钟和 10 分钟(T6~T9);皮肤切开时(T10)。记录了低血压和心动过缓的发生率以及血管活性药物的剂量:与 T0 相比,给药后 HR、MAP、SV、CO 均有不同程度的下降,B 组和 C 组的下降时间早于其他两组(P<0.05)。各组 T4 后 SVR 均缓慢增加,但无显著差异(P > 0.05)。与 E 组相比,A 组和 B 组的去甲肾上腺素剂量明显降低(均 P < 0.05)。从 T7 到 T10,C 组的 CO 和 SV 下降幅度大于其他三组(P < 0.05),而 A 组和 E 组的 CO 以及 A 组、B 组和 E 组的 SV 没有明显差异(P > 0.05)。结论:0.2 mg/kg ciprofol 对心脏手术患者的血流动力学影响最小,并能减少去甲肾上腺素的使用。
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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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