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那屈肝素与镇痛药、镇静剂和肌肉松弛剂在治疗 2019 年冠状病毒病中的物理相容性。

Physical Compatibility of Nafamostat with Analgesics, Sedatives, and Muscle Relaxants for Treatment of Coronavirus Disease 2019.

机构信息

Department of Pharmacy, Nippon Medical School Tama Nagayama Hospital.

出版信息

J Nippon Med Sch. 2021 Dec 29;88(6):533-539. doi: 10.1272/jnms.JNMS.2022_89-104. Epub 2021 Mar 9.

Abstract

BACKGROUND

Severe coronavirus disease 2019 (COVID-19) may require continuous administration of analgesics, sedatives, and muscle relaxants. Nafamostat has recently been reported as a therapeutic agent for COVID-19. However, there is a lack of information on the compatibility of nafamostat with the aforementioned drug classes. This study evaluated the physical compatibility of nafamostat with these drug classes.

METHODS

Nafamostat was combined with 1-3 target drugs (fentanyl, morphine, midazolam, dexmedetomidine, and rocuronium). Fifteen physical compatibility tests were conducted. Nafamostat was dissolved in 5% glucose solution; the final concentration was 10 mg/mL. All other medications were diluted in 0.9% sodium chloride to obtain clinically relevant concentrations. The power of hydrogen (pH) of all medications was measured during each test. Compatibility tests were conducted with 4 test solutions in which nafamostat and the target drugs were compounded at equal volume ratios (1:1, 1:1:1, or 1:1:1:1). Visual appearance, turbidity, and pH were evaluated immediately after mixing and at 1 and 3 hours. Physical incompatibilities were defined as gross precipitation, cloudiness, appearance of the Tyndall effect, or a turbidity change of ≥0.5 nephelometric turbidity units (NTU) based on nafamostat.

RESULTS

The mean pH of nafamostat was 3.13 ± 0.03. The combination of nafamostat, fentanyl, and dexmedetomidine had the highest pH (3.39 ± 0.01; 3 hours after mixing). All drugs were compatible with nafamostat until 3 hours after admixture, with a mean turbidity value of ≤0.03 NTU.

CONCLUSIONS

Infusions combining nafamostat with the tested sedatives, analgesics, and muscle relaxants could be safely administered.

摘要

背景

严重的 2019 年冠状病毒病(COVID-19)可能需要持续给予镇痛药、镇静剂和肌肉松弛剂。那屈肝素最近被报道为 COVID-19 的治疗药物。然而,关于那屈肝素与上述药物类别的相容性的信息有限。本研究评估了那屈肝素与这些药物类别的物理相容性。

方法

将那屈肝素与 1-3 种目标药物(芬太尼、吗啡、咪达唑仑、右美托咪定和罗库溴铵)联合使用。进行了 15 项物理相容性测试。将那屈肝素溶解在 5%葡萄糖溶液中;最终浓度为 10mg/mL。所有其他药物均用 0.9%氯化钠稀释至临床相关浓度。在每次测试中测量所有药物的氢离子(pH)。在纳屈肝素与目标药物以等体积比(1:1、1:1:1 或 1:1:1:1)混合的 4 种测试溶液中进行相容性测试。混合后立即以及 1 小时和 3 小时评估外观、浑浊度和 pH。物理不相容性定义为根据那屈肝素出现明显沉淀、浑浊、出现丁达尔效应或浊度变化≥0.5 奈氏浊度单位(NTU)。

结果

那屈肝素的平均 pH 值为 3.13 ± 0.03。那屈肝素、芬太尼和右美托咪定的组合 pH 值最高(3.39 ± 0.01;混合 3 小时后)。所有药物在混合后 3 小时内均与那屈肝素相容,平均浊度值≤0.03 NTU。

结论

那屈肝素与测试用镇静剂、镇痛药和肌肉松弛剂联合输注可安全给药。

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