Sobuwa Simpiwe, Singh Thishana, Kalicharan Kerusha
Faculty of Health & Wellness Sciences, Department of Emergency Medical Sciences, Cape Peninsula University of Technology, Cape Town, South Africa.
School of Chemistry and Physics, College of Agriculture, Engineering and Science, University of KwaZulu-Natal, Durban, South Africa.
Afr J Emerg Med. 2024 Mar;14(1):7-10. doi: 10.1016/j.afjem.2023.11.009. Epub 2023 Dec 13.
Temperature conditions vary in emergency service vehicles, which may pose a risk to the integrity of the drugs on board, possibly rendering them ineffective and increasing morbidity and mortality in patients.
This study assessed the stability of four emergency care drugs (adrenaline, etomidate, ketamine, and rocuronium) after eight weeks of deployment in the prehospital context.
The study adopted a longitudinal quantitative design to evaluate the chemical stability of emergency care drugs. The study was conducted at four emergency medical service bases in Ballito, Durban and Pietermaritzburg, South Africa. The primary outcome was the relative reduction in drug concentration from the labelled concentration after four and eight weeks. High-performance liquid chromatography-mass spectrometry (HPLC-MS) analysed samples to determine the concentration of active ingredients in the drug samples.
HPLC analysis was done on 176 samples. The ambient temperature ranged from 18.7 to 44 °C in the first four weeks, averaging 26.8 °C ± 3.0. At 4 and 8 weeks, Adrenaline decreased 24.93 % and 22.73 %, respectively. Etomidate's control had 3.06 mg/ml, not the 2 mg/ml on the bottle. After 4 and 8 weeks, the samples had 3.10 and 3.15 mg/ml active components, respectively. Ketamine degraded over 30 % after four weeks but not beyond that. The Ketamine package states 10 mg/ml. However, we found 17.46 mg/ml. Rocuronium was 6.45 mg/ml in the control, although the manufacturer specified 10 mg/ml. At four weeks, the concentration was 6.70 mg/ml; at eight weeks, 6.56.
This study suggests that adrenaline and ketamine degrade by more than 20 % within four weeks of deployment in the prehospital field, whereas etomidate and rocuronium remain stable after eight weeks.
急救车辆中的温度条件各不相同,这可能会对车上药品的完整性构成风险,有可能使其失效,并增加患者的发病率和死亡率。
本研究评估了四种急救药物(肾上腺素、依托咪酯、氯胺酮和罗库溴铵)在院前环境中部署八周后的稳定性。
本研究采用纵向定量设计来评估急救药物的化学稳定性。该研究在南非贝利托、德班和彼得马里茨堡的四个紧急医疗服务基地进行。主要结果是四周和八周后药物浓度相对于标签浓度的相对降低。采用高效液相色谱 - 质谱联用仪(HPLC-MS)分析样品,以确定药物样品中活性成分的浓度。
对176个样品进行了HPLC分析。前四周环境温度范围为18.7至44°C,平均为26.8°C±3.0。在4周和8周时,肾上腺素分别下降了24.93%和22.73%。依托咪酯对照品为3.06mg/ml,而非瓶身上标注的2mg/ml。4周和8周后,样品中活性成分分别为3.10mg/ml和3.15mg/ml。氯胺酮在四周后降解超过30%,但之后不再降解。氯胺酮包装标注为10mg/ml。然而,我们测得为17.46mg/ml。罗库溴铵对照品为6.45mg/ml,尽管制造商规定为10mg/ml。四周时浓度为6.70mg/ml;八周时为6.56mg/ml。
本研究表明,肾上腺素和氯胺酮在院前环境中部署四周内降解超过20%,而依托咪酯和罗库溴铵在八周后仍保持稳定。