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河北省人民医院药学部
纸质出版日期:2021,
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庞国勋, 闫彬, 靳会欣. 多种微量元素注射液相关药品不良反应及联合用药中配伍禁忌分析与预防策略[J]. 中国医院用药评价与分析, 2021,21(7):881-885.
PANG Guoxun, YAN Bin, Jin Huixin. Analysis and Prevention Strategies of Adverse Drug Reactions Related to Multi-Trace Elements Injection and Incompatibility in Drug Combination[J]. 2021,21(7):881-885.
庞国勋, 闫彬, 靳会欣. 多种微量元素注射液相关药品不良反应及联合用药中配伍禁忌分析与预防策略[J]. 中国医院用药评价与分析, 2021,21(7):881-885. DOI: 10.14009/j.issn.1672-2124.2021.07.025.
PANG Guoxun, YAN Bin, Jin Huixin. Analysis and Prevention Strategies of Adverse Drug Reactions Related to Multi-Trace Elements Injection and Incompatibility in Drug Combination[J]. 2021,21(7):881-885. DOI: 10.14009/j.issn.1672-2124.2021.07.025.
目的:了解多种微量元素注射液相关药品不良反应(adverse drug reaction
ADR)及联合用药中的配伍禁忌
探讨预防策略
以期为该药的临床应用及药品说明书修订提供参考。方法:检索中国知网、万方数据库以及维普数据库
检索时间段为2007—2020年
纳入多种微量元素注射液相关ADR及联合用药中配伍禁忌的文献报道
进行整理分析。结果:共检索到相关文献53篇
其中多种微量元素注射液致ADR文献8篇(1篇为多病例报告
7篇为个案报告)
联合用药中配伍禁忌相关文献45篇。所有ADR均为静脉滴注给药
除1例使用果糖注射液作为溶剂且多种微量元素注射液浓度较高之外
其余患者均按照药品说明书中规定的正常用法与用量用药
滴注速度亦符合要求;多病例报告中
多种微量元素注射液致ADR发生在输注开始后15 min左右
9例个案报告中
6例(占66.67%) ADR发生于给药后1~6 h; ADR的临床表现包括血管局部疼痛明显
血管呈条索状内陷、闭塞且周围皮肤痛感明显
输注部位红肿、疼痛、硬结
静脉炎
输液反应和皮肤坏死等;所有ADR预后基本良好
未出现严重的ADR及死亡病例。多种微量元素注射液(Ⅱ)与多种药物存在配伍禁忌。结论:多种微量元素注射液的ADR发生率不高
以静脉炎为主; ADR、配伍禁忌的发生与溶剂选择、输注速度、输注顺序和用药监护等诸多因素有关
临床应用时
应严格遵照药品说明书的用法、用量及注意事项
尽量单独、缓慢滴注
并加强用药监护
确保用药安全。目前
多种微量元素注射液致ADR以及配伍禁忌的报道多来自于临床一线护理人员
其物质基础和作用机制尚需药学专业人员进一步研究。
OBJECTIVE: To investigate the adverse drug reaction( ADR) related to multi-trace element injection and and incompatibility in drug combination
and to discuss the prevention strategies
so as to provide reference for the clinical application of the drug and the revision of drug instructions. METHODS: CNKI
Wanfang database and VIP database were retrieved
the retrieval time was from 2007 to 2020. Literature with ADR related to multi-trace element injection and incompatibility in drug combination were extracted and analyzed. RESULTS: A total of 53 relevant literature were retrieved
including 8 literature with ADR induced by multi-trace element injection( 1 for multiple case report
7 for case report)
and 45 literature with incompatibility of drug combination. All ADR were administered by intravenous drip. Except for one case with fructose injection as the solvent and the high concentration of multi-trace element injection
the rest of the patients were administered in accordance with the normal usage and dosage specified in the drug instructions
and the drip rate also met the requirements. In multiple case reports
ADR induced by multitrace element injection occurred about 15 min after the start of the infusion. In 9 case reports
6 cases( 66. 67%) of ADR occurred 1 to 6 h after administration. The clinical manifestations of ADR included localized pain in the blood vessels
streak-like invagination
occlusion and pain in the surrounding skin
redness
swelling
pain and stiffness at the infusion site
phlebitis
infusion reaction and skin necrosis. The prognosis of all ADR was basically good
and no severe ADR or death cases were found. There were contraindications in the compatibility of multi-trace element injection( Ⅱ) and a variety of drugs. CONCLUSIONS: The incidence of ADR for multi-trace element injection is not high
mainly for phlebitis. The occurrence of ADR and contraindications is related to many factors such as solvent selection
infusion speed
infusion sequence and medication monitoring. In clinical application
the usage
dosage and precautions in the drug instructions should be strictly followed
and the drug should be infused individually and slowly as far as possible
and medication monitoring should be strengthened to ensure medication safety. At present
the reports on ADR and incompatibility induced by multi-trace element injection are mostly from front-line clinical nursing staff
and the material basis and mechanism of action still need to be further studied by pharmaceutical professionals.
多种微量元素注射液药品不良反应配伍禁忌预防策略
Multi-trace elements injectionAdverse drug reactionsIncompatibilityPrevention strategies
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