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1.重庆医科大学附属第三医院药剂科,重庆 401120
2.重庆市药品不良反应监测中心,重庆 401120
药师,硕士。研究方向:临床药学、药物不良反应。E-mail:15123054472@163.com
主管药师。研究方向:临床药学、药物警戒。E-mail:650101@hospital.cqmu.edu.cn
收稿日期:2023-03-17,
修回日期:2023-07-07,
录用日期:2023-08-02,
纸质出版日期:2023-09-30
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陈诚,王彦,邓莉,等.重庆市2015-2022年药物过敏性休克救治使用肾上腺素情况的回顾性研究[J].中国药房,2023,34(18):2238-2242.
CHEN Cheng,WANG Yan,DENG Li,et al.Retrospective study on the use of epinephrine in patients with drug-induced anaphylactic shock in Chongqing from 2015 to 2022[J].ZHONGGUO YAOFANG,2023,34(18):2238-2242.
陈诚,王彦,邓莉,等.重庆市2015-2022年药物过敏性休克救治使用肾上腺素情况的回顾性研究[J].中国药房,2023,34(18):2238-2242. DOI: 10.6039/j.issn.1001-0408.2023.18.12.
CHEN Cheng,WANG Yan,DENG Li,et al.Retrospective study on the use of epinephrine in patients with drug-induced anaphylactic shock in Chongqing from 2015 to 2022[J].ZHONGGUO YAOFANG,2023,34(18):2238-2242. DOI: 10.6039/j.issn.1001-0408.2023.18.12.
目的
2
评价肾上腺素在药物过敏性休克救治中使用的合理性,为进一步规范过敏性休克的救治提供参考。
方法
2
依据重庆市药品不良反应(ADR)监测中心提供的2015-2022年药物过敏性休克严重ADR报告的相关数据,回顾性分析患者的救治药物选择及肾上腺素使用情况,探讨不同肾上腺素救治方案下过敏性休克患者的临床转归情况。
结果
2
共纳入1 415份药物过敏性休克严重ADR报告,所涉患者男女比例为1.04∶1;引发过敏性休克的药物主要为抗感染药(47.92%)、中药注射剂(9.12%);43.96%患者的ADR发生于用药后1
0 min内;97.24%的患者治愈或好转,2.76%的患者死亡或未好转。1 415例患者中,使用肾上腺素救治的占63.39%,首选肾上腺素救治的占53.14%;肌内注射、皮下注射、静脉注射和静脉滴注分别占33.78%、30.32%、25.75%和1.23%;肾上腺素的初始剂量范围为0.01~10 mg,单次剂量以1 mg居多(44.70%);肌内注射、皮下注射和静脉注射单次剂量过量的分别有148例(51.03%)、136例(53.13%)和193例(91.47%),静脉注射给药更有可能出现单次剂量过量(
P
<0.05)。初始救治使用肾上腺素者的好转/痊愈率显著高于非肾上腺素使用者(98.14% vs. 96.23%,
P
=0.029),首选肾上腺素者的好转/痊愈率显著高于非首选肾上腺素者(98.14% vs. 95.17%,
P
=0.031),肌内注射者的好转/痊愈率显著高于非肌内注射者(99.01% vs. 96.69%,
P
=0.038)。
结论
2
在药物过敏性休克的救治中,存在救治药物选择不适宜和肾上腺素使用不足、给药延迟、给药途径不适宜及单次剂量过高等不合理现象。
OBJECTIVE
2
To evaluate the rationality of epinephrine in the treatment of drug-induced anaphylactic shock, and to provide a reference for further standardizing the treatment measures of anaphylactic shock.
METHODS
2
According to the relevant data of the reports of severe adverse drug reaction (ADR) of drug-induced anaphylactic shock provided by Chongqing ADR Monitoring Center from 2015 to 2022, the selection of treatment drugs, and the application of epinephrine in anaphylactic shock were analyzed retrospectively; the clinical outcomes of anaphylactic shock with different epinephrine administration methods were investigated.
RESULTS
2
A total of 1 415 cases of severe ADR related to drug-induced anaphylactic shock were reported, with a male-to-female ratio of 1.04∶1; the drugs that caused allergic shock mainly included anti-infective drugs (47.92%), TCM injections (9.12%); the patients who suffered from drug-induced anaphylactic shock within 10 min after medication accounted for 43.96%; 97.24% of patients were cured or improved, and 2.76% of patients died or did not been improved. Among 1 415 patients, 63.39% of patients were treated with epinephrine, and the patients who preferred epinephrine treatment accounted for 53.14%; the intramuscular injection, subcutaneous injection, intrav
enous injection and intravenous drip accounted for 33.78%, 30.32%, 25.75% and 1.23%, respectively. The initial dose range of epinephrine was 0.01-10 mg, and the most frequent single dose was 1 mg (44.70%). Excessive single doses of intramuscular injection, subcutaneous injection and intravenous injection accounted for 51.03% (148 cases), 53.13% (136 cases) and 91.47% (193 cases) respectively, and the risk of overdose in intravenous injection was higher (
P
<0.05). The patients receiving initial treatment with epinephrine had a higher improvement rate/cure rate than those who did not use epinephrine (98.14% vs. 96.23%,
P
=0.029); the patients who preferred epinephrine had a higher improvement rate/cure rate than those who did not preferred epinephrine (98.14% vs. 95.17%,
P
=0.031); the improvement rate/cure rate of patients receiving intramuscular injection of epinephrine was higher than those without intramuscular injection (99.01% vs. 96.69%,
P
=0.038).
CONCLUSIONS
2
There are some unreasonable phenomena in the treatment of drug-induced anaphylactic shock, such as inappropriate selection of drugs, insufficient use of epinephrine, delay of administration, inappropriate route of administration and excessive single dose.
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