Fujizuka Kenji, Nakamura Mitsunobu, Tamura Junichi, Kawai-Kowase Keiko
Advanced Medical Emergency Department and Critical Care Center Japanese Red Cross Maebashi Hospital Maebashi Japan.
Department of General Medicine Gunma University Graduate School of Medicine Maebashi Japan.
Acute Med Surg. 2022 Oct 20;9(1):e790. doi: 10.1002/ams2.790. eCollection 2022 Jan-Dec.
Continuous intravenous (CIV) infusion of epinephrine for the treatment of anaphylaxis may be required if symptoms do not improve after intramuscular (IM) injection. As CIV infusion permits precise dose adjustment, we compared treatment course and adverse events following CIV infusion and IM injection of epinephrine for the management of anaphylaxis.
Medical records of patients, who were treated for anaphylaxis with epinephrine, were 18 years or older, and were admitted to our department from April 2005 to March 2016, were retrospectively reviewed. The cases were categorized as CIV infusion or IM injection, and treatment course and outcomes were compared between the two groups.
Of the 142 eligible cases, there were 78 in the CIV infusion group and 64 in the IM injection group. The CIV infusion group had lower systolic blood pressure, more respiratory symptoms, and higher Acute Physiology and Chronic Health Evaluation II (APACHE II) scores, but required a lower total dose of epinephrine, had fewer adverse events after epinephrine administration, and showed lower incidence of biphasic reactions. In addition, compared with the IM injection group, time to administration of epinephrine was significantly longer ( < 0.001), but time to resolution of symptoms, both from contact and epinephrine administration, was significantly shorter ( < 0.01 and = 0.03, respectively).
Continuous intravenous infusion of epinephrine for the treatment of anaphylaxis may be safe, has fewer adverse events, improves symptoms, and is relatively easy to administer under ready conditions. CIV infusion of epinephrine may also reduce the incidence of biphasic reactions.
如果肌内注射肾上腺素后症状未改善,则可能需要持续静脉输注肾上腺素来治疗过敏反应。由于持续静脉输注允许精确调整剂量,我们比较了持续静脉输注和肌内注射肾上腺素治疗过敏反应的疗程及不良事件。
回顾性分析2005年4月至2016年3月期间在我科就诊、年龄18岁及以上、接受肾上腺素治疗过敏反应的患者的病历。将病例分为持续静脉输注组或肌内注射组,并比较两组的治疗过程和结果。
在142例符合条件的病例中,持续静脉输注组78例,肌内注射组64例。持续静脉输注组收缩压较低,呼吸道症状较多,急性生理与慢性健康状况评分II(APACHE II)较高,但所需肾上腺素总剂量较低,肾上腺素给药后不良事件较少,双相反应发生率较低。此外,与肌内注射组相比,肾上腺素给药时间明显更长(<0.001),但从接触过敏原和给予肾上腺素到症状缓解的时间明显更短(分别为<0.01和=0.03)。
持续静脉输注肾上腺素治疗过敏反应可能是安全的,不良事件较少,可改善症状,且在现有条件下相对易于给药。持续静脉输注肾上腺素还可能降低双相反应的发生率。