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药物不良反应的发生率:在半乳糖-α-1,3-半乳糖(α-半乳糖)流行地区比较响尾蛇科免疫多价抗蛇毒血清F(ab')和F(ab)

Prevalence of Adverse Drug Reactions: Comparing Crotalidae Immune Polyvalent Antivenoms F(ab') and F(ab) in a Galactose-alpha-1,3-galactose (alpha-gal) Endemic Area.

作者信息

Filip Ari B, Mahmood Lina, Tilly Collette, Foster Howell R, Jackson Fawn, Banner William, Platts-Mills Thomas A E, Wilson Jeffrey, Bortz Pamela Schoppee, Charlton Nathan, Kennedy Joshua L

机构信息

Arkansas Poison and Drug Information Center, University of Arkansas for Medical Sciences College of Pharmacy, Little Rock, AR.

Department of Pediatrics, University of Arkansas for Medical Sciences, Little Rock, AR.

出版信息

Ann Emerg Med. 2025 Aug 16. doi: 10.1016/j.annemergmed.2025.06.618.

Abstract

STUDY OBJECTIVES

North American pit viper antivenoms, CroFab® and ANAVIP®, contain galactose-α-1,3-galactose (α-GAL) oligosaccharide. We compared adverse drug reactions, including presumed anaphylaxis, following administration of these antivenoms and investigated biological plausibility of these antivenoms leading to anaphylaxis in α-GAL-immunoglobulin (Ig) E-sensitized individuals.

METHODS

We performed 2 studies. A retrospective chart review from the Arkansas Poison Center (May 2021 to July 2023) identified adverse drug reactions and presumed anaphylaxis in patients treated with crotaline antivenom. Two allergists (JK, LM), blinded to the antivenom used, adjudicated presumed anaphylaxis cases. To assess whether antivenoms could activate basophils from α-GAL-IgE-sensitized individuals, basophil activation tests were performed on blood from 5 α-GAL-IgE-sensitized participants with a history of mammalian meat allergy. Basophil activation was assessed by %CD63 upregulation.

RESULTS

Adverse drug reactions without presumed anaphylaxis occurred in 7 out of 171 (4.1%) Fab recipients versus 8 out of 37 (21.6%) F(ab') recipients (Δ=17.5%, 95% confidence interval [CI] [4.0 to 31.0]). Presumed anaphylaxis was observed in 3 out of 171 (1.8%) for Fab and 6/37 (16.2%) for F(ab') (Δ=14.3%, 95% CI 2.5 to 26.2). In the basophil activation tests, the mean EC for basophil CD63 activation was 144-fold higher for Fab (mean, [standard deviation]; 647 μg/mL of antivenom [627]) compared to F(ab') (4.48 μg/mL of antivenom [2.75]).

CONCLUSION

We demonstrate a substantial incidence of adverse drug reactions and presumed anaphylaxis to crotaline antivenoms in an α-GAL endemic region, with F(ab') antivenom associated with more reactions than F(ab). Clinicians in α-GAL endemic regions should be cautious in the use of antivenoms, especially for patients with α-GAL allergy.

摘要

研究目的

北美蝰蛇抗蛇毒血清CroFab®和ANAVIP®含有半乳糖-α-1,3-半乳糖(α-GAL)寡糖。我们比较了使用这些抗蛇毒血清后发生的药物不良反应(包括疑似过敏反应),并研究了这些抗蛇毒血清导致α-GAL免疫球蛋白(Ig)E致敏个体发生过敏反应的生物学合理性。

方法

我们进行了两项研究。对阿肯色州中毒中心(2021年5月至2023年7月)的病历进行回顾性分析,确定接受响尾蛇科抗蛇毒血清治疗的患者的药物不良反应和疑似过敏反应。两名过敏症专科医生(JK、LM)在不知道所使用抗蛇毒血清的情况下,对疑似过敏反应病例进行判定。为评估抗蛇毒血清是否能激活α-GAL-IgE致敏个体的嗜碱性粒细胞,对5名有哺乳动物肉类过敏史的α-GAL-IgE致敏参与者的血液进行了嗜碱性粒细胞活化试验。通过%CD63上调评估嗜碱性粒细胞活化情况。

结果

171名接受Fab治疗的患者中有7名(4.1%)出现无疑似过敏反应的药物不良反应,而37名接受F(ab')治疗的患者中有8名(21.6%)出现此类反应(差异=17.5%,95%置信区间[CI][4.0至31.0])。171名接受Fab治疗的患者中有3名(1.8%)出现疑似过敏反应,37名接受F(ab')治疗的患者中有6名(16.2%)出现此类反应(差异=14.3%,95%CI 2.5至26.2)。在嗜碱性粒细胞活化试验中,Fab使嗜碱性粒细胞CD63活化的平均有效浓度(EC)(平均值,[标准差];抗蛇毒血清647μg/mL[627])比F(ab')(抗蛇毒血清4.48μg/mL[2.75])高144倍。

结论

我们证明在α-GAL流行地区,使用响尾蛇科抗蛇毒血清后药物不良反应和疑似过敏反应的发生率很高,F(ab')抗蛇毒血清比Fab引发的反应更多。α-GAL流行地区的临床医生在使用抗蛇毒血清时应谨慎,尤其是对于有α-GAL过敏的患者。

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