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首页> 外文期刊>Annals of allergy, asthma, and immunology >Allergic reactions to the coronavirus disease 2019 vaccine (ARCOV) study: The McGill University Health Centre experience: The McGill University Health Centre experience
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Allergic reactions to the coronavirus disease 2019 vaccine (ARCOV) study: The McGill University Health Centre experience: The McGill University Health Centre experience

机译:对 2019 年冠状病毒病疫苗 (ARCOV) 研究的过敏反应: 麦吉尔大学健康中心的经验: 麦吉尔大学健康中心的经验

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? 2022 American College of Allergy, Asthma ImmunologyBackground: Messenger RNA coronavirus disease 2019 (COVID-19) vaccines have been associated with allergic reactions. A history of anaphylaxis has been suggested as a risk factor for such reactions. Polyethylene glycol (PEG) has been proposed as a possible culprit allergen. Objective: To investigate possible PEG or polysorbate allergy among patients reporting prior reactions to COVID-19 vaccines or PEG and to report their subsequent tolerance of COVID-19 vaccines. Methods: From January 1, 2021, to October 31, 2021, adult patients referred to the McGill University Health Centre allergy clinics who were considered at risk of anaphylaxis were prospectively recruited. The entry criteria were any documented history of reaction to a COVID-19 vaccine or reported allergy to PEG or polysorbate. Evaluated patients underwent skin prick testing (SPT) with PEG and polysorbate. After SPT, placebo-controlled vaccine challenges were carried out. Results: Of the 44 patients recruited, 40 (90.1) had reacted to the first vaccine dose, with 18 (45) of them had anaphylactic reaction. All patients underwent SPT and 5 (11.3) had a positive test result. A total of 39 patients (88.6) underwent COVID-19 vaccine challenge at the allergy clinic. Most tolerated the vaccine, with 18 (40.1) received a single full dose, 20 (45.4) 2 split doses, and 6 (13.6) a graded dosing protocol. Of the 40 patients who reacted to the first dose, 2 had immediate nonsevere allergic reactions to the second dose. Conclusion: In this cohort of patients with a history of anaphylaxis and increased risk of allergic reactions to the COVID-19 vaccines, after allergist evaluation, including negative PEG skin testing result, the vaccine was safely administered without any serious adverse events.
机译:?2022 年美国过敏、哮喘和免疫学会背景:2019 年信使 RNA 冠状病毒病 (COVID-19) 疫苗与过敏反应有关。全身性过敏反应史被认为是此类反应的危险因素。聚乙二醇 (PEG) 已被提议作为可能的罪魁祸首过敏原。目的:调查既往对 COVID-19 疫苗或 PEG 有反应的患者可能对 PEG 或聚山梨酯过敏,并报告他们随后对 COVID-19 疫苗的耐受性。方法:前瞻性招募2021年1月1日至2021年10月31日转诊至麦吉尔大学健康中心过敏门诊的被认为有过敏反应风险的成年患者。入组标准是对 COVID-19 疫苗的任何记录在案的反应史或报告的对 PEG 或聚山梨酯过敏。被评估的患者接受了PEG和聚山梨醇酯的皮肤点刺试验(SPT)。在SPT之后,进行了安慰剂对照的疫苗挑战。结果:在招募的44例患者中,40例(90.1%)对第一剂疫苗有反应,其中18例(45%)有过敏反应。所有患者均行SPT,5例(11.3%)检测结果呈阳性。共有 39 名患者 (88.6%) 在过敏门诊接受了 COVID-19 疫苗挑战。大多数疫苗耐受性,18 例 (40.1%) 接种了单剂全剂量疫苗,20 例 (45.4%) 接种了分两次剂量,6 例 (13.6%) 接种了分级给药方案。在对第一剂有反应的 40 名患者中,有 2 名对第二剂有立即非严重过敏反应。结论:在这组有过敏反应史且对 COVID-19 疫苗过敏反应风险增加的患者中,经过敏症专科医生评估,包括 PEG 皮肤试验阴性结果,疫苗安全接种,无任何严重不良事件。

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