Institute for Epidemiology, Statistics and Informatics GmbH, Frankfurt, Germany.
Northern Clinical School, Sydney Medical School, Faculty of Medicine and Health, University of Sydney, Sydney, New South Wales, Australia.
Clin Exp Immunol. 2021 Dec;206(3):384-394. doi: 10.1111/cei.13665. Epub 2021 Oct 17.
This large cohort study from the US Premier Healthcare Database evaluated the risk and predictors of anaphylaxis in association with intravenous immunoglobulin (IvIg) therapy in the inpatient and outpatient setting. Data were collected retrospectively (January 2009-December 2018) from 24 919 patients administered IgPro10 IvIg, median age 54 years. Immunoglobulins of interest were IgPro10 and other IvIg given before or after IgPro10. Moderate and severe anaphylaxis was identified from same-day parenteral epinephrine and IvIg use and reviews of patient record summaries. Predictors for first anaphylactic reactions associated with IvIg administration were derived from adjusted incidence rate ratios (IRR) using Poisson regression. Moderate anaphylaxis in IvIg use was rare and severe anaphylaxis very rare based on a total of 124 moderate and four non-fatal severe first anaphylactic events, incidence rate of 7.11 and 0.23/10 000 IvIg administrations, respectively. Age under 18 years was an independent predictor of moderate or severe anaphylactic events [adjusted incidence rate ratio = 2.94, 0.95 confidence interval = 1.91-4.52] compared with those aged 18 years and older. First IvIg administration was a strong predictor of anaphylaxis. The IRR in those with a subsequent IvIg administration in the preceding 42 days decreased to 0.27 (0.17-0.42) and in those effectively IvIg-naive (no IvIg for > 42 days) to 0.76 (0.44-1.32) compared with first IvIg use. The key conclusions from this study are that the risk of anaphylaxis has progressively reduced over the last decade, from 14.87 of 10 000 in 2009-10 to 4.39 of 10 000 IvIg administrations in 2017-18 and is rare overall, and that the risk of anaphylaxis is increased in those aged under 18 years.
这项来自美国 Premier Healthcare Database 的大型队列研究评估了静脉注射免疫球蛋白 (IvIg) 治疗与住院和门诊环境下过敏反应风险的相关性及其预测因素。数据通过回顾性收集(2009 年 1 月至 2018 年 12 月)来自 24919 例接受 IgPro10 IvIg 治疗的患者,中位年龄为 54 岁。感兴趣的免疫球蛋白是 IgPro10 和其他在 IgPro10 之前或之后给予的 IvIg。中度和重度过敏反应是根据当天使用的静脉内肾上腺素和 IvIg 以及患者病历摘要的审查来确定的。使用泊松回归分析得出与 IvIg 给药相关的首次过敏反应的预测因素。根据总共 124 例中度和 4 例非致命性重度首次过敏反应事件,IgPro10 使用率中过敏反应发生率为 7.11/10000 IvIg 给药,IvIg 使用率中严重过敏反应发生率为 0.23/10000 IvIg 给药,发生率较低。与 18 岁及以上患者相比,18 岁以下患者为中度或重度过敏反应的独立预测因素[调整后发病率比=2.94,95%置信区间 1.91-4.52]。首次 IvIg 给药是过敏反应的强烈预测因素。在之前 42 天内随后进行 IvIg 给药的患者中,IRR 降至 0.27(0.17-0.42),在真正 IvIg 无反应(>42 天无 IvIg)的患者中降至 0.76(0.44-1.32),与首次 IvIg 使用相比。这项研究的主要结论是,过敏反应的风险在过去十年中逐渐降低,从 2009-10 年的每 10000 例 14.87 例降至 2017-18 年的每 10000 例 IvIg 治疗 4.39 例,总体而言较为罕见,18 岁以下患者过敏反应风险增加。