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药物不良反应评估中测试剂量的安全性和结果:一项 5 年回顾性研究。

Safety and outcomes of test doses for the evaluation of adverse drug reactions: a 5-year retrospective review.

机构信息

Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, Mass.

Division of Rheumatology, Allergy, and Immunology, Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, Mass.

出版信息

J Allergy Clin Immunol Pract. 2014 Nov-Dec;2(6):768-74. doi: 10.1016/j.jaip.2014.08.001. Epub 2014 Sep 10.

Abstract

BACKGROUND

Graded challenges are the criterion standard for evaluating adverse drug reactions (ADR). Evidence-based guidelines regarding the optimal number of steps for challenges are lacking.

OBJECTIVE

To determine the safety and outcomes of 1- or 2-step test doses among patients with ADRs seen by the allergy/immunology consult service and to compare the outcomes of 1- or 2-step test doses with multistep challenges performed during the same time period.

METHODS

We conducted a retrospective chart review of all 1- or 2-step test doses and multistep challenges at a single academic center between 2008 and 2013. Patient demographics, symptoms of initial ADRs, and outcomes of test doses and multistep challenges were reviewed. ADRs were classified by type and were graded by severity. Outcomes of 1- or 2-step test doses were compared with multistep challenges.

RESULTS

We identified 456 patients who underwent 497 one- or 2-step test doses (mean age, 51 years; 67.5% female patients). The most common drugs that prompted test doses were β-lactams (62%). The majority of patients (n = 444 [89%]) did not experience any ADRs during test doses. ADRs that occurred during test doses (n = 53 [11%]) were most commonly non-immune-mediated (45%) or IgE-mediated (32%), with grade 1 or 2 severity (100%). Forty-nine percent of ADRs during test doses did not receive any treatment. The ADR rate during multistep challenges (10/82 [12%]) was similar to test doses.

CONCLUSION

One- or 2-step test doses were safe for evaluation of ADRs. Multistep challenges did not confer added safety. Furthermore, 1- or 2-step test doses did not raise concern for induction of tolerance.

摘要

背景

递增量挑战是评估药物不良反应(ADR)的标准。缺乏有关最佳递增量步骤数的循证指南。

目的

确定过敏/免疫学咨询服务中出现 ADR 的患者接受 1 步或 2 步测试剂量的安全性和结果,并比较同一时期进行的 1 步或 2 步测试剂量与多步挑战的结果。

方法

我们对 2008 年至 2013 年间在一家学术中心进行的所有 1 步或 2 步测试剂量和多步挑战进行了回顾性图表审查。回顾了患者的人口统计学数据、初始 ADR 的症状以及测试剂量和多步挑战的结果。根据类型对 ADR 进行分类,并根据严重程度进行分级。比较了 1 步或 2 步测试剂量的结果与多步挑战。

结果

我们确定了 456 名接受 497 次 1 步或 2 步测试剂量的患者(平均年龄为 51 岁;67.5%为女性患者)。引发测试剂量的最常见药物是β-内酰胺类药物(62%)。大多数患者(n = 444 [89%])在测试剂量期间未发生任何 ADR。在测试剂量期间发生的 ADR(n = 53 [11%])最常见为非免疫介导(45%)或 IgE 介导(32%),严重程度为 1 级或 2 级(100%)。49%的测试剂量期间的 ADR 未接受任何治疗。多步挑战期间的 ADR 率(10/82 [12%])与测试剂量相似。

结论

1 步或 2 步测试剂量可安全评估 ADR。多步挑战并不能提高安全性。此外,1 步或 2 步测试剂量不会引起耐受诱导的担忧。

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