Abu Esba Laila Carolina, Alhoraibi Reham, Abu Al-Burak Salem, Ardah Husam I
Pharmaceutical Care Department, Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia.
King Abdullah International Medical Research Center (KAIMRC), Riyadh, Saudi Arabia.
Front Allergy. 2025 Jul 29;6:1611309. doi: 10.3389/falgy.2025.1611309. eCollection 2025.
NSAIDs are widely used for pain management but are second only to antibiotics in causing drug hypersensitivity reactions. Misclassification of these reactions often leads to unnecessary avoidance of the entire drug class, potentially resulting in increased opioid prescribing. This study aimed to assess the prevalence and characteristics of NSAID hypersensitivity, cross-reactivity patterns, and the association between NSAID hypersensitivity and opioid prescribing. The use of COX-2 selective inhibitors as a safe alternative was also explored.
A retrospective cohort study was conducted at a tertiary care hospital, including patients with documented NSAID hypersensitivity between 2016 and 2023. Data on demographics, hypersensitivity reactions, NSAID cross-reactivity, and opioid prescriptions were collected. Patients with penicillin hypersensitivity were included for comparison. Logistic regression was used to analyze the association between NSAID hypersensitivity and opioid prescribing.
Among 319 patients with NSAID hypersensitivity, 30% ( = 96) were classified as true allergy, 12.5% ( = 40) as pseudo-allergy, and 57% ( = 183) were unclassified. Cross-reactivity between NSAIDs was observed in 13%, although 52% tolerated at least one other NSAID. Patients with NSAID hypersensitivity were 62% more likely to be prescribed opioids compared to those with penicillin hypersensitivity [adjusted OR 1.62 (95% CI: 1.40-1.88), < 0.001]. Celecoxib was underutilized, prescribed to only 10% of hypersensitive patients.
NSAID hypersensitivity is associated with increased opioid prescribing due to class-wide avoidance. Despite concerns about cross-reactivity, many patients can tolerate alternative NSAIDs. Improved classification tools and clinical decision support systems are needed to guide prescribers.
非甾体抗炎药(NSAIDs)广泛用于疼痛管理,但在引起药物过敏反应方面仅次于抗生素。这些反应的错误分类常常导致对整个药物类别不必要的回避,可能导致阿片类药物处方增加。本研究旨在评估NSAIDs过敏的患病率和特征、交叉反应模式,以及NSAIDs过敏与阿片类药物处方之间的关联。还探讨了使用COX-2选择性抑制剂作为安全替代药物的情况。
在一家三级医疗中心进行了一项回顾性队列研究,纳入2016年至2023年期间有NSAIDs过敏记录的患者。收集了人口统计学、过敏反应、NSAIDs交叉反应和阿片类药物处方的数据。纳入青霉素过敏患者作为对照。采用逻辑回归分析NSAIDs过敏与阿片类药物处方之间的关联。
在319例NSAIDs过敏患者中,30%(n = 96)被分类为真正过敏,12.5%(n = 40)为假性过敏,57%(n = 183)未分类。观察到13%的NSAIDs之间存在交叉反应,尽管52%的患者至少耐受一种其他NSAIDs。与青霉素过敏患者相比,NSAIDs过敏患者开具阿片类药物的可能性高62%[调整后的比值比为1.62(95%置信区间:1.40 - 1.88),P < 0.001]。塞来昔布未得到充分利用,仅10%的过敏患者使用。
由于对整个药物类别的回避,NSAIDs过敏与阿片类药物处方增加有关。尽管存在交叉反应的担忧,但许多患者可以耐受其他NSAIDs。需要改进分类工具和临床决策支持系统来指导处方医生用药。