-内酰胺过敏标签对骨髓移植患者的影响。

Benjamin M Haxby, Kendall J Tucker, Caitlin M McCracken, YoungYoon Ham, Jon P Furuno, Jessina C McGregor
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引用次数: 0

摘要

背景:大约95%的医疗记录中记录的β -内酰胺过敏患者在测试时并不真正过敏。这些患者可能不必要地避免使用一线抗生素,导致治疗失败增加、费用增加和抗生素耐药性增加。骨髓移植(BMT)患者由于免疫系统减弱和严重感染的高风险,可能面临这些不良后果的更高风险。我们的目的是评估β -内酰胺过敏标签及其对BMT患者预后的影响。方法:我们对2018年4月至2020年3月期间接受BMT的成年住院患者进行了回顾性队列研究。评估青霉素过敏试验/去标签的资格。采用多变量logistic回归来衡量β -内酰胺过敏标签对100天结局的独立影响:死亡率、ICU入院率、再住院率和静脉抗生素使用。结果:在358例BMT患者中,75例(21%)在基线时有β -内酰胺过敏标签。有过敏标签的患者死亡率更高(14.7% vs 7.8%, P = 0.067)。在多变量分析中,有过敏标签的患者的死亡风险并没有显著增加(OR = 1.60;95% CI = 0.68 - 3.78),但更有可能接受碳青霉烯类药物(OR = 6.27;95% ci = 2.81-13.98)。所有贴有青霉素类过敏标签的患者均符合过敏试验/去标签的条件。结论:我们没有观察到有β -内酰胺过敏标签的BMT患者死亡风险显著增加;然而,碳青霉烯的使用有所增加。青霉素过敏去标签程序可能有助于优化BMT患者的抗生素处方。需要更大规模的研究来量化β -内酰胺过敏标签对BMT患者预后的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of beta-lactam allergy labels on bone marrow transplant patients.

Background: Approximately 95% of patients with a beta-lactam allergy noted in their medical record are not truly allergic when tested. These patients may unnecessarily avoid first-line antibiotics, resulting in increased treatment failure, higher costs, and antibiotic resistance. Bone marrow transplant (BMT) patients may be at higher risk for these adverse outcomes due to weakened immune systems and high risk for severe infections. Our objective was to evaluate beta-lactam allergy labels and their influence on BMT patient outcomes.

Methods: We conducted a retrospective cohort study of adult inpatients undergoing BMT during April 2018-March 2020. Eligibility for penicillin allergy testing/de-labeling was evaluated. Multivariable logistic regression was performed to measure independent effects of beta-lactam allergy labels on 100-day outcomes: mortality, ICU admission, rehospitalization, and intravenous antibiotic use.

Results: Among 358 BMT patients, 75 (21%) had a beta-lactam allergy label at baseline. Mortality was higher in patients with an allergy label (14.7% vs 7.8%, P = 0.067). In multivariable analysis, patients with allergy labels were not at a significantly greater risk of mortality (OR = 1.60; 95% CI = 0.68 - 3.78) but were significantly more likely to receive carbapenems (OR = 6.27; 95% CI = 2.81-13.98). All patients with penicillin-class allergy labels were eligible for allergy testing/de-labeling.

Conclusion: We did not observe a significant increased risk of mortality in BMT patients with beta-lactam allergy labels; however, increased carbapenem use was observed. Penicillin allergy de-labeling programs may help optimize antibiotic prescribing in BMT patients. Larger studies are needed to quantify the impact of beta-lactam allergy labels on BMT patient outcomes.

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