Department of Clinical Pharmacy, University of Colorado Skaggs School of Pharmacy and Pharmaceutical Sciences, Aurora, Colo.
Department of Pharmacy, Mayo Clinic Hospital-Rochester, Rochester, Minn.
J Allergy Clin Immunol. 2016 Apr;137(4):1148-1153. doi: 10.1016/j.jaci.2015.10.026. Epub 2015 Dec 11.
The choice of empiric antibiotics for the treatment of gram-negative bacilli (GNB) bloodstream infections (BSIs) in patients presenting with a β-lactam (BL) allergy is often a difficult decision given that these agents are first-line treatment in many guidelines.
We sought to compare rates of clinical failure between patients with a history of BL allergy who received either a BL or a non-β-lactam (NBL).
Adult patients with a past medical history of BL allergy and receipt of antibiotics for treatment of a GNB BSI were included from 3 academic medical centers. Treatment groups were classified as BL or NBL groups based on the empiric antibiotics received. Clinical failure was assessed 72 to 96 hours after initiation of empiric antibiotics. Hypersensitivity reactions during receipt of antibiotic therapy for the index BSI were recorded.
A total of 552 patients were included for analysis: 433 patients in the BL group and 119 patients in the NBL group. Clinical failure was higher in the NBL group compared with the BL group (38.7% vs 27.4%, P = .030). The most common cause of clinical failure was a temperature of greater than 38.0°C 72 to 96 hours after receipt of empiric antibiotics (NBL group: 22.7% vs BL group: 13.9%, P = .016). Hypersensitivity occurred in 16 (2.9%) of 552 patients. Thirteen (2.5%) of 552 patients experiencing hypersensitivity reactions were exposed to a BL during treatment for GNB BSI.
Among patients with a BL allergy, use of BL antibiotics is associated with a lower rate of clinical failure. The low rate of hypersensitivity provides further evidence about the risk of cross-reactivity between BL classes. These results support the practice of using a BL from an alternative class for patients in need of gram-negative antibiotic coverage.
对于β-内酰胺(BL)过敏的患者,在革兰氏阴性杆菌(GNB)血流感染(BSI)中选择经验性抗生素治疗时,通常需要做出艰难的决策,因为这些药物是许多指南中的一线治疗药物。
我们旨在比较有 BL 过敏史的患者中,接受 BL 或非β-内酰胺(NBL)治疗的患者的临床失败率。
从 3 所学术医疗中心纳入有 BL 过敏史并接受抗生素治疗 GNB BSI 的成年患者。根据接受的经验性抗生素,将治疗组分为 BL 或 NBL 组。在开始经验性抗生素治疗后 72 至 96 小时评估临床失败。记录在 GNB BSI 治疗期间接受抗生素治疗时发生的过敏反应。
共纳入 552 例患者进行分析:BL 组 433 例,NBL 组 119 例。NBL 组的临床失败率高于 BL 组(38.7% vs. 27.4%,P = 0.030)。临床失败的最常见原因是在接受经验性抗生素治疗后 72 至 96 小时体温大于 38.0°C(NBL 组:22.7% vs. BL 组:13.9%,P = 0.016)。552 例患者中有 16 例(2.9%)发生过敏(NBL 组:2.5% vs. BL 组:13.9%,P = 0.016)。在因 GNB BSI 接受治疗时发生过敏反应的 552 例患者中,有 13 例(2.5%)接触了 BL。
在 BL 过敏患者中,使用 BL 抗生素与较低的临床失败率相关。低过敏率进一步证明了 BL 类之间交叉反应的风险。这些结果支持在需要革兰氏阴性抗生素覆盖的情况下,使用来自替代类别的 BL 的做法。