Department of Pharmaceutical Services, Vanderbilt University Medical Center, Nashville, Tennessee.
Department of Pharmaceutical Services, Vanderbilt University Medical Center, Nashville, Tennessee.
Transplant Cell Ther. 2024 Oct;30(10):1031.e1-1031.e9. doi: 10.1016/j.jtct.2024.07.020. Epub 2024 Jul 27.
Febrile neutropenia (FN) is a complication in approximately 90% of autologous stem cell transplant (SCT) patients. Guidelines support early broad-spectrum antibiotics (BSA) to prevent morbidity and mortality. However, in patients who are clinically stable and deemed to have a fever of unknown origin, the optimal duration of BSA is unknown. Accumulating evidence suggests that de-escalation of BSA in select patients may decrease duration of BSA exposure without compromising clinical outcomes such as infection, recurrent fever, and readmission. With this, a de-escalation protocol was implemented at Vanderbilt University Medical Center (VUMC) to identify autologous SCT patients who may benefit from early de-escalation of BSA. The objectives of this study were to analyze the impact of early empiric antibiotic de-escalation on the duration of BSA as well as its impact on the incidence of recurrent fever and documented infection in autologous SCT patients. This was a single-center, retrospective study evaluating patients older than 18 years of age who underwent autologous SCT and experienced an episode of FN from January 2018 to December 2022 at VUMC (N = 195). The protocol was initiated on January 1, 2020, to de-escalate BSA back to prophylaxis in stable neutropenic patients determined to have a fever of unknown origin. The primary outcome was the number of BSA days within 30 days. Secondary clinical outcomes included recurrent fever, documented infection, readmission, 30-day mortality, and 90-day non-relapsed mortality (NRM). Outcomes were compared across pre- and postprotocol groups with a Wilcoxon rank sum test, Pearson chi-square test, or regression analysis as appropriate. The median BSA duration was 4.7 and 2.7 days in the pre- and postprotocol groups, respectively (P < .001). Recurrent fever (14.2% versus 16.0%, P = .726), documented infection (1.7% versus 6.7%, P = .068), and readmission (13.3% versus 22.7%, P = .091) within 30 days were not significantly different between the two groups. Neither 30-day mortality (0.8% versus 1.3%, P = .736) nor 90-day NRM (0.8% versus 1.3%, P = .736) differed. The implementation of an early de-escalation protocol for autologous SCT patients who develop FN was associated with a reduction in duration of BSA compared to the preprotocol group without a significant difference in readmission, recurrent fevers, and documented infections. This study adds to existing evidence that early de-escalation of BSA in FN patients with a fever of unknown origin who are afebrile and clinically stable is safe and reduces unnecessary antibiotic use.
发热性中性粒细胞减少症(FN)是大约 90%自体干细胞移植(SCT)患者的并发症。指南支持早期使用广谱抗生素(BSA)以预防发病率和死亡率。然而,对于临床稳定且被认为发热原因不明的患者,BSA 的最佳持续时间尚不清楚。越来越多的证据表明,在选择的患者中降低 BSA 的级别可能会减少 BSA 暴露的持续时间,而不会影响感染、复发性发热和再入院等临床结果。因此,范德比尔特大学医学中心(VUMC)实施了一项降级方案,以确定可能从 BSA 早期降级中受益的自体 SCT 患者。本研究的目的是分析早期经验性抗生素降级对 BSA 持续时间的影响,以及对自体 SCT 患者复发性发热和已记录感染发生率的影响。这是一项单中心、回顾性研究,评估了 2018 年 1 月至 2022 年 12 月期间在 VUMC 接受自体 SCT 并发生 FN 的年龄大于 18 岁的患者(N=195)。该方案于 2020 年 1 月 1 日启动,旨在将稳定中性粒细胞减少症患者的 BSA 降级回预防,这些患者被认为发热原因不明。主要结局是 30 天内 BSA 的天数。次要临床结局包括复发性发热、已记录感染、再入院、30 天死亡率和 90 天非复发死亡率(NRM)。使用 Wilcoxon 秩和检验、Pearson 卡方检验或适当的回归分析比较了方案前组和方案后组之间的结果。方案前组和方案后组的中位 BSA 持续时间分别为 4.7 天和 2.7 天(P<.001)。两组 30 天内复发性发热(14.2%与 16.0%,P=.726)、已记录感染(1.7%与 6.7%,P=.068)和再入院(13.3%与 22.7%,P=.091)无显著差异。两组 30 天死亡率(0.8%与 1.3%,P=.736)和 90 天 NRM(0.8%与 1.3%,P=.736)也无差异。与方案前组相比,为发生 FN 的自体 SCT 患者实施早期降级方案与 BSA 持续时间缩短相关,且再入院、复发性发热和已记录感染无显著差异。本研究增加了现有证据,即对发热原因不明且无发热、临床稳定的 FN 患者进行早期 BSA 降级是安全的,可减少不必要的抗生素使用。