Damlaj M, Bartoo G, Cartin-Ceba R, Gijima D, Alkhateeb H B, Merten J, Hashmi S, Litzow M, Gastineau D, Hogan W, Patnaik M M
Division of Hematology, Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Department of Pharmacy Services, Mayo Clinic, Rochester, Minnesota, USA.
Transpl Infect Dis. 2016 Apr;18(2):216-26. doi: 10.1111/tid.12513. Epub 2016 Apr 1.
Respiratory syncytial virus (RSV) infection causes significant morbidity and mortality in allogeneic stem cell transplant (allo-SCT) recipients. Although ribavirin and immunoglobulins are common components of therapy, the role of adjunct corticosteroids is not established.
We sought to evaluate corticosteroid utilization in the setting of post-allo-SCT RSV infection in our center and assess post-transplant outcomes including pulmonary function decline.
Patients with a history of RSV infection from 2008 to 2014 seen at our institution were identified. Treatment and outcome data were retrospectively collected. Forced expiratory volume at 1 s (FEV1) and carbon monoxide diffusion capacity (DLCO) were collected pre- and post-RSV infection.
During the observation period, RSV was isolated in 53 of 552 patients undergoing allo-SCT (10%) and 45 had evaluable therapy data. RSV-related mortality in this cohort was 4/45 (9%). Twenty-one (47%) were on corticosteroids prior to RSV diagnosis, of whom 11 (24%) had a dose increase post symptom onset. Eight (18%) patients were started on corticosteroids at the time of RSV infection. Corticosteroid therapy at symptom onset was associated with a higher rate of upper respiratory infection (URTI) to lower respiratory infection (LRTI) progression risk ratio (RR) 2.49 (1.21-5.13; P = 0.016), hospital admission RR 2.05 (1.24-3.37; P = 0.005), or intensive care unit admission RR 2.91 (1.89-5.01; P = 0.002). No significant difference was seen with FEV1 and DLCO decline (P = 0.3 and 0.24, respectively) or mortality (P = 0.26).
Adjunct corticosteroid use in the setting of RSV infection did not improve RSV-related outcomes including long-term pulmonary function. Our results do not support the routine use of corticosteroids; however, this finding does need to be verified in a larger cohort of patients.
呼吸道合胞病毒(RSV)感染在异基因造血干细胞移植(allo-SCT)受者中可导致显著的发病率和死亡率。尽管利巴韦林和免疫球蛋白是治疗的常用成分,但辅助性皮质类固醇的作用尚未明确。
我们试图评估本中心在allo-SCT后RSV感染情况下皮质类固醇的使用情况,并评估移植后的结局,包括肺功能下降情况。
确定2008年至2014年在本机构就诊的有RSV感染病史的患者。回顾性收集治疗和结局数据。在RSV感染前后收集第1秒用力呼气量(FEV1)和一氧化碳弥散量(DLCO)。
在观察期内,552例接受allo-SCT的患者中有53例分离出RSV(10%),45例有可评估的治疗数据。该队列中RSV相关死亡率为4/45(9%)。21例(47%)在RSV诊断前使用皮质类固醇,其中11例(24%)在症状出现后增加了剂量。8例(18%)患者在RSV感染时开始使用皮质类固醇。症状出现时使用皮质类固醇治疗与上呼吸道感染(URTI)进展为下呼吸道感染(LRTI)的风险比更高相关(RR 2.49,1.21 - 5.13;P = 0.016),住院风险比RR 2.05(1.24 - 3.37;P = 0.005),或重症监护病房入院风险比RR 2.91(1.89 - 5.01;P = 0.002)。FEV₁和DLCO下降(分别为P = 0.3和0.24)或死亡率(P = 0.26)未见显著差异。
在RSV感染情况下使用辅助性皮质类固醇并不能改善包括长期肺功能在内的RSV相关结局。我们的结果不支持常规使用皮质类固醇;然而,这一发现需要在更大规模的患者队列中得到验证。