Camou Fabrice, Issa Nahéma, Hessamfar Mojgan, Guisset Olivier, Mourissoux Gaëlle, Pedeboscq Stéphane, Minot Aimée, Bonnet Fabrice
CHU BORDEAUX, Intensive Care and Infectious Diseases Department, Saint-Andre Hospital, 33075 Bordeaux, France.
CHU BORDEAUX, Internal Medicine and Infectious Diseases Department, Saint-Andre Hospital, 33075 Bordeaux, France.
J Clin Med. 2022 Sep 22;11(19):5559. doi: 10.3390/jcm11195559.
Dexamethasone and tocilizumab are used to treat severely ill COVID-19 patients admitted to intensive care units (ICUs). We explored whether combination therapy increased the risk of superinfection compared to dexamethasone alone.
This observational, retrospective study included critically ill COVID-19 adult patients admitted to our ICU because of respiratory failure. Patients received dexamethasone with (Group 1) or without (Group 2) tocilizumab. Data were collected from electronic medical files.
A total of 246 patients were included, of whom 150 received dexamethasone and tocilizumab, while 96 received dexamethasone alone. Acute respiratory distress syndrome was evident on admission in 226 patients, 56 of whom required mechanical ventilation (MV). Superinfections, mainly respiratory, were diagnosed in 59 patients, including 34/150 (23%) in Group 1 and 25/96 (26%) in Group 2 ( = 0.32). After multivariate analysis, the factors associated with a higher risk of superinfection included hematological malignancy (hazard ratio (HR): 2.47 (1.11-5.47), = 0.03), MV (HR: 3.74 (1.92-7.26), = 0.0001), and a higher SAPS-II score on admission (HR: 1.03 (1.01-1.06), = 0.006).
In critically ill COVID-19 patients, the addition of tocilizumab to dexamethasone was not associated with an increased risk of superinfection.
地塞米松和托珠单抗用于治疗入住重症监护病房(ICU)的重症新型冠状病毒肺炎(COVID-19)患者。我们探讨了联合治疗与单独使用地塞米松相比是否会增加二重感染的风险。
这项观察性、回顾性研究纳入了因呼吸衰竭入住我们ICU的重症成年COVID-19患者。患者接受了地塞米松联合(第1组)或不联合(第2组)托珠单抗治疗。数据从电子病历中收集。
共纳入246例患者,其中150例接受了地塞米松和托珠单抗治疗,而96例仅接受了地塞米松治疗。226例患者入院时出现急性呼吸窘迫综合征,其中56例需要机械通气(MV)。59例患者被诊断为二重感染,主要为呼吸道感染,包括第1组中的34/150(23%)和第2组中的25/96(26%)(P = 0.32)。多因素分析后,与二重感染风险较高相关的因素包括血液系统恶性肿瘤(风险比(HR):2.47(1.11 - 5.47),P = 0.03)、MV(HR:3.74(1.92 - 7.26),P = 0.0001)以及入院时较高的简化急性生理学评分-II(SAPS-II)(HR:1.03(1.01 - 1.06),P = 0.006)。
在重症COVID-19患者中,地塞米松联合托珠单抗治疗与二重感染风险增加无关。