Department of Anesthesiology and Reanimation, Acibadem Mehmet Ali Aydinlar University School of Medicine, Istanbul, Turkey.
General Intensive Care Unit, Acibadem Altunizade Hospital, Istanbul, Turkey.
Sci Rep. 2024 Sep 9;14(1):20991. doi: 10.1038/s41598-024-71912-3.
Although COVID-19 infection is an immunosuppressant disease, many immunosuppressant agents, such as pulse methylprednisolone (PMP), dexamethasone (DXM), and tocilizumab (TCZ), were used during the pandemic. Secondary infections in patients with COVID-19 have been reported recently. This study investigated these agents' effects on secondary infections and outcomes in patients with COVID-19 in intensive care units (ICUs). This study was designed retrospectively, and all data were collected from the tertiary intensive care units of six hospitals between March 2020 and October 2021. All patients were divided into three groups: Group I [GI, PMP (-), DXM (-) and TCZ (-)], Group II [GII, PMP (+), DXM (+)], and Group III [GIII, PMP (+), DXM (+), TCZ (+)]. Demographic data, PO/FiO ratio, laboratory parameters, culture results, and outcomes were recorded. To compare GI-GII and GI-GIII, propensity score matching (PSM) was used by matching 14 parameters. Four hundred twelve patients with COVID-19 in the ICU were included in the study. The number of patients with microorganisms ≥ 2 was 279 (67.7%). After PSM, in GII and GIII, the number of (+) tracheal cultures and (+) bloodstream cultures detected different microorganisms ≥ 2 during the ICU period, neuropathy, tracheotomized patients, duration of IMV, and length of ICU stay were significantly higher than GI. The mortality rate was similar in GI and GII, whereas it was significantly higher in GIII than in GI. The use of immunosuppressant agents in COVID-19 patients may lead to an increase in secondary infections. In addition, increased secondary infections may lead to prolonged ICU stay, prolonged IMV duration, and increased mortality.
尽管 COVID-19 感染是一种免疫抑制性疾病,但在大流行期间,许多免疫抑制剂,如脉冲甲基泼尼松龙(PMP)、地塞米松(DXM)和托珠单抗(TCZ),都被用于治疗 COVID-19 患者。最近有报道称 COVID-19 患者发生了继发性感染。本研究调查了这些药物在重症监护病房(ICU)中 COVID-19 患者中的继发性感染和结局的影响。本研究设计为回顾性研究,所有数据均来自 2020 年 3 月至 2021 年 10 月六家医院的三级重症监护病房。所有患者分为三组:I 组[GI,PMP(-),DXM(-)和 TCZ(-)]、II 组[GII,PMP(+),DXM(+)]和 III 组[GIII,PMP(+),DXM(+),TCZ(+)]。记录人口统计学数据、PO/FiO 比值、实验室参数、培养结果和结局。为了比较 GI-GII 和 GI-GIII,通过匹配 14 个参数使用倾向评分匹配(PSM)。本研究共纳入 412 例 COVID-19 重症监护病房患者。有 279 例(67.7%)患者的微生物培养结果≥2 个。经 PSM 后,GII 和 GIII 组 ICU 期间气管培养和血培养(+)检出不同微生物≥2 的例数、神经病变、气管切开患者、有创机械通气(IMV)时间、ICU 住院时间明显高于 GI 组。GI 和 GII 组死亡率相似,而 GIII 组死亡率明显高于 GI 组。COVID-19 患者使用免疫抑制剂可能导致继发性感染增加。此外,继发性感染的增加可能导致 ICU 住院时间延长、IMV 时间延长和死亡率增加。