Martos-Benítez Frank D, Betancourt-Plaza Iliovanys, Osorio-Carmenates Isleidys, González-Martínez Nadieska J, Moráles-Suárez Ileana, Peña-García Carilda E, Pérez-Matos Yudeily L, Lestayo-O'Farrill Zurina, de Armas-Fernández José R, Cárdenas-González Raysa C, Izquierdo-Castañeda Judet, la Rosa Ernesto Sánchez-de, Orama-Requejo Versis
Intensive Care Unit, National Institute of Neurology and Neurosurgery, Havana, Cuba.
National Department of Urgency, Emergency, and Transplant of the Ministry of Public Health, Havana, Cuba.
J Peripher Nerv Syst. 2025 Mar;30(1):e12683. doi: 10.1111/jns.12683.
A recent study reported that Oropouche virus (OROV) infection may play a role in the etiology of Guillain-Barré syndrome. We aimed to identify the neurological performance, disease-modifying therapies, and clinical outcomes related to patients with Oropouche-associated Guillain-Barré syndrome admitted to the critical care unit.
This was an analysis of 210 patients diagnosed with Guillain-Barré syndrome and suspicion of Oropouche viral infection admitted to the critical care units from June 2024 to September 2024 using the national administrative healthcare data. OROV was identified by reverse-transcriptase-polymerase-chain-reaction. Patients with Guillain-Barré syndrome and Oropouche infection were compared with those without Oropouche infection in terms of demography features, neurological performance, disease-modifying therapies, and clinical outcomes.
Most patients had a severe disease. Mechanical ventilation was required in 28.6%. Overall mortality rate was 14.3%. The median time from onset of weakness to intensive care unit discharge, and the median time from hospital admission to intensive care unit discharge was 18 days (IQR: 13-24.3 days) and 13 days (IQR: 9-19 days), respectively. Oropouche viral infection was detected in 43 (20.5%) patients. There were no differences among patients with and without Oropouche viral infection regarding general characteristics, neurological performance, disease-modifying therapies, and outcomes. After adjusting for confounders in multivariate logistic regression analysis, Oropouche viral infection (OR: 1.94; 95% CI: 0.72-5.20; p = 0.189) was not related to increased mortality.
Oropouche viral infection does not modify the clinical course, disease severity, and outcomes of patients with Guillain-Barré syndrome.
最近一项研究报告称,奥罗普切病毒(OROV)感染可能在吉兰 - 巴雷综合征的病因中起作用。我们旨在确定入住重症监护病房的奥罗普切相关吉兰 - 巴雷综合征患者的神经功能表现、疾病改善治疗方法及临床结局。
这是一项对210例被诊断为吉兰 - 巴雷综合征且疑似奥罗普切病毒感染的患者进行的分析,这些患者于2024年6月至2024年9月入住重症监护病房,使用的是国家行政医疗保健数据。通过逆转录 - 聚合酶链反应鉴定OROV。将吉兰 - 巴雷综合征合并奥罗普切感染的患者与未感染奥罗普切的患者在人口统计学特征、神经功能表现、疾病改善治疗方法及临床结局方面进行比较。
大多数患者病情严重。28.6%的患者需要机械通气。总体死亡率为14.3%。从肌无力发作到重症监护病房出院的中位时间,以及从入院到重症监护病房出院的中位时间分别为18天(四分位间距:13 - 24.3天)和13天(四分位间距:9 - 19天)。43例(20.5%)患者检测到奥罗普切病毒感染。在一般特征(人口统计学特征)方面、神经功能表现、疾病改善治疗方法及结局方面,感染奥罗普切病毒的患者与未感染的患者之间没有差异。在多因素逻辑回归分析中对混杂因素进行校正后,奥罗普切病毒感染(比值比:1.94;95%置信区间:0.72 - 5.20;p = 0.189)与死亡率增加无关。
奥罗普切病毒感染不会改变吉兰 - 巴雷综合征患者的临床病程、疾病严重程度及结局。