Lopez Roa Paula, Hill Joshua A, Kirby Katharine A, Leisenring Wendy M, Huang Meei-Li, Santo Tracy K, Jerome Keith R, Boeckh Michael, Limaye Ajit P
1Department of Microbiology and Infectious Diseases, Hospital Gregorio Maranon, Madrid, Spain. 2Department of Medicine, University of Washington, Seattle, WA. 3Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA. 4Department of Medicine, University of California San Francisco, San Francisco, CA. 5Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA. 6Department of Laboratory Medicine, University of Washington, Seattle, WA.
Crit Care Med. 2015 Jul;43(7):1415-22. doi: 10.1097/CCM.0000000000000969.
Human herpesvirus 6 is associated with a variety of complications in immunocompromised patients, but no studies have systematically and comprehensively assessed the impact of human herpesvirus 6 reactivation, and its interaction with cytomegalovirus, in ICU patients.
We prospectively assessed human herpesvirus 6 and cytomegalovirus viremia by twice-weekly plasma polymerase chain reaction in a longitudinal cohort study of 115 adult, immunocompetent ICU patients. The association of human herpesvirus 6 and cytomegalovirus reactivation with death or continued hospitalization by day 30 (primary endpoint) was assessed by multivariable logistic regression analyses.
This study was performed in trauma, medical, surgical, and cardiac ICUs at two separate hospitals of a large tertiary care academic medical center.
A total of 115 cytomegalovirus seropositive, immunocompetent adults with critical illness were enrolled in this study.
None.
Human herpesvirus 6 viremia occurred in 23% of patients at a median of 10 days. Human herpesvirus 6B was the species detected in eight samples available for testing. Most patients with human herpesvirus 6 reactivation also reactivated cytomegalovirus (70%). Severity of illness was not associated with viral reactivation. Mechanical ventilation, burn ICU, major infection, human herpesvirus 6 reactivation, and cytomegalovirus reactivation were associated with the primary endpoint in unadjusted analyses. In a multivariable model adjusting for mechanical ventilation and ICU type, only coreactivation of human herpesvirus 6 and cytomegalovirus was significantly associated with the primary endpoint (adjusted odds ratio, 7.5; 95% CI, 1.9-29.9; p = 0.005) compared to patients with only human herpesvirus 6, only cytomegalovirus, or no viral reactivation.
Coreactivation of both human herpesvirus 6 and cytomegalovirus in ICU patients is associated with worse outcome than reactivation of either virus alone. Future studies should define the underlying mechanism(s) and determine whether prevention or treatment of viral reactivation improves clinical outcome.
人疱疹病毒6与免疫功能低下患者的多种并发症相关,但尚无研究系统全面地评估人疱疹病毒6激活及其与巨细胞病毒的相互作用对重症监护病房(ICU)患者的影响。
在一项对115名具有免疫能力的成年ICU患者的纵向队列研究中,我们通过每周两次的血浆聚合酶链反应前瞻性评估人疱疹病毒6和巨细胞病毒血症。通过多变量逻辑回归分析评估人疱疹病毒6和巨细胞病毒激活与30天时死亡或持续住院(主要终点)之间的关联。
本研究在一家大型三级医疗学术中心的两家不同医院的创伤、内科、外科和心脏ICU中进行。
共有115名巨细胞病毒血清阳性、具有免疫能力的成年危重症患者纳入本研究。
无。
23%的患者出现人疱疹病毒6血症,中位时间为10天。在可用于检测的8个样本中检测到的是人疱疹病毒6B型。大多数人疱疹病毒6激活的患者也激活了巨细胞病毒(70%)。疾病严重程度与病毒激活无关。在未校正分析中,机械通气、烧伤ICU、严重感染、人疱疹病毒6激活和巨细胞病毒激活与主要终点相关。在调整了机械通气和ICU类型的多变量模型中,与人疱疹病毒6单独激活、巨细胞病毒单独激活或无病毒激活的患者相比,只有人疱疹病毒6和巨细胞病毒共同激活与主要终点显著相关(校正比值比,7.5;95%可信区间,1.9 - 29.9;p = 0.005)。
ICU患者中人疱疹病毒6和巨细胞病毒共同激活与单独一种病毒激活相比,结局更差。未来的研究应明确潜在机制,并确定预防或治疗病毒激活是否能改善临床结局。