首页> 外文期刊>JAMA: the Journal of the American Medical Association >Cytomegalovirus reactivation in critically ill immunocompetent patients.
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Cytomegalovirus reactivation in critically ill immunocompetent patients.

机译:危重免疫能力强的患者的巨细胞病毒再激活。

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CONTEXT: Cytomegalovirus (CMV) infection is associated with adverse clinical outcomes in immunosuppressed persons, but the incidence and association of CMV reactivation with adverse outcomes in critically ill persons lacking evidence of immunosuppression have not been well defined. OBJECTIVE: To determine the association of CMV reactivation with intensive care unit (ICU) and hospital length of stay in critically ill immunocompetent persons. DESIGN, SETTING, AND PARTICIPANTS: We prospectively assessed CMV plasma DNAemia by thrice-weekly real-time polymerase chain reaction (PCR) and clinical outcomes in a cohort of 120 CMV-seropositive, immunocompetent adults admitted to 1 of 6 ICUs at 2 separate hospitals at a large US tertiary care academic medical center between 2004 and 2006. Clinical measurements were assessed by personnel blinded to CMV PCR results. Risk factors for CMV reactivation and association with hospital and ICU length of stay were assessed by multivariable logistic regression and proportional odds models. MAIN OUTCOME MEASURES: Association of CMV reactivation with prolonged hospital length of stay or death. RESULTS: The primary composite end point of continued hospitalization (n = 35) or death (n = 10) by 30 days occurred in 45 (35%) of the 120 patients. Cytomegalovirus viremia at any level occurred in 33% (39/120; 95% confidence interval [CI], 24%-41%) at a median of 12 days (range, 3-57 days) and CMV viremia greater than 1000 copies/mL occurred in 20% (24/120; 95% CI, 13%-28%) at a median of 26 days (range, 9-56 days). By logistic regression, CMV infection at any level (adjusted odds ratio [OR], 4.3; 95% CI, 1.6-11.9; P = .005) and at greater than 1000 copies/mL (adjusted OR, 13.9; 95% CI, 3.2-60; P .001) and the average CMV area under the curve (AUC) in log(10) copies per milliliter (adjusted OR, 2.1; 95% CI, 1.3-3.2; P .001) were independently associated with hospitalization or death by 30 days. In multivariable partial proportional odds models, both CMV 7-day moving average (OR, 5.1; 95% CI, 2.9-9.1; P .001) and CMV AUC (OR, 3.2; 95% CI, 2.1-4.7; P .001) were independently associated with a hospital length of stay of at least 14 days. CONCLUSIONS: These preliminary findings suggest that reactivation of CMV occurs frequently in critically ill immunocompetent patients and is associated with prolonged hospitalization or death. A controlled trial of CMV prophylaxis in this setting is warranted.
机译:背景:巨细胞病毒(CMV)感染与免疫抑制患者的不良临床预后相关,但对于缺乏免疫抑制证据的重症患者,CMV激活与不良反应的发生率及相关性尚未明确。目的:确定重症免疫功能正常者CMV再激活与重症监护病房(ICU)和住院时间之间的关系。设计,地点和参与者:我们通过每周两次实时实时聚合酶链反应(PCR)评估了CMV血浆DNA含量,并在2家独立医院的6个ICU中纳入了120个CMV血清阳性,具有免疫能力的成年人,在2004年至2006年期间,在美国一家大型三级医疗学术医学中心就诊。临床测量由对CMV PCR结果不了解的人员进行评估。通过多变量logistic回归和比例赔率模型评估了CMV复活以及与医院和ICU住院时间相关的危险因素。主要观察指标:CMV再激活与住院或死亡时间延长的关联。结果:120例患者中有45例(35%)持续住院(n = 35)或30天死亡(n = 10)的主要复合终点。任何水平的巨细胞病毒毒血症的发生率为33%(39/120; 95%置信区间[CI],24%-41%),中位数为12天(范围3-57天),CMV病毒血症大于1000份/ mL以20%(24/120; 95%CI,13%-28%)的中位数为26天(范围9-56天)出现。通过Logistic回归分析,可以发现任何水平的CMV感染(调整后的优势比[OR]为4.3; 95%CI为1.6-11.9; P = 0.005),且感染量大于1000拷贝/ mL(调整后的OR为13.9; 95%CI 3.2-60; P <.001)和log(10)每毫升拷贝数下曲线下的平均CMV面积(AUC)(校正OR,2.1; 95%CI,1.3-3.2; P <.001)独立相关30天之内住院或死亡。在多变量部分比例赔率模型中,CMV 7天移动平均值(OR,5.1; 95%CI,2.9-9.1; P <.001)和CMV AUC(OR,3.2; 95%CI,2.1-4.7; P < .001)与至少14天的住院时间独立相关。结论:这些初步发现表明,CMV的重新激活经常发生在危重的免疫功能正常的患者中,并且与住院或死亡时间延长有关。在这种情况下,有必要进行CMV预防性对照试验。

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