Sun Bing, He Hangyong, Wang Zheng, Qu Jiuxin, Li Xuyan, Ban Chengjun, Wan Jun, Cao Bin, Tong Zhaohui, Wang Chen
Crit Care. 2014 Aug 12;18(4):456. doi: 10.1186/s13054-014-0456-6.
Since 2008, severe cases of emerging human adenovirus type 55 (HAdV-55) in immunocompetent adults have been reported sporadically in China. The clinical features and outcomes of the most critically ill patients with severe acute respiratory distress syndrome (ARDS) caused by HAdV-55 requiring invasive mechanical ventilation (IMV) and/or extracorporeal membrane oxygenation (ECMO) are lacking.
We conducted a prospective, single-center observational study of pneumonia with ARDS in immunocompetent adults admitted to our respiratory ICU. We prospectively collected and analyzed clinical, laboratory, radiological characteristics, sequential tests of viral load in respiratory tract and blood, treatments and outcomes.
The results for a total of five consecutive patients with severe ARDS with confirmed HAdV-55 infection were included. All five patients were immunocompetent young men with a median age of 32 years. The mean time from onset to dyspnea was 5 days. Arterial blood gas analysis at ICU admission revealed profound hypoxia. Mean partial oxygen pressure/fraction of inspired oxygen was 58.1. Mean durations from onset to a single-lobe consolidation shown on chest X-rays (CXRs) and, from the first positive CXR to bilateral multilobar lung infiltrates, were 2 days and 4.8 days, respectively. The viral load was higher than 1 × 108 copies in three patients and was 1 × 104 in one patient. It was negative in the only patient who survived. The mean duration for noninvasive positive pressure ventilation (NPPV) failure and IMV failure were 30.8 hours and 6.2 days, respectively. Four patients received venovenous ECMO. Four (80%) of the five patients died despite receiving appropriate respiratory support.
HAdV-55 may cause severe ARDS in immunocompetent young men. Persistent high fever, dyspnea and rapid progression to respiratory failure within 2 weeks, together with bilateral consolidations and infiltrates, are the most frequent clinical manifestations of HAdV-55-induced severe ARDS. Viral load monitoring may help predict disease severity and outcome. The NPPV and IMV failure rates were very high, but ECMO may still be the respiratory support therapy of choice.
Clinicaltrials.gov NCT01585922. Registered 20 April 2012.
自2008年以来,中国已零星报告免疫功能正常的成年人感染新型55型人类腺病毒(HAdV-55)的严重病例。目前尚缺乏关于因HAdV-55导致严重急性呼吸窘迫综合征(ARDS)并需要有创机械通气(IMV)和/或体外膜肺氧合(ECMO)的最危重患者的临床特征及预后情况。
我们对收入我院呼吸重症监护病房(ICU)的免疫功能正常的成年ARDS肺炎患者进行了一项前瞻性、单中心观察性研究。我们前瞻性地收集并分析了临床、实验室、影像学特征,呼吸道和血液中病毒载量的系列检测结果、治疗方法及预后情况。
共纳入连续5例确诊为HAdV-55感染的严重ARDS患者。所有5例患者均为免疫功能正常的青年男性,中位年龄32岁。从发病到出现呼吸困难的平均时间为5天。入住ICU时的动脉血气分析显示严重缺氧。平均氧分压/吸入氧分数为58.1。胸部X线片(CXR)显示单叶实变从发病到出现的平均时间以及从首次CXR阳性到双侧多叶肺浸润的平均时间分别为2天和4.8天。3例患者的病毒载量高于1×108拷贝,1例患者为1×104拷贝。唯一存活的患者病毒载量为阴性。无创正压通气(NPPV)失败和IMV失败的平均持续时间分别为30.8小时和6.2天。4例患者接受了静脉-静脉ECMO治疗。尽管给予了适当的呼吸支持,5例患者中有4例(80%)死亡。
HAdV-55可能在免疫功能正常的青年男性中引起严重ARDS。持续高热、呼吸困难以及在2周内迅速进展为呼吸衰竭,伴双侧实变和浸润,是HAdV-55所致严重ARDS最常见的临床表现。病毒载量监测可能有助于预测疾病严重程度及预后。NPPV和IMV失败率很高,但ECMO可能仍是首选的呼吸支持治疗方法。
Clinicaltrials.gov NCT01585922。于2012年4月20日注册。