Cheng Jia Lu, Peng Chun-Chih, Chiu Nan-Chang, Weng Li-Chuan, Chiu Yu-Ying, Chang Lung, Huang Daniel Tsung-Ning, Huang Fu-Yuan, Liu Chang-Pan, Chi Hsin
Department of Pediatrics, MacKay Children's Hospital, Taipei, Taiwan.
Department of Pediatrics, MacKay Children's Hospital, Taipei, Taiwan; Department of Medicine, MacKay Medical College, New Taipei City, Taiwan.
J Microbiol Immunol Infect. 2017 Aug;50(4):418-426. doi: 10.1016/j.jmii.2015.08.006. Epub 2015 Sep 9.
BACKGROUND/PURPOSE: Respiratory infections caused by human adenoviruses (HAdV) are worldwide, and have significantly increased recently in Taiwan. This study aimed to clarify the molecular epidemiology and risk factors of HAdV severe infections and pneumonia among Taiwanese children.
Patients with HAdV infections and hospitalized in a medical center between 2009 and 2013 were divided into severe or nonsevere HAdV infections based on whether or not they received intensive care. HAdV pneumonia was identified for comparison. The HAdV genotype was determined by sequencing the partial hexon and fiber genes. The nucleotide sequences were compared by phylogenetic analysis.
The 176 patients (97 boys, 79 girls) had a median age of 3.7 years. The HAdV infections circulated year-round. HAdV B3 (54.5%) was the most common genotype, followed by HAdV C2 (21%), HAdV E4 (8%), and HAdV B7 (6.8%). Thirty-two patients needed intensive care. In multivariate analysis, the risk factors for severe HAdV infections were underlying neurologic diseases [odds ratio (OR): 164.9; p < 0.001], prematurity (OR: 10.9; p = 0.042), and HAdV B7 (OR: 39.5; p = 0.011). Twenty-nine patients had HAdV pneumonia. Patients with underlying neurologic diseases (OR 76.8; p < 0.001), airway anomaly (OR 15.1; p = 0.033), chronic lung diseases (OR 12.5; p = 0.047), weight < 3 percentile (OR 5.5; p = 0.027), and HAdV B7 (OR 4.2; p = 0.002) had higher incidences of pneumonia. Four with underlying neurologic diseases died of acute respiratory distress syndrome.
HAdV infections circulate all year-round. HAdV B7 is strongly related to severe infections and pneumonia. Underlying neurologic diseases and prematurity are risk factors for severe HAdV infections.
背景/目的:人腺病毒(HAdV)引起的呼吸道感染在全球范围内存在,且近期在台湾地区显著增加。本研究旨在阐明台湾儿童中HAdV严重感染和肺炎的分子流行病学及危险因素。
2009年至2013年期间在某医疗中心住院的HAdV感染患者,根据是否接受重症监护分为严重或非严重HAdV感染。确定HAdV肺炎以作比较。通过对部分六邻体和纤维基因进行测序来确定HAdV基因型。通过系统发育分析比较核苷酸序列。
176例患者(97例男孩,79例女孩)的中位年龄为3.7岁。HAdV感染全年均有发生。HAdV B3(54.5%)是最常见的基因型,其次是HAdV C2(21%)、HAdV E4(8%)和HAdV B7(6.8%)。32例患者需要重症监护。在多变量分析中,严重HAdV感染的危险因素为潜在神经系统疾病[比值比(OR):164.9;p < 0.001]、早产(OR:10.9;p = 0.042)和HAdV B7(OR:39.5;p = 0.011)。29例患者患有HAdV肺炎。患有潜在神经系统疾病(OR 76.8;p < 0.001)、气道异常(OR 15.1;p = 0.033)、慢性肺部疾病(OR 12.5;p = 0.047)、体重<第3百分位数(OR 5.5;p = 0.027)和HAdV B7(OR 4.2;p = 0.002)的患者肺炎发病率较高。4例患有潜在神经系统疾病的患者死于急性呼吸窘迫综合征。
HAdV感染全年均有发生。HAdV B7与严重感染和肺炎密切相关。潜在神经系统疾病和早产是严重HAdV感染的危险因素。