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2002~2005年期间萨斯喀彻温省儿科三级医疗中心因呼吸道合胞病毒感染住院的儿童病例分析(英文) 被引量:3

Children hospitalized with respiratory syncytial virus infection in Saskatchewan pediatric tertiary care centers,2002-2005
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摘要 中文概呼吸道合胞病毒(RSV)是2岁以下儿童呼吸道感染最常见的病原体,也是引起婴儿病毒感染所致死亡的主要原因。到目前为止,尚未见加拿大萨斯喀彻温省RSV流行病学的研究报道。本研究的目的是描述2002年7月至2005年6月期间在萨斯喀彻温省的两个儿科三级医疗中心,即皇家大学医院(RUH)和萨斯卡通和里贾纳总医院(RGH),因RSV感染住院的儿童的流行病学特点及疾病严重程度,其中部分患儿有帕利珠单抗(palivizumab)预防史。 在上述2个医疗中心住院时间≥24h的儿童(年龄:从出生到16岁11个月)经实验室病毒鉴定确诊为RSV感染的儿童纳入本研究。在RUH中心,患儿鼻咽部分泌物经直接荧光抗体(DFA)检测阳性者确诊为RSV感染。如果DFA为阴性,则对该标本进行病毒培养。在RGH中心,所有患儿鼻咽部分泌物标本均进行DFA检测和病毒培养。确诊后对患儿的健康记录进行回顾性分析,内容包括患儿的人口统计信息、转诊模式、帕利珠单抗预防史、感染严重程度及转归。目前尚无统一的感染严重程度的判断标准,本研究根据住院时间、是否需要小儿重症监护及持续时间、是否机械通气等进行评估。在研究期间,萨斯喀彻温省的帕利珠单抗预防的标准与加拿大儿科学会(CPS)的建议一致。 2002年7月至2005年6月3年期间,总共有590名RSV儿童(包括324名男童)住院治疗,共602次住院记录,其中12名儿童住院1次以上。入院时患儿中位实足年龄为5.3个月,平均住院时间为4.0d(范围:〈1d至121.2个月)。82.4%的患儿出生时胎龄≥36周,7.5%为33-35周,9.5%≤32周。RSV感染住院情况呈现季节性模式,其中大部分发生在三月和六月。患儿最常见的临床表现为细支气管炎(70.2%),38.1%表现为肺炎,17.3%为上呼吸道感染,0.5%表现为哮吼(患儿可能同时有1个以上的临床表现)。478例(81.0%)为RSV轻度至中度感染,110例(18.6%)为重度感染。25.1%的患儿有继发性细菌感染。共有39例(6.7%)需要入住儿科重症监护病房(PICU),中位入住时间为5.0d。其中,22例重症患儿(56%)需要机械通气(通气时间中位数6.0d),14例重症患儿(36%)有继发性细菌感染。与入住普通病房的患儿比较,PICU患儿大多有如下情况:入院时年龄较小(P〈0.01),有潜在的肺部疾病(P〈0.01)或先天性心脏疾病(P=0.01),有两个或更多潜在的疾病(P〈0.01),与其他儿童共同居住(P=0.02)。在本研究过程中,2例儿童死亡,但均与RSV感染无关。 本研究有22例患儿在入院前接受过帕利珠单抗预防RSV感染,其中18例已完成至少2个月的剂量,17例(77%)有1个或以上的慢性疾病,14例(64%)出生时胎龄不超过32周。入院时中位实足年龄为5.6个月(范围0-27.5个月),中位住院时间为9.5d(范围2-271d)。大多数儿童(17/22)为轻度至中度RSV感染。 小结:RSV在萨斯喀彻温省保持较高的发病率,男性、实足年龄小于1岁的足月儿或晚期早产儿发病率较高。细支气管炎是最常见的临床表现。大多数患儿呈轻度至中度感染,但约7%的患儿需要重症监护。较小的实足年龄、潜在的肺部或心脏疾病或多个潜在疾病等因素均有可能导致患儿需要重症监护。此外,与其他孩子同住也有可能是导致患儿需要重症监护的一个因素。需要重症监护的患儿往往胎龄大于35周。虽然部分接受过帕利珠单抗预防的患儿也感染了RSV,但是其大部分患儿的病情为轻度至中度。这些曾接受过帕利珠单抗预防的患儿更可能有潜在疾病,并且出生时胎龄往往小于32周。在本研究中,无一例因RSV感染而引起的死亡病例。本研究尚浅,需要开展更深入的研究,以进一步确定RSV患儿,特别是PICU患儿以及曾接受过帕利珠单抗预防却仍然受到RSV感染的患儿的特征。 Objective To describe the epidemiology and severity of illness of children hospitalized with respiratory syncytial virus (RSV) infection, including those who received palivizumab prophylaxis, at Royal University Hospital (RUH), Saskatoon and Regina General Hospital (RGH) from July 2002 to June 2005. Methods Children hospitalized for ≥ 24 hours with laboratory-confirmed RSV infection were enrolled, and their health records were retrospectively reviewed for patient demographics and referral patterns, use of palivizumab prophylaxis, severity of infection (length of hospitalization, need for and duration of pediatric intensive care and mechanical ventilation) and outcome of infection. Results A total of 590 children (324 males) were hospitalized over the three years. The median chronological age at admission was 5.3 months, and median hospital stay was 4.0 days. Gestational age at birth was≥36 weeks in 82.4%of patients. RSV disease severity was mild to moderate in 478 patients (81.0%) and severe in 110 (18.6%). Thirty-nine patients (6.6%) required pediatric intensive care unit admission, for a median of 5.0 days. Twenty-two of these patients (56%) were mechanically ventilated for a median of 6.0 days. Two children died, not attributed to RSV infection. Twenty-two patients had received palivizumab prophylaxis before hospital admission, with 18 completing at least 2 of the monthly doses. Most of these children (17/22) had mild to moderate illness. Conclusions RSV causes signiifcant morbidity in Saskatchewan, affecting predominantly term infants. The majority of illness is mild to moderate. Some patients who have received palivizumab may still develop signiifcant RSV disease.
出处 《中国当代儿科杂志》 CAS CSCD 北大核心 2014年第10期1005-1013,共9页 Chinese Journal of Contemporary Pediatrics
关键词 呼吸道合胞病毒 帕利珠单抗 儿童 Respiratory syncytial virus Palivizumab Child
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  • 1Paes BA, Mitchell I, Banerji A, et al. A decade of respiratorysyncytial virus epidemiology and pophylaxis: translatingevidence into everyday prophylaxis[J/OL]. Can Respir J,2011,18(2):el0-el9.
  • 2Greenough A, Cox S, Alexander J, et al. Health care utilizationof infants with chronic lung disease, related to hospitalizationfor RSV infection[J]. Arch Dis Child, 2001, 85(6): 463-468.
  • 3Meissner HC. Selected populations at increased risk fromrespiratory syncytial virus infection[J]. Pediatr Infect Dis J,2003,22(2 Suppl): S40-S44.
  • 4Mitchell A, Tough S, Gillis L, et al. Beyond randomizedcontrolled trials: a “real life” experience of respiratorysyncytial virus infection prevention in infancy with and withoutpalivizumab[J]. Pediatr Pulmonol, 2006,41(12): 1167-1174.
  • 5Nair H, Nokes DJ, Gessner BD, et al. Global burden of acutelower respiratory infection due to respiratory syncytial virus inyoung children: a systematic reiew and meta-analysis[J]. Lancet,2010,375(9725): 1545-1555.
  • 6Shay DK,Holman RC, Roosevelt GE,et al. Bronchiolitis-associated mortality and estimates of respiratory syncytial virus-associated deaths among US children, 1979-1997[J]. J InfectDis, 2001, 183(1): 16-22.
  • 7Resch B, Sommer C, Nuitjen M, et al. Cost-effectiveness ofpalivizumab for respiratory syncytial virus infection in high riskchildren, based on long-term epidemiologic data from Austria[J/OL]. Pediatr Infect Dis J, 2012, 31 (1): el-e8.
  • 8Canadian Pediatric Society Infectious Diseases andImmunization Committee. Prevention of respiratory syncytialvirus infection[J]. Pediatr Child Health, 2009, 14(8): 521-526.
  • 9Langley GF, Anderson LJ. Epidemiology and prevention ofrespiratory syncytial virus infections among infants and youngchildren[J]. Pediatr Infect Dis J, 2011, 30(6): 510-517.
  • 10Welliver RC Sr, Checchia PA, Bauman JH, et al. Fatality rates inpublished reports of RSV hospitalizations among high-risk andotherwise healthy children[J]. Curr Med Res Opin, 2010, 26(9):2175-2181.

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