Li Y A, Tsang R, Desai S, Deehan H
Public Health Agency of Canada, Centre for Immunization and Respiratory Infectious Diseases, Ottawa, Ontario.
Public Health Agency of Canada, National Microbiology Laboratory, Winnipeg, Manitoba.
Can Commun Dis Rep. 2014 May 1;40(9):160-169. doi: 10.14745/ccdr.v40i09a01.
The purpose of this report is to describe the epidemiology of invasive meningococcal disease (IMD) in Canada from 2006 to 2011.
Data from the Enhanced Invasive Meningococcal Disease Surveillance System and national population estimates were selected for descriptive and inferential analyses. The geographic, demographic, seasonal and subtype distributions as well as clinical characteristics of the IMD cases were examined. Incidence and mortality rates were calculated per 100,000 population per year; 95% confidence intervals (CI) were calculated for rate comparison. The direct method was used for age standardization. Proportions were compared using the chi-squared test at a p<0.05 significance level.
During the study period, the mean incidence rates of IMD were 0.58 (total), 0.33 (serogroup B), 0.07 (serogroup C), 0.03 (serogroup W-135) and 0.10 (serogroup Y). The median age for serogroups B, C, W-135 and Y was 16, 43, 38 and 47 years respectively. The mean age-specific incidence rates among infants under 1 year of age (7.35, CI: 5.38-9.32) and children from 1 to 4 years of age (1.89, CI: 1.54-2.24) were significantly higher than those in any other age group. The mean case fatality ratio was 8.1% (range 4.3%-14.3%). The average number of cases that occurred per month was significantly higher (p<0.0001) in winter (18 cases) than in summer (12 cases).
IMD is still endemic in Canada. Although individuals at any age can be affected, infants under 1 year of age are at the greatest risk, followed by children aged 1-4 years and individuals aged 15-19 years. Following the implementation of routine childhood immunization programs with monovalent meningococcal C conjugate vaccines (MenC) in all provinces and territories (beginning in 2007), the incidence of serogroup C has decreased significantly over the study period and is now at an all-time low. Serogroup B is the leading cause of IMD, and diseases of serogroup W-135 and Y have stabilized at relatively lower incidence rates. With the addition of immunization programs using quadrivalent conjugate meningococcal vaccines (MCV4), we would expect further reductions in the incidence of meningococcal infection in Canada.
本报告旨在描述2006年至2011年加拿大侵袭性脑膜炎球菌病(IMD)的流行病学情况。
选取强化侵袭性脑膜炎球菌病监测系统的数据和全国人口估计数进行描述性和推断性分析。研究了IMD病例的地理、人口统计学、季节和亚型分布以及临床特征。计算每年每10万人口的发病率和死亡率;计算95%置信区间(CI)用于率的比较。采用直接法进行年龄标准化。使用卡方检验在p<0.05显著性水平下比较比例。
在研究期间,IMD的平均发病率分别为0.58(总计)、0.33(B血清群)、0.07(C血清群)、0.03(W-135血清群)和0.10(Y血清群)。B、C、W-135和Y血清群的中位年龄分别为16岁、43岁、38岁和47岁。1岁以下婴儿(7.35,CI:5.38 - 9.32)和1至4岁儿童(1.89,CI:1.54 - 2.24)的年龄特异性平均发病率显著高于其他任何年龄组。平均病死率为8.1%(范围4.3% - 14.3%)。冬季每月发生的病例平均数(18例)显著高于夏季(12例)(p<0.0001)。
IMD在加拿大仍为地方病。尽管任何年龄的个体都可能受到影响,但1岁以下婴儿风险最高,其次是1至4岁儿童和15至19岁个体。在所有省份和地区实施常规儿童单价C群脑膜炎球菌结合疫苗(MenC)免疫规划后(从2007年开始),研究期间C血清群的发病率显著下降,目前处于历史最低水平。B血清群是IMD的主要病因,W-135和Y血清群疾病的发病率稳定在相对较低水平。随着使用四价结合脑膜炎球菌疫苗(MCV4)免疫规划的增加,我们预计加拿大脑膜炎球菌感染的发病率将进一步降低。