Fujii Yoshiyuki, Noguchi Atsuko, Miura Shinobu, Ishii Haruka, Nakagomi Toyoko, Nakagomi Osamu, Takahashi Tsutomu
Department of Pediatrics, Akita University Graduate School of Medicine, Hondo 1-1-1, Akita, 010-8543, Japan.
Department of Pediatrics, Yuri-Kumiai General Hospital, 38 Kawaguti Aza Yago,Yurihonjo, Akita, 015-8511, Japan.
BMC Pediatr. 2017 Jul 11;17(1):156. doi: 10.1186/s12887-017-0916-7.
In Japan, rotavirus hospitalisation occurs at a rate from 2.8 to 13.7 per 1000 child-years among children age less than 5 years, and it imposes a substantial burden to the healthcare system in the country. While both monovalent (RV1) and pentavalent (RV5) rotavirus vaccines are licensed in Japan, neither has been incorporated in the national infant immunization programme. In this study, we estimated vaccine effectiveness (VE) in Japan.
This study was conducted in Yuri-Kumiai General Hospital located in a city in the north-western part of Japan. Age-eligible children for rotavirus vaccination were enrolled if they were hospitalized for rotavirus gastroenteritis between September 2013 and August 2016. Rotavirus gastroenteritis was defined by the detection of rotavirus antigen by immunochromatography. "Vaccinated" was defined as infant inoculated with at least one dose of either RV1 or RV5. A conditional logistic regression analysis was performed by modelling the year of birth, year of admission, residence of the children and vaccination status, and by matching the age of cases with that of test-negative controls. The adjusted odds ratio of the vaccinated over unvaccinated was then used to calculate VE in the formula of (1 - adjusted odds ratio) × 100.
Out of the 244 patients enrolled, rotavirus antigen was detected in 55 (22.5%) of whom 10 (18.2%) were vaccinated, whereas 94 (49.7%) of 189 test-negative controls were vaccinated. During the study period, the vaccine uptake rate in the controls increased from 36.2% to 61.8%. On the other hand, the vaccination coverage over the three years was 64.2% in Yuri-Honjo city (three quarters of the catchment), and 91.4% in Nikaho city (one quarter of the catchment). The VE was calculated to be 70.4% (95% confidence interval: 36.0-86.4%, P = 0.002). The point estimate of the VE was lower but its 95% confidence interval overlaps those of the efficacies obtained from clinical trials in Japan.
The rotavirus vaccine was effective in the real-world setting in Japan as in the clinical trials, and the introduction of rotavirus vaccine in the national infant immunization schedule will substantially reduce the number of rotavirus gastroenteritis hospitalisation in Japan.
在日本,5岁以下儿童轮状病毒住院率为每1000儿童年2.8至13.7例,给该国医疗系统带来了沉重负担。虽然单价(RV1)和五价(RV5)轮状病毒疫苗在日本均已获得许可,但均未纳入国家婴儿免疫规划。在本研究中,我们估计了日本的疫苗效力(VE)。
本研究在日本西北部一个城市的百合共济综合医院进行。符合轮状病毒疫苗接种年龄的儿童,若在2013年9月至2016年8月期间因轮状病毒胃肠炎住院,则纳入研究。轮状病毒胃肠炎通过免疫层析法检测轮状病毒抗原进行定义。“接种疫苗”定义为接种过至少一剂RV1或RV5的婴儿。通过对出生年份、入院年份、儿童居住地和疫苗接种状况进行建模,并将病例年龄与检测阴性对照的年龄进行匹配,进行条件逻辑回归分析。然后,将接种疫苗者与未接种疫苗者的调整优势比用于公式(1 - 调整优势比)×100中计算VE。
在纳入的244例患者中,55例(22.5%)检测到轮状病毒抗原,其中10例(18.2%)接种过疫苗,而189例检测阴性对照中有94例(49.7%)接种过疫苗。在研究期间,对照中的疫苗接种率从36.2%增至61.8%。另一方面,三年来百合本庄市(集水区的四分之三)的疫苗接种覆盖率为64.2%,二瓶市(集水区的四分之一)为91.4%。计算得出VE为70.4%(95%置信区间:36.0 - 86.4%,P = 0.002)。VE的点估计值较低,但其95%置信区间与日本临床试验获得的效力的置信区间重叠。
轮状病毒疫苗在日本的实际应用中与临床试验一样有效,在国家婴儿免疫计划中引入轮状病毒疫苗将大幅减少日本轮状病毒胃肠炎住院病例数。