Vaccine impact on long-term trends in invasive bacterial disease in New Zealand children
Authors: Walls T et al.
Summary: This article describes long-term trends in
hospital discharge rates and notifications for invasive
bacterial infections caused by Streptococcus pneumoniae
(IPD), Neisseria meningitidis and Haemophilus influenzae
type B (Hib) in NZ children (aged <15 years), the impact
of vaccines on the rates of these diseases and rates in
comparison to UK data. Two datasets were used: the
National Minimum Dataset for data on hospital discharges
from all private and public hospitals in NZ and EpiSurv,
NZ’s national database for notifiable disease surveillance.
Hospitalisation rates for Hib fell by 84% within 2 years
after the introduction of the vaccine (from 13.53/100,000
in 1993 to 2.19/100,000 in 1995). Hospitalisation and
notification rates were similar for Hib. After the introduction
of MeNZB vaccine in 2004, hospitalisation rates for
meningococcal disease fell by 73% within 3 years: from
36.68 per 100,000 in 2003 to 10.05 per 100,000 in
2006. Over the 8 years after the introduction of MeNZB
vaccine, notification rates for meningococcal disease
declined by 75%, from 26.15 per 100,000 to 2.48 per
100,000 and continued to decline. From 2007 to 2011,
the rates of meningococcal disease in NZ were lower than
those in the UK (8.16 vs 10.37/100,000), despite NZ not
having a meningococcal vaccine on the immunisation
schedule for those years. NZ hospitalisation rates for IPD
fell by 62% within 2 years of the introduction of PCV7
vaccine (from 7.80/100,000 in 2007 to 2.98/100,000
in 2009). Notification rates were 3–6-fold higher than
the hospitalisation rates, but also fell markedly after the
introduction of PCV7 vaccine. Rates of invasive bacterial
disease have fallen substantially in NZ children since
the introduction of meningococcal and pneumococcal
vaccines, with the greatest absolute reductions in disease
incidence amongst Māori children, although disparities are
still apparent between Māori and non-Māori children.
Reference: Pediatr Infect Dis J. 2018;37(10):1041-7
Abstract