Abstract

BackgroundNew Zealand initiated HPV vaccination in 2008, and has attained 3-dose coverage of ~50 % in 12–13 year old girls. Due to the success of program initiatives in Māori girls, higher coverage rates of ~60 % have been achieved in this group. We have previously reported a benchmark overall pre-vaccination prevalence of oncogenic HPV infection in high grade cervical lesions in New Zealand. The current extended analysis provides separate pre-vaccination benchmark prevalence for Māori and non-Māori women.MethodsThe National Cervical Screening Programme Register (NCSP-R) was used to identify any woman aged 20–69 years of age with an index high grade cytology report from 2009–2011. Extended recruitment was performed until 2012 in clinics with a high proportion of Māori women. Ethnicity status was based on self-reported information by participating women through phone contact supplemented by recordings on the study questionnaire (the NCSP-R was not used to extract ethnicity status). A total of 730 women consented to participate and had a valid HPV test result; 418 of these had histologically-confirmed cervical intraepithelial neoplasia (CIN) 2/3 lesions (149 Māori, 269 non-Māori). The prevalence of any cervical oncogenic HPV infection, HPV16, and HPV18 was calculated in women with CIN2/3.ResultsIn confirmed CIN2/3, the prevalence of any oncogenic HPV, HPV16 and HPV18 was 96 % (95 % CI:91–99 %), 54 % (95 % CI:46–63 %), 11 % (95 % CI:7–18 %) in Māori and 96 % (95 % CI:93–98 %), 54 % (95 % CI:48–60 %), 11 % (95 % CI:7–15 %) in non-Māori women, respectively. Age-specific patterns of infection for HPV16/18 in confirmed CIN2/3 differed between the two groups (Pinteraction = 0.02), with a lower prevalence in younger vs. older Māori women (57 % in 20–29 years vs 75 % in 40–69 years) but a higher prevalence in younger vs. older non-Māori women (70 % in 20–29 years vs 49 % in 40–69 years); the difference in the age-specific patterns of infection for HPV16/18 was not significant either when considering confirmed CIN2 alone (p = 0.09) or CIN3 alone (p = 0.22).ConclusionsThe overall prevalence of vaccine-included types in CIN2/3 was similar in Māori and non-Māori women, implying that the long-term effects of vaccination will be similar in the two groups.Electronic supplementary materialThe online version of this article (doi:10.1186/s12879-015-1034-5) contains supplementary material, which is available to authorized users.

Highlights

  • New Zealand initiated Human Papillomavirus (HPV) vaccination in 2008, and has attained 3-dose coverage of ~50 % in 12–13 year old girls

  • We have previously reported the overall population prevalence of pre-vaccination oncogenic HPV infection in New Zealand in both high grade cytology and histologically-confirmed high grade lesions, in a sample of women identified via the New Zealand National Cervical Screening Programme (NCSP) [7]

  • A total of 96 % of confirmed CIN2+ lesions were associated with any HPV positivity

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Summary

Introduction

New Zealand initiated HPV vaccination in 2008, and has attained 3-dose coverage of ~50 % in 12–13 year old girls. We have previously reported a benchmark overall pre-vaccination prevalence of oncogenic HPV infection in high grade cervical lesions in New Zealand. The current extended analysis provides separate pre-vaccination benchmark prevalence for Māori and non-Māori women. A higher coverage rate has been achieved in Māori compared to non-Māori and non-Pacific girls (60 vs 50 % as of February 2014, in girls born in 2000) [3]: this was due to the success of specific program initiatives, which included engagement with Māori and Pacific stakeholders nationally and regionally, the involvement of Māori and Pacific Equity Advisory Groups to guide the design and roll out of the immunisation program at the regional level, and the use of the existing evidence-base to identify service delivery processes most effective for Māori and Pacific young women [4]. A major factor likely to underlie this difference in cancer rates is screening behaviour, and recent screening program initiatives have been ‘closing the gap’; recent (2012) 3-yearly screening coverage rates for women aged 25–69 years in Māori and non-Māori women have been reported as 61.6 and 83.5 %, respectively [6]

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