Gynaecology

Cervical Screening in Aotearoa

4 min

โ At a glance

  • New Zealand moved to primary HPV-based cervical screening in 2023. Eligible people are those with a cervix aged 25-69, regardless of sexual history or HPV vaccination status. Screening interval is every 5 years for most people - longer than the old cytology programme, with improved detection of significant disease.1
  • HPV 16/18 detected with any cytology abnormality: refer to colposcopy. HPV 16/18 detected with negative cytology: still refer to colposcopy within 3 months (high-risk combination regardless of cytology). Other high-risk HPV with negative cytology: repeat combined test in 12 months.
  • Self-testing is now a formal part of the NZ programme. Offer it proactively to Maori and Pacific women and others with barriers to clinician-collected testing. Sensitivity for HPV detection is similar to clinician-collected samples.3
  • Postcoital bleeding always warrants cervical examination, regardless of screening history. A normal HPV screen does not exclude a visible cervical lesion. Refer urgently if a visible abnormality is present.

New Zealand transitioned to primary HPV-based cervical screening in 2023, replacing the cytology-based programme in place since 1990. The new programme offers longer screening intervals (every 5 years rather than 3), broader eligibility, self-testing as an option, and improved detection of significant cervical disease - particularly for Maori and Pacific women, who have historically had lower participation rates and higher cervical cancer rates.

โ Programme pathway and result interpretation

Eligibility: any person with a cervix aged 25-69, free, regardless of sexual history or vaccination status. People who have never been sexually active can be offered screening - shared decision-making is appropriate given very low HPV exposure risk. Vaccinated people should still screen.

Test: clinician-collected cervical sample or self-collected vaginal swab, tested for high-risk HPV. Reflex cytology is performed on the same sample if high-risk HPV is detected.

Results: HPV not detected - return to routine 5-yearly screening. HPV 16 or 18 detected with any cytology abnormality - refer to colposcopy. HPV 16 or 18 detected with negative or inadequate cytology - refer to colposcopy within 3 months (these types carry high risk regardless of cytology). Other high-risk HPV detected with any cytology abnormality - refer to colposcopy. Other high-risk HPV with negative cytology - repeat combined test in 12 months; if HPV still detected, refer to colposcopy; if negative, return to routine 5-yearly screening. Inadequate sample - repeat within 3 months.

Self-testing: appropriate for people who decline clinician-collected testing due to discomfort, cultural reasons, previous trauma, or access barriers. Similar HPV sensitivity to clinician-collected tests. Offer proactively to Maori and Pacific women - this is a deliberate equity tool. Offering self-testing in a culturally safe, non-judgmental way is as important as the technical aspects.

Colposcopy: specialist examination of the transformation zone with targeted biopsies. In NZ, provided through DHB/hospital gynaecology. Most referrals seen within 4-8 weeks; urgent referrals within 2 weeks. CIN 2/3 is typically treated by LLETZ. CIN 1 is managed conservatively. After treatment: enhanced surveillance with combined HPV and cytology at defined intervals before return to routine screening.

โ HPV vaccination and referral criteria

Gardasil 9 is funded for people aged 9-26 under the NZ immunisation schedule, covering HPV types 6, 11, 16, 18, 31, 33, 45, 52, and 58. Surveillance data from vaccinated NZ cohorts shows significant reductions in CIN 2/3 incidence. Catch-up for ages 27-45 is available but not funded.

Urgent colposcopy (within 2 weeks): visible cervical lesion suspicious for invasive cancer; persistent unexplained postcoital bleeding with abnormal-appearing cervix. Routine colposcopy: as per HPV pathway above. Postcoital bleeding always requires cervical examination - a normal HPV screen does not exclude ectropion, cervicitis, or visible lesion. Check local HealthPathways for current colposcopy referral thresholds and wait times.

References

  1. Ronco G, Dillner J, Elfstrom KM, et al. Efficacy of HPV-based screening for prevention of invasive cervical cancer: follow-up of four European randomised controlled trials. Lancet. 2014;383(9916):524-532.
  2. Cuzick J, Cadman L, Mesher D, et al. Comparing the performance of six human papillomavirus tests in a screening population. Br J Cancer. 2013;108(4):908-913.
  3. Ministry of Health New Zealand. Cervical Screening Programme Overview. Wellington: MoH; 2023.