Abstract

Background:Initial introduction of HPV vaccination from 2006 to 2008 was largely confined to high-income countries (HIC), such as Australia, the United States, and Europe, where cervical cancer incidence is lowest. Much of the post-introduction literature has come from HICs, with a focus on coverage levels achieved, provider acceptability and early impact of vaccination on disease endpoints. However, there are a few literature evaluating the mechanics of delivery, feasibility of the health system and acceptability from low and middle income countries (LMICs). The primary objective was to evaluate the feasibility, acceptability and safety of two dose HPV vaccination in adolescent girls between 9-14 years. Methods:After an orientation camp followed by filling up of prevaccine questionnaires by parents on HPV related diseases and its vaccines and informed consent, girls between9-14years were vaccinated. They were asked to report any side effects in the next 24 hours after each dose. Parents were contacted on Day 7 and Day 30 to enquire about any side effects . Total 3 visits were required i.e two for the vaccination and one visit at 7th month post completion of second dose. To estimate the acceptability, successful completion of two doses by at least 80% of the girls were measured. For measurement of acceptability, either of the parents were recalled along with their daughter at 7th month and were asked to fill up a pre-set questionnaire. Results:After institutional ethical clearance, 555 girls were recruited in the study from rural parts of West Bengal, India between July, 2017 to November, 2017. Out of which, 544 girls (98%) received their 2nd dose between January, 2018 and May, 2018 without any serious adverse effects. No serious adverse effect was reported on follow up till December, 2019. Conclusion:The introduction of HPV vaccination is feasible in large scale and the vaccine is well accepted and safe.

Highlights

  • Since the introduction of cervical cancer screening by Papanicolaou smear from cervical cytology in 1940s, various methods have evolved with latest addition of Human papillomavirus Deoxyribonucleic acid (DNA) and/ Ribonucleic acid (RNA) test to detect the causative agent and treat

  • The number of girls attended these camps were 612, out of which 57 girls were not included in the project The major reason for exclusion were age >15 years, high fever on previous night and one girl had a history of epileptic attack in previous week.Total 555 girls between 9-14 years were recruited in the study, number of girls between 9-11 years and 12-14 years are 276 (49.7%) and 279 (50.3%) respectively

  • Inc.) targets an additional five oncogenic genotypes 31, 33, 45, 52 and 58 (Zhai and Tumban, 2016) Between 2007 and 2012, several countries conducted Human papillomavirus (HPV) demonstration projects with vaccines provided by the GARDASIL® Access Program (GAP), Merck & Co., the Bill & Melinda Gates Foundation through PATH, or through other means (Luciani et al, 2018; Zhai and Tumban, 2016; Gallagher et al, 2017).In 2012 GAVI, the Vaccine Alliance, commenced support for demonstration projects and national introductions to increase access to HPV vaccine worldwide (Ladner et al, 2016)

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Summary

Introduction

Background: Since the introduction of cervical cancer screening by Papanicolaou smear from cervical cytology in 1940s, various methods have evolved with latest addition of Human papillomavirus Deoxyribonucleic acid (DNA) and/ Ribonucleic acid (RNA) test to detect the causative agent and treat . Much of the post-introduction literature has come from high-income countries, with a focus on coverage levels achieved, provider acceptability, and early impact of vaccination on disease endpoints (Malloy et al, 2000). Methods: After an orientation camp followed by filling up of prevaccine questionnaires by parents on HPV related diseases and its vaccines and informed consent, girls between9-14years were vaccinated. They were asked to report any side effects in the 24 hours after each dose. Conclusion: The introduction of HPV vaccination is feasible in large scale and the vaccine is well accepted and safe

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