Thursday, October 15, 2015

Human Papillomavirus Vaccination Coverage Among School Girls in a Demonstration Project — Botswana, 2013

Cervical cancer, caused by human papillomavirus (HPV), is the leading cause of cancer mortality among women in Botswana (1). Three vaccines prevent infection with HPV types responsible for the majority of cervical cancer worldwide. Two of these vaccines also protect against types that cause anogenital warts. Two vaccines are currently prequalified by the World Health Organization (WHO); these were >90% efficacious in preventing precancerous lesions caused by HPV types 16 and 18 (the cause of 70% of cervical cancers) in clinical trials studying women who received the recommended 3-dose series before exposure to targeted HPV types. WHO recommends targeting HPV vaccination to girls aged 9–13, before initiation of sexual activity and thus HPV exposure (2). This report summarizes HPV vaccination coverage among girls aged ≥9 years enrolled in grades 4–6 in 23 primary schools in Molepolole, Botswana, during a 2013 HPV vaccination demonstration project conducted by the Botswana Ministry of Health (MOH). Of the 2,488 eligible school girls, 83% received the first dose and 79% completed the 3-dose HPV vaccination series. Drop out between first and third dose was 5%. No serious adverse events were reported. Given the successful pilot, the project was expanded to immunize approximately 6,000 girls in 2014, followed by national rollout of the HPV vaccine in 2015.

Botswana is an upper middle income country with a population of 2 million in southern Africa. Approximately 22,000 females are born annually. Human immunodeficiency virus (HIV) prevalence among women aged 15–49 years is 28%.* Cervical cancer, the fourth most common cancer worldwide (3), is the most common cancer among women aged 15–44 years and the leading cause of cancer mortality among women in Botswana, reflecting the 4–5 times increased risk for cervical cancer among HIV-infected women (3). Primary prevention of cervical cancer via HPV vaccination might be particularly beneficial to Botswana, given the country's challenges with both HIV infection and cervical cancer. However, establishing a sustainable program to deliver HPV vaccine to a population not previously targeted for immunizations can be challenging in resource-limited countries.

In 2012, the Botswana MOH initiated its National Cervical Cancer Prevention Program Comprehensive Strategy (2012–2016). The same year, the Pink Ribbon Red Ribbon (PRRR) initiative, a public-private partnership for breast and cervical cancer prevention and treatment, was implemented to expand cervical cancer screening and treatment with a focus on HPV-related disease. With PRRR and other donor support, the Botswana MOH decided to conduct a grade-based HPV vaccination demonstration project in primary schools. The project was completed during the 2013 school year (January–December) in Molepolole, a town with a population of 63,000 located 31 miles (50 kilometers) from the national capital. The objectives were to evaluate HPV vaccine implementation among age-eligible girls enrolled in school and to improve planning for possible expansion of HPV vaccine activities.

A multidisciplinary team, with representatives from the Botswana MOH, including Expanded Program on Immunization, Ministry of Education, WHO, nongovernmental organizations, and other key stakeholders, developed the project protocol, educational materials, a parental consent form, and data-gathering tools. The Botswana MOH determined the project to be public health practice. Multiple educational meetings for community stakeholders, sensitization meetings for parents and educators, and training sessions for local public health providers participating in the project were held before implementation. All girls aged ≥9 years attending grades 4–6 at any of Molepolole's 17 public primary schools, five private primary schools, or one school for special needs students, and who had written parental consent, were eligible for vaccination. Participating schools provided enrollment lists of female students. The quadrivalent HPV vaccine, Gardasil (Merck and Co.), was administered in schools by public health workers in March, May (approximately 2 months after the first dose), and early October 2013 (approximately 6 months after the first dose). Immunization teams visited each school twice during each of the three vaccination campaign rounds. Girls who missed a dose at school could receive it at Scottish Livingston Hospital in Molepolole. Vaccination data on each girl were collected on paper-based records and transferred to a spreadsheet. To identify the number of girls who received HPV vaccination during March–December 2013, staff reviewed the line lists of girls by school, which contained birthdate, grade, documentation of parental consent, and HPV vaccination date.

There were 2,742 girls registered in grades 4–6 in the 23 participating schools (median enrollment = 135 girls; range = 12–227 girls). Of the 2,590 (94%) girls with a recorded date of birth, 2,488 (96%) were aged ≥9 years on the first day of school vaccination in March 2013. Among these girls, 83% (n = 2,075) received the first dose, 82% (n = 2,049) received 2 doses, and 79% (n = 1,967) completed the 3-dose series (Table). Overall vaccination completion among girls who received the first dose was 95%. Approximately one fifth (431/2488) of girls with known date of birth were without documented parental consent, 88 of whom received vaccination. The proportion of school girls vaccinated increased with increasing age (Cochran-Armitage trend test p<0.001) and was higher among girls who attended public school compared with those who attended private school (p<0.001). Passive surveillance for adverse events (following girls for 30 days postimmunization) was designed for this campaign. No serious adverse events were reported.


By: Mmakgomo Mimi Raesima, MD1Sara E. Forhan, MD2Andrew C. Voetsch, PhD2Shannon Hewitt3Susan Hariri, PhD4Susan A. Wang, MD5Andrew R. Pelletier, MD2Mpho Letebele, MD2Tlhomamo Pheto1Doreen Ramogola-Masire, MD6,7Shenaaz El-Halabi, MPH1
  

No comments:

Post a Comment