Abstract
Introduction
Although the burden of cervical cancer in Africa is highest, HPV vaccination coverage remains alarmingly low in this region. Providers’ knowledge and recommendation are key drivers of HPV vaccination uptake. Yet, evidence about providers’ knowledge and recommendation practices about the HPV vaccine against a backdrop of emerging vaccine hesitancy fueled by the COVID-19 pandemic is lacking in Africa.
Methods
A cross-sectional study was conducted in 2021–2022 among healthcare providers involved in cervical cancer prevention activities in Africa. They were invited to report prior training, the availability of the HPV vaccine in their practice, whether they recommended the HPV vaccine, and, if not, the reasons for not recommending it. Their knowledge about the HPV vaccine was assessed through self-reporting (perceived knowledge) and with three pre-tested knowledge questions (measured knowledge).
Results
Of the 153 providers from 23 African countries who responded to the survey (mean age: 38.5 years, SD: 10.1), 75 (54.0%) were female and 97 (63.4%) were based In countries with national HPV immunization programs. Overall, 57 (43.8%) reported having received prior training on HPV vaccine education/counseling, and 40 (37.4%) indicated that the HPV vaccine was available at the facility where they work. Most respondents (109, 83.2%) reported recommending the HPV vaccine in their practice. Vaccine unavailability (57.1%), lack of effective communication tools and informational material (28.6%), and need for adequate training (28.6%) were the most commonly reported reasons for not recommending the HPV vaccine. While 63 providers (52.9%) reported that their knowledge about HPV vaccination was adequate for their practice, only 9.9% responded correctly to the 3 knowledge questions.
Conclusion
To increase HPV vaccination coverage and counter misinformation about this vaccine in Africa, adequate training of providers and culturally appropriate educational materials are needed to improve their knowledge of the HPV vaccine and to facilitate effective communication with their patients and the community.
Keywords: HPV, cervical cancer, HPV-related disease, HPV vaccination, vaccine recommendation, vaccine hesitancy, cancer control, healthcare providers
Introduction
Human papillomavirus (HPV) – the most common sexually transmitted virus globally - is responsible for cervical cancer, a leading cause of cancer morbidity and mortality among women in Africa, where approximately 415 million women aged 15 years and older are at risk of developing this preventable condition (1). Just like women, men in Africa are exposed to HPV-associated cancers (oropharyngeal, anal, and penile cancers) as well as genital warts (2). The prevalence of HPV infection was reported to be twice as higher in Africa compared to global estimates (22–24% versus 11–12%) (3).
In 2009, the HPV vaccine was endorsed by the World Health Organization (WHO) for girls aged 9 to 14 to prevent HPV-associated diseases (4). Although in use in the private sector in some urban African settings, HPV vaccines were not introduced in National Immunization Programs (NIPs) until 2011, when Rwanda became the first African country to successfully implement an HPV vaccination program (5). Between 2013 and 2016, GAVI (the Vaccine Alliance) initiated the provision of support to eligible countries (e.g., Zambia in 2013, Malawi in 2013, Uganda in 2015) for 2-year HPV vaccine demonstration projects, and GAVI funding for national rollouts in these countries became available in mid-2016 (6). As of 2022, only 40% (22 out of 54) of African countries had effectively included HPV vaccine in their NIPs (7) (Figure 1).
The HPV vaccination schedule has evolved since the vaccine was approved, from a three-dose regimen recommended by the WHO between 2009 and 2014; to a two-dose regimen (for girls below the age of 15) between 2014 and 2022. Since December 2022, WHO has updated its recommendations in light of new scientific evidence for a cost-effective single-dose HPV vaccine to endorse a one-dose regimen for girls and women below the age of 21 (8). With the reduction in the number of doses, vaccine uptake in limited resource settings is expected to increase even faster through the reduction of system-related barriers such as logistic constraints, workforce shortage, and vaccine prices (9).
While the HPV vaccine has been available for about a decade in some parts of Africa, dose completion in 2022 was as low as 20% (on average) in African countries that introduced the HPV vaccine in their NIP (10). Despite the progress made so far, this rate is far below the WHO target of 90% vaccination coverage to be achieved by 2030 to accelerate the elimination of cervical cancer by the end of the millennium.
The effect of high HPV vaccine coverage on mitigating the burden of HPV-related conditions is now observed in high-income settings where organized HPV immunization programs are widely implemented (11). In a recent report of a cohort of vaccinated girls in Rwanda, a reduction in the prevalence of vaccine-targeted HPV types from 12% (in 2013–2014) to 5% (in 2019–2020) was observed in sexually active women aged 17–29 years (12). Despite this strong evidence, many African countries are still lagging behind in implementing HPV immunization programs in a context where HPV-related morbidity and mortality remain high (13). Further, the growing access to health information through the internet and social media in recent years in Africa, combined with the limited involvement of frontline healthcare providers, has accelerated the spread of vaccine hesitancy in the African population, especially in the COVID-19 era where misbeliefs and misconceptions about vaccines have been exacerbated (14).
While providers’ recommendation has been consistently recognized as a driving factor for HPV vaccine uptake (15), little is known about providers’ practices and recommendation for HPV vaccination in Africa. Further, the low level of knowledge about HPV vaccination which is also recognized as a strong barrier to HPV vaccine acceptance has not been characterized in Africa. In this study, we assessed the training, knowledge, and recommendation of the HPV vaccine among African providers involved in cervical cancer prevention activities. These findings will serve as a basis for developing and evaluating targeted interventions to improve provider communication about the HPV vaccine against a backdrop of increased vaccine hesitancy and increased population access to health information through social media and the internet in Africa.
Methods
Study population and study design
The study population consisted of healthcare providers involved in cervical cancer prevention activities from 23 African countries who were enrolled in a distance learning program focusing on cervical cancer and other HPV-related anogenital diseases (16, 17). Between 2021 and 2022, providers were invited to take an online survey (in English or French) to assess their training, knowledge, and practices toward cervical cancer screening, management of pre-invasive lesions, and HPV vaccination (Supplementary Figure S1). The questionnaire was pre-tested and validated before being administered to the target population. This was done in two steps: In a first step, after developing the survey tool, we shared it with 4 experts to get their feedback and remarks regarding content validity. Suggestions from these experts were then incorporated into the survey tool. In a second step, the self-administered survey was pilot tested with a convenience sample of 20 individuals of varying healthcare provider professions based in Africa to ensure clarity of questions and ease of administration. Further comments from this set of HCPs were accounted for in the final revision of the questionnaire. Participation was anonymous and voluntary, and refusal to take the survey had no consequence on participation in the distance learning program. A detailed description of the survey design, content, and administration has been published elsewhere (16).
Measures
Main variable
We assessed whether African-based providers involved in cervical cancer prevention activities were recommending HPV vaccination in their practice using the following questions. “Do you currently recommend HPV vaccination in your practice?” If the answer to this question was “yes,” a follow-up question was asked: “Who do you recommend the HPV vaccine for?” The possible responses to this follow-up question included: “I recommend HPV vaccine for girls only,” and “I recommend HPV vaccine for both girls and boys.” If the answer to the first question was “no,” the follow-up question was: “What is/are the reason(s) for not recommending HPV vaccination in your practice?.” Possible responses to the latter included: “HPV vaccination is not available in my practice,” “I delegate these activities to other staff in my practice,” “Additional training would be needed to perform some of these activities,” “Not enough time,” “Lack of effective tools and information to give to patients,” “Patient/family cannot afford the cost of the HPV vaccine,” “I chose not to perform these activities,” “Not needed because cervical cancer screening is effective,” and “Some other reasons.”
Additional variables
Prior training on HPV vaccine counseling was assessed with the following question: “Have you previously had training in how to educate your patients, their family members, and the population about HPV vaccination?” (Yes/No). Availability of HPV vaccine was assessed with the following question: “Is HPV vaccine currently available at the facility where you work?” (Yes/No).
To better describe the study population, we collected the following socio-demographic variables: age (years), gender (Male/Female), location according to the United Nation’s classification of African regions (Eastern Africa, Middle Africa, Western Africa, Southern Africa, and Northern Africa), and setting (urban/rural). Age was described as a continuous variable. Providers were also classified according to their educational background into doctors (including family medicine physicians, internists, obstetricians-gynecologists, oncologists, pediatricians, surgeons, pathologists, etc.), nurses (including midwives), and non-clinician providers (including health administrators, project managers, and community health workers involved in cervical cancer prevention activities).
Knowledge questions
Measured knowledge
The level of knowledge about HPV vaccination was assessed with three statements to which participants were asked to provide either of the three possible responses: “true,” “false,” or “I do not know.” The first statement was about vaccine efficacy: (i) “A 13-year-old girl receives two doses of the quadrivalent HPV vaccine. By doing so she expects a 90–100% protection rate against future development of cervical cancer.” The second statement was about the vaccine administration schedule: (ii) “A 16-year-old girl has received only one dose of HPV vaccine when she was 13 years old. To complete her vaccination schedule, she should restart HPV vaccination from the first dose.” The third statement was about vaccine safety: (iii) “HPV vaccination reduces fertility of women.”
Perceived knowledge
In addition to the measured knowledge, self-reported knowledge about the HPV vaccine was assessed with the following statement: “My knowledge about HPV vaccination is adequate for my current practice.” Possible responses to this statement included: “Agree,” “Disagree,” “Neither Agree nor Disagree,” and “I do not know.”
Statistical analysis
Analyses were performed using statistical analysis software The SAS (v9.4). We classified healthcare providers into 2 groups according to the introduction status of the HPV vaccine into the NIP: providers working in countries with national HPV immunization programs and those working in countries without national HPV immunization programs (Figure 1). Descriptive statistics were tabulated in each group. We also examined the gender difference (female providers versus male providers) in HPV vaccine knowledge and recommendation practices. Comparisons between groups were carried out using Fisher’s exact test for categorical variables and the likelihood ratio chi-square test for continuous variables. Missing data were excluded by listwise deletion. Two-sided p < 0.05 was considered statistically significant.
This study was conducted according to the strengthening the Reporting of observational studies in epidemiology (STROBE) guidelines (Supplementary Table S1).
Ethics approval
This research conformed to the principles embodied in the Declaration of Helsinki. All participants provided written informed consent. The study protocol was approved by the University of Texas MD Anderson Cancer Center’s IRB.
Patient and public involvement
Patients or public were not involved in the design, or conduct, or reporting, or dissemination plans of our research.
Results
Characteristics of the study population
Of the 153 (mean [SD] age, 38.5 [10.1] years) respondents who completed the survey, most were female (75 [54.0%]) and working in urban areas [113 (89.7%)]. Participants were from 23 African countries, including 16 providers (10.5%) from Eastern Africa, 64 (41.8%) from Middle Africa, 10 (6.5%) from Northern Africa, 6 (3.9%) from Southern Africa, and 57 (37.3%) from Western Africa (Table 1).
Table 1.
Variables a | Total | HPV vaccine included in the National Immunization Program | HPV vaccine not included in the National Immunization Program | |||
---|---|---|---|---|---|---|
N = 153 (100.0) | Range | n = 97 (63.4) | Range | n = 56 (36.6) | Range | |
Age (mean, SD, years), n = 139 | 38.5 (10.1) | 20–69 | 36.3 (9.2) | 20–59 | 42.9 (10.4) | 25–69 |
n (%) | 95% CI | n (%) | 95% CI | n (%) | 95% CI | |
Gender | n = 139 | |||||
Female | 75 (54.0) | 45.6–62.3 | 56 (61.5) | 51.4–71.7 | 19 (39.6) | 25.6–53.6 |
Male | 64 (46.0) | 37.7–54.4 | 35 (38.5) | 28.3–48.6 | 29 (60.4) | 46.4–74.4 |
Country by region b | n = 153 | |||||
Eastern Africa | 16 (10.5) | 5.6–15.4 | 7 (7.2) | 2.0–12.4 | 9 (16.1) | 6.3–25.8 |
Middle Africa | 64 (41.8) | 33.9–49.7 | 52 (53.6) | 43.6–63.6 | 12 (21.4) | 10.6–32.3 |
Northern Africa | 10 (6.5) | 2.6–10.5 | 9 (9.3) | 3.4–15.1 | 1 (1.8) | 0.0–5.3 |
Southern Africa | 6 (3.9) | 0.8–7.0 | 6 (6.2) | 1.3–11.0 | 0 | - |
Western Africa | 57 (37.3) | 29.5–45.0 | 23 (23.7) | 15.2–32.3 | 34 (60.7) | 47.8–73.7 |
Provider | n = 134 | |||||
Doctors/Residents | 87 (64.9) | 56.7–73.1 | 54 (60) | 49.7–70.3 | 33 (75) | 62.0–88.0 |
Nurses/Midwives | 25 (18.7) | 12–25.3 | 18 (20) | 11.6–28.4 | 7 (15.9) | 5.0–26.9 |
Otherc | 22 (16.4) | 10.1–22.8 | 18 (20) | 11.6–28.4 | 4 (9.1) | 0.5–17.7 |
Setting | n = 126 | |||||
Rural | 13 (10.3) | 4.9–15.7 | 10 (11.4) | 4.6–18.1 | 3 (7.9) | 0.0–16.6 |
Urban | 113 (89.7) | 84.3–95.1 | 78 (88.6) | 81.9–95.4 | 35 (92.1) | 83.4–100.0 |
aFor some variables, the total number of observations does not add up to 153 because of missing data. bThe UN Statistics Division has subdivided the African continent into five regions: Northern Africa (Algeria, Egypt, Libya, Morocco, Sudan, Tunisia, Western Sahara), Central or Middle Africa (Angola, Cameroon, Central African Republic, Chad, Equatorial Guinea, Congo, Democratic Republic of Congo, Gabon, Sao Tome and Principe), Southern Africa (Eswatini, Lesotho, Namibia, Botswana, South Africa), Eastern Africa (Eritrea, Djibouti, Somalia, Burundi, Rwanda, Uganda, South Sudan, Kenya, Tanzania, Seychelles, Comoros, Malawi, Madagascar, Mozambique, Zambia, Mauritius, Zimbabwe), and Western Africa (Burkina Faso, Benin, Togo, Ghana, Cote d’Ivoire, Liberia, Sierra Leone, Guinea, Guinea-Bissau, Senegal, Gambia, Cape Verde, Mauritania, Mali, Niger, Nigeria). cThe “other” category included health administrators, community health workers, and program managers.
HPV vaccine availability and training of providers to perform HPV vaccine education
We assessed providers’ prior training on HPV vaccine education and the availability of the HPV vaccine in their practice according to the HPV vaccine national introduction status of the country where they work (Table 2). Up to 73 respondents (56.2%) indicated having received no prior training on HPV vaccine administration and related counseling; this proportion did not differ between countries with HPV NIPs and countries without HPV NIPs (54.1% versus 60.0%, p = 0.58) or between female providers compared to male providers (60.0% versus 51.7%, p = 0.38) (Supplementary Table S2). Only about one-third (40, 37.4%) of providers reported that the HPV vaccine was available at the facility where they work; this proportion was twice as high among participants in countries with HPV NIPs compared to those in countries without HPV NIPs (43.8% versus 23.5%, p = 0.05) (Table 2).
Table 2.
Variables a | Total | Are you working in a country that has introduced HPV vaccine in the National Immunization Program? | |||||||
---|---|---|---|---|---|---|---|---|---|
Yes | No | p-value b | |||||||
N (%) | 95% CI | N (%) | 95% CI | N (%) | 95% CI | ||||
Have you previously had training in how to educate your patients, their family members, and the population about HPV vaccination? | 0.58 | ||||||||
No | 73 (56.2) | 47.5–64.8 | 46 (54.1) | 43.4–64.9 | 27 (60.0) | 45.5–74.5 | |||
Yes | 57 (43.8) | 35.2–52.5 | 39 (45.9) | 35.1–56.6 | 18 (40.0) | 25.5–54.5 | |||
My knowledge about HPV vaccination is adequate for my current practice | 0.06 | ||||||||
Agree | 63 (52.9) | 43.8–62.0 | 43 (55.8) | 44.6–67.1 | 20 (47.6) | 32.3–62.9 | |||
Disagree | 36 (30.3) | 21.9–38.6 | 18 (23.4) | 13.8–33.0 | 18 (42.9) | 27.7–58.0 | |||
Neutral | 20 (16.8) | 10.0–23.6 | 16 (20.8) | 11.6–30.0 | 4 (9.5) | 0.5–18.5 | |||
Is HPV vaccine available at the facility where you work? | 0.05 | ||||||||
No | 67 (62.6) | 53.3–71.9 | 41 (56.2) | 44.6–67.7 | 26 (76.5) | 62.0–91.0 | |||
Yes | 40 (37.4) | 28.1–46.7 | 32 (43.8) | 32.3–55.4 | 8 (23.5) | 9.0–38.0 | |||
Do you currently recommend HPV vaccination in your practice? | 0.05 | ||||||||
No | 22 (16.8) | 10.3–23.3 | 10 (11.8) | 4.8–18.7 | 12 (26.1) | 13.2–38.9 | |||
Yes | 109 (83.2) | 76.7–89.7 | 75 (88.3) | 81.3–95.2 | 34 (73.9) | 61.1–86.8 | |||
Who do you recommend the HPV vaccine for? | 0.49 | ||||||||
Girls only | 87 (82.1) | 74.7–89.5 | 62 (83.8) | 75.2–92.3 | 25 (78.1) | 63.6–92.7 | |||
Girls and boys | 19 (17.9) | 10.5–25.3 | 12 (16.2) | 7.7–24.8 | 7 (21.9) | 7.3–36.4 |
aFor some variables, the total number of observations does not add up to 153 because of missing data. bThe p-value was calculated using the likelihood ratio chi-square test for continuous variables and the Fisher’s exact test for categorical variables.Bold values are highlight statistically significant p-values.
HPV vaccine recommendation practices
A majority of providers (109, 83.2%) reported that they were recommending the HPV vaccine in their practice; this proportion was significantly higher among providers based in countries with HPV NIPs compared to those in countries without HPV NIPs (88.3% versus 73.9%, p = 0.05) (Table 2). The proportion of providers who reported recommending the HPV vaccine was higher among female providers compared to male providers (87.3% versus 78.3%), although the difference was not statistically significant (p = 0.17) (Supplementary Table S2).
Among providers who reported recommending the HPV vaccine in their practice, 87 (82.1%) recommended it for girls only (per the WHO guidelines), and 19 (17.9%) recommended it for both girls and boys (gender-neutral vaccination, per the US CDC guidelines). There was no significant difference in the proportion of providers who reported girl-only recommendation according to the HPV vaccine national introduction status of the country where they work (83.8% versus 78.1%, p = 0.49), and according to gender (78.7% versus 86.7%, p = 0.29).
Among providers who did not recommend the HPV vaccine (16.8%), the most frequent reasons for not recommending it included: vaccine unavailability (57.1%), lack of effective tools and information to give to patients (28.6%), and need for additional training (28.6%) (Figure 2A). The proportion of providers who reported either of these reasons was higher among respondents based in countries without HPV NIPs compared to those based in countries with HPV NIPs (Figure 2B), and among male providers compared to female providers (Supplementary Figure S2).
HPV vaccine knowledge among African healthcare providers
Perceived knowledge
Providers were also asked if their knowledge about HPV vaccination was adequate for their current practice. Of the 119 providers who responded to this question, 63 (52.9%) agreed with this statement; there was no difference between providers working in countries with HPV NIPs and those working in countries without HPV NIPs (55.8% versus 47.6%, p = 0.06) (Table 2), and between female providers and male providers (53.1% versus 52.7%, p = 0.45) (Supplementary Table S2).
Measured knowledge
Providers’ knowledge about the HPV vaccine was measured with three knowledge questions. Of the 121 providers who responded to the knowledge questions, 17 (14.0%) respondents provided the correct answer to the question about vaccine efficacy (question i); 32 (26.4%) provided the correct answer to the question about vaccine administration schedule (question ii); and 111 (91.7%) provided the correct answer to the question about vaccine safety (question iii). Overall, 9.9% of providers answered correctly to all three knowledge questions; this proportion was twice as high among providers based in countries with HPV NIPs compared to providers in countries without HPV NIPs (12.3% versus 5.0%, p = 0.34), and among female providers compared to male providers (13.4% versus 5.6%, p = 0.26), although the difference was not statistically significant.
Discussion
In this study, we examined the training and knowledge of African healthcare providers involved in cervical cancer prevention activities, as well as their recommendation practices for the HPV vaccine. While a majority of providers reported recommending the HPV vaccine, their level of knowledge about this vaccine was relatively low. Further, most providers have not been trained in performing HPV vaccine education/counseling and reported that the HPV vaccine remains unavailable in their practice.
Provider’s recommendation of HPV vaccine has been examined in different regions of the world. In a survey conducted in China before the COVID-19 pandemic, 66.4% of HCPs reported recommending (either sometimes, usually, or always) HPV vaccination in their practice (18). In two recent surveys conducted during the COVID-19 pandemic, the proportion of HCPs who recommended HPV vaccination was 57% in Japan (19), and 59% in the State of New York in the US (20). The higher prevalence of HPV vaccine recommendation observed in our study sample is likely explained by our target population which consisted of HCPs involved in cervical cancer prevention activities, and thus, who were more actively engaged in addressing cervical cancer and HPV-related diseases in their practice.
Our findings suggest a relatively low level of training and knowledge about the HPV vaccine among healthcare providers in Africa, including in countries that have introduced HPV immunization in their NIPs. The poor compliance with HPV vaccination in many of these countries may be explained by a limited experience in implementing routine immunization programs for adolescents, as vaccines administered through NIPs in most African settings were primarily targeting newborns and/or infants (21). Corroborating previous reports (22), our findings suggest that adequate training to increase healthcare providers’ knowledge about the HPV vaccine will contribute to the success of HPV NIPs in Africa. Since adolescent immunization is not routinely practiced in many African countries, the introduction of HPV vaccines has created a unique opportunity to build platforms for adolescent immunization and related sexual and reproductive health services.
Vaccination is considered to be the most effective intervention for controlling infectious diseases and other vaccine-preventable diseases like cancers (23). However, the emergence of vaccine hesitancy, fueled by the COVID-19 pandemic, and its penetration into mainstream media may adversely affect the impact of immunization programs, especially in Africa, where access to the internet and social media networks are rapidly growing. Our study was conducted in the midst of the COVID-19 pandemic and provides insights about African providers’ HPV vaccination knowledge and recommendation against a backdrop of increased distrust toward the healthcare system and increased vaccine hesitancy (24). In many parts of Africa, inaccurate messages about HPV vaccine safety were often disseminated through social media (25). In a recent systematic review assessing barriers and facilitators of HPV vaccination in sub-Saharan Africa, limited health system capacities, socio-economic status, stigma, fear and costs of vaccines, negative experience with vaccinations, COVID-19 pandemic, lack of adequate information were identified as the main barriers (26). Further, the inadequate training of the workforce in Africa that was observed in this study, has emerged as the major constraint to the implementation of HPV vaccination programs in the region (27), and highlights the need for targeted interventions to improve providers’ education on this highly effective vaccine. There is strong evidence that training providers to improve their recommendation practices can be accomplished with evidence-based communication interventions (28). In our study, only one-fourth of providers responded correctly to the question about the vaccine administration schedule, suggesting that vaccine stock could be better utilized with prior appropriate training of providers and other stakeholders, especially in the context of a global shortage of HPV vaccines. The recent recommendation by the WHO of a single-dose regimen to achieve adequate protection against HPV-related diseases may further simplify the vaccine administration schedule, thereby facilitating the communication about the vaccine, and reducing the logistics for deploying and administering the vaccine, particularly to the population in remote areas. This may contribute to reducing disparities in access to the HPV vaccine in Africa.
A majority of African providers in this study reported recommending HPV vaccination only for girls per the WHO guidelines, as opposed to the gender-neutral strategy which has been adopted in most high-income countries. While the recently updated WHO recommendations for HPV vaccination remained focused on females, the single-dose strategy may provide an opportunity to introduce gender-neutral vaccination in high-burden settings like Africa, which may further accelerate herd immunity and the subsequent elimination of cervical cancer while reducing the growing burden of other HPV related diseases in the region (29). By removing the stigma associated with a female-only health intervention, the gender-neutral vaccination approach may improve population engagement and political involvement in a setting where community leaders and decision-makers are predominantly male. In our study, a gender-difference (although not statistically significant) was observed in the knowledge and recommendation practices for the HPV vaccine, with the proportion of providers who responded correctly to the knowledge questions and that of providers who reported recommending the HPV vaccine being higher among women compared to men.
Our study had some limitations. First, most respondents to the survey were clinicians working in urban settings, suggesting that our findings may not representatively reflect the status of HPV vaccine knowledge and recommendation practices among providers living in rural areas. Second, respondents were selected among participants in a continuing education e-learning program aimed at building the capacity of African providers in the field of cervical cancer prevention and management, and the survey was administered online. As a result, providers in areas with limited internet penetration were underrepresented in our study sample.
Our study reports pertinent data on provider HPV vaccine knowledge and recommendation against a backdrop of increasing vaccine hesitancy in the African population (24). Because provider recommendation is one of the major facilitators of vaccination uptake, culturally relevant programs should focus on reducing barriers and enhancing factors that promote providers’ recommendation of HPV vaccination. In developed country settings, relevant organizations have worked to increase the frequency and quality of HPV vaccination recommendations. The American Cancer Society has developed a guidebook for clinicians that uses evidence-based strategies to increase HPV vaccination (30). In the same way, African-based organizations, and immunization advisory bodies of African Ministries of Health should develop context-specific and evidence-based recommendations for increasing HPV vaccine recommendations by African providers. About a decade ago, a sub-Saharan African Cervical Cancer Working Group expert panel developed consensus recommendations for the prevention of cervical cancer in the region (including the importance of the HPV vaccine based on the latest clinical data) (31), such recommendations should be updated in the light of scientific advances and emerging needs of the African population.
Conclusion
Despite a high rate of HPV vaccine recommendation among providers in Africa, provider training and knowledge about HPV vaccination remain suboptimal, and vaccine availability remains limited. To increase HPV vaccine uptake in a context of increased vaccine hesitancy in the region, further training is needed to improve providers’ knowledge and engagement. In addition, efforts to develop tailored educational material should be reinforced to facilitate culturally sensitive communication of providers with their patients and the community.
The recent recommendation by the WHO of a single-dose HPV vaccination regimen to prevent HPV-related diseases provides a unique opportunity for African countries to increase HPV vaccination coverage in an economically and logistically viable way. To that end, further training to improve healthcare providers’ knowledge about the HPV vaccine is needed in the region to enhance patient-provider communication, promote mass sensitization, and counter misinformation about the HPV vaccine. Context-specific and culturally sensitive educational tools and informational material to boost HPV vaccination in Africa should be developed.
Data availability statement
The original contributions presented in the study are included in the article/Supplementary material, further inquiries can be directed to the corresponding author.
Ethics statement
The studies involving humans were approved by the study protocol was approved by the University of Texas MD Anderson Cancer Center’s IRB. The studies were conducted in accordance with the local legislation and institutional requirements. The participants provided their written informed consent to participate in this study.
Author contributions
JF: Conceptualization, Data curation, Formal analysis, Methodology, Project administration, Writing – original draft. ID: Conceptualization, Project administration, Writing – review & editing. SK: Writing – review & editing. RY: Data curation, Formal analysis, Methodology, Writing – review & editing. FG: Project administration, Writing – review & editing. LC: Writing – review & editing. GM: Writing – review & editing. NM: Project administration, Writing – review & editing. MPa: Data curation, Methodology, Supervision, Writing – review & editing. FS: Writing – review & editing. JK: Conceptualization, Methodology, Supervision, Writing – review & editing. BT: Project administration, Writing – review & editing. HE: Supervision, Writing – review & editing. MD: Supervision, Writing – review & editing. P-MT: Supervision, Writing – review & editing. MID: Supervision, Writing – review & editing. FL: Supervision, Writing – review & editing. IA: Conceptualization, Supervision, Writing – review & editing. MPl: Conceptualization, Supervision, Writing – review & editing. PB: Conceptualization, Supervision, Writing – review & editing. J-MD: Conceptualization, Supervision, Writing – original draft. SS: Conceptualization, Data curation, Formal analysis, Funding acquisition, Methodology, Project administration, Supervision, Writing – original draft.
Acknowledgments
The authors would like to acknowledge the Leadership of the Division of Cancer Prevention and Population science of the University of Texas MD Anderson Cancer Center, the International Agency for Research in Cancer (IARC), and the African Regional office of the World Health Organization for their support, as well as the REDCap team of the University of Texas MD Anderson Cancer Center for their assistance in data collection. We thank our colleagues and collaborators from various African countries who participated in this survey.
Funding Statement
The author(s) declare financial support was received for the research, authorship, and/or publication of this article. The study was funded by the National Cancer Institute (P30CA016672), the Betty B. Marcus Chair in Cancer Prevention, and the Duncan Family Institute for Cancer Prevention and Risk Assessment. The funders had no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; and in the decision to submit the paper for publication.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Author disclaimer
Where authors are identified as personnel of the International Agency for Research on Cancer/World Health Organization, the authors alone are responsible for the views expressed in this article, and they do not necessarily represent the decisions, policies, or views of the International Agency for Research on Cancer/World Health Organization.
Supplementary material
The Supplementary material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fpubh.2024.1343064/full#supplementary-material
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Data Availability Statement
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