Skip to main content

Far behind 90-70-90’s screening target: the prevalence and determinants of cervical cancer screening among Sub-Saharan African women: evidence from Demographic and Health Survey

Abstract

Background

Cervical cancer screening is the primary goal in 90-70-90 targets to reduce cervical cancer incidence and mortality by identifying and treating women with precancerous lesions. Although several studies have been conducted in Sub-Saharan African (SSA) countries on cervical cancer screening, their coverage was limited to the regional or national level, and/or did not address individual- and community-level determinants, with existing evidence gaps to the wider SSA region using the most recent data. Hence, this study aimed to assess the pooled prevalence and multilevel correlates of cervical cancer screening among women with SSA.

Methods

This study was conducted using the Demographic Health Survey data (2015–2022) from 11 countries, and a total weighted sample of 124,787 women was considered in the analysis. Using multilevel mixed-effects logistic regression, the influence of each factor on cervical cancer screening uptake was investigated, and significant predictors were reported using the adjusted odds ratio (aOR) with their respective 95% confidence intervals (95% CI).

Results

The overall weighted prevalence of cervical cancer screening was 10.29 (95% CI: 7.77, 11.26), with the highest and lowest screening rates detected in Namibia and Benin at 39.3% (95% CI: 38.05, 40.54) and 0.5% (95% CI: 0.36, 0.69), respectively. Higher cervical screening uptake was observed among women aged 35–49 [aOR = 4.11; 95% CI: 3.69, 4.58] compared to 15–24 years, attending higher education [aOR = 2.71; 95% CI: 2.35, 3.23] than no formal education, being in the richest wealth quintile [aOR = 1.45; 95% CI: 1.26, 1.67], having a recent visit to a health facility [aOR = 1.83; 95% CI: 1.71, 1.95], using contraception [aOR = 1.54; 95% CI: 1.45, 1.64], recent sexual activity [aOR = 3.59; 95% CI: 2.97, 4.34], and listening to the radio [aOR = 1.78; 95%CI: 1.60, 2.15].

Conclusion

The overall prevalence of cervical cancer screening in SSA countries was found to be low; only one in every ten women has been screened. Strengthening universal health coverage, and promoting screening programs with an emphasis on rural areas and low socioeconomic status are key to improving screening rates and equity. Additionally, integrating cervical cancer screening with existing reproductive health programs, e.g. contraceptive service would be important.

Peer Review reports

Background

Cervical cancer is one of the most common cancers and causes of cancer-related death in women worldwide [1]. One of its main causes is persistent infection with one or more of the high-risk oncogenic forms of human papillomavirus (HPV), which disrupt normal cell functioning and result in alterations in cervical epithelial cells [2]. Cervical cancer is the fourth most frequent malignancy in women globally, with 604,127 new cases and 341,831 deaths in 2020, with low- and middle-income countries, including Africa, accounting for 90% of the deaths [3]. In 2040, over four-fifths of the increase is projected for cases (847,306) and deaths (524,214), with about a double increase in Africa (e.g., 93.3% for deaths), while only a quarter increase in Europe (e.g., 28.7% for deaths) [3]. Sub-Saharan Africa (SSA) is among the highest regards poor cervical cancer outcomes, including high mortality and low survival, reflecting late diagnosis, low access to screening and treatment services as well as the existence of its risks such as high HIV prevalence and low socioeconomic factors and poverty [1, 3,4,5].

Early identification of cervical cancer through screening is related to improved outcomes, and the World Health Organization (WHO) has released a Global Strategy to Accelerate Cervical Cancer Elimination, which outlines three critical measures: immunisation for human papillomavirus (HPV), screening and treatment [1]. In resource-constrained settings, visual inspection of the cervix with acetic acid followed by treatment (screen and treat) provides an alternative strategy to secondary prevention [6, 7]. If executed properly, this three-pronged strategy is predicted to avert more than 40% of new incidents of the disease and five million related deaths by 2050 [8]. Similarly, the WHO Secretariat modeled the health and socioeconomic implications of meeting the 90-70-90 targets by 2030 in 78 low- and lower-middle-income countries that focus on the following: (i) 90% of girls will be properly vaccinated for HPV, (ii) 70% of women will be screened for cervical cancer, and (iii) 90% of women diagnosed with cervical cancer will receive treatment at the end of 2030 [9].

Effective screening programs and interventions for screening identified abnormal results can reduce cervical cancer cases by 80% [10]. The key strategies to achieve this 70% screening are understanding barriers to services, integrating screening packages with the existing primary healthcare, promoting a screen-and-treat approach, ensuring affordable and high-performance screening tests and treatment devices, and strengthening laboratory capacity and quality assurance programs [9, 11, 12].

Despite the ongoing activities and targets, cervical screening uptake is suboptimal in most low and middle-income countries, including in Sub-Saharan Africa, highlighting unmet needs and less attention to implementing screening initiatives [13,14,15]. For example, in 2020, only below half of women had been screened for cervical cancer in low-income (35%) or lower-middle-income countries (55%), which is lower compared to the rates in high-income countries (80%) [1]. Cervical cancer screening uptake could be attributed to individual factors, including low awareness about cancer or the screening program, limited time to attend the screening, or low preference and acceptance, and community and system-level factors, including limited coverage and access, low health insurance coverage, limited resources, including educational and screening materials [16].

Although several studies have been conducted in SSA countries, they were undertaken at one country or sub-country level, and there was a lack of evidence showing the pooled prevalence of screening in the region using the most recent data [17,18,19]. In addition, those previous studies did not explore the individual and beyond individual contextual factors that affect screening uptake. Hence, the current study addressed the evidence gap by estimating the prevalence and identifying multilevel correlates of cervical cancer screening among women in SSA using the most recent standard Demographic Health Survey data (2015–2022). To do this, this study employed a multilevel regression analysis, which allowed it to demonstrate the influence of factors at the individual and community levels, independently and collectively. The quantitative evidence from screening uptake will provide insights into the coverage, optimal participation, and effectiveness of existing screening programs, which often motivates collective efforts to scale up screening implementation. In addition, the evidence from the pooled prevalence is essential in guiding clinical practice and policy decisions and advancing research efforts to reduce the burden of cervical cancer globally. Moreover, identification of the factors that facilitate or impede cervical cancer screening would be crucial for tailoring interventions by leveraging the facilitators and tackling the barriers through targeted awareness campaigns, educational initiatives, resource allocation, and mobilisation. The WHO’s 90-70-90 targets for cervical cancer elimination by 2030 underscore the urgency of ensuring early detection and improving screening rates [9]. This study could provide the SSA’s progress toward these ambitious goals, allowing for evidence-based adjustments and refinements to strategies, ultimately promoting equity in screening access and uptake and ensuring equity in cervical cancer prevention and outcome.

Methods

Data source, study period, and population

The study was based on the appended woman file (IR) of the most recent Demographic and Health Surveys (DHS) of 11 African countries (2015–2022). The data was accessed from DHS office on a reasonable request via https://dhsprogram.com/Countries/. The study comprised all women who had complete information on the variables of interest: a total of 124,787 women aged 15 to 49 years. In the analysis of DHS data, weighting was performed using a weighting factor ‘wgt’ which was calculated by dividing the variable v005 (women’s individual sample weight of six decimal point) by 1,000,000. All the descriptive statistics were performed by running a STATA command ‘tab varlist [iw = wgt]’, where varlist = variable of interest and wgt = weighting factor. For instance, the weighted sample sizes listed in Table 1 were generated using the STATA command ‘tab v000 [iw = wgt]’. This approach was employed to ensure that the data accurately represented the population being studied, thus allowing for more reliable and meaningful conclusions to be drawn from the analysis (Table 1).

Table 1 Description of the countries included in the analysis with their respective sample size, 2015–2022

Sampling procedures and data collection tools, and sample size

The respondents were accessed using a stratified two-stage cluster sampling technique and the data were collected through face-to-face interviews by trained data collectors. A detailed elaboration of the sampling technique is described in the DHS Sampling and Household Listing Manual [20]. Initially, women’s (IR) files of 12 countries containing data on cervical cancer screening were appended. After excluding missing values, the final analysis was based on 125,756 records (weighted sample size of 124,787) (Fig. 1).

Fig. 1
figure 1

Schematic presentation of the sampling procedure and sample size determination for the study

Measurement of variables of the study

Outcome variable

Cervical cancer screening was defined if the women reported yes to either of the following questions prior to the survey [15]: ‘Have you ever been screened for cervical cancer?’ or ‘Have you ever been tested for cervical cancer?’ ‘Have you had a cervical examination before?’ Further details on the cervical cancer screening questionnaires can be found elsewhere [21]. The response was dichotomised as yes = 1 or no = 0 and was used as an outcome variable [15].

Explanatory variables

Potential variables at the individual and community levels were identified considering prior literature on the area of interest [15, 22]. Individual-level factors comprised socio-demographic, obstetric, and healthcare-related aspects unique to each woman, while community-level factors were shared by all women living in the same community (cluster), such as residency and community poverty (Table 2).

Table 2 List of individual and community-level factors that were supposed to affect the uptake of cervical cancer screening in SSA, 2015–2022

Statistical analysis and data management

The most recent datasets from the 11 SSA countries were appended, recoded, cleaned, and analyzed using STATA version 16. A weighting factor (wgt)\(\:\left(\frac{\mathbf{v}005}{1000000}\right)\) was applied to ensure the representativeness of the data by averting under- and over-representation, where v005 = women’s individual sample weight (in six decimal point). All the descriptive statistics were performed by running a command ‘tab varlist [iw = wgt]’, where varlist = variable of interest and wgt = weighting factor. Frequencies and percentages were computed to determine the characteristics of the respondents across the overall sample size. There was no multicollinearity among the variables (the VIF ranged from 1.08 to 1.88, with a mean of 1.39).

Multilevel mixed-effect logistic regression

Given that the DHS data were hierarchical, we used multilevel modelling; as the outcome variable was binary, we used multilevel multivariable regression analysis.

Model building and selection

Fixed effects (measures of association)

A multilevel bivariable logistic regression analysis was performed to assess the association between each explanatory variable and the response variable, and variables with p-values < 0.25 were entered into multilevel mixed-effect multivariable logistic regression. Finally, multilevel multivariable logistic regression analysis was used to identify significant predictors of cervical cancer screening; statistical significance was declared at p < 0.05, and adjusted odds ratios (AOR) with respective 95% confidence intervals.

Random effects

Using multilevel approaches, four distinct models were fitted: model one (null model) contained no explanatory variables, model two (had eligible individual-level factors), model three (with selected community-level factors), and model four (containing all variables). The intraclass correlation coefficient (ICC) and proportionate change in variance (PCV) were estimated to quantify the random effects in each model (variability in screening levels between and across clusters).

\(\:ICC=\frac{\text{v}\text{a}\text{r}\left(\text{b}\right)}{\text{V}\text{a}\text{r}\left(\text{b}\right)+\text{V}\text{a}\text{r}\left(\text{w}\right)}\), where Var(b) is the variance at the group level and Var(w) is the predicted individual variance component, which is π2/3 ≈ 3.29.

Proportional Change in Variance (PCV) was estimated as.

\(\:PCV=\frac{(\text{V}\text{a}-\text{V}\text{b})}{\text{V}\text{a}}*100\), where Va is the variance of the initial model (null model) and Vb=variance of the subsequent models (models 2, 3, and 4).

Goodness of fit

To evaluate the goodness of fit, deviance = (-2 * (Log Likelihood (LL) of each model), Schwarz’s Bayesian Information Criterion (BIC), and Akaike’s Information Criterion (AIC) were estimated for each model. Following the comparison, the best-fit model for this study was determined to be the fourth model with the lowest deviance, AIC, and BIC values (Table 3).

Table 3 Distribution of sociodemographic characteristics of respondents: cervical cancer screening participation rate and bivariable analysis, SSA, 2015–2022

Results

Sociodemographic characteristics

This study examined a weighted sample of 124,787 women with a mean (± SD) age of 29.38 (± 8.61) years. Burkina Faso had the highest number of respondents (14.2%), while Namibia had the lowest (4.8%). Two-thirds (68.6%) of women have cohabited marital status, and a quarter (24.8%) were in the richest wealth quintile. Women residing in rural areas and those without formal education constituted 53.4% and 26.5% of the respondents, respectively (Table 4).

Table 4 Distribution of obstetric and health service-related characteristics of respondents: status of cervical cancer screening and bivariable analysis, SSA, 2015–2022

Obstetric and health service-related characteristics

More than half of women were multiparous (2–4 living children) (53.8%) and did not use contraception (68.4%) (Table 5). About half of the women had a recent history of sexual activity within the last four weeks (52.0%) or had not visited a health facility within the last 12 months (49.2%). Three-quarters (78.6%) of women never read newspapers, while a comparable proportion never listen to the radio (45.0%) or watch television (45.4%). Obtaining money, traveling long distances, and getting permission were major barriers to seeking maternity care for 53.4%, 34.7%, and 20% of women in the region, respectively (Table 5).

Table 5 Random intercept variances and model fit statistics comparison of multilevel mixed effect logistic regression model

The pooled estimate of women screened for cervical cancer

The overall weighted prevalence of cervical screening in SSA countries was 10.29 (95% CI: 7.77, 11.26). The highest and lowest screening rates were detected in Namibia and Benin at 39.3% (95% CI: 38.05, 40.54) and 0.5% (95% CI: 0.36, 0.69), respectively (Fig. 2).

Fig. 2
figure 2

A forest plot depicting the weighted prevalence of cervical cancer screening in SSA countries, 2015–2022

Results of multilevel mixed effect logistic regression

Random effect (measures of variation)

The null model (Model I) results revealed that the variability between clusters accounted for 17.13% of the total variation in cervical cancer screening in SSA. Furthermore, individual- and community-level characteristics independently accounted for 13.6% and 15.64% of the disparities in cervical cancer screening uptake. In contrast, individual- and community-level factors together accounted for 52.94% of the variation observed in the null model (PCV = 52.94%) (Table 6).

Table 6 Results of a multilevel mixed-effect multivariable logistic regression analysis to identify the factors affecting the uptake of cervical screening in SSA, 2015–2022

Determinants of screening for cervical cancer (fixed effect analysis)

Women’s age, educational level, wealth index, residency, parity, history of recent sexual activity, contraceptive uptake, visiting health facilities, and listening to radio all had a significant association with cervical cancer screening in the multilevel multivariable logistic regression (Table 3). The odds of cervical screening were 4.11 [aOR = 4.11; 95% CI: 3.69, 4.58] times higher among women aged 35–49 than women aged 15–24 years. Women who attended higher education were 2.71 [aOR = 2.71; 95% CI: 2.35, 3.23] times more likely to have a cervical screening than their counterparts with no formal education. The odds of having cervical cancer screening were 3.59 [aOR = 3.59; 95% CI: 2.97, 4.34] times higher in women who had sexual activity within the last 4 weeks than in those who had never had sex. Contraceptive users were 1.54 [aOR = 1.54; 95% CI: 1.45, 1.64] times more likely to be screened than non-users. Similarly, the odds of being screened for cervical cancer were 1.83[aOR = 1.83; 95% CI: 1.71, 1.95] times higher among women who had visited a health facility within the last 12 months than among their non-visited counterparts. Women who listened to the radio at least once a week had a 1.78 [aOR = 1.78; 95%CI: 1.60, 2.15] greater chance of being screened than those who never listened to the radio. (Table 3).

Discussion

The pooled prevalence of cervical cancer screening in SSA was 10.29% (95% CI: 7.77, 11.26), which varied significantly across countries. The likelihood of screening for cervical cancer was higher among women of advanced age (35–49 years), urban residents, higher educational levels, and richest wealth quintile, multiparous, with a recent history of sexual activity, contraceptive users, visiting health facilities, and listening to radio. This prevalence is lower than in a previous study conducted on DHS data from five SSA countries (19.0%) [15], a systematic review and meta-analysis in the same region by using 29 primary studies (12.87%) [22], the United States (77.5%) [25], and Europe(60.3%) [26]. The low screening rate in the current study compared to the previous study in the same region could be attributed to variations in sample size (124,787 vs. 28,976) and number of countries included (11 vs. 5). Overall, low coverage in the region may be due to limited access and coverage of the screening programs, limited awareness about the screening, location of the program and preferences, unmet need of resources, low prioritization by governments due to multiple competing priorities including infectious disease, limited support during the screening process, and cultural and societal factors such as stigma [16, 27]. Overcoming these challenges and implementing targeted measures are critical for increasing the cervical cancer screening rates in the region. Thus, screening necessitates political support, multisectoral collaboration, equitable access in the context of universal health coverage, effective resource mobilisation, health system strengthening, and active health promotion at all levels [1, 9, 28].

Women with a higher level of education are more likely to receive screening services, which is supported by previous studies [15, 22, 26, 29,30,31]. This could be because women with a higher level of education have better access to health information about the benefits of regular cervical cancer screening, the risks associated with the disease, and the available screening methods, which motivate them to prioritise their health and seek regular screening. Furthermore, women with higher education levels may have better health literacy, decision-making autonomy [32, 33], empowerment [34, 35], and a larger social network, all of which make them more proactive in pursuing preventive measures such as cervical cancer screening. This finding emphasises the need to increase access to cervical cancer screening in women with no formal education.

Women who recently engaged in sexual activity were more likely to be screened for cervical cancer. This is supported by other studies [31, 36]. This may be because of various reasons. To begin, sexually active women are often more cognizant of the risks of cervical cancer and are more inclined to seek regular screenings as part of their overall healthcare [36]. In addition, healthcare providers may prioritise screening for sexually active women because of the higher risk associated with certain sexually transmitted viruses such as human papillomavirus (HPV), which is a key risk factor for cervical cancer. Despite this, the WHO recommends two strategies for cervical cancer prevention in the general population of women: screen-and-treat and screening, triage, and treatment commencing at the age of 30 years with regular screening every 5–10 years [37].

The odds of screening were higher among contraceptive users, which is consistent with previous studies [15, 22, 38]. These women may have better access to healthcare services related to increase screening uptake in the current study. These are more likely to contact healthcare providers for contraception counselling or follow-up, and the health visiting experience was related to a better screening rate in our study. Furthermore, contraception use may be a marker of sexual activity and the perceived risk of sexually transmitted illnesses, such as human papillomavirus (HPV). As a result, they may be more motivated to seek cervical cancer screening [38], pointing the importance of integrating cervical cancer screening with existing contraceptive programs.

Urban residents and those in higher wealth quintiles had a higher chance of being screened for cervical cancer, which is in line with similar studies [15, 22, 39,40,41,42]. Women from urban settings have better access to healthcare facilities that offer cervical cancer screening services and better access to health education, and information on preventive healthcare measures [42]. Similarly, women in higher wealth quintiles may have better access to information and resources as well as financial means to access health service delivery points where screening is readily available [40]. Thus, stakeholders in the health sector need to devise policies that promote universal access to healthcare services to address residential and economic disparities in cervical cancer screening rates.

In line with other studies [43, 44], the likelihood of getting screened was higher among multiparous women. As those women are more likely to be in an age group (over 30 years) where cervical screening is highly recommended, they have a higher chance of being included in regular screening programs [37]. This was also supported by another finding of this study that there was a significant positive association between cervical cancer screening and advanced age (35–49 years). These findings should be interpreted with caution, and healthcare providers should encourage all women, regardless of parity status, to be checked for cervical cancer.

This study had both strengths and limitations. To the best of our knowledge, this is the first study in the SSA region to investigate the prevalence and determinants of cervical cancer screening with a larger sample size and most recent data from multiple countries; this makes the findings generalised to women across the region. Furthermore, due to the clustering effect of the DHS data, a multilevel analysis was performed, and the findings at the individual and community levels are vital for developing contextual interventions to improve cervical cancer screening in these regions. As the study was relied on secondary data, there were a possibilities of inherent bias (i.e. bias present in the data process itself due to sampling design, data collection methods, or respondent characteristics). In addition, because the responses were self-reported, there was a chance of social desirability and recall bias. Furthermore, due to the cross-sectional nature of the initial survey, establishing a causal relationship between the outcome of interest and predictors may be difficult.

Conclusion

The prevalence of cervical cancer screening in SSA was found to be low. Higher screening was observed among women of advanced age (35–49 years), living in urban, had higher educational levels, being in the richest wealth quintile, multiparous, had recent history of sexual activity, used contraceptive, visited health facilities, and listened radio. Strengthening awareness campaigns, health education, promoting universal health coverage, and screening program access with an emphasis on rural areas and low socioeconomic status are key to improving cervical cancer screening rates and equity. Additionally, integrating cervical cancer screening with existing reproductive health programs, e.g. contraceptive service would be important. Finally, the DHS office should enhance efforts to disseminate a consistent approach to data collection on cervical cancer (knowledge, screening, and treatment) across all countries.

Data availability

The data for this study were obtained from the DHS program with a reasonable request. Thus, the one who needs the data supporting the findings of this study can get it in anonymised form from the DHS website at https://dhsprogram.com/Countries/ upon reasonable request in the same manner as the authors did.

Abbreviations

AOR:

Adjusted odds ratio

AIC:

Akaike’s Information Criterion

BIC:

Bayesian Information Criterion

ICC:

Intraclass Correlation Coefficient

HPV:

Human Papilloma Virus

PCV:

Proportionate Change in Variance

SSA:

Sub-Saharan African

WHO:

World Health Organization

References

  1. Organization WH. Global strategy to accelerate the elimination of cervical cancer as a public health problem. World Health Organization; 2020.

  2. Johnson CA, et al. Cervical cancer: an overview of pathophysiology and management. Seminars in oncology nursing. Elsevier; 2019.

  3. Bizuayehu HM et al. Global burden of 34 cancers among women in 2020 and projections to 2040: Population-based data from 185 countries/territories. Int J Cancer, 2023.

  4. World Health Organisation, Cervical cancer. Key Facts, 2023 https://www.who.int/news-room/fact-sheets/detail/cervical-cancer#:~:text=Key%20facts,-%20and%20middle-income%20countries

  5. Buskwofie A, David-West G, Clare CA. A review of cervical cancer: incidence and disparities. J Natl Med Assoc. 2020;112(2):229–32.

    PubMed  Google Scholar 

  6. Megevand E, et al. Acetic acid visualization of the cervix: an alternative to cytologic screening. Obstet Gynecol. 1996;88(3):383–6.

    Article  PubMed  CAS  Google Scholar 

  7. Sheth TM, Maitra N. Study to assess the acceptability and feasibility of cervical cancer screening using visual inspection with acetic acid and treatment of precancerous lesions using cryotherapy in low resource settings. Int J Reprod Contracept Obstet Gynecol. 2014;3(3):615–22.

    Article  Google Scholar 

  8. Arbyn M, et al. Estimates of incidence and mortality of cervical cancer in 2018: a worldwide analysis. Lancet Global Health. 2020;8(2):e191–203.

    Article  PubMed  Google Scholar 

  9. Organization WH. Accelerating the elimination of cervical cancer as a public health problem: towards achieving 90-70-90 targets by 2030. World Health Organization. Regional Office for South-East Asia; 2022.

  10. Chakkalakal RJ, et al. Implementing clinical guidelines in low-income settings: a review of literature. Glob Public Health. 2013;8(7):784–95.

    Article  PubMed  Google Scholar 

  11. Pimple S, Mishra G, Shastri S. Global strategies for cervical cancer prevention. Curr Opin Obstet Gynecol. 2016;28(1):4–10.

    Article  PubMed  Google Scholar 

  12. Johnson LG, et al. Implementation strategies to improve cervical cancer prevention in sub-saharan Africa: a systematic review. Implement Sci. 2018;13:1–18.

    Article  Google Scholar 

  13. Lemp JM, et al. Lifetime prevalence of cervical cancer screening in 55 low-and middle-income countries. JAMA. 2020;324(15):1532–42.

    Article  PubMed  PubMed Central  Google Scholar 

  14. Olson B, et al. Cervical cancer screening programs and guidelines in low-and middle-income countries. Int J Gynecol Obstet. 2016;134(3):239–46.

    Article  Google Scholar 

  15. Ba DM, et al. Prevalence and determinants of cervical cancer screening in five sub-saharan African countries: a population-based study. Cancer Epidemiol. 2021;72:101930.

    Article  PubMed  PubMed Central  Google Scholar 

  16. Anaman-Torgbor J et al. Cervical cancer screening behaviours and challenges: a sub-saharan Africa perspective. Pan Afr Med J, 2020. 36(1).

  17. Hoque ME, et al. Cervical cancer screening among university students in South Africa: a theory based study. PLoS ONE. 2014;9(11):e111557.

    Article  PubMed  PubMed Central  Google Scholar 

  18. Rosser JI, et al. Barriers to cervical cancer screening in rural Kenya: perspectives from a provider survey. J Community Health. 2015;40:756–61.

    Article  PubMed  PubMed Central  Google Scholar 

  19. Nwobodo H, Ba-Break M. Analysis of the determinants of low cervical cancer screening uptake among Nigerian women. J Public Health Afr, 2015. 6(2).

  20. ICF International. 2012. Demographic and Health Survey Sampling and Household Listing Manual. MEASURE DHS, Calverton, Maryland, U.S.A.: ICF International https://www.dhsprogram.com/pubs/pdf/DHSM4/DHS6_Sampling_Manual_Sept2012_DHSM4.pdf

  21. Viens L, et al. Questions about cervical and breast cancer screening knowledge, practice, and outcomes: a review of demographic and health surveys. J Women’s Health. 2017;26(5):403–12.

    Article  Google Scholar 

  22. Yimer NB, et al. Cervical cancer screening uptake in Sub-saharan Africa: a systematic review and meta-analysis. Public Health. 2021;195:105–11.

    Article  PubMed  CAS  Google Scholar 

  23. Asabu MD, Altaseb DK. The trends of women’s autonomy in health care decision making and associated factors in Ethiopia: evidence from 2005, 2011 and 2016 DHS data. BMC Womens Health. 2021;21:1–9.

    Article  Google Scholar 

  24. Habte A, Tamene A, Bogale B. Women empowerment domains and unmet need for contraception among married and cohabiting fecund women in Sub-saharan Africa: a multilevel analysis based on gender role framework. PLoS ONE. 2023;18(9):e0291110.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  25. Watson M, Benard V, W Flagg E. Assessment of trends in cervical cancer screening rates using healthcare claims data: United States, 2003–2014. Prev Med Rep. 2018;9:124–30.

    Article  PubMed  PubMed Central  Google Scholar 

  26. Palència L, et al. Socio-economic inequalities in breast and cervical cancer screening practices in Europe: influence of the type of screening program. Int J Epidemiol. 2010;39(3):757–65.

    Article  PubMed  Google Scholar 

  27. Tsu VD, et al. Opportunities and challenges for introducing HPV testing for cervical cancer screening in sub-saharan Africa. Prev Med. 2018;114:205–8.

    Article  PubMed  PubMed Central  Google Scholar 

  28. Buang SN et al. Making multisectoral collaboration work: human papillomavirus immunisation of adolescent girls: improving coverage through multisectoral collaboration in Malaysia. BMJ, 2018. 363.

  29. Damiani G, et al. The impact of level of education on adherence to breast and cervical cancer screening: evidence from a systematic review and meta-analysis. Prev Med. 2015;81:281–9.

    Article  PubMed  Google Scholar 

  30. Akinyemiju TF. Socio-economic and health access determinants of breast and cervical cancer screening in low-income countries: analysis of the World Health Survey. PLoS ONE. 2012;7(11):e48834.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  31. Gu C, Chan CW, Twinn S. How sexual history and knowledge of cervical cancer and screening influence Chinese women’s screening behavior in mainland China. Cancer Nurs. 2010;33(6):445–53.

    Article  PubMed  Google Scholar 

  32. Sultana AM. Factors effect on women autonomy and decision-making power within the household in rural communities. J Appl Sci Res. 2011;7(1):18–22.

    Google Scholar 

  33. Rizkianti A, et al. Women’s decision-making autonomy in the household and the use of maternal health services: an Indonesian case study. Midwifery. 2020;90:102816.

    Article  PubMed  Google Scholar 

  34. Sundaram MS, Sekar M, Subburaj A. Women empowerment: role of education. Int J Manage Social Sci. 2014;2(12):76–85.

    Google Scholar 

  35. Shetty S, Hans V. Role of education in women empowerment and development: Issues and impact Role of Education in Women Empowerment and Development: Issues and ImpactSeptember 26, (2015), 2015.

  36. Wilson KL, et al. Characteristics associated with HPV diagnosis and perceived risk for cervical cancer among unmarried, sexually active college women. J Cancer Educ. 2018;33:404–16.

    Article  PubMed  Google Scholar 

  37. Web Annex A. WHO guideline for screening and treatment of cervical pre-cancer lesions for cervical cancer prevention. World Health Organization; 2021.

  38. Leno D et al. Integration of family planning counselling to mass screening campaign for cervical cancer: Experience from Guinea Obstetrics and Gynecology International, 2018. 2018.

  39. Muthuramalingam M, Muraleedharan V. Patterns in the prevalence and wealth-based inequality of cervical cancer screening in India. BMC Womens Health. 2023;23(1):337.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  40. Mahumud RA, et al. Wealth-related inequalities of women’s knowledge of cervical cancer screening and service utilisation in 18 resource-constrained countries: evidence from a pooled decomposition analysis. Int J Equity Health. 2020;19:1–15.

    Article  Google Scholar 

  41. Locklar LR, Do DP. Rural-urban differences in HPV testing for cervical cancer screening. J Rural Health. 2022;38(2):409–15.

    Article  PubMed  Google Scholar 

  42. Walji LT, et al. Exploring the influence of rural residence on uptake of organized cancer screening–A systematic review of international literature. Cancer Epidemiol. 2021;74:101995.

    Article  PubMed  Google Scholar 

  43. Eshete M, Abdulwuhab Atta M, Yeshita HY. Cervical cancer screening acceptance among women in Dabat district, Northwest Ethiopia, 2017: an institution-based cross-sectional study Obstetrics and Gynecology International, 2020. 2020.

  44. Ugwu UP et al. Cervical Cancer screening knowledge among women of Childbearing Age in Nsukka Local Government Area, Enugu State. Int J Hum Kinetics Health Educ, 2022. 7(1).

Download references

Acknowledgements

We would like to acknowledge the the DHS office to access the data based on a reasonable request.

Funding

Not Applicable.

Author information

Authors and Affiliations

Authors

Contributions

AHH was involved in the design, Literature review, Screening, analysis and interpretation, and manuscript writing from the beginning. HMB and LLT contributed to data analysis and interpretation, as well as drafting and editing the manuscript for final submission. All authors read and approved the final manuscript prior to submission.

Corresponding author

Correspondence to Aklilu Habte Hailegebireal.

Ethics declarations

Ethics approval and consent to participate

All methods and procedures were carried out per the relevant guidelines and regulations of the Declaration of Helsinki. The DHS office provided written permission to use the DHS datasets following registration. Furthermore, as this is secondary data, the ethics committee of Wachemo University College of Medicine and Health Sciences declared that no formal ethics approval was required, with a written letter at the reference number (WCU/337/2023).

Consent for publication

Not applicable.

Competing interests

The authors declare no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Hailegebireal, A.H., Bizuayehu, H.M. & Tirore, L.L. Far behind 90-70-90’s screening target: the prevalence and determinants of cervical cancer screening among Sub-Saharan African women: evidence from Demographic and Health Survey. BMC Cancer 24, 1050 (2024). https://doi.org/10.1186/s12885-024-12789-3

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12885-024-12789-3

Keywords