Skip to main content

Patterns in the prevalence and wealth-based inequality of cervical cancer screening in India

Abstract

Background

Cervical cancer is the second leading cause of deaths due to cancer among women in India. This study assesses the prevalence of cervical cancer screening among women in the 30 to 49 years age-group and its relation to demographic, social and economic factors. The equity in the prevalence of screening is studied with respect to the women’s household wealth.

Methods

Data from the fifth National Family Health Survey are analyzed. The adjusted odds ratio is used to assess the prevalence of screening. The Concentration Index (CIX) and the Slope Index of Inequality (SII) are analyzed to assess the inequality.

Results

The average national prevalence of cervical cancer screening is found to be 1.97% (95% C.I, 1.8–2.1), ranging from 0.2% in West Bengal and Assam to 10.1% in Tamil Nadu. Screening is significantly more prevalent among the following demographics: educated, higher age group, Christian, scheduled caste, Government health insurance coverage, and high household wealth. Significantly lower prevalence is found among Muslim women, women from scheduled tribes, general category castes, non-Government health insurance coverage, high parity, and those who use oral contraceptive pills and tobacco. Marital status, place of residence, age at first sexual activity, and IUD usage are not significant influencers. At the national level, CIX (0.22 (95% C.I, 0.20–0.24)) and SII (0.018 (95% C.I, 0.015–0.020)) indicate significantly higher prevalence of screening among women from the wealthier quintiles. Significantly higher screening prevalence among wealthier quintiles in the North-East (0.1), West (0.21) and Southern (0.05) regions and among the poor quintiles in the Central (-0.05) region. Equiplot analysis shows a “top inequality pattern” in the North, North-East and Eastern regions, with overall low performance where the rich alone manage to avail screening. The Southern region exhibits an overall progress in screening prevalence with the exception of the poorest quintile, which is left behind. Pro-poor inequality exists in the Central region, with significantly higher prevalence of screening among poor.

Conclusion

The prevalence of cervical cancer screening is very low (2%) in India. Cervical cancer screening is substantially higher among women with education and Government Health insurance coverage. Wealth-based inequality exists in the prevalence of cervical cancer screening and the prevalence is concentrated among the women from wealthier quintiles.

Peer Review reports

Introduction

The burden of cervical cancer

Cervical cancer (cancer of the uterine cervix) was the fourth most common cancer and the fourth leading cause of cancer deaths in women worldwide during the year 2020, with an estimated 6,04,127 new cases and 3,41,831 deaths [1]. In India, cervical cancer is the second most common cancer among women with 1,23,907 new cases, and the second leading cause of cancer deaths in women with 77,348 estimated deaths during 2020. In the same year, India accounted for 21% of new cases of cervical cancer and 23% of deaths due to cervical cancer in the world. This makes India the country with the highest number of new cases of cervical cancer and the highest number of deaths due to cervical cancer, surpassing China, which was leading in incidence of cervical cancer until 2018 [2].

The peak age of incidence for cervical cancer in India is 50–59 years, compared to 35–44 years in developed countries [3]. This high age group is partially attributable to the considerable proportion of women in India who are diagnosed with cervical cancer when they are already in the advanced and late stages of the disease: 32.8% of patients have localized disease and for 67.2% of patients, the disease has spread beyond the uterine cervix at the time of initial diagnosis [4, 5]. This makes treatment costly and provides a poor prognosis, resulting in higher mortality rates. The 5-year relative survival rate of cervical cancer (all stages combined for all people) is 46% in India compared to 66% in the United States [3, 6]. With the current population growth rate, the absolute number of new cases of cervical cancer for all ages in India in 2040 is estimated to be 1,91,347 – an increase of 54% over the number of new cases reported during 2020. The corresponding mortalities due to cervical cancer in India in 2040 are estimated to be 1,24,677 – an increase of 61% over the estimated number of deaths due to cervical cancer in 2020 [7, 8].

Cervical cancer screening

The importance of screening for cervical cancer cannot be overemphasized, because diagnosis at the earliest stage of disease is the key to achieving a complete cure without recurrence. Cervical Intraepithelial Neoplasia (CIN) is the precancerous lesion that could lead to cervical cancer. CIN is graded into Low grade Squamous Intraepithelial Lesion (LSIL) also called CIN I and High grade Squamous Intraepithelial Lesion (HSIL). HSIL is subdivided into CIN II and CIN III [9].

  • CIN II: Moderate cervical dysplasia; high rate of regression to normal.

  • CIN III: Marked full thickness atypia and loss of maturation; carries highest risk of progression to invasive squamous cell carcinoma.

A patient with lesions diagnosed and treated at stage CIN III is at significantly higher hazard risk (4.88) for persistence / recurrence than a patient with lesions that are diagnosed and treated during CIN II [10]. Early-stage cervical cancer is amenable to treatment, resulting in 95% disease-free survival and 98% overall survival at ten years [11].

In India, the prevalence of cervical cancer screening was reported as 29.8% among women aged 30–49 years and 22.3% among women aged 15–49 years, as per the fourth round of the National Family Health Survey (NFHS-4) conducted during the year 2015–16 [12, 13]. NFHS-4 collected responses to the question “Have you ever had cervix examination?” from the participant women to assess the prevalence of cervical cancer screening. Responses from the 6,99,686 women aged 15–49 years who participated in the survey revealed that 22.3% of them have had a cervix examination [12]. The fifth round of NFHS, conducted in 2019–21, rephrased the question more specifically as “Have you ever undergone a screening test for cervical cancer?”, which is more specific to cervical cancer, unlike the non-specific question posed during the previous round. Responses from 7,65,805 women aged 15–49 years (during NFHS-5) showed that 1.2% of them have undergone a screening test for cervical cancer [14]. This is far below the prevalence rate based on the NFHS-4 (22.3%), which is primarily due to the formulation of the question.

Considering the marked difference in the prevalence of screening for cervical cancer between NFHS-4 and NFHS-5 and the reason that NFHS-5 is based on the response to a more specific question on cervical cancer screening, the baseline for prevalence needs to be reset according to the NFHS-5 data. Our study, therefore, analyzes the baseline characteristics of cervical cancer screening in India based on the NFHS-5 data. We consider it inappropriate to analyze the prevalence trends over time, as the data from the previous rounds of the NFHS are not comparable with NFHS-5 with respect to the question on the prevalence of cervical cancer screening.

This paper is organized as follows:

  • Introduction” section presents the burden of cervical cancer and the need for resetting the baseline for cervical cancer screening prevalence.

  • Methods” section describes the methodology of the study and the indices used to assess the data.

  • Results” section elaborates the results of the analysis – the socio-demographic profile, the prevalence of cervical cancer screening, and the wealth-based inequality associated with it.

  • Discussion” section discusses the results of the study.

Methods

Database

The fifth round of the National Family Health Survey was conducted between June 2019 and April 2021, covering all the 28 states and eight union territories of India, comprising 707 districts. This survey, organized by the Ministry of Health and Family Welfare, gathered information from 6,36,699 households, 7,24,115 women, and 1,01,839 men. The sample is a stratified two-stage sample derived from the 2011 census representative at the national, state/union territory, and district level. A detailed description of the sampling design is presented in the NFHS-5 national report [14]. No ethical clearance is required, since this study involves the secondary analysis of the NFHS survey dataset, which is freely downloadable following a successful registration in the Demographic and Health Survey program. The data does not contain respondents’ names or any other identifiers.

Data and variables

The NFHS-5 questionnaire contains information from women between 15–49 years of age who were identified as eligible for the survey. From this dataset, the data pertaining to the women in the age group of 30–49 years who answered the question “Have you ever undergone a screening test for cervical cancer?” were filtered and analyzed. The dependent variable was the response to the above question. The independent variables were socio-demographic factors – age in five-year groups, highest educational level, ever been married or in union, religion, caste, household wealth index, type of place of residence (rural vs urban), health insurance coverage (government vs non-government), occupation, partner’s education, region of residence (at the sub-national level – North, Central & others) – and the risk factors for cervical cancer – age at first sexual activity, number of child births, have used IUDs (intrauterine contraceptive devices), have used OCPs (oral contraceptive pills), tobacco use, and history of STI (Sexually Transmitted Infections).

Analysis

Analysis was carried out using the statistical software STATA 15.1 (StataCorp LLC, Texas, USA). Sampling weights, stratification and clustering were accounted for in the analysis and datasets were declared as survey-type using the “svyset” command. Proportion, unweighted and weighted prevalence, and unadjusted and adjusted odds ratios with a 95% confidence interval were analyzed for the prevalence of cervical cancer screening. The national and sub-national prevalence of screening for cervical cancer among women in the 30-to-49-year age group and their relation to demographic, social and economic factors were analyzed. A collinearity check was performed to avoid multicollinearity. A test for goodness of fit was also performed to check whether the sample data fit an expected set of data from a population with normal distribution. The variable inflation factor (VIF) and tolerance were also checked. The adjusted odds ratio was calculated to compare the prevalence of screening with one predictor after adjusting for the other predictors.

The Concentration Index and the Slope Index of Inequality were analyzed to assess the inequality in the prevalence of cervical cancer screening with respect to the household wealth of the respondents. The data related to the quintile-wise wealth inequality of screening prevalence was plotted using the equiplot creator to study the impact of wealth inequality. The district- as well as state-level weighted prevalence was plotted in graphs to create maps. The indices of inequality and the equiplot are discussed in the results section.

Results

Socio-demographic profile

The NFHS-5 questionnaire collected information from 7,47,176 women between the ages of 15 and 49 who were identified as eligible for the survey. Among them, 7,24,115 women completed the questionnaire with a response rate of 96.9.%. Out of these responses, 3,57,353 were from the 30–49 years age group. The 30–34 age group constituted 27.5% and the 35–39 age group had 26.7% of the participants; the 40–44- and 45–49-years’ groups constituted 22.4% and 23.4%, respectively. Women with no formal education comprised 35.4% of respondents whereas 15.5% had primary education (5 years of schooling), 38.7% had completed secondary education (10 years of schooling), and 10.4% higher education (10 + years of schooling). A majority of the women (91.0%) were currently married, 7.4% were formerly married, and 1.6% were never married. 82.3% of participants were Hindu by religion, and 12.1% and 2.6% were Muslims and Christians, respectively. With respect to caste, OBC (Other Backward Castes) constituted 42.9% of the participants, general caste comprised 21.3%, scheduled castes 21.2% and scheduled tribes 9.1%. A majority of the participants were residents of rural areas (66.1%). By household wealth, 17.8% belonged to the poorest quintile, 19.1% to the poorer (the next highest quintile), 20.5% were in the middle quintile, 21.2% in the richer quintile, and 21.3% were from the richest quintile. Health insurance coverage was available to 34.4% of the participants – 24.2% were covered by either one or more government-sponsored or administrated health insurance schemes, and 9.7% possessed one or more non-government health insurance policies. Both government and non-government health insurance cover was available to 0.5% of the participants. Responses were not available from 85.1% for the question on respondents’ occupation, and less than 15% responded to the question on their partner’s education (Table 1).

Table 1 Socio-demographic characteristics of participants (women aged 30–49 years)

Age at first sexual activity was less than 18 years of completed age for 41.6% of the participants. 47.5% of the participants had given birth more than twice. IUDs were used by 5.0% of participants as the method of contraception, while 13.5% have used OCPs. Tobacco use was present among 6.2% of the participants. Only 15% of respondents answered the question related to history of STI – 0.7% have had STIs in the past. Since the response rate for participant’s occupation, partner’s education and history of STI were very low, these three were not included for calculating the adjusted odds of prevalence for cervical cancer screening. Also, the response “Don’t know/Not recorded” for IUD use, OCP use and age at first sexual activity were not included while calculating the adjusted odds, in order to avoid collinearity.

Prevalence of screening

The following observations are derived from Table 2. The prevalence of screening significantly increases with increasing age. The adjusted odds of screening for cervical cancer increase with increasing age – they are 1.21, 1.46 and 1.64 for the age groups 35–39, 40–44 and 45–49 years, respectively, with reference to the 30–34 years age group. The prevalence of screening for cervical cancer is significantly higher among women with some level of education (primary, secondary or tertiary) when compared to women with no education. The adjusted odds of having been screened for cervical cancer are 1.42, 1.44 and 1.51 for women with primary, secondary and higher education respectively, when compared to women with no education. Christian women have significantly higher adjusted odds (1.82) for having undergone screening for cervical cancer, while Muslim women have significantly lower adjusted odds (0.73) for having undergone screening for cervical cancer in comparison to Hindu women. With respect to caste and with scheduled caste women as reference, the adjusted odds are significantly lower for women from scheduled tribes and the general category (0.45, and 0.56 respectively), while those of women from other backward castes are not significantly different. The marital status of the women and the type of place of residence do not show any association with the prevalence of screening for cervical cancer. Among the women with different household wealth, the odds (adjusted) of having undergone screening for cervical cancer are significantly higher among the wealthier quintiles—poorest (reference, 1.0), poorer (1.32), middle (1.59), richer (1.54) and richest (1.55). The availability of government health insurance coverage is associated with significantly higher prevalence of cervical cancer screening, either with a single scheme (adjusted odds 1.22) or multiple schemes (adjusted odds 2.08). Non-government health insurance schemes are associated with significantly lower prevalence of cervical cancer screening (adjusted odds 0.53).

Table 2 Prevalence of cervical cancer screening

Analysis of the prevalence of screening among women with risk factors for cervical cancer shows that high parity (more than two births), oral contraceptive pill usage and tobacco use significantly influence the odds of screening negatively and are associated with lower prevalence of screening. Age at first sexual activity and intrauterine contraceptive device use are not significant factors in determining the prevalence of cervical cancer screening.

The prevalence pattern of cervical cancer screening among different types of health insurance schemes is presented in Table 3. Women with state government–sponsored health insurance schemes have significantly higher prevalence of cervical cancer screening with odds of 1.57 when compared to women without any health insurance coverage. Participants covered under more than one government insurance scheme have significantly higher screening prevalence (2.44). Women covered only under Rashtriya Swasthya Bima Yojana Scheme or certain non-government health insurance schemes have significantly lower screening prevalence.

Table 3 Cervical cancer screening among Health insurance coverage

The nationwide average prevalence of screening for cervical cancer among women in the age group 30–49 years is 1.97% (1.85–2.09%, 95% C.I). Screening prevalence is comparatively higher in the Southern region (5.0) than the other regions – West (1.7), Central (1.2), North (0.9), North-East (0.6) and the East (0.6) (Table 4).

Table 4 Region-wise prevalence of cervical cancer screening

The prevalence ranges widely between the states, from the lowest (0.2%) in West Bengal and Assam to the highest (10.1%) in Tamil Nadu. The state-wise prevalence among women aged 30–49 years is presented in Table 5. Tamil Nadu, Puducherry, Mizoram, Andhra Pradesh, Kerala, Telangana, Punjab, Maharashtra, Andaman & Nicobar and Manipur have higher prevalence of screening than the national average. The district-wise prevalence of cervical cancer screening is depicted in the Fig. 1.

Table 5 Cervical cancer screening. State / Union Territory-wise weighted prevalence among women aged 30–49 years
Fig. 1
figure 1

Cervical cancer screening: district-wise prevalence (%) among women aged 30–49 years, India, NFHS-5+. + Map is not representative of the borders of the Country. Areas that were not included in the DHS survey are not shown in the map

Wealth-based inequality

The Relative Concentration Index (RCI), Corrected Concentration Index (CCI) and the Slope Index of Inequality (SII) are measures used to assess the level of inequality in the prevalence of cervical cancer screening with respect to the wealth quintiles – poorest, poorer, middle, richer and richest. A negative value for an index indicates that the concentration of the health variable is among the poor, and a positive value indicates that the concentration of the health variable is among the richer groups. The results of the analysis show pro-rich wealth-based inequality at the national level, as indicated by the significantly positive values of all three indexing measures of inequality (Table 6). The concentration curve lies below the line of equality, indicating a significantly higher concentration of screening prevalence among women from wealthier quintiles (Fig. 2). The graph for Slope Index of Inequality shows the line rising from left to right, a positive slope, which indicates higher prevalence of cervical cancer screening among the wealthier quintiles (Fig. 3).

Table 6 Wealth-based inequality in cervical cancer screening. Measures of inequality
Fig. 2
figure 2

Wealth-based inequality in cervical cancer screening. Concentration Index

Fig. 3
figure 3

Wealth-based inequality in cervical cancer screening. Slope Index of Inequality

At the regional level, the West and North-East regions show significantly positive values of RCI, CCI and SII, indicating significantly higher prevalence of cervical cancer screening among the richer quintiles. Analysis shows significantly positive values for RCI & CCI for the South, while the Northern region returns a significantly positive value for SII only. These are also indicative of a higher concentration of cervical cancer screening prevalence among wealthier women. The values for the Eastern region are insignificant and hence inconclusive. The Central region shows significant negative values for the RCI, CCI and SII, indicating a significantly higher concentration of cervical cancer screening among the women belonging to poor quintiles (Table 7). The concentration curves for the five regions North, North-East, West, East and South are below the line of equality, implying significantly higher prevalence of cervical cancer screening among wealthier quintiles. The Central region’s concentration curve is above the line of equality, meaning cervical cancer screening prevalence is significantly higher among the poor (Fig. 4). In line with the concentration curves, the SII curves also show significantly higher prevalence of cervical cancer screening among wealthier women in the North, North-East, West, East and South regions and women belonging to poor quintiles in the Central region (Fig. 5).

Table 7 Region-wise – Wealth-based inequality in cervical cancer screening
Fig. 4
figure 4

Region-wise – Wealth-based inequality in cervical cancer screening. Concentration curve

Fig. 5
figure 5

Region-wise – Wealth-based inequality in cervical cancer screening. Slope Index of Inequality

An equiplot is a graphical way to present the patterns of inequality among different groups within a population. The equiplot in Fig. 6, built based on the data in Table 8, presents the relative prevalence of cervical cancer screening among the wealth quintiles of the six sub-national regions based on the inequality patterns “top, linear and bottom” described by Victora CG et al. and Barros AJ et al. [15, 16]. The colored dots depict the prevalence of cervical cancer screening in the wealth quintiles. In the eastern region the dots are closely packed – the poor and rich are intertwined without any distinctive pattern of hierarchical order of prevalence, indicating an absence of significant inequality in cervical cancer screening based on household wealth. In the central region the darker dots depicting the poor quintiles are on the right side, showing higher prevalence of cervical cancer screening among the poor than the rich, a pattern of pro-poor inequality. The North, North-East and Western regions show a “top-inequality pattern” with the richest quintile placed way ahead of the rest, which is typical of regions with overall lower prevalence where the richest alone manage to avail screening. The southern region shows a “bottom-inequality pattern” with the poorest quintile alone lagging behind all others, typical of a region which is actually beginning to gain acceleration in overall prevalence. This shows that although the poorest quintile of the southern region is placed ahead of the richest quintiles of other regions and the overall prevalence is improving in the southern region, the poorest sections of the southern region are not progressing at the same pace and are left behind compared to other quintiles.

Fig. 6
figure 6

Region-wise – Wealth-based inequality in cervical cancer screening

Table 8 Prevalence of cervical cancer screening (%) in wealth quintiles across regions

Discussion

The ideal way to avoid morbidity and mortality due to cervical cancer is by preventing the acquisition / chronic persistence of the causative agent, the Human Papilloma Virus in the uterine cervix. This can be achieved by HPV immunization at the appropriate age before the initiation of sexual activity, i.e., risk of exposure to HPV. This prevents risk for the development of squamous cell carcinoma of the cervix. Even though cervical cancer can be completely cured without further recurrences when diagnosed in its initial stages, surgical treatment of CIN has been associated with an increased risk of preterm delivery, lower birth weight, preterm premature rupture of membrane and obstetrical outcomes, especially following “large loop excision of transformation zone (LLETZ)” and “cold-knife conization (CKC) procedures on the uterine cervix” [17]. This emphasizes the importance of preventing an HPV infection.

Diagnosis of cervical cancer in its initial stages by screening is the next best way to prevent mortality due to cervical cancer, because the disease is amenable to treatment if diagnosed early. In its initial stages, cervical cancer does not cause any symptoms, and hence affected people do not seek medical attention. Screening for cervical cancer is considered crucial because it enables detection of the disease in its early stages. Unless identified by screening, cervical cancer will be left undiagnosed and the disease will progress unnoticed. The affected person will develop symptoms as the disease progresses to an advanced stage, making it difficult to achieve a complete cure and thereby prevent mortality [4, 5]. Moreover, early detection by screening is the only way to prevent death due to cervical cancer among people who are already exposed to HPV infection and people who are not suitable candidates for receiving HPV vaccination [18]. In addition, screening is important irrespective of having received an HPV vaccination, because strains not included in the vaccine are also oncogenic [1]. Considering the important role of screening in the elimination of cervical cancer, the WHO’s global strategy to accelerate the elimination of cervical cancer targets covering 70% of women with two episodes of screening, with a high-performance screening test by the year 2030, one episode at 35 years of age and another episode at 45 years of age.

Baseline information on key indicators is necessary to devise implementation strategies for achieving the WHO targets and also to measure periodical progress towards achieving the targets. The baseline parameters on the prevalence of cervical cancer screening derived from NFHS-4 data were reported by Van Dyne et al. [19]. The subsequent survey, NFHS-5, used a more specific question for collecting data on prevalence of cervical cancer screening. Consequently, NFHS-5 presents a markedly lower prevalence of cervical cancer screening across India in comparison to NFHS-4 [19, 13]. An independent study conducted in July 2019 among women aged 25–65 years in a South Indian community revealed that 14.3% had a pelvic exam in their lifetime while only 7.1% had undergone cervical cancer screening at least once in their lifetime [20]. This explains the reason for difference in results when the survey question was about cervical examination (NFHS-4) compared to the survey question about screening for cervical cancer (NFHS-5). As discussed by Van Dyne EA et al., women might have reported cervical examinations that were not related to cervical cancer screening as a positive response to the NFHS-4 questionnaire. This could have led to the perception of a higher prevalence of cervical cancer screening in NFHS-4 compared to NFHS-5 [1519]. A systematic review of 78 studies published between 1993–2017 (52 of them between 2012–17) revealed that the percentage of women from the general population of India who have participated in cervical cancer screening ranged from 0.7% to 12.2% [21]. This is in line with the results of the NFHS-5’s reporting of 0.2% to 10.1% of screening prevalence between the states. Moreover, the National Noncommunicable Diseases Monitoring Survey, a national representative survey conducted during 2017–18, reported that 2.3% of women aged 30–49 years had undergone screening for cervical cancer by visual inspection with acetic acid, pap smear or HPV test [22]. This is much more in correlation with the NHFS-5’s prevalence rate of 1.97% for cervical cancer screening among women aged 30–49 years than the NFHS-4’s, where it is reported as 29.8% [19]. Hence, the results presented in this study are appropriate as a baseline for devising implementation strategies and also for measuring the progress towards achieving the WHO targets when future rounds of NFHS data or another data from national representative sample become available.

Inequity in the prevalence of cervical cancer screening exists worldwide based on different factors. In Europe, women living in Eastern, Southern and Northern Europe, with a low or intermediate educational level, widowed women or never-married women, and those with low household income were associated with a lower likelihood of having had a cervical smear test in the past three years when compared to women living in Western Europe, women of a high educational level, married women, and those with a higher household income, respectively. In comparison, India’s pattern shows inequality in the prevalence of cervical cancer screening with higher prevalence among educated women and those with a higher household income. The earlier implementation of organized screening programs in Northern and Western European countries compared to the rest of Europe is proposed as the reason for the higher prevalence of screening [23]. In India, the South, West and Central regions have significantly higher prevalence of cervical cancer screening when compared to East, North-East and Northern regions. The National Program for Control of Cancer, Diabetes, Cardiovascular diseases and Stroke (NPCDCS) was launched in the year 2010, implemented in phases, and it covered the entire nation by the year 2017 [24]. A few states in India were already implementing their own state-level cancer control programs and were in an advantageous position to easily adopt the NPCDCS when it was launched. Tamil Nadu implemented the World Bank–supported NCD control program from the year 2008 using the VIA testing method in facility-based opportunistic mode, and later switched to the NPCDCS program [25, 26]. The early implementation of the program could be one of the reasons for the relatively higher prevalence of cervical cancer screening in Tamil Nadu.

Utilization of cervical cancer tests is higher among women who are daily or occasional smokers in Europe [23]. This is in contrast to India, where the prevalence of cervical cancer screening is lower among women using tobacco. In Zimbabwe, religious affiliations and usage of health facilities act as determinants of participation in cervical cancer screening. Women affiliated with Roman Catholic, Protestant, Pentecostal and Apostolic sects were less likely to screen for cervical cancer compared to those in other religions [27]. Our study also shows that religious affiliations are associated with inequity in prevalence of cervical cancer screening. Christian women in India have significantly higher adjusted odds (1.82) for having undergone screening for cervical cancer, while Muslim women have significantly lower adjusted odds (0.73) for having undergone screening for cervical cancer in comparison to Hindu women. In South Africa, Nigeria, Uganda and Peru, women in rural areas were disproportionately affected by distance and the travel costs incurred in assessing the health facilities for cervical cancer screening [28,29,30,31]. For women living in the rural areas of these countries, lack of time due to home care commitments, travel costs and personal safety issues on the way to the health facility are mentioned as the barriers in availing cervical cancer screening. Our study does not find any significant difference in the prevalence of cervical cancer screening among women based on the type of place of residence in India (rural vs urban areas).

A study among United States women aged 21–65 years reported that cervical cancer screening rates varied significantly by type of insurance coverage. Compared with women with employer-based insurance or Medicare (aged ≥ 65 years), women with other types of insurance were 2%–4% less likely to receive a Pap test [32]. A systematic review of 29 observational studies conducted in the United States revealed that lack of health insurance coverage or disruptions in health insurance coverage were consistently statistically significantly associated with lesser receipt of cervical cancer prevention services as well as with advanced stages of cancer at diagnosis and worse survival [33]. Our study shows that government-sponsored health insurance schemes, particularly state government–sponsored schemes, are associated with significantly higher prevalence of cervical cancer screening (O.R-1.57, p < 0.001). Women covered under more than one government health insurance scheme have even higher prevalence of cervical cancer screening (O.R-2.44, p < 0.001). In Tamil Nadu, the state with the highest prevalence of cervical cancer screening among the Indian states, the state-sponsored Chief Minister’s Comprehensive Health Insurance Scheme covers the confirmatory colposcopy test for women tested VIA positive, and also covers cryotherapy and all other treatments for cervical cancer. The relationship between the availability of further diagnostic tests and treatment for cervical cancer under health insurance and the prevalence of cancer screening has to be studied, as it may be a possible cause for the higher prevalence of cervical cancer screening among women covered under these schemes [34].

The significant difference in prevalence among states, religious groups, caste groups and wealth quintiles necessitate the exploration of reasons for the same. Further studies are required to find the reason for the higher prevalence of cervical cancer screening among women covered under state government–sponsored health insurance schemes when compared to women without insurance coverage and women covered under other types of health insurance schemes. Apart from the social, economic and demographic factors discussed in this study, other influences like behavioral and belief patterns need to be studied and addressed to successfully achieve the targeted coverage of cervical cancer screening. It is established that the majority of women who perceived their health status to be poor had taken a Pap smear test compared to those with perceived excellent health status [35]. Similarly, a fear of screening (that the test would be painful) and a fear of the detection of any abnormal pathology, particularly in the absence of support mechanisms, have been proved to be a reason for the low acceptance of screening tests in rural India [36, 37]. Health education campaigns that address specific religious and cultural issues regarding cervical cancer prevention need to be explored for their effectiveness [38, 39]. The validity of providing alternative choices to women, like offering self-sample collection methods for undergoing screening, needs to be studied with respect to women who did not respond to health education and for whom privacy is the major concern [40, 41]. We conclude that demystifying the reasons for the socio-demographic and economic patterns of difference in prevalence presented above hold the key to achieving the target screening levels and preventing deaths due to cervical cancer.

Strengths of the study

This is the first study about the prevalence of cervical cancer screening based on the NFHS-5 data, which contains specific information on cervical cancer screening. The role of health insurance on cervical cancer screening is explored for the first time from a national representative database, and wealth-based inequality is explored with relation to cervical cancer screening.

Limitations of the study

The types of tests commonly used for screening (VIA/Pap/HPV), places of screening (primary/secondary/tertiary care facility/mobile health units/home) and types of facility (public or private) are not described in this study. Moreover, the behaviors, beliefs, social and economic levels, and demographic patterns are dynamic and constantly changing. Hence periodical assessment is necessary for the suitable modification of cancer control programs at required time intervals.

Availability of data and materials

The datasets analyzed during the current study are available in the Demographic Health Survey website, the datasets are downloaded from the website after registration and approval. The website can be accessed from https://dhsprogram.com/data/available-datasets.cfm.

Abbreviations

CaCx:

Cervical Cancer

CCI:

Corrected Concentration Index (Erreygers)

C.I:

Confidence Interval

CIX:

Concentration Index

CKC:

Cold-knife conization

Co. Eff:

Co-efficient

Govt:

Government

HPV:

Human Papilloma Virus

HSIL:

High grade Squamous Intraepithelial Lesion

IUD:

Intra Uterine contraceptive Device

LLETZ:

Large loop excision of transformation zone

LSIL:

Low grade Squamous Intraepithelial Lesion

NCD:

Non-Communicable Diseases

NFHS:

National Family Health Survey

NPCDCS:

National Program for Control of Cancer, Diabetes, Cardiovascular diseases and Stroke

OBC:

Other Backward Castes

OCP:

Oral Contraceptive Pills

Pap:

Papanicolaou test

RCI:

Relative Concentration Index

RSBY:

Rashtriya Swasthya Bima Yojana

SII:

Slope Index of Inequality

STI:

Sexually Transmitted Infections

VIA:

Visual Inspection with Acetic acid

VIF:

Variable Inflation Factor

WHO:

World Health Organization

References

  1. Sung H, Ferlay J, Siegel RL, Laversanne M, Soerjomataram I, Jemal A, Bray F. Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA Cancer J Clin. 2021;71(3):209–49. https://doi.org/10.3322/caac.21660. Epub 2021 Feb 4 PMID: 33538338.

    Article  PubMed  Google Scholar 

  2. Arbyn M, Weiderpass E, Bruni L, de Sanjosé S, Saraiya M, Ferlay J, Bray F. Estimates of incidence and mortality of cervical cancer in 2018: a worldwide analysis. Lancet Glob Health. 2020;8(2):e191–203. https://doi.org/10.1016/S2214-109X(19)30482-6. Epub 2019 Dec 4. Erratum in: Lancet Glob Health. 2022 Jan;10(1):e41. PMID: 31812369; PMCID: PMC7025157.

    Article  PubMed  Google Scholar 

  3. Bobdey S, Sathwara J, Jain A, Balasubramaniam G. Burden of cervical cancer and role of screening in India. Indian J Med Paediatr Oncol. 2016;37(4):278–85. https://doi.org/10.4103/0971-5851.195751. PMID: 28144096; PMCID: PMC5234166.

    Article  PubMed  PubMed Central  Google Scholar 

  4. Mathur P, Sathishkumar K, Chaturvedi M, Das P, Sudarshan KL, Santhappan S, Nallasamy V, John A, Narasimhan S, Roselind FS, ICMR-NCDIR-NCRP Investigator Group. Cancer Statistics, 2020: Report From National Cancer Registry Programme, India. JCO Glob Oncol. 2020;6:1063–75. https://doi.org/10.1200/GO.20.00122. PMID: 32673076; PMCID: PMC7392737.

    Article  PubMed  Google Scholar 

  5. Sreedevi A, Javed R, Dinesh A. Epidemiology of cervical cancer with special focus on India. Int J Womens Health. 2015;16(7):405–14. https://doi.org/10.2147/IJWH.S50001.PMID:25931830;PMCID:PMC4404964.

    Article  Google Scholar 

  6. American Cancer Society. Cancer Facts & Figures 2021. Atlanta: American Cancer Society; 2021. https://www.cancer.org/content/dam/cancer-org/research/cancer-facts-and-statistics/annual-cancer-facts-and-figures/2021/cancer-facts-and-figures-2021.pdf. Accessed on 14 Feb 2023.

  7. International Agency for Research on Cancer, WHO. https://gco.iarc.fr/tomorrow/en/dataviz/tables?sexes=2&single_unit=5000&cancers=23&populations=356&group_populations=1&multiple_populations=1&mode=population&key=total&show_bar_mode_prop=0&types=0. Accessed on 14 Feb 2023.

  8. International Agency for Research on Cancer, WHO. https://gco.iarc.fr/tomorrow/en/dataviz/tables?sexes=2&single_unit=5000&cancers=23&populations=356&group_populations=1&multiple_populations=1&mode=population&key=total&show_bar_mode_prop=0&types=1. Accessed on 14 Feb 2023.

  9. Khieu M, Butler SL. High Grade Squamous Intraepithelial Lesion. 2022 . In: StatPearls. Treasure Island (FL): StatPearls Publishing; 2023 Jan–. PMID: 28613479.

  10. Giannini A, Di Donato V, Sopracordevole F, Ciavattini A, Ghelardi A, Vizza E, D’Oria O, Simoncini T, Plotti F, Casarin J, GoliaD’Augè T, Cuccu I, Serati M, Pinelli C, Bergamini A, Gardella B, Dell’Acqua A, Monti E, Vercellini P, D’Ippolito G, Aguzzoli L, Dario Mandato V, Giannella L, Scaffa C, Ditto A, Falcone F, Borghi C, Malzoni M, Di Giovanni A, Salerno MG, Liberale V, Contino B, Donfrancesco C, Desiato M, Perrone AM, De Iaco P, Ferrero S, Sarpietro G, Matarazzo MG, Cianci A, Cianci S, Bosio S, Ruisi S, Mosca L, Tinelli R, De Vincenzo R, Zannoni GF, Ferrandina G, Petrillo M, Capobianco G, Carlea A, Zullo F, Muschiato B, Palomba S, Greggi S, Spinillo A, Ghezzi F, Colacurci N, Angioli R, Benedetti Panici P, Muzii L, Scambia G, Raspagliesi F, Bogani G. Outcomes of High-Grade Cervical Dysplasia with Positive Margins and HPV Persistence after Cervical Conization. Vaccines (Basel). 2023;11(3):698. https://doi.org/10.3390/vaccines11030698. PMID:36992282;PMCID:PMC10051663.

    Article  PubMed  Google Scholar 

  11. Di Donato V, Bogani G, Casarin J, Ghezzi F, Malzoni M, Falcone F, Petrillo M, Capobianco G, Calò F, D’Augè TG, Muzii L, Benedetti Panici P, Ervas E, Ditto A, Raspagliesi F, Sopracordevole F, Vizza E, Giannini A. Ten-year outcomes following laparoscopic and open abdominal radical hysterectomy for “low-risk” early-stage cervical cancer: a propensity-score based analysis. Gynecol Oncol. 2023;174:49–54. https://doi.org/10.1016/j.ygyno.2023.04.030. Epub ahead of print. PMID: 37149905.

    Article  PubMed  Google Scholar 

  12. International Institute for Population Sciences (IIPS) and ICF. 2017. National Family Health Survey (NFHS-4), 2015–16: India. Mumbai: IIPS

  13. Krishnamoorthy Y, Ganesh K, Sakthivel M. Prevalence and determinants of breast and cervical cancer screening among women aged between 30 and 49 years in India: Secondary data analysis of National Family Health Survey - 4. Indian J Cancer. 2022;59(1):54–64. https://doi.org/10.4103/ijc.IJC_576_19. PMID: 33753601.

    Article  PubMed  Google Scholar 

  14. International Institute for Population Sciences (IIPS) and ICF. 2021. National Family Health Survey (NFHS-5), 2019–21: India. Mumbai: IIPS

  15. Victora CG, Fenn B, Bryce J, Kirkwood BR. Co-coverage of preventive interventions and implications for child-survival strategies: evidence from national surveys. Lancet. 2005;366(9495):1460–6. https://doi.org/10.1016/S0140-6736(05)67599-X. PMID: 16243091.

    Article  PubMed  Google Scholar 

  16. Barros AJ, Victora CG. Measuring coverage in MNCH: determining and interpreting inequalities in coverage of maternal, newborn, and child health interventions. PLoS Med. 2013;10(5):e1001390. https://doi.org/10.1371/journal.pmed.1001390. Epub 2013 May 7. PMID: 23667332; PMCID: PMC3646214.

    Article  PubMed  PubMed Central  Google Scholar 

  17. Monti M, D’Aniello D, Scopelliti A, Tibaldi V, Santangelo G, Colagiovanni V, Giannini A, DI Donato V, Palaia I, Perniola G, Giancotti A, Muzii L, Benedetti Panici P. Relationship between cervical excisional treatment for cervical intraepithelial neoplasia and obstetrical outcome. Minerva Obstet Gynecol. 2021;73(2):233–46. https://doi.org/10.23736/S2724-606X.20.04678-X.

    Article  PubMed  Google Scholar 

  18. ICMR. Consensus Document for The Management of Cancer Cervix. 2016 https://main.icmr.nic.in/sites/default/files/guidelines/Consensus%20Document%20for%20The%20Management%20of%20Cancer%20Cervix_0.pdf. Accessed on 14 Feb 2023.

  19. Van Dyne EA, Hallowell BD, Saraiya M, Senkomago V, Patel SA, Agrawal S, Ghosh A, Saraf D, Mehrotra R, Dhillon PK. Establishing Baseline Cervical Cancer Screening Coverage - India, 2015–2016. MMWR Morb Mortal Wkly Rep. 2019;68(1):14–9. https://doi.org/10.15585/mmwr.mm6801a4. PMID: 30629571.

    Article  PubMed  Google Scholar 

  20. Reichheld A, Mukherjee PK, Rahman SM, David KV, Pricilla RA. Prevalence of Cervical Cancer Screening and Awareness among Women in an Urban Community in South India-A Cross Sectional Study. Ann Glob Health. 2020;86(1):30. https://doi.org/10.5334/aogh.2735. PMID:32211300;PMCID:PMC7082824.

    Article  PubMed  PubMed Central  Google Scholar 

  21. Thulaseedharan JV, Frie KG, Sankaranarayanan R. Challenges of health promotion and education strategies to prevent cervical cancer in India: a systematic review. J Educ Health Promot. 2019;29(8):216. https://doi.org/10.4103/jehp.jehp_156_19. PMID:31867380;PMCID:PMC6905291.

    Article  Google Scholar 

  22. ICMR-NCDIR, National Noncommunicable Disease Monitoring Survey (NNMS) 2017–18, Bengaluru, India. https://www.ncdirindia.org/nnms/resources/NNMS2017-18-Report.pdf. Accessed on 09 June 2023.

  23. Bozhar H, McKee M, Spadea T, Veerus P, Heinävaara S, Anttila A, Senore C, Zielonke N, de Kok IMCM, van Ravesteyn NT, Lansdorp-Vogelaar I, de Koning HJ, Heijnsdijk EAM, EU-TOPIA consortium. Socio-economic inequality of utilization of cancer testing in Europe: a cross-sectional study. Prev Med Rep. 2022;26:101733. https://doi.org/10.1016/j.pmedr.2022.101733. PMID: 35198362; PMCID: PMC8850331.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  24. DGHS, MoHFW. Operational Guidelines (Revised 2013–17): NPCDCS, 2013. https://main.mohfw.gov.in/sites/default/files/Operational%20Guidelines%20of%20NPCDCS%20%28Revised%20-%202013-17%29_1.pdf. Last accessed on 14 Feb 2023.

  25. Aoki ES, Yin R, Li K, Bhatla N, Singhal S, Ocviyanti D, Saika K, Suh M, Kim M, Termrungruanglert W. National screening programs for cervical cancer in Asian countries. J Gynecol Oncol. 2020;31(3):e55. https://doi.org/10.3802/jgo.2020.31.e55. Epub 2020 Feb 26. PMID: 32266804; PMCID: PMC7189071.

    Article  PubMed  PubMed Central  Google Scholar 

  26. Tamil Nadu Health Systems Project, Government of Tamil Nadu, Implementation completion results report, 2015. https://tnhsp.org/tnhsp/images/Completion-Report.pdf. Accessed on 14 Feb 2023.

  27. Tapera O, Kadzatsa W, Nyakabau AM, Mavhu W, Dreyer G, Stray-Pedersen B, Sjh H. Sociodemographic inequities in cervical cancer screening, treatment and care amongst women aged at least 25 years: evidence from surveys in Harare, Zimbabwe. BMC Public Health. 2019;19(1):428. https://doi.org/10.1186/s12889-019-6749-6. PMID:31014308;PMCID:PMC6480834.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  28. Harries J, Scott SE, Walter FM, Mwaka AD, Moodley J. Women’s appraisal, interpretation and help-seeking for possible symptoms of breast and cervical cancer in South Africa: a qualitative study. BMC Womens Health. 2020;20(1):251. https://doi.org/10.1186/s12905-020-01120-4. PMID:33187501;PMCID:PMC7666481.

    Article  PubMed  PubMed Central  Google Scholar 

  29. Stewart K, Li M, Xia Z, Adewole SA, Adeyemo O, Adebamowo C. Modeling spatial access to cervical cancer screening services in Ondo State, Nigeria. Int J Health Geogr. 2020;19(1):28. https://doi.org/10.1186/s12942-020-00222-4.PMID:32693815;PMCID:PMC7374833.

    Article  PubMed  PubMed Central  Google Scholar 

  30. Hasahya OT, Berggren V, Sematimba D, Nabirye RC, Kumakech E. Beliefs, perceptions and health-seeking behaviours in relation to cervical cancer: a qualitative study among women in Uganda following completion of an HPV vaccination campaign. Glob Health Action. 2016;16(9):29336. https://doi.org/10.3402/gha.v9.29336. PMID:26895145;PMCID:PMC4759844.

    Article  Google Scholar 

  31. Barrett BW, Paz-Soldan VA, Mendoza-Cervantes D, Sánchez GM, CórdovaLópez JJ, Gravitt PE, Rositch AF, Proyecto Precancer Study Group. Understanding Geospatial Factors Associated With Cervical Cancer Screening Uptake in Amazonian Peruvian Women. JCO Glob Oncol. 2020;6:1237–47. https://doi.org/10.1200/GO.20.00096. PMID: 32755481; PMCID: PMC7456312.

    Article  PubMed  Google Scholar 

  32. Zhao G, Okoro CA, Li J, Town M. Health insurance status and clinical cancer screenings among U.S. adults. Am J Prev Med. 2018;54(1):e11–9. https://doi.org/10.1016/j.amepre.2017.08.024. PMID: 29102459.

    Article  PubMed  Google Scholar 

  33. Yabroff KR, Reeder-Hayes K, Zhao J, Halpern MT, Lopez AM, Bernal-Mizrachi L, Collier AB, Neuner J, Phillips J, Blackstock W, Patel M. Health insurance coverage disruptions and cancer care and outcomes: systematic review of published research. J Natl Cancer Inst. 2020;112(7):671–87. https://doi.org/10.1093/jnci/djaa048. PMID:32337585;PMCID:PMC7357319.

    Article  PubMed  PubMed Central  Google Scholar 

  34. Chief Minister's Comprehensive Health Insurance Scheme (cmchistn.com). https://www.cmchistn.com/prate.php?category=Diagnostic%20center. Accessed on 10 Jun 2023.

  35. Akokuwebe ME, Idemudia ES, Lekulo AM, Motlogeloa OW. Determinants and levels of cervical Cancer screening uptake among women of reproductive age in South Africa: evidence from South Africa Demographic and health survey data, 2016. BMC Public Health. 2021;21(1):2013. https://doi.org/10.1186/s12889-021-12020-z. PMID:34740352;PMCID:PMC8571865.

    Article  PubMed  PubMed Central  Google Scholar 

  36. Srivastava AN, Misra JS, Srivastava S, Das BC, Gupta S. Cervical cancer screening in rural India: status & current concepts. Indian J Med Res. 2018;148(6):687–96. https://doi.org/10.4103/ijmr.IJMR_5_17. PMID:30778002;PMCID:PMC6396551.

    Article  PubMed  PubMed Central  Google Scholar 

  37. Misra J, Srivastava A, Gupta H. Impact of Literacy Status on the Cervical Cancer Screening in Rural Women of India. Invest Gynecol Res Women’s Health. 1(2). IGRWH.000510: 2017. https://doi.org/10.31031/IGRWH.2017.01.000510.

  38. SaeiGharenaz M, Kariman N, Ebadi A, Ozgoli G, Ghasemi V, RashidiFakari F. Educational interventions for cervical cancer screening behavior of women: a systematic review. Asian Pac J Cancer Prev. 2018;19(4):875–84. https://doi.org/10.22034/APJCP.2018.19.4.875. PMID: 29693331; PMCID: PMC6031778.

    Article  Google Scholar 

  39. AL-Hammadi FA, Al-Tahri F, Al-Ali A, Nair SC, Abdulrahman M. Limited understanding of pap smear testing among women, a barrier to cervical cancer screening in the United Arab Emirates. Asian Pac J Cancer Prev. 2017;18(12):3379–87. https://doi.org/10.22034/APJCP.2017.18.12.3379. PMID: 29286607; PMCID: PMC5980898.

    Article  PubMed  PubMed Central  Google Scholar 

  40. Arbyn M, Smith SB, Temin S, Sultana F, Castle P, Collaboration on Self-Sampling and HPV Testing. Detecting cervical precancer and reaching underscreened women by using HPV testing on self samples: updated meta-analyses. BMJ. 2018;363:k4823. https://doi.org/10.1136/bmj.k4823. PMID: 30518635; PMCID: PMC6278587.

    Article  PubMed  PubMed Central  Google Scholar 

  41. Musa J, Achenbach CJ, O’Dwyer LC, Evans CT, McHugh M, Hou L, Simon MA, Murphy RL, Jordan N. Effect of cervical cancer education and provider recommendation for screening on screening rates: a systematic review and meta-analysis. PLoS One. 2017;12(9):e0183924. https://doi.org/10.1371/journal.pone.0183924. Erratum in: PLoS One. 2017 Dec 29;12 (12 ):e0190661. PMID: 28873092; PMCID: PMC5584806.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

Download references

Acknowledgements

The equiplot graph presented in this paper was made with the equiplot creator tool available in the International Center for Equity in Health’s website, https://equidade.org/equiplot_creator.

Funding

Authors did not receive any funding for the completion of this study. No funding involved.

Author information

Authors and Affiliations

Authors

Contributions

MR and VRM have made contributions to the conception; MR has contributed to the analysis, interpretation of results and have drafted the work. VRM has contributed to the interpretation of results and reviewed the study; and all authors have read the manuscript and contributed substantially to the work. All the authors have read and approved the study.

Corresponding author

Correspondence to M. R. Muthuramalingam.

Ethics declarations

Ethics approval and consent to participate

The current study is an analysis of the data collected by the National Family Health Survey—5 (NFHS-5) of India also called Demographic Health Survey VII (DHS-VII, 2019–21). The NFHS-5 (DHS-VII, 2019–21) survey was reviewed for ethical clearance by the Institutional Review Board (IRB) of ICF (Project Number—190308.0.001.00, Project Name: DHS/2019–20 India National Family Health Survey). The project description and the supporting materials were reviewed and the IRB considered the project as “The Activity is Not Research or Not Human Subjects Research” due to the activity being “Public health surveillance requested/authorized by a public health authority”. The NFHS-5 India final report states that, “The protocol for the NFHS-5 survey, including the content of all the survey questionnaires, was approved by the International Institute for Population Sciences, Mumbai (IIPS)—Institutional Review Board and the ICF’s Institutional Review Board. The protocol was also reviewed by the U.S. Centers for Disease Control and Prevention (CDC)” (page.3 of the NFHS-5 final report—International Institute for Population Sciences (IIPS) and ICF. 2021. National Family Health Survey (NFHS-5), 2019–21: India. Mumbai: IIPS). ICF IRB ensured that the survey complies with the U.S. Department of Health and Human Services regulations for the protection of human subjects (45 CFR 46), while IIPS-Mumbai, the host country IRB ensured that the survey complies with laws and norms of the nation. Moreover, Informed consent was obtained from the NFHS-5 survey participants and data is publicly available with no identifiable information about the survey participants. Being an analysis of the survey data of NFHS-5 which is conducted with required ethical approvals, no ethical approval was required for this study. The data was downloaded from the Demographic Health Survey Program after registration and obtaining permission for analysis. All methods were carried out in accordance with relevant guidelines and regulations.

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 4.0 International License, which permits use, sharing, adaptation, 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 changes were made. 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/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Muthuramalingam, M.R., Muraleedharan, V.R. Patterns in the prevalence and wealth-based inequality of cervical cancer screening in India. BMC Women's Health 23, 337 (2023). https://doi.org/10.1186/s12905-023-02504-y

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12905-023-02504-y

Keywords