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. 2021 Nov 4;16(11):e0259339. doi: 10.1371/journal.pone.0259339

Cervical cancer screening utilization and predictors among eligible women in Ethiopia: A systematic review and meta-analysis

Melaku Desta 1,*, Temesgen Getaneh 1, Bewuket Yeserah 1, Yichalem Worku 1, Tewodros Eshete 2, Molla Yigzaw Birhanu 3, Getachew Mullu Kassa 1, Fentahun Adane 4, Yordanos Gizachew Yeshitila 5
Editor: Gizachew Tessema6
PMCID: PMC8568159  PMID: 34735507

Abstract

Background

Despite a remarkable progress in the reduction of global rate of maternal mortality, cervical cancer has been identified as the leading cause of maternal morbidity and mortality, particularly in sub-Saharan African countries. The uptake of cervical cancer screening service has been consistently shown to be effective in reducing the incidence rate and mortality from cervical cancer. Despite this, there are limited studies in Ethiopia that were conducted to assess the uptake of cervical cancer screening and its predictors, and these studies showed inconsistent and inconclusive findings. Therefore, this systematic review and meta-analysis was conducted to estimate the pooled cervical cancer screening utilization and its predictors among eligible women in Ethiopia.

Methods and findings

Databases like PubMed, Web of Science, SCOPUS, CINAHL, Psychinfo, Google Scholar, Science Direct, and the Cochrane Library were systematically searched. All observational studies reporting cervical cancer screening utilization and/ or its predictors in Ethiopia were included. Two authors independently extracted all necessary data using a standardized data extraction format. Quality assessment criteria for prevalence studies were adapted from the Newcastle Ottawa quality assessment scale. The Cochrane Q test statistics and I2 test were used to assess the heterogeneity of studies. A random effects model of analysis was used to estimate the pooled prevalence of cervical cancer screening utilization and factors associated with it with the 95% confidence intervals (CIs). From 850 potentially relevant articles, twenty-five studies with a total of 18,067 eligible women were included in this study. The pooled national cervical cancer screening utilization was 14.79% (95% CI: 11.75, 17.83). The highest utilization of cervical cancer screening (18.59%) was observed in Southern Nations Nationalities and Peoples’ region (SNNPR), and lowest was in Amhara region (13.62%). The sub-group analysis showed that the pooled cervical cancer screening was highest among HIV positive women (20.71%). This meta-analysis also showed that absence of women’s formal education reduces cervical cancer screening utilization by 67% [POR = 0.33, 95% CI: 0.23, 0.46]. Women who had good knowledge towards cervical screening [POR = 3.01, 95%CI: 2.2.6, 4.00], perceived susceptibility to cervical cancer [POR = 4.9, 95% CI: 3.67, 6.54], severity to cervical cancer [POR = 6.57, 95% CI: 3.99, 10.8] and those with a history of sexually transmitted infections (STIs) [POR = 5.39, 95% CI: 1.41, 20.58] were more likely to utilize cervical cancer screening. Additionally, the major barriers of cervical cancer screening utilization were considering oneself as healthy (48.97%) and lack of information on cervical cancer screening (34.34%).

Conclusions

This meta-analysis found that the percentage of cervical cancer screening among eligible women was much lower than the WHO recommendations. Only one in every seven women utilized cervical cancer screening in Ethiopia. There were significant variations in the cervical cancer screening based on geographical regions and characteristics of women. Educational status, knowledge towards cervical cancer screening, perceived susceptibility and severity to cervical cancer and history of STIs significantly increased the uptake of screening practice. Therefore, women empowerment, improving knowledge towards cervical cancer screening, enhancing perceived susceptibility and severity to cancer and identifying previous history of women are essential strategies to improve cervical cancer screening practice.

Background

Despite a remarkable progress in the reduction of maternal mortality, cervical cancer is the second most commonly diagnosed cancer and the leading cause of cancer related death among African women [1]. There were approximately 236,000 deaths from cervical cancer worldwide and it was the most common cancer in east and middle Africa [2, 3]. About 90% of cases and 85% of these deaths have occurred in Low and Middle-Income Countries (LMICs); the highest has occurred in Sub-Saharan Africa (SSA) and approximately 311,000 women died from cervical cancer [2]. The incidence, the death rate and morbidities associated with cervical cancer significantly varies across the world; higher in the developing nations compared to the developed countries [4]. The high burden of cervical cancer is mainly due to the early onset of sexual intercourse, multiple sexual partners, human immunodeficiency virus (HIV) infection, history of sexually transmitted infections (STIs), human papilloma virus (HPV) infection, cigarette smoking, limited resources for early detection and poor HPV vaccination coverage [5, 6].

Almost all of the maternal deaths associated with cervical cancer could be prevented if early and effective interventions mechanisms to cervical cancer control were available to all women. In particular, a comprehensive approach such as prevention, early diagnosis, effective screening and treatment programmes of pre-cervical lesions are essential for prevention of cervical cancer [7]. Visual inspection with Acetic Acid (VIA) and Visual Inspection with Lugol’s Iodine (VILI) are commonly used in low-resource settings [6]. VIA combined with the immediate treatment of women who tested positive at the first visit was cost saving and was the next most effective strategy, with a 26% decrease in the incidence of CC, further reduce mortality due to CC. A large-cluster randomized trial from rural India showed that a single round of HPV screening could reduce the incidence and mortality from CC of approximately 50% [8].

The guidelines of the World Health Organization (WHO), the United States Preventive Services Task Force (USPSTF) and the American Cancer Society (ACS) recommends that all eligible women should have cervical cancer screening at least once every three years [9]. Ethiopia adopted WHO’s recommendation that woman aged 30 and above should begin screening for cervical cancer at least one to three years of age with a see- and -treat approach. However, sexually active and HIV-positive women (start screening at HIV diagnosis) are suggested to be screened every 3 years regardless of their age [10]. The prevalence of cervical cancer screening is much higher at the Western countries than SSA [11, 12]; 85.0% in the United States, 78.6% in the United Kingdom [13], and ranges from 2% in Ethiopia, 6% in Kenya [14], to 8% in Nigeria [15]. The lower rate of cervical cancer screening programme at LMICs may be related to the complexity of the screening process and the common inherent barriers in the setting such as poverty, limited access to information, lack of knowledge of cervical cancer, lack of healthcare infrastructure required, lack of trained practitioners and the absence of sustained prevention programmes [16].

The government of Ethiopia launched a cervical cancer screening service and has given more emphasis on programs focusing on the early detection of cervical cancer using advocacy efforts by different stakeholders such as academia, professionals, media and partners. However, the prevalence of cervical cancer remains a major problem, and it is one of the leading causes of morbidity and mortality among women in the country [17, 18]. Evidence show success of cervical screening initiatives depend on high participation of the target population, which in turn is determined by the women’s knowledge, perceptions, health orientations and other socio-cultural issues. It is also affected by factors including early marriage, early sexual practice, delivery of the first baby before the age of 20, multiple sexual partners and low socio economic status. Therefore, addressing the different barriers for poor utilization of cervical cancer screening is essential component of intervention. Although, there were previous pocket studies conducted on these issues in Ethiopia, the studies showed fragmented, inconsistent and inconclusive findings. Even the studies were fragmented in different specific population characteristics like among HIV positive women and reproductive age women. Therefore, this systematic review and meta-analysis aimed to estimate the pooled cervical cancer screening utilization and its predictors among all eligible women in Ethiopia. It also aimed to address the common barriers of cervical cancer screening.

Methods

Registration of systematic review, data sources and search strategies

The purpose of this systematic review and meta-analysis was to estimate the pooled utilization level of cervical cancer screening and its predictors among women of reproductive-aged in Ethiopia. The protocol has been registered with the International Prospective Register of Systematic Review (PROSPERO), the University of York Center for Reviews and Dissemination (https://www.crd.york.ac.uk/), registration number CRD42019119626. The findings of this review have been reported as recommended by the Preferred Reporting Items for Systematic Review and Meta-Analysis (PRISMA-P) 2009 statement checklist [19] (S1 Table). All published articles were searched from major international databases like PubMed, Cochrane Library, Psych Info, Scopus, CINAHL, Web of Science, Science Direct, Google Scholar and African Journals Online. Additionally, Google hand searches were used mainly for unpublished studies. A search was also made for the reference list of studies already identified in order to retrieve additional articles. The Population, Exposure, Comparison and Outcomes (PECO) search formula was used to retrieve articles.

All eligible women for cervical cancer screening Ethiopia were the population of interest for this study. The outcome of interest was the utilization of cervical cancer screening among women. The predictor variables of cervical cancer screening utilization included in this study were age of women, educational status, and occupational status, knowledge of cervical cancer screening, perceived susceptibility and severity to cervical cancer and history of sexually transmitted infections. Comparisons were defined for each predictor based on the reported reference group for each predictor in each respective variable.

For each of the selected components of PECO, electronic databases were searched using the keyword search and the medical subject heading [MeSH] words. The keywords include “utilization, uptake, cervical cancer, screening, and women of reproductive age as well as Ethiopia”. The search terms were combined by the Boolean operators "OR" and "AND. The specific searching detail in PubMed was putted in S1 Appendix.

Eligibility criteria and study selection

This review included studies that reported either the use of cervical cancer screening or the cervical cancer screening predictors in Ethiopia. All published and unpublished studies through April 7, 2020 and reported in English language were retrieved to assess eligibility for inclusion in this review. However, this review excluded studies that were case reports of populations, surveillance data (demographic health survey), and abstracts of conferences, articles without full access and the outcome of interest not reported. The article selection underwent several steps. Two reviewers (MD and TE) evaluated the retrieved articles for inclusion using their title, abstract and full text review. Any disagreement during the selection process between the reviewers was resolved by consensus. Full texts of selected articles were then evaluated using the prior eligibility. During the encounter of duplication; only the full-text article was retained.

Quality assessment and data collection

The Newcastle-Ottawa Scale (NOS) quality assessment tool was used to assess the quality of the included studies. The tool contains three components- selection of the study groups, comparability of the study groups, and ascertainment of exposure or outcome [20]. The main component of the tool was graded from five stars and mainly emphasized on the methodological quality of each primary study. The other component of the tool graded from two stars and mainly concerned with the comparability of each study. The last component of the tool was graded from three stars and was used to evaluate the results and statistical analysis of each original study. The NOS included three categorical criteria with a maximum score of 9 points. The quality of each study was assessed using the following score algorithms: ≥7 points were considered as “good”, 4 to 6 points were considered as “moderate”, and ≤ 3 point was considered as “poor” quality studies. In order to improve the validity of this systematic review result, only primary studies of fair to good quality have been included. The two reviewers (MD and TE) independently assessed articles for overall study quality and extracted data using a standardized data extraction format. The data extraction format included primary author, year of publication, region of the study, sample size, prevalence, and the selected predictors of cervical cancer screening utilization.

Publication bias and statistical analysis

The publication bias was assessed using the Egger’s [21] and Begg’s [22] tests with a p-value of less than 0.05. The I2 statistic was used to assess heterogeneity between studies and a p-value of less than 0.05 was used to detect heterogeneity. As a result of the presence of heterogeneity, a random-effects model was used as a method of analysis [23]. Data were extracted in Microsoft Excel and exported to Stata version 11 for analysis. Subgroup analysis was conducted by geographic region, population’s characteristics and design or type of study. Moreover, a meta-regression model based on sample size and year of publication was used to identify the sources of random variations in the included studies. The effect of selected determinant variables was analyzed using separate categories of meta-analysis [24]. The findings of the meta-analysis were presented using forest plots and Odds Ratio (OR) with its 95% Confidence intervals (CI). In addition, we conducted a sensitivity analysis to assess whether the pooled prevalence estimates were influenced by individual studies.

Results

Study identification and characteristics of included studies

This systematic review and meta-analysis included both published and unpublished studies on the use of cervical cancer screening in Ethiopia. A total of 850 articles were found from the review. Of these, 250 duplicated records were removed and 581 articles were excluded by screening using their titles and abstracts. Subsequently, a total of 38 full-text papers were assessed for eligibility on the basis of the inclusion and exclusion criteria. Thus, four studies were excluded due to lack of the outcome of interest [2530], three due to low quality [3133], five due to difference in the study population [3439] and only one study was excluded due to lack of access to the full text [40]. Finally, 25 studies were included in the final quantitative meta-analysis (Fig 1).

Fig 1. PRISMA flow diagram of cervical cancer screening utilization in Ethiopia.

Fig 1

All of the included studies were cross-sectional. From this, twelve studies were facility- based cross sectional studies (FBCS) and thirteen were community- based cross-sectional studies (CBCS). The review was conducted among 18,067 women to estimate the pooled prevalence of cervical cancer screening. Publication of articles was between 2016 and 2020. The largest sample size was 5,823 women in a national level study [41] and the smallest sample was 250 women from a study conducted in Oromia region [42]. All studies were conducted in five geographic regions of Ethiopia. Four studies (16%) were from Addis Ababa [4346], nine (36%) were from Amhara [4755], four (16%) were from Southern Nations, Nationalities and Peoples Representative (SNNPR) [5660], four (16%) were from Oromia [42, 6163], two (8%) were from Tigray [64, 65], and the remaining one study [41] was a national- level study. Twelve studies were conducted among eligible women with no specific characteristics of their HIV status [44, 47], five studies on HIV-positive women [43, 48, 53, 61, 63], four studies among healthcare workers [59, 63, 65, 66] and the remaining one study [51] was conducted among women who were commercial sex workers (Table 1).

Table 1. Characteristics of the included studies in the meta-analysis, Ethiopia.

Author Year Region Prevalence Design Sample Population
Shiferaw H et al. [43] 2018 AA 10.8 FBCS 598 HIV+
Getachew S et al. [44] 2018 AA 25 FBCS 520 All
Bante SA et al. [47] 2019 Amhara 20.9 CBCS 577 All
Aweke YH et al. [56] 2017 SNNPR 9.9 CBCS 583 all
Nega AD et al. [48] 2018 Amhara 10 FBCS 496 HIV+
Nigussie T et al. [49] 2019 Amhara 15.5 CBCS 737 all
Bayu H et al. [64] 2016 Tigray 19.8 CBCS 1186 all
Assefa AA et al. [57] 2019 SNNPR 40.1 FBCS 342 all
Gebreegziabher M et al. [65] 2016 Tigray 10.7 FBCS 225 all
Solomon K et al. [61] 2019 Oromia 25 FBCS 475 HIV+
Tefera and Mitiku [50] 2017 Amhara 11 CBCS 620 All
Muluneh BA et al. [51] 2019 Amhara 13.28 CBCS 467 CSWs
Seyoum T et al. [58] 2017 SNNPR 9.6 FBCS 281 all
Geremew AB et al. [26] 2018 Amhara no data 1152 98.7
Michael E et al. [42] Unpub Oromia 17.6 CBCS 250 all
Galibo T et al. [41] 2017 National 2.9 CBCS 5823 all
Kassa AS et al. [52] 2018 Amhara 7.3 CBCS 735 all
Erku DA et al. [53] 2017 Amhara 23.5 FBCS 302 HIV+
Woldetsadik AB [45] 2020 AA 12.2 FBCS 425 All
Aynalem BY et al. [54] 2020 Amhara 5.4 CBCS 822 All
Asres T [55] Unpub Amhara 18 FBCS 322 Healthcare
Dulla D et al. [59] 2017 SNNPR 11.4 FBCS 367 Healthcare
Heyi WD et al. [62] 2018 Oromia 5.8 CBCS 845 All
Berhanu T et al. [66] 2019 AA 9.3 CBCS 291 Healthcare
Tekle T et al. [60] 2020 SNNPR 22.9 CBCS 520 All
Ashagrie A [63] Unpub Oromia 16 FBCS 318 HIV+

AA: Addis Ababa; CSWs: Commercial sex workers.

CBCS: community based cross-sectional study; FBCS: facility based cross-sectional study.

Meta-analysis of cervical cancer screening utilization in Ethiopia

The highest cervical cancer screening utilization was observed in SNNPR, a study conducted at ART health facilities of Hawassa, 40% [57] and Wolayita hospitals, 22.9% [60]. Whereas, the lowest was 2.9% in a national level study [41] and 5.4% from a study conducted in Amhara region [54].

The meta-analysis of twenty-five studies showed that the pooled national level of cervical cancer screening utilization was 14.79% (95% CI: 11.75, 17.83). A random-effect model of analysis was used due to significant heterogeneity (I2 = 97.9%, p-value<0.05) (Fig 2). Publication bias was assessed using Eggers test and it was statistically significant, p-value less than 0.0001. To account for publication bias, the duval and trimmed full analysis was performed. The univariate meta-regression model was also used to identify possible sources of heterogeneity using different covariates like year of publication and sample size. However, none of these variables were found to be statistically significant, p-value > 0.05. Moreover, the sensitivity analysis using a random-effects model showed that no single study had unduly influenced the overall estimate of the use of cervical cancer screening among Ethiopian women (S1 Fig). The funnel plot also showed that there was symmetrical distribution (Fig 3).

Fig 2. The pooled utilization of cervical cancer screening among women in Ethiopia.

Fig 2

Fig 3. Funnel plot of the prevalence of cervical cancer screening utilization in Ethiopia.

Fig 3

Subgroup analysis

The subgroup analysis was conducted based on region of studies, the study design and women’s characteristics. Therefore, this random effect meta-analysis based on the geographic region revealed that the highest cervical cancer screening utilization was observed in the SNNPR, 18.59 (95% CI: 9.65, 27.53) followed by Oromia region, 16.00% (95% CI: 16.00% (95% CI: 6.31, 25.7) and lowest occurred in Amhara region, 13.62% (95% CI: 9.92, 17.32) (Table 2). In addition, the pooled subgroup analysis showed that cervical cancer screening was highest in studies that were institution- based cross-sectional studies, 17.54% (95% CI: 13.16, 21.93). The highest cervical cancer screening was among HIV- positive women, 20.71% (95% CI: 12.8, 28.63) and the lowest was among reproductive age women, 11.54% (95% CI: 8.00, 15.05) (Table 2).

Table 2. Sub-group analysis of cervical cancer screening utilization in Ethiopia: A meta-analysis.

Subgroup type Category No of studies Prevalence(95%CI) I2 P-value
Study design FBCS 12 17.54 (13.16,21.93) 94.6% <0.0001
CBCS 13 12.29 (8.70,15.88) 98.0% <0.0001
Region Addis Ababa 4 14.32 (8.09,20.56) 93.7% <0.0001
Amhara 9 13.62 (9.92,17.32) 94.5% <0.0001
SNNPR 5 18.59 (9.65,27.53) 97.3% <0.001
Oromia 4 16.00 (6.31, 25.7) 97.1% <0.001
Tigray 2 15.41 (6.5, 24.32) 93.3% <0.001
National level 1 2.9 (2.47,3.33) -
Women characteristics HIV positive 5 20.71 (12.8,28.63) 96.6% <0.0001
All women 12 11.54 (8.00, 15.05) 97.9% <0.0001
Healthcare workers 4 12.21 (8.71,15.71) 72.4% 0.012
Commercial sex worker 1 13.28 (10.2,16.36) - -

Predictors of cervical cancer screening utilization

Association of educational status and utilization of cervical cancer screening

In regard to the social inequities, the effects of three predictors on cervical cancer screening utilization were estimated. Thus, age of women and occupational status were not significantly associated with cervical cancer screening utilization (S2 and S3 Figs). While, women’s educational status was significantly associated with utilization of cervical cancer screening. Accordingly, the pooled random effect of eight studies [4850, 54, 57, 62, 63, 60] found that women who have no formal education were 66% (POR:0.33, 95% CI: 0.23,0.46) times less likely to utilize cervical cancer screening than those who attended any formal education (Fig 4).

Fig 4. Association of educational status with cervical cancer screening in Ethiopia.

Fig 4

Association of knowledge and perception of cancer and screening utilization

The meta-analysis of 14 studies revealed [42, 45, 4951, 53, 54, 57, 58, 60, 6265] that women’s knowledge of cervical cancer screening uptake was the commonest predictor of screening utilization. Women who had good knowledge of cervical cancer screening reuptake were 3.97 times (POR: 3.49, 95% CI: 1.67, 7.33) more likely to have cervical cancer screening than women who had poor knowledge (Fig 5).

Fig 5. Association of knowledge of the screening with cervical cancer screening utilization.

Fig 5

The pooled effect of six studies [33, 42, 45, 49, 53, 64] also revealed that the perceived susceptibility to cervical cancer was another major predictor of cervical cancer screening utilization in Ethiopia. Women who had perceived susceptibility to cervical cancer were 5.5 times more likely to reuptake cervical cancer screening than their counterparts (POR = 5.54, 95% CI: 4.28, 7.16) (Fig 6). Similarly, women who had perceived severity of cervical cancer were more likely to utilize cervical cancer screening (POR = 6.57, 95% CI: 3.99, 10.82) (Fig 7).

Fig 6. Association of perceived susceptibility to cervical cancer with cervical cancer screening.

Fig 6

Fig 7. Association of perceived severity of cancer and cervical cancer screening utilization.

Fig 7

Association of history of sexual transmitted infection and cervical cancer screening uptake

Based on the pooled analysis of four studies [47, 51, 54, 64], women who had history of sexual transmitted infection were more likely to utilize cervical cancer screening (POR: 3.32, 95% CI: 1.07, 10.34) (Fig 8).

Fig 8. Association of history of sexual transmitted infection with cervical cancer screening utilization.

Fig 8

Barriers of cervical cancer screening uptake

The pooled analysis also revealed that the most common reasons that hinder the use of cervical cancer screening were associated with women considered to be healthy, 48.97% (95% CI: 38.3, 59.59) and lack of information on screening, 34.34% (95% CI: (17.93, 50.75) (Table 3).

Table 3. Barriers of the cervical cancer screening utilization in Ethiopia: A meta-analysis.

Barriers Studies Prevalence [95% CI] I2 P-value
Consider as healthy 11 48.97% [38.3, 59.59] 98.7% <0.0001
Fear of screening 11 15.25% [6.77,23.73] 99.4% <0.0001
Lack of information 7 34.34% [17.93, 50.75] 99.4% <0.0001
Embarrassment 8 11.16% [5.76,16.56] 99.3 <0.0001
Long waiting time 7 21.58% [6.87,36.28] 99.6 <0.0001
Don’t know place 5 10.06% [3.53,16.59] 97.0 <0.0001

Discussions

The uptake of cervical cancer screening services in Ethiopia is not well established. Despite, WHO recommends cervical cancer screening tests to be included as part of well-planned and implemented programs in every country’s health care policy. This systematic review and meta-analysis was conducted to estimate the pooled level of cervical cancer screening and its associated factors in Ethiopia. Accordingly, the pooled national level of cervical cancer screening utilization was 14.79 (95% CI: 11.75, 17.83). This was lower than 85% from a study conducted in United States [13], 21.4% in China national population based survey [67], 19.4% in Kenya [68], 19% - 63% from studies conducted in 54 countries [69], 48.9% in Malaysia [70], and also lower than 67% from a national-based study conducted among Vietnamese women [71]. The difference could be explained by the variation in the population characteristics, study settings and quality of health care services and screening programs. Besides, this could be explained by socio-economic inequalities, higher birth order and poor access to reproductive health care service utilization in Ethiopia could lower the cervical screening utilization. Previous report also showed that women with high birth order and poor women are less likely to receive cervical screening service [69]. In Ethiopia, a small proportion of women are in contact with obstetric or gynecological health services and that the health system may not have the capacity to provide effective screening to a larger number of women. Therefore, intervention programs to improve the quality of cervical cancer screening clinics are essential.

The findings of this meta-analysis also showed that the highest prevalence of cervical cancer screening occurred in the SNNPR followed by Oromia region and the lowest was in Amhara region. Regional variation in the burden of cervical cancer screening in Ethiopia might be explained by the difference in maternal health care service utilization that could be explained by in the difference in spousal support, cultural and linguistic diversity across the regions and societal stigmatization. Additionally, health service-related reason like cost of access to services, proximity to facilities, navigation of the facilities, waiting time and attitude of the health care staff may be the reasons for the regional difference and lower use of cervical cancer screening in the country.

The highest screening utilization in SNNPR and Oromia may be due to the nature of included studies in the respective regions. For example, 60% of the studies from SNNP region were institutional based cross-sectional studies and 50% of the included studies from Oromia region were conducted among HIV-positive women. Such differences may have contributed to the higher prevalence of cervical cancer screening in SNNPR and Oromia regions. Furthermore, socio-demographic characteristics and lifestyle activities could also be mentioned as reasons for the variation in screening across the different regions in the country. The pooled cervical cancer screening was also highest among HIV- positive women (20.71%). This may be due to the fact that these women may be given information about the disease during their follow-up visit to antiretroviral therapy [57], which may improve their knowledge about cervical cancer, and therefore, increase service utilization.

This systematic review and meta-analysis found that educational status of women was one of the significant predictors of cervical cancer screening utilization. No formal education reduces the cervical cancer screening uptake by 67%, and this finding was supported by a study done in China [67] and a meta-analysis conducted in developed countries [72]. The possible justification for this might be due to the fact that women who have no formal education are less likely to have gynecological examinations and maternal health service utilization. As the result, they are likely to have limited exposure to visit health institution for antenatal care, health facility delivery and post-natal care.

Uneducated women also have lower possibilities to read and fully understand the information and instructions provided by healthcare providers, and therefore, reduce the rate of cervical cancer screening. Cervical cancer educational interventions and provider recommendation for screening increases the rates of cervical cancer screening [73]. Therefore, more integrated interventions to improve women’s empowerment should be done at national level to improve the rate of cervical cancer screening utilization, and therefore, reduce cervical cancer related morbidity and mortality.

This study also found that women’s knowledge of screening for cervical cancer was a significant predictor of cervical cancer screening service uptake. The finding was supported by studies done in Uganda [74], Malaysia [70], a review done in LMICs [75] and among Arab women [76]. This could be explained by the fact that those women who had good knowledge for cervical cancer screening are more likely to give priority to the issue and improves their decisions on health- seeking screening behavior. Accordingly, findings in Ethiopia, Malawi, Tanzania and Thailand [64, 7779] have shown that a good flow of information and awareness creation campaigns about cervical cancer increase the uptake of cervical cancer screening.

This meta-analysis also showed that women with a history of STI were more likely to use screening for cervical cancer compared to those with no history of STI. This result was supported by the findings of other studies [64, 80]. This may be explained by the fact that women who have STIs and history of STI will have an increased chance of visiting health institutions for treatment and medical check-ups, and therefore, more likely to get the screening information from the healthcare provider.

This systematic review and meta-analysis also found that perceived susceptibility and severity were also predictors of the use of cervical cancer screening as supported by Wanyenze et al. [74]. This may be those who perceive their susceptibility or severity of cancer may be aware of the severity of the cancer and higher level of education about the disease as a result of the increased screening rate. As a result, those women who have an increased perception of susceptibility or severity of the disease may have higher education that has increased adherence to the cervical cancer screening [68]. These may include those women who are perceived to be more acutely aware of their risk, more interested and knowledgeable about health and behavioral issues, and better access to health information and resources [81]. This finding was also supported by recent studies done in Ghana [82] and Kenya [83] which found that women who perceived the severity of disease were more likely to accept screening due to increased perception of the benefits and barriers to cervical cancer, which increases their cancer screening.

Furthermore, the results of this systematic review and meta-analysis found that the common barriers to the utilization of cervical cancer screening were considered healthy and lack of information by women. This is supported by additional studies [47, 49, 51, 56, 64]. This may be due to the fact that those who consider their status to be healthy and who have poor knowledge are less likely to perceive the benefits of screening and the severity of cervical cancer., Therefore, multi-disciplinary interventions across the life course, community education and social mobilization on cervical cancer risk and its screening should be improved and emphasized to increase the cervical cancer screening utilization.

This review’s strengths include the very extensive systematic search conducted and the inclusion of articles identified without specifying the population characteristics and period of publications. Our review adopted the international standard definitions to measure the quality of studies. This meta-analysis has its strengths because it has used a pre-specified protocol for search strategy and data abstraction and used internationally accepted tools for a critical appraisal system for the quality assessment of individual studies.

However, the results of this review should be interpreted with some limitation. The high heterogeneity in the characteristics of the studies might lead to insufficient statistical power to detect significant association. However, a meta-regression analysis revealed that there was no variation due to sample size and publication year. This meta-analysis was also unable to assess the type of screening, and therefore, an area of research for future studies. Additionally, the studies included in this review were from only five regions out of the nine regional states and the two administrative cities that might reduce its representativeness for the country. Some studies have small sample size, affect the estimation.

Conclusions

This meta-analysis found that cervical cancer screening rate was lower than the WHO recommendations. Only one in every seven eligible women were screened in Ethiopia, and there was a significant variation in the screening level based on geographical regions and characteristics of women. Women’s educational status, knowledge towards cervical cancer screening, perceived susceptibility and severity to cervical cancer and history of sexual transmitted infections significantly increased uptake of the screening practice. Therefore, women empowerment, improving knowledge towards cervical cancer screening, enhancing perceived susceptibility and severity to cervical cancer and identifying previous history of women are an essential strategy to increase utilization of cancer screening. Moreover, adoption of the better strategies and addressing the barriers of cervical cancer screening uptake mainly improving of the provision of adequate information on cervical cancer screening has a paramount importance to improve cervical cancer screening among reproductive age women.

Supporting information

S1 Fig. Sensitivity analysis of cervical cancer screening utilization.

(TIF)

S2 Fig. Association of women’s age and cervical cancer screening utilization.

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S3 Fig. Association of occupational status and cervical cancer screening utilization.

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S1 Table. PRISMA check list.

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S2 Table. Included studies for the barriers of cervical cancer screening.

(DOCX)

S3 Table. Quality assessment of included studies.

(DOCX)

S1 Appendix. Specific searching on PubMed database.

(DOCX)

Abbreviations

CBCS

Community Based Cross-sectional Studies

FBCS

Facility- Based Cross-sectional Studies

HIV

Human Immunodeficiency Virus

HPV

Human Papilloma Virus

LMICs

Low and Middle-Income Countries

POR

Pooled Odds Ratio

SNNPR

Southern Nations, Nationalities and Peoples Representative

SSA

Sub Saharan Africa

STI

Sexually Transmitted Infection, WHO: World Health Organization

Data Availability

All relevant data are within the manuscript and its Supporting Information files.

Funding Statement

The author(s) received no specific funding for this work.

References

  • 1.WHO U, PATH. cryosurgical equipment for the treatment of precancerous cervical lesions and prevention of cervical cancer. 2012.
  • 2.WHO/NMH/NMA. UN Joint Global Programme on Cervical Cancer Prevention and Control. The United Nations Global Cervical Cancer Programme 2016.
  • 3.Bruni L, Albero G, Serrano B, Mena M, Gómez D, Muñoz J, et al. Human Papillomavirus and Related Diseases in Ethiopia. 2017. [Google Scholar]
  • 4.Fitzmaurice C, Dicker D, Pain A, Hamavid H, Moradi-Lakeh M, MacIntyre MF, et al. The Global Burden of Cancer 2013. JAMA oncology. 2015;1(4):505–27. Epub 2015/07/17. doi: 10.1001/jamaoncol.2015.0735 ; PubMed Central PMCID: PMC4500822. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Hendry M, Lewis R, Clements A, Damery S, Clare W. "HPV? Never heard of it!": A systematic review of girls’ and parents’ information needs, views and preferences about human papillomavirus vaccination 2013. doi: 10.1016/j.vaccine.2013.08.091 [DOI] [PubMed] [Google Scholar]
  • 6.Health WHOR, Diseases WHOC, Promotion H. Comprehensive cervical cancer control: a guide to essential practice: World Health Organization; 2006. [PubMed]
  • 7.Denny L, Quinn M, Sankaranarayanan R. Screening for cervical cancer in developing countries. Vaccine. 2006;24:S71–S7. doi: 10.1016/j.vaccine.2006.05.121 [DOI] [PubMed] [Google Scholar]
  • 8.Sankaranarayanan R et al. HPV screening for cervical cancer in rural India. N Engl J Med. 2009;360: 1385–1394. doi: 10.1056/NEJMoa0808516 [DOI] [PubMed] [Google Scholar]
  • 9.Moyer VA. Screening for cervical cancer: US Preventive Services Task Force recommendation statement. Annals of internal medicine. 2012;156(12):880–91. doi: 10.7326/0003-4819-156-12-201206190-00424 [DOI] [PubMed] [Google Scholar]
  • 10.FMOH. National cancer control plan of Ethiopia. 2015.
  • 11.Campos NG, Castle PE, Wright TC Jr, Kim JJ. Cervical cancer screening in low‐resource settings: A cost‐effectiveness framework for valuing tradeoffs between test performance and program coverage. International journal of cancer. 2015;137(9):2208–19. doi: 10.1002/ijc.29594 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Pimple S, Mishra G, Shastri S. Global strategies for cervical cancer prevention. Current Opinion in Obstetrics and Gynecology. 2016;28(1):4–10. doi: 10.1097/GCO.0000000000000241 [DOI] [PubMed] [Google Scholar]
  • 13.(OECD. StatExtracts; 2013. http://stats.oecd.org/Index.aspx?DataSetCode=HEALTH_PROC. Cited May 6 2020.).
  • 14.Sudenga SL, Rositch AF, Otieno WA, Smith JS. Knowledge, attitudes, practices, and perceived risk of cervical cancer among Kenyan women: brief report. International Journal of Gynecologic Cancer. 2013;23(5):895–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Idowu A, Olowookere SA, Fagbemi AT, Ogunlaja OA. Determinants of cervical cancer screening uptake among women in Ilorin, North Central Nigeria: a community-based study. Journal of cancer epidemiology. 2016;2016. doi: 10.1155/2016/6469240 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Ngugi CW BH, Muigai AW, Wanzala P, Mbithi JN. Factors affecting uptake of cervical cancer early detection measures among women in Thika, Kenya. Health Care Women Int. 2012;33(595–613 doi: 10.1080/07399332.2011.646367 ]. [DOI] [PubMed] [Google Scholar]
  • 17.De Sanjosé S, Serrano B, Castellsagué X, Brotons M, Muñoz J, Bruni L, et al. Human papillomavirus (HPV) and related cancers in the Global Alliance for Vaccines and Immunization (GAVI) countries. A WHO/ICO HPV Information Centre Report. Vaccine. 2012;30(Suppl 4):D1–83. [DOI] [PubMed] [Google Scholar]
  • 18.Chidyaonga-Maseko F, Chirwa ML, Muula AS. Underutilization of cervical cancer prevention services in low and middle income countries: a review of contributing factors. Pan African medical journal. 2015;21(1). doi: 10.11604/pamj.2015.21.231.6350 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Moher D et al. Preferred reporting items for systematic review and meta-analysis protocols (PRISMA-P) 2015 statement. Systematic reviews. 2015;4(1). doi: 10.1186/2046-4053-4-1 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Singer M, Deutschman CS, Seymour CW, Shankar-Hari M, Annane D, Bauer M, et al. The third international consensus definitions for sepsis and septic shock (Sepsis-3). Jama. 2016;315(8):801–10. doi: 10.1001/jama.2016.0287 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Egger M SG, Schneider M, Minder C. Bias in meta-analysis detected by a simple, graphical test. BMJ. 1997;315(7109):629–34. doi: 10.1136/bmj.315.7109.629 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Begg CB MM. Operating characteristics of a rank correlation testfor publication bias. Biometrics. 1994;50(4):1088–101. [PubMed] [Google Scholar]
  • 23.Higgins JP TS, Deeks JJ, Altman DG. Measuring inconsistency in meta-analyses. BMJ. 2003;327(7414):557. doi: 10.1136/bmj.327.7414.557 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Deeks JJ, Higgins JP, Altman DG. Analysing data and undertaking meta‐analyses. Cochrane handbook for systematic reviews of interventions. 2008:241–84. [Google Scholar]
  • 25.Teame H, Gebremariam L, Kahsay T, Berhe K, Gebreheat G. Factors affecting utilization of cervical cancer screening services among women attending public hospitals in Tigray region, Ethiopia, 2018; Case control study. 2019;14(3):e0213546. doi: 10.1371/journal.pone.0213546 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Geremew AB, Gelagay AA, Azale T. Comprehensive knowledge on cervical cancer, attitude towards its screening and associated factors among women aged 30–49 years in Finote Selam town, northwest Ethiopia. Reproductive health. 2018;15(1):29. Epub 2018/02/16. doi: 10.1186/s12978-018-0471-1 ; PubMed Central PMCID: PMC5813403. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Petros H, Ayele AA. Cervical Cancer Screening and Treatment Services in South West Shoa Zone of Oromia Region. Ethiopian Journal of Reproductive Health. 2018;10(1):7–. [Google Scholar]
  • 28.Gebrie MH, Belete MA, Lemlem SB, Woreta HK. Knowledge, preventive practice and associated factors of female nurses’ towards cervical cancer in the selected government hospitals in Addis Ababa, Ethiopia. J Diabetes Metab. 2015;6(7):569. [Google Scholar]
  • 29.Tarekegn AA, Mengistu MY, Mirach TH. Health professionals’ willingness to pay and associated factors for cervical cancer screening program at College of Medicine and Health Sciences, University of Gondar, Northwest Ethiopia. PloS one. 2019;14(4). doi: 10.1371/journal.pone.0215904 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Bejiga B. Acceptability of cervical cancer screening using See and Treat (SAT) approachand determinant factors among women of reproductive age in health centers in Addis Ababa, Ethiopia 2017. [Google Scholar]
  • 31.Boka A, Nigatu D. Cervical cancer screening and associated factors among women attending gynecology out-patient department and maternal and child health atmettu karlreferralhospital, South West, Ethiopia, 2019. International Journal of Current Research in Life Sciences. 8(01):2934–44. [Google Scholar]
  • 32.Deribe L. cervical cancer screening service utilization and associated factors among HIV positive and women with unknown hiv status in alamata generalized hospital, Tigray, Ethiopia 2018: comparative cross sectional study: Addis Ababa Universty; 2018. [Google Scholar]
  • 33.Gebru Z, Gerbaba M, Dirar A. Utilization of Cervical Carcinoma Screening Service and Associated Factors among Currently Married Women in Arba Minch Town, Southern Ethiopia Journal of Womens Health Care. 2016;5(1). [Google Scholar]
  • 34.Tilahun T, Tulu T, Dechasa W. Knowledge, attitude and practice of cervical cancer screening and associated factors amongst female students at Wollega University, western Ethiopia. BMC research notes. 2019;12(1):518. doi: 10.1186/s13104-019-4564-x [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Mulatu K, Motma A, Seid M, Tadesse M. Assessment of knowledge, attitude and practice on cervical cancer screening among female students of Mizan Tepi University, Ethiopia, 2016. Cancer Biol Ther Oncol. 2017;1(1):1–5. [Google Scholar]
  • 36.Mekuria R. cervical cancer screening behavior and associated factors among women attending gynecology out-patient department and maternal and child health Atdilla university referral hospital, Ethiopia, 2018: Addis Ababa University; 2018. [Google Scholar]
  • 37.Tsegaye S. Knowledge, Attitude, Practice of Cervical Cancer Screening and Its Associated Factors Among Female Students in Hawassa Universitycollege of Medicine and Health Science Hawassa: Addis Ababa University; 2015. [Google Scholar]
  • 38.Abdulkadir IR. Level of knowledge toward human papillomavirus/cervical cancer & practice of Papanicolaou test screening among female Addis Ababa university students in Ethiopia: California State University, Northridge; 2013. [Google Scholar]
  • 39.Gebregziabher D, Berhanie E, Birhanu T, Tesfamariam K. Correlates of cervical cancer screening uptake among female under graduate students of Aksum University, College of Health Sciences, Tigray, Ethiopia. BMC research notes. 2019;12(1):520. Epub 2019/08/21. doi: 10.1186/s13104-019-4570-z ; PubMed Central PMCID: PMC6701026. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Mersha A. Comprehensive knowledge and uptake of cervical cancer screening is low among women living with HIV/AIDS in Northwest Ethiopia. Value in Health. 2017;20(9):A493. doi: 10.1186/s40661-017-0057-6 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.Gelibo T, Roets L, Getachew T, Bekele A. Coverage and factors associated with cervical Cancer screening: results from a population-based WHO steps Study in Ethiopia. Adv Oncol Res Treat. 2017;1(115):2. [Google Scholar]
  • 42.Michael E. Cervical cancer screening utilization and its associated factors among women aged 30 years and above in Woliso town, South West Showa Zone, Oromia region, Ethiopia: Addis Ababa Universty; 2018. [Google Scholar]
  • 43.Shiferaw S, Addissie A. Knowledge about cervical cancer and barriers toward cervical cancer screening among HIV-positive women attending public health centers in Addis Ababa city, Ethiopia. 2018;7(3):903–12. doi: 10.1002/cam4.1334 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.Getachew S, Getachew E. Cervical cancer screening knowledge and barriers among women in Addis Ababa, Ethiopia. 2019;14(5):e0216522. doi: 10.1371/journal.pone.0216522 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45.Woldetsadik AB, Amhare AF, Bitew ST, Pei L, Lei J, Han J. Socio-demographic characteristics and associated factors influencing cervical cancer screening among women attending in St. Paul’s Teaching and Referral Hospital, Ethiopia. BMC women’s health. 2020;20(1):70. Epub 2020/04/08. doi: 10.1186/s12905-020-00927-5 ; PubMed Central PMCID: PMC7137499. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 46.Birhanu Z, Abdissa A, Belachew T, Deribew A, Segni H, Tsu V, et al. Health seeking behavior for cervical cancer in Ethiopia: a qualitative study. International journal for equity in health. 2012;11:83. Epub 2013/01/01. doi: 10.1186/1475-9276-11-83 ; PubMed Central PMCID: PMC3544623. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 47.Bante SA, Getie SA, Getu AA, Mulatu K, Fenta SL. Uptake of pre-cervical cancer screening and associated factors among reproductive age women in Debre Markos town, Northwest Ethiopia, 2017. BMC public health. 2019;19(1):1102. Epub 2019/08/16. doi: 10.1186/s12889-019-7398-5 ; PubMed Central PMCID: PMC6692942. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 48.Nega AD, Woldetsadik MA, Gelagay AA. Low uptake of cervical cancer screening among HIV positive women in Gondar University referral hospital, Northwest Ethiopia: cross-sectional study design. 2018;18(1):87. Epub 2018/07/10. doi: 10.1186/s12905-018-0579-z . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 49.Nigussie T, Admassu B, Nigussie A. Cervical cancer screening service utilization and associated factors among age-eligible women in Jimma town using health belief model, South West Ethiopia. BMC women’s health. 2019;19(1):127. Epub 2019/10/30. doi: 10.1186/s12905-019-0826-y ; PubMed Central PMCID: PMC6819648. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 50.Tefera F, Mitiku I. Uptake of Cervical Cancer Screening and Associated Factors Among 15-49-Year-Old Women in Dessie Town, Northeast Ethiopia. Journal of cancer education: the official journal of the American Association for Cancer Education. 2017;32(4):901–7. Epub 2016/04/15. doi: 10.1007/s13187-016-1021-6 . [DOI] [PubMed] [Google Scholar]
  • 51.Muluneh BA, Atnafu DD, Wassie B. Predictors of cervical cancer screening service utilization among commercial sex workers in Northwest Ethiopia: a case-control study. BMC women’s health. 2019;19(1):162. doi: 10.1186/s12905-019-0862-7 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 52.Kasa AS, Tesfaye TD, Temesgen WA. Knowledge, attitude and practice towards cervical cancer among women in Finote Selam city administration, West Gojjam Zone, Amhara Region, North West Ethiopia, 2017. African health sciences. 2018;18(3):623–36. doi: 10.4314/ahs.v18i3.20 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 53.Erku DA, Netere AK, Mersha AG, Abebe SA, Mekuria AB, Belachew SA. Comprehensive knowledge and uptake of cervical cancer screening is low among women living with HIV/AIDS in Northwest Ethiopia. Gynecologic oncology research and practice. 2017;4(1):20. doi: 10.1186/s40661-017-0057-6 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 54.Aynalem BY, Anteneh KT, Enyew MM. Utilization of cervical cancer screening and associated factors among women in Debremarkos town, Amhara region, Northwest Ethiopia: Community based cross-sectional study. PloS one. 2020;15(4):e0231307. Epub 2020/04/08. doi: 10.1371/journal.pone.0231307 ; PubMed Central PMCID: PMC7138328. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 55.ASERES T. KNOWLEDGE, PRACTICE AND ASSOCIATED FACTORS OF CERVICAL CANCER SCREENING AMONG WOMEN HEALTH WORKERS IN GONDAR UNIVERSITY TEACHING AND REFERRAL HOSPITAL, GONDAR, ETHIOPIA, 2016 2017.
  • 56.Aweke YH, Ayanto SY, Ersado TL. Knowledge, attitude and practice for cervical cancer prevention and control among women of childbearing age in Hossana Town, Hadiya zone, Southern Ethiopia: Community-based cross-sectional study. PloS one. 2017;12(7):e0181415. Epub 2017/07/26. doi: 10.1371/journal.pone.0181415 ; PubMed Central PMCID: PMC5526548. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 57.Assefa AA, Astawesegn FH, Eshetu B. Cervical cancer screening service utilization and associated factors among HIV positive women attending adult ART clinic in public health facilities, Hawassa town, Ethiopia: a cross-sectional study. BMC health services research. 2019;19(1):847. Epub 2019/11/21. doi: 10.1186/s12913-019-4718-5 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 58.Seyoum T, Yesuf A, Kejela G, Gebremeskel F. Utilization of cervical cancer screening and associated factors among female health Workers in Governmental Health Institution of Arba Minch town and Zuria District, Gamo Gofa zone, Arba Minch, Ethiopia, 2016. Arch Cancer Res. 2017;5(4):165. [Google Scholar]
  • 59.Dulla D, Daka D, Wakgari N. Knowledge about cervical cancer screening and its practice among female health care workers in southern Ethiopia: a cross-sectional study. International journal of women’s health. 2017;9:365. doi: 10.2147/IJWH.S132202 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 60.Tekle T, Wolka E, Nega B, Kumma WP, Koyira MM. Knowledge, Attitude and Practice Towards Cervical Cancer Screening Among Women and Associated Factors in Hospitals of Wolaita Zone, Southern Ethiopia. Cancer management and research. 2020;12:993. doi: 10.2147/CMAR.S240364 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 61.Solomon K, Tamire M, Kaba M. Predictors of cervical cancer screening practice among HIV positive women attending adult anti-retroviral treatment clinics in Bishoftu town, Ethiopia: the application of a health belief model. BMC cancer. 2019;19(1):989. Epub 2019/10/28. doi: 10.1186/s12885-019-6171-6 ; PubMed Central PMCID: PMC6813043. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 62.Heyi WD, Bekabil TT, Ebo GG. KNOWLEDGE, ATTITUDE AND PRACTICE OF CERVICAL CANCER SCREENING AMONG WOMEN AGED 15–49 YEARS IN BISHOFTU TOWN, EAST SHEWA ZONE, OROMIA REGION, ETHIOPIA, 2016. Ethiopian Journal of Reproductive Health. 2018;10(2):10–. [Google Scholar]
  • 63.Ashagrie A. Knowledge and screening practice on cervical cancer and associated factors among HIV positive women in Adama, Ethiopia: Addis Ababa Universty; 2017. doi: 10.1186/s13104-017-2887-z [DOI] [Google Scholar]
  • 64.Bayu H, Berhe Y, Mulat A, Alemu A. Cervical Cancer Screening Service Uptake and Associated Factors among Age Eligible Women in Mekelle Zone, Northern Ethiopia, 2015: A Community Based Study Using Health Belief Model. PloS one. 2016;11(3):e0149908. Epub 2016/03/11. doi: 10.1371/journal.pone.0149908 ; PubMed Central PMCID: PMC4786115. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 65.Gebreegziabher M, Asefa NG, Berhe S. Factors Affecting the Practices of Cervical Cancer Screening among Female Nurses at Public Health Institutions in Mekelle Town, Northern Ethiopia, 2014: A Cross-Sectional Study. Journal of Cancer Research. 2016;2016. [Google Scholar]
  • 66.Berhanu T, Mamo E, Tewolde T, Beshir M. Knowledge of Cervical Cancer and Its Screening Practice among Health Extension Workers in Addis Ababa, Ethiopia. Primary Health Care: Open Access. 2019;9(1):1–5. [Google Scholar]
  • 67.Bao H, Zhang L, Wang L, Zhang M, Zhao Z, Fang L, et al. Significant variations in the cervical cancer screening rate in China by individual‐level and geographical measures of socioeconomic status: a multilevel model analysis of a nationally representative survey dataset. Cancer medicine. 2018;7(5):2089–100. doi: 10.1002/cam4.1321 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 68.Tiruneh FN, Chuang K-Y, Ntenda PAM, Chuang Y-C. Individual-level and community-level determinants of cervical cancer screening among Kenyan women: a multilevel analysis of a Nationwide survey. BMC women’s health. 2017;17(1):109. doi: 10.1186/s12905-017-0469-9 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 69.Gakidou E, Nordhagen S, Obermeyer Z. Coverage of cervical cancer screening in 57 countries: low average levels and large inequalities. PLoS medicine. 2008;5(6). doi: 10.1371/journal.pmed.0050132 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 70.Gan DEH, Dahlui M. Cervical screening uptake and its predictors among rural women in Malaysia. Singapore medical journal. 2013;54(3):163–8. doi: 10.11622/smedj.2013047 [DOI] [PubMed] [Google Scholar]
  • 71.Ho V, Yamal JM, Atkinson EN, Basen-Engquist K, Tortolero-Luna G, Follen M. Predictors of Breast and Cervical Screening in Vietnamese Women in Harris County, Houston, Texas. Cancer Nursing. 2005;28(2):119–29. 00002820-200503000-00005. doi: 10.1097/00002820-200503000-00005 [DOI] [PubMed] [Google Scholar]
  • 72.Damiani G, Basso D, Acampora A, Bianchi CB, Silvestrini G, Frisicale EM, et al. The impact of level of education on adherence to breast and cervical cancer screening: evidence from a systematic review and meta-analysis. Preventive medicine. 2015;81:281–9. doi: 10.1016/j.ypmed.2015.09.011 [DOI] [PubMed] [Google Scholar]
  • 73.Musa J, Achenbach CJ, O’Dwyer LC, Evans CT, McHugh M, Hou L, et al. Effect of cervical cancer education and provider recommendation for screening on screening rates: A systematic review and meta-analysis. PloS one. 2017;12(9). doi: 10.1371/journal.pone.0183924 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 74.Wanyenze RK, Bwanika JB, Beyeza-Kashesya J, Mugerwa S, Arinaitwe J, Matovu JK, et al. Uptake and correlates of cervical cancer screening among HIV-infected women attending HIV care in Uganda. Global health action. 2017;10(1):1380361. doi: 10.1080/16549716.2017.1380361 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 75.Devarapalli P, Labani S, Nagarjuna N, Panchal P, Asthana S. Barriers affecting uptake of cervical cancer screening in low and middle income countries: A systematic review. Indian journal of cancer. 2018;55(4):318. doi: 10.4103/ijc.IJC_253_18 [DOI] [PubMed] [Google Scholar]
  • 76.Abboud S, De Penning E, Brawner BM, Menon U, Glanz K, Sommers MS, editors. Cervical cancer screening among Arab women in the United States: an integrative review. Oncology nursing forum; 2017: NIH Public Access. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 77.Lyimo FS, Beran TN. Demographic, knowledge, attitudinal, and accessibility factors associated with uptake of cervical cancer screening among women in a rural district of Tanzania: three public policy implications. BMC public health. 2012;12(1):22. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 78.Chosamata MS, Hong SA, Tiraphat S. Determinants of cervical cancer screening utilization among women aged 30–45 years in Blantyre district, Malawi. 2015. [Google Scholar]
  • 79.Visanuyothin S, Chompikul J, Mongkolchati A. Determinants of cervical cancer screening adherence in urban areas of Nakhon Ratchasima Province, Thailand. Journal of infection and public health. 2015;8(6):543–52. doi: 10.1016/j.jiph.2015.04.018 . [DOI] [PubMed] [Google Scholar]
  • 80.Teame H, Addissie A, Ayele W, Hirpa S, Gebremariam A, Gebreheat G, et al. Factors associated with cervical precancerous lesions among women screened for cervical cancer in Addis Ababa, Ethiopia: A case control study. PLOS ONE. 2018;13(1):e0191506. doi: 10.1371/journal.pone.0191506 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 81.Ross CE, Wu C-l. The links between education and health. American sociological review. 1995:719–45.
  • 82.Ebu NI, Ogah JK. Predictors of cervical cancer screening intention of HIV-positive women in the central region of Ghana. BMC women’s health. 2018;18(1):43. doi: 10.1186/s12905-018-0534-z [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 83.KAMBAGA EM. Determinants of provider-initiated HIV testing and counselling uptake in Jaramogi Oginga Odinga teaching and referral hospital, Kisumu, Kenya: Maseno University; 2017. [Google Scholar]

Decision Letter 0

Nicola Stead

16 Dec 2020

PONE-D-20-22948

Cervical cancer screening utilization and predictors among reproductive-age women in Ethiopia: a systematic review and meta-analysis

PLOS ONE

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Reviewer #2: Yes

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3. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

Reviewer #2: Yes

**********

4. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: Yes

Reviewer #2: Yes

**********

5. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: General comment: Very good and useful review that could provide evidence on barrier to CC screening in Ethiopia

Specific comments

IN the abstract as well as under background section, it is stated “Despite a remarkable progress in the reduction of maternal mortality, cervical cancer is the 73 second most commonly diagnosed cancer and the leading cause of cancer related death among 74 African women”. I agree with the reduction of MM. However, in view of the fact that CC is a major public health challenge and with its continued pressure, is it not naïve to argue about reduction of maternal mortality without showing how CC screening has contributed to that or contrary to this maintained MM in consequence higher.

Mention is made “The incidence, death rate and morbidities associated with cervical cancer is 79 significantly varies across the world; higher in the developing nations than compared to the 80 developed countries”(4), while again it is stated “The prevalence of cervical cancer screening is much higher at the Western countries than SSA” (11, 12); The two statements looks contradictory

Method

There is no clarity on whether this review is ‘systematic’ or ‘met-analysis’ or ‘both’. If it is both, it is imperative to clarify which part of it is systematic and meta-analysis OR clarify why both were considered.

From the statement “All published and unpublished studies through April 7, 2020” there were quite few concerns. Firstly what was the lower time frame. Could it be any document from time immemorial to April 7, 2020? Secondly, how were the unpublished reports captured? Were there any criterion set to identify those?

While WHO’s recommended age of CC screening is 30-50, it is not clear why in this study age 18-49 years was chosen? Is it not contradictory?

Results

The studies were drawn from five geographic regions: Addis Ababa, Amhara, Southern Nations, Nationalities and Peoples, Oromia and Tigray with only one from the national- level study. Couple of concern here. Firstly, how was the 18,067 women considered to estimate the pooled… proportionated in light of population size. Given the fact that studies are not proportional to the population of the regions, it would be difficult to reach conclusion as desired – this is about comparability of results. Secondly, I am wondering if this study could mirror realities for the country at large. Perhaps clarifying those and stating limitations may help.

I am not convinced that what are stated as ‘most common reasons that hinder the use of cervical cancer screening’ in the result section and conclusion section are aligned. This needs to be checked against the finding and corrected

Discussion

The fact that it was not clear on what of this review is meta and systematic, the discussion suffers much missing what is being discussed. Perhaps with clarification on how the two contributed to this review may

Reviewer #2: Generally a good paper, congratulations, however, the work needs some grammatic revision for clarity. I have listed some below but kindly revise the entire paper checking for grammatic and punctuation errors.

Line 74- Update the reference and use more recent data than 2013

Line 77- Be consistent in presenting figures i.e 311000 should have a comma as with other figures

Line 78- Correct the grammar of the sentence which start as "The incidence, death ......"

Line 85-6- Correct the grammar of the sentence

Line 97-98- Correct grammar

Line 99-100- Correct grammar

Line 103- Correct the punctuation

Line 292-295- Sentence needs revision for clarity, attend to the grammar

Line 295-298- Sentence needs some revision for clarity

Line 307 - Clarify what "tall reproductive age" refers, sentence may need some revisions

Line 309- Add reference of relevant papers to support your interpretation

Line 367- Replace "representative" with representativeness

**********

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Reviewer #1: Yes: Mirgissa Kaba

Reviewer #2: Yes: Dr. Oscar Tapera

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Attachment

Submitted filename: CC meta-systematic analysis-Review comment.docx

PLoS One. 2021 Nov 4;16(11):e0259339. doi: 10.1371/journal.pone.0259339.r002

Author response to Decision Letter 0


8 Apr 2021

Dear editors and reviewer of Plos One

We would like to extend our deepest appreciation for devoting your time to review our manuscript entitled “cervical cancer screening utilization and predictors among eligible women in Ethiopia: a systematic review and meta- analysis”. Cervical cancer is the second most commonly diagnosed cancer and the leading cause of cancer death in African women. In 2013, there were approximately 236,000 deaths from cervical cancer worldwide and it is the most common cancer in east and middle Africa. Cervical cancer screening is an important intervention to redcue cervical cancer and its associated maternal mortality. Even though, the utilization of the screening is inconsistent across the country and affected by different barrier. Therefore, this systematic review and meta-analysis estimates the pooled utilization of cervical cancer screening and its predictors in Ethiopia. Overall the main finding of this review is means of an intervention based on the pooled cervical cancer screening utilization and its predictors, which might be used to improve maternal adverse outcomes in Low and middle income countries, subsequently means of achieving SDGs.

Dear reviewer, there has been a major revision of the whole structure of the manuscript (Abstract, introduction, methods, results, discussion and conclusions) mainly with a correction of grammar errors. The further details regarding the choice of age range as well as outlining the limitations of the study and it's generalizability for the study areas are addressed. The reproductive group is substituted by eligible women as the global and who recommendations. We hope now the manuscript is clear and more acceptable than its previous version. We tried to state the limitations and generalizability issues in the limitation and strength section of the discussion. We have tried to present the response for each reviewer according to your comment what to suppose to do so. For this, here we have given our responses to each of the concerns you raised, highlighted by red color. Again, we would like to remind our strongest gratitude for your effort for the improvement of this manuscript and the response for each the points were addressed in the response to reviewers’ section. For this, I kindly request you to consider the paper for publication. Again, we would like to remind our strongest gratitude for your effort for the improvement of this manuscript.

Regards

Reviewer #1

1. Abstract

1.1. In the abstract as well as under background section, it is stated “Despite a remarkable progress in the reduction of maternal mortality, cervical cancer is the 73 second most commonly diagnosed cancer and the leading cause of cancer related death among 74 African women”. I agree with the reduction of MM. However, in view of the fact that CC is a major public health challenge and with its continued pressure, is it not naïve to argue about reduction of maternal mortality without showing how CC screening has contributed to that or contrary to this maintained MM in consequence higher.

Response: thank you for the highly valuable scholarly comments and suggestions. Revision was made on the abstract and background section stating that maternal mortality reduction achieved with cervical cancer screening.

1.2. Mention is made “The incidence, death rate and morbidities associated with cervical cancer is significantly varies across the world; higher in the developing nations than compared to the 80 developed countries”. While again it is stated “The prevalence of cervical cancer screening is much higher at the Western countries than SSA” (11, 12); the two statements looks contradictory.

Response: Thank you for the comments, but, the two statements is non-contradictory. Hence, the incidence, death rate and morbidities associated with cervical cancer is significantly varies across the world, which is higher in developing countries like SSA. This is explained due to high prevalence and severity of the problem among in low income countries and the fact that it is the only gynaecologic cancer which can be prevented and treated through early screening and follow-up, and the cervical cancer screening practice in low income countries is significantly low. Therefore, the two statements support each other.

#2. Method

2.1. There is no clarity on whether this review is ‘systematic’ or ‘met-analysis’ or ‘both’. If it is both, it is imperative to clarify which part of it is systematic and meta-analysis OR clarify why both were considered.

Response: Thank you for the valuable comments. We used the PRISMA diagram or recommendations of the systematic review and meta-analysis including the report of this study like the search strategy and the overall written was based on the recommendations. The meta-analysis commands and software were used based on the meta-analysis Cochrane handbooks. The meta-analysis was done to get the pooled estimate using Stata 14 using a meta-analysis written command. To do a good review and meta-analysis it should be searched systematically and other quality measures should be addressed what we have tried.

2.2. From the statement “All published and unpublished studies through April 7, 2020” there were quite few concerns. Firstly what was the lower time frame? Could it be any document from time immemorial to April 7, 2020? Secondly, how were the unpublished reports captured? Was there any criterion set to identify those?

Response: accepted and specific lower time frame was putted (2016) and the criteria used to identify unpublished articles were those fully access during manual search, found in university repositories and those studies fulfilling quality score to be included in this study.

2.3. While WHO’s recommended age of CC screening is 30-50, it is not clear why in this study age 18-49 years was chosen? Is it not contradictory?

Response: Thank you for the highly valuable comments. I completely agree what you supposed to do so and revision was made throughout the manuscript. The reproductive age group is not representative for all the all age eligible women for cervical cancer screening for the population charactertics we included. The recommendation was for the general population Evidence show success of cervical screening initiatives depend on high participation of the target population, which in turn is determined by the women’s knowledge, perceptions, health orientations and other socio-cultural issues. It is also affected by factors including early marriage, early sexual practice, delivery of the first baby before the age of 20, too many or too frequent childbirths, multiple sexual partners and low socio economic status. Women with early sexual practice, multiple partners, having HIV AIDS and sexual transmitted disease should have more screening schedule.

According to world health organization (WHO) guideline, every sexually active woman aged 30–49 years should undergo cervical cancer screening at least every 5 years. However, sexually active and HIV-positive women are suggested to be screened every 3 years regardless of their age. HIV positive women Ethiopia adopted the WHO recommendation in 2015 and recommended HIV positive women to start screening at HIV diagnosis, regardless of age once the woman is sexually exposed. In this meta-analysis age all age eligible women or from different population charactertics for cervical cancer screening such as women from 30-50 years old, HIV positive women, healthcare workers, and commercial sex workers were included. Thus, eligible women are better than reproductive age and we have accepted your comment.

#3. Results

3.1. The studies were drawn from five geographic regions: Addis Ababa, Amhara, Southern Nations, Nationalities and Peoples, Oromia and Tigray with only one from the national- level study. Couple of concern here. Firstly, how was the 18,067 women considered to estimate the pooled… proportionated in light of population size. Given the fact that studies are not proportional to the population of the regions, it would be difficult to reach conclusion as desired – this is about comparability of results. Secondly, I am wondering if this study could mirror realities for the country at large. Perhaps clarifying those and stating limitations may help.

Response: accepted and revision was made. The limitations were stated in regard to the less representativeness of five studies out of nine regions in Ethiopia in our meta-analysis.

3.2. I am not convinced that what are stated as ‘most common reasons that hinder the use of cervical cancer screening’ in the result section and conclusion section are aligned. This needs to be checked against the finding and corrected

Response: thank you for the comments suggest being.

We have checked it and the barriers in the result section and conclusion section are aligned

#4. Discussion

4.1. The fact that it was not clear on what of this review is Meta and systematic, the discussion suffers much missing what is being discussed. Perhaps with clarification on how the two contributed to this review may help refine the discussion section.

Response: Highly valuable comment, I completely agree what you supposed and revision was made. In the last two paragraphs of the discussion section narrates about the meta-analysis and systematic review mainly the strength and weakness.

Reviewer #2

1. Generally a good paper, congratulations, however, the work needs some grammatical revision for clarity. I have listed some below but kindly revise the entire paper checking for grammatical and punctuation errors.

Response: Thank you for your scholarly comments.

The major grammatical errors were revised and seen by sinor experts.

2. Line 74- update the reference and use more recent data than 2013

Response: Accepted and data published in 2016 by WHO and Bruni et al 2017 was cited.

3. Line 77- Be consistent in presenting figures i.e. 311000 should have a comma as with other figures

4. Response: accepted and revision was made. Comma as with other figures is putted.

5. Line 78- Correct the grammar of the sentence which starts as "The incidence, death ......"

Response: accepted and the grammar error was revised.

6. Line 85-6- Correct the grammar of the sentence, Line 97-98- Correct grammar, Line 99-100- Correct grammar, Line 103- Correct the punctuation, Line 292-295- Sentence needs revision for clarity, attend to the grammar, Line 295-298- Sentence needs some revision for clarity.

Response: all grammar and punctuation errors was corrected

7. Line 307 - Clarify what "tall reproductive age" refers, sentence may need some revisions

Response: valuable comment and revised. The editing "tall reproductive age" is an error, we want to instead want to spell as all reproductive age and revision was made. Fortunately, hence, it was not clear for reader we remove from the document.

8. Line 309- Add reference of relevant papers to support your interpretation

Response: reference number 73 was cited.

9. Line 367- Replace "representative" with representativeness

10. Response: representative" was replaced by with representativeness.

Attachment

Submitted filename: Point by Point reponse .docx

Decision Letter 1

Gizachew Tessema

19 Oct 2021

Cervical cancer screening utilization and predictors among eligible women in Ethiopia: a systematic review and meta-analysis

PONE-D-20-22948R1

Dear Mr Desta,

We’re pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it meets all outstanding technical requirements.

Within one week, you’ll receive an e-mail detailing the required amendments. When these have been addressed, you’ll receive a formal acceptance letter and your manuscript will be scheduled for publication.

An invoice for payment will follow shortly after the formal acceptance. To ensure an efficient process, please log into Editorial Manager at http://www.editorialmanager.com/pone/, click the 'Update My Information' link at the top of the page, and double check that your user information is up-to-date. If you have any billing related questions, please contact our Author Billing department directly at authorbilling@plos.org.

If your institution or institutions have a press office, please notify them about your upcoming paper to help maximize its impact. If they’ll be preparing press materials, please inform our press team as soon as possible -- no later than 48 hours after receiving the formal acceptance. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information, please contact onepress@plos.org.

Kind regards,

Gizachew Tessema, PhD

Academic Editor

PLOS ONE

Additional Editor Comments.

I would suggest to shorten the description related to key words and search terms. Instead put the details search terms and key words presented in lines 158-172 in a supplementary appendix. Revise the statement in the methods section of the abstract. Indicate that databases were searched for peer-review articles whereas Google scholar was used to search grey literature

Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. If the authors have adequately addressed your comments raised in a previous round of review and you feel that this manuscript is now acceptable for publication, you may indicate that here to bypass the “Comments to the Author” section, enter your conflict of interest statement in the “Confidential to Editor” section, and submit your "Accept" recommendation.

Reviewer #1: All comments have been addressed

Reviewer #2: (No Response)

**********

2. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: Yes

Reviewer #2: Yes

**********

3. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: Yes

Reviewer #2: Yes

**********

4. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: (No Response)

Reviewer #2: Yes

**********

5. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: Yes

Reviewer #2: Yes

**********

6. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: Authors revised the manuscript following the comments. They considered the comments useful which helped them to refine the manuscript

Reviewer #2: Great paper that contribute to knowledge in LMICs. Please see a few comments below:

-Some grammar and punctuation corrections are needful throughout the paper to aid clarity

-Line 74 Use more recent data e.g GLOBOCAN 2020

-Line 77 Be consistent in presentation of figures use the format 311,000

**********

7. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

If you choose “no”, your identity will remain anonymous but your review may still be made public.

Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #1: Yes: Mirgissa Kaba, School of Public Health, Addis Ababa University

Reviewer #2: Yes: Oscar Tapera

Acceptance letter

Gizachew Tessema

26 Oct 2021

PONE-D-20-22948R1

Cervical cancer screening utilization and predictors among eligible women in Ethiopia: a systematic review and meta-analysis

Dear Dr. Desta:

I'm pleased to inform you that your manuscript has been deemed suitable for publication in PLOS ONE. Congratulations! Your manuscript is now with our production department.

If your institution or institutions have a press office, please let them know about your upcoming paper now to help maximize its impact. If they'll be preparing press materials, please inform our press team within the next 48 hours. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information please contact onepress@plos.org.

If we can help with anything else, please email us at plosone@plos.org.

Thank you for submitting your work to PLOS ONE and supporting open access.

Kind regards,

PLOS ONE Editorial Office Staff

on behalf of

Dr. Gizachew Tessema

Academic Editor

PLOS ONE

Associated Data

    This section collects any data citations, data availability statements, or supplementary materials included in this article.

    Supplementary Materials

    S1 Fig. Sensitivity analysis of cervical cancer screening utilization.

    (TIF)

    S2 Fig. Association of women’s age and cervical cancer screening utilization.

    (TIF)

    S3 Fig. Association of occupational status and cervical cancer screening utilization.

    (TIF)

    S1 Table. PRISMA check list.

    (DOC)

    S2 Table. Included studies for the barriers of cervical cancer screening.

    (DOCX)

    S3 Table. Quality assessment of included studies.

    (DOCX)

    S1 Appendix. Specific searching on PubMed database.

    (DOCX)

    Attachment

    Submitted filename: CC meta-systematic analysis-Review comment.docx

    Attachment

    Submitted filename: Point by Point reponse .docx

    Data Availability Statement

    All relevant data are within the manuscript and its Supporting Information files.


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