Literature DB >> 34228766

Cervical cancer risk and access: Utilizing three statistical tools to assess Haitian women in South Florida.

Rhoda K Moise1, Raymond Balise2, Camille Ragin3, Erin Kobetz2.   

Abstract

Although decreasing rates of cervical cancer in the U.S. are attributable to health policy, immigrant women, particularly Haitians, experience disproportionate disease burden related to delayed detection and treatment. However, risk prediction and dynamics of access remain largely underexplored and unresolved in this population. This study seeks to assess cervical cancer risk and access of unscreened Haitian women. Extracted and merged from two studies, this sample includes n = 346 at-risk Haitian women in South Florida, the largest U.S. enclave of Haitians (ages 30-65 and unscreened in the previous three years). Three approaches (logistic regression [LR]; classification and regression trees [CART]; and random forest [RF]) were employed to assess the association between screening history and sociodemographic variables. LR results indicated women who reported US citizenship (OR = 3.22, 95% CI = 1.52-6.84), access to routine care (OR = 2.11, 95%CI = 1.04-4.30), and spent more years in the US (OR = 1.01, 95%CI = 1.00-1.03) were significantly more likely to report previous screening. CART results returned an accuracy of 0.75 with a tree initially splitting on women who were not citizens, then on 43 or fewer years in the U.S., and without access to routine care. RF model identified U.S. years, citizenship, and access to routine care as variables of highest importance indicated by greatest mean decreases in Gini index. The model was .79 accurate (95% CI = 0.74-0.84). This multi-pronged analysis identifies previously undocumented barriers to health screening for Haitian women. Recent US immigrants without citizenship or perceived access to routine care may be at higher risk for disease due to barriers in accessing U.S. health-systems.

Entities:  

Mesh:

Year:  2021        PMID: 34228766      PMCID: PMC8259954          DOI: 10.1371/journal.pone.0254089

Source DB:  PubMed          Journal:  PLoS One        ISSN: 1932-6203            Impact factor:   3.240


Introduction

Worldwide, sexual and reproductive cancer, such as that of the cervix, remains a leading cause of death for women despite being preventable with early detection and treatment of cancerous lesions [1-5]. Although mortality from cervical cancer in the United States (U.S.) has significantly decreased over recent decades due to vaccination policies and screening recommendations, immigrants who are women of African ancestry still experience disproportionate rates of disease [2, 4, 6–11]. Specifically, Haitian women have been found to have increased risk for cervical cancer in part due to delayed detection and subsequent treatment [4, 6–8, 12]. Yet, the literature to date under-investigates the risk factors that characterize health and health behavior for unscreened Haitian women living in the U.S. Individuals of African ancestry may be African American or may belong to a multitude of other groups (e.g., French-, Dutch-, or English-speaking Caribbean/West Indian, African, American, European, Canadian). The African ancestry immigrant population has quadrupled since 1980 with over half of these immigrants originating from the Caribbean [13]. The Census Bureau projects that the number of immigrants of African ancestry will double again by 2060 with Haitian immigrants contributing a significant portion to the statistics [13]. Thus, Haitian women’s health must be contextualized at the intersection of science, health, and policy, as well as through a syndemic, medical, and anthropological lens of structural violence [12, 14–18]. Structural violence may not be physical and refers to social institutions which harm groups of people by impeding their ability to achieve basic human needs such as healthcare, education, and other resources [19-21]. For instance, colonialism, sexism, racism, and xenophobia are so deeply embedded in society that they may go largely unnoticed while directly and indirectly impacting health and health behavior [20, 21]. Colonialism, sexism, racism, and xenophobia create a dynamic interplay of poverty, gendered experiences, and race consciousness, which must be exposed and rectified in order to promote health and prevent disease for all with efficiency and sustainability [12, 14–17]. Notably, xenophobia, the hatred of people from other countries, persists in the U.S. For instance, the CDC initially categorized four risks for HIV (referred to as 4H) including the following: hemophilia, heroin use, homosexuality, and people of Haitian ancestry [22, 23]. Although the CDC has redacted the wrongful statement regarding Haitian ancestry as a risk factor, Haitians still carry the burden of stigmatization and medical mistrust associated with the incident [15]. Haitians’ unfavorable context of reception in the U.S. (e.g., government policies and local labor market, social relationships, and perceptions) predicts cultural dissonance, poor self-esteem, and depression which all consequently influence health and wellness [16, 17]. Thus, hostile context of reception may also provide insight into poor health outcomes in Haitian women [15-17]. Furthermore, Haitian women’s native language is not English which may also cause challenges in navigating the U.S. health system. Overall, Haitian women are impacted by multiple structures of violence which may translate into restricted access to health preserving care like preventive gynecological measures against cervical cancer [12, 24, 25].

Purpose of the study

This paper explores literature-supported variables including socio-demographic (age, marital and employment status, education), immigrant history (citizenship, length in U.S.), and health care utilization (insurance, access to routine care) to predict cervical cancer risk in Haitian women living in the U.S. [26]. Each variable has specific justification for inclusion in data analysis. For instance, socio-demographic variables are standard in statistics. Immigrant history adds contextual detail in data analysis for meaningful interpretation, and health care utilization links to health care outcomes [26]. We utilize three statistical methods: a) logistic regression (LR); b) classification and regression trees (CART); and c) random forest (RF) for comprehensive analytics. Statistical approaches vary in their degree of responding to scientific inquiry due to intrinsic assumptions for each methodology; therefore, this study includes three different methods to curate a comprehensive view of Haitian women’s risk profiles for cervical cancer using predictors across immigration history, patterns of healthcare utilization, and key socio-demographic characteristics. Further, multiple statistical methodology allows for examination of similarities and nuances across analysis, producing more reliable results and more detailed findings. Each statistical methodology holds inherent and applied (to this dataset) strengths and weaknesses. LR, RF, and CART models are all evaluated using a myriad of assessments, and this study uses accuracy, the systematic correctness of the model’s predictions compared to the true classifications in the dataset where a high percentage is favored, as a common assessor of result comparison [27-29]. Further, through incorporating all three of the detailed statistical approaches, this study leverages strengths and minimizes weaknesses for a more comprehensive grasp of cervical cancer risk prediction [30].

Theoretical rationale: PEN 3 Cultural Model’s relationships and expectations via perceptions, enablers, and nurturers

The PEN-3 Cultural Model (Fig 1) has been developed particularly for research in ethnic populations [31-34]. Further, the PEN-3 Cultural Model has several domains which help researchers approach data analysis and interpretation with cultural sensitivity [31-34]. This study relates to the dimension of relationships and expectations (one’s perceptions, enablers, and nurturers) by employing a series of quantitative analyses to assess the relationship between cervical cancer screening behaviors, immigration history, patterns of healthcare utilization, and key socio-demographic characteristics of Haitian immigrant women in the Miami metropolitan area (Fig 2). The PEN-3 Cultural Model includes categories to organize the data and aids in data interpretation to advance knowledge of socio-cultural influences of Haitian women’s navigation of healthcare. Accordingly, we theoretically organized variables by perceptions, enablers, and nurturers of health and health behavior for the population [35]. For instance, participants’ reports of age, access to routine care, and length of time in the U.S. make up the subdimension of perceptions. Enablers include participants’ insurance and citizenship status. Education, employment, and marriage may nurture a participants’ health and wellness.
Fig 1

The PEN-3 Cultural Model.

PEN-3 domain of relationships and expectations are the key serves as the theoretical framework element for this study.

Fig 2

The PEN-3 Cultural Model relationships and expectations domain.

Relationships and expectations of the PEN-3 Cultural Model were applied to theoretically organize the study variables.

The PEN-3 Cultural Model.

PEN-3 domain of relationships and expectations are the key serves as the theoretical framework element for this study.

The PEN-3 Cultural Model relationships and expectations domain.

Relationships and expectations of the PEN-3 Cultural Model were applied to theoretically organize the study variables. Overall, this study aims to understand the characteristics of a Haitian woman living in South Florida who is at-risk for cervical cancer defined by her self-reported health history including absence of cervical cancer screening with a Pap test. Statistical findings may help to provide better comprehension of socio-cultural and socio-environmental factors fostering (or impeding) women immigrants’ ability to navigate the U.S. healthcare system. Results may inform public health planning and delivery for Haitian women as well as other underserved immigrants living in the U.S. for equitable access to disease prevention and control.

Materials and methods

Sample

Data were extracted and merged from two larger studies, namely Health in Your Hands (HIYA; Clinical Trial Registration Number NCT02970136) and South Florida Center for the Reduction of Cancer Health Disparities (SUCCESS; Clinical Trial Registration Number NCT02121548). HIYA and SUCCESS tested modality, the fashion in which participants were screened (i.e., mailed self-sampler, community health worker [CHW] support). Both studies were ethically approved prior to the study by the University of Miami ethics committee as well as with an updated University of Miami IRB approval to be merged and analyzed (IRB #20180129). Both studies, HIYA and SUCCESS, included purposive convenience sampling. SUCCESS sought to bypass barriers to screening through delivering HPV self-sampling tools to women via a CHW [36]. Indeed, the study produced significant results indicating efficacy in screening uptake despite women’s lack of knowledge, insurance, and access [37]. HIYA sought to clarify the viability of HPV self-sampling tools delivered by mail in order to circumvent conflict or confusion with scheduling an appointment with a CHW [4]. Findings from HIYA suggested no statistical differences in screening uptake by CHW compared to mailed kit, validating the feasibility of a new format for screening via a mailed self-sampling tool approach. Details of these studies may be found elsewhere [4, 36]. We also conducted preliminary data analysis to ensure there were no significant differences in the data to further justify merging. The sample was fairly split across both datasets (n = 148 SUCCESS; n = 198 HIYA) to include n = 346 Haitian women living in South Florida who were at risk for cervical cancer, defined as self-reported age of 30–65 and unscreened in the previous three years.

Measures and analyses

Measures included self-reported information on previous Pap smear history, demographics, and health access. The response variable for all analyses was a binary, yes/no, outcome of whether women ever underwent a Pap smear. Study investigation focused on screening as compared to vaccination due to the demographics of the sample who immigrated to the U.S. on average at an age beyond the recommended vaccination window of early adolescence. Explanatory measures included self-reported variables pertaining to immigration history, patterns of healthcare utilization, and socio-demographic characteristics. Measures were recoded into binary (yes/no) predictors. Immigration history included U.S. citizenship, where permanent resident status was coded as non-citizen. Healthcare utilization encompassed insurance and perceived access to routine medical care. Socio-demographic variables included marital status, education, and employment. For marital status, cohabitation, separated, divorced, and widowed were coded as not married. Education included less than high school or high school educated and above. Dataset (HIYA or SUCCESS) was also coded as binary. Although initially collected as continuous variables, age and length in U.S., both in years, were recoded categorically. Age was coded into terciles including 30–40 years of age or early-adulthood, 41–50 years of age or middle-adulthood, and 51–65 years of age or older-adulthood. Length of time spent in the U.S. was coded into quartiles including the following: = <5 years or recent immigrants, 6–25 years, 26–40 years, 41–50 years, and 51–65 years. All analyses were completed using R software version 3.5.1 [38]. All corresponding package numbers are included below.

Three risk prediction processes across LR, CART, and RF

To craft the most parsimonious model, data analysis included a manual hierarchal stepwise approach [39]. Each predictor was inputted for univariate logistic regression models to assess the association between screening history and various predictors. All predictors were fitted for a multivariate model to ascertain the variable inflation factor (VIF), a measure of violating the assumption of collinearity, and then predictors with a low VIF (<2.5) were then fitted for another multivariate model using the “step” function in R. All theory and literature-supported variables carried over from LR and were inputted for CART and RF. CART graphs were created for ease of interpretability with R packages including “rpart” version 4.1–13 and “rattle” version 5.2.0. The procedure of randomly creating 70:30 ratio for training (n = 241) to test (n = 105) sets, respectively, sufficed for considerations of model fit and accurate data representation. RF packages included “caret” version 6.0–80 with the default of n = 500 trees [40, 41].

Results

Sample characteristics

The sample included women who were on average 46 years of age (interquartile range = 39, 53; median = 46; SD = 9.2) with 30.5 years spent in the U.S. (interquartile range = 8, 47; median = 36; SD = 20.4). Women displayed low levels of citizenship (23.1%), insurance (19.4%), access to routine care (22.0%), and employment (28.3%). Slightly more than half of the sample was married (56.1%) with less than high school education (57.4%). The entire sample was foreign-born in Haiti, with the exception of three participants born in other parts of the Caribbean and Latin America. Although income data were collected, analyses were not viable as more than half of the sample lived below the poverty line (n = 190, 54.9%), with a sizeable portion of the sample reporting unknown income (n = 138, 39.9%). Overall the sample distribution presented as skewed with categorical binary variables representing a low socio-economic status (SES) sample with recent immigration to the U.S. (<5 years), indicative of hyper-vulnerability to poor health outcomes [42]. The sample was fairly split across both datasets. Although none of the women adhered to U.S. recommendations of undergoing Pap smear screening every three years, classifying them as at risk for undetected cell abnormalities and potential infection, approximately two thirds of the sample (n = 226; 65.3%) had history of a previous Pap smear in general. Sample descriptive statistics are summarized in Tables 1 and 2. Results are described in detail below by statistical approach.
Table 1

Sample descriptive statistics categorical variables (n = 346).

Variablen(Percent)
Previous Pap226 (65.3)
U.S. Citizens80 (23.1)
Insured67 (19.4) 
Routine Care76 (22.0) 
Married194 (56.1) 
Employed 98 (28.3)
HS Educated152 (43.9)
Dataset (HIYA)148 (42.8)
Table 2

Sample descriptive statistics continuous variables (n = 346).

VariableAverage (Interquartile Range)
Age46 (39, 53)
Length in U.S. (years)30.5 (8, 47)

LR, CART, and RF analytics

Results from both single predictor and multivariable logistic regression, predicting being screened, are depicted in Table 3. The models show increased odds of screening for women who were middle or older age, in the country for longer than five years, U.S. citizens, insured, employed, and able to access routine care. Marital status, education, and dataset did not produce significant univariate results.
Table 3

Bivariate and multivariate logistic regression statistics.

VariablesBivariate OR, (95%CI)Multivariate OR, (95%CI)
Age 
A (30–40 years)1 (ref)1 (ref)
B (41–50 years)2.10 (1.19, 3.72) *3.10 (1.19, 8.10) *
C (51–65 years)2.29 (1.27, 4.11) **2.56 (0.95, 6.89)
Length in U.S.
A (= <5 years)1 (ref)1 (ref)
B (6–25 years)3.92 (1.81, 8.50) ***1.85 (0.76, 4.54)
C (26–40 years)2.45 (1.23, 4.86) *2.89 (1.14, 7.35) *
D (41–50 years)3.19 (1.59, 6.38) **1.52 (0.64, 3.63)
E (51–65 years)3.83 (1.79, 8.19) ***1.72 (0.63, 4.67)
U.S. Citizenship4.94 (2.44, 10.00) ***3.19 (1.36, 7.49) **
Insured2.09 (1.12, 3.90) *1.12 (0.51, 2.46)
Routine Care3.18 (1.67, 6.06) ***2.60 (1.16, 5.81) *
Married1.01 (0.65, 1.59)0.94 (0.55, 1.59)
Employed 2.09 (1.23, 3.57) **1.06 (0.55, 2.02)
HS Educated1.10 (0.07, 1.74)1.58 (0.89, 2.82)
Dataset (HIYA)1.41 (0.90, 2.21)N/A

Logistic regression statistics for the bivariate and multivariate analyses.

Note: Significance codes: 0 ‘***’ 0.001 ‘**’ 0.01 ‘*’ 0.05 ‘.’ 0.1 ‘ ‘ 1.

OR = Odds ratio; CI = confidence interval; Ref = Referent group; N/A = Not applicable.

Logistic regression statistics for the bivariate and multivariate analyses. Note: Significance codes: 0 ‘***’ 0.001 ‘**’ 0.01 ‘*’ 0.05 ‘.’ 0.1 ‘ ‘ 1. OR = Odds ratio; CI = confidence interval; Ref = Referent group; N/A = Not applicable. A multivariate model was built including all variables to ascertain VIF. Two variables (years in the U.S. and dataset) were collinear, indicated by high VIF (>2.5). Given previous justification of merging across datasets as well as the insignificance of dataset in the univariate analyses, the dataset variable was consequently removed from the multivariate model, and categorical length in U.S. was maintained. In the next iteration of multivariate analyses, excluding the dataset variable, no predictors returned high VIF results. Further, middle and older age, mid-range length in the U.S., U.S. citizenship, and routine access to care were significant predictors of likelihood in presence of previous screening history. According to the C-statistic, 72% of the time this model would correctly guess, when presented with two women where only one of which was screened, which one was screened. To further assess predictors, the R “step” function was employed to select the most parsimonious model. This required omitting 13 women from the categorical age and length in the U.S. predictors for model execution, leading to an n = 333 down from n = 346. The ultimate model shown in Table 4 was selected according to the PEN-3 Cultural Model and parsimony (AIC = 367.5) with age, citizenship, access to routine care, and education as predictors. Ultimately, women reporting middle or older age, U.S. citizenship, and access to routine care were most likely to report previous history of Pap smear screening. The C-statistic of 73% reflects a similar level of accuracy compared to the manually built model described above.
Table 4

Stepwise regression model (n = 333).

VariablesStepwise OR, (95%CI)
Age
A (30–40 years)1 (ref)
B (41–50 years)2.21 (1.17, 4.17) *
C (51–65 years)1.96 (0.98, 3.94)
U.S. Citizenship4.11 (1.83, 9.26) ***
Routine Care2.69 (1.26, 5.71) *
HS Educated1.60 (0.91, 2.80)

Stepwise regression statistics for the multivariate analysis.

Note: Significance codes: 0 ‘***’ 0.001 ‘**’ 0.01 ‘*’ 0.05 ‘.’ 0.1 ‘ ‘ 1.

OR = Odds ratio; CI = confidence interval; Ref = Referent group; N/A = Not applicable.

Stepwise regression statistics for the multivariate analysis. Note: Significance codes: 0 ‘***’ 0.001 ‘**’ 0.01 ‘*’ 0.05 ‘.’ 0.1 ‘ ‘ 1. OR = Odds ratio; CI = confidence interval; Ref = Referent group; N/A = Not applicable. CART results, using the same dataset from initial analyses in LR with n = 346, returned an accuracy of 71.9% when predicting women’s Pap smear history and a kappa of .37. The tree mainly split on women who were not citizens, in the U.S. for five years or fewer, and without routine access to medical care. Results of CART are depicted in graph form in Fig 3. Attempts to prune tree (c = .04) resulted with a notification that the fit was not a tree, just a root.
Fig 3

Decision tree–CART model, fancy rpart plot.

There are numeric and text outputs associated with respective splits to aid in result interpretation. The figure featured at the top represents the predicted value per split. The number featured at the lower left represents the likelihood of the predicted split value. The number featured at the lower right represents the likelihood of the opposite endorsement value. The percentage at the bottom represents the size of the sample passing through the node per split. For example, with node number 2, the group is inclined to take on the activity, “yes” regarding screening history. The probability for people to say “yes” in this group is .41 while the probability for the group to take on the opposite activity, “no,” is .59. Of the 346 study subjects, 74% of the data passed through this node. Overall, the decision tree selected citizenship, length of time in the U.S., and age as important predictors in ascertaining a women’s screening history. For example, with node 1, the model asks if the participant is not a citizen. If the participant responds affirmatively, she is not a citizen, she will be classified into the node on the left. If the participant responds in opposition, “no” they are indeed as citizen, she will be classified in the node on the right.

Decision tree–CART model, fancy rpart plot.

There are numeric and text outputs associated with respective splits to aid in result interpretation. The figure featured at the top represents the predicted value per split. The number featured at the lower left represents the likelihood of the predicted split value. The number featured at the lower right represents the likelihood of the opposite endorsement value. The percentage at the bottom represents the size of the sample passing through the node per split. For example, with node number 2, the group is inclined to take on the activity, “yes” regarding screening history. The probability for people to say “yes” in this group is .41 while the probability for the group to take on the opposite activity, “no,” is .59. Of the 346 study subjects, 74% of the data passed through this node. Overall, the decision tree selected citizenship, length of time in the U.S., and age as important predictors in ascertaining a women’s screening history. For example, with node 1, the model asks if the participant is not a citizen. If the participant responds affirmatively, she is not a citizen, she will be classified into the node on the left. If the participant responds in opposition, “no” they are indeed as citizen, she will be classified in the node on the right. RF results, also using the same dataset from analyses in LR and CART with n = 346, identified years spent in the U.S., citizenship, and age as variables of highest importance indicated by greatest mean decreases in the Gini index. A loop function to identify best settings confirmed the defaults were ideally maintained as 500 trees and mtry three for a 37.6% error. The training model was 78% accurate (95% CI = 0.72–0.83) with specificity of 0.94, the predictive ability to correctly identify women who had not been screened, and a Positive Predictive Value (PPV) of 82%. The testing model was 72% accurate (95% CI = 0.61–0.81) with specificity of 0.80, the predictive ability to correctly identify women who had not been screened, and a Positive Predictive Value (PPV) of 50%. Table 5 contains statistical results for the RF confusion matrices of the training and test sets. Fig 4 displays variables of importance accordingly.
Table 5

Confusion matrix statistics for random forest (RF) training (n = 241) and test sets (n = 105).

Statistic TypeTraining Set ResultTest Set
Accuracy0.780.72
95% CI(0.72, 0.83)(0.61, 0.81)
No Information Rate0.650.72
P-Value [Acc > NIR]3.01e-050.55
Pos Pred Value0.820.50
Neg Pred Value0.770.81
Specificity0.940.80
Sensitivity0.470.52
McNemar’s Test P-Value4.84e-061.00
Kappa0.460.31
Prevalence0.350.28
Detection Prevalence0.200.29
Balanced Accuracy0.710.66
Fig 4

Random Forest (RF) important variables.

Results of RF variables of importance are featured including order of ranked importance.

Random Forest (RF) important variables.

Results of RF variables of importance are featured including order of ranked importance.

Discussion

This study utilizes three quantitative methods (LR, CART, and RF) for improved assessment of risk of cancer for Haitian women who have never undergone screening, based in Miami-Dade County, FL, the largest enclave of Haitians living in the U.S. [37]. This study uniquely applies classic analysis of LR, an innovative application of CART, and rigorous assessment of RF, to understand cervical cancer risk in Haitian women. This study utilized three statistical methods to explore risk prediction for Haitian women who had never undergone screening for cervical cancer from a sample of women who reported no screening in the previous three years. Results indicated numerous factors may influence the disproportionate burden of HPV infection and related cancer in Haitian women including lack of screening, non-citizenship status, recent immigration to the U.S., and routine access to care. Reports of non-citizenship were the strongest predictors of absence of screening history across all analytic tools followed by younger (<40 years of age), recent immigrants (<5 years). LR results suggest perceived access to routine care outperforms insurance in predictive power which underscores the interplay of multilevel factors influencing access to health care for immigrant populations [4, 37, 43, 44]. However, uncertainty remains regarding the importance of other socio-demographic variables. For instance, education, employment, access to care, marital status, and insurance did not significantly appear in CART yet were present in varying degrees of LR analyses as well as the output of important variables produced by the random forest. RF models were specific, yet not very sensitive, meaning the model functioned better in predicting those under-screened than those who were screened. This finding is meaningful and useful due to the study’s purpose of identifying women at risk [41]. Although no cutoff was provided for the length in the U.S. predictor, it was the most important variable. Such findings demonstrate the need to further tease out levels of risk by immigration time [24, 45–47].

PEN-3 Cultural Model–relationships and expectations via perceptions, enablers, and nurturers

Framed by the PEN-3 Cultural Model, results indicate enablers as the most influential portion of the model considering citizenship status appearing as a key predictive variable across all analytics while insurance had little effect. Next, perceptions followed in significance with length of time in the U.S. and access to care. Finally, nurturing variables (theorized as education, employment, and marriage) had mild influence in predicting a participant’s screening history. These findings add complexity to the literature on the healthy migrant effect which suggests a selection bias of groups in better health tend to immigrate [42, 48, 49]. Although the theory may hold true for baseline health, it may not accurately describe health behaviors. Future studies should consider qualitatively exploring drivers of HPV screening knowledge, attitudes, and behaviors (KAB) as well as access and barriers to improve Haitian women’s uptake [44, 50].

Strengths and limitations

This study should be considered in light of both strengths and weaknesses. For instance, this study includes vigorous statistical methodology and robust data analysis [27]. Additionally, the sample size was relatively small for the type of analyses typically used for machine learning tools [51-55]. The sample also included a skewed sample of Haitian women with low SES indicated by a majority of below poverty or unknown income. In spite of the limited, medium sample size, with low SES Haitian women, the consistency of results along with their associated data validation metrics producing accuracy across all methods are encouraging.

Conclusions

Although some recognize systemic, structural violence as a problem and are working to address it, women still encounter related difficulties and barriers to accessing care such as sexual and reproductive health [20, 56]. Particularly, Black women experience hyper-vulnerability to inequity and societal exclusion at the intersection of sexism and racism [57, 58]. Health and research policies and procedures have been institutionalized in order to account for such biases and prevent poor practices in the future. These practices included, for examples, federal entities requiring assessments of inclusion of women and minorities in grants, institutional review boards, and informed consent. However, detrimental effects on vulnerable populations still carry over from historical context [59]. Further, findings imply the need to address related systematic barriers blocking Haitian women from successfully navigating the U.S. healthcare system due to colonialism, sexism, racism, and xenophobia [32, 60]. Citizenship status may supersede literature supported variables in driving health and health behavior [12, 26, 46]. Overall, results mainly highlighted younger, recent women immigrants, without citizenship, as the most at risk for cervical cancer due to lack of screening. There may also be implications for compounded factors and cumulative effects of other variables such as employment, education, and marital status. Future studies must consider holistic ecological approaches to population health to best serve Haitian women spanning their individual insights (i.e., KAB) to institutional influences (i.e., SES, citizenship). Implications for health equity and public health entail policy and systems level consideration for vulnerable populations in light of structural violence linked to gender, racial/ethnic and, nativity. 12 Jan 2021 PONE-D-20-21793 Cervical Cancer Risk and Access: Utilizing Three Statistical Tools to Assess Haitian Women in South Florida PLOS ONE Dear Dr. Moise, Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process. I would like to sincerely apologise for the delay you have incurred with your submission. It has been exceptionally difficult to secure reviewers to evaluate your study. 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For instructions see: http://journals.plos.org/plosone/s/submission-guidelines#loc-laboratory-protocols We look forward to receiving your revised manuscript. Kind regards, Miquel Vall-llosera Camps Senior Editor PLOS ONE Journal Requirements: When submitting your revision, we need you to address these additional requirements. 1. Please ensure that your manuscript meets PLOS ONE's style requirements, including those for file naming. The PLOS ONE style templates can be found at https://journals.plos.org/plosone/s/file?id=wjVg/PLOSOne_formatting_sample_main_body.pdf and https://journals.plos.org/plosone/s/file?id=ba62/PLOSOne_formatting_sample_title_authors_affiliations.pdf 2. Please provide more information on the data sources used. We note that two different clinical trials are cited as  data sources ; please ensure that you provide more information on the two trials (settings,  participants included, etc) and discuss what type of data were used in your study (baseline/ post-intervention). Moreover, please clarify the eligibility criteria used for inclusion in your analysis; and provide a participant flowchart. 3. Please specify whether you had access to any identifying information, and provide the IRB approval number for your study. 4. We suggest you thoroughly copyedit your manuscript for language usage, spelling, and grammar. If you do not know anyone who can help you do this, you may wish to consider employing a professional scientific editing service. Whilst you may use any professional scientific editing service of your choice, PLOS has partnered with both American Journal Experts (AJE) and Editage to provide discounted services to PLOS authors. Both organizations have experience helping authors meet PLOS guidelines and can provide language editing, translation, manuscript formatting, and figure formatting to ensure your manuscript meets our submission guidelines. To take advantage of our partnership with AJE, visit the AJE website (http://learn.aje.com/plos/) for a 15% discount off AJE services. To take advantage of our partnership with Editage, visit the Editage website (www.editage.com) and enter referral code PLOSEDIT for a 15% discount off Editage services.  If the PLOS editorial team finds any language issues in text that either AJE or Editage has edited, the service provider will re-edit the text for free. Upon resubmission, please provide the following: The name of the colleague or the details of the professional service that edited your manuscript A copy of your manuscript showing your changes by either highlighting them or using track changes (uploaded as a *supporting information* file) A clean copy of the edited manuscript (uploaded as the new *manuscript* file) 5. We note that you have indicated that data from this study are available upon request. PLOS only allows data to be available upon request if there are legal or ethical restrictions on sharing data publicly. For information on unacceptable data access restrictions, please see http://journals.plos.org/plosone/s/data-availability#loc-unacceptable-data-access-restrictions. In your revised cover letter, please address the following prompts: a) If there are ethical or legal restrictions on sharing a de-identified data set, please explain them in detail (e.g., data contain potentially identifying or sensitive patient information) and who has imposed them (e.g., an ethics committee). Please also provide contact information for a data access committee, ethics committee, or other institutional body to which data requests may be sent. b) If there are no restrictions, please upload the minimal anonymized data set necessary to replicate your study findings as either Supporting Information files or to a stable, public repository and provide us with the relevant URLs, DOIs, or accession numbers. Please see http://www.bmj.com/content/340/bmj.c181.long for guidelines on how to de-identify and prepare clinical data for publication. For a list of acceptable repositories, please see http://journals.plos.org/plosone/s/data-availability#loc-recommended-repositories. We will update your Data Availability statement on your behalf to reflect the information you provide. 6. Please respond by return e-mail with an updated version of your manuscript to include your abstract after the title page. 7. Please include a separate caption for each figure in your manuscript. [Note: HTML markup is below. Please do not edit.] Comments to the Author 1. 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 ********** 2. Has the statistical analysis been performed appropriately and rigorously? Reviewer #1: Yes Reviewer #2: Yes ********** 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: No 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: No ********** 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: This study examined factors associated with cervical cancer screening among Haitian women. Specifically, the authors used three different statistical methods to determine salient factors related to lack of screening among. I have offered a few suggestions for the authors’ consideration: Abstract •The authors state, “This study seeks to assess cancer risk and access of unscreened Haitian women.” The statement seems to indicate an examination of general cancer risk as opposed to risk and access specific to cervical cancer. Introduction •The first sentence of the second paragraph is missing a closed parenthesis. Same issue for the last sentence of paragraph three. •The description of the influence of how structural violence influence health behaviors is an interesting concept. However, since the study focuses on specific determinants of cancer screening, which have been examined in previous immigrant health literature, it would be helpful to provide further justification for choosing the specific screening determinants in this study. •The authors indicate that the study utilizes three distinct statistical methods to examine factors associated with Pap screening. It seems to me that the focus of the paper is on the use of the statistical methods, so it would be helpful to provide additional justification for using this approach. Methods • The theoretical rationale seems a bit out of place in the methods sections. I suggest including this in the introduction section. Perhaps, it may bolster the arguments for examining factors associated with Pap screening using three statistical methods. • Why were data from the two studies merged, I assume both data were very similar? What was the sample sizes for each data? Results • In subsection 3.2 (LRC, CART, and…) include the relevant statics, e.g. the ORs and CIs. Discussion • The first paragraph of the discussion provides more detailed rationale for utilizing the three statistical methods in this paper. I suggest incorporating some of the information here in the introduction section. Tables • In table 1, I suggest including information for the categorical variables. For instance, what is the breakdown of length in the US, education, age etc.? Reviewer #2: Introduction: Your problem specification needs to be clearer, for example in page 8, you mentioned “structural violence, colonialism, racism and xenophobia” which are note in your aim of study. You should specify the reference for each sentence in your introduction, for example in page 9 the sentence:” Colonialism, sexism, racism, and xenophobia create a dynamic interplay of poverty, gendered experiences, and race consciousness, which must be exposed and rectified in order to promote health and prevent disease for all with efficiency and sustainability.” Has not any references. There are many such sentences that you need to add references for them. At the end of the introduction, please mention the aim of your study. Methods: Please explain why you chose PEN 3-Cultural Model for your study. In page 10, part 2.1 the last sentence should be transferred to the introduction. Please also mention the criteria and reason you considered for selecting each predictor. Since the number of your data is low, the results are not reliable, so please try applying cross validation to gain more reliable results. Results: The accuracy obtained from the approaches may be improved, try selecting more important variables for your prediction and report them if the results improved. ********** 6. 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: No Reviewer #2: Yes: Farkhondeh Asadi [NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files.] While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Registration is free. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email PLOS at figures@plos.org. Please note that Supporting Information files do not need this step. 24 Mar 2021 Thank you for the feedback. I responded to all comments in an uploaded attached file. Submitted filename: PLOS_Rresponse to Reviewers_2021March01.docx Click here for additional data file. 14 May 2021 PONE-D-20-21793R1 Cervical Cancer Risk and Access: Utilizing Three Statistical Tools to Assess Haitian Women in South Florida PLOS ONE Dear Dr. Moise, Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process. Please submit your revised manuscript by Jun 28 2021 11:59PM. If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at plosone@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pone/ and select the 'Submissions Needing Revision' folder to locate your manuscript file. Please include the following items when submitting your revised manuscript: A rebuttal letter that responds to each point raised by the academic editor and reviewer(s). You should upload this letter as a separate file labeled 'Response to Reviewers'. A marked-up copy of your manuscript that highlights changes made to the original version. You should upload this as a separate file labeled 'Revised Manuscript with Track Changes'. An unmarked version of your revised paper without tracked changes. You should upload this as a separate file labeled 'Manuscript'. If you would like to make changes to your financial disclosure, please include your updated statement in your cover letter. Guidelines for resubmitting your figure files are available below the reviewer comments at the end of this letter. If applicable, we recommend that you deposit your laboratory protocols in protocols.io to enhance the reproducibility of your results. Protocols.io assigns your protocol its own identifier (DOI) so that it can be cited independently in the future. For instructions see: http://journals.plos.org/plosone/s/submission-guidelines#loc-laboratory-protocols. Additionally, PLOS ONE offers an option for publishing peer-reviewed Lab Protocol articles, which describe protocols hosted on protocols.io. Read more information on sharing protocols at https://plos.org/protocols?utm_medium=editorial-email&utm_source=authorletters&utm_campaign=protocols. We look forward to receiving your revised manuscript. Kind regards, Farkhondeh Asadi Academic Editor PLOS ONE Journal Requirements: Please review your reference list to ensure that it is complete and correct. If you have cited papers that have been retracted, please include the rationale for doing so in the manuscript text, or remove these references and replace them with relevant current references. Any changes to the reference list should be mentioned in the rebuttal letter that accompanies your revised manuscript. If you need to cite a retracted article, indicate the article’s retracted status in the References list and also include a citation and full reference for the retraction notice. Additional Editor Comments (if provided): Dear Authors, Thanks for addressing some of reviewers' comment. According to reviews' 1 comment he/she believes that his/her comment did not address well so, I invite you to response to his/her comment again correctly. [Note: HTML markup is below. Please do not edit.] 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: (No Response) Reviewer #2: All comments have been addressed ********** 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: (No Response) Reviewer #2: Dear authors, Thank you very much for improving your manuscript, all the comments are well addressed. ********** 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: No Reviewer #2: Yes: Farkhondeh Asadi [NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files.] While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Registration is free. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email PLOS at figures@plos.org. Please note that Supporting Information files do not need this step. 21 May 2021 May 18, 2021 PLOS ONE Re: Manuscript Submission PONE-D-20-21793 Dear Dr. Miquel Vall-llosera Camps, My colleagues and I would like to thank you for allowing us to revise and resubmit our manuscript, “Cervical Cancer Risk and Access: Utilizing Three Statistical Tools to Assess Haitian Women in South Florida”. My colleagues and I feel that the comments and concerned raised by you and the reviewers have significantly strengthened the manuscript. There was confusion regarding the submission process and Response to Reviewers letter. I have resubmitted our response letter (please see the end of this PDF) where we list each comment made by each of the reviewers, followed by a narrative response to the comment. We have also included requested editorial revisions. We have track changes for ease of reference as well as a clean, updated document. As previously mentioned, Dr. Elizabeth Metzger, a professor in the English department at University of South Florida, provided copyediting services. In order to incorporate responses to the many excellent comments of the reviewers, the manuscript is over length. If there are additional comments from Reviewer 1 who felt their feedback was not incorporated, please have them specify their concerns. Please communicate the confusion to them to ensure they note that their comments were considered, but due to confusion where I included responses to reviewers previously, then got an admin request for updates, the original track changed document and responses were not sent to them. I valued their insights. I also maintain the following by kindly offering more clarification in response to your previous request to make the data publicly available. The data includes a vulnerable group facing stigma. Further, the IRB did not include approval of data sharing. Thus, we are ethically unable to grant public availability of the data. However, there may be potential opportunities to collaborate with interested researchers. The data findings of the larger studies are available in published in peer-reviewed journals as indicated in the manuscript. The corresponding author’s information is available for contact accordingly. I hope this addresses the data issue. I noted in my previous resubmission that "Data cannot be shared publicly because of confidentiality. Data are available from the Dr. Erin Kobetz at University of Miami (contact via ekobetz@med.miami.edu) for researchers who meet the criteria for access to confidential data. Indeed, there are legal and ethical restrictions being placed upon the data. Data contain potentially identifying or sensitive patient information and the University of Miami IRB has imposed them. Feel free to contact them through Cynthia Gates, JD, ADN, CIP, their Executive Director of Human Subjects Research Office (email:cmg345@med.miami.edu)" Please let me know if you need anything else from me in order to move forward. Thank you in advance for considering our manuscript for publication. Overall, we hope that you and the reviewers will find our revised manuscript acceptable for publication in PLOS ONE. We have been corresponding for quite some time with minor updates. Please note, this paper is time sensitive as my access to funds to pay for the publication will expire in July. Should you have any questions or concerns, please feel free to contact me. Sincerely, Rhoda Moise, Ph.D. rmoise@reessi.com Submitted filename: PLOS_Rresponse to Reviewers_2021MAY18.docx Click here for additional data file. 21 Jun 2021 Cervical Cancer Risk and Access: Utilizing Three Statistical Tools to Assess Haitian Women in South Florida PONE-D-20-21793R2 Dear Dr. Moise, 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, Farkhondeh Asadi Guest Editor PLOS ONE Additional Editor Comments (optional): 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 ********** 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 ********** 3. Has the statistical analysis been performed appropriately and rigorously? Reviewer #1: 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 ********** 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 ********** 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: (No Response) ********** 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: No 24 Jun 2021 PONE-D-20-21793R2 Cervical cancer risk and access: Utilizing three statistical tools to assess Haitian women in South Florida Dear Dr. Moise: 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. Farkhondeh Asadi Guest Editor PLOS ONE
  40 in total

1.  The Latino mortality paradox: a test of the "salmon bias" and healthy migrant hypotheses.

Authors:  A F Abraído-Lanza; B P Dohrenwend; D S Ng-Mak; J B Turner
Journal:  Am J Public Health       Date:  1999-10       Impact factor: 9.308

2.  Models to predict cardiovascular risk: comparison of CART, multilayer perceptron and logistic regression.

Authors:  I Colombet; A Ruelland; G Chatellier; F Gueyffier; P Degoulet; M C Jaulent
Journal:  Proc AMIA Symp       Date:  2000

3.  AIDS: the early years and CDC's response.

Authors:  James W Curran; Harold W Jaffe
Journal:  MMWR Suppl       Date:  2011-10-07

4.  HIV/AIDS Knowledge and Beliefs Among Haitian Adolescents in Miami-Dade County, Florida.

Authors:  Louis Herns Marcelin; H Virginia McCoy; Ralph J Diclemente
Journal:  J HIV AIDS Prev Child Youth       Date:  2006

5.  Cervical cancer screening rates in the United States and the potential impact of implementation of screening guidelines.

Authors:  Diane Solomon; Nancy Breen; Timothy McNeel
Journal:  CA Cancer J Clin       Date:  2007 Mar-Apr       Impact factor: 508.702

6.  Health literacy, cervical cancer risk factors, and distress in low-income African-American women seeking colposcopy.

Authors:  Lisa K Sharp; Jill M Zurawski; Phillip Y Roland; Cheryl O'Toole; Jane Hines
Journal:  Ethn Dis       Date:  2002       Impact factor: 1.847

7.  Black Heterogeneity in Cancer Mortality: US-Blacks, Haitians, and Jamaicans.

Authors:  Paulo S Pinheiro; Karen E Callahan; Camille Ragin; Robert W Hage; Tara Hylton; Erin N Kobetz
Journal:  Cancer Control       Date:  2016-10       Impact factor: 3.302

8.  Awareness of Cervical Cancer Causes and Predeterminants of Likelihood to Screen Among Women in Haiti.

Authors:  Schatzi H McCarthy; Kathy A Walmer; Joel C Boggan; Margaret W Gichane; William A Calo; Harry A Beauvais; Noel T Brewer
Journal:  J Low Genit Tract Dis       Date:  2017-01       Impact factor: 1.925

Review 9.  The global burden of women's cancers: a grand challenge in global health.

Authors:  Ophira Ginsburg; Freddie Bray; Michel P Coleman; Verna Vanderpuye; Alexandru Eniu; S Rani Kotha; Malabika Sarker; Tran Thanh Huong; Claudia Allemani; Allison Dvaladze; Julie Gralow; Karen Yeates; Carolyn Taylor; Nandini Oomman; Suneeta Krishnan; Richard Sullivan; Dominista Kombe; Magaly M Blas; Groesbeck Parham; Natasha Kassami; Lesong Conteh
Journal:  Lancet       Date:  2016-11-01       Impact factor: 79.321

10.  Rationale and design of the research project of the South Florida Center for the Reduction of Cancer Health Disparities (SUCCESS): study protocol for a randomized controlled trial.

Authors:  Olveen Carrasquillo; Sheila McCann; Antony Amofah; Larry Pierre; Brendaly Rodriguez; Yisel Alonzo; Kumar Ilangovan; Martha Gonzalez; Dinah Trevil; Margaret M Byrne; Tulay Koru-Sengul; Erin Kobetz
Journal:  Trials       Date:  2014-07-23       Impact factor: 2.279

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