“I did not know it was a medical condition”: Predictors, severity and help seeking behaviors of women with female sexual dysfunction in the Volta region of Ghana
Authors:
Bolade Ibine aff001; Linda Sefakor Ametepe aff001; Maxfield Okere aff003; Martina Anto-Ocrah aff004
Authors place of work:
Obstetrics and Gynecology, University of Health and Allied Sciences, School of Medicine, Ho, Volta Region, Ghana
aff001; Department of Obstetrics and Gynecology, Family Health Medical School, Accra, Ghana
aff002; Department of Biostatistics, Korle Bu Teaching Hospital, Accra, Greater Accra Region, Ghana
aff003; Department of Emergency Medicine University of Rochester School of Medicine and Dentistry, Rochester, New York, United States of America
aff004; Department of Obstetrics and Gynecology, University of Rochester School of Medicine and Dentistry, Rochester, New York, United States of America
aff005; Department of Neurology, University of Rochester School of Medicine and Dentistry, Rochester, New York, United States of America
aff006
Published in the journal:
PLoS ONE 15(1)
Category:
Research Article
doi:
https://doi.org/10.1371/journal.pone.0226404
Summary
Objectives
The study’s main objective was to describe the prevalence and severity of female sexual dysfunction (FSD) amongst a group of Ghanaian women in the outpatient setting of the predominantly rural Volta region of Ghana. Additionally we determine the predictors of FSD severity and care seeking behaviors of women with the condition.
Study design and setting
This was a cross sectional study conducted in the outpatient setting of the Ho Teaching Hospital in the rural-savannah, agro-ecological zone of Volta Region, Ghana.
Methods and procedures
FSD was assessed using the Female Sexual Function Index (FSFI) questionnaire. FSD was defined with a cutoff of ≤23 so as not to under-estimate the prevalence in this conservative setting. FSFI score >23 was designated “no FSD”. We further categorized women with FSD as having mild (FSFI Total score 18–23), moderate (FSFI Total score <18 to >10) or severe (FSFI Total score ≤10) FSD. Due to sample size restrictions, we combined the moderate and severe FSD groups in our analyses and defined “moderate/severe FSD” as an FSFI Total score < 18. Participants with FSD were further asked to indicate whether or not they sought help for their conditions, the reasons they sought help, and the types of help they sought. We used p<0.05 to determine statistical significance for all analyses and logistic regression models were used to determine crude and age-adjusted effect estimates.
Results
FSD Prevalence: Out of 407 women approached, 300 (83.8%) agreed and consented to participate in the study. The prevalence of FSD was 48.3% (n = 145). Compared to those without FSD, over a third of the FSD women resided in rural settings (37.90% vs 20.60%; p = 0.001) and tended to be multiparous, with a significantly greater proportion having at least three children (31.70% vs 18.10%; p = 0.033).
FSD Severity: Over a quarter of the sample (27.6%, n = 40) met the cut-off for moderate to severe FSD. In age-adjusted models, lubrication disorder was associated with 45 times the odds of moderate/severe FSD (age-adj. OR: 45.38, 95% CI: 8.37, 246.00; p<0.001), pain with 17times the odds (age-adj. OR: 17.18, 95% CI: 4.50, 65.50; p<0.001) and satisfaction almost 5times the odds (age-adj. OR: 4.69, 95% CI: 1.09, 20.2; p = 0.04). Compared to those with 1–3 children, nulliparous women had 3.5 times higher odds of moderate/severe sexual dysfunction as well (age-adj. OR:3.51, 95% CI:1.37,8.98; p = 0.009).
FSD-related Health Seeking Behaviors: Statistically significant predictors of FSD-related care seeking included having FSD of pain disorder (age-adj. OR: 5.91, 95% CI:1.29, 27.15; p = 0.02), having ≥4 children (age-adj. OR: 6.29, 95%CI: 1.53, 25.76; p = 0.01). Of those who sought help, seven in 10 sought formal help from a healthcare provider, with General Practitioners preferred over Gynecologist. About one in 3 (31.3%) who did not seek help indicated that they did not know their sexual dysfunction was a medical condition, over a quarter (28.9%) “thought it was normal” to have FSD, and interestingly, 14.1% did not think a medical provider would be able to provide them with assistance.
Conclusions
Sexual dysfunctions are prevalent yet taboo subjects in many countries, including Ghana. Awareness raising and efforts to feminize the physician workforce are necessary to meet the healthcare needs of vulnerable members of Ghanaian society.
Keywords:
Health care providers – Physicians – children – Outpatients – Ghana – Sexual dysfunction – Global health – Lubrication
Introduction
The World Health Organization defines sexuality as a state of physical, emotional, mental and social well-being; a central aspect of “being human” that encompasses the possibility of having pleasurable and safe sexual experiences [1, 2]. Although sexual functioning is an essential aspect of human life, sexual problems are pervasive, and can result in severe consequences for the individual (and potentially their partner), if not addressed. Sexual dysfunction, defined as difficulty experienced by an individual or a couple during any stage of a normal sexual activity, including physical pleasure, desire, preference, arousal or orgasm [3, 4] has been associated with depression and other common mental disorders, relationship discord, poor self-rated health, infertility and overall quality of life [4–11]. Per the published literature, the prevalence of sexual dysfunctions is extremely high, and ranges from 10–63% across various global populations [7, 11–14].
Sexual problems are often multifactorial and can be classified into four broad categories, which are: biomedical (biological factors such as pregnancy, injury and disability, cardiovascular and other chronic diseases that can interfere with intercourse); intrapsychic (psychological elements within the individual, that influence their sexual expression e.g., values learned about one’s body, nudity, “where babies come from”, puberty, etc); interpersonal (factors that influence one’s ability to engage in sexual relationships, such as communication difficulties with a partner, the extent to which partners share compatible visions of sex, eroticism, pleasure etc.); and socio-cultural/economic/political (‘blueprints’ for sexual norms, beliefs, values, practices and attitudes that are created and imposed on an individual based on the ‘moral code’ of their society. Includes religion.) [4, 15]. These four factors often overlap, and rarely occur in isolation to cause the sexual dysfunction [4]. Though sexual dysfunctions are common in both sexes, the greatest morbidity has been reported in women, particularly those in the African region [7]. In many African cultures, the discussion of sexual issues is generally considered a taboo [15, 16]; with conversations of sexuality heavily focused on religion, “moral behavior” and abstinence [15]. The mere mention of sex is often synonymous with deviant behavior [15], suppressing discussions of sexuality as a whole, and sexual dysfunctions in particular. Female sexual dysfunction (FSD), defined as persistent or recurring decrease in a woman’s sexual desire, sexual arousal, painful sex (dyspareunia) and/or difficulty in or inability to achieve orgasm [7, 17], is rarely acknowledged in many societies and cultures [7, 18, 19]; though emerging literature suggests that the condition is quite common amongst African women in particular [7, 20, 21]. In the West African country of Ghana, the prevalence of FSD has been estimated to be as high as 72% [20, 21], 30% higher than the global prevalence [7]. These estimates however, are based on mostly urban heterosexual populations [21], limiting their generalizability to women in rural settings, who may be most vulnerable to adverse gynecological and mental health outcomes [22–25]. Moreover, the landmark evaluation of FSD amongst Ghanaian women [20], was based on a subpopulation of female urology patients, a clinical subgroup that would have greater predisposition for, and higher awareness of the dysfunction [26] than the average Ghanaian woman. Thus current prevalence estimates of FSD in Ghana may have some inherent biases.
The government of Ghana and the Ministry of Health, as part of the national agenda, have adopted sexual health as a component of reproductive health [16, 20]. Emphasis, however, has often been placed on sexually transmitted infections and contraception use, with little attention to, or a total neglect for sexual dysfunctions (SD) [20, 27]. In this paper, we describe the prevalence and severity of FSD amongst a group of Ghanaian women in the outpatient setting of the predominantly rural Volta region of Ghana. We describe the predictors of FSD severity and the care seeking behaviors of women with the condition; in the hopes of identifying possible opportunities for developing contextually appropriate interventions for this subpopulation of women.
Methods
Study Setting
Ghana is a West African country with a population of 26.7 million and an annual gross domestic product (GDP) per capita income of $4,100 [28–31]. With a land mass of 92,099 square miles, the country is comparable in size to the United Kingdom, with its’ western border delineated by the Ivory Coast, the north by Burkina Faso, east by Togo, and the Atlantic Ocean covering its’ southernmost borders [31]. English is the official language, even though Ghanaians and non-Ghanaians of various ethnic, linguistic and religious backgrounds call the country home [28, 32, 33]. Similar to the 50 American states, Ghana is currently divided into 16 regions, with 45% of the population spread over large and rural expanses of land [28, 30, 34–36]. Volta Region, the site of the study, is considered part of the ‘rural-savannah’ agro-ecological zone of the country. The region is the farthest east, and shares boundaries with the Republic of Togo. Over a third of the residents (37.9%) are in rural settings and agriculture and fishery account for 71% of employment [36]. Volta is one of Ghana’s 16 administrative regions, with Ho designated as its capital. The total population of the Ho capital is estimated at 177,281, which represents 8.4% of the region’s total population. Females constitute 53% of the population, and an estimated 26.5% of the 11 and over population have no formal education compared to the national rate of 25.9%; with literacy rates for males being higher than that of females [37, 38].
A convenient sample of women in the outpatient setting of the Ho Teaching Hospital were recruited for this study. The Ho Teaching Hospital is a government-owned, 340-bed capacity hospital, equipped to provide services for several out-and in-patient departments including (but not limited to) surgery, medicine, obstetrics and gynaecology, diagnostics, paediatrics and psychiatry.
Eligibility criteria
All women were encouraged to participate in this cross-sectional study, irrespective of their relationship status. To be eligible, participants had to be consenting adults over the age of 18years, who were seeking care in the outpatient setting of the Ho Teaching Hospital during the period of data collection, which spanned April 17th 2019 to May 22nd 2019. Women who were admitted, or had major mental or cognitive impairment, speech impairment and major morbidity like stroke and psychiatric illness were excluded from the study, as were those who refused consent. The study was approved by the University of Health and Allied Sciences’ Research Ethics Committee, with permission obtained from the Ho Teaching Hospital administration. As specified and approved by the University of Health and Allied Sciences’ Research Ethics Committee, we obtained written consent from all participants to conduct this study. All consent forms were kept separately from the de-identified survey questionnaires, in a secure location under the supervision of the final author. Keeping the signed consents separate from the survey questionnaires was to ensure that participants’ responses could not be connected to their identities.
Sample size determination
Based on a prevalence estimate of 72%, an alpha of 0.05 and a 95% confidence interval, an estimated sample size of 301 was required to complete the study [39].
Data collection instrument & measures
Demographics
A standard questionnaire (see Appendix) was used to collect socio-demographic data about participants’ demographic (age, educational attainment, employment status, religious affiliation, residential setting), relational (marital status, parity), and recruitment (i.e. outpatient department recruited from e.g. surgery, medicine, obstetrics and gynaecology, etc.) characteristics.
Sexual functioning
Female sexual function was assessed using the 19-item Female Sexual Function Index (FSFI) questionnaire [11, 40, 41]. With an internal consistency of 0.89–0.96, the FSFI is the most frequently used questionnaire for assessing FSD in various populations across the literature [11, 41]. The measure has been deemed reliable for Ghanaian populations, and used previously in clinical, community and population-based assessments of sexual functioning in Ghanaian women [18, 21]. The FSFI evaluates six domains of female sexual functioning: desire (2 items:Q1,Q2), arousal (4 items:Q3-Q6), lubrication (4 items: Q7-Q10), orgasm (3 items: Q11-Q13), satisfaction (3 items: Q14-Q16) and pain (3 items: Q17-Q19) during sexual intercourse. Study participants are asked to choose the response option that best suited their sexual function during the past four weeks. Scores for items 3–14 and 17–19 range from 0 (“No Sexual Activity”) to 5 (“Very high” or “Almost always/ Always”), and for items 1, 2, 15 and 16, range from 1 (“Almost never/Never” or “Very low/None at all” to 5 (“Very high/satisfied” or “Almost always/Always”). Each domain is ascribed a factor (0.6 for desire, 0.3 for arousal & lubrication, and 0.4 for orgasm, satisfaction and pain) [11, 40, 41]. The scores for each domain are calculated by adding the scores of the individual domain items and multiplying the sum by the domain factor. Total score is obtained by adding the six domain scores. The full-scale score range is from 2.0 to 36.0, with lower scores indicative of poor sexual functioning. Since the typical cutoff of FSFI score of ≤26.55 for FSD is less sensitive in conservative settings, we used an FSFI score ≤23 to designate FSD [11], so as not to underestimate the FSD prevalence. Thus women with FSD had an FSFI Total score of 23 or lower, and “no FSD” was designated as an FSFI Total score >23. We further used the following criteria to categorize FSD severity [11]: mild FSD (FSFI Total score 18–23), moderate FSD (FSFI Total score <18 to >10), severe FSD (FSFI Total score ≤10). Due to sample size restrictions, we combined the moderate and severe FSD groups in our analyses and defined “moderate/severe FSD” as an FSFI Total score below 18.
Help seeking behaviors
Participants with FSD were further asked to indicate whether or not they sought help for their sexual dysfunction, the reasons they sought help, and the types of help sought. Help sought from medical providers were designated as “formal help” whereas “Informal help” was ascribed to friends, family and prayer camps. Responses of “Other” were prompted for further elaboration.
All surveys were interviewer led and completed in-person (i.e. face-to-face) with each respondent. A translated version of the questionnaire was used for those who were not English speaking. The questionnaire was translated into the local dialect, pre-tested to ensure accuracy of translation, and administered by trained study personnel. All interviews were conducted in a screen-protected and discrete study-designated area of the outpatient departments of the Ho Teaching Hospital where the study was conducted. Though there are many languages spoken in the Volta region, from our training and pre-testing phases preparatory to the study, we found most respondents could comfortably speak Ewe, Twi, English or combinations of these. We pretested the survey questionnaire in the following two steps: i) Interviewing of random respondents within the Ho Teaching Hospital to determine participants’ language preferences and to ensure uniformity among study personnel, and 2) under the supervision of the senior author (BI), interviewers practiced administering the survey to ensure consistency of delivery and translation of questions by all study personnel.
Statistical analyses
We considered in our analyses, several covariates that are associated with sexual functioning, including age, relationship status, parity, education, religious affiliation and residential setting (urban/rural). Univariate analyses and descriptive statistics were used to examine the frequencies and distributions of the study population by FSD group (Has FSD/No FSD), domain (desire, arousal, lubrication, orgasm, satisfaction, pain) and severity (mild, moderate, severe). Categorical variables were compared using chi-square (Х2) or Fisher’s Exact tests, where appropriate, while comparisons of continuous outcomes were done using t-tests and Anova estimates, with a parametric distribution of FSD in the study sample.
Age was found to be associated with several other covariates and predictors, and was the most significant predictor of FSD outcome in this study. Adjusting for age only in logistic regression analyses gave us the most parsimonious models. Thus in our logistic regression models, we present both crude and age-adjusted effect estimates. All computations were done at the 95% confidence level, and we report odds ratios and their associated 95% confidence intervals. We used p <0.05 to determine statistical significance for all analyses.
Results
Demographics and FSD prevalence
Of 407 women approached, 341 (83.8%) agreed and consented to participate in the study. Fourty one (12%) had incomplete questionnaires, where subjects declined further participation because they found the questionnaire exhausting or intrusive or because of time constraints. The attributes of the final 300 subjects are presented in Table 1. The majority of participants were recruited from the Gynecological and General Outpatient departments of the Ho Teaching Hospital. As depicted, the prevalence of FSD was 48.3% (n = 145), with women who endorsed the dysfunction being significantly older than those without the dysfunction (mean age 34.0(+/-9.5) versus 29.3(+/-6.7) years; p<0.001). Of the women with FSD, the majority (73.8%) were below the age of 40, with most (42.1%) spanning ages 30 and 39 years, and about a third (31.7%) between ages 18 and 29. Approximating the rural population of the Volta Region, over a third of the FSD women resided in rural settings (37.9% vs 20.6% p = 0.001) and tended to be multiparous, with a significantly greater proportion having at least three children (31.7% vs 18.1; p = 0.033), compared to those without FSD.
There were also significant differences in education between the groups. Three out of every 25 women with FSD (12.4%) had no formal education, compared to 1 in 25 (3.9%) uneducated women in the “No FSD” group; and the proportion of those with tertiary education was also lower for FSD women compared to those without the dysfunction (31.7% vs 50.3%; p = 0.002). The employment rates for women in the FSD group was slightly higher than those without the dysfunction, though the difference was not statistically significant (77.9% vs 70.3%; p = 0.148).
Amongst women with FSD, the most commonly endorsed domains were Desire (97.2%), Orgasm (82.8%) and Arousal (80.0%), with one in five (20%) women endorsing dysfunctions in all 6 domains. Forty women (27.6%), representing over a quarter of the sample, met the cut-off for moderate to severe FSD. Women with severe FSD were on average, significantly younger than the rest of the group (Fig 1). Six in 10 (63.6%) women with severe FSD was between the ages of 18 and 29; and 91% of all women with severe FSD were under the age of 40 (Fig 1). These age distributions were significantly greater than any of the others groups’.
Age was found to be associated with several other covariates and predictors, and was the most significant predictor of FSD outcome in this study. Adjusting for age only in logistic regression analyses gave us the most parsimonious models, thus Table 2 shows crude and age-adjusted effect estimates for the predictors of FSD severity.
FSD severity
In both crude and age-adjusted models, women with lubrication, pain and satisfaction disorders had statistically greater odds of reporting moderate/severe FSD (Table 2). Lubrication disorder was associated with 45 times the odds of moderate/severe FSD (95% CI: 8.37, 246.00; p<0.001) whilst pain (OR: 17.18, 95% CI: 4.50, 65.50; p<0.001) and satisfaction (OR: 4.69, 95% CI: 1.09, 20.20; p = 0.04) were lower in comparison, but highly significant. Compared to those with 1–3 children, women at both ends of the parity spectrum had higher odds of moderate/severe sexual dysfunction; though the effect estimate for those with no children (OR: 3.51; 95% CI: 1.37, 8.98; p = 0.009) was much greater than those with 4 or more offspring (OR:1.64; 95% CI: 0.61, 4.39; p = 0.32). It is important to note that 21.0% (n = 19) of women with no children were married.
Lower educational attainment and residing in a rural setting were, surprisingly, protective for moderate/severe FSD. At all levels of education, FSD women without tertiary training had consistently lower odds of reporting moderate/severe sexual dysfunction compared to those with university level education or higher. Residing in a rural setting was also associated with lower odds of moderate/severe FSD, though residential setting was not a significant predictor of the outcome.
Care seeking behaviors
Out of the 145 women with FSD, 17 (11.7%) sought help for their dysfunction (Table 1). Statistically significant predictors of FSD-related care seeking, depicted in Table 3, included dissatisfied (age-adj. OR: 0.30, 95% CI: 0.10, 0.86; p = 0.03) or painful sex (age-adj OR: 5.91, 95% CI:1.29, 27.15; p = 0.02), having 4 more children (age-adj OR: 6.29; 95% CI: 1.53, 25.76; p = 0.01), or residing in a rural setting (age-adj. OR: 2.87, 95%CI: 1.00, 8.24; p = 0.05).
Eight in ten women (82.4%) were prompted to seek help due to the emotional strain of the sexual dysfunction, 12% cited relationship strain as a prompt for their care-seeking, and one woman (5.8%) sought help upon the advice of her pastor (Table 3). Of those who sought help, seven in 10 sought formal assistance from a healthcare provider, with the majority (83%) consulting a General Practitioner for their dysfunctions; and only 16.7% seeking the care of a Gynecologist.
Of the 128 women with FSD who did not seek help, about one in 3 (31.3%) indicated that they did not know their sexual dysfunction was a medical condition. Over a quarter (28.9%) “thought it was normal” to have FSD, and interestingly, 14.1% did not think a medical provider would be able to provide them with assistance.
Discussion
Though human sexual function has requisite biological underpinnings, it is usually experienced as a complex interaction of biological, intrapsychic, interpersonal and socio-cultural/economic/political factors [4, 15]. In many parts of the world, sexuality is considered a sensitive topic, and sexual discussions-whether they be of displeasure or not, are discouraged. Female sexuality is especially taboo; particularly in religious countries like Ghana. Thus women with pathological disorders in sexual functioning may not seek and/or receive the diagnosis and treatment that they may need for their clinically diagnosable and treatable sexual disorders. This is the first study that to our knowledge, evaluates the prevalence, severity and help-seeking behaviors of women with FSD in the mostly rural and agrarian setting of the Volta region of Ghana. Almost half of the women in our study met the cutoff for female sexual dysfunction. The FSD prevalence estimate of 48.3% in our study, approximates the global prevalence of 40.9% [7] and is similar to rates reported for non-clinical, mostly urban Ghanaian females in heterosexual relationships (45.6%) who hailed from the Greater Accra, Ashanti, Western, Central, Brong-Ahafo and Eastern regions. [21]. Though often shrouded in taboo and stigma, research shows that sexual and reproductive health is fundamental to the economic development of nations, to people’s health and survival, and to the wellbeing of humanity [42]. Compared to those in urban settings and of higher socio-economic status, women in rural settings, and those of lower socio-economic standing, tend to be more vulnerable to adverse physical, mental, obstetric and gynecological health outcomes [22, 43–53]. They often report poorer self-rated mental and physical health [43, 52], have less access to necessary obstetric care [22, 46, 47, 50], and have higher rates of trauma and mortality [23, 24, 46, 54–59]. Poor sexual functioning may further exacerbate these and other adverse health conditions in this subpopulation. Not surprisingly, women with FSD in our study were most likely to be rural residents, have lower educational attainment and on average, have more children than those without sexual dysfunctions. Given the associations between sexual health, economic growth and overall population health, future studies should engage government stakeholders and policy makers to incorporate sexual dysfunctions as a core component of the government’s reproductive health agenda. The Ministry of Health’s reproductive health policy could be expanded beyond the prevention of unwanted pregnancies and sexually transmitted infections [15, 16, 20] to more holistically encourage providers to discuss sexual health and sexual dysfunctions (both male and female forms) with their patients. We acknowledge that such a recommendation would require an enormous psycho-socio-cultural shift across all facets of the country’s healthcare system, but
without such a strategy, it will be difficult to recognize the discriminant impact that sexual dysfunctions have on some of the most vulnerable members of Ghanaian society.
It is often assumed that sexual dysfunctions in women are associated with increasing age, the onset of menopause, and several associated hormonal changes [5, 6, 13, 60–65]. However, our results show that FSD is quite common in premenopausal women, particularly those between the ages of 18 and 39 years. Women in this age group were most likely to report that their FSD was severe, with lubrication disorders being the most common disturbance. Compared to those who did not endorse problems with lubrication, women with lubrication disorders had close to 50 times the odds of reporting moderate/severe sexual dysfunction. These findings are similar to those reported by Imbeah et al [21], who reported that 72% of Ghanaian women surveyed in their six region study, cited lubrication difficulties as causes of their dysfunctions. The root cause of FSD for these “young” women may have less to do with age and/or biological changes in hormonal regulation, and are most likely attributable to the physical/mechanical stress imposed on the vaginal tissue during sexual encounters. For women, vaginal lubrication is an important part of sex [66]. Lubrication readies the vagina for penetration, and reduces any accompanying friction or irritation during intercourse [4, 66, 67]. Without adequate lubrication, the frictional force imposed on the delicate vaginal tissue can result in bruising and tearing [66], which may lead to infections, painful sexual experiences and overall dissatisfaction with sex. Not surprisingly, lubrication, pain and satisfaction were the three FSD domains most associated with FSD severity in our study. And although sexual pain was the only statistically significant predictor of FSD-associated care seeking behavior, likely at the root of the woman’s dyspareunia is inadequate lubrication. Though lubrication usually occurs naturally, some women become more lubricated than others [66]. It is important that women and their partners understand the role that lubrication plays in comfortable intercourse to reduce the woman’s susceptibility for infections, as well as their painful sexual experiences. More studies are needed to evaluate the access, utilization and perception of personal lubricants amongst Ghanaian women and couples.
In our study, Women with FSD often normalized their dysfunctions, with one in three women indicating that they did not know that FSD was a medical condition and 14% noting that a healthcare provider would not be able to resolve their issue. These results again echo the findings of Imbeah and team [21] who indicated that 50%(n = 80) of the women in their study did not seek help because they were under the impression that FSD was normal, and 19.2% (n = 31) were embarrassed to seek help. Through targeted educational efforts, Ghanaian women should be made aware that persistent or recurring decreases in a woman’s sexual desire, sexual arousal, painful sex (dyspareunia) and/or difficulty in or inability to achieve orgasm [7, 17] is a medical condition that can be treated by healthcare providers. This awareness raising is necessary, given that 82.4% of those who sought help in our study point to emotional strain as their reasons for seeking care for their sexual dysfunction. These women fit the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) criteria for the clinical diagnosis of FSD [3, 68–70], and would require referral and treatment by an appropriate healthcare provider. Appropriately, most women in our study sought formal help from a General Practitioner (GP) or a Gynecologist for their conditions.
Ghana, like most countries, is undergoing a gender redistribution of the physician workforce [71–74]. The estimated 1:8,481 patient to provider ratio [75] has traditionally tipped in favor of male doctors [76–79], including Obstetric/Gynecologists (ObGyns) [80], even though there is ample literature to support the notion that women, particularly those in conservative cultures, prefer female OB-GYNs, given the intimacy of the services rendered by these providers [81–83]. Research shows that when patients are treated by physicians “who look like them” or have life experiences that closely match that of their patients’, patients perceive their care to be of higher quality, are more satisfied with their care, have greater adherence to medical advice, and overall, have better health outcomes [84–88]. Providers also show a preference for same-gender consultations for sexual health matters [89].The global trend towards feminization of the healthcare workforce promises to bring changes to the patient–physician relationship, the local delivery of care, the global delivery of care to the society as a whole, as well as to the medical profession itself [72, 74]. Female physicians it has been shown, spend more time with their patients [72, 74, 90], write fewer prescriptions and are more attuned to their patients’ needs enough to refer more cases to specialists than their male colleagues [72, 74, 91]. The female patient may be more comfortable raising sexual concerns with a female physician. There is however, a glaring male dominance of the ObGyn specialty in Ghana, with less than 10% female representation among practicing gynecologists [92]. Improving the gender balance of the Ghanaian physician workforce would decrease the patient:provider gender mismatch, and potentially improve discussions around the traditionally taboo details of female sexuality. Feminization could result in more women being screened by their GPs, and referred to ObGyns for proper diagnosis and treatment. Gender redistribution of Ghanaian doctors is a necessary step in reducing the “personal embarrassment” associated with women’s reluctance to seek help for their sexual dysfunctions, as reported by our study participants. More female doctors are needed to provide care for the majority female Ghanaian population [35] and serve the needs and priorities of the health system. Transitioning to this model of care however, may take a long time to achieve, as it requires not only an attitudinal and cultural shift in the existing healthcare infrastructure, but may also require a dismantling of pre-existing institutional and structural barriers. Bridging this transition, may be a healthcare model that utilizes Advanced Practice Providers (APPs) such as nurse midwives, who often serve as primary caregivers for patients with obstetric and gynecological needs. Not only is the provider:patient ratio higher for these APPs, but the gender balance between patients and providers is not as disproportional. Nurse midwives could be trained to screen for FSD as part of their “routine” patient care; relieving the workload expectations of other providers.
In spite of these healthcare workforce trends, providers, male or female, should be made aware of and encouraged to discuss sexual health and sexual dysfunctions with their patients. Insufficient assessment of sexual health concerns by Physicians, is at the core of the barriers against appropriate diagnosis and outcome of FSD. Literature has emphasized the inconsistent and avoidant approach by providers to exploring women’s sexual concerns [26, 93, 94]. Often times, the burden of reporting embarrassing symptoms and diagnosing of a dysfunction is shifted to the patient [26, 89, 95, 96]. The physician is often unintentionally constrained by multifaceted reasons, prominent among which is confidence in assessment skills. In Ghana, the ObGyn is expected in most cases, to deal with female reproductive and sexual health concerns. Hence the GP and other providers rarely explore detailed sexual history or lack proactivity and social empathy for discussing and identifying clients with sexual health needs. In addition to raising the awareness of patients about the detriments of FSD, there is a corresponding need to improve social empathy, assessment and management skills of Ghanaian physicians, particularly non-ObGyns, who often serve as the first point of contact for patients suffering from the condition.
Because of the social stigma around female sexuality, women tend to avoid and/or are embarrassed to discuss their sexual health with their health care professionals (HCPs) [94]. HCPs-both physicians and APPs-can be trained to improve their empathetic responses to their patients’ sexual frustrations by initiating (and maintaining) a sexual health conversation in a manner that is comfortable for the woman to convey her concerns. This initial step is crucial to the trust building necessary for the trained provider to assess the patient, diagnose, treat and manage their FSD [89, 93, 94]. These tools-educating women, training HCPs, and providing communication tools to HCPs-may serve to decrease the stigma associated with sexual health discussions, and facilitate the treatment-oriented dialogue between patients and their providers when dealing with FSDs [94].
Strengths and limitations
This study, to our knowledge is the first of its kind in the rural-savannah, agro-ecological zone of Ghana’s Volta region. Even though most of the study participants were recruited from the Gynecological and General Outpatient departments, we had representation from women in the Surgical, Dental, Ear/Nose/Throat and Ophthalmology departments as well. Our study did not exclude single women, or women who were not in heterosexual relationships, making our findings generalizable to a broad reach of Ghanaian women with varying sexual and relationship experiences. Despite these strengths, our study has a few limitations that bear mentioning. Firstly, restricting the study to women 18 years and older limits the generalizability of our findings to females below this age, particularly teenagers, whose sexual health tends to be under-studied in the Ghanaian context. The sexual experiences of the average Ghanaian teenager may be higher and more likely to be deemed “immoral” [19] than that of the “older” female; putting such adolescents at greater risk for gynecological infections, psychological distress and other FSD-related sequelae. More research is needed to better understand the impact of sexual dysfunctions across the spectrum of a Ghanaian woman’s reproductive years. Another limitation of our study is in the sample size limitations imposed upon our analyses. Even though the study was well powered at a prevalence estimate of 72%, the low prevalence of moderate/severe FSD (27.6%, n = 40) resulted in wide and imprecise confidence intervals for the effect estimates in our adjusted analyses. This estimate, as discussed earlier, is likely over-estimated and reflects the prevalence amongst a care-seeking subpopulation of urology patients. The prevalence rate of our sample is in line with other non-clinical Ghanaian populations [18, 21], and also in range with global FSD prevalence estimates [7]. Studies that are powered at the lower prevalence estimates of our findings may yield more robust results from larger studies, that reflect the true population estimates. Such studies are needed to replicate and validate the current findings. Finally, our study does not account for differences in FSD outcomes based on the women’s pregnancy status or sexual preferences. Though the FSFI was designed to be used non-discriminately, and has in fact been used to evaluate FSD outcomes in pregnant and non-pregnant heterosexual, lesbian and bisexual populations [13, 97–99], because we do not explicitly compare outcomes within these subgroups in our study, the findings should be interpreted cautiously. As is common in most sexuality studies, our results may be more reflective of a heterosexual majority and/or those with less conservative sexual attitudes and values [4, 100], than that of sexual minorities and/or others with conservative sexual attitudes. This is particularly salient in a country like Ghana, where overt discussions of sexual matters are frowned upon [15]. Those who are most reticent about sexual issues may be most vulnerable to adverse sexual outcomes, and may require greater clinical interventions. Thus future studies should attempt to evaluate FSD outcomes in pregnant Ghanaian women, as well as non-heterosexual individuals, who may have these and other unique challenges. Future research endeavors should also consider qualitative research methodologies that will better contextualize and support the study findings, through the use of narratives and theoretical frameworks. The contribution of this paper may be better appreciated if it were supported with qualitative theories/frameworks/models.
Conclusions
The study’s main objective was to describe the prevalence and severity of female sexual dysfunction (FSD) amongst a group of Ghanaian women in the outpatient setting of the predominantly rural Volta region of Ghana. Additionally we determine the predictors of FSD severity and care seeking behaviors of women with the condition.
We found that FSD is highly prevalent amongst women in rural settings of the Ghanaian community, with lubrication, pain and satisfaction disorders being the most associated with severity. These conditions leave women vulnerable to preventable sexually transmitted infections, physical pain and psychological distress. Most women deem the dysfunctions to be normal, and are unaware that FSD is a clinically diagnosable condition that can be treated by expert physicians. In order to attain the World Health Organization’s agenda of “Health for All” by the year 2030 [101, 102], sexual dysfunctions should be incorporated into Ghana’s national health agenda to improve the health of some of the most vulnerable members of Ghanaian society.
Appendix
DATA COLLECTION TOOL
FEMALE SEXUAL DYSFUNCTION: PREVALENCE AND HELP- SEEKING BEHAVIOUR AMONG WOMEN ATTENDING THE HO TEACHING HOSPITAL OUT–PATIENT DEPARTMENT.
Section A
Demographic Data of Participant
Part A
A1. AGE: ………………………
A2. MARITAL STATUS: single (), married (), cohabiting (), deceased ()
A3.RELIGIOUS AFFILIATION: Christianity () Islam () others ()
A4.EDUCATIONAL LEVEL: no education () JHS () High School () Tertiary ()
A5.EMPLOYMENT STATUS: employed () unemployed ()
A6.OCCUPATION…………………………………
A7.AVERAGE MONTHLY INCOME: GHS………….
A8.NUMBER OF CHILDREN …………….
A9.NUMER OF DEPENDANTS……………….
A10.PLACE OF RESIDENCE…………………………..
A11.CLINIC SPECIALTY (OPD in what specialty)…………………………………………
Part B
B1. Over the past 4 weeks, how often did you feel sexual desire or interest?
5 = Almost always or always
4 = Most times (more than half the time)
3 = Sometimes (about half the time)
2 = A few times (less than half the time)
1 = Almost never or never
B2. Over the past 4 weeks, how would you rate your level (degree) of sexual desire or interest?
5 = Very high
4 = High
3 = Moderate
2 = Low
1 = Very low or none at all
B3. Over the past 4 weeks, how often did you feel sexually aroused ("turned on") during sexual activity or intercourse?
0 = No sexual activity
5 = Almost always or always
4 = Most times (more than half the time)
3 = Sometimes (about half the time)
2 = A few times (less than half the time)
1 = Almost never or never
B4. Over the past 4 weeks, how would you rate your level of sexual arousal ("turn on") during sexual activity or intercourse?
0 = No sexual activity
5 = Very high
4 = High
3 = Moderate
2 = Low
1 = Very low or none at all
B5. Over the past 4 weeks, how confident were you about becoming sexually aroused during sexual activity or intercourse?
0 = No sexual activity
5 = Very high confidence
4 = High confidence
3 = Moderate confidence
2 = Low confidence
1 = Very low or no confidence
B6. Over the past 4 weeks, how often have you been satisfied with your arousal (excitement) during sexual activity or intercourse?
0 = No sexual activity
5 = Almost always or always
4 = Most times (more than half the time)
3 = Sometimes (about half the time)
2 = A few times (less than half the time)
1 = Almost never or never
B7. Over the past 4 weeks, how often did you become lubricated ("wet") during sexual activity or intercourse?
0 = No sexual activity
5 = Almost always or always
4 = Most times (more than half the time)
3 = Sometimes (about half the time)
2 = A few times (less than half the time)
1 = Almost never or never
B8. Over the past 4 weeks, how difficult was it to become lubricated ("wet") during sexual activity or intercourse?
0 = No sexual activity
1 = Extremely difficult or impossible
2 = Very difficult
3 = Difficult
4 = Slightly difficult
5 = Not difficult
B9. Over the past 4 weeks, how often did you maintain your lubrication ("wetness") until completion of sexual activity or intercourse?
0 = No sexual activity
5 = Almost always or always
4 = Most times (more than half the time)
3 = Sometimes (about half the time)
2 = A few times (less than half the time)
1 = Almost never or never
B10. Over the past 4 weeks, how difficult was it to maintain your lubrication ("wetness") until completion of sexual activity or intercourse?
0 = No sexual activity
1 = Extremely difficult or impossible
2 = Very difficult
3 = Difficult
4 = Slightly difficult
5 = Not difficult
B11. Over the past 4 weeks, when you had sexual stimulation or intercourse, how often did you reach orgasm (climax)?
0 = No sexual activity
5 = Almost always or always
4 = Most times (more than half the time)
3 = Sometimes (about half the time)
2 = A few times (less than half the time)
1 = Almost never or never
B12. Over the past 4 weeks, when you had sexual stimulation or intercourse, how difficult was it for you to reach orgasm (climax)?
0 = No sexual activity
1 = Extremely difficult or impossible
2 = Very difficult
3 = Difficult
4 = Slightly difficult
5 = Not difficult
B13. Over the past 4 weeks, how satisfied were you with your ability to reach orgasm (climax) during sexual activity or intercourse?
0 = No sexual activity
5 = Very satisfied
4 = Moderately satisfied
3 = About equally satisfied and dissatisfied
2 = Moderately dissatisfied
1 = Very dissatisfied
B14. Over the past 4 weeks, how satisfied have you been with the amount of emotional closeness during sexual activity between you and your partner?
0 = No sexual activity
5 = Very satisfied
4 = Moderately satisfied
3 = About equally satisfied and dissatisfied
2 = Moderately dissatisfied
1 = Very dissatisfied
B15. Over the past 4 weeks, how satisfied have you been with your sexual relationship with your partner?
5 = Very satisfied
4 = Moderately satisfied
3 = About equally satisfied and dissatisfied
2 = Moderately dissatisfied
1 = Very dissatisfied
B16. Over the past 4 weeks, how satisfied have you been with your overall sexual life?
5 = Very satisfied
4 = Moderately satisfied
3 = About equally satisfied and dissatisfied
2 = Moderately dissatisfied
1 = Very dissatisfied
B17. Over the past 4 weeks, how often did you experience discomfort or pain during vaginal penetration?
0 = Did not attempt intercourse
1 = Almost always or always
2 = Most times (more than half the time)
3 = Sometimes (about half the time)
4 = A few times (less than half the time)
5 = Almost never or never
B18. Over the past 4 weeks, how often did you experience discomfort or pain following vaginal penetration?
0 = Did not attempt intercourse
1 = Almost always or always
2 = Most times (more than half the time)
3 = Sometimes (about half the time)
4 = A few times (less than half the time)
5 = Almost never or never
B19. Over the past 4 weeks, how would you rate your level (degree) of discomfort or pain during or following vaginal penetration?
0 = Did not attempt intercourse
1 = Very high
2 = High
3 = Moderate
4 = Low
5 = Very low or none at all
Part c
C1.Did you seek for help when you experienced the female sexual dysfunction?
Yes [] No []
C2. If no to C1, why didn’t you seek for help?
Health provider cannot help me [] time constraints []
Others………………………………
c3. If yes to C1, where did you seek help from?
Gynecologist () general practitioner () Herbalist () friends () family () Prayer camp ()
Others…………………
C4. If yes to C1, why did you seek help?
Advised to by relatives/friends/pastor [] Referred from a formal healthcare personnel [] condition is causing relationship/marriage strains [] condition is causing emotional strains []
Others……………………………………………………
Supporting information
S1 File [zip]
Female Sexual Dysfunction Data_Deidentified for submission.
Zdroje
1. World Health Organization. Sexual and reproductive health: Defining Sexual Health. 2006a 7/16/2019]; Available from: https://www.who.int/reproductivehealth/topics/sexual_health/sh_definitions/en/.
2. Sandfort T.G. and Ehrhardt A.A., Sexual health: a useful public health paradigm or a moral imperative? Arch Sex Behav, 2004. 33(3): p. 181–7. doi: 10.1023/B:ASEB.0000026618.16408.e0 15129037
3. Association, A.P., Highlights of Changes from DSM-IV-TR to DSM-5. 2013.
4. McAnulty Richard D and Burnette M. Michele, Sex and Sexuality: Sexual function and dysfunction. 2006, Greenwood Press: Westport, CT [u.a.].
5. Nappi R.E. and Lachowsky M., Menopause and sexuality: prevalence of symptoms and impact on quality of life. Maturitas, 2009. 63(2): p. 138–41. doi: 10.1016/j.maturitas.2009.03.021 19464129
6. Nappi R.E., Cucinella L., Martella S., Rossi M., Tiranini L., and Martini E., Female sexual dysfunction (FSD): Prevalence and impact on quality of life (QoL). Maturitas, 2016. 94: p. 87–91. doi: 10.1016/j.maturitas.2016.09.013 27823751
7. McCool M.E., Zuelke A., Theurich M.A., Knuettel H., Ricci C., and Apfelbacher C., Prevalence of Female Sexual Dysfunction Among Premenopausal Women: A Systematic Review and Meta-Analysis of Observational Studies. Sex Med Rev, 2016. 4(3): p. 197–212. doi: 10.1016/j.sxmr.2016.03.002 27871953
8. Smith N.K., Madeira J., and Millard H.R., Sexual function and fertility quality of life in women using in vitro fertilization. J Sex Med, 2015. 12(4): p. 985–93. doi: 10.1111/jsm.12824 25639162
9. Smith L.J., Mulhall J.P., Deveci S., Monaghan N., and Reid M.C., Sex after seventy: a pilot study of sexual function in older persons. J Sex Med, 2007. 4(5): p. 1247–53. doi: 10.1111/j.1743-6109.2007.00568.x 17727349
10. Flynn K.E., Lin L., Bruner D.W., Cyranowski J.M., Hahn E.A., Jeffery D.D., Reese J.B., Reeve B.B., Shelby R.A., and Weinfurt K.P., Sexual Satisfaction and the Importance of Sexual Health to Quality of Life Throughout the Life Course of U.S. Adults. J Sex Med, 2016.
11. Safarinejad M.R., Female sexual dysfunction in a population-based study in Iran: prevalence and associated risk factors. Int J Impot Res, 2006. 18(4): p. 382–95. doi: 10.1038/sj.ijir.3901440 16395324
12. Laumann E.O., Paik A., and Rosen R.C., Sexual dysfunction in the United States: prevalence and predictors. JAMA, 1999. 281(6): p. 537–44. doi: 10.1001/jama.281.6.537 10022110
13. West S.L., Vinikoor L.C., and Zolnoun D., A systematic review of the literature on female sexual dysfunction prevalence and predictors. Annu Rev Sex Res, 2004. 15: p. 40–172. 16913279
14. Rahman S., Female Sexual Dysfunction Among Muslim Women: Increasing Awareness to Improve Overall Evaluation and Treatment. Sex Med Rev, 2018. 6(4): p. 535–547. doi: 10.1016/j.sxmr.2018.02.006 29678473
15. John Kwasi Anarfi and Adobea Yaa Owusu, The Making of a Sexual Being in Ghana: The State, Religion and the Influence of Society as Agents of Sexual Socialization. Sexuality & Culture, 2010. 15(1): p. 1–18.
16. Adanu R.M., Seffah J., Anarfi J.K., Lince N., and Blanchard K., Sexual and reproductive health in Accra, Ghana. Ghana medical journal, 2012. 46(2): p. 58–65. 22942453
17. Basson R., Berman J., Burnett A., Derogatis L., Ferguson D., Fourcroy J., Goldstein I., Graziottin A., Heiman J., Laan E., et al., Report of the international consensus development conference on female sexual dysfunction: definitions and classifications. J Urol, 2000. 163(3): p. 888–93. 10688001
18. Erica Goldstein and Charles Takyi, Female Sexual Dysfunction:Prevalence and Risk in Ghana. November 2015: Physicians For Human Rights National Student Conference
19. Fiaveh D.Y. and Okyerefo Michael PK, Femininity, Sexual Positions and Choice. Sexualities, 2019. 22(1–2): p. 131–147.
20. Amidu N., Quaye L., Afoko A.A., Karikari P., Gandau B.B., Amoah E.O., and Nuwoku E., Golombok Rust Inventory of Sexual Satisfaction for the presence of sexual dysfunction within a Ghanaian urological population. Int J Impot Res, 2014. 26(4): p. 135–40. doi: 10.1038/ijir.2013.52 24430277
21. Imbeah Emelia P, Afrane Barima A, Kretchy Irene A, Sarkodie Joseph A, Acheampong Franklin, Oppong Samuel and Amoateng Patrick, Prevalence and Self-Management of Female Sexual Dysfunction among Women in Six Regions of Ghana: A Cross-Sectional Study. J Womens Health Issues Care, 2015. 4(6).
22. Thaddeus S. and Maine D., Too far to walk: maternal mortality in context. Soc Sci Med, 1994. 38(8): p. 1091–110. doi: 10.1016/0277-9536(94)90226-7 8042057
23. Kyei-Nimakoh M., Carolan-Olah M., and McCann T.V., Access barriers to obstetric care at health facilities in sub-Saharan Africa-a systematic review. Syst Rev, 2017. 6(1): p. 110. doi: 10.1186/s13643-017-0503-x 28587676
24. Say L., Chou D., Gemmill A., Tuncalp O., Moller A.B., Daniels J., Gulmezoglu A.M., Temmerman M., and Alkema L., Global causes of maternal death: a WHO systematic analysis. Lancet Glob Health, 2014. 2(6): p. e323–33. doi: 10.1016/S2214-109X(14)70227-X 25103301
25. Cong J., Li P., Zheng L., and Tan J., Prevalence and Risk Factors of Infertility at a Rural Site of Northern China. PLoS One, 2016. 11(5): p. e0155563. doi: 10.1371/journal.pone.0155563 27177147
26. Roos A.M., Sultan A.H., and Thakar R., Sexual problems in the gynecology clinic: are we making a mountain out of a molehill? Int Urogynecol J, 2012. 23(2): p. 145–52. doi: 10.1007/s00192-011-1516-y 21796468
27. Ghana Health Service; Family Health Division. 7/16/2019]; Available from: http://www.ghanahealthservice.org/division-scat.php?ghsdid=2&ghsscid=26.
28. United States Central Intelligence Agency. CIA World Factbook. 2018 9/28/2018]; Available from: https://www.cia.gov/library/publications/the-world-factbook/geos/gh.html.
29. Zakariah A., Stewart B.T., Boateng E., Achena C., Tansley G., and Mock C., The Birth and Growth of the National Ambulance Service in Ghana. Prehosp Disaster Med, 2017. 32(1): p. 83–93. doi: 10.1017/S1049023X16001151 27938469
30. Ghana Health Service and Center for Health and Information Management subdivision of the Policy Planning, Monitoring and Evaluation Division (PPMED) of the Ghana Health Service, The Health Sector in Ghana Facts and Figures 2016, Technical Working Group of the Center for Health and Information Management subdivision of the Policy Planning, Monitoring and Evaluation Division (PPMED) of the Ghana Health Service, and World Health Organization, Editors. 2016: Accra, Ghana.
31. World Population Review. Ghana Population 2019. 2019 7/17/2019]; Available from: http://worldpopulationreview.com/countries/ghana-population/.
32. Ghana Statistical Service. 2010 Population Projection by Sex, 2010–2016. 2018 9/28/2018]; Available from: http://www.statsghana.gov.gh/pop_stats.html.
33. UNICEF. At a glance: Ghana, Statistics. 26 December 2013 9/17/2018]; Available from: https://www.unicef.org/infobycountry/ghana_statistics.html.
34. World Population Review. Ghana Population 2018. 2018 10/1/2018]; Available from: http://worldpopulationreview.com/countries/ghana-population/.
35. CIA World Factbook. Ghana Demographics Profile 2018. January 2018 8/1/2019]; Available from: https://www.indexmundi.com/ghana/demographics_profile.html.
36. Development Initiatives 2018. Ghana’s rural savannah areas suffer persistently high poverty. 4/5/205 8/1/2019]; Available from: http://devinit.org/post/ghanas-rural-savannah-areas-suffer-persistently-high-poverty/.
37. Zindzy Gracia Current literacy rate in Ghana by regions. 2018 8/2/2019]; Available from: https://yen.com.gh/106652-current-literacy-rate-ghana-by-regions.html#106652.
38. Ghana Statistical Service, 2010 Population and Housing Census Summary Report of Final Results. May 2012.
39. Philippe Glaziou. Sampsize. 2003–2005 7/17/2019]; Available from: http://sampsize.sourceforge.net/iface/.
40. Female Sexual Functioning Website. Available from: http://fsfi-questionnaire.com/.
41. Rosen R., Brown C., Heiman J., Leiblum S., Meston C., Shabsigh R., Ferguson D., and D'Agostino R. Jr., The Female Sexual Function Index (FSFI): a multidimensional self-report instrument for the assessment of female sexual function. J Sex Marital Ther, 2000. 26(2): p. 191–208. doi: 10.1080/009262300278597 10782451
42. Starrs A.M., Ezeh A.C., Barker G., Basu A., Bertrand J.T., Blum R., Coll-Seck A.M., Grover A., Laski L., Roa M., et al., Accelerate progress-sexual and reproductive health and rights for all: report of the Guttmacher-Lancet Commission. Lancet, 2018. 391(10140): p. 2642–2692. doi: 10.1016/S0140-6736(18)30293-9 29753597
43. ACOG Committee Opinion No. 586: Health disparities in rural women. Obstet Gynecol, 2014. 123(2 Pt 1): p. 384–8. doi: 10.1097/01.AOG.0000443278.06393.d6 24451676
44. Awoonor-Williams J.K., Bailey P.E., Yeji F., Adongo A.E., Baffoe P., Williams A., and Mercer S., Conducting an audit to improve the facilitation of emergency maternal and newborn referral in northern Ghana. Glob Public Health, 2015. 10(9): p. 1118–33. doi: 10.1080/17441692.2015.1027247 25833654
45. Kyei-Nimakoh M., Carolan-Olah M., and McCann T.V., Millennium development Goal 5: progress and challenges in reducing maternal deaths in Ghana. BMC Pregnancy Childbirth, 2016. 16: p. 51. doi: 10.1186/s12884-016-0840-0 26960599
46. Barnes-Josiah D., Myntti C., and Augustin A., The "three delays" as a framework for examining maternal mortality in Haiti. Soc Sci Med, 1998. 46(8): p. 981–93. doi: 10.1016/s0277-9536(97)10018-1 9579750
47. Bazzano A.N., Kirkwood B., Tawiah-Agyemang C., Owusu-Agyei S., and Adongo P., Social costs of skilled attendance at birth in rural Ghana. Int J Gynaecol Obstet, 2008. 102(1): p. 91–4. doi: 10.1016/j.ijgo.2008.02.004 18395724
48. Sikder S.S., Labrique A.B., Craig I.M., Wakil M.A., Shamim A.A., Ali H., Mehra S., Wu L., Shaikh S., West K.P. Jr., et al., Patterns and determinants of care seeking for obstetric complications in rural northwest Bangladesh: analysis from a prospective cohort study. BMC Health Serv Res, 2015. 15: p. 166. doi: 10.1186/s12913-015-0832-1 25985774
49. Tansley G., Stewart B., Zakariah A., Boateng E., Achena C., Lewis D., and Mock C., Population-level Spatial Access to Prehospital Care by the National Ambulance Service in Ghana. Prehosp Emerg Care, 2016. 20(6): p. 768–775. doi: 10.3109/10903127.2016.1164775 27074588
50. Newell R., Spillman I., and Newell M.L., The Use of Facilities for Labor and Delivery: The Views of Women in Rural Uganda. J Public Health Afr, 2017. 8(1): p. 592. doi: 10.4081/jphia.2017.592 28890773
51. Dube E., Mtapuri O., and Matunhu J., Managing flood disasters on the built environment in the rural communities of Zimbabwe: Lessons learnt. Jamba, 2018. 10(1): p. 542. doi: 10.4102/jamba.v10i1.542 29955273
52. Mark T, LaTulipe R, Anto-Ocrah M, Adler D, and J. Lanning, Depression and Food Insecurity amongst breastfeeding mothers in rural Malawi, in Consortium of Universities of Global Health (CUGH), The Lancet Global Health Selection for Best Research in Session, Editor. March 2018: New York, NY.
53. Amalba A., Abantanga F.A., Scherpbier A., and van Mook W., Working among the rural communities in Ghana—why doctors choose to engage in rural practice. BMC Med Educ, 2018. 18(1): p. 133. doi: 10.1186/s12909-018-1234-y 29884172
54. The Guardian. Maternal mortality down 45% globally, but 33 women an hour are still dying. The Guardian June 2014 8/28/2018]; Available from: https://www.theguardian.com/news/datablog/2014/may/07/maternal-mortality-rate-drops-half-report-who-childbirth-pregnancy.
55. Baravilala, W., at the Global Burden of Surgical Disease 3rd International Medical Development Symposium Melbourne and RACS, Spring St, Melbourne. Challenges of Obstetrics & Gynaecology: Strategies to Reduce Maternal Mortality. 9/19/2018]; Available from: https://pdfs.semanticscholar.org/presentation/7233/c82c737f610d0e3cc5c9e4bba05a24022d67.pdf.
56. Knight H.E., Self A., and Kennedy S.H., Why are women dying when they reach hospital on time? A systematic review of the 'third delay'. PLoS One, 2013. 8(5): p. e63846. doi: 10.1371/journal.pone.0063846 23704943
57. Kacker S., Bishai D., Mballa G.A., Monono M.E., Schneider E.B., Ngamby M.K., Hyder A.A., and Juillard C.J., Socioeconomic correlates of trauma: An analysis of emergency ward patients in Yaounde, Cameroon. Injury, 2015.
58. Kyei-Nimakoh M., Carolan-Olah M., and McCann T.V., Barriers to obstetric care at health facilities in sub-Saharan Africa—a systematic review protocol. Syst Rev, 2015. 4: p. 54. doi: 10.1186/s13643-015-0045-z 25900086
59. Alkema L., Chou D., Hogan D., Zhang S., Moller A.B., Gemmill A., Fat D.M., Boerma T., Temmerman M., Mathers C., et al., Global, regional, and national levels and trends in maternal mortality between 1990 and 2015, with scenario-based projections to 2030: a systematic analysis by the UN Maternal Mortality Estimation Inter-Agency Group. Lancet, 2016. 387(10017): p. 462–74. doi: 10.1016/S0140-6736(15)00838-7 26584737
60. Coelho G., Frange C., Siegler M., Andersen M.L., Tufik S., and Hachul H., Menopause Transition Symptom Clusters: Sleep Disturbances and Sexual Dysfunction. J Womens Health (Larchmt), 2015. 24(11): p. 958–9.
61. Prairie B.A., Wisniewski S.R., Luther J., Hess R., Thurston R.C., Wisner K.L., and Bromberger J.T., Symptoms of depressed mood, disturbed sleep, and sexual problems in midlife women: cross-sectional data from the Study of Women's Health Across the Nation. J Womens Health (Larchmt), 2015. 24(2): p. 119–26.
62. Makara-Studzinska M.T., Krys-Noszczyk K.M., and Jakiel G., Epidemiology of the symptoms of menopause—an intercontinental review. Prz Menopauzalny, 2014. 13(3): p. 203–11. doi: 10.5114/pm.2014.43827 26327856
63. Bachmann G.A. and Leiblum S.R., The impact of hormones on menopausal sexuality: a literature review. Menopause, 2004. 11(1): p. 120–30. doi: 10.1097/01.GME.0000075502.60230.28 14716193
64. Bachmann G.A., Influence of menopause on sexuality. Int J Fertil Menopausal Stud, 1995. 40 Suppl 1: p. 16–22.
65. Remez, L. Multiple Factors, Including Genetic and Environmental Components, Influence When Menopause Begins. 8/9/2016]; Available from: https://www.guttmacher.org/about/journals/psrh/2001/09/multiple-factors-including-genetic-and-environmental-components.
66. International Society for Sexual Medicine. Why is vaginal lubrication important for women? 7/31/2019]; Available from: https://www.issm.info/sexual-health-qa/why-is-vaginal-lubrication-important-for-women/.
67. Jennifer Huizen for Medical News Today. Causes and treatment of vaginal cuts. May 2nd, 2019 7/31/2019]; Available from: https://www.medicalnewstoday.com/articles/325100.php.
68. Simons J.S. and Carey M.P., Prevalence of sexual dysfunctions: results from a decade of research. Arch Sex Behav, 2001. 30(2): p. 177–219. doi: 10.1023/a:1002729318254 11329727
69. Shifren, J., R. Barbieri, and S. Falk. Sexual dysfunction in women: Epidemiology, risk factors, and evaluation. 12/31/2015]; Available from: http://www.uptodate.com/contents/sexual-dysfunction-in-women-epidemiology-risk-factors-and-evaluation#H1.
70. Heiman J.R., Sexual dysfunction: overview of prevalence, etiological factors, and treatments. J Sex Res, 2002. 39(1): p. 73–8. doi: 10.1080/00224490209552124 12476261
71. Mohamed N.A., Abdulhadi N.N., Al-Maniri A.A., Al-Lawati N.R., and Al-Qasmi A.M., The trend of feminization of doctors' workforce in Oman: is it a phenomenon that could rouse the health system? Hum Resour Health, 2018. 16(1): p. 19. doi: 10.1186/s12960-018-0283-y 29699562
72. Russo G., Goncalves L., Craveiro I., and Dussault G., Feminization of the medical workforce in low-income settings; findings from surveys in three African capital cities. Hum Resour Health, 2015. 13: p. 64. doi: 10.1186/s12960-015-0064-9 26228911
73. World Health Organization. The World Health Report 2006 2006 8/1/2019]; Available from: http://www.who.int/whr/2006/en/.
74. Levinson W. and Lurie N., When most doctors are women: what lies ahead? Ann Intern Med, 2004. 141(6): p. 471–4. doi: 10.7326/0003-4819-141-6-200409210-00013 15381521
75. Ghana Health Service, The Health Sector In Ghana: Facts and Figures. 2017.
76. Abdulai, T., D.A. Abobi-Kanbigs, S.K. Joseph, A. J, G. Adiiboka, and C. Solomon, Bridging the Inequitable Distribution of Physicians in Ghana: Factors Medical Students and House Officers at UDS and TTH Will Consider in Accepting Postings to Northern Ghana.
77. Lassey A.T., Lassey P.D., and Boamah M., Career destinations of University of Ghana Medical School graduates of various year groups. Ghana Med J, 2013. 47(2): p. 87–91. 23966746
78. Newman-Nartey M.A., Nartey N.O., Amoah K.G., Buckman V.A., Ndanu T.A., and Achempong A.A.O., Residency training in Ghana: the residents' perspective. Ghana Med J, 2019. 53(1): p. 13–19. doi: 10.4314/gmj.v53i1.3 31138939
79. Menes Tau. Ghanaian Medical Doctors–The Ungrateful Bastards. 2013 8/1/2019]; Available from: http://grandmotherafrica.com/ghanaian-medical-doctors-the-ungrateful-bastards/.
80. Clinton Y., Anderson F.W., and Kwawukume E.Y., Factors related to retention of postgraduate trainees in obstetrics-gynecology at the Korle-Bu Teaching Hospital in Ghana. Acad Med, 2010. 85(10): p. 1564–70. doi: 10.1097/ACM.0b013e3181f09112 20881676
81. Buck K.S. and Littleton H.L., Stereotyped beliefs about male and female OB-GYNS: relationship to provider choice and patient satisfaction. J Psychosom Obstet Gynaecol, 2014. 35(1): p. 1–7. doi: 10.3109/0167482X.2013.866646 24320840
82. Amir H., Abokaf H., Levy Y.A., Azem F., and Sheiner E., Bedouin Women's Gender Preferences When Choosing Obstetricians and Gynecologists. J Immigr Minor Health, 2018. 20(1): p. 51–58. doi: 10.1007/s10903-016-0522-z 27796701
83. Somaia Ragab Eid, Hassan H.E., Fathy W., and Abou-Shabana K.R., Study Women Verbal and Nonverbal Response, during Their First Gynecological Examination. American Journal of Nursing Research, 2019. 7(1): p. 1–7.
84. Erika Stallings. Black patients, black physicians and the need to improve health outcomes for African Americans. May 5th, 2019 8/1/2019]; Available from: https://www.nbcnews.com/news/nbcblk/black-patients-black-physicians-need-improve-health-outcomes-african-americans-n1000696.
85. Nicole Torres. Research: Having a Black Doctor Led Black Men to Receive More-Effective Care. August 10 2018 8/1/2019]; Available from: https://hbr.org/2018/08/research-having-a-black-doctor-led-black-men-to-receive-more-effective-care.
86. Levy D.R., White doctors and black patients: influence of race on the doctor-patient relationship. Pediatrics, 1985. 75(4): p. 639–43. 3982895
87. Shields C.G., Griggs J.J., Fiscella K., Elias C.M., Christ S.L., Colbert J., Henry S.G., Hoh B.G., Hunte H.E.R., Marshall M., et al., The Influence of Patient Race and Activation on Pain Management in Advanced Lung Cancer: a Randomized Field Experiment. J Gen Intern Med, 2019. 34(3): p. 435–442. doi: 10.1007/s11606-018-4785-z 30632104
88. Silver J.K., Bean A.C., Slocum C., Poorman J.A., Tenforde A., Blauwet C.A., Kirch R.A., Parekh R., Amonoo H.L., Zafonte R., et al., Physician Workforce Disparities and Patient Care: A Narrative Review. Health Equity, 2019. 3(1): p. 360–377. doi: 10.1089/heq.2019.0040 31312783
89. Gott M., Galena E., Hinchliff S., and Elford H., "Opening a can of worms": GP and practice nurse barriers to talking about sexual health in primary care. Fam Pract, 2004. 21(5): p. 528–36. doi: 10.1093/fampra/cmh509 15367475
90. French F., Andrew J., Awramenko M., Coutts H., Leighton-Beck L., Mollison J., Needham G., Scott A., and Walker K., Why do work patterns differ between men and women GPs? J Health Organ Manag, 2006. 20(2–3): p. 163–72. doi: 10.1108/14777260610661556 16869352
91. Hedden L., Barer M.L., Cardiff K., McGrail K.M., Law M.R., and Bourgeault I.L., The implications of the feminization of the primary care physician workforce on service supply: a systematic review. Human resources for health, 2014. 12: p. 32–32. doi: 10.1186/1478-4491-12-32 24898264
92. Ghana College of Physicians and Surgeons. 2018 [cited 2019; Available from: https://gcps.edu.gh/members-of-the-college/#.
93. Feldhaus-Dahir M., Female sexual dysfunction: barriers to treatment. Urol Nurs, 2009. 29(2): p. 81–5; quiz 86. 19507405
94. Kingsberg S.A., Schaffir J., Faught B.M., Pinkerton J.V., Parish S.J., Iglesia C.B., Gudeman J., Krop J., and Simon J.A., Female Sexual Health: Barriers to Optimal Outcomes and a Roadmap for Improved Patient-Clinician Communications. J Womens Health (Larchmt), 2019. 28(4): p. 432–443.
95. Gott M. and Hinchliff S., Barriers to seeking treatment for sexual problems in primary care: a qualitative study with older people. Fam Pract, 2003. 20(6): p. 690–5. doi: 10.1093/fampra/cmg612 14701894
96. Seftel A.D., Re: What we don't talk about when we don't talk about sex(1): results of a national survey of U.S. obstetrician/gynecologists. J Urol, 2012. 188(4): p. 1265–6. doi: 10.1016/j.juro.2012.06.115 22971395
97. Khalesi Z.B., Bokaie M., and Attari S.M., Effect of pregnancy on sexual function of couples. Afr Health Sci, 2018. 18(2): p. 227–234. doi: 10.4314/ahs.v18i2.5 30602947
98. Duarte-Guterman P., Leuner B., and Galea L.A.M., The long and short term effects of motherhood on the brain. Front Neuroendocrinol, 2019. 53: p. 100740. doi: 10.1016/j.yfrne.2019.02.004 30826374
99. Breyer B.N., Smith J.F., Eisenberg M.L., Ando K.A., Rowen T.S., and Shindel A.W., The impact of sexual orientation on sexuality and sexual practices in North American medical students. J Sex Med, 2010. 7(7): p. 2391–400. doi: 10.1111/j.1743-6109.2010.01794.x 20384941
100. Anto-Ocrah M., Bazarian J., Lewis V., Jones C.M., Jusko T.A., and Van Wijngaarden E., Risk of female sexual dysfunction following concussion in women of reproductive age. Brain Inj, 2019. 33(11): p. 1449–1459. doi: 10.1080/02699052.2019.1644377 31322004
101. Campbell J., Buchan J., Cometto G., David B., Dussault G., Fogstad H., Fronteira I., Lozano R., Nyonator F., Pablos-Mendez A., et al., Human resources for health and universal health coverage: fostering equity and effective coverage. Bull World Health Organ, 2013. 91(11): p. 853–63. doi: 10.2471/BLT.13.118729 24347710
102. World Health Organization. Global strategy on human resources for health: workforce 2030. 2016 8/1/2019]; Available from: http://www.who.int/hrh/resources/pub_globstrathrh-2030/en/.
Článek vyšel v časopise
PLOS One
2020 Číslo 1
- S diagnostikou Parkinsonovy nemoci může nově pomoci AI nástroj pro hodnocení mrkacího reflexu
- Je libo čepici místo mozkového implantátu?
- Pomůže v budoucnu s triáží na pohotovostech umělá inteligence?
- AI může chirurgům poskytnout cenná data i zpětnou vazbu v reálném čase
- Nová metoda odlišení nádorové tkáně může zpřesnit resekci glioblastomů
Nejčtenější v tomto čísle
- Severity of misophonia symptoms is associated with worse cognitive control when exposed to misophonia trigger sounds
- Chemical analysis of snus products from the United States and northern Europe
- Calcium dobesilate reduces VEGF signaling by interfering with heparan sulfate binding site and protects from vascular complications in diabetic mice
- Effect of Lactobacillus acidophilus D2/CSL (CECT 4529) supplementation in drinking water on chicken crop and caeca microbiome