Current patient perspectives of vulvovaginal candidiasis: incidence, symptoms, management and post-treatment outcomes

Vulvovaginal candidiasis (VVC) is a common fungal infection caused by Candida species, predominantly C. albicans [1]. Historical reports approximate that 70% of all women will have at least one episode of VVC during their reproductive years [2]. The pathological hallmark of the disease is an acute inflammatory condition of the vulva and vaginal mucosa induced by and accompanied with overgrowth of Candida organisms that normally exists as a quiescent vaginal commensal [3]. Signs/symptoms of VVC are typically characterized by white clumpy discharge, burning, redness and itching in the vulva and vagina, and dyspareunia [4]. The onset of most VVC cases is believed to be associated with a wide range of predisposing factors or triggering events including the use of antibiotics, increased estrogen levels (e.g. high estrogen oral contraceptives, hormone replacement therapies, pregnancy), uncontrolled diabetes mellitus, sexual activities and tight-fit clothing [2, 5]. In addition, an estimated 8 to 10% of women are susceptible to recurrent VVC (RVVC), having 4 or more episodes per annum [4]. Multiple recurring infections are often idiopathic without regard to the array of potential risk factors. Unlike most episodic or sporadic VVC, RVVC cases require maintenance regimens with long-term use of antifungals over several months or longer to avoid recurrence [4, 6].

Despite the high incidence rates worldwide, epidemiological data supporting the current estimates of VVC or RVVC prevalence rates had been limited, largely historical, and often anecdotal. More recently, however, several global studies have been reported. One reports the worldwide prevalence of RVVC at approximately 138 million women annually, and an additional 372 million over one’s lifetime, causing substantial morbidity and economic burden [7]. Another large-scale multi-country internet panel survey indicated a lifetime RVVC prevalence rate of 9% by age 50 with the vast majority of episodes occurring between 19 to 35 years of age [8], which was remarkably similar to the historical estimates [9]. Despite these global studies on incidence/prevalence rates worldwide, current information/perspectives on VVC/RVVC disease trends is still needed and critical for reporting on aspects of vaginal infections, including diagnostics and therapeutic approaches, understanding host immunity and pathogenesis, and behavioral factors associated with disease etiology. Indeed, a large body of current literature on host defense mechanisms against VVC/RVVC and associated immunopathology [10‐14] has relied on long past historical epidemiological citations for VVC/RVVC that may not accurately reflect current disease-associated trends.

The objective of this study was to conduct a contemporary survey of women with a history of VVC and RVVC among general populations and those seeking standard or elective care at several university-affiliated Obstetrics and Gynecology clinics or referral clinics, to determine current trends including diagnostic/management parameters, ranking of disease symptomatology, and post-treatment outcomes, in addition to prevalence rates.

Despite decades of research and high global prevalence, VVC and RVVC continue to present major health issues in affected women [2, 7]. Until very recently, general epidemiological information has been limited in contemporary literature and consequently, reports of current research in a variety of areas related to VVC/RVVC have referenced predominantly long past historical epidemiological data/observations. Results from the current survey provide a current patient perspective for several aspects of VVC/RVVC that can be used to compare to historical data and provide a contemporary resource for citation.

Data collected from 284 women showed a high proportion with a history of at least one previous episode of VVC (78%), with the majority of women with 3 or less annual episodes (65%) and a smaller proportion of those with 4 or more annual episodes (35%, i.e., RVVC). If one removes the RVVC sub-population, the lifetime prevalence is reduced to 68%. In either case, the reported lifetime history of VVC in this population of women is remarkably similar to historical reports (~ 75%) [15‐18]. Although the proportion of the RVVC group in this population was relatively high, owing to the inclusion of many women seeking specialist gynecologic care, this provided a large sample size of women with a history of VVC/RVVC (n = 204) to provide their perspectives. The race distribution (78% Caucasian, 14% African American, and 8% Asian) was reflective of the participant pool and not designed for matching by age or race.

The current survey estimates that approximately 38% of VVC cases are associated with antibiotic use, similar to previous estimates of 33% [9]. Interestingly, the high rate of responses (55%) denoting ‘no known cause’ for their episodes (idiopathic) was not dominated by RVVC respondents who are characteristically in the idiopathic category relative to cause [4]. Quite the contrary, there was a similar percentage of women with VVC and RVVC noting ‘no known cause’ (52 vs. 63%, respectively). This suggests that while the cause of episodic VVC is often known, there is an equally high proportion of acute VVC cases that are idiopathic similar to RVVC.

As historically reported, signs/symptoms associated with vulvovaginal inflammation (i.e. pruritus, burning, redness) and vaginal discharge are the hallmark manifestations of an acute VVC episode [19], which was also clearly indicated in the current survey. Interestingly, ranking of symptoms reported by those with episodic VVC was comparable to those experienced during RVVC when analyzed independently. Based on the sufficient numbers of women with VVC and RVVC in the survey, these data have significant power to suggest that the clinical pathology of RVVC is quite similar, if not identical, to acute VVC. It is noteworthy, however, that the frequency of women reporting multiple symptoms was higher in those with RVVC. This may be due simply to the relative frequency of the infection and a higher level of attentiveness to the accompanying signs/symptoms.

Among the RVVC population, the highest proportion were in the age ranging from 26 to 40. This is consistent with historical data and likely reflects the reported hormonal and behavioral predisposing factors to infection [20]. The relatively high proportions of RVVC rates in the perimenopausal (41 to 55 years of age) and postmenopausal (56 or older) populations may reflect potential age-related health conditions such as exogenous estrogen use to treat atrophy. Indeed, a study conducted in patients attending a vulvar disease referral clinic reported that nearly 50% of women diagnosed with VVC/RVVC were on hormone replacement therapy [21].

Regarding diagnosis and treatment, results showed that a significantly greater proportion of respondents had their episodes physician-diagnosed and treated with prescription antifungal drugs, leading to control/relief of symptoms in 84% of cases. These observations closely parallel previously reported estimates of 80 to 90% cure rates (defined by resolution of signs/symptoms and negative mycological tests) by treatment with topical or oral azoles [22, 23]. Also, consistent with a previous report estimating that only 38% of cases can be diagnosed correctly by symptomatology alone [19], our survey showed poor relief rate (57%) among women who reported they self-diagnosed and self-medicated with OTC drugs. For RVVC, a previous study reported that relapse occurred in 50% of women who failed to initiate a maintenance regimen [24]. This was reflective in the current survey where > 71% of women with RVVC reported requiring constant/as needed antifungal therapy to sustain relief. The overall relapse rate noted by the respondents (53%) is likely reflective of the relatively large RVVC population surveyed.

We acknowledge several limitations to the current study. It is important to note that the VVC diagnosis/cure data described was solely based on self-reported data as no formal chart screening was performed. As a result, we acknowledge that the open survey format leaves room for inaccuracies that should not be overlooked. For example, poor relief rate among women relying on self-diagnosis may have resulted from self-misdiagnosis. Indeed, signs and symptoms of RVVC are frequently mistaken for many other conditions such as bacterial vaginosis or persistent vulvar vestibulitis, and inadequate diagnosis without clinical examinations often leads to chronic vulvovaginal conditions [7, 25]. But despite potential inaccuracies, these current data are remarkably similar to historical information [19, 22, 23]. The relatively small sample size (n = 284) represented another limitation, especially considering the recent internet-based multi-country survey on RVVC prevalence that included 6100 respondents [26]. However, most clinic-based VVC/RVVC studies consist of sample sizes typical of the present study [3, 27‐32]. More importantly, however, is the recognition of selection/accrual bias in the current dataset owing to the fact that the participants were mainly comprised of women seeking care or continued care by a gynecologist, and often those specializing in chronic/recurrent VVC. Indeed, > 34% of the respondents reported RVVC. This introduced a significant bias in the participant pool that likely resulted in overestimation of the number of physician-diagnosed VVC/RVVC cases although the overall lifetime VVC incidence rate (~ 78%) were comparable to historical estimates (~ 75%) [15‐18]. It is assumed that the proportion of self-diagnosed VVC/RVVC cases would be higher in a more randomized population with all respondents devoid of attending established clinics. We recognize that these results may not be fully representative of a broader general population and thus may be another potential limitation. On the other hand, the inclusion of women with higher than average incidence rates of RVVC may actually be considered advantageous as it provided the opportunity to collect more relevant and informative data with respect to symptomatology, diagnosis, treatment and post-treatment outcomes.

In summary, we provide a contemporary patient perspective of several aspects of VVC and RVVC that while largely confirm historical reports, also include some new insights. Taking into account the overall similarity to historical reports, it bears noting that there has not been any substantial reduction in lifetime or annual prevalence rates of VVC over the past 30+ years despite a number of new drugs and effective maintenance therapy for RVVC. In fact, a study by Denning, et al. predicts an upward trend in RVVC cases by 2030 [7]. This is also despite a plethora of data regarding the pathogenesis of disease and potential immunotherapeutic strategies. Hence, continued research is still needed to impact the incidence of VVC/RVVC. On the positive side, the fact that VVC and RVVC appear to manifest a similar, if not identical, clinical pathology suggests that any diagnostic or immunotherapeutic advances will benefit either condition. Though we recognize the limitations of this study and selection bias of the respondents, these data represent a current set of patient trends in several areas that can serve as a useful resource in future research/publications involving VVC/RVVC.

A contemporary survey of women with a history of VVC and RVVC provides current trends in prevalence rates, ranking of disease symptomatology, diagnostic/management parameters, and post-treatment outcomes. These current patient perspectives closely reflect previously documented estimates and validate historical reports.