Journal of
Public Health and Epidemiology

  • Abbreviation: J. Public Health Epidemiol.
  • Language: English
  • ISSN: 2141-2316
  • DOI: 10.5897/JPHE
  • Start Year: 2009
  • Published Articles: 653

Full Length Research Paper

Prevalence of vulvo-vaginal candidiasis among women attending clinics in selected Hospitals in Oyo State, Southwest, Nigeria

Michael Oladimeji Idowu
  • Michael Oladimeji Idowu
  • Department of Community Medicine, College of Medicine, University of Ibadan, Ibadan, Oyo State, Nigeria.
  • Google Scholar
Gabriel Ifeoluwa Makinde
  • Gabriel Ifeoluwa Makinde
  • Department of Community Medicine, College of Medicine, University of Ibadan, Ibadan, Oyo State, Nigeria.
  • Google Scholar
Olayinka Oluyemi Oluranti
  • Olayinka Oluyemi Oluranti
  • Microbiology Programme, Bowen University, Iwo, Osun State, Nigeria.
  • Google Scholar
Matthew Ayodeji Adebayo
  • Matthew Ayodeji Adebayo
  • Department of Community Medicine, College of Medicine, University of Ibadan, Ibadan, Oyo State, Nigeria.
  • Google Scholar
Olajide Ayodele Adekunle
  • Olajide Ayodele Adekunle
  • Department of Epidemiology and Medical Statistics, College of Medicine, University of Ibadan, Nigeria.
  • Google Scholar


  •  Received: 05 January 2021
  •  Accepted: 21 May 2021
  •  Published: 31 March 2022

 ABSTRACT

Vulvo-vaginal candidiasis (VVC) is a pathogenic fungal infection with a high burden among women of reproductive age (WRA). Healthcare delivery system related constraints in developing countries have made its diagnosis and management unnecessarily complicated leading to poor management of the infection. The study was conducted to determine the prevalence of VVC among women attending clinics in selected hospitals in Oyo State, Nigeria. Two hundred high vaginal swabs were collected from the selected hospitals. These were streaked on chocolate agar, blood agar and sabouraud dextrose agar. Structured tool was used in collecting patients’ basic clinical information. The prevalence of Candida species among the 200 subjects was 40% and 45.0% of those infected were aged 20-30 years. Across all Candida species, Candida albicans (83.8%) had the highest prevalence and mostly occurred among patients aged 20-30 years (47.8%). Higher proportion of Candida species infection was detected among patients without vaginal discharge (65.0%) and pelvic inflammation diseases (88.8%) than those with symptoms. Higher proportion of those without vaginal itching (34.5%, n=69) had positive Candida albicans culture compared with those who had symptoms. Among the Candida species reported in this study, C. albicans was the most vulvo-vaginal candida infection. Majority of patients without pelvic inflammatory disease, vaginal discharge and itching symptoms tested positive for VVC. Health education and awareness for routine screening are highly recommended for WRA to aid in early candida diagnosis and treatment. Also, clinicians are advised to essentially emphasize on empirical laboratory diagnosis for speciation of Candida species as against syndromic approach.

Key words: Vulvo-vaginal candidiasis, prevalence, Candida species, routine screening, diagnosis.


 INTRODUCTION

Vulvo-vaginal candidiasis is a fungal or yeast infection of the female lower genital tract (Sobel, 2007) and is characterized by curd-like vaginal discharge, itching, and erythema, (Achkar and Fries, 2010). It can be referred to as candidiasis  or  moniliasis.  About  70-75%  of  healthy women will at least either experience one episode of vulvo-vaginal candidiasis during their lifetime or during their reproductive life (Ferris et al., 2002). It can be recurrent or relapsing when a woman presents with four or  more  episodes  per  year and  this condition has been reported among less than 5% of healthy women (Rex et al., 2000).

Also, half of college women by age of 25 years would have had one episode of vulvo-vaginal candidiasis diagnosed by a physician (Sobel, 1997). Candida species are part of the lower genital tract flora in 20-50% of healthy asymptomatic women (Akah et al., 2010) and in most cases prevalence of vaginal colonization and symptomatic vaginitis is higher in pregnant women than in those who are not pregnant. This is due to high concentration of reproductive hormones that increase the glycogen content in the vaginal tissue thereby providing a carbon source for candida organisms (Dennerstein and Ellis, 2001). Increasing Candida infection colonization had been found among women who douche (Rathod et al., 2012). Infectious Disesse Of Obsterics and Gynecology, and women using certain types of contraceptives, (Tarry et al., 2005) although this is not found in a study among some college students (Demirezen et al., 2005).

Vulvo-vaginal candidiasis has been associated with considerable direct and indirect economic costs (Foxman et al., 2000), enhanced susceptibility to HIV infection (Røttingen et al., 2001) and is being investigated for a potential relationship with preterm birth (Roberts et al., 2011). Carrier rates are higher in women treated with broad spectrum antibiotics (Singh, 2003) pregnant women, diabetic women (Donders et al., 2002; Reed et al., 2003) and women with HIV/AIDS (Nelson et al., 2013). Treatment of vulvo-vaginal candidiasis is warranted when a woman presents with a complaint of symptoms of this condition and laboratory confirmation of the presence of candida from a vaginal specimen.  

A study conducted in Ghana, West Africa reported that among a cohort of apparently healthy women, 30% had confirmed cases of diagnosed vulvo-vaginal candidiasis (Maccato and Kaufman, 1991). Also, in a study conducted by Okonofua et al. (1995) reported a prevalence of 36.0% VVC among pregnant women in south-western, Nigeria. Okonkwo (2010) in Nigerian study found no significant difference among patients who were positive with vulvo-vaginal candidiasis and their socioeconomic status. C. albicans is the most frequent colonizer, and is incriminated in most cases of vulvo-vaginal candidiasis (Ugwa, 2015). Nelson et al. (2013), showed C. albicans as the most common Candida species followed by Candida glabrata causing vaginal candidiasis among pregnant women. Okonofua et al. (1995), a high prevalence of C. albicans among infertile women compared with controls.  Over the last 10 years, research evidence has revealed an increase in frequency of  cases caused by non - albicans species, with C. glabrata consistently being the leading species (Cheesbrough, 2000). Candida species that rarely cause candidiasis include Candida parapsilosis, Candida pseudotropicalis, Candida krusei, Candida guilliermondi and Candida stellatoidea.

Vulvo-vaginal candidiasis remains a common problem worldwide affecting all strata of society. They are much more so in the developing country context because of various health care delivery related constraints such as work force shortages and regulatory inadequacies. The absence of rapid, simple, and inexpensive diagnostic tests continues to result in either over-diagnosis, under diagnosis or misdiagnosis, leading to inappropriate treatment (Mohamadi et al., 2015). Although commonly caused by C. albicans, non-albicans species immunosuppression has led to the development of recurrent diseases some of which are nonresponsive to conventional antifungal regimes (Mohamadi et al., 2015).

This study aimed to determine, the prevalence of vulvo-vaginal candidiasis and the pattern of Candida species in women who attend some selected hospitals in Ibadan, Oyo state, Nigeria. The findings of the study will inform the need for a well sustained health education and awareness programme targeted at women of reproductive age on need for routine and periodic Candida specie diagnosis. The findings will also re-affirm the orthodoxy of physicians’ basic and mandatory requirement for empirical laboratory diagnosis as a gold-standard for management of vulvo vaginal candidiasis. 


 MATERIALS AND METHODS

Study area, sampling technique and data collection

A descriptive cross-sectional study was conducted using a purposive selection of a combination of tertiary, secondary and primary health care facilities located in Oyo State namely University College Hospitals, State Hospital; Adeoyo, Ring road and Bowen University Teaching Hospital. Purposive sampling technique was also applied in recruiting women of reproductive age attending General Out-Patient and Ante-natal Clinics of participating hospitals who consented to participate in the study. Women on hormonal contraceptives, who had documented records of HIV antibodies 1 and 2, who were diabetic and those on steroid or antifungal, therapy within the previous 2 weeks or broad-spectrum antibiotics in the past month were excluded from the study. An average of eight to ten samples of women of reproductive age were collected by trained medical personnel on each centre’s clinic days for a period of 3 months till sample size was reached. The 200 subjects enrolled into the study were estimated from prevalence of Candida specie among women in a previous study (Lisiak et al., 2000) using Leslie Kish formula for cross-sectional study.

where n = z2 p q/d2

(n = Sample size, z = Standard normal deviation = 1.96 at 95% confidence limit, p = Prevalence rate = 14.0%, q = 1 = 1–14.0% =0.86, d = Error margin = 5%).

This study was conducted, in principle with the Helsinki Declaration, and the protocol was approved by the Human Research Ethical Committee of the University College Hospital, Ibadan. All subjects gave written informed consent prior to being included in the study. All data were analyzed anonymously throughout the study. A pro-forma was used to obtain basic information such as age, clinical diagnosis and test result. Data were analyzed using the SPSS version 21. Descriptive statistics were presented as proportions in tables and charts. Inferential statistics were limited to bivariate analysis conducted between Candida species test outcome and clinical symptoms at p=0.05.

Sample collection and laboratory analysis

Paired high vaginal swab and endocervical swab samples were collected from each of the 200 participating subjects and analyzed in medical microbiology laboratory of the hospital for the isolation and identification of both C. albicans and non-C. albicans species.

The specimens were routinely cultured for Candida species using sabouraud’s dextrose agar, incubated in paired sets, one set at 25ºC for 3 to 7 days and the other at 37ºC for 24 h.

The culture revealed whitish soft cream colonies. Direct gram staining was done with standard procedures to differentiate positive slides of large purple oval yeast cells. Microscopic examination also showed bacteria which are normal cocci and bacilli forms of floral of the body. Wet preparation processes were done and showed budding yeasts and hyphae with buds at points of constriction. C. albicans was identified by the production of germ tubes. Other candida isolates were speciated with a battery of biochemical tests using sugar fermentation such as glucose, sucrose, lactose, maltose, urease tests. CHROMagar (CAC, Becton Dickinson, Heidelberg, Germany) was also used in the speciation of C. albicans, C. tropicalis, C. krusei, C. glabrata by colony, color and morphology.


 RESULTS

Of the 200 subjects recruited, 80 respondents had Candida-positive cultures from both High Vaginal Swab and Endocervical Swab samples, giving a prevalence of vulvo-vaginal candidiasis as 40.0%.

Candida-positive cultures were observed mostly among those aged 20–30 years, at 36 (45.0%) and lowest among those less than 20 years, 2 (1%) (Figure1). There was no significant statistical relationship between the prevalence of vulvo-vaginal candidiasis and age (P>0.05).

With respect to speciation of cultures, C. albicans had the highest prevalence 67 (83.8%) (Figure 2) and was diagnosed mostly among patients aged 20-30 years (47.8%) followed by  those aged 31-40, 32 (37.30%). The laboratory investigations yield low prevalence of the remaining Candida species; C. tropicalis 10 (12.5%); C. glabrata 2 (2.5%) and C. krusei 1 (1.25%). The Bar-chart representation of Candida-positive cultures among  those with vulvo-vaginal discomfort of itching and those with no vulvo-vaginal discomfort (Figure 3).

There were unequal Candida-positive cultures between women  who  presented with clinical symptoms of vaginal discharge and those who were without discharge. Of the 79 test subjects who are presented with vaginal discharge 28 (35.0%) had candidiasis while those without discharge accounted for 52 (65.0%). High prevalence of C. albicans (64.2 %) and C. tropicalis (60.0%) were diagnosed in women without vaginal discharge symptoms. Table 1 shows the age distribution of Candida species speciation in the study of the work.

This pattern was also observed for pelvic inflammatory disease. Positive cultures of individuals without PID (88.8%) were higher than those with symptoms of PID (11.2%). Also C. albicans and C. tropicalis had the highest prevalence of 89.6% and 90.0% among those without PID symptoms compared to 10.4% and 10.0% among those with the symptoms respectively (Table 2). A higher prevalence of 34.5% positive cultures of Candidiasis was reported among those without clinical diagnosis of vaginal itching compared with those who had symptoms (5.5%).


 DISCUSSION

Vulvo-vaginal candidiasis is a common fungal infection among women worldwide. The infection occurs  commonly  at  the  lower  female  genitalia and is reported in 35% - 80% of cases without any symptoms (Mohamadi et al., 2015). Symptomatic vulvo-vaginal candidiasis has been found in up to 70% of the sexually active women (Lisiak et al., 2000). Chronic vulvo-vaginal candidiasis severely affects the quality of life for millions of women in the world and is frequently refractory to antifungal treatments (Sobel, 2007).

The prevalences of vaginal candidiasis reported by different studies were 14, 16.5, 21.31, and 19% (Emeribe et al., 2015; Yadav et al., 2016; Mahadani et al., 1998; Nandan et al., 2011). In this study, the prevalence was found to be 40%. This relatively high prevalence of vaginal candidiasis among women in this study may be due to a combination of habits such as poor personal hygiene, the use of contraceptives, and drug abuse (Lisiak et al., 2000; Mahadani et al., 1998). The disparity in prevalence in studies of vulvo-vaginal candidiasis might be due to the fact that vulvo-vaginal candidiasis shows different frequency of occurrence from region to region and some studies have disclosed that the incidence differs in various areas. It can be related to geographical conditions, social and cultural factors, hygiene practices, and diagnostic techniques (Salvi, 2019).

Candida-positive cultures were observed mostly among  women  aged  20–30  years (45.0 %). The high prevalence is consistent with Emeribe et al. (2015) which reported a prevalence of 60.0% among the specified age-group.

Salvi (2019) and Ugwa (2015) in a similar study of prevalence of vulvo-vaginal candidiasis among reproductive age group of pregnant and non-pregnant women done separately in Dubai and North-west Nigeria reported of 39.1 and 53.0% of VVC among mid-upper interval of 26-30 years age group, respectively. While Yadav and Prakash (2016) found the highest of vulvo-vaginal candidiasis among 21-25 years age group (40.4%) followed by 26-30 years with 32.6%. These findings could essentially be attributed to exposure to risk of sexually transmitted diseases of the group because of their high sexual activity during this period for procreative purposes and possibly due to financial benefits that arise from prostitution.

Whereas, the lowest prevalence among those less than 20 years of age in this study corroborates the finding of (Ugwa, 2015) who reported that women above 40 years had the lowest rate of infection (14.0%). Except women of this age group are still using contraceptives (Tarry et al., 2005), their risk of candida infections are likely to be low due to the fact that they have entered menopausal period of their lives. The study also  revealed  the  isolation  of  C.  albicans and non-C.albicans organisms to be the causative fungal agents associated with vulvo-vaginal candidiasis among women in selected hospitals in Oyo-state. C. albicans showed the highest prevalence at 83.8% followed by C. tropicalis (12.5%) while C. glabrata (2.5%) and C. krusei (1.25%) recording the lowest.

C. albicans having the highest prevalence in this study corroborate different previous studies. For example, (Shekufe et al., (2017) in an Iranian study among women of reproductive age conducted traditional tests such as gram-staining, microscopic examination, and culture for species identification and reported C. albicans as the most prevalent species (83.5%), followed by Candida glabrata (16%). (Mucci et al., (2016) showed that the occurrence of vulvo-vaginal candidiasis was 25% among pregnant women and C. albicans with a prevalence of 80.7% was the predominant Candida species. Also, the study of Nnadi and Singh (2017) reported that out of 288 pregnant women, 212 were positive for c. albicans giving a prevalence rate of 73.7%. C. albicans can colonize on the mucous membrane of genitourinary tracts of healthy humans (Singh, 2003). In contrast to this study, (Emeribe et al., (2015) revealed a lower prevalence of C. albicans 13 (6.5%), than  that  of  non-albicans candidiasis 15 (7.5%). Their study reported that among the non-albicans species, C. glabrata was the commonest type (10.5%) and C. krusei the least among the Candida species (3.5%). The reasons for the increase in incidence of C. glabrata in their study were as a result of single-dose antifungal treatment, low-dosage azole-maintenance regimens, and the use of over-the-counter antimycotics (Alo et al., 2012). Therefore, for effective control of candidiasis, laboratory diagnosis must be a pre-requisite for candida infection management.

In this study, cultures from the patients who did not present with clinically diagnosed symptoms of vagina discharge and pelvic inflammatory disease had higher rate of VVC than those with symptoms. Of the 79 subjects who presented with vaginal discharge, 28 (35.0%) had candidiasis while those without discharge had 65.0% (n=52). Also, positive cultures of individuals without PID (88.8%) were higher than those with symptoms of PID (11.2%). The Subjects whose cultures were positive, for Candida species and were without symptoms of PID and vaginal discharge are likely to have built some level of resistance to the infection as a result of drug abuse of antifungal prescription and self-medication  (Mucci  et  al.,  2016).  Also,  those  who  had symptoms of discharge and PID but did not have Candida specie positive cultures could have other diseases causing infectious agents which could be from known or unknown origin (Hofs et al., 2016). Subjects with no vulvo-vaginal discomfort of itching had a higher percentage of Candida-positive cultures (34.5%) than those with no discomfort (5.5%). This report is in agreement with the findings of (Emeribe et al., 2015) Vaginal discomfort of itching irrespective of the fungal test outcome could be as a result of infections such as enterobiosis from poor personal hygiene and some deep socio-cultural beliefs that encourage poor hygiene (Burkhart et al., (2005). Itching could also be as a result of sexually transmitted diseases. According to (Aurora and Aurora (2014) approximately 10% of vulvo-vaginitis is due to infection of Trichomonas vaginalis (Hofs et al., 2016).


 LIMITATION OF THE STUDY

This is a cross-sectional study to assess the pattern and prevalence of candida spp to strengthen the need for careful diagnosis of VVC infection. This study did not assess life-style and behavioral information that could be associated with incidence of VVC.


 CONCLUSION

The highest prevalence of candida infection was among respondents age 20-30 years. C albicans was the commonest pattern of species in the area. The findings also revealed the that majority of the respondents without symptoms of pelvic inflammatory disease, vaginal discharge tested positive for Candida infection.


 RECOMMENDATIONS

The prevalence of vulvo-vaginal candidiasis among women has been a fast growing and serious burden in our environment which can result in a lot of future health challenges. Emergence of C. albicans and non-albicans species among clinical specimens are crucial concern in medical mycology. For better management of fungal infections like vulvo-vaginal candidiasis this study thus recommend that medical practitioners through their various channels of engagement such as workshop and conferences should  emphasis on laboratory diagnosis of Candida infection for precise identification of fungal isolates prior to commencement of treatment. Also, health education and awareness for routine screening are highly recommended for women of reproductive age to aid early Candida diagnosis and treatment.


 CONFLICT OF INTERESTS

The author has not declared any conflict of interests.



 REFERENCES

Alo MN, Anyim C, Onyebuchi AK, Okonkwo EC (2012). Prevalence of asymptomatic co-infection of candidiasis and vaginal trichomoniasis among pregnant women in Abakaliki, South-Eastern Nigeria. Prevalence 2(7):87-91.

 

Achkar JM, Fries BC (2010). Candida infections of the genitourinary tract, Clinical Microbiology Reviews 23(2):253-273.
Crossref

 

Akah PA, Nnamani CE, Nnamani PO (2010). Prevalence and treatment outcome of vulvovaginal candidiasis in pregnancy in a rural community in Enugu State, Nigeria. Journal of Medicine and Medical Sciences 1(10):447-452.

 

Aring BJ, Mankodi PJ, Jasani JH (2012). Incidence of vaginal Candidiasis in leucorrhoea in women Attending in OPD of Gynecology and Obstetrics Department. International Journal of Biomedical and Advance Research 3(12):867-869.
Crossref

 

Arora DR, Arora BB (2014). Medical Parasitology, 4e 4th Edition, Kindle Edition (46):41-71.

 

Burkhart CN, Burkhart CG (2005). Assessment of frequency, transmission, and genitourinary complications of enterobiasis (pinworms). International journal of dermatology 44(10):837-840.
Crossref

 

Cheesbrough M (2000). Fungal pathogens. In: District Laboratory Practice in Tropical Countries. Cambridge, UK: Cambridge University Press pp. 235-248.

 

Demirezen S, Dirlik OO, Beksaç MS (2005). The association of Candida infection with intrauterine contraceptive device. Central European Journal of Public Health 13:32-34.

 

Dennerstein GJ, Ellis DH (2001). Oestrogen, glycogen and vaginal candidiasis. Australian and New Zealand Journal of Obstetrics and Gynaecology 41(3):326-328.
Crossref

 

Donders GG, Prenen H, Verbeke G, Reybrouck R (2002). Impaired tolerance for glucose in women with recurrent vaginal candidiasis. American Journal of Obstetrics and Gynecology 187(4):989-993.
Crossref

 

Emeribe AU, Nasir IA, Onyia J, Ifunanya AL (2015). Prevalence of vulvovaginal candidiasis among nonpregnant women attending a tertiary health care facility in Abuja, Nigeria. Research and Reports in Tropical Medicine 6:37-42.
Crossref

 

Ferris DG. Nyirjesy P, Sobel JD, Soper D, Pavletic A, Litaker MS (2002).Over-the-counter antifungal drug misuse associated with patient diagnosed vulvovaginal candidiasis. Obstetrics Gynecology 99(3):419-425.
Crossref

 

Foxman B, Barlow RH, D'Arcy H, Gillespie B, Sobel JD (2000). Candida vaginitis: self-reported incidence and associated costs, Sexually Transmitted Diseases 27(4):230-235.
Crossref

 

Hofs S, Mogavero S, Hube B (2016). Interaction of Candida albicans with host cells: virulence factors, host defense, escape strategies, and the microbiota. Journal of Microbiology 54(3):149-169.
Crossref

 

Jombo GT, Opajobi SO, Egah DZ, Banwat EB, Akaa PD (2010). Symptomatic vulvovaginal candidiasis and genital colonization by Candida species in Nigeria. Journal of Public Health and Epidemiology 2(6):147-151.

 

Kwawukume EY, Arhin RA (2002). Vulvovaginitis. In: Kwawukume EY, Emuveyan EE, editors. Comprehensive Gynaecology in the Tropics.1st ed. Dansoman: Asante and Hittscher pp. 72-74.

 

Lisiak M, K?yszejko C, Pierzcha?o T, Marcinkowski Z (2000).Vaginal candidiasis: frequency of occurrence and risk factors. Ginekologia polska 71(9):964-970.

 

Maccato ML, Kaufman RH (1991). Fungal vulvovaginitis. Current opinion in obstetrics and gynecology 3(6):849-852.
Crossref

 

Mahadani JW, Dekate RR, Shrikhande AV (1998). Diagnosis of discharge per vaginum. Indian Journal of Pathology and Microbiology 41(4):403-411.

 

McCormack Jr WM, Zinner SH, McCormack WM (1994). The incidence of genitourinary infections in a cohort of healthy women. Sexually Transmitted Diseases 21(2):63-64.
Crossref

 

Mirza NB, Nsanze H, D'Costa LJ, Piot P (1983). Microbiology of vaginal discharge in Nairobi, Kenya. British Journal on Venereal Diseases 59(3):186-188.
Crossref

 

Mohamadi J, Havasian MR, Panahi J, Pakzad I (2015). Antifungal drug resistance pattern of Candida. spp isolated from vaginitis in Ilam-Iran during 2013-2014. Bioinformation 11(4):203-206.
Crossref

 

Mucci MJ, Cuestas ML, Cervetto MM, Landaburu MF, Mujica MT (2016). A prospective observational study of vulvovaginitis in pregnant women in Argentina, with special reference to candidiasis. Mycoses. 59(7):429-435.
Crossref

 

Nandan D, Gupta YP, Krishnan V, Sharma A, Misra SK (2011) Reproductive tract infection in women of reproductive age group in Sitapur/ Shahjahanpur district of Uttar Pradesh. Indian Journal of Public Health 45(1):8-13.

 

Nelson M, Wanjiru W, Margaret MW (2013). Prevalence of Vaginal Candidiasis and Determination of the Occurrence of Candida Species in Pregnant Women Attending the Antenatal Clinic of Thika District Hospital, Kenya. Open Journal of Medical Microbiology 3:264-272.
Crossref

 

Nnadi DC, Singh S (2017). The prevalence of genital Candida species among pregnant women attending antenatal clinic in a tertiary health center in North-west Nigeria. Sahel Medical Journal 20(1):33-37.

 

Okonkwo NJ (2010). Prevalence of vaginal candidiasis among pregnant women in Nnewi town of Anambra State, Nigeria. African Research Review 24:539-548.
Crossref

 

Okonofua FE, Ako-Nai KA, Dighitoghi MD (1995). Lower genital tract infections in infertile Nigerian women compared with controls. Genitourinary Medicine 71(3):163-168.
Crossref

 

Parveen N, Munir AA, Din I, Majeed R (2008). Frequency of vaginal candidiasis in pregnant women attending routine antenatal clinic. Journal of College Physicians and Surgoens Pakistan 18:154-157.

 

Rathod SD, Klausner JD, Krupp K, Reingold AL, Madhivanan P (2012). Epidemiologic features of vulvovaginal candidiasis among reproductive-age women in India. Infectious Diseases of Obstetrics and Gynecology, 859071.
Crossref

 

Ray D, Goswami R, Banerjee U, Dadhwal V, Goswami D, Mandal P, Kochupillai N (2007). Prevalence of Candida glabrata and its response to boric acid vaginal suppositories in comparison with oral fluconazole in patients with diabetes and vulvovaginal candidiasis. Diabetes Care 30(2):312-317.
Crossref

 

Reed BD, Zazove P, Pierson CL, Gorenflo DW, Horrocks JJ ((2003). Candida transmission and sexual behaviors as risks for a repeat episode of Candida vulvovaginitis. Journal of Women's Health 12(10):979-989.
Crossref

 

Rex JH, Walsh TJ, Sobel JD, Filler SG, Pappas PG, Dismukes WE, Edwards JE (2000). Practice guidelines for the treatment of candidiasis. Clinical Infectious Diseases 30(4):662-678.
Crossref

 

Roberts CL, Morris JM, Rickard KR, Giles WB, Simpson JM, Kotsiou G, Bowen JR (2011). Protocol for a randomised controlled trial of treatment of asymptomatic candidiasis for the prevention of preterm birth [ACTRN12610000607077]. BMC Pregnancy and Childbirth 11(1):1-9.
Crossref

 

Røttingen JA, Cameron DW, Garnett GP (2001). A systematic review of the epidemiologic interactions between classic sexually transmitted diseases and HIV: how much really is known? Sexually Transmitted Diseases 28(10):579-597.
Crossref

 

Salvi M (2019). Prevalence of vulvovaginal candidiasis in females in the reproductive age group. International Journal of Reproduction, Contraception Obstetrics and Gynecology 8(2):647-651.
Crossref

 

Shekufeh P, Minoo M, Rasoul M (2017). Clinical and Mycological study of vulvovaginal candidiasis (VVC), Identification of clinical isolates by polymerase chain-fragment size polymorphyim (PCR-FSP) technique. Archives of Clinical Infectious Diseases 12(2):e62761.

 

Singh SI (2003). Treatment of vulvovaginal candidiasis. Clinical Review 136(9):26-30.

 

Sobel JD (2007). Vulvovaginal candidosis. Lancet 369(9577):1961-1971.
Crossref

 

Sobel TD (1997). Vaginitis. New England Journal of Medicine 337(26):1896-1903.
Crossref

 

Tarry W, Fisher M, Shen S (2005). Mawhinney M. Candida albicans: The estrogen target for vaginal colonization. Journal of Surgical Research 129(2):278-282.
Crossref

 

Ugwa EA (2015). Vulvovaginal Candidiasis in Aminu Kano Teaching Hospital, North West Nigeria: Hospital Based Epidemiological Study. Annals of Medical and Health Science Research 5(4):274-278.
Crossref

 

Yadav K, Prakash S (2016). Prevalence of vulvovaginal candidiasis in pregnancy. Global Journal of Medical Sciences 4(1):108-106.

 




          */?>