|Year : 2021 | Volume
| Issue : 1 | Page : 57-61
Clinicomycological study of vulvovaginal candidiasis
S Seeniammal, M Selvakumar, P Nirmaladevi
Department of Dermato-Venereo-Leprology, Tirunelveli Medical College, Tirunelveli, Tamil Nadu, India
|Date of Submission||27-Jun-2018|
|Date of Decision||11-Dec-2018|
|Date of Acceptance||30-Dec-2019|
|Date of Web Publication||31-Jul-2020|
Dr. S Seeniammal
Department of Dermato-Venereo-Leprology, Tirunelveli Medical College, Tirunelveli, Tamil Nadu
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Background: Vaginal candidiasis is one of the most common vaginal infections in women of reproductive age group caused by Candida species of fungi, a normal inhabitant of vagina. Aims: The aim is to study the culture characteristics, species prevalence, and drug sensitivity of vulvovaginal candidiasis (VVC) among females with genital pruritus and discharge per vaginum who are proved to have Candida infection by a vaginal smear study. Materials and Methods: A prospective study was done on female patients aged 18 years attending the Sexually Transmitted Diseases Clinic of the Department of Dermato-Venereo-Leprology (DVL), Tirunelveli Medical College, with complaints of genital pruritus and vaginal discharge over a period of 1½ years from 2013 to 2015. After clinical examination, vaginal discharge was smeared for wet mount, potassium hydroxide mount, and Gram stain. Those with pseudohyphae were chosen for culture, speciation, and drug sensitivity. Results: The most common age group affected was 18–35 years. The most common predisposing factor was HIV infection-induced immunosuppression (48.7%), followed by antibiotic usage and diabetes mellitus. Clinical presentation of VVC was similar in HIV-positive and HIV-negative patients. Recurrent VVC makes up 12% of total cases with most common species being Candida albicans whereas Candida glabrata among the non-C. albicans. Drug sensitivity pattern of C. albicans showed the highest sensitivity to nystatin 85.7%, followed by triazoles (75%–85%) with ketoconazole being more resistant (40%–60%), and was similar in C. albicans and non-C. albicans. Limitations: Exclusion of unmarried and pregnant women and lack of follow-up were limitations in our study. Conclusions: According to our study, elimination of predisposing factors, speciation of fungus, and treatment based on drug sensitivity pattern will reduce the incidence of VVC.
Keywords: Candida, fungal infection, vaginal discharge
|How to cite this article:|
Seeniammal S, Selvakumar M, Nirmaladevi P. Clinicomycological study of vulvovaginal candidiasis. Indian J Sex Transm Dis 2021;42:57-61
|How to cite this URL:|
Seeniammal S, Selvakumar M, Nirmaladevi P. Clinicomycological study of vulvovaginal candidiasis. Indian J Sex Transm Dis [serial online] 2021 [cited 2021 Jun 12];42:57-61. Available from: https://www.ijstd.org/text.asp?2021/42/1/57/291212
| Introduction|| |
Vaginal Candidiasis (vaginal thrush) is the most common fungal infection of the vulva and vagina affecting nearly 75% of adult women during their lifetime. It is caused by Candida species and is the second most common cause of vaginitis after bacterial vaginosis. Candida albicans constitutes 85%–90% of cases. Candida is a normal inhabitant of oral cavity, gastrointestinal tract, and vagina and is a true opportunistic pathogen. The genus Candida is comprised of more than 200 species. The medically significant Candida species include C. albicans, Candida glabrata, Candida tropicalis, Candida krusei, Candida parapsilosis, Candida lusitaniae, Candida kefyr, Candida stellatoidea, Candida guilliermondii, and Candida dubliniensis. In recent years, drug-resistant non-C. albicans species are emerging. Over-the-counter medications favor infection by drug-resistant species. Hence, speciation and drug sensitivity of vulvovaginal candidiasis (VVC) was done, and the results were analyzed.
Aims and objectives
This study was done in adult females in the Department of Dermato-Venereo-Leprology (DVL) in our tertiary care hospital with the following objectives.
- To diagnose VVC among female patients with genital pruritus and discharge per vaginum by clinical and laboratory methods including wet mount, 10% potassium hydroxide (KOH) mount, and Gram staining
- To identify the culture characteristics and species prevalence of Candida species
- To study the drug sensitivity pattern of VVC those who were proved to have Candida infection by a vaginal smear study.
| Materials and Methods|| |
This is an open prospective study which was conducted in the Department of DVL after obtaining clearance from the Ethical Committee over a period of 1½ years.
- All female patients aged more than 18 years with complaints of genital pruritus and discharge per vaginum attending the STD clinic
- Those cases proved to have Candida infection by vaginal smear for wet mount, KOH, and Gram stain in the laboratory.
- Female patients aged less than 18 years
- Patients already treated with antifungals
- Vaginal smear negative for Candida
- Pregnant women.
Oral and written consent in their local language was obtained before starting the study including consent for photographs. Clinical history regarding the duration of vaginal discharge, number of recurrences per year, extramarital contact, comorbidities such as diabetes, drug history, and contraceptive usage was taken.
A thorough genital examination regarding sites involved, nature of the discharge (colour and consistency), and surrounding skin was done. Speculum examination was also done and vaginal discharge was smeared in three separate slides. Wet mount, KOH mount, and Gram staining were done. The patients whose vaginal smear showed candidal pseudohyphae as elongated structure with cell wall constrictions in KOH mount [Figure 1] and Gram-positive rods in Gram staining were chosen for the study of culture, species identification, and drug sensitivity. The vaginal swabs were inoculated in Sabouraud dextrose agar and incubated at 37°C for 48 h. The candidal isolates were inoculated in the CHROMagar, and various species were identified based on the pigmentation [Figure 2], [Figure 3], [Figure 4]. All the isolates were subjected for antifungal susceptibility testing for fluconazole, itraconazole, voriconazole, clotrimazole, nystatin, miconazole, and ketoconazole by disc diffusion method. The basic investigations such as blood sugar, urea, creatinine, urine routine, and complete hemogram were done to look for precipitating factors. The cases were treated with antifungals according to the sensitivity and followed up after the 1st and 2nd weeks.
|Figure 1: Potassium hydroxide mount of vaginal smear with branched hyphae and cysts|
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|Figure 2: HiCrome agar media showing smooth green-colored wet colonies of Candida albicans|
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|Figure 3: HiCrome agar media showing pink-colored wet colonies of Candida glabrata|
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|Figure 4: HiCrome agar media showing metallic blue-colored colonies of Candida tropicalis|
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| Results|| |
The most common age group affected was 18–35 years. The most common predisposing factor was HIV infection-induced immunosuppression (48.7%), followed by antibiotic usage and diabetes mellitus. Clinical presentation of VVC was similar in HIV-positive and HIV-negative patients.
Recurrent VVC (RVVC) makes up 12% of total cases with most common species being C. albicans whereas C. glabrata among the non-C. albicans. Drug sensitivity pattern of C. albicans showed the highest sensitivity to nystatin 85.7%, followed by triazoles (75%–85%) with ketoconazole being more resistant (40%–60%), and was similar in C. albicans and non-C. albicans.
| Discussion|| |
The speciation of Candida and non-Candida organisms in our study was consistent with literature. Our study revealed the highest frequency of vaginal candidiasis in the age group of 18–35 years (55%) which was similar to literature. The least frequency of around 6.3% is observed in menopausal age group., Among the study group, 97% were symptomatic patients. All had itching of the vulva and vagina [Table 1]. HIV-negative and HIV-positive patients had more or less similar symptoms. However, severe forms of VVC were more common in HIV-negative patients infected with non-C. albicans species.
In our study, HIV infection was the major predisposing factor [Table 2]. Out of 80 cases, 39 were HIV positives. VVC was one of the most common opportunistic fungal infections in HIV-positive women. This was found to be because of depressed cell-mediated immunity, followed by diabetes mellitus, prolonged antibiotic use, IUCD, etc.,,
The genital coinfections which occurred in higher frequencies were bacterial vaginosis (6.25%), trichomonas vaginalis (5%), herpes genitalis (3.75%), and genital warts (1.25%) in decreasing order of frequency. Twenty-two women (27.5%) had no associated infections with HIV being the most common association.
We observed that the most prevalent species was C. albicans (82%) and 18% were non-C. albicans [Table 3] and [Table 4]. We isolated nine cases of non-Candida species, of which four (8%) belonged to C. glabrata, three (6%) C. tropicalis, and two (4%) C. krusei. Reports from Mahmoudi Rad et al. and Fan et al., have also documented similar results. In our study, C. glabrata was most common, followed by C. tropicalis and C. krusei. The emphasis on non-C. albicans was very essential because of drug resistance. Various study reports done by Study reports done by Redondo Lopez et al. was similar to our results., Hence, speciation by reliable culture methods is beneficial in the diagnostic aspect.
|Table 4: Prevalence of Candida and non-Candida species in HIV-positive patients|
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Over the past few years, there has been increasing incidence of primary and acquired resistance to azoles in Candida species. Some studies documented that the in vitro resistance to antifungal medication was common for non-C. albicans., The rate of fluconazole resistance varies from 5% to 25% with high resistance in ketoconazole and itraconazole (5%–56%). Similar observations were noted in our study [Table 5] which revealed the highest susceptibility to nystatin (90%), followed by fluconazole (82%), itraconazole (80%), voriconazole (75%), and clotrimazole (75%). Ketoconazole and miconazole were less sensitive. Regarding resistance pattern, ketoconazole (61%) was more resistant, followed by miconazole (47%). We also compared the susceptibility of C. albicans and non-C. albicans drug sensitivity. For C. albicans, sensitivity to nystatin (87.8%) was high, followed by itraconazole (85.3%), fluconazole (82%) clotrimazole (75%), and voriconazole (75%). Ketoconazole showed high-level resistance. Regarding non-C. albicans, three out of four (75%) C. glabrata showed sensitivity to fluconazole, voriconazole, and miconazole and only 25% were resistant to fluconazole. Two cases were sensitive (50%) and two cases (50%) were resistant to Itraconazole. Drug sensitivity in C. tropicalis showed all the three cases (100%) to be sensitive to fluconazole, itraconazole, and nystatin, and one case was resistant to clotrimazole and miconazole. Two cases of C. krusei showed sensitivity to nystatin. Azoles (fluconazole, itraconazole, and voriconazole) were only 50% sensitive. Both the cases were resistant to miconazole. While comparing our results with other studies done on drug susceptibility pattern, all the three non-C. albicans species showed the highest sensitivity to nystatin. Out of nine cases of non-C. albicans, all were sensitive to nystatin. 66%–78% sensitivity was observed to fluconazole, voriconazole, clotrimazole, and itraconazole. Ketoconazole showed the least sensitivity (55%). Further analysis of drug sensitivity pattern in large study group is necessary. Our study showed similarity with a study done by Panchal et al. in Western India.,
|Table 5: Analysis of drug sensitivity pattern in vulvovaginal candidiasis|
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We compared the drug susceptibility pattern of C. albicans and non-C. albicans in this study which showed a similar pattern of sensitivity and resistance in both groups. Nystatin scored the highest sensitivity, followed by fluconazole, itraconazole, and voriconazole. Ketoconazole showed the highest resistance in both groups.
Unmarried women were excluded in the study as speculum examination should be avoided in them. Speculum examination was avoided in pregnant women as organisms were identified in them from secretions from vulva itself. Follow-up was not analyzed for our patients as our study confined to clinicomycological study only.
| Conclusion|| |
VVC is common among women in the reproductive age group. Species identification by culture methods showed C. albicans to be the most prevalent species including the HIV-positive patients in this study. Fluconazole, itraconazole, and voriconazole were sensitive in both C. albicans and non-C. albicans infections. Nystatin was found to be a highly sensitive drug, followed by triazoles. Ketoconazole and miconazole were highly resistant to both Candida and non-C. albicans species. According to our study results, elimination of predisposing factors and ensuring good immunity with identification of causative fungal species and treatment according to the drug sensitivity pattern will reduce the incidence of VVC.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| References|| |
Hurley R, de Louvois J. Candida
vaginitis. Postgrad Med J 1979;55:645-7.
Nyirjesy P, Weitz MV, Grody MH, Lorber B. Over-the-counter and alternative medicines in the treatment of chronic vaginal symptoms. Obstet Gynecol 1997;90:50-3.
Ako-Nai AK, Kassim OO, Adeniran MO, Taiwo O. A study of urinary tract infections at Ile-Ife, Nigeria. East Afr Med J 1993;70:10-4.
Sehgal SC. Epidemiology of male urethritis in Nigeria. J Trop Med Hyg 1990;93:151-2.
White MH. Is vulvovaginal candidiasis an AIDS-related illness? Clin Infect Dis 1996;22 Suppl 2:S124-7.
Duerr A, Sierra MF, Feldman J, Clarke LM, Ehrlich I, DeHovitz J. Immune compromise and prevalence of Candida
vulvovaginitis in human immunodeficiency virus-infected women. Obstet Gynecol 1997;90:252-6.
Spinillo A, Michelone G, Cavanna C, Colonna L, Capuzzo E, Nicola S. Clinical and microbiological characteristics of symptomatic vulvovaginal candidiasis in HIV-seropositive women. Genitourin Med 1994;70:268-72.
Fichtenbaum CJ, Koletar S, Yiannoutsos C, Holland F, Pottage J, Cohn SE, et al
. Refractory mucosal candidiasis in advanced human immunodeficiency virus infection. Clin Infect Dis 2000;30:749-56.
Mahmoudi Rad M, Zafarghandi S, Abbasabadi B, Tavallaee M. The epidemiology of Candida
species associated with vulvovaginal candidiasis in an Iranian patient population. Eur J Obstet Gynecol Reprod Biol 2011;155:199-203.
Redondo-Lopez V, Lynch M, Schmitt C, Cook R, Sobel JD. Torulopsis glabrata
vaginitis: Clinical aspects and susceptibility to antifungal agents. Obstet Gynecol 1990;76:651-5.
Ahmad A, Khan AU. Prevalence of Candida
species and potential risk factors for vulvovaginal candidiasis in Aligarh, India. Eur J Obstet Gynecol Reprod Biol 2009;144:68-71.
Fan SR, Liu XP, Li JW. Clinical characteristics of vulvovaginal candidiasis and antifungal susceptibilities of Candida
species isolates among patients in southern China from 2003 to 2006. J Obstet Gynaecol Res 2008;34:561-6.
Panchal PA, Katara RK, Mehta RC, Soni ST, Nanera A, Trivedi NA, et al
. Microbiological study of various Candida
species and its antifungal sensitivity testing isolated from antenatal women with vaginitis, in tertiary care teaching hospital, Western India. Int J Microbiol Res 2013;5:486-9.
Mutua F, Revathi G, Machoki JM. Species distribution and antifungal sensitivity patterns of vaginal yeasts. East Afr Med J 2010;87:156-62.
[Figure 1], [Figure 2], [Figure 3], [Figure 4]
[Table 1], [Table 2], [Table 3], [Table 4], [Table 5]