Cited by 120Antifungal resistance and susceptibilityReproductive tract infections researchYeasts and Rust Fungi Studies

Guideline: Vulvovaginal Candidosis (AWMF 015/072), S2k (Excluding Chronic Mucocutaneous Candidosis)

Open access
Mendling, Werner·2015·Mycoses

Abstract

The oestrogenised vagina is colonised by Candida species in at least 20% of women; in late pregnancy and in immunosuppressed patients, this increases to at least 30%. In most cases, Candida albicans is involved. Host factors, particularly local defence mechanisms, gene polymorphisms, allergies, serum glucose levels, antibiotics, psycho-social stress and oestrogens influence the risk of candidal vulvovaginitis. Non-albicans species, particularly Candida glabrata, and in rare cases also Saccharomyces cerevisiae, cause less than 10% of all cases of vulvovaginitis with some regional variation; these are generally associated with milder signs and symptoms than normally seen with a C. albicans-associated vaginitis. Typical symptoms include premenstrual itching, burning, redness and odourless discharge. Although itching and redness of the introitus and vagina are typical symptoms, only 35-40% of women reporting genital itching in fact suffer from vulvovaginal candidosis. Medical history, clinical examination and microscopic examination of vaginal content using 400× optical magnification, or preferably phase contrast microscopy, are essential for diagnosis. In clinically and microscopically unclear cases and in chronically recurring cases, a fungal culture for pathogen determination should be performed. In the event of non-C. albicans species, the minimum inhibitory concentration (MIC) should also be determined. Chronic mucocutaneous candidosis, a rarer disorder which can occur in both sexes, has other causes and requires different diagnostic and treatment measures. Treatment with all antimycotic agents on the market (polyenes such as nystatin; imidazoles such as clotrimazole; and many others including ciclopirox olamine) is easy to administer in acute cases and is successful in more than 80% of cases. All vaginal preparations of polyenes, imidazoles and ciclopirox olamine and oral triazoles (fluconazole, itraconazole) are equally effective (Table ); however, oral triazoles should not be administered during pregnancy according to the manufacturers. C. glabrata is not sufficiently sensitive to the usual dosages of antimycotic agents approved for gynaecological use. In other countries, vaginal suppositories of boric acid (600 mg, 1-2 times daily for 14 days) or flucytosine are recommended. Boric acid treatment is not allowed in Germany and flucytosine is not available. Eight hundred-milligram oral fluconazole per day for 2-3 weeks is therefore recommended in Germany. Due to the clinical persistence of C. glabrata despite treatment with high-dose fluconazole, oral posaconazole and, more recently, echinocandins such as micafungin are under discussion; echinocandins are very expensive, are not approved for this indication and are not supported by clinical evidence of their efficacy. In cases of vulvovaginal candidosis, resistance to C. albicans does not play a significant role in the use of polyenes or azoles. Candida krusei is resistant to the triazoles, fluconazole and itraconazole. For this reason, local imidazole, ciclopirox olamine or nystatin should be used. There are no studies to support this recommendation, however. Side effects, toxicity, embryotoxicity and allergies are not clinically significant. Vaginal treatment with clotrimazole in the first trimester of a pregnancy reduces the rate of premature births. Although it is not necessary to treat a vaginal colonisation of Candida in healthy women, vaginal administration of antimycotics is often recommended in the third trimester of pregnancy in Germany to reduce the rate of oral thrush and napkin dermatitis in healthy full-term newborns. Chronic recurrent vulvovaginal candidosis continues to be treated in intervals using suppressive therapy as long as immunological treatments are not available. The relapse rate associated with weekly or monthly oral fluconazole treatment over 6 months is approximately 50% after the conclusion of suppressive therapy according to current studies. Good results have been achieved with a fluconazole regimen using an initial 200 mg fluconazole per day on 3 days in the first week and a dosage-reduced maintenance therapy with 200 mg once a month for 1 year when the patient is free of symptoms and fungal infection (Table ). Future studies should include Candida autovaccination, antibodies to Candida virulence factors and other immunological experiments. Probiotics with appropriate lactobacillus strains should also be examined in future studies on the basis of encouraging initial results. Because of the high rate of false indications, OTC treatment (self-treatment by the patient) should be discouraged.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1111/myc.12292

Cites

162 of 162 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Cites

Flagged first, then by citations

Research works printed but not linked: 25

  1. Anderson MR, Klink K, Cohrssen A. Evaluation of vaginal com- plaints. JAMA 2004; 291: 1368-79.
  2. Davidson F, Mould RF. Recurrent vaginal candidosis in women and the effect of intermittent prophylactic treatment. BJ Vener Dis 1978; 54: 176-83.
  3. Farrell SM, Hawkins DF, Ryder TT. Scanning electron microscope study of Candida albicans, invasion of cultural human cervical epi- thelial cells. Sabouraudia 1983; 25: 251-4.
  4. Ferwerda B, Ferwerda B, Platinga TS et al. Human lectin-1 defi- ciency and mucocutaneous fungal infections. N Engl J Med 2009; 361: 1760-7.
  5. Jeavons HS. Prevention and treatment of vulvovaginal candidosis using exogenous lactobacilli. J Obstet Gynecol Neonatal Nurs 2003; 32: 287-96.
  6. Li J, Fan SR, Liu XP et al. Biased genotype distributions of Candida albicans strains associated with vulvovaginal candidosis and candi- dal balanoposthitis in China. Clin Infect Dis 2008; 47: 1119-25.
  7. Loeffler W. Terminologie der Humanmykosen. Mykosen 1983; 26: 346.
  8. Mendling W. Die Torulopsidose in der Frauenheilkunde. Geburtsh Frauenheilk 1984; 44: 583-6.
  9. Mendling W, Koldovsky U. Investigations by cell-mediated immuno- logic tests of therapeutic trials with thymopentin in vaginal myco- ses. Inf Dis Obstet Gynecol 1996a; 4: 225-31.
  10. Mendling W, Niemann D, Tintelnot K. Vaginal Colonisation with Candida Species with Special Focus on Candida dubliniensis. A Pro- spective Study. Geburtsh Frauenheilk 2007; 67: 1132-7.
  11. Mendling W, Schlegelmilch R. Die 3t€ agige Kombinationsbehand- lung der Vulvovaginalkandidose mit Clotrimazol 200 mg Vaginalta- bletten und Clotrimazol Cr eme f€ ur die Vulva ist significant besser als die mit Vaginaltabletten allein. Eine € altere multizentrische, Pla- zebo-kontrollierte Doppelblindstudie und ihre Bedeutung f€ ur Thera- pieempfehlungen. Geburtsh Frauenheilk 2014; 74: 355-60.
  12. M€ uller J, Nold B, Kubitza D, Baumert J. Quantitative Untersuchun- gen € uber die D€ oderlein-Flora gesunder sowie mykosekranker Prob- andinnen unter lokaler Isoconazol-Nitrat-Therapie. In: Seeliger HPR (ed) Gyno -Travogen, Monographie Excerpta Medica. Amsterdam: Oxford Princeton 1981: 81-93.
  13. Niewerth M, Kunze D, Seibold M, Schaller M, Korting HC, Hube B. Ciclopirox olamine treatment affects the expression pattern of metabolism proteins, and drug resistance factors. Antimicrob Agents Chemother 2003; 47: 1805-17.
  14. Powell BL. Identification of a 173 -estradiol -binding protein in Candida albicans and Candida (Torulopsis) glabrata. Exp Mycology 1984; 8: 304. 108
  15. Reed BD, Zazone P, Pierson LL, Gorenflo DW, Horreocks J. Candida transmission and sexual behaviour as risk for a repeated episode of Candida vulvovaginitis. J Womens Health (Larchmt) 2003; 12: 979- 89. 112
  16. Rusch K, Schwiertz A. Candida autovaccination in the treatment of vulvovaginal Candida infections. Int J Gynecol Obstet 2007; 96: 130. 122
  17. Scheklakow ND, Deletorski WW, Goldoa OA. Ver€ anderungen der Ultrastruktur von Candida albicans unter Einwirkung von Polyen- Antibiotika. Mykosen 1980; 24: 140-52. 125
  18. Schnell JD, Voigt WH. Das Verhalten von Sprosspilzen am nicht verhornenden Plattenepithel. Arch Gynaekol 1974; 217: 377-82. 127
  19. Spinillo A, Capuzzo E, Egbe TO, Baltaro P, Nicola S, Piazzi G. Torul- opsis glabrata vaginitis. Obstet Gynecol 1995; 85: 993-8. 139
  20. Wajnberg M, Wajnberg A. Doppelblind-Vergleichsstudie mit Cic- lopyroxolamin-und Miconazol-Vaginalcreme bei vulvovaginaler Kandidose. Mykosen 1981; 24: 721-30. 149
  21. Watson MC, Grimshaw JM, Bond CM, Mollison J, Ludbrook A. Oval versus intravaginal imidazole and triazole antifungal treatment of uncomplicated Candidiasis (thrush): a systemic review. BJOG 2002; 109: 85-89. 151
  22. Wilson C. Recurrent vulvovaginal candidiasis; an overview of tradi- tional and alternative therapies. Adv Nurse Pract. 2005; 13: 24-29. 155
  23. Witkin SS, Giraldo P, Linhares D. New insights into the immune pathogenesis of recurrent vulvovaginal candidiasis. Int J Gynecol Obestet 2000; 3: 114-8. 157
  24. Young GL, Jewell D. Topical treatment for vaginal candidiasis (thrush in pregnancy) (review). The Cochrane Database of systematic Reviews 2001; 4:CD 000225. 161
  25. Von Zglinicki W. Die Hormonspirale als Ursache f€ ur chronische Infektionen. Dissertation (Prof. HJ Tietz), Charit e 2011.

Cited by

Sorted by citations

Authors
Mendling, W.
Affiliations
Deutsches Zentrum für Infektionen in Gynäkologie und Geburtshilfe Vogelsangstrasse 106 42109 Wuppertal Germany
Corresponding author
Mendling, Werner
Venue
Mycoses
Publisher
Wiley
Published
2015-02-24
Volume
58
Issue
S1
Pages
1-15
ISSN
  • 0027-5557 (ISSN-L)
  • 0933-7407
  • 1439-0507
OpenAlex
W2164957395
Cited by
117
References
161
Citations by year
2026: 1 · 2025: 6 · 2024: 7 · 2023: 6 · 2022: 12 · 2021: 19 · 2020: 17 · 2019: 8 · 2018: 11 · 2017: 11 · 2016: 12 · 2015: 7
FWCI
10.64
Type
journal article
Language
en
Open access
Locations
  • Mycoses (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Infectious Diseases › Antifungal resistance and susceptibility
  • Life Sciences › Immunology and Microbiology › Microbiology › Reproductive tract infections research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Yeasts and Rust Fungi Studies
Keywords
candidal vaginitis, Candida albicans, Candida glabrata, non-albicans Candida, fungal culture, polyenes, imidazole, ciclopirox olamine, 5-fluorocytosine
MeSH terms
Antifungal Agents, Candida albicans, Candidiasis, Vulvovaginal, Female, Germany, Humans, Infant, Newborn, Microbial Sensitivity Tests, Microscopy, Phase-Contrast, Pregnancy, Pregnancy Complications, Infectious, Vaginal Discharge, Candida glabrata

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review