treatment of oral candidiasis
Last edited 06/2021 and last reviewed 10/2023
Initial management includes identifying and correcting any underlying factors that may predispose or contribute to oral candidosis- exclude any deficiency states (iron, folate and vitamins B12 and C), diabetes
and any immunodeficiencies
- this condition is uncommon in people other than infants, denture wearers, and the elderly
- identify any drugs which might be the cause and if practical, substituted for an alternative
- in denture‐associated erythematous candidosis
- check for the adequacy of the dentures
- evaluate oral and denture hygiene measures and make necessary corrections if required
- avoid nocturnal denture wearing (1,2)
If underlying predisposing factors cannot be corrected, pharmacological treatment is indicated
- treatment involves topical or systemic antifungals
- management options vary with respect to patient population:
- oral candidiasis in children
- exclude risk factors for candidiasis (1,2,3)
- topical antifungal treatment
- first line therapy
- miconazole oral gel first-line for 7 days
- note that this medication is unlicensed for use in a child aged younger than 4 months (or 5-6 months for an infant born pre-term)
- an alternative is oral nystatin suspension for 7 days
- note that this medication is unlicensed for use in neonates
- miconazole oral gel first-line for 7 days
- first line therapy
- if persistent oral candidiasis after 7 day treatment regime (and
adequate adherence to regime)
- if evidence of partial response to miconazole oral gel then extension of treatment for a further 7 day course
- if minimal or no effect from miconazol oral gel regime then treat with nystatin suspension for 7 day course
- seek specialist advice
- if inadequate response to 14 day treatment for oral thrush or
- there are recurrent episodes of oral thrush (3) or
- a clinical suspicion of immunosuppression
- oral candidiasis in adults and young people
- oral candidiasis is uncommon in people other than infants, denture wearers, and the elderly. In otherwise healthy people, it may be the first presentation of an undiagnosed risk factor.
- Prescribe antifungal treatment.
- If the infection is mild and localized, prescribe topical antifungal treatment for 7 days.
- miconazole oral gel is first-line therapy
- If miconazole is unsuitable, offer nystatin suspension.
- If the infection is extensive or severe infection, consider one of the following:
- oral fluconazole 50 mg a day for 7 days or
- seek specialist advice or refer to an oral surgeon (3)
- follow up people who have extensive or severe oral candidiasis (requiring oral fluconazole) after 7 days
- if complete resolution of infection then stop treatment
- if there has not been complete resolution of the infection then various options are appropriate (3):
- extension of the course of fluconazole for a further 7 days (refer to an oral surgeon if the infection persists after this)
- take an oral swab in order to identify the causative organism
- seek further advicce
- either seek specialist advice or
- undertake specialist referral (to an oral surgeon)
- when making this decision then the clinician must consider
- a) severity of infection - there should be a low threshold for early referral if infection is severe (3)
- b) the level of immunocompromise
- c) response to first-line therapy.
- If the infection is mild and localized, prescribe topical antifungal treatment for 7 days.
- oral candidiasis in immunosuppressed adults
- mild, localized oral candidiasis
- miconazole oral gel first-line for 7 days
- nystatin suspension for 7 days is an alternative
- if severe and extensive infection then consider
- systemic treatment with oral fluclonazole (check the summary of product characteristics before prescribing) and/or
- seeking specialist advice
- be aware of the potential interactions of systemic antifungal
therapy with medication prescribed
- for example fluconazole can increase ciclosporin or tacrolimus levels if prescribed concurrently with either of these agents (4,5)
- seek specialist advice if patient on chemotherapy regime
- if there is a concern that oral candidiasis may be related to immunosuppression
caused by disease-modifying anti-rheumatic drugs (DMARDS)
- seek specialist advice
- ensure monitoring blood tests are undertaken
- mild, localized oral candidiasis
- oral candidiasis in children
Notes:
- general principles for use of systemic agents such as fluconazole, ketoconazole, and itraconazole (1)
- these may be used in the following groups
- patients who have candidiasis refractory to topical therapy
- patients intolerant of topical agents
- patients at high risk of developing systemic infection (1,2)
- oral candidiasis
- uncommon in people other than infants, denture wearers, and the elderly
- it may be the first presentation of an undiagnosed risk factor
- evidence from randomised controlled trials that miconazole and fluconazole increased clinical cure of oropharyngeal candidiasis in immunocompetent and immunocompromised infants and children when compared with nystatin (6,7).
Reference:
- (1) Farah CS et al. Oral fungal infections: an update for the general practitioner. Aust Dent J. 2010;55 Suppl 1:48-54.
- (2) Singh A, Verma R, Murari A, Agrawal A. Oral candidiasis: An overview. Journal of Oral and Maxillofacial Pathology : JOMFP. 2014;18(Suppl 1):S81-S85.
- (3) NICE. CKS - Oral Candida (accessed June 26th 2021)
- (4) Canafax DM et al. Interaction between cyclosporine and fluconazole in renal allograft recipients.Transplantation. 1991 May;51(5):1014-8.
- (5) Mathis AS et al. Sex and ethnicity may chiefly influence the interaction of fluconazole with calcineurin inhibitors.Transplantation. 2001 Apr 27;71(8):1069-75.
- (6) Hoppe J, Burr R, Ebeling H, et al. Treatment of oropharyngeal candidiasis in immunocompetent infants: a randomized multicenter study of miconazole gel vs. nystatin suspension. Pediatr Infect Dis J 1997;16:288-293.
- (7) Goins RA, Ascher D, Waecker N, et al. Comparison of fluconazole and nystatin oral suspensions for treatment of oral candidiasis in infants. Pediatr Infect Dis J 2002;21:1165-1167.