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Otomycosis: Clinical Features and Treatment Implications: Tang Ho, MD, MSC, Jeffrey T. Vrabec, MD, Donald Yoo, BS
Otomycosis: Clinical Features and Treatment Implications: Tang Ho, MD, MSC, Jeffrey T. Vrabec, MD, Donald Yoo, BS
ORIGINAL RESEARCH
From the Bobby R. Alford Department of Otolaryngology–Head and Reprint request: Jeffrey T. Vrabec, MD, Neurosensory Center, 6501
Neck Surgery, Baylor College of Medicine, Houston, Texas. Fannin, Rm NA 102, Houston, TX 77030-3498.
Presented at the Annual Meeting of the American Academy of Otolar- E-mail address: jvrabec@bcm.tmc.edu.
yngology–Head and Neck Surgery, Toronto, Canada, September 17-20,
2006.
0194-5998/$32.00 © 2006 American Academy of Otolaryngology–Head and Neck Surgery Foundation. All rights reserved.
doi:10.1016/j.otohns.2006.07.008
788 Otolaryngology–Head and Neck Surgery, Vol 135, No 5, November 2006
Table 2
Treatment received before diagnosis
Number of Percentage
Treatment patients (%)
Ototopical drops 59 45
Ciprofloxacin 14 11
Neomycin-polymyxin
B-hydrocortisone 14 11
Ofloxacin 9 7
Other* 8 6
Unknown 14 11
Oral antimicrobials 32 24
*Includes acetic acid, alcohol, clotrimazole, and other anti-
microbial otic drops.
Figure 1 Clinical appearance of otomycosis.
Ho et al Otomycosis: Clinical features and treatment . . . 789
Table 4
Treatment success and failure rates
pearance like Aspergillus and can present as otorrhea not pears to convey an increased risk for development of oto-
responding to aural antimicrobials. Otomycosis attributed to mycosis.
Candida is often identified by culture data. Prior otologic procedures were noted in more than one-
Although multiple in vitro studies have examined the effi- third of the patients in the study and appear to increase the
cacy of various antifungal agents, there is no consensus on the risk for developing otomycosis. This is higher than that
most effective agent.10,11 Various agents have also been used reported in other series such as that by Pradhan et al7 where
clinically with variable rates success.12-14 Nevertheless, ap- 4.6% of the subjects were postmastoidectomy patients. Al-
plication of appropriate topical antifungal agents coupled though this may represent a referral bias inherent to a
with frequent mechanical debridements usually results in tertiary otology practice, the data appear to support prior
prompt resolution of symptoms, although recurrence or re- otologic procedures, particularly those that result in a mas-
sidual disease can be common. In this series, more than 80% toid cavity, as a potential risk factor for otomycosis. Several
of the patients had resolution of the infection with initial factors may contribute to development of otomycosis in the
treatment, often in less than 2 weeks. Topical ketoconazole previously operated ear. First, recurrent drainage or subse-
is our preferred antifungal agent for its efficacy against both quent antibiotic/antiseptic application may alter the local
Aspergillus and Candida species. There were no cases of environment of the external canal and allow superinfection
local sensitivity to ketoconazole, and the infections seemed by nosocomial fungi. Second, alteration of the anatomy by
to resolve faster and display a lower recurrence rate. The use CWD procedures may also produce changes in cerumen
of cresylate otic drops should be avoided in patients with production or relative humidity that favor fungal growth.
TM perforation given its potential complications. In our The incidence of both recurrent and residual fungal dis-
practice, we have observed transient sensorineural hearing ease for postmastoidectomy patients in this series is higher
loss associated with such use. than that in patients with an intact canal wall (residual, 23%
Complications such as TM perforation and serous otitis vs 13%; recurrent, 27% vs 12%); this suggests that eradi-
media as a result of otomycosis are not uncommon and tend cation of disease is more difficult in the presence of a
to resolve with treatment. The pathophysiology of the TM mastoid cavity. Further analysis found that the patients with
perforations may be attributed to avascular necrosis of the CWD cavities were more likely to receive cresylate as
TM as a result of mycotic thrombosis in the adjacent blood initial therapy. However, treatment of CWD cavities with
vessels.15 The rate (14%) of TM perforation in this series is ketoconazole was also more difficult and more prone to
similar to that observed by Pradhan et al7 (16%) and Kur- recurrence. Because both agents were highly effective over-
natowski and Filipiak12 (12%). There were no clinical fea- all, as demonstrated by the ⬎80% resolution rate after initial
tures predictive of TM perforation. TM involvement is treatment (Table 4), we conclude that the anatomic differ-
likely a consequence of fungal inoculation in the most ences imposed by CWD surgery are responsible for the
medial aspects of the external canal or direct extension of doubling of residual/recurrent disease rates. One obvious
disease from adjacent skin. explanation for this finding is the difficulty in applying
There appears to be little consensus with respect to the topical medications in the relatively large surface area of the
predisposing factors for otomycosis. For instance, the pres- cavity. This is especially problematic when the focus of
ence of cerumen has been speculated to be supportive of infection is in the superior or posterior aspects of the cavity.
fungal growth by some yet inhibitory by others.1,5,14 There In this situation we recommend filling the cavity with top-
have also been reports of autoinoculation of the ear canal ical ketoconazole cream and then packing the cavity with
that result in otomycosis by patients with untreated der- gauze to ensure the topical medication stays in contact with
matomycoses.16 However, autoinoculation of the external the infected epithelium. The addition of oral antifungals is
canal does not appear to be a significant factor in our patient reserved for cases with severe disease and poor response to
population as the history of fungal infections of the skin or therapy, though it is rarely necessary. We have observed
nails was rare. patients treated with oral agents before referrals that con-
More recently, there has been increasing concern with tinued to have persistent disease. We believe oral antifun-
respect to increasing incidence of otomycosis from wide- gals are unlikely to succeed in the absence of adequate local
spread use of fluoroquinolone otic drops.17-19 It is interest- care.
ing to note that similar concerns had been raised nearly 2 The limitations of this study include the possible selec-
decades ago with the introduction of topical antibiotic/ste- tion bias given the referral pattern of our practice. Never-
roid preparations, yet they have subsequently been shown to theless, to our knowledge this series is one of the largest
have little or no effect on the incidence of otomycosis.1,14 In otomycosis surveys reported. In addition, the increased heat
this series, ciprofloxacin and neomycin-polymyxin B-hy- and humidity in our geographical region may limit the
drocortisone drops were the most frequently prescribed oto- applicability of these findings in regions with a more tem-
topical therapy before presentation. Although the chronic perate climate. Future research may include better charac-
use of ototopical antimicrobial preparations remains a po- terization of the effective treatment dose and duration of the
tential predisposing risk factor, no specific preparation ap- various available antifungal agents.
Ho et al Otomycosis: Clinical features and treatment . . . 791
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