2021
DOI: 10.1007/s11046-021-00581-x
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A Case of Topical Ofloxacin-Induced Otomycosis and Literature Review

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Cited by 9 publications
(5 citation statements)
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“…Therefore, the use of Telipidal ear drops is necessary for adjuvant treatment, which can produce a good secretion of pathogenic bacteria in children. Only by suppressing the pathogenic bacteria in children can we truly and effectively remove the infection lesions, which is an important step in reducing the disease recurrence rate and the incidence of adverse reactions in children [ 20 ].…”
Section: Discussionmentioning
confidence: 99%
“…Therefore, the use of Telipidal ear drops is necessary for adjuvant treatment, which can produce a good secretion of pathogenic bacteria in children. Only by suppressing the pathogenic bacteria in children can we truly and effectively remove the infection lesions, which is an important step in reducing the disease recurrence rate and the incidence of adverse reactions in children [ 20 ].…”
Section: Discussionmentioning
confidence: 99%
“…Furthermore, in patients receiving long‐term ototopical antibiotic therapy, M . furfur may cause subsidiary infections, affecting the flora in the outer ear canal 20 . Particular attention should be given to M .…”
Section: Discussionmentioning
confidence: 99%
“…19 Furthermore, in patients receiving long-term ototopical antibiotic therapy, M. furfur may cause subsidiary infections, affecting the flora in the outer ear canal. 20 Particular attention should be given to M. furfur strains exhibiting strong resistance to antifungal drugs. 11 In this respect, FastFung agar would be helpful, as it demonstrated better results in M. furfur isolation than mDixon agar, although there was no difference in the variety of isolated species between the two media (Wilcoxon p = .28, McNemar p = .004; Table 3).…”
Section: Discussionmentioning
confidence: 99%
“…Isolates that we were unable to appropriately identify were subjected to molecular analysis using DNA extracted by a Kaneka Easy DNA Extraction Kit (KANEKA Corp., Tokyo, Japan) in accordance with the manufacturer’s instructions. Using the two primer pairs 28SF1/635 and ITS1/ITS4 [ 1 , 3 ], we respectively amplified fragments of the 28S rDNA D1/D2 domain and the rDNA internal transcribed spacer (ITS) region, which were subsequently sequenced using an Applied Biosystems model 3130 sequencer. To identify the generated sequences, sequence similarity was assessed based on searches using the Basic Local Alignment Search Tool (BLAST) ( http://blast.ncbi.nlm.nih.gov/Blast.cgi ).…”
Section: Methodsmentioning
confidence: 99%