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Management of otitis externa with an led-illuminated gel: a randomized controlled clinical trial in dogs

DOI:10.1186/s12917-020-02311-9 期刊:BMC Veterinary Research 出版年份:2020 更新时间:2025-09-23 15:19:57
摘要: Background: Canine otitis externa is a painful condition which can be challenging to treat due to difficulties in the administration of otic medication. This can be due to lack of owner compliance in the application of ear drops or due to the resentment that some dogs demonstrate when attempts are made to administer topical medication into a sensitive ear canal. The aim of the study was to assess the efficacy of a topical LED-illuminated gel (LIG) in canine otitis externa in comparison to standard of care therapy. Dogs with spontaneous otitis externa were randomly allocated in three groups: groups QW received LIG once weekly; BW received LIG twice weekly; group C received enrofloxacin and silver sulfadiazine twice daily. LIG consists of a topical application of a gel containing chromophores that, when illuminated by a LED lamp, re-emit fluorescent light which can stimulate physiological responses, promoting healing and controlling bacteria. The evaluation protocol (T0 to T5) considered clinical assessment (OTIS-3-index-scoring-system; pruritus-severity-scale; pain-severity-score; aural temperature), cytological scoring system, quali-quantitative bacteriologic assessment. Results: All groups (QW, n = 21; BW, n = 23; C, n = 20) showed improvement during the study (QW: P < 0.02 for cytological and pain scores, P < 0.003 for bacteriologic assessment, P < 10? 4 for pruritus, total OTIS-3 and temperature assessments; BW: P < 10? 4 for all clinical, cytological and bacteriologic assessments; C: P < 0.02 for all clinical and cytological assessments, P < 10? 4 for bacteriologic assessment). The highest clinical score reduction occurred in Group BW (P < 0.014 in T3; P < 0.001 in T4 and P < 10? 4 in T5). BW reached the clinically relevant effect level at T3 (? 3.26 ± 1.21 levels), QW reached it at T4 (? 3.24 ± 0.99), C did not reach it. No differences between groups were seen in the reduction of CFU/mL (T0-T5). Conclusions: All treatment groups showed a positive clinical effect. LIG administered twice-a-week was the most favourable protocol of the study. LIG may be considered beneficial in the management of canine otitis externa; it seems to be effective in controlling the clinical condition, including the signs of inflammation and local pain, the bacterial growth, and it may help increasing treatment compliance.
作者: Adolfo Maria Tambella,Anna Rita Attili,Francesca Beribè,Margherita Galosi,Andrea Marchegiani,Matteo Cerquetella,Angela Palumbo Piccionello,Cecilia Vullo,Andrea Spaterna,Alessandro Fruganti
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The aim of the study was to assess the efficacy of a topical LED-illuminated gel (LIG) in canine otitis externa in comparison to standard of care therapy.

An overall effect was found during the study both for LIG and for standard of care. The LIG administered twice weekly was the protocol that showed the greatest overall reduction in OTIS-3 score from start to finish of therapy course. The LED-Illuminated Gel (LIG) may be considered beneficial in the management of canine otitis externa; it seems to be effective in improving clinical condition, modulating inflammation and controlling bacteria. Having demonstrated similar efficacy to SOC, it may help reducing or avoiding antibiotic treatment in otitis cases. The lower frequency of application of LIG compared to standard of care could also increase therapeutic compliance.

One of the limitations of the study is the difference in OTIS-3 scores between groups at enrolment, with the BW group averaging a higher condition severity than QW and C. This is also observed in some of the secondary parameters measured, although baseline demographic and clinical data did not show significant statistical differences. This limitation is intrinsic to the fact that it is a clinical trial with patients suffering from spontaneous pathology. Another limitation was that, to be included in this trial, dogs had to have an intact tympanic membrane visible by otoscopy before treatment.

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