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DOI 10.3109/00016489.2014.975893

Медицинская библиотека · Acta oto-laryngologica · 2015

Clinical effects of clarithromycin on persistent inflammation following Haemophilus influenzae-positive acute otitis media.

Iino Yukiko, Yoshida Naohiro, Kato Toshinori, Kakizaki Keiko, Miyazawa Tetsuo, Kakuta Hiroyuki

СтатьяРандомизированное исследованиеПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

CONCLUSION

Additional treatment with clarithromycin (CAM) reduced persistent middle ear inflammation after acute otitis media (AOM) caused by Haemophilus influenzae in children. CAM is a treatment option for persistent inflammation following AOM and to prevent continuing otitis media with effusion.

OBJECTIVE

We conducted a clinical study to evaluate a new method of treatment for persistent inflammation after AOM in children.

METHODS

H. influenzae-infected children with AOM were treated acutely with antimicrobial agents, after which those still demonstrating effusion of the middle ear cavity received additional treatment with carbocysteine (S-CMC) alone or S-CMC combined with clarithromycin (CAM) for 1 week. The two regimens were compared in terms of clinical effects.

RESULTS

After the initial acute treatment, many patients still showed abnormal otoscopic findings. At the completion of additional treatment, there were no significant differences between the two treatment groups. However, 1 week after completion of additional treatment, the prevalence of a diminished light reflex was significantly lower in the CAM + S-CMC group than in the S-CMC group (p = 0.017). The prevalence of redness of the tympanic membrane also tended to be lower in the combined treatment group than in those receiving a single drug (p = 0.097).

Для цитирования: Iino Yukiko, Yoshida Naohiro, Kato Toshinori, Kakizaki Keiko, Miyazawa Tetsuo, Kakuta Hiroyuki. Clinical effects of clarithromycin on persistent inflammation following Haemophilus influenzae-positive acute otitis media.. Acta oto-laryngologica. 2015. DOI: 10.3109/00016489.2014.975893.

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