Efficacy and Safety of Long-Term Low-Dose Clarithromycin in Patients With Refractory Chronic Sinusitis After Endoscopic Sinus Surgery: A Prospective Clinical Trial

• Published in: Ear, nose, & throat journal nose, & throat journal, 2024-01, Vol.103 (1), p.NP31-NP39
• Main Authors: Chen, Han, Zhou, Bing, Huang, Qian, Li, Cheng, Wu, Yubin, Huang, Zhenxiao, Li, Yunxia, Qu, Jing, Xiao, Nianci, Wang, Mingjie
• Format: Article
• Language: English
• Subjects: Antibiotics; Chronic Disease; Clarithromycin - adverse effects; Endoscopy; Humans; Microbiota; Nasal Polyps - surgery; Oral administration; Otolaryngology; Prospective Studies; Rhinitis - chemically induced; Rhinitis - drug therapy; Rhinitis - surgery; Rhinorrhea; Sinusitis - chemically induced; Sinusitis - drug therapy; Sinusitis - surgery; Streptococcus infections; Treatment Outcome
• ISSN: 0145-5613; 1942-7522
• DOI: 10.1177/01455613211032020

Objective: To observe the efficacy and safety of postoperative long-term low-dose oral administration of clarithromycin in patients with refractory chronic rhinosinusitis (RCRS), to explore the characteristics of postoperative microbiota in the nasal cavity in patients with RCRS, and to compare the differences and changes in microbiota in the nasal cavity before and after medication. Methods: This was a prospective, self-controlled study. Eighteen patients with RCRS who had persistent symptoms after endoscopic sinus surgery and standard therapy with normal immunoglobulin E and eosinophil level were included. Low dose (250 mg, once daily) clarithromycin was orally administrated for 12 weeks. Symptom severity and endoscopic findings were evaluated before, after 4 weeks, and 12 weeks of treatment, and nasal cavity microbiota was analyzed simultaneously. Results: A total of 18 patients with RCRS were enrolled and 17 patients completed the study. Four weeks after oral administration of clarithromycin, significant improvement was observed in subjective symptoms including nasal congestion, rhinorrhea, postnasal drip, and general discomfort, as well as endoscopic findings including general surgical cavity condition, rhinedema, and rhinorrhea (P < .05). After continuous treatment to the 12th week, symptoms showed significant improvement compared with baseline, and endoscopic score showed significant improvement compared with both baseline and 4 weeks after treatment. Analysis of middle nasal meatus flora revealed a significant decrease of Streptococcus pneumoniae after 12 weeks of clarithromycin treatment (P < .05), while the richness, composition, and diversity were similar before and after treatment. Patients enrolled experienced no adverse drug reaction or allergic reaction, nor clinical significant liver function impairment observed. Conclusion: Postoperative low-dose long-term oral administration of clarithromycin in patients with RCRS can improve the clinical symptoms and facilitate the mucosal epithelialization, with good tolerance and safety. The efficacy of clarithromycin in patients with RCRS may be related to its regulatory effect on nasal cavity microbiota.