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Research Articles

Doxycycline may be more clinically effective in type 2 chronic rhinosinusitis nasal polyp comorbid with asthma

, MD, , MD & , MD
Pages 20-26 | Received 19 Feb 2023, Accepted 10 Jul 2023, Published online: 20 Jul 2023
 

Abstract

Objective

Chronic rhinosinusitis with nasal polyp (CRSwNP) is one of the major phenotypes of chronic rhinosinusitis (CRS) with a high symptom burden. Doxycycline can be used as add-on therapy in CRSwNP. We aimed to evaluate short-term efficacy of oral doxycycline on visual analog scale (VAS) and SNOT-22 (Sino-nasal outcome test) score for CRSwNP.

Methods

Visual analog score (VAS) for nasal symptoms and total SNOT-22 scores of 28 patients who applied with the diagnosis of CRSwNP and received 100 mg doxycycline for 21 days were analyzed in this retrospective cohort study. Doxycycline efficacy was also evaluated in subgroups determined according to asthma, presence of atopy, total IgE and eosinophil levels.

Results

After 21-day doxycycline treatment, there was a significant improvement in VAS score for post-nasal drip, nasal discharge, nasal congestion, and sneeze, and total SNOT-22 score (p = 0.001, p < 0.001, p < 0.001, p < 0.001, p < 0.001, respectively). No significant improvement was observed in VAS score for the loss of smell (p = 0.18). In the asthmatic subgroup, there were significant improvements in all VAS scores and total SNOT-22 score after doxycycline. In the non-asthmatic subgroup, there was no significant change in any of the VAS scores, but total SNOT-22 score was significantly improved (42 [21–78] vs. 18 [9–33]; p = 0.043). Improvement in VAS score for loss of smell is significant in only some subgroups like asthmatic patients, non-atopic patients, and patients with eosinophil >300 cell/µL.

Conclusions

Doxycycline can be considered as an add-on treatment for symptom control in patients especially with CRSwNP comorbid with asthma.

Acknowledgments

All of these authors worked in the writing, control and statistical analysis sections of the study designed by İnsu Yılmaz. We also thank Murat Türk and Seçkin Özsaydı for their technical support and assistance.

Disclosure statement

Gülden Paçacı Çetin reports congress travel support from and speaker fees form GSK. İnsu Yılmaz reports advisory board, speaker fees, and congress travel support from Novartis, Bahar Arslan declare no conflict of interest.

Additional information

Funding

The author(s) reported there is no funding associated with the work featured in this article.

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