Caballero Anyull D B, Candelo Estephania, Avila-Castano Karol, Alhalabi Alaa, Donaldson Angela M
Department of Otolaryngology Mayo Clinic Florida Jacksonville Florida USA.
OTO Open. 2024 Sep 18;8(3):e70013. doi: 10.1002/oto2.70013. eCollection 2024 Jul-Sep.
This study aimed to evaluate the impact of endoscopic sinus surgery (ESS) on asthma severity up to 12 months after surgical intervention.
Retrospective cohort.
Tertiary care center.
Patients with a history of asthma and Chronic Rhinosinusitis (CRS) who underwent ESS between 2013 and 2023 were included. Asthma severity was assessed according to current Global Initiative for Asthma (GINA) guidelines, classifying patients into mild, moderate, and severe based on medication requirements. Asthma severity was evaluated up to 3 months prior to ESS and 1-year post-ESS. Patients with aspirin-exacerbated respiratory disease (AERD) were excluded. Statistical analysis was performed using McNemar test and Wilcoxon signed-rank test to assess differences in asthma severity, medication doses, and number of medications.
Sixty-five patients were included, of which 44 (67.7%) had CRS with nasal polyps (CRSwNP) and 21 (32.3%) had CRS without nasal polyps (CRSsNP). No significant differences were found in asthma severity pre- and post-ESS ( = .175). Similarly, no differences were found in ICS doses ( = .999), total number of prescribed medications ( = .157) or presence of exacerbations before and after ESS ( = .078). However, a significant increase in time from last rescue inhaler use was noted after ESS, increasing from a median of 6.71 to 23.1 weeks ( = .004).
This study is the first to assess the impact of ESS on asthma severity in a real-world setting. Our findings suggest that ESS does not impact asthma severity classification. However, it might provide relief of asthma symptoms in the early postoperative period.
本研究旨在评估内镜鼻窦手术(ESS)对手术干预后长达12个月的哮喘严重程度的影响。
回顾性队列研究。
三级医疗中心。
纳入2013年至2023年间接受ESS的哮喘和慢性鼻窦炎(CRS)患者。根据当前全球哮喘防治创议(GINA)指南评估哮喘严重程度,根据药物需求将患者分为轻度、中度和重度。在ESS前3个月和ESS后1年评估哮喘严重程度。排除阿司匹林诱发的呼吸道疾病(AERD)患者。使用McNemar检验和Wilcoxon符号秩检验进行统计分析,以评估哮喘严重程度、药物剂量和药物数量的差异。
纳入65例患者,其中44例(67.7%)患有伴鼻息肉的CRS(CRSwNP),21例(32.3%)患有不伴鼻息肉的CRS(CRSsNP)。ESS前后哮喘严重程度无显著差异(P = 0.175)。同样,ICS剂量(P = 0.999)、处方药物总数(P = 0.157)或ESS前后发作情况(P = 0.078)也无差异。然而,ESS后从最后一次使用急救吸入器到下次使用的时间显著增加,从中位数6.71周增加到23.1周(P = 0.004)。
本研究是首次在现实环境中评估ESS对哮喘严重程度的影响。我们的研究结果表明,ESS不会影响哮喘严重程度分类。然而,它可能在术后早期缓解哮喘症状。