Plantier Diogo Barreto, Pinna Fábio de Rezende, Olm Mary Anne Kowal, Athanázio Rodrigo, Pilan Renata Ribeiro de Mendonça, Voegels Richard Louis
Department of Otorhinolaryngology and Ophthalmology, School of Medicine, Universidade de São Paulo, São Paulo, SP, Brazil.
Department of Pathology, School of Medicine, Universidade de São Paulo, São Paulo, SP, Brazil.
Int Arch Otorhinolaryngol. 2023 Aug 4;27(3):e423-e427. doi: 10.1055/s-0042-1746193. eCollection 2023 Jul.
Primary ciliary dyskinesia (PCD) is a rare inherited disease associated with impairment of mucociliary transport and, consequently, with a high incidence of chronic rhinosinusitis. For patients with chronic rhinosinusitis who remain symptomatic despite medical treatment, endoscopic sinus surgery is a safe and effective therapeutic option. However, to date, no studies have been found evaluating the effect of surgery on the quality of life associated with the effect on olfaction and nasal endoscopy findings of patients with primary ciliary dyskinesia and chronic rhinosinusitis. To describe the effect of endoscopic sinus surgery on the quality of life, on olfaction, and on nasal endoscopy findings of adults with PCD and chronic rhinosinusitis. Four patients who underwent endoscopic sinus surgery were included. The Sinonasal Outcome Test-22 (SNOT-22) score, the Nasal Obstruction Symptom Evaluation (NOSE) questionnaire, and the Lund-Kennedy score were collected preoperatively and at 3 and 6 months postoperatively. The olfaction as assessed with the University of Pennsylvania Smell Identification Test (UPSIT), which was administered preoperatively and 3 months postoperatively. A total of 4 patients with a mean age of 39.3 years old (3 men and 1 woman) completed the study. All patients showed clinically significant improvement in the SNOT-22, NOSE, and Lund-Kennedy scores at 3 months postoperatively, and this improvement was sustained throughout the follow-up period. However, olfaction did not improve after surgery. The endoscopic sinus surgery treatment of chronic rhinosinusitis in adults with PCD was associated with improvement in quality of life and endoscopic findings. However, no improvement in olfaction was demonstrated. Studies with a larger number of patients and control groups should help confirm these findings.
原发性纤毛运动障碍(PCD)是一种罕见的遗传性疾病,与黏液纤毛运输功能受损相关,因此慢性鼻窦炎的发病率较高。对于经药物治疗后仍有症状的慢性鼻窦炎患者,鼻内镜鼻窦手术是一种安全有效的治疗选择。然而,迄今为止,尚未发现有研究评估手术对原发性纤毛运动障碍合并慢性鼻窦炎患者嗅觉及鼻内镜检查结果的影响以及对生活质量的作用。
描述鼻内镜鼻窦手术对原发性纤毛运动障碍合并慢性鼻窦炎的成年患者生活质量、嗅觉及鼻内镜检查结果的影响。
纳入4例行鼻内镜鼻窦手术的患者。术前及术后3个月和6个月收集鼻窦结局测试-22(SNOT-22)评分、鼻阻塞症状评估(NOSE)问卷及Lund-Kennedy评分。术前及术后3个月采用宾夕法尼亚大学嗅觉识别测试(UPSIT)评估嗅觉。
共有4例患者(平均年龄39.3岁,3例男性,1例女性)完成了研究。所有患者术后3个月时SNOT-22、NOSE及Lund-Kennedy评分均有显著临床改善,且在整个随访期内这种改善持续存在。然而,术后嗅觉并未改善。
鼻内镜鼻窦手术治疗原发性纤毛运动障碍合并慢性鼻窦炎的成年患者可改善生活质量及鼻内镜检查结果。然而,未显示嗅觉有改善。纳入更多患者及对照组的研究应有助于证实这些发现。