Lavigne François, Miller Steven K, Gould Andrew R, Lanier Brent J, Romett J Lewis
Department of Otolaryngology, Centre hospitalier de l'Université de Montréal (CHUM), Hôpital Notre-Dame, Montréal, Québec, Canada.
Int Forum Allergy Rhinol. 2014 May;4(5):381-9. doi: 10.1002/alr.21309. Epub 2014 Mar 5.
Treatment options for chronic rhinosinusitis with recurrent polyposis (CRSwNP) after endoscopic sinus surgery (ESS) are limited, and include frequent use of systemic steroids and revision surgery. A bioabsorbable, steroid-eluting implant was studied for its ability to dilate sinuses obstructed by polyps and provide localized, controlled steroid delivery to reestablish sinus patency. This study assessed the initial feasibility, safety, and efficacy of steroid-eluting implants placed in the office setting in patients who were candidates for revision ESS.
Prospective, multicenter study enrolling 12 patients who had prior ESS but experienced recurrent polyposis refractory to medical therapy. Implants were placed bilaterally under topical anesthesia in-office. Follow-up through 6 months included endoscopic grading, patient-reported outcomes (22-item Sino-Nasal Outcomes Test [SNOT-22]) and need for revision ESS.
Implants were successfully inserted in 21 of 24 (88%) ethmoid sinuses, resulting in 11 evaluable patients. No serious adverse events occurred. Within 1 month, mean bilateral polyp grade was reduced from 4.5 at baseline to 2.3 (p = 0.008) and sustained through 6 months (2.33; p = 0.008). Mean SNOT-22 score was significantly improved from 2.19 at baseline to 0.90 within 1 month (p = 0.001) and sustained to 6 months (1.03; p = 0.012). Sixty-four percent of patients were no longer revision ESS candidates at 6 months.
The study provided initial clinical evidence of the feasibility, safety, and efficacy of in-office steroid-eluting implant placement in CRS patients with recurrent polyposis after ESS. Although further studies are needed, the results suggest this therapy may provide a safe and effective, office-based option for the treatment of obstructive polyposis.
内镜鼻窦手术(ESS)后复发性息肉的慢性鼻-鼻窦炎(CRSwNP)的治疗选择有限,包括频繁使用全身类固醇和再次手术。一种可生物吸收的、释放类固醇的植入物被研究用于扩张被息肉阻塞的鼻窦,并提供局部、可控的类固醇释放以重建鼻窦通畅。本研究评估了在门诊环境中为接受ESS翻修手术的患者植入类固醇释放植入物的初步可行性、安全性和有效性。
一项前瞻性、多中心研究,纳入12例曾接受ESS但药物治疗难治性复发性息肉的患者。在门诊局部麻醉下双侧植入植入物。随访6个月,包括内镜分级、患者报告的结局(22项鼻-鼻窦结局测试[SNOT-22])以及ESS翻修的必要性。
24个筛窦中的21个(88%)成功植入植入物,产生了11例可评估患者。未发生严重不良事件。1个月内,双侧息肉平均分级从基线时的4.5降至2.3(p = 0.008),并持续至6个月(2.33;p = 0.008)。SNOT-22平均评分从基线时的2.19显著改善至1个月内的0.90(p = 0.001),并持续至6个月(1.03;p = 0.012)。64%的患者在6个月时不再是ESS翻修的候选者。
该研究为ESS后复发性息肉的CRS患者在门诊植入类固醇释放植入物的可行性、安全性和有效性提供了初步临床证据。尽管需要进一步研究,但结果表明这种治疗可能为阻塞性息肉的治疗提供一种安全有效的门诊治疗选择。