Gao William Z, Paoletti Marcus F, Bensoussan Yael, Bhatt Neel K, van der Woerd Benjamin, Shuman Elizabeth A, Grant Nazaneen, O'Dell Karla, Johns Michael M
UChicago Voice Center, Department of Surgery, Section of Otolaryngology-Head & Neck Surgery, University of Chicago, Chicago, Illinois, U.S.A.
Keck School of Medicine of University of Southern California, Los Angeles, California, U.S.A.
Laryngoscope. 2024 Aug;134(8):3679-3685. doi: 10.1002/lary.31039. Epub 2023 Sep 7.
Vocal fold injection medialization (VFIM) is widely used as an initial treatment for unilateral vocal fold paralysis (UVFP). Current practices employ materials that share the limitation of temporary clinical effect from variable resorption rates. A novel silk protein microparticle-hyaluronic acid-based material (silk-HA) has demonstrated cellular infiltration and tissue deposition that may portend a durable medialization effect. We report on ≥12 months outcomes after VFIM with silk-HA.
Prospective open-label study of patients with UVFP that elected treatment with VFIM with silk-HA. Blinded experts rated laryngeal stroboscopic exams.
Seventeen patients with UVFP underwent VFIM with silk-HA. Twelve of the 17 patients have ≥12 months follow-up. Seven patients demonstrated durable treatment benefit ≥12 months after injection with median improvement of 19 (p = 0.0156) in VHI-10. There was no significant change in VHI-10 between 1 and 12 months for these patients. Blinded ratings indicated that 5/7 patients with sustained improvements in VHI-10 exhibited complete or touch glottal closure at 12 months. Two of the seven patients exhibited a small (<1 mm) glottal gap at 12 months. Seven patients experienced initial benefit with later regression 3-4 months after injection.
VFIM with silk-HA can offer durable improvement in voice-related outcomes for UVFP past 12 months. A subset of patients treated with silk-HA experienced early loss of effect around 3-4 months postinjection. Clinical factors predictive of sustained treatment response to silk-HA injection require further exploration.
3 Laryngoscope, 134:3679-3685, 2024.
声带注射内移术(VFIM)被广泛用作单侧声带麻痹(UVFP)的初始治疗方法。目前的做法所使用的材料存在共同的局限性,即由于吸收率不同,临床效果是暂时的。一种新型的基于丝蛋白微粒-透明质酸的材料(丝-透明质酸)已显示出细胞浸润和组织沉积,这可能预示着持久的内移效果。我们报告了使用丝-透明质酸进行VFIM术后≥12个月的结果。
对选择使用丝-透明质酸进行VFIM治疗的UVFP患者进行前瞻性开放标签研究。由盲法专家对喉动态喉镜检查进行评分。
17例UVFP患者接受了丝-透明质酸VFIM治疗。17例患者中有12例进行了≥12个月的随访。7例患者在注射后≥12个月显示出持久的治疗益处,嗓音障碍指数(VHI)-10的中位数改善为19(p = 0.0156)。这些患者在1至12个月期间VHI-10没有显著变化。盲法评分表明,VHI-10持续改善的7例患者中有5例在12个月时表现为完全或接近声门闭合。7例患者中有2例在12个月时出现小的(<1毫米)声门间隙。7例患者在注射后3至4个月出现初始益处,随后病情复发。
使用丝-透明质酸进行VFIM可在12个月后为UVFP患者的嗓音相关结局提供持久改善。一部分接受丝-透明质酸治疗的患者在注射后约3至4个月出现早期疗效丧失。预测对丝-透明质酸注射持续治疗反应的临床因素需要进一步探索。
3 《喉镜》,134:3679 - 3685,2024年。