Suppr超能文献

患者定义的乔雅登(透明质酸)注射性喉成形术中获益持续时间。

Patient-defined duration of benefit from juvederm (hyaluronic acid) used in injection laryngoplasty.

机构信息

Department of Otolaryngology-Head and Neck Surgery, Washington University in St. Louis School of Medicine, St. Louis, Missouri, U.S.A.

出版信息

Laryngoscope. 2019 Dec;129(12):2744-2747. doi: 10.1002/lary.27842. Epub 2019 Jan 30.

Abstract

OBJECTIVES/HYPOTHESIS: Injection laryngoplasty has become valuable in treating laryngologic disorders including vocal cord atrophy, paralysis, and paresis. Although materials such as carboxymethylcellulose and calcium hydroxylapatite are Food and Drug Administration (FDA) approved, they are not without limitations. Juvederm (hyaluronic acid) is an alternative treatment that is not FDA approved. Although studies have examined Juvederm's longevity in cutaneous injections, there are limited data examining durability of Juvederm used in laryngoplasty. We aimed to determine the longevity and effectiveness of Juvederm used in injection laryngoplasty.

STUDY DESIGN

Retrospective cohort study.

METHODS

Subjects who underwent injection laryngoplasty using Juvederm were reviewed. Longevity was defined as the time between injection and the date that a patient first noted subjective deterioration of their voice. All subjects were subsequently followed using videostroboscopy to evaluate for Juvederm resorption. Longevity was analyzed using a Kaplan-Meier survival model, and effectiveness of laryngoplasty was determined using the Voice-Related Quality of Life index scores and analyzed using a Wilcoxon signed ranks test.

RESULTS

Fifty-nine subjects met inclusion criteria and underwent Juvederm injection laryngoplasty. Kaplan-Meier survival analysis revealed a mean longevity of 10.6 months (95% confidence interval: 9.1-12.0 months). Wilcoxon signed ranks analysis of the pre- and postinjection Voice Related Quality of Life (VRQOL) scores revealed improvement, with a mean preinjection VRQOL of 49.2 (standard deviation [SD] = 25.8) and mean postinjection VRQOL of 68.2 (SD = 27.5) (P < .001).

CONCLUSIONS

Injection laryngoplasty using Juvederm is an effective treatment for vocal cord atrophy, paralysis, and paresis. Knowledge of the patient-defined duration of benefit following laryngoplasty using Juvederm plays an important role in counseling patients as well as in the planning of future interventions.

LEVEL OF EVIDENCE

4 Laryngoscope, 129:2744-2747, 2019.

摘要

目的/假设:注射性声门成形术已成为治疗声带萎缩、麻痹和瘫痪等喉部疾病的有效方法。尽管羧甲基纤维素和羟基磷灰石等材料已获得美国食品和药物管理局(FDA)批准,但它们并非没有局限性。Juve derm(透明质酸)是一种替代治疗方法,尚未获得 FDA 批准。虽然有研究检查了 Juve derm 在皮内注射中的持久性,但关于 Juve derm 用于声门成形术的耐久性的数据有限。我们旨在确定 Juve derm 在注射性声门成形术中的持久性和有效性。

研究设计

回顾性队列研究。

方法

回顾性分析接受 Juve derm 注射性声门成形术的患者。将持久性定义为注射后至患者首次注意到声音主观恶化的时间。所有患者随后均通过频闪喉镜进行随访,以评估 Juve derm 的吸收情况。使用 Kaplan-Meier 生存模型分析持久性,并使用嗓音相关生活质量指数(Voice-Related Quality of Life index,VRQOL)评分分析声门成形术的效果,并使用 Wilcoxon 符号秩检验进行分析。

结果

59 例患者符合纳入标准,并接受 Juve derm 注射性声门成形术。Kaplan-Meier 生存分析显示平均持久性为 10.6 个月(95%置信区间:9.1-12.0 个月)。Wilcoxon 符号秩检验分析注射前后 VRQOL 评分显示有改善,注射前 VRQOL 平均为 49.2(标准差 [SD] = 25.8),注射后 VRQOL 平均为 68.2(SD = 27.5)(P <.001)。

结论

Juve derm 注射性声门成形术是治疗声带萎缩、麻痹和瘫痪的有效方法。了解患者接受 Juve derm 注射性声门成形术后的获益持续时间,对于向患者提供咨询以及规划未来干预措施非常重要。

证据水平

4 Laryngoscope, 129:2744-2747, 2019.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验