Venkatraman Anumitha, Davis Ruth J, Thibeault Susan
Department of Otolaryngology Head and Neck Surgery University of Wisconsin Madison USA.
Laryngoscope Investig Otolaryngol. 2025 Aug 6;10(4):e70223. doi: 10.1002/lio2.70223. eCollection 2025 Aug.
Injection augmentation (or injection laryngoplasty) is a common treatment for presbyphonia. As current injection materials are temporary, it is anticipated that patients injected for presbyphonia will either need a repeat injection or framework surgery to maintain glottal competence (or sufficient glottal closure). Despite the expected temporary nature of these injections, patients report variable durability of effect, and some do not require a repeat injection. The primary aim of this investigation was to identify factors that affect treatment durability of injection augmentation among patients with presbyphonia.
Patients who underwent one or multiple injection augmentations for presbyphonia between May 2008 and September 2017 were extracted from the UW Madison Voice and Swallow Outcomes Database. Variables collected included demographics (age, sex), injection material, volume, duration between injections, date of first and last follow-up, voice therapy (yes/no, number of sessions), and pre- and post-injection voice measures (Maximum Phonation Time, Dysphonia Severity Index, Glottal Function Index score, Vocal Handicap Index Score) in an observational cohort design. For patients receiving one injection (TF group), duration between injection and last follow-up was taken as a durability measure termed "time to follow up." For patients receiving multiple injections (TR group), duration between injection treatments were termed "time to reinjection." Patients receiving one or more injections were compared separately and together (where treatment durability refers to the combined TF + TR group) in different statistical analyses.
Thirty-five patients with presbyphonia met inclusion criteria (mean age 74.3 years [SD 7.6], 78% male). Twenty patients received only one injection. Repeat injection augmentation was performed in 40% of patients ( = 15, ranging from 1 to 6 additional injection augmentations). Maximum phonation time increased after injection augmentation (or injection laryngoplasty) and was similar across injection materials (HA (mean change (SD)): +6 s (3) [95% CI 0.1-0.8], CaHa: +4 s (2.8) [95% CI 0.2-0.7], < 0.001). Treatment durability was longer for hyaluronic acid injectables when compared to calcium hydroxyapatite injectables (1232 days [CI: 552-1911] vs. 257 days [168-345], (2) = 7.505, = 0.023). Voice therapy extended treatment durability TF for injection augmentation compared to no voice therapy (1388 [95% CI: 772-2003] vs. 277 days [206-349 days], (1) = 9.173, = 0.002). Age did not affect treatment durability TF ( (1) 1.01, = 0.67).
Factors that affected treatment durability TF for injection augmentation treatments were the type of injectable and whether patients underwent adjuvant voice therapy.
III, Retrospective cohort study.
注射填充(或注射喉成形术)是治疗老年嗓音障碍的常用方法。由于目前的注射材料是临时性的,预计接受老年嗓音障碍注射治疗的患者要么需要重复注射,要么需要进行支架手术以维持声门功能(或足够的声门闭合)。尽管这些注射预期具有临时性,但患者报告的疗效持续时间各不相同,有些患者不需要重复注射。本研究的主要目的是确定影响老年嗓音障碍患者注射填充治疗疗效持久性的因素。
从威斯康星大学麦迪逊分校嗓音与吞咽结果数据库中提取2008年5月至2017年9月期间接受一次或多次老年嗓音障碍注射填充治疗的患者。收集的变量包括人口统计学信息(年龄、性别)、注射材料、注射量、两次注射之间的时间间隔、首次和末次随访日期、嗓音治疗(是/否、治疗次数)以及注射前后的嗓音测量指标(最长发声时间、嗓音障碍严重程度指数、声门功能指数评分、嗓音障碍指数评分),采用观察性队列设计。对于接受一次注射的患者(TF组),将注射至末次随访的时间作为疗效持久性的衡量指标,称为“随访时间”。对于接受多次注射的患者(TR组),将两次注射治疗之间的时间间隔称为“再次注射时间”。在不同的统计分析中,分别对接受一次或多次注射的患者进行比较,并将两者合并在一起进行比较(此处治疗持久性指TF + TR合并组)。
35例老年嗓音障碍患者符合纳入标准(平均年龄74.3岁[标准差7.6],78%为男性)。20例患者仅接受了一次注射。40%的患者(n = 15)进行了重复注射填充(额外注射填充1至6次)。注射填充(或注射喉成形术)后最长发声时间增加,且不同注射材料之间相似(透明质酸(平均变化[标准差]):+6秒(3)[95%置信区间0.1 - 0.8],羟基磷灰石钙:+4秒(2.8)[95%置信区间0.2 - 0.7],P < 0.001)。与羟基磷灰石钙注射剂相比,透明质酸注射剂的治疗持久性更长(1232天[置信区间:552 - 1911]对257天[168 - 345],t(2) = 7.505,P = 0.023)。与未接受嗓音治疗相比,嗓音治疗延长了注射填充治疗的TF疗效持久性(1388天[95%置信区间:772 - 2003]对277天[206 - 349天],t(1) = 9.173,P = 0.002)。年龄不影响TF治疗持久性(t(1) = 1.01,P = 0.67)。
影响注射填充治疗TF疗效持久性的因素是注射剂类型以及患者是否接受辅助嗓音治疗。
III级,回顾性队列研究。