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球囊扩张治疗儿童阻塞性咽鼓管功能障碍。

Balloon Dilation for Obstructive Eustachian Tube Dysfunction in Children.

机构信息

Department of Otolaryngology and Communication Enhancement, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts.

Department of Otorhinolaryngology-Head and Neck Surgery, Turku University Hospital, University of Turku, Turku, Finland.

出版信息

Otol Neurotol. 2021 Apr 1;42(4):566-572. doi: 10.1097/MAO.0000000000003009.

DOI:10.1097/MAO.0000000000003009
PMID:33351568
Abstract

OBJECTIVE

Determine the safety and efficacy of balloon dilation of the Eustachian tube (ET) in pediatric patients.

STUDY DESIGN

Retrospective matched cohort study.

SETTING

Tertiary medical center.

PATIENTS

Pediatric patients (<18 yr) with persistent (>1.5 yr) chronic Eustachian tube dysfunction (ETD) with previous tympanostomy tube (TT) insertion versus matched controls.

INTERVENTIONS

Balloon dilation of the cartilaginous ET (BDET) was performed using concomitant myringotomy with/without tube placement and adjunctive procedures if indicated versus controls (TT).

MAIN OUTCOME MEASURES

Otitis media with effusion (OME)/retraction with need for additional tube, tympanogram, audiogram, otomicroscopy, ET mucosal inflammation/opening score, and Valsalva maneuver.

RESULTS

Forty six ETs (26 patients), ages 7 to 17 years (mean 12.5) underwent BDET. Mean follow-up was 2.3 years (standard deviation [SD], 1.1; range, 6 mo-5 yr). Significant improvements were observed for all measures. Tympanic membranes were healthy in 9% preoperatively, 38% at 6 months, 55% at 12 months, and 93% at 36 months postoperatively. Tympanograms improved to type A in 50% at 6 months, 59% at 12 months, and 85% at 36 months. Mean scores of mucosal inflammation declined from 3.2 (±0.6) preoperatively to 2.5 (±0.7) at 6 months and 1.7 (±0.6) at 36 months postoperatively. BDET had lower risk of failure versus TT insertion (adjusted hazard ratio [HR] 0.26; 95% confidence interval [CI]: 0.10, 0.70; p = 0.007). Probability of being failure free at 2 years was 87% (95% CI: 70, 94%) after BDET and 56% (95% CI: 40, 70%) after TT insertions.

CONCLUSIONS

BDET is a safe and possibly effective procedure in selected pediatric patients with chronic ETD.

摘要

目的

确定球囊扩张咽鼓管(ET)在儿科患者中的安全性和疗效。

研究设计

回顾性匹配队列研究。

设置

三级医疗中心。

患者

患有持续性(> 1.5 年)慢性咽鼓管功能障碍(ETD)的小儿患者(< 18 岁),既往行鼓膜切开置管术(TT)与匹配对照组。

干预措施

行软骨 ET 球囊扩张术(BDET),同时行鼓膜切开术/置管术,并根据需要进行附加手术,与对照组(TT)进行比较。

主要观察指标

分泌性中耳炎(OME)/伴有需要再次置管的鼓膜内陷、鼓室图、听力图、耳镜检查、ET 黏膜炎症/开放评分和瓦尔萨尔瓦动作。

结果

46 例 ET(26 例患者),年龄 7-17 岁(平均 12.5 岁)行 BDET。平均随访时间为 2.3 年(标准差 [SD],1.1;范围,6 个月-5 年)。所有指标均有显著改善。术前鼓膜正常占 9%,6 个月时为 38%,12 个月时为 55%,36 个月时为 93%。鼓室图在 6 个月时改善为 A 型占 50%,12 个月时为 59%,36 个月时为 85%。黏膜炎症评分从术前的 3.2(±0.6)降至 6 个月时的 2.5(±0.7)和 36 个月时的 1.7(±0.6)。与 TT 插入相比,BDET 失败的风险较低(调整后的危险比 [HR] 0.26;95%置信区间 [CI]:0.10,0.70;p=0.007)。BDET 组 2 年时无失败率为 87%(95% CI:70%,94%),TT 组为 56%(95% CI:40%,70%)。

结论

BDET 是一种安全且可能有效的治疗方法,适用于有慢性 ETD 的特定儿科患者。

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