Endobronchial silicone spigot in prolonged air leaks: Nationwide study on outcomes and risk factors for treatment failure

IF 2.4 Q2 RESPIRATORY SYSTEM
Jumpei Taniguchi , Shotaro Aso , Jo Taisuke , Hiroki Matsui , Kiyohide Fushimi , Hideo Yasunaga
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引用次数: 0

Abstract

Background

The endobronchial silicone spigot, also known as the endobronchial Watanabe spigot, is used in bronchoscopic interventions to manage prolonged pulmonary air leakage. However, the outcomes of this procedure have not been thoroughly investigated.

Methods

Using a Japanese national inpatient database from April 2014 to March 2022, we assessed the clinical characteristics and outcomes of all eligible patients who received the endobronchial spigot. We also investigated risk factors associated with treatment failure. Treatment failure was defined as in-hospital death or the need for surgery after bronchial occlusion.

Results

We analyzed data of 1095 patients who underwent bronchial occlusion using the endobronchial spigot. Among them, 252 patients (23.0%) died during hospitalization, and 403 patients (36.8%) experienced treatment failure. Factors associated with treatment failure included age between 85 and 94 years (odds ratio [OR] 1.83; 95% confidence intervals [CI], 1.04–3.21); male sex (OR 2.43; 95% CI, 1.44–4.11); low Barthel index score; comorbidities of interstitial pneumonia (OR 1.71; 95% CI, 1.18–2.48); antibiotics treatment (OR 1.45; 95% CI, 1.02–2.07); steroids treatment (OR 1.59; 95% CI, 1.07–2.36); and surgery prior to bronchial occlusion (OR 2.08; 95% CI, 1.29–3.35). In contrast, pleurodesis after bronchial occlusion (OR 0.49; 95% CI, 0.32–0.75), and admission to high-volume hospitals were inversely associated with treatment failure (OR 0.58; 95% CI, 0.37–0.90).

Conclusions

The endobronchial Watanabe spigot could be a nonsurgical treatment option for patients with prolonged pulmonary air leaks. Our findings will help identify patients who may benefit from such bronchial interventions.

治疗长期漏气的支气管内硅胶塞:关于治疗结果和治疗失败风险因素的全国性研究
背景支气管内硅胶塞(又称支气管内渡边塞)用于支气管镜介入治疗,以控制长期肺漏气。方法利用 2014 年 4 月至 2022 年 3 月的日本全国住院患者数据库,我们评估了所有符合条件的接受支气管内塞子治疗的患者的临床特征和治疗结果。我们还调查了与治疗失败相关的风险因素。结果 我们分析了 1095 名使用支气管内插管进行支气管闭塞的患者的数据。其中,252 名患者(23.0%)在住院期间死亡,403 名患者(36.8%)治疗失败。与治疗失败相关的因素包括:年龄在 85 至 94 岁之间(比值比 [OR] 1.83;95% 置信区间 [CI],1.04-3.21);男性(OR 2.43;95% CI,1.44-4.11);低 Barthel 指数评分;合并间质性肺炎(OR 1.71;95% CI,1.18-2.48);抗生素治疗(OR 1.45;95% CI,1.02-2.07);类固醇治疗(OR 1.59;95% CI,1.07-2.36);支气管闭塞前手术(OR 2.08;95% CI,1.29-3.35)。相比之下,支气管闭塞后进行胸膜腔穿刺术(OR 0.49;95% CI,0.32-0.75)和入住大容量医院与治疗失败成反比(OR 0.58;95% CI,0.37-0.90)。我们的研究结果将有助于识别可能从此类支气管介入治疗中获益的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Respiratory investigation
Respiratory investigation RESPIRATORY SYSTEM-
CiteScore
4.90
自引率
6.50%
发文量
114
审稿时长
64 days
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