Rapid Pleurodesis in Patients With Chronic Noninfectious Pleural Effusion: Twenty Years of Real-world Performance Data.

IF 3.3 Q2 RESPIRATORY SYSTEM
Chan Yeu Pu, Camilo A Avendano, Makayla Durant, Daniel Ospina-Delgado, Alma V Burbano, Kai E Swenson, Jason Beattie, Mihir Parikh, Adnan Majid
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Abstract

Background: Small cohort studies have shown rapid pleurodesis protocol's (RPP) effectiveness and capacity to expedite pleurodesis for malignant pleural effusion (MPE). This study intends to evaluate the effectiveness of the RPP in inducing pleurodesis in patients with pleural effusions from either malignant or benign etiologies.

Methods: In this single-center, retrospective cohort study spanning 2 decades, we assessed patients with recurrent symptomatic chronic noninfectious pleural effusion, both benign and malignant. Post-RPP, chest tubes were removed when fluid output dropped below 150 mL/d, and patients were discharged with daily indwelling pleural catheter (IPC) drainage. Exclusion criteria included nonexpandable lung and active pleural infection. Treatment success was defined as IPC removal on reduced output (<50 mL) on 3 consecutive drainages and radiologic effusion resolution. Recurrence was defined as the occurrence of pleural effusion requiring additional pleural procedures postsuccess. Duration outcome was expressed as median with IPC placement as time zero.

Results: Of the 210 patients studied, 72% had MPE, and 28% had benign effusions. The median hospital stay was 4 days post-RPP. Treatment was successful in 177 (84%) patients within a median of 12 days, with no significant differences between MPE and benign cases. Nine patients (5%) experienced recurrence within a median of 152 days. Complications included hemothorax in 4 (1.9%) and empyema in 2 (1%). The thirty-day mortality rate was 9%, with a median survival time of 245 days postprocedure.

Conclusion: The RPP combines the benefit of chemical pleurodesis and IPC and appears to be a reasonable option for patients with recurrent and symptomatic pleural effusion.

慢性非感染性胸腔积液患者的快速胸膜腔穿刺术:二十年来的实际应用数据。
背景:小型队列研究显示,快速胸腔穿刺方案(RPP)可有效加快恶性胸腔积液(MPE)的胸腔穿刺。本研究旨在评估快速胸膜腔穿刺术在诱导恶性或良性胸腔积液患者进行胸膜腔穿刺方面的有效性:在这项跨越 20 年的单中心回顾性队列研究中,我们评估了复发性症状性慢性非感染性胸腔积液患者,包括良性和恶性患者。RPP术后,当液体排出量低于150毫升/天时拔除胸管,患者每日留置胸膜导管(IPC)引流后出院。排除标准包括无扩张肺和活动性胸膜感染。治疗成功的定义是在排液量减少的情况下拔除IPC(结果:在接受研究的 210 名患者中,72% 患有 MPE,28% 患有良性积液。RPP 术后的中位住院时间为 4 天。有 177 名患者(84%)在中位 12 天内治疗成功,良性和恶性积液病例之间无明显差异。9名患者(5%)在中位 152 天内复发。并发症包括血气胸 4 例(1.9%)和肺水肿 2 例(1%)。30天死亡率为9%,术后中位生存时间为245天:结论:RPP结合了化学胸膜穿刺术和IPC的优点,似乎是复发性和无症状胸腔积液患者的合理选择。
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
CiteScore
4.40
自引率
6.10%
发文量
121
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