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首页> 外文期刊>Journal of palliative medicine >Use of a subcutaneous implantable pleural port in the management of recurrent malignant pleurisy: five-year experience based on 168 subcutaneous implantable pleural ports.
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Use of a subcutaneous implantable pleural port in the management of recurrent malignant pleurisy: five-year experience based on 168 subcutaneous implantable pleural ports.

机译:皮下植入性胸膜端口在复发性恶性胸膜炎治疗中的应用:基于168个皮下可植入胸膜端口的五年经验。

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摘要

INTRODUCTION: The authors report their experience in the use of subcutaneous implantable pleural port (SIPP) catheters for the treatment of symptomatic recurrent malignant pleurisy. MATERIALS AND METHODS: Single-center, prospective follow-up of 137 patients (168 SIPPs). RESULTS: No SIPP placement failures were observed. All but 3 of the 125 evaluable patients obtained complete or partial relief of their dyspnea. Seventy-six patients (60.3%) were receiving chemotherapy. Spontaneous pleurodesis was observed within 2 months in 46 patients (36.8%). Twenty-six patients (20.8%) died during the month following SIPP placement. Forty-one patients (32%) survived for more than 6 months. The overall median survival time was 344 days. Three infectious complications (1 empyema, 2 cellulitis) and 3 mechanical complications were observed. The role of pleurodesis as prognostic factor was assessed. Seventy-one patients survived for more than 2 months, 36 with pleurodesis, 35 without pleurodesis, requiring repeated pleural aspiration. The difference observed between the two groups by the 120th day was no longer significant when chemotherapy was taken into account. CONCLUSION: SIPP is a safe and effective option for the outpatient management of recurrent malignant effusions and could be considered as first-line treatment in all patients with bilateral, compressive pleural effusion or poor lung reexpansion.
机译:简介:作者报告了他们在使用皮下植入式胸膜开口(SIPP)导管治疗症状性复发性恶性胸膜炎的经验。材料与方法:单中心,前瞻性随访137例患者(168 SIPP)。结果:未观察到SIPP放置失败。在125位可评估患者中,除3位外,所有患者均获得了呼吸困难的全部或部分缓解。七十六名患者(60.3%)正在接受化疗。 46例患者(36.8%)在两个月内观察到自发性胸膜固定术。 SIPP放置后的一个月内有26名患者(20.8%)死亡。 41名患者(32%)存活超过6个月。总体中位生存时间为344天。观察到三种感染性并发症(1例脓胸,2例蜂窝织炎)和3例机械性并发症。评估了胸膜固定作为预后因素的作用。 71例患者存活超过2个月,其中36例有胸膜固定术,35例无胸膜固定术,需要反复胸膜穿刺。考虑到化疗,两组在第120天时观察到的差异不再显着。结论:SIPP是门诊复发性恶性积液的安全有效选择,可作为所有双侧,压缩性胸腔积液或肺扩张不良的患者的一线治疗。

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