首页> 外文期刊>Journal of the Medical Association of Thailand =: Chotmaihet thangphaet >The efficacy of Jackson drain in the application to be a tunnel pleural catheter (TPC) in the management of malignant pleural effusion.
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The efficacy of Jackson drain in the application to be a tunnel pleural catheter (TPC) in the management of malignant pleural effusion.

机译:杰克逊引流在恶性胸腔积液管理中应用隧道胸膜导管(TPC)的功效。

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BACKGROUND: Malignant pleural effusion (MPE) is a common clinical problem in patients with advanced cancer and portends a poor prognosis, which means survival of less than six months. In June 1997, the US-FDA approved an indwelling TPC with a one-way drainage valve to be used in the management of MPE. Although popularity of this TPC has increased over the past few years, the experience with this device remains limited in Thai patients. One of the reasons is its high cost. OBJECTIVE: Assess the efficacy and the safety of customary indwelling TPC by using Jackson drain in the management of patients with symptomatic MPE. MATERIAL AND METHOD: Ten patients with symptomatic MPE were receiving these catheters (18 Fr Silicone catheters with 25 cm fenestrated length) to drain effusion via plastic vacuum bottles (250 ml) every other day or as needed to relieve dyspnea. The patient's dyspnic respiration, quality of life, and comfort during the catheter's application were quantified with a Borg score, the St. George Respiratory Disease Questionnaire (SGRQ), and the comfort's score, respectively. These parameters were recorded at initial (before insertion) and 2-week follow-up visit. Pain after 24 hours of each insertion was quantified by visual pain analogue scale (VPAS). Patients were followed until either death or catheter removal. RESULTS: The Borg score, SGRQ, and comfort's score showed significant improvement at 2-week visit (p < 0.05). Mean VPAS was 2.44. There was no early (2-week) complication, but the catheters were obstructed in three patients (mean = 60 days) and slipped out in two (day 18, day 50). CONCLUSION: This modified Jackson drain was effective in the treatment of MPE as a TPC without early complications.
机译:背景:恶性胸腔积液(MPE)是晚期癌症患者的常见临床问题,预后不良,意味着生存期不到六个月。 1997年6月,美国食品药品监督管理局(FDA)批准了带有单向排水阀的留置TPC用于MPE的管理。尽管在过去的几年中,这种TPC的普及程度有所提高,但是在泰国患者中使用该设备的经验仍然有限。原因之一是其成本高。目的:使用杰克逊引流术评估有症状的MPE患者的常规留置TPC的疗效和安全性。材料和方法:10例有症状MPE的患者每隔一天或根据需要通过塑料真空瓶(250 ml)接受这些导管(开窗长度为25 cm的18 Fr硅胶导管)引流,以缓解呼吸困难。使用Borg评分,圣乔治呼吸系统疾病问卷(SGRQ)和舒适度评分分别量化患者在应用导管过程中的呼吸困难,生活质量和舒适度。这些参数在初次(插入之前)和2周的随访中记录。通过视觉疼痛类似物量表(VPAS)量化每次插入24小时后的疼痛。随访患者直至死亡或拔除导管。结果:Borg评分,SGRQ和舒适度评分显示2周访视时有显着改善(p <0.05)。平均VPAS为2.44。没有早期(2周)并发症,但是3名患者(平均= 60天)阻塞了导管,有2例(第18天,第50天)滑出。结论:改良的杰克逊引流管可有效治疗TPE且无早期并发症。

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