Effective palliation of refractory ascites in cirrhosis is challenging.

Jane Abbott, Sumita Verma, Sushma Saksena
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Abstract

Background: Palliative care is often suboptimal for patients with end-stage liver disease (ESLD). Ascites remains the most common complication in ESLD. Though long-term abdominal drains (LTAD) are commonly used in refractory malignant ascites, the standard care for ESLD is hospital drainage (large volume paracentesis (LVP)). There is an ongoing National Institute for Health and Care Research (NIHR) funded trial (REDUCe 2 Study) (ISRCTN269936824) comparing palliative LTAD to LVP in ESLD. This 35-site trial is being conducted in England, Scotland and Wales.

Aim: To understand the views and experience of healthcare professionals (HCP) on the use of palliative LTAD in ESLD.

Methods: An electronic survey comprised of seven questions with fixed quantitative options and three exploratory questions was used between August-December 2019. The survey was distributed electronically via the British Association for Study of Liver newsletter and to relevant hospital departments in Southeast England and Northeast London. An email reminder was sent at 4 and 8 weeks after the initial invitation to the survey.

Results: There were 211 respondents (hepatologists (36.5%), specialist nurses (24.6%), gastroenterologists (16.6%), trainees (17%) and others (5.2%)). All respondents had access to LVP, 86% to a transjugular intrahepatic portosystemic shunt procedure for patients, 67% to LTADs and 10% to other options, such as the automated low-flow ascites (ALFA) pump. The majority of respondents to the survey (68%) reported their experience of using LTAD. Almost all respondents (91%) were willing to consider LTAD in ESLD. However, the main deterrents of this were the perceived risk of infection (90%), followed by LTAD management in community (57%). Some 51% of those with prior experience of using LTAD reported clinical complications for patients (including bleeding, infection and renal impairment), 41% reported technical issues and 35% inadequate community support.

Conclusions: Almost all HCPs are willing to consider palliative LTAD in refractory ascites due to ESLD, but the main deterrents are the perceived infection risk and lack of published data to guide community management. The REDUCe 2 trial will clarify if these concerns are real and provide conclusive evidence on role, if any, of palliative LTADs in this vulnerable and under researched cohort with ESLD.

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有效缓解肝硬化难治性腹水具有挑战性。
背景:对于终末期肝病(ESLD)患者来说,姑息治疗往往并不理想。腹水仍是 ESLD 最常见的并发症。虽然长期腹腔引流术(LTAD)常用于难治性恶性腹水,但 ESLD 的标准治疗方法是医院引流(大容量腹腔穿刺术(LVP))。美国国家健康与护理研究所(NIHR)资助的一项试验(REDUCe 2 研究)(ISRCTN269936824)正在对 ESLD 的姑息性 LTAD 和 LVP 进行比较。该试验在英格兰、苏格兰和威尔士的35个地点进行。目的:了解医护人员(HCP)对在ESLD中使用姑息性LTAD的看法和经验:在 2019 年 8 月至 12 月期间进行了一项电子调查,其中包括 7 个具有固定定量选项的问题和 3 个探索性问题。调查表通过英国肝脏研究协会通讯以及英格兰东南部和伦敦东北部的相关医院部门进行电子分发。在发出首次调查邀请后的 4 周和 8 周,还发送了电子邮件提醒:共有 211 名受访者(肝病专家(36.5%)、专科护士(24.6%)、肠胃病专家(16.6%)、实习生(17%)和其他人员(5.2%))。所有受访者都可以使用 LVP,86% 的患者可以使用经颈静脉肝内门体分流术,67% 的患者可以使用 LTAD,10% 的患者可以使用其他方法,如自动低流量腹水(ALFA)泵。大多数受访者(68%)报告了他们使用低流量腹水分流术的经历。几乎所有受访者(91%)都愿意考虑在 ESLD 中使用 LTAD。然而,主要的阻碍因素是认为存在感染风险(90%),其次是LTAD在社区的管理(57%)。在有过使用LTAD经验的人中,约有51%报告了患者的临床并发症(包括出血、感染和肾功能损害),41%报告了技术问题,35%报告了社区支持不足:几乎所有的保健医生都愿意考虑对 ESLD 引起的难治性腹水患者使用姑息性 LTAD,但主要的阻碍因素是感染风险和缺乏已发表的数据来指导社区管理。REDUCe 2 试验将澄清这些顾虑是否属实,并提供确凿证据,说明姑息性 LTAD 在 ESLD 这一研究不足的弱势人群中的作用。
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