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临床试验/NCT03058874
NCT03058874已完成不适用

The Effect of a Dry-weight Probing Guided by Lung Ultrasound on Ambulatory Blood Pressure and Arterial Stiffness in Hemodialysis Patients. A LUST Sub-study.

Carmine Zoccali2 个研究点 分布在 2 个国家目标入组 71 人开始时间: 2016年9月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
71
试验地点
2
主要终点
Difference between groups in changes in 48-hour Brachial Systolic Blood Pressure, obtained with the Mobilograph device

研究概览

简要总结

The most common co-morbidity accompanying Chronic Kidney Disease (CKD) is hypertension, which appears in approximately 80% of all patients with renal dysfunction, whereas its prevalence in general population is remarkably lower appearing in approximately 30% of adults.Defining hypertension in ESRD patients under maintenance dialysis is a challenging procedure. Ambulatory blood pressure monitoring (ABPM) is considered the "gold standard" for the diagnosis of hypertension in hemodialysis patients over the last years. The major pathophysiologic mechanism underlying hypertension development in patients with ESRD under hemodialysis is water and sodium overload.

Identifying an accurate and objective method of dry weight evaluation has been a matter of intensive nephrology research for more than two decades. Assessment of the water balance in hemodialysis patients on the basis of common clinical criteria (e.g. leg or face swelling or signs of lung congestion) is a subjective method with limited reliability, despite its widespread use. Recently, a novel technique has been developed to quantify water excess by conducting an ultrasound lung scan. Pilot studies have shown significant changes in lung water in hemodialysis patients according to body weight changes during interdialytic days and dialysis sessions. Moreover, results from previous studies indicate significant benefits from dry weight probing with regards to blood pressure (BP).

The clinical application of a lung-ultrasound-based volume control strategy in hemodialysis patients is currently being tested by the randomized study entitled "Lung water by ultrasound guided treatment to prevent death and cardiovascular complications in high risk end stage renal disease patients with cardiomyopathy (The LUST Study)". This clinical trial aims at evaluating whether the use of the number of US-B lines could be used as a biomarker to guide a per-protocol intensification of ultrafiltration (UF) in order to reduce volume overload, improve cardiac function and prolong survival.

Cardiovascular disease in patients with CKD is attributed to a spectrum of structural and functional alterations of the large and the small branches of the arterial tree. The most important process in patients with advanced CKD is that of arteriosclerosis, which is developed in parallel to atherosclerosis and is typically associated with impaired cushioning function of the aorta and the large conduit arteries. Accelerated arterial stiffening is involved in the development of isolated systolic hypertension, left ventricular hypertrophy (LVH) and congestive heart failure (CHF), which predispose to arrhythmias and sudden cardiac death. In the context of the phenomenon of "aortic-to-brachial BP amplification", systolic BP (SBP) and pulse pressure (PP) conventionally measured at the level of brachial artery are higher than the relevant pressures in the ascending aorta. Due to extreme elevation of arterial stiffness, BP amplification is disturbed in patients with ESRD. Prospective cohort studies have demonstrated that elevated central PP, wave reflections and arterial stiffness, as well as, reduced PP amplification represent strong and independent predictors of all-cause and cardiovascular mortality in hemodialysis patients. On this basis, estimation of central BP indices appears as an important tool towards optimisation of cardiovascular risk stratification in ESRD as well as in other diseased populations.

Until recently, available devices for ABPM evaluated BP levels only at the level of brachial artery. The newly developed Mobil-O-Graph NG (IEM, Stolberg, Germany) provides the ability to monitor central aortic pressure and indices of vascular resistance, such as wave reflections (augmentation index, AIx) and arterial stiffness (pulse wave velocity, PWV).This device has recently been validated in hemodialysis patients and showed comparable performance with the widely used tonometric SphygmoCor device (ArtCor, Sydney, Australia). Accumulated evidence over central BP and PWV in hemodialysis patients derives mostly from studies that included only static pre-dialysis and post-dialysis measurements. However, variations of BP levels during intra- and interdialytic intervals combined with the superiority of aortic BP measurements, as analysed above, indicate that ambulatory monitoring of central BP is the best available method.

This study aims for the first time to evaluate the outcome of a treatment strategy for dry weight probing, based on volume overload quantification with lung ultrasound, on 48-hour peripheral systolic BP, aortic BP and arterial stiffness in hemodialysis hypertensive patients.

This is a Lust Sub-Study. Additional information can be found at: NCT02310061.

详细描述

Patient selection and study preparations

Potentially eligible hemodialysis patients, not fitting the exclusion criteria, will provide written informed consent and will be evaluated for the diagnosis of hypertension. If patients are treated with antihypertensive therapy, a brief-wash out from medications period will take place and home BP will be monitored up to a maximum of 4 weeks. During this period BP ≥160/110 mmHg will be a threshold for further medication withdrawal.

Hypertension diagnosis will be based on mean BP values ≥135/85 mmHg with home BP monitoring the days after the mid and last dialysis of the week for 2 consecutive weeks using a validated self-inflating automatic oscillometric device (cuff with bladder size encircling at least 80% of arm circumference and covering two thirds of arm length). Every patient will be asked to conduct both morning and evening BP measurements at the level of brachial artery after 5 min of rest and with two measurements per occasion taken 2 min apart according to the European Society of Hypertension 2013 guidelines. The mean of the last measurements would be used.

Study period

A total number of 70 eligible patients undergoing hemodialysis in the Hemodialysis Unit of the Department of Nephrology, Hippokration Hospital, Aristotle University of Thessaloniki, Greece and in affiliated Hemodialysis Units in Northern Greece, as well in the Hemodialysis Units of the Department of Nephrology University Clinical Centre Maribor, Slovenia will participate in the study. In all potentially eligible patients full medical history, as well as demographic characteristics and drug treatment will be recorded, followed by a detailed physical examination. Patients that meet the inclusion and exclusion criteria, will be randomized with a ratio of 1:1 into two equal groups consisting of 35 patients. In the intervention group a specific treatment strategy for dry-weight reduction will be applied guided by lung ultrasound, whereas in the control group standard-of-care treatment will be applied guided by conventional clinical criteria. Blood samples for hematological and biochemical laboratory tests will be collected at baseline prior to a mid-week dialysis session; these tests will correspond to the routine monthly laboratory tests of the patients.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age > 18 years
  • Dialysis vintage > 3 months
  • A history of hypertension, confirmed by valid Home BP readings
  • Written consent to take part in the study

排除标准

  • Cancer or other advanced non cardiac disease or co-morbidity (e.g. end-stage liver failure) imposing a very poor short-term prognosis
  • Active infections or relevant inter-current disease
  • Inadequate lung scanning and echocardiographic studies
  • Hemodynamic instability during dialysis session that require intravenous fluid administration to restore BP, in over 30% of sessions during the past 3 months
  • Patients with modification of their dry weight and antihypertensive treatment during one month prior to study enrolment
  • Nonfunctional arteriovenous fistula in the contralateral arm of the one used as vascular access for the hemodialysis session
  • Patients with Home BP readings >180/110 mmHg
  • Patients with history of drug or alcohol abuse or known severe mental disorder
  • Pregnancy at study entry or during study period

结局指标

主要结局

Difference between groups in changes in 48-hour Brachial Systolic Blood Pressure, obtained with the Mobilograph device

时间窗: 0, 2, 12 months

次要结局

  • Difference between groups in changes in 48-hour Brachial Diastolic Blood Pressure, obtained with the Mobilograph device(0, 2, 12 months)
  • Difference between groups in changes in 48-hour Aortic Systolic Blood Pressure, obtained with the Mobilograph device(0, 2, 12 months)
  • Difference between groups in changes in 48-hour Aortic Diastolic Blood Pressure, obtained with the Mobilograph device(0, 2, 12 months)
  • Difference between groups in changes in ambulatory pulse pressure (PP), obtained with the Mobilograph device(0, 2, 12 months)
  • Difference between groups in changes in ambulatory augmentation index (AIx), obtained with the Mobilograph device(0, 2, 12 months)
  • Difference between groups in changes in ambulatory pulse wave velocity (PWV), obtained with the Mobilograph device(0, 2, 12 months)
  • Difference between groups in changes in echocardiographic indices of left ventricular function(0, 2, 12 months)
  • Difference between groups in changes in Body composition assessed with bioelectrical impedance analysis(0, 2, 12 months)
  • Difference between groups in changes in PWV, obtained with the Sphygmocor device(0, 2, 12 months)
  • Difference between groups in changes in AIx, obtained with the Sphygmocor device(0, 2, 12 months)

研究者

发起方
Carmine Zoccali
申办方类型
Other Gov
责任方
Sponsor Investigator
主要研究者

Carmine Zoccali

MD, FASN, Professor of Nephrology (PG)

Fondazione C.N.R./Regione Toscana "G. Monasterio", Pisa, Italy

研究点 (2)

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