standard hemodialysis
Devicehemodialysis with high-flux dialyzer; prescription of dialysate temperature: 36.5 degrees Celsius; convection volume: not applicable
NCT Number: NCT03249532
Online hemodiafiltration confers a reduced mortality risk. However, it is not clear why HDF improved survival. To gain more insight in this issue, the effect of 4 dialysis techniques (differing in dialysate temperature and the absence/presence of convective clearance) on intradialytic hemodynamic stability and cardiac function will be investigated in a prospective cross over trial.
Looking for future studies?
Notify Me18 year and older
All sexes
Interventional
Not applicable
St Antonius Ziekenhuis, Nieuwegein, Utrecht, Netherlands
Despite the use of high permeable dialyzers, which combine diffusive with convective clearance, the clinical outcome of hemodialysis (HD) patients remains poor. In post-dilution online hemodiafiltration (denoted further on as HDF) diffusive clearance is similar to HD, while the amount of convective transport is considerable increased. Recently, 4 randomized controlled trails have been published which compared HD with HDF. Although the results of the individual studies were inconclusive, a recent meta-analysis, using individual patient data of these studies, showed a superior outcome for patients treated with HDF. The largest mortality reduction was obtained in patients receiving the highest convection volume (high-volume HDF [HV-HDF] >23 L/1.73 m2/session): all-cause mortality [22% (95 % confidence interval [CI] 2-38)], cardiovascular disease (CVD) mortality [31% (95 % CI 0-53)].
It is far from clear, however, why (HV)HDF is associated with an improved survival. Both long term and short term effects may be involved. With respect to the latter, the intra-dialytic removal of middle molecular weight (MMW) uremic retention products and a superior bio-incompatibility (BI) profile may play a role. In addition, treatment with HDF may induce less intra-dialytic hypotension (IDH) and less tissue injury. Enhanced removal of the MMW substance FGF23 may reduce the intra-dialytic acute phase reaction (APR), which is regarded a chief element of HD-induced BI. Other key components which may contribute to IDH and are supposed to be alleviated by HDF, include dialysis-induced hypoxia and intra-dialytic extracellular vesicle release. Patho-physiologically, IDH depends both on a decline in the circulating blood volume and an impaired response to hypovolaemia. As a result, venous return, cardiac output and peripheral vascular resistance are impaired. Since IDH is reduced by HD with cool dialysate (C-HD), thermal factors may play an important role.
Microcirculatory dysfunction is a prominent feature of HD patients. Since IDH occurs in 20-30% of the sessions, any interference with an already abnormal perfusion may further deteriorate the structure and function of vital organs, such as the brain, gut and heart. HD-associated cardiomyopathy, which is considered a model of repetitive organ ischemia-reperfusion injury, is superimposed on the cardiac changes resulting from the various inflammatory and metabolic derangements of pre-dialysis kidney disease. As measured by imaging techniques and biomarkers, HD induces a fall in cardiac perfusion and elicits tissue injury. While cardiac MRI is considered the reference method for LV quantification, intra-dialytic measurements can only be obtained in stable patients who can be safely transferred to the radiology department. Echocardiography, though, can be performed in all individuals at the bed-side, including hypotension-prone patients. Because of its superiority over standard echocardiography, especially with respect to diastolic (dys)function, speckle tracking echocardiography will be used in the present study.
As mentioned, the effect on long term survival is especially prominent when HV-HDF is applied. Theoretically, HV-HDF is also the preferred treatment to circumvent dialysis-induced IDH, and hence, to alleviate the repetitive intra-dialytic tissue damage. Therefore, the following hypotheses will be tested:
Worldwide, however, (HV)HDF is only limited available. Since intradialytic hemodynamic instability may contribute substantially to the poor clinical prospects of end-stage-kidney-disease (ESKD) patients, these individuals may benefit from each maneuver that minimizes the number and severity of intradialytic hypotensive episodes. Therefore, the question which of the comparator treatments [(S)-HD, C-HD and LV-HDF] has the best intradialytic hemodynamic stability, appears relevant as well.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
hemodialysis with high-flux dialyzer; prescription of dialysate temperature: 36.5 degrees Celsius; convection volume: not applicable
hemodialysis with high-flux dialyzer; prescription of dialysate temperature: 35.5 degrees Celsius; convection volume: not applicable
hemodiafiltration; prescription of dialysate temperature: 36.5 degrees celsius prescription of convection volume: 15 L
hemodiafiltration; prescription of dialysate temperature: 36.5 degrees celsius prescription of convection volume: 25 L
Time frame: up to 4 hours (= one dialysis treatment); assessed during 3 treatments on each modality
nadir in systolic blood pressure (SBP) of 90 mmHg for patient with predialysis SBP <160mmHg and a nadir of 100 mmHg for patients with predialysis SBP ≥160 mmHg during treatment (blood pressure will be measured before and every 15 minutes after the start of dialysis during the treatment)
Time frame: up to 4 hours (= one dialysis treatment); assessed during 1 treatment on each modality
speckle tracking echocardiography will be performed before, after 60 minutes of dialysis and after and after 3,5 hours
Time frame: up to 4 hours(= one dialysis treatment); assessed during 3 treatments on each modality
change in systolic blood pressure (mmHg)
Time frame: up to 4 hours(= one dialysis treatment); assessed during 3 treatments on each modality
change in diastolic blood pressure (mmHg)
Time frame: up to 4 hours(= one dialysis treatment); assessed during 3 treatments on each modality
change in mean arterial blood pressure (mmHg)
Time frame: up to 4 hours(= one dialysis treatment); assessed during 3 treatments on each modality
change in pulse pressure (systolic - diastolic blood pressure; mmHg)
Time frame: up to 4 hours(= one dialysis treatment); assessed during 1 treatment on each modality
change in beat-to-beat blood pressure (finger cuff; mmHg)
Time frame: up to 4 hours(= one dialysis treatment); assessed during 1 treatment on each modality
change in heart rate (finger cuff assessment)
Time frame: up to 4 hours(= one dialysis treatment); assessed during 1 treatment on each modality
change in stroke volume (finger cuff assessment)
Time frame: up to 4 hours(= one dialysis treatment); assessed during 1 treatment on each modality
change in cardiac output (finger cuff assessment)
Time frame: up to 4 hours(= one dialysis treatment); assessed during 1 treatment on each modality
change in total peripheral resistance (finger cuff assessment)
Time frame: up to 4 hours(= one dialysis treatment); assessed during 3 treatments on each modality
number of sessions with reached target dry weight (kg)
Time frame: up to 4 hours(= one dialysis treatment); assessed during 2 treatments on each modality
relative blood volume (%) during dialysis treatment
Time frame: up to 4 hours(= one dialysis treatment); assessed during 2 treatments on each modality
oxygen saturation in the arterial line of the extracorporeal system (%) during dialysis treatment; patients with central venous catheters and fistulas/grafts will be analyzed separately
Time frame: up to 4 hours(= one dialysis treatment); assessed during 1 treatment on each modality
pO2 in the arterial line of the extracorporeal system (mmHg or kiloPascal [kPa], assessed by a point of care device) during dialysis treatment; patients with central venous catheters and fistulas/grafts will be analyzed separately
Time frame: up to 4 hours(= one dialysis treatment); assessed during 1 treatment on each modality
marker of cardiac damage, assessment in blood from arterial line of extracorporeal circuit, before and after dialysis treatment
Time frame: up to 4 hours(= one dialysis treatment); assessed during 1 treatment on each modality
marker of gut ischemia, assessment in blood from arterial line of extracorporeal circuit, before and after dialysis treatment
Time frame: up to 4 hours(= one dialysis treatment); assessed during 1 treatment on each modality
marker of gut ischemia, assessment in blood from arterial line of extracorporeal circuit, before and after dialysis treatment
Time frame: up to 4 hours(= one dialysis treatment); assessed during 1 treatment on each modality
marker of endothelial damage, assessment in blood from arterial line of extracorporeal circuit, before and after dialysis treatment
Time frame: up to 4 hours(= one dialysis treatment); assessed during 1 treatment on each modality
marker of endothelial damage, assessment in blood from arterial line of extracorporeal circuit, before and after dialysis treatment
Time frame: up to 4 hours(= one dialysis treatment); assessed during 1 treatment on each modality
marker of inflammation, assessment in blood from arterial line of extracorporeal circuit, before and after dialysis treatment
Time frame: up to 4 hours(= one dialysis treatment); assessed during 1 treatment on each modality
marker of inflammation, assessment in blood from arterial line of extracorporeal circuit, before and after dialysis treatment
Time frame: up to 4 hours(= one dialysis treatment); assessed during 1 treatment on each modality
marker of inflammation/mineral bone disease, assessment in blood from arterial line of extracorporeal circuit, before and after dialysis treatment
Amsterdam UMC, location VUmc
Other
Effect of High-volume Online hemodiafiLtration on Intra-diaLytic hemodynAmic (iN)sTability and Cardiac Function in Chronic Hemodialysis Patients (the HOLLANT Study)
Acronym: HOLLANT
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07348536
Bronchial Diseases, Bronchiolitis
Mexico City, Mexico
View Trial DetailsNCT07531186
Chronic Disease, Disease Attributes
Al Mansurah, Dakahlia Governorate, Egypt
View Trial DetailsNCT06802679
Chronic Disease, Dialysis Access Dysfunction
Singapore
View Trial DetailsNCT01950819
Chronic Disease, Chronic Kidney Disease (CKD)
Birmingham, Alabama, United States
View Trial Details