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Completed

NCT Number: NCT03249532

Effect of Dialysis Techniques on Blood Pressure and Cardiac Function During Dialysis

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.

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Key information

About this study

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:

  • intra-dialytic hemodynamic stability is better preserved during HV-HDF as compared to standard (S)-HD, C-HD and low volume (LV)-HDF;
  • mainly as a result of a better intra-dialytic hemodynamic stability, the severity of organ injury, especially the heart, is least evident during HV-HDF;
  • the mechanism of a better preserved intra-dialytic hemodynamic stability during HV-HDF depends on its superior thermal balance and/or bio-incompatibility, clearance of MMW substances, or a combination of these items.

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • treatment with HD or HDF 3 x per week during at least 4 hours for at least 2 months
  • ability to understand study procedures
  • willingness to provide informed consent
  • single pool Kt/V urea (spKt/Vurea) ≥ 1.2
  • achievement of blood flow of ≥360 ml/min and/or convection volume of >23 Liter per treatment during the run-in phase

Exclusion criteria

  • - current age < 18 years
  • severe incompliance to dialysis procedure and accompanying prescriptions, especially frequency and duration of dialysis treatment
  • life expectancy < 3 months
  • participation in another clinical intervention trial

Treatment and study plan

standard hemodialysis

Device

hemodialysis with high-flux dialyzer; prescription of dialysate temperature: 36.5 degrees Celsius; convection volume: not applicable

cool hemodialysis

Device

hemodialysis with high-flux dialyzer; prescription of dialysate temperature: 35.5 degrees Celsius; convection volume: not applicable

low volume hemodiafiltration

Device

hemodiafiltration; prescription of dialysate temperature: 36.5 degrees celsius prescription of convection volume: 15 L

high volume hemodiafiltration

Device

hemodiafiltration; prescription of dialysate temperature: 36.5 degrees celsius prescription of convection volume: 25 L

Primary outcomes

  1. intradialytic hypotension

    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)

Secondary outcomes

  1. diastolic dysfunction during 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

Other outcomes

  1. systolic blood pressure

    Time frame: up to 4 hours(= one dialysis treatment); assessed during 3 treatments on each modality

    change in systolic blood pressure (mmHg)

  2. diastolic blood pressure

    Time frame: up to 4 hours(= one dialysis treatment); assessed during 3 treatments on each modality

    change in diastolic blood pressure (mmHg)

  3. mean arterial blood pressure

    Time frame: up to 4 hours(= one dialysis treatment); assessed during 3 treatments on each modality

    change in mean arterial blood pressure (mmHg)

  4. pulse pressure

    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)

  5. beat-to-beat blood pressure

    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)

  6. heart rate

    Time frame: up to 4 hours(= one dialysis treatment); assessed during 1 treatment on each modality

    change in heart rate (finger cuff assessment)

  7. stroke volume

    Time frame: up to 4 hours(= one dialysis treatment); assessed during 1 treatment on each modality

    change in stroke volume (finger cuff assessment)

  8. cardiac output

    Time frame: up to 4 hours(= one dialysis treatment); assessed during 1 treatment on each modality

    change in cardiac output (finger cuff assessment)

  9. total peripheral resistance

    Time frame: up to 4 hours(= one dialysis treatment); assessed during 1 treatment on each modality

    change in total peripheral resistance (finger cuff assessment)

  10. number of sessions with reached target dry weight

    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)

  11. relative blood volume

    Time frame: up to 4 hours(= one dialysis treatment); assessed during 2 treatments on each modality

    relative blood volume (%) during dialysis treatment

  12. oxygen saturation

    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

  13. oxygen partial pressure (pO2)

    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

  14. change in creatine kinase (CK)-MB

    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

  15. change in bacterial DNA in blood

    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

  16. change in soluble CD14

    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

  17. change in extracellular vesicles (EVs)

    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

  18. change in soluble intercellular adhesion molecule-1 (s-ICAM-1)

    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

  19. change in high sensitivity C-reactive protein (hs-CRP)

    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

  20. change in interleukin-6 (IL-6)

    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

  21. change in fibroblast growth factor-23 (FGF-23)

    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

Sponsors and collaborators

Lead sponsor

Amsterdam UMC, location VUmc

Other

Collaborators

  • B.Braun Avitum AG
  • Niercentrum aan de Amstel, Amstelveen, Netherlands

Registry information

Official study title

Effect of High-volume Online hemodiafiLtration on Intra-diaLytic hemodynAmic (iN)sTability and Cardiac Function in Chronic Hemodialysis Patients (the HOLLANT Study)

Acronym: HOLLANT

Important dates

Study start
2018
Primary completion
2021
Study completion
2021
First posted
Aug 15, 2017
Registry last updated
Nov 30, 2021

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.

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