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The concept of renal rehabilitation has become increasingly important with the increasing age of patients with severe or even terminal chronic kidney disease (CKD). It combines physical exercise and nutritional monitoring programs for patients with terminal CKD who are most often treated with conventional hemodialysis (HD) at a rate of 3 sessions of 4 hours per week.
Sarcopenia is a very common phenomenon in patients with CKD. The prevalence found in recent meta-analyses varies between 25.6 and 28.5% in patients treated with dialysis. It is even higher in patients treated with HD than in patients treated with peritoneal dialysis (PD). Younger and more active patients will more often choose PD. The conventional HD modality preserves residual renal function less well, which is important for better elimination of uremic toxins bound to plasma proteins. Conventional HD requires a higher immobilization time and causes more post-dialysis symptoms, leaving less time for the patient to be physically active.
The phenomenon of sarcopenia is not insignificant. It is associated in dialysis patients with a higher mortality rate (risk x 1.8) and a higher incidence of cardiovascular events (risk x 3.8). The association with higher mortality is well demonstrated for the 2 main components of sarcopenia, namely reduced muscle mass and reduced muscle strength. Sarcopenia also increases the risk of falls and fractures, it decreases the physical performance of patients and their ability to perform activities of daily living. The quality of life of patients is reduced and the probability of social placement is high.
The phenomena of sarcopenia and physical deconditioning are even more problematic in patients in HD after an acute medical problem. The need for rehabilitation is even higher. "Classical" HD treatment can be a burden for these patients, leaving no room for integrating a complete rehabilitation program.
Daily low dialysate flow rate hemodialysis (LDF) is a type of hemodialysis in which patients benefit from more frequent but shorter and hemodynamically better tolerated HD sessions. This new technique potentially presents certain advantages over conventional HD, particularly at the cardiovascular level: better blood pressure control and better reduction of left ventricular hypertrophy. LDF also allows better control of hyperphosphatemia with a reduced need for phosphorus binders. Thanks to more frequent dialysis (5 to 6 sessions per week), inter-dialytic weight gain is often less significant, allowing less aggressive ultrafiltration, with better hemodynamic tolerance, and better post-dialysis recovery. In this perspective, this study aims to examine the interest of integrating HDQ dialysis into a renal rehabilitation program in patients with terminal CKD whose dialysis must continue after an acute event requiring hospitalization. The investigators want to study whether this technique allows the implementation of a more effective rehabilitation program, while maintaining the same dialysis efficiency as with the conventional HD technique. To the investigator's knowledge, no study concerning patients under HDQ has been conducted during their renal rehabilitation phase.
The objectives of the current study are:
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Hemodialysis patients | Experimental | Patients under hemodialysis |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Low flow rate hemodialysis | Procedure | Low flow rate hemodialysis five times per week |
|
| Measure | Description | Time Frame |
|---|---|---|
| Hand grip test | Grip strength (measured by means of a dynamometer) is recommended as a good simple measure of muscle strength. Low grip strength is a powerful predictor of poor patient outcomes such as longer hospital stays, increased functional limitations, poor health-related quality of life and death. Cut-off points for men <27 kg Cut-off points for women <16 kg | At admission in the rehabilitation ward |
| Hand grip test | Grip strength (measured by means of a dynamometer) is recommended as a good simple measure of muscle strength. Low grip strength is a powerful predictor of poor patient outcomes such as longer hospital stays, increased functional limitations, poor health-related quality of life and death. Cut-off points for men <27 kg Cut-off points for women <16 kg | At discharge from the rehabilitation ward, in general up to 24 weeks after admission |
| Measure | Description | Time Frame |
|---|---|---|
| Short physical performance battery test (SPPB) | The short physical performance battery (SPPB) is a group of measures that combines the results of the gait speed, chair stand and balance tests. It has been used as a predictive tool for possible disability. The scores range from 0 (worst performance) to 12 (best performance). The SPPB has been shown to have predictive validity showing a gradient of risk for mortality, nursing home admission, and disability. The maximum score is 12 points, and a score of ≤ 8 points indicates poor physical performance. |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Joris Vanparys, MD | Contact | +32 2475 52 64 | Joris.VANPARYS@chu-brugmann.be |
| Name | Affiliation | Role |
|---|---|---|
| Joris Vanparys, MD | CHU Brugmann | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| CHU Brugmann | Recruiting | Brussels | 1020 | Belgium |
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| Multidisciplinary rehabilitation program | Other | Tailor made rehabilitation program |
|
| At admission in the rehabilitation ward |
| Short physical performance battery test (SPPB) | The short physical performance battery (SPPB) is a group of measures that combines the results of the gait speed, chair stand and balance tests. It has been used as a predictive tool for possible disability. The scores range from 0 (worst performance) to 12 (best performance). The SPPB has been shown to have predictive validity showing a gradient of risk for mortality, nursing home admission, and disability. The maximum score is 12 points, and a score of ≤ 8 points indicates poor physical performance. | At discharge from the rehabilitation ward, in general up to 24 weeks after admission |
| Six minutes walking test (6 MWT) | The 6-minute walk test (6MWT) is a commonly used test to assess functional exercise capacity. It evaluates the functional capacity of the individual and it provides information over the pulmonary and cardiovascular systems, blood circulation, neuromuscular system, body metabolism, and peripheral circulation. An increase in the distance walked indicates improvement in basic mobility. In the geriatric population: Small meaningful change 20 m, Substantial meaningful change 50 m. | At admission in the rehabilitation ward |
| Six minutes walking test (6 MWT) | The 6-minute walk test (6MWT) is a commonly used test to assess functional exercise capacity. It evaluates the functional capacity of the individual and it provides information over the pulmonary and cardiovascular systems, blood circulation, neuromuscular system, body metabolism, and peripheral circulation. An increase in the distance walked indicates improvement in basic mobility. In the geriatric population: Small meaningful change 20 m, Substantial meaningful change 50 m. | At discharge from the rehabilitation ward, in general up to 24 weeks after admission |
| Muscle ultrasound conclusion | Assessment of pennate muscles such as the quadriceps femoris can detect a decrease in muscle thickness and cross-sectional area within a relatively short period of time, the use of ultrasound has been expanded in clinical practice to support the diagnosis of sarcopenia in older adults. | At admission in the rehabilitation ward |
| Muscle ultrasound conclusion | Assessment of pennate muscles such as the quadriceps femoris can detect a decrease in muscle thickness and cross-sectional area within a relatively short period of time, the use of ultrasound has been expanded in clinical practice to support the diagnosis of sarcopenia in older adults. | At discharge from the rehabilitation ward, in general up to 24 weeks after admission |
| SF-36 | Short Form Health Survey (SF-36) Standardised questionnaire measuring quality of life, reporting a physical componant summary score and a mental componant summary score, both ranging from 0 to 100, with lower scores indicating more disability and higher scores indicating less disability. | At admission in the rehabilitation ward |
| SF-36 | Short Form Health Survey (SF-36) Standardised questionnaire measuring quality of life, reporting a physical componant summary score and a mental componant summary score, both ranging from 0 to 100, with lower scores indicating more disability and higher scores indicating less disability. | At discharge from the rehabilitation ward, in general up to 24 weeks after admission |
| Kt/V | Blood test evaluating the quality of the dialysis on weekly basis | At admission in the rehabilitation ward |
| Kt/V | Blood test evaluating the quality of the dialysis on weekly basis | At discharge from the rehabilitation ward, in general up to 24 weeks after admission |
| Myostatin blood levels | Blood levels of Myostatin (sarcopenia biomarker) | At admission in the rehabilitation ward |
| Myostatin blood levels | Blood levels of Myostatin (sarcopenia biomarker) | At discharge from the rehabilitation ward, in general up to 24 weeks after admission |
| Activin A blood levels | Blood levels of Activin A (sarcopenia biomarker) | At admission in the rehabilitation ward |
| Activin A blood levels | Blood levels of Activin A (sarcopenia biomarker) | At discharge from the rehabilitation ward, in general up to 24 weeks after admission |
| IGF1 blood levels | Blood levels of IGF1 (biomarker) | At admission in the rehabilitation ward |
| IGF1 blood levels | Blood levels of IGF1 (biomarker) | At discharge from the rehabilitation ward, in general up to 24 weeks after admission |
| ID | Term |
|---|---|
| D055948 | Sarcopenia |
| ID | Term |
|---|---|
| D009133 | Muscular Atrophy |
| D020879 | Neuromuscular Manifestations |
| D009461 | Neurologic Manifestations |
| D009422 | Nervous System Diseases |
| D001284 | Atrophy |
| D020763 | Pathological Conditions, Anatomical |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D012816 | Signs and Symptoms |
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