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Efficacy and Safety of Incremental Hemodialysis

কেবল নিবন্ধিত ব্যবহারকারীরা নিবন্ধগুলি অনুবাদ করতে পারবেন
প্রবেশ করুন - নিবন্ধন করুন
লিঙ্কটি ক্লিপবোর্ডে সংরক্ষিত হয়েছে
স্থিতিএখনও নিয়োগ হচ্ছে না
স্পনসর
Carlo Basile, M.D.
সহযোগী
Miulli General Hospital

কীওয়ার্ডস

বিমূর্ত

Background: The thrice-weekly hemodialysis (HD) regimen is widely accepted as a standard prescription. The concept of incremental dialysis has been established as a possible alternative for patients with preserved diuresis and end-stage renal failure in need of HD. The main problems related to prescription of incremental HD are an arbitrary use of infrequent regimens and the lack of clear standards for incorporating residual kidney function (RKF) in the assessment of HD dose. Several models have been proposed for prescription of incremental dialysis. The latest, the variable target model (VTM) (Casino&Basile, NDT, 2018), gives more clinical weight to the RKF and allows less frequent HD treatments at lower RKF. Despite increasing evidence derived from observational studies to support the use of incremental HD, RCTs are lacking and, then, urgently needed.
Methods/Design:
The Division of Nephrology of the Miulli General Hospital, Acquaviva delle Fonti, Italy, the EUDIAL Working Group of the European Renal Association - European Dialysis Transplant Association (ERA-EDTA) and the Department of Nephrology, Dialysis and Transplantation of the Azienda Ospedaliero-Universitaria ConsorzialePoliclinico, Bari, Italy are starting a randomized clinical trial (RCT) in incident HD patients, whose name is "REAL LIFE", by using the acronym of its whole definition: RandomizEd clinicAL triaL on the effIcacy and saFety of incremental haEmodialysis. REAL LIFE is a pragmatic, prospective, multicentre, open label RCT, investigator-initiated, comparing the intervention arm (incremental HD) with the control arm (standard 3HD/wk). It consists in starting the HD treatment adopting the new incremental approach guided by the VTM. The primary outcome is the survival of kidney function, with the event defined as urinary output (UO) ≤ 100 mL/day, confirmed by a further collection after 2 weeks to exclude temporary illness.
Discussion: REAL LIFE will enable the investigators to know with the highest level of scientific evidence the safety and efficacy of an incremental approach to the start of HD treatment.

বর্ণনা

The majority of dialysis patients are currently treated with a fixed dose thrice-weekly haemodialysis (HD) (3HD/wk). The 3HD/wk regimen has been assumed, until recently, almost as a dogma in the dialysis community. Incremental HD is based on the simple idea of adjusting its dose according to the metrics of RKF. REAL LIFE is a pragmatic, prospective, multicentre, open label RCT, investigator-initiated, comparing the intervention arm (incremental HD) with the control arm (standard 3HD/wk). A Variable Target Model (VTM) has been suggested, which gives more clinical weight to the RKF and allows less frequent HD treatments in patients with lower RKF. The investigators recommend to start and keep on with once-weekly HD, which should be possible until residual renal urea clearance (KRU) falls below 2.5 - 3.0 mL/min/35 L, i.e., glomerular filtration rate (GFR) ≈ 4 mL/min/1.73 m2. The primary outcome is the survival of kidney function, with the event defined as urinary output (UO) ≤ 100 mL/day, confirmed by a further collection after 2 weeks to exclude temporary illness. Secondary outcomes are: composite primary cardiovascular endpoint (cardiovascular death, non fatal myocardial infarction and/or or non fatal stroke); intima-media thickness of the carotid arteries; specific cardiomyopathy control; RKF preservation; survival of the patients; hospital admissions; anemia control; mineral and bone disorder control; middle molecules and RKF. Considering a type I error of 0.05 and type II error of 0.20, the study must enroll 49 patients in the conventional HD arm and 49 patients in the incremental HD arm, totaling 98 patients enrolled into the trial. Finally, under the assumption of an expected drop-out rate of 15%, 58 patients per group should be enrolled for a total of 116. The assessment of the key kinetic parameters as well as the guide to the selection of operative parameters, as required to get the required equilibrated Kt/V (eKt/V = 1.2), will be done by using SPEEDY, a spreadsheet prescription tool that uses essentially the same equations used by Solute Solver, the software based on the double pool UKM recommended by the 2015 KDOQI guidelines. SPEEDY is freely available at the European Nephrology Portal (ENP). The link is https://enp-era-edta.org/174/page/home. The control arm includes patients put on a thrice-weekly HD schedule, as detailed above. The dialysis dose (eKt/V) should be about 1.2.

তারিখ

সর্বশেষ যাচাই করা হয়েছে: 03/31/2020
প্রথম জমা দেওয়া: 04/16/2020
আনুমানিক তালিকাভুক্তি জমা দেওয়া হয়েছে: 04/20/2020
প্রথম পোস্ট: 04/23/2020
সর্বশেষ আপডেট জমা দেওয়া হয়েছে: 04/20/2020
সর্বশেষ আপডেট পোস্ট: 04/23/2020
আসল অধ্যয়ন শুরুর তারিখ: 08/31/2020
আনুমানিক প্রাথমিক সমাপ্তির তারিখ: 11/30/2023
আনুমানিক অধ্যয়ন সমাপ্তির তারিখ: 11/30/2024

অবস্থা বা রোগ

End Stage Renal Disease on Dialysis

হস্তক্ষেপ / চিকিত্সা

Procedure: Incremental hemodialysis

Procedure: Conventional hemodialysis

পর্যায়

-

বাহু গ্রুপ

বাহুহস্তক্ষেপ / চিকিত্সা
Experimental: Incremental hemodialysis
Procedure: Incremental hemodialysis. It consists in reducing the frequency or number of sessions per week with which patients start the HD treatment. The experimental group will start with one session/week, then the number of weekly sessions will be increased to two and later to three as per criteria for progression
Procedure: Incremental hemodialysis
58 patients will start renal replacement therapy (RRT) with an incremental hemodialysis (once-weekly or twice-weekly) regimen.
Active Comparator: Conventional hemodialysis
Procedure: Conventional hemodialysis. It is controlled through usual clinical practice, based on starting the HD treatment with three sessions per week (control group).
Procedure: Conventional hemodialysis
58 patients will start renal replacement therapy (RRT) with the standard (thrice-weekly) hemodialysis regimen.

যোগ্যতার মানদণ্ড

বয়স অধ্যয়নের জন্য যোগ্য 18 Years প্রতি 18 Years
লিঙ্গ অধ্যয়নের জন্য যোগ্যAll
স্বাস্থ্যকর স্বেচ্ছাসেবীদের গ্রহণ করেহ্যাঁ
নির্ণায়ক

Inclusion Criteria:

- Adults aged > 18 years

- Start of maintenance hemodialysis treatment due to advanced CKD stage 5D

- Glomerular filtration rate (GFR) ranging from 4 to 10 mL/min/1.73 m2, as estimated by means of CKD-EPI formula or as a mean of the measured urea and creatinine clearances.

Exclusion Criteria:

- Age < 18 years

- Acute kidney injury or acute on chronic kidney injury

- Tranferred from other dialysis modalities (peritoneal dialysis) or restarting HD after kidney transplant rejection

- eGFR lesser than 4 mL/min/1.73 m2 or greater than 10 mL/min/1.73 m2

- UO < 500 mL/day

- Unable or unwilling to give informed consent.

- Unable to comply with trial procedures, e.g., collection of UO.

- Likely survival prognosis or planned modality or centre transfer < 6 months.

- Associated diseases: active neoplastic disease; refractory congestive heart failure (type IV NYHA) requiring high ultrafiltration volumes per session.

ফলাফল

প্রাথমিক ফলাফল ব্যবস্থা

1. Survival of kidney function [24 months]

The survival of kidney function is defined as a time to the event (anuria): the anuria is defined as urinary output (UO) ≤ 100 mL/day, confirmed by a further collection after 2 weeks to exclude temporary illness

মাধ্যমিক ফলাফলের ব্যবস্থা

1. Composite primary cardiovascular endpoint [24 months]

Cardiovascular death, non fatal myocardial infarction and/or or non fatal stroke

2. Intima-media thickness of the carotid arteries [24 months]

Echographic evaluation of intima-media thickness of the carotid arteries

3. Specific cardiomyopathy control [24 months]

Ecocardiography reporting data on the left ventricular ejection fraction (LVEF)

4. Residual kidney function (RKF) preservation [24 months]

The rate of decline in RKF defined as the slope of decline of residual renal urea clearance

5. Survival of the patients [24 months]

The follow-up time will be determined in days. It will be defined as the difference in days from the date of the end of the follow-up minus the date of the baseline visit. Events will be counted either as deaths (follow-up of less than 24 months) or as end of the follow-up

6. Hospital admissions [24 months]

The number of admissions will be registered.

7. Anemia control [24 months]

The hemoglobin levels (in g/dl) will be measured.

8. Mineral and bone disorder control [24 months]

Serum phosphorus and calcium levels (in mg/dl), and intact PTH (in pg/dl) will be measured.

9. Middle molecules and RKF [24 months]

The rate of change in serum β2-microglobulin concentrations over time will be evaluated

আমাদের ফেসবুক
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