Description

Data from approximately 50 patients with chronic end-stage renal disease treated consecutively during the considered study period with HDx with Theranova filter, with HF HD, with OL-HDF, and with HFR with HFR17 filter at the Dialysis Center of the O.U. of Nephrology, Dialysis and Transplantation, directed by Prof. Gaetano La Manna, of IRCCS AOUBO Policlinico Sant'Orsola in the period from 01/01/2018 to 30/11/2022 will be analyzed. It should be noted that these membranes were used as part of the normal course of care.

The study is observational, non-interventional in nature. Patients will be treated according to clinical practice in accordance with the judgment of the physician and the information in the Technical Data Sheet of each individual product of any concomitant therapies administered according to clinical practice.

There will be about 50 patients, divided into 4 cohorts: patients undergoing HDx treatment with Theranova filter (group A), patients undergoing HFR treatment with HFR17 filter (group B), patients undergoing OL- HDF treatment (group C) and patients undergoing HD treatment with HF filter (HF HD) (group D). Each group will consist of at least 10 patients with chronic terminal kidney disease undergoing dialysis treatment at the O.U. of Nephrology, Dialysis and Transplantation, directed by Prof. Gaetano La Manna, of IRCCS AOUBO Policlinico Sant'Orsola from 01/01/2018 to 30/11/2022.

Inclusion criteria.

• Age ≥ 18 years
• Chronic hemodialytic treatment (on dialysis for at least 6 months), hemodialytic treatment with MCO filter (Theranova) or HF filter, OL- HDF or HFR with HFR filter17.
• Continuous use of the same filter for at least 12 months.
• Diuresis < 200 ml/day.
• Tri-weekly hemodialysis treatment.
• Duration of session ≥ 210 minutes.
• Availability of clinical data collected during the follow-up occurred at the OU of Nephrology, Dialysis and Transplantation - La Manna.

Exclusion criteria.

• Intradialytic hypotension
• Need for dialysis without heparin
• Active bleeding
• Active hematologic diseases
• Thrombocytopenia
• Chronic hepatopathies
• Active systemic inflammatory diseases
• Uncontrolled diabetes mellitus
• Temporary vascular access
• Recurrent vascular access infections

A sample size of approximately 50 patients treated consecutively during the study period under consideration and within the inclusion criteria with HDx with Theranova filter, HF HD, OL-HDF or HFR with HFR filter17 is estimated. The study will be initiated after formal notification to the Ethics Committee. Only patients undergoing chronic dialysis treatment at the OU of Nephrology, Dialysis and Transplantation, directed by Prof. Gaetano La Manna, of IRCCS AOUBO Policlinico Sant'Orsola will be enrolled.

Study Duration:

Patient data will be collected for the period from 01/01/2018 to 30/11/2022. A total duration of 18 months is estimated for data collection and analysis, starting from the approval of the Ethics Committee and issuance of the Nulla Osta by the General Management.

Treatments, visits and evaluations:

There are no study-specific treatments other than those provided by normal clinical practice.

For the purpose of this clinical trial, no study-specific visits are planned, but patients eligible in the study, still in follow-up, will be asked to read the information sheet and sign a study-specific informed consent for the collection and evaluation of the specified clinical-anamnestic data specified below. Clinical data will be collected in a structured manner from patients' medical records. It is specified that patient data will be collected for the period from 01/01/2018 to 30/11/2022.

The clinical data required by the protocol will be collected in pseudonymized form by the Principal Investigator's designated personnel in an electronic Data Collection Form (CRF) and will be managed through the REDCap platform. The eCRF in REDCap will be requested and implemented according to the procedure described in the "Corporate Operational Instruction for the Management and Use of the REDCap Platform" (IOA119). The Principal Investigator must indicate the names of personnel delegated to data management by specifying their relative functions within the study in the Delegation log.

Analysis Methodology:

The demographic and clinical characteristics of patients treated in the period 01/01/2018- 30/11/2022 at the Center, enrolled and evaluated in the study, will be reported in summary tables. Given the large number of patients under study (n=10 per group), descriptive statistics such as median, minimum value and maximum value for continuous type variables; absolute frequencies and percentage relative frequencies (when appropriate) for discrete or nominal type variables will be reported.

Summary data of blood parameters, relevant clinical events, etc., taken during the observation period will be summarized in summary tables.

Summary data of blood parameters, relevant clinical events, etc., collected during the observation period will be summarized in summary tables.

Data analysis will be carried out using SPSS software. For variables with normal distribution the Anova test will be used, for variables with distribution the Kruskal-Wallis test will be used.