Lipoprotein-apheresis DFPP has been performed in patients with Lp(a) levels greater than 125 nmol/L. In this report, data will be presented on five hemodialysis patients with significantly elevated Lp(a) levels (\>200 nmol/L) who had a history of cardiovascular disease and notable thromboembolic events.
The biological and clinical outcomes related to Lipoprotein-apheresis DFPP treatment and the associated cardiovascular and thromboembolic events will be described in these patients. Additionally, the impact of DFPP on biological and clinical markers including LDL cholesterol, triglycerides, fibrinogen, hemoglobin, platelet count, C-reactive protein (CRP), blood pressure, plasma volume treated, volume of albumin substitution, volume of plasma rejected, and duration of each Lipoprotein-apheresis DFPP session will be evaluated .
Study Type
OBSERVATIONAL
Enrollment
5
CHR Metz-Thionville Hopital de Mercy
Metz, France
serum Lp(a) concentration (nmol/L), on routine venous blood sampling
Before and after each DFPP session (repeated measures) during the study period
Time frame: up to 15 months after inclusion
serum LDL and serum triglycerides concentration (g/L), on routine venous blood sampling
before and after each DFPP session (repeated measures) during the study period
Time frame: up to 15 months after inclusion
serum triglycerides concentration (g/L), on routine venous blood sampling
before and after each DFPP session (repeated measures) during the study period
Time frame: up to 15 months after inclusion
cardiovascular or thromboembolic events
Myocardial infarction, stroke, Deep vein thrombosis, Pulmonary embolism, Systemic arterial embolism, aortiques complictions, thrombosis, Based on patient questioning and clinical examination during routine follow-up consultations
Time frame: during all the study period: up to 15 months after inclusion
Hemodynamic status:blood pressure
follow-up of patients' blood pressure (mmHg) before and after each DFPP session (repeated measures) during the study period
Time frame: up to 15 months after inclusion
Hemodynamic status: ultrafiltration rate
follow-up of patients' ultrafiltration rate (grams) before and after each DFPP session (repeated measures) during the study period
Time frame: up to 15 months after inclusion
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