Citrate, Hemodialysis, Heparin
Conditions
Brief summary
Acetate-free citrate containing dialysate is expected to be clinically effective in maintaining hemodynamic stability during hemodialysis (HD). It has been demonstrated that citrate dialysate help produce a local anticoagulant effect by chelating ionized calcium. Moreover, citrate can improve phosphate and beta2 macroglobulin and better control of arterial hypertension and hemoglobinemia. We therefore would like to study the effect of citrate dialysate on clot formation and anemia while reducing heparin in chronic hemodialysis patients.
Detailed description
This is the prospective comparison study. This study enrolled chronic hemodialysis patients age more than 18 who undergo hemodialysis 3 times per week for at least 3 months. All the patients should have serum ferritin 200-1000 ng/L and TSAT of 15-50%. The investigators exclude patients with age more than 70 years, comorbidities influencing citrate metabolism (hepatic failure,liver transplantation,cancer with bone metastasis), patients using heparin free protocol, hyperkalemia worsened by hypocalcemia, contraindication to heparin, treatment with cinacalcet or oral anticoagulant, patients using central venous catheter with blood flow less than 300 ml/min, and patients using low molecular weight heparin. The study will be conducted in three phases over a period of 4 months. After run-in period for 2 weeks using acetate dialysate, the heparin dose will be titrated to lowest effective dose. During the first phase, citrate was replaced for acetate and heparin will be reduced to 50%. The second and third phase will be performed by reducing heparin doses to 25 % and heparin free consecutively. Each phase lasts for 4 weeks. Washout period for 2 weeks will be alternated after each phase. Data collection: The investigators measure blood chemistries such as CBC, BUN creatinine electrolytes calcium phosphorus and KT/V at the beginning and at the end of each session. Ionized calcium will be monitored pre and post dialysis in each session. In addition, the investigators record clot score and erythropoietin dosage in each session and each phase.
Interventions
DEVICECitrate dialysate
Change form acetate to citrate dialysate
Sponsors
Bangkok Metropolitan Administration Medical College and Vajira Hospital
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Intervention model description
prospective comparison study
Eligibility
Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No
Inclusion criteria
* This study enrolled chronic hemodialysis patients age more than 18 who undergo hemodialysis 3 times per week for at least 3 months. * Serum ferritin 200-1000 ng/L and TSAT of 15-50%.
Exclusion criteria
* age more than 70 years, * comorbidities influencing citrate metabolism (hepatic failure,liver transplantation,cancer with bone metastasis), * patients using heparin free protocol,hyperkalemia worsened by hypocalcemia * contraindication to heparin, * treatment with cinacalcet, or oral anticoagulant * patients using central venous catheter with blood flow less than 300 ml/min * patients using low molecular weight heparin
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Effect of citrate dialysate to anemia | 3 months | Hemoglobin in gram per dL |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Effect of citrate dialysate to dialyzer clotting | 3 months | clot score.The clot score ranges from 1-4.Score 1 means no residual blood or less than 10 % in the fibers Score 2 means residual blood in \< 10-25% of the fiber score 3 means residual blood in 25-50 % of the fiber Score 4 means more than 50 % of the fiber Score3 |
| effect of citrate dialysate to electrolyte changes | 3 months | electrolyte in mmoll/L(Sodium,Potassium,Chloride and bicarbonate) |
| effect of citrate dialysate to dialysis adequacy | 3 months | Kt/V |
Countries
Thailand
Outcome results
None listed