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Intraperitoneal heparin ameliorates the systemic inflammatory response in PD patients
Jonas Angel Sjøland1, Robert Smith Pedersen, Jørgen Jespersen
1Department of Clinical Biochemistry, Ribe County Hospital, Esbjerg, Denmark. sjoland@dadlnet.dk
Nephron. Clinical Practice
|April 26, 2005
Summary
Long-term intraperitoneal tinzaparin treatment in peritoneal dialysis (PD) patients with end-stage renal disease (ESRD) significantly reduced key inflammatory markers. This suggests a potential therapeutic benefit for managing inflammation in PD patients.
Area of Science:
- Nephrology
- Immunology
- Pharmacology
Background:
- End-stage renal disease (ESRD) patients exhibit high cardiovascular mortality linked to chronic inflammation.
- Heparins show potential anti-inflammatory effects.
- Investigating intraperitoneal heparin's impact on inflammation in peritoneal dialysis (PD) patients is crucial.
Purpose of the Study:
- To evaluate the long-term effects of intraperitoneal tinzaparin on local and systemic inflammation in PD patients.
- To assess changes in inflammatory markers during tinzaparin treatment compared to placebo.
Main Methods:
- A double-blinded, cross-over study involving 21 PD patients with ESRD.
- Patients received either tinzaparin (4,500 anti-Xa IU) or placebo daily in dialysis bags for 3-month periods, with a 1-month wash-out.
- Blood and dialysate samples were analyzed for inflammatory markers, with dialysate marker rates adjusted for ultrafiltration variations.
Main Results:
- Intraperitoneal tinzaparin treatment led to a 25.8% reduction in plasma C-reactive protein (p = 0.032).
- Plasma fibrinogen concentration decreased by 7.3% (p = 0.042).
- Dialysate interleukin-6 appearance rate showed a significant 54.5% reduction (p = 0.007) compared to placebo.
Conclusions:
- Long-term intraperitoneal tinzaparin administration effectively reduces local and systemic inflammatory markers in ESRD patients undergoing PD.
- This treatment may offer a strategy to mitigate inflammation-associated risks in PD patients.