PMID- 20185164 OWN - NLM STAT- MEDLINE DCOM- 20100922 LR - 20131121 IS - 1879-2472 (Electronic) IS - 0049-3848 (Linking) VI - 126 IP - 1 DP - 2010 Jul TI - Heparin versus prostacyclin in continuous hemodiafiltration for acute renal failure: effects on platelet function in the systemic circulation and across the filter. PG - 24-31 LID - 10.1016/j.thromres.2010.01.048 [doi] AB - Continuous venovenous hemodiafiltration (CVVHDF) is the treatment of choice for critically-ill patients suffering from acute renal failure (ARF). One major problem of extracorporeal circuits is their thrombogenicity, which requires pharmacological blockade of primary (platelet-dependent) or secondary (plasmatic) haemostasis, increasing the patient's bleeding risk. Our study assessed platelet function during CVVHDF, comparing anticoagulant versus antiplatelet pharmacological strategies, commonly used to avoid circuit clotting. Twenty-three critically-ill patients with ARF, requiring CVVHDF were randomized to a prostacyclin analogue (PGI) or to unfractionated heparin (UFH). Ex vivo platelet function, assessed by optical aggregometry (OPA) induced by collagen or ADP, was studied in peripheral blood at baseline, 4 and 24 hrs after starting CVVHDF, and at 4 hrs within the circuit, before and after the filter (n=9). Coagulation was also monitored. PGI significantly inhibited ADP-induced OPA of peripheral platelets: maximal aggregation (Tmax) was reduced at 4 and 24 hrs by 20%, while collagen-induced Tmax was significantly reduced at 4 hrs only. In the UFH group, collagen-induced OPA in peripheral platelets was significantly inhibited: slopes of OPA tracings were decreased by 25%, lag time was prolonged by 22%, Tmax decreased by 10% already at 4 hrs. ADP-induced OPA showed a similar, but non-significant trend. UFH expectedly prolonged aPTT. In the UFH group, platelet responsiveness to collagen was significantly increased by 30% in post-filter versus pre-filter samples. This effect was blunted in the PGI group. UFH does not protect platelets from filter-induced activation and is associated with a reduced function of systemic platelets. Platelet-inhibiting agents might better prevent the activatory effect of the filter. CI - Copyright (c) 2010 Elsevier Ltd. All rights reserved. FAU - Arcangeli, Andrea AU - Arcangeli A AD - Istituto Anestesia e Rianimazione, Policlinico Agostino Gemelli, Catholic University School of Medicine, Largo Francesco Vito 1, 00168 Rome, Italy. andrea.arcangeli@rm.unicatt.it FAU - Rocca, Bianca AU - Rocca B FAU - Salvatori, Gabriella AU - Salvatori G FAU - Ciancia, Mariano AU - Ciancia M FAU - De Cristofaro, Raimondo AU - De Cristofaro R FAU - Antonelli, Massimo AU - Antonelli M LA - eng PT - Comparative Study PT - Journal Article PT - Randomized Controlled Trial PT - Research Support, Non-U.S. Gov't DEP - 20100224 PL - United States TA - Thromb Res JT - Thrombosis research JID - 0326377 RN - 0 (Anticoagulants) RN - 9005-49-6 (Heparin) RN - DCR9Z582X0 (Epoprostenol) SB - IM MH - Acute Kidney Injury/blood/drug therapy/*therapy MH - Aged MH - Anticoagulants/pharmacology/therapeutic use MH - Blood Coagulation/drug effects MH - Blood Coagulation Disorders/drug therapy/therapy MH - Blood Platelets/drug effects MH - Critical Illness/therapy MH - Epoprostenol/pharmacology MH - Female MH - Filtration MH - Hemodiafiltration MH - Hemorrhage/drug therapy/therapy MH - Hemostasis/*drug effects MH - Heparin/*pharmacology/*therapeutic use MH - Humans MH - Male MH - Middle Aged MH - Partial Thromboplastin Time MH - Platelet Count MH - Prospective Studies MH - Renal Dialysis EDAT- 2010/02/27 06:00 MHDA- 2010/09/24 06:00 CRDT- 2010/02/27 06:00 PHST- 2009/11/24 00:00 [received] PHST- 2010/01/27 00:00 [revised] PHST- 2010/01/27 00:00 [accepted] PHST- 2010/02/27 06:00 [entrez] PHST- 2010/02/27 06:00 [pubmed] PHST- 2010/09/24 06:00 [medline] AID - S0049-3848(10)00103-9 [pii] AID - 10.1016/j.thromres.2010.01.048 [doi] PST - ppublish SO - Thromb Res. 2010 Jul;126(1):24-31. doi: 10.1016/j.thromres.2010.01.048. Epub 2010 Feb 24.