Hämodialyse

Wetzels, E; Colombi, Aldo; Dittrich, P.; Gurland, Hans J.; Kessel, Michael; Klinkmann, H

doi:10.1007/978-3-642-70908-1_1

Cited by 2 publications

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“…This is about twice the amount measured during anticoagulation with unfractionated heparin. These data are in agreement with the literature [10][11][12][13][14][15]. aXa-like activity The differences between the three anti-factor Xa test systems during anticoagulation with LMW heparin were similar to those found during anticoagulation with unfractionated heparin (see Table 2).…”

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confidence: 91%

“…Anticoagulation during haemodialysis with lowmolecular-weight heparin can be monitored by chromogenic substrate assays. Values of 0.6 to 1.0 aXa V/mI plasma are typically measured during effective anticoagulation [9,10,12,13]. The aXa levels measured during anticoagulation with unfractionated heparins are somewhat tower.…”

Section: Discussionmentioning

confidence: 99%

“…Measurement of LMW heparins requires a specific chromogenic substrate assays to determine the inhibition of factor Xa [9][10][11]. In contrast, unfractionated heparin is monitared using whole-blood clotting methods [12,13]. These whole-blood clotting methods are not sensitive to LMW heparins and the chromogenic assays are time consuming and quite laborious.…”

Section: Introductionmentioning

confidence: 99%

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Monitoring of heparins in haemodialysis using an anti-factor-Xa-specific whole-blood clotting assay

1995

Nephrology Dialysis Transplantation

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In haemodialysis low-molecular-weight (LMW) heparin is increasingly used für anticoagulation. The advantages over unfractionated (UF) heparin are the lower bleeding risk and the lack of infiuence on lipid metabolism. However, no reliable and rapid method is available so rar to control the efficacy and safety of LMW heparin during haemodialysis. The specific anti-factor Xa (aXa) chromogenic substrate assays are laborious and time consuming. In the present study we have compared chromogenic assay with a coagulation assay (heptest), which was performed from plasma and whole-blood sampIes. The effects were compared with unfractionated heparin during haemodialysis. The aXa activity in the chromogenic S2222 assay ranged between 0.2 and 0.5 V/mI with UF heparin and between 0.4 and 0.8 V/mI with LMW heparin during haemodialysis. The coagulometric aXa activity in heptest assay from plasma was 0.6-1.0 V/mI with UF heparin and 1.2-2.0 V/mI with LMW heparin. The Heptest coagulation values from citrated whole blood sampIes ranged from 0.4 to 0.8 V/mI with UF heparin and from 0.8 to 1.4 U/ml with LMW heparin. The prolongation of the heptest clotting times with UF and LMW heparin was in the range of 4.4 für UF heparin and 5.2 für LMW heparin using the whole-blood assay. Heptest assay from plasma sampIes yielded prolongations of 6.1 with UF heparin and 6.6 with LMW heparin. The data show thai the coagulation assay is rapid and reproducible using plasma ar uncentrifuged whole-blood sampIes and is valid to monitor UF heparin or LMW heparin in patients undergoing chronic intermittent haemodialysis.

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confidence: 91%