PMID- 31837560 OWN - NLM STAT- MEDLINE DCOM- 20210617 LR - 20210617 IS - 1879-2472 (Electronic) IS - 0049-3848 (Linking) VI - 186 DP - 2020 Feb TI - Monitoring unfractionated heparin therapy. 4 hour-stability of anti-Xa activity in unspun citrated tubes. PG - 7-12 LID - S0049-3848(19)30464-5 [pii] LID - 10.1016/j.thromres.2019.10.019 [doi] AB - Current guidelines recommend performing laboratory tests aimed at monitoring unfractionated heparin (UFH) treatments within a delay not exceeding 1 to 2 h(s) after sampling when blood is collected into citrated tubes. As such a short delay could be an issue, we evaluated the potential impact of longer delays. For that purpose, two citrated tubes were obtained from patients on UFH: one was centrifuged and tested for anti-Xa activity and aPTT within 1 h after collection (T1 h) and one was stored for 4 h at room temperature (T4 h) before being processed. A total of 123 paired tubes were investigated. Anti-Xa activity was significantly lower at T4 h than at T1 h, with a mean bias, calculated according to Bland-Altman, of 0.05 IU/mL. Considering 0.30 to 0.70 IU/mL as the therapeutic range, there were 12 cases of discrepant test results (9.8%). Most of them being around the lower limit of the therapeutic range had no impact on patients' management. APTT was significantly shortened (p < 0.0001) at T4 h vs. T1 h, with a mean bias of -7.9 s. Considering anti-Xa correlated aPTT therapeutic range, 29 cases of discrepant test results (23.6%) were found, 10% would have induce dosage changes. The concordance between anti-Xa activities measured at T4 h and T1 h was excellent (kappa = 0.813) and good for aPTT (kappa = 0.661). In conclusion, extending the delay between blood collection and measurement of tests prescribed for monitoring UFH therapy up to 4 h was found to lead to a systematic reduction in both anti-Xa activity and aPTT in unspun citrated tubes. As changes at T4 h were limited and had few clinically relevance than the ones observed with aPTT testing, a 4 h-delay was found to be acceptable for anti-Xa activity. The maximum delay for aPTT should remain around 1-2 h as changes were more relevant. CI - Copyright (c) 2019. Published by Elsevier Ltd. FAU - Toulon, Pierre AU - Toulon P AD - Universite Cote d'Azur, CHU Nice, Hematology Department, Nice, France. Electronic address: toulon.p@chu-nice.fr. FAU - Appert-Flory, Anny AU - Appert-Flory A AD - Universite Cote d'Azur, CHU Nice, Hematology Department, Nice, France. FAU - Fischer, Florence AU - Fischer F AD - Universite Cote d'Azur, CHU Nice, Hematology Department, Nice, France. FAU - Buvat, Sylvain AU - Buvat S AD - Universite Cote d'Azur, CHU Nice, Hematology Department, Nice, France. FAU - Jambou, Didier AU - Jambou D AD - Universite Cote d'Azur, CHU Nice, Hematology Department, Nice, France. FAU - Mahagne, Marie-Helene AU - Mahagne MH AD - Universite Cote d'Azur, CHU Nice, Neurology Department, Nice, France. LA - eng PT - Journal Article DEP - 20191024 PL - United States TA - Thromb Res JT - Thrombosis research JID - 0326377 RN - 0 (Anticoagulants) RN - 0 (Factor Xa Inhibitors) RN - 0 (Heparin, Low-Molecular-Weight) RN - 9005-49-6 (Heparin) SB - IM MH - Anticoagulants/therapeutic use MH - *Drug Monitoring MH - Factor Xa Inhibitors/therapeutic use MH - *Heparin/therapeutic use MH - Heparin, Low-Molecular-Weight MH - Humans MH - Partial Thromboplastin Time OTO - NOTNLM OT - Anti-Xa activity OT - Monitoring OT - Stability OT - Unfractionated heparin OT - aPTT EDAT- 2019/12/15 06:00 MHDA- 2021/06/22 06:00 CRDT- 2019/12/15 06:00 PHST- 2019/05/31 00:00 [received] PHST- 2019/10/18 00:00 [revised] PHST- 2019/10/19 00:00 [accepted] PHST- 2019/12/15 06:00 [pubmed] PHST- 2021/06/22 06:00 [medline] PHST- 2019/12/15 06:00 [entrez] AID - S0049-3848(19)30464-5 [pii] AID - 10.1016/j.thromres.2019.10.019 [doi] PST - ppublish SO - Thromb Res. 2020 Feb;186:7-12. doi: 10.1016/j.thromres.2019.10.019. Epub 2019 Oct 24.