Thromb Haemost 2010; 104(04): 837-844
DOI: 10.1160/TH10-02-0099
New Technologies, Diagnostic Tools and Drugs
Schattauer GmbH

Interlaboratory variation in heparin monitoring: Lessons from the Quality Management Program of Ontario coagulation surveys

Adam Cuker
1   University of Pennsylvania, Philadelphia, Pennsylvania, USA
,
Anne Raby
2   Quality Management Program – Laboratory Services, Toronto, Ontario, Canada
,
Karen A. Moffat
2   Quality Management Program – Laboratory Services, Toronto, Ontario, Canada
3   McMaster University and St. Joseph’s Hospital, Hamilton, Ontario, Canada
,
Greg Flynn
2   Quality Management Program – Laboratory Services, Toronto, Ontario, Canada
,
Mark A. Crowther
3   McMaster University and St. Joseph’s Hospital, Hamilton, Ontario, Canada
› Author Affiliations

Financial support:This work was funded in part by K12 HL087064–03 and a grant from the University of Pennsylvania Institute of Translational Medicine and Therapeutics (to AC). Dr. Crowther holds a Career Investigator Award from the Heart and Stroke Foundation of Ontario.
Further Information

Publication History

Received: 05 February 2010

Accepted after minor revision: 14 May 2010

Publication Date:
24 November 2017 (online)

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Summary

Unfractionated heparin (UFH) monitoring is subject to substantial inter-laboratory variation. We analysed results of annual coagulation surveys administered by the Quality Management Program – Laboratory Services (Toronto, ON, Canada) from 2003 to 2007 to evaluate variation in UFH monitoring across Ontario. Participating laboratories performed an activated partial thromboplastin time (APTT) utilising their local methodology on lyophilised human plasma spiked with UFH. In the 2006 and 2007 surveys, laboratories licensed to perform anti-Xa assays also reported anti-Xa activity results. The APTT differed significantly between heparin-sensitive and heparin-insensitive methods (p<0.0005). Within-method variation was observed and increased with increasing heparin concentration. Among laboratories performing an APTT and anti-Xa, the coefficient of variation was greater in the anti-Xa than in the APTT for both the 2006 (64.0% vs. 10.5%) and 2007 (15.0% vs. 11.6%) surveys. Substantial interlaboratory variation in UFH monitoring, both between and within APTT methods, was observed and was not reduced by use of an anti-Xa assay.