Improving the specificity of the PF4 ELISA in diagnosing heparin-induced thrombocytopenia

被引:27
作者
McFarland, Janice [1 ]
Lochowicz, Andrew
Aster, Richard
Chappell, Bryan
Curtis, Brian
机构
[1] Blood Ctr Wisconsin, Platelet & Neutrophil Immunol Lab, Milwaukee, WI 53201 USA
关键词
CARDIAC-SURGERY; UNFRACTIONATED HEPARIN; CLINICAL-SIGNIFICANCE; DEPENDENT ANTIBODIES; CONFIRMATORY TEST; PLATELET; PLATELET-FACTOR-4; THROMBOSIS; COMPLEXES; PATIENT;
D O I
10.1002/ajh.23248
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Heparin induced thrombocytopenia (HIT) is a serious complication of heparin therapy. The PF4 ELISA is a serologic assay that provides laboratory support for the clinical diagnosis of HIT, but it is often positive in patients who do not have the syndrome. We examined whether the specificity of the PF4 ELISA can be improved by 1) taking antibody potency into consideration, 2) by measuring only IgG antibodies, and 3) by utilizing a high concentration heparin inhibition step. We reviewed clinical information on 116 patients whose samples were referred for HIT antibody testing and assigned each a clinical score related to the likelihood of the patient having HIT. The scores were then correlated with serologic findings. Patients with strongly positive PF4ELISA results (OD = 1.0) using both versions of the assay (IgG/A/M and IgG only) had clinical scores and SRA activity that were significantly higher than those having reactive or negative results. When the IgG-only PF4 ELISA was used, only the strongly positive result group had significantly higher clinical scores and SRA release, and fewer samples were classified as weakly positive or reactive, suggesting that detection of IgG only in the PF4 ELISA improves the assay's specificity. The heparin inhibition step identified reactive samples that were associated with clinical scores and SRA release indistinguishable from the negative result groups, confirming that this step further improves specificity of the test. This study supports utilizing these 3 modifications of the PF4 ELISA to improve specificity in supporting the clinical diagnosis of HIT. Am. J. Hematol., 2012. (c) 2012 Wiley Periodicals, Inc.
引用
收藏
页码:776 / 781
页数:6
相关论文
共 30 条
[11]  
Lee DH, 2004, HEPARIN INDUCED THRO, P107
[12]   Evaluation of pretest clinical score (4 T's) for the diagnosis of heparin-induced thrombocytopenia in two clinical settings [J].
Lo, GK ;
Juhl, D ;
Warkentin, TE ;
Sigouin, CS ;
Eichler, P ;
Greinacher, A .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2006, 4 (04) :759-765
[13]   What is the potential for overdiagnosis of heparin-induced thrombocytopenia? [J].
Lo, Gregory K. ;
Sigouin, Christopher S. ;
Warkentin, Theodore E. .
AMERICAN JOURNAL OF HEMATOLOGY, 2007, 82 (12) :1037-1043
[14]  
Pouplard C, 1999, AM J CLIN PATHOL, V111, P700
[15]   Changes in platelet count after cardiac surgery can effectively predict the development of pathogenic heparin-dependent antibodies [J].
Pouplard, C ;
May, MA ;
Regina, S ;
Marchand, M ;
Fusciardi, J ;
Gruel, Y .
BRITISH JOURNAL OF HAEMATOLOGY, 2005, 128 (06) :837-841
[16]   Platelet and monocyte antigenic complexes in the pathogenesis of heparin-induced thrombocytopenia (HIT) [J].
Rauova, L. ;
Arepally, G. ;
McKenzie, S. E. ;
Konkle, B. A. ;
Cines, D. B. ;
Poncz, M. .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2009, 7 :249-252
[17]   The Diagnostic Value of the Anti-PF4/Heparin Immunoassay High-Dose Heparin Confirmatory Test in Cardiac Surgery Patients [J].
Selleng, Sixten ;
Schreier, Natalie ;
Wollert, Hans-Georg ;
Greinacher, Andreas .
ANESTHESIA AND ANALGESIA, 2011, 112 (04) :774-776
[18]   Incidence and clinical relevance of anti-platelet factor 4/heparin antibodies before cardiac surgery [J].
Selleng, Sixten ;
Malowsky, Birgit ;
Itterman, Till ;
Bagemuehl, Jessica ;
Wessel, Antje ;
Wollert, Hans-Georg ;
Warkentin, Theodore E. ;
Greinacher, Andreas .
AMERICAN HEART JOURNAL, 2010, 160 (02) :362-369
[19]  
SHERIDAN D, 1986, BLOOD, V67, P27
[20]   ANTIBODIES FROM PATIENTS WITH HEPARIN-INDUCED THROMBOCYTOPENIA/THROMBOSIS ARE SPECIFIC FOR PLATELET FACTOR-4 COMPLEXED WITH HEPARIN OR BOUND TO ENDOTHELIAL-CELLS [J].
VISENTIN, GP ;
FORD, SE ;
SCOTT, JP ;
ASTER, RH .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 93 (01) :81-88