Combinations of rapid immunoassays for a speedy diagnosis of heparin-induced thrombocytopenia.


Journal

Journal of thrombosis and haemostasis : JTH
ISSN: 1538-7836
Titre abrégé: J Thromb Haemost
Pays: England
ID NLM: 101170508

Informations de publication

Date de publication:
10 2022
Historique:
revised: 23 05 2022
received: 11 01 2022
accepted: 27 06 2022
pubmed: 10 7 2022
medline: 23 9 2022
entrez: 9 7 2022
Statut: ppublish

Résumé

Early recognition and treatment of heparin-induced thrombocytopenia (HIT) are key to prevent severe complications. To assess the diagnostic performance of rapid immunoassays (IA) in detecting anti-PF4/heparin-antibodies. Diagnostic performances of lateral-flow IA (LFIA; STic Expert HIT) and latex IA (LIA; HemosIL HIT-Ab) were analyzed in pilot (n = 74) and derivation cohorts (n = 267). Two novel algorithms based on the combination of HIT clinical probability with sequentially performed LIA and chemiluminescent IA (CLIA; HemosIL AcuStar-HIT-IgG) were compared with published rapid diagnostic algorithms: the "Lausanne algorithm" sequentially combining CLIA and particle-gel IA (PaGIA) and the "Hamilton algorithm" based on simultaneously performed LIA and CLIA. LFIA missed 6/30 HIT. The sensitivity and specificity of LIA were 90.9% and 93.5%. The Lausanne algorithm correctly predicted HIT in 19/267 (7.1%), excluded it in 240/267 (89.9%), leaving 8/267 (3%) cases unsolved. The algorithm sequentially combining CLIA and LIA predicted HIT in 19/267 (7.1%) with 1/19 wrong prediction, excluded it in 236/267 (88.4%), leaving 11/267 (4.1%) cases unsolved. The algorithm employing LIA as a first assay predicted HIT in 22/267 (8.2%), excluded it in 235/267 (88%), leaving 9/267 (3.4%) cases unsolved. Finally, the Hamilton algorithm correctly predicted HIT in 10/267 (3.7%), excluded it in 229/267 (85.7%), leaving 28/267 (10.5%) cases unsolved. LFIA cannot be used to exclude or predict HIT when using frozen plasma. A Bayesian approach sequentially employing two rapid immunoassays for anti-PF4/heparin antibodies is most effective for the accurate diagnosis of HIT. Based on retrospective data, the combination LIA/CLIA is a candidate for a prospective validation.

Sections du résumé

BACKGROUND
Early recognition and treatment of heparin-induced thrombocytopenia (HIT) are key to prevent severe complications.
OBJECTIVE
To assess the diagnostic performance of rapid immunoassays (IA) in detecting anti-PF4/heparin-antibodies.
METHODS
Diagnostic performances of lateral-flow IA (LFIA; STic Expert HIT) and latex IA (LIA; HemosIL HIT-Ab) were analyzed in pilot (n = 74) and derivation cohorts (n = 267). Two novel algorithms based on the combination of HIT clinical probability with sequentially performed LIA and chemiluminescent IA (CLIA; HemosIL AcuStar-HIT-IgG) were compared with published rapid diagnostic algorithms: the "Lausanne algorithm" sequentially combining CLIA and particle-gel IA (PaGIA) and the "Hamilton algorithm" based on simultaneously performed LIA and CLIA.
RESULTS
LFIA missed 6/30 HIT. The sensitivity and specificity of LIA were 90.9% and 93.5%. The Lausanne algorithm correctly predicted HIT in 19/267 (7.1%), excluded it in 240/267 (89.9%), leaving 8/267 (3%) cases unsolved. The algorithm sequentially combining CLIA and LIA predicted HIT in 19/267 (7.1%) with 1/19 wrong prediction, excluded it in 236/267 (88.4%), leaving 11/267 (4.1%) cases unsolved. The algorithm employing LIA as a first assay predicted HIT in 22/267 (8.2%), excluded it in 235/267 (88%), leaving 9/267 (3.4%) cases unsolved. Finally, the Hamilton algorithm correctly predicted HIT in 10/267 (3.7%), excluded it in 229/267 (85.7%), leaving 28/267 (10.5%) cases unsolved.
CONCLUSION
LFIA cannot be used to exclude or predict HIT when using frozen plasma. A Bayesian approach sequentially employing two rapid immunoassays for anti-PF4/heparin antibodies is most effective for the accurate diagnosis of HIT. Based on retrospective data, the combination LIA/CLIA is a candidate for a prospective validation.

Identifiants

pubmed: 35808841
doi: 10.1111/jth.15811
pmc: PMC9796930
pii: S1538-7836(22)19045-8
doi:

Substances chimiques

Anticoagulants 0
Immunoglobulin G 0
Latex 0
Platelet Factor 4 37270-94-3
Heparin 9005-49-6

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2407-2418

Informations de copyright

© 2022 The Authors. Journal of Thrombosis and Haemostasis published by Wiley Periodicals LLC on behalf of International Society on Thrombosis and Haemostasis.

Références

Swiss Med Wkly. 2020 Apr 24;150:w20210
pubmed: 32329806
J Thromb Haemost. 2020 Jun;18(6):1435-1446
pubmed: 32167669
Br J Haematol. 2022 Jun;197(6):766-790
pubmed: 35358358
Blood. 2016 Feb 4;127(5):546-57
pubmed: 26518436
J Thromb Haemost. 2009 Oct;7(10):1649-55
pubmed: 19515091
Thromb Haemost. 2011 Dec;106(6):1197-202
pubmed: 21979237
Haematologica. 2012 Jan;97(1):89-97
pubmed: 21933856
Br J Haematol. 2014 Sep;166(5):774-82
pubmed: 24815503
Br J Haematol. 2003 May;121(4):535-55
pubmed: 12752095
Thromb Res. 2017 May;153:108-117
pubmed: 28391124
Lancet. 1999 Oct 30;354(9189):1525-6
pubmed: 10551503
Blood. 2017 May 25;129(21):2864-2872
pubmed: 28416511
Thromb Haemost. 2016 May 2;115(5):1044-55
pubmed: 26763074
Ann Intern Med. 1993 Nov 1;119(9):874-81
pubmed: 8214998
Clin Chem Lab Med. 2020 Nov 23;:
pubmed: 33554568
J Thromb Haemost. 2011 Jul;9 Suppl 1:105-17
pubmed: 21781246
Curr Opin Hematol. 2008 Sep;15(5):456-64
pubmed: 18695368
Hamostaseologie. 2020 Nov;40(4):472-484
pubmed: 33091948
J Clin Med. 2021 Feb 10;10(4):
pubmed: 33578859
Blood. 2020 Apr 2;135(14):1171-1184
pubmed: 31945147
Thromb Haemost. 2010 Aug;104(2):402-9
pubmed: 20539902
N Engl J Med. 2015 Jul 16;373(3):252-61
pubmed: 26176382
J Thromb Haemost. 2022 Oct;20(10):2407-2418
pubmed: 35808841
Blood Adv. 2018 Nov 27;2(22):3360-3392
pubmed: 30482768
Blood. 2012 Nov 15;120(20):4160-7
pubmed: 22990018
Thromb Res. 2012 Apr;129(4):426-33
pubmed: 22178575
Semin Thromb Hemost. 2016 Feb;42(1):69-74
pubmed: 26595149
Pathology. 2018 Jun;50(4):426-436
pubmed: 29678479
Blood. 2020 Apr 2;135(14):1082-1083
pubmed: 32243513
Rev Med Interne. 2009 Apr;30(4):331-4
pubmed: 18814940

Auteurs

Luana Rittener-Ruff (L)

Division of Haematology and Central Haematology Laboratory, Lausanne University Hospital (CHUV) and University of Lausanne (UNIL), Lausanne, Switzerland.

Matteo Marchetti (M)

Division of Haematology and Central Haematology Laboratory, Lausanne University Hospital (CHUV) and University of Lausanne (UNIL), Lausanne, Switzerland.

Elena Matthey-Guirao (E)

Division of Haematology and Central Haematology Laboratory, Lausanne University Hospital (CHUV) and University of Lausanne (UNIL), Lausanne, Switzerland.

Francesco Grandoni (F)

Division of Haematology and Central Haematology Laboratory, Lausanne University Hospital (CHUV) and University of Lausanne (UNIL), Lausanne, Switzerland.

Francisco J Gomez (FJ)

Division of Haematology and Central Haematology Laboratory, Lausanne University Hospital (CHUV) and University of Lausanne (UNIL), Lausanne, Switzerland.

Lorenzo Alberio (L)

Division of Haematology and Central Haematology Laboratory, Lausanne University Hospital (CHUV) and University of Lausanne (UNIL), Lausanne, Switzerland.

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Classifications MeSH