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Combinations of rapid immunoassays for a speedy diagnosis of heparin‐induced thrombocytopenia
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 (LFI...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9796930/ https://www.ncbi.nlm.nih.gov/pubmed/35808841 http://dx.doi.org/10.1111/jth.15811 |
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author | Rittener‐Ruff, Luana Marchetti, Matteo Matthey‐Guirao, Elena Grandoni, Francesco Gomez, Francisco J. Alberio, Lorenzo |
author_facet | Rittener‐Ruff, Luana Marchetti, Matteo Matthey‐Guirao, Elena Grandoni, Francesco Gomez, Francisco J. Alberio, Lorenzo |
author_sort | Rittener‐Ruff, Luana |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-9796930 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97969302023-01-04 Combinations of rapid immunoassays for a speedy diagnosis of heparin‐induced thrombocytopenia Rittener‐Ruff, Luana Marchetti, Matteo Matthey‐Guirao, Elena Grandoni, Francesco Gomez, Francisco J. Alberio, Lorenzo J Thromb Haemost PLATELETS 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. John Wiley and Sons Inc. 2022-07-27 2022-10 /pmc/articles/PMC9796930/ /pubmed/35808841 http://dx.doi.org/10.1111/jth.15811 Text en © 2022 The Authors. Journal of Thrombosis and Haemostasis published by Wiley Periodicals LLC on behalf of International Society on Thrombosis and Haemostasis. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | PLATELETS Rittener‐Ruff, Luana Marchetti, Matteo Matthey‐Guirao, Elena Grandoni, Francesco Gomez, Francisco J. Alberio, Lorenzo Combinations of rapid immunoassays for a speedy diagnosis of heparin‐induced thrombocytopenia |
title | Combinations of rapid immunoassays for a speedy diagnosis of heparin‐induced thrombocytopenia |
title_full | Combinations of rapid immunoassays for a speedy diagnosis of heparin‐induced thrombocytopenia |
title_fullStr | Combinations of rapid immunoassays for a speedy diagnosis of heparin‐induced thrombocytopenia |
title_full_unstemmed | Combinations of rapid immunoassays for a speedy diagnosis of heparin‐induced thrombocytopenia |
title_short | Combinations of rapid immunoassays for a speedy diagnosis of heparin‐induced thrombocytopenia |
title_sort | combinations of rapid immunoassays for a speedy diagnosis of heparin‐induced thrombocytopenia |
topic | PLATELETS |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9796930/ https://www.ncbi.nlm.nih.gov/pubmed/35808841 http://dx.doi.org/10.1111/jth.15811 |
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