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Heparin ‘flush’ induced thrombocytopenia triggered by total hip replacement: a case report
BACKGROUND: Heparin-induced thrombocytopenia (HIT) typically responds to heparin termination. Some types of HIT can persist after heparin discontinuation. CASE SUMMARY: A 95-year-old woman was referred to the cardiology from orthopaedics because of acute limb ischaemia (ALI) 1 day after surgery of a...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7180709/ https://www.ncbi.nlm.nih.gov/pubmed/32352075 http://dx.doi.org/10.1093/ehjcr/ytaa036 |
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author | Yoshida, Ruka Tanaka, Akihito Yoshioka, Naoki Yokote, Jun |
author_facet | Yoshida, Ruka Tanaka, Akihito Yoshioka, Naoki Yokote, Jun |
author_sort | Yoshida, Ruka |
collection | PubMed |
description | BACKGROUND: Heparin-induced thrombocytopenia (HIT) typically responds to heparin termination. Some types of HIT can persist after heparin discontinuation. CASE SUMMARY: A 95-year-old woman was referred to the cardiology from orthopaedics because of acute limb ischaemia (ALI) 1 day after surgery of a femoral neck fracture. Despite thrombectomy, ALI relapsed the next day. She had been treated with intravenous antibiotics with a diagnosis of aspiration pneumonia for 1 week until 3 days before surgery, together with heparin flush twice a day. Of note, no intra-/post-operative heparin was administered, no cell salvage device, central venous, nor arterial catheters were used before development of ALI. The patient and her family refused reattempting invasive therapies; consequently, the patient continued to worsen and died on post-operative day 3. Diagnosis of autoimmune HIT, which was prompted by surgery without re-exposure to heparin, was confirmed posthumously. DISCUSSION: This case emphasizes the significance of suspecting autoimmune HIT in any patient presenting with thrombosis, even if the heparin exposure dates back more than a few days or even without heparin exposure. |
format | Online Article Text |
id | pubmed-7180709 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-71807092020-04-29 Heparin ‘flush’ induced thrombocytopenia triggered by total hip replacement: a case report Yoshida, Ruka Tanaka, Akihito Yoshioka, Naoki Yokote, Jun Eur Heart J Case Rep Case Report BACKGROUND: Heparin-induced thrombocytopenia (HIT) typically responds to heparin termination. Some types of HIT can persist after heparin discontinuation. CASE SUMMARY: A 95-year-old woman was referred to the cardiology from orthopaedics because of acute limb ischaemia (ALI) 1 day after surgery of a femoral neck fracture. Despite thrombectomy, ALI relapsed the next day. She had been treated with intravenous antibiotics with a diagnosis of aspiration pneumonia for 1 week until 3 days before surgery, together with heparin flush twice a day. Of note, no intra-/post-operative heparin was administered, no cell salvage device, central venous, nor arterial catheters were used before development of ALI. The patient and her family refused reattempting invasive therapies; consequently, the patient continued to worsen and died on post-operative day 3. Diagnosis of autoimmune HIT, which was prompted by surgery without re-exposure to heparin, was confirmed posthumously. DISCUSSION: This case emphasizes the significance of suspecting autoimmune HIT in any patient presenting with thrombosis, even if the heparin exposure dates back more than a few days or even without heparin exposure. Oxford University Press 2020-02-27 /pmc/articles/PMC7180709/ /pubmed/32352075 http://dx.doi.org/10.1093/ehjcr/ytaa036 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the European Society of Cardiology. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Case Report Yoshida, Ruka Tanaka, Akihito Yoshioka, Naoki Yokote, Jun Heparin ‘flush’ induced thrombocytopenia triggered by total hip replacement: a case report |
title | Heparin ‘flush’ induced thrombocytopenia triggered by total hip replacement: a case report |
title_full | Heparin ‘flush’ induced thrombocytopenia triggered by total hip replacement: a case report |
title_fullStr | Heparin ‘flush’ induced thrombocytopenia triggered by total hip replacement: a case report |
title_full_unstemmed | Heparin ‘flush’ induced thrombocytopenia triggered by total hip replacement: a case report |
title_short | Heparin ‘flush’ induced thrombocytopenia triggered by total hip replacement: a case report |
title_sort | heparin ‘flush’ induced thrombocytopenia triggered by total hip replacement: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7180709/ https://www.ncbi.nlm.nih.gov/pubmed/32352075 http://dx.doi.org/10.1093/ehjcr/ytaa036 |
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