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Outcomes of catheter‐directed interventions in high‐risk pulmonary embolism‐a retrospective analysis
BACKGROUND: First‐line treatment of high‐risk pulmonary embolism with persistent hypotension and/or signs of shock is intravenous thrombolysis. However, if thrombolysis is contraindicated due to risk of serious bleeding, or if it yields insufficient effect, surgical thrombectomy or catheter‐directed...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7986106/ https://www.ncbi.nlm.nih.gov/pubmed/33245785 http://dx.doi.org/10.1111/aas.13753 |
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author | Einarsson, Freyr Sandström, Charlotte Svennerholm, Kristina Oras, Jonatan Rylander, Christian |
author_facet | Einarsson, Freyr Sandström, Charlotte Svennerholm, Kristina Oras, Jonatan Rylander, Christian |
author_sort | Einarsson, Freyr |
collection | PubMed |
description | BACKGROUND: First‐line treatment of high‐risk pulmonary embolism with persistent hypotension and/or signs of shock is intravenous thrombolysis. However, if thrombolysis is contraindicated due to risk of serious bleeding, or if it yields insufficient effect, surgical thrombectomy or catheter‐directed intervention (CDI) plus anticoagulation is recommended. The aim of this study was to assess the outcomes of the CDI modality introduced in a tertiary referral centre in 2013. METHODS: Retrospective comparison between patients treated with CDI plus anticoagulation (n = 22) and patients treated with anticoagulation only (n = 23) as used before the CDI technique was available. The main outcomes of interest were 90‐day survival and reduction of right to left ventricle diameter (RV/LV) ratio, using the Fischer's exact test and a mixed model, respectively, for statistical analysis. RESULTS: Ninety‐day survival was 59% after CDI and 61% after anticoagulation only; P = .903. The rate of RV/LV ratio reduction was 0.4 units higher per 24 hours in the CDI group (median 2.1 pre‐treatment), than in the anticoagulation only group (median 1.3 pre‐treatment); P = .007. CONCLUSION: In patients with high‐risk pulmonary embolism, 90‐day survival was similar after treatment with CDI plus anticoagulation compared to anticoagulation only. The mean reduction in RV/LV ratio was larger in the CDI group. Our results support the use of CDI in selected patients, respecting the limitations and potential side effects of each technical device used. |
format | Online Article Text |
id | pubmed-7986106 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-79861062021-03-25 Outcomes of catheter‐directed interventions in high‐risk pulmonary embolism‐a retrospective analysis Einarsson, Freyr Sandström, Charlotte Svennerholm, Kristina Oras, Jonatan Rylander, Christian Acta Anaesthesiol Scand Intensive Care and Physiology BACKGROUND: First‐line treatment of high‐risk pulmonary embolism with persistent hypotension and/or signs of shock is intravenous thrombolysis. However, if thrombolysis is contraindicated due to risk of serious bleeding, or if it yields insufficient effect, surgical thrombectomy or catheter‐directed intervention (CDI) plus anticoagulation is recommended. The aim of this study was to assess the outcomes of the CDI modality introduced in a tertiary referral centre in 2013. METHODS: Retrospective comparison between patients treated with CDI plus anticoagulation (n = 22) and patients treated with anticoagulation only (n = 23) as used before the CDI technique was available. The main outcomes of interest were 90‐day survival and reduction of right to left ventricle diameter (RV/LV) ratio, using the Fischer's exact test and a mixed model, respectively, for statistical analysis. RESULTS: Ninety‐day survival was 59% after CDI and 61% after anticoagulation only; P = .903. The rate of RV/LV ratio reduction was 0.4 units higher per 24 hours in the CDI group (median 2.1 pre‐treatment), than in the anticoagulation only group (median 1.3 pre‐treatment); P = .007. CONCLUSION: In patients with high‐risk pulmonary embolism, 90‐day survival was similar after treatment with CDI plus anticoagulation compared to anticoagulation only. The mean reduction in RV/LV ratio was larger in the CDI group. Our results support the use of CDI in selected patients, respecting the limitations and potential side effects of each technical device used. John Wiley and Sons Inc. 2020-12-25 2021-04 /pmc/articles/PMC7986106/ /pubmed/33245785 http://dx.doi.org/10.1111/aas.13753 Text en © 2020 The Authors. Acta Anaesthesiologica Scandinavica published by John Wiley & Sons Ltd on behalf of Acta Anaesthesiologica Scandinavica Foundation This is an open access article under the terms of the http://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 | Intensive Care and Physiology Einarsson, Freyr Sandström, Charlotte Svennerholm, Kristina Oras, Jonatan Rylander, Christian Outcomes of catheter‐directed interventions in high‐risk pulmonary embolism‐a retrospective analysis |
title | Outcomes of catheter‐directed interventions in high‐risk pulmonary embolism‐a retrospective analysis |
title_full | Outcomes of catheter‐directed interventions in high‐risk pulmonary embolism‐a retrospective analysis |
title_fullStr | Outcomes of catheter‐directed interventions in high‐risk pulmonary embolism‐a retrospective analysis |
title_full_unstemmed | Outcomes of catheter‐directed interventions in high‐risk pulmonary embolism‐a retrospective analysis |
title_short | Outcomes of catheter‐directed interventions in high‐risk pulmonary embolism‐a retrospective analysis |
title_sort | outcomes of catheter‐directed interventions in high‐risk pulmonary embolism‐a retrospective analysis |
topic | Intensive Care and Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7986106/ https://www.ncbi.nlm.nih.gov/pubmed/33245785 http://dx.doi.org/10.1111/aas.13753 |
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