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Evaluation of the “hemoptysis” item in clinical decision rules for the diagnosis of pulmonary embolism in the emergency department
BACKGROUND: Hemoptysis is not common in pulmonary embolism (PE) and lacks specificity for its diagnosis. However, this item is present in different validated scores that estimate the clinical probability of PE. The relevance of this item in clinical decision rules (CDRs) is not clearly established....
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/PMC9804711/ https://www.ncbi.nlm.nih.gov/pubmed/35975482 http://dx.doi.org/10.1111/acem.14574 |
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author | Bannelier, Héloïse Gorlicki, Judith Penaloza, Andrea Douillet, Delphine Roy, Pierre‐Marie Freund, Yonathan Roussel, Melanie |
author_facet | Bannelier, Héloïse Gorlicki, Judith Penaloza, Andrea Douillet, Delphine Roy, Pierre‐Marie Freund, Yonathan Roussel, Melanie |
author_sort | Bannelier, Héloïse |
collection | PubMed |
description | BACKGROUND: Hemoptysis is not common in pulmonary embolism (PE) and lacks specificity for its diagnosis. However, this item is present in different validated scores that estimate the clinical probability of PE. The relevance of this item in clinical decision rules (CDRs) is not clearly established. OBJECTIVE: The aim of this study was to evaluate the impact of removing the “hemoptysis” item from the PERC, YEARS, and PEGeD CDR in patients with low clinical probability of PE. DESIGN: This was a post hoc analysis of two European prospective cohorts, which included 2968 patients presenting to the ED with a low clinical probability of PE (PROPER and PERCEPIC) and a 3‐month follow‐up. The primary endpoint was the false‐negative rate of a CDR score without the hemoptysis item. Secondary endpoints included the potential reduction of chest imaging if the item hemoptysis was to be removed and risk stratification of the Geneva and Wells scores without the hemoptysis item. RESULTS: Of 2968 patients included (mean ± SD age 46 ± 18 years, 53% female), 87 patients (3%) had a PE diagnosed at 3 months. A total of 2908 were followed‐up at 3 months and analyzed. Using the PERC rule with and without the hemoptysis item, there were 13 and 14 missed cases of PE, respectively (failure rate 0.45% [95% CI 0.25%–0.78%] and 0.48% [95% CI 0.27%–0.82%]). Using the YEARS strategy, there were 11 missed PE cases with or without the hemoptysis item (false‐negative rate 0.57% [95% CI 0.30%–1.05%]). With the PERC and YEARS rule, removing the hemoptysis item would have led to a 1% reduction in chest imaging. The PEGeD strategy was not modified by the removal of the hemoptysis item. CONCLUSIONS: The hemoptysis item could be safely removed from the PERC, YEARS, and PEGeD CDRs. However, there was no subsequent clinically relevant reduction of chest imaging. |
format | Online Article Text |
id | pubmed-9804711 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98047112023-01-06 Evaluation of the “hemoptysis” item in clinical decision rules for the diagnosis of pulmonary embolism in the emergency department Bannelier, Héloïse Gorlicki, Judith Penaloza, Andrea Douillet, Delphine Roy, Pierre‐Marie Freund, Yonathan Roussel, Melanie Acad Emerg Med Original Contributions BACKGROUND: Hemoptysis is not common in pulmonary embolism (PE) and lacks specificity for its diagnosis. However, this item is present in different validated scores that estimate the clinical probability of PE. The relevance of this item in clinical decision rules (CDRs) is not clearly established. OBJECTIVE: The aim of this study was to evaluate the impact of removing the “hemoptysis” item from the PERC, YEARS, and PEGeD CDR in patients with low clinical probability of PE. DESIGN: This was a post hoc analysis of two European prospective cohorts, which included 2968 patients presenting to the ED with a low clinical probability of PE (PROPER and PERCEPIC) and a 3‐month follow‐up. The primary endpoint was the false‐negative rate of a CDR score without the hemoptysis item. Secondary endpoints included the potential reduction of chest imaging if the item hemoptysis was to be removed and risk stratification of the Geneva and Wells scores without the hemoptysis item. RESULTS: Of 2968 patients included (mean ± SD age 46 ± 18 years, 53% female), 87 patients (3%) had a PE diagnosed at 3 months. A total of 2908 were followed‐up at 3 months and analyzed. Using the PERC rule with and without the hemoptysis item, there were 13 and 14 missed cases of PE, respectively (failure rate 0.45% [95% CI 0.25%–0.78%] and 0.48% [95% CI 0.27%–0.82%]). Using the YEARS strategy, there were 11 missed PE cases with or without the hemoptysis item (false‐negative rate 0.57% [95% CI 0.30%–1.05%]). With the PERC and YEARS rule, removing the hemoptysis item would have led to a 1% reduction in chest imaging. The PEGeD strategy was not modified by the removal of the hemoptysis item. CONCLUSIONS: The hemoptysis item could be safely removed from the PERC, YEARS, and PEGeD CDRs. However, there was no subsequent clinically relevant reduction of chest imaging. John Wiley and Sons Inc. 2022-08-17 2022-10 /pmc/articles/PMC9804711/ /pubmed/35975482 http://dx.doi.org/10.1111/acem.14574 Text en © 2022 The Authors. Academic Emergency Medicine published by Wiley Periodicals LLC on behalf of Society for Academic Emergency Medicine. 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 | Original Contributions Bannelier, Héloïse Gorlicki, Judith Penaloza, Andrea Douillet, Delphine Roy, Pierre‐Marie Freund, Yonathan Roussel, Melanie Evaluation of the “hemoptysis” item in clinical decision rules for the diagnosis of pulmonary embolism in the emergency department |
title | Evaluation of the “hemoptysis” item in clinical decision rules for the diagnosis of pulmonary embolism in the emergency department |
title_full | Evaluation of the “hemoptysis” item in clinical decision rules for the diagnosis of pulmonary embolism in the emergency department |
title_fullStr | Evaluation of the “hemoptysis” item in clinical decision rules for the diagnosis of pulmonary embolism in the emergency department |
title_full_unstemmed | Evaluation of the “hemoptysis” item in clinical decision rules for the diagnosis of pulmonary embolism in the emergency department |
title_short | Evaluation of the “hemoptysis” item in clinical decision rules for the diagnosis of pulmonary embolism in the emergency department |
title_sort | evaluation of the “hemoptysis” item in clinical decision rules for the diagnosis of pulmonary embolism in the emergency department |
topic | Original Contributions |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9804711/ https://www.ncbi.nlm.nih.gov/pubmed/35975482 http://dx.doi.org/10.1111/acem.14574 |
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