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Thirty-day readmissions due to Venous thromboembolism in patients discharged with syncope

A recent study found that approximately 1 in every 6 patients hospitalized for the 1st episode of syncope had an underlying pulmonary embolism (PE). As current guidelines do not strongly emphasize evaluation for PE in the workup of syncope, we hypothesize that there might be a higher rate of 30-day...

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Autores principales: Siddappa Malleshappa, Sudeep K., Valecha, Gautam K., Mehta, Tapan, Patel, Smit, Giri, Smith, Smith, Roy E., Parikh, Rahul A., Mehta, Kathan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7153877/
https://www.ncbi.nlm.nih.gov/pubmed/32282801
http://dx.doi.org/10.1371/journal.pone.0230859
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author Siddappa Malleshappa, Sudeep K.
Valecha, Gautam K.
Mehta, Tapan
Patel, Smit
Giri, Smith
Smith, Roy E.
Parikh, Rahul A.
Mehta, Kathan
author_facet Siddappa Malleshappa, Sudeep K.
Valecha, Gautam K.
Mehta, Tapan
Patel, Smit
Giri, Smith
Smith, Roy E.
Parikh, Rahul A.
Mehta, Kathan
author_sort Siddappa Malleshappa, Sudeep K.
collection PubMed
description A recent study found that approximately 1 in every 6 patients hospitalized for the 1st episode of syncope had an underlying pulmonary embolism (PE). As current guidelines do not strongly emphasize evaluation for PE in the workup of syncope, we hypothesize that there might be a higher rate of 30-day readmission due to untreated venous thromboembolism (VTE). The objective of this study is to measure the 30-day readmission rate due to VTE and identify predictors of 30-day readmission with VTE among syncope patients. We identified patients admitted with syncope with ICD9 diagnoses code 780.2 in the Nationwide Readmission Database (NRD-2013), Healthcare Cost and Utilization Project (HCUP). The 30-day readmission rate was calculated using methods described by HCUP. Logistic-regression was used to identify predictors of 30-day readmission with VTE. Discharge weights provided by HCUP were used to generate national estimates. In 2013, NRD included 207,339 eligible patients admitted with syncope. The prevalence rates of PE and DVT were 1.1% and 1.4%, respectively. At least one syncope associated condition was present in 60.9% of the patients. Among the patients who were not diagnosed with VTE during index admission for syncope (N = 188,015), 30-day readmission rate with VTE was 0.5% (0.2% with PE and 0.4% with DVT). In conclusion, low prevalence of VTE in patients with syncope and extremely low 30-day readmission rate with VTE argues against missed diagnoses of VTE in index admission for syncope. These results warrant further studies to determine clinical impact of work up for PE in syncope patients without risk factors.
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spelling pubmed-71538772020-04-16 Thirty-day readmissions due to Venous thromboembolism in patients discharged with syncope Siddappa Malleshappa, Sudeep K. Valecha, Gautam K. Mehta, Tapan Patel, Smit Giri, Smith Smith, Roy E. Parikh, Rahul A. Mehta, Kathan PLoS One Research Article A recent study found that approximately 1 in every 6 patients hospitalized for the 1st episode of syncope had an underlying pulmonary embolism (PE). As current guidelines do not strongly emphasize evaluation for PE in the workup of syncope, we hypothesize that there might be a higher rate of 30-day readmission due to untreated venous thromboembolism (VTE). The objective of this study is to measure the 30-day readmission rate due to VTE and identify predictors of 30-day readmission with VTE among syncope patients. We identified patients admitted with syncope with ICD9 diagnoses code 780.2 in the Nationwide Readmission Database (NRD-2013), Healthcare Cost and Utilization Project (HCUP). The 30-day readmission rate was calculated using methods described by HCUP. Logistic-regression was used to identify predictors of 30-day readmission with VTE. Discharge weights provided by HCUP were used to generate national estimates. In 2013, NRD included 207,339 eligible patients admitted with syncope. The prevalence rates of PE and DVT were 1.1% and 1.4%, respectively. At least one syncope associated condition was present in 60.9% of the patients. Among the patients who were not diagnosed with VTE during index admission for syncope (N = 188,015), 30-day readmission rate with VTE was 0.5% (0.2% with PE and 0.4% with DVT). In conclusion, low prevalence of VTE in patients with syncope and extremely low 30-day readmission rate with VTE argues against missed diagnoses of VTE in index admission for syncope. These results warrant further studies to determine clinical impact of work up for PE in syncope patients without risk factors. Public Library of Science 2020-04-13 /pmc/articles/PMC7153877/ /pubmed/32282801 http://dx.doi.org/10.1371/journal.pone.0230859 Text en © 2020 Siddappa Malleshappa et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Siddappa Malleshappa, Sudeep K.
Valecha, Gautam K.
Mehta, Tapan
Patel, Smit
Giri, Smith
Smith, Roy E.
Parikh, Rahul A.
Mehta, Kathan
Thirty-day readmissions due to Venous thromboembolism in patients discharged with syncope
title Thirty-day readmissions due to Venous thromboembolism in patients discharged with syncope
title_full Thirty-day readmissions due to Venous thromboembolism in patients discharged with syncope
title_fullStr Thirty-day readmissions due to Venous thromboembolism in patients discharged with syncope
title_full_unstemmed Thirty-day readmissions due to Venous thromboembolism in patients discharged with syncope
title_short Thirty-day readmissions due to Venous thromboembolism in patients discharged with syncope
title_sort thirty-day readmissions due to venous thromboembolism in patients discharged with syncope
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7153877/
https://www.ncbi.nlm.nih.gov/pubmed/32282801
http://dx.doi.org/10.1371/journal.pone.0230859
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