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The Impact of a Nurse‐Led Syncope Clinic: Experience from a single UK tertiary center
BACKGROUND: Syncope is a leading cause of hospital admission and is associated with significant morbidity and mortality. Our Syncope Clinic commenced in 2014 and we sought to evaluate its impact on outcomes (1‐yr mortality and syncope re‐hospitalization) in patients discharged following syncope admi...
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/PMC7532277/ https://www.ncbi.nlm.nih.gov/pubmed/33024463 http://dx.doi.org/10.1002/joa3.12420 |
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author | Adlan, Ahmed M. Eftekhari, Helen Paul, Geeta Hayat, Sajad Osman, Faizel |
author_facet | Adlan, Ahmed M. Eftekhari, Helen Paul, Geeta Hayat, Sajad Osman, Faizel |
author_sort | Adlan, Ahmed M. |
collection | PubMed |
description | BACKGROUND: Syncope is a leading cause of hospital admission and is associated with significant morbidity and mortality. Our Syncope Clinic commenced in 2014 and we sought to evaluate its impact on outcomes (1‐yr mortality and syncope re‐hospitalization) in patients discharged following syncope admission. METHODS: A single‐center study of all consecutive patients discharged with syncope (ICD‐10 R55) between April 2012 and 2017. Patient demographics, comorbidities, hospital stay, syncope re‐hospitalization, and mortality at one‐year were collected. Those subsequently referred and seen in Syncope Clinic were compared with those who were not and predictors of poor outcome were evaluated. RESULTS: In total 2950 patients were discharged from hospital with syncope (median age: 73years, 51% male) with 1220 (41%) discharged same‐day; after commencement of Syncope Clinic 231were subsequently reviewed here. Overall mortality was 11%, which was lower in the Syncope Clinic group (3% vs 12%, P < .001). Temporal analysis revealed reduced re‐hospitalization following commencement of Syncope Clinic (2% vs 6%, P = .027). Independent predictors of mortality were increasing age (HR 1.03, 95% CI 1.03‐1.04), AF (HR 1.6, 95% CI 1.2‐2.1), HF (HR 2.2, 95% CI 1.6‐3.0), COPD (HR 1.9, 95% CI 1.4‐2.7), and CHADS(2) score ≥ 1 (HR 1.45, 95% CI 1,12‐1.87). Syncope Clinic attendance was associated with reduced mortality (HR 0.3, 95% CI 0.1‐0.6). CONCLUSIONS: Syncope patients discharged from hospital had reduced 1yr mortality if seen in subsequent Syncope Clinic. Independent predictors of mortality were COPD, HF, AF, and CHADS(2 )≥1. Prospective randomized trials of Syncope Clinics are warranted. |
format | Online Article Text |
id | pubmed-7532277 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75322772020-10-05 The Impact of a Nurse‐Led Syncope Clinic: Experience from a single UK tertiary center Adlan, Ahmed M. Eftekhari, Helen Paul, Geeta Hayat, Sajad Osman, Faizel J Arrhythm Original Articles BACKGROUND: Syncope is a leading cause of hospital admission and is associated with significant morbidity and mortality. Our Syncope Clinic commenced in 2014 and we sought to evaluate its impact on outcomes (1‐yr mortality and syncope re‐hospitalization) in patients discharged following syncope admission. METHODS: A single‐center study of all consecutive patients discharged with syncope (ICD‐10 R55) between April 2012 and 2017. Patient demographics, comorbidities, hospital stay, syncope re‐hospitalization, and mortality at one‐year were collected. Those subsequently referred and seen in Syncope Clinic were compared with those who were not and predictors of poor outcome were evaluated. RESULTS: In total 2950 patients were discharged from hospital with syncope (median age: 73years, 51% male) with 1220 (41%) discharged same‐day; after commencement of Syncope Clinic 231were subsequently reviewed here. Overall mortality was 11%, which was lower in the Syncope Clinic group (3% vs 12%, P < .001). Temporal analysis revealed reduced re‐hospitalization following commencement of Syncope Clinic (2% vs 6%, P = .027). Independent predictors of mortality were increasing age (HR 1.03, 95% CI 1.03‐1.04), AF (HR 1.6, 95% CI 1.2‐2.1), HF (HR 2.2, 95% CI 1.6‐3.0), COPD (HR 1.9, 95% CI 1.4‐2.7), and CHADS(2) score ≥ 1 (HR 1.45, 95% CI 1,12‐1.87). Syncope Clinic attendance was associated with reduced mortality (HR 0.3, 95% CI 0.1‐0.6). CONCLUSIONS: Syncope patients discharged from hospital had reduced 1yr mortality if seen in subsequent Syncope Clinic. Independent predictors of mortality were COPD, HF, AF, and CHADS(2 )≥1. Prospective randomized trials of Syncope Clinics are warranted. John Wiley and Sons Inc. 2020-08-31 /pmc/articles/PMC7532277/ /pubmed/33024463 http://dx.doi.org/10.1002/joa3.12420 Text en © 2020 The Authors. Journal of Arrhythmia published by John Wiley & Sons Australia, Ltd on behalf of Japanese Heart Rhythm Society 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 | Original Articles Adlan, Ahmed M. Eftekhari, Helen Paul, Geeta Hayat, Sajad Osman, Faizel The Impact of a Nurse‐Led Syncope Clinic: Experience from a single UK tertiary center |
title | The Impact of a Nurse‐Led Syncope Clinic: Experience from a single UK tertiary center |
title_full | The Impact of a Nurse‐Led Syncope Clinic: Experience from a single UK tertiary center |
title_fullStr | The Impact of a Nurse‐Led Syncope Clinic: Experience from a single UK tertiary center |
title_full_unstemmed | The Impact of a Nurse‐Led Syncope Clinic: Experience from a single UK tertiary center |
title_short | The Impact of a Nurse‐Led Syncope Clinic: Experience from a single UK tertiary center |
title_sort | impact of a nurse‐led syncope clinic: experience from a single uk tertiary center |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7532277/ https://www.ncbi.nlm.nih.gov/pubmed/33024463 http://dx.doi.org/10.1002/joa3.12420 |
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