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New hemodynamic criteria to separate classical orthostatic hypotension from vasovagal syncope
OBJECTIVE: To define and evaluate hemodynamic criteria to distinguish between classical orthostatic hypotension (cOH) and vasovagal syncope (VVS) in tilt table testing (TTT). METHODS: Inclusion criteria for VVS were a history of VVS and tilt‐induced syncope defined as a blood pressure (BP) decrease...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8351382/ https://www.ncbi.nlm.nih.gov/pubmed/34166574 http://dx.doi.org/10.1002/acn3.51412 |
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author | Ghariq, Maryam Kerkhof, Fabian I. Reijntjes, Robert H. Thijs, Roland D. van Dijk, J. Gert |
author_facet | Ghariq, Maryam Kerkhof, Fabian I. Reijntjes, Robert H. Thijs, Roland D. van Dijk, J. Gert |
author_sort | Ghariq, Maryam |
collection | PubMed |
description | OBJECTIVE: To define and evaluate hemodynamic criteria to distinguish between classical orthostatic hypotension (cOH) and vasovagal syncope (VVS) in tilt table testing (TTT). METHODS: Inclusion criteria for VVS were a history of VVS and tilt‐induced syncope defined as a blood pressure (BP) decrease and electroencephalographic changes during syncope with complaint recognition. Criteria for cOH were a history of cOH and a BP decrease meeting published criteria. Clinical diagnoses were established prior to TTT. We assessed (1) whether the decrease of systolic BP accelerated, “convex,” or decelerated, “concave”; (2) the time from head‐up tilt to when BP reached one‐half its maximal decrease; (3) the difference between baseline heart rate (HR) and HR at BP nadir. We calculated the diagnostic yield of optimized thresholds of these features and their combinations. RESULTS: We included 82 VVS cases (40% men, median age 44 years) and 65 cOH cases (66% men, median age 70 years). BP decrease was concave in cOH in 79% and convex in VVS in 94% (p < 0.001). The time to reach half the BP decrease was shorter in cOH (median 34 sec, interquartile range (IQR) 19–98 sec) than in VVS (median 1571 sec, IQR 1381–1775 sec, p < 0.001). Mean HR increased by 11 ± 11 bpm in cOH and decreased by 20 ± 19 bpm in VVS (p < 0.001). When all three features pointed to VVS, sensitivity for VVS was 82% and specificity was 100%. When all three pointed to cOH, sensitivity for cOH was 71% and specificity was 100%. INTERPRETATION: These new hemodynamic criteria reliably differentiate cOH from VVS. |
format | Online Article Text |
id | pubmed-8351382 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-83513822021-08-15 New hemodynamic criteria to separate classical orthostatic hypotension from vasovagal syncope Ghariq, Maryam Kerkhof, Fabian I. Reijntjes, Robert H. Thijs, Roland D. van Dijk, J. Gert Ann Clin Transl Neurol Research Articles OBJECTIVE: To define and evaluate hemodynamic criteria to distinguish between classical orthostatic hypotension (cOH) and vasovagal syncope (VVS) in tilt table testing (TTT). METHODS: Inclusion criteria for VVS were a history of VVS and tilt‐induced syncope defined as a blood pressure (BP) decrease and electroencephalographic changes during syncope with complaint recognition. Criteria for cOH were a history of cOH and a BP decrease meeting published criteria. Clinical diagnoses were established prior to TTT. We assessed (1) whether the decrease of systolic BP accelerated, “convex,” or decelerated, “concave”; (2) the time from head‐up tilt to when BP reached one‐half its maximal decrease; (3) the difference between baseline heart rate (HR) and HR at BP nadir. We calculated the diagnostic yield of optimized thresholds of these features and their combinations. RESULTS: We included 82 VVS cases (40% men, median age 44 years) and 65 cOH cases (66% men, median age 70 years). BP decrease was concave in cOH in 79% and convex in VVS in 94% (p < 0.001). The time to reach half the BP decrease was shorter in cOH (median 34 sec, interquartile range (IQR) 19–98 sec) than in VVS (median 1571 sec, IQR 1381–1775 sec, p < 0.001). Mean HR increased by 11 ± 11 bpm in cOH and decreased by 20 ± 19 bpm in VVS (p < 0.001). When all three features pointed to VVS, sensitivity for VVS was 82% and specificity was 100%. When all three pointed to cOH, sensitivity for cOH was 71% and specificity was 100%. INTERPRETATION: These new hemodynamic criteria reliably differentiate cOH from VVS. John Wiley and Sons Inc. 2021-06-24 /pmc/articles/PMC8351382/ /pubmed/34166574 http://dx.doi.org/10.1002/acn3.51412 Text en © 2021 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Ghariq, Maryam Kerkhof, Fabian I. Reijntjes, Robert H. Thijs, Roland D. van Dijk, J. Gert New hemodynamic criteria to separate classical orthostatic hypotension from vasovagal syncope |
title | New hemodynamic criteria to separate classical orthostatic hypotension from vasovagal syncope |
title_full | New hemodynamic criteria to separate classical orthostatic hypotension from vasovagal syncope |
title_fullStr | New hemodynamic criteria to separate classical orthostatic hypotension from vasovagal syncope |
title_full_unstemmed | New hemodynamic criteria to separate classical orthostatic hypotension from vasovagal syncope |
title_short | New hemodynamic criteria to separate classical orthostatic hypotension from vasovagal syncope |
title_sort | new hemodynamic criteria to separate classical orthostatic hypotension from vasovagal syncope |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8351382/ https://www.ncbi.nlm.nih.gov/pubmed/34166574 http://dx.doi.org/10.1002/acn3.51412 |
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