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Subarachnoid hemorrhage admissions retrospectively identified using a prediction model
OBJECTIVE: To create an accurate prediction model using variables collected in widely available health administrative data records to identify hospitalizations for primary subarachnoid hemorrhage (SAH). METHODS: A previously established complete cohort of consecutive primary SAH patients was combine...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5067543/ https://www.ncbi.nlm.nih.gov/pubmed/27629096 http://dx.doi.org/10.1212/WNL.0000000000003204 |
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author | English, Shane W. McIntyre, Lauralyn Fergusson, Dean Turgeon, Alexis dos Santos, Marlise P. Lum, Cheemun Chassé, Michaël Sinclair, John Forster, Alan van Walraven, Carl |
author_facet | English, Shane W. McIntyre, Lauralyn Fergusson, Dean Turgeon, Alexis dos Santos, Marlise P. Lum, Cheemun Chassé, Michaël Sinclair, John Forster, Alan van Walraven, Carl |
author_sort | English, Shane W. |
collection | PubMed |
description | OBJECTIVE: To create an accurate prediction model using variables collected in widely available health administrative data records to identify hospitalizations for primary subarachnoid hemorrhage (SAH). METHODS: A previously established complete cohort of consecutive primary SAH patients was combined with a random sample of control hospitalizations. Chi-square recursive partitioning was used to derive and internally validate a model to predict the probability that a patient had primary SAH (due to aneurysm or arteriovenous malformation) using health administrative data. RESULTS: A total of 10,322 hospitalizations with 631 having primary SAH (6.1%) were included in the study (5,122 derivation, 5,200 validation). In the validation patients, our recursive partitioning algorithm had a sensitivity of 96.5% (95% confidence interval [CI] 93.9–98.0), a specificity of 99.8% (95% CI 99.6–99.9), and a positive likelihood ratio of 483 (95% CI 254–879). In this population, patients meeting criteria for the algorithm had a probability of 45% of truly having primary SAH. CONCLUSIONS: Routinely collected health administrative data can be used to accurately identify hospitalized patients with a high probability of having a primary SAH. This algorithm may allow, upon validation, an easy and accurate method to create validated cohorts of primary SAH from either ruptured aneurysm or arteriovenous malformation. |
format | Online Article Text |
id | pubmed-5067543 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-50675432016-10-25 Subarachnoid hemorrhage admissions retrospectively identified using a prediction model English, Shane W. McIntyre, Lauralyn Fergusson, Dean Turgeon, Alexis dos Santos, Marlise P. Lum, Cheemun Chassé, Michaël Sinclair, John Forster, Alan van Walraven, Carl Neurology Article OBJECTIVE: To create an accurate prediction model using variables collected in widely available health administrative data records to identify hospitalizations for primary subarachnoid hemorrhage (SAH). METHODS: A previously established complete cohort of consecutive primary SAH patients was combined with a random sample of control hospitalizations. Chi-square recursive partitioning was used to derive and internally validate a model to predict the probability that a patient had primary SAH (due to aneurysm or arteriovenous malformation) using health administrative data. RESULTS: A total of 10,322 hospitalizations with 631 having primary SAH (6.1%) were included in the study (5,122 derivation, 5,200 validation). In the validation patients, our recursive partitioning algorithm had a sensitivity of 96.5% (95% confidence interval [CI] 93.9–98.0), a specificity of 99.8% (95% CI 99.6–99.9), and a positive likelihood ratio of 483 (95% CI 254–879). In this population, patients meeting criteria for the algorithm had a probability of 45% of truly having primary SAH. CONCLUSIONS: Routinely collected health administrative data can be used to accurately identify hospitalized patients with a high probability of having a primary SAH. This algorithm may allow, upon validation, an easy and accurate method to create validated cohorts of primary SAH from either ruptured aneurysm or arteriovenous malformation. Lippincott Williams & Wilkins 2016-10-11 /pmc/articles/PMC5067543/ /pubmed/27629096 http://dx.doi.org/10.1212/WNL.0000000000003204 Text en © 2016 American Academy of Neurology https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially. |
spellingShingle | Article English, Shane W. McIntyre, Lauralyn Fergusson, Dean Turgeon, Alexis dos Santos, Marlise P. Lum, Cheemun Chassé, Michaël Sinclair, John Forster, Alan van Walraven, Carl Subarachnoid hemorrhage admissions retrospectively identified using a prediction model |
title | Subarachnoid hemorrhage admissions retrospectively identified using a prediction model |
title_full | Subarachnoid hemorrhage admissions retrospectively identified using a prediction model |
title_fullStr | Subarachnoid hemorrhage admissions retrospectively identified using a prediction model |
title_full_unstemmed | Subarachnoid hemorrhage admissions retrospectively identified using a prediction model |
title_short | Subarachnoid hemorrhage admissions retrospectively identified using a prediction model |
title_sort | subarachnoid hemorrhage admissions retrospectively identified using a prediction model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5067543/ https://www.ncbi.nlm.nih.gov/pubmed/27629096 http://dx.doi.org/10.1212/WNL.0000000000003204 |
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