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Informing patients that they are at high risk for serious complications of viral infection increases vaccination rates
For many vaccine-preventable diseases like influenza, vaccination rates are lower than optimal to achieve community protection. Those at high risk for infection and serious complications are especially advised to be vaccinated to protect themselves. Using influenza as a model, we studied one method...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7924279/ https://www.ncbi.nlm.nih.gov/pubmed/33655258 http://dx.doi.org/10.1101/2021.02.20.21252015 |
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author | Shermohammed, Maheen Goren, Amir Lanyado, Alon Yesharim, Rachel Wolk, Donna M. Doyle, Joseph Meyer, Michelle N. Chabris, Christopher F. |
author_facet | Shermohammed, Maheen Goren, Amir Lanyado, Alon Yesharim, Rachel Wolk, Donna M. Doyle, Joseph Meyer, Michelle N. Chabris, Christopher F. |
author_sort | Shermohammed, Maheen |
collection | PubMed |
description | For many vaccine-preventable diseases like influenza, vaccination rates are lower than optimal to achieve community protection. Those at high risk for infection and serious complications are especially advised to be vaccinated to protect themselves. Using influenza as a model, we studied one method of increasing vaccine uptake: informing high-risk patients, identified by a machine learning model, about their risk status. Patients (N=39,717) were evenly randomized to (1) a control condition (exposure only to standard direct mail or patient portal vaccine promotion efforts) or to be told via direct mail, patient portal, and/or SMS that they were (2) at high risk for influenza and its complications if not vaccinated; (3) at high risk according to a review of their medical records; or (4) at high risk according to a computer algorithm analysis of their medical records. Patients in the three treatment conditions were 5.7% more likely to get vaccinated during the 112 days post-intervention (p < .001), and did so 1.4 days earlier (p < .001), on average, than those in the control group. There were no significant differences among risk messages, suggesting that patients are neither especially averse to nor uniquely appreciative of learning their records had been reviewed or that computer algorithms were involved. Similar approaches should be considered for COVID-19 vaccination campaigns. |
format | Online Article Text |
id | pubmed-7924279 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-79242792021-03-03 Informing patients that they are at high risk for serious complications of viral infection increases vaccination rates Shermohammed, Maheen Goren, Amir Lanyado, Alon Yesharim, Rachel Wolk, Donna M. Doyle, Joseph Meyer, Michelle N. Chabris, Christopher F. medRxiv Article For many vaccine-preventable diseases like influenza, vaccination rates are lower than optimal to achieve community protection. Those at high risk for infection and serious complications are especially advised to be vaccinated to protect themselves. Using influenza as a model, we studied one method of increasing vaccine uptake: informing high-risk patients, identified by a machine learning model, about their risk status. Patients (N=39,717) were evenly randomized to (1) a control condition (exposure only to standard direct mail or patient portal vaccine promotion efforts) or to be told via direct mail, patient portal, and/or SMS that they were (2) at high risk for influenza and its complications if not vaccinated; (3) at high risk according to a review of their medical records; or (4) at high risk according to a computer algorithm analysis of their medical records. Patients in the three treatment conditions were 5.7% more likely to get vaccinated during the 112 days post-intervention (p < .001), and did so 1.4 days earlier (p < .001), on average, than those in the control group. There were no significant differences among risk messages, suggesting that patients are neither especially averse to nor uniquely appreciative of learning their records had been reviewed or that computer algorithms were involved. Similar approaches should be considered for COVID-19 vaccination campaigns. Cold Spring Harbor Laboratory 2021-02-23 /pmc/articles/PMC7924279/ /pubmed/33655258 http://dx.doi.org/10.1101/2021.02.20.21252015 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Shermohammed, Maheen Goren, Amir Lanyado, Alon Yesharim, Rachel Wolk, Donna M. Doyle, Joseph Meyer, Michelle N. Chabris, Christopher F. Informing patients that they are at high risk for serious complications of viral infection increases vaccination rates |
title | Informing patients that they are at high risk for serious complications of viral infection increases vaccination rates |
title_full | Informing patients that they are at high risk for serious complications of viral infection increases vaccination rates |
title_fullStr | Informing patients that they are at high risk for serious complications of viral infection increases vaccination rates |
title_full_unstemmed | Informing patients that they are at high risk for serious complications of viral infection increases vaccination rates |
title_short | Informing patients that they are at high risk for serious complications of viral infection increases vaccination rates |
title_sort | informing patients that they are at high risk for serious complications of viral infection increases vaccination rates |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7924279/ https://www.ncbi.nlm.nih.gov/pubmed/33655258 http://dx.doi.org/10.1101/2021.02.20.21252015 |
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