Secondary Analysis of Electronic Health Records

Diagnostic and therapeutic technologies continue to evolve rapidly, and both individual practitioners and clinical teams face increasingly complex decisions. Unfortunately, the current state of medical knowledge does not provide the guid- ance to make the majority of clinical decisions on the basis...

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Autores:
Tipo de recurso:
Book
Fecha de publicación:
2016
Institución:
Universidad de Bogotá Jorge Tadeo Lozano
Repositorio:
Expeditio: repositorio UTadeo
Idioma:
eng
OAI Identifier:
oai:expeditiorepositorio.utadeo.edu.co:20.500.12010/18740
Acceso en línea:
https://directory.doabooks.org/handle/20.500.12854/35747
http://hdl.handle.net/20.500.12010/18740
Palabra clave:
Health Informatics
Data Mining and Knowledge Discovery
Statistics for Life Sciences
Historias clínicas - Control de acceso
Ética médica
Secreto médico
Rights
License
Abierto (Texto Completo)
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dc.title.spa.fl_str_mv Secondary Analysis of Electronic Health Records
title Secondary Analysis of Electronic Health Records
spellingShingle Secondary Analysis of Electronic Health Records
Health Informatics
Data Mining and Knowledge Discovery
Statistics for Life Sciences
Historias clínicas - Control de acceso
Ética médica
Secreto médico
title_short Secondary Analysis of Electronic Health Records
title_full Secondary Analysis of Electronic Health Records
title_fullStr Secondary Analysis of Electronic Health Records
title_full_unstemmed Secondary Analysis of Electronic Health Records
title_sort Secondary Analysis of Electronic Health Records
dc.subject.spa.fl_str_mv Health Informatics
Data Mining and Knowledge Discovery
Statistics for Life Sciences
topic Health Informatics
Data Mining and Knowledge Discovery
Statistics for Life Sciences
Historias clínicas - Control de acceso
Ética médica
Secreto médico
dc.subject.lemb.spa.fl_str_mv Historias clínicas - Control de acceso
Ética médica
Secreto médico
description Diagnostic and therapeutic technologies continue to evolve rapidly, and both individual practitioners and clinical teams face increasingly complex decisions. Unfortunately, the current state of medical knowledge does not provide the guid- ance to make the majority of clinical decisions on the basis of evidence. According to the 2012 Institute of Medicine Committee Report, only 10–20 % of clinical decisions are evidence based. The problem even extends to the creation of clinical practice guidelines (CPGs). Nearly 50 % of recommendations made in specialty society guidelines rely on expert opinion rather than experimental data. Furthermore, the creation process of CPGs is “marred by weak methods and financial conflicts of interest,” rendering current CPGs potentially less trustworthy. The present research infrastructure is inefficient and frequently produces unre- liable results that cannot be replicated. Even randomized controlled trials (RCTs), the traditional gold standards of the research reliability hierarchy, are not without limitations. They can be costly, labor-intensive, slow, and can return results that are seldom generalizable to every patient population. It is impossible for a tightly controlled RCT to capture the full, interactive, and contextual details of the clinical issues that arise in real clinics and inpatient units. Furthermore, many pertinent but unresolved clinical and medical systems issues do not seem to have attracted the interest of the research enterprise, which has come to focus instead on cellular and molecular investigations and single-agent (e.g., a drug or device) effects. For clinicians, the end result is a “data desert” when it comes to making decisions. Electronic health record (EHR) data are frequently digitally archived and can subsequently be extracted and analyzed. Between 2011 and 2019, the prevalence of EHRs is expected to grow from 34 to 90 % among office-based practices, and the majority of hospitals have replaced or are in the process of replacing paper systems with comprehensive, enterprise EHRs. The power of scale intrinsic to this digital transformation opens the door to a massive amount of currently untapped infor- mation. The data, if properly analyzed and meaningfully interpreted, could vastly improve our conception and development of best practices.
publishDate 2016
dc.date.created.none.fl_str_mv 2016
dc.date.accessioned.none.fl_str_mv 2021-04-15T18:54:37Z
dc.date.available.none.fl_str_mv 2021-04-15T18:54:37Z
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dc.identifier.isbn.none.fl_str_mv 9784431551119
dc.identifier.other.none.fl_str_mv https://directory.doabooks.org/handle/20.500.12854/35747
dc.identifier.uri.none.fl_str_mv http://hdl.handle.net/20.500.12010/18740
dc.identifier.doi.none.fl_str_mv 10.1007/978-3-319-43742-2
identifier_str_mv 9784431551119
10.1007/978-3-319-43742-2
url https://directory.doabooks.org/handle/20.500.12854/35747
http://hdl.handle.net/20.500.12010/18740
dc.language.iso.spa.fl_str_mv eng
language eng
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rights_invalid_str_mv Abierto (Texto Completo)
https://creativecommons.org/licenses/by-nc/4.0/
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dc.format.extent.spa.fl_str_mv 427 páginas
dc.format.mimetype.spa.fl_str_mv application/pdf
dc.publisher.spa.fl_str_mv Springer Nature
institution Universidad de Bogotá Jorge Tadeo Lozano
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spelling 2021-04-15T18:54:37Z2021-04-15T18:54:37Z20169784431551119https://directory.doabooks.org/handle/20.500.12854/35747http://hdl.handle.net/20.500.12010/1874010.1007/978-3-319-43742-2Diagnostic and therapeutic technologies continue to evolve rapidly, and both individual practitioners and clinical teams face increasingly complex decisions. Unfortunately, the current state of medical knowledge does not provide the guid- ance to make the majority of clinical decisions on the basis of evidence. According to the 2012 Institute of Medicine Committee Report, only 10–20 % of clinical decisions are evidence based. The problem even extends to the creation of clinical practice guidelines (CPGs). Nearly 50 % of recommendations made in specialty society guidelines rely on expert opinion rather than experimental data. Furthermore, the creation process of CPGs is “marred by weak methods and financial conflicts of interest,” rendering current CPGs potentially less trustworthy. The present research infrastructure is inefficient and frequently produces unre- liable results that cannot be replicated. Even randomized controlled trials (RCTs), the traditional gold standards of the research reliability hierarchy, are not without limitations. They can be costly, labor-intensive, slow, and can return results that are seldom generalizable to every patient population. It is impossible for a tightly controlled RCT to capture the full, interactive, and contextual details of the clinical issues that arise in real clinics and inpatient units. Furthermore, many pertinent but unresolved clinical and medical systems issues do not seem to have attracted the interest of the research enterprise, which has come to focus instead on cellular and molecular investigations and single-agent (e.g., a drug or device) effects. For clinicians, the end result is a “data desert” when it comes to making decisions. Electronic health record (EHR) data are frequently digitally archived and can subsequently be extracted and analyzed. Between 2011 and 2019, the prevalence of EHRs is expected to grow from 34 to 90 % among office-based practices, and the majority of hospitals have replaced or are in the process of replacing paper systems with comprehensive, enterprise EHRs. The power of scale intrinsic to this digital transformation opens the door to a massive amount of currently untapped infor- mation. 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