Personalizing prenatal care using family health history

Identifying a panel of conditions for a novel electronic genetic screening tool

Bruce K. Lin, Emily Edelman, Joseph D. McInerney, James O'leary, Vaughn Edelson, Kevin S. Hughes, Brian Drohan, Penny Kyler, Michele Lloyd-Puryear, Joan Scott, Siobhan M. Dolan

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

In the age of genomic medicine, family health history (FHH) remains an important tool for personalized risk assessment as it can inform approaches to disease prevention and management. In primary care, including in prenatal settings, providers recognize that FHH enables them to assess the risk for birth defects and complex conditions that not only affect the fetus health, but also the mother's. However, many providers lack the time to gather FHH or the knowledge to confidently interpret the data. Electronic tools providing clinical decision support using FHH data can aid the busy provider with data collection and interpretation. We describe the scope of conditions included in a patient-entered FHH tool that provides clinical decision support and point-of-care education to assist with patient management. This report details how we selected the conditions for which it is appropriate to use FHH as a means to promote personalized medicine in primary prenatal care.

Original languageEnglish (US)
Pages (from-to)307-318
Number of pages12
JournalPersonalized Medicine
Volume10
Issue number3
DOIs
StatePublished - May 2013
Externally publishedYes

Fingerprint

Medical History Taking
Prenatal Care
Genetic Testing
Clinical Decision Support Systems
Primary Health Care
Point-of-Care Systems
Precision Medicine
Disease Management
Fetus
Mothers
Medicine
Education
Health

Keywords

  • clinical decision support
  • family health history
  • genetic screening
  • personalized risk assessment
  • prenatal care

ASJC Scopus subject areas

  • Molecular Medicine
  • Pharmacology
  • Medicine(all)

Cite this

Personalizing prenatal care using family health history : Identifying a panel of conditions for a novel electronic genetic screening tool. / Lin, Bruce K.; Edelman, Emily; McInerney, Joseph D.; O'leary, James; Edelson, Vaughn; Hughes, Kevin S.; Drohan, Brian; Kyler, Penny; Lloyd-Puryear, Michele; Scott, Joan; Dolan, Siobhan M.

In: Personalized Medicine, Vol. 10, No. 3, 05.2013, p. 307-318.

Research output: Contribution to journalArticle

Lin, BK, Edelman, E, McInerney, JD, O'leary, J, Edelson, V, Hughes, KS, Drohan, B, Kyler, P, Lloyd-Puryear, M, Scott, J & Dolan, SM 2013, 'Personalizing prenatal care using family health history: Identifying a panel of conditions for a novel electronic genetic screening tool', Personalized Medicine, vol. 10, no. 3, pp. 307-318. https://doi.org/10.2217/pme.13.18
Lin, Bruce K. ; Edelman, Emily ; McInerney, Joseph D. ; O'leary, James ; Edelson, Vaughn ; Hughes, Kevin S. ; Drohan, Brian ; Kyler, Penny ; Lloyd-Puryear, Michele ; Scott, Joan ; Dolan, Siobhan M. / Personalizing prenatal care using family health history : Identifying a panel of conditions for a novel electronic genetic screening tool. In: Personalized Medicine. 2013 ; Vol. 10, No. 3. pp. 307-318.
@article{86b830faef3e426e89e61633e72e1b49,
title = "Personalizing prenatal care using family health history: Identifying a panel of conditions for a novel electronic genetic screening tool",
abstract = "In the age of genomic medicine, family health history (FHH) remains an important tool for personalized risk assessment as it can inform approaches to disease prevention and management. In primary care, including in prenatal settings, providers recognize that FHH enables them to assess the risk for birth defects and complex conditions that not only affect the fetus health, but also the mother's. However, many providers lack the time to gather FHH or the knowledge to confidently interpret the data. Electronic tools providing clinical decision support using FHH data can aid the busy provider with data collection and interpretation. We describe the scope of conditions included in a patient-entered FHH tool that provides clinical decision support and point-of-care education to assist with patient management. This report details how we selected the conditions for which it is appropriate to use FHH as a means to promote personalized medicine in primary prenatal care.",
keywords = "clinical decision support, family health history, genetic screening, personalized risk assessment, prenatal care",
author = "Lin, {Bruce K.} and Emily Edelman and McInerney, {Joseph D.} and James O'leary and Vaughn Edelson and Hughes, {Kevin S.} and Brian Drohan and Penny Kyler and Michele Lloyd-Puryear and Joan Scott and Dolan, {Siobhan M.}",
year = "2013",
month = "5",
doi = "10.2217/pme.13.18",
language = "English (US)",
volume = "10",
pages = "307--318",
journal = "Personalized Medicine",
issn = "1741-0541",
publisher = "Future Medicine Ltd.",
number = "3",

}

TY - JOUR

T1 - Personalizing prenatal care using family health history

T2 - Identifying a panel of conditions for a novel electronic genetic screening tool

AU - Lin, Bruce K.

AU - Edelman, Emily

AU - McInerney, Joseph D.

AU - O'leary, James

AU - Edelson, Vaughn

AU - Hughes, Kevin S.

AU - Drohan, Brian

AU - Kyler, Penny

AU - Lloyd-Puryear, Michele

AU - Scott, Joan

AU - Dolan, Siobhan M.

PY - 2013/5

Y1 - 2013/5

N2 - In the age of genomic medicine, family health history (FHH) remains an important tool for personalized risk assessment as it can inform approaches to disease prevention and management. In primary care, including in prenatal settings, providers recognize that FHH enables them to assess the risk for birth defects and complex conditions that not only affect the fetus health, but also the mother's. However, many providers lack the time to gather FHH or the knowledge to confidently interpret the data. Electronic tools providing clinical decision support using FHH data can aid the busy provider with data collection and interpretation. We describe the scope of conditions included in a patient-entered FHH tool that provides clinical decision support and point-of-care education to assist with patient management. This report details how we selected the conditions for which it is appropriate to use FHH as a means to promote personalized medicine in primary prenatal care.

AB - In the age of genomic medicine, family health history (FHH) remains an important tool for personalized risk assessment as it can inform approaches to disease prevention and management. In primary care, including in prenatal settings, providers recognize that FHH enables them to assess the risk for birth defects and complex conditions that not only affect the fetus health, but also the mother's. However, many providers lack the time to gather FHH or the knowledge to confidently interpret the data. Electronic tools providing clinical decision support using FHH data can aid the busy provider with data collection and interpretation. We describe the scope of conditions included in a patient-entered FHH tool that provides clinical decision support and point-of-care education to assist with patient management. This report details how we selected the conditions for which it is appropriate to use FHH as a means to promote personalized medicine in primary prenatal care.

KW - clinical decision support

KW - family health history

KW - genetic screening

KW - personalized risk assessment

KW - prenatal care

UR - http://www.scopus.com/inward/record.url?scp=84877587599&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84877587599&partnerID=8YFLogxK

U2 - 10.2217/pme.13.18

DO - 10.2217/pme.13.18

M3 - Article

VL - 10

SP - 307

EP - 318

JO - Personalized Medicine

JF - Personalized Medicine

SN - 1741-0541

IS - 3

ER -