Evaluation of a novel electronic genetic screening and clinical decision support tool in prenatal clinical settings

Maternal and Child Health Journal

Volumn 18, Issue 5, 2014, Pages 1233-1245

  Edelman, Emily A ^a   Lin, Bruce K ^b   Doksum, Teresa ^c   Drohan, Brian ^d   Edelson, Vaughn ^e   Dolan, Siobhan M ^b,f   Hughes, Kevin ^d   O'Leary, James ^e   Vasquez, Lisa ^g   Copeland, Sara ^g   Galvin, Shelley L ^h   DeGroat, Nicole ⁱ   Pardanani, Setul ^f   Feero, W Gregory ^j   Adams, Claire ^j   Jones, Renee ^k   Scott, Joan ^a  

^a National Coalition for Health Professional Education in Genetics   (United States)

^b March of Dimes Birth Defects Foundation   (United States)

^c Doksum Consulting   (United States)

^d MASSACHUSETTS GENERAL HOSPITAL   (United States)

^e GENETIC ALLIANCE   (United States)

^f ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

^g HEALTH RESOURCES AND SERVICES ADMINISTRATION   (United States)

^h Mountain Area Health Education Center   (United States)

ⁱ MONTEFIORE MEDICAL CENTER   (United States)

^j Maine Dartmouth Family Practice Residency   (United States)

^k Ariosa Diagnostics   (United States)

more..

Author keywords

Clinical decision support; Family health history; Genetic screening; Personalized risk assessment; Prenatal care

Indexed keywords

ADOLESCENT; ADULT; ANAMNESIS; CLINICAL PRACTICE; CLINICAL TRIAL; COMPUTER PROGRAM; DECISION SUPPORT SYSTEM; DEMOGRAPHY; FEMALE; GENETIC SCREENING; HEALTH PERSONNEL ATTITUDE; HUMAN; INTERVIEW; MIDDLE AGED; MULTICENTER STUDY; PREGNANCY; PRENATAL CARE; PRIMARY HEALTH CARE; PROCEDURES; QUESTIONNAIRE; RISK ASSESSMENT; STATISTICS AND NUMERICAL DATA; UNITED STATES;

ADOLESCENT; ADULT; ATTITUDE OF HEALTH PERSONNEL; DECISION SUPPORT TECHNIQUES; DEMOGRAPHY; FEMALE; GENETIC TESTING; HUMANS; INTERVIEWS AS TOPIC; MEDICAL HISTORY TAKING; MIDDLE AGED; PHYSICIAN'S PRACTICE PATTERNS; PREGNANCY; PRENATAL CARE; PRIMARY HEALTH CARE; QUESTIONNAIRES; RISK ASSESSMENT; SOFTWARE; UNITED STATES;

EID: 84904440804     PISSN: 10927875     EISSN: 15736628     Source Type: Journal    
DOI: 10.1007/s10995-013-1358-y     Document Type: Article

References (35)

1. Guttmacher, A. E., Collins, F. S., & Carmona, R. H. (2004). The family history-more important than ever. New England Journal of Medicine, 351(22), 2333-2336. (Pubitemid 39552752)
2. Pyeritz, R. E. (2012). The family history: the first genetic test, and still useful after all those years? Genetics in Medicine, 14(1), 3-9.
3. ACOG. (2011). Committee Opinion No. 478: Family history as a risk assessment tool. Obstetrics and Gynecology, 117(3), 747-750.
4. Bhattacharya, S., Raja, E. A., Mirazo, E. R., et al. (2010). Inherited predisposition to spontaneous preterm delivery. Obstetrics and Gynecology, 115(6), 1125-1133.
5. Oyen, N., Poulsen, G., Boyd, H. A., et al. (2009). Recurrence of congenital heart defects in families. Circulation, 120(4), 295-301.
6. Forty, L., Jones, L., Macgregor, S., et al. (2006). Familiality of postpartum depression in unipolar disorder: Results of a family study. American Journal of Psychiatry, 163(9), 1549-1553. (Pubitemid 44465754)
7. Hampel, H., Frankel, W. L., Martin, E., et al. (2005). Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer). New England Journal of Medicine, 352(18), 1851-1860.
8. ACOG. (2012). Practice bulletin: Clinical management guidelines for obstetrician-gynecologists. http://www.acog.org//media/List%20of%20Titles/ PBListOfTitles.pdf.
9. Lin, B. K., Edelman, E. A., McInerney, J. D., et al. (2013). Personalizing prenatal care using family health history: Identifying and integrating a panel of conditions into a novel screening tool. Personalized Medicine, 10(3), 307-318.
10. Darcy, D., Tian, L., Taylor, J., et al. (2011). Cystic fibrosis carrier screening in obstetric clinical practice: Knowledge, practices, and barriers, a decade after publication of screening guidelines. Genet Test Mol Biomarkers, 15(7-8), 517-523.
11. SACGHS. (2011). Genetics education and training: Report of the secretary's advisory committee on genetics, health, and society. Bethesda, MD: Department of Health and Human Services.
12. Nippert, I., Harris, H. J., Julian-Reynier, C., et al. (2011). Confidence of primary care physicians in their ability to carry out basic medical genetic tasks-a European survey in five countries-Part 1. Journal of Community Genetics, 2(1), 1-11.
13. Hoffman, M. A., & Williams, M. S. (2011). Electronic medical records and personalized medicine. Human Genetics, 130(1), 33-39.
14. Osheroff, J. A., Teich, J. M., Middleton, B., et al. (2007). A roadmap for national action on clinical decision support. Journal of the American Medical Informatics Association, 14(2), 141-145. (Pubitemid 46275496)
15. Litvin, C. B., Davis, K. S., Moran, W. P., et al. (2012). The use of clinical decision-support tools to facilitate geriatric education. Journal of the American Geriatrics Society, 60(6), 1145-1149.
16. Welch, B. M., & Kawamoto, K. (2013). Clinical decision support for genetically guided personalized medicine: A systematic review. Journal of the American Medical Informatics Association, 20(2), 388-400.
17. Rubinstein, W. S., Acheson, L. S., O'Neill, S. M., et al. (2011). Clinical utility of family history for cancer screening and referral in primary care: A report from the family healthware impact trial. Genetics in Medicine, 13(11), 956-965.
18. Ozanne, E. M., Loberg, A., Hughes, S., et al. (2009). Identification and management of women at high risk for hereditary breast/ovarian cancer syndrome. The Breast Journal, 15(2), 155-162.
19. Orlando, L. A., Hauser, E. R., Christianson, C., et al. (2011). Protocol for implementation of family health history collection and decision support into primary care using a computerized family health history system. BMC Health Services Research, 11, 264.
20. NCHPEG. (2013). The pregnancy and health profile: A screening and risk assessment tool. Accessed July 15, 2013, from http://www.nchpeg.org/index.php? option=com-content&view=article&id=410&Itemid=277.
21. Ralston, J. D., Carrell, D., Reid, R., et al. (2007). Patient web services integrated with a shared medical record: Patient use and satisfaction. Journal of the American Medical Informatics Association, 14(6), 798-806. (Pubitemid 350026418)
22. Arar, N., Seo, J., Abboud, H. E., et al. (2011). Veterans' experience in using the online surgeon general's family health history tool. Personalized Medicine, 8(5), 523-532. doi:10.2217/pme.11.53.
23. Westman, J., Hampel, H., & Bradley, T. (2000). Efficacy of a touchscreen computer based family cancer history questionnaire and subsequent cancer risk assessment. Journal of Medical Genetics, 37(5), 354-360. (Pubitemid 30261267)
24. Facio, F. M., Feero, W. G., Linn, A., et al. (2010). Validation of my Family health Portrait for six common heritable conditions. Genetics in Medicine, 12(6), 370-375.
25. ACOG. (2013). ACOG Resource Center. Accessed February 4, 2013, from fromhttp://www.acog.org/About-ACOG/ACOG-Departments/Resource-Center.
26. van der Sijs, H., Aarts, J., Vulto, A., et al. (2006). Overriding of drug safety alerts in computerized physician order entry. Journal of the American Medical Informatics Association, 13(2), 138-147. (Pubitemid 43332904)
27. Shah, N. R., Seger, A. C., Seger, D. L., et al. (2006). Improving acceptance of computerized prescribing alerts in ambulatory care. Journal of the American Medical Informatics Association, 13(1), 5-11. (Pubitemid 41828329)
28. Toriello, H. V., & Goldenberg, P. (2009). Evidence-based medicine and practice guidelines: Application to genetics. American Journal of Medical Genetics Part C: Seminars in Medical Genetics, 151C(3), 235-240.
29. Wilson, B. J., Carroll, J. C., Allanson, J., et al. (2012). Family history tools in primary care: Does one size fit all? Public Health Genomics, 15(3-4), 181-188.
30. Kawamoto, K., Houlihan, C. A., Balas, E. A., et al. (2005). Improving clinical practice using clinical decision support systems: A systematic review of trials to identify features critical to success. BMJ, 330(7494), 765.
31. Bauer, N. S., & Carroll, A. E. (2013). Downs SM. Journal of the American Medical Informatics Association: Understanding the acceptability of a computer decision support system in pediatric primary care.
32. VanGeest, J. B., Johnson, T. P., & Welch, V. L. (2007). Methodologies for improving response rates in surveys of physicians: A systematic review. Evaluation and the Health Professions, 30(4), 303-321.
33. Ruffin, M. T., Jr Nease, D. E., Sen, A., et al. (2011). Effect of preventive messages tailored to family history on health behaviors: The family healthware impact trial. The Annals of Family Medicine, 9(1), 3-11.
34. Qureshi, N., Armstrong, S., Dhiman, P., et al. (2012). Effect of adding systematic family history enquiry to cardiovascular disease risk assessment in primary care. Annals of Internal Medicine, 156(4), 253-262.
35. NIH. (2009). Family history and improving health. National Institutes of Health State of the Science Consensus Conference; Bethesda, Maryland.