Newborn blood spot screening and genetic services: A survey of Minnesota primary care physicians

Genetics in Medicine

Volumn 7, Issue 8, 2005, Pages 564-570

  Thompson, Diane B ^a,d   Ahrens, Mary J ^a   LeRoy, Bonnie S ^a   Brown, Dana ^c   Berry, Susan A ^a,b,e  

^a UNIVERSITY OF MINNESOTA   (United States)

^b UNIVERSITY OF MINNESOTA MEDICAL SCHOOL   (United States)

^c MINNESOTA DEPARTMENT OF HEALTH   (United States)

^d MERCY MEDICAL CENTER   (United States)

^e NONE   (United States)

Author keywords

Genetic counseling; Genetic services; Newborn blood spot screening; Primary care physicians; Tandem mass spectrometry

Indexed keywords

ANXIETY; CLINICAL PRACTICE; EMOTION; FOLLOW UP; GENERAL PRACTITIONER; GENETIC ANALYSIS; GENETIC COUNSELING; HUMAN; NEWBORN SCREENING; PEDIATRICIAN; PRIMARY MEDICAL CARE; PUBLIC HEALTH SERVICE; QUESTIONNAIRE; REVIEW; SATISFACTION; UNITED STATES;

ATTITUDE OF HEALTH PERSONNEL; COMMUNICATION; EDUCATION, CONTINUING; GENETIC COUNSELING; GENETIC SCREENING; GENETIC SERVICES; HUMANS; INFANT, NEWBORN; MINNESOTA; NEONATAL SCREENING; PHYSICIAN-PATIENT RELATIONS; PHYSICIANS, FAMILY;

EID: 27644485020     PISSN: 10983600     EISSN: None     Source Type: Journal    
DOI: 10.1097/01.GIM.0000177417.61006.a6     Document Type: Review

References (22)

1. Desposito F, Lloyd-Puryear MA, Tonniges TF, Rhein F, Mann M. Survey of pediatrician practices in retrieving statewide authorized newborn screening results. Pediatrics 2001;108:E22.
2. American Academy of Pediatrics Newborn Screening Task Force, Serving the family from birth to the medical home: newborn screening. A blueprint for the future: a call for a national agenda on state newborn screening programs. Pediatrics 2000;106:389-427.
3. Minnesota Department of Health. http://www.health.state.mn.us.divs/fh/ mcshn/ nbshome.htm. Minnesota Newborn Blood Spot Screening Accessed May 31, 2005.
4. Centers for Disease Control and Prevention. Using tandem mass spectrometry for metabolic disease screening among newborns: a report of a work group. Morb Mortal Wkly Rep April 13, 2001;50:1-34.
5. Lloyd-Puryear MA, Forsman I. Newborn screening and genetic testing. J Obstet Gynecol Neonatal Nurs 2002;31:200-207.
6. Korson MS. Advances in newborn screening for metabolic disorders: what the pediatrician needs to know. Pediatr Ann 2000;29:294-301.
7. Kim S, Lloyd-Puryear MA, Tonniges TF. Examination of the communication practices between state newborn screening programs and the medical home. Pediatrics 2003;111:e120-e126.
8. Steinberg Warren N, Carter TP, Humbert JR, Rowley PT. Newborn screening for hemoglobinopathies in New York State: experience of physicians and parents of affected children. J Pediatr 1982;100:373-377.
9. Ciske DJ, Haavisto A, Laxova A, Rock LZM, Farrell PM. Genetic counseling and neonatal screening for Cystic Fibrosis: an assessment of the communication process. Pediatrics 2001;107:699-705.
10. U.S. Department of Health and Human Services, Health Resources and Services Administration, Maternal and Child Health Bureau Newborn Screening: Toward a Uniform Screening Panel and System Report for Public Comment http://www. mchb.hrsa.gov/screening. Accessed May 31, 2005.
11. American College of Medical Genetics/American Society of Hum Genet Test and Technology Transfer Committee Working Group. Tandem mass spectrometry in newborn screening. Genet Med 2000;2:267-269.
12. Bleiker, EM, Aaronson NK, Menko FH, Hahn DE, et al. Genetic counseling for hereditary cancer: a pilot study on experiences of patients and family members. Patient Educ Couns. 1997;32:107-116.
13. Berkenstadt M, Shiloh S, Barkai G, Katznelson MBM, Goldman B. Perceived personal control (PPe): a new concept in measuring outcome of genetic counseling. Am J Med Genet 1999;82:53-59.
14. Stockdill SH. How to evaluate foundation programs. St, Paul: St Paul Foundation, 1998.
15. The R Development Core Team 2003. [web based free software]. Version 1.6.2. http://rweb.statumn.edu/cgi-bin/Rweb/Rweb.cgi. Accessed May 31, 2005.
16. Wheeler PG, Smith R, Dorkin H, Parad RB, Comeau AM, Bianchi DW. Genetic counseling after implementation of statewide cystic fibrosis newborn screening: two years' experience in one medical center. Genet Med 2001;3:411-415.
17. Farrell MH, Certain LK, Farrell PM. Genetic counseling and risk communication services of newborn screening programs. Arch Pediatr Adolesc Med 2001;155:120-126.
18. Bernhardt BA, Biesecker BB, Mastromarino CL. Goals, benefits, and outcomes of genetic counseling: client and genetic counselor assessment. Am J Med Genet 2000;94:189-197.
19. National Society of Genetic Counselors, 1983. Available at: http://www.nsgc. org!about!definition.asp. Accessed May 31, 2005.
20. Kaye CI, Laxova R, Livingston JE, Lloyd-Puryear MA, et al. Integrating genetic services into public health- guidance for state and territorial programs from the National Newborn Screening and Genetics Resource Center (NNSGRC). Community Genet 2001;4:175-196.
21. Korf BR. Integration of genetics into clinical teaching in medical school education. Genet Med 2002 4, Supplement:33S-38S. Newborn blood spot screening
22. Reddy H, Harris I, Galle B, Seaquist ER. Continuing medical education: what do Minnesota physicians want? Minn Med 2001;84:58-61.