Education in the genetics of hearing loss: A survey of early hearing detection and intervention programs

被引:5
作者
Burton, Sarah K.
Blanton, Susan H.
Culpepper, Brandt
White, Karl R.
Pandya, Arti
Nance, Walter E.
Arnos, Kathleen S.
机构
[1] Gallaudet Univ, Dept Biol, Genet Program, Washington, DC 20002 USA
[2] Virginia Commonwealth Univ, Dept Human Genet, Richmond, VA 23298 USA
[3] Univ Virginia, Dept Pediat, Charlottesville, VA USA
[4] Northside Hosp, Audiol Serv, Atlanta, GA USA
[5] Utah State Univ, Natl Ctr Hearing Assessment & Management, Logan, UT 84322 USA
关键词
genetics education; hearing loss; early hearing detection and intervention;
D O I
10.1097/01.gim.0000232462.55966.92
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Purpose: Permanent hearing loss at birth or in early childhood is common and has many genetic and environmental causes. Advances in the identification and characterization of genetic forms, combined with the early identification of children through the implementation of state-based Early Hearing Detection and Intervention programs suggests the need for education about the causes of hearing loss among professionals who work in these programs. Methods: An online survey was directed to state program coordinators of Early Hearing Detection and Intervention programs to identify gaps in knowledge about the genetic causes of hearing loss and to assess interest in continuing education on this topic. Results: The study identified clear gaps in respondents' knowledge about genetic causes of hearing loss. Twenty percent of respondents indicated that they had received no training in genetics. When asked to rate their knowledge about the genetics of hearing loss, most rated their knowledge as "not adequate." Respondents expressed interest in genetics training through several modalities, including a distance learning format. Conclusion: This study provides documentation of the need for education of health care professionals involved in the early identification of hearing loss. Suggestions for suitable educational formats based on respondent needs and interests are provided.
引用
收藏
页码:510 / 517
页数:8
相关论文
共 20 条
[1]  
Arnos Kathleen S, 2004, Am J Audiol, V13, P126, DOI 10.1044/1059-0889(2004/017)
[2]   Clinical studies of families with hearing loss attributable to mutations in the connexin 26 gene (GJB2/DFNB1) [J].
Cohn, ES ;
Kelley, PM ;
Fowler, TW ;
Gorga, MP ;
Lefkowitz, DM ;
Kuehn, HJ ;
Schaefer, GB ;
Gobar, LS ;
Hahn, FJ ;
Harris, DJ ;
Kimberling, WJ .
PEDIATRICS, 1999, 103 (03) :546-550
[3]   A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairment [J].
del Castillo, FJ ;
Rodríguez-Ballesteros, M ;
Alvarez, A ;
Hutchin, T ;
Leonardi, E ;
de Oliveira, CA ;
Azaiez, H ;
Brownstein, Z ;
Avenarius, MR ;
Marlin, S ;
Pandya, A ;
Shahin, H ;
Siemering, KR ;
Weil, D ;
Wuyts, W ;
Aguirre, LA ;
Martín, Y ;
Moreno-Pelayo, MA ;
Villamar, M ;
Avraham, KB ;
Dahl, HHM ;
Kanaan, M ;
Nance, W ;
Petit, C ;
Smith, RJH ;
Van Camp, G ;
Sartorato, EL ;
Murgia, A ;
Moreno, F ;
del Castillo, I .
JOURNAL OF MEDICAL GENETICS, 2005, 42 (07) :588-594
[4]   A deletion involving the connexin 30 gene in nonsyndromic hearing impairment. [J].
del Castillo, I ;
Villamar, M ;
Moreno-Pelayo, MA ;
del Castillo, FJ ;
Alvarez, A ;
Tellería, D ;
Menéndez, I ;
Moreno, F .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 346 (04) :243-U1
[5]   The efficacy of early identification and intervention for children with hearing impairment [J].
Downs, MP ;
Yoshinaga-Itano, C .
PEDIATRIC CLINICS OF NORTH AMERICA, 1999, 46 (01) :79-+
[6]  
Finitzo T, 2000, PEDIATRICS, V106, P798, DOI 10.1044/1059-0889(2000/005)
[7]   Assessment of the genetic causes of recessive childhood non-syndromic deafness in the UK - implications for genetic testing [J].
Hutchin, T ;
Coy, NN ;
Conlon, H ;
Telford, E ;
Bromelow, K ;
Blaydon, D ;
Taylor, G ;
Coghill, E ;
Brown, S ;
Trembath, R ;
Liu, XZ ;
Bitner-Glindzicz, M ;
Mueller, R .
CLINICAL GENETICS, 2005, 68 (06) :506-512
[8]   GJB2 (connexin 26) variants and nonsyndromic sensorineural hearing loss: A HuGE review [J].
Kenneson, A ;
Braun, KV ;
Boyle, C .
GENETICS IN MEDICINE, 2002, 4 (04) :258-274
[9]   GENETIC EPIDEMIOLOGIC STUDIES OF EARLY-ONSET DEAFNESS IN THE UNITED-STATES SCHOOL-AGE POPULATION [J].
MARAZITA, ML ;
PLOUGHMAN, LM ;
RAWLINGS, B ;
REMINGTON, E ;
ARNOS, KS ;
NANCE, WE .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1993, 46 (05) :486-491
[10]  
MOELLER MP, 2006, 2006 NAT EARL HEAR D