Experiences of cystic fibrosis newborn screening and genetic counseling

被引:0
|
作者
Foil, Kimberly [1 ]
Christon, Lillian [2 ]
Kerrigan, Cheryl [3 ]
Flume, Patrick A. [1 ,3 ]
Drinkwater, Jaclyn [3 ]
Szentpetery, Sylvia [3 ]
机构
[1] Med Univ South Carolina, Dept Med, 30 Courtenay Dr Room 113, Charleston, SC 29425 USA
[2] Med Univ South Carolina, Dept Psychiat & Behav Sci, Charleston, SC 29425 USA
[3] Med Univ South Carolina, Dept Pediat, Charleston, SC 29425 USA
关键词
Cystic fibrosis; Newborn screening; Genetic counseling; Parents; Distress; Comprehension; DIAGNOSIS;
D O I
10.1007/s12687-023-00666-8
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The South Carolina cystic fibrosis (CF) newborn screening (NBS) program changed in 2019 to include CFTR genotyping for babies with top 4% immunoreactive trypsinogen, which improves sensitivity and timeliness but increases carrier detection. Carrier identification has genetic implications for the family and parents of NBS+ babies have increased emotional distress. Genetic counseling (GC) may increase parent understanding and reduce anxiety yet is not uniformly offered at CF centers. We report our early results after implementing GC for NBS+ families at the time of sweat chloride testing based on GC availability, which resulted in an unselected GC- control arm. Sixteen mothers (GC+ = 9, GC- = 7) participated in an online survey about their experience. Responses were analyzed in aggregate and for differences between GC+ and GC- groups. All-respondent sadness and anxiety increased with notification of the NBS+ result and decreased after sweat test results. Anxiety and sadness were greater in GC- compared to GC+ until after the diagnosis was resolved, though emotional differences between the groups were not statistically significant. On a scale of 0 = not at all to 10 = extremely, GC was rated very helpful (mean 9.0, range 5-10), informative (mean 8.9, range 4-10), comforting (mean 9.1, range 6-10), and minimally distracting (mean 1.8, range 0-9). All participants correctly identified that a risk for a child to have CF exists when both parents are (at least) carriers. Delivery of NBS results to respondents varied by timing, informant, and information given. The child's pediatrician notified 10 (62.5%) of the NBS+ result. Parents felt they were notified in a timely manner (68.8%), by someone knowledgeable about NBS (62.5%), the sweat test (62.5%), CF (43.8%), and genetics (43.8%) and who cared about them (81.3%). Parents felt worried (81.3%), confused (81.3%), empowered (25%), and other (sad, shocked, scared, overwhelmed, devastated, defeated). Data from this single-center study suggest benefit of GC, that families would value earlier contact with an expert, and that prompt diagnostic resolution may reduce duration of parental distress.
引用
收藏
页码:621 / 626
页数:6
相关论文
共 50 条
  • [1] Experiences of cystic fibrosis newborn screening and genetic counseling
    Kimberly Foil
    Lillian Christon
    Cheryl Kerrigan
    Patrick A. Flume
    Jaclyn Drinkwater
    Sylvia Szentpetery
    [J]. Journal of Community Genetics, 2023, 14 : 621 - 626
  • [2] Evaluation of genetic counseling among cystic fibrosis carriers, Michigan Newborn Screening
    Kleyn, Mary J.
    Langbo, Carrie
    Abdulhamid, Ibrahim
    Adamski, Craig R.
    Allan, Catherine
    Carmany, Erin P.
    Gregoire-Bottex, M. Myrtha
    Homnick, Douglas
    Schuen, John
    Nasr, Samya Z.
    [J]. PEDIATRIC PULMONOLOGY, 2013, 48 (02) : 123 - 129
  • [3] Cystic fibrosis newborn screening: Impact on reproductive behavior and implications for genetic counseling
    Mischler, EH
    Wilfond, BS
    Fost, N
    Laxova, A
    Reiser, C
    Sauer, CM
    Makholm, LM
    Shen, GH
    Feenan, L
    McCarthy, C
    Farrell, PM
    [J]. PEDIATRICS, 1998, 102 (01) : 44 - 52
  • [4] Improvement in cystic fibrosis newborn screening program outcomes with genetic counseling via telemedicine
    Stalker, Heather J.
    Jonasson, Amy R.
    Hopfer, Sidney M.
    Collins, Melanie Sue
    [J]. PEDIATRIC PULMONOLOGY, 2023, 58 (12) : 3478 - 3486
  • [5] EVALUATION OF GENETIC COUNSELING FOR A COHORT OF CYSTIC FIBROSIS CARRIERS IN THE MICHIGAN NEWBORN SCREENING PROGRAM
    Langbo, C.
    Kleyn, M.
    Andruszewski, K.
    Abdulhamid, I
    Homnick, D. N.
    Schuen, J. N.
    Nasr, S. Z.
    Gregoire-Bottex, M.
    [J]. PEDIATRIC PULMONOLOGY, 2011, : 367 - 368
  • [6] A TAILORED APPROACH TO FAMILY-CENTERED GENETIC COUNSELING FOR CYSTIC FIBROSIS NEWBORN SCREENING
    Tluczek, A.
    Zaleski, C.
    Stachiw-Hietpas, D.
    Modaff, P.
    Adamski, C. R.
    Nelson, M. R.
    Reiser, C. A.
    Ghate, S.
    Josephson, K. D.
    [J]. PEDIATRIC PULMONOLOGY, 2010, : 406 - 406
  • [7] A Tailored Approach to Family-Centered Genetic Counseling for Cystic Fibrosis Newborn Screening: The Wisconsin Model
    Tluczek, Audrey
    Zaleski, Christina
    Stachiw-Hietpas, Dania
    Modaff, Peggy
    Adamski, Craig R.
    Nelson, Megan R.
    Reiser, Catherine A.
    Ghate, Sumedha
    Josephson, Kevin D.
    [J]. JOURNAL OF GENETIC COUNSELING, 2011, 20 (02) : 115 - 128
  • [8] Genetic counseling and cystic fibrosis
    Julia, S
    Beth, E
    [J]. REVUE DES MALADIES RESPIRATOIRES, 2000, 17 (3BIS) : 807 - 811
  • [9] Newborn screening for cystic fibrosis
    LeGrys, VA
    [J]. LABORATORY MEDICINE, 2002, 33 (03) : 212 - 213
  • [10] Newborn screening for cystic fibrosis
    David, TJ
    [J]. JOURNAL OF THE ROYAL SOCIETY OF MEDICINE, 2004, 97 (05) : 209 - 210