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Volumn 36, Issue 3, 2016, Pages 252-259

What results to disclose, when, and who decides? Healthcare professionals' views on prenatal chromosomal microarray analysis

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME ANALYSIS; FEMALE; HEALTH CARE PERSONNEL; HUMAN; INFORMATION DISSEMINATION; MALE; METHODOLOGY; MICROARRAY ANALYSIS; PARENT; PREGNANCY; PRENATAL SCREENING; PRIORITY JOURNAL; UNITED KINGDOM; ADULT; CHROMOSOME DISORDERS; DECISION MAKING; HEALTH PERSONNEL ATTITUDE; INTERPERSONAL COMMUNICATION; ONSET AGE; PRENATAL DIAGNOSIS; PROCEDURES; PROFESSIONAL-PATIENT RELATIONSHIP; PSYCHOLOGY; QUESTIONNAIRE; TIME FACTOR; UNCERTAINTY;

EID: 84975763680     PISSN: 01973851     EISSN: 10970223     Source Type: Journal    
DOI: 10.1002/pd.4772     Document Type: Article
Times cited : (25)

References (38)
  • 1
    • 77952032690 scopus 로고    scopus 로고
    • Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies
    • Miller DT, Adam MP, Aradhya S, et al. Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies. Am J Hum Genet 2010;86:749-64.
    • (2010) Am J Hum Genet , vol.86 , pp. 749-764
    • Miller, D.T.1    Adam, M.P.2    Aradhya, S.3
  • 2
    • 84875818687 scopus 로고    scopus 로고
    • Array CGH as a first line diagnostic test in place of karyotyping for postnatal referrals-results from four years' clinical application for over 8,700 patients
    • Ahn JW, Bint S, Bergbaum A, et al. Array CGH as a first line diagnostic test in place of karyotyping for postnatal referrals-results from four years' clinical application for over 8, 700 patients. Mol Cytogenet 2013;6:10-16.
    • (2013) Mol Cytogenet , vol.6 , pp. 10-16
    • Ahn, J.W.1    Bint, S.2    Bergbaum, A.3
  • 3
    • 84898033264 scopus 로고    scopus 로고
    • Implementation of genomic arrays in prenatal diagnosis: the Belgian approach to meet the challenges
    • Vanakker O, Vilain C, Janssens K, et al. Implementation of genomic arrays in prenatal diagnosis: the Belgian approach to meet the challenges. Eur J Med Genet 2014;57:151-6.
    • (2014) Eur J Med Genet , vol.57 , pp. 151-156
    • Vanakker, O.1    Vilain, C.2    Janssens, K.3
  • 4
    • 84893182999 scopus 로고    scopus 로고
    • Committee opinion no. 581: the use of chromosomal microarray analysis in prenatal diagnosis
    • Obstetricians ACo, Gynecologists
    • Obstetricians ACo, Gynecologists. Committee opinion no. 581: the use of chromosomal microarray analysis in prenatal diagnosis. Obstet Gynecol 2013;122:1374-7.
    • (2013) Obstet Gynecol , vol.122 , pp. 1374-1377
  • 5
    • 84879099857 scopus 로고    scopus 로고
    • Use of prenatal chromosomal microarray: prospective cohort study and systematic review and meta-analysis
    • Hillman S, McMullan D, Hall G, et al. Use of prenatal chromosomal microarray: prospective cohort study and systematic review and meta-analysis. Ultrasound Obstet Gynecol 2013;41:610-20.
    • (2013) Ultrasound Obstet Gynecol , vol.41 , pp. 610-620
    • Hillman, S.1    McMullan, D.2    Hall, G.3
  • 6
    • 84878873338 scopus 로고    scopus 로고
    • Estimates of penetrance for recurrent pathogenic copy-number variations
    • Rosenfeld JA, Coe BP, Eichler EE, et al. Estimates of penetrance for recurrent pathogenic copy-number variations. Genet Med 2012;15:478-81.
    • (2012) Genet Med , vol.15 , pp. 478-481
    • Rosenfeld, J.A.1    Coe, B.P.2    Eichler, E.E.3
  • 7
    • 84859494373 scopus 로고    scopus 로고
    • Clinical utility of chromosomal microarray analysis in invasive prenatal diagnosis
    • Armengol L, Nevado J, Serra-Juhé C, et al. Clinical utility of chromosomal microarray analysis in invasive prenatal diagnosis. Hum Genet 2012;131:513-23.
    • (2012) Hum Genet , vol.131 , pp. 513-523
    • Armengol, L.1    Nevado, J.2    Serra-Juhé, C.3
  • 8
    • 84863438703 scopus 로고    scopus 로고
    • Array CGH in routine prenatal diagnosis practice
    • Cavalli P, Cavallari U, Novelli A. Array CGH in routine prenatal diagnosis practice. Prenat Diagn 2012;32:708-9.
    • (2012) Prenat Diagn , vol.32 , pp. 708-709
    • Cavalli, P.1    Cavallari, U.2    Novelli, A.3
  • 9
    • 79961128043 scopus 로고    scopus 로고
    • Unexpected findings in cancer predisposition genes detected by array comparative genomic hybridisation: what are the issues?
    • Pichert G, Mohammed SN, Ahn JW, et al. Unexpected findings in cancer predisposition genes detected by array comparative genomic hybridisation: what are the issues? J Med Genet 2011;48:535-9.
    • (2011) J Med Genet , vol.48 , pp. 535-539
    • Pichert, G.1    Mohammed, S.N.2    Ahn, J.W.3
  • 10
    • 84911986477 scopus 로고    scopus 로고
    • An exploration of genetic counselors' needs and experiences with prenatal chromosomal microarray testing
    • Bernhardt BA, Kellom K, Barbarese A, et al. An exploration of genetic counselors' needs and experiences with prenatal chromosomal microarray testing. J Genet Couns 2014;23:938-47.
    • (2014) J Genet Couns , vol.23 , pp. 938-947
    • Bernhardt, B.A.1    Kellom, K.2    Barbarese, A.3
  • 11
    • 84875653819 scopus 로고    scopus 로고
    • Prenatal chromosomal microarray analysis: a survey of prenatal genetic counselors' experiences and attitudes
    • Mikhaelian M, Veach PM, MacFarlane I, et al. Prenatal chromosomal microarray analysis: a survey of prenatal genetic counselors' experiences and attitudes. Prenat Diagn 2013;33:371-7.
    • (2013) Prenat Diagn , vol.33 , pp. 371-377
    • Mikhaelian, M.1    Veach, P.M.2    MacFarlane, I.3
  • 12
    • 84940791610 scopus 로고    scopus 로고
    • Comparing genetic counselor's and patient's perceptions of needs in prenatal chromosomal microarray testing
    • Walser SA, Kellom KS, Palmer SC, Bernhardt BA. Comparing genetic counselor's and patient's perceptions of needs in prenatal chromosomal microarray testing. Prenat Diagn 2015;35:870-8.
    • (2015) Prenat Diagn , vol.35 , pp. 870-878
    • Walser, S.A.1    Kellom, K.S.2    Palmer, S.C.3    Bernhardt, B.A.4
  • 13
    • 79954571974 scopus 로고    scopus 로고
    • A systematic literature review of the applications of Q-technique and its methodology
    • Dziopa F, Ahern K. A systematic literature review of the applications of Q-technique and its methodology. Meth: Eur J Res Meth Behav Soc Sci 2011;7:39-55.
    • (2011) Meth: Eur J Res Meth Behav Soc Sci , vol.7 , pp. 39-55
    • Dziopa, F.1    Ahern, K.2
  • 15
    • 84857913732 scopus 로고    scopus 로고
    • Interpretations of informed choice in antenatal screening: a cross-cultural, Q-methodology study
    • Ahmed S, Bryant LD, Tizro Z, Shickle D. Interpretations of informed choice in antenatal screening: a cross-cultural, Q-methodology study. Soc Sci Med 2012;74:997-1004.
    • (2012) Soc Sci Med , vol.74 , pp. 997-1004
    • Ahmed, S.1    Bryant, L.D.2    Tizro, Z.3    Shickle, D.4
  • 16
    • 84857038661 scopus 로고    scopus 로고
    • Non-invasive prenatal genetic testing: a study of public attitudes
    • Kelly SE, Farrimond HR. Non-invasive prenatal genetic testing: a study of public attitudes. Public Health Genomics 2012;15:73-81.
    • (2012) Public Health Genomics , vol.15 , pp. 73-81
    • Kelly, S.E.1    Farrimond, H.R.2
  • 17
    • 84880733682 scopus 로고    scopus 로고
    • Public viewpoints on new non-invasive prenatal genetic tests
    • Farrimond HR, Kelly SE. Public viewpoints on new non-invasive prenatal genetic tests. Publ Understand Sci 2013;22:730-44.
    • (2013) Publ Understand Sci , vol.22 , pp. 730-744
    • Farrimond, H.R.1    Kelly, S.E.2
  • 18
    • 84942295467 scopus 로고    scopus 로고
    • Presenting life with cystic fibrosis: a Q-methodological approach to developing balanced, experience-based prenatal screening information
    • Wright KF, Bryant LD, Morley S, et al. Presenting life with cystic fibrosis: a Q-methodological approach to developing balanced, experience-based prenatal screening information. Health Expect 2015;18(5):1349-62. DOI:10.1111/hex.12113.
    • (2015) Health Expect , vol.18 , Issue.5 , pp. 1349-1362
    • Wright, K.F.1    Bryant, L.D.2    Morley, S.3
  • 19
    • 0002673411 scopus 로고
    • Q methodology
    • In, Smith JA, Harre R, Langenhove LV (eds). SAGE Publication Ltd: London
    • Rogers RS. Q methodology. In Rethinking Methods in Psychology, Smith JA, Harre R, Langenhove LV (eds). SAGE Publication Ltd: London, 1995;178-92.
    • (1995) Rethinking Methods in Psychology , pp. 178-192
    • Rogers, R.S.1
  • 20
    • 84978325397 scopus 로고    scopus 로고
    • EACH study. Available at:[Accessed on 1 December 2015].
    • EACH study. Available at: http://www.nets.nihr.ac.uk/__data/assets/pdf_file/0010/55468/PRO-10-60-03.pdf [Accessed on 1 December 2015].
  • 21
    • 84978319510 scopus 로고    scopus 로고
    • The Joint Committee on Genomics in Medicine (JCGM). Recommendations for the use of chromosome microarray in pregnancy. Available at:[Accessed on January 2016].
    • The Joint Committee on Genomics in Medicine (JCGM). 2015. Recommendations for the use of chromosome microarray in pregnancy. Available at: http://www.bsgm.org.uk/media/956141/g144_useofcmapregnancy_jun15.pdf [Accessed on January 2016].
    • (2015)
  • 22
    • 84978325395 scopus 로고    scopus 로고
    • Genethics Club. Available at:[Accessed on 1 December 2015].
    • Genethics Club. Available at: www.genethicsclub.org [Accessed on 1 December 2015].
  • 23
    • 84873547792 scopus 로고    scopus 로고
    • Women's experiences receiving abnormal prenatal chromosomal microarray testing results
    • Bernhardt BA, Soucier D, Hanson K, et al. Women's experiences receiving abnormal prenatal chromosomal microarray testing results. Genet Med 2012;15:139-45.
    • (2012) Genet Med , vol.15 , pp. 139-145
    • Bernhardt, B.A.1    Soucier, D.2    Hanson, K.3
  • 24
    • 84930389541 scopus 로고    scopus 로고
    • Pregnant couples at increased risk for common aneuploidies choose maximal information from invasive genetic testing
    • Van der Steen S, Diderich K, Riedijk S, et al. Pregnant couples at increased risk for common aneuploidies choose maximal information from invasive genetic testing. Clin Genet 2014;88:25-31.
    • (2014) Clin Genet , vol.88 , pp. 25-31
    • Van der Steen, S.1    Diderich, K.2    Riedijk, S.3
  • 25
    • 81455144813 scopus 로고    scopus 로고
    • Application of SNP array for rapid prenatal diagnosis: implementation, genetic counselling and diagnostic flow
    • Srebniak M, Boter M, Oudesluijs G, et al. Application of SNP array for rapid prenatal diagnosis: implementation, genetic counselling and diagnostic flow. Eur J Hum Genet 2011;19:1230-7.
    • (2011) Eur J Hum Genet , vol.19 , pp. 1230-1237
    • Srebniak, M.1    Boter, M.2    Oudesluijs, G.3
  • 26
    • 84943359380 scopus 로고    scopus 로고
    • Prenatal whole exome sequencing: parental attitudes
    • e-pub ahead of print 17 June 2015
    • Kalynchuk EJ, Althouse A, Parker LS, et al. Prenatal whole exome sequencing: parental attitudes. Prenat Diag 2015; e-pub ahead of print 17 June 2015. DOI:10.1002/pd.4635.
    • (2015) Prenat Diag
    • Kalynchuk, E.J.1    Althouse, A.2    Parker, L.S.3
  • 27
    • 84879463781 scopus 로고    scopus 로고
    • "If it helps..." the use of microarray technology in prenatal testing: patient and partners reflections
    • Hillman SC, Skelton J, Quinlan-Jones E, et al. "If it helps..." the use of microarray technology in prenatal testing: patient and partners reflections. Am J Med Genet A 2013;161:1619-27.
    • (2013) Am J Med Genet A , vol.161 , pp. 1619-1627
    • Hillman, S.C.1    Skelton, J.2    Quinlan-Jones, E.3
  • 29
    • 84893182999 scopus 로고    scopus 로고
    • Committee Opinion No. 581: the use of chromosomal microarray analysis in prenatal diagnosis
    • Genetics ACoOaGCo. Committee Opinion No. 581: the use of chromosomal microarray analysis in prenatal diagnosis. Obstet Gynecol 2013;122:1374-7.
    • (2013) Obstet Gynecol , vol.122 , pp. 1374-1377
  • 30
    • 84859358210 scopus 로고    scopus 로고
    • Microarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011
    • Novelli A, Grati F, Ballarati L, et al. Microarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011. Ultrasound Obstet Gynecol 2012;39:384-8.
    • (2012) Ultrasound Obstet Gynecol , vol.39 , pp. 384-388
    • Novelli, A.1    Grati, F.2    Ballarati, L.3
  • 31
    • 84860440226 scopus 로고    scopus 로고
    • Re: Microarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011
    • Fiorentino F, Baldi M. Re: Microarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011. Ultrasound Obstet Gynecol 2012;39:601-2.
    • (2012) Ultrasound Obstet Gynecol , vol.39 , pp. 601-602
    • Fiorentino, F.1    Baldi, M.2
  • 32
    • 84879422370 scopus 로고    scopus 로고
    • Chromosomal microarray analysis as a first-line test in pregnancies with a priori low risk for the detection of submicroscopic chromosomal abnormalities
    • Fiorentino F, Napoletano S, Caiazzo F, et al. Chromosomal microarray analysis as a first-line test in pregnancies with a priori low risk for the detection of submicroscopic chromosomal abnormalities. Eur J Hum Genet 2012;21:725-30.
    • (2012) Eur J Hum Genet , vol.21 , pp. 725-730
    • Fiorentino, F.1    Napoletano, S.2    Caiazzo, F.3
  • 33
    • 84862118837 scopus 로고    scopus 로고
    • Noninvasive whole-genome sequencing of a human fetus
    • 137ra76.
    • Kitzman JO, Snyder MW, Ventura M, et al. Noninvasive whole-genome sequencing of a human fetus. Sci Trans Med 2012;4:137ra76.
    • (2012) Sci Trans Med , vol.4
    • Kitzman, J.O.1    Snyder, M.W.2    Ventura, M.3
  • 34
    • 84873711791 scopus 로고    scopus 로고
    • Noninvasive detection of fetal subchromosome abnormalities via deep sequencing of maternal plasma
    • Srinivasan A, Bianchi DW, Huang H, et al. Noninvasive detection of fetal subchromosome abnormalities via deep sequencing of maternal plasma. Am J Hum Genet 2013;92:167-76.
    • (2013) Am J Hum Genet , vol.92 , pp. 167-176
    • Srinivasan, A.1    Bianchi, D.W.2    Huang, H.3
  • 35
    • 85027922912 scopus 로고    scopus 로고
    • Attitudes of pregnant women and male partners towards non-invasive prenatal testing and widening the scope of prenatal screening
    • van Schendel RV, Kleinveld JH, Dondorp WJ, et al. Attitudes of pregnant women and male partners towards non-invasive prenatal testing and widening the scope of prenatal screening. Eur J Hum Genet 2014;22:1345-50.
    • (2014) Eur J Hum Genet , vol.22 , pp. 1345-1350
    • van Schendel, R.V.1    Kleinveld, J.H.2    Dondorp, W.J.3
  • 36
    • 77952087607 scopus 로고    scopus 로고
    • A toolkit for incorporating genetics into mainstream medical services: learning from service development pilots in England
    • Bennett CL, Burke SE, Burton H, Farndon PA. A toolkit for incorporating genetics into mainstream medical services: learning from service development pilots in England. BMC Health Serv Res 2010;10:125.
    • (2010) BMC Health Serv Res , vol.10 , pp. 125
    • Bennett, C.L.1    Burke, S.E.2    Burton, H.3    Farndon, P.A.4
  • 37
    • 84865195385 scopus 로고    scopus 로고
    • The introduction of arrays in prenatal diagnosis: a special challenge
    • Vetro A, Bouman K, Hastings R, et al. The introduction of arrays in prenatal diagnosis: a special challenge. Hum Mutat 2012;33:923-9.
    • (2012) Hum Mutat , vol.33 , pp. 923-929
    • Vetro, A.1    Bouman, K.2    Hastings, R.3
  • 38
    • 84876566173 scopus 로고    scopus 로고
    • Prenatal diagnosis using combined quantitative fluorescent polymerase chain reaction and array comparative genomic hybridization analysis as a first-line test: results from over 1000 consecutive cases
    • Scott F, Murphy K, Carey L, et al. Prenatal diagnosis using combined quantitative fluorescent polymerase chain reaction and array comparative genomic hybridization analysis as a first-line test: results from over 1000 consecutive cases. Ultrasound Obstet Gynecol 2013;41:500-7.
    • (2013) Ultrasound Obstet Gynecol , vol.41 , pp. 500-507
    • Scott, F.1    Murphy, K.2    Carey, L.3


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