Modes of risk explanation in telephone consultations between nurses and parents for a genetic condition

Health, Risk and Society

Volumn 15, Issue 2, 2013, Pages 194-215

  Zayts, Olga ^a   Sarangi, Srikant ^b  

^a UNIVERSITY OF HONG KONG   (Hong Kong)

^b CARDIFF UNIVERSITY   (United Kingdom)

Author keywords

advice giving; G6PD deficiency; Hong Kong; nurse parent interactions; reassurance; risk; risk explanations; telephone consultations

Indexed keywords

BILIRUBIN;

ARTICLE; AUDIO RECORDING; FAVISM; FEMALE; GENETIC RISK; GENETICS; GLUCOSE 6 PHOSPHATE DEHYDROGENASE DEFICIENCY; HEMOLYSIS; HUMAN; JAUNDICE; NURSE; PARENT; PHYSIOLOGY; QUESTIONNAIRE; RISK EXPLANATION; SEMI STRUCTURED INTERVIEW; TELECONSULTATION;

EID: 84876339988     PISSN: 13698575     EISSN: 14698331     Source Type: Journal    
DOI: 10.1080/13698575.2013.764975     Document Type: Article

References (27)

1. Adelswärd, V. and Sachs, L. 1996. The meaning of 6.8: numeracy and normality in health information talks. Social science and medicine, 43 (8): 1179-1187.
2. Adelswärd, V. and Sachs, L. 1998. Risk discourse: recontextualization of numerical values in clinical practice. Text, 18 (2): 191-210.
3. Arribas-Ayllon, M., Sarangi, S. and Clarke, A. 2008. Managing self-responsibility through other-oriented blame: family accounts of genetic testing. Social science and medicine, 66 (7): 1521-1532.
4. Clarke, A., Sarangi, S. and Verrier-Jones, K. 2011. Voicing the lifeworld: parental accounts of responsibility in genetic consultations for polycystic kidney disease. Social science and medicine, 72: 1743-1751.
5. Etchegary, H. and Perrier, C. 2007. Information processing in the context of genetic risk: implications for genetic-risk communication. Journal of genetic counseling, 16 (4): 419-432.
6. Farhud, D. and Yazdanpanah, L. 2008. Glucose-6-phosphate dehydrogenase (G6PD) deficiency. Iranian journal of public health, 37 (4): 1-18.
7. Henneman, L., Marteau, T.M. and Timmermans, D.R.M. 2008. Clinical geneticists' and genetic counselors' view on the communication of genetic risk: a qualitative study. Patient education and counseling, 73: 42-49.
8. Heyman, B. 2010. Editorial. Screening for health risks: a social science perspective. Health, risk and society, 12 (1): 1-6.
9. Lam, S.T. and Cheng, M.L. 2003. Neonatal screening in Hong Kong and Macau. Southeast Asian Journal of Tropical Medicine and Public Health, 34 (3): 73-75.
10. Li, K.C., Lai, S.S. and Lam, S.T. 1999. Adequacy and pitfalls of G6PD deficiency counseling in Hong Kong. Southeast Asian Journal of Tropical Medicine and Public Health, 30 (2): 79-83.
11. Marteau, T.M., Dormandy, E. and Michie, S. 2001. A measure of informed choice. Health expectations, 4: 99-108.
12. Peräkylä, A. 1995. AIDS Counselling: Institutional interaction and clinical practice, Cambridge: Cambridge University Press.
13. Roberts, C. and Sarangi, S. 2005. Theme-oriented discourse analysis of medical encounters. Medical education, 39 (6): 632-640.
14. Sarangi, S. 2000. " Activity types, discourse types and interactional hybridity: the case of genetic counseling ". In Discourse and social life, Edited by: Sarangi, S. and Coulthard, M. 1-27. London: Pearson.
15. Sarangi, S. 2002. The language of likelihood in genetic counseling discourse. Journal of language and social psychology, 21 (1): 7-31.
16. Sarangi, S. 2006. " Genetic counselling communication: a discourse analytic approach ". In Encyclopaedia of life sciences, Edited by: Cooper, D.N. 1-6. Oxford: Wiley.
17. Sarangi, S. 2007. " Other-orientation in patient-centred healthcare communication: unveiled ideology or discoursal ecology? ". In Discourse, ideology and specialised communication, Edited by: Garzone, G. and Sarangi, S. 39-71. Berne: Peter Lang.
18. Sarangi, S. 2010. " Practising discourse analysis in healthcare settings ". In The SAGE handbook of qualitative methods in health research, Edited by: Bourgeault, I., DeVries, R. and Dingwall, R. 397-416. London: Sage.
19. Sarangi, S. 2003a. Relatively speaking': relativisation of genetic risk in counseling for predictive testing. Health, risk & society, 5 (2): 155-170.
20. Sarangi, S. 2003b. " Categorisation practices across professional boundaries: some analytic insights from genetic counselling ". In Applied linguistics and communities of practice, Edited by: Sarangi, S. and van Leeuwen, T. 150-168. London: Continuum.
21. Sarangi, S. and Clarke, A. 2002a. Constructing an account by contrast in counselling for childhood testing. Social science and medicine, 54: 295-308.
22. Sarangi, S. and Clarke, A. 2002b. Zones of expertise and the management of uncertainty in genetics risk communication. Research on language and social interaction, 35 (2): 139-171.
23. Sarangi, S. 2004. Initiation of reflective frames in counselling for Huntington's Disease predictive testing. Journal of genetic counselling, 13 (2): 135-155.
24. Sarangi, S. 2005. (Mis)alignments in counseling for Huntington's Disease predictive testing: clients' responses to reflective frames. Journal of genetic counseling, 14 (1): 29-42.
25. Sivell, T. 2008. How risk is perceived, constructed, and interpreted by clients in clinical genetics, and the effects on decision making: systematic review. Journal of genetic counseling, 17: 30-63.
26. Thomassen, G. and Sarangi, S. 2012. Evidence-based familial risk explanations in cancer genetic counselling. Health, risk and society, 14 (7-8): 607-626.
27. Thomson, R., Edwards, A. and Grey, J. 2005. Risk in the clinical consultation. Clinical Medicine, 5: 465-469.