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OBJECTIVES: To describe women's information needs prior to genetic counselling for familial breast or ovarian cancer. DESIGN: Prospective study including semistructured telephone interviews before genetic counselling, observations of consultations, completion of postal questionnaires, and face-to face interviews within two months of counselling. SUBJECTS: 46 women attending genetic counselling for familial breast or ovarian cancer. MAIN OUTCOME MEASURES: Subjects' understanding of process and content of genetic counselling before attending and attitudes about their preparation for the counselling session. RESULTS: Although all women interviewed before the clinic expected to discuss their risk of developing cancer and risk management options, there was evidence of a lack of knowledge about the process and content of genetic counselling, 17 (37%) women said they did not know what else would happen. Most women interviewed after counselling viewed it positively, but 26 (65%) felt they had been inadequately prepared and 11 (28%) felt that their lack of preparation meant that they could not be given an accurate estimation of their risk of cancer. CONCLUSIONS: Some women felt that they did not obtain optimum benefit from genetic counselling because they were inadequately prepared for it. We suggest that cancer family history clinics should provide women with written information about the process and content of genetic counselling before their clinic attendance.

Original publication

DOI

10.1136/bmj.314.7076.281

Type

Journal article

Journal

BMJ

Publication Date

25/01/1997

Volume

314

Pages

281 - 283

Keywords

Empirical Approach, Genetics and Reproduction, Adult, Attitude to Health, Breast Neoplasms, Communication, Comprehension, England, Female, Genetic Counseling, Health Services Needs and Demand, Humans, Medical Informatics, Middle Aged, Ovarian Neoplasms, Patient Education as Topic, Patient Satisfaction, Prospective Studies, Surveys and Questionnaires