Ethical issues in cancer register follow-up of hormone treatment in adolescence
M. Hultman Christina, Mats Ann-Christin Lindgren, Jan Carlstedt-Duke G. Hansson, Ingemar Persson Martin Ritzen & Helle Kieler
Public Health Ethics 2 (1) (2009)
| Abstract | Karolinska Institutet, Stockholm, Sweden Mats G. Hansson Uppsala University, Sweden Jan Carlstedt-Duke Karolinska Institutet, Stockholm, Sweden Martin Ritzen Karolinska Institutet, Stockholm, Sweden Ingemar Persson Karolinska Institutet, Stockholm, Sweden Helle Kieler Karolinska Institutet, Stockholm, Sweden * Corresponding author: Christina M. Hultman, Department of Medical Epidemiology and Biostatistics, Box 281, SE-171 77 Stockholm, Sweden. Tel.: +46 8 52483893; +46 70 3621031; Fax: +46 8 314975; Email: Christina.Hultman{at}ki.se ' + u + '@' + d + ' '//--> Abstract Since the 1970s, estrogen have sometimes been used in adolescent girls to reduce very tall adult expected height. Worries about long-term effects have led to a proposal to link treatment data with cancer registers. How should one deal with informed consent for such a study? We designed a qualitative study with semi-structured telephone interviews. From 1200 women who were to be followed-up in cancer registers, we randomly selected 22 women. Major themes were a wish to be involved and a positive attitude to the proposed register research. The women did not express worry after reading the study protocol, but did convey considerable frustration that this research had not been initiated earlier. Active consent was not seen as crucial. We found strong interest in a high participation rate and a concern over missing data. The selection of information and consent or the decision to go ahead without consent in register follow-up is a delicate balancing act. Study participants wish to be contacted, but acknowledge the primary goal of answering important questions. Our study provides support for safeguarding privacy in epidemiological linkage studies and in follow-up of medical treatment without losing the scientific value by requesting for informed consent. CiteULike Connotea Del.icio.us What's this? | |||||||||
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Roy Gilbar & Ora Gilbar (2009). The Medical Decision-Making Process and the Family: The Case of Breast Cancer Patients and Their Husbands. Bioethics 23 (3):183-192.
James R. P. Ogloff & Randy K. Otto (1991). Are Research Participants Truly Informed? Readability of Informed Consent Forms Used in Research. Ethics and Behavior 1 (4):239 – 252.
K. W. Arafat (1999). C. G ILLIS , B. W ELLS , G. N ORDQUIST , M. F RISELL , M. E LLIOTT : Corpus Vasorum Antiquorum: Sweden, 4: Medelhavsmuseet and Nationalmuseum, Stockholm, 2 . Pp. 88, 220 Figs, 35 Pls. Stockholm: Kungl. Vitterhets Historie Och Antikvitets Akademien, 1995. SEK 260. ISBN: 91-7402-254-. [REVIEW] The Classical Review 49 (01):298-.
Howard B. Degenholtz, Lisa S. Parker & Charles F. Reynolds (2002). Trial Design and Informed Consent for a Clinic-Based Study with a Treatment as Usual Control Arm. Ethics and Behavior 12 (1):43 – 62.
Jerry Menikoff (2006). What the Doctor Didn't Say: The Hidden Truth About Medical Research. Oxford University Press.
Christian Munthe, Susanna Radovic & Henrik Anckarsäter (2010). Ethical Issues in Forensic Psychiatric Research on Mentally Disordered Offenders. Bioethics 24 (1):35-44.
M. P. M. Richards (2003). Issues of Consent and Feedback in a Genetic Epidemiological Study of Women with Breast Cancer. Journal of Medical Ethics 29 (2):93-96.
Edward Wilson Grandin Rajiv Sarkar, Jayaprakash Muliyil Beryl Primrose Gladstone & Gagandeep Kang (2009). Comprehension and Recall of Informed Consent Among Participating Families in a Birth Cohort Study on Diarrhoeal Disease. Public Health Ethics 2 (1).
C. M. Hultman, A. -C. Lindgren, M. G. Hansson, J. Carlstedt-Duke, M. Ritzen, I. Persson & H. Kieler (2009). Ethical Issues in Cancer Register Follow-Up of Hormone Treatment in Adolescence. Public Health Ethics 2 (1):30-36.
Michelle H. Biros (2007). Research Without Consent: Exception From and Waiver of Informed Consent in Resuscitation Research. Science and Engineering Ethics 13 (3).
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