59 articles – 21 Notices  [english version]
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Information for patients undergoing a prenatal diagnosis.
Alouini S., Moutel G., Venslauskaite G., Gaillard M., Truc J.-B., Hervé C.
European Journal of Obstetrics & Gynecology and Reproductive Biology / European Journal of Obstetrics and Gynaecology and Reproductive Biology 134, 1 (2007) 9-14 - http://www.hal.inserm.fr/inserm-00255875
(17045386)
Information for patients undergoing a prenatal diagnosis.
Souhail Alouini1, Grégoire Moutel1, Goda Venslauskaite2, Martine Gaillard1, Jean-Bernard Truc3, Christian Hervé1
1 :  LEM - Laboratoire d'éthique médicale et médecine légale
Université Paris V - Paris Descartes
Faculté de médecine, 45 rue des Saints-Pères, Paris 75006
France
2 :  Department of Philosophy
Vilnius University
Lituanie
3 :  Service de Gynècologie-Obstetrique
Hôpital Lariboisière – Assistance publique - Hôpitaux de Paris (AP-HP)
2 rue Ambroise Paré 75010 Paris
France
OBJECTIVES: Lack of information is a frequent complaint with regard to physicians dealing with prenatal diagnosis (PD). The aim of the study was to find out how information on PD was perceived by patients and if they considered that they had been correctly informed by their physicians. METHODS: We conducted a prospective study in Lariboisi? Hospital (Paris) with 86 patients undergoing prenatal diagnosis between 2001 and 2003. A 23-item questionnaire was given to patients after delivery or termination of pregnancy (TP). RESULTS: Fifty patients out of 86 answered the questionnaire. Twelve patients out of 50 underwent a TP. Information on foetal anomaly was insufficient for 11 patients out of 50 (22%). Some patients found the information too technical; others would like to see photos to illustrate the anomalies and the possible surgical repairs to be performed. Information was insufficient for one in four patients concerning maternal serum screening for Down's syndrome. Information before amniocentesis was considered sufficient by 9 out of 10 patients. Information on the risks of TP was not given or not understood by 10 out of 12 patients. CONCLUSION: Information on prenatal diagnosis could be improved by using simple and accessible language, supported by written documents and photos for certain anomalies. More information should be given in cases of abstract anomalies and should be adapted to the social, ethnic and cultural background of the patient.
Sciences du Vivant/Ethique
Anglais
0301-2115

Articles dans des revues avec comité de lecture
10.1016/j.ejogrb.2006.07.056
European Journal of Obstetrics & Gynecology and Reproductive Biology / European Journal of Obstetrics and Gynaecology and Reproductive Biology
internationale
09/2007
11/10/2006
134
1
9-14

Abortion – Therapeutic – Emigrants and Immigrants – Female – Genetic Counseling – Health Knowledge – Attitudes – Practice – Hospitals – University – Humans – Paris – Patient Education as Topic – Physician-Patient Relations – Pregnancy – Prenatal Diagnosis – Prospective Studies