Bioethics and Informed Consent in Prenatal Diagnostics

dc.contributor.authorSerapinas, Danielius
dc.contributor.authorNarbekovas, Andrius
dc.date.accessioned2024-12-03T13:31:40Z
dc.date.available2024-12-03T13:31:40Z
dc.date.issued2023
dc.description.abstractInnovative methods of prenatal diagnosis allow us to see the development of the fetus and to detect early disorders of fetal development, which may lead to an early diagnosis and possible treatment, or to a woman’s decision to terminate the pregnancy. Therefore, it is very important to accurately inform a woman about the risks and consequences of this life-related issue, even before deciding to perform prenatal tests; and after the results, when a misinterpreted diagnosis may lead a woman to terminate her pregnancy. The obligation of d octors to i nform patients is inseparable from the requirement to receive informed consent. The two parts are mandatory for any medical procedure and intervention. The main requirements for the informed consent include rationality, sufficient and clear information, free will, and the form of consent conforming to the legal acts. However, informed consent is not an absolute requirement, as the patient has a right to remain uninformed. Additionally, under certain circumstances, it might be impossible to inform patients, or to receive consent from patients or their duly authorized representatives. Prenatal testing is an integral part of ante-natal care that aims to verify the proper development of the fetus, or to identify potential hereditary or chromosomal diseases at the earliest possible stage. Prenatal testing can be classified as noninvasive or invasive measures, according to the types of procedures In addition to this, according to the aim of the procedure, into diagnostic prenatal testing with the aim of prenatal therapy, and purely diagnostic prenatal testing. Purely diagnostic prenatal testing is closely connected with the problem of selective abortion. Part of this article covers the main problems of informed consent in prenatal diagnostics, by outlining two stages of the process: conveyance before prenatal testing, and interpretation of the results alongside presentation of the possible choices. The legal implications we consider are based on information from other European countries: we name the main questions analyzed by courts, including cases of “wrongful birth” and “wrongful life”; inappropriate information regarding possibilities of abortion; the right of a woman to use all available diagnostic methods; and the allocation of damages to the claimants.
dc.identifier.citationThe Person and the Challenges, 2023, Vol. 13, No. 1, p. 97-113.
dc.identifier.issn2083-8018
dc.identifier.urihttps://theo-logos.pl/handle/123456789/24891
dc.language.isoen
dc.publisherThe Pontifical University of John Paul II in Cracow
dc.rightsCC-BY-NC-ND - Uznanie autorstwa - Użycie niekomercyjne - Bez utworów zależnych
dc.subjectinformed consent
dc.subjectethics
dc.subjectbioethics
dc.subjectchromosomal anomalies
dc.subjectprenatal diagnostics
dc.subjectmedicine
dc.subjectmedical ethics
dc.subjectświadoma zgoda
dc.subjectetyka
dc.subjectbioetyka
dc.subjectanomalie chromosomalne
dc.subjectdiagnostyka prenatalna
dc.subjectmedycyna
dc.subjectetyka lekarska
dc.subjectetyka medyczna
dc.titleBioethics and Informed Consent in Prenatal Diagnostics
dc.typeArticle

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