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The Reconfiguration of the Relationship to Care for a Rare Disease ; The Reconfiguration of the Relationship to Care for a Rare Disease: Neonatal Expended Screening in a Socio-material Perspective

Title: The Reconfiguration of the Relationship to Care for a Rare Disease ; The Reconfiguration of the Relationship to Care for a Rare Disease: Neonatal Expended Screening in a Socio-material Perspective
Authors: Langeard, Chloé; Minguet, Guy; Gueganton, Laetitia; Cam, Pierre; Faquet, Christine; Lombrail, Pierre; Rault, Gilles
Contributors: Groupe de Recherche Angevin en Economie et Management (GRANEM); Université d'Angers (UA)-AGROCAMPUS OUEST-Institut National de l'Horticulture et du Paysage; Laboratoire d'économie et de management de Nantes Atlantique (LEMNA); Institut d'Économie et de Management de Nantes - Institut d'Administration des Entreprises - Nantes (IEMN-IAE Nantes); Université de Nantes (UN)-Université de Nantes (UN); Centre de Ressources et de Compétences de la Mucoviscidose (CRCM); Centre de Perharidy-Cellule de Coordination du Réseau Mucoviscidose (CECOREM)
Source: ISSN: 0971-7218 ; Science Technology and Society ; https://imt-atlantique.hal.science/hal-01371528 ; Science Technology and Society, 2013, 18 (1), pp.115-138. ⟨10.1177/0971721813484382⟩.
Publisher Information: CCSD; SAGE Publications
Publication Year: 2013
Collection: Université de Nantes: HAL-UNIV-NANTES
Subject Terms: Neonatal Expended Screening; [SHS.SOCIO]Humanities and Social Sciences/Sociology; [SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie; [SDV.ETH]Life Sciences [q-bio]/Ethics
Description: International audience ; Neonatal Screening (NBS) is a mass screening, secondary prevention policy aimed at detecting one or several often congenital disorders in all neonates in a given country. The French CF NBS programme is completely functional since the middle of 2003. Drawing its inspiration from the socio-material approach, this article advances a description and analysis of the interactions between the biomedical technologies used in neonatal cystic fibrosis screening and the resulting changes in clinical practice, the bioethical debate and finally in the interstice between voluntary individual consent to screening and the management of a population’s health. The analysis grid focuses on four dimensions: institutional, techno-scientific, regulatory and socio-professional. Backed up by a field survey conducted in the specialised healthcare centres, this study explores two major aspects of the repercussions of NBS: first, the genesis and institutionalisation of this public policy and the impact of a more flexible form of Evidence Based Medicine (EBM) and the sustained controversy on the neonatal screening programme uniting the community of cystic fibrosis paediatrics. This study suggests that institutional stability remains fragile and in this respect constitutes a paradoxical form of production with incompleteness and uncertainty as constituting factors.
Document Type: article in journal/newspaper
Language: English
DOI: 10.1177/0971721813484382
Availability: https://imt-atlantique.hal.science/hal-01371528; https://imt-atlantique.hal.science/hal-01371528v1/document; https://imt-atlantique.hal.science/hal-01371528v1/file/SST_special_issue__Gm_CL_V2_5mars.pdf; https://doi.org/10.1177/0971721813484382
Rights: info:eu-repo/semantics/OpenAccess
Accession Number: edsbas.8A450A67
Database: BASE