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  • 1
    Online Resource
    Online Resource
    John Libbey Eurotext ; 2000
    In:  Sciences sociales et santé Vol. 18, No. 2 ( 2000), p. 11-42
    In: Sciences sociales et santé, John Libbey Eurotext, Vol. 18, No. 2 ( 2000), p. 11-42
    Abstract: Le nouveau concept de biomédicalisation retient de la théorie initiale de la médicalisation cette particularité d'étendre les juridictions professionnelles, mais son modus operandi passe par des innovations que les technosciences construisent et organisent et qui ne se contentent pas d'ajouter à ce qui existe, mais le transforment. Nous exposerons dans ce texte les pivots conceptuels de cette transformation et les éléments-clefs de la théorie de la nouvelle biomédicalisation : risque et surveillance, technoscientifisation de la biomédecine, transformations de la production des connaissances et de la gestion et distribution de l'information, transformations des corps, constitution politique et économique du Complexe biomédical de technoservices™, Inc. En conclusion, nous réfléchirons à la mondialisation rhizomique de la nouvelle biomédecine et de la nouvelle biomédicalisation.
    Type of Medium: Online Resource
    ISSN: 0294-0337
    Language: French
    Publisher: John Libbey Eurotext
    Publication Date: 2000
    detail.hit.zdb_id: 2178377-9
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  • 2
    Online Resource
    Online Resource
    SAGE Publications ; 2003
    In:  American Sociological Review Vol. 68, No. 2 ( 2003-04), p. 161-
    In: American Sociological Review, SAGE Publications, Vol. 68, No. 2 ( 2003-04), p. 161-
    Type of Medium: Online Resource
    ISSN: 0003-1224
    RVK:
    Language: Unknown
    Publisher: SAGE Publications
    Publication Date: 2003
    detail.hit.zdb_id: 203405-0
    detail.hit.zdb_id: 2010058-9
    SSG: 2,1
    SSG: 3,4
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  • 3
    Online Resource
    Online Resource
    SAGE Publications ; 2003
    In:  American Sociological Review Vol. 68, No. 2 ( 2003-04), p. 161-194
    In: American Sociological Review, SAGE Publications, Vol. 68, No. 2 ( 2003-04), p. 161-194
    Abstract: The first social transformation of American medicine institutionally established medicine by the end of World War II. In the next decades, medicalization—the expansion of medical jurisdiction, authority, and practices into new realms—became widespread. Since about 1985, dramatic changes in both the organization and practices of contemporary biomedicine, implemented largely through the integration of technoscientific innovations, have been coalescing into what the authors call biomedicalization, a second “transformation “ of American medicine. Biomedicalization describes the increasingly complex, multisited, multidirectional processes of medicalization, both extended and reconstituted through the new social forms of highly technoscientific biomedicine. The historical shift from medicalization to biomedicalization is one from control over biomedical phenomena to transformations of them. Five key interactive processes both engender biomedicalization and are produced through it: (1) the political economic reconstitution of the vast sector of biomedicine; (2) the focus on health itself and the elaboration of risk and surveillance biomedicines; (3) the increasingly technological and scientific nature of biomedicine; (4) transformations in how biomedical knowledges are produced, distributed, and consumed, and in medical information management; and (5) transformations of bodies to include new properties and the production of new individual and collective technoscientific identities.
    Type of Medium: Online Resource
    ISSN: 0003-1224 , 1939-8271
    RVK:
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2003
    detail.hit.zdb_id: 203405-0
    detail.hit.zdb_id: 2010058-9
    SSG: 2,1
    SSG: 3,4
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  • 4
    Online Resource
    Online Resource
    Informa UK Limited ; 2002
    In:  Women & Therapy Vol. 24, No. 1-2 ( 2002-03-05), p. 179-193
    In: Women & Therapy, Informa UK Limited, Vol. 24, No. 1-2 ( 2002-03-05), p. 179-193
    Type of Medium: Online Resource
    ISSN: 0270-3149 , 1541-0315
    Language: English
    Publisher: Informa UK Limited
    Publication Date: 2002
    detail.hit.zdb_id: 2068122-7
    SSG: 5,2
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  • 5
    Online Resource
    Online Resource
    SAGE Publications ; 2004
    In:  Social Studies of Science Vol. 34, No. 2 ( 2004-04), p. 187-218
    In: Social Studies of Science, SAGE Publications, Vol. 34, No. 2 ( 2004-04), p. 187-218
    Abstract: The process of bringing new drugs to market interweaves commercialism, science, clinical medicine, and governmental regulation. Through their authority and public persona as medical experts, academic clinical trial researchers studying these pharmaceuticals are integral to this process, serving as mediators between producers (the pharmaceutical companies) and consumers (clinicians and patients) of new drugs through a complex set of exchange networks. Using examples from my ethnographic research on the search for pharmaceuticals to treat what has become known as female sexual dysfunction, this paper explores the links academic researchers make with drug manufacturers and consumer markets. Academic researchers have become an integral aspect of drug development, not only by conducting clinical trial research, but also by participating in a number of other activities that assist pharmaceutical companies in identifying and creating new markets. In this paper, I examine how researchers attend professional meetings where they present clinical trial data, lecture at continuing medical education conferences, and offer themselves as ‘experts’ to raise awareness about disorders and their treatments. Modifying a sociology of technology approach, this paper focuses on the actors in the social network who mediate the junctions between technological producers and consumers. This extends work in this area through theorizing the linkages between exchange networks, commodification techniques, and technoscientific developments.
    Type of Medium: Online Resource
    ISSN: 0306-3127 , 1460-3659
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2004
    detail.hit.zdb_id: 1482712-8
    SSG: 11
    SSG: 3,4
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  • 6
    Online Resource
    Online Resource
    Elsevier BV ; 2008
    In:  Journal of Aging Studies Vol. 22, No. 4 ( 2008-12), p. 295-303
    In: Journal of Aging Studies, Elsevier BV, Vol. 22, No. 4 ( 2008-12), p. 295-303
    Type of Medium: Online Resource
    ISSN: 0890-4065
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2008
    detail.hit.zdb_id: 2006012-9
    SSG: 3,4
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  • 7
    Online Resource
    Online Resource
    SAGE Publications ; 2000
    In:  Nursing Ethics Vol. 7, No. 3 ( 2000-05), p. 237-249
    In: Nursing Ethics, SAGE Publications, Vol. 7, No. 3 ( 2000-05), p. 237-249
    Abstract: The purpose of this article is to provide a critical examination of two aspects of culture and biomedicine that have helped to shape the meaning and practice of genetic testing for breast cancer. These are: (1) the cultural construction of fear of breast cancer, which has been fuelled in part by (2) the predominance of a ‘risk’ paradigm in contemporary biomedicine. The increasing elaboration and delineation of risk factors and risk numbers are in part intended to help women to contend with their fear of breast cancer. However, because there is no known cure or foolproof prevention for breast cancer, risk designations bring with them recommendations for vigilant surveillance strategies and screening guidelines. We argue that these in effect exacerbate women’s fears of breast cancer itself. The volatile combination of discourses of fear, risk and surveillance have significant ethical and social consequences for women’s lives and well-being. Genetic testing decisions are made within this context; if nurses understand this context they can play an important role in helping women to cope with the anxiety and fear of breast cancer risk.
    Type of Medium: Online Resource
    ISSN: 0969-7330 , 1477-0989
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2000
    detail.hit.zdb_id: 2031461-9
    SSG: 0
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  • 8
    In: Journal of Clinical Oncology, American Society of Clinical Oncology (ASCO), Vol. 41, No. 16_suppl ( 2023-06-01), p. 3037-3037
    Abstract: 3037 Background: Less than 20% of cancers are diagnosed as a result of standard-of-care (SOC) screening in the US. MCED tests may expand screening to more cancers, but the long-term outcomes of MCED test-detected cancers are unknown. DETECT-A was the first large prospective interventional clinical trial to evaluate an MCED blood test. The test used was an early version of CancerSEEK and was evaluated in 9,911 women without history of cancer ( Science 369:6499, 2020). CancerSEEK, coupled with diagnostic PET-CT, safely identified cancers including those not detected by SOC screening, the majority of which were localized or regional. This follow-up observational study evaluated longitudinal clinical outcomes of cancers diagnosed as a result of an abnormal CancerSEEK test with a median follow up of 4.4 (IQR:4.1-4.6) years from initial CancerSEEK testing. Methods: Nine cancer types were diagnosed in 26 participants whose cancers were first detected by CancerSEEK. Information on cancer diagnosis, treatment, treatment response, remission status, recurrence, secondary cancer diagnoses, and mortality (cancer-related and all-cause) was extracted from electronic medical records through November 2022. Data collection for living participants took place a median of 3.7 years following cancer diagnosis (IQR: 3.3-3.9) and a median of 4.3 years (IQR: 4.1-4.7) following initial CancerSEEK screen. Results: Fourteen (53.8%) participants underwent surgery; 5 had surgery alone, 9 had surgery with adjuvant and/or neoadjuvant chemotherapy, radiation, or hormone therapy. Twelve of 14 (85.7%) surgically treated participants were in remission as of November 2022, including 10 with localized or regional disease at diagnosis. Among patients whose treatment was non-surgical (11) or unknown (1), 1 (8.3%) was in remission (stage I at diagnosis), 9 (75.0%) were deceased (all stage III or IV at diagnosis), and 2 (16.7%) were in surveillance or ongoing treatment (stage II and stage III at diagnosis). Overall, 13 of 26 (50%) participants were in remission [ovarian (4), thyroid (1), uterus (2), breast (1), colorectal (2), and lung (3)] ; 7 of these 13 (54%) had cancers without recommended SOC screening modalities. Eleven of 17 (64.7%) participants with localized or regional disease (stage I, II, or III) were in remission, whereas 2 of 9 (22.2%) with stage IV disease at diagnosis were in remission. Conclusions: CancerSEEK detected cancers earlier in patients who, when treated subsequently with conventional methods, achieved long-term survival. Half of all patients with a CancerSEEK-detected cancer remain cancer-free after treatment 〉 4 years (median) after their initial CancerSEEK test. This includes 7 patients with cancer types for which no SOC screening option exists. Additional biomarkers, new analytic methods and algorithms are being incorporated in the development of the next generation of the MCED test.
    Type of Medium: Online Resource
    ISSN: 0732-183X , 1527-7755
    RVK:
    RVK:
    Language: English
    Publisher: American Society of Clinical Oncology (ASCO)
    Publication Date: 2023
    detail.hit.zdb_id: 2005181-5
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  • 9
    Online Resource
    Online Resource
    Mary Ann Liebert Inc ; 2006
    In:  Rejuvenation Research Vol. 9, No. 4 ( 2006-12), p. 433-435
    In: Rejuvenation Research, Mary Ann Liebert Inc, Vol. 9, No. 4 ( 2006-12), p. 433-435
    Type of Medium: Online Resource
    ISSN: 1549-1684 , 1557-8577
    Language: English
    Publisher: Mary Ann Liebert Inc
    Publication Date: 2006
    detail.hit.zdb_id: 2155984-3
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  • 10
    Online Resource
    Online Resource
    Informa UK Limited ; 2017
    In:  The American Journal of Bioethics Vol. 17, No. 1 ( 2017-01-02), p. 45-60
    In: The American Journal of Bioethics, Informa UK Limited, Vol. 17, No. 1 ( 2017-01-02), p. 45-60
    Type of Medium: Online Resource
    ISSN: 1526-5161 , 1536-0075
    RVK:
    Language: English
    Publisher: Informa UK Limited
    Publication Date: 2017
    detail.hit.zdb_id: 2035206-2
    SSG: 12
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