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1.
Organ Stud ; 44(9): 1439-1464, 2023 Sep.
Article de Anglais | MEDLINE | ID: mdl-37671086

RÉSUMÉ

We examine how actors engage in temporal self-discipline so as to achieve entrainment of a practice to temporal norms. Temporal self-discipline is about imposing self-created temporal structures on one's future behaviour and goes along with the (re-)production of a time-conscious self. Based on our fieldwork, we show how such self-discipline materializes both in the form of a very detailed temporal plan and in spaces for coordination to ensure sticking to this plan. We demonstrate that practising temporal self-discipline provides accountants with a sense of control over the budgeting process - a way to achieve 'controlled' entrainment to the temporal norm. We also show how temporal disruptions may challenge controlled entrainment, forcing actors into a passive mode of reaction and potential deviation from their intended plan.

2.
Soc Sci Med ; 287: 114349, 2021 10.
Article de Anglais | MEDLINE | ID: mdl-34525419

RÉSUMÉ

This article explores how temporal structuring of clinical activities affects nurses' establishment of caring relationships with patients, based on an ethnographic study in a Norwegian cancer ward in January-June 2017. By drawing on practice-based perspectives on time and care, the article shows how 'medical time', 'patient time' and 'hospital time' represent three distinct but interconnected clinical rhythms affecting caring relationships. In this way, the article provides insights into how caring relationships are established in nurses' intermediate role as temporal agents, accommodation various temporal structures associated with the biomedical and person-centred care models. Second, it contributes insights into how caring practices are temporally structured and reproduced in a hospital context. Finally, the article describes factors that influence different ways of structuring time, emphasising the need for temporal reflexivity and flexibility in meeting patients' care needs, and the role time to care plays in facilitating this.


Sujet(s)
Soins infirmiers , Personnel infirmier hospitalier , Anthropologie culturelle , Humains , Norvège , Rôle de l'infirmier , Relations infirmier-patient
3.
Infect Genet Evol ; 43: 186-96, 2016 09.
Article de Anglais | MEDLINE | ID: mdl-27234841

RÉSUMÉ

Five patients (P) were followed-up for an average of 7.73years after highly active antiretroviral therapy (HAART) initiation. Patients' immune and virological status were determined by periodical CD4+T-cell counts and HIV and HCV viral load. HCV populations were studied using longitudinal high throughput sequence data obtained in parallel by virological and immunological parameters. Two patients (P7, P28) with sub-optimal responses to HAART presented HCV viral loads significantly higher than those recorded for two patients (P1, P18) that achieved good responses to HAART. Interestingly, HCV populations from P7 and P28 displayed a stable phylogenetic structure, whereas HCV populations from P1 and P18showeda significant increase in their phylogenetic structure, followed by a decrease after achieving acceptable CD4+T-cell counts (>500 cell/µl). The fifth patient (P25) presented high HCV viral loads, preserved CD4+T-cell counts from baseline and all along the follow-up, and displayed a constant viral phylogenetic structure. These results strongly suggest that HAART-induced immune recovery induces a decrease in HCV viral load and an increase in the HCV population phylogenetic structure likely reflecting the virus diversification in response to the afresh immune response. The relatively low HCV viral load observed in the HAART responder patients suggests that once HCV is adapted it reaches a maximum number of haplotypes higher than that achieved during the initial stages of the immune response as inferred from the two recovering patients. Future studies using larger number of patients are needed to corroborate these hypotheses.


Sujet(s)
Agents antiVIH/usage thérapeutique , Évolution moléculaire , Infections à VIH/traitement médicamenteux , Hepacivirus/génétique , Phylogenèse , ARN viral/génétique , Adulte , Thérapie antirétrovirale hautement active , Numération des lymphocytes CD4 , Lymphocytes T CD4+/virologie , Co-infection , Variation génétique , Infections à VIH/immunologie , Infections à VIH/virologie , VIH-1 (Virus de l'Immunodéficience Humaine de type 1)/génétique , VIH-1 (Virus de l'Immunodéficience Humaine de type 1)/croissance et développement , VIH-1 (Virus de l'Immunodéficience Humaine de type 1)/pathogénicité , Haplotypes , Hepacivirus/classification , Hepacivirus/croissance et développement , Hepacivirus/pathogénicité , Hépatite C chronique/traitement médicamenteux , Hépatite C chronique/immunologie , Hépatite C chronique/virologie , Humains , Études longitudinales , Charge virale
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