Publications

Jeannic, A. Le; Quelen, C.; Alberti, C.; Durand-Zaleski, I.

Comparison of two data collection processes in clinical studies: electronic and paper case report forms Article de journal

Dans: BMC Med Res Methodol, vol. 14, p. 7, 2014, ISSN: 1471-2288.

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Léger, J.; Kaguelidou, F.; Alberti, C.; Carel, J. C.

Graves' disease in children Article de journal

Dans: Best Pract Res Clin Endocrinol Metab, vol. 28, no. 2, p. 233-43, 2014, ISSN: 1521-690x.

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Levy, C.; Pereira, M.; Guedj, R.; Abt-Nord, C.; Gelbert, N. B.; Cohen, R.; Alberti, C.; Gajdos, V.; Angoulvant, F.

Impact of 2011 French guidelines on antibiotic prescription for acute otitis media in infants Article de journal

Dans: Med Mal Infect, vol. 44, no. 3, p. 102-6, 2014, ISSN: 0399-077x.

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Lugosi, M.; Alberti, C.; Zahar, J. R.; Garrouste, M.; Lemiale, V.; Descorps-Desclère, A.; Ricard, J. D.; Goldgran-Tolédano, D.; Cohen, Y.; Schwebel, C.; Vésin, A.; Timsit, J. F.; Azoulay, E.

Aspergillus in the lower respiratory tract of immunocompetent critically ill patients Article de journal

Dans: J Infect, vol. 69, no. 3, p. 284-92, 2014, ISSN: 0163-4453.

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Mellerio, H.; Alberti, C.; Labèguerie, M.; Andriss, B.; Savoye, E.; Lassalle, M.; Jacquelinet, C.; Loirat, C.

Adult social and professional outcomes of pediatric renal transplant recipients Article de journal

Dans: Transplantation, vol. 97, no. 2, p. 196-205, 2014, ISSN: 0041-1337.

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Oguri, A.; Yamamoto, M.; Mouillet, G.; Gilard, M.; Laskar, M.; Eltchaninoff, H.; Fajadet, J.; Iung, B.; Donzeau-Gouge, P.; Leprince, P.; Leguerrier, A.; Prat, A.; Lievre, M.; Chevreul, K.; Dubois-Rande, J. L.; Chopard, R.; Belle, E. Van; Otsuka, T.; Teiger, E.; Investigators, France Registry

Clinical outcomes and safety of transfemoral aortic valve implantation under general versus local anesthesia: subanalysis of the French Aortic National CoreValve and Edwards 2 registry Article de journal

Dans: Circ Cardiovasc Interv, vol. 7, no. 4, p. 602-10, 2014, ISSN: 1941-7632 (Electronic) 1941-7640 (Linking).

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Prigent, A.; Auraaen, A.; Kamendje-Tchokobou, B.; Durand-Zaleski, I.; Chevreul, K.

Dans: Int J Environ Res Public Health, vol. 11, no. 3, p. 2804-17, 2014, ISSN: 1660-4601 (Electronic) 1660-4601 (Linking).

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Prigent, A.; Simon, S.; Durand-Zaleski, I.; Leboyer, M.; Chevreul, K.

Quality of life instruments used in mental health research: properties and utilization Article de journal

Dans: Psychiatry Res, vol. 215, no. 1, p. 1-8, 2014, ISSN: 1872-7123 (Electronic) 0165-1781 (Linking).

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Prot-Labarthe, S.; Weil, T.; Angoulvant, F.; Boulkedid, R.; Alberti, C.; Bourdon, O.

POPI (Pediatrics: Omission of Prescriptions and Inappropriate prescriptions): development of a tool to identify inappropriate prescribing Article de journal

Dans: PLoS One, vol. 9, no. 6, p. e101171, 2014, ISSN: 1932-6203.

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Sartor, A.; Arthurs, O.; Alberti, C.; Belarbi, N.; Tilea, B.; Boizeau, P.; Oury, J. F.; Elmaleh-Berges, M.; Gressens, P.; Sebag, G.; Alison, M.

Apparent diffusion coefficient measurements of the fetal brain during the third trimester of pregnancy: how reliable are they in clinical practice? Article de journal

Dans: Prenat Diagn, vol. 34, no. 4, p. 357-66, 2014, ISSN: 0197-3851.

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Schmitz, T.; Alberti, C.; Andriss, B.; Moutafoff, C.; Oury, J. F.; Sibony, O.

Identification of women at high risk for severe perineal lacerations Article de journal

Dans: Eur J Obstet Gynecol Reprod Biol, vol. 182, p. 11-5, 2014, ISSN: 0301-2115.

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Strullu, M.; Caye, A.; Lachenaud, J.; Cassinat, B.; Gazal, S.; Fenneteau, O.; Pouvreau, N.; Pereira, S.; Baumann, C.; Contet, A.; Sirvent, N.; Méchinaud, F.; Guellec, I.; Adjaoud, D.; Paillard, C.; Alberti, C.; Zenker, M.; Chomienne, C.; Bertrand, Y.; Baruchel, A.; Verloes, A.; Cavé, H.

Juvenile myelomonocytic leukaemia and Noonan syndrome Article de journal

Dans: J Med Genet, vol. 51, no. 10, p. 689-97, 2014, ISSN: 0022-2593.

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Stylianidis, S.; Pantelidou, S.; Chondros, P.; Roelandt, J. L.; Barbato, A.

Prevalence of mental disorders in a Greek island Article de journal

Dans: Psychiatriki, vol. 25, no. 1, p. 19-26, 2014, ISSN: 1105-2333 (Print) 1105-2333.

BibTeX

Tchetche, D.; Farah, B.; Misuraca, L.; Pierri, A.; Vahdat, O.; Lereun, C.; Dumonteil, N.; Modine, T.; Laskar, M.; Eltchaninoff, H.; Himbert, D.; Iung, B.; Teiger, E.; Chevreul, K.; Lievre, M.; Lefevre, T.; Donzeau-Gouge, P.; Gilard, M.; Fajadet, J.

Cerebrovascular events post-transcatheter aortic valve replacement in a large cohort of patients: a FRANCE-2 registry substudy Article de journal

Dans: JACC Cardiovasc Interv, vol. 7, no. 10, p. 1138-45, 2014, ISSN: 1876-7605 (Electronic) 1936-8798 (Linking).

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Belle, E. Van; Juthier, F.; Susen, S.; Vincentelli, A.; Iung, B.; Dallongeville, J.; Eltchaninoff, H.; Laskar, M.; Leprince, P.; Lievre, M.; Banfi, C.; Auffray, J. L.; Delhaye, C.; Donzeau-Gouge, P.; Chevreul, K.; Fajadet, J.; Leguerrier, A.; Prat, A.; Gilard, M.; Teiger, E.; Investigators, France

Postprocedural aortic regurgitation in balloon-expandable and self-expandable transcatheter aortic valve replacement procedures: analysis of predictors and impact on long-term mortality: insights from the FRANCE2 Registry Article de journal

Dans: Circulation, vol. 129, no. 13, p. 1415-27, 2014, ISSN: 1524-4539 (Electronic) 0009-7322 (Linking).

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Zoppei, S.; Lasalvia, A.; Bonetto, C.; Bortel, T. Van; Nyqvist, F.; Webber, M.; Aromaa, E.; Weeghel, J. Van; Lanfredi, M.; Harangozó, J.; Wahlbeck, K.; Thornicroft, G.

Social capital and reported discrimination among people with depression in 15 European countries Article de journal

Dans: Soc Psychiatry Psychiatr Epidemiol, vol. 49, no. 10, p. 1589-98, 2014, ISSN: 0933-7954.

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Aujoulat, Isabelle; Marcolongo, Renzo; Bonadiman, Leopoldo; Deccache, Alain

Reconsidering patient empowerment in chronic illness: A critique of models of self-efficacy and bodily control Article de journal

Dans: Social Science and Medicine, vol. 66, no. 5, p. 1228–1239, 2008, ISSN: 0277-9536.

Résumé | Liens | BibTeX

@article{aujoulat_reconsidering_2008,

title = {Reconsidering patient empowerment in chronic illness: A critique of models of self-efficacy and bodily control},

author = {Isabelle Aujoulat and Renzo Marcolongo and Leopoldo Bonadiman and Alain Deccache},

url = {https://www.sciencedirect.com/science/article/pii/S0277953607006223},

doi = {10.1016/j.socscimed.2007.11.034},

issn = {0277-9536},

year  = {2008},

date = {2008-01-01},

urldate = {2021-02-14},

journal = {Social Science and Medicine},

volume = {66},

number = {5},

pages = {1228--1239},

abstract = {Studies that focus on patient empowerment tend to address more specifically two issues of patients' experience of illness: managing regimens and relating to health-care providers. Other aspects of illness experience, such as coming to terms with disrupted identities, tend to be overlooked. The outcome of empowerment is therefore usually referred to as achieving self-efficacy, mastery and control. We conducted an inductive exploratory study, based on individual in-depth interviews with 40 chronically ill patients in Belgium and Italy, in order to understand the process of empowerment as it may occur in patients whose experience of illness has at some point induced a feeling of powerlessness, which we conceptualised as a threat to their senses of security and identity. Our findings show that empowerment and control are not one and the same thing. We describe patient empowerment as a process of personal transformation which occurs through a double process of (i) “holding on” to previous self-representations and roles and learning to control the disease and treatment, so as to differentiate one's self from illness on the one hand, and on the other hand (ii) “letting go”, by accepting to relinquish control, so as to integrate illness and illness-driven boundaries as being part of a reconciled self. Whereas the process of separating identities (“holding on”) was indeed found to be linked to efforts aimed at taking control and maintaining or regaining a sense of mastery, the process of reconciling identities (“letting go”) was found to be linked to a need for coherence, which included a search for meaning and the acceptance that not everything is controllable. We argue that the process of relinquishing control is as central to empowerment as is the process of gaining control. As a “successful” process of empowerment occurs when patients come to terms with their threatened security and identity, not only with their treatment, it may be facilitated by health-care providers through the use of narratives.},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

Fermer

Studies that focus on patient empowerment tend to address more specifically two issues of patients' experience of illness: managing regimens and relating to health-care providers. Other aspects of illness experience, such as coming to terms with disrupted identities, tend to be overlooked. The outcome of empowerment is therefore usually referred to as achieving self-efficacy, mastery and control. We conducted an inductive exploratory study, based on individual in-depth interviews with 40 chronically ill patients in Belgium and Italy, in order to understand the process of empowerment as it may occur in patients whose experience of illness has at some point induced a feeling of powerlessness, which we conceptualised as a threat to their senses of security and identity. Our findings show that empowerment and control are not one and the same thing. We describe patient empowerment as a process of personal transformation which occurs through a double process of (i) “holding on” to previous self-representations and roles and learning to control the disease and treatment, so as to differentiate one's self from illness on the one hand, and on the other hand (ii) “letting go”, by accepting to relinquish control, so as to integrate illness and illness-driven boundaries as being part of a reconciled self. Whereas the process of separating identities (“holding on”) was indeed found to be linked to efforts aimed at taking control and maintaining or regaining a sense of mastery, the process of reconciling identities (“letting go”) was found to be linked to a need for coherence, which included a search for meaning and the acceptance that not everything is controllable. We argue that the process of relinquishing control is as central to empowerment as is the process of gaining control. As a “successful” process of empowerment occurs when patients come to terms with their threatened security and identity, not only with their treatment, it may be facilitated by health-care providers through the use of narratives.

Fermer

Aujoulat, Isabelle; d’Hoore, William; Deccache, Alain

Patient empowerment in theory and practice: Polysemy or cacophony? Article de journal

Dans: Patient Education and Counseling, vol. 66, no. 1, p. 13–20, 2007, ISSN: 0738-3991.

Résumé | Liens | BibTeX

@article{aujoulat_patient_2007,

title = {Patient empowerment in theory and practice: Polysemy or cacophony?},

author = {Isabelle Aujoulat and William d’Hoore and Alain Deccache},

url = {https://www.sciencedirect.com/science/article/pii/S0738399106003247},

doi = {10.1016/j.pec.2006.09.008},

issn = {0738-3991},

year  = {2007},

date = {2007-04-01},

urldate = {2021-02-14},

journal = {Patient Education and Counseling},

volume = {66},

number = {1},

pages = {13--20},

abstract = {Objective 

This paper examines how the term “empowerment” has been used in relation to the care and education of patients with chronic conditions over the past decade. 

Methods 

Fifty-five articles were analysed, using a qualitative method of thematic analysis. 

Results 

Empowerment is more often defined according to some of its anticipated outcomes rather than to its very nature. However, because they do not respect the principle of self-determination, most anticipated outcomes and most evaluation criteria are not specific to empowerment. Concerning the process of empowerment, our analysis shows that (i) the educational objectives of an empowerment-based approach are not disease-specific, but concern the reinforcement or development of general psychosocial skills instead; (ii) empowering methods of education are necessarily patient-centred and based on experiential learning; and (iii) the provider–patient relationship needs to be continuous and self-involving on both sides. 

Conclusion 

Our analysis did not allow for the unfolding of a well-articulated theory on patient empowerment but revealed a number of guiding principles and values. 

Practice implications 

The goals and outcomes of patient empowerment should neither be predefined by the health-care professionals, nor restricted to some disease and treatment-related outcomes, but should be discussed and negotiated with every patient, according to his/her own particular situation and life priorities.},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

Fermer

Deccache, Alain; Aujoulat, Isabelle

A European perspective: common developments, differences and challenges in patient education Article de journal

Dans: Patient Education and Counseling, vol. 44, no. 1, p. 7–14, 2001, ISSN: 0738-3991.

Résumé | Liens | BibTeX

Deccache, Alain; Aujoulat, Isabelle

A European perspective: common developments, differences and challenges in patient education Article de journal

Dans: Patient Education and Counseling, vol. 44, no. 1, p. 7–14, 2001, ISSN: 0738-3991.

Résumé | Liens | BibTeX