D. Rey

Satisfaction with care in HIV-infected patients treated with long-term follow-up antiretroviral therapy: the role of social vulnerability

Abstract The aim of this study was to determine factors associated with complete satisfaction with the care provided (satisfaction with physicians and satisfaction with services and organization) among HIV-infected patients followed up in the French ANRS CO8 APROCO-COPILOTE cohort. Analyses focused on cross-sectional data collected during the ninth year of cohort follow-up. Satisfaction with care, sociodemographic characteristics, and behavioral data were collected using self-administered questionnaires, while clinical data were derived from medical records. Complete satisfaction with care was defined as being 100% satisfied. Two logistic regression models were used to identify predictors of (1) complete satisfaction with physicians (n=404) and (2) complete satisfaction with services and organization (n=396). Sixteen percent of patients were completely satisfied with physicians, while 15.9% were completely satisfied with services and organization. Being older and reporting fewer discomforting antiretroviral therapy (ART) side effects were factors independently associated with complete satisfaction with both physicians and services and organization. Strong support from friends and absence of hepatitis C (HCV) co-infection were independently associated with complete satisfaction with physicians, while strong support from ones family and comfortable housing conditions were independently associated with complete satisfaction with services and organization. Even after nine years of follow-up, social vulnerabilities still strongly influence HIV-infected patients’ interactions with the health care system. Day-to-day experience with the disease, including perceived treatment side effects, appears to play a key role in the quality of these interactions. More attention should be given to patient satisfaction, especially for socially vulnerable patients, in order to avoid potentially detrimental consequences such as poor adherence to ART.

Barriers to procreational intentions among cancer survivors 2 years after diagnosis: a French national cross-sectional survey.

Objectives: To determine the procreational intention rates among cancer survivors whose fertility was unimpaired and to identify the factors associated with their procreational intentions.

Impact du cancer du sein sur la vie professionnelle. Enquête parmi les femmes de la cohorte ELIPPSE

Working people who are diagnosed with cancer must generally stop working, and returning to work after treatment is a very important issue for them. This article investigates the impact of cancer on professional trajectory among working women after a breast cancer diagnosis. We conducted in-depth interviews with 21 women from the ELIPPSE cohort. They were aged under 40 at cancer diagnosis, and they were interviewed from 16 months to 3 years after diagnosis. Several participants reported a deterioration of their professional situation even before they stopped working, with long-lasting consequences on their daily allowance. Others reported such deterioration during their sick leave. For all of them, returning to work after cancer treatment was very important, but they faced several obstacles. For example, some of them had to give up their former profession because of treatment side-effects. Moreover, the cancer experience frequently changed their attitude and expectations toward their working career. Finally, in order to find a new job these women were prone to hide their cancer experience and to resort to their social network (this network was also helpful to face the financial consequences of their sick leave).