Home care organization impacts patient management and survival in ALS

Article indépendant

LAVERNHE, Sylvie | ANTOINE, Jean-Christophe | COURT-FORTUNE, Isabelle | DIMIER, Nathalie | COSTES, Frédéric | LACOUR, Arnaud | CAMDESSANCHE, Jean-Philippe

Objective: Progression of amyotrophic lateral sclerosis (ALS) depends on several factors linked to the disease. However, both the patient’s living place and care organization role need to be evaluated. Methods: We analysed the effect on survival of factors linked to ALS or the socio-geographical context in a prospective cohort of 203 patients followed between 2003 and 2011. Results: Patients were 97 females and 106 males with a mean age of 65.5 years. Survival was longer in younger patients, in case of upper limb involvement, longer time to diagnosis, and initially higher forced vital capacity. Non-invasive positive pressure ventilation (NIPPV) and percutaneous gastrostomy (PEG) failed to demonstrate benefit. Patients who lived at home had longer survival. The nature of non-medical organization at home statistically influenced survival, which was longer with an organized network than with an unorganized one and shorter in absence of non-medical organization. In patients with indication of PEG and NIPPV, the proposition was statistically different according to the care givers. Conclusions: Besides the natural history of ALS, survival depended on home organization and the presence or the nature of a home-care system. Home organization was an important factor of decision for NIPPV and PEG proposals.

http://dx.doi.org/10.1080/21678421.2017.1332076

Voir la revue «Amyotrophic lateral sclerosis and frontotemporal degeneration, 18»

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