The National Center for Palliative and End-of-Life Care was established in 2016 in conjunction with the passage of the Claes-Leonetti Act, which identified the difficulty of providing information on end-of-life, and therefore palliative, issues. care In 2022, his missions expanded. For its director, Giovanna Marsico, there is still much to do with patients and their families, but also with caregivers.
LE FIGARO: Why do you think caregivers are so uncomfortable with palliative care?
Giovanna MARSICO: Our health care system is more focused on “treatment” (treatment) than “care” (caring). For many health workers, medicine must lead to a cure; the application of palliative care can therefore be perceived as a kind of failure, abandonment of the patient. Furthermore, physicians are poorly educated in end-of-life discussions and have limited knowledge of what a palliative approach actually is. It seems important to me that…
Source: Le Figaro
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