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  • 8/14/2019 Zambelli Agostino

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    ABSTRACT FORM

    Presenting author

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    Pain and other symptoms

    Palliative care for cancer patients

    Palliative care for non cancer

    patients

    Paediatric palliative care

    Palliative care for the elderly

    The actors of palliative care

    Latest on drugs

    Pain

    Illness and suffering through

    media

    Marginalisation and social stigma

    at the end of life

    Palliative care advocacy projects

    Prognosis and diagnosis

    communication in

    different cultures

    Communication between doctor-

    patient and patient-

    equipe

    Religions and cultures versus

    suffering, death and

    bereavement

    Public institution in the world:

    palliative care policies

    and law

    Palliative care: from villages to

    metropolies

    Space, light and gardens for the

    terminally ill patient

    End-of-life ethics

    Complementary therapies

    Education, training and research

    Fund-raising and no-profit

    Bereavement support Volunteering in palliative care

    Palliative care for HIV people in Milan: three years of experience in Hospice

    Author: Agostino Zambelli

    Luigi Sacco Hospital has always been involved in caring AIDS last phases of life.Our hospital has 90 beds for infectious disease patients, and supported a strong burden during allthe HIV epidemic, in spite of the global number of HIV positive people followed in Milan (about10% of the whole Italian cases).The deaths of HIV people till 1995, year of introduction of HAART, were daily and personnelwas not prepared to face this problem.We started with experimental home care in 1992 and, finally we arrived to open the Hospice inapril 2005. This was an important event because, before the opening, all patients died in thehospital or had to be sent in the only Hospice which accepted HIV positive people, far fromMilan.Our Hospice was born for HIV positive patients, but from the first moment it was open to allterminal patients, trying to avoid the stigma that burden HIV people.

    Our Hospice is a part of the network for AIDS patients, comprehending Shelters, Home Care,Outpatients and Day hospital.From the opening we followed in the Hospice 335 pts, mean age 66y, 212 males and 123Females. 123 HIV pos, 56 Infectious non HIV (hepatitis B, C, Creutzfeldt Jakob disease), and156 not infectious (neoplasm, cardiac failure, cerebral failure, etc).The most important differences we evidenced between HIV positive and the other terminal

    patients in our Hospice could be resumed in four groups: prognosis (difficult to establish anddefine in HIV people), fever and other symptoms due to infections (opportunistic or not), privacy(a big problem in HIV patients), social burden (familial problems, strangers, transsexuals, etc)

    Need of pain therapy is lower in HIV patients than in cancer patients, while the use of sedativedrugs is usually higher.A special training has been established for nurses, doctors, psychologists, volunteers working inthe Hospice, both initial and permanent.

    Session: Non cancer palliative care

    Chair: Dott. M. Fantoni

    Antea Worldwide Palliative Care ConferenceRome, 12-14 November 2008

    Agostino Zambelli

    [email protected]

    mailto:[email protected]:[email protected]:[email protected]
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    Rehabilitation in palliative care

    Palliative care quality indicators

    Neurology in palliative care