Background: Idiopathic Pulmonary Fibrosis (IPF) is a lethal disease; most patients die in hospitals because palliative care (PC) is not wildly and early available. We aimed to determine the impact of an early PC program in IPF patients on place of death, emergency department (ED) admission, unplanned medical visits and survival before and after its implementation at our clinic. Methods: IPF patients from our ILD clinic who died between January 1st, 2018 and December 31th, 2023 were included in the analysis. Primary outcomes were location of death, number of ED access and unplanned medical visits; secondary outcomes was survival from diagnosis. Results: A total of 46 decedents between 2018 and 2023 were analysed: (median age 71,5 +/- 5,5 years, 89 % male): 26 died before the implementation of the early PC program and 20 after. Through chi 2 test, location of death resulted significantly different in the two groups, showing the capacity of early PC to favor at home or in hospice death (p = 0,02); similarly, the number of unplanned visits was significantly lower (p = 0,03). Finally, survival was significantly lower in patients not receiving the early PC program (p = 0,01). Conclusion: The availability of an early PC program since the diagnosis significantly reduced both the death rate in hospital settings, favoring dying in hospice or at home, and the number of unplanned medical visits. Furthermore, IPF patients receiving early PC showed a longer survival than those who did not.

Bassi, I., Pastorello, S., Guerrieri, A., Giancotti, G., Cuomo, A.M., Rizzelli, C., et al. (2024). Early palliative care program in idiopathic pulmonary fibrosis patients favors at-home and hospice deaths, reduces unplanned medical visits, and prolongs survival: A pilot study. EUROPEAN JOURNAL OF INTERNAL MEDICINE, 128, 81-86 [10.1016/j.ejim.2024.05.024].

Early palliative care program in idiopathic pulmonary fibrosis patients favors at-home and hospice deaths, reduces unplanned medical visits, and prolongs survival: A pilot study

Bassi I.
Primo
;
Guerrieri A.;Giancotti G.;Cuomo A. M.;Nava S.
2024

Abstract

Background: Idiopathic Pulmonary Fibrosis (IPF) is a lethal disease; most patients die in hospitals because palliative care (PC) is not wildly and early available. We aimed to determine the impact of an early PC program in IPF patients on place of death, emergency department (ED) admission, unplanned medical visits and survival before and after its implementation at our clinic. Methods: IPF patients from our ILD clinic who died between January 1st, 2018 and December 31th, 2023 were included in the analysis. Primary outcomes were location of death, number of ED access and unplanned medical visits; secondary outcomes was survival from diagnosis. Results: A total of 46 decedents between 2018 and 2023 were analysed: (median age 71,5 +/- 5,5 years, 89 % male): 26 died before the implementation of the early PC program and 20 after. Through chi 2 test, location of death resulted significantly different in the two groups, showing the capacity of early PC to favor at home or in hospice death (p = 0,02); similarly, the number of unplanned visits was significantly lower (p = 0,03). Finally, survival was significantly lower in patients not receiving the early PC program (p = 0,01). Conclusion: The availability of an early PC program since the diagnosis significantly reduced both the death rate in hospital settings, favoring dying in hospice or at home, and the number of unplanned medical visits. Furthermore, IPF patients receiving early PC showed a longer survival than those who did not.
2024
Bassi, I., Pastorello, S., Guerrieri, A., Giancotti, G., Cuomo, A.M., Rizzelli, C., et al. (2024). Early palliative care program in idiopathic pulmonary fibrosis patients favors at-home and hospice deaths, reduces unplanned medical visits, and prolongs survival: A pilot study. EUROPEAN JOURNAL OF INTERNAL MEDICINE, 128, 81-86 [10.1016/j.ejim.2024.05.024].
Bassi, I.; Pastorello, S.; Guerrieri, A.; Giancotti, G.; Cuomo, A. M.; Rizzelli, C.; Coppola, M.; Valenti, D.; Nava, S.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/1007955
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