Palliative Care and Location of Death in Decedents With Idiopathic Pulmonary Fibrosis

被引:124
作者
Lindell, Kathleen O. [1 ,2 ]
Liang, Zhan [3 ]
Hoffman, Leslie A. [3 ]
Rosenzweig, Margaret Q. [3 ]
Saul, Melissa I. [4 ]
Pilewski, Joseph M. [2 ]
Gibson, Kevin F. [1 ,2 ]
Kaminski, Naftali [5 ]
机构
[1] Univ Pittsburgh, Dorothy P & Richard P Simmons Ctr Interstitial Lu, UPMC, Pittsburgh, PA USA
[2] Univ Pittsburgh, Div Pulm Allergy & Crit Care Med, Pittsburgh, PA USA
[3] Univ Pittsburgh, Sch Nursing, Pittsburgh, PA 15261 USA
[4] Univ Pittsburgh, Dept Biomed Informat, Sch Med, Pittsburgh, PA 15261 USA
[5] Yale Univ, Sch Med, New Haven, CT USA
基金
美国国家卫生研究院;
关键词
INTERSTITIAL LUNG-DISEASE; QUALITY-OF-LIFE; SURVIVAL; MANAGEMENT; PATIENT; SYSTEM;
D O I
10.1378/chest.14-1127
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
BACKGROUND: Palliative care, integrated early, may reduce symptom burden in patients with idiopathic pulmonary fibrosis (IPF). However, limited information exists on timing and clinical practice. The purpose of this study was to describe the time course of events prior to death in patients with IPF managed at a specialty center with a focus on location of death and timing of referral for palliative care. METHODS: Data were retrospectively extracted from the health system's data repository and obituary listings. The sample included all decedents, excluding lung transplant recipients, who had their first visit to the center between 2000 and 2012. RESULTS: Median survival for 404 decedents was 3 years from diagnosis and 1 year from first center visit. Of 277 decedents whose location of death could be determined, > 50% died in the hospital (57%). Only 38 (13.7%) had a formal palliative care referral and the majority (71%) was referred within 1 month of their death. Decedents who died in the academic medical center ICU were significantly younger than those who died in a community hospital ward (P = .04) or hospice (P = .001). CONCLUSIONS: The majority of patients with IPF died in a hospital setting and only a minority received a formal palliative care referral. Referral to palliative care occurred late in the disease. These findings indicate the need to study adequacy of end-of-life management in IPF and promote earlier discussion and referral to palliative care.
引用
收藏
页码:423 / 429
页数:7
相关论文
共 50 条
  • [31] Care programs and their components for patients with idiopathic pulmonary fibrosis: a systematic review
    Delameillieure, Anouk
    Vandekerkhof, Sarah
    Van Grootven, Bastiaan
    Wuyts, Wim A.
    Dobbels, Fabienne
    RESPIRATORY RESEARCH, 2021, 22 (01)
  • [32] Cough in Idiopathic Pulmonary Fibrosis
    Mann, Jennifer
    Goh, Nicole S. L.
    Holland, Anne E.
    Khor, Yet Hong
    FRONTIERS IN REHABILITATION SCIENCES, 2021, 2
  • [33] Management of Idiopathic Pulmonary Fibrosis
    Salisbury, Margaret L.
    Wijsenbeek, Marlies S.
    CLINICS IN CHEST MEDICINE, 2021, 42 (02) : 275 - 285
  • [34] Management of Idiopathic Pulmonary Fibrosis
    Pleasants, Roy
    Tighe, Robert M.
    ANNALS OF PHARMACOTHERAPY, 2019, 53 (12) : 1238 - 1248
  • [35] Idiopathic Pulmonary Fibrosis With Emphysema: Evidence of Synergy Among Emphysema and Idiopathic Pulmonary Fibrosis in Smokers
    Mitchell, Patrick D.
    Das, Jeeban P.
    Murphy, David J.
    Keane, Michael P.
    Donnelly, Seamas C.
    Dodd, Jonathan D.
    Butler, Marcus W.
    RESPIRATORY CARE, 2015, 60 (02) : 259 - 268
  • [36] The impact of palliative care on quality of life, anxiety, and depression in idiopathic pulmonary fibrosis: a randomized controlled pilot study
    Katherine Janssen
    Drew Rosielle
    Qi Wang
    Hyun Joo Kim
    Respiratory Research, 21
  • [37] PULMONARY HYPERTENSION IN IDIOPATHIC PULMONARY FIBROSIS: A REVIEW
    Corte, T. J.
    Wort, S. J.
    Wells, A. U.
    SARCOIDOSIS VASCULITIS AND DIFFUSE LUNG DISEASES, 2009, 26 (01) : 7 - 19
  • [38] It takes a village to care for the patient with idiopathic pulmonary fibrosis
    Fischer, Aryeh
    CLEVELAND CLINIC JOURNAL OF MEDICINE, 2018, 85 (05) : 387 - 389
  • [39] Titrated oxygen requirement and prognostication in idiopathic pulmonary fibrosis
    Hook, J. L.
    Arcasoy, S. M.
    Zemmel, D.
    Bartels, M. N.
    Kawut, S. M.
    Lederer, D. J.
    EUROPEAN RESPIRATORY JOURNAL, 2012, 39 (02) : 359 - 365
  • [40] Comparing effectiveness of prognostic tests in idiopathic pulmonary fibrosis
    Moua, Teng
    Lee, Augustine S.
    Ryu, Jay H.
    EXPERT REVIEW OF RESPIRATORY MEDICINE, 2019, 13 (10) : 993 - 1004