In-hospital mortality trends among patients with idiopathic pulmonary fibrosis in the United States between 2013-2017: a comparison of academic and non-academic programs

被引:15
作者
Alqalyoobi, Shehabaldin [1 ,2 ]
Fernandez Perez, Evans R. [3 ]
Oldham, Justin M. [4 ]
机构
[1] East Carolina Univ, Brody Sch Med, Dept Med, Div Pulm Crit Care & Sleep Med, Greenville, NC 27858 USA
[2] Brody Sch Med, Internal Med Pulm Crit Care & Sleep Med, Mail Stop 628,3E-149, Greenville, NC 27834 USA
[3] Natl Jewish Hlth, Div Pulm Crit Care & Sleep Med, Denver, CO USA
[4] Univ Calif Davis, Div Pulm Crit Care & Sleep Med, Dept Internal Med, Sacramento, CA 95817 USA
关键词
Idiopathic pulmonary fibrosis; Mortality; Academic hospital; Respiratory failure; Mechanical ventilation; END-POINTS; SURVIVAL; PIRFENIDONE; NINTEDANIB; COHORT;
D O I
10.1186/s12890-020-01328-y
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background Idiopathic pulmonary fibrosis (IPF) is a devastating condition characterized by progressive lung function decline and early mortality. While early accurate diagnosis is essential for IPF treatment, data evaluating the impact of hospital academic status on IPF-related mortality remains limited. Here we examined in-hospital mortality trends for patients with IPF from 2013 to 2017. We hypothesized that in-hospital IPF mortality would be influenced by hospital academic setting. Methods Hospitalization data was extracted from the National Inpatient Sample (NIS) for subjects with an international classification of disease code for IPF. In-hospital mortality stratified by hospital setting (academic versus non-academic) was the primary outcome of interest, with secondary analyses performed for subgroups with and without respiratory failure and requiring mechanical ventilation. Predictors of mortality were then assessed. Results Among 93,680 patients with IPF requiring hospitalization, 58,450 (62.4%) were admitted to academic institutions. In-hospital mortality decreased significantly in those admitted to an academic hospital (p < 0.001) but remained unchanged in patients admitted to a non-academic hospital. A plateau in-hospital mortality was observed among all hospitalized patients (p = 0.12), with a significant decrease observed for patients with admitted respiratory failure (p < 0.001) and those placed on mechanic ventilation (p < 0.001). Conclusion In-hospital mortality decreased significantly for patients with IPF admitted to an academic hospital, suggesting that management strategies may differ by hospital setting. Mortality among those with respiratory failure and those requiring mechanical ventilation has dropped significantly. Our findings may underscore the importance of promoting early referral to an academic institution and adherence to international treatment guidelines.
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页数:11
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共 49 条
  • [1] African-American race and mortality in interstitial lung disease: a multicentre propensity-matched analysis
    Adegunsoye, Ayodeji
    Oldham, Justin M.
    Bellam, Shashi K.
    Chung, Jonathan H.
    Chung, Paul A.
    Biblowitz, Kathleen M.
    Montner, Steven
    Lee, Cathryn
    Hsu, Scully
    Husain, Aliya N.
    Vij, Rekha
    Mutlu, Gokhan
    Noth, Imre
    Churpek, Matthew M.
    Strek, Mary E.
    [J]. EUROPEAN RESPIRATORY JOURNAL, 2018, 51 (06)
  • [2] Body mass index and mortality in patients with idiopathic pulmonary fibrosis
    Alakhras, Mazen
    Decker, Paul A.
    Nadrous, Hassan F.
    Collazo-Clavell, Maria
    Ryu, Jay H.
    [J]. CHEST, 2007, 131 (05) : 1448 - 1453
  • [3] [Anonymous], **NON-TRADITIONAL**
  • [4] [Anonymous], **NON-TRADITIONAL**
  • [5] [Anonymous], **NON-TRADITIONAL**
  • [6] [Anonymous], **NON-TRADITIONAL**
  • [7] Comorbidities in idiopathic pulmonary fibrosis: an underestimated issue
    Caminati, Antonella
    Lonati, Chiara
    Cassandro, Roberto
    Elia, Davide
    Pelosi, Giuseppe
    Torre, Olga
    Zompatori, Maurizio
    Uslenghi, Elisabetta
    Harari, Sergio
    [J]. EUROPEAN RESPIRATORY REVIEW, 2019, 28 (153)
  • [8] Acute exacerbations in the INPULSIS trials of nintedanib in idiopathic pulmonary fibrosis
    Collard, Harold R.
    Richeldi, Luca
    Kim, Dong Soon
    Taniguchi, Hiroyuki
    Tschoepe, Inga
    Luisetti, Maurizio
    Roman, Jesse
    Tino, Gregory
    Schlenker-Herceg, Rozsa
    Hallmann, Christoph
    du Bois, Roland M.
    [J]. EUROPEAN RESPIRATORY JOURNAL, 2017, 49 (05)
  • [9] Acute Exacerbation of Idiopathic Pulmonary Fibrosis An International Working Group Report
    Collard, Harold R.
    Ryerson, Christopher J.
    Corte, Tamera J.
    Jenkins, Gisli
    Kondoh, Yasuhiro
    Lederer, David J.
    Lee, Joyce S.
    Maher, Toby M.
    Wells, Athol U.
    Antoniou, Katerina M.
    Behr, Juergen
    Brown, Kevin K.
    Cottin, Vincent
    Flaherty, Kevin R.
    Fukuoka, Junya
    Hansell, David M.
    Johkoh, Takeshi
    Kaminski, Naftali
    Kim, Dong Soon
    Kolb, Martin
    Lynch, David A.
    Myers, Jeffrey L.
    Raghu, Ganesh
    Richeldi, Luca
    Taniguchi, Hiroyuki
    Martinez, Fernando J.
    [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2016, 194 (03) : 265 - 275
  • [10] Study Design Implications of Death and Hospitalization as End Points in Idiopathic Pulmonary Fibrosis
    Collard, Harold R.
    Brown, Kevin K.
    Martinez, Fernando J.
    Raghu, Ganesh
    Roberts, Rhonda S.
    Anstrom, Kevin J.
    [J]. CHEST, 2014, 146 (05) : 1256 - 1262