دورية أكاديمية

Disparities in Lung Transplant among Patients with Idiopathic Pulmonary Fibrosis: An Analysis of the IPF-PRO Registry.

التفاصيل البيبلوغرافية
العنوان: Disparities in Lung Transplant among Patients with Idiopathic Pulmonary Fibrosis: An Analysis of the IPF-PRO Registry.
المؤلفون: Swaminathan AC; Duke Clinical Research Institute, Durham, North Carolina.; Duke University Medical Center, Durham, North Carolina., Hellkamp AS; Duke Clinical Research Institute, Durham, North Carolina.; Duke University Medical Center, Durham, North Carolina., Neely ML; Duke Clinical Research Institute, Durham, North Carolina.; Duke University Medical Center, Durham, North Carolina., Bender S; Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, Connecticut., Paoletti L; Division of Pulmonary, Critical Care, and Sleep Medicine, Department of Medicine, Medical University of South Carolina, Charleston, South Carolina; and., White ES; Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, Connecticut., Palmer SM; Duke Clinical Research Institute, Durham, North Carolina.; Duke University Medical Center, Durham, North Carolina., Whelan TPM; Division of Pulmonary, Critical Care, and Sleep Medicine, Department of Medicine, Medical University of South Carolina, Charleston, South Carolina; and., Dilling DF; Division of Pulmonary and Critical Care, Loyola University Chicago Stritch School of Medicine, Maywood, Illinois.
مؤلفون مشاركون: Idiopathic Pulmonary Fibrosis Prospective Outcomes Registry investigators
المصدر: Annals of the American Thoracic Society [Ann Am Thorac Soc] 2022 Jun; Vol. 19 (6), pp. 981-990.
نوع المنشور: Journal Article; Multicenter Study
اللغة: English
بيانات الدورية: Publisher: American Thoracic Society Country of Publication: United States NLM ID: 101600811 Publication Model: Print Cited Medium: Internet ISSN: 2325-6621 (Electronic) Linking ISSN: 23256621 NLM ISO Abbreviation: Ann Am Thorac Soc Subsets: MEDLINE
أسماء مطبوعة: Original Publication: New York, NY : American Thoracic Society, [2013]-
مواضيع طبية MeSH: Idiopathic Pulmonary Fibrosis*/diagnosis , Idiopathic Pulmonary Fibrosis*/surgery , Lung Transplantation*, Humans ; Proportional Hazards Models ; Prospective Studies ; Registries
مستخلص: Rationale: Lung transplant offers the potential to extend life for patients with idiopathic pulmonary fibrosis (IPF); yet, this therapeutic modality is only available to a small proportion of patients. Objectives: To identify clinical characteristics and social determinants of health that differentially associate with lung transplant compared with death in patients with IPF. Methods: We evaluated data from the Idiopathic Pulmonary Fibrosis Prospective Outcomes (IPF-PRO) Registry, a multicenter U.S. registry of patients with IPF that was diagnosed or confirmed at the enrolling center in the previous 6 months. Patients were enrolled between June 2014 and October 2018. Patients who were listed for lung transplant were not eligible to enroll in the registry, but patients could be listed for transplant after enrollment. We performed a multivariable time-to-event analysis incorporating competing risks methodology to examine differential associations between prespecified covariates and the risk of lung transplant versus death. Covariates included factors related to lung transplant eligibility, clinical characteristics of IPF, and social determinants of health. Covariates were modeled as time independent or time dependent as appropriate. Results: Among 955 patients with IPF, event rates of lung transplant and death were 7.4% and 16.3%, respectively, at 2 years. Covariates with the strongest differential association were age, median zip code income, and enrollment at a center with a lung transplant program. Lung transplant was less likely (hazard ratio [HR], 0.13 [95% confidence interval (CI), 0.06-0.28] per 5-yr increase) and death more likely (HR, 1.41 [95% CI, 1.22-1.64] per 5-yr increase) among those older than 70 years of age. Higher median zip code income was associated with lung transplant (HR, 1.22 [95% CI, 1.13-1.31] per $10,000 increase) but not death (HR, 0.99 [95% CI, 0.94-1.04] per $10,000 increase). Enrollment at a center with a lung transplant program was associated with lung transplant (HR, 4.31 [95% CI, 1.76-10.54]) but not death (HR, 0.99 [95% CI, 0.69-1.43]). Oxygen use with activity was associated with both lung transplant and death, but more strongly with lung transplant. A higher number of comorbidities was associated with an increased likelihood of death but not lung transplant. Conclusions: For patients in the Idiopathic Pulmonary Fibrosis Prospective Outcomes Registry, median zip code income and access to a lung transplant center differentially impact the risk of lung transplant compared with death, regardless of disease severity measures or other transplant eligibility factors. Interventions are needed to mitigate inequalities in lung transplantation based on socioeconomic status. Clinical trial registered with www.clinicaltrials.gov (NCT01915511).
التعليقات: Comment in: Ann Am Thorac Soc. 2022 Jun;19(6):899-901. (PMID: 35648085)
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فهرسة مساهمة: Investigator: A Baker; S Beegle; JA Belperio; R Condos; F Cordova; DA Culver; J Fitzgerald; KR Flaherty; K Gibson; M Gulati; K Guntupalli; N Gupta; AH Case; D Hotchkin; TJ Huie; RJ Kaner; HJ Kim; LH Lancaster; JA Lasky; D Lee; T Liesching; R Lipchik; J Lobo; TR Luckhardt; Y Mageto; P Menon; L Morrison; A Namen; JM Oldham; T Paul; D Zhang; M Porteous; R Raj; M Ramaswamy; T Russell; P Sachs; Z Safdar; S Shafazand; A Siddiqi; B Sigal; ME Strek; S Suliman; J Tabak; R Walia
Keywords: interstitial lung disease; lung transplantation; organ transplants; pulmonary fibrosis
سلسلة جزيئية: ClinicalTrials.gov NCT01915511
تواريخ الأحداث: Date Created: 20220124 Date Completed: 20220603 Latest Revision: 20221229
رمز التحديث: 20231215
مُعرف محوري في PubMed: PMC9169123
DOI: 10.1513/AnnalsATS.202105-589OC
PMID: 35073248
قاعدة البيانات: MEDLINE
الوصف
تدمد:2325-6621
DOI:10.1513/AnnalsATS.202105-589OC