The DOI matches its Crossref record; 33 of the 33 references it cites were found in a registry or an index.
Adoption of the Antifibrotic Medications Pirfenidone and Nintedanib for Patients with Idiopathic Pulmonary Fibrosis
Abstract
Abstract Rationale In October 2014, the antifibrotic medications pirfenidone and nintedanib became the first medications approved by the U.S. Food and Drug Administration for use in patients with idiopathic pulmonary fibrosis (IPF). Since approval, there has been no nonregistry analysis of the real-world adoption of these medications in everyday clinical practice. Objectives To evaluate the adoption, persistence, and out-of-pocket (OOP) costs of pirfenidone and nintedanib since their approval in the United States in 2014. Methods A retrospective cohort analysis was performed by identifying privately insured and Medicare Advantage beneficiaries with IPF. We then split the patients into three cohorts: those who were untreated and those who filled a prescription for either pirfenidone or nintedanib between October 1, 2014, and July 31, 2019. The primary outcome was adoption of the medications. Secondary outcomes included medication persistence and prescription drug costs. Results A total of 10,996 patients with IPF were identified in the data set. A minority of patients (26.4%) with IPF identified in the cohort had started either medication since approval in 2014, with the adoption of both medications being comparable at around 13.2%. Those receiving the medications were younger (72 vs. 73.9 yr; P < 0.0001) and healthier (3.9 vs. 4.9 comorbidities; P < 0.0001) than those not receiving treatment. Men were significantly more likely to receive treatment than woman (30.0% vs. 21.9%; P < 0.0001). Among treated patients, 42.8% discontinued the medications during the study period. Patients’ OOP expenses per month were high for both drugs (mean, $397.51 for nintedanib; mean, $394.49 for pirfenidone). Conclusions The adoption of both the antifibrotic medications in the United States in everyday practice has been low since approval and may be associated with the high OOP cost.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Their limited efficacy, combined with tolerability challenges, contributes to low treatment uptake, frequent discontinuation of both treatments, and impaired quality of life.6-8”
From Deupirfenidone Compared with Pirfenidone and Placebo in Idiopathic Pulmonary Fibrosis (ELEVATE-IPF): a Phase 2b Randomized Placebo-Controlled Trial (2026) · cites this paper as [7]
Citations
Cites
Coding algorithms for defining comorbidities in ICD-9-CM and ICD-10 administrative data
Quan, H., Sundararajan, V., Halfon, P., Fong, A., Burnand, B., Luthi, J.-C., Saunders, L. D., Beck, C. A., Feasby, T. E., & Ghali, W. A. (2005) · Medical Care · doi:10.1097/01.mlr.0000182534.19832.83 · Cited by 10,669
Efficacy and Safety of Nintedanib in Idiopathic Pulmonary Fibrosis
Richeldi, L., du Bois, R. M., Raghu, G., Azuma, A., Brown, K. K., Costabel, U., Cottin, V., Flaherty, K. R., Hansell, D. M., Inoue, Y., et al. (2014) · New England Journal of Medicine · doi:10.1056/nejmoa1402584 · Cited by 4,654
A phase 3 trial of pirfenidone in patients with idiopathic pulmonary fibrosis.
King, T. E., Bradford, W. Z., Castro-Bernardini, S., Fagan, E. A., Glaspole, I., Glassberg, M. K., Gorina, E., Hopkins, P. M., Kardatzke, D., Lancaster, L., et al. (2014) · New England Journal of Medicine · doi:10.1056/nejmoa1402582 · Cited by 3,975
Medication compliance and persistence: terminology and definitions
Cramer, J. A., Roy, A., Burrell, A., Fairchild, C. J., Fuldeore, M. J., Ollendorf, D. A., & Wong, P. K. (2008) · Value in Health · doi:10.1111/j.1524-4733.2007.00213.x · Cited by 2,220
Raghu, G., Rochwerg, B., Zhang, Y., Garcia, C. A. C., Azuma, A., Behr, J., Brozek, J. L., Collard, H. R., Cunningham, W., Homma, S., et al. (2015) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201506-1063st · Cited by 1,916
Prednisone, Azathioprine, and N -Acetylcysteine for Pulmonary Fibrosis
The Idiopathic Pulmonary Fibrosis Clinical Research Network (2012) · New England Journal of Medicine · doi:10.1056/nejmoa1113354 · Cited by 1,654
Incidence and Prevalence of Idiopathic Pulmonary Fibrosis
Raghu, G., Weycker, D., Edelsberg, J., Bradford, W. Z., & Oster, G. (2006) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.200602-163oc · Cited by 1,310
Idiopathic Interstitial Pneumonia
Flaherty, K. R., King, T. E., Raghu, G., Lynch, J. P., Colby, T. V., Travis, W. D., Gross, B. H., Kazerooni, E. A., Toews, G. B., Long, Q., et al. (2004) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.200402-147oc · Cited by 672
Treatment of Idiopathic Pulmonary Fibrosis With Ambrisentan: A Parallel, Randomized Trial
Raghu, G., Behr, J., Brown, K. K., Egan, J. J., Kawut, S. M., Flaherty, K. R., Martinez, F. J., Nathan, S. D., Wells, A. U., Collard, H. R., et al. (2013) · Annals of Internal Medicine · doi:10.7326/0003-4819-158-9-201305070-00003 · Cited by 553
King, T. E., Albera, C., Bradford, W. Z., Costabel, U., Hormel, P., Lancaster, L., Noble, P. W., Sahn, S. A., Szwarcberg, J., Thomeer, M., et al. (2009) · The Lancet · doi:10.1016/s0140-6736(09)60551-1 · Cited by 531
Research works printed but not linked: 4
- Flaherty, 2018, Baseline characteristics of 1461 participants in the pulmonary fibrosis foundation patient registry [abstract], Eur Respir J, 52, PA2199
- Wong, 2018, Direct oral anticoagulant prescription trends, switching patterns, and adherence in Texas Medicaid, Am J Manag Care, 24, SP309
- Achaiah, 2017, Tolerability and efficacy of pirfenidone and nintedanib for patients with IPF in real world clinical practice [abstract], Eur Respir J, 50, PA4879
- Eaddy, 2012, How patient cost-sharing trends affect adherence and outcomes: a literature review, P&T, 37, 45
Cited by
Sorted by citations
Idiopathic pulmonary fibrosis: Current and future treatment
Glass, D. S., Grossfeld, D. J., Renna, H. A., Agarwala, P., Spiegler, P. A., DeLeon, J. R., & Reiss, A. B. (2022) · The Clinical Respiratory Journal · doi:10.1111/crj.13466 · Cited by 322
Pirfenidone and Nintedanib in Pulmonary Fibrosis: Lights and Shadows
Chianese, M. I., Screm, G., Salton, F., Confalonieri, P., Trotta, L., Barbieri, M., Ruggero, L., Mari, M., Reccardini, N., Geri, P., et al. (2024) · Pharmaceuticals · doi:10.3390/ph17060709 · Cited by 113
Sex and gender in interstitial lung diseases
Kawano-Dourado, L. B., Glassberg, M. K., Assayag, D., Borie, R., & Johannson, K. A. (2021) · European Respiratory Review · doi:10.1183/16000617.0105-2021 · Cited by 67
Idiopathic pulmonary fibrosis in the United States: time to diagnosis and treatment
Herberts, M. B., Teague, T., Thao, V., Sangaralingham, L. R., Henk, H. J., Hovde, K. T., Dempsey, T. M., & LIMPER, A. H. (2023) · BMC Pulmonary Medicine · doi:10.1186/s12890-023-02565-7 · Cited by 47
Self-citationShi, X., Chen, Y., Shi, M., Gao, F., Huang, L., Wang, W. J., Wei, D., Shi, C., Yu, Y., Xia, X., et al. (2024) · Lipids in Health and Disease · doi:10.1186/s12944-024-02062-8 · Cited by 44
Teague, T., Payne, S. R., Kelly, B. T., Dempsey, T. M., McCoy, R. G., Sangaralingham, L. R., & LIMPER, A. H. (2022) · Respiratory Research · doi:10.1186/s12931-022-02001-0 · Cited by 50
Self-citationPCSK6 and Survival in Idiopathic Pulmonary Fibrosis
Oldham, J. M., Allen, R. J., Lorenzo-Salazar, J. M., Molyneaux, P. L., Ma, S., Joseph, C., Kim, J. S., Guillén‐Guío, B., Hernández-Beeftink, T., Kropski, J. A., et al. (2023) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.202205-0845oc · Cited by 42
Progressive lung fibrosis: reprogramming a genetically vulnerable bronchoalveolar epithelium
Bridges, J. P., Vladar, E. K., Kurche, J. S., Krivoi, A., Stancil, I. T., Dobrinskikh, E., Hu, Y., Sasse, S. K., Lee, J. S., Blumhagen, R. Z., et al. (2025) · Journal of Clinical Investigation · doi:10.1172/jci183836 · Cited by 40
Inhaled Treprostinil for Idiopathic Pulmonary Fibrosis
Nathan, S. D., Smith, P., Deng, C., Salvo, M. D., Wuyts, W. A., Gallegos, J. P., Song, J. M., Kramer, M. R., King, C., Mackintosh, J. A., et al. (2026) · New England Journal of Medicine · doi:10.1056/nejmoa2512911 · Cited by 33
Man, R. K., Gogikar, A., Nanda, A., Janga, L. S. N., Sambe, H. G., Yasir, M., & Ramphall, S. (2024) · Cureus · doi:10.7759/cureus.54268 · Cited by 30
Relative environmental and social disadvantage in patients with idiopathic pulmonary fibrosis
Avitzur, N., Noth, E. M., Lamidi, M., Nathan, S. D., Collard, H. R., DeDent, A. M., Thakur, N., & Johannson, K. A. (2021) · Thorax · doi:10.1136/thoraxjnl-2021-217652 · Cited by 27
Dempsey, T. M., Thao, V., Moriarty, J. P., Borah, B. J., & LIMPER, A. H. (2022) · BMC Pulmonary Medicine · doi:10.1186/s12890-021-01811-0 · Cited by 25
Self-citationIdiopathic pulmonary fibrosis: Diagnosis, biomarkers and newer treatment protocols
Patel, H., Shah, J. R., Patel, D., Avanthika, C., Jhaveri, S., & Gor, K. (2022) · Disease-a-Month · doi:10.1016/j.disamonth.2022.101484 · Cited by 21
Regulator of Cell Cycle Protein (RGCC/RGC-32) Protects Against Pulmonary Fibrosis
Luzina, I. G., Rus, V., Lockatell, V., Courneya, J.-P., Hampton, B., Fishelevich, R., Misharin, A. V., Todd, N. W., Badea, T. C., Rus, H., et al. (2021) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2021-0022oc · Cited by 19
Interstitial lung disease progression after genomic usual interstitial pneumonia testing
Chaudhary, S., Weigt, S. S., Neto, M. L. R., Benn, B. S., Pugashetti, J. V., Keith, R. C., Chand, A., Oh, S., Kheir, F. M., Ramalingam, V. S., et al. (2022) · European Respiratory Journal · doi:10.1183/13993003.01245-2022 · Cited by 20
Chen, M. C., Korth, C. C., Harnett, M. D., Elenko, E., & Lickliter, J. D. (2022) · Clinical Pharmacology in Drug Development · doi:10.1002/cpdd.1040 · Cited by 18
Calabrese, F., Lunardi, F., Tauro, V., Pezzuto, F., Fortarezza, F., Vedovelli, L., Faccioli, E., Balestro, E., Schiavon, M., Esposito, G., et al. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23063323 · Cited by 18
Disparities in Antifibrotic Medication Utilization Among Veterans With Idiopathic Pulmonary Fibrosis
Kaul, B., Lee, J. S., Petersen, L. A., McCulloch, C. E., Rosas, I. O., Bandi, V., Zhang, N., DeDent, A. M., Collard, H. R., & Whooley, M. A. (2023) · CHEST Journal · doi:10.1016/j.chest.2023.02.027 · Cited by 18
Racial and ethnic disparities in antifibrotic therapy in idiopathic pulmonary fibrosis
Zhao, J. L., Fares, J., George, G., Maheu, A. R., Loizidis, G., Roman, J., Kramer, D., Li, M., & Summer, R. S. (2023) · Respirology · doi:10.1111/resp.14563 · Cited by 18
Jiang, H., Zheng, B., Hu, G., Kuang, L., Zhou, T., Li, S., Chen, X., Li, C., Zhang, D., Zhang, J., et al. (2024) · Journal of Pharmaceutical Analysis · doi:10.1016/j.jpha.2024.100971 · Cited by 15
Tikellis, G., & Holland, A. E. (2025) · European Respiratory Review · doi:10.1183/16000617.0176-2024 · Cited by 14
Citrus pectin-coated inhalable PLGA nanoparticles for treatment of pulmonary fibrosis
Perera, K. D. C., Ghumman, M., Sorkhdini, P., Norbrun, C., Negash, S., Zhou, Y., & Menon, J. U. (2025) · Journal of Materials Chemistry B · doi:10.1039/d4tb01682c · Cited by 14
Challenges in the Management of Post-COVID-19 Pulmonary Fibrosis for the Latin American Population
Chérrez-Ojeda, I., Cortés-Telles, A., Gochicoa‐Rangel, L., Camacho-Leon, G., Mautong, H., Robles‐Velasco, K., & Faytong‐Haro, M. (2022) · Journal of Personalized Medicine · doi:10.3390/jpm12091393 · Cited by 15
Lee, C. T., Hao, W., Burg, C., Best, J. H., Kolenic, G. E., & Strek, M. E. (2024) · Respiratory Research · doi:10.1186/s12931-024-02883-2 · Cited by 13
Interstitial Lung Disease and Sarcoidosis
Sharp, M., Mustafa, A., Farah, N., & Bonham, C. A. (2023) · Clinics in Chest Medicine · doi:10.1016/j.ccm.2023.06.003 · Cited by 12
Pirfenidone: A Promising Drug in Ocular Therapeutics
Bisen, A. C., Agrawal, S., Rayiti, R., Sanap, S. N., Biswas, A., Mishra, A., Gupta, N. M., & Bhatta, R. S. (2024) · Chemistry & Biodiversity · doi:10.1002/cbdv.202301389 · Cited by 11
Use of pirfenidone in fibrotic interstitial lung diseases and beyond: a review
Han, M., Liu, Q., Ji, Z., Jin, L., Jin, W., & Gao, Z. (2024) · Frontiers in Medicine · doi:10.3389/fmed.2024.1411279 · Cited by 11
Phase 3 Trials of Inhaled Treprostinil for Idiopathic Pulmonary Fibrosis
Nathan, S. D., Smith, P., Deng, C., King, C. S., Salvo, M. D., Weigt, S. S., Pandya, S., Bandyopadhyay, D., Lasky, J. A., Krishna, R., et al. (2026) · New England Journal of Medicine · doi:10.1056/nejmoa2501488 · Cited by 10
Focal adhesion kinase inhibitors in fibrotic diseases therapy: Development and therapeutic potential
Gan, C., Wei, W., Xue, T., Xie, Y., Yue, L., Su, X., Yan, Y., Liu, Z., & Ye, T. (2025) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2025.117882 · Cited by 12
Assayag, D., Adegunsoye, A., Sheehy, R. D., Morisset, J., Khalil, N., Johannson, K. A., Marcoux, V. S., Kolb, M. R. J., Fisher, J. H., Manganas, H., et al. (2023) · CHEST Journal · doi:10.1016/j.chest.2022.12.039 · Cited by 10
Safety of Nintedanib in a Patient with Chronic Pulmonary Fibrosis and Kidney Disease
Maggisano, M., Mondini, L., Chernovsky, M., Confalonieri, P., Salton, F., Reccardini, N., Kodric, M., Geri, P., Confalonieri, M., Hughes, M., et al. (2024) · Pharmaceuticals · doi:10.3390/ph17091147 · Cited by 9
Wong, S. L., Gan, J. S., Rubis, G. D., Paudel, K. R., Yeung, S., Chellappan, D. K., Keng, P. S., & Dua, K. (2024) · Journal of Drug Delivery Science and Technology · doi:10.1016/j.jddst.2024.105942 · Cited by 8
Effect of Antifibrotic Use on Mortality in Patients with Idiopathic Pulmonary Fibrosis
Xu, H., Hui, S. L., Lee, J. S., Zhang, Z., & Boente, R. (2024) · Annals of the American Thoracic Society · doi:10.1513/annalsats.202312-1054oc · Cited by 8
Qiaolongbatu, X., Zhao, W., Huang, X., Qian, F., Yang, X., Wu, J., Ma, C., Qu, H., Wang, L., Fan, G., et al. (2023) · Drug Design Development and Therapy · doi:10.2147/dddt.s391503 · Cited by 8
Uptake of Antifibrotics for Patients with Idiopathic Pulmonary Fibrosis: 2016–2022
Shankar, D. A., Hawkins, F. J., Alysandratos, K., Wilson, K. C., Walkey, A. J., Bosch, N. A., & Law, A. C. (2023) · Annals of the American Thoracic Society · doi:10.1513/annalsats.202308-697rl · Cited by 8
Meng, Y., Han, X., Ji, Q., Zhang, A., Zhan, Y., & Chen, X. (2024) · BMJ Open Respiratory Research · doi:10.1136/bmjresp-2024-002296 · Cited by 7
Salonen, J., Purokivi, M., Hodgson, U., & Kaarteenaho, R. L. (2022) · BMJ Open Respiratory Research · doi:10.1136/bmjresp-2022-001363 · Cited by 9
An, B., Fang, Y., Wang, L., Nie, W., Wang, M., Nie, H., Wu, C., & Wang, R. (2024) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2024.107374 · Cited by 6
Qiu, Y., Zhu, J., Chopra, P., Elpers, B., Dieyi, C., Byrne, C., Tang, J., Ye, W., Govindaraj, K., & Fischer, A. (2024) · Therapeutic Advances in Respiratory Disease · doi:10.1177/17534666241280704 · Cited by 6
Assayag, D., Adegunsoye, A., Khor, Y. H., Bonella, F., Borie, R., Buendía-Roldán, I., Chaudhuri, N., Gibson, K. F., Johannson, K. A., Kaminski, N., et al. (2025) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.202509-2336st · Cited by 7
The Impact of Nintedanib Dosing on Clinical Outcomes
LIMPER, A. H., Thao, V., Helfinstine, D. A., Sangaralingham, L. R., & Dempsey, T. M. (2024) · CHEST Journal · doi:10.1016/j.chest.2024.09.030 · Cited by 6
Self-citationBroad Adoption of Antifibrotics in Idiopathic Pulmonary Fibrosis: Still a Long Way to Go
Assayag, D. (2021) · Annals of the American Thoracic Society · doi:10.1513/annalsats.202102-123ed · Cited by 6
Antifibrotic Therapy for Idiopathic Pulmonary Fibrosis
Khor, Y. H. (2021) · CHEST Journal · doi:10.1016/j.chest.2021.07.033 · Cited by 7
Baig, S. H., & Yoo, E. J. (2024) · Life · doi:10.3390/life14010156 · Cited by 7
Maher, T. M., Hamblin, M. J., Choi, W.-I., Case, A. H., Tomos, I. P., Tzouvelekis, A. E., Shore, J. E., Bergna, M. A., Golod, D., Elenko, E., et al. (2026) · American Journal of Respiratory and Critical Care Medicine · doi:10.1093/ajrccm/aamag155 · Cited by 4
Majewski, S., Górska, K., Lewandowska, K. B., Martusewicz-Boros, M. M., Sobiecka, M., & Piotrowski, W. J. (2025) · Frontiers in Pharmacology · doi:10.3389/fphar.2025.1586197 · Cited by 4
Zhang, M., Wu, X., Zhu, H., Fu, C., Yang, W., Jing, X. B., Liu, W., & Cheng, Y. (2024) · Biochemical Genetics · doi:10.1007/s10528-024-10853-y · Cited by 4
Wang, Z., Sriram, S., Ugwoke, C., Gale, Z., Tabrizi, M. E. A., & Griffin, M. (2025) · Cells · doi:10.3390/cells14070497 · Cited by 4
Graham, C. S., Bisson, B., Shore, J. E., Pardy, E., Salisbury, F., LANCASTER, L. H., & Kulkarni, T. (2025) · BMC Pulmonary Medicine · doi:10.1186/s12890-025-03689-8 · Cited by 4
Editorial: Epidemiology and risk factors for interstitial lung diseases
Jeganathan, N., Corte, T. J., & Spagnolo, P. (2024) · Frontiers in Medicine · doi:10.3389/fmed.2024.1384825 · Cited by 4
Transcription factor MEOX1 accelerates pulmonary fibrosis by regulating mitophagy and senescence
Fang, L., Lyu, L., Zhong, H., Lin, J., Ren, P., Wang, Y., Yin, Y., Zhang, M., & Qu, Y.-Q. (2025) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2025.178043 · Cited by 3
Zhu, S., Zhou, J. Q., Wang, K., Guo, M., & Sanders, Y. Y. (2026) · Aging · doi:10.18632/aging.206357 · Cited by 4
Targeted Drug Delivery System for Pulmonary Fibrosis: Design and Development of Biomaterials
Liu, J., Pan, Z., Khan, A., & Li, H. (2025) · BIO Integration · doi:10.15212/bioi-2025-0016 · Cited by 5
Guidot, D. M., Pepin, M. J., Hastings, S. N., Tighe, R. M., & Schmader, K. E. (2025) · BMC Pulmonary Medicine · doi:10.1186/s12890-025-03611-2 · Cited by 3
Han, M. K., Shteinberg, M., Assayag, D., Schleich, F., Pengo, M. F., Scicluna, V. M., Lombardi, C., Barrecheguren, M., & Jara‐Palomares, L. (2024) · Archivos de Bronconeumología · doi:10.1016/j.arbres.2024.10.009 · Cited by 3
Comparing the Utilization of Antifibrotic Medications Based on Income Level
Dempsey, T. M., Thao, V., Helfinstine, D. A., Sangaralingham, L. R., & LIMPER, A. H. (2023) · CHEST Journal · doi:10.1016/j.chest.2023.07.4215 · Cited by 2
Self-citationCaring for Rural Patients With Interstitial Lung Disease
DeDent, A. M., Shore, J. E., Bascom, R., Reichuber, J., Scholand, M. B., Boente, R., Nambiar, A. M., Danoff, S. K., Rahaghi, F., Kulkarni, T., et al. (2025) · CHEST Pulmonary · doi:10.1016/j.chpulm.2025.100136 · Cited by 2
Luo, Y., Assassi, S., Mayes, M. D., Frech, T., Steen, V. D., Richardson, C., Chung, L. S., Sandorfi, N., VanBuren, J. M., Harding, M. L., et al. (2025) · Annals of the American Thoracic Society · doi:10.1513/annalsats.202410-1045rl · Cited by 2
Mefunidone treats pulmonary fibrosis by targeting SDH to regulate fibro-promoting macrophages
Zhang, X., He, Y., Long, L., Jiang, G., Yao, T., Cheng, X., Peng, Z., Hu, G., Tao, L., & Meng, J. (2025) · International Immunopharmacology · doi:10.1016/j.intimp.2025.114971 · Cited by 2
Aiming to Improve Equity in Lung Health: Sex and Gender
Wojcik, R. M., & Morris, A. M. (2023) · Clinics in Chest Medicine · doi:10.1016/j.ccm.2023.03.014 · Cited by 2
Polat, G., Özdemir, Ö., Ermin, S., Unat, D. S., & Üçsular, F. D. (2024) · Sarcoidosis vasculitis and diffuse lung diseases · doi:10.36141/svdld.v41i2.13779 · Cited by 2
Yue, L., Jiang, N., Fan, X., Xu, S., Yi, R., Lei, H., & Zhai, X. (2025) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2025.118013 · Cited by 2
Johannson, K. A., Collard, H. R., & Richeldi, L. (2021) · Clinics in Chest Medicine · doi:10.1016/j.ccm.2021.03.014 · Cited by 2
Research advances in self-assembled peptide delivery systems for fibrosis treatment
Zhang, Y., Su, D., & Wang, Y. (2025) · Precision medicine and engineering. · doi:10.1016/j.preme.2025.100043 · Cited by 1
Fares, W. H., & Castagna, M. (2026) · Journal of Aerosol Medicine and Pulmonary Drug Delivery · doi:10.1177/19412711251414386 · Cited by 1
Farrand, E. D., Chung, A., Joshua, J., Dong, H., Mills, H., Lee, A., Ieong, M. M., Radhakrishnan, L., Gologorskaya, O., & Butte, A. J. (2026) · EClinicalMedicine · doi:10.1016/j.eclinm.2026.103790 · Cited by 1
Geriatric nutritional risk index in antifibrotic therapy can predict tolerability and mortality risk
Masuda, T., Mochizuka, Y., Suzuki, Y., Kono, M., Matsushima, S., Kato, S., Suzuki, K., Tanaka, K., Koda, K., Masuda, T., et al. (2026) · Scientific Reports · doi:10.1038/s41598-026-45792-8 · Cited by 1
Braverman, G., Aronson, K. I., Thomas, C., & Spiera, R. (2026) · Rheumatology Advances in Practice · doi:10.1093/rap/rkag050 · Cited by 1
Foudah, A. I., & Alam, A. (2026) · Chinese Herbal Medicines · doi:10.1016/j.chmed.2026.05.008 · Cited by 1
Suzuki, Y., Kono, M., Matsushima, S., Kato, S., Suzuki, K., Tanaka, K., Koda, K., Masuda, T., Kanai, M., Ikeda, M., et al. (2026) · ERJ Open Research · doi:10.1183/23120541.00402-2026 · Cited by 1
Zhang, S.-M., Huang, M.-Z., Wang, Y.-W., Wang, X.-F., Ding, Y., Li, J. Q., Zou, X.-M., & Ma, C. (2026) · Respiratory Medicine · doi:10.1016/j.rmed.2026.108946 · Cited by 1
Xu, L., 臧丹阳, Yan, R., Liang, Z., Yang, S., Yu, N., & Yu, X. (2026) · BMC Pulmonary Medicine · doi:10.1186/s12890-026-04400-1 · Cited by 1
Interstitial Lung Disease in Veterans: Leveraging Big Data to Bridge Evidence and Practice Gaps
Kaul, B., Petersen, L. A., Rosas, I. O., Lee, J. S., Martínez, F. J., Bandi, V., Helmer, D. A., Wolters, P. J., Collard, H. R., & Whooley, M. A. (2023) · Annals of the American Thoracic Society · doi:10.1513/annalsats.202211-942ps · Cited by 1
Lee, H. Y., Jung, S. Y., Jang, J. H., Ko, J., Kim, D.-W., Her, M., & Lee, J. H. (2023) · Life · doi:10.3390/life13112118 · Cited by 1
Gaffney, A. W., & Podolanczuk, A. J. (2022) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.202111-2652ed · Cited by 1
Ma, A., & Montesi, S. B. (2025) · ERJ Open Research · doi:10.1183/23120541.01395-2024 · Cited by 1
Adoption of Antifibrotic Medications: A Closer Look at the Data
White, E. S., Nili, M., Shetty, S. S., & Leonard, T. B. (2021) · Annals of the American Thoracic Society · doi:10.1513/annalsats.202103-359le
Reply: Adoption of Antifibrotic Medications: A Closer Look at the Data
Dempsey, T. M., Payne, S. R., Sangaralingham, L. R., & LIMPER, A. H. (2021) · Annals of the American Thoracic Society · doi:10.1513/annalsats.202104-516le
Self-citationEinsatz antifibrotischer Medikamente bei interstitiellen Lungenerkrankungen
Kreutz, C.-P., Gesierich, W., Behr, J., & Kneidinger, N. (2022) · DMW - Deutsche Medizinische Wochenschrift · doi:10.1055/a-1825-4967
Jain, S., Witt, L. J., & Ferrante, L. E. (2022) · Journal of the American Geriatrics Society · doi:10.1111/jgs.18196
Locke, B. W., & Callahan, S. J. (2023) · CHEST Journal · doi:10.1016/j.chest.2023.03.037
Geschlechtsspezifische Aspekte bei interstitiellen Lungenerkrankungen
Buschulte, K., & Polke, M. (2024) · Zeitschrift für Pneumologie · doi:10.1007/s10405-024-00551-2
李, 亚. (2024) · Journal of Clinical Personalized Medicine · doi:10.12677/jcpm.2024.33091
The Impact of Obstructive Sleep Apnea on Idiopathic Pulmonary Fibrosis Clinical Outcomes
Hamza, A., Helfinstine, D. A., Herberts, M. B., Olson, E. J., Dempsey, T. M., & Limper, A. H. (2025) · Journal of Clinical Sleep Medicine · doi:10.1007/s44470-026-00054-2
Self-citationBig Data: Pearls and Pitfalls for Precision Medicine in Interstitial Lung Disease
Kaul, B., Collard, H. R., & Petersen, L. A. (2025) · Respiratory medicine · doi:10.1007/978-3-031-87183-2_10
A phase 1 pharmacokinetics study of deupirfenidone (LYT-100) in healthy older adults
Maher, T. M., Chen, M. J., Korth, C. C., Elenko, E., Harnett, M. D., Garg, V., & Graham, C. S. (2025) · ERJ Open Research · doi:10.1183/23120541.00469-2025
Trends in Medicare Part D Spending on Antifibrotic Therapies for Pulmonary Fibrosis: 2019–2023Preprint
RIZLY, S., VAITHISWARAN, D., Lorenzana, A. M., & Saleh, A. G. (2025) · medRxiv · doi:10.1101/2025.08.01.25332591
Herberts, M. B., Teague, T., Thao, V., Sangaralingham, L. R., Henk, H. J., Hovde, K. T., Dempsey, T. M., & LIMPER, A. H. (2023) · Figshare · doi:10.6084/m9.figshare.23826911
Self-citationLee, C. T., Hao, W., Burg, C., Best, J. H., Kolenic, G. E., & Strek, M. E. (2024) · Figshare · doi:10.6084/m9.figshare.26737635
Economic Burden of Idiopathic Pulmonary Fibrosis: Updated Evidence on Costs and Resource Use
Diamantopoulos, A., Pople, O., Godman, A., & Papastergios, E. (2026) · PharmacoEconomics · doi:10.1007/s40273-026-01600-9
Bao, H., Jian, Y., Penaloza-Ramos, C. M., Kanakapura, M., Deng, Z., Xuan, J., & Zhao, H. (2026) · Pharmacoeconomics and Policy · doi:10.1016/j.pharp.2026.03.005
Kourlaba, G., Stefanou, G., Ravanidis, S., Mathioudakis, K., Tsolakidis, A., & Zografopoulos, D. (2026) · Respiratory Medicine and Research · doi:10.1016/j.resmer.2026.101269
Xu, H., Meier, E., Chhabria, M., DeDent, A. M., Hui, S. L., Zhang, Z., & Boente, R. (2026) · CHEST Journal · doi:10.1016/j.chest.2026.03.040
Yang, J., Fee, R. M., Steffens, A., Le, L., Bui, B. H., & Borah, B. J. (2026) · Journal of health economics and outcomes research · doi:10.36469/jheor.2026.161503
Chee, M., Khor, Y. H., Jackson, D., Cooper, W., D’Costa, J., de Boer, S., Edwards, A., Ellis, S. J., Gabbay, E., Gallagher, H., et al. (2026) · Internal Medicine Journal · doi:10.1111/imj.70490
Senescent fibroblasts in aging and pulmonary fibrosis
Palega, S., Borengasser, A. Y., & Sanders, Y. Y. (2026) · Frontiers in Aging · doi:10.3389/fragi.2026.1816071
Zhang, Q., Ouyang, X., Tan, Y., Qian, Y., Song, M., & Peng, H. (2026) · Annals of Medicine · doi:10.1080/07853890.2026.2689565
Jafari, A., Manzari‐Tavakoli, A., Tavakoli, M. M., Hashemian, S. M., Jamaati, H., Akhtari, M., Tabarsi, P., & Omrani, M. (2026) · Expert Review of Molecular Diagnostics · doi:10.1080/14737159.2026.2714060
The anti-fibrotic effects of irisolidone via peroxisome proliferator-activated receptor gamma
Pan, Z.-A., Tong, L.-T., & Wang, Z.-M. (2026) · Tissue and Cell · doi:10.1016/j.tice.2026.103916
Bajpai, J., Pradhan, A. K., Manek, G., Maurya, S., Kant, S., & Perrone, M. A. (2026) · Advances in respiratory medicine · doi:10.3390/arm94050073
Metadata
- Authors
- Dempsey, T. M., Payne, S., Sangaralingham, L., Yao, X., Shah, N. D., & Limper, A. H.
- Affiliations
- Department of Pulmonary and Critical Care Medicine
- Robert D. and Patricia E. Kern Center for the Science of Health Care Delivery
- Mayo Clinic (US)
- Corresponding author
- Dempsey, Timothy M.
- ORCID
- Venue
- Annals of the American Thoracic Society
- Publisher
- Oxford University Press (OUP)
- Published
- 2021-07-01
- Volume
- 18
- Issue
- 7
- Pages
- 1121-1128
- ISSN
- 2325-6621 (ISSN-L)
- 2329-6933
- OpenAlex
- W3122584685
- Cited by
- 101
- References
- 33
- Citations by year
- 2026: 24 · 2025: 21 · 2024: 22 · 2023: 14 · 2022: 11 · 2021: 9
- FWCI
- 9.09
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Annals of the American Thoracic Society (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Chronic Obstructive Pulmonary Disease (COPD) Research
- Social Sciences › Economics, Econometrics and Finance › Economics and Econometrics › Pharmaceutical Economics and Policy
- Keywords
- idiopathic pulmonary fibrosis, pirfenidone, nintedanib, antifibrotic agents, treatment persistence, out-of-pocket costs, prescription drug costs, Medicare Advantage beneficiaries, real-world applications, drug approval
- MeSH terms
- Aged, Pharmaceutical Preparations, Female, Medicare, Humans, Indoles, Male, Pyridones, Retrospective Studies, United States, Treatment Outcome, Idiopathic Pulmonary Fibrosis
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review