176 results on '"Weatherald J"'
Search Results
2. The Clinical Impact of Heart Failure With Preserved Ejection Fraction in Interstitial Lung Diseases
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Zanini, U., primary, Ferrara, G., additional, Moitra, S., additional, Varughese, R.A., additional, Kalluri, M., additional, and Weatherald, J., additional
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- 2024
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3. Predicting Renal Function After Lung Transplantation
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Gouda, J., primary, Kaur, K., additional, Hirji, A., additional, Weinkauf, J., additional, Lien, D., additional, Varughese, R., additional, van den Bosch, L., additional, Weatherald, J., additional, Gauthier, P., additional, and Halloran, K., additional
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- 2024
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4. Investigating Pulmonary Vascular Disease in Patients with Long COVID Using Methylation Patterns in Cell-Free DNA
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Iqbal, F., primary, Ehteshami Afshar, E., additional, Lewis, J., additional, Thakrar, M., additional, Kularatne, M., additional, Helmersen, D., additional, Hirani, N., additional, Mak, S., additional, Granton, J., additional, Greenway, S., additional, and Weatherald, J., additional
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- 2024
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5. SEVERITY OF ILLNESS IN INDIGENOUS PATIENTS WITH PULMONARY ARTERIAL HYPERTENSION IN CANADA
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Cheung, A., primary, Marchand, M., additional, Kolkman, L., additional, Swiston, J., additional, Kapasi, A., additional, Weatherald, J., additional, and Brunner, N., additional
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- 2023
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6. Klippel-Trenaunay syndrome as a rare cause of chronic thromboemboembolic pulmonary hypertension
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Seferian, A., Jaïs, X., Savale, L., Jevnikar, M., Ghigna, M.-R., Weatherald, J., Assoun, S., Fadel, E., Simonneau, G., Sitbon, O., Humbert, M., and Montani, D.
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- 2019
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7. Transitioning Patients With Pulmonary Arterial Hypertension From Parenteral Prostacyclin Therapy to Oral Selexipag: A Multi-center Retrospective Cohort Study
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Budhram, B., primary, Spence, E., additional, Weatherald, J., additional, Gardner, A., additional, Kemp, K., additional, Fox, G.A., additional, Legkaia, L., additional, Swiston, J.R., additional, Thakrar, M., additional, Liu, J., additional, Helmerson, D., additional, Harper, L., additional, Kularatne, M., additional, Hirani, N., additional, Wadden, D., additional, Foxall, J., additional, Chandy, G., additional, Provencher, S., additional, and Hambly, N., additional
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- 2023
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8. Persistence and Predictors of Persistency for Pulmonary Arterial Hypertension (PAH) Patients on Selexipag in Canada: A Retrospective Claims Database Study
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Ibrahim, E., primary, Mielniczuk, L., additional, Provencher, S., additional, Swiston, J., additional, Weatherald, J., additional, Yip, C., additional, Zhang, C., additional, Murray, J., additional, Badin, M., additional, Golden, S., additional, and Millson, B., additional
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- 2023
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9. VENTRICULAR-ARTERIAL DECOUPLING IS ASSOCIATED WITH IN-HOSPITAL ADVERSE EVENTS IN NORMOTENSIVE PULMONARY EMNBOLISM
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Prosperi-Porta, G., primary, Kiamanesh, O., additional, Fine, N., additional, Ferland, A., additional, Harper, L., additional, Solverson, K., additional, Boiteau, P., additional, Helmerson, D., additional, and Weatherald, J., additional
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- 2022
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10. Validation of EmPHasis-10 health-related quality of life assessment tool in Canadian patients with pulmonary hypertension.
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McBride, A, primary, Helmersen, D, additional, Hirani, N, additional, Thakrar, M, additional, Kularatne, M, additional, Liu, J, additional, Harper, L, additional, Iqbal, H, additional, Naser, A, additional, Varughese, R, additional, and Weatherald, J, additional
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- 2022
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11. Awake Prone Positioning for COVID-19 Hypoxemic Respiratory Failure: A Systematic Review and Meta-Analysis of Randomized Trials
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Weatherald, J, primary, Parhar, K K S, additional, Al Duhailib, Z, additional, Chu, D, additional, Granholm, A, additional, Solverson, K, additional, Lewis, K, additional, Hylander Møller, M, additional, Alshahrani, M, additional, Belley-Côté, E, additional, Loroff, N, additional, Gatto, C, additional, Qian, E T, additional, Rice, T, additional, Niven, D, additional, Stelfox, H T, additional, Fiest, K, additional, Cook, D, additional, Arabi, Y, additional, and Alhazzani, W, additional
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- 2022
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12. Awake Prone Positioning in Acute Hypoxemic Respiratory Failure from COVID-19: A Randomized Clinical Trial
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Alhazzani, W, primary, Parhar, K K S, additional, Weatherald, J, additional, Al Duhailib, Z, additional, Alshahrani, M, additional, Al-Fares, A, additional, Buabbas, S, additional, Cherian, S V, additional, Munshi, L, additional, Fan, E, additional, Al-Hameed, F, additional, Chalabi, J, additional, Rahmatullah, A A, additional, Duan, E, additional, Tsang, J L, additional, Lewis, K, additional, Lauzier, F, additional, Centofanti, J, additional, Rochwerg, B, additional, Culgin, S, additional, Nelson, K, additional, Abdukahil, S A, additional, Fiest, K M, additional, Stelfox, H T, additional, Tlayjeh, H, additional, Meade, M O, additional, Perri, D, additional, Solverson, K, additional, Niven, D J, additional, Lim, R, additional, Møller, M H, additional, Belley-Cote, E, additional, Thabane, L, additional, Tamim, H, additional, Cook, D J, additional, and Arabi, Y M, additional
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- 2022
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13. Research priorities for future pulmonary hypertension research: a James Lind Alliance priority setting partnership
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Weatherald, J, primary, Iqbal, H, additional, Mielniczuk, L, additional, Syed, A R, additional, Howard, J, additional, Dempsey, N, additional, Rader, T, additional, Swiston, J, additional, and Provencher, S, additional
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- 2022
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14. Change in Lung Function and Health Related Quality of Life in Post-COVID-19 Infection: A Provincial, 3-Month Follow-Up Study in Canada
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Smith, M., primary, Moitra, S., additional, Fuhr, D.P., additional, Befus, D., additional, Chen, J., additional, Damant, R.W., additional, Ferrara, G., additional, Laratta, C., additional, Lau, A., additional, Liu, J., additional, Lim, R., additional, Sorril, L., additional, Stickland, M.K., additional, Weatherald, J., additional, Varughese, R., additional, Wong, E.Y., additional, and Lam, G.Y., additional
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- 2022
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15. Successful Use of Mepolizumab for Steroid-Dependent Chronic Eosinophilic Pneumonia
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Cyca, P., primary, Walker, B.L., additional, Mitchell, P., additional, and Weatherald, J., additional
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- 2022
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16. (642) - Investigating Pulmonary Vascular Disease in Patients with Long COVID Using Methylation Patterns in Cell-Free DNA
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Ehteshami Afshar, E., Lewis, J., Thakrar, M., Kularatne, M., Helmersen, D., Hirani, N., Mak, S., Granton, J., Greenway, S., and Weatherald, J.
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- 2024
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17. (632) - Predicting Renal Function After Lung Transplantation
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Kaur, K., Hirji, A., Weinkauf, J., Lien, D., Varughese, R., van den Bosch, L., Weatherald, J., Gauthier, P., and Halloran, K.
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- 2024
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18. SEVERITY OF ILLNESS IN INDIGENOUS PATIENTS WITH PULMONARY ARTERIAL HYPERTENSION IN CANADA
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Cheung, A., Marchand, M., Kolkman, L., Swiston, J., Kapasi, A., Weatherald, J., and Brunner, N.
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- 2023
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19. Early Echocardiographic Improvements with Upfront Riociguat and Ambrisentan Combination Therapy for Incident Pulmonary Arterial Hypertension
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Thornton, C.S., primary, Helmersen, D., additional, Thakrar, M.V., additional, Varughese, R.A., additional, Fine, N.M., additional, Hirani, N., additional, and Weatherald, J., additional
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- 2020
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20. Validation of a Nurse Led Triage Algorithm for New Referrals in a Specialized Pulmonary Hypertension Clinic
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Kularatne, M., primary, Weatherald, J., additional, Varughese, R., additional, Helmersen, D., additional, Hirani, N., additional, Chou, J., additional, Janovcik, J., additional, Livingston, N., additional, Petkau, J., additional, Lee, M., additional, and Thakrar, M., additional
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- 2020
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21. Hypertension pulmonaire et exposition au léflunomide : données du registre français de l’hypertension pulmonaire
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Lacoste Palasset, T., primary, Chaumais, M.C., additional, Savale, L., additional, Jais, X., additional, Weatherald, J., additional, Chabanne, C., additional, Ahmad, K., additional, Guillaumot, A., additional, Favrolt, N., additional, Reynaud-Gaubert, M., additional, Lamblin, N., additional, Sitbon, O., additional, Humbert, M., additional, and Montani, D., additional
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- 2020
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22. PULMONARY ARTERY MORPHOLOGY AS A BIOMARKER OF PULMONARY HYPERTENSION
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Hong, Z., Garcia, J., Howarth, A., Lydell, C., Weatherald, J., and White, J.
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- 2018
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23. P4690Effects of pulmonary artery wedge pressure on right ventricular pulsatile loading in pulmonary hypertension: a reappraisal based on pulmonary arterial isobaric stiffness
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Chemla, D, primary, Berthelot, E, additional, Weatherald, J, additional, Lau, E, additional, Attal, P, additional, Boulate, D, additional, Montani, D, additional, Jourdain, P, additional, Humbert, M, additional, Assayag, P, additional, and Herve, P, additional
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- 2019
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24. IMPACT OF SALINE LOADING AT CATHETERIZATION ON THE CLASSIFICATION AND MANAGEMENT OF PATIENTS EVALUATED FOR PULMONARY HYPERTENSION
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Moghaddam, N., primary, Swiston, J., additional, Kapasi, A., additional, Mielniczuk, L., additional, Hambly, N., additional, Weatherald, J., additional, and Brunner, N., additional
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- 2018
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25. ROLES OF WALL SHEAR STRESS AND PRESSURE MAPPING AS BIOMARKERS OF PULMONARY HYPERTENSION
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Hong, Z., primary, Garcia, J., additional, Howarth, A., additional, Lydell, C., additional, Weatherald, J., additional, and White, J., additional
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- 2018
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26. P2614Factors associated with survival in patients with not-operated chronic thromboembolic pulmonary hypertension (CTEPH) in the modern management era
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Taniguchi, Y, primary, Jais, X, additional, Boucly, A, additional, Weatherald, J, additional, Jevnikar, M, additional, Brenot, P, additional, Planche, O, additional, Parent, F, additional, Savale, L, additional, Montani, D, additional, Fadel, E, additional, Humbert, M, additional, Simonneau, G, additional, and Sitbon, O, additional
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- 2018
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27. Hypertension pulmonaire sévère associée aux maladies pulmonaires chroniques post-tabagiques bronchiques ou emphysémateuses
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Chelabi, S., primary, Chassagnon, G., additional, Savale, L., additional, Weatherald, J., additional, Jais, X., additional, Boucly, A., additional, Mal, H., additional, Burgel, P.R., additional, Simonneau, G., additional, Sitbon, O., additional, Humbert, M., additional, and Montani, D., additional
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- 2018
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28. Influence de la stratégie thérapeutique initiale sur la survie des patients atteints d’HTAP : trithérapie d’emblée, le tiercé gagnant
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Boucly, A., primary, Weatherald, J., additional, Saval, L., additional, Montani, D., additional, Jevnikar, M., additional, Jaïs, X., additional, Simonneau, G., additional, Humbert, M., additional, and Sitbon, O., additional
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- 2018
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29. (642) - Investigating Pulmonary Vascular Disease in Patients with Long COVID Using Methylation Patterns in Cell-Free DNA.
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Iqbal, F., Ehteshami Afshar, E., Lewis, J., Thakrar, M., Kularatne, M., Helmersen, D., Hirani, N., Mak, S., Granton, J., Greenway, S., and Weatherald, J.
- Subjects
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POST-acute COVID-19 syndrome , *CELL-free DNA , *METHYLATION , *CIRCULATING tumor DNA ,PULMONARY artery diseases - Published
- 2024
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30. (632) - Predicting Renal Function After Lung Transplantation.
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Gouda, J., Kaur, K., Hirji, A., Weinkauf, J., Lien, D., Varughese, R., van den Bosch, L., Weatherald, J., Gauthier, P., and Halloran, K.
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LUNG transplantation , *KIDNEY physiology , *FORECASTING - Published
- 2024
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31. Phenotypes in pulmonary hypertension.
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Weatherald J, Hemnes AR, Maron BA, Mielniczuk LM, Gerges C, Price LC, Hoeper MM, and Humbert M
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- Humans, Prognosis, Pulmonary Arterial Hypertension physiopathology, Pulmonary Arterial Hypertension diagnosis, Pulmonary Arterial Hypertension classification, Phenotype, Hypertension, Pulmonary classification, Hypertension, Pulmonary physiopathology, Hypertension, Pulmonary diagnosis, Hypertension, Pulmonary therapy
- Abstract
The clinical classification of pulmonary hypertension (PH) has guided diagnosis and treatment of patients with PH for several decades. Discoveries relating to underlying mechanisms, pathobiology and responses to treatments for PH have informed the evolution in this clinical classification to describe the heterogeneity in PH phenotypes. In more recent years, advances in imaging, computational science and multi-omic approaches have yielded new insights into potential phenotypes and sub-phenotypes within the existing clinical classification. Identification of novel phenotypes in pulmonary arterial hypertension (PAH) with unique molecular profiles, for example, could lead to new precision therapies. Recent phenotyping studies have also identified groups of patients with PAH that more closely resemble patients with left heart disease (group 2 PH) and lung disease (group 3 PH), which has important prognostic and therapeutic implications. Within group 2 and group 3 PH, novel phenotypes have emerged that reflect a persistent and severe pulmonary vasculopathy that is associated with worse prognosis but still distinct from PAH. In group 4 PH (chronic thromboembolic pulmonary disease) and sarcoidosis (group 5 PH), the current approach to patient phenotyping integrates clinical, haemodynamic and imaging characteristics to guide treatment but applications of multi-omic approaches to sub-phenotyping in these areas are sparse. The next iterations of the PH clinical classification are likely to reflect several emerging PH phenotypes and improve the next generation of prognostication tools and clinical trial design, and improve treatment selection in clinical practice., Competing Interests: Conflict of interest: J. Weatherald reports grants from Janssen, Bayer, Merck and AstraZeneca; consulting fees and lecture honoraria from Janssen and Merck; payment for expert testimony from Sprigings Intellectual Property Law; travel support from Janssen; advisory board participation with Janssen, Acceleron and Université Laval; and a leadership role on the medical advisory committee for Pulmonary Hypertension Association of Canada, outside the submitted work. A.R. Hemnes reports grants from NIH; consulting fees from Gossamer Bio, United Therapeutics, Bayer, Janssen, Merch and Tenax Therapeutics; advisory board participation with NIH/NHLBI; leadership roles with the Nashville Ballet and Pulmonary Vascular Research Institute; and stock or stock options with Tenax Therapeutics, outside the submitted work. B.A. Maron reports grants from NIH/NHLBI; consulting fees from Actelion and Tenax Therapeutics; and the following patents: PCT/US2019/059890, #9605047 and PCT/US2020/066886, outside the submitted work. L.M. Mielniczuk reports consulting fees from Bayer, Merck and Janssen; lecture honoraria from Janssen and Merck; and leadership roles as Chair of Pulmonary Hypertension Association of Canada and Vice President of Canadian Heart Failure Society, outside the submitted work. C. Gerges reports support for the present manuscript from OrphaCare; outside the submitted work, C. Gerges reports lecture honoraria from AOPHealth, AstraZeneca, Janssen and Ferrer; and travel support from AOPHealth, AstraZeneca, Cordis, Janssen and MSD. L.C. Price reports grants from Ferrer; lecture honoraria from Janssen, Ferrer and MSD; travel support from Janssen, Ferrer Pharmaceuticals and Altavant; and advisory board participation with Janssen, outside the submitted work. M.M. Hoeper reports consulting fees from Acceleron, Actelion, Altavant, AOP Health, Bayer, Ferrer, Gossamer Bio, Janssen, Keros and MSD; lecture honoraria from Acceleron, Actelion, AOP Health, Bayer, Ferrer, Janssen and MSD; and US patent application #63466014 (Methods of improving lung diffusion capacity in a patients with pulmonary arterial hypertension, application filed by MSD), outside the submitted work. M. Humbert reports grants from Acceleron, AOP Orphan, Janssen, Merck and Shou Ti; consulting fees from Acceleron, Aerovate, Altavant, AOP Orphan, Bayer, Chiesi, Ferrer, Janssen, Merck, MorphogenIX, Shou Ti and United Therapeutics; lecture honoraria from Janssen and Merck; and advisory board participation with Acceleron, Altavant, Janssen, Merck and United Therapeutics, outside the submitted work., (Copyright ©The authors 2024. For reproduction rights and permissions contact permissions@ersnet.org.)
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- 2024
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32. Impact of COVID-19 Pandemic on Chronic Obstructive Pulmonary Disease Healthcare Use, Exacerbations, and Mortality: A Population Study.
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Lam GY, Wen C, Ronksley PE, Bakal JA, Bhutani M, Soril LJJ, Stickland MK, Gross DP, and Weatherald J
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- Humans, Male, Female, Retrospective Studies, Aged, Alberta epidemiology, Middle Aged, Patient Acceptance of Health Care statistics & numerical data, Aged, 80 and over, Ambulatory Care statistics & numerical data, Disease Progression, Pandemics, COVID-19 mortality, COVID-19 epidemiology, COVID-19 therapy, Pulmonary Disease, Chronic Obstructive mortality, Pulmonary Disease, Chronic Obstructive epidemiology, Hospitalization statistics & numerical data, SARS-CoV-2, Emergency Service, Hospital statistics & numerical data
- Abstract
Rationale: Existing work suggests that patients with chronic obstructive pulmonary disease (pwCOPD) presented less frequently to the emergency department and were less likely to be hospitalized during the coronavirus disease (COVID-19) pandemic, but it is unclear if this was due to improved health and disease management or to increased barriers and/or avoidance of health care. Objectives: The objective of this study was to determine the impact of the pandemic on inpatient and outpatient healthcare use, disease incidence, and mortality rates in pwCOPD. Methods: A retrospective population-based analysis using linked administrative datasets from Alberta, Canada 18 months before and after March 12, 2020 was conducted to measure hospitalization, emergency department and outpatient visits, and COPD outpatient exacerbations during these time periods. Mortality data were also analyzed before versus after the pandemic, taking confirmed COVID-19 infection within 30 days into account. Subgroup analysis based on COPD exacerbation risk stratification was undertaken to determine if healthcare use differed based on exacerbation risk. Finally, sex-based analysis of healthcare use during the pandemic was also completed. Results: Hospitalization or emergency department visits and outpatient treatment for acute exacerbations of COPD dropped, whereas total outpatient COPD visits, including both virtual and in person, increased during the pandemic for pwCOPD. The mortality rate increased even after adjusting for COVID-19-associated deaths. Sex-based subgroup analysis showed a greater drop in acute care use for females, but the rise in mortality was seen for both sexes, with men experiencing a greater rate of mortality than women. Conclusions: Overall, pwCOPD accessed acute care resources less during the pandemic, which may have contributed to a rise in non-COVID-19 all-cause mortality.
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- 2024
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33. Clinical trial design, end-points, and emerging therapies in pulmonary arterial hypertension.
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Weatherald J, Fleming TR, Wilkins MR, Cascino TM, Psotka MA, Zamanian R, Seeger W, Galiè N, and Gomberg-Maitland M
- Abstract
Clinical trials in pulmonary arterial hypertension (PAH) have led to the approval of several effective treatments that improve symptoms, exercise capacity and clinical outcomes. In phase 3 clinical trials, primary end-points must reflect how a patient "feels, functions or survives". In a rare disease like PAH, with an ever-growing number of treatment options and numerous candidate therapies being studied, future clinical trials are now faced with challenges related to sample size requirements, efficiency and demonstration of incremental benefit on traditional end-points in patients receiving background therapy with multiple drugs. Novel clinical trial end-points, innovative trial designs and statistical approaches and new technologies may be potential solutions to tackle the challenges facing future PAH trials, but these must be acceptable to patients and regulatory bodies while preserving methodological rigour. In this World Symposium on Pulmonary Hypertension task force article, we address emerging trial end-points and designs, biomarkers and surrogate end-point validation, the concept of disease modification, challenges and opportunities to address diversity and representativeness, and the use of new technologies such as artificial intelligence in PAH clinical trials., Competing Interests: Conflict of interest: J. Weatherald declares grants or contracts to their institution from Janssen, Bayer, Merck, AstraZeneca and Sanofi; consulting fees, payment or honoraria to themselves, travel support and paid membership of an Advisory Board from Janssen and Merck; payment for expert testimony from Sprigings Intellectual Property Law; unpaid membership of a Data Safety Monitoring Board drom Université Laval; and unpaid membership of the medical advisory committee of the Pulmonary Hypertension Association of Canada and the scientific medical advisory committee of the Pulmonary Vascular Research Institute. T.R. Fleming declares no competing interests. M.R. Wilkins declares grants or contracts from the British Heart Foundation (RE/18/4/34215 centre support); consulting fees from MorphogenIX (advisory committee), VIVUS (study protocol advisory meeting), Janssen and Kinaset (study advisory boards) and Chiesi, Aerami and Benevolent AI (consultancy); payment for expert testimony from Pennington Marches and Sprigings; support for travel to scientific meetings from Apollo Therapeutics; patents planned, issued or pending (Imperial Innovations: patent submitted for prognostic protein model presented in this manuscript; patent for ZIP12 as a drug target; patent for TSPO as a drug target); membership of an adjudication committee for three clinical trials for Acceleron; membership of study safety committees for GSK and Novartis; a role as a trustee of the Pulmonary Vascular Research Institute; and stock options in W12 Therapeutics. T.M. Cascino delares grants from NHLBI (K12 HL138039) and Johnson & Johnson Innovative Medicine; consulting fees from and participation on a Data Safety Monitoring Board or Advisory Board for Merck; and payment or honoraria from Total CME. M.A. Psotka declares no competing interests. R. Zamanian declares grants to their institution from Gossamer Bio, Merck, United Therapeutics and Janssen; consulting fees from Gossamer Bio, Morphogen IX, Merck and Aerovate; patents planned, issued or pending for FK506 for treatment of pulmonary hypertension; participation on a Data Safety Monitoring Board or Advisory Board for Aerovate; and stock options in REVIVA. W. Seeger declares consulting fees from United Therapeutics, Abivax, Tiakis Biotech AG, Pfizer, Liquidia, Medspray BV and Pieris Pharmaceuticals. N. Galiè declares grants or contracts from Janssen, Actelion and Merck; consulting fees from Janssen, Actelion, Chiesi and Ferrer; payment or honoraria from Janssen, Actelion and Chiesi; support for attending meetings and/or travel from Dompe; and participation on a Data Safety Monitoring Board or Advisory Board from Janssen, Actelion and Ferrer. M. Gomberg-Maitland declares consulting fees from Acceleron/Merck (steering committee), Aerami (until 2023), Janssen (consultancy), JucaBio (steering committee), Keros (steering committee) and United Therapeutics (Jenesis Young Investigator Grant Chairman); support for attending the ERS Congress from Merck; participation on a Data Safety Monitoring board for Acceleron/Merck (until 2023) and Janssen (until 2023); and unpaid roles as Treasurer of ISHLT and a member of the United Therapeutics Scientific Advisory Board., (Copyright ©The authors 2024.)
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- 2024
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34. Sex Differences in Venous Thromboembolism after Covid-19 Infection: A Retrospective Population-based Matched Cohort Study.
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Weatherald J, Wen C, Stickland MK, Damant R, Smith MP, Soril LJ, Zhang Z, D'Souza AG, Rennert-May E, Leal J, and Lam GY
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- 2024
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35. Moving the needle on proteasome inhibitor-induced pulmonary arterial hypertension: a definite maybe.
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Budhram B, Zamanian RT, and Weatherald J
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- Humans, Hypertension, Pulmonary chemically induced, Hypertension, Pulmonary drug therapy, Bortezomib adverse effects, Proteasome Inhibitors adverse effects, Proteasome Inhibitors therapeutic use, Pulmonary Arterial Hypertension chemically induced, Pulmonary Arterial Hypertension drug therapy
- Abstract
Competing Interests: Conflict of interest: R.T. Zamanian reports grants from National Institutes of Health, Merck, United Therapeutics and GossamerBio, consultancy fees from GossamerBio, Merck and Aerovate, patents planned, issued or pending (FK-506 for treatment of PAH), participation on a data safety monitoring board or advisory board with Aerovate, and stock (or stock options) with Reviva Pharma and Genentech. J. Weatherald reports grants from Janssen, Bayer, Merck, AstraZeneca and Sanofi, consultancy fees from Janssen and Merck, payment or honoraria for lectures, presentations, manuscript writing or educational events from Janssen and Merck, payment for expert testimony from Sprigings Intellectual Property Law, support for attending meetings from Janssen and Merck, participation on a data safety monitoring board or advisory board with Janssen, Merck and Université Laval, and is member of a Medical Advisory Committee for the Pulmonary Hypertension Association of Canada and member of a Scientific Medical Advisory Committee for the Pulmonary Vascular Research Institute. B. Budhram has no potential conflicts of interest to disclose.
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- 2024
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36. Pulmonary Hypertension in Connective Tissue Diseases Other than Systemic Sclerosis.
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Budhram B, Weatherald J, and Humbert M
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- Humans, Scleroderma, Systemic complications, Scleroderma, Systemic physiopathology, Scleroderma, Systemic therapy, Lupus Erythematosus, Systemic complications, Lupus Erythematosus, Systemic physiopathology, Sjogren's Syndrome complications, Sjogren's Syndrome physiopathology, Prognosis, Hypertension, Pulmonary etiology, Hypertension, Pulmonary physiopathology, Hypertension, Pulmonary therapy, Connective Tissue Diseases complications, Connective Tissue Diseases physiopathology
- Abstract
Pulmonary hypertension (PH) is a known complication of certain connective tissue diseases (CTDs), with systemic sclerosis (SSc) being the most common in the Western world. However, PH in association with non-SSc CTD such as systemic lupus erythematous, mixed connective tissue disease, and primary Sjögren's syndrome constitutes a distinct subset of patients with inherently different epidemiologic profiles, pathophysiologic mechanisms, clinical features, therapeutic options, and prognostic implications. The purpose of this review is to inform a practical approach for clinicians evaluating patients with non-SSc CTD-associated PH.The development of PH in these patients involves a complex interplay between genetic factors, immune-mediated mechanisms, and endothelial cell dysfunction. Furthermore, the broad spectrum of CTD manifestations can contribute to the development of PH through various pathophysiologic mechanisms, including intrinsic pulmonary arteriolar vasculopathy (pulmonary arterial hypertension, Group 1 PH), left-heart disease (Group 2), chronic lung disease (Group 3), chronic pulmonary artery obstruction (Group 4), and unclear and/or multifactorial mechanisms (Group 5). The importance of diagnosing PH early in symptomatic patients with non-SSc CTD is highlighted, with a review of the relevant biomarkers, imaging, and diagnostic procedures required to establish a diagnosis.Therapeutic strategies for non-SSc PH associated with CTD are explored with an in-depth review of the medical, interventional, and surgical options available to these patients, emphasizing the CTD-specific considerations that guide treatment and aid in prognosis. By identifying gaps in the current literature, we offer insights into future research priorities that may prove valuable for patients with PH associated with non-SSc CTD., Competing Interests: None declared., (Thieme. All rights reserved.)
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- 2024
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37. The clinical impact of heart failure with preserved ejection fraction in interstitial lung diseases.
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Zanini U, Ferrara G, Moitra S, Varughese R, Kalluri M, and Weatherald J
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- Humans, Male, Female, Aged, Middle Aged, Lung Diseases, Interstitial physiopathology, Heart Failure physiopathology, Stroke Volume physiology
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- 2024
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38. Increased Virtual Visits to Physicians During the COVID-19 Pandemic and Estimated Impact on Physician Compensation: The Case of Lung and Colorectal Cancers, Chronic Obstructive Pulmonary Diseases, and Heart Failure in Alberta, Canada.
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Thanh NX, Waye A, Stewart D, Weatherald J, Lam GY, Stickland MK, Hill MD, Choy J, Chuck AW, and Wasylak T
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- Humans, Alberta epidemiology, Male, Female, Lung Neoplasms therapy, Lung Neoplasms epidemiology, Pandemics, SARS-CoV-2, Middle Aged, Aged, COVID-19 epidemiology, Pulmonary Disease, Chronic Obstructive therapy, Pulmonary Disease, Chronic Obstructive epidemiology, Heart Failure therapy, Heart Failure epidemiology, Telemedicine statistics & numerical data, Telemedicine economics, Colorectal Neoplasms therapy, Colorectal Neoplasms epidemiology
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Introduction: The COVID-19 pandemic started in Alberta in March 2020 and significantly increased telehealth service use and provision reducing the risk of virus transmission. We examined the change in the number and proportion of virtual visits by physician specialty and condition (chronic obstructive pulmonary diseases [COPD], heart failure [HF], colorectal and lung cancers), as well as associated changes in physician compensation. Methods: A population-based design was used to analyze all processed physician claims comparing the number and proportion of virtual visits and associated physician billings relative to in-person between pre- (2019/2020) and intra-pandemic (2020/2021). Physician compensations were the claim amounts paid by the health insurance. Results: Pre-pandemic (intra-), there were 8,981 (8,897) lung cancer, 9,245 (9,029) colorectal, 37,558 (36,292) HF, and 68,270 (52,308) COPD patients. Each patient had totally 2.3-4.7 (of which 0.4-0.6% were virtual) general practitioner (GP) visits and 0.9-2.3 (0.2-0.7% were virtual) specialist visits per year pre-pandemic. The average number and proportion of per-patient virtual visits to GPs and specialists grew significantly pre- to intra-pandemic by 2,138-4,567%, and 2,201-7,104%, respectively. Given the lower fees of virtual compared with in-person visits, the reduction in physician compensation associated with the increased use of virtual care was estimated at $3.85 million, with $2.44 million attributed to specialist and $1.41 million to GP. Discussion: Utilization of telehealth increased significantly, while the physician billings per patient and physician compensation declined early in the pandemic in Alberta for the four chronic diseases considered. This study forms the basis for future study in understanding the impact of virtual care, now part of the fabric of health care delivery, on quality of care and patient safety, overall health service utilization (such as diagnostic imaging and other investigations), as well as economic impacts to patients, health care systems, and society.
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- 2024
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39. Randomized trial of routine versus on-demand intraoperative extracorporeal membrane oxygenation in lung transplantation: A feasibility study.
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Nasir BS, Weatherald J, Ramsay T, Cypel M, Donahoe L, Durkin C, Schisler T, Nagendran J, Liberman M, Landry C, Overbeek C, Moore A, and Ferraro P
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- Humans, Male, Prospective Studies, Female, Adult, Middle Aged, Lung Transplantation, Extracorporeal Membrane Oxygenation methods, Feasibility Studies, Intraoperative Care methods
- Abstract
In most centers, extracorporeal membrane oxygenation (ECMO) is the preferred means to provide cardiopulmonary support during lung transplantation. However, there is controversy about whether intraoperative venoarterial (VA) ECMO should be used routinely or selectively. A randomized controlled trial is the best way to address this controversy. In this publication, we describe a feasibility study to assess the practicality of a protocol comparing routine versus selective VA-ECMO during lung transplantation. This prospective, single-center, randomized controlled trial screened all patients undergoing lung transplantation. Exclusion criteria include retransplantation, multiorgan transplantation, and cases where ECMO is mandatory. We determined that the trial would be feasible if we could recruit 19 participants over 6 months with less than 10% protocol violations. Based on the completed feasibility study, we conclude that the protocol is feasible and safe, giving us the impetus to pursue a multicenter trial with little risk of failure due to low recruitment., (Copyright © 2024 The Authors. Published by Elsevier Inc. All rights reserved.)
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- 2024
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40. Treatments for pulmonary arterial hypertension: navigating through a network of choices.
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Pitre T, Weatherald J, and Humbert M
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- Humans, Antihypertensive Agents therapeutic use, Hypertension, Pulmonary therapy, Hypertension, Pulmonary physiopathology, Pulmonary Arterial Hypertension physiopathology, Pulmonary Arterial Hypertension therapy
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- 2024
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41. Constructing the Framework for Disease Modification in Pulmonary Arterial Hypertension.
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Zamanian RT, Weatherald J, Sweatt AJ, Hemnes A, Rashid M, Psotka MA, Bogaard HJ, and de Jesus Perez V
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- Humans, Hypertension, Pulmonary physiopathology, Pulmonary Arterial Hypertension physiopathology
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- 2024
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42. Inhaled treprostinil in patients with pulmonary hypertension associated with interstitial lung disease with less severe haemodynamics: a post hoc analysis of the INCREASE study.
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Weatherald J, Nathan SD, El-Kersh K, Argula RG, DuBrock HM, Rischard FP, Cassady SJ, Tarver J, Levine DJ, Tapson VF, Deng C, Shen E, Das M, and Waxman AB
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- Humans, Bayes Theorem, Hemodynamics, Randomized Controlled Trials as Topic, Epoprostenol analogs & derivatives, Hypertension, Pulmonary drug therapy, Hypertension, Pulmonary etiology, Lung Diseases, Interstitial complications, Lung Diseases, Interstitial drug therapy
- Abstract
Background: Inhaled treprostinil (iTre) is the only treatment approved for pulmonary hypertension due to interstitial lung disease (PH-ILD) to improve exercise capacity. This post hoc analysis evaluated clinical worsening and PH-ILD exacerbations from the 16-week INCREASE study and change in 6-minute walking distance (6MWD) in the INCREASE open-label extension (OLE) in patients with less severe haemodynamics., Methods: Patients were stratified by baseline pulmonary vascular resistance (PVR) of <4 Wood units (WU) versus ≥4 WU and <5 WU versus ≥5 WU. Exacerbations of underlying lung disease, clinical worsening and change in N-terminal prohormone of brain natriuretic peptide (NT-proBNP) in INCREASE were evaluated. For the OLE, patients previously assigned to placebo were considered to have a 16-week treatment delay. 6MWD and clinical events in the OLE were evaluated by PVR subgroup., Results: Of the 326 patients enrolled in INCREASE, patients with less severe haemodynamics receiving iTre had fewer exacerbations of underlying lung disease and clinical worsening events. This was supported by the Bayesian analysis of the risk of disease progression (HR<1), and significant decreases in NT-proBNP levels. In the OLE, patients without a treatment delay had improved exercise capacity after 1-year compared with those with a 16-week treatment delay (22.1 m vs -10.3 m). Patients with a PVR of ≤5 WU without a treatment delay had a change of 5.5 m compared with -8.2 m for those with a treatment delay. Patients without a treatment delay had a prolonged time to hospitalisation, lung disease exacerbation and death., Conclusion: Treatment with iTre led to consistent benefits in clinical outcomes in patients with PH-ILD and less severe haemodynamics. Earlier treatment in less severe PH-ILD may lead to better exercise capacity long-term, however, the subgroup analyses in this post hoc study were underpowered and confirmation of these findings is needed., Competing Interests: Competing interests: ABW has received grant support or consulting fees from AI Therapeutics, ARIA-CV, Acceleron/Merck, Janssen Pharmaceuticals, and has participated on a data and safety monitoring board for Insmed. SDN has received consulting fees or payment or honoraria, from United Therapeutics, Boehringer-Ingelheim, Roche, Bellerophon Therapeutics, Altavant Sciences, and Merck. JW has received grants or contracts to his institution from AstraZeneca, Bayer, Janssen and Merck; consulting fees from Janssen and Merck; honoraria from Janssen and Merck; payment for expert testimony from Sprigings Intellectual Property Law; travel support from Janssen; participation on Data Safety and Monitoring Board or advisory board from Janssen, Acceleron, and the Université de Laval; and has unpaid leadership role at the Pulmonary Hypertension Association of Canada. CQD, ES and MD are employees of and may have received stock or stock options from United Therapeutics. RGA has participated in advisory boards, disease state-specific speaking engagements and clinical trials sponsored by United Therapeutics. VFT reports research grants paid to institution from Boston Scientific Corporation, Bristol Myers Squibb and Genentech, speaker and consulting fees from Janssen, fees from Boston Scientific Corporation for participating in an executive committee for a clinical trial, that he serves as President for PE Response Team Consortium (unpaid), owns stock in Thrombolex and Inari Medical, and that he is employed as VP of Medical Affairs at Inari Medical. HMD is a consultant for Janssen Pharmaceuticals, has received grant funding from Bayer and has served on advisory boards for United Therapeutics and Janssen Pharmaceuticals. FR is a consultant for Acceleron and United Therapeutics and is on a steering committee for Acceleron, Ismed, United Therapeutics, Bayer, Acceleron, Janssen and AADI. SJC is a consultant for Iota Biosciences, Inc. KE-K is a consultant for Acceleron, Merck, United Therapeutics, J&J Actelion and served on advisory boards for J&J Actelion, Merck and United Therapeutics, received institutional research funding from J&J Actelion and United Therapeutics and participated in United Therapeutics speaker bureau, steering committee and clinical studies. JT has received consulting fees or payment or honoraria from United Therapeutics and Medtronic, Inc., (© Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.)
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- 2024
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43. "I Had to Know About It, I Had to Find It, I Had to Know How to Access it": Experiences of Access to Rehabilitation Services Among People Living with Long COVID.
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Hung P, Brehon K, Miciak M, Brown DA, Bostick G, Brown C, Churchill K, Hall M, Hoddinott L, Hudon A, Hunter S, Perreault K, Wieler M, Skolnik K, Lam GY, Weatherald J, and Gross DP
- Abstract
Purpose: The aim of this qualitative study is to understand the need for, access to, and quality of rehabilitation services for people living with Long COVID. Little is known about the experiences of people living with Long COVID accessing rehabilitation services. Therefore, we explored health concerns leading people living with Long COVID to seek help to address functional concerns and their experiences with accessing and participating in rehabilitation., Method: Interpretive description guided exploration of participants' experiences with Long COVID rehabilitation in Alberta, Canada. Semi-structured interviews were completed with 56 participants recruited from: three publicly funded Long COVID clinics, a specialized private physiotherapy clinic, a telephone-based rehabilitation advice line, and a Workers' Compensation Board-funded Long COVID rehabilitation program. Recruitment through mass media coverage allowed us to include people who did not access rehabilitation services. Data analysis was informed by Braun and Clarke's reflexive thematic analysis., Results: Four themes were identified: (1) the burden of searching for guidance to address challenges with functioning and disability; (2) supportive relationships promote engagement in rehabilitation; (3) conditions for participation in safe rehabilitation; and (4) looking forward - provision of appropriate interventions at the right time., Conclusions: Our findings highlight the experiences of accessing rehabilitation services for people living with Long COVID. Results suggest approaches to Long COVID rehabilitation should be accessible, multi-disciplinary, flexible, and person-centred., Competing Interests: Competing Interests: DPG is chief investigator or co-investigator on multiple previous and current research grants from government research agencies in Canada (e.g Canadian Institutes for Health Research, Alberta Innovates, Alberta Labour and Immigration) and the Netherlands (e.g TechForFuture Centre of Expertise HTSM Oost). His research has also received funding from philanthropy and quasi-governmental agencies (e.g Workers’ Compensation Board of Alberta, Workers’ Compensation Board of Manitoba, WorkSafeBC, Institute for Health Economics) and charities linked to professional body membership (e.g Physiotherapy Foundation of Canada, Canadian Occupational Therapy Foundation). Additionally, he has received research grants from industry (Medtronics). His travel expenses have been covered when he has been an invited speaker at conferences and he has received honoraria for talks, reviewing grants and theses (no honoraria or travel expenses from pharmaceutical or device companies). JW has received research grants (paid to institution) from Canadian Institutes for Health Research, Heart and Stroke Foundation of Canada, outside the current work. He has also received research grants (paid to the institution) from Janssen, Astra Zeneca, Merck, and Bayer. JW has also received honoraria and speaker's fees (paid to him) from Janssen and Merck, as well as travel support from Janssen. JW has received payments for attending advisory boards (paid to him) from Janssen and Merck. GL has received research grants from Roche Diagnostics, Alberta Lung, and Canadian Institute of Health Research (CIHR) as well as honoraria from Boehringer Ingelheim (honoraria for educational event) and Alberta Lung (honoraria for educational event). All other authors declare no conflicts of interest., (© Canadian Physiotherapy Association, 2024.)
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- 2024
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44. Rebuttal From Drs Weatherald and Sitbon.
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Weatherald J and Sitbon O
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Competing Interests: Financial/Nonfinancial Disclosures The authors have reported to CHEST the following: J. W. has received grants or contracts to his institution from Astra Zeneca, Bayer, Janssen, and Merck; consulting fees from Janssen and Merck; honoraria from Janssen and Merck; payment for expert testimony from Sprigings Intellectual Property Law; travel support from Janssen; participation on Data Safety and Monitoring Board or advisory board from Janssen, Acceleron, and the Université de Laval; and has unpaid leadership role at the Pulmonary Hypertension Association of Canada. O. S. has received grants or contracts to his institution from Acceleron, AOP Orphan, Janssen, and MSD; consulting fees from Altavant, Gossamer Bio, Janssen, and MSD; honoraria from AOP Orphan, Janssen, Ferrer, and MSD; and has participated on a Data Safety Monitoring Board or Advisory Board from Acceleron, Altavant, Gossamer Bio, Janssen, MSD, and Ferrer.
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- 2024
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45. POINT: Should the Use of Upfront Triple Combination Therapy Be Standard of Care in Pulmonary Arterial Hypertension? Yes.
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Weatherald J and Sitbon O
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- Humans, Standard of Care, Familial Primary Pulmonary Hypertension, Drug Therapy, Combination, Antihypertensive Agents therapeutic use, Pulmonary Arterial Hypertension drug therapy, Hypertension, Pulmonary drug therapy
- Abstract
Competing Interests: Financial/Nonfinancial Disclosures The authors have reported to CHEST the following: J. W. has received grants or contracts to his institution from Astra Zeneca, Bayer, Janssen, and Merck; consulting fees from Janssen and Merck; honoraria from Janssen and Merck; payment for expert testimony from Sprigings Intellectual Property Law; travel support from Janssen; participation on Data Safety and Monitoring Board or advisory board from Janssen, Acceleron, and the Université de Laval; and has unpaid leadership role at the Pulmonary Hypertension Association of Canada. O. S. has received grants or contracts to his institution from Acceleron, AOP Orphan, Janssen, and MSD; consulting fees from Altavant, Gossamer Bio, Janssen, and MSD; honoraria from AOP Orphan, Janssen, Ferrer, and MSD; and has participated on a Data Safety Monitoring Board or Advisory Board from Acceleron, Altavant, Gossamer Bio, Janssen, MSD, and Ferrer.
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- 2024
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46. Real-world evidence to advance knowledge in pulmonary hypertension: Status, challenges, and opportunities. A consensus statement from the Pulmonary Vascular Research Institute's Innovative Drug Development Initiative's Real-world Evidence Working Group.
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Morland K, Gerges C, Elwing J, Visovatti SH, Weatherald J, Gillmeyer KR, Sahay S, Mathai SC, Boucly A, Williams PG, Harikrishnan S, Minty EP, Hobohm L, Jose A, Badagliacca R, Lau EMT, Jing ZC, Vanderpool RR, Fauvel C, Leonidas Alves J Jr, Strange G, Pulido T, Qian J, Li M, Mercurio V, Zelt JGE, Moles VM, Cirulis MM, Nikkho SM, Benza RL, and Elliott CG
- Abstract
This manuscript on real-world evidence (RWE) in pulmonary hypertension (PH) incorporates the broad experience of members of the Pulmonary Vascular Research Institute's Innovative Drug Development Initiative Real-World Evidence Working Group. We aim to strengthen the research community's understanding of RWE in PH to facilitate clinical research advances and ultimately improve patient care. Herein, we review real-world data (RWD) sources, discuss challenges and opportunities when using RWD sources to study PH populations, and identify resources needed to support the generation of meaningful RWE for the global PH community., Competing Interests: Boucly reports consulting fees from AOP Orphan; payment, honoraria for lectures, presentations, speakers bureaus, manuscript writing or educational events from AOP Orphan, MSD, and Janssen; and support for attending meetings/travel from MSD and Janssen. Moles reports grants or contracts from Acceleron Pharma, Janssen, and CVS Caremark; and leadership or fiduciary role in other board, society, committee, or advocacy group, paid or unpaid, for Gossamer Bio. Elwing reports grants or contracts from United Therapeutics Corporation, Gossamer Bio, Bayer, Acceleron/Merck, Altavant, Aerovate, Tenax, Pharmosa, Actelion/Janssen, Arena, Lung, Liquidia, and Phase Bio; consulting fees for United Therapeutics Corporation; support for attending meetings and/or travel for United Therapeutics, Altavant, Aerovate, Bayer, Gossamer Bio, Liquida, Acceleron/Merck, Janssen/Actelion, and Insmed; and other financial or nonfinancial interests from Bayer as a grant reviewer. Jose reports grants or contracts from Team Phenomenal Hope Charity, Francis Family Foundation, United Therapeutics, and Janssen/Johnson & Johnson. Alves Jr. reports payment or honoraria from Bayer and Janssen; and support for attending meetings and/or travel from Janssen. Minty reports consulting fees from Janssen Pharmaceuticals and Orpyx Medical Technologies; and stock or stock options from Orpyx Medical Technologies. Weatherald reports grants or contracts from Janssen, Bayer, Merck, Canadian Institutes for Health Research, and the Heart & Stroke Foundation of Canada; consulting fees from Janssen and Merck; payment or honoraria for lectures, presentations, speakers bureaus, manuscript writing or educational events from Janssen and Merck; payment for expert testimony from Sprigings Intellectual Property Law; support for attending meetings and/or travel from Janssen; participation on a data safety monitoring board or advisory board from Janssen, Acceleron, and Université Laval; and leadership or fiduciary role in other board, society, committee or advocacy group, paid or unpaid, from the Pulmonary Hypertension Association of Canada. Mathai reports grants or contracts from NIH/NHLBI (HL125175) and DOD (W81XWH‐20‐1‐0768); consulting fees from Actelion/Janssen, Aerovate, Merck, United Therapeutics Corporation, and Theravance; and participation on a data safety monitoring board or advisory board from Bayer. Sahay reports grants or contracts from United Therapeutics Corporation, Janssen, Bayer, Merck, Liquidia, and Gossamer; consulting fees from Merck, Liquidia, and Gossamer; payment or honoraria for lectures, presentations, speakers bureaus, manuscript writing or educational events from United Therapeutics Corporation (received by hospital rather than self); patents planned, issued, or pending with Janssen; and participation on a data safety monitoring board or advisory board with GSK, Bayer, United Therapeutics, and Janssen. Pulido reports grants or contracts from Janssen, MSD, and United Therapeutics; consulting fees from Janssen, Bayer, Gossamer, and MSD; and payment or honoraria for lectures, presentations, speakers bureaus, manuscript writing or educational events from Bayer, Janssen, and Pfizer. Badagliacca reports grants or contracts from United Therapeutics Corporation, Ferrer, and Janssen; consulting fees from MSD, United Therapeutics Corporation, Ferrer, Janssen, and AOP; payment or honoraria for lectures, presentations, speakers bureaus, manuscript writing or educational events from MSD, United Therapeutics Corporation, Ferrer, Janssen, and AOP; and support for attending meetings and/or travel from MSD, United Therapeutics Corporation, Ferrer, Janssen, and AOP. Cirulis reports grants or contracts from Entelligence (now ATS); and leadership or fiduciary role in other board, society, committee or advocacy group, paid or unpaid, with ATS Web Committee Co‐Director and ATS Program Committee. Gerges reports grants or contracts from AOP Health; payment or honoraria for lectures, presentations, speakers bureaus, manuscript writing or educational events from AOP Health, Actelion/Janssen, and Ferrer; and support for attending meetings and/or travel from AOP Health, Actelion/Janssen, Ferrer, Daiichi Sankyo, and MSD. Gillmeyer reports grants or contracts from Parker B. Francis Fellowship Award, Doris Duke Charitable Foundation Award, and National Center for Advancing Translational Sciences, National Institutes of Health (BU‐CTSI Grant Number 1UL1TR001430); and leadership or fiduciary role in other board, society, committee or advocacy group, paid or unpaid, for the American Thoracic Society Program Committee (unpaid). Hobohm reports consulting fees for Janssen, Boston Consulting, and MSD. Lau reports grants or contracts from Janssen and GSK; consulting fees for Janssen; and payment or honoraria for lectures, presentations, speakers bureaus, manuscript writing or educational events from Janssen. Morland reports grants or contracts from United Therapeutics Corporation; leadership or fiduciary role in other board, society, committee or advocacy group, paid or unpaid, from the PVRI Innovative Drug Development Initiative (unpaid); and stock or stock options from United Therapeutics Corporation. Nikkho reports grants or contracts from Bayer AG; and leadership or fiduciary role in other board, society, committee or advocacy group, paid or unpaid, from the PVRI Innovative Drug Development Initiative (unpaid). The remaining authors declare no conflict of interest., (© 2023 The Authors. Pulmonary Circulation published by John Wiley & Sons Ltd on behalf of Pulmonary Vascular Research Institute.)
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- 2023
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47. "None of us are lying": an interpretive description of the search for legitimacy and the journey to access quality health services by individuals living with Long COVID.
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Brehon K, Miciak M, Hung P, Chen SP, Perreault K, Hudon A, Wieler M, Hunter S, Hoddinott L, Hall M, Churchill K, Brown DA, Brown CA, Bostick G, Skolnik K, Lam G, Weatherald J, and Gross DP
- Subjects
- Humans, Qualitative Research, Health Services, Delivery of Health Care, Health Services Accessibility, Post-Acute COVID-19 Syndrome, COVID-19 epidemiology
- Abstract
Background: Understanding of Long COVID has advanced through patient-led initiatives. However, research about barriers to accessing Long COVID services is limited. This study aimed to better understand the need for, access to, and quality of, Long COVID services. We explored health needs and experiences of services, including ability of services to address needs., Methods: Our study was informed by the Levesque et al.'s (2013) "conceptual framework of access to health care." We used Interpretive Description, a qualitative approach partly aimed at informing clinical decisions. We recruited participants across five settings. Participants engaged in one-time, semi-structured, virtual interviews. Interviews were transcribed verbatim. We used reflexive thematic analysis. Best practice to ensure methodological rigour was employed., Results: Three key themes were generated from 56 interviews. The first theme illustrated the rollercoaster-like nature of participants' Long COVID symptoms and the resulting impact on function and health. The second theme highlighted participants' attempts to access Long COVID services. Guidance received from healthcare professionals and self-advocacy impacted initial access. When navigating Long COVID services within the broader system, participants encountered barriers to access around stigma; appointment logistics; testing and 'normal' results; and financial precarity and affordability of services. The third theme illuminated common factors participants liked and disliked about Long COVID services. We framed each sub-theme as the key lesson (stemming from all likes and dislikes) that, if acted upon, the health system can use to improve the quality of Long COVID services. This provides tangible ways to improve the system based directly on what we heard from participants., Conclusion: With Long COVID services continuously evolving, our findings can inform decision makers within the health system to better understand the lived experiences of Long COVID and tailor services and policies appropriately., (© 2023. The Author(s).)
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- 2023
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48. Esophageal motility in systemic sclerosis before and after autologous hematopoietic cell transplantation.
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Woo MMK, Levin D, Li DY, David J, Buresi M, Gupta M, Nasser Y, Andrews CN, Durand C, Osman MS, Jamani K, Weatherald J, Johannson KA, Howlett JG, Hemmati I, Kim H, Curley M, and Storek J
- Subjects
- Humans, Recurrence, Esophageal Motility Disorders diagnosis, Scleroderma, Systemic complications, Hematopoietic Stem Cell Transplantation
- Abstract
Introduction: Systemic sclerosis (SSc) is associated with esophageal dysmotility. Autologous hematopoietic cell transplantation (HCT) results in improvement of skin tightness and lung function. Whether esophageal motility improves after HCT is unknown., Methods: Esophageal motility was studied using high-resolution esophageal manometry in 21 SSc patients before and at multiple time points after autologous HCT. Median posttransplant follow-up was 2 years (range, 6 months to 5 years)., Results: Prior to HCT, all 21 patients had abnormal motility-10 (48%) had unmeasurable and 11 (52%) had measurable peristalsis. Manometric diagnosis in the former 10 patients was "absent contractility" and in the latter 11 patients "ineffective esophageal motility (IEM)." After HCT, among the 10 patients with absent contractility, 9 continued to have absent contractility and one demonstrated weak measurable peristalsis. Of the 11 patients with IEM, 5 experienced SSc relapse, and 2 out of these 5 patients developed absent contractility. Among the 6 non-relapsed patients, 4 continued to have IEM, and 2 developed normal motility., Conclusions: HCT appears to have no beneficial effect on motility in patients with unmeasurable peristalsis. In patients with measurable peristalsis, HCT appears to stabilize and in some normalize motility, unless relapse occurs. Key Points • In patients with systemic sclerosis, esophageal dysmotility is a significant contributor to morbidity and so far, there has been no data describing the effects of hematopoietic cell transplantation on esophageal motility. • Our work demonstrated that in patients with systemic sclerosis and unmeasurable esophageal peristalsis prehematopoietic cell transplantation, there was no measurable beneficial effect of transplantation on esophageal motility. • In patients with systemic sclerosis and measurable peristalsis prehematopoietic cell transplantation, esophageal motility stabilized, except in relapsed patients., (© 2023. The Author(s), under exclusive licence to International League of Associations for Rheumatology (ILAR).)
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- 2023
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49. Ambitions for Pulmonary Arterial Hypertension Composite End Points: A Chain Is Only as Strong as Its Weakest Link.
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Zelt JGE, Weatherald J, and Mathai SC
- Abstract
Competing Interests: Financial/Nonfinancial Disclosures The authors have reported to CHEST the following: J. W. has received grants or contracts to his institution from Astra Zeneca, Bayer, Janssen, and Merck; has received consulting fees from Janssen and Merck; honoraria from Janssen and Merck; has received payment for expert testimony from Sprigings Intellectual Property Law; travel support from Janssen; participates in Data Safety and Monitoring Board or advisory board from Janssen, Acceleron, and the Université de Laval; and has an unpaid leadership role at the Pulmonary Hypertension Association of Canada. S. C. M. has received consulting fees from Actelion/Janssen, Bayer, Merck, and Aerovate; has received honoraria from Clinical Viewpoints; and has leadership roles as Scientific Secretariat, World Symposia on Pulmonary Hypertension Association and with Patient-Centered Outcomes Research Institute, Rare Disease Panel. None declared (J. G. E. Z.).
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- 2023
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50. Systemic corticosteroids for outpatient respiratory viral infections in lung transplant recipients.
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Ghandi V, Li D, Weinkauf J, Lien D, Hirji A, Varughese R, Weatherald J, Sligl W, Kabbani D, Schwartz I, Doucette K, Cervera C, and Halloran K
- Subjects
- Adult, Humans, Transplant Recipients, Outpatients, Lung, Adrenal Cortex Hormones therapeutic use, Steroids, Forced Expiratory Volume, Lung Transplantation adverse effects, Virus Diseases drug therapy, Virus Diseases epidemiology, Virus Diseases diagnosis
- Abstract
Introduction: Respiratory viral infections (RVI) in lung transplant recipients (LTR) have variably been associated with rejection and chronic lung allograft dysfunction. Our center has used systemic corticosteroids to treat outpatient RVI in some cases, but evidence is limited. We reviewed all adult LTR diagnosed with outpatient RVI January 2017 to December 2019. The primary outcome was recovery of lung function (forced expiratory volume in 1 s [FEV1]) at next stable visit between 1 and 12 months postinfection, expressed as a ratio over stable preinfection FEV1 (FEV1 recovery ratio)., Methods: We identified 100 adult LTR with outpatient RVI diagnoses eligible for study, 36% of whom received corticosteroids. We modelled the adjusted association between corticosteroid use and FEV1 recovery ratio using linear regression., Results: Steroid-treated patients had a lower FEV1 presentation ratio (0.92 vs. 1.04, p = .0070) and were more likely to have chronic lung allograft dysfunction at time of infection (25% vs. 5%, p = .0077). Mean FEV1 recovery ratio was 1.02 (SD 0.19) with no association with corticosteroid therapy via multivariable linear regression (p = .5888)., Conclusions: Steroid treatment was not associated with FEV1 recovery. This suggests corticosteroids may not have a role in the management of RVI in this population., (© 2023 Wiley Periodicals LLC.)
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- 2023
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