Iatrogenic esophageal dysmotility as a barrier to transplantation in pulmonary arterial hypertension

Autor: Michael S. Miller, Shelsey W. Johnson, Alexander R. Opotowsky, Michael J. Landzberg, Nirmal S. Sharma, Hilary J. Goldberg, Alexandra K. Wong, Alison S. Witkin, Josanna Rodriguez-Lopez, Ronald H. Goldstein, Bradley A. Maron, Bradley M. Wertheim

Publikováno v: JHLT Open, Vol 5, Iss , Pp 100098- (2024)

Esophageal dysmotility is identified as a contraindication to lung transplantation at some centers due to increased risks of acute rejection, pulmonary infection, and chronic lung allograft dysfunction. Phosphodiesterase-type 5 inhibitors (PDE5i) are

Externí odkaz: https://doaj.org/article/4145d27170eb4e76b982c3e6fb360f36

Room for improvement in pulmonary capillary wedge pressure reporting: a review of hemodynamic tracings at a large academic medical center

Autor: Shelsey W. Johnson, Alison Witkin, Josanna Rodriguez-Lopez, Richard Channick

Publikováno v: Pulmonary Circulation, Vol 10 (2020)

To describe the frequency with which pulmonary capillary wedge pressure measurements, obtained during right heart catheterization, are falsely elevated and to educate operators on techniques to improve accuracy of pulmonary capillary wedge pressure r

Externí odkaz: https://doaj.org/article/a27ea734980844b8a2c565966fef5c1d

Anticoagulation and antiplatelet therapy in hereditary hemorrhagic telangiectasia: A scoping review

Autor: Ellen Zhang, Zain M. Virk, Josanna Rodriguez-Lopez, Hanny Al-Samkari

Publikováno v: Thrombosis Research. 226:150-155

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::0f225e096dcb03a37eb3ea8d856b802b
https://doi.org/10.1016/j.thromres.2023.04.017

Perfusion imaging heterogeneity during NO inhalation distinguishes pulmonary arterial hypertension (PAH) from healthy subjects and has potential as an imaging biomarker

Autor: Tilo Winkler, Puja Kohli, Vanessa J Kelly, Ekaterina G. Kehl, Alison S. Witkin, Josanna Rodriguez-Lopez, Kathryn A. Hibbert, Mamary Kone, David M. Systrom, Aaron B. Waxman, Jose G. Venegas, Richard Channick, R. Scott Harris

Publikováno v: Respiratory Research. 23

Background Without aggressive treatment, pulmonary arterial hypertension (PAH) has a 5-year mortality of approximately 40%. A patient’s response to vasodilators at diagnosis impacts the therapeutic options and prognosis. We hypothesized that analyz

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f06cc112fe0994775e7e8bc9cf55892
https://doi.org/10.1186/s12931-022-02239-8

Second International Guidelines for the Diagnosis and Management of Hereditary Hemorrhagic Telangiectasia

Autor: Justin P. McWilliams, Miles Conrad, Mary Porteous, Mary E. Meek, James R. Gossage, Jay F. Piccirillo, Masaki Komiyama, Elisabetta Buscarini, Carlo Sabbà, Andrea Lausman, Paul J. Rochon, Ketil Heimdal, Rose Pantalone, Claire L. Shovlin, Valerie A. Palda, Hanny Al-Samkari, Kevin Korenblatt, Marianne S. Clancy, Jamie McDonald, Katharine J. Henderson, Marie E. Faughnan, Claudia Crocione, Steven W. Hetts, Erik Deslandres, Urban W. Geisthoff, Ingrid Winship, Els de Gussem, Vivek N. Iyer, Daniel Cortes, Sophie Dupuis-Girod, Beth Plahn, Kelly Lang-Robertson, Patrick Foy, Mark S. Chesnutt, Ivan Radovanovic, Anette Drøhse Kjeldsen, Felix Ratjen, Johannes J. Mager, Carol Derksen, Adrienne M. Hammill, Sara Palmer, Marcelo M. Serra, Jack McMahon, Josanna Rodriguez-Lopez, Andrew J. White, Roberto Zarrabeitia, Raj S. Kasthuri, Marco C. Post, Jama M. Darling, Scott E. Olitsky, Dennis L. Sprecher, Murali M. Chakinala, Kevin J. Whitehead, David M. Poetker, Meir Mei-Zahav

Publikováno v: Faughnan, M E, Mager, J J, Hetts, S W, Palda, V A, Lang-Robertson, K, Buscarini, E, Deslandres, E, Kasthuri, R S, Lausman, A, Poetker, D, Ratjen, F, Chesnutt, M S, Clancy, M, Whitehead, K J, Al-Samkari, H, Chakinala, M, Conrad, M, Cortes, D, Crocione, C, Darling, J, de Gussem, E, Derksen, C, Dupuis-Girod, S, Foy, P, Geisthoff, U, Gossage, J R, Hammill, A, Heimdal, K, Henderson, K, Iyer, V N, Kjeldsen, A D, Komiyama, M, Korenblatt, K, McDonald, J, McMahon, J, McWilliams, J, Meek, M E, Mei-Zahav, M, Olitsky, S, Palmer, S, Pantalone, R, Piccirillo, J F, Plahn, B, Porteous, M E M, Post, M C, Radovanovic, I, Rochon, P J, Rodriguez-Lopez, J, Sabba, C, Serra, M, Shovlin, C, Sprecher, D, White, A J, Winship, I & Zarrabeitia, R 2020, ' Second International Guidelines for the Diagnosis and Management of Hereditary Hemorrhagic Telangiectasia ', Annals of Internal Medicine, vol. 173, no. 12, pp. 989-1001 . https://doi.org/10.7326/M20-1443

Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant disease with an estimated prevalence of 1 in 5000 that is characterized by the presence of vascular malformations (VMs). These result in chronic bleeding, acute hemorrhage, and comp

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4ee4994475518c545cc94de43b382bf
https://doi.org/10.7326/m20-1443