Initial combination therapy with ambrisentan + tadalafil on pulmonary arterial hypertension‒related hospitalization in the AMBITION trial
Background: In the randomized, double-blind, event-driven AMBITION study, initial combination therapy with ambrisentan and tadalafil was associated with a 50% reduction in risk of clinical failure (first occurrence of all-cause death, hospitalization for worsening pulmonary arterial hypertension [PA...
| Autores: | , , , , , , , , , , , , , |
|---|---|
| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2019 |
| País: | España |
| Institución: | Universidad de Barcelona |
| Repositorio: | Dipòsit Digital de la UB |
| OAI Identifier: | oai:diposit.ub.edu:2445/183972 |
| Acceso en línea: | https://hdl.handle.net/2445/183972 |
| Access Level: | acceso abierto |
| Palabra clave: | Hipertensió pulmonar Vasodilatadors Pulmonary hypertension Vasodilators |
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Initial combination therapy with ambrisentan + tadalafil on pulmonary arterial hypertension‒related hospitalization in the AMBITION trialVachiéry, Jean-LucGaliè, NazzarenoBarberà i Mir, Joan AlbertFrost, Adaani E.Ghofrani, Hossein-ArdeschirHoeper, Marius MMcLaughlin, Vallerie V.Peacock, Andrew J.Simonneau, GéraldBlair, ChristianaMiller, Karen L.Langley, JonathanRubin, Lewis J.AMBITION InvestigatorsHipertensió pulmonarVasodilatadorsPulmonary hypertensionVasodilatorsBackground: In the randomized, double-blind, event-driven AMBITION study, initial combination therapy with ambrisentan and tadalafil was associated with a 50% reduction in risk of clinical failure (first occurrence of all-cause death, hospitalization for worsening pulmonary arterial hypertension [PAH], disease progression, or unsatisfactory long-term clinical response) vs pooled monotherapy. These results were primarily driven by a reduction in PAH-related hospitalization in the combination therapy group, although a significant effect was not observed in a post-hoc analysis of all-cause hospitalization. Methods: The effect of initial combination therapy with ambrisentan and tadalafil in AMBITION was further explored to study PAH-related hospitalization, which was not reported in the primary publication. Results: Initial combination therapy was associated with a 63% reduction in risk of PAH-related hospitalization when compared with pooled monotherapy (hazard ratio [HR] 0.372, 95% confidence interval [CI] 0.217 to 0.639, p = 0.0002). For every 9 patients treated with combination therapy vs monotherapy, 1 PAH-related hospitalization could be prevented over a 1-year period. Serious adverse events leading to hospitalization, not necessarily PAH-related, occurred in 87 of 253 (34%) and 89 of 247 (36%) of patients on combination therapy and pooled monotherapy, respectively (post-hoc summary). Conclusions: Initial combination therapy with ambrisentan and tadalafil was found to reduce the risk of PAH-related hospitalization by 63% compared with pooled monotherapy.Elsevier2019info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://hdl.handle.net/2445/183972Articles publicats en revistes (Medicina)reponame:Dipòsit Digital de la UBinstname:Universidad de BarcelonaInglésReproducció del document publicat a: https://doi.org/10.1016/j.healun.2018.11.006Journal of Heart and Lung Transplantation, 2019, vol. 38, num. 2, p. 194-202https://doi.org/10.1016/j.healun.2018.11.006cc-by-nc-nd (c) Elsevier, 2019https://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessoai:diposit.ub.edu:2445/1839722026-05-27T06:46:51Z |
| dc.title.none.fl_str_mv |
Initial combination therapy with ambrisentan + tadalafil on pulmonary arterial hypertension‒related hospitalization in the AMBITION trial |
| title |
Initial combination therapy with ambrisentan + tadalafil on pulmonary arterial hypertension‒related hospitalization in the AMBITION trial |
| spellingShingle |
Initial combination therapy with ambrisentan + tadalafil on pulmonary arterial hypertension‒related hospitalization in the AMBITION trial Vachiéry, Jean-Luc Hipertensió pulmonar Vasodilatadors Pulmonary hypertension Vasodilators |
| title_short |
Initial combination therapy with ambrisentan + tadalafil on pulmonary arterial hypertension‒related hospitalization in the AMBITION trial |
| title_full |
Initial combination therapy with ambrisentan + tadalafil on pulmonary arterial hypertension‒related hospitalization in the AMBITION trial |
| title_fullStr |
Initial combination therapy with ambrisentan + tadalafil on pulmonary arterial hypertension‒related hospitalization in the AMBITION trial |
| title_full_unstemmed |
Initial combination therapy with ambrisentan + tadalafil on pulmonary arterial hypertension‒related hospitalization in the AMBITION trial |
| title_sort |
Initial combination therapy with ambrisentan + tadalafil on pulmonary arterial hypertension‒related hospitalization in the AMBITION trial |
| dc.creator.none.fl_str_mv |
Vachiéry, Jean-Luc Galiè, Nazzareno Barberà i Mir, Joan Albert Frost, Adaani E. Ghofrani, Hossein-Ardeschir Hoeper, Marius M McLaughlin, Vallerie V. Peacock, Andrew J. Simonneau, Gérald Blair, Christiana Miller, Karen L. Langley, Jonathan Rubin, Lewis J. AMBITION Investigators |
| author |
Vachiéry, Jean-Luc |
| author_facet |
Vachiéry, Jean-Luc Galiè, Nazzareno Barberà i Mir, Joan Albert Frost, Adaani E. Ghofrani, Hossein-Ardeschir Hoeper, Marius M McLaughlin, Vallerie V. Peacock, Andrew J. Simonneau, Gérald Blair, Christiana Miller, Karen L. Langley, Jonathan Rubin, Lewis J. AMBITION Investigators |
| author_role |
author |
| author2 |
Galiè, Nazzareno Barberà i Mir, Joan Albert Frost, Adaani E. Ghofrani, Hossein-Ardeschir Hoeper, Marius M McLaughlin, Vallerie V. Peacock, Andrew J. Simonneau, Gérald Blair, Christiana Miller, Karen L. Langley, Jonathan Rubin, Lewis J. AMBITION Investigators |
| author2_role |
author author author author author author author author author author author author author |
| dc.subject.none.fl_str_mv |
Hipertensió pulmonar Vasodilatadors Pulmonary hypertension Vasodilators |
| topic |
Hipertensió pulmonar Vasodilatadors Pulmonary hypertension Vasodilators |
| description |
Background: In the randomized, double-blind, event-driven AMBITION study, initial combination therapy with ambrisentan and tadalafil was associated with a 50% reduction in risk of clinical failure (first occurrence of all-cause death, hospitalization for worsening pulmonary arterial hypertension [PAH], disease progression, or unsatisfactory long-term clinical response) vs pooled monotherapy. These results were primarily driven by a reduction in PAH-related hospitalization in the combination therapy group, although a significant effect was not observed in a post-hoc analysis of all-cause hospitalization. Methods: The effect of initial combination therapy with ambrisentan and tadalafil in AMBITION was further explored to study PAH-related hospitalization, which was not reported in the primary publication. Results: Initial combination therapy was associated with a 63% reduction in risk of PAH-related hospitalization when compared with pooled monotherapy (hazard ratio [HR] 0.372, 95% confidence interval [CI] 0.217 to 0.639, p = 0.0002). For every 9 patients treated with combination therapy vs monotherapy, 1 PAH-related hospitalization could be prevented over a 1-year period. Serious adverse events leading to hospitalization, not necessarily PAH-related, occurred in 87 of 253 (34%) and 89 of 247 (36%) of patients on combination therapy and pooled monotherapy, respectively (post-hoc summary). Conclusions: Initial combination therapy with ambrisentan and tadalafil was found to reduce the risk of PAH-related hospitalization by 63% compared with pooled monotherapy. |
| publishDate |
2019 |
| dc.date.none.fl_str_mv |
2019 |
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info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
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article |
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publishedVersion |
| dc.identifier.none.fl_str_mv |
https://hdl.handle.net/2445/183972 |
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https://hdl.handle.net/2445/183972 |
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Inglés |
| language_invalid_str_mv |
Inglés |
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Reproducció del document publicat a: https://doi.org/10.1016/j.healun.2018.11.006 Journal of Heart and Lung Transplantation, 2019, vol. 38, num. 2, p. 194-202 https://doi.org/10.1016/j.healun.2018.11.006 |
| dc.rights.none.fl_str_mv |
cc-by-nc-nd (c) Elsevier, 2019 https://creativecommons.org/licenses/by-nc-nd/4.0/ info:eu-repo/semantics/openAccess |
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cc-by-nc-nd (c) Elsevier, 2019 https://creativecommons.org/licenses/by-nc-nd/4.0/ |
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openAccess |
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application/pdf |
| dc.publisher.none.fl_str_mv |
Elsevier |
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Elsevier |
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Articles publicats en revistes (Medicina) reponame:Dipòsit Digital de la UB instname:Universidad de Barcelona |
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Universidad de Barcelona |
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Dipòsit Digital de la UB |
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Dipòsit Digital de la UB |
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15,300719 |