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PAH in ACHD: Research, Global Perspective and Future Prospects. An Epilogue

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Book cover Pulmonary Hypertension in Adult Congenital Heart Disease

Abstract

Medical and scientific research in the field of pulmonary arterial hypertension (PAH) in adults with congenital heart disease (ACHD) in the past few years has gradually become globalized, inclusive and collaborative. Education of physicians, health administrators and patients in congenital heart disease (CHD), especially in the field of PAH, is of paramount importance. It is also crucial for ACHD patients with PAH to be followed in tertiary centres where they can benefit from a multidisciplinary approach. Shared care models dictate closer collaboration between tertiary expert centres and local non-specialist services, as well as networking between CHD and PAH physicians and geneticists/epidemiologists, with inclusion of PAH–CHD patients in national and international registries, and detailed genotypic/phenotypic characterization.

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Abbreviations

ACHD:

Adult congenital heart disease

CHD:

Congenital heart disease

PAH:

Pulmonary arterial hypertension

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Correspondence to Michael A. Gatzoulis M.D., Ph.D., F.A.C.C., F.E.S.C. .

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Giannakoulas, G., Gatzoulis, M.A. (2017). PAH in ACHD: Research, Global Perspective and Future Prospects. An Epilogue. In: Dimopoulos, K., Diller, GP. (eds) Pulmonary Hypertension in Adult Congenital Heart Disease. Congenital Heart Disease in Adolescents and Adults. Springer, Cham. https://doi.org/10.1007/978-3-319-46028-4_24

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  • DOI: https://doi.org/10.1007/978-3-319-46028-4_24

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  • Publisher Name: Springer, Cham

  • Print ISBN: 978-3-319-46026-0

  • Online ISBN: 978-3-319-46028-4

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