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| 001 | 96514 | ||
| 003 | ES-MaUEC | ||
| 005 | 20230102112757.0 | ||
| 006 | m o d | ||
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| 008 | 170913s2017 sz ob 000 0 eng d | ||
| 020 |
_a3319460285 _q(electronic bk.) |
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| 020 |
_a9783319460284 _q(electronic bk.) |
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| 020 | _z3319460269 | ||
| 020 | _z9783319460260 | ||
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_aYDX _beng _erda _cYDX _dN$T _dEBLCP _dGW5XE _dN$T _dOCLCF _dYDX _dAZU _dUPM _dMERER _dUAB _dIOG _dCOO _dOCLCO _dOCLCQ _dOCLCA _dES-MaUEC _bspa |
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| 050 | 4 |
_aRC776.P87 _b2017 EB |
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| 245 | 0 | 0 |
_aPulmonary hypertension in adult congenital heart disease _cKonstantinos Dimopoulos, Gerhard-Paul Diller, editors. |
| 264 | 1 |
_aCham, Switzerland _bSpringer International Publishing _c2017 |
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| 264 | 4 | _c2017 | |
| 300 | _a1 recurso en línea | ||
| 336 |
_aTexto _btxt _2rdacontent |
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| 337 |
_aelectrónico _bc _2rdamedia |
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| 338 |
_arecurso electrónico _bcr _2rdacarrier |
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| 347 |
_atext file _bPDF |
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| 490 | 0 |
_aCongenital heart disease in adolescents and adults _x2364-6659 |
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| 504 | _aIncluye referencias bibliográficas | ||
| 505 | 0 | _aPreface to the Series; Foreword; Preface; Contents; Part I: Pathophysiology and Classification of Pulmonary Hypertension in Adult Congenital Heart Disease; 1: Congenital Heart Defects and Pulmonary Hypertension: The Heath-Edwards Paradigm; 1.1 Introduction; 1.2 The Morphology of PAH Related to CHD: Pulmonary Vascular Disease; 1.3 The Evolution of Pulmonary Vascular Disease in Common Types of CHD; 1.4 Operability and Survival After Cardiac Repair; 1.5 Eisenmenger Syndrome: Viktor Eisenmenger and Paul Wood | |
| 505 | 8 | _a1.6 The Effect of PAH on the Heart: RV Adaptation and Maladaptation and the Vicious Cycle of Heterometric Adaptation1.7 The Effect of PAH on the Large Pulmonary Arteries; References; 2: Definition and Classification of Pulmonary Hypertension in Congenital Heart Disease; 2.1 Definition of Pulmonary Hypertension; 2.2 Classification of Pulmonary Hypertension; References; 3: Eisenmenger Syndrome: Pathophysiology and Haematologic Effects; 3.1 Introduction; 3.2 Pathology; 3.3 Haematologic Considerations; 3.3.1 Secondary Erythrocytosis; 3.3.2 Iron Deficiency; 3.3.3 Hyperviscosity | |
| 505 | 8 | _a3.3.4 Pulmonary Thrombosis and Haemoptysis3.3.5 Non-haematologic Considerations; 3.3.5.1 Cerebral Vascular Events; 3.3.5.2 Pulmonary Mechanics and Gas Exchange; 3.3.6 Exercise Physiology; 3.3.6.1 Pulmonary Vasodilator Therapy; 3.3.7 Prognosis; References; 4: PAH in Patients with Prevalent Systemic-Pulmonary Shunts and PAH in Patients with Small Cardiac Defects; 4.1 Introduction; 4.2 Classification of PAH Associated with Systemic-to-Pulmonary Shunts; 4.3 PAH in Patients with Prevalent Systemic-Pulmonary Shunts and PAH in Patients with Small Cardiac Defects | |
| 505 | 8 | _a4.4 PAH Associated with Prevalent Systemic-Pulmonary Shunts4.4.1 Prognostic Relevance of the Appropriate Identification of Correctable versus Non-correctable CHD; 4.4.2 Assessment of Operability; 4.4.3 Treat-and-Repair Approach; 4.5 PAH Associated with Small Cardiac Defects; 4.5.1 Epidemiology; 4.5.2 Clinical Picture; 4.5.3 Therapy; References; 5: Pulmonary Arterial Hypertension in Patients with Previous Reparative Surgery; 5.1 Introduction; 5.2 Classification and Epidemiology; 5.3 Mechanisms for the Development of Late Postoperative PAH; 5.3.1 Maladaptation/Developmental Factors | |
| 505 | 8 | _a5.3.2 PAH Late After Repair5.4 Genetic Factors; 5.5 Treatment; 5.6 Natural Course: Outcome; References; 6: Segmental Pulmonary Hypertension; 6.1 Introduction; 6.2 Segmental Pulmonary Hypertension: Definition and Classification; 6.2.1 Pulmonary Atresia; 6.2.2 PH in Repaired Pulmonary Atresia; 6.2.3 Unilateral Absence of Pulmonary Artery; 6.2.4 Hemitruncus Arteriosus; 6.2.5 Truncus Arteriosus with Stenosis of a Single Pulmonary Artery; 6.2.6 Large Post-tricuspid Defects with Peripheral Pulmonary Stenosis; 6.2.7 Waterston and Potts Shunts to a Single Lung; 6.2.8 Scimitar Syndrome | |
| 520 | 3 | _aThis book is intended as a comprehensive, practically oriented reference on pulmonary hypertension within the context of adult congenital heart disease (ACHD). After an introductory chapter on pathophysiology, the various types of pulmonary hypertension that may be encountered in ACHD are discussed, highlighting the specifics observed within different patient categories. The diagnostic approach is then addressed in detail, and the last section of the book is devoted to management options, from conservative approaches to interventional treatment and the concept of treat and repair. Management in specific patient subjects, such as pregnant women, Fontan patients, and Down syndrome patients with Eisenmenger syndrome, is fully discussed, and guidance is also provided on palliative care. Pulmonary arterial hypertension related to congenital heart disease (PAH-CHD), despite significant similarities in lung pathohysiology, differs significantly from other types of PAH in terms of mechanism of onset, natural history and management. Mistakes and pitfalls in the management of patients with PAH-CHD are often related to a lack of knowledge or expertise in this condition. Pulmonary Hypertension in Adult Congenital Heart Disease will be a valuable resource and learning tool for all who care for patients with ACHD, both in tertiary practice and general cardiology. | |
| 650 | 7 |
_aCardiopatías congénitas _2embne _0(OCoLC)fst00875104 _0 _9168001 |
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| 700 | 1 |
_aDiller, Gerhard-Paul, _eeditor literario |
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| 700 | 1 |
_aDimopoulos, K. _q(Konstantinos), _eeditor literario |
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| 856 | 4 | 0 |
_uhttps://go.openathens.net/redirector/universidadeuropea.es?url=http://link.springer.com/10.1007/978-3-319-46028-4 _zAcceso a este recurso digital (usuarios Universidad Europea de Madrid) |
| 988 | _aSpringer_Medicine_2017 | ||
| 998 |
_b02/2018 _dz _e- _zSI |
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| 999 |
_c96514 _d96514 _x1 |
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