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دسته بندی: قلب و عروق ویرایش: نویسندگان: Ramiah Rajeshkannan, Vimal Raj, Sanjaya Viswamitra سری: ISBN (شابک) : 9811567549, 9789811567544 ناشر: Springer Singapore سال نشر: 2021 تعداد صفحات: 584 زبان: English فرمت فایل : PDF (درصورت درخواست کاربر به PDF، EPUB یا AZW3 تبدیل می شود) حجم فایل: 64 مگابایت
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در صورت تبدیل فایل کتاب CT and MRI in Congenital Heart Diseases به فرمت های PDF، EPUB، AZW3، MOBI و یا DJVU می توانید به پشتیبان اطلاع دهید تا فایل مورد نظر را تبدیل نمایند.
توجه داشته باشید کتاب سی تی و ام آر آی در بیماری های مادرزادی قلب نسخه زبان اصلی می باشد و کتاب ترجمه شده به فارسی نمی باشد. وبسایت اینترنشنال لایبرری ارائه دهنده کتاب های زبان اصلی می باشد و هیچ گونه کتاب ترجمه شده یا نوشته شده به فارسی را ارائه نمی دهد.
این کتاب تصویربرداری مقطعی از بیماریهای مادرزادی قلب را پوشش میدهد و تعداد زیادی از تصاویر سیتی و امآرآی مرتبط را ارائه میکند. جزئیات مهم در مورد آناتومی، فیزیولوژی، جنین شناسی و گزینه های مدیریت مورد بحث قرار می گیرد و جنبه های فنی کلیدی انجام تصویربرداری گام به گام توضیح داده می شود. این کتاب که توسط تیمی از نویسندگان محترم نوشته شده است، دارای مصور فراوان است و با دسترسی به تعدادی فیلم بالینی تکمیل شده است.
این کتاب با هدف ارائه دسترسی سریع و قابل اعتماد به تصاویر با کیفیت بالا MRI و CT از ناهنجاریهای مادرزادی و ساختاری قلب که اغلب با آنها مواجه میشوند، یک راهنمای کامل برای پزشکان تصویربرداری ارائه میکند که به آنها کمک میکند بر منحنی یادگیری شیبدار غلبه کنند. برای تصویربرداری قلب کودکان.
This book covers the cross-sectional imaging of congenital heart diseases, and features a wealth of relevant CT and MRI images. Important details concerning anatomy, physiology, embryology and management options are discussed, and the key technical aspects of performing the imaging are explained step by step. Written by a team of respected authors, the book is richly illustrated and supplemented with access to a number of clinical videos.
Intended to provide quick and reliable access to high-quality MRI and CT images of frequently encountered congenital and structural heart abnormalities, the book offers a go-to guide for imaging physicians, helping them overcome the steep learning curve for pediatric cardiac imaging.
Foreword Preface Contents About the Editors and Contributors About the Editors Contributors Part I: The Basics of CHD imaging 1: CMR Physics 1.1 Introduction 1.2 Hardware 1.2.1 Magnets 1.2.2 Coils 1.3 Principle 1.4 MR Signal Formation 1.4.1 Radio-frequency Excitation 1.4.2 180° and 90° Pulse 1.4.3 T1 Relaxation/Spin: Lattice Relaxation 1.4.4 T2 Decay or Spin: Spin Relaxation 1.4.5 T2* Relaxation 1.5 MR Signal Localization 1.5.1 Slice Selection 1.5.2 Phase Encoding 1.5.3 Frequency Encoding 1.5.4 k-Space 1.5.5 Scan Time 1.6 Sequences 1.6.1 Spin-Echo (SE) Imaging 1.6.2 Gradient-Echo (GRE) Imaging 1.6.3 Parallel Imaging 1.6.4 Myocardial Tagging 1.6.5 Contrast-Enhanced (CE) Imaging 1.6.6 Mapping Sequences 1.7 ECG Gating 1.8 MR Artifacts 1.8.1 Equipment-Related Artifacts 1.8.2 Aliasing or Wrap-Around Artifact 1.8.3 Aliasing During Flow Analysis 1.8.4 Chemical Shift Artifact 1.8.5 Truncation or Gibbs Artifact or Dark Rim Artifact 1.8.6 Magnetic Susceptibility Artifact 1.8.7 Trigger Artifact 1.8.8 Blood Flow Artifact 1.9 Conclusion References 2: Cardiac Embryology 2.1 Introduction 2.2 Early Embryonic Development 2.3 Cardiac Development 2.3.1 Formation of the Endocardial Tube 2.3.1.1 Clinical Correlate 2.4 Determination of Right-Left Symmetry 2.4.1 Clinical Correlate 2.5 Formation of the Myocardium 2.5.1 Clinical Correlate 2.6 Formation of the Four-Chambered Heart 2.7 Formation of the Right and Left Atrioventricular Canals 2.7.1 Clinical Correlate 2.8 Formation of the Interventricular Septum (IVS) 2.8.1 Clinical Correlate 2.9 Formation of the Interatrial Septum 2.9.1 Clinical Correlates 2.10 Separation of the Outflow Tracts 2.10.1 Clinical Correlate 2.10.1.1 Conotruncal Anomalies 2.10.1.2 Truncus Arteriosus 2.10.1.3 D: Transposition of the Great Arteries 2.10.1.4 Tetralogy of Fallot (TOF) 2.10.1.5 Double Outlet Right Ventricle (DORV) 2.11 Development of the Aortic Arches and the Great Vessels 2.11.1 Clinical Correlate 2.11.1.1 Double Aortic Arch 2.11.1.2 Right Aortic Arch 2.11.1.3 Aberrant Right Subclavian Artery 2.11.1.4 Interruption of the Aortic Arch 2.11.1.5 Patent Ductus Arteriosus (PDA) 2.11.1.6 Coarctation of the Aorta 2.12 Formation of the Venous System 2.12.1 Clinical Correlate 2.12.1.1 Persistent Left Superior Vena Cava 2.12.1.2 Isolated Left Superior Vena Cava 2.12.1.3 Azygous Continuation of the Inferior Vena Cava 2.12.1.4 Double Interior Vena Cavae 2.13 Fetal Circulation References 3: Cross-Sectional Imaging Atlas 4: Technical Aspects of Pediatric Cardiac CT 4.1 Introduction 4.2 Common Indications for Pediatric CCT 4.3 Technical Requirements for Pediatric Cardiac CT 4.4 Technical Parameters for a Successful Cardiac CT 4.4.1 Intravenous (IV) Access 4.4.2 Sedation 4.4.3 Fasting 4.4.4 Contrast Media 4.4.5 CT Angiography Procedure 4.4.6 Timing of CTA Scan 4.4.7 Scan Range 4.4.8 Single-Phase Versus Multiphase CT Angio 4.4.9 ECG-Gated Versus Non-ECG Gated Study 4.4.9.1 Non-ECG Gated Scan 4.4.9.2 Retrospective ECG-Gated Spiral Scan 4.4.9.3 Prospective ECG-Gated Sequential Scan 4.4.9.4 Prospectively ECG-Triggered High-Pitch Helical CT 4.5 Processing the Raw Data 4.6 Image Reconstruction 4.7 Keep Radiation to Minimum (ALARA) 4.8 Documentation and Storage of Data 4.9 3D Printing References 5: Scan Techniques for Pediatric Cardiac MRI 5.1 Introduction 5.2 Paediatric CMR Set-Up 5.3 Sedation/Anaesthesia 5.4 Patient Positioning and Coil Placement 5.5 ECG Placement 5.6 Breath-Holding Versus Free-Breathing Scan 5.7 MRI Scanner 5.8 Contrast Media for MRI 5.9 MRI Acquisition Protocol 5.10 CMR Pulse Sequences 5.10.1 Black Blood Sequences 5.10.2 Bright Blood Cine Imaging 5.10.3 MR Angiography 5.10.3.1 Contrast MRA Technique Contrast Timing 5.10.3.2 Non-contrast MRA 5.10.4 Phase-Contrast Velocity Mapping Imaging 5.10.5 Myocardial Viability Imaging 5.11 MRI Imaging Planes 5.12 Standard CMR Pulse Sequences for CHD 5.13 Postprocessing 5.14 MR Imaging Safety References 6: Sequential Segmental Approach to CHD 6.1 Introduction 6.2 Basic Concepts of Sequential and Segmental Approach 6.3 Morphologic Features of Different Cardiac Chambers 6.3.1 Atria 6.3.2 Ventricles 6.3.3 Great Arteries 6.4 Anatomical Analysis of Each Segment 6.5 Conclusion References Part II: Imaging in Congenital Heart Disease 7: Congenital Aortic Anomalies 7.1 Introduction 7.2 Normal Embryology 7.3 Imaging Protocols 7.3.1 CT Aortogram 7.3.2 MR Angiogram 7.4 Aortic Root Anomalies 7.4.1 Truncus Arteriosus 7.4.2 Aorto-Pulmonary Window (AP Window: APW) 7.4.3 Transposition of Great Arteries (TGA) 7.4.4 Sinus of Valsalva Aneurysm 7.4.5 Supravalvar Aortic Stenosis 7.4.6 Aorta to LV Fistula 7.4.7 Aortic Valve Anomalies 7.4.8 Ascending Aortic Atresia 7.5 Aortic Arch Anomalies 7.5.1 Hypoplastic Aortic Arch 7.5.2 Coarctation of Aorta 7.5.3 Interrupted Aortic Arch 7.5.4 Congenital Ductus Arteriosus Aneurysm 7.6 Genetic Anomalies Affecting the Aorta 7.6.1 Marfan Syndrome 7.6.2 Arterial Tortuosity Syndrome (ATS) References 8: Vascular Rings and Slings 8.1 Introduction 8.2 Embryology 8.3 Types of Vascular Rings and Slings 8.3.1 Double Aortic Arch 8.3.1.1 Double Aortic Arch with Both Arches Patent 8.3.1.2 Double Aortic Arch with Atresia or Hypoplasia of One Arch with Fibrous Remnant 8.3.2 Left Aortic Arch with Aberrant Right Subclavian Artery and Kommerrell’s Diverticulum 8.3.3 Right Aortic Arch with Aberrant Left Subclavian Artery and Kommerrell’s Diverticulum 8.3.4 Right Circumflex Aorta and Left Circumflex Aorta 8.3.5 Left Aortic Arch with Aberrant Course of Right Subclavian Artery 8.3.6 Right Aortic Arch with Aberrant Course of Left Subclavian Artery Without Retroesophageal Diverticulum 8.3.7 Right Aortic Arch with Mirror-Image Branching 8.3.8 Innominate Artery Compression Syndrome 8.3.9 Pulmonary Sling 8.4 Conclusion References 9: Radiological Review of Coronary Artery Anomalies 9.1 Introduction 9.2 Normal Anatomy of the Coronary Arteries 9.2.1 Coronary Artery Dominance 9.2.2 Right Coronary Artery (RCA) 9.2.3 Left Main Coronary Artery (LMCA) 9.2.4 Left Anterior Descending Artery (LAD) 9.2.5 Left Circumflex Artery (LCx) 9.2.6 Ramus Intermedius (RI)/(Medianus) 9.3 Normal Variants 9.3.1 Right Superior Septal Perforator 9.3.2 Supernumerary Coronary Ostia 9.3.3 Myocardial Bridging 9.4 Coronary Anomalies 9.5 Hemodynamically Significant Anomalies 9.5.1 Coronary Ostial Stenosis or Atresia (COSA) 9.5.2 Anomalous Origin of the Coronary Artery from a Ventricle 9.5.3 Anomalous Origin of the Coronary Artery from the Pulmonary Artery 9.5.4 Inter-arterial/Malignant course 9.5.5 Coronary Arterial Fistula 9.5.6 Aorto-Atrial Tunnel 9.6 Hemodynamically Less Significant Anomalies 9.6.1 Duplication 9.6.2 High Origin/High “Takeoff” 9.6.3 Single Coronary Artery (SCA) 9.6.4 Pre-pulmonic Course 9.6.5 Trans-Septal Course 9.6.6 Retro-Aortic Course 9.6.7 Acute Takeoff of LCx 9.6.8 Shepherd’s Crook RCA 9.6.9 Coronary Arcade 9.6.10 Extracardiac Termination 9.7 Conclusion References 10: Imaging in Pulmonary Atresia with Ventricular Septal Defect 10.1 Introduction 10.2 Etiology 10.3 Embryology 10.4 Morphology 10.5 Classification 10.6 Pathophysiology 10.7 Clinical Presentation 10.8 Imaging Modalities 10.8.1 Chest X-Ray 10.8.2 Echocardiography 10.8.3 Cardiac Catheterization 10.8.4 MR Angiography (MRA) 10.8.4.1 Assessment of Morphology 10.8.4.2 Functional Assessment 10.8.5 CT Angiography (CTA) 10.8.5.1 Technical Factors 10.8.5.2 Image Post-processing 10.9 MDCT and MRI Evaluation of PA-VSD 10.9.1 Pulmonary Arteries 10.9.2 PDA 10.9.3 MAPCAs 10.9.4 Z-Score 10.9.5 McGoon’s Ratio 10.9.6 Nakata Index 10.9.7 Total Neo-pulmonary Artery Index (TNPAI) 10.9.8 Lung Arborization (Distribution) 10.9.9 Aortic Anomalies 10.9.10 Coronary and Intracardiac Abnormalities 10.9.11 Septal Defects 10.9.12 Intracardiac Morphology 10.9.13 Pulmonary and Systemic Venous System 10.9.14 Situs Anomalies 10.10 Management 10.10.1 Single-Stage Versus Multi-Stage Approach 10.10.1.1 Single-Stage Approach 10.10.1.2 Multi-Stage Approach 10.10.1.3 Comparison Between Multi- and Single-Stage Repair 10.11 Postoperative Assessment Using MDCT and MRI 10.11.1 Aortopulmonary Shunts 10.11.2 Classic Cavopulmonary Shunt (Glenn Operation) 10.11.3 The Bidirectional Glenn Shunt 10.11.4 Fontan Procedure 10.12 Limitations of MDCT References 11: Congenital Pulmonary Venous Anomalies 11.1 Introduction 11.2 Embryology of the Pulmonary Veins 11.3 Normal Pulmonary Venous Anatomy 11.4 Normal Variant Pulmonary Venous Drainage 11.5 Imaging Modalities 11.5.1 Chest Radiography 11.5.2 Echocardiography 11.5.3 CT Scan 11.5.4 MRI 11.6 Congenital Pulmonary Vein Anomalies 11.6.1 Total Anomalous Pulmonary Venous Drainage (TAPVD) 11.6.1.1 Imaging of TAPVD: Chest Radiography 11.6.2 Partial Anomalous Pulmonary Venous Drainage (PAPVD) 11.6.2.1 Imaging of PAPVD: Chest Radiography 11.6.2.2 CT/MRA 11.6.3 Sinus Venosus Defect 11.6.4 Congenital Pulmonary Venolobar Syndrome 11.6.4.1 Scimitar Syndrome 11.6.4.2 Pulmonary Sequestrations and Variants 11.6.4.3 Horseshoe Lung 11.7 Malposition of the Septum Primum 11.8 Meandering Pulmonary Vein 11.9 Levoatriocardinal Vein 11.10 Cor Triatriatum 11.11 Pulmonary Vein Stenosis/Hypoplasia/Atresia 11.12 Pulmonary Vein Varix 11.13 Pulmonary Arteriovenous Malformation 11.14 Post-operative TAPVD 11.15 Summary References 12: CT and MRI of Simple Cardiovascular Shunts 12.1 Introduction 12.2 Atrial Septal Defect (ASD) 12.2.1 Introduction 12.2.2 Normal Anatomy of Inter-Atrial Septum (Fig. 12.2) 12.2.3 Classification of ASD (Fig. 12.3) 12.2.4 Ostium Secundum ASD (Fig. 12.4) 12.2.5 Ostium Primum ASD (Fig. 12.5) 12.2.6 Sinus Venosus ASD (Figs. 12.6 and 12.7) 12.2.7 Unroofed Coronary Sinus (Fig. 12.8) 12.2.8 Common Atrium 12.2.9 Patent Foramen Ovale (PFO) (Figs. 12.9 and 12.10) 12.2.10 Clinical Features 12.2.11 Imaging Findings 12.2.12 Treatment 12.3 Ventricular Septal Defect (VSD) 12.3.1 Introduction 12.3.2 Embryology (Figs. 12.11 and 12.12) 12.3.3 Normal Anatomy of Interventricular Septum (Figs. 12.13, 12.14, and 12.15) 12.3.4 Pathophysiology of VSD 12.3.5 Complications of VSD 12.3.6 Classification 12.3.7 Imaging Findings 12.3.7.1 Central Perimembranous VSD (Figs. 12.16 and 12.17) 12.3.7.2 Muscular: Trabecular VSD (Figs. 12.18 and 12.19) 12.3.7.3 Inlet VSD (Fig. 12.20) 12.3.7.4 Outlet VSD (Fig. 12.21) 12.3.8 Clinical Presentation 12.3.9 Treatment 12.4 Atrio-Ventricular Septal Defect (AVSD) 12.4.1 Introduction 12.4.2 Classification [15] (Table 12.3) 12.4.3 Associations 12.4.4 Pathophysiology 12.4.5 Clinical Presentation 12.4.6 Imaging Findings (Fig. 12.22) 12.4.7 Treatment 12.5 Patent Ductus Arteriosus (PDA) 12.5.1 Introduction 12.5.2 Embryology 12.5.3 Morphology 12.5.4 Pathophysiology 12.5.5 Clinical Features 12.5.6 Imaging Findings 12.5.7 Treatment 12.6 MRI Quantification of Shunts [26, 27] 12.6.1 Calculating Shunt Across Atrial Septal Defect (Fig. 12.30) 12.6.2 Calculating Shunt Across Ventricular Septal Defect (Fig. 12.31) 12.6.3 Calculating Shunt Across Patent Ductus Arteriosus (Fig. 12.32) 12.6.4 Illustrative Examples References 13: Ebstein Anomaly 13.1 Introduction 13.2 Epidemiology and Risk Factors 13.3 Embryology 13.4 Pathological Anatomy 13.5 Associated Abnormalities 13.6 Pathophysiology 13.7 Classifications 13.8 Clinical Presentation 13.9 Approach to Diagnosis and Evaluation 13.10 Imaging Tests 13.10.1 Chest Radiograph (CXR) 13.10.2 Echocardiography 13.10.2.1 Transesophageal Echocardiogram (TEE) 13.10.3 CT 13.10.3.1 Indications for CT 13.10.4 CMR 13.10.5 CMR Protocol 13.10.6 Preoperative CMR Imaging Checklist 13.10.7 Postoperative CMR Imaging Checklist 13.11 Treatment 13.11.1 Prenatal 13.11.2 Neonates 13.11.3 Children, Adolescents, and Adults 13.12 Ebsteinoid Malformation of Left AV Valve in L-TGA 13.13 Differential Diagnosis References 14: Pre- and Postoperative Imaging in Tetralogy of Fallot 14.1 Definition 14.2 Introduction 14.3 Pathophysiology 14.4 Management of TOF 14.4.1 Single-Stage Repair 14.4.2 Multi-stage Repair 14.4.3 Natural History Post Surgery 14.5 Imaging Techniques 14.5.1 Chest Radiograph 14.5.2 Echocardiography 14.5.3 Cardiac Catheterization 14.5.4 Computed Tomography Angiography (CTA) 14.5.5 Cardiac MR (CMR) 14.6 Preoperative Imaging of TOF 14.6.1 Characterization of Primary Lesion 14.6.1.1 Right Ventricle Outflow Tract Obstruction (RVOTO) 14.6.1.2 Ventricular Septal Defect 14.6.2 Pulmonary Arteries 14.6.2.1 Aortic Anatomy 14.6.2.2 Coronary Anatomy 14.6.2.3 Atrial Septal Defects 14.6.2.4 Pulmonary Venous Return 14.6.2.5 Airway Compression 14.7 Postoperative Imaging in TOF 14.7.1 Imaging Post BT Shunt 14.7.2 Imaging Post Intracardiac Repair (ICR) 14.8 Conclusion References 15: Double Outlet Right Ventricle: Morphology and Function 15.1 Introduction 15.2 History 15.3 Embryology 15.4 Pathophysiology 15.5 CT and MR Imaging Techniques 15.5.1 MSCT 15.5.2 MRI Techniques 15.6 Morphology of DORV 15.7 Common Variants of DORV (Summarized in Table 15.1) 15.7.1 Tetralogy of Fallot (TOF)-Like Variant (Figs. 15.5, 15.6, and 15.7) 15.7.2 Transposition of Great Arteries (TGA)-Like Variant (Taussig–Bing Anomaly) (Figs. 15.8, 15.9, 15.10, 15.11, and 15.12) 15.7.3 Variant Resembling VSD (Fig. 15.13) 15.7.4 Variant Resembling a Univentricular Heart (Figs. 15.14, 15.15, and 15.16) 15.8 Less Frequent Variants of DORV 15.8.1 DORV with Subaortic VSD, Aorta Left to Pulmonary Trunk with PS (Figs. 15.17 and 15.18) 15.8.2 DORV with Noncommitted VSD (Fig. 15.19) 15.8.3 DORV with Discordant Atrioventricular Connection (Figs. 15.20 and 15.21) 15.8.4 DORV with Mirror-Image Atrial Arrangement (Fig. 15.22) 15.8.5 DORV with Isomeric Atrial Appendages (Ambiguous AV Connection) 15.8.6 DORV Without VSD 15.9 Associated Other Cardiac Anomalies 15.9.1 Juxtaposition of the Atrial Appendages (Fig. 15.28) 15.9.2 Abnormalities of the Atrioventricular Valves 15.10 3D Printing in DORV 15.11 Surgical Repair [29–33] 15.11.1 LV to Aorta Routability 15.11.2 Postoperative Complications 15.12 Double Outlet Left Ventricle (DOLV) 15.13 Conclusion References 16: Pre- and Postoperative Imaging in Transposition of Great Arteries 16.1 Introduction 16.2 Embryology 16.3 Morphology 16.3.1 Coronary Arteries in TGA [5, 6] 16.4 Differential Diagnosis 16.5 Pathophysiology 16.6 Clinical Aspects 16.7 Management of TGA 16.7.1 Surgical Options 16.8 Expected Complications of Surgery 16.9 Imaging in TGA 16.10 Postoperative evaluation [15] 16.10.1 Senning and Mustard Repair 16.10.2 Arterial Switch Operation 16.10.3 Rastelli Operation 16.10.4 Double Switch Surgery 16.10.5 Nikaidoh Procedure 16.11 Comparison Between Cardiac CT Versus Cardiac MRI References 17: Imaging of Single Ventricle 17.1 Introduction 17.2 Evolution of Concept of Single Ventricle 17.3 Classification 17.3.1 True Univentricular Heart 17.3.2 Functionally Univentricular Heart 17.4 Physiology of Univentricular Hearts 17.5 Pattern/Arrangement of Univentricular Heart 17.5.1 Univentricular Hearts That Are Morphological LV 17.5.2 Univentricular Heart with Morphological Right Ventricle 17.6 Epidemiology and Natural History 17.7 Fontan Circulation 17.8 Imaging of the Single Ventricle 17.8.1 ECG 17.8.2 X-Ray 17.8.3 Echocardigraphy (Figs. 17.9, 17.10, 17.11, and 17.12) 17.8.3.1 Approach 17.8.3.2 AV Valve 17.8.3.3 Great Arteries 17.8.4 Cardiac MRI (Figs. 17.13, 17.14, 17.15, and 17.16) 17.8.5 Cardiac CT (Figs. 17.16, 17.17, 17.18, 17.19, and 17.20) 17.8.5.1 Scanning Protocol 17.8.5.2 Image Analysis 17.8.6 Cardiac Catheterisation 17.9 Common Conditions Producing Univentricular Heart 17.9.1 Tricuspid Atresia 17.9.2 Double Inlet Left Ventricle (DILV) 17.9.3 Hypoplastic Left Heart Syndrome 17.10 Conclusion References 18: CT and MR Imaging in Post-operative CHD 18.1 Introduction 18.2 Suggested Imaging Protocol 18.2.1 CMR Protocol 18.2.2 CTA Protocol 18.3 Common Surgical Procedures Used for Palliation and Correction of CHDs and Their Imaging Findings 18.4 Palliative Procedures 18.4.1 Other Palliative Procedures 18.5 Corrective Surgeries for Common CHDs 18.5.1 Tetralogy of Fallot (TOF) 18.5.2 Transposition of Great Arteries (TGA) 18.5.3 Double Outlet Right Ventricle (DORV) 18.5.4 Coarctation of Aorta 18.6 Imaging of Complications of Palliative Shunts 18.7 Imaging of Complications of Repaired CHDs 18.7.1 Tetralogy of Fallot (TOF) and TOF-Type Double Outlet Right Ventricle (DORV) 18.7.2 Transposition of Great Arteries (TGA) and TGA-Type Double Outlet Right Ventricle (DORV) 18.7.3 Coarctation of Aorta 18.8 Conclusion References 19: Valvular Heart Disease 19.1 Introduction 19.1.1 MRI Assessment of Valve Morphology 19.1.2 Flow Mechanics and Valve Mathematics 19.1.2.1 Normal Flow Patterns 19.1.2.2 Abnormal Flow Patterns 19.1.3 MRI Techniques to Evaluate Valvular Function 19.1.3.1 Qualitative Assessment of Valve Function 19.1.3.2 Quantitative Assessment of Valve Function Potential Pitfalls of Flow Quantification Using Phase-Contrast Imaging Interpretation of Phase-Contrast Flow Maps 19.2 Merits and Limitations of Echocardiography and CMR 19.3 Role of CT in the Assessment of VHD 19.4 Aortic Valve 19.4.1 Aortic Stenosis 19.4.1.1 Ventricular Mass, Function, and Tissue Characterization 19.4.1.2 Aortic Root Evaluation 19.4.2 Aortic Regurgitation 19.5 Mitral Valve 19.5.1 Mitral Stenosis 19.5.2 Mitral Regurgitation 19.6 Pulmonary Valve 19.6.1 Pulmonary Stenosis 19.6.2 Pulmonary Regurgitation 19.7 Tricuspid Valve 19.7.1 Tricuspid Stenosis 19.7.2 Tricuspid Regurgitation 19.8 Prosthetic Valves 19.9 Conclusion References Part III: Special Topics in CHD 20: Techniques and Clinical Applications of Phase-Contrast MRI in CHD 20.1 Introduction 20.2 Phase-Contrast MRI: Basic Concepts 20.3 Imaging Technique 20.3.1 Basic Scan Parameters 20.3.2 Recommended Velocities 20.4 Planning for Specific Vessels 20.4.1 Ascending Aorta 20.4.2 Main Pulmonary Artery 20.4.3 Branch Pulmonary Arteries 20.4.4 Superior Vena Cava 20.4.5 Descending Aorta 20.4.6 Pulmonary Veins 20.4.7 Atrio Ventricular Valve 20.5 Image Post-processing 20.5.1 Practical Pearls for PC Flow study Post Processing 20.5.2 Internal Checking 20.6 Comparison with Doppler USG 20.7 Pitfalls of PC-MRI and the Remedies 20.7.1 Improper Selection of VENC 20.7.2 Improper Vessel Alignment 20.7.3 Inadequate Temporal Resolution 20.7.4 Inadequate Spatial Resolution 20.7.5 Magnetic Field Inhomogeneity 20.7.6 Flow-Related Signal Loss 20.7.7 Pulsation Artifacts 20.7.8 Phase Offset Error 20.7.9 Prospective Gating 20.8 Clinical Applications of PC-MRI 20.8.1 Presence of Flow 20.8.2 To Know the Direction of Blood Flow 20.8.3 Gradient Across the Stenosis 20.8.4 Calculation of Valve Regurgitation 20.8.4.1 Methods to Calculate Isolated Pulmonary Regurgitant Volume 20.8.4.2 Methods to Calculate Isolated Tricuspid Regurgitant Volume 20.8.5 Calculation of Shunts 20.8.6 Evaluation of Collateral Flow Circulation 20.8.7 Assessment of Differential Lung Perfusion 20.8.8 Velocity Waveforms and Flow Patterns 20.8.8.1 Diastolic Function Assessment by Transmitral Flow 20.8.8.2 Pulmonary Venous PC 20.8.8.3 Assessment of Pulmonary Hypertension 20.8.9 Practical Pearls 20.9 Newer Applications 20.9.1 “Real-Time” Flow Imaging 20.9.2 Coronary Artery Blood Flow (CBF) 20.9.3 3D and 4D Flow 20.10 Conclusions References 21: Imaging of Pulmonary Hypertension in Congenital Heart Disease 21.1 What Is Pulmonary Hypertension? 21.2 Classification of PH 21.3 Pathophysiology of PH 21.4 Pathophysiology of PAH in CHD 21.5 Prevalence of PAH in CHD 21.6 Cross-Sectional Imaging 21.6.1 CT Protocols 21.6.2 MRI Protocols 21.7 Diagnosis and Detection of PAH 21.7.1 CT Assessment 21.7.2 MRI Assessment 21.8 Functional Assessment 21.8.1 Cine Imaging 21.8.2 Phase-Contrast Imaging 21.8.3 Other Functional Parameters 21.9 Role of CT/MRI in PAH Associated with CHD 21.10 Newer Advances in MRI 21.11 Practical Tips 21.12 Summary References 22: CT Versus MRI in Congenital Heart Disease 22.1 Introduction 22.2 CT Imaging in CHD 22.2.1 Technical and Equipment Requirements for Cardiac CT 22.2.1.1 Spatial Resolution 22.2.1.2 Temporal Resolution 22.2.1.3 Pitch 22.2.1.4 High-Pitch CT Scan 22.2.1.5 ECG Gated Versus Non-gated Study 22.2.2 Protocoling a CT CHD Study 22.3 MR in Congenital Heart Disease 22.3.1 Morphological Imaging 22.3.2 Cine Imaging 22.3.3 Phase-Contrast Imaging (PC) 22.3.4 Delayed Enhancement Imaging 22.3.5 Contrast-Enhanced Magnetic Resonance Angiography (CE-MRA) 22.3.5.1 3D CE-MRA 22.4 Protocols for Common Conditions (Table 22.1) 22.5 CT Versus CMR for Congenital Heart Disease 22.6 3D Printing 22.7 Imaging in Cardiac Shunts 22.7.1 MRI 22.7.2 Atrial Septal Defects 22.7.2.1 Types of ASD 22.7.2.2 Ostium Primum ASD 22.7.2.3 Ostium Secundum ASD 22.7.2.4 Sinus Venosus ASD 22.7.2.5 Coronary Sinus (CS) Defect 22.7.2.6 CT and MRI: When and Why 22.7.2.7 Practical Pearl 22.7.2.8 Atrioventricular Cushion/Septal Defects (AVCD/AVSD) 22.7.2.9 Types of AVSD 22.7.2.10 CT and MRI: When and Why 22.7.2.11 Practical Pearls 22.7.3 Ventricular Septal Defects 22.7.3.1 Type 1 22.7.3.2 Type 2 22.7.3.3 Type 3 22.7.3.4 Type 4 22.7.3.5 CT and MR: When and Why 22.7.3.6 Practical Pearl 22.8 Venoatrial Anomalies 22.8.1 Partial Anomalous Pulmonary Venous Connection 22.8.2 Total Anomalous Pulmonary Venous Return (TAPVC) 22.8.3 CT and MR Imaging: Where and Why 22.8.3.1 Practical Pearls 22.9 Tetralogy of Fallot (TOF) 22.9.1 Anatomy 22.9.2 Associated Anomalies 22.9.3 CT and MRI: When and Why 22.9.4 CMR in TOF 22.9.5 Practical Pearls 22.10 Double-Outlet Ventricles: DORV 22.10.1 CT and MRI: When and Why 22.11 Transposition of Great Arteries (TGA) 22.11.1 D-TGA (Ventriculoarterial Discordance, Atrioventricular Concordance) 22.11.2 L-TGA or ccTGA (Atrioventricular and Ventriculoarterial Discordance: Double Discordance) 22.11.3 Surgical Modalities in TGA 22.11.4 CT and MRI: When and Why 22.12 Post-surgical TGA 22.12.1 Ebstein’s Anomaly 22.12.2 CT and MRI: When and Why 22.12.3 Carpentier Classification [75] 22.12.4 Practical Pearls 22.13 Coarctation of Aorta (CoA) 22.13.1 CT and MRI: When and Why 22.13.2 Imaging in Repaired Coarctation of Aorta 22.14 Conclusion References 23: Echocardiography for Congenital Heart Disease: Fundamental Approach 23.1 Introduction 23.2 History of Echocardiography 23.3 Advantages of Echocardiography 23.4 Objectives of Echocardiography 23.5 General Guidelines for Echocardiography 23.6 Optimal Image Acquisition 23.6.1 Choice of Transducer and Frequency 23.6.2 Standardization and Optimization 23.6.3 Imaging Protocols 23.6.4 The Segmental Approach 23.7 Views and Scanning Techniques 23.8 Specific Views 23.8.1 Subxiphoid Views 23.8.2 Subxiphoid Long-Axis Sweep 23.8.3 Subxiphoid Short-Axis Sweep 23.8.4 Apical Views 23.8.5 Parasternal Views 23.8.6 High-Parasternal (“Ductal”) View 23.8.7 Suprasternal Views 23.9 Hemodynamic Assessment 23.10 Summary References 24: 3D Prototyping: Technology and Applications for CHD 24.1 Introduction 24.2 What Is 3D Printing or Additive Manufacturing? 24.3 Different Types of 3D Printing Technologies and How They Work 24.4 Brief History of Additive Manufacturing 24.5 3D Printing in Medicine and in Cardiovascular Sciences 24.6 Steps in Cardiovascular 3D Printing 24.6.1 Step 1: Imaging 24.6.2 Step 2: Segmentation, Design, and Creation of the Digital 3D Object 24.6.3 Step 3: Consideration of the Printing Technology and Material to Be Used 24.6.4 Step 4: Export of Digital 3D File to 3D Printer Software and Hardware 24.6.5 Step 5: Printing and Post-processing 24.7 Caveats of 3D Models 24.8 Illustrative Case Examples 24.9 Summary References 25: Radiation Issues in Pediatric Cardiac CT Imaging 25.1 Introduction 25.2 Basic Radiation Dosimetry Parameters 25.2.1 Absorbed Dose 25.2.2 Equivalent Dose 25.2.3 Effective Dose 25.3 Radiation Risks from Performing Cardiac CT in Pediatric Age Group 25.4 Steps for Lowering the Radiation Dose from CT to Pediatric Population 25.4.1 Appropriate Selection of Patient 25.4.2 Patient Centering in the Gantry 25.4.3 Contrast Delivery 25.4.4 Appropriate Coverage 25.4.5 mAs and kVp Settings 25.4.6 Pitch of Scan 25.4.7 Thicker Detector Width 25.4.8 Iterative Reconstruction 25.4.9 Prospective/Retrospective ECG Gating and Non-ECG Pulsing References