8 PART 3: Maternal Disease PROTOCOL 11: Maternal Anemia Definition Consequences Diagnostic work‐up and treatment Macrocytic anemia Suggested reading PROTOCOL 12: Hemoglobinopathies in Pregnancy Clinical significance Diagnosis Role of transfusion therapy Pregnancy management of sickle cell disease Pregnancy management of thalassemias Suggested reading PROTOCOL 13: Fetal and Neonatal Alloimmune Thrombocytopenia Introduction Diagnosis Management Conclusion Suggested reading PROTOCOL 14: Rheumatological Disorders Introduction Systemic lupus erythematosus Rheumatoid arthritis Scleroderma Suggested reading PROTOCOL 15: Antiphospholipid Syndrome Overview Pathophysiology Diagnosis Effect on pregnancy Antepartum management Conclusion Suggested reading PROTOCOL 16: Inherited Thrombophilias Overview Mechanisms of hemostasis Mechanisms of thrombosis Genetic risk factors for thrombosis Adverse pregnancy outcome Evaluation and treatment Suggested reading PROTOCOL 17: Valvular Heart Disease in Pregnancy Introduction Diagnosis and work‐up Etiology of VHD Maternal risk stratification Stages of progression of valvular heart disease Cardiac medications in pregnancy Stenotic versus regurgitant valve lesions Mixed anomalies Artificial valves Cardiac surgery in pregnancy Preconception and early pregnancy counseling Antepartum management Anticoagulation Delivery planning Medications on L&D Delivery and the immediate postpartum period Prophylactic antibiotics Anesthesia Follow‐up Suggested reading PROTOCOL 18: Peripartum Cardiomyopathy Peripartum cardiomyopathy and the obstetric care provider Clinical presentation and diagnosis Etiopathogenesis of peripartum and other cardiomyopathies Stabilization and treatment Cardiomyopathy pearls for the obstetric care provider
Автор: | Группа авторов |
Издательство: | John Wiley & Sons Limited |
Серия: | |
Жанр произведения: | Медицина |
Год издания: | 0 |
isbn: | 9781119635291 |
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PROTOCOL 10: Preconception Genetic Screening
Overview
Cystic fibrosis
Spinal muscular atrophy
Hemoglobinopathies
Fragile X syndrome
Tay–Sachs disease and other disorders more prevalent in individuals of Ashkenazi Jewish descent
Management and follow‐up
Conclusion
Suggested reading