Professional Documents
Culture Documents
Pekerjaan
Dokter PTTT / Kepala Puskesmas Nusajaya, Kabupaten Halmahera Timur, Provinsi Maluku Utara, 2003 - 2005 Staf Dinas Kesehatan Provinsi Sumatera Staf Divisi Kardiologi, Departemen Ilmu Kesehatan Anak
Special Tools
Pediatric Echocardiography Pediatric Cardiac Catheterization
Special Problems
Pediatric Heart Failure Pediatric Hypertension, etc
Selected Aspects of History Taking GESTATIONAL AND NATAL HISTORY Infections, medications, excessive smoking or alcohol intake during pregnancy; Birth weight POSTNATAL, PAST AND PRESENT HISTORY Weight gain, development, and feeding pattern Cyanosis, cyanotic spells, and squatting Tachypnea, dyspnea, puffy eyelids Frequency of respiratory infection Exercise intolerance; Heart murmur Chest pain; Syncope; Palpitations; Joint symptoms; Neurologic symptoms; Medications FAMILY HISTORY Hereditary disease; Congenital heart defect; Rheumatic fever; Sudden unexpected death; Diabetes mellitus, arteriosclerotic heart disease, hypertension, and so on
Major Syndromes Associated with Cardiovascular Abnormalities CV Abnormalities: Disorders Major Features Etiology Frequency and Types Hypotonic, flat facies, slanted palpebral Down syndrome Frequent (40%50%); fissure, small eyes, Trisomy 21 (trisomy 21) ECD, VSD mental deficiency, simian crease Prenatal growth retardation, Occasional (25% microcephaly, short Fetal alcohol Ethanol or its 30%); VSD, PDA, ASD, palpebral fissure, syndrome byproducts TOF mental deficiency, irritable infant or hyperactive child Macrosomia, hypoglycemia and CHDs (3%5%); TGA, hypocalcemia, Infant of diabetic VSD, COA; Fetal exposure to high polycythemia, mother cardiomyopathy glucose levels hyperbilirubinemia, (10%20%); PPHN other congenital anomalies
Major Syndromes Associated with Cardiovascular Abnormalities CV Abnormalities: Disorders Major Features Etiology Frequency and Types Congenital deafness (not in Romano-Ward syndrome), syncope Very common; long resulting from Long QT syndrome: QT interval on ventricular arrhythmias, family history of sudden death () Frequent; aortic Arachnodactyly with aneurysm, aortic Marfan syndrome hyperextensibility, AD and/or mitral subluxation of lens regurgitation Similar to Turner's Frequent; PS syndrome but may Noonan's syndrome (dystrophic occur in phenotypic (Turner-like pulmonary valve), Usually sporadic male and without syndrome) LVH (or anterior chromosomal septal hypertrophy) abnormality
Major Syndromes Associated with Cardiovascular Abnormalities CV Abnormalities: Disorders Major Features Etiology Frequency and Types Excessive bone Occasional; aortic fragility with Osteogenesis dilatation, aortic deformities of AD/AR imperfecta regurgitation, MVP skeleton, blue sclera, hyperlaxity of joints Triad of the syndrome: deafness, cataract, and CHDs. Others include intrauterine growth Maternal rubella Frequent (>95%); PDA Rubella syndrome retardation, infection during the and PA stenosis microcephaly, first trimester microphthalmia, hepatitis, neonatal thrombocytopenic purpura
Major Syndromes Associated with Cardiovascular Abnormalities CV Abnormalities: Disorders Major Features Etiology Frequency and Types Low birth weight, central facial Very common (80%); anomalies, Trisomy 13 syndrome VSD, PDA, polydactyly, chronic Trisomy 13 (Patau's syndrome) dextrocardia hemangiomas, lowset ears, visceral and genital anomalies Low birth weight, microcephaly, Trisomy 18 syndrome Very common (90%); micrognathia, rockerTrisomy 18 (Edwards' syndrome) VSD, PDA, PS bottom feet, closed fists with overlapping fingers
Major Syndromes Associated with Cardiovascular Abnormalities CV Abnormalities: Disorders Major Features Etiology Frequency and Types Vertebral anomalies, anal atresia, congenital heart VATER association defects, Common (>50%); (VATER/VACTERL tracheoesophageal Sporadic VSD, other defects syndrome) (TE) fistula, renal dysplasia, limb anomalies (e.g., radial dysplasia)
Etc
Prevalence of Associated Congenital Heart Defects in Patients with Other System Malformations
Organ System and Malformation Central Nervous System Hydrocephalus Dandy-Walker syndrome Agenesis of corpus callosum Meckel-Gruber syndrome Thoracic Cavity TE fistula and/or esophageal atresia Diaphragmatic hernia Gastrointestinal Duodenal atresia Jejunal atresia Anorectal anomalies Imperforate anus Ventral Wall Omphalocele Gastroschisis Genitourinary Renal agenesis Bilateral Unilateral Horseshoe kidney Renal dysplasia Frequency (Range) (%) 6 (4.514.9) 3 (2.54.3) 15 14 Specific Cardiac Defects VSD, ECD, TOF VSD No specific defects No specific defects
21 (1539) 11 (9.622.9)
17 5 22 12 21 (1932) 3 (07.7)
43 17 39 5