Codes Discussed: Q21 (Congenital malformations of cardiac septa), Q21.0 (Ventricular septal defect), Q21.11 (Secundum atrial septal defect), Q21.12 (Patent foramen ovale), Q21.13 (Coronary sinus atrial septal defect), Q21.14 (Superior sinus venosus atrial septal defect), Q21.15 (Inferior sinus venosus atrial septal defect), Q21.16 (Sinus venosus atrial septal defect, unspecified), Q21.19 (Other specified atrial septal defect), Q21.2 (Atrioventricular septal defect category), Q21.20 (Atrioventricular septal defect, unspecified), Q21.21 (Partial atrioventricular septal defect/incomplete AVSD), Q21.22 (Transitional atrioventricular septal defect/intermediate AVSD), Q21.23 (Complete atrioventricular septal defect), Q23.0 (Congenital stenosis of aortic valve), Q23.81 (Bicuspid aortic valve), Q23.2 (Congenital mitral stenosis), Q23.88 (Other congenital malformations of aortic and mitral valves/double-orifice mitral valve), Q25.6 (Stenosis of pulmonary artery), Q25.5 (Atresia of pulmonary artery), Q25.0 (Patent ductus arteriosus), Q25.1 (Coarctation of aorta), Q26.4 (Anomalous pulmonary venous return), Q26.2 (Total anomalous pulmonary venous return), Q26.3 (Partial anomalous pulmonary venous return), Q20.1 (Double outlet right ventricle), Q21.3 (Tetralogy of Fallot), Q23.4 (Hypoplastic left heart syndrome), I27.840 (Fontan-associated liver disease), I27.841 (Fontan-associated lymphatic dysfunction), J94.0 (Chylothorax), K90.49 (Fontan-associated protein-losing enteropathy), J44.89 (Plastic obstructive bronchitis), I27.848 (Other Fontan-associated condition), I27.849 (Fontan-related circulation, unspecified), R09.02 (Hypoxemia), Z87.74 (Personal history of corrected congenital malformations of heart and circulatory system), Q00-Q89 (Congenital malformations code range), Z48.21 (Encounter for aftercare following heart transplant), Z94.1 (Heart transplant status), T86.21 (Heart transplant rejection), Z45.010 (Encounter for checking and testing of cardiac pacemaker pulse generator/pacemaker battery management), Z45.02 (Encounter for adjustment and management of automatic implantable cardiac defibrillator/ICD management), Z95.0 (Presence of cardiac pacemaker), Z95.820 (Peripheral vascular angioplasty status with implants and grafts/pulmonary vein stent status), T82.857A (Stenosis of other cardiac prosthetic devices, implants and grafts, initial encounter/prosthetic pulmonary valve stenosis), T82.858A (Stenosis of other vascular prosthetic devices, implants and grafts, initial encounter/aortic stent stenosis), Z48 (Aftercare code category), T code (Complication code category), Z45 (Device management code category), Z95 (Device presence/status code category), Z87 (Personal history code category), Z94 (Transplant status code category)
Topics Covered: congenital cardiac cath diagnostic coding, pediatric cardiac catheterization diagnosis coding, congenital heart defect coding, major congenital heart defect coding, ICD-10-CM congenital cardiac coding, atrial septal defect coding, ASD coding, secundum ASD coding, coronary sinus ASD coding, superior sinus venosus ASD coding, inferior sinus venosus ASD coding, sinus venosus ASD coding, patent foramen ovale coding, PFO coding, normal newborn variant coding, ventricular septal defect coding, VSD coding, VSD with Tetralogy of Fallot coding, integral congenital defect coding, atrioventricular septal defect coding, AVSD coding, atrioventricular canal coding, AV canal coding, endocardial cushion defect coding, partial AVSD coding, transitional AVSD coding, complete AVSD coding, congenital aortic valve disorder coding, congenital aortic valve stenosis coding, bicuspid aortic valve coding, aortic valve calcification risk, aortic aneurysm risk, congenital mitral valve disorder coding, congenital mitral stenosis coding, double-orifice mitral valve coding, DOMV coding, other specified aortic and mitral valve malformation coding, congenital pulmonary artery defect coding, pulmonary artery stenosis coding, pulmonary artery atresia coding, supravalvular pulmonary artery narrowing, right ventricular hypertrophy, patent ductus arteriosus coding, PDA coding, ductus arteriosus, fetal blood vessel closure, aorta to pulmonary artery connection, heart failure risk with PDA, lung damage risk with PDA, coarctation of aorta coding, congenital aortic narrowing, systemic blood flow obstruction, restricted lower body blood flow, congenital hypertension risk, anomalous pulmonary venous return coding, anomalous pulmonary venous connection coding, pulmonary veins to right atrium, total anomalous pulmonary venous return coding, TAPVR coding, partial anomalous pulmonary venous return coding, PAPVR coding, oxygenated and deoxygenated blood mixing, double outlet right ventricle coding, DORV coding, aorta connected to right ventricle, pulmonary artery and aorta arising from right ventricle, DORV with VSD, Tetralogy of Fallot coding, TOF coding, pulmonary valve stenosis, right ventricular hypertrophy, overriding aorta, cyanotic congenital heart disease, hypoplastic left heart syndrome coding, HLHS coding, hypoplastic left ventricle, hypoplastic aorta, hypoplastic aortic valve, hypoplastic mitral valve, Norwood procedure, Glenn procedure, Fontan procedure, Fontan physiology coding, Fontan circulation coding, single ventricle physiology, chronic venous hypertension, low cardiac output, Fontan-associated liver disease coding, FALD coding, liver fibrosis, cirrhosis, regenerative arterialized liver nodules, hepatocellular carcinoma, Fontan-associated lymphatic dysfunction coding, impaired lymphatic flow, protein-losing enteropathy, plastic bronchitis, ascites, edema, Fontan-associated condition coding, hypoxemia with Fontan circulation coding, repaired congenital defect coding, personal history of corrected congenital malformation coding, clinically relevant history coding, repaired VSD coding, repaired ASD coding, repaired TOF coding, partially repaired congenital malformation coding, active congenital defect coding, congenital defect still requiring treatment, heart transplant aftercare coding, heart transplant status coding, heart transplant rejection coding, routine transplant surveillance coding, endomyocardial biopsy coding, transplant rejection surveillance coding, active transplant complication coding, pathology-confirmed rejection coding, aftercare versus complication coding, transplant status informational coding, device management encounter coding, cardiac device coding, pacemaker generator replacement coding, pacemaker battery end-of-life coding, ICD removal coding, implantable cardiac defibrillator management coding, device status code coding, pacemaker presence coding, pulmonary vein stent status coding, cardiac prosthetic device complication coding, vascular prosthetic device complication coding, prosthetic pulmonary valve stenosis coding, aortic stent stenosis coding, routine device management versus device complication, device replacement coding, device removal coding, initial device insertion diagnosis coding, status code versus complication code, key takeaways for congenital cardiac cath coding, active condition versus history code, transplant aftercare versus rejection, device management versus device complication, device presence status coding, congenital cardiac cath coding scenarios, pediatric cardiology coding education, congenital heart disease diagnosis coding webinar content
Kimberly Maupin, CPC, RCC, AAPC Approved Instructor
Kimberly Maupin, CPC, RCC, is an AAPC Approved Instructor at Haugen Academy with more than 25 years of experience in medical billing, coding, and health information management. She has worked across multiple healthcare settings, developing deep expertise throughout the entire revenue cycle, with a strong focus on diagnostic and interventional radiology coding and coder education. Kimberly is passionate about helping coders succeed. She has developed and delivered engaging online and in-person courses, educational resources, and webinars designed to prepare professionals for coding certification exams and keep them informed about the latest industry updates in this rapidly evolving field.
