Diagnosis Codes in MS-DRG 306 - Cardiac Congenital And Valvular Disorders With MCC
The Medicare Severity Diagnosis-Related Group (MS-DRG) is a patient classification system used to categorize hospital cases based on clinical similarity and expected resource use. MS-DRGs organize all possible principal diagnoses into mutually exclusive groups known as Major Diagnostic Categories (MDCs), which help determine reimbursement under the Medicare Inpatient Prospective Payment System.
This section lists the diagnosis codes included in MS-DRG V42.0: Cardiac Congenital and Valvular Disorders with MCC from October 1, 2024, through September 30, 2025.
MS-DRG: 306
MS-DRG Title: Cardiac Congenital and Valvular Disorders with MCC
MCD: 05
Relative Weight: 1.4974 Relative Weight
The relative weight of a diagnostic related group determines the reimbursement rate based on the severity of a patient's illness and the associated cost of care during hospitalization.
Arithmetic LOS: 3.90 Arithmetic Length of Stay
The average length of stay (ALOS) reflects the average number of days a patient spends in a hospital for each admission.
- A52.0 - Cardiovascular and cerebrovascular syphilis
- B33.2 - Viral carditis
- I01 - Rheumatic fever with heart involvement
- I05 - Rheumatic mitral valve diseases
- I06 - Rheumatic aortic valve diseases
- I07 - Rheumatic tricuspid valve diseases
- I08 - Multiple valve diseases
- I09 - Other rheumatic heart diseases
- I09.8 - Other specified rheumatic heart diseases
- I23 - Certain current complications following ST elevation (
- I34 - Nonrheumatic mitral valve disorders
- I34.8 - Other nonrheumatic mitral valve disorders
- I35 - Nonrheumatic aortic valve disorders
- I36 - Nonrheumatic tricuspid valve disorders
- I37 - Nonrheumatic pulmonary valve disorders
- I51 - Complications and ill-defined descriptions of heart di
- Q20 - Congenital malformations of cardiac chambers and conne
- Q21 - Congenital malformations of cardiac septa
- Q21.1 - Atrial septal defect
- Q21.2 - Atrioventricular septal defect
- Q22 - Congenital malformations of pulmonary and tricuspid va
- Q23 - Congenital malformations of aortic and mitral valves
- Q23.8 - Other congenital malformations of aortic and mitral
- Q24 - Other congenital malformations of heart
- Q25 - Congenital malformations of great arteries
- Q25.2 - Atresia of aorta
- Q25.4 - Other congenital malformations of aorta
- Q25.7 - Other congenital malformations of pulmonary artery
- Q26 - Congenital malformations of great veins
- Q87.4 - Marfan syndrome
- Q87.41 - Marfan syndrome with cardiovascular manifestations
- R01 - Cardiac murmurs and other cardiac sounds
- T82.01 - Breakdown (mechanical) of heart valve prosthesis
- T82.02 - Displacement of heart valve prosthesis
- T82.03 - Leakage of heart valve prosthesis
- T82.09 - Other mechanical complication of heart valve prosth
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A52.0 - Cardiovascular and cerebrovascular syphilis
I01 - Rheumatic fever with heart involvement
I01.1 - Acute rheumatic endocarditis
I05 - Rheumatic mitral valve diseases
I06 - Rheumatic aortic valve diseases
I07 - Rheumatic tricuspid valve diseases
I08 - Multiple valve diseases
I08.0 - Rheumatic disorders of both mitral and aortic valves
I08.1 - Rheumatic disorders of both mitral and tricuspid valves
I08.2 - Rheumatic disorders of both aortic and tricuspid valves
I08.3 - Combined rheumatic disorders of mitral, aortic and tricuspid valves
I08.8 - Other rheumatic multiple valve diseases
I08.9 - Rheumatic multiple valve disease, unspecified
I09 - Other rheumatic heart diseases
I09.1 - Rheumatic diseases of endocardium, valve unspecified
I09.8 - Other specified rheumatic heart diseases
I09.89 - Other specified rheumatic heart diseases
I23 - Certain current complications following ST elevation (STEMI) and non-ST elevation (NSTEMI) myocardial infarction (within the 28 day period)
I34 - Nonrheumatic mitral valve disorders
I34.8 - Other nonrheumatic mitral valve disorders
I35 - Nonrheumatic aortic valve disorders
I36 - Nonrheumatic tricuspid valve disorders
I37 - Nonrheumatic pulmonary valve disorders
I51 - Complications and ill-defined descriptions of heart disease
Q20 - Congenital malformations of cardiac chambers and connections
Q20.0 - Common arterial trunk
Q20.1 - Double outlet right ventricle
Q20.2 - Double outlet left ventricle
Q20.3 - Discordant ventriculoarterial connection
Q20.4 - Double inlet ventricle
Q20.5 - Discordant atrioventricular connection
Q20.6 - Isomerism of atrial appendages
Q20.8 - Other congenital malformations of cardiac chambers and connections
Q20.9 - Congenital malformation of cardiac chambers and connections, unspecified
Q21 - Congenital malformations of cardiac septa
Q21.1 - Atrial septal defect
Q21.10 - Atrial septal defect, unspecified
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
Q22 - Congenital malformations of pulmonary and tricuspid valves
Q22.0 - Pulmonary valve atresia
Q22.1 - Congenital pulmonary valve stenosis
Q22.2 - Congenital pulmonary valve insufficiency
Q22.3 - Other congenital malformations of pulmonary valve
Q22.4 - Congenital tricuspid stenosis
Q22.5 - Ebstein's anomaly
Q22.6 - Hypoplastic right heart syndrome
Q22.8 - Other congenital malformations of tricuspid valve
Q22.9 - Congenital malformation of tricuspid valve, unspecified
Q23 - Congenital malformations of aortic and mitral valves
Q23.8 - Other congenital malformations of aortic and mitral valves
Q24 - Other congenital malformations of heart
Q25 - Congenital malformations of great arteries
Q25.2 - Atresia of aorta
Q25.4 - Other congenital malformations of aorta
Q25.40 - Congenital malformation of aorta unspecified
Q25.41 - Absence and aplasia of aorta
Q25.42 - Hypoplasia of aorta
Q25.43 - Congenital aneurysm of aorta
Q25.44 - Congenital dilation of aorta
Q25.45 - Double aortic arch
Q25.46 - Tortuous aortic arch
Q25.47 - Right aortic arch
Q25.48 - Anomalous origin of subclavian artery
Q25.49 - Other congenital malformations of aorta
Q25.7 - Other congenital malformations of pulmonary artery
Q26 - Congenital malformations of great veins
Q26.0 - Congenital stenosis of vena cava
Q26.1 - Persistent left superior vena cava
Q26.2 - Total anomalous pulmonary venous connection
Q26.3 - Partial anomalous pulmonary venous connection
Q26.4 - Anomalous pulmonary venous connection, unspecified
Q26.8 - Other congenital malformations of great veins
Q26.9 - Congenital malformation of great vein, unspecified
Q87.4 - Marfan syndrome
Q87.41 - Marfan syndrome with cardiovascular manifestations
R01 - Cardiac murmurs and other cardiac sounds
T82.01 - Breakdown (mechanical) of heart valve prosthesis
T82.01XA - Breakdown (mechanical) of heart valve prosthesis, initial encounter
T82.02 - Displacement of heart valve prosthesis
T82.02XA - Displacement of heart valve prosthesis, initial encounter
T82.03 - Leakage of heart valve prosthesis
T82.03XA - Leakage of heart valve prosthesis, initial encounter
T82.09 - Other mechanical complication of heart valve prosthesis
T82.09XA - Other mechanical complication of heart valve prosthesis, initial encounter