| Common Diagnoses | ICD10 |
|---|---|
| Tetralogy of Fallot | Q21.3 |
| Total anomalous pulmonary venous connection | Q26.2 |
| Malformation of coronary vessels | Q24.5 |
| Myocarditis | I40.0-I40.9 |
ICD-10 code Q21.3 for Tetralogy of Fallot is a medical classification as listed by WHO under the range - Congenital malformations, deformations and chromosomal abnormalities . Subscribe to Codify and get the code details in a flash.
Tetralogy of Fallot. The 2019 edition of ICD-10-CM Q21.3 became effective on October 1, 2018. This is the American ICD-10-CM version of Q21.3 - other international versions of ICD-10 Q21.3 may differ.
Tetralogy of Fallot (TOF) is a congenital heart defect which is classically understood to involve four anatomical abnormalities of the heart (although only three of them are always present). It is the most common cyanotic heart defect and the most common cause of blue baby syndrome.
The surgeon accomplished a repair of Tetralogy of Fallot. At surgery, cardiopulmonary bypass was established; the ligamentum was ligated; the thymus was resected; the right ventricle outflow tract (RVOT) was divided and widened; and closure of VSD was done with a Gore-tex® patch.
3: Tetralogy of Fallot.
Q22. 0 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
Tetralogy of Fallot is a heart defect made up of four different heart problems: ventricular septal defect, overriding aorta, pulmonary stenosis and right ventricular hypertrophy. These problems result in cyanotic, or blue, skin on babies because of a lack of oxygen.
Tetralogy of Fallot is a combination of four congenital heart defects. The four defects are a ventricular septal defect (VSD), pulmonary stenosis, a misplaced aorta and a thickened right ventricular wall (right ventricular hypertrophy). They usually result in a lack of oxygen-rich blood reaching the body.
Tetralogy of Fallot with Pulmonary Atresia is an extreme form of tetralogy characterized by absence of flow from the right ventricle to the pulmonary arteries.
Q24. 9 - Congenital malformation of heart, unspecified. ICD-10-CM.
This condition results in mixing oxygen-rich and oxygen-poor blood across the ventricular septal defect, which causes an overall decrease in the amount of oxygen in the blood. It is called tetralogy of Fallot because "tetralogy" means "four" in Greek and there are four defining features of this heart defect.
Tetralogy of Fallot (pronounced te-tral-uh-jee of Fal-oh) is a birth defect that affects normal blood flow through the heart. It happens when a baby's heart does not form correctly as the baby grows and develops in the mother's womb during pregnancy.
The acronym “PROVe” can be used to help remember the four specific abnormalities generally associated with TOF: P for pulmonary infundibular stenosis, R for RVH, O for overriding aorta, V for VSD, and the “e” is silent without an associated pathology.
The most common type of right-to-left shunt is the tetralogy of Fallot, which accounts for up to 6% of congenital heart disease (see Fig. 7-21D). Tetralogy of Fallot corresponds to anatomic stenosis of the pulmonary outflow tract in the right ventricle in combination with a ventricular septal defect.
Tetralogy of Fallot (fah-LO) is a congenital (present at birth) heart defect. In tetralogy of Fallot (TOF), four related heart defects change the way blood flows to the lungs and through the heart. TOF is repaired through open-heart surgery soon after birth or later in infancy.
The difference between TOF and the Fallot–DORV type is in the degree of aortic overriding. Although there is still some controversy, it is generally accepted that the diagnosis of DORV is considered when at least half of the aorta arises from the right ventricle. 3.
Tetralogy of Fallot (TOF) is a congenital heart defect which is classically understood to involve four anatomical abnormalities of the heart (although only three of them are always present). It is the most common cyanotic heart defect and the most common cause of blue baby syndrome.
Inclusion Terms are a list of concepts for which a specific code is used. The list of Inclusion Terms is useful for determining the correct code in some cases, but the list is not necessarily exhaustive.
DRG Group #306-307 - Cardiac congenital and valvular disorders with MCC.
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code Q21.3. Click on any term below to browse the alphabetical index.
This is the official exact match mapping between ICD9 and ICD10, as provided by the General Equivalency mapping crosswalk. This means that in all cases where the ICD9 code 745.2 was previously used, Q21.3 is the appropriate modern ICD10 code.