Diagnosis Code Q25.1
Information for Medical Professionals
The diagnosis code Q25.1 is grouped in the following Diagnostic Related Group(s) (MS-DRG V34.0)
- 306 - CARDIAC CONGENITAL AND VALVULAR DISORDERS WITH MCC
- 307 - CARDIAC CONGENITAL AND VALVULAR DISORDERS WITHOUT MCC
Convert to ICD-9 General Equivalence Map
The ICD-10 and ICD-9 GEMs are used to facilitate linking between the diagnosis codes in ICD-9-CM and the new ICD-10-CM code set. The GEMs are the raw material from which providers, health information vendors and payers can derive specific applied mappings to meet their needs.
- 747.10 - Coarctation of aorta
Present on Admission (POA) Present on Admission
The Present on Admission (POA) indicator is used for diagnosis codes included in claims involving inpatient admissions to general acute care hospitals. POA indicators must be reported to CMS on each claim to facilitate the grouping of diagnoses codes into the proper Diagnostic Related Groups (DRG). CMS publishes a listing of specific diagnosis codes that are exempt from the POA reporting requirement.
The code Q25.1 is exempt from POA reporting.
- Abdominal aortic coarctation
- Abnormality within thorax due to coarctation of aorta
- Abscess at site of aortic coarctation
- Abscess of aorta
- Coarctation of aorta
- Coarctation of aorta between left common carotid artery and right common carotid artery
- Coarctation of aorta between subclavian artery and common carotid artery
- Coarctation of infrarenal abdominal aorta
- Coarctation of suprarenal abdominal aorta
- Congenital stenosis of aorta
- Congenital stenosis of aortic arch
- Double aortic arch with left arch dominant
- Double aortic arch with left arch dominant and coarctation of right arch
- Double aortic arch with right arch dominant
- Double aortic arch with right arch dominant and coarctation of left arch
- Infective endarteritis at site of aortic coarctation
- Juxtaductal aortic coarctation
- Obstruction of aortic arch
- Parachute malformation of mitral valve
- Postductal coarctation of aorta
- Posterior fossa brain malformation, haemaniogma, arterial anomaly, cardiac defect and aortic coarctation, eye abnormality synodrome and sternal anomaly syndrome
- Posterior fossa brain malformation, hemangioma, arterial anomaly, cardiac defect and aortic coarctation, and eye abnormality syndrome
- Preductal coarctation of aorta
- Recoarctation of aorta
- Shone complex
- Stenosis of thoracic aorta
- Supramitral left atrial ring
- Thoracic aortic coarctation
Index of Diseases and Injuries
References found for the code Q25.1 in the Index of Diseases and Injuries:
- Inclusion Terms: Inclusion terms
List of terms is included under some codes. These terms are the conditions for which that code is to be used. The terms may be synonyms of the code title, or, in the case of "other specified" codes, the terms are a list of the various conditions assigned to that code. The inclusion terms are not necessarily exhaustive. Additional terms found only in the Alphabetic Index may also be assigned to a code.
- Coarctation of aorta (preductal) (postductal)
- Stenosis of aorta
Information for Patients
Congenital Heart Defects
A congenital heart defect is a problem with the structure of the heart. It is present at birth. Congenital heart defects are the most common type of birth defect. The defects can involve the walls of the heart, the valves of the heart, and the arteries and veins near the heart. They can disrupt the normal flow of blood through the heart. The blood flow can slow down, go in the wrong direction or to the wrong place, or be blocked completely.
Doctors use a physical exam and special heart tests to diagnose congenital heart defects. They often find severe defects during pregnancy or soon after birth. Signs and symptoms of severe defects in newborns include
- Rapid breathing
- Cyanosis - a bluish tint to the skin, lips, and fingernails
- Poor blood circulation
Many congenital heart defects cause few or no signs and symptoms. They are often not diagnosed until children are older.
Many children with congenital heart defects don't need treatment, but others do. Treatment can include medicines, catheter procedures, surgery, and heart transplants. The treatment depends on the type of the defect, how severe it is, and a child's age, size, and general health.
NIH: National Heart, Lung, and Blood Institute
- Atrial septal defect (Medical Encyclopedia)
- Bicuspid aortic valve (Medical Encyclopedia)
- Congenital heart defect corrective surgeries (Medical Encyclopedia)
- Congenital heart disease (Medical Encyclopedia)
- Cyanotic heart disease (Medical Encyclopedia)
- Dextrocardia (Medical Encyclopedia)
- Echocardiogram -- children (Medical Encyclopedia)
- Heart murmurs and other sounds (Medical Encyclopedia)
- Patent ductus arteriosus (Medical Encyclopedia)
- Ventricular septal defect (Medical Encyclopedia)
Critical congenital heart disease Critical congenital heart disease (CCHD) is a term that refers to a group of serious heart defects that are present from birth. These abnormalities result from problems with the formation of one or more parts of the heart during the early stages of embryonic development. CCHD prevents the heart from pumping blood effectively or reduces the amount of oxygen in the blood. As a result, organs and tissues throughout the body do not receive enough oxygen, which can lead to organ damage and life-threatening complications. Individuals with CCHD usually require surgery soon after birth.Although babies with CCHD may appear healthy for the first few hours or days of life, signs and symptoms soon become apparent. These can include an abnormal heart sound during a heartbeat (heart murmur), rapid breathing (tachypnea), low blood pressure (hypotension), low levels of oxygen in the blood (hypoxemia), and a blue or purple tint to the skin caused by a shortage of oxygen (cyanosis). If untreated, CCHD can lead to shock, coma, and death. However, most people with CCHD now survive past infancy due to improvements in early detection, diagnosis, and treatment.Some people with treated CCHD have few related health problems later in life. However, long-term effects of CCHD can include delayed development and reduced stamina during exercise. Adults with these heart defects have an increased risk of abnormal heart rhythms, heart failure, sudden cardiac arrest, stroke, and premature death.Each of the heart defects associated with CCHD affects the flow of blood into, out of, or through the heart. Some of the heart defects involve structures within the heart itself, such as the two lower chambers of the heart (the ventricles) or the valves that control blood flow through the heart. Others affect the structure of the large blood vessels leading into and out of the heart (including the aorta and pulmonary artery). Still others involve a combination of these structural abnormalities.People with CCHD have one or more specific heart defects. The heart defects classified as CCHD include coarctation of the aorta, double-outlet right ventricle, D-transposition of the great arteries, Ebstein anomaly, hypoplastic left heart syndrome, interrupted aortic arch, pulmonary atresia with intact septum, single ventricle, total anomalous pulmonary venous connection, tetralogy of Fallot, tricuspid atresia, and truncus arteriosus.