This is the American ICD-10-CM version of Q23.4 - other international versions of ICD-10 Q23.4 may differ. A condition caused by underdevelopment of the whole left half of the heart. It is characterized by hypoplasia of the left cardiac chambers (heart atrium; heart ventricle), the aorta, the aortic valve, and the mitral valve.
Hypoplastic left heart syndrome (HLHS) is a rare congenital heart defect in which the left heart is severely underdeveloped. The International Working Group for Mapping and Coding of Nomenclatures for Paediatric and Congenital Heart Disease defined HLHS as
Q23.4 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2019 edition of ICD-10-CM Q23.4 became effective on October 1, 2018.
This is the American ICD-10-CM version of Q23.4 - other international versions of ICD-10 Q23.4 may differ. A condition caused by underdevelopment of the whole left half of the heart.
Hypoplastic left heart syndrome (HLHS) is a birth defect that affects normal blood flow through the heart. As the baby develops during pregnancy, the left side of the heart does not form correctly. Hypoplastic left heart syndrome is one type of congenital heart defect. Congenital means present at birth.
Q22. 6 - Hypoplastic right heart syndrome | ICD-10-CM.
It consists of a bilateral pulmonary artery banding and a stent placement in ductus arteriosus to secure the right to left shunt (1, 29). This grants a restrictive blood flow to the lungs, while maintaining a systemic perfusion.
The series of three reconstructive operations to repair HLHS — the Norwood, Glenn and Fontan procedures — is known as " Staged Reconstruction ." Frequent surveillance in infancy and early childhood is important to minimize risk factors for the eventual Fontan operation.
It is caused by underdevelopment of the structures on the right side of the heart (tricuspid valve, right ventricle, pulmonary valve, and pulmonary artery) and commonly associated with atrial septal defect.
746.1 - Tricuspid atresia and stenosis, congenital. ICD-10-CM.
Before birth It's possible for a baby to be diagnosed with hypoplastic left heart syndrome while still in the womb. Your doctor might be able to identify the condition on a routine ultrasound exam during the second trimester of pregnancy.
The oldest living person with HLHS is their 30s. Ultimately, the Cribbs hope and pray that Leigh Ann has a long life ahead of her. Texas Children's Hospital – part of the Children's Miracle Network Hospitals is excited to celebrate the third annual Children's Hospital Week from March 18-24.
Most infants die within the first two weeks of life, with an average age at death of 4.5 days (31,33,34). Some patients with HLHS, however, can survive beyond sixty days, without any surgical intervention through the development of pulmonary hypertension (8,33).
Babies born with hypoplastic left heart syndrome need the Norwood procedure because their left ventricle and aorta are too small to pump blood to the body. The Norwood procedure lets the right ventricle pump blood to the body (usually it only pumps blood to the lungs).
The Fontan procedure refers to any surgical procedure that leads to systemic flow of venous blood to the lungs without passing through a ventricle. In 1971, Fontan and Baudet (1) described a surgical procedure for repair of tricuspid atresia that built on experimental and clinical research from the 1940s.
Surgical Treatment Treatment for hypoplastic left heart syndrome requires either a three-step surgical procedure called staged palliation or a heart transplant. Staged palliation is considered one of the major achievements of congenital heart surgery in recent years.
Hypoplastic left heart syndrome (HLHS) is a rare congenital heart defect in which the left heart is severely underdeveloped. The International Working Group for Mapping and Coding of Nomenclatures for Paediatric and Congenital Heart Disease defined HLHS as
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 Q23.4. 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 746.7 was previously used, Q23.4 is the appropriate modern ICD10 code.
DESCRIPTION. Hypoplastic Left Heart Syndrome (HLHS) is a rare congenital heart defect in which the left side of the heart is severely under-developed. The structures of the heart that are usually affected include the mitral valve, left ventricle, aortic valve and the aorta. Because the left side of the heart is unable to send enough blood to ...
Because the left side of the heart is unable to send enough blood to the body, the right side of the heart must maintain the circulation for both the lungs and the body . This extra work eventually causes the right side of the heart to fail. Approximately 20% of children with HLHS have other birth defects or genetic syndromes.
Diagnostic testing: A physical exam showing signs of heart failure (faster than normal heart rate, lethargy, liver enlargement, and rapid breathing) weak pulses at various locations (wrist, groin, and others); and abnormal heart sounds when listening to the chest. Other imaging studies as appropriate.
The child may need a heart transplant as time goes on. Congenital heart defects can be chronic conditions with health implications across the lifespan. Children with HLHS who survive into adulthood may require additional surgical intervention. Lifelong medical follow-up by a cardiologist will be required.
DESCRIPTION. Hypoplastic Left Heart Syndrome (HLHS) is a rare congenital heart defect in which the left side of the heart is severely under-developed. The structures of the heart that are usually affected include the mitral valve, left ventricle, aortic valve and the aorta. Because the left side of the heart is unable to send enough blood to ...
Because the left side of the heart is unable to send enough blood to the body, the right side of the heart must maintain the circulation for both the lungs and the body . This extra work eventually causes the right side of the heart to fail. Approximately 20% of children with HLHS have other birth defects or genetic syndromes.
Diagnostic testing: A physical exam showing signs of heart failure (faster than normal heart rate, lethargy, liver enlargement, and rapid breathing) weak pulses at various locations (wrist, groin, and others); and abnormal heart sounds when listening to the chest. Other imaging studies as appropriate.
The child may need a heart transplant as time goes on. Congenital heart defects can be chronic conditions with health implications across the lifespan. Children with HLHS who survive into adulthood may require additional surgical intervention. Lifelong medical follow-up by a cardiologist will be required.