Coronary Angiography (CAG) is a specialized diagnostic procedure used to visualize the coronary arteries — the blood vessels that supply the heart muscle. It helps detect blockages, narrowing, or abnormalities in the arteries that may cause chest pain, heart attacks, or other cardiac conditions. What is CAG? CAG is performed using a contrast dye and X-ray imaging (fluoroscopy). A thin, flexible catheter is inserted through the wrist or groin artery and guided to the coronary arteries. Once the contrast dye is injected, X-ray images are taken to show the flow of blood through the coronary vessels. When is Coronary Angiography recommended? Chest pain (angina) or tightness Positive stress test or abnormal ECG Suspected or confirmed heart attack (MI) Coronary artery disease risk in diabetic or high-risk patients Prior to angioplasty (PCI) or cardiac surgery What does it reveal? Location and severity of arterial narrowing or blockage Condition of the heart chambers and valves Need for further intervention such as angioplasty or bypass surgery Procedure Highlights Minimally invasive, typically done under local anesthesia Takes about 20–30 minutes Most patients are discharged the same or next day Performed in a dedicated Cath Lab by expert interventional cardiologist Dr.Chetan Jain

Angioplasty and Stent Placement Angioplasty and stent placement is a minimally invasive, image-guided procedure used to treat coronary artery disease (CAD) — a condition caused by the narrowing or blockage of the heart's blood vessels due to plaque buildup. What is Angioplasty? Angioplasty, also known as Percutaneous Coronary Intervention (PCI), involves the insertion of a small balloon through a catheter into a narrowed coronary artery. The balloon is gently inflated to widen the artery and restore blood flow to the heart muscle. What is a Stent? In most cases, a stent — a small, mesh-like metallic scaffold — is placed at the site of the blockage to keep the artery open permanently. Drug-eluting stents are commonly used to reduce the risk of re-narrowing (restenosis). When is it recommended? Acute heart attack (STEMI/NSTEMI) Unstable angina or chest pain not relieved by medication Significant coronary artery narrowing found on angiography High-risk coronary lesions with compromised blood flow Benefits of Angioplasty and Stenting Rapid symptom relief (e.g., chest pain, breathlessness) Minimally invasive with faster recovery Improved heart function and reduced risk of heart attacks Short hospital stay (typically 1–2 days) Advanced Techniques Available For patients with complex or calcified lesions, we also offer: Rotational Atherectomy (ROTA) Intravascular Lithotripsy (IVL) Intravascular Ultrasound (IVUS) CHIP angioplasty for high-risk cases

Congenital Heart Disease – Pediatric Overview Overview Congenital heart disease (CHD) refers to structural abnormalities in the heart present from birth. These defects can vary from mild (requiring only observation) to severe (requiring intervention). Treatment and follow-up depend on the specific defect and its impact on heart function. Types of Congenital Heart Defects Atrial Septal Defect (ASD) Ventricular Septal Defect (VSD) Patent Ductus Arteriosus (PDA) Pulmonary or Aortic Valve Stenosis Coarctation of the Aorta Ebstein’s Anomaly Single Ventricle Defects (e.g., Hypoplastic Left Heart Syndrome) Tetralogy of Fallot Total Anomalous Pulmonary Venous Connection (TAPVC) Transposition of the Great Arteries (TGA) Symptoms Symptoms vary by defect but may include: Breathing difficulties Poor feeding and growth Fatigue Cyanosis (bluish skin) Frequent respiratory infections Heart murmur Causes Most congenital heart defects arise from unknown causes, though genetics and environmental factors during pregnancy (e.g., infections, medication use, or maternal conditions) may play a role. Diagnosis Echocardiography (ECHO) Electrocardiogram (ECG) Chest X-ray Cardiac MRI or CT Cardiac catheterization Treatment Treatment depends on the severity and type of defect: Observation: For small, asymptomatic defects Medication: To control symptoms or stabilize the patient before surgery (e.g., diuretics, digoxin, prostaglandins) Catheter-Based Interventions: For PDA, ASD, VSD closures, and valvuloplasty Surgery: Required for more complex or severe defects Multistage Surgery: For single ventricle conditions (e.g., Norwood, Glenn, Fontan procedures) Valve Replacement: In stenotic or leaky valves, either surgically or via catheter Arterial Switch Operation: For TGA within the first month of life Complications Heart rhythm issues Heart failure Valve dysfunction Need for repeat procedures Pulmonary hypertension Endocarditis Growth and development delays Prevention While not all CHDs are preventable: Prenatal care and screening Managing maternal health conditions Avoiding teratogenic drugs Genetic counseling for high-risk families