Childhood Pulmonary Arterial Hypertension treatment

Childhood pulmonary arterial hypertension (PAH) is a serious condition where the blood vessels in the lungs become narrow, making it hard for the heart to pump blood. Treatment focuses on improving blood flow and may include medications like vasodilators to widen blood vessels, diuretics to reduce fluid buildup, and anticoagulants to prevent blood clots. In some cases, oxygen therapy or more advanced options like lung transplants may be recommended. Careful monitoring and regular check-ups with pediatric pulmonologists are crucial to managing the condition and improving the child’s quality of life.