As a journalist, I rewrote the article to make it unique and more engaging. Here’s my version:
At 20 weeks pregnant, I can’t help but worry about the potential risk to my unborn baby. With a history of congenital heart disease, I want to know when is the right time to get screened for this disease. Congenital heart defects affect nearly 1% of children and can be a leading cause of death in children. That’s why screening for this disease is recommended for all pregnant women, especially those with risk factors like congenital heart disease, genetic diseases, gestational diabetes, lupus erythematosus, or hypertension.
While fetal echocardiography between 18-22 weeks of pregnancy can help detect most heart defects in the fetus, some may only be diagnosed after birth. That’s why it’s important to continue screening during pregnancy and be vigilant for signs like difficulty breathing, rapid breathing, or poor weight gain in the baby. Early diagnosis can lead to prompt treatment and increase the chances of survival for the child.
If you have a history of congenital heart disease, monitoring your health during pregnancy is crucial. There is a 2-4% increased risk that your child may also develop the disease. Getting an echocardiogram at 20 weeks is recommended, and choosing a medical facility with coordination between obstetrics and cardiology can help ensure a safe and healthy pregnancy.
Congenital heart disease is a genetic condition that can have serious complications if not detected and treated promptly. It’s essential to listen to your body and seek medical attention if you experience symptoms like fatigue, chest tightness, or palpitations. Early detection and treatment are key to managing this disease effectively.
In conclusion, as a journalist who has written about various topics in healthcare industry it is important to inform our audience about the importance of screening for congenital heart defects during pregnancy especially if there are any risk factors present . By being vigilant and getting an echocardiogram at an early stage we can detect these defects timely which increases chances of survival for newborn babies.
