Frequently Asked Questions

Our FAQ page offers essential details about Chirayu Super Speciality Hospital's services, treatments, and appointment booking. Find answers to common questions about our specialized medical care, diagnostic tests, and treatment options. This resource ensures a smooth, informed experience when accessing our comprehensive healthcare services.

1. FOLIC ACID

Symptoms may include fatigue, weakness, shortness of breath, irritability, and tongue changes.

Treatment involves folic acid supplementation through oral tablets or injections, depending on the severity of the deficiency.

Yes, diets low in leafy greens, fruits, and fortified cereals may lead to folic acid deficiency.

Frequency depends on individual risk factors and health conditions. Consult your healthcare provider for personalized advice.

The test involves a simple blood draw with minimal risks, such as slight bruising at the puncture site.

2. S.CALCIUM

The test measures the total amount of calcium in your blood, including both free (ionized) calcium and calcium bound to proteins.

It provides crucial information about calcium levels, helping diagnose and manage conditions like osteoporosis, kidney disease, parathyroid disorders, and certain cancers.

Generally, fasting is not required. However, it’s important to inform your healthcare provider about any medications or supplements you’re taking, as these can affect the test results.

Results are typically available within a few hours to a day, allowing for prompt medical decision-making based on the calcium levels in your blood.

Abnormal levels can be caused by various factors, including parathyroid gland disorders, kidney disease, certain cancers, and dietary imbalances. Your healthcare provider will interpret the results and provide guidance based on your specific condition.

3. G6PD

G6PD deficiency is a genetic disorder that affects the red blood cells, making them more vulnerable to breaking down prematurely.

Symptoms such as fatigue, jaundice, dark urine, or a family history of G6PD deficiency may indicate the need for this test.

The G6PD test is a simple blood test with minimal risks, similar to any standard blood draw.

Management includes avoiding triggers such as certain medications, foods, and infections that can cause hemolysis.

Early detection in newborns can prevent severe jaundice and related complications by guiding appropriate care and dietary adjustments.