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What is PSMA Therapy?

Prostate-specific membrane antigen (PSMA) therapy is a targeted radiopharmaceutical treatment used for certain types of prostate cancer. It involves the administration of a radioactive substance that specifically targets and destroys prostate cancer cells.

What is the Cost of PSMA Therapy?

The cost of PSMA Therapy is between Rs. 7,00,000 to Rs. 8,00,000 approximately.

Who Performs PSMA Therapy?

PSMA therapy is performed by a specialized team of healthcare professionals, including:

Nuclear medicine physician: A physician who specializes in nuclear medicine and is responsible for overseeing the PSMA therapy treatment.

Radiation oncologist: A medical doctor who specializes in using radiation therapy to treat cancer and provides guidance on the overall treatment plan.

Nuclear medicine technologist: A trained heal

Technology Used in PSMA Therapy:

Technology Used in PSMA Therapy:

Precautions Before PSMA Therapy:

Before undergoing PSMA therapy, certain precautions may be advised by the healthcare provider, including:

Medical evaluation: A thorough medical evaluation, including blood tests and imaging studies, may be conducted to assess the patient's overall health and suitability for the treatment.

Medication adjustments: The healthcare provider may recommend temporary discontinuation or adjustment of certain medications before the therapy to minimize

Key Tests and Assessments During PSMA Therapy:

During PSMA therapy, the following steps are typically involved:

  • Radiotracer injection, A radioactive substance, typically labeled with lutetium-177 (Lu-177), is injected into a vein.
  • Monitoring and observation, The patient is closely monitored during the therapy session to ensure safety and to assess any immediate side effects.
  • Follow-up assessments, After the therapy, the healthcare team may conduct follow-up tests, such as blood tests and imaging studies, to evaluate the treatment response and assess the patient's progress.

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Frequently Asked Questions

Yes, congenital heart disease can be passed down from a parent to a child. If one or both parents have a congenital heart defect, there is an increased risk of their child having the condition as well. However, it is important to note that not all congenital heart defects are inherited and some can occur due to other factors such as infections during pregnancy or exposure to certain medications or substances.

The initial treatment process for a child with congenital heart disorder depends on the type and severity of the condition. This could include medications for visible symptoms and monitoring with regular checkups.

The tests for congenital heart disorders do not always require hospitalization. Many of the tests can be performed on an outpatient basis, which means the patient can leave the hospital or clinic on the same day. However, some tests may require a short hospital stay, particularly if the patient is an infant or young child.

The treatment options for congenital heart disease may depend on the type and severity of the condition. These options may include medications or procedures like cardiac catheterization.