Intravenous pyelogram (IVP) factsheet

Introduction

An intravenous pyelogram (IVP) is a scan used to look at the urinary system and check how well it is working.

The urinary system includes:

  • the kidneys – filter waste from the blood, turning it into urine, also called wee
  • the ureters – thin tubes that carry urine from the kidneys to the bladder
  • the bladder – stores urine
  • the urethra – the tube that carries urine out of the body.

An IVP uses a type of imaging called fluoroscopy. Fluoroscopy is where many X-ray pictures are taken and then put together as a moving picture to show how the organs work.

 Before the scan

You will get instructions from the hospital or your child’s doctor about how to prepare for the scan. 

These may include:

  • when to stop eating
  • when to drink clear fluids
  • what medicines your child should take or stop taking.

A special fluid called contrast is used in an IVP to help show the urinary system clearly. In rare cases, contrast can cause a serious allergic reaction called anaphylaxis.

Tell your child’s treatment team if your child has:

 During the scan

The scan usually includes the following steps:

  1. your child will lie on an X-ray table with a camera above
  2. a small tube called an intravenous (IV) cannula is placed into a vein in their arm
  3. the doctor injects contrast fluid through the IV cannula
  4. your child may feel warm or have a funny taste in their mouth as the contrast enters the body
  5. X-ray images are taken of the kidneys, ureters, and bladder.

The scan takes about 30 minutes to 2 hours.

 After the scan

Your child’s treatment team will let you know if there are any special instructions to follow after the scan is finished. 

Most children can eat, drink, and play as normal afterwards.

Your child’s doctor will arrange a follow-up appointment to talk about the results.

Disclaimer

This factsheet is provided for general information only. It does not constitute health advice and should not be used to diagnose or treat any health condition.

Please consult with your doctor or other health professional to make sure this information is right for you and/or your child.

The Sydney Children’s Hospitals Network does not accept responsibility for inaccuracies or omissions, the interpretation of the information, or for success or appropriateness of any treatment described in the factsheet.

© Sydney Children’s Hospitals Network 2025


This factsheet was produced with support from John Hunter Children's Hospital.