![]() kidshealth is a joint initiative between the Starship Foundation and the Paediatric Society of New Zealand. www.kidshealth.co.nz / Content Page / Content Page Disclaimer: This fact sheet is for educational use only. Please consult your doctor or other health professional to make sure this information is right for your child. Drips (intravenous fluids or IV )Disclaimer: This fact sheet is for educational use only. Please consult your doctor or other health professional to make sure this information is right for your child. Key points to remember
Back to TopWhat is a drip?![]() A drip is also sometimes known as a cannula, intravenous cannula,
needle or intravenous fluids or IV. It is a short, small plastic tube that is put into your child's vein using a needle. The plastic tube is then left in so that fluids and medicines can be given directly into the blood via the vein. It can also sometimes be used to take blood samples as well. Back to TopWhy would my child need a drip?The drip will allow your child to be given fluid or medicines directly into a vein quickly and for up to several days. It is usually used when children are too sick to swallow fluids and medicines, or when the medicine can only be given this way. Back to TopHow is it put in?The doctor or nurse may put a local anaesthetic patch on the skin first to numb the area where the needle is to be put. It takes about half an hour for the patch to work. If the drip needs to be inserted urgently there may not be time to wait for the local anaesthetic to work. A tourniquet (elastic belt) is put around your child's arm or leg. Your child will need to be held still while a small needle is put into a vein. Once the needle is in the vein, the 'steel' part of the needle is removed and a plastic tube is left in the vein. The plastic tube will be held in place with tape and bandages and a padded board placed to keep the closest joint still. The needle and keeping still can hurt, but once the steel part is removed this does not cause your child any discomfort. If possible, blood tests will be taken from the needle at the time of putting it in. At times there may not be enough blood collected from the needle. If that happens, a separate blood test will need to be taken. Back to TopWhat happens after the drip is put in?Long tubing or syringes can then be attached to the drip and fluids and medicines can be given. Often the long tubing will be put into a special (IV) pump on a drip stand that will control the amount of fluid that will go in. Most of the time the long tubing will stay connected and your child will need to take the drip pump and stand wherever they go. The nurses will explain and show you how to do this. Your doctor will discuss with you how long the drip will need to stay in. This will depend on why it is being put in, and how quickly your child gets better. Back to TopWhat problems can occur?Drips can become blocked, leak or become infected. The nurses will need to regularly check the drip and the area around the drip (cannula). The nurses will look for redness, swelling, leakage and pain at the drip site. If any problems occur the drip may need to be put in again in another spot. At times a bruise may form when the needle is taken out of the vein. This will soon fade. If you are worried please ask the nurses to check you child's drip. Back to TopWhat can I do to help?Cuddling your child while the drip is being put in can help comfort them. If you cannot stay with your child then a staff member will hold your child instead. If your child asks about the tests being done, reassure them and explain in simple terms what is being done and why. Always tell the truth. At times it is helpful to tell stories, talk about the family or anything else that may help to take their mind off the procedure. Remain calm and comfort your child. If you get upset so will your child. The staff are there to help you and your child. If you would like more information please ask the nurse or doctor caring for your child. Back to TopAcknowledgementsStarship Foundation and the Paediatric Society of New Zealand acknowledge the co-operation of The Children's Hospital at Westmead, Sydney Children's Hospital at Randwick, and Kaleidoscope - Hunter Children's Health Network in making this fact sheet available to patients and families.
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This fact sheet was endorsed by PSNZ - 24/03/2011
CopyrightFact sheets are subject to copyright. In the interests of information sharing they may be copied but acknowledgement must be given to PSNZ and Starship Foundation. © The Paediatric Society of New Zealand and Starship Foundation 2005 - 2012
© The Paediatric Society of New Zealand and Starship Foundation 2005 - 2012
This fact sheet was printed on: 10-Feb-2012 03:46am |