|Leukemia: Central venous line||2852.00000000000||Leukemia: Central venous line||Leukemia: Central Venous Line||L||English||Oncology||Child (0-12 years);Teen (13-18 years)||Body||Skeletal system||Procedures||Adult (19+)||NA||2018-03-06T05:00:00Z||6.50000000000000||75.5000000000000||1094.00000000000||Flat Content||Health A-Z||<p> Learn why your child acute myeloid leukemia (AML) will receive a central venous line (CVL) and how to care for it.</p>||<p>Once your child is diagnosed with acute myeloid leukemia (AML), they will receive a central venous line (CVL).</p>
<p>A CVL is a long, soft, thin, flexible tube that is inserted into one of the large veins leading to the heart. It is a special intravenous (IV) line that is used in children who need IV therapy for a long time. IV therapy means medicine that is put into a vein. A CVL makes it easier and more comfortable for your child to receive medicines such as chemotherapy and IV fluids, and to have blood samples taken. </p>||<h2> Key points </h2>
<ul><li>Children with acute myeloid leukemia (AML) will receive a central venous line (CVL).
</li><li> A CVL is a special intravenous (IV) line inserted into the major blood vessels leading to the heart.
</li><li> A CVL allows children with AML to receive chemotherapy and other medicines more easily and comfortably. </li>
<li> Your child will have a general anesthetic before the procedure to insert the CVL.</li>
<li> There must always be a bandage over the CVL site on the chest to keep it clean and secure.</li>
<li> It is important to ensure the CVL and end of the catheter are always taped to prevent them from being pulled out.</li></ul>||<figure>
<span class="asset-image-title">Central venous line</span>
<img src="https://assets.aboutkidshealth.ca/akhassets/Central_venous_line_MED_ILL_EN.jpg" alt="Catheter inserted into superior vena cava through the internal jugular vein, external jugular vein or right subclavian vein" />
<figcaption class="asset-image-caption">A central venous line is a tube that is inserted into the major blood vessels leading to your child’s heart.</figcaption>
<h2>What happens during the procedure</h2><p>Your child will have a general anesthetic before the procedure to make sure that they sleep through the procedure and will not feel any pain. The procedure will take place in the interventional radiology suite or in the operating room (OR). During the procedure, an interventional radiologist or surgeon threads the CVL tube through a vein in the neck and places it in the large vein leading to the heart, where the blood flow is fast. This placement allows for better mixing of medicines and IV fluids. </p><p>A chest X-ray may be taken after the procedure to ensure the CVL is in the correct position. </p><p>It will take about 1 hour to insert the CVL.</p><h2>What to expect after the procedure</h2><p>After the procedure, your child will have 2 large bandages, 1 on their neck and 1 over their chest area. These bandages are sterile. This means that they are put on in a special way to keep the site as germ-free as possible. </p><p>The neck dressing is cloth-like and will be removed within a few hours. There will also be a bandage over the CVL exit site on the chest wall. It is normal to see some blood under this bandage. You will see a small stitch in both the neck and chest area. These stitches will dissolve and fall off on their own, usually within a few weeks. </p><p>The CVL can be used right away.</p><p>Your child may feel some pain or discomfort in their neck or chest for the first day or two after the procedure. Your child may take Tylenol or morphine, in some cases.</p><p>Often, children feel like they have a stiff neck due to the neck bandage. It is safe for your child to move their neck as usual. </p><p>Your child should not feel any pain when the CVL is being used.</p><h2>How to care for the CVL</h2><p>There must always be a bandage over the CVL site on the chest. This bandage keeps the CVL clean and secure. The end of the catheter tube, called the hub, will be closed with a cap. </p><p>While you are in the hospital, the nurses will care for your child’s CVL. </p><p>When you go home, a Community Care Nurse will care for your child’s CVL. As you become more comfortable caring for the CVL, the Community Care Nurses will teach you how to provide some of this care yourself. </p><p>The CVL will always have either an infusion or a heparin lock. An infusion means that fluids are passed through tubing and a pump. Heparin is a medication that helps prevent the CVL from becoming blocked so that it will work well every time your child needs IV medications or fluids. New heparin will be flushed into the CVL after each use. If it is not being used each day, the heparin flush will be done every 24 hours. </p><p>It is always important to keep the CVL dry. If the CVL gets wet, it can become infected. Your nurse will teach you how to cover the CVL to keep it dry when your child bathes. If the bandage gets wet, it should be changed right away. </p><h2>Protect the CVL</h2><p>Although the CVL is quite secure, it can come out if it is pulled. It is very important to make sure the CVL is always taped in a looped position and covered with a bandage. It is also important that the end of the catheter, called the hub, is taped to your child’s chest or tummy to prevent it from being damaged, broken or pulled out by accident.</p><p>Contact your Community Care Nurse if the CVL comes out a little or is hard to flush. </p><h2>What to look out for after the CVL insertion</h2><p>Contact your Community Care Nurse, the Vascular Access Service at the hospital, or your doctor or clinic nurse if your child has: </p><ul><li>Fever or chills</li><li>Bleeding, redness, or swelling around the CVL or neck.</li><li>Leaking or drainage at the CVL site.</li><li>Pain when the CVL is being used.</li></ul><p>Because each child’s situation is different, you should also ask your doctor if there are any specific instructions for your child. </p><h2>Activities</h2><p>After the CVL is inserted, your child will be able to go back to most activities within a day or two as long as they are not experiencing any pain. This includes going to day care or school. Tell your child’s caregivers or teachers about the CVL. </p><p>Your child may also be able to play some sports and games such as bike riding and tennis. It is important for your child to maintain as many usual activities as possible. Your child should avoid: </p><ul><li>Water sports or swimming. A wet bandage increases the risk of infection. If the bandage becomes wet, it should be changed right away. </li><li>Using scissors anywhere near the CVL. </li><li> Sports that might result in a hit to the CVL or cause the catheter to be pulled out, such as hockey, football, gymnastics, or basketball. </li><li>Letting other children touch or play with the CVL.</li></ul>||https://assets.aboutkidshealth.ca/akhassets/Central_venous_line_MED_ILL_EN.jpg||Leukemia: Central venous line||False|