Childhood Brain and Spinal Cord Tumors
Low blood cell counts
Bone marrow—the spongy material that fills the inside of the bones—produces red cells, white cells, and platelets. Chemotherapy drugs damage or destroy the cells inside the bone marrow and can dramatically lower the number of cells circulating in the blood. Frequent blood tests are crucial in determining whether your child needs transfusions. Many children treated for brain or spinal cord tumors require transfusions of red cells and sometimes platelets. When the number of infection-fighting white cells is low, your child is in danger of developing serious infections.
Absolute neutrophil count (ANC)
The activities of families of children with cancer revolve around the sick child’s white blood cell (WBC) count, and, specifically the absolute neutrophil count (ANC). The ANC provides an indication of the child’s ability to fight infection.
When a child has blood drawn for a complete blood count (CBC), one section of the lab report will state the total WBC count and a “differential.” This means each type of WBC will be listed as a percentage of the total. For example, if the total WBC count is 1500 mm3, the differential might appear as follows:
White Blood Cell Type | Percentage of Total WBC |
Segmented neutrophils (also called polys or segs) | 49% |
Band neutrophils (also called bands) | 1% |
Basophils (also called basos) | 1% |
Eosinophils (also called eos) | 1% |
Lymphocytes (also called lymphs) | 38% |
Monocytes (also called monos) | 10% |
To calculate the ANC, add the percentages of segmented and band neutrophils, then multiply by the total WBC. Using the example above, the ANC is 49% + 1% = 50%; 50% of 1,500 (.50 x 1500) = 750; so the ANC is 750.
How to protect a child with a low ANC
Erica ran a fever whenever her counts were low, but nothing ever grew in her cultures. They would hospitalize her for 48 hours as a precaution. She was never on a full dose of medicine because of her chronically low counts. She’s 2 years off treatment now and doing great.
Generally, an ANC of 500 to 1,000 provides children with enough protective neutrophils to fight off exposure to infection due to bacteria and viruses. With an ANC this high, you can usually allow your child to attend all normal functions such as school, athletic events, and parties. However, it is wise to keep close track of the pattern of the rise and fall of your child’s ANC. If you know the ANC is 1,000, but is on the way down, it will affect what activities are appropriate for your child. Each hospital has different guidelines concerning activities for children with low ANCs.
Following are parents’ suggestions for ways to prevent and detect infections:
Insist on frequent, lengthy (at least 1 to 2 minutes), and thorough hand washing for every member of the family. Use plenty of soap and warm water, lather well, and rub all portions of the hands, including between all the fingers and under the fingernails. Children and parents need to wash before preparing meals, before eating, after playing outdoors, and after using the bathroom.
We always had antibacterial baby wipes in our car. We washed Justin’s hands, and our own, after going to any public places such as parks, museums, or restaurants. They can also be used to wipe off tables or high chairs at restaurants.
- Make sure all medical personnel at the hospital or doctor’s office thoroughly wash their hands before touching your child.
- Keep your young child’s diaper area and skin creases clean and dry.
- Whenever your child needs a needle stick, make sure the technician cleans your child’s skin thoroughly with both betadine and alcohol.
- If your child gets a small cut, wash it with soap and water, rinse it with hydrogen peroxide, and cover it with a small bandage.
- When your child is ill, take his temperature every 2 to 3 hours. Call the doctor if your child’s temperature is 101o F (38.5° C) or above.
- Do not permit anyone to take your child’s temperature rectally (in the anus) or use rectal suppositories, as these may cause anal tears and increase the risk of infection and bleeding.
Believe it or not, we once stopped the nursing assistant from doing a rectal temp during an inpatient admission. When we had a room on the pediatric oncology side, this never happened. But for that admission those rooms were full, and we were on the other side of the floor.
- Do not use a humidifier, as the stagnant water can become a reservoir for contamination.
- Apply sunscreen whenever your child plays outdoors. The skin of children taking certain chemotherapy drugs or who have recently received cranial radiation therapy is sun sensitive, and a bad sunburn can easily become infected.
- Your child should not receive routine immunizations while on chemotherapy. Your child’s doctor or nurse can complete medical exemption forms for your child’s school.
- Siblings should not be vaccinated with the live polio virus (OPV); they should get the killed polio virus (IPV). Verify that your pediatrician is using the appropriate vaccine for the siblings.
Katy was diagnosed just a week after her younger sister, Alison, had been given the live polio vaccine. Because there was a small risk that Alison could infect any immunosup-presed child with polio, she was not allowed to visit the oncology floor of the hospital.
My daughter kept getting ear infections while on chemotherapy. They would find them during routine exams. I felt guilty because she never told me her ears were hurting. I told her doctor that I was worried because she didn’t complain of pain, and he reassured me by telling me that she probably felt no pain because she didn’t have enough white cells to cause swelling inside her ear.
Shawn had continual ear infections while on treatment. He had two sets of tubes surgically implanted while on chemotherapy.
- Never give aspirin for fever, because aspirin and drugs containing aspirin interfere with blood clotting. Aspirin is not recommended for children in general. Ibuprofen may be given if approved by your child’s oncologist. If your child has a fever, call the doctor before giving any medication.
- Ask your child’s oncologist about using a stool softener if your child has problems with constipation. Stool softeners can help prevent anal tears.
- Call the doctor if any of the following symptoms appear: fever above 101° F (38.5° C), chills, cough, shortness of breath, sore throat, severe diarrhea, bloody urine or stool, and pain or burning while urinating. Bring your child immediately to the hospital if there is a fever and you know that your child is neutropenic (low ANC) because if not treated immediately, this could be a life-threatening situation.
Some people choose to keep their kids away from everything and everyone during treatment, while others restrict their activities when they’re neutropenic or receiving a particularly heavy dose of chemo. You will learn how to trust your instincts and your doctor’s advice, and also learn how to take your cues from your child. For us, we try to walk a fine line between keeping Hunter’s life as normal and stimulating as possible, while not taking any foolish risks with his health. When he’s neutropenic (ANC below 500), when he’s in a particularly heavy round of chemo, or when there’s chicken pox going around we keep him at home. When he’s doing well then we take him out a bit more, but sensibly: no shopping malls on Saturdays, no contact with anyone who’s sick, and limited contact with other kids. During the week, I will take him with me to the grocery store, or to see his grandparents or cousins, provided everyone is healthy. When he’s feeling well, we also go to the park, ride our bikes, and do normal kid stuff. I carry around antibacterial hand wipes with me so I can keep him clean after playgrounds.
Table of Contents
All Guides- Introduction
- 1. Diagnosis
- 2. The Brain and Spinal Cord
- 3. Types of Tumors
- 4. Telling Your Child and Others
- 5. Choosing a Treatment
- 6. Coping with Procedures
- 7. Forming a Partnership with the Treatment Team
- 8. Hospitalization
- 9. Venous Catheters
- 10. Surgery
- 11. Chemotherapy
- 12. Common Side Effects of Chemotherapy
- 13. Radiation Therapy
- 14. Peripheral Blood Stem Cell Transplantation
- 15. Siblings
- 16. Family and Friends
- 17. Communication and Behavior
- 18. School
- 19. Sources of Support
- 20. Nutrition
- 21. Medical and Financial Record-keeping
- 22. End of Treatment and Beyond
- 23. Recurrence
- 24. Death and Bereavement
- 25. Looking Forward
- Appendix A. Blood Tests and What They Mean
- Appendix C. Books and Websites