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Specialist Haematology Services

CVP


Introduction Show [+]Hide [-]

This information sheet is a guide to you and your family. Your treatment will be fully explained by your doctor or nurse, who will be happy to answer any questions.

Your Treatment: Your doctor has prescribed for you a treatment known as CVP. You will be asked to attend the unit every three weeks for this treatment, for up to a maximum of six to eight visits. The treatment consists of the following chemotherapy drugs: -

1. Cyclophosphamide injection
2. Vincristine injection
3. Prednisolone E.C. tablets

Two of these drugs are administered as an intravenous injection via a ‘drip’ into a vein in your arm. Prednisolone is given in tablet form for five days following treatment. Prednisolone tablets should be taken with food and not on an empty stomach as they may cause indigestion. They may also cause an increase in appetite. It is better to take them earlier in the day – with breakfast and lunch – since they can make you feel more alert and prevent sleep.

How long will I be in the department?
You can expect to spend at least two hours in the department.

Can I bring someone with me?
Yes you may also wish to bring in some items to pass the time such as books and personal stereos.

Do I need to take any special precautions before I come to the day unit?
You can eat and drink as usual. You can also take any medication that has been prescribed by your GP providing you have told your hospital doctor you are taking this medication. A packed lunch will be provided.

Will I be able to drive home?
Yes it is extremely uncommon for people to feel unwell immediately after their treatment.

Common side effectsShow [+]Hide [-]

As each patient is an individual your experience will be different to other patients receiving chemotherapy. Common side effects that you may experience during treatment are:

• Nausea and vomiting (sickness)
The severity of any nausea and vomiting will vary from person to person. An anti-sickness injection will be given before your chemotherapy. You will also be given some anti-sickness tablets to take home. If you continue to feel sick, contact the day unit (telephone numbers at the end of this leaflet) as your anti-sickness medication may need to be changed or increased.

• Sore Mouth
Following treatment you may develop a sore mouth and may notice mouth ulcers. Avoid very hot spicy foods. To help prevent oral infections brush your teeth at least twice a day and drink plenty of fluids. To prevent any mouth ulcers becoming infected you should use an anti-bacterial mouthwash. Ask your doctor or nurse to recommend one that is suitable. Occasionally during treatment you may experience a strange taste sometimes described as a metallic or bitter. A strong flavoured sweet or mint may help disguise this.

• Bone Marrow Suppression
Your bone marrow is where your blood cells are made (these are the red cells, white cells, and platelets) to replace those naturally worn out by the body. Chemotherapy interferes with this process and the number of the cells in your blood can become lower than normal. This means following your treatment you could become:

• Prone to infection: White cells fight infection. A low white count can make you prone to infection. You may develop a sore throat, cough, high temperature, shivering or other symptoms, which may be due to infection. A normal temperature is between 36°C and 37°C. A raised temperature is:

Above 38°C (100.4F) at any time or
Above 37.5°C (99.5F) at any two readings taken an hour apart.

• Anaemic: Red cells carry oxygen around your body. A shortage of these cells is called anaemia. You may feel dizzy, out of breath or unusually tired and you may look pale.

• Prone to bleeding: Platelets help to clot your blood and slow down bleeding. A low platelet count may make you prone to bleeding, this usually takes the form of nose-bleeds, bruising or bleeding gums.
You will have a routine blood test before each treatment to monitor the effects of the chemotherapy. Please contact Ward 6b or Ward 8 if you experience any of these symptoms.

• Hair loss
Unfortunately as a result of your treatment you will experience hair loss. The hair falls out gradually 10 to 14 days following your first course of treatment. The time scale varies from person to person. Please remember that this is a temporary side effect and your hair will grow back when your treatment is completed. Your nurse will arrange for you to be provided with a wig if required. A scalp cooling service to prevent or reduce hair loss is available in this trust and is located at the Northern Centre for Cancer Treatment (NCCT) .If you wish to have further details please ask your nurse or doctor. An information sheet is available re managing hair loss.

• Sex, pregnancy and family planning
If you are having chemotherapy it doesn’t mean that you shouldn’t have sex, but you may not feel like it. If there is a chance of pregnancy, you must use effective contraception while on chemotherapy. If you suspect that you or your partner may be pregnant please tell your doctor immediately. Chemotherapy may affect your ability to have children in the future – please discuss this with your doctor or chemotherapy nurse before treatment.

• Fatigue
Many people feel tired and have low energy levels whilst undergoing chemotherapy. There is very little you can do to avoid this but research has shown that patients who suffer fatigue need to take gentle exercise and rest often. This feeling of fatigue is quite normal and energy levels will begin to improve once treatment is completed.
Please remember side effects are usually temporary. If you experience any of them, discuss them with your doctor or nurse.

• Tingling or numbness in fingers and toes
Occasionally, loss of feeling, tingling and numbness of the hands and feet may occur. This is usually temporary and may decrease over several months when your treatment is completed. If you experience any of these symptoms please report them to your doctor or nurse as the drug responsible can be changed.

• Cystitis
Cyclophosphamide may cause a burning sensation or irritation on passing urine because the drug irritates the bladder wall. To prevent cystitis drink a large glass of water both before and after treatment with this drug. Also, try to pass urine as soon as the urge is felt.

• Constipation
Try to drink plenty of fluids and eat foods high in fibre such as fruits and cereals. Report this to your hospital doctor who may prescribe a suitable laxative.

• Skin colouring
Sometimes as a result of the chemotherapy, your skin may appear darker in colour or lightly tanned, especially around the joints. This is known as hyperpigmentation. The skin will return to normal when treatment is finished.

• Extravasation
The drugs you are about to receive are known as “cytotoxic “ or “chemotherapy” drugs. Most of these drugs need to be administered directly into the blood stream through a cannula (a plastic needle inserted directly into a vein.) In most cases it should not cause pain as it is given and often the only sensation you may experience is a “coldness “ running up your arm. However if the drip becomes dislodged from the vein an “extravasation” could occur with chemotherapy leaking outside the vein, causing damage to the surrounding tissues. This happens very rarely. Indications of this are pain, redness or swelling around the cannula site. Your nurse will be looking for any signs of extravasation while your chemotherapy is in progress but it is essential that you inform your nurse if problems arise. Very occasionally patients may notice pain and discomfort around the area only after their chemotherapy has been completed. This also must be reported immediately so that appropriate treatment may be prescribed.

After your TreatmentShow [+]Hide [-]

Please note that alcohol is best avoided for 48 hours after each course of treatment.

Contact numbers

If you have any questions or concerns regarding your treatment please contact:

  • Ward 6b Monday to Friday, 8.00am to 5.00pm - tel: 0191 282 4388
  • Ward 8 Available at all times, tel: 0191 282 5008 (Direct line)

Further information

For further information regarding the drugs you receive, contact Macmillan Cancer Support.

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