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LUPUS AND TREATMENT WITH DRUGS

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Title: LUPUS AND TREATMENT WITH DRUGS


1
LUPUS AND TREATMENT WITH DRUGS
2
Aims of Treatment
  • The aim of drug treatment in Lupus is to treat
    the disease with minimal side affects from the
    drugs.
  • We aim to make you feel as well as possible so
    that you can continue life as you would wish to.
  • Although this is our aim it may take time to get
    the right combination of drugs. For this we
    require your help and patience.

3
Ways of Treating You
  • Over the years it has been found that the best
    way of making you feel better with the least risk
    of developing drug side effects may be to use
    several different drugs at lower doses rather
    than a single drug alone at higher doses.
  • This means you may end up on several different
    drugs to take during the day.

4
First Line of Treatment
  • We give you different drugs depending on how ill
    you are.
  • If you have mild Lupus we or you GP may start
    with Non Steroidal Anti Inflammatory Drugs such
    as Ibuprofen.
  • You may also need other pain killers as well such
    as paracetamol.
  • You should always use sunblock from April to
    October, especially if you get sun induced
    rashes.

5
Anti Malarial Tablets
  • If Anti Inflammatory Drugs are not enough then we
    often give antimalarial drugs next.
  • This is usually Hydroxychloroquine. This
    particularly helps with joint pains and mild
    rashes.
  • Most patients tolerate this drug well. Some
    patients may develop side effects such as nausea
    or allergic rashes. A rare side effect can be
    problems with the vision, although this is
    usually the result of other causes.

6
Steroids
  • This is the fastest acting treatment for Lupus.
  • The dose given and the method of administration
    varies depending on how bad your symptoms are.
  • Our aim is to give the smallest dose possible
    while keeping your Lupus under control.

7
Steroids Continued
  • The steroid we use is different to the one you
    read about athletes taking.
  • It is dangerous to stop steroids suddenly. They
    must be reduced gradually under medical
    supervision.
  • Steroids can be given as creams, ointment, eye
    drops or injections into the joints, muscles or
    veins.

8
Steroid Sparing Drugs
  • If we cannot get your dose of steroids down, or
    if you have required drips of steroids or other
    drugs. We will then recommend other drugs to keep
    your Lupus under control.
  • The drug we choose to put you on depends on your
    symptoms, blood results and whether or not you
    plan to become pregnant.
  • These drugs usually take 12 weeks to have an
    effect on your Lupus. Therefore you use them in
    combination with steroids or other drugs.

9
What are the steroid sparing drugs?
  • Azathioprine is one of the most commonly used
    drugs that we use to help reduce the steroid
    dose.
  • It can be used in pregnancy and breast feeding.
  • We sometimes do not use it if there are concerns
    about a low white cell count (blood cells that
    fight infection). However, this depends on the
    cause of the low count.

10
Cyclosporin
  • Cyclosporin is usually used in patients who
    cannot use Azathioprine to reduce the steroid
    dose.
  • Sometimes we cannot use it if there are certain
    problems with the kidneys or high blood pressure.
  • Can be used in pregnancy.

11
Methotrexate
  • Methotrexate is particularly good for arthritis
    symptoms.
  • It is only taken once a week
  • It cannot be used in pregnancy or while breast
    feeding.

12
Mycophenolate mofetil (MMF)
  • Good for many Lupus symptoms, although it is
    still being tested
  • Appears to be good when Lupus has not responded
    to other treatments.
  • You should not get pregnant while taking this
    this drug. There is a risk of congenital
    abnormalities in the baby.
  • This drug is not yet routinely available.

13
Blood Tests
  • You need regular blood tests while taking steroid
    sparing drugs.
  • These tests are usually done once every two weeks
    to begin with, until you are established on the
    drug.
  • The blood tests are then done monthly to 3
    monthly until you stop the drug.
  • These blood tests are important as they show
    problems that you will not be aware of until you
    are very sick due to side effects on the bone
    marrow (where blood cells are made), the liver or
    kidneys.

14
Drips or Pulses
  • The main two drugs we use as drips or pulses are
    steroids and cyclophosphamide.
  • These are used when you Lupus is severe and we
    want to get it under control quickly.
  • Once under control we can consider other
    treatments for long term use.
  • You must not get pregnant whilst been treated
    with cyclophosphamide as it causes abnormalities
    in the unborn baby.

15
Ways of treating yourself
  • From April to October you should wear a sun
    block. Factor 25 or above. You can get this on
    prescription.
  • Fatigue is a constant problem for many Lupus
    patients. It is important to balance rest, work
    and gentle exercise.
  • Keeping your weight within recommended limits on
    a low fat diet will help, particularly with joint
    pains. It will also reduce the risk of heart
    disease in later life.

16
Alternative Therapy
  • The only alternative therapies that we do not
    recommend are herbal treatments and Chinese
    medicine. These can react with conventional
    treatment and cause liver and kidney problems.
  • St Johns Wort also interacts with many of the
    drugs used for Lupus.
  • Other alternative therapies are considered safe,
    but the potential benefits are uncertain. For
    example acupuncture, shiatsu, massage,
    reflexology or homeopathy.
  • Please discuss any forms of therapy that you are
    having or considering with the doctor or nurse in
    clinic.

17
Final Comment
  • This is only an outline of how we choose which
    drugs to treat your Lupus.
  • If you have comments or strong feelings about
    your treatment please discuss this with your
    Lupus doctor.
  • If you have other questions or comments please
    discuss them with me
  • Kate Peers, Lupus UK funded Nurse
  • Phone numbers 0121 414 6875 or 0776 558 7885
    Works Tuesday to Friday 8am - 4pm
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