nsaid, dr. siti s..ppt

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    Siti SupartiDepart. Of. Pharmacology & Therapy

    Faculty Of MedicinePadjadjaran University

    NON STEROID ANTIINFLAMMATORY DRUGS& DRUGS USE IN THE TREATMENT OF GOUT

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    What is NSAID ?

    The antiinflamatory, analgesic, antipyretic

    drugs are heterogenous group of

    compounds, often chemically unrelated(most of them are organic acids), which

    nevertheless share certain therapeutic

    actions and side effects The prototype is aspirin, named: Aspirin

    like drugs or NSAIDs

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    Chemical classification of

    NSAIDs Salicylic acid dervatives

    Para-aminophenol derivatives

    Indole and Indene acetic acids

    Heteroaryl acetic acids

    Anthranilic acids (fenamates) Enolic acids

    Alkanones

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    Therapeutic Activities

    Analgesic - against pain of low to moderate

    intensity

    Chronic post operative pain or pain arising

    from inflammation => (+)

    Pain arising from the hollow viscera => (-)

    Antipyretics - reduce the body temperature

    in febrile states

    Anti inflammatory agents - musculosceletal

    disorder

    Treatment of primary dysmenorrhea

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    Side Effects

    Induce gastric or intestinal ulceration - erosions,ulcers

    GI side effects

    Disturbances in platelet function

    Prolongation of gestation

    spontaneous labor

    Changes in renal function

    Prolongation of bleeding time Intolerance => to Aspirin = to all NSAIDs

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    Choice of NSAIDs in varying

    clinical situationThe choice among NSAIDs for the tretment of

    arthritides is largely empirical.

    Choice of the drug, given for a week or more.

    If the drug is effective => treament should be

    continued.

    Mild arthropaties => together with rest andphysical therapy.

    For children: aspirin, naproxen, tolmetin.

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    Precaution when patients given salicylates or

    phenylbutazone together with warfarin,sulfonylurea, hypoglycemic agents, methotrexate.

    If patients can not tolerate NSAIDs => choice the

    other form of therapy.Gold, hydrochloroquine, penicillamine,

    imunosuppressive agents and glucocorticoids are

    another choice.

    The selection of an NSAIDs for patient accordingto cost of therapy, Aspirin is very inexpensive.

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    SALICYLATE

    Pharmacological Properties

    Effects: analgesia, antipyretic, on CNS,

    respiration, acid base balance and

    electrolyte pattern, CV, GI, hepatic and

    renal, uricosuric, the blood, on rheumatic,

    inflammatory and immunological process,

    on connective tissue metabolism, on CH, N,fat metabolism, on endocrine, salicylate and

    pregnancy, local irritant effects.

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    Absorbtion: orally - absorbed rapidly

    rectal - absorped slower than

    orally.Distribution: salicylates is distributed

    throughout most body tissues and

    most trancellular fluids.Biotransformation: in many tissues,

    particularly in the hepatic

    endoplasmic reticulum and

    mitochondria.

    Excretion: renal (GF and proximal tubular

    secretion)

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    THERAPEUTIC USE

    Systemic uses: antipyresis, analgesia,

    rheumatoid arthritis.

    Other uses: in the treatment or prophylaxis

    of diseases associated with

    hyperaggregability.

    Local uses; per rectal, local on skin.

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    TOXIC EFFECT OF SALICYLATES

    => May be fatal

    Salicylate intoxication: 10 - 30 g (adult)

    4,7 mg methyl salicylate

    in children.

    Simptoms and Signs (SALICYLISM)

    Disturbances in acid balance

    CNS disturbances

    Fever

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    Dehydration

    GI symptoms

    Acidosis

    Toxic encephalopathy.

    In adult - toxic effects occured by therapeuticdose:

    Non cardiogenic pulmonary edem

    Non focal neurologic abnormalities Acid base abnormalities (ketosis)

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    Aspirin Hypersensitivity

    Vasomotor rhinitis

    Angioedema

    Generalized urticaria

    Bronchial asthma

    Hypotension Shock.

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    PARAAMINOPHENOL

    DERIVATIES ACETAMMINOPHEN

    An effective alternative to aspirin

    Available without prescription Acute overdosage causes fatal hepatic

    damage

    ( hepetotoxicity )For Analgesicantipyretic uses, a weak

    antiinflammatory activity.

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    INDOMETHACIN

    Congener of indomethacin : Sulindac

    Used in rheumatoid arthritis and related

    disorder as antiinflamatory drugs, includingacute gout.

    Toxicity often limit its use

    There is entherohepatic cycling of theconjugate and probably indomethacin usedas an antipyretic in Hodgkins disease.

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    Precaution : In concurrentadministration with probenecid,

    ancoagulant agents, furosemide,

    thiazide diuretics, Betaadrenergicblocking agents, inhibitor of

    angiotensin converting enzyme.

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    Toxic effect of indomethacin

    - Most adverse effect are close dependent : GIT complaints

    Occult blood loss

    Acute pancreatitis Hepatic abnormalities

    Severe frontal headache ( CNS effect )

    Hemopoietic reaction Hypersensitivity

    - Contraindication : renal disease, ulcus in

    GIT

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    MEFENAMIC ACID

    Have antiimflammatory, analgesic andantipyretic properties

    Inhibit cyclooxygenase

    Meclofenamic acid may antagonize certaineffect of prostaglandis

    Pharmacokinetic properties :

    Meclofenamate reaches the peak concentrationfaster than mefenamic acid

    50 % of mefenamic acid excreted in urine 20% is recovered in the feces

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    Toxic Effect and Precautions GIT disorder

    Hemolytic anemia of an autoimmune

    type

    Contraindicated on patients with a

    history of gastrointestinal diseases

    Diarrhea or skin rash : drug should be

    stopped.

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    NAPROXEN

    Fully absorbed. Influenced by food

    Accelerated by sod.bicarbonate and reduce byMg oxide or Aluminium hydroxide.

    Crosses the placenta , 1 % of the materialplasma concentration appears in milk oflactating mother

    GIT effect and CNS effect Ototoxicity

    Dermatological Problems

    Other effect

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    PIROXICAM

    Has antiinflammatory, analgesic andantipyretic activity

    For long term treatment of RA or OAequivalent of aspirin indomethacin ornaproxen, be tolerated better

    T 1 / 2 is long single daily dose

    For the treatment of AS, acutemusculoskeletal disorders, dysmenorrhea,postop.pain and acute gout

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    PHENYLBUTAZONE

    For the treatment of RA etc.

    In long term therapy serious toxicity

    Can cause agranulocytosis Sulfinpyrazone much more effective

    uricosuric agent for chronic gout

    Can cause edema

    Death especially caused aplastic anemia andagranulositosis

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    Do not give drug more than 7 days.

    Contraindicated in patient with

    hypertension, cardiac, renal or hepatic

    dysfuncion, a history of peptic ulcer, blood

    dyscrasia, or hypersensitivity to the drug

    Not advisable for elderly persons and not

    recommended in children under the age of

    14

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    GOLD

    Can supress or prevent, but not cure

    experimental arthritis and synovitis due to a

    number of infectious and chemical agents The best hypothesis related to the capacity

    of gold compounds to inhibit maturation

    and function of mononuclear phagocytesand of Tcell supressing immune

    responsiviness

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    Aurothioglucose and gold sodium thiomalate :Parenteral and oral

    Interaction with dimercaprol, penicillamine

    and Nacethylcystein

    increase theexretion of gold

    Auranofin :

    Per oral, par enteralPredominantly exccreated in the feces.

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    Contraindication

    Renal disease, hepatic dysfunction, a historyof infectious hapatitis, hematologicaldisorders.

    Pregnancy, breast feeding Concomitant use of antimalarials,

    immunosupressants, phenylbutazone,

    oxyphenbutazone Urticaria, eczema, colitis

    Poorly tolerated by elderly persons

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    Colchicine

    Only againts gouty arthritis dramatic

    relief of acute attack of gout

    Effective prophylactic agent

    An antimitotic agent

    Inhibit the migration of granulocytes into

    the inflammed area and a decreasedmetabolic and phagosytic activity of

    granulocytes

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    Allopurinol

    Effective for the treatment of :

    Primary hyperuricemia of gout

    Secondary to hematological disorders

    Antineoplastic therapy

    Inhibit the terminal step in uric acid

    biosyntesis Well tolerated by most patients