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CHRONIC ITP By DR Falak abro

Chronic itp

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Page 1: Chronic itp

CHRONIC ITP

By DR Falak abro

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• chronic ITP persists for more than 6-12 months.

• Chronic ITP has more insidious onset with easy bruising and petechiae

•Age 8-14 years.

• male : female ratio is 1:2

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PATHOPHYSIOLOGY

• Increased platelet destruction .

• Spleen is key organ in Pathophysiology

.platelet autoantibodies formed in white pulp

. Macrophages in red pulp destroy immunoglobulin coated platelets.

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PATHOPHYSIOLOGY

•Autoantibody coated platelets induce Fc receptor-mediated phagocytosis by mononuclear macrophages

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Clinical Signs and symptoms

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*Bruise

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Petechiae

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PurPura

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Gingival bleeding

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Epistaxsis

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INVESTIGATION

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PERIPHERAL BLOOD FILM

• ITP with low platelet count usually (<100,000 usually) with normal hemoglobin and WBC count

• thrombocytopenia with platelet count <20 x 109/L is common and platelet size may be normal or increased

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Bone Marrow Examination

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•The bone marrow in patients with ITP contains normal or increased number of megakaryocytes indicates that :

a: plateletes production is normal

b: thrombocytpenia is due to increased platelet destruction.

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TREATMENT

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• Wait and Watch if platelets are below 50,000 or there is no signs of bleeding.

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INTRAVENOUS IMMUNOGLOBULINS

•Mechanism:

blocking FC receptors of RE (reticuloendothelial) phagocytes.

• preventing them from binding and destroying IgG antibody-coated platelets.

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LNH PHARMACY

1 vial= 250 mgPrice= approx Rs: 1500

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Dose : safe dose is 400mg/kg/day using 5 days continuously or 1g/kg/day for 2 days.

Merits: IVIG is preferable to steroids because it causes faster elevation of platelete count greater than 20,000 within 24 hours.

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Demerits :• Its expensive

• Long infusion time of 6-8 hours

• Headache

• vomiting

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Corticosteroids:

Mechanism

• inhibit platelet destruction.

•Rapid action that reduces RE destruction of antibody coated platelet.

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Dose:•Oral prednisone 1-2mg/kg/day for two weeks then tapered over third week

• In chronic ITP with recurrent bleeding intravenous methyl predinisolone20-30mg/kg/day for 3 days can be given.

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Intravenous Anti D therapy :MECHANISM:• Specific red blood cell antibodies coat red blood cells, which are taken by RE system in place of antibody coated platelets.

•Anti Rh-D immunoglobulin produces mild hemolytic anemia that saturates Fc receptors of phagocytic elements of RE system.

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•Dose I/V 50ug -75ug/kg for two days platelet rise within 48 hours to 72 hours.

•Merits: Lower side effects than IVIG doesnot cause headach or vomiting

•Demerit: causes hemolysis.

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LNH PHARMACY

1 vial= 300 ugPrice = RS: 5500

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SPLEENECTOMY:

•Indicated in chronic, symptomatic ITP when other options fail.

•About 64-88% of patient with chronic Itp achieve complete remission.

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It is done because It removes:• primary site of platelete destruction and

site of antiplatelete-antibody production

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RITUXIMAB:MECHANISM:

• it is monoclonal antibody which depletes B-cells by binding to the CD-20 antigen surface •Therapy effect remains for 6-12 months as it prevents activity of autoreactive cells specially against gp-IIb/IIIa.

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Dose : 375mg/m2 per dose weekly for 4 weeks.

Price : 100mg vial approx RS: 17000 500mg vial approx RS: 85000

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Time to respond therapy : 1-7 weeks

Side-effects: fever, chills, allergy reactions which can be prevented by slow infusion and premedication with antihistamine or steroids.

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(Thrombopoeitin) TPO receptor agonists

•Mechanism of action

•Endogenous TPO made in liver which regulates platelet production by increasing the number and maturation of bone marrow megakaryocytes.

•2 TPO receptor agonists : a: romiplostim with dose 1-10ug/kg/dose subcutanously weekly.

b: Eltrombopag with dose is 50mg orally.

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•ROMIPLOSTIM is a subcutaneous thrombopoiesis stimulating FC-peptide fusion protein.

•ELTROMBOPAG is orally active non peptide agonist, it acts by stimulating platelet production.

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Side effects

• Romiplostim : headache, phyrangitis, fatigue

•Eltrombopag : nausea and vomiting, hepatic toxicity

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THANKYOU…