Immune thrombocytopenic purpura: Difference between revisions
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==Treatment== | ==Treatment== | ||
===Options=== | === Options === | ||
##Corticosteroids | |||
###First-line in adults | ##Corticosteroids | ||
###Prednisone 60-100 mg/d w/ taper after count reaches normal | ###First-line in adults | ||
###Prednisone 60-100 mg/d w/ taper after count reaches normal | |||
###Methylprednisolone 30mg/kg/d IV x3d (for life-threatening bleeding) | ###Methylprednisolone 30mg/kg/d IV x3d (for life-threatening bleeding) | ||
##IVIG | ##IVIG | ||
###First-line in children | ###First-line in children | ||
###1gm/kg/d x2d | ###1gm/kg/d x2d | ||
##Anti-D (RhoGAM) | ##Anti-D (RhoGAM) | ||
###Pt must be Rh+ for it to work | ###Pt must be Rh+ for it to work | ||
##Transfusion (platelets) | ##Transfusion (platelets) | ||
###Indicated for life-threatening bleeding | ###Indicated for life-threatening bleeding | ||
###Transfuse only following first dose of methylprednisolone or IVIG | ###Transfuse only following first dose of methylprednisolone or IVIG | ||
####Holding transfusion until after first dose results in greater rise in plt count | ####Holding transfusion until after first dose results in greater rise in plt count | ||
##Estrogen (uterine bleeding) | ##Estrogen (uterine bleeding) | ||
###25mg IV x1 | ###25mg IV x1 | ||
6. Emergent splenectomy - uncontrolled/life threatening hemorrhage | |||
1. after tranfusion, IVIG, and steroids | |||
===Indications=== | ===Indications=== | ||
Revision as of 00:28, 13 May 2012
Background
- Acquired autoimmune disease resulting in destruction of platelets
- Because circulating plts are functional, life-threatening bleeding only once plt <10K
- Types
- Acute
- More common among younger children
- Affects men/women equally
- Resolves in 1-2mo
- Chronic
- Lasts >3mo
- More common in adults and women
- Rarely remits spontaneously or with tx
- More likely to have an ynderlying disease or autoimmune disorder (e.g. SLE)
- Acute
Clinical Features
- Petechiae
- Epistaxis, ginigival bleeding, menorrhagia
Diagnosis
- Diagnosis of exclusion
- Must differentiate from chronic ITP, which suggests an underlying disorder
- CBC shows normal cell lines except for the platelets (may have mild anemia)
Treatment
Options
- Corticosteroids
- First-line in adults
- Prednisone 60-100 mg/d w/ taper after count reaches normal
- Methylprednisolone 30mg/kg/d IV x3d (for life-threatening bleeding)
- IVIG
- First-line in children
- 1gm/kg/d x2d
- Anti-D (RhoGAM)
- Pt must be Rh+ for it to work
- Transfusion (platelets)
- Indicated for life-threatening bleeding
- Transfuse only following first dose of methylprednisolone or IVIG
- Holding transfusion until after first dose results in greater rise in plt count
- Estrogen (uterine bleeding)
- 25mg IV x1
- Corticosteroids
6. Emergent splenectomy - uncontrolled/life threatening hemorrhage
1. after tranfusion, IVIG, and steroids
Indications
Adults
- Plt >30K and asymptomatic: Usually do not require treatment
- Plt count <30K: Prednisone
- Plt <50K AND bleeding: Prednisone
- Life-threatening bleeding
- IVIG, methylprednisolone, platelet transfusion
Children
- Plt count >30K: Usually do not require treatment
- Plt count <20K + significant bleeding: IVIG
- Plt count <10K: IVIG
- Life-threatening bleeding
- IVIG, methylprednisolone, platelet transfusion
Disposition
- Admit:
- Pts w/ plt count <20K or those who have significant mucous membrane bleeding
- Discharge:
- Plt counts >20K AND asymptomatic or have only minor petechiae
Complications
- Rare; more common in elderly
- Intracerebral bleeding
- Severe GI bleeding
See Also
Source
- Tintinalli
- UpToDate
