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Thrombocytopaenic Purpura
Dr Zanapiah Zakaria
Haematology Update 2007
Hospital Ampang
Outline
• ITP in Adults
- Clinical features
- Diagnosis
-Management
• ITP in Pregnancy
-Diagnosis
-Management
Immune Thrombocytopaenic purpura
• an autoimmune disorder
• characterised by persistent
thrombocytopenia (peripheral platelet
count of less than 150 x109/L)
• due to autoantibody binding to platelet
antigen(s)
• causing their premature destruction by the
reticuloendothelial system, in particular the
spleen.
ITP in Adults
Clinical features
• Insidious onset
• Signs and symptoms variable
• Most common- mucocutaneous bleeding
with purpura, epitaxis, gingival bleeding
and menorrhagia
ITP in Adults
Diagnosis
- Remains clinical
- can be defined as isolated
thrombocytopenia with no clinically
apparent associated conditions or other
causes of thrombocytopenia
George et al 1998
ITP in Adults
Laboratory
- Thrombocytopenia needs to be confirmed on PBF
- Autoimmune screen and HIV serology
- Indications for BMA:
> 60 y old
Prior splenectomy
Presence of atypical features
Poor response to first line treatment( eg
prednisolone)
Relapsed ITP following complete remission
- Anti-platelet antibodies: not sensitive
ITP in Adults
• When to treat
- treat when symptomatic or when
platelet count < 30 x 109/L unless they
are undergoing surgical procedures
ITP in Adults
ITP in Adults
ITP in Adults
• Refractory ITP
ITP in Adults
ITP in Pregnancy
ITP only accounts for approximately 3%1
thrombocytopenia in pregnancy as
compared to gestational or incidental
thrombocytopaenia of pregnancy (74%)
and hypertensive disorders of pregnancy
(21%) 2
1Karim ,R. et al 2004
2Burrows, R.F. et al 1993
ITP in Pregnancy
ITP in Pregnancy
• Diagnosis of exclusion
• Aim of investigation :
1. to confirm thrombocytopenia and
2. to exclude secondary causes
ITP in Pregnancy
ITP in Pregnancy
Management: close collaboration between
haematologist, obstetrician, neonatologist
and anaesthetist
Monitoring of platelet counts:
AND/ OR
AND