Immune-mediated thrombocytopenic purpura: Difference between revisions

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== Definition ==
==Definition==


* Acquired autoimmune bleeding disorder characterized by autoimmune autobody-mediated destruction of platelets
*Acquired autoimmune bleeding disorder characterized by autoimmune autobody-mediated destruction of platelets


== Differential Diagnosis ==
==Differential Diagnosis==


* Primary
*Primary
* Secondary
*Secondary
** Infection
**Infection
*** HIV
***[[HIV]]
*** Hepatitis C
***[[Hepatitis C virus]]
*** CMV
***[[CMV]]
*** VZV
***[[VZV]]
*** H. pylori
***[[Helicobacter pylori]]
** Inflammatory/Autoimmune
**Inflammatory/Autoimmune
*** Antiphospholipid syndrome
***[[Antiphospholipid antibody syndrome]]
*** Autoimmune thrombocytopenia (Evans syndrome)
***[[Autoimmune thrombocytopenia]] (Evans syndrome)
** Congenital
**Congenital: [[common variable immune deficiency]]
**Neoplasm: [[lymphoproliferative disorder]]
*** Common variable immune deficiency
**Medications
** Neoplasm
*** Lymphoproliferative disorders
** Medications


== Investigations ==
==Investigations==


* CBC
*CBC
** Mean platelet volume can suggest high platelet turnover
**Mean platelet volume can suggest high platelet turnover
* Peripheral blood film
*Peripheral blood film
* HIV and HCV testing
*HIV and HCV testing
* Additional
*Additional
** Abdo ultrasound for splenomegaly and liver disease
**Abdo ultrasound for splenomegaly and liver disease
** Rh status
**Rh status
** DAT for Evan's syndrome
**DAT for Evan's syndrome
** Quantitative immunoglobulins
**Quantitative immunoglobulins
** Hep B testing
**Hep B testing
** H. pylori, if at risk
**H. pylori, if at risk
** Antiphospholipid antibodies
**Antiphospholipid antibodies
** ANA, anti-dsDNA
**ANA, anti-dsDNA
** Thyroid tests
**Thyroid tests
** vWF testing (for type 2B vWD)
**vWF testing (for type 2B vWD)
** Bone marrow biopsy
**Bone marrow biopsy


== Management ==
==Management==


=== Acute management ===
* Only needs treatment if platelets lower than 30 or if bleeding

* First-line:
*Only needs treatment if platelets lower than 30 or if bleeding
** Steroids
*'''First-line:'''
*** Prednisone 1-2mg/kg/day x3weeks then taper (70-80% response but high relapses over next 10 years)
**Steroids
*** Dexamethasone 40mg/d po x4days ever 2-4 weeks, repeated for 3-6 cycles (90% response)
***Prednisone 1-2mg/kg/day x3weeks then taper (70-80% response but high relapses over next 10 years)
** IVIg 1-2g/kg x1-2 days, if refractory to steroids or requires rapid treatment
***Dexamethasone 40mg/d po x4days ever 2-4 weeks, repeated for 3-6 cycles (90% response)
** Anti-D if Rh positive and has a spleen
**IVIg 1-2g/kg x1-2 days, if refractory to steroids or requires rapid treatment
* Second-line:
**Anti-D if Rh positive and has a spleen
** Splenectomy
*'''Second-line:'''
*** Ensure vaccinated for Hib, Strep pneumo, and N. meningitidis
**Splenectomy
** Rituximab
***Ensure vaccinated for Hib, Strep pneumo, and N. meningitidis
** Thrombopoeitin agonists: eltrombopag or romiplostim
**Rituximab
** Immunosuppressive therapies: azathioprine, cyclosporin A, cyclophosphomide, danazol, dapsone, mycofenolate mofetil, vina alkaloids
**Thrombopoeitin agonists: eltrombopag or romiplostim
* Third-line:
**Immunosuppressive therapies: azathioprine, cyclosporin A, cyclophosphomide, danazol, dapsone, mycofenolate mofetil, vina alkaloids
** Almtuzumab, chemotherapy, stem cell transplant
*'''Third-line:'''
* For life-threatening bleed:
**Almtuzumab, chemotherapy, stem cell transplant
** IVIG 1g/kg, repeated once more if platelets remain below 50 the next day
*'''For life-threatening bleed:'''
** Pulse steroids: methylprednisolone 30mg/kg IV daily x2-3 days)
**IVIG 1g/kg, repeated once more if platelets remain below 50 the next day
** Tranexamic acid 1G IV q6h
**Pulse steroids: methylprednisolone 30mg/kg IV daily x2-3 days)
** Platelet transfusion
**Tranexamic acid 1G IV q6h
** Emergency splenectomy
**Platelet transfusion
** Last-ditch: recombinant factor VIIa 90mcg/kg IV q2h
**Emergency splenectomy
*** High risk for clotting
**Last-ditch: recombinant factor VIIa 90mcg/kg IV q2h
***High risk for clotting


[[Category:Hematology]]
[[Category:Hematology]]

Revision as of 15:12, 29 July 2020

Definition

  • Acquired autoimmune bleeding disorder characterized by autoimmune autobody-mediated destruction of platelets

Differential Diagnosis

Investigations

  • CBC
    • Mean platelet volume can suggest high platelet turnover
  • Peripheral blood film
  • HIV and HCV testing
  • Additional
    • Abdo ultrasound for splenomegaly and liver disease
    • Rh status
    • DAT for Evan's syndrome
    • Quantitative immunoglobulins
    • Hep B testing
    • H. pylori, if at risk
    • Antiphospholipid antibodies
    • ANA, anti-dsDNA
    • Thyroid tests
    • vWF testing (for type 2B vWD)
    • Bone marrow biopsy

Management

Acute management

  • Only needs treatment if platelets lower than 30 or if bleeding
  • First-line:
    • Steroids
      • Prednisone 1-2mg/kg/day x3weeks then taper (70-80% response but high relapses over next 10 years)
      • Dexamethasone 40mg/d po x4days ever 2-4 weeks, repeated for 3-6 cycles (90% response)
    • IVIg 1-2g/kg x1-2 days, if refractory to steroids or requires rapid treatment
    • Anti-D if Rh positive and has a spleen
  • Second-line:
    • Splenectomy
      • Ensure vaccinated for Hib, Strep pneumo, and N. meningitidis
    • Rituximab
    • Thrombopoeitin agonists: eltrombopag or romiplostim
    • Immunosuppressive therapies: azathioprine, cyclosporin A, cyclophosphomide, danazol, dapsone, mycofenolate mofetil, vina alkaloids
  • Third-line:
    • Almtuzumab, chemotherapy, stem cell transplant
  • For life-threatening bleed:
    • IVIG 1g/kg, repeated once more if platelets remain below 50 the next day
    • Pulse steroids: methylprednisolone 30mg/kg IV daily x2-3 days)
    • Tranexamic acid 1G IV q6h
    • Platelet transfusion
    • Emergency splenectomy
    • Last-ditch: recombinant factor VIIa 90mcg/kg IV q2h
      • High risk for clotting