Thrombocytopenia resident survival guide: Difference between revisions

Jump to navigation Jump to search
No edit summary
No edit summary
Line 75: Line 75:
*Bone marrow biopsy should be done for patients that are older than 60 years of age to rule out myelodysplastic syndrome or lymphoproliferative disorders.
*Bone marrow biopsy should be done for patients that are older than 60 years of age to rule out myelodysplastic syndrome or lymphoproliferative disorders.
*Treatment should be considered for patients with platelet counts less than 30,000 per microliter.
*Treatment should be considered for patients with platelet counts less than 30,000 per microliter.


==Dont's==
==Dont's==

Revision as of 18:45, 17 January 2014

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ogheneochuko Ajari, MB.BS, MS [2]

Introduction

Thrombocytopenia refers to relatively few platelets in blood. A normal platelet count ranges from 150,000 to 450,000 per microliter of blood, determined by the 2.5th lower percentile of the normal platelet count distribution.

Causes

Life Threatening Causes

Life-threatening causes include conditions which may result in death or permanent disability within 24 hours if left untreated.

Common Causes

Management

Shown below are algorithms summarizing the approach to thrombocytopenia.

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Characterize the symptoms:
❑ Easy bruising
❑Petechiae
❑ Rashes
❑ Melena
Fevers
Bleeding
Headaches
Abdominal pain
❑ Visual disturbances
Weight loss
❑ Night sweats
❑ Bone pain
History/Epidemiological factors:
❑ Recent medications
❑ Pregnancy
❑ Family history
❑ Medical history
❑ Recent vaccinations
❑ Recent travels
❑ Recent transfusions
❑ Chronic alcohol use
❑ Recent hospitalization
❑ Recent organ transplantation
❑ Recent valve replacement surgery
❑ Dietary habits
❑ Sexual history
❑ Ingestion of quinine containing beverages
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Examine the patient:
❑ Bleeding location
❑ Assess bleeding severity
Hepatomegaly
Splenomegaly
❑ Mucocutaneous bleeding
❑ Skeletal abnormalities
❑ Joint or soft tissue bleeding
Rash
❑ Generalized lymphadenopathy
❑ Ischemic limb/Skin necrosis
❑ Neurologic
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Order tests
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Peripheral blood smear
CBC
Reticulocyte count
LDH
LFT
❑ Renal function test
Blood group (Rh)
 
 
Viral screening
HIV
HCV
HBV
 
 
Clotting screen:
PT
aPTT
Fibrinogen
Haptoglobin
D-dimer
FDP
 
 
Bone marrow examination:
Bone marrow aspiration
Bone marrow biopsy
 
Other Investigations:
H. pylori
❑ Abdominal ultrasound scan
Chest X-ray
Flow cytometry
Antiphospholipid antibody
ANA
ELISA
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Any abnormality, suspect
DIC
TTP/HUS
 
 
Bone marrow disorder
 
 
 
 
 
 
 
 
 
 
 
 



Algorithm for Diagnosis of Thrombocytopenia based on the Peripheral Blood Smear

 
 
 
 
 
 
 
 
 
 
 
 
Thrombocytopenia
Platelet count <150,000 per microliter
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Platelet clumping
 
Examine peripheral blood smear
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Pseudothrombocytopenia
 
True thrombocytopenia
 
Giant platelets
±WBC inclusions
 
Congenital/Hereditary thrombocytopenia
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Schistocytes
 
Spherocytes
 
Dacrocytes
 
Hypersegmented neurophils
Macrocytosis
 
Neutrophilia
Lymphocytosis
Leukopenia
Toxic granulations
 
Blasts
 
Isolated thrombocytopenia
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
DIC
TTP/HUS
 
Evans syndrome
Hypersplenism
 
Myelofibrosis
 
Vit. B12 deficiency
Folate deficiency
 
Infections
 
Bone marrow disorders
 
ITP
DITP
HIV, HCV
H. pylori
HIT
DIC
Gestational thrombocytopenia
 
 
 
 
 

Algorithm based on the 2012 American Society of Hematology Evidence-Based Approaches to Cytopenias.[5]


Treatment of Thrombocytopenia

The treatment of thrombocytopenia depends on or is determined by the underlying cause of thrombocytopenia.

Do's

  • Bone marrow biopsy should be done for patients that are older than 60 years of age to rule out myelodysplastic syndrome or lymphoproliferative disorders.
  • Treatment should be considered for patients with platelet counts less than 30,000 per microliter.

Dont's

  • Do not initiate cancer chemotherapy or antiviral therapy in the presence of thrombocytopenia.[5]
  • Do not start treatment for platelet counts greater than 50,000 per microliter unless actively bleeding.
  • Don't give warfarin (coumadin) monotherapy to an acutely bleeding patient because it may induce thrombosis.

References

  1. 1.0 1.1 1.2 1.3 Greenberg EM, Kaled ES (2013). "Thrombocytopenia". Crit Care Nurs Clin North Am. 25 (4): 427–34, v. doi:10.1016/j.ccell.2013.08.003. PMID 24267279.
  2. Nisha S, Amita D, Uma S, Tripathi AK, Pushplata S (2012). "Prevalence and characterization of thrombocytopenia in pregnancy in Indian women". Indian J Hematol Blood Transfus. 28 (2): 77–81. doi:10.1007/s12288-011-0107-x. PMC 3332269. PMID 23730013.
  3. Farid J, Gul N, Qureshi WU, Idris M (2012). "Clinical presentations in immune thrombocytopenic purpura". J Ayub Med Coll Abbottabad. 24 (2): 39–40. PMID 24397048.
  4. Abdel Karim N, Haider S, Siegrist C, Ahmad N, Zarzour A, Ying J; et al. (2013). "Approach to management of thrombotic thrombocytopenic purpura at university of cincinnati". Adv Hematol. 2013: 195746. doi:10.1155/2013/195746. PMC 3876823. PMID 24396345.
  5. 5.0 5.1 Stasi R (2012). "How to approach thrombocytopenia". Hematology Am Soc Hematol Educ Program. 2012: 191–7. doi:10.1182/asheducation-2012.1.191. PMID 23233580.

Template:WH Template:WS