Thrombocytopenia resident survival guide: Difference between revisions
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*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
- Bone marrow suppression (for example chemotherapy, irradiation)
- Chronic alcohol use
- Chronic liver disease[1]
- Congenital thrombocytopenia
- Disseminated intravascular coagulation[1]
- Drug-induced thrombocytopenia (DITP)[1]
- Gestational thrombocytopenia[2]
- HELLP syndrome
- Hemolytic uremic syndrome
- Heparin-induced thrombocytopenia
- Immune thrombocytopenic purpura[3]
- Infections[1]
- Preeclampsia
- Pseudothrombocytopenia
- Thrombotic thrombocytopenic purpura[4]
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) | 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
- ↑ 1.0 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.
- ↑ 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.
- ↑ 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.
- ↑ 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.
- ↑ 5.0 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.