Thrombocytopenia (Low Platelet Count) (cont.)
Siamak T. Nabili, MD, MPH
Dr. Nabili received his undergraduate degree from the University of California, San Diego (UCSD), majoring in chemistry and biochemistry. He then completed his graduate degree at the University of California, Los Angeles (UCLA). His graduate training included a specialized fellowship in public health where his research focused on environmental health and health-care delivery and management.
William C. Shiel Jr., MD, FACP, FACR
Dr. Shiel received a Bachelor of Science degree with honors from the University of Notre Dame. There he was involved in research in radiation biology and received the Huisking Scholarship. After graduating from St. Louis University School of Medicine, he completed his Internal Medicine residency and Rheumatology fellowship at the University of California, Irvine. He is board-certified in Internal Medicine and Rheumatology.
In this Article
- What is thrombocytopenia?
- What causes thrombocytopenia?
- What are the symptoms of thrombocytopenia?
- When should I seek medical care for thrombocytopenia?
- How is thrombocytopenia diagnosed?
- How is thrombocytopenia treated?
- What are the complications of thrombocytopenia?
- Can thrombocytopenia be prevented?
- Thrombocytopenia At A Glance
- Find a local Hematologist in your town
What causes thrombocytopenia?
Low platelet counts, thrombocytopenia, can be caused by a variety of reasons. In general, they can be divided into:
- decreased platelet production,
- increased platelet destruction or consumption, or
- increased splenic sequestration (capturing of circulating platelets in the spleen).
Some of the most common and important causes or thrombocytopenia are outlined below.
Decreased platelet production
Decreased platelet production is usually related to a bone marrow problem
(agranulocytosis). In most of these conditions,
red blood cell and white blood cell productions may also be affected.
- Viral infections affecting the marrow for example:
- parvovirus,
- rubella,
- mumps,
- varicella
(chickenpox),
- hepatitis C,
- Epstein-Barr virus,
and
- HIV.
- parvovirus,
- Aplastic anemia is a general term used when the bone
marrow fails to produce any blood cells (red cells, white cells, and platelets), also called
pancytopenia. This can
be caused by some viral infections (parvovirus or HIV), medications (gold,
chloramphenicol, Dilantin, valproate (Depacon), or
radiation, or rarely, it can be
congenital (Fanconi's anemia).
- Chemotherapy drugs frequently cause bone marrow suppression resulting in
thrombocytopenia.
- Some drugs other than chemotherapy can suppress platelet production, such
as thiazide diuretics.
- Cancers of the bone marrow and blood (leukemia) or
cancers of the lymph
nodes (lymphoma) can cause various degrees of thrombocytopenia.
- Cancers from other organs can sometimes infiltrate
(invade) the bone marrow
and result in impaired production of platelets.
- Long term alcohol can cause direct
toxicity of the bone marrow.
- Deficiency of vitamin B12 and
folic acid can result in low platelet
production by the bone marrow.
Increased platelet destruction or consumption
Increased platelet destruction or consumption can be
seen a number of medical conditions. They can be divided into immune related and non-immune related
causes.
Many medications can cause low platelet count by
causing immunologic reaction against platelets, called drug-induced
thrombocytopenia. Some examples may include:
- sulfonamide antibiotics,
- carbamazepine [(Tegretol, Tegretol XR , Equetro, Carbatrol) anti-seizure drug],
- digoxin (Lanoxin),
- quinine (Quinerva,
Quinite, QM-260),
- quinidine
(Quinaglute, Quinidex),
- acetaminophen
(Tylenol and others), and
- rifampin.
- carbamazepine [(Tegretol, Tegretol XR , Equetro, Carbatrol) anti-seizure drug],
- Heparin, a commonly used blood thinner, and similar medications [low
molecular weight heparin or
enoxaparin (Lovenox)] can occasionally induce an
immune response
against platelets resulting in rapid destruction of platelets. This condition is
termed heparin-induced thrombocytopenia or HIT.
- Idiopathic thrombocytopenic
purpura (ITP) is a condition where the immune system
attacks platelets. In severe conditions, ITP can result in very low platelet
counts. In adults, this is usually a chronic (long standing) condition,
whereas, in children, it can be caused acutely after a
viral infection. This
is usually a diagnosis of exclusion, meaning other more common causes need to be
ruled out.
-
Some rheumatologic condition, such as systemic lupus erythematosus (SLE) or other autoimmune conditions (connective tissue diseases), can cause platelet destruction.
- Transfusion of blood
products and organ transplantation can sometimes cause
immunologic disturbances resulting in thrombocytopenia.
- Thrombotic thrombocytopenic
purpura (TTP) and
hemolytic uremic syndrome (HUS) are similar conditions that can cause non-immune related
consumptive thrombocytopenia resulting from some viral illnesses,
pregnancy,
some metastatic cancers, or chemotherapy. Other manifestations of these
conditions include kidney insufficiency,
confusion,
anemia (hemolytic), and
fever.
HUS is largely seen in children and is generally thought of as an aftermath of
an infection with a certain strain of
Escherichia coli bacteria (E. coli
O157:H7) which causes infectious diarrhea.
- HELLP syndrome (hemolysis,
elevated
liver tests, low platelets) is another non-immune thrombocytopenia that may
occur during pregnancy and can include elevation of liver enzyme and anemia (specifically,
hemolytic anemia or
rupturing of red blood cells).
- Disseminated intravascular coagulopathy (DIC) is a rare but severe
condition that may be a complication of overwhelming infections, traumas,
burns,
or pregnancy.
- Injury to or inflammation of blood
vessels (vasculitis) and, sometimes,
artificial heart valves can cause increased destruction of platelets as they
pass by.
- Severe infections (sepsis) or trauma can sometimes cause consumptive
thrombocytopenia (without DIC).
Splenic sequestration
Splenic sequestration can also lead to low platelet counts as a result of
enlargement of the spleen for a variety of reasons. When the spleen enlarges, it
can retain (sequester) more than the usual amount of platelets. Common causes of
thrombocytopenia due to splenic enlargement may include advanced
liver disease (cirrhosis, for example, from chronic
hepatitis B or
C) and blood cancers
(leukemias or lymphomas).
- Dilutional thrombocytopenia can result from severe bleeding and transfusion
of several units transfused red blood cells in a short time.
- Pseudothrombocytopenia (false thrombocytopenia) is also
one of a commonly encountered condition where the number of platelets seen on a
complete blood count analysis (CBC) may falsely appear low because of the clumping of platelets
together. This can lead to a smaller number of platelets seen throughout the
slide reviewed by the technician. If this is suspected, the blood can be redrawn
in a tube with a material that prevents clumping of platelets for repeat
analysis.
- Thrombocytopenia can also be present at birth, called neonatal thrombocytopenia. Most of these cases can be caused by processes similar to above, although, they are occasionally related to rare genetic conditions.
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