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Heparin Induced Thrombocytopenia
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Heparin Induced Thrombocytopenia
, Heparin-Induced Thrombocytopenia
See Also
Low Molecular Weight Heparin
Heparin
Epidemiology
Incidence
: 1 to 3% of those on
Heparin
>4 days
LMWH
is much less likely (only 1/6 of
Heparin
risk)
Pathophysiology
Immune mediated disorder
IgG
Antibody
against
Heparin
-
Platelet
factor 4 (PF4) complex
Onset 4-10 days after
Heparin
exposure
Onset earlier with prior
Heparin
exposure
Two types
Type I is mild, and just requires monitoring
Type II is severe, life-threatening
Risk Factors
Heparin
type
Bovine is higher risk than porcine is higher risk than
Low Molecular Weight Heparin
Patient type
Surgical patients are more likely than medical patients to have HIT
Orthopedic surgery is most likely to have
Clinically Significant
HIT
Cardiovascular surgery is most likely to form heparin
Antibody
But typically do not manifest HIT clinically
Medical patients are moderately likely to have HIT
Obstetrics patients are very low risk for developing HIT
Signs
Onset typically 5-10 days after initial
Heparin
exposure (range is 4-14 days)
May present in first 24 hours if prior
Heparin
exposure (within last 90 days)
Often presents as a new thrombotic event while on
Heparin
therapy
Thrombosis (skin necrosis, extremity gangrene, CVA) occurs in up to one third of HIT patients
Type II HIT is a clinically devastating event
Associated with DIC-type findings
Bleeding is uncommon despite
Thrombocytopenia
Signs
Presentations
Deep Vein Thrombosis
(50%)
Pulmonary Embolism
(25%)
Skin lesions at injection site (10–20%)
Acute Limb Ischemia
(5–10%)
Warfarin
-associated venous limb gangrene (5–10%)
Acute thrombotic stroke or
Myocardial Infarction
(3–5%)
Acute systemic reactions following intravenous bolus (25%)
Diagnosis
Identify
Thrombocytopenia
Absolute
Thrombocytopenia
or
Relative
Thrombocytopenia
(30-50%
Platelet Count
decrease from baseline)
Consider other
Thrombocytopenia Causes
See
Thrombocytopenia Causes
Evaluate
Pre-Test Probability
See
Heparin Induced Thrombocytopenia Pre-Test Scoring System
Low probability for HIT
Do not obtain Hep-PF4
Antibody
ELISA
Consider alternative causes of
Thrombocytopenia
Moderate probability for HIT
Treat if Hep-PF4
Antibody
ELISA
positive and
Platelet
SRA positive
Consider other causes of
Thrombocytopenia
if testing negative
High probability for HIT
Treat if Hep-PF4
Antibody
ELISA
Positive
Consider other causes of
Thrombocytopenia
if testing negative
Labs
Complete Blood Count
Platelet Count
decrease
Marked and sudden
Thrombocytopenia
following
Heparin
therapy initiation
Platelet Count
drops 30-50% from baseline
Median
Platelet
nadir is 50,000 (drops to 15,000 in only 5% of patients)
Labs
Diagnosis
HIT is a clinical diagnosis driving initial withdrawal of
Heparin
and testing should be considered confirmatory
Start with the Hep-PF4
Antibody
ELISA
and if positive, confirm with
Platelet
SRA
If Hep-PF4
Antibody
ELISA
is negative, or
Platelet
SRA on confirmation is negative, HIT is unlikely
May reintroduce
Heparin
on
Consultation
with hematology
Hep-PF4
Antibody
ELISA
First line test due to ready availability, speed of testing, and high sensitivity
Efficacy in diagnosis of HIT
High
Test Sensitivity
(>97%)
Low
Test Specificity
(74 to 86%)
False Positive Rate
:1% in
Dialysis
patients
False Positive Rate
: 20% following vascular surgery
Incidence
of positive
Antibody
in patients on
Heparin
(UFH) with
Thrombocytopenia
Orthopedic surgery patient: 14% positive
Antibody
(with 3-5% with clinical HIT)
Cardiac surgery patient: 25-50% positive
Antibody
(with 1-2% with clinical HIT)
Gene
ral medicine patient: 8-20% positive
Antibody
(with 0.8-3% with clinical HIT)
References
Arepally (2006) N Engl J Med 355: 809-17 [PubMed]
Serotonin
release assay (
Platelet
SRA)
High
Test Sensitivity
and
Test Specificity
Slow and difficult test with limited testing locations
Second-line test
Used as a confirmatory test
Imaging
Venous
Doppler Ultrasound
Evaluate for asymptomatic DVT in legs (and arms if upper extremity central venous catheter) in all HIT patients
Management
Intermediate to High Probability for HIT
Stop all
Heparin
forms (including
Low Molecular Weight Heparin
and line flushes)
Consult hematology
Screen for
Deep Vein Thrombosis
with all four limbs
Start non-heparin
Anticoagulant
(consult with hematology regarding choice of agent)
Agents confer risk - do not use if low index of suspicion
Direct Thrombin Inhibitor
(
Lepirudin
,
Argatroban
or
Bivalirudin
) OR
Fondaparinux
(
Arixtra
) OR
Factor Xa Inhibitor
(
Apixaban
,
Rivaroxaban
)
Continue
Anticoagulation
for at least 4 weeks to 3 months (up to 3 to 6 months if HIT induced thrombosis)
Do not transfuse
Platelet
s unless bleeding (bleeding is rare in HIT)
Transfused
Platelet
s can activate in HIT and result in thrombosis
Do not use
Warfarin
alone (prothrombotic)
If on
Warfarin
, at HIT diagnosis
Stop
Warfarin
and give
Vitamin K
Do not restart
Warfarin
until
Platelet Count
normalizes
Only start
Warfarin
after
Platelet Count
has recovered to >100,000 and preferably 150,000
When
Warfarin
started, do not exceed 5 mg daily dose initially
Overlap non-heparin
Anticoagulant
and
Coumadin
concurrent use
Use together for at least 5 days and
Platelet Count
should be constant and stable and
INR therapeutic for at least 2 days
Duration of
Warfarin
therapy
Thrombosis present: Set duration based on clot type, site and
Thrombophilia
risks
Thrombosis absent: Variable recommendations (1-6 months)
Prognosis
Life and limb threatening thrombotic events in 20-50% of untreated HIT
Thrombotic risk can persist for weeks after
Platelet Count
normalizes
References
Merrill and Gillen (2016) Crit Dec Emerg Med 30(3): 3-8
Reding (2009) UMN CME Internal Medicine Review, Minneapolis
Arepally (2006) N Engl J Med 355: 809-17 [PubMed]
Castelli (2007) Cardiovasc Hematol Disord Drug Targets 7(3):153-62 [PubMed]
Fabris (2000) Haematologica 85(1):72-81 [PubMed]
Shantsila (2009) Chest 135(6):1651-64 [PubMed]
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