hit cdh
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Heparin Induced Thrombocytopenia
Dr. Imad Hassan El-SadekKuwaiti Board of Anesthesia (PGY3)
March 21st, 2012
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Outline
• Definition &Types• Incidence• Pathophysiology• Diagnosis• Treatment• HIT in CABG patients• Protocol
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Definition
• HIT is an antibody-mediated adverse drug reaction to heparin that can lead to devastating thromboembolic complications
Types Type 1 Type 2
Nature Non immune Immune-mediated
Onset 1-4 5-10
Incidence 10-20% 0.2-5%.
Pathophysiology Heparin-induced platelet aggregation
Platelet Count nadir 100,000 30,000-60,000
Manifestation Asymptomatic Thrombosis (30-80%): venous-arterial (3– 4:1)
Management Strategy Observation; improves while on heparin
Heparin alternatives
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HOW DOES HIT HAPPEN?
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PathogenesisHeparin or Heparin/PF4 complex: trigger an antibody response (IgG, IgM, and IgA).
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WHO WOULD GET HIT?
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Risk factors for developing HITRisk Factor Risk
Prolonged Heparin use
UFH > LMWH (2.6% with UFH and 0.2% with LMWH) RR 5.3; 95% CI 2.8-9.9
Surgical > medical patients RR 3.2; 95% CI 2.0-5.4
Female > male patients RR 2.4; 95% CI 1.4-4.1
The highest risk for HIT was seen in female surgical patients receiving UFH
RR 17; 95% CI 4.2-72
Prior Exposure to Heparin (UFH or LMWH) 1.7 vs 0.3%,OR 4.9; 95% CI 1.5-16
Cardiac and Orthopedic Surgery have a higher risk of HIT (1%-5%) than medical or obstetric patients (0.1%-1%)
• Warkentin TE, Sheppard JA, Sigouin CS, et al. Gender imbalance and risk factor interactions in heparin-induced thrombocytopenia. Blood 2006; 108:2937.• Warkentin TE, Sheppard JA, Horsewood P, et al. Impact of the patient population on the risk for heparin-induced thrombocytopenia. Blood 2000; 96:1703.• Prandoni P, Siragusa S, Girolami B, et al. The incidence of heparin-induced thrombocytopenia in medical patients treated with low-molecular-weight heparin: a
prospective cohort study. Blood 2005; 106:3049.
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Cardiac and Orthopedic Population
Patient population
Days of treatment
Frequency of HIT antibodies Frequency of clinical HIT
Activation assay
Antigen assay
Cardiac, UFH 5.1 ± 2.2 (SD) 20.0 % 50.0 % 1.0 %
Orthopedic, UFH
9.2 ± 2.2 9.3 % 14.1 % 4.9 %
Orthopedic, LMWH
9.5 ± 3.0 3.2 % 7.5 % 0.9 %
Warkentin TE, Sheppard JA, Horsewood P, et al. Impact of the patient population on the risk for heparin-induced thrombocytopenia. Blood 2000; 96:1703.
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Iceberg Model of HIT
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HOW DOES HIT PRESENT
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Diagnosis of HIT
HIT is a clinico-pathologic syndrome
• Onset Variations– Typical-onset HIT: 5-10 days
– Rapid-onset HIT: within 24 hrs
– Delayed-onset HIT: as long as 3 weeks after cessation of heparin
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Diagnosis of HIT
Gruel Y, Pouplard C. Post-operative platelet count profile: the most reliable tool for identifying patients with true heparin-induced thrombocypenia after cardiac surgery. J Thromb Haemost 2010; 8:27.
90% to 95%<150,000 or 30-50% fall
Thrombocytopenia
• Rarely severe, platelet counts typically >20,000/µL; median platelet count nadir of about 60,000/µL
• Cardiac Surgical Patients: “a secondary fall in the platelet count ≥50 percent that begins between the 5th-10th postop day appears to be highly predictive of HIT”
30-80%Thrombosis
• venous-arterial (3-4:1)• Manifestations: DVT, PE, distal ischemic necrosis following DVT, cerebral sinus thrombosis,
adrenal hemorrhage secondary to adrenal vein thrombosis, and transient global amnesia.• Necrotic skin lesions at heparin injection sites.
Within 30min of exposureAcute Systemic
Reactions• fever/chills, tachycardia, hypertension, dyspnea, cardiopulmonary arrest occurring after IV
heparin bolus administration.
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Differential Diagnosis
DIC ITP TTP-HUS
Drug-induced Thrombocytopenia SLE
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4T’s for Diagnosis of HIT
6-8Very likely
4-5Possible
0-3Unlikely
Pretest Probability
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Laboratory Diagnosis of HIT
ELISA
particle gel immunoassay
Antigen Assays
SRAserotonin release assay
HIPAHeparin-induced platelet activation
Functional Assays
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MANAGEMENT OF HIT
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BivalirudinDesirudin
Fondaparinux
argatroban
Danaparoid
Management of HITTACCP 2012 Recommendations
1. Stop Heparin2. Treatment With Nonheparin Anticoagulants
Recommendation LoE
In patients with HIT/HITT, we recommend the use of nonheparin anticoagulants, in particular lepirudin, argatroban, and danaparoid, over the further use of heparin or LMWH or initiation/continuation of VKA
1C
No prospective head-to-head trials comparing one agent with another
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Characteristics of Anticoagulants Used to Treat Patients with HIT
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Management of Clinically suspected HITPharmacological Treatment
• Two DTIs are available in the United States:Lepirudin Argatroban
Caution Prolonged in Renal Failure Prolonged in liver dysfunction (decrease by 75%)
Initial Dose: IVI: 0.10 mg/kg/h Recommended: 2mcg/kg/minACCP: 0.5-1.2 mcg/kg/min
Dose adjustment aPTT: 1.5-2.0 x baseline aPTT: 1.5-3 x baseline
Effect on INR Minimal Substantial
Adverse Effects Anaphylaxis (1st: 0.015%; re-exposure:0.16%)
According to systematic review (2004): • Lepirudin results in RRR of clinical outcome (death, amputation, etc.) to be 0.52 and 0.42
when compared to patient controls. • Argatroban showed a RRR of the above clinical outcomes to be 0.20 and 0.18.[8]
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Dosing of Heparin Alternatives
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Management of HITTACCP 2012 Recommendations
• Treatment With Nonheparin AnticoagulantsRecommendation LoE
In patients with HIT/ HITT who have normal renal function, we suggest the use of argatroban or lepirudin or danaparoid over other nonheparin anticoagulants
2C
In patients with HIT/HITT and renal insufficiency, we suggest the use of argatroban over other nonheparin anticoagulants
2C
LoE
In patients with HIT and severe thrombocytopenia, we suggest giving platelet transfusions only if bleeding or during the performance of an invasive procedure with a high risk of bleeding.
2C
2. Platelet Transfusions
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Management of Clinically suspected HITPharmacological Treatment
For how long?• HIT– Therapeutic anticoagulation: Until platelet count
recovers to stable plateau.– Prophylactic anticoagulation: for up to 4 weeks
• Risk of thrombosis for 2-4 weeks after initiation of Rx.
• HITT– Transition to warfarin after platelet count > 150– Overlap warfarin with DTI for >= 5 days, with >= 48 hrs
INR >2
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SUSPECTED HIT MANAGEMENT PROTOCOL
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Confirm HIT
• 4T’s: - Low: May continue Heparin, consider alternative diagnosis• - Intermediate: immunoassay, if positive Send functional assay• - High: Stop Heparin and initiate alternative
Stop
Heparin
• Stop all heparin or LMWH, including flushes or locks• Label all IV sites or catheters as “NO HEPARIN”
Rule-out Thrombu
s
• Order bilateral lower extremity ultrasound for DVT
Heparin alternative
• HIT/HITT: lepirudin, argatroban, and danaparoid• Renal impairment: Argatroban; RRT: argatroban or danaparoid• Pregnant: danaparoid. lepirudin or fondaparinux only if danaparoid is not available
Overlap warfarin
• Initiate late (Plt >150,000) and low( Max 5mg/d)• Overlap with nonheparin anticoagulant for >=5days and Target INR reached• If already on warfarin when HIT Reverse with Vitamin K
Avoid
Platelet
s
• Usually no bleeding• Can result in acute thrombosis
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MANAGEMENT OF HIT IN PATIENTS UNDERGOING CARDIAC SURGERY
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Factors Influencing HIT Management Options in Cardiac Surgery Patients
Disease Activity• Acute, Subacute, history of HIT
Patient’s Co-morbidities• Renal Impairment, liver impairment
Drug Availability• UFH, Heparin Alternatives, Plasmapheresis
Surgical Urgency• Postponement vs. Proceeding
Drug Monitoring• ACT, aPTT, ECT
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Management of HITin Patients Undergoing Cardiac Surgery
Cardiac Surgery
Acute or Subacute HIT
Urgent
Bivalirudinover other nonheparin
anticoagulants and over heparin plus antiplatelet agents
Non-Urgent
Delaying the surgery until HIT has resolved and HIT antibodies are negative
History of HIT
Ab Negative
Short-term Heparin
Ab Positive
Non Heparin anticoagulant
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Management of HITin Patients Undergoing Cardiac Surgery
Recommendation LoE
Acute
HIT
In patients with acute HIT (thrombocytopenic, HIT antibody positive) or subacute HIT (platelets recovered, but still HIT antibody positive) who require urgent cardiac surgery, we suggest the use of bivalirudin over other nonheparin anticoagulants and over heparin plus antiplatelet agents
2C
In patients with acute HIT who require nonurgent cardiac surgery, we recommend delaying the surgery (if possible) until HIT has resolved and HIT antibodies are negative
2C
History of HIT
In patients with a history of HIT in whom heparin antibodies have been shown to be absent who require cardiac surgery, we suggest the use of heparin (short-term use only) over nonheparin anticoagulants
2C
In patients with a history of HIT in whom heparin antibodies are still present who require cardiac surgery, we suggest the use of nonheparin anticoagulants over heparin or LMWH
2C
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Possible Treatment Options for HIT patients Undergoing CBP
Heparin Based• Non-urgent: Postpone• Semi-Urgent: Brief intra-op UFH• Urgent: UFH with intra-op Plasmapheresis
Heparin with Antiplatelets• Heparin + Iloprost
• Drawback: severe hypotension• Hepain + Tirofebam (Glycoprotein IIb-IIIa antagonist)
• In renal imapirment patients (2001)
Hepain Alternatives• DTI: Lepirudin, Argatroban• Danaparoid• Defibrinogenating Agent (ancorod)
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Heparin Based Treatment1. Non-Urgent CPB: Postponement
• Rationale:– A secondary immune response after reexposure to
heparin should not occur until at least three days after exposure.
– Thus, a brief exposure to heparin during CPB should not immediately elicit HIT antibodies.
– Furthermore, since the heparin would be rapidly cleared after the procedure, even if antibodies appeared, they would not be thrombogenic in the absence of heparin.
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Thank You