Bleeding Disorders

Morey A. Blinder, M.D.

Associate Professor of Medicine
and Pathology & Immunology
 Objectives

 Coagulation factor disorders and treatment

 Disorders of platelets and platelet transfusion
 Adjunctive drug therapy for bleeding
Coagulation factor disorders
requiring blood products
 Coagulation factor disorders

 Inherited bleeding disorders  Acquired bleeding disorders

• Hemophilia A and B • Liver disease

• vonWillebrands disease • Vitamin K deficiency/warfarin
• Other factor deficiencies overdose
• DIC
Ecchymoses

(typical of
coagulation factor
disorders)
 Hemophilia A and B
Hemophilia A Hemophilia B

Coagulation factor deficiency Factor VIII Factor IX

Inheritance X-linked X-linked

recessive recessive

Incidence 1/10,000 males 1/50,000 males

Severity Related to factor level

<1% - Severe - spontaneous bleeding
1-5% - Moderate - bleeding with mild injury
5-25% - Mild - bleeding with surgery or trauma

Complications Soft tissue bleeding

Hemophilia
Clinical manifestations (hemophilia A & B
indistinguishable)
Hemarthrosis (most common)
Fixed joints
Soft tissue hematomas (e.g., muscle)
Muscle atrophy
Shortened tendons
Other sites of bleeding
Urinary tract
CNS, neck (may be life-threatening)
Prolonged bleeding after surgery or dental extractions
Treatment of hemophilia A

 Intermediate purity plasma products

• Virucidally treated
• May contain von Willebrand factor

 High purity (monoclonal) plasma products

• Virucidally treated
• No functional von Willebrand factor

 Recombinant factor VIII

• Virus free/No apparent risk
• No functional von Willebrand factor
Factor VIII Infusion
Dosing guidelines for hemophilia A
 Mild bleeding
• Target: 30% dosing q8-12h; 1-2 days (15U/kg)
• Hemarthrosis, oropharyngeal or dental, epistaxis, hematuria

 Major bleeding
• Target: 80-100% q8-12h; 7-14 days (50U/kg)
• CNS trauma, hemorrhage, lumbar puncture
• Surgery
• Retroperitoneal hemorrhage
• GI bleeding

 Adjunctive therapy
•  amino caproic acid (Amicar) or DDAVP (for mild disease only)
Complications of therapy

 Formation of inhibitors (antibodies)

• 10-15% of severe hemophilia A patients
• 1-2% of severe hemophilia B patients
 Viral infections
• Hepatitis B Human parvovirus
• Hepatitis C Hepatitis A
• HIV Other
Treatment of hemophilia B
 Agent
• High purity factor IX
• Recombinant human factor IX

 Dose
• Initial dose: 100U/kg
• Subsequent: 50 U/kg every 24 hours
 von Willebrand Disease
Clinical features
 von Willebrand factor Carrier of factor VIII
Anchors platelets to subendothelium
Bridge between platelets

 Inheritance Autosomal dominant

 Incidence 1/10,000

 Clinical features Mucocutaneous bleeding

Laboratory evaluation of
von Willebrand disease
Classification
• Type 1 Partial quantitative deficiency
• Type 2 Qualitative deficiency
• Type 3 Total quantitative deficiency
 Diagnostic tests:
vonWillebrand type
Assay 1 2 3

vWF antigen  Normal 

vWF activity   
Multimer analysis Normal Normal Absent
Treatment of von Willebrand disease
Varies by Classification
 Cryoprecipitate
• Source of fibrinogen, factor VIII and VWF
• Only plasma fraction that consistently contains VWF multimers
• Correction of bleeding time is variable

 DDAVP (Deamino-8-arginine vasopressin)

• Increases plasma VWF levels by stimulating secretion from endothelium
• Duration of response is variable
• Used for type 1 disease
• Dosage 0.3 µg/kg q 12 hr IV

 Factor VIII concentrate (Humate-P)

• Virally inactivated product
• Used for type 2 and 3
 Vitamin K deficiency
 Source of vitamin K Green vegetables
Synthesized by intestinal flora
 Required for synthesis Factors II, VII, IX ,X
Protein C and S
 Causes of deficiency Malnutrition
Biliary obstruction
Malabsorption
Antibiotic therapy
 Treatment Vitamin K
Fresh frozen plasma
Vitamin K deficiency due to warfarin overdose
Managing high INR values

Clinical situation Guidelines

INR therapeutic-5 Lower or omit next dose;

Resume therapy when INR is therapeutic

INR 5-9; no bleeding Lower or omit next dose;

Resume therapy when INR is therapeutic
Omit dose and give vitamin K (1-2.5mg po)
Rapid reversal: vitamin K 2-4 mg po (repeat)

INR >9; no bleeding Omit dose; vitamin K 3-5 mg po; repeat as necessary
Resume therapy at lower dose when INR therapeutic

Chest 2001:119;22-38s (supplement)

Vitamin K deficiency due to warfarin overdose
Managing high INR values in bleeding patients

Clinical situation Guidelines

INR > 20; serious bleeding Omit warfarin

Any life-threatening bleeding Vitamin K 10 mg slow IV infusion
FFP ± factor rhVIIa (depending on urgency)
Repeat vitamin K injections every 12 hrs as needed
Disseminated Intravascular Coagulation (DIC)
Mechanism
Systemic activation
of coagulation

Intravascular Depletion of platelets

deposition of fibrin and coagulation factors

Thrombosis of small Bleeding

and midsize vessels
with organ failure
Common clinical conditions
associated with DIC
 Sepsis  Vascular disorders

 Trauma  Reaction to toxin (e.g. snake

• Head injury
venom, drugs)
• Fat embolism  Immunologic disorders
• Severe allergic reaction
 Malignancy • Transplant rejection

 Obstetrical complications
• Amniotic fluid embolism
• Abruptio placentae
DIC
Treatment approaches
 Treatment of underlying disorder
 Anticoagulation with heparin
 Platelet transfusion
 Fresh frozen plasma
Liver Disease

Decreased synthesis of II, VII, IX, X, XI, and fibrinogen

Prolongation of PT, aPTT and Thrombin Time

Often complicated by
Gastritis, esophageal varices, DIC

Treatment
Fresh-frozen plasma infusion (immediate but temporary effect)
Vitamin K (usually ineffective)
Coagulation cascade
Intrinsic system (surface contact) Extrinsic system (tissue damage)

XII XIIa Tissue factor

XI XIa

IX IXa VIIa VII

VIII VIIIa

X Xa
V Va

II IIa (Thrombin)
Fibrinogen Fibrin

Vitamin K dependant factors

Laboratory Evaluation of the Coagulation
Pathways
Partial thromboplastin time Prothrombin time
(PTT) (PT)
Surface activating agent Thromboplastin
(Ellagic acid, kaolin) Tissue factor
Phospholipid Phospholipid
Calcium Calcium

Intrinsic pathway Extrinsic pathway

Thrombin time Common pathway

Thrombin

Fibrin clot
 Pre-analytic errors

 Problems with blue-top tube  Biological effects

• Partial fill tubes • Hct ≥55 or ≤15
• Vacuum leak and citrate evaporation • Lipemia, hyperbilirubinemia,
hemolysis
 Problems with phlebotomy
• Heparin contamination
 Laboratory errors
• Wrong label
• Slow fill
• Delay in testing
• Underfill • Prolonged incubation at 37°C
• Vigorous shaking • Freeze/thaw deterioration
Initial Evaluation of a Bleeding Patient - 1
Normal PT
Normal PTT

Abnormal
Urea Factor XIII
solubility deficiency

Normal

Consider evaluating for:

Mild factor deficiency Monoclonal gammopathy
Abnormal fibrinolysis Platelet disorder
(2 anti-plasmin def) Vascular disorder
Elevated FDPs
Initial Evaluation of a Bleeding Patient - 2
Normal PT
Abnormal PTT
50:50 mix is
Repeat abnormal
with Test for inhibitor activity:
50:50 Specific factors: VIII,IX, XI
mix Non-specific (anti-phospholipid Ab)

50:50 mix is normal

Test for factor deficiency:

Isolated deficiency in intrinsic pathway (factors VIII, IX, XI)
Multiple factor deficiencies (rare)
Initial Evaluation of a Bleeding Patient - 3
Abnormal PT
Normal PTT
50:50 mix is
Repeat abnormal
with Test for inhibitor activity:
50:50 Specific: Factor VII (rare)
mix Non-specific: Anti-phospholipid (rare)

50:50 mix is normal

Test for factor deficiency:

Isolated deficiency of factor VII (rare)
Multiple factor deficiencies (common)
(Liver disease, vitamin K deficiency, warfarin, DIC)
Initial Evaluation of a Bleeding Patient - 4

Abnormal PT
Abnormal PTT
50:50 mix is
Repeat abnormal
with Test for inhibitor activity:
50:50 Specific : Factors V, X, Prothrombin,
mix fibrinogen (rare)
Non-specific: anti-phospholipid (common)

50:50 mix is normal

Test for factor deficiency:

Isolated deficiency in common pathway: Factors V, X,
Prothrombin, Fibrinogen
Multiple factor deficiencies (common)
(Liver disease, vitamin K deficiency, warfarin, DIC)
Coagulation factor deficiencies
Summary

Sex-linked recessive
 Factors VIII and IX deficiencies cause bleeding
Prolonged PTT; PT normal

Autosomal recessive (rare)

 Factors II, V, VII, X, XI, fibrinogen deficiencies cause bleeding
Prolonged PT and/or PTT

 Factor XIII deficiency is associated with bleeding and

impaired wound healing
PT/ PTT normal; clot solubility abnormal

 Factor XII, prekallikrein, HMWK deficiencies

do not cause bleeding
Disorders of Platelets and Platelet
Transfusion
Sites of bleeding in thrombocytopenia
 Skin and mucous membranes
• Petechiae
• Ecchymosis
• Hemorrhagic vesicles
• Gingival bleeding and epistaxis
 Menorrhagia
 Gastrointestinal bleeding
 Intracranial bleeding
 Petechiae

Do not blanch with pressure

(cf. angiomas)
Not palpable
(cf. vasculitis)
Classification of platelet disorders

 Quantitative disorders  Qualitative disorders

• Abnormal distribution • Inherited disorders (rare)

• Dilution effect • Acquired disorders
• Decreased production – Medications
• Increased destruction – Chronic renal failure
– Cardiopulmonary bypass
 Acquired thrombocytopenia with
shortened platelet survival

 Associated with  Associated with

bleeding thrombosis

• Immune-mediated • Thrombotic
thrombocytopenia (ITP) thrombocytopenic purpura
• Most drug-induced • DIC
thrombocytopenias • Trousseau’s syndrome
• Most others • Heparin-associated
thrombocytopenia
Platelet function screen
 Replaces the bleeding time as a
test of platelet function
 PFA-100; ordered as “platelet
function screen”
 Blue top tube
 Measures the time it takes for
blood to block membrane coated
with either collagen/epinephrine
or collagen/ADP
Platelet function screen
Results

Epi ADP Interpretation

Normal Normal Normal platelet function
Abnormal Normal “Aspirin effect”
Abnormal Abnormal Abnormal platelet function
Valvular heart disease
Renal failure
Von Willebrand disease
 Platelet transfusions
 Source
• Platelet concentrate (Random donor)
Each donor unit should increase platelet count ~10,000 /µl
• Pheresis platelets (Single donor)

 Storage
• Up to 5 days at room temperature

 “Platelet trigger”
• Bone marrow suppressed patient (>10-20,000/µl)
• Bleeding/surgical patient (>50,000/µl)
Platelet transfusions - complications
 Transfusion reactions
• Higher incidence than in RBC transfusions
• Related to length of storage/leukocytes/RBC mismatch
• Bacterial contamination

 Platelet transfusion refractoriness

• Alloimmune destruction of platelets (HLA antigens)
• Non-immune refractoriness
– Microangiopathic hemolytic anemia
– Coagulopathy
– Splenic sequestration
– Fever and infection
– Medications (Amphotericin, vancomycin, ATG, Interferons)
 Laboratory Evaluation of Bleeding
Overview

CBC and smear Platelet count Thrombocytopenia

RBC and platelet morphology TTP, DIC, etc.

Coagulation Prothrombin time Extrinsic/common pathways

Partial thromboplastin time Intrinsic/common pathways
Coagulation factor assays Specific factor deficiencies
50:50 mix Inhibitors (e.g., antibodies)
Fibrinogen assay Decreased fibrinogen
Thrombin time Qualitative/quantitative
fibrinogen defects
FDPs or D-dimer Fibrinolysis (DIC)

Platelet function von Willebrand factor vWD

Bleeding time In vivo test (non-specific)
Platelet function analyzer (PFA) Qualitative platelet disorders
and vWD
Platelet function tests Qualitative platelet disorders
Adjunctive therapy for
bleeding disorders
Adjunctive drug therapy for bleeding

Fresh frozen plasma

Cryoprecipitate
Epsilon-amino-caproic acid (Amicar)
DDAVP
Recombinant human factor VIIa (Novoseven)
 Fresh frozen plasma

 Content - plasma (decreased factor V and VIII)

 Indications
• Multiple coagulation deficiencies (liver disease, trauma)
• DIC
• Warfarin reversal
• Coagulation deficiency (factor XI or VII)
 Dose (225 ml/unit)
• 10-15 ml/kg
 Note
• Viral screened product
• ABO compatible
Cryoprecipitate
 Prepared from FFP
 Content
• Factor VIII, von Willebrand factor, fibrinogen
 Indications
• Fibrinogen deficiency
• Uremia
• von Willebrand disease
 Dose (1 unit = 1 bag)
• 1-2 units/10 kg body weight
Aminocaproic acid (Amicar)
 Mechanism
• Prevent activation plaminogen -> plasmin

 Dose
• 50mg/kg po or IV q 4 hr

 Uses
• Primary menorrhagia
• Oral bleeding
• Bleeding in patients with thrombocytopenia
• Blood loss during cardiac surgery

 Side effects
• GI toxicity
• Thrombi formation
Desmopressin (DDAVP)
 Mechanism
• Increased release of VWF from endothelium

 Dose
• 0.3µg/kg IV q12 hrs
• 150mg intranasal q12hrs

 Uses
• Most patients with von Willebrand disease
• Mild hemophilia A

 Side effects
• Facial flushing and headache
• Water retention and hyponatremia
Recombinant human factor VIIa
(rhVIIa; Novoseven)
 Mechanism
• Activates coagulation system through extrinsic pathway

 Approved Use
• Factor VIII inhibitors in hemophiliacs

 Dose: (1.2 mg/vial)

• 90 µg/kg q 2 hr
• “Adjust as clinically indicated”

 Cost (70 kg person) @ $1/µg

• ~$5,000/dose or $60,000/day
Recombinant human factor VIIa
in non-approved settings
 Surgery or trauma with profuse bleeding
• Consider in patients with excessive bleeding without apparent
surgical source and no response to other components
• Dose: 50-100ug/kg for 1-2 doses
• Risk of thrombotic complications not well defined

 Anticoagulation therapy with bleeding

• 20ug/kg with FFP if life or limb at risk; repeat if needed for bleeding
Approach to bleeding:
Summary
 Identify and correct any specific defect of hemostasis
 Use non-transfusional drugs whenever possible
 RBC transfusion for surgical procedures or large
blood loss