1 coagulation disorderin pregnancy ch06 --dic
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7/25/2019 1 Coagulation Disorderin Pregnancy CH06 --DIC
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Coagulation Disorders
International
Coagulation Disorders
in Pregnancy
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Coagulation Disorders
International
Objectives
• Definition
• Causes
• Pathophysiology
• Clinical Features
• Diagnosis
• Management
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Coagulation Disorders
International
Definition
• Abnormal coagulation
– consumptive - disseminated intravascular coagulation (DI
- increased split products and fibrinolysis
– dilutional - secondary to massive volume replacement
- crystalloid or PRBC without clotting
factors
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Coagulation Disorders
International
Causes - Consumptive
• Abruptio placentae
• Pre-eclampsia/Eclampsia
• Sepsis - including septic abortion• Amniotic fluid embolus
• Intrauterine Fetal Demise
• Sickle Cell Crisis
• Trophoblastic Disease
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Coagulation Disorders
International
Causes - Dilutional
• Massive resuscitation due to hypovolemia
– post-partum hemorrhage
– placenta abruption
– placenta previa – uterine rupture
– ectopic pregnancy / incomplete abortion
– trauma
– non-pregnancy related bleeding
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Coagulation Disorders
International
Activation of Clotting System
• Thromboplastin release
– acute - abruption, AF embolus, uterine rupture
– sub-acute - intrauterine death, missed abortion
• Endothelial cell injury
– pre-eclampsia, sepsis
• Uterine Rupture
• Phospholipid release
– sepsis, transfusion reactions
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Coagulation Disorders
International TABLE – Couses and Pathophysiology of
Disseminated Intravascular Coagulation
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Coagulation Disorders
International
Clinical Features• signs and symptoms of underlying cause
• bleeding
– bruising, purpura, epistaxis, venipunctureoozing
– operative sites, PPH
• hypotension and hypoperfusion
• thrombotic complications are rare
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Coagulation Disorders
International
Diagnosis• recognize triggering conditions
• high index of suspicion
• Clot Test - simple bedside test – abnormal if no clot formed in 10 -12 minutes
– clot occupies 50% of blood sample volume
–clot withstands inversion of tube after 30
minutes
– no clot lysis within 1 hour
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Coagulation Disorders
International
Diagnosis
• decreased platelets
• prolonged INR and PTT may not be seen initially
• thrombin time usually prolonged
• fibrinogen level decreased
– normally increased to 4 - 8 mM in pregnancy
– levels < 2 mM may indicate coagulopathy
• increase in fibrin split products• evidence of RBC damage - blood smear
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Coagulation Disorders
International
Management - Principles
• rapidly developing and evolving condition
• lab results may not reflect current situation
• serious threat to life
• rapid and rational treatment essential
• multi-specialty approach
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Coagulation Disorders
International
Management - Initiating Cause
• rapid identification of underlying condition
• appropriate treatment of underlying condition
• removes cause and allows homeostatic
mechanisms to recover
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Coagulation Disorders
International
Management - Resuscitation• oxygen
• maintain organ perfusion
–
promotes clearance of anticoagulants – prevents ischemic injury - liver, kidney
– allows clotting factor synthesis
• rapid crystalloid infusion - saline, Ringer’s
• RBC replacement - situation specific
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Coagulation Disorders
International
Management - Procoagulant Replacement
• component replacement - situation specific
– Fresh whole blood
– Fresh Frozen Plasma
– Fresh Plasma
– Cryoprecipitate - infection risk
– Platelets
• management aided by hematologist
• anticoagulants not indicated
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Coagulation Disorders
International
Summary
• identify and treat underlying cause
• rapid resuscitation
• airway and oxygen
• volume replacement
• RBC replacement
• clotting factor replacement
• multi-specialty approach in severe cases
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Coagulation Disorders
International
Replacement of procoagulants
- Fresh frozen plasma replaces most clotting factors and has the least risk
of transmitting hepatitis.
1 unit after the initial 4-6 units of whole blood and thereafter 1 unit for
every 2 units of wholeblood required.
- Cryoprecipitates may be necessary if fibrinogen levels are low.
- Platelets can be transfused in severe cases of thrombocytopenia.
1 unit of platelets can raise the number of platelets to about
5000-10 000.
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Coagulation Disorders
International
Inhibition of the DIC and fibrinolysis
The use of heparin has been advocated as a method of blocking DIC. It is
especially recommended in cases of chronis DIC, as is the intrauterine
death syndrome. It is not recommended if the patient is bleeding
profusely.
Epsilon aminocaproic acid (EACA) inhibits the conversion of plasminogen
to plasmin and its use has been suggested as a means to counteract
secondary fibrinolysis. It is not recommended in these cases.
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Coagulation Disorders
Internationalanagement option
Quality of
evidence
Strength of recommendation
DIC/massive
hemorrhage
Interdisciplinary approach
Obstetrics/hematology)
IV C
Treat cause IV C
Resuscitation volume
replacement to maintain
tissue perfusion
IV C
Replace fresh frozen
plasma, cryoprecipitate and
platelets on basis of
laboratory results and
clinical condition
IV C
Consider heparin in severe
DIC due to amniotic fluid
embolism
IV C
Acquired inhibitors of
coagulation
Interdisciplinary approach
obstetrics/hematology)
IV C
Specific clotting factor
concentrates individualized
management)
IV
III
C
B
Immunosuppressive therapy IV
III
C
B
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Coagulation Disorders
International
Disseminated intravascular coagulation
Management option Quality of evidenceStrength of
recommendation
Involve hematologist and support
services (blood transfusion etc.) early- √
Treat/remove cause (e.g.empty uterus,antibiotics for sepsis) - √
Hematological priorities are to replace
blood constituents and coagulation
factors
III B
Heparin and antithrombolytic therapy
have both been used in DIC to break thecycle of consumptive coagulopathy.
Neither has been subjected to controlled
trials
IV C
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Coagulation Disorders
International
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