Download - Disseminated Intravascular Coagulation
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Disseminated Intravascular Coagulation
D I CBy
Prof. Rifaat Al-Shimmy Al-azhar U2010 ِ
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Definition of DIC
A pathological condition associated with activation of both:
• Coagulation system and • Fibrinolytic one
It should be considered as a secondary phenomena of an underlying disease as.……………………………
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Common Obstetric ConditionsAssociated with:• Inadequate replacement of blood loss• Pre-eclampsia-Eclampsia….HELP syndrome• Ante partum hge (abruptio placenta and P.P.)• I U F D when prolonged more than 4 weeks• Blood transfusion when massive or incompatible• Septic abortion or massive tissue injury• Amniotic fluid embolism • Saline I U infusion
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Massive Transfusion
Is defined as the replacement of a patient's total blood volume in less than 24
hours, or as the acute administration of more than half the patient's estimated blood
volume per hour.
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DIC is commonly a DIC is commonly a consequence of delayed consequence of delayed
or inadequate or inadequate resuscitationresuscitation
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DIC: Is it Predictable?
• It can probably be predicted in all the previously mentioned high risk groups, except amniotic fluid embolism, as it is an unpredictable condition.
• However, in AFE, DIC it always occurs only after resuscitation from the primary shocked state.
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Is it Preventable ?
• It can be avoided in most cases by proper ‘in time’ resuscitation and management of the underlying disease in proper time, e.g. Pre-eclampsia
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Pathogenesis• The most accepted theory is the Cascade
theory in which there is activation of both Extrinsic and Intrinsic pathways leading to
activation of factor xa leading to formation of thrombin from prothrombin to form fibrin from fibrinogen
• With associated activation of fibrinolytic system as a protective mechanism.
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Path physiology, continued
Pregnancy is considered as a hypercoagulable state by:
• An increase in all coagulation factors except FXI/FXIII. Fibrinogen which increases to 400-650mg/dl in late pregnancy.
• The fibrinolytic system is depressed during normal pregnancy and labor but returns to normal one hour after delivery of the placenta.
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Path physiology, continued
Decrease in platelets count is a result of :
1. Consumption
2. Aggregation of platelets
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Path physiology, continued
• So DIC is a state of increase thrombin activity at first, followed by increased fibrinolytic activity, leading to…
• consumption of coagulation factor (source of old name consumptive coagulopathy) and the formation of FDP impairing homeostasis.
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Path physiology, continued
• Deposition of fibrin in organs and tissues may lead to ischemic tissue damage.
• The decreased number of platelets and elevated FDP increase the problem of homeostasis.
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Symptoms of DIC
It is variable according to the cause, the presentation of the primary cause with:
• Generalized or localized hemorrhage• Peticheae• Thromboembolc manifestation, organ failure as:
liver, lung, kidneys, brain and frank gangrene have been described.
• Chronic DIC, (that occurs with IUFD) may be asymptomatic.
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Diagnosis Although the definite diagnosis is only by histological
finding of fibrin deposits, there are many indirect tests as:
• Bedside clot retraction test• Skin puncture test, measure clotting time (fibrinogen)• D. Diamer (90%d) • Platelets count (90%)• FDP (90%)• Thrombin time (80%)• PTT and PT (60%)
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Bedside Clot Retraction Tes(CT)
• It simply tests the clotting time - a test of decreased fibrinogen
• 2 ml blood in test tube - no clot formed but if occurs it is prolonged, soft and not retracted after half an hour, leaving a clot volume more than serum volume.
(the clot doesn't retract)
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Skin Puncture Test (bleeding time)
• Prolonged skin puncture ooze is observed when the platelets count is less than 100,000/ul
• Continuous bleeding at puncture site occurs when pl count is less than 30,000 /ul
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Other laboratory tests
• Platelets count decreases in 90% of cases (count less than 100,000/dl)
• PT, which measures the time required by extrinsic pathway, elevated in 80% of DIC
• PPT which measure the time required by intrinsic pathway - not helpful.
• Thrombin time elevated in 80% of cases
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Other laboratory tests
• Fibrinogen level/ less than150mg. This is present in 70% of cases.
• Fibrin split product >40ug/dl, 90% of cases• D-Diamer - an antigen formed as a result of
plasmin digestion, elevated in 90%of cases.
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Treatment of DIC
• Essentially treat the underlying cause. In most cases prompt termination of pregnancy is required.
• Supportive therapy should be directed to the correction of shock, acidosis and tissue ischemia.
• Cardiopulmonary support including inotropic therapy, blood transfusion and assisted ventilation
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Guidelines by the Scottish Executive Committee of the RCOG
RESUSCITATEMONITOR / INVESTIGATESTOP THE BLEEDINGCOMMUNICATE
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Help….be ready expecting a catastrophe
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Call Help ……ALB…….
• Set up IV Infusion• O2 administration• Airway control end otracheal intubations maximal ventilation and oxygenation.
A= ANESTHESIA AND INTENSIVE CARE IN DUTY
L = lab group in dutyB= Blood bank in duty
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Treatment
• Careful monitoring of fluid balance
• Serial evaluation of coagulation parameters
• If sepsis is suspected, antibiotic is indicated with evacuation of the septic focus
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Inform blood bank that it is an emergency
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Obtain and send 2 blood samples:
1) To blood bank for grouping and cross matching
2) To lab to obtain baseline for Hb, Htc, PT, PTT, platelet count and fibrinogen levels
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GENERAL ROLE in Treatment of DIC
• Vaginal delivery if possible is preferable than Cesarean section
• Episiotomy should be avoided if possible
• Central invasive monitoring as pulmonary catheterization is contraindicated
• Failure of response after delivery suggest other cause of coagulopathy or persistent sepsis
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DIC Treatment• Treatment of hypovolemia should be applied
according to the guideline of National Institute of Health.
• Crystalloid first• Plenty blood transfusion• Treat hypothermia• Red cell transfusion, if bleeding. (anticipated) Wies et al2007
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Treatment of Coagulopathy
• FFP for a prolonged PT - The idea is to keep it 2 to 3
seconds from control, (it contains coagulation factors), each unit volume is 250ml
2-Cryoprecipitate
• For a fibrinogen level less than 100 mg/dL. it is a fresh frozen plasma concentrate, (each bag volume is 10ml), contains 100mg fibrinogen raising f by 10mg/dl.
1-Fresh Frozen PASMA
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Platelet Transfusion
• Transfuse platelets for platelet counts less than 20,000/mm3in active bleeding or less than 50,000 if c s is planned.
• The rate of pl transfusion is one unit to every 10 kg/body w.
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Treat Coagulopathy
• Parental vitamin k and folic acid as pt of DICare deficient in these vitamins
• There is much data not in favor of use of the antifibrinolytic drugs
• In DIC 10 UNITES OF CRYOPPT, FOE 2/3 UNITE OF FF PLASMA SHOUID BE READY
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Role of Heparin in low dose
• Although there is a controversy in regards to giving a low dose of LMWH, its idea is to stop the consumption of coagulation factors, however its role is established in case of chronic DIC, (as in case IUFD of single twin for example or any case of IUFD before termination with follow up with fibrinogen level)
• Full dose if thrombosis is definitely diagnosed
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PREPARE
AT LEAST:
• 10 units of cryoprecipitate• 4 units of fresh frozen plasma• 10 units of platelet concentrate• Blood and packed RBC’s
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Whole Whole bloodblood
Blood componentsBlood components Plasma fractionsPlasma fractions
-FreshFresh-oldold
Packed Packed red cellsred cells
plateletsplatelets Fresh Fresh Frozrn Frozrn PlasmaPlasma
CryoprecCryoprecipitateipitate
DIVCMassive
haemorrhage
Major liver trauma
Bleeding associated with liver
disease
-Washed -Washed RBC’sRBC’sPts with allergic reactions to plasma proteins
-Leuko--Leuko-poor poor RBC’sRBC’sPts with febrile, non-hemolytic reactions to plasma WBC’s
when platelet. count less than 50000/cmm or when massive blood loss or replacement has occurred
when PT & PTT are
higher than 1.5 times
control levels All clotting factors; no plateletsCan supplement RBC’s when whole blood not available for exchange transfusion
when fibrinogen
level is less than
80-100mg/dl
Initially a tx for VW Dz, HemophiliaNow a source of fibrinogen in obstetric emergencies
–Clotting factor Clotting factor concentratesconcentrates–Immunoglobulin Immunoglobulin preparationspreparations–Saline albumin Saline albumin solutionsolution–Salt-poor albuminSalt-poor albumin
Platelet concentrates (1 pack/10kg) dose : 6units RDP or 1 unit SDP
normal dose: 12 - 15ml/ kg (4-5packs)
dose: 1- 1.5 -2 packs/ 10 kg
(8-10 packs)
Clotting disorders Haemophilia
Liver disease
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Prognosis
• Most cases of obstetric DIC will improve with delivery of the fetus or evacuation of the uterus
• This improved prognosis seems to be related to the recent advance in critical care
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Conclusion
• DIC is a secondary phenomena, therefore it is mostly predictable
• It occurs in an acute or chronic form, therefore it can be anticipated in the later form.
• The commonest cause is inadequate resuscitation, therefore it is preventable by early intervention.
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Take Home Message
DIC can be predicted and even prevented in most of the cases.
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Thank you