Disseminated intravascular coagulation (DIC) is a serious disorder occurring in response to an illness or disease process which results in dysregulated blood clotting.
In DIC there is an inappropriate activation of clotting and/or fibrinolytic system
Leads to tendency to both bleeding and thrombosis simultaneously
Causes:
Shock
Sepsis/severe infection - massive release of pro-inflammatory cytokines that activate the coagulation cascade
Major trauma or burns
Malignancies - acute promyelocytic leukaemia is strongly associated
Severe immune-mediated reactions - haemolytic transfusion reaction
Severe organ dysfunction - acute hepatic failure and severe acute pancreatitis
Pathophysiology:
Release of pro-inflammatory cytokines or pro-coagulant factors such as tissue factor
Intravascular activation of the coagulation cascade throughout the body
Microvascular thrombosis results due to the formation of fibrin webs and the activation and aggregation of platelets - multi organ failure due to tissue ischaemia
Concentration of available clotting factors falls - risk of bleeding
Platelets being used up - thrombocytopenia
DIC can be acute or chronic. Acute DIC is the most common subtype, with rapid-onset conditions such as trauma, sepsis and haemolytic transfusion reactions. Chronic DIC tends to occur with less rapid-onset conditions such as cancer.
History:
For a diagnosis of DIC to be made, there must be some objective evidence of a precipitating factor
Typical symptoms:
Bleeding from unusual sites - ears, node, GI tract, respiratory tract or sites of venepuncture/cannulation
Bleeding from three unrelated sites is highly suggestive of DIC
Widespread or unexpected bruising without a history of trauma
New confusion or disorientation - microvascular thrombosis affecting cerebral perfusion
Clinical exam findings:
Signs of haemorrhage: bleeding from cannula sites/venepuncture sites, melaena, haematemesis, rectal bleeding, epistaxis, haemoptysis, haematuria
Petechiae or purpura
Livedo reticularis - mottled lace like patterning of the skin
Purpura fulminans - widespread skin necrosis due to microvascular thrombosis leading to localised infarction
Localised infarction and gangrene e.g. of the fingers
Confusion
Signs of circulatory collapse - oliguria, hypotension and/or tachycardia
ISTH scoring system:
The international society of thrombosis and haemostasis
Make the diagnosis of DIC more objective
Platelet count
D-dimer
Prothrombin time
Fibrinogen levels
Lab investigations:
FBC - thrombocytopenia due to excessive platelet consumption
Coagulation screen - prolonged PT and/or APTT
Clauss fibrinogen - decreased as fibrinogen is converted to fibrin
D-dimer - raised, providing evidence of degradation of fibrin clots around the body
Other investigations depend on the underlying cause e.g. blood cultures in sepsis
Management:
Transfusion should be based on whether the patient is actively bleeding
Platelet transfusions should be considered if the patient is bleeding to maintain >50
In bleeding patients with a prolonged PT and/or APTT, fresh frozen plasma can be considered
Concentrated solutions of clotting factors such as prothrombin complex concentrate
If there is severely low fibrinogen then transfusions of cryoprecipitate should be considered
If thrombosis is a prominent feature - therapeutic doses of heparin
Complications:
Multi-organ failure
Life-threatening haemorrhage
Cardiac tamponade - bleeding into the pericardial space