Disseminated intravascular coagulation: Difference between revisions

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==Background==
==Background==
*Abbreviation = DIC
*Widespread and inappropriate activation of the coagulation and fibrinolytic systems
*Widespread and inappropriate activation of the coagulation and fibrinolytic systems
**Exposure of blood to procoagulants such as tissue factor and cancer procoagulant
**Exposure of blood to procoagulants such as tissue factor and cancer procoagulant
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===Causes===
===Causes===
*Infection
*[[Sepsis]](most common cause)
**Most common cause of DIC
**10%–20% of pts w/ Gram-neg sepsis have DIC
***Septic pts more likely to have bleeding than thrombosis
**More likely to develop in asplenic pts or cirrhosis
*Carcinoma
*Carcinoma
*Leukemia
*[[Leukemia]]
*Trauma
*[[Trauma]]
**Brain injury, crush injury, burns, rhabdo, fat embolism
*[[Pancreatitis]]
*Liver disease
**Brain injury, [[crush injury]], [[burns]], [[rhabdomyolysis]], [[fat embolism]]
*Pregnancy
*[[hepatic failure|Liver disease]]
**Abruption, [[Amniotic Fluid Embolus]], septic abortion, HELLP syndrome
*[[Pregnancy]]-related
**[[Placental Abruption]], [[Amniotic Fluid Embolus]], [[septic abortion]], [[HELLP Syndrome]], [[acute fatty liver of pregnancy]]
*[[Snake bite]]
*[[Snake bite]]
*[[ARDS]]
*[[ARDS]]
*[[Transfusion reaction]]
*[[Transfusion reaction]]
*[[Transplant complications|Transplant rejection]]


==Clinical Features==
==Clinical Features==
*In given pt either bleeding or thrombosis will predominate
''[[hemorrhage|Bleeding]] or [[thromboembolism|thrombosis]] can predominate (bleeding is more common ~65%)''
**Bleeding is more common (65% of pts)
*[[Shoc]]k (15%)
***Ranges from petechiae/ecchymosis to life-threatening GI/CNS/pulm bleeding
*[[Acute renal failure]] (25-40%)
***Shock occurs in 15%
*[[hepatic failure|Hepatic dysfunction]] (19%)
**Renal failure (25-40%)
*Respiratory dysfunction (16%)
**Hepatic dysfunction (19%)
*[[Thromboembolism]] (7%)
**Respiratory dysfunction (16%)
*CNS involvement (2%)
**Thromboembolism (7%)
*[[Purpura fulminans]] (widespread arterial and venous thromboses)
**CNS involvement (2%)
**Associated with significant [[bacteremia]]
**Purpura fulminans (widespread arterial and venous thromboses)
***Associated w/ significant bacteremia


==Differential Diagnosis==
==Differential Diagnosis==
*[[TTP]]-[[HUS]]
{{Hemolytic anemia DDX}}
**Pts usually have little or no prolongation of PT or PTT
{{Thrombocytopenia}}
*Severe liver disease
{{Increased bleeding DDX}}
**Also a/w prolonged PT/PTT, thrombocytopenia, incr D-dimer, incr FDPs
{{Bullous rashes DDX}}
***However, D-dimer is usually only mildly elevated
*Heparin-induced thrombocytopenia


{{Thrombocytopenia}}
==Evaluation==
===Acute===
*Platelets<ref>Spero JA, Lewis JH, Hasiba U. Disseminated intravascular coagulation. Findings in 346 patients. Thromb Haemost. 1980 Feb 29. 43(1):28-33.</ref>
**[[thrombocytopenia|Low]] (or dropping) in 98% of DIC patients
**Sn, not Sp
**Repeat platelets may be necessary if first level normal or if need to trend
*PT and PTT
**[[coagulopathy|Prolonged]]
**May be normal in as many as 50% of DIC patients<ref>Olson JD, Kaufman HH, Moake J, O'Gorman TW, Hoots K, Wagner K, et al. The incidence and significance of hemostatic abnormalities in patients with head injuries. Neurosurgery. 1989 Jun. 24(6):825-32.</ref>
**Serial coagulation testing may be necessary
**PT, not INR, is used for monitoring<ref>Levi M, Toh CH, Thachil J, Watson HG. Guidelines for the diagnosis and management of disseminated intravascular coagulation. British Committee for Standards in Haematology. Br J Haematol. 2009 Apr. 145(1):24-33.</ref>
*Fibrinogen
**Low
**<100 correlates with severe DIC
**May be normal (acute phase reactant), up to 57% in  DIC patients<ref>Spero JA, Lewis JH, Hasiba U. Disseminated intravascular coagulation. Findings in 346 patients. Thromb Haemost. 1980 Feb 29. 43(1):28-33.</ref>
*FDP
**Elevated
*[[D-dimer]]
**Elevated
**Sn but not Sp: may also see in patients with chronic liver or renal disease
**Combination of elevated FDP and d-dimer may increase sensitivity and specificity
*RBCs
**Fragmented (not specific)


==Diagnosis==
===Chronic===
*Acute DIC
*FDP: Elevated
**Platlets
*[[D-dimer]]: Elevated
***Low (or dropping)
*Platelet: Variable
***Sn, not Sp
*Fibrinogen: Normal-elevated
**PT
*PT: Normal
***Prolonged
*PTT: Normal
**Fibrinogen
*RBCs
***Low
**Fragmented
***<100 correlates w/ severe DIC
***May be normal (acute phase reactant)
**PTT
***Prolonged
**FDP
***Elevated
**D-dimer
***Elevated
***Sn but not Sp: may also see in pts w/ chronic liver or renal disease
**RBCs
***Fragmented (not specific)
*Chronic DIC
**FDP: Elevated
**D-dimer: Elevated
**Platelet: Variable
**Fibrinogen: Normal-elevated
**PT: Normal
**PTT: Normal
**RBCs
***Fragmented


==Treatment==
==Management==
*Treat underlying illness
*Treat underlying illness
*Replacement tx
*Replacement treatment
**Only indicated in pts w/ documented DIC + bleeding or impending procedure
**Only indicated in with documented DIC + bleeding or impending procedure
***Fibrinogen
***Fibrinogen
****Consider repletion w/ cryoprecipitate to raise level to 100-150
****Consider repletion with [[cryoprecipitate]] to raise level to 100-150
***Platelets
***[[Platelets]]
****Consider repletion if <50K w/ bleeding or <20K without bleeding
****Consider repletion if <50K with bleeding or <20K without bleeding
***FFP
***[[FFP]]
***Vitamin K
****Consider repletion to goal of PT and PTT < 1.5 times the normal limit
***Folate
***[[Vitamin K]]
**Heparin
***[[Folate]]
***Consider only in pts w/ thromboembolic predominant symptoms from chronic DIC
**[[Heparin]]
***Consider only if thromboembolic are predominant symptoms from chronic DIC
 
==Disposition==
*Admit


==See Also==
==See Also==
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==References==
==References==
 
<references/>
[[Category:Heme/Onc]]
[[Category:Heme/Onc]]

Latest revision as of 00:24, 1 October 2019

Background

  • Abbreviation = DIC
  • Widespread and inappropriate activation of the coagulation and fibrinolytic systems
    • Exposure of blood to procoagulants such as tissue factor and cancer procoagulant
    • Formation of fibrin within the circulation
    • Fibrinolysis
    • Depletion of clotting factors
    • End-organ damage
  • Chronic DIC occurs when hepatic/bone marrow production balances coag factor consumption

Causes

Clinical Features

Bleeding or thrombosis can predominate (bleeding is more common ~65%)

Differential Diagnosis

Microangiopathic Hemolytic Anemia (MAHA)

Thrombocytopenia

Decreased production

Increased platelet destruction or use

Drug Induced

Comparison by Etiology

ITP TTP HUS HIT DIC
↓ PLT Yes Yes Yes Yes Yes
↑PT/INR No No No +/- Yes
MAHA No Yes Yes No Yes
↓ Fibrinogen No No No No Yes
Ok to give PLT Yes No No No Yes

Coagulopathy

Platelet Related

Factor Related

Vesiculobullous rashes

Febrile

Afebrile

Evaluation

Acute

  • Platelets[1]
    • Low (or dropping) in 98% of DIC patients
    • Sn, not Sp
    • Repeat platelets may be necessary if first level normal or if need to trend
  • PT and PTT
    • Prolonged
    • May be normal in as many as 50% of DIC patients[2]
    • Serial coagulation testing may be necessary
    • PT, not INR, is used for monitoring[3]
  • Fibrinogen
    • Low
    • <100 correlates with severe DIC
    • May be normal (acute phase reactant), up to 57% in DIC patients[4]
  • FDP
    • Elevated
  • D-dimer
    • Elevated
    • Sn but not Sp: may also see in patients with chronic liver or renal disease
    • Combination of elevated FDP and d-dimer may increase sensitivity and specificity
  • RBCs
    • Fragmented (not specific)

Chronic

  • FDP: Elevated
  • D-dimer: Elevated
  • Platelet: Variable
  • Fibrinogen: Normal-elevated
  • PT: Normal
  • PTT: Normal
  • RBCs
    • Fragmented

Management

  • Treat underlying illness
  • Replacement treatment
    • Only indicated in with documented DIC + bleeding or impending procedure
      • Fibrinogen
      • Platelets
        • Consider repletion if <50K with bleeding or <20K without bleeding
      • FFP
        • Consider repletion to goal of PT and PTT < 1.5 times the normal limit
      • Vitamin K
      • Folate
    • Heparin
      • Consider only if thromboembolic are predominant symptoms from chronic DIC

Disposition

  • Admit

See Also

References

  1. Spero JA, Lewis JH, Hasiba U. Disseminated intravascular coagulation. Findings in 346 patients. Thromb Haemost. 1980 Feb 29. 43(1):28-33.
  2. Olson JD, Kaufman HH, Moake J, O'Gorman TW, Hoots K, Wagner K, et al. The incidence and significance of hemostatic abnormalities in patients with head injuries. Neurosurgery. 1989 Jun. 24(6):825-32.
  3. Levi M, Toh CH, Thachil J, Watson HG. Guidelines for the diagnosis and management of disseminated intravascular coagulation. British Committee for Standards in Haematology. Br J Haematol. 2009 Apr. 145(1):24-33.
  4. Spero JA, Lewis JH, Hasiba U. Disseminated intravascular coagulation. Findings in 346 patients. Thromb Haemost. 1980 Feb 29. 43(1):28-33.