Disseminated Intravascular Coagulation
) (Transfusion Alternatives in Transfusion Medicine VOLUME 4 NUMBER 6 MARCH 2003( Pa ge 21 2 ) isseminated intravascular coagulation (DIC) in a patient may lead to considerable confusion among physicians, in particular concerning its proper management. In fact, the syndrome is often viewed differently depending on the specialist. Surgeons, for example, may consider DIC a severe bleeding disorder whereas intensive care specialists may focus on the role of disseminated fibrin deposition in multiple organ failure (MOF). This variable perception is also reflected by the many names for the syndrome, ranging from disseminated intravascular fibrin formation to consumptive hemorrhagic coagulopathy.The reason for this confusion is not because DIC is a new syndrome. The medical literature of the 1950s includes precise accounts of what we would now call DIC.1 Even centuries earlier, Celsus described diffuse hemorrhage from several sites after a snake bite and Dupuy, in 1834, noted that the injection of brain material resulted in widespread intravascular clotting in dogs. DIC is also not a syndrome that has been altogether ignored in the medical literature. A search of the MEDLINE database from 1966 to 2002 using the search term "disseminated intravascular coagulation" and related text words yields an impressive number of manuscripts -some 1400. Most are case reports and studies dealing with the pathophysiology of disseminated intravascular coagulation, which, in its main features, is indeed well understood now. Very few of the published papers -only about 1.5% -report on clinical studies that may be helpful in guiding the clinician to appropriate and "evidence-based" management strategies applicable to patients with DIC. The lack of useful literature can probably be explained by the fact that DIC is a poorly defined syndrome whose intensity varies widely. It often occurs with a broad range of severe disorders, which, individually, are associated with extensive morbidity and mortality, thus complicating them even further.
Definition, Relevance, and Clinical Setting of DICDIC is not a disease or a symptom, but a syndrome that is always secondary to an underlying disorder. The syndrome is characterized by a systemic activation of the blood coagulation system, which results in the generation and deposition of fibrin, leading to microvascular thrombi in various organs and contributing to the development of MOF. Consumption and subsequent depletion of coagulation proteins and platelets, due to the ongoing activation of the coagulation system, may induce severe bleeding complications, although microclot formation may occur in the absence of severe clotting factor depletion and bleeding. 4 Hence, a patient with DIC can present with a simultaneously occurring thrombotic and bleeding problem (Figure 1) The clinical importance of severe platelet and coagulation factor depletion in patients with diffuse widespread bleeding or requiring an invasive procedure is obviously indisputable. However, i...