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Abstract Hematologic disorders are frequently encountered in the intensive care unit, which include anemia, coagulation disorders, hematological malignancies and eosinophil disorders. Anemia often develops early in the course of a critical illness. The causes of anemia in ICU include blood loss, blunted erythropoietin response, inflammation and increased RBCs destruction. The established method for managing anaemia in the ICU is allogeneic red cell transfusion. The key question in deciding how to use red cell transfusion in the ICU is identifying the most appropriate transfusion trigger and the target haemoglobin range for each patient. Recombinant human erythropoietin (rHuEPO) may represent a therapeutic option for the treatment of anemia of critical illness and an additional way to conserve RBCs in the ICU. Coagulation disorders are commonly found in critically ill patients. They include bleeding disorders (hemorrhagic disorders) and clotting disorders (thrombotic disorders or hypercoagulable states). Hypercoagulable states can be defined as a group of inherited or acquired conditions associated with a predisposition to venous thrombosis (including upper and lower extremity deep venous thrombosis (DVT) with or without pulmonary embolism (PE), cerebral venous thrombosis, and intra-abdominal venous thrombosis), arterial thrombosis (including Summary 107 myocardial infarction, stroke, acute limb ischemia, and splanchnic ischemia), or both. Bleeding disorders can arise from disorders of the coagulation system, platelets and vessel wall. The most common bleeding disorders in ICU is acute traumatic hemorrhage. Massive haemorrhage has been reported to account for up to 50% of all trauma-related deaths. In addition to blood loss alone, haemorrhage produces a cascade of three key physiological interactions encapsulated by the term the “lethal triad”. It is this combination of coagulopathy, hypothermia and acidosis that results in a global haemostatic deficit, increasing the risk of exsanguination. Damage control resuscitation (DCR) is a treatment strategy that targets the conditions that exacerbate hemorrhage in trauma patients. DCR differs from current resuscitation approaches by attempting an earlier and more aggressive correction of coagulopathy and metabolic derangement. Thrombocytopenia is very common in critically ill patients treated in the intensive care unit (ICU). Thrombocytopenia in the ICU is caused by many causes such as immune-medicated thrombocytopenia, drugs or toxins, intra-aortic balloon pump/intravascular device use, hypersplenism and microangiopathic hemolytic anemia as DIC. Summary 108 DIC is common in ICU patients, as it is a comorbidity of many of the diagnoses, which lead to ICU admission. While DIC is not a primary disorder, it is a marker of an underlying systemic process. Treatment of DIC is treatment of the underlying disorder aggressively, restoration of adequate circulatory volume and coagulation potential as quickly as possible. Patients with haematological malignancy may develop critical illness either as part of their first presentation with the malignancy or more commonly after chemotherapy or haematopoietic stem cell transplant (HSCT). ICU admission for patients with haematological malignancies, and particularly after bone marrow transplantation, has been associated with very poor outcomes, and in some cases, critical care has been withheld because it was perceived to be futile. Newer studies suggest that ICU outcomes have improved, probably as a result of changes in both haematological treatments and ICU care. The normal eosinophil count in the peripheral blood ranges from 50 to 500 × 109/l. Blood eosinophilia can be divided into mild eosinophilia (up to 1500 × 109/l) and marked eosinophilia (>1500 × 109/l). Eosinophils and their products play an essential role in the pathogenesis of various reactive and neoplastic disorders. Early therapeutic intervention with agents reducing eosinophil counts can be effective in limiting or preventing irreversible organ damage |