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diagnosis hematology tls tumor activation arteritis catatonia dermatology differential gca giantcell hemeonc hemophagocytic hlh hyperkalemia k leukostasis lymphohistiocytosis macrophage malignant
Comparison - Serotonin Syndrome, Neuroleptic Malignant Syndrome, and Malignant Catatonia - BWH Medicine Chiefs @BrighamChiefs #Serotonin #Syndrome #Neuroleptic
Comparison - Serotonin ... Malignant #Catatonia #NMS ... #SS #comparison ... #diagnosis #management ... #treatment #table
Leukostasis vs Tumor Lysis Syndrome Leukostasis: • Pathophysiology: Large, immature blasts and high WBC count cause hyperviscosity
: - Neuro: AMS ... organ damage • Treatment ... unless worrisome EKG ... #diagnosis #management ... #hematology
Acquired von Willebrand Syndrome - Diagnosis and Management • Autoantibodies to vWF: Lymphoproliferative disorders (e.g. lymphoma,
Acquired von Willebrand ... Syndrome - Diagnosis ... and Management ... vonWillebrand #Syndrome ... #treatment #hematology
Tumor Lysis Syndrome An acute, life-threatening condition that appears within 7 days of starting cytotoxic therapies in
Tumor Lysis Syndrome ... with Ca only if EKG ... Walid Malki, MD, MS ... #Syndrome #TLS ... #oncology #management
Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
the secondary or acquired ... • Infection (eg ... Treatment: • Corticosteroids ... #Diagnosis #Management ... #Hematology #Rheumatology
Hyperkalemia - Diagnosis and Management - GrepMed Handbook S/Sx: Most pts asymptomatic. Weakness, cramping, nausea, paresthesias, palpitations,
Acidosis, Cell Lysis ... heparinized tube) • ECG ... acidosis), CK+LDH (lysis ... Elimination (see Table ... Bicarb<22) - avoid NS
Giant cell arteritis (GCA) Giant cell arteritis (GCA) definition: Most common systemic inflammatory vasculitis in older adults
vision changes, etc ... of the steroid treatment ... Treatment of GCA ... them, but urgent rheumatology ... Symptoms #Diagnosis #Management
SAPHO Syndrome Summary What? SAPHO syndrome is a rare chronic inflammatory disorder of bone, joint, and skin characterized
and lower jaw Treatment ... antiinflammatory properties e.g ... Tetracyclines etc ... #Rheumatology # ... diagnosis #management
Hemophagocytic Lymphohistiocytosis (HLH) High mortality without prompt recognition and management. HLH is a critical diagnostic consideration in
recognition and management ... hyperinflammatory syndrome ... • Secondary (Acquired ... Treatment Approach ... #Hematology #HemeOnc
TAFRO TAFRO syndrome was first described in 2010, standing for: - Thrombocytopenia - Anasarca - Fever - Reticulin fibrosis - Organomegaly TAFRO syndrome
without TAFRO (iMCD-NOS ... mesothelioma, etc ... Hypoalbuminemia Treatment ... TAFRO #diagnosis #management ... #rheumatology #
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