11 results
diagnosis hepatology neurology hematology nephrology nutrition rheumatology activation b1 cerebritis cns compartment deficiency differential erythematosus gitelman hemeonc hemophagocytic hepatic hepatopulmonary
Wernicke Encephalopathy - Acute B1 (Thiamine) Deficiency - Diagnosis and Management Diagnosis - Caine Criteria (2 of
Diagnosis and Management ... Diagnosis - Caine Criteria ... Anorexia nervosa Treatment ... • A prompt treatment ... development of Korsakoff syndrome
CNS Manifestations of Systemic Lupus Erythematosus (SLE) Clinical Manifestations: Demyelinating Syndrome, Headache, Movement disorders, Seizure disorders, Aseptic
Demyelinating Syndrome ... Meningitis, Myelopathy, Encephalopathy ... Disease, PRES Pathophysiology ... inflammation, leading ... cerebritis #diagnosis #management
Hepatic Encephalopathy - Diagnosis and Management Summary Definition: • Alteration in brain function manifested by neuropsychiatric symptoms
Hepatic Encephalopathy ... Diagnosis and Management ... TIPS West Haven Criteria ... #Grading #Classification ... #Diagnosis #Management
Refeeding Syndrome Overview What Is It? • Electrolyte/fluid shifts caused by initiation of nutrition in severely malnourished patient.
Refeeding Syndrome ... • Wernicke encephalopathy ... hyperparathyroidism Treatment ... Arrhythmias are the leading ... Differential #Diagnosis #Pathophysiology
Posterior Reversible Encephalopathy Syndrome (PRES) Overview Clinico-Radiological Syndrome, characterized by: • Headache • Seizures • Altered mental
Posterior Reversible Encephalopathy ... Etiology: • Pathophysiology ... epilepticus Treatment ... underlying cause • Treatment ... #management #neurology
Hepatopulmonary Syndrome - Diagnosis and Management Summary A defect in arterial oxygenation due to a gas exchange
Hepatopulmonary Syndrome ... HPS Diagnostic Criteria ... 80mmHg or A-a gradient ... ) on room air Treatment ... #treatment #hepatology
Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
Macrophage Activation Syndrome ... IL-1 and IL-6, leading ... Histopathologic criteria ... Treatment: • Corticosteroids ... #Diagnosis #Management
Gitelman Syndrome Overview What? • Inherited (AR) hypokalemic salt-losing tubulopathies affecting the thiazide-sensitive sodium chloride cotransporter • Gitelman's syndrome
Gitelman Syndrome ... abuse • Salt craving ... Rhabdomyolysis Treatment ... diagnosis #nephrology #management ... #pathophysiology
Compartment Syndrome Pearls A vicious cycle of increased pressure within a facial compartment leading to compression of
Compartment Syndrome ... facial compartment leading ... Pathophysiology: ... onset of ischemia Treatment ... #diagnosis #management
Hemophagocytic Lymphohistiocytosis (HLH) High mortality without prompt recognition and management. HLH is a critical diagnostic consideration in
recognition and management ... hyperinflammatory syndrome ... Pathophysiology ... Diagnostic Criteria ... of 8 HLH-2004 criteria
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