27 results
diagnosis management signs hematology psychiatry syndrome differential endocrinology neurology treatment behavioraldisorder criteria disorders gastroenterology hepatology obstruction oncology sbo 21hydroxylasedeficiency 21ohd
Eosinophil Disorders Testing Algorithm INDICATIONS FOR TESTING: • Peripheral blood eosinophilia/hypereosinophilia uncovered incidentally during medical evaluation or
Algorithm INDICATIONS ... evaluation or workup ... for specific symptoms ... 1,500 cells/µL Workup ... for secondary causes
Hematuria Workup and Diagnosis Algorithm • Confirm hematuria → Urinalysis >3 RBCs/HPF, exclude mimics, repeat testing
Hematuria Workup ... and Diagnosis Algorithm ... mimics, repeat testing ... nephrolithiasis • Symptoms ... #Workup #urology
Hypereosinophilia Different Diagnosis and Workup Secondary causes are broad so start with a med review, the most
Diagnosis and Workup ... Secondary causes ... the most common cause ... the US inpatient setting ... #algorithm
Causes of Thrombocytopenia and Platelet Disorders - Differential Diagnosis and Workup History: - Prior platelet count, family
Causes of Thrombocytopenia ... Diagnosis and Workup ... smear, HIV/HCV testing ... pylori test (GI symptoms ... #Workup #hematology
Diabetic Ketoacidosis (DKA) - Pathogenesis and Clinical Findings • Note: in DKA, body K+ is lost
out of cells may cause ... Treating DKA: 1) ... Signs/Symptoms/Complications ... tachycardia, Incr resting ... DiabeticKetoacidosis #DKA #pathophysiology
Mechanical Bowel Obstruction and Ileus - Pathogenesis and Clinical Findings Ileus: Functional bowel "blockage", no peristalsis Mechanical Obstruction:
pain and related symptoms ... Flat/low JVP, resting ... percussion • Nausea ... obstruction #sbo #ileus #pathophysiology
Primary Biliary Cirrhosis (PBC) - Summary PBC Epidemiology: • Female:Male 9:1 • Common European descent • Age:
65 years PBC Pathophysiology ... intralobular bile ducts causes ... PBC Signs and Symptoms ... Proximal limb muscle wasting ... cholangitis #diagnosis #workup
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... glands • Salt wasting ... infants with "salt wasting ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology
Scurvy (Vitamin C Deficiency) - Diagnosis and Management Vitamin C is required for hydroxylation of proline residues
musculoskeletal symptoms ... Psychiatric symptoms ... , or any other cause ... weeks #Scurvy #Pathophysiology ... #AscorbicAcid #Pathophysiology
Attention Deficit Hyperactive Disorder (ADHD): Pathogenesis and clinical findings - For diagnosis, must have either 26
have either 26 symptoms ... 2 settings - Symptoms ... their turn • Causes ... finish assigned work ... BehavioralDisorder #Pathophysiology
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