19 results
diagnosis heartfailure hfref cardiology disease gastroenterology nutrition celiac chf indications pathophysiology peds schf 21hydroxylasedeficiency 21ohd ascorbicacid b12 chagas ckd cobalamin
Diagnostic Algorithm for Treatment of Iron Deficiency in Patients With Heart Failure Consensus Recommendations #Iron #Deficiency
Diagnostic Algorithm ... for Treatment of ... Iron Deficiency ... #Deficiency #Management ... #Diagnosis #Algorithm
Iron Deficiency in Heart Failure - Diagnosis and Treatment Algorithm Diagnosis: Ferritin <100 ng/mL (absolute ID) OR
Iron Deficiency ... Diagnosis and Treatment ... Algorithm Diagnosis ... to alleviate symptoms ... heartfailure #diagnosis #management
Algorithm for screening/diagnosis and treatment/follow‐up of iron deficiency in patients with chronic heart failure. Hb, haemoglobin;
Algorithm for screening ... /diagnosis and treatment ... /follow‐up of iron ... deficiency in patients ... #Deficiency #Management
Suspected Celiac Disease - Diagnosis Algorithm Celiac disease suspected: • Signs and symptoms of celiac disease •
Disease - Diagnosis Algorithm ... suspected: • Signs ... and symptoms of ... celiac disease • Iron-deficiency ... unresponsive to treatment
Iron Deficiency in Heart Failure Pathophysiology: Chronic heart failure leads to an increase in inflammatory cytokines → Inflammation
Iron Deficiency ... functional ID) Treatment ... improvement in symptoms ... #deficiency #CHF ... heartfailure #diagnosis #management
Risk Factors and Signs of Copper Deficiency Risk Factors: • Gastrointestinal: Previous upper bowel resection/bariatric surgery, Inflammatory
of Copper Deficiency ... dental fixatives, Treatment ... , Optic neuropathy ... drkeithsiau #Copper #Deficiency ... #riskfactors #symptoms
Pediatric SVT - Management Algorithm Identify SVT: • HR not variable • Abrupt rate changes • Infants:
Pediatric SVT - ... Management Algorithm ... Signs of shock or ... #Algorithm #peds ... #Pediatric #treatment
Polycythemia Vera (PV) - Diagnosis and Management Summary Diagnostic Criteria: • Elevated hemoglobin and/or hematocrit AND •
Diagnosis and Management ... When present, symptoms ... , signs, and complications ... • Treatment algorithms ... PV #Diagnosis #Management
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
21-Hydroxylase Deficiency ... maintains appropriate ion ... amount of enzyme deficiency ... Signs/Symptoms/Complications ... endocrinology #peds #pediatrics
Algorithm regarding the diagnosis and treatment of Hereditary Hemochromatosis HH. Step 1: In the patient with
Algorithm regarding ... diagnosis and treatment ... suspected HH based on symptoms ... hemochromatosis #algorithm ... #diagnosis #management
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