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management febrile stepbystep lp risk stratification 21hydroxylasedeficiency 21ohd acute causes cough differential discitis disease ebm endocrinology genetics hematology hemophagocytic hlh
Validation of the Step-By-Step Approach to Febrile Infants #Diagnosis #Management #Pediatrics #Peds #Febrile #Infant #StepByStep #Algorithm #LP
#Diagnosis #Management ... #Pediatrics #Peds ... #StepByStep #Algorithm ... #LP #Antibiotics ... Stratification #Fever
Step by Step Algorithmic Approach to Pediatric Fever Age < 21 days old (or 28 days for
Step by Step Algorithmic ... Approach to Pediatric ... Fever Age < 21 ... #Peds #Diagnosis ... #Infant #Fever
Clinical Algorithm for Emergency Department Evaluation and Management of UTI in Febrile Infants and Young Children Urinary
Clinical Algorithm ... department with fever ... #Diagnosis #Management ... #Peds #UrinaryTract ... #Pediatrics #Fever
Practical Pediatric Viral Rash Algorithm Child presenting with rash and current/ recent symptoms of viral illness but
Practical Pediatric ... Viral Rash Algorithm ... but is well with fever ... #Pediatrics #Peds ... #Diagnosis
The Febrile Infant Step-by-Step Algorithm This is an algorithm developed by European emergency physicians to identify low-risk
92.0% and 46.9% #Diagnosis ... EBM #Management #Pediatrics ... #Peds #Febrile ... #Antibiotics #Risk ... Stratification #Fever
“Step by Step” – the new kid on the block – aims to risk stratify this
CRP < 20 mg/L #Diagnosis ... #Management #Pediatrics ... #Peds #Febrile ... #Algorithm #LP ... #Antibiotics #Risk
Pediatric Discitis - Inflammation of intervertebral disc Etiology • Bacterial or viral Clinical •
Pediatric Discitis ... Bacterial or viral Clinical ... Absent or low grade fever ... • Radicular symptoms ... #Peds #Diagnosis
Causes of Acute Pediatric Cough - Differential Diagnosis Algorithm No Fever, No Tachypnea - Normal Chest Auscultation
Causes of Acute Pediatric ... - Differential Diagnosis ... Algorithm No Fever ... Bronchitis - No URTI Symptoms ... #Peds #Pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... deficiencies present in infants ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics
Evaluation of suspected incomplete Kawasaki Disease 1. AHA consensus recommendations 2. Infants ≤6 months old on day ≥7
Infants ≤6 months ... old on day ≥7 of fever ... if they have no clinical ... #Diagnosis #Peds ... #Pediatrics #Kawasaki
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