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algorithm antibiotics febrile fever lp stepbystep stratification 21hydroxylasedeficiency 21ohd bronchiolitis causes cthead decisionaid differential disease ebm endocrinology features genetics guidelines
Validation of the Step-By-Step Approach to Febrile Infants #Diagnosis #Management #Pediatrics #Peds #Febrile #Infant #StepByStep #Algorithm #LP
Approach to Febrile Infants ... #Diagnosis #Management ... #Pediatrics #Peds ... #Febrile #Infant ... #Antibiotics #Risk
Causes of Sudden Unexpected Death in Infancy (SUDI) - Differential Diagnosis Algorithm Congenital Anomaly / Disorder: •
- Differential Diagnosis ... • Deliberate (abuse ... 80% of SUDI • Risk ... #Causes #Peds # ... Pediatrics
Standardized Physical Abuse Guideline <6 months of age • Social work consult • Skeletal survey • Head
Standardized Physical Abuse ... • Troponin for infants ... AST or ALT> 80, signs ... Guidelines #Workup #Peds ... #Pediatrics #Diagnosis
“Step by Step” – the new kid on the block – aims to risk stratify this
” an infant with ... CRP < 20 mg/L #Diagnosis ... #Management #Pediatrics ... #Peds #Febrile ... #Infant #StepByStep
Kawasaki Disease (Mucocutaneous Lymph Node Syndrome) An rare systemic acute febrile vasculitic syndrome. Aetiology unknown. Affects
Early diagnosis ... immunoglobulin reduces the risk ... Disease #Features #Signs ... #Symptoms #Diagnosis ... #Peds #Pediatrics
PECARN Head CT Decision Aid The Head CT Choice decision aid was developed in Rochester, Minnesota. Full
TBIs, the child’s risk ... observation, and signs ... and symptoms that ... #PatientInfo #Peds ... #Pediatrics #DecisionAid
The Febrile Infant Step-by-Step Algorithm This is an algorithm developed by European emergency physicians to identify low-risk
to identify low-risk ... 92.0% and 46.9% #Diagnosis ... #EBM #Management ... #Pediatrics #Peds ... #Antibiotics #Risk
Bronchiolitis Bronchiolitis is a viral inflamation of the bronchioles and the commonest LRTI in under 1s'. It's
symptoms for 1 ... REMEMBER - infants ... Bronchiolitis #pediatrics ... #diagnosis #management ... #peds #treatment
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
deficiencies present in infants ... Signs/Symptoms/Complications ... Hirsutism & acne • Infertility ... endocrinology #peds ... #pediatrics
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