13 results
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 ... 80% of SUDI • Risk ... #Diagnosis #Algorithm ... #Causes #Peds # ... Pediatrics
Clinical features of shock from dehydration in an infant

Decreased level of consciousness 
Sunken fontanelle 
Dry mucous
dehydration in an infant ... Extremities #PhysicalExam ... #Signs #Symptoms ... #Dehydration #Peds ... #Pediatrics
The Febrile Child - some diagnostic clues to evaluating the febrile child.

#Febrile #Fever #Evaluation #Assessment #Signs
Febrile Child - some diagnostic ... Assessment #Signs #Symptoms ... #PhysicalExam # ... Diagnosis #Peds ... #Pediatrics
“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
The infant with tachypnea or wheeze - Clinical Conditions to Consider
 - Bronchiolitis 
 - Pneumonia
The infant with ... viral infections, risk ... Other causes #Diagnosis ... #Peds #Pediatrics ... #Infant #Tachypnea
Kawasaki Disease (Mucocutaneous Lymph Node Syndrome) 
An rare systemic acute febrile vasculitic syndrome. Aetiology unknown. 
Affects
Early diagnosis ... immunoglobulin reduces the risk ... Features #Signs #Symptoms ... #Diagnosis #Peds ... #Pediatrics
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 #Febrile ... #Antibiotics #Risk
Bronchiolitis
Bronchiolitis is a viral inflamation of the bronchioles and the commonest LRTI in under 1s'. It's
Diagnosis - Coryzal ... symptoms for 1 ... REMEMBER - infants ... Bronchiolitis #pediatrics ... #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