11 results
MoCA: Montreal Cognitive Assessment 

#Diagnosis #Geriatrics #Dementia #Montreal #Cognitive #Assessment #MoCA #MSE #Evaluation #Score
Montreal Cognitive Assessment ... #Diagnosis #Geriatrics ... #Dementia #Montreal ... #Cognitive #Assessment
Initial assessment and management of coma in pediatric population.

Airway - is it secure? 
Breathing — is
Initial assessment ... management of coma in pediatric ... treatable: - hypoglycaemia ... care unit #Assessment ... #Coma #Pediatrics
The Mini-Mental State Examination (MMSE) is commonly used as a screening tool to detect dementia. However,
tool to detect dementia ... #Diagnosis #Geriatrics ... #Dementia #SLUMS ... Examination #Score #Assessment
Major neurocognitive disorders (MNCD): Diagnosis and workup 

1) Clinical diagnosis Cognitive impairment + loss of autonomy
2)
neuropsychological assessment ... atrophy Lewy body dementia ... Frontotemporal dementia ... atrophy Vascular Dementia ... Workup #Diagnosis #Geriatrics
Lewy Body Dementia: Pathogenesis and Clinical Findings
Lewy Body Dementia is a sub-category of major or mild
Lewy Body Dementia ... Findings Lewy Body Dementia ... Dementia should ... #pathophysiology ... #geriatrics #diagnosis
Fecal Incontinence - Pathogenesis and Complications
Continence mechanisms are impaired
 • Local neuronal damage
 • External and
(e.g. stroke, dementia ... #Incontinence #geriatrics ... #pathophysiology
Assessment of diabetic control:
 - Any episodes of hypoglycaemia, diabetic ketoacidosis, hospital admission? 
 - Is
Assessment of diabetic ... Any episodes of hypoglycaemia ... still awareness of hypoglycaemia ... primarycare #DM1 #Peds #Pediatrics ... #Assessment
Alzheimer’s Disease: Pathogenesis and Clinical Findings
Risk factor for Late Onset Alzheimer's (99% of cases):
 - Increasing
AlzheimersDisease #Dementia ... #pathophysiology ... #geriatrics #diagnosis
SLU Mental Status Examination Tool
What does the SLU Mental Status Exam Test Do?
Q1-Q3: Attention, immediate recall,
extrapolation #Diagnosis #Geriatrics ... #Dementia #SLUMS ... #Examination #Assessment
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Hyperkalemia, Hypoglycemia ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds #pediatrics