Mnemonic: ABCD
Mnemonic: PPM
Malnourished (depleted intracellular Phosphate, Potassium, Magnesium) → Refeeding → Increased glucose load → Insulin spikes → Drives PPM into cells → Hypophosphatemia (major abnormality), hypokalemia, hypomagnesemia
If patient hasn’t not eaten for >5 days, aim to refeed at <50% energy and protein levels.
Monitor and aggresively supplement PPM.
Indications for surgery Age group Spondylolisthesis Indications Pediatric Low grade Failure to respond to conservative treatment (9-12 months)Progressive slippageIntractable low back or radicular painNeurological deficit and deterioration High grade Neurological symptomsSevere sagittal plane spinal deformity Adult Low grade Failure of non-operative treatmentProgressive slippageSymptomatic and radiographically unstable isthmic spondylolisthesis High grade…
Among the common lysosomal storage disorders: Two of them are Mucopolysaccharidoses (Hunter and Hurler syndrome) Pompe’s disease is Glycogen Storage Disease. Others are Sphingolipidoses. Inheritance of Lysosomal Storage Diseases All are inherited as Autosomal Recessive (AR) condition except: Hunter syndrome (X-linked recessive) Fabry’s disease (X-linked recessive) Higher risk in Ashkenazi…
Type Description Treatment 1 Boutonniere (most common) Synovectomy with extensor hood reconstruction; MCP fusion or arthroplasty 2 Boutonniere with CMC subluxation (uncommon; Type 1 + Type 3) Same as type 1 and type 3 3 Swan neck deformity (2nd most common) Splinting vs CMC arthroplasty; MCP fusion 4 Gamekeeper deformity…