Severe Hypertriglyceridemia¶
Chloe de Crecy
Background¶
- Elevated triglycerides (TG) on a fasting lipid panel
- Normal: <150 mg/dL
 - Moderate HTG: 150-499 mg/dL
 - Moderate to severe HTG: 500-999 mg/dL
 - Severe HTG: >1000 mg/dL
 
 - Nearly all pts with severe HTG have a genetic predisposition + additional risk factor (e.g. DM, alcohol abuse, oral estrogen, hypothyroidism, nephrotic syndrome, propofol, ART)
 - Risks of hypertriglyceridemia: pancreatitis (requires serum TG >500 mg/dL), ASCVD
 - Signs: xanthomas, hepatosplenomegaly, lipemia retinalis, milky appearance of plasma
 - Sxs: short-term memory loss, abdominal pain, flushing with ETOH
 
Evaluation¶
- Lipid panel: usual outpt screening, acute pancreatitis, cutaneous xanthomas, familial HTG, monitoring HTG treatment
 - Note: Na, glucose, amylase, LDL readings can be affected by HTG
 - Consider sending A1c, Cr, TSH
 - Assess medication list for secondary causes
 
Management¶
- HTG induced pancreatitis
- If pt has hypocalcemia, lactic acidosis, or multi-organ dysfunction
- Initiate plasmapheresis and monitor serum TG after each cycle until <500
 - Severe dietary fat restriction (<5%) until TG <1000
 
 - If none of the above and pt is hyperglycemic
- Start insulin gtt, IVF, monitor q1h BG and q12h TG
 - Discontinue insulin when serum TG <500
 - Severe dietary fat restriction (<5%) until TG <1000
 
 - If none of the above and pt is euglycemic
- Start insulin gtt + dextrose, Monitor q12h TG until <500
 - Severe dietary fat restriction (<5%) until TG <1000
 
 
 - If pt has hypocalcemia, lactic acidosis, or multi-organ dysfunction
 - Long-term Management (once TG <1000, otherwise decreased efficacy)
- Pharmacologic: fibrates (most commonly fenofibrate), statins, niacin, omega-3 fatty acids
 - Nonpharmacologic: discontinue ETOH use, dietary fat and sugar restriction (target fat intake at <10% of calorie intake), exercise