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Joshua J. Zaritsky M.D., Julian A. Martinez M.D., Ora Yadin M.D.

Continuous Veno-venous Hemodiafiltration Therapy for Acute Decompensation with Cerebral Edema in Maple Syrup Urine Disease. Joshua J. Zaritsky M.D., Julian A. Martinez M.D., Ora Yadin M.D. David Geffen School of Medicine, Mattel Children’s Hospital at UCLA, Los Angeles, United States.

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Joshua J. Zaritsky M.D., Julian A. Martinez M.D., Ora Yadin M.D.

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  1. Continuous Veno-venous Hemodiafiltration Therapy for Acute Decompensation with Cerebral Edema in Maple Syrup Urine Disease Joshua J. Zaritsky M.D., Julian A. Martinez M.D., Ora Yadin M.D. David Geffen School of Medicine, Mattel Children’s Hospital at UCLA, Los Angeles, United States

  2. Maple Syrup Urine Disease • Autosomal recessive disorder characterized by psychomotor retardation, feeding problems and maple syrup odor of the urine • Caused by deficiency of branched-chained alpha-ketoacid dehydrogenase complex • Results in increased plasma concentrations of the branched-chained amino acids: leucine, isoleucine and valine • Five phenotypes have been described based on both clinical and biochemical findings

  3. Management of MSUD • Dietary therapy to promote normal growth and development • Prompt recognition and treatment of acute metabolic decompensation usually triggered by an intercurrent illness • Characterized by acute rises in the BCAA with leucine accumulation leading to neurotoxicty

  4. Cerebral Edema during Episodes of Metabolic Decompenstation • Cerebral edema is the leading cause of death during periods of acute decompensation • Remains unclear why MSUD patients are prone to cerebral edema (Morton et.al. 2002) • Intracellular entrapment of osmotically active amino acids caused by high intracellular leucine levels • Impairment of normal regulatory volume defense- disrupution of intracellular protein synthesis • Pathological or iatrogenic decreases in serum sodium and osmolarity with rapid water flux into cells

  5. Treatment of Acute Decompensation • Native urinary clearance is low so strategies for removal of BCAA include • Nutritional support: • Inhibition of protein catabolism • Enhancement of protein synthesis with amino acid supplementation aimed at promoting leucine incorporation • Extracorporeal Removal • Exchange transfusions • Dialysis; PD, HD and CRRT

  6. Choice of Dialysis Modality • Literature is largely case based • Guoyon et. al. (1994) compared BCAA clearance between PD, CAVH and CAVHD in a rabbit model of MSUD • PD was less efficient than CRRT • Using CRRT; BCAA clearance paralleled that of urea • No comparisons of HD vs. CRRT in cases complicated by cerebral edema

  7. Case Presentation • 7 yo male with neonatal diagnosis of MSUD presented to outside hospital with a 2 week history of URI symptoms and difficulty walking • Diagnosed with pneumonia with a superimposed asthma exacerbation • Over the period of one week he became progressively encephalopathic with new onset spastic diplegia despite dietary modifications • CT upon arrival at UCLA revealed diffuse cerebral edema with no visible sulcation • Initial leucine level of 285 µmoles/L at outside hospital. At time of transfer had reached a peak of 1581 µmoles/L

  8. Therapeutic CVVHDF • Based on his cerebral edema decision made to initiate CVVHDF • Gambro circuit with M60 filter; Qb of 100ml/min, Qd of 1500ml/hr and Qr of 750ml/hr , no net ultrafiltration • Predicted small molecule clearance of 57ml/min/1.73m2 • Given an estimated Vd of leucine of 17L (Based on a weight of 27kg; see Jouvet et.al. 2001)acceptable steady state levels of leucine were predicted to be reached in 16 hours

  9. CVVHDF 36 4 8 12 16 Plasma Amino Acid Levels

  10. Amino Acid Clearances

  11. Summary • CRRT clearances of BCAA are similar to those of other small molecules • CVVHDF is effective in acutely lowering serum leucine levels during acute decompensation in MSUD • CVVHDF is a safe therapy for decompensation in MSUD when complicated by cerebral edema

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