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Nutritional Management of Hepatic Encephalopathy Presented by Chris Theberge & Sara Murkowski
Presentation At A Glance ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Let’s Take It From The Top ,[object Object]
Functions of the Liver: A Brief Overview ,[object Object],[object Object],[object Object]
Functions of the Liver ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Alanine Transaminase (ALT) Aspartate Transaminase(AST)  The Urea Cycle
Liver Diseases  ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Classifications
Liver Diseases ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Liver Diseases ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Inherited   Liver Disorders
Liver Diseases ,[object Object],[object Object],[object Object],[object Object],[object Object]
Progression of Liver Diseases
Normal Liver
Alcoholic Fatty Liver
Cirrhotic Liver
Prognosis of Cirrhosis Child-Pugh and MELD Score Both used to determine prognosis of  Cirrhosis (mortality and survival) Determine Need For Transplantation Used in studies to determine effect of treatment on liver function
Malnutrition In Liver Disease ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
And Now Our Featured Presentation…
What is Hepatic Encephalopathy? ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Incidence & Prognosis ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Clinical Manifestations of HE ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Variants of Hepatic Encephalopathy ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Precipitants of Hepatic Encephalopathy ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Primary Hepatocellular Carcinoma
Variants of Hepatic Encephalopathy ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Stages of Hepatic Encephalophay Stage Symptoms I Mild Confusion, agitation, irritability, sleep disturbance, decreased attention II Lethargy, disorientation, inappropriate behavior, drowsiness III Somnolent but arousable, slurred speech, confused, aggressive  IV Coma
Pathogenesis Theories ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Neurotoxic Action of Ammonia ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Pathogenesis Theories:  False Neurotransmitter Hypothesis   ,[object Object],[object Object],[object Object],[object Object],[object Object]
Abnormal plasma amino acids: chronic liver disease Val 400 350 300 250 150 200 100 50 Thr Leu Ileu Lys Try Meth Phe Tau Asp Glu Ser Pro Gly Ala Tyr Orn His Arg Essential Non-Essential % of Normal Cerra, et al; JPEN, 1985 J. Y. Pang
Pathogenesis Theories:  False Neurotransmitter Hypothesis ,[object Object]
Pathogenesis Theories: Change In Neurotransmitters and Receptors ,[object Object],[object Object]
Increase Permeability of Blood-Brain Barrier ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Symptoms of HE ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Diagnosing HE ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Diagnostic Criteria ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Differential Diagnosis ,[object Object],[object Object],[object Object],Table 3. Differential diagnostic considerations in hepatic encephalopathy
Treatment of Hepatic Encephalopathy ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Nutritional Management of HE ,[object Object],[object Object],[object Object],[object Object],[object Object]
Historical Treatment Theories: Protein Restriction ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Dispelling the Myth ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Dispelling the Myth ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Protein and HE Considerations ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Other Considerations ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Branched Chain Amino Acids (BCAA) Valine Leucine Isoleucine ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object]
Nutritional Supplementation with Branched-Chain Amino Acids in Advanced Cirrhosis: A Double-Blind, Randomized Trial ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Nutritional Supplementation with Branched-Chain Amino Acids in Advanced Cirrhosis: A Double-Blind, Randomized Trial ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
*  Significantly different from both lactoalbumin and maltodextrin.  1  Some individuals were removed based on more than 1 criterion.  2  Cases with HCC were censored at the time of HCC diagnosis.  3  The number of withdrawn patients who died or progressed to exclusion criteria within 12 mo from entry into the study is reported in parentheses.  4  Including the patient lost to follow-up. Study Profile of BCAA Trial BCAA Lactoalbumin Maltodextrin Total number 59 56 59 Lost to follow-up 1 — — Intention-to-treat analysis 58 56 59 Events (death, any cause, or progression of liver failure to exclusion criteria) 9 (15.5%) * 18 (32.1%) 16 (27.1%) Removed from systematic follow-up 1 7 4 4      Development of HCC 2 1 1 2      Noncompliance to treatment 3 5 (1) 2 (1) 0      Side effects 3 4 4  (1) 2 (1) 2      Treatment-unrelated diseases — 1 — Regular 3-mo follow-up 42 (71.2%) * 34 (60.7%) 39 (66.1%)      Admission to hospital 15 (35.7%) * 27 (79.4%) 28 (71.8)      Admission rate (patients/y) 0.6 ± 0.2 * 2.1 ± 0.5 1.9 ± 0.4      Total no. d in hospital 195 * 327 520
Primary Outcome Results ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Anorexia and Health-Related Quality of Life ,[object Object],[object Object],[object Object],[object Object],[object Object]
Conclusions ,[object Object],[object Object],[object Object],[object Object],[object Object]
The Mother of All BCAA Trials? Randomized Study Limitations ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
The Mother of All BCAA Trials? Further Study Limitations ,[object Object],[object Object]
[object Object],[object Object]
Branched-Chain Amino Acids For Hepatic Encephalopathy ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Branched-Chain Amino Acids For Hepatic Encephalopathy ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Branched-Chain Amino Acids For Hepatic Encephalopathy ,[object Object],[object Object],[object Object],[object Object]
Branched-Chain Amino Acids For Hepatic Encephalopathy: Results ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Significant
Not significant Combining survival data regardless of window of f/u showed no significant Difference in survival between BCAA and controls
Branched-Chain Amino Acids For Hepatic Encephalopathy: Results ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Conclusions ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Conclusions ,[object Object],[object Object]
TABLE 1   Randomized controlled trials of BCAA treatment in cirrhosis 1   1  bw, body weight; co, crossover study; pg, parallel group design.  2  Dietary BCAA not included. Data are in g/d except as noted.  3  Positive, BCAA significantly different; negative, BCAA not significantly different.
Limitations  ,[object Object],[object Object],[object Object],[object Object]
Implications For Future Research ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Implications For Future Research ,[object Object],[object Object],[object Object],[object Object],[object Object]
BCAA Enteral Formulations ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
The Child-Turcotte-Pugh Classification                                                                                     
Goals of MNT for HE ,[object Object],[object Object],[object Object],[object Object],[object Object]
Nutritional Implications: PCM associated Liver Dz ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
MNT in Advanced Liver Disease ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
MNT in Advanced Liver Disease ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
MNT in Advanced Liver Disease ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
How Much Protein:  That is the Question ,[object Object],[object Object],[object Object],[object Object],[object Object]
MNT Specifically in HE ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
MNT Specifically in HE ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Conclusions in HE Management ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Thank You! ,[object Object],[object Object],[object Object]
References ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
References ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
References ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]

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Nutritional Management of Hepatic Encephalopathy

  • 1. Nutritional Management of Hepatic Encephalopathy Presented by Chris Theberge & Sara Murkowski
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  • 6. Alanine Transaminase (ALT) Aspartate Transaminase(AST) The Urea Cycle
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  • 16. Prognosis of Cirrhosis Child-Pugh and MELD Score Both used to determine prognosis of Cirrhosis (mortality and survival) Determine Need For Transplantation Used in studies to determine effect of treatment on liver function
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  • 19. And Now Our Featured Presentation…
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  • 26. Stages of Hepatic Encephalophay Stage Symptoms I Mild Confusion, agitation, irritability, sleep disturbance, decreased attention II Lethargy, disorientation, inappropriate behavior, drowsiness III Somnolent but arousable, slurred speech, confused, aggressive IV Coma
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  • 30. Abnormal plasma amino acids: chronic liver disease Val 400 350 300 250 150 200 100 50 Thr Leu Ileu Lys Try Meth Phe Tau Asp Glu Ser Pro Gly Ala Tyr Orn His Arg Essential Non-Essential % of Normal Cerra, et al; JPEN, 1985 J. Y. Pang
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  • 50. * Significantly different from both lactoalbumin and maltodextrin. 1 Some individuals were removed based on more than 1 criterion. 2 Cases with HCC were censored at the time of HCC diagnosis. 3 The number of withdrawn patients who died or progressed to exclusion criteria within 12 mo from entry into the study is reported in parentheses. 4 Including the patient lost to follow-up. Study Profile of BCAA Trial BCAA Lactoalbumin Maltodextrin Total number 59 56 59 Lost to follow-up 1 — — Intention-to-treat analysis 58 56 59 Events (death, any cause, or progression of liver failure to exclusion criteria) 9 (15.5%) * 18 (32.1%) 16 (27.1%) Removed from systematic follow-up 1 7 4 4      Development of HCC 2 1 1 2      Noncompliance to treatment 3 5 (1) 2 (1) 0      Side effects 3 4 4 (1) 2 (1) 2      Treatment-unrelated diseases — 1 — Regular 3-mo follow-up 42 (71.2%) * 34 (60.7%) 39 (66.1%)      Admission to hospital 15 (35.7%) * 27 (79.4%) 28 (71.8)      Admission rate (patients/y) 0.6 ± 0.2 * 2.1 ± 0.5 1.9 ± 0.4      Total no. d in hospital 195 * 327 520
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  • 63. Not significant Combining survival data regardless of window of f/u showed no significant Difference in survival between BCAA and controls
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  • 67. TABLE 1 Randomized controlled trials of BCAA treatment in cirrhosis 1 1 bw, body weight; co, crossover study; pg, parallel group design. 2 Dietary BCAA not included. Data are in g/d except as noted. 3 Positive, BCAA significantly different; negative, BCAA not significantly different.
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  • 72. The Child-Turcotte-Pugh Classification                                                                                     
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Notes de l'éditeur

  1. CHO metabolism : glycogenesis, glycogenolysis, gluconeogenesis Protein metabolism: deamination and transamination, synthesis of serum protein, blood clotting protein, lipoprotein Fat: converts fatty acids from diet and adipose tissue Acetyl-CoA, also synthesis of cholesterol and phospholipids Storage: fat soluble vitamins, B12, and other minerals Conversion of Vit. D to active form, carotenes to vit. A, vit. K to prothrombin