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Intestinal Transplantation

Intestinal Transplantation. Jonathan Fryer MD Associate Professor of Surgery Feinberg School of Medicine Northwestern University. Objectives. To review the indications for intestinal transplant. To review the types of intestinal transplant.

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Intestinal Transplantation

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  1. Intestinal Transplantation Jonathan Fryer MD Associate Professor of Surgery Feinberg School of Medicine Northwestern University

  2. Objectives • To review the indications for intestinal transplant. • To review the types of intestinal transplant. • To review management of intestinal transplant candidates and recipients. • To review the outcomes and potential complication of intestinal transplants.

  3. Intestinal Failure • Inability to maintain adequate protein calorie and/or micronutrient nutritional balance despite maximal delivery of enteral nutrients. • Intestinal Failure = PN dependence.

  4. Intestinal TransplantCandidates • Intestinal Failure patients that are permanently dependent on Parenteral Nutrition (PN) or are anticipated to be. • Short Bowel (70%) (i.e. < 100 cm of functional SB) • Dysmotility (15%) • Malabsorption (15%)

  5. Intestinal Failure (TPN dependency) Intestinal Rehabilitation -Dietary optimization -Hormonal Enhancement Therapy -Gut lengthening Surgery TPN reduced (50%) (lower-risk?) -Monitor closely TPN not reducible (20%) (high-risk) -Transplant TPN free (30%)

  6. Intestinal Transplantation Indications • PN failure (Medicare criteria) • Impending or overt liver failure: •  bili,  liver enzymes,  spleen,  PT,  INR,  plts, varices, stomal bleeding, fibrosis, cirrhosis • Thrombosis of central veins: •  2 of subclavian, jugular, or fem veins • Frequent central line-related sepsis: • 2 line sepsis per year, 1 if fungemia, septic shock, or ARDS • Frequent severe dehydration.

  7. Referral for SB transplantUnresolved Issues re: timing of referral • Referral when liver complications develop. • PNALD is often benign / reversible. • Risk of transplanting too early. • Referral before liver complications develop. • High risk groups identifiable. • Parameters of PNALD progression poorly defined. • Transition to lethal / irreversible – unpredictable. • Candidates often unsalvageable when referred for transplant. • Outcomes worse when liver + intestine needed. • Optimal utility of donor livers?

  8. Number of UNOS Listings for Intestinal Transplants (1987-2004) (1,159) IBL 185 (400) (74.3%) (25.7%)

  9. Annual Waiting List Death Rates All organs(per 1,000 Patient-Years at Risk Waiting)

  10. Waiting List Mortality (1999-2004)ALI – All patients ever listed for bothLiver andIntestine-vs-INL – listed forIntestine,Never forLiver Death rate % 0-17 Years 18 + years Death rate % PELD PELD PELD PELD (4/99-2/02) (2/02-12/04) (4/99-2/02) (2/02-12/04)

  11. Figure 3A Intestinal Transplant Waiting List Outcomes Based On Their Liver Transplant Listing Status

  12. Types of Intestinal Transplants Adult Pediatric 28.9% 36.2% 39.2% 50.3% 34.9% 10.5%

  13. Preop Considerations • Organs to be included. • SB, Liver, Pancreas, Stomach, Colon, Kidney. • Multivisceral transplant – definition? when? why? • Donor : Recipient size match • Usually 0.5-0.75 D:R size ratio preferred. • If D>R size ratio- abdominal wall reconstruction strategy? • Recipient pre-sensitization (PRA) • Higher risk of rejection? • Desensitization or other strategy required? • Donor and recipient CMV and EBV status. • +ve  -ve at highest risk • Antiviral / immunosuppression strategy modified?

  14. Post-operative considerations Immunosuppression • Induction • Anti-lymphocyte products • Polyclonals: Thymoglobulin, Atgam • Monoclonals: Campath (anti –CD52), Zenepax/Simulect (anti-CD25) • Maintenance • Prograf • Rapamycin • Anti-rejection therapy • Solumedrol • Antilymphocyte products • Polyclonals: Thymoglobulin, Atgam • Monoclonals: OKT3 (anti-CD3)

  15. Post-operative considerations Monitoring • Rejection surveillance (No reliable serum marker): • Protocol biopsies (Initially weekly) • If rejection: mildSteroids; Severe  anti-lymphocyte products • Viral surveillance (CMV, EBV, adeno): • PCR (Initially weekly) • If progressive  replication  immunosuppression and/or antiviral therapy • Immunusuppression monitoring: • Drug level: (Prograf, Rapammune) • Immune monitoring (Lymphocyte count, Cylex)

  16. Post-op managementOther issues • Parenteral  enteral nutrition transition • Generally well tolerated early • Fat-free diet until lymphatics reform (chylous ascites) • PN catheter removal • When PN and IV hydration no longer required • G-tube / J-tube • Initial enteral nutrition administration • Safety line for admin of meds / nutrition • Loop ileostomy (all patients) • Easy access for protocol biopsies • Usually closed at 6 mos- 12 mos postop

  17. 1 YEAR PATIENT SURVIVAL 1994 T0 2004 SOURCE: OPTN/SRTR 2005 ANNUAL REPORT

  18. 2005-07 Graft Survival – Transplant Type p = 0.255 2 yr Analysis Intestinal Transplant Registry March 31, 2005

  19. 2005-07 Patient Survival - Transplant Type p = 0.001 2 yr Analysis Intestinal Transplant Registry March 31, 2005

  20. Causes of All Deaths % Distribution

  21. Causes of Death - % Distribution

  22. Alive Patient Status > 6 Months Post Tx2005 - 2007 Modified Karnofsky Performance Score(N=163) Graft Function (N=178)

  23. Summary • Intestinal transplantation is indicated for intestinal failure patients that are at high risk for life- threatening PN associated complications: • Consensus on “high risk” patients controversial • Timing of referral remains controversial • Additional organs are included with Intestinal transplants based on: • Failure /dysfunction of native organs (liver, stomach, colon) • Potential for reducing rejection (liver, spleen) • Technical considerations (pancreas)

  24. Summary (cont’d) • Due to high infection and rejection risk post-transplant surveillance is critical to optimize level of immunosuppression. • Viral activity (PCR) • Histologic evaluation for rejection (Endoscopic Biopsy) • Level of immunosuppression (Prograf, etc.) • Overall outcomes with intestinal transplant are improving: • Outcomes with intestine only candidates are superior to intestine + liver candidates • 1st year patient and graft loss is higher with intestine + liver • Liver has survival benefit for SB graft in >1 yr survivors

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