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An adult cadaver liver is split, and the left lobe or lateral segment is transplanted to the child.
Adult living donors donate their left lateral segment to the child.
E Operative strategy
The procedure generally requires 6–10 hours to perform.
Removal of the diseased liver requires dissection of the porta hepatitis, the inferior vena cava, and the diaphragmatic and retroperitoneal attachments of the liver. The blood flow to the diseased liver is interrupted, and the liver is removed. The patient is then anhepatic and requires intensive monitoring to maintain homeostasis. A segment of the retrohepatic vena cava may be removed with the liver, interrupting venous return.
Implantation of the new liver
External venovenous bypass from the femoral and portal veins to the axillary vein may be used to bypass the inferior vena cava.
Venous anastomoses are created for the suprahepatic vena cava, infrahepatic vena cava, and portal vein. These veins can then be opened, supplying the liver with warm, oxygenated blood and reestablishing caval flow. Alternatively, a piggyback method is used. The donor suprahepatic cava is anastomosed to the preserved recipient vena cava, and the donor infrahepatic cava is closed.
Hemostasis is obtained, the hepatic artery is reconstructed, and the biliary tract is reconstituted to complete the procedure. The donor bile duct is anastomosed either to the recipient's bile duct or a Roux -en -Y segment of jejunum (see Chapter 11).
F
Postoperatively the function of the new liver can be ascertained by production of bile, uptake of potassium by hepatocytes (hypokalemia), correction of coagulopathy, and metabolism of the citrate anticoagulant of blood products (alkalosis).
Nonfunction of the liver graft is manifest by the absence of bile, persistent coagulopathy, and the inability to fully awaken. This uncommon complication (<10%) requires urgent retransplantation.
P.450
Immunosuppression is achieved by either cyclosporine or tacrolimus with steroids and often an antimetabolite.
G Complications and results
Surgical complications requiring reoperation are common, and they relate to any of the five anastomoses between the donor and the recipient. Hepatic artery thrombosis is especially common in children (5%– 10%) and often requires retransplantation. Biliary complications are also fairly common. Anastomotic strictures are more common than leaks, and these usually happen early. Late strictures can be related to rejection.
Acute rejection usually manifests as increased liver function tests and occurs in about 40% of recipients. Fever or jaundice can occur with rejection. Diagnosis is made by liver biopsy. Rejection is almost always reversible.
Chronic rejection , also called vanishing bile duct syndrome, represents immunologic attack on the bile ducts and the small arteries that nourish them. This is uncommon but may require retransplantation because it is generally untreatable.
Post -transplant death is usually related to multiple organ failure. It is usually brought on by a combination of infection or rejection plus nephrotoxicity from cyclosporine or tacrolimus.
Recurrence of hepatitis. Hepatitis B recurrence can be treated with lamivudine. Recurrence of hepatitis C is universal and usually takes an insidious course. The long-term outcome of recurrent hepatitis C is mild or no hepatitis in 40%, moderate hepatitis in 45%, and recurrent cirrhosis in 15% (at 5 years).
Survival of pediatric patients after liver transplantation is slightly better than that of adults.
Survival of adult patients is more variable than survival of children (Table 24 -3). Again, two factors have strong statistical influence.
Diagnosis. The diagnoses of cancer and fulminant hepatic failure are associated with poorer outcomes.
Patients who are more ill at the time of transplantation do not fare as well as those who are less ill.
TABLE 24-3 Patient Survival after Liver Transplantation
Pre-operative Status |
Patient Survival (%) (1 year)Patient Survival (%) (5 years) |
|
Pediatric recipients (all) |
80 |
74 |
|
|
|
Age <1 Year |
74 |
67 |
|
|
|
Age <10 years |
84 |
77 |
|
|
|
Patient status |
|
|
|
|
|
Life support |
61 |
58 |
|
|
|
ICU |
80 |
71 |
|
|
|
Hospitalized |
77 |
71 |
|
|
|
At home |
86 |
80 |
|
|
|
Adult recipients (all) |
81 |
67 |
|
|
|
Patient status |
|
|
|
|
|
Life support |
64 |
55 |
|
|
|
ICU |
74 |
60 |
|
|
|
Hospitalized |
79 |
62 |
|
|
|
|
|
|
|
At home |
86 |
72 |
|
|
|
|
|
|
|
Diagnosis |
|
|
|
|
|
|
|
|
|
Hepatitis C |
82 |
65 |
|
|
|
|
|
|
|
Hepatitis B |
78 |
59 |
|
|
|
|
|
|
|
Cancer |
67 |
32 |
|
|
|
|
|
|
|
Fulminant hepatic failure |
71 |
63 |
|
|
|
|
|
|
|
ICU, intensive care unit. |
|
|
|
|
|
|
|
|
|
|
|
|
|
P.451
V Renal Transplantation
When renal transplantation is successful, patients return to normal lives unencumbered by dialysis.
A Candidates
Patients from newborn to 70 years of age with end -stage renal disease and on maintenance dialysis are typical candidates. Patients with declining renal function who are almost at the stage of requiring dialysis are also candidates.
Renal transplantation is elective in the sense that dialysis is always an option. Therefore, candidates should be stable before transplantation.
Common indications for renal transplant in adults include glomerulonephritis (41%), diabetes mellitus (16%), polycystic disease (13%), hypertension (12%), and pyelonephritis or interstitial nephritis (6%). In children, approximately 50% of candidates have congenital or hereditary renal disease, and the remaining 50% have acquired renal disease.
B Donors
Living related donors represent 30% of kidney transplants. A related donor and recipient share more genes than do unrelated pairs. Three types of histocompatibility match occur between related individuals.
A perfect match (two haplotypes). Two siblings share the same HLA haplotype from both their mother and father. Siblings have a 25% chance of being a perfect match.
A half match (one haplotype). The donor and recipient share one of two HLA haplotypes. Siblings have a 50% chance of being a half match; all parent–child pairs are a half match.
A zero match (no haplotypes). Two siblings share neither haplotype. This situation occurs in 25% of sibling pairs.
Cadaver donors represent 70% of kidney transplant donors. The donor and the recipient can match from zero to six of their HLA antigens (see I F 3 c).
Living unrelated donors represent 3%–4% of kidney transplants and have the same types of matches as