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Bronchial, pulmonary artery, and donor left atrial anastomoses (left atrial patch includes the pulmonary vein orifices) are performed.

The bronchial anastomosis is performed by using a telescoping interrupted suture technique. Wrapping the bronchial anastomosis with a vascularized pedicle of omentum has also been used.

Induction therapy with antilymphocyte sera and avoidance of high-dose steroids (which inhibit bronchial anastomotic healing) is often chosen.

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Double-lung transplants are usually performed through a transverse anterior thoracotomy with or without cardiopulmonary bypass, and the procedure resembles two single -lung transplants. The two bronchial anastomoses are performed like single -lung transplants.

D Postoperatively

the new lung(s) rapidly accommodate, and prompt extubation is the rule. Both rejection and infection are monitored with serial chest radiographs, bronchoscopy with bronchoalveolar lavage or transbronchial biopsy, and measurements of forced expiratory volume in 1 second (FEV 1 , only for rejection surveillance).

E

Donors are scarce because prolonged intubation, chest contusions, aspiration injury, and pneumonia—any of which may contraindicate lung donation—are all common in brain-dead individuals. Bronchoscopy is required before donation and is often performed in the operating room just before the donor surgery.

F Complications and results

Acute rejection is characterized by fever, infiltrates on a chest radiograph, worsened blood gas exchange, and exclusion of infection by bronchoalveolar lavage. The incidence of acute rejection is 60%.

Bronchial anastomotic complications occur in approximately 15% of recipients and are treated with various methods from observation through surgical repair or stent placement. Complete breakdown or dehiscence of the bronchial anastomosis requires surgical repair or retransplantation.

Pneumonia is a common source of morbidity and potential mortality. The prevalence of bacterial pneumonia is 50%. The prevalence of CMV pneumonia varies with the serostatus (prior infection) of the donor and the recipient, but it can be fatal and prophylaxis is required. Fungal infection is uncommon (<10%) but is usually lethal.

Survival is similar for single -lung, double -lung, and heart -lung transplantation, with a 70% 1-year survival rate. Chronic rejection is a significant long-term problem. It is diagnosed histologically as bronchiolitis obliterans or clinically as bronchiolitis obliterans syndrome. Mortality with this diagnosis is high (40% within 2 years).

Survival by diagnosis , from best to worst, is as follows:

Obstructive lung disease

Cystic fibrosis

Restrictive lung disease

Pulmonary hypertension

IV Hepatic Transplantation


Hepatic transplantation is technically difficult because portal hypertension, portosystemic venous collaterals, and coagulopathy are usually present. The postoperative course depends on the initial condition of the patient, the function of the new liver, and technical problems in the perioperative period.

A

Candidates have end -stage liver disease and are likely to die within 1–2 years without transplantation. Most candidates are between 6 months and 70 years of age. Careful evaluation of cardiopulmonary and renal function is essential. Once listed, priority is based on their MELD (Model for End -stage Liver Disease) score. The score is based on bilirubin, creatinine, and international normalized ratio (INR) and ranges from a minimum of 6 to a maximum of 40. The sicker the patient, the higher the values, and the higher the MELD score. Since priority is based on MELD, severity of disease is emphasized rather than waiting time.

B Indications for liver transplantation

Approximately 95% of candidates have chronic disease; the remaining 5% have fulminant hepatic failure , which is a disorder that progresses rapidly.

Adults. In adults, the common chronic diseases that require liver transplantation include cirrhosis from chronic hepatitis C (40%), alcoholic cirrhosis (15%), chronic hepatitis B (<10%), primary biliary cirrhosis (<10%), and primary sclerosing cholangitis (<10%).

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Children. In children who require liver transplantation, more than 50% have biliary atresia as the cause of liver failure.

Three major complications herald end -stage liver disease and indicate the need to consider liver transplantation.

Difficult-to -manage ascites (refractory to treatment, associated with spontaneous bacterial peritonitis, or hydrothorax from peritoneal–pleural leaks)

Encephalopathy

Esophageal variceal hemorrhage (recurrent or associated with hepatic decompensation)

C Four areas of controversy

Alcoholic patients with cirrhosis have the same chance for successful transplantation as do patients with other diagnoses. However, they require screening to identify and exclude those who are likely to return to drinking. Most programs require a minimum of 6 months of abstinence. Alcoholic patients with cardiomyopathy and cerebral atrophy must be excluded.

Patients with fulminant hepatic failure can develop cerebral edema, herniation, and brain death. When fulminant hepatic failure results from a suicide attempt (classically from acetaminophen overdose), the patient can be excluded if the psychiatric history has documented multiple suicide attempts.

Patients with primary hepatic malignancies treated with transplantation have high recurrence rates and a poorer outcome. Therefore, their suitability as candidates is controversial. However, candidates with cirrhosis and a single, small (<5 cm) hepatocellular carcinoma that is not amenable to resection do not have a substantial risk of recurrence and are good candidates.

Patients with cirrhosis from chronic viral hepatitis face risks of recurrent hepatitis and the potential for recurrent cirrhosis. Treatment varies with the causative virus.

D

Donors must match the recipient for size. For small children, the number of size -appropriate donors is insufficient. This problem has alternatives, including:


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.

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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.

 

 

 

 

 

 

 

 

 

 

 

 

 

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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