Transplantation Flashcards
The most appropriate treatment of a lymphocoele following renal transplantation is
A. Observation until resolution
B. Percutaneous aspiration
C. Laparoscopic or open peritoneal window
D. Open exploration with sclerotherapy
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A positive crossmatch means:
A. There are no immunologic problems so one may proceed with the transplant
B. Will likely result in only mild rejection sometime after the 1st week
C. The recipient has preformed antibodies to donor antigens
D. Both the donor and recipient are CMV positive
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Hyperacute rejection following organ transplantation is most often due to:
A. ABO incompatibility
B. Rh incompatibility
C. Previous sensitized T cells
D. Macrophages
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Which of the following immunosuppressive drugs inhibits IL-2 synthesis?
A. Azathioprine
B. Mycophenolate mofetil
C. Tacrolimus
D. Sirolimus
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Post transplant lymphoproliferative disorder has been most commonly linked to:
A. HSV
B. RSV
C. EBV
D. Influenza virus
EBV
Two weeks following kidney transplantation, a patient develops respiratory insufficiency requiring admission to the ICU. Chest x-ray shows diffuse infiltrations and bronchial washings show cells with inclusion bodies. The most appropriate therapy is:
A. Ganciclovir
B. Acyclovir
C. Bactrim
D. Penicillin
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A 35-year-old male POD 6 from a cadaveric renal transplantation develops a rise in creatinine. Ultrasound of the graft is normal. The biopsy shows acute tubulitis. This is consistent with?
A. Acute rejection
B. Urinary tract infection
C. Chronic rejection
D. Renal vein thrombosis
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Tacrolimus levels may be decreased in patients who are also taking:
A. Phenytoin
B. Erythromycin
C. Cimetidine
D. Fluconazole
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The most common etiology of liver failure in patients undergoing liver transplantation is:
A. Alcoholic cirrhosis
B. Metabolic disease
C. Chronic hepatitis
D. Fulminant (acute) liver failure
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Hyperacute rejection is caused by
A. Preformed antibodies
B. B-cell–generatedantidonorantibodies
C. T-cell–mediated allorejection
D. Nonimmunemechanism
Answer: A
Hyperacute rejection, a very rapid type o rejection, results in irreversible damage and graft loss within minutes to hours after organ reperfusion.
It is triggered by preformed antibodies against the donor’s human leukocyte antigen (HLA) or ABO blood group antigens.
These antibodies activate a series of events that result in diffuse intravascular coagulation, causing ischemic necrosis of the graft.
Fortunately, pretransplant blood group typing and cross-matching (in which the donor’s cells are mixed with the recipient’s serum, and then destruction of the cells is observed) have virtually eliminated the incidence of hyper acute rejection. (SeeSchwartz10thed.,p.324.)
The mechanism of action of Azathioprine is:
A. Inhibition of calcineurin
B. Interference with DNA synthesis
C. Binding of FK-506 binding proteins
D. Inhibition of P7056 kinase
Answer: B
An antimetabolite, azathioprine (AZA) is converted to 6-mercaptopurine and inhibits both the de novo purine synthe- sis and salvage purine synthesis.
AZA decreases T-lymphocyte activity and decreases antibody production.
It has been used in transplant recipients or more than 40 years, but became an adjunctive agent after the introduction of cyclosporine. With the development of newer agents such as mycophenolate mofetil (MMF), the use of AZA has decreased significantly. However, it is preferred in recipients who are considering conceiving a child, because MMF is teratogenic in females and can cause birth defects. AZA might be an option or recipients who cannot tolerate the gastrointestinal (GI) side effects of MMF.
The most significant side effect of AZA, often dose-related, is bone marrow suppression.
Leukopenia is often reversible with dose reduction or temporary cessation of the drug. Other significant side effects include hepatotoxicity, pancreatitis, neoplasia, anemia, and pulmonary fibrosis. Its most significant drug interaction is with allopurinol, which blocks AZA’s metabolism, increasing the risk of pancytopenia.
Recommendations are to not use AZA and allopurinol together, or if doing so is unavoidable, to decrease the dose of AZA by 75%. (See Schwartz 10th ed., p. 326.)
Which of the following is NOT a side effect of cyclosporine?
A. Interstitial fibrosis of the renal parenchyma
B. Gingival hyperplasia
C. Hirsutism
D. Pancreatitis
Answer: D
(See Schwartz 10th ed.,
Table 11-4, p. 327.)
Post-renal transplant graft thrombosis usually occurs
A. Within 2 to 3 days
B. Within 2 weeks
C. Within 1 month
D. Within 3 months
Answer: A
One of the most devastating postoperative complications in kidney recipients is graft thrombosis. It is rare, occurring in fewer than 1% of recipients.
The recipient risk factors include a history of recipient hypercoagulopathy and severe peripheral vascular disease; donor-related risk actors include the use of enbloc or pediatric donor kidneys, procurement damage, technical factors such as intimal dissection or torsion of vessels, and hyperacute rejection. Graft thrombosis usually occurs within the first several days posttransplant.
Acute cessation of urine output in recipients with brittle posttransplant diuresis and the sudden onset of hematuria or graft pain should arouse suspicion of graft thrombosis.
Doppler ultrasound may help confirm the diagnosis. In cases of graft thrombosis, an urgent thrombectomy is indicated; however, it rarely results in graft salvage. (See Schwartz 10th ed., p. 339.)
The 1-year graft survival after renal transplantation is
A. 35–40%
B. 50–55%
C. 75–80%
D. 92–96.5%
Answer: D
According to the 2010 Scientific Registry of Transplant Recipients (SRTR) annual report, a total of 84,614 adult patients were on the kidney transplant waiting list, including 33,215 added just that year.
Yet in 2009, only 15,964 adult kidney transplants were performed in the United States (9912 with a deceased donor and 6052 with a living donor). Of note, the number of patients added to the kidney transplant waiting list has increased every year, but the number of kidney transplants performed has been declining since 2006.
On the positive side, posttransplant outcomes have continued to improve: in 2009, the 1-year graft survival rate with a living donor kidney was 96.5%; with a deceased donor kidney, the rate was 92.0%. (See Schwartz 10th ed., p. 334.)
After completion of the vascular anastomoses, drainage of a transplanted pancreas is accomplished by anastomosis to
A. Right colon
B. Left colon
C. Duodenum
D. Bladder or small bowel
Answer: D
Over the years, different surgical techniques have been described for (1) the management of exocrine pancreatic secretions and (2) the type of venous drainage.
For the secretions, the two most common techniques are drainage of the duodenal segment to the bladder (bladder drainage) or to the small bowel (enteric drainage) (Figs. 11-1 and 11-2).
For venous drainage, systemic venous drainage is preferred over portal venous drainage. (See Schwartz 10th ed., Figures 11-12 and 11-13, pp. 341–343.)