《肝移植术后管理》PPT课件

1、Long-Term Management of the Successful Adult Liver Transplant (2012 Practice Guideline) 感染内科科内业务学习陈洪涛2016-03-17Background-中国肝移植现状Background-中国肝移植现状Background-中国肝移植现状Background-中国肝移植现状Background-中国肝移植现状Background-中国肝移植现状Background-中国肝移植现状Background-中国肝移植现状Background-中国肝移植现状Survival 85%, 4years 75%, 5

2、yearsRecurrence 8%, 4yearsBackground-中国肝移植现状 杭州标准Background-美国肝移植现状 Background-美国肝移植现状 Characteristics of adult liver transplant recipients, 2002 & 2012Background1. Liver Transplantation (LT) as a Treatment for End-stage Liver Disease / Mortality After LT / Morbidity After LT2. Complications of

3、Portal Hypertension After LT3. Liver Tests / Vascular Thrombosis4. Immunosuppression5. Late Rejection6. Promoting Health After LT7. Bone Health. Contents8. Systemic Disease9. Nutrition and Obesity10. Oncology11. Reproductive Health12. Infectious Disease13. Immunizations14. Hepatitis（Viral, PBC/PSC,

4、AIH, ALD, NASH/NAFLD ） Contents Recommendations and Rationales Morbidity After LT Clinical features of liver failure and portal hypertension resolve rapidly after LT. The exception is splenomegaly, which may persist for years Variceal hemorrhage is very unusual unless the patient has an occluded por

5、tal vein. The late emergence of hepatic encephalopathy suggests the development of clandestine cirrhosis or a persistent portosystemic shunt Late-onset ascites or peripheral edema may indicate stenosis of the inferior vena cava or portal vein anastomosis. Recommendations and Rationales Complications

6、 of Portal Hypertension After LT Recommendations and Rationales LIVER TESTS Recommendations and Rationales Vascular ThrombosisHepatic artery thrombosis (HAT) or stenosis may present clinically after 3 months, as : intrahepatic non-anastomotic strictures and/or sterile or infected fluid collections w

7、ithin the liver, sometimes referred to as bilomas ischemic cholangiopathy or biliary cast syndrome. Recommendations and Rationales Immunosuppression the target levels after 3 months, whole blood trough levels Tacrolimus - 5 to 10 ng/mL Cyclosporine-100 to 150 ng/mL Sirolimus - 5 ng/ mL. Recommendati

8、ons and Rationales Late Rejection Cellular rejection (also known as acute cellular rejection and late-onset rejection) Liver tests nonspecific abnormalities with a rise in serum bilirubin and aminotransferases Histologically, cellular rejection is characterized by the triad of inflammatory bile duct

9、 damage, subendothelial inflammation of the portal, central, or perivenular veins, and a predominantly lymphocytic portal inflammatory infiltrate with neu- trophils and eosinophils in addition Ductopenic rejection (also known as vanishing bile duct syndrome) Recommendations and Rationales Late Rejec

10、tionCellular rejection-Risk factors Reduction of immunosuppression (whether iatro- genic or due to noncompliance). Pre-LT autoimmune liver disease. Concurrent administration of interferon (for HCV treatment). The differential diagnosis includes infection, recurrent and de novo autoimmune disease, an

11、d drug toxicity Recommendations and Rationales Late RejectionCellular rejection-Treatment Mild : an increase in maintenance levels of immunosuppression Moderate or severe: a short course of increased immunosuppression (eg, methyl predni- sone at 500 mg/day or prednisolone at 200 mg/day for 3 days) f

12、ollowed by an increase in the baseline immunosuppression Only approximately half of patients, with approximately 25% developing a further episode of cellular rejection and 25% developing ductopenic rejection. Recommendations and Rationales Late RejectionDuctopenic rejection -Risk factors Recurrent a

13、nd unresponsive cellular rejection. Transplantation for autoimmune disease. Exposure to interferon Loss of a previous graft to ductopenic rejection. The differential diagnosis includes recurrent disease (PBC or PSC) and drug toxicity. Recommendations and Rationales Late RejectionDuctopenic rejection

14、 Treatment ncreased immunosuppression, and an increase in or switch to tacrolimus may be effective in some early cases. when fewer than 50% of the portal tracts contain bile ducts, the condition progresses to graft failure. Recommendations and RationalesPromoting Health After LT Frequent handwashing

15、 reduces the risk of infection with pathogens acquired by direct contact, including Clostridium difficile, community-acquired viral infections, and pathogens found in soil Shoes, socks, long-sleeve shirts, and long pants should be worn for activities that will involve soil exposure and tick exposure

16、 and also to avoid unnecessary sun exposure During periods of maximal immunosuppression, LT recipients should avoid crowds to minimize exposures to respiratory illnesses Work in high-risk areas, such as construction, animal care settings, gardening, landscaping, and farming, should be reviewed with

17、the transplant team Recommendations and RationalesPromoting Health After LT LT recipients should avoid the consumption of water from lakes and rivers LT recipients should avoid unpasteurized milk products and raw and undercooked eggs and meats LT recipients should avoid high-risk pets All LT recipie

18、nts should be educated about the importance of sun avoidance and sun protection through the use of a sun block with a sun protection factor of at least 15 and protective clothing. They should be encouraged to examine their skin on a regular basis and report any suspicious or concerning lesions to th

19、eir physicians the sustained cessation of smoking is the most important pre- ventative intervention Recommendations and RationalesBone HealthRecommendations and RationalesBone Health In the first 5 years after transplantation, screening by BMD should be done yearly for osteopenic patients and every

20、2 to 3 years for patients with normal BMD; thereafter, screen- ing depends on the progression of BMD and on risk factors If osteopenic bone disease is confirmed or if atraumatic fractures are present, then patients should be assessed for risk factors for bone loss; in particular, this should include

21、 an assessment of calcium intake and 25-hydroxy- vitamin D levels, an evaluation of gonadal and thyroid function, a full medication history, and thoracolumbar radiography The osteopenic LT recipient should perform regular weight-bearing exercise and receive calcium and vitamin D supplements Recommen

22、dations and RationalesSystemic DiseaseKidney Disease Urinary protein quantification using the concentration ratio of protein to creatinine in a spot urine specimen should be evaluated at least once yearly The reduction or withdrawal of CNI-associated immunosuppression is an appropriate response to t

23、he development of CKD in LT recipientsMetabolic Syndrome Metabolic Syndrome Recommendations and RationalesSystemic DiseaseMetabolic Syndrome The treatment of DM after LT should aim for an HBA1c target goal of 40 U of blood products), Choledocho-jejunostomy, reoperation, retransplantation, hepatic ir

24、on overload, renal replacement therapy extended intervals of intensive care Recommendations and RationalesINFECTIOUS DISEASE Fungal Infections Blood cultures are most helpful for the diagnosis of Candida bloodstream infections and Blastomyces Cryptococcal antigen testing of cerebrospinal fluid or bl

25、ood is most helpful for the diagnosis of Cryptococcus Urinary histoplasmosis and Blastomyces antigens are useful for the diagnosis of disseminated histoplasmosis and blastomycosis, respectivelyRecommendations and RationalesINFECTIOUS DISEASE Pneumocystis jirovecii All LT recipients should receive pr

26、ophylaxis against P. jirovecii with trimethoprim-sulphame- thoxazole (single strength daily or double strength 3 times per week) for a minimum of 6 to 12 months after transplantation (grade 1, level A). Atovaquone and dapsone are the preferred alternatives for patients who are intolerant of tri- met

27、hoprim sulfamethoxazole Recommendations and RationalesINFECTIOUS DISEASE Tuberculosis Because of the risk of a marked reduction in CNI and mTOR inhibitor levels with rifampin coadministration, the doses of CNIs will need to be increased 2- to 5-fold at the initiation of treatment. Rifabutin may be substituted for rifampin to reduce the impact on drug levels, or nonrifampin-con