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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 2016-03-17 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 Background- 中国肝移植现状 Survival 85%, 4years 75%, 5years Recurrence 8%, 4years Background- 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 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 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 Recommendations and Rationales Systemic Disease Kidney 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 the development of CKD in LT recipients Metabolic Syndrome Metabolic Syndrome Recommendations and Rationales Systemic Disease Metabolic 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 iron overload, renal replacement therapy extended intervals of intensive care Recommendations and Rationales INFECTIOUS DISEASE Fungal Infections Blood cultures are most helpful for the diagnosis of Candida bloodstream infections and Blastomyces Cryptococcal antigen testing of cerebrospinal fluid or blood is most helpful for the diagnosis of Cryptococcus Urinary histoplasmosis and Blastomyces antigens are useful for the diagnosis of disseminated histoplasmosis and blastomycosis, respectively Recommendations and Rationales INFECTIOUS DISEASE Pneumocystis jirovecii All LT recipients should receive prophylaxis 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- methoprim sulfamethoxazole Recommendations and Rationales INFECTIOUS 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-containing regimens can be consid- ered, although the duration of treatment will need to be extended. Recommendations and Rationales INFECTIOUS DISEASE HIV HIV-infected LT recipients receiving HAART require frequent monitoring of CNI levels because of the significant interaction between antiretrovirals and CNIs Standard prophylaxis for CMV is recommended for HIV- infected LT recipients receiving HAART, and lifelong Pneumocystis pneumonia prophy laxis is the norm Recommendations and Rationales INFECTIOUS DISEASE Recommendations and Rationales IMMUNIZATIONS Recommendations and Rationales IMMUNIZATIONS All LT recipients should receive an annual influenza vaccination All LT recipients should avoid live virus vac- cines (g
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