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Methylprednisolone (Solu-Medrol®)/Prednisone
Day 1: 2 x 50 mg
Day 2: 2 x 40 mg
Day 3: 2 x 30 mg
Day 4: 2 x 20 mg
Day 5: 2 x 10 mg
Day 6 to end of third week: 20 mg
Week 4: 17.5 mg
Month 2: 15 mg
Month 3: 10 mg
Month 4: 7.5 mg
Month 6: 5 mg which is then titrated down
to 2.5 mg at a time every two weeks until
**Specific patients may be tapered off at 6

Day 1: 2 mg PO BID and titrated to maintain
a tacrolimus level of 12-15 ng/dl and then
blood levels of,
Week 2: 12-15 ng/dl
Week 4: 10-12 ng/dl
Month 9: 8-10 ng/dl
Month 12: 5-8 ng/dl
Week 1-4: 250-300 ng/dl
Week 4: 250 ng/dl
Day 1 to Month 5: 500 mg BID
Month 6: 250 mg BID
Month 9: 250 QD and then discontinued one
year post transplant
**Used only if patient is intolerant to other
medications or in case of calcineurin

Start on Day 3 and continue until for 3 mo (Valcyte®) Trimethoprim/Sulfamethoxazole (Septra®) Dosed MWF beginning on Day 3 for 12 mo. If a patient is allergic then he/she receive a Pentamidine treatment monthly for one year Initiated Day 0 and dosed BID until one month post transplant at which time it is reduced to daily dosing if no history of PUD/GERD 500 mg PO TID initiated one month post transplant Resumed or initiated if osteopenia or osteoporosis diagnosed
Our basic immunosuppressive protocol is steroids and tacrolimus

If the patient presents with any of the following fever, jaundice, ascites, elevation of liver tests we recommend that the trasplant hepatologist be contacted immediately. We may request that the following tests be preformed either locally or at LLUMC. 1. Doppler ultrasound of liver /MRI/MRA/MRCP to evaluate for bile duct stricture, vessel 2. Liver biopsy to evaluate for rejection; recurrent disease; preservation injury; other conditions ACUTE CELLULAR REJECTION PROTOCOL

Methylprednisolone (Solu-Medrol®) Give 500 mg IV per day for three days in a peripheral
vein. Anti-thymocyte globulin (Thymoglobulin®) (1.5 mg/kg via central venous catheter daily
x 5 days) can be given in event of steroid resistant rejection. A follow-up liver biopsy should be
if liver tests are not normalizing 3-5 days after completion of the treatment.
The decision to treat the patient for hepatitis C after liver transplantation is individualized based upon recurrence of the disease, time from transplantation, elevation of liver tests, Immunosuppression level, and the liver biopsy. Treatment id individualized by genotype, biopsy results, and viral load. At this time we are using Pegilated interferon and ribavirin. In conjunction with our nurse practitioner we provide individualized patient education and monitoring though an education class and close evaluation for 6 months to 1 year for efficacy of treatment. HEPATITIS B IMMUNE GLOBULIN (HBIG) PROTOCOL
HBIG is now standard therapy for patients undergoing transplantation for acute or chronic
hepatitis B. Intravenous use of HBIG for this indication is not experimental, but off label. The
first dose is given in the operating room during the anhepatic phase of the surgery. The dose is
10,000 IU (35 ml when concentration is approximately 250 IU/ml). Patients will then receive a
daily dose for the first 7 postoperative days and then as needed as an outpatient based upon blood
levels. The goal is to maintain anti-HBs level > 150 mIU/ml. Intramuscular doses of 5-10 ml
according to HB surface antibody level done on an outpatient basis.
Intravenous HBIG:
• Dose: 35 ml (approximately 10,000 IU) every day through POD 7 then monthly • Dilute each dose in 200 cc of normal saline
• Meperidine: 50 mg IV for patients with a history of significant muscular or back pain Monitoring:
• Hepatitis surface quantitative antibody monthly (maintain a level > 150 mIU/ml) • May calculate anti-HBs clearance to aid in determining redose timing and development • HBsAg every 2 months for the first year and then less frequently (3-4 times/year) ANTIVIRAL THERAPY
• Lamivudine: 100 mg PO daily/Adefovir: 10 mg PO or Enteivir 0.5mg PO daily continued indefinitely.
• Monthly HBV DNA (quantitative) in addition to regular laboratory testing during • HBV DNA PCR qualitative testing done when undetectable virus level by quantitative • After viral suppression achieved (HBV DNA-) follow HBsAg and HBeAg assays every month and recheck HBV DNA (qualitative) only with evidence of increase in liver enzymes • Adjust dose for patients with renal impairment PROCEDURAL ANTIBIOTIC PROPHYLAXIS PROTOCOL

I. Infective Endocarditis Prophylaxis (SBE) - per LLUMC guidelines
• Amoxicillin 3 gm PO1 hr before procedure and 1.5 gm PO 6 hours after the first dose Mitral valve prolapse with regurgitation, murmur or auscultation -Clindamycin 300 mg PO 1 hr before and 6 hours later for dental and upper GI procedures -Ciprofloxacin 750 mg PO 1 hr before and 6 hours after first dose for lower GI procedures (colon, rectum, bladder) -Cefotaxime 1 gm IV before cholangiogram; repeat in 12 hours for T-tube cholangiogram/biliary tract manipulations (i.e. ERCP) I. Liver Biopsy Prophylaxis
• Cefotaxime 1 gm IV before procedure or Levofloxacin 250-500 mg PO or IV before
III. Biliary Tract Procedures
• Ciprofloxacin 750 mg PO 1 hr before and 6 hours after first dose if patient is allergic DIABETES MELLITUS PROTOCOL*
Patient will be monitored postoperatively for the development and management of diabetes mellitus. Dietary consultation and when appropriate, referral to the endocrinologist/Diabetes Treatment Center, will be initiated. SKIN CANCER PROTOCOL*
Patients will be counseled regarding the need for skin cancer prevention methods, e.g. sunscreen, minimal exposure, use of hats. When appropriate, referral to dermatology service will be initiated. OSTEOPOROSIS PROTOCOL*
Patients will be screened for osteopenia and osteoporosis using bone mineral density scans. Treatment with Fosamax®, Actonel®, or Miacalcin® spray will be initiated along with calcium plus Vitamin D as needed. Yearly repeat bone mineral density will be obtained to follow for disease progression or improvement. When necessary, referral to the Loma Linda Osteoporosis Center will be initiated. TRAVEL/IMMUNIZATIONS
Patients will be discouraged from international travel for the first 3 months post-transplant. After
three months they are to alert their coordinator regarding foreign travel and receive education on
vaccinations (no live vaccines), dietary and sanitary issues, medications (need to carry extra
doses), etc.
Patients will need to receive boosters or additional vaccinations : Flu vaccination yearly,
pneumovax every five years, HBV booster at 7 years following initial series.

* At 3 months post-transplant, patients are transitioned to their
Hepatologist/Gastroenterologist for long-term care and follow-up.
Patients will be monitored long-term for the following issues:

Management of graft function
Recurrent liver disease


Microsoft word - guidelines for poster.doc

National Symposium on Innovation in TB Diagnostics, Drug Targets and Biomarkers C.M.E. On Innovation in Molecular and Immunodiagnostics for PTB & EPTB in India (*Supported by KHS, AstraZeneca, ICMR, DBT, CSIR, DST & MCI) January 27 –28, 2014 JB Tropical Disease Research Centre, Mahatma Gandhi Institute of Medical Sciences, Sevagram - Poster Session: There

Microsoft word - doc_c7ccd459231fa209d193ed6696d906ae_1261472873630_40

THERAPEUTIC USE EXEMPTION (TUE) APPLICATION FORM Please complete all sections in capital letters or type. Incomplete applications will be returned. I apply for approval from the International Cricket Council’s Therapeutic Use Exemption Committee (the ICC’s TUEC) for the therapeutic use of a Prohibited Substance or Method on the current WADA Prohibited List, a copy of which ca

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