The effect of mannitol in living-donor renal graft function : A randomized controlled trial / Basma Gaber Elbaz ; Supervised Manar Mahmod Elkholy , Nazmy Edward Seif , Saheer Alkhashab
Material type:
- تأثير المانيتول على زراعة الكلى و المأخوذة من متبرعين احياء : دراسة مقارنة مستقبلية عشوائية [Added title page title]
- Issued also as CD
Item type | Current library | Home library | Call number | Copy number | Status | Barcode | |
---|---|---|---|---|---|---|---|
![]() |
قاعة الرسائل الجامعية - الدور الاول | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.11.01.M.Sc.2014.Ba.E (Browse shelf(Opens below)) | Not for loan | 01010110064919000 | ||
![]() |
مخـــزن الرســائل الجـــامعية - البدروم | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.11.01.M.Sc.2014.Ba.E (Browse shelf(Opens below)) | 64919.CD | Not for loan | 01020110064919000 |
Browsing المكتبة المركزبة الجديدة - جامعة القاهرة shelves Close shelf browser (Hides shelf browser)
Thesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Anaesthesia
Renal transplant (RT) is the optimal treatment for the majority of patient with end - stage renal failure (ESRF). Many studies had tried to express various roles allowing for a successful renal transplantation using many techniques and drugs applied on both donors and recipients. The only setting in which the mannitol is thought to be a useful renal protectant is in renal transplantation, however, much of the work in this area was completed in the 1980s and early in 1990s. And according to some investigators most of these studies lack scientific rigors. The study included 30 recipient patients (age 18-60), suffering from end stage renal failure because of deferent etiology, of both sex, they were divided into two group according to intra - operative kidney protective management strategy given to their living donors either containing mannitol or not. Each consists of 15 patients: In one group; the donors received a solution of mannitol 20%, at a dose of 0.5 mg / kg IV infusion intra operative, 30 minutes before vascular clamping. The other group received routine intra-operative fluids. Follow up data of early post operative graft function was collected over 14 days, and at 1, 2, and 3 months
Issued also as CD
There are no comments on this title.