Therapeutic window of mycophenolate mofetil for preventing acute graft rejection following renal transplantation.
- Author:
Lixin YU
1
;
Minjie ZHOU
;
Min LUO
Author Information
- Publication Type:Journal Article
- MeSH: Graft Rejection; drug therapy; prevention & control; Graft Survival; Humans; Immunosuppressive Agents; administration & dosage; therapeutic use; Kidney Transplantation; Methylprednisolone; Mycophenolic Acid; administration & dosage; analogs & derivatives; therapeutic use; Survival Rate; Time Factors
- From: Journal of Southern Medical University 2014;34(12):1842-1845
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo determine the optimal dose range (therapeutic window) of mycophenolate mofetil (MMF) for preventing acute graft rejection following renal transplantation.
METHODSThe trough concentration of MMF (MPA-C0) at 12 h after oral administration of the drug (two doses daily given at an interval of 12 h) was monitored in 110 renal transplant recipients within a month, in 2-3 months, and over 4 months after the transplantation using EMIT method. The occurrence of acute graft rejection and drug toxicity were observed in all the patients during the one-year follow-up.
RESULTSs The incidence of acute graft rejection after transplantation was 13.64% (15/110) in these patients. Drug toxicity and complications occurred in 32.73% (36/110) of the patients, including 12 cases with reduced white blood cell counts, 10 with MMF cid-associated diarrhea, 10 with infection, 4 with liver function damage. Acute rejection was successfully reversed after methylprednisolone treatment and drug toxicity was managed by corresponding treatment and adjustment of MMF dose. No deaths or graft removal occurred in these patients. The ROC curve showed that a MPA-C0 of 1.40-2.80 mg/L was optimal in preventing acute rejection after the transplantation and reducing adverse drug effects.
CONCLUSIONMonitoring MPA-C0 and individualized MMF dosing help to prevent acute graft rejection, reducing drug toxicity and complications, and improving graft survival rate after renal transplantation.