Most bacterial and fungal infections occur in the number one period of time postoperatively, hence the rationale for fastener prophylaxis at 2 months. If the affected role is receiving an anticonvulsant drug or some other strong hepatic microsomal enzyme communicator, then we continue fluconazole indefinitely in arrangement to maintain reference calcineurin inhibitor levels, or postiche to some other strong hepatic enzyme inhibitor (ie, erythromycin, diltiazem).
I have little content with (or secret in) nystatin and clotrimazole as effective agents in pancreas animal tissue recipients, although we use these agents routinely after kidney operation in lieu of fluconazole. The newer antifungal agents (itraconazole, voriconazole, posaconazole, caspofungin, micafungin) and amphotericin preparations are not indicated unless Aspergillus is identified or the affected role has a chronicle of Cryptococcus or resistant Candida pathological process. Probably one of the most important points is to avoid prolonged use of broad-spectrum antibiotics and to remove indwelling devices in a timely vogue. Using the described anti-infective prophylaxis regimen, our incidences of resistant bacterial and any fungal infections after pancreas organ transplant have been extremely low.
Subscribe to:
Post Comments (Atom)
No comments:
Post a Comment