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Analysis of Infectious Complications Occurring After Solid-Organ Transplantation
Kenneth L. Brayman, MD, PhD;
Edic Stephanian, MD;
Arthur J. Matas, MD;
Walter Schmidt;
William D. Payne, MD;
David E. R. Sutherland, MD, PhD;
Paul F. Gores, MD;
John S. Najarian, MD;
David L. Dunn, MD, PhD
Arch Surg. 1992;127(1):38-48.
Abstract
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To improve our understanding of posttransplant infections, we analyzed bacterial, viral, fungal, parasitic, and other infections in 604 consecutive recipients of kidney (n = 518), kidney-pancreas (n = 82), kidney-liver (n = 3), or kidney-islet (n = 1) allografts (355 cadaveric, 14 living-unrelated, 235 living-related donors) who also received cyclosporine, azathioprine, and prednisone immunosuppression. Recipients of cadaveric grafts received additional induction immunosuppression (antilymphocyte globulin or murine monoclonal antibody OKT3). Rejection episodes were treated with high-dose steroids, and either antilymphocyte globulin or OKT3 was administered when clinically indicated. Perioperative antibiotics and posttransplant prophylactic acyclovir sodium or ganciclovir sodium, trimethoprim-sulfamethoxazole, and clotrimazole or nystatin (Mycostatin) were administered to all recipients. Two hundred thirteen patients (35.3%) were found to have had no identifiable infections, while 391 (64.7%) had either isolated bacterial (97 [16.1 %]), viral (53 [8.8%]), or fungal (34 [5.6%]) infections or combination (concurrent or sequential) infections with bacterial plus viral (46 [7.6%]), bacterial plus fungal (66 [10.9%]), viral plus fungal (20 [3.3%]), bacterial plus viral plus fungal (64 [10.6%]), or bacterial plus viral plus fungal plus parasitic (11 [1.8%]) pathogens in the posttransplantation period. Renal allograft survival (percentage, actuarial method) was diminished in patients with infections at both 1 year (91% vs 83%) and 3 years (81% vs 76%) after transplantation, as was actuarial patient survival (1 year, 97% vs 92%; 3 years, 93% vs 88%). We conclude that infection remains a major cause of both patient demise and allograft loss following successful solid-organ transplantation.
(Arch Surg. 1992;127:38-48)
Author Affiliations
From the Department of Surgery, University of Minnesota, Minneapolis. Dr Brayman is a recipient of the American Society of Transplant Surgeons Sandoz Transplant Fellowship and the American Philosophical Society Daland Fellowship.
Footnotes
Accepted for publication September 8, 1991.
Presented at the Eleventh Annual Meeting of the Surgical Infection Society, Ft Lauderdale, Fla, April 10, 1991.
Reprints not available.
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