POSTTRANSPLANT CONVERSION FROM CYCLOSPORINE TO AZATHIOPRINE - EFFECT ON CARDIOVASCULAR RISK PROFILE

被引:16
作者
SUTHERLAND, F
BURGESS, E
KLASSEN, J
BUCKLE, S
PAUL, LC
机构
[1] Department of Surgery, University of Calgary Foothills Hospital, Calgary, T2N 2T9, Alberta
[2] Department of Medicine, University of Calgary, Foothills Hospital, Calgary, T2N 2T9, Alberta
关键词
CONVERSION; CYCLOSPORINE; KIDNEY TRANSPLANTATION; CARDIOVASCULAR RISK;
D O I
10.1007/BF00336354
中图分类号
R61 [外科手术学];
学科分类号
摘要
The benefits of long-term cyclosporin (CyA) therapy are not yet established and must be weighed against its toxicity. We studied cardiovascular risk factors in 25 patients who received a kidney transplant between 1985 and 1989 and in whom CyA was discontinued. The protocol for discontinuing CyA involved starting azathioprine (Aza) and then weaning CyA over 6 weeks without changing the prednisone dose. Parameters collected from the patients' charts 3 months before (pre) and 3 months after conversion (post) and at the most current follow-up (cur) included serum creatinine, cholesterol, blood pressure, and anti-hypertensive medication. The severity of the hypertension was graded, based on a hypertension index reflecting the nature and dose of the anti-hypertensive medication. Of the 25 patients in whom CyA was discontinued, 2 experienced a rejection episode during conversion and were switched back to CyA; 1 patient had a rejection episode after conversion but remained on Aza. Converted patients demonstrated improved renal function (1/Cr pre 0.69 +/- 0.20, post 0.84 +/- 0.23, P < 0.05), lower serum cholesterol levels (pre 6.8 +/- 1.0, post 5.8 +/- 1.2, P < 0.05), lower mean arterial pressure (pre 111 +/- 14, post 102 +/- 8, P < 0.05) and a lower hypertension index (pre 2.45 +/- 2.77, cur 1.62 +/- 1.70, P < 0.05). Although conversion may carry some risk of acute rejection, it improves graft function and, the cardiovascular risk profile significantly.
引用
收藏
页码:129 / 132
页数:4
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共 21 条
[1]  
Ballantyne C.M., Podet E.J., Patsch W.P., Harati Y., Appel V., Gotto A.M., Young J.B., Effect of cyclosporine therapy on plasma lipoprotein levels, JAMA, 262, pp. 53-56, (1989)
[2]  
Bennett W., Porter G., Cyclosporine associated hypertension, Am J Med, 85, pp. 131-139, (1980)
[3]  
Brunchman T.E., Brookshire C.A., Smooth muscle cell proliferation by conditioned media from cyclosporine-treated endothelial cells: a role of endothelin, Transplant Proc, 2, pp. 967-969, (1991)
[4]  
Chan M.K., Varghese Z., Moorhead J., Lipid abnormalities in uremia dialysis and transplantation, Kidney Int, 19, pp. 625-637, (1981)
[5]  
Chan M.K., Varghese Z., Persuad J.W., The role of multiple pharmacotherapy in the pathogenesis of hyperlipidemia after renal transplantation, Clin Nephrol, 15, pp. 309-316, (1981)
[6]  
Ellis C.N., Gorsulowsky D.C., Hamilton T.A., Billings J.K., Brown M.D., Headington J.T., Cooper K.D., Boodsguard O., Duell E.A., Annesly T.M., Turcotte J.G., Voorhees J.J., Cyclosporine improves psoriasis in double-blind study, JAMA: The Journal of the American Medical Association, 256, pp. 3110-3116, (1986)
[7]  
Harris K.P.G., Russell G.I., Parvin S.D., Veitch P.S., Walls J., Alteration in lipid and carbohydrate metabolism attributable to cyclosporine A in renal transplant patients, BMJ, 292, (1986)
[8]  
Higgins R.M., Ratcliffe P.J., Hypercholesterolaemia and vascular disease after transplantation, Transplantation Reviews, 5, pp. 131-149, (1991)
[9]  
Ibels L.S., Stewart J.H., Mahony J.F., Sheil A.G.R., Deaths from occlusive arterial disease in renal allograft recipients, BMJ, 3, pp. 522-554, (1974)
[10]  
Jackson J.M., Lee H.A., The role of propranolol therapy and proteinuria in the etiology of post renal transplantation hyperlipidaemia, Clin Nephrol, 18, pp. 95-100, (1982)