Graft function 5-7 years after renal transplantation in early childhood

被引:34
作者
Qvist, E [1 ]
Laine, J [1 ]
Rönnholm, K [1 ]
Jalanko, H [1 ]
Leijala, M [1 ]
Holmberg, C [1 ]
机构
[1] Univ Helsinki, Hosp Children & Adolescents, FIN-00290 Helsinki, Finland
关键词
D O I
10.1097/00007890-199904150-00018
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Low recipient age is still a risk factor for graft failure after kidney transplantation (Tx), Detailed prospective reports on long-term graft function in small children after renal Tx are still lacking, Methods. Forty-nine kidney allograft recipients who received transplants before the age of 5 years were followed prospectively. The most common disease was congenital nephrotic syndrome of the Finnish type. Twenty patients were recipients of living related donors (LRD), and 29 were cadaveric kidney (CAD) recipients. All patients received triple immunosuppression. Glomerular filtration rate (GFR), effective renal plasma now (ERPF), sodium, urate, and potassium handling, and concentrating capacity were studied for up to 7 years after Tx. Results. Patient survival 7 years after Tx was 100% for LRD and 96% for CAD recipients. Graft survival was 94% for LRD and 79% for CAD recipients (P=NS) and 89% and 83% for children >2 years and <2 years of age at Tx, respectively (P=NS). Five years after Tx, GFR was 70 vs. 64 and ERPF was 380 vs. 310 ml/min/1.73 m(2) for LRD and CAD recipients, respectively (P=NS). Mean absolute GFR remained stable. GFR was lower in children who received transplants at <2 years than in children who received transplants at >2 years of age, 54 vs. 75 ml/min/1.73 m(2) (P=0.02), Sodium handling remained intact, but hyperuricemia was seen in 43-67%; 17-33% showed abnormal handling of potassium; and most patients had a subnormal concentrating capacity. Conclusions. Excellent long-term graft survival and good graft function can be achieved with triple immunosuppression, even in young CAD kidney recipients.
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页码:1043 / 1049
页数:7
相关论文
共 37 条
[11]   Tubular dysfunction following kidney transplantation [J].
Heering, P ;
Degenhardt, S ;
Grabensee, B .
NEPHRON, 1996, 74 (03) :501-511
[12]   MANAGEMENT OF CONGENITAL NEPHROTIC SYNDROME OF THE FINNISH TYPE [J].
HOLMBERG, C ;
ANTIKAINEN, M ;
RONNHOLM, K ;
ALAHOUHALA, M ;
JALANKO, H .
PEDIATRIC NEPHROLOGY, 1995, 9 (01) :87-93
[13]   PHARMACOKINETICALLY DETERMINED CYCLOSPORINE DOSAGE IN YOUNG-CHILDREN [J].
HOPPU, K ;
KOSKIMIES, O ;
HOLMBERG, C ;
HIRVISALO, EL .
PEDIATRIC NEPHROLOGY, 1991, 5 (01) :1-4
[14]  
HOYER PF, 1990, TRANSPLANT P, V22, P1711
[15]  
KAMEL KS, 1992, J AM SOC NEPHROL, V2, P1279
[16]   Positionally cloned gene for a novel glomerular protein - nephrin - is mutated in congenital nephrotic syndrome [J].
Kestila, M ;
Lenkkeri, U ;
Mannikko, M ;
Lamerdin, J ;
McCready, P ;
Putaala, H ;
Ruotsalainen, V ;
Morita, T ;
Nissinen, M ;
Herva, R ;
Kashtan, CE ;
Peltonen, L ;
Holmberg, C ;
Olsen, A ;
Tryggvason, K .
MOLECULAR CELL, 1998, 1 (04) :575-582
[17]   RENAL AND ADRENAL MECHANISMS IN CYCLOSPORINE-INDUCED HYPERKALEMIA AFTER RENAL-TRANSPLANTATION [J].
LAINE, J ;
HOLMBERG, C .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 1995, 25 (09) :670-676
[18]   RENAL-FUNCTION AND HISTOPATHOLOGIC CHANGES IN CHILDREN AFTER LIVER-TRANSPLANTATION [J].
LAINE, J ;
KROGERUS, L ;
FYHRQUIST, F ;
JALANKO, H ;
RONNHOLM, K ;
HOLMBERG, C .
JOURNAL OF PEDIATRICS, 1994, 125 (06) :863-869
[19]  
LAINE J, 1994, NEPHROL DIAL TRANSPL, V9, P1468
[20]   POSTTRANSPLANTATION NEPHROSIS IN CONGENITAL NEPHROTIC SYNDROME OF THE FINNISH TYPE [J].
LAINE, J ;
JALANKO, H ;
HOLTHOFER, H ;
KROGERUS, L ;
RAPOLA, J ;
VONWILLEBRAND, E ;
LAUTENSCHLAGER, I ;
SALMELA, K ;
HOLMBERG, C .
KIDNEY INTERNATIONAL, 1993, 44 (04) :867-874