Clinical study of 18 pediatric cadaveric renal transplantations : organ sharing in pediatric renal transplantation after enforcement of the organ transplant law in Japan

Renal transplantation is considered to be the optimal replacement therapy for children with end stage renal disease. However, the number of pediatric renal transplants in Japan is much lower than in the USA and/or Europe. Since October 1997, pediatric (< 15 years) recipients are given priority ov...

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Published inNihon Jinzo Gakkai shi Vol. 42; no. 4; pp. 327 - 332
Main Authors HATTORI, Motoshi, ASANO, Takako, ISHIKAWA, Nobuo, TANABE, Kazunari, AKIOKA, Yuko, TOMA, Hiroshi, SHIRAGA, Hiroshi, ITO, Katsumi
Format Journal Article
LanguageJapanese
Published Japan Japanese Society of Nephrology 01.05.2000
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ISSN0385-2385
1884-0728
DOI10.14842/jpnjnephrol1959.42.327

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Abstract Renal transplantation is considered to be the optimal replacement therapy for children with end stage renal disease. However, the number of pediatric renal transplants in Japan is much lower than in the USA and/or Europe. Since October 1997, pediatric (< 15 years) recipients are given priority over adult recipients for organ sharing, only if one or two HLA-DR antigen (s) are matched between the recipient and pediatric (< 15 years) donor. However, the number of pediatric transplants is not increasing. One hundred and twenty-four pediatric renal transplantations were performed in Tokyo Women's Medical University between 1983 and 1999, of which 18(14.5 %) were cadaveric transplants and the others (106, 85.5 %) were livingrelated transplants. We examined 18 pediatric cadaveric renal transplantations. Seven patients received their graft from pediatric donors less than 15 years of age and 11 from adult donors . The mean age at transplantation was 13.2 years (range 4.5-18.7 years) . Major etiologies of renal disease are hereditary renal disease (38.8 %), chronic glomerulonephritis (33 .3 %), and focal segmental glomerulosclerosis [FSGS] (16.7 %). Zero matches in HLA-DR locus were observed in 72.2 %. Patient survival rate was 100 %. Graft survival rates at 1 and 5 years after transplantation were 83 % and 64 % successively . There was no significant difference between the graft survival of cadaveric and livingrelated transplantation at 1 and 5 years. All 5 patients who received their graft between 1994 and 1998 have maintained normal graft function. Causes of their graft loss were chronic rejection in 3, recurrence of FSGS in 2, primary non function in 1, and graft thrombosis in 1. Donor age and HLA-DR mismatching did not affect the outcome. We propose that pediatric renal grafts should be provided to children with priority, regardless of their HLA-A, B and HLA-DR matching.
AbstractList Renal transplantation is considered to be the optimal replacement therapy for children with end-stage renal disease. However, the number of pediatric renal transplants in Japan is much lower than in the USA and/or Europe. Since October 1997, pediatric(< 15 years) recipients are given priority over adult recipients for organ sharing, only if one or two HLA-DR antigen(s) are matched between the recipient and pediatric(< 15 years) donor. However, the number of pediatric transplants is not increasing. One hundred and twenty-four pediatric renal transplantations were performed in Tokyo Women's Medical University between 1983 and 1999, of which 18(14.5%) were cadaveric transplants and the others (106, 85.5%) were living-related transplants. We examined 18 pediatric cadaveric renal transplantations. Seven patients received their graft from pediatric donors less than 15 years of age and 11 from adult donors. The mean age at transplantation was 13.2 years (range 4.5-18.7 years). Major etiologies of renal disease are hereditary renal disease(38.8%), chronic glomerulonephritis(33.3%), and focal segmental glomerulosclerosis[FSGS] (16.7%). Zero matches in HLA-DR locus were observed in 72.2%. Patient survival rate was 100%. Graft survival rates at 1 and 5 years after transplantation were 83% and 64% successively. There was no significant difference between the graft survival of cadaveric and living-related transplantation at 1 and 5 years. All 5 patients who received their graft between 1994 and 1998 have maintained normal graft function. Causes of their graft loss were chronic rejection in 3, recurrence of FSGS in 2, primary non-function in 1, and graft thrombosis in 1. Donor age and HLA-DR mismatching did not affect the outcome. We propose that pediatric renal grafts should be provided to children with priority, regardless of their HLA-A, B and HLA-DR matching.
Renal transplantation is considered to be the optimal replacement therapy for children with end-stage renal disease. However, the number of pediatric renal transplants in Japan is much lower than in the USA and/or Europe. Since October 1997, pediatric(< 15 years) recipients are given priority over adult recipients for organ sharing, only if one or two HLA-DR antigen(s) are matched between the recipient and pediatric(< 15 years) donor. However, the number of pediatric transplants is not increasing. One hundred and twenty-four pediatric renal transplantations were performed in Tokyo Women's Medical University between 1983 and 1999, of which 18(14.5%) were cadaveric transplants and the others (106, 85.5%) were living-related transplants. We examined 18 pediatric cadaveric renal transplantations. Seven patients received their graft from pediatric donors less than 15 years of age and 11 from adult donors. The mean age at transplantation was 13.2 years (range 4.5-18.7 years). Major etiologies of renal disease are hereditary renal disease(38.8%), chronic glomerulonephritis(33.3%), and focal segmental glomerulosclerosis[FSGS] (16.7%). Zero matches in HLA-DR locus were observed in 72.2%. Patient survival rate was 100%. Graft survival rates at 1 and 5 years after transplantation were 83% and 64% successively. There was no significant difference between the graft survival of cadaveric and living-related transplantation at 1 and 5 years. All 5 patients who received their graft between 1994 and 1998 have maintained normal graft function. Causes of their graft loss were chronic rejection in 3, recurrence of FSGS in 2, primary non-function in 1, and graft thrombosis in 1. Donor age and HLA-DR mismatching did not affect the outcome. We propose that pediatric renal grafts should be provided to children with priority, regardless of their HLA-A, B and HLA-DR matching.Renal transplantation is considered to be the optimal replacement therapy for children with end-stage renal disease. However, the number of pediatric renal transplants in Japan is much lower than in the USA and/or Europe. Since October 1997, pediatric(< 15 years) recipients are given priority over adult recipients for organ sharing, only if one or two HLA-DR antigen(s) are matched between the recipient and pediatric(< 15 years) donor. However, the number of pediatric transplants is not increasing. One hundred and twenty-four pediatric renal transplantations were performed in Tokyo Women's Medical University between 1983 and 1999, of which 18(14.5%) were cadaveric transplants and the others (106, 85.5%) were living-related transplants. We examined 18 pediatric cadaveric renal transplantations. Seven patients received their graft from pediatric donors less than 15 years of age and 11 from adult donors. The mean age at transplantation was 13.2 years (range 4.5-18.7 years). Major etiologies of renal disease are hereditary renal disease(38.8%), chronic glomerulonephritis(33.3%), and focal segmental glomerulosclerosis[FSGS] (16.7%). Zero matches in HLA-DR locus were observed in 72.2%. Patient survival rate was 100%. Graft survival rates at 1 and 5 years after transplantation were 83% and 64% successively. There was no significant difference between the graft survival of cadaveric and living-related transplantation at 1 and 5 years. All 5 patients who received their graft between 1994 and 1998 have maintained normal graft function. Causes of their graft loss were chronic rejection in 3, recurrence of FSGS in 2, primary non-function in 1, and graft thrombosis in 1. Donor age and HLA-DR mismatching did not affect the outcome. We propose that pediatric renal grafts should be provided to children with priority, regardless of their HLA-A, B and HLA-DR matching.
Renal transplantation is considered to be the optimal replacement therapy for children with end stage renal disease. However, the number of pediatric renal transplants in Japan is much lower than in the USA and/or Europe. Since October 1997, pediatric (< 15 years) recipients are given priority over adult recipients for organ sharing, only if one or two HLA-DR antigen (s) are matched between the recipient and pediatric (< 15 years) donor. However, the number of pediatric transplants is not increasing. One hundred and twenty-four pediatric renal transplantations were performed in Tokyo Women's Medical University between 1983 and 1999, of which 18(14.5 %) were cadaveric transplants and the others (106, 85.5 %) were livingrelated transplants. We examined 18 pediatric cadaveric renal transplantations. Seven patients received their graft from pediatric donors less than 15 years of age and 11 from adult donors . The mean age at transplantation was 13.2 years (range 4.5-18.7 years) . Major etiologies of renal disease are hereditary renal disease (38.8 %), chronic glomerulonephritis (33 .3 %), and focal segmental glomerulosclerosis [FSGS] (16.7 %). Zero matches in HLA-DR locus were observed in 72.2 %. Patient survival rate was 100 %. Graft survival rates at 1 and 5 years after transplantation were 83 % and 64 % successively . There was no significant difference between the graft survival of cadaveric and livingrelated transplantation at 1 and 5 years. All 5 patients who received their graft between 1994 and 1998 have maintained normal graft function. Causes of their graft loss were chronic rejection in 3, recurrence of FSGS in 2, primary non function in 1, and graft thrombosis in 1. Donor age and HLA-DR mismatching did not affect the outcome. We propose that pediatric renal grafts should be provided to children with priority, regardless of their HLA-A, B and HLA-DR matching.
Author AKIOKA, Yuko
ISHIKAWA, Nobuo
ASANO, Takako
SHIRAGA, Hiroshi
TANABE, Kazunari
TOMA, Hiroshi
ITO, Katsumi
HATTORI, Motoshi
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References 5. 秋岡祐子,白髪宏司,伊藤克己,石川暢夫,山崎雄一郎,田邉一成,東間紘,富松宏文,中澤誠.献腎移植が成功し,尿毒症性心筋症による高度心機能低下から救命された1例.日小児腎不全会誌1999;19:23-5.
3. 長谷川昭.小児の献腎移植.今日の移植1998;11:810-8
4. 白髪宏司.こどもの腎移布直透析ケア1996;冬期増刊:55-66
8. First MR. Living-related donor transplants should be per formed with caution in patients with focal segmental glomerulonephritis. Pediatric Nephrol 1995 ; 9 : S40-2.
11. Feld LG, Stablein D, Fivush B, Harmon W, Tejani A. Renal transplantation in children from 1987-1996 : The annual report of the North American Pediatric Renal Transplant Cooperative Study. Pediatr Transplant 1997 ; 1 :146 -62.
15. 石川暢夫,田邉一成,大田敏之,八木沢 隆,合谷信行,中沢速和,中島一朗,渕之上昌平,白髪宏司,川口 洋,伊藤克己,高橋公太,東間 紘,阿岸鉄三,太田和夫.小児ドナーからの献腎移植についての検討―成績,適応,問題点移植1998;33:359-66.
12. USRDS 1998 Annual Data Report : Pediatric endstage renal disease. Am J Kidney Dis 1998 ; 32(Suppl 1) : 598- 108.
6. Cameron JS. Recurrent primary disease and de novo nephritis following renal transplantation. In : Tej ani AH, Fine RN (eds) Pediatric renal transplantation. New York Wiley-Liss, 1994 ; 503-23.
13. Harmon WE, Stablein D, Alexander SR, Tejani A. Graft thrombosis in pediatric renal transplant recipients. Trans plant 1991 ; 51: 406-12.
9. 星井桜子.小児透析患者の腎移植の選択を阻む要因はなにか.透析会 1996;29:375-82.
10. 大田敏之,川口 洋,服部元史,水島和一郎,此元隆雄,秋岡祐子,伊藤克己,田邉一成,石川暢夫,東間 紘,高橋公太.小児ABO血液型不適合間生体腎移植9例の経験.今日の移植1997;10:884-7.
14, Alexander JW, Bennett LE, Breen TJ. Effect of donor age on outcome of kidney transplantation. Transplant 1994 ; 57 871-6.
7. Tejani A, Stablein DH. Recurrence of focal segmental gromerulosclerosis post transplantation : a special report of the North American Pediatric Renal Transplantation Coop erative Study. J Am Soc Nephrol 1991 ; 2 (Suppl 3) : S256- 63.
1. 両角國男,福田道雄,杉戸健二.組織適合性検査方法と公正公平な死体腎移植レシピエント選択基準.内科1995;76:581-3
16. Filler G, Lindeke A, Bohme K, Devaux S, Schonberger B, Ehrich JHH. Renal transplantation from donors aged <6 years into children yields equal graft survival when compared to older donors. Pediatr Transplant 1997 ; 1 : 119-23.
2. 高橋公太,斉藤和英,金井利雄,中川由紀,片桐明善,冨田善彦,谷川俊貴,武田正之,成田一衛,上野光博,西慎一,荒川正昭,早川広史,内山聖,若月俊二,今井智之,高橋等,坂田安之輔,柳原俊雄,原正則,吉田和清3歳以下のドナーからの小児腎移植.高橋公太編小児腎移植を増やすには.東京:日本医学館,1998;39-54.
References_xml – reference: 9. 星井桜子.小児透析患者の腎移植の選択を阻む要因はなにか.透析会 1996;29:375-82.
– reference: 14, Alexander JW, Bennett LE, Breen TJ. Effect of donor age on outcome of kidney transplantation. Transplant 1994 ; 57 871-6.
– reference: 13. Harmon WE, Stablein D, Alexander SR, Tejani A. Graft thrombosis in pediatric renal transplant recipients. Trans plant 1991 ; 51: 406-12.
– reference: 6. Cameron JS. Recurrent primary disease and de novo nephritis following renal transplantation. In : Tej ani AH, Fine RN (eds) Pediatric renal transplantation. New York Wiley-Liss, 1994 ; 503-23.
– reference: 7. Tejani A, Stablein DH. Recurrence of focal segmental gromerulosclerosis post transplantation : a special report of the North American Pediatric Renal Transplantation Coop erative Study. J Am Soc Nephrol 1991 ; 2 (Suppl 3) : S256- 63.
– reference: 1. 両角國男,福田道雄,杉戸健二.組織適合性検査方法と公正公平な死体腎移植レシピエント選択基準.内科1995;76:581-3
– reference: 2. 高橋公太,斉藤和英,金井利雄,中川由紀,片桐明善,冨田善彦,谷川俊貴,武田正之,成田一衛,上野光博,西慎一,荒川正昭,早川広史,内山聖,若月俊二,今井智之,高橋等,坂田安之輔,柳原俊雄,原正則,吉田和清3歳以下のドナーからの小児腎移植.高橋公太編小児腎移植を増やすには.東京:日本医学館,1998;39-54.
– reference: 12. USRDS 1998 Annual Data Report : Pediatric endstage renal disease. Am J Kidney Dis 1998 ; 32(Suppl 1) : 598- 108.
– reference: 5. 秋岡祐子,白髪宏司,伊藤克己,石川暢夫,山崎雄一郎,田邉一成,東間紘,富松宏文,中澤誠.献腎移植が成功し,尿毒症性心筋症による高度心機能低下から救命された1例.日小児腎不全会誌1999;19:23-5.
– reference: 10. 大田敏之,川口 洋,服部元史,水島和一郎,此元隆雄,秋岡祐子,伊藤克己,田邉一成,石川暢夫,東間 紘,高橋公太.小児ABO血液型不適合間生体腎移植9例の経験.今日の移植1997;10:884-7.
– reference: 8. First MR. Living-related donor transplants should be per formed with caution in patients with focal segmental glomerulonephritis. Pediatric Nephrol 1995 ; 9 : S40-2.
– reference: 16. Filler G, Lindeke A, Bohme K, Devaux S, Schonberger B, Ehrich JHH. Renal transplantation from donors aged <6 years into children yields equal graft survival when compared to older donors. Pediatr Transplant 1997 ; 1 : 119-23.
– reference: 15. 石川暢夫,田邉一成,大田敏之,八木沢 隆,合谷信行,中沢速和,中島一朗,渕之上昌平,白髪宏司,川口 洋,伊藤克己,高橋公太,東間 紘,阿岸鉄三,太田和夫.小児ドナーからの献腎移植についての検討―成績,適応,問題点移植1998;33:359-66.
– reference: 11. Feld LG, Stablein D, Fivush B, Harmon W, Tejani A. Renal transplantation in children from 1987-1996 : The annual report of the North American Pediatric Renal Transplant Cooperative Study. Pediatr Transplant 1997 ; 1 :146 -62.
– reference: 3. 長谷川昭.小児の献腎移植.今日の移植1998;11:810-8
– reference: 4. 白髪宏司.こどもの腎移布直透析ケア1996;冬期増刊:55-66
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Snippet Renal transplantation is considered to be the optimal replacement therapy for children with end stage renal disease. However, the number of pediatric renal...
Renal transplantation is considered to be the optimal replacement therapy for children with end-stage renal disease. However, the number of pediatric renal...
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SubjectTerms Adolescent
Adult
Cadaver
cadaveric renal transplantation, pediatric donor, pediatric recipient , HLA, organ sharing
Child
Child, Preschool
Graft Rejection - epidemiology
Graft Survival
Humans
Japan - epidemiology
Kidney Diseases - therapy
Kidney Transplantation - mortality
Kidney Transplantation - statistics & numerical data
Male
Organ Transplantation - legislation & jurisprudence
Survival Rate
Tissue Donors
Title Clinical study of 18 pediatric cadaveric renal transplantations : organ sharing in pediatric renal transplantation after enforcement of the organ transplant law in Japan
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