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  • 1
    ISSN: 1432-198X
    Keywords: Key words: Renal transplantation   ;   Graft rejection
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract. Infants are thought to be more immunoreactive and at a greater risk for developing irreversible rejection compared with older children. We investigated this by analyzing patient and graft survival rates, incidence of acute rejection, reversibility of acute rejection, development of a subsequent acute rejection, and incidence of graft loss due to rejection in 154 children (〈18 years of age) after primary renal transplantation. Most patients (n = 139) were treated with quadruple immunosuppression (antibody, azathioprine, prednisone, cyclosporine). Treatment of the first acute rejection episode (ARE) consisted of antibody and increased prednisone (68%) or increased prednisone alone (30%), and was not significantly different between the age groups. Transplants were from living donors (LRD) in 80% of cases. Patients were followed for at least 1 year (mean 58±30 months); 68% (105/154) of recipients experienced 1 or more ARE. The incidence of ARE was significantly lower in patients 〈2 years of age (45%) compared with patients 2 – 5 (76%, P = 0.01), 6 – 12 (78%, P = 0.005), and 13 – 17 (76%, P = 0.009) years of age. There was no significant difference in the 1-, 2- and 5-year patient or graft survival rates, the development of a subsequent acute rejection, or the incidence of graft loss due to acute rejection when analyzed by age group. These data suggest that the impact of an ARE is similar for younger and older children in our population receiving predominantly LRD transplants and quadruple immunosuppression.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-198X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Pediatric nephrology 11 (1997), S. 399-403 
    ISSN: 1432-198X
    Keywords: Key words:  Renal transplantation ; Hospital readmissions ; Infections
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract.   We asked whether pediatric renal transplant recipients, subgrouped by age, differed in the percentage and number of hospital readmissions and in the incidence of infectious complications post transplant. Between 1 August 1985 and 31 October 1993, a total of 164 patients 〈18 years of age underwent primary transplants, with cyclosporine-based immunosuppression, at the University of Minnesota. The percentage of readmissions (P = NS), the mean number of readmissions (P = NS), and the length of hospital stay during readmission (P = NS) did not differ significantly among age groups. The overall incidence of acute rejection was greater in those ≥2 years than those 〈2 years (P = 0.002), and in living donor recipients ≥2 years versus those 〈2 years (P = 0.02). The incidence of bacterial infection (〈2 years, 87%; 2 – 5 years, 72%; 6 – 12 years, 51%; 13 – 17 years, 40%) was greater in younger recipients (P = 0.0001). The most common bacterial infection in recipients ≤5 years was Clostridium difficile-associated diarrhea; in those 〉5 years, urinary tract infection. The overall incidence of viral infection did not differ among groups (P = NS). The most common viral infection in recipients ≤5 years was varicella and those 〉5 years, cytomegalovirus infection. Risk factors for infection in the first 6 months post transplant included age 〈2 years and Solu-Medrol treatment for acute rejection. In conclusion, young recipients 〈2 years of age at the time of transplant are at a higher risk for bacterial infection post transplant.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-198X
    Keywords: Key words: Renal transplantation ; Acute rejection ; Chronic rejection ; Risk factors
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract. Chronic rejection (CR) is the most common cause of graft loss beyond the 1st posttransplant year. The aim of this analysis was to identify the risk factors for the development of CR in pediatric renal transplant recipients. Between June 1984 and March 1994, 217 renal transplants were performed in children at our center. Immunosuppression included prednisone, azathioprine, cyclosporine (CsA), and prophylactic antibody. Using multivariate analysis, we studied the impact of the following variables on the development of biopsy-proven CR: age at transplant (≤5 years, 〉5 years), gender, race, transplant number (primary, retransplant), donor source (cadaver, living donor), donor age (〈20 years, 20 – 49 years, 〉49 years), number of ABDR mismatches (0, 1 – 2, 3 – 4, 5 – 6), number of DR mismatches (0, 1, 2), percentage peak panel reactive antibody (PRA) (≤50%, 〉50%), percentage PRA at transplantation (≤50%, 〉50%), dialysis pretransplant, preservation time 〉24 h, acute tubular necrosis requiring dialysis, initial CsA dosage (≤5 mg/kg per day, 〉5 mg/kg per day), CsA dosage at 1 year posttransplant (≤5 mg/kg per day, 〉5 mg/kg per day), acute rejection (AR), number of AR episodes (ARE) (1, 〉1), timing of AR (≤6 months, 〉6 months), reversibility of AR (complete, partial), and infection [cytomegalovirus (CMV), non-CMV viral, bacterial]. Risk factors for the development of CR in pediatric renal transplant recipients were: AR (P 〈0.0001, odds ratio 19.4), multiple ARE (〉1 vs. 1) (P 〈0.0001, odds ratio 30.1), and high percentage peak PRA (〉50%) (P 〈0.03, odds ratio 3.6).
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-198X
    Keywords: Allograft loss ; Causes ; Large single-center pediatric population
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract At our institution, 521 kidney transplants were performed in 429 children (mean age 8.7±5.6-years) between 1969 and 1991. Of these transplants, 408 were primary, 113 were retransplants, 347 were living related, 171 were cadaver, and 3 were living nonrelated. Immunosuppression consisted of prednisone, azathioprine, and Minnesota antilymphocyte globulin (non-CSA) in 339 patients, total lymphoid irradiation in 8, and, more recently, cyclosporine (CSA) in addition in 168 patients. Average followup was 8.8±6.0 years. Actuarial graft survival in the non-CSA versus CSA groups at 1 year was 77.0% versus 85.7%; at 5 years, 59.6% versus 71.9%. Of 136 non-CSA patients, causes of graft loss at 5 years included: chronic rejection in 55 (40.4%), acute rejection in 27 (19.9%), recurrent disease in 16 (11.8%), technical complications in 8 (5.9%), infectious complications in 4 (2.9%), other causes in 5 (3.7%), and death with a functioning graft in 21 (15.4%). Of 40 CSA patients, causes of graft loss at 5 years included: chronic rejection in 16 (40.0%), acute rejection in 8 (20.0%), recurrent disease in 6 (15.0%), technical complications in 3 (7.5%), other causes in 2 (5.0%), and death with a functioning graft in 5 (12.5%). The causes of graft loss did not significantly differ in the non-CSA and CSA groups. Chronic rejection was the most common cause of graft loss in both groups. Research focusing on chronic rejection is needed to improve graft outcome in pediatric kidney transplantation.
    Type of Medium: Electronic Resource
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