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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Scandinavian journal of immunology 16 (1982), S. 0 
    ISSN: 1365-3083
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: We have made an attempt to define a more ‘economical’ method for glucocorticosteroid (GS) administration in renal transplantation in man by shifting most of the GS to the immediate post-operative period. Thirty cadaver kidney recipients were prerandomized in 2 groups of 15 patients and monitored by transplant aspiration cytology (TAC). After transplantation the high-dose experimental group received 3.5 mg/kg/day of methyl-predinisolone (MP), tapered to 0.4 mg/kg/day in 14 days, and the low-dose control group 1.0 mg/kg/day, tapered to 0.4 mg/kg/day in 5 days. Upon rejection the patients in the high-dose experimental group were treated with at most 7 mg/kg/day of oral MP divided into four doses daily, whereas the low-dose control group received 1–3 intravenous boluses of 14 mg/kg (approximately 1000 mg/70 kg). Within 30 days after the transplantation, 7 clinically manifest rejection episodes and 2 episodes of in situ inflammation (without signs of rejection) were recorded in the experimental group, compared with 18 clinically manifest rejection episodes and 6 episodes of inflammation in the control group. The onset of the first episode of inflammation was delayed from 5.0±1.5 days in the control group to 6.6 ± 1.0 days (P=0.00) in the experimental group, and the onset of the first clinical rejection from 5.4±2.1 days to 8.5±1.0 days (P=0.00), respectively. TAC analysis documented that the first episode of inflammation was significantly smaller in the experimental group than in the control group (P=0.001), although the frequency of T lymphoblasts and monocytes was similar to that in the control group (P= 1.00 and 0.20), the frequency of in situ B lymphoblasts and lymphocytes was moderately depressed (P=0.04 and 0.04), and the accumulation of macrophages was both depressed (P=0.07) and delayed. After high initial MP administration the rejections were shorter and easier to overcome: the duration of the first inflammation episode was reduced from 10.5±4.4 days in the control group to 5.9±4.0 days (P=0.02) in the experimental group and the duration of clinical rejection from 8.4±4.1 days to 3.9±3.4 days, respectively (P=0.01). After 18-month follow-up study 12 patients in the experimental group had a life-supporting graft, compared with 7 patients in the control group. There was no difference in the frequency or type of complications between the two groups.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1365-3083
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Twenty cadaveric kidney allograft recipients were prerandomized into two groups. Ten patients (control group) were treated postoperatively with azathioprine (AZA) plus methylprednisolone (MP); the other ten received cyclosporin A (CyA) as the only immunosuppressive agent. Both groups received MP during rejection. One patient was excluded from the CyA group because of an early postoperative cardiac infarction and death. All transplants were monitored by alternate-day fine-needle aspiration biopsy and transplant aspiration cytology. Some patients treated with CyA had a significant initial decrease in urine output, reaching control values approximately 1 week postoperatively. The mechanism behind this deteriorated renal function is not clear, but it seemed to have been caused by injuries to the kidney tubular component, since a distinct monocytic-lymphocytic inflammation and severe cytological changes resembling pronounced acute tubular necrosis were observed concomitantly in transplant aspiration cytology. The CyA-treated patients had normal levels of blood leucocytes, thrombocytes and lymphocytes but displayed a strong early blood eosinophilia that was absent in the control subjects. During the first 30 days after transplantation 15 in situ episodes of inflammation were recorded in the nine transplants treated with CyA, whereas only 6 episodes were found in the 10 transplants receiving AZA + MP (P〈0.01). The first inflammatory episode in the CyA-treated transplants peaked between days 5 and 8 after transplantation and was followed by another distinct inflammatory episode between days 23 and 26. In the AZA- plus MP-treated transplants, only one inflammation episode was observed, with a peak on day 14 postoperatively. The inflammatory cell types most prominently present in the CyA-treated transplants were lymphocytes, B plasmablasts and monocytes. The early inflammatory episodes in the CyA-treated transplants may have been related to the fact that during the initial intramuscular administration, therapeutic CyA concentrations in patient serum were not achieved until the fourth postoperative day during peroral administration. The onset of transplant function had no impact on the in situ inflammatory response of rejection in the CyA-treated transplants or on the concentration of CyA in patient serum. This indicates that CyA may also be used in initially non functioning transplants. Confirming our earlier results, we were unable to demonstrate the major histocompatibility complex (MHC) antigens on the healthy grafts treated with AZA plus MP. However, in healthy allografts treated with CyA, both classes of MHC antigens were nearly invariably demonstrable on the graft endothelial cell surface. Approximately 60% allograft survivals were recorded in both groups at 6 months, and all patients with functioning grafts were able to work.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Journal of Molecular and Cellular Cardiology 9 (1977), S. 23 
    ISSN: 0022-2828
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Scandinavian journal of immunology 19 (1984), S. 0 
    ISSN: 1365-3083
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: In a previous clinical trial we demonstrated that. by increasing the postoperative administration of methylprednisolone from 1.0 to 3.5 mg/kg/day. ihe onset of the first inflammatory rejection episode was significantly delayed and the size of the inflammation was reduced. The ‘high initial’ steroid treatment specifically depleted blast cells and macrophages from the in situ inflammatory infiltraie. In ihis trial we demonstrate that the ‘high initial’ glueocorticosteroid administration significantly improves 1-year cadaver allograft survival from 44% to 68% (P = 0.00.3) without increasing the number of complications. Although the ‘high initial’ steroid administration only partially overcomes the impact of HLA-AB incompatibility, it seems to overcome entirely the impact of absence of blood transfusions. The ‘high initial’ steroid administration also makes the first episodes of inflammation easier to overcome: less steroids are needed to counteract the first rejection, and, as a consequence, only 30% more steroids were used in the ‘high initial’ versus the ‘low intial’ steroid programme.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Prostaglandins 20 (1980), S. 333-347 
    ISSN: 0090-6980
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Prostaglandins 17 (1979), S. 821-830 
    ISSN: 0090-6980
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1432-2277
    Keywords: Key words Kidney transplantation ; Delayed graft function ; Acute rejection ; Long-term results
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract We studied the effect of initial graft function and acute rejection on graft survival in 1047 cadaveric renal transplantations during 1991–1997 with a constant policy of donor selection, graft allocation, and immunosuppression. The overall 1- and 5-year patient survival rates were 96 % and 88 %, and the 1- and 5-year graft survival (GS) rates were 92 % and 78 %. Delayed graft function (DGF) occurred in 31 % and there were 1.2 % never-functioning grafts. One-year GS in transplantations with early graft function (EGF) was 95 % compared to 87 % in DGF (P 〈 0.001). Donor age and cause of death, type of graft perfusion and cold ischemia time, and type and length of dialysis treatment were significant factors in determining the onset of graft function. These factors did not have a significant direct effect on GS. Early ( 〈 100 days) acute rejection occurred in 25 %. In transplantations without rejection, the 1 and 5-year GS was 93.3 % and 80.8 %. In acute rejection responding to steroids, the GS was equal to that up to 3 years, but after that a significantly worse survival rate was observed (1- and 5-year GS: 93.6 % and 73.4 %). DGF was detrimental to GS both in transplantations without rejection and in all rejection types.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Transplant international 3 (1990), S. 92-97 
    ISSN: 1432-2277
    Keywords: Kidney transplantation ; triple drug therapy—Cyclosporin monotherapy ; in kidney transplantation—Triple drug ; double drug, and monodrug therapy ; in kidney transplantation—Fine needle aspiration ; in kidney transplantation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract We have investigated the impact of triple drug immunosuppression on the occurrence of early inflammatory episodes, as detected by fine needle aspiration biopsy, and of episodes of clinical rejection during the immediate postoperative period. The prospective component of this study includes 128 consecutive first cadaveric renal transplant recipients receiving triple drug treatment consisting of azathioprine (Aza), cyclosporin (CyA) and methylprednisolone (MP). For controls we have used three historical groups: one immunosuppressed with Aza and MP (group A), another with CyA monotherapy (group B), and the third with CyA together with MP (group C) in equivalent drug dosages. On the average, 0.8 episodes of inflammation per patient were recorded during the immediate postoperative period of 30 days with triple drug treatment. This was significantly less than the 1.3 episodes in patients receiving Aza and MP (P〈0.01), the 1.7 episodes in patients on CyA monotherapy (P〈0.001), or the 1.6 episodes in patients receiving CyA together with MP (P〈0.001). Although the first episode of inflammation commenced concurrently in each group and the peak intensity of inflammation was the same, the mean duration of inflammation was significantly shorter-2.7 days-under triple drug treatment than the 7.8–11.7 days for controls (P〈0.001). The frequency of rejection episodes under triple treatment was also significantly lower-0.2 per patient-than the 0.8 per patient in controls (P〈0.001). The first rejection episode occurred later in the triple drug treatment group-on the average, on day 15.2-than in the historical controls (on days 7.7–11.7). There was, however, no difference in the duration of rejection. There were no differences in patient survival between the four groups. Graft survival was 97% at 10 weeks for triple drug-treated recipients and 79%, 68%, and 87% for first grafts in groups A, B, and C, respectively. Disregarding a minor demographic bias for the triple drugtreated group with respect to preformed antibodies and preoperative dialysis treatment, the study suggests that the triple drug protocol, in the short run, is superior to any conceivable double drug combination or CyA monotherapy.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1432-0428
    Keywords: Arterial insulin ; venous insulin ; arterial glucose ; venous glucose ; human ; forearm ; muscle ; early response ; glucose infusion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The concentrations of glucose and insulin were determined with high precision at half minute intervals in arterial and deep forearm vein blood after a bolus injection of glucose (4 g), followed by a constant i. v. infusion (200 mg/min), in four healthy subjects. The values for the deep vein were corrected for the transit time, which was determined by injection of Cardio-green. Arterial glucose peaked at the end of the bolus injection, venous glucose 1 1/2 min later. Arterial insulin reached its maximum later than glucose, after 2 1/2–4 min. The venous insulin reached its maximum later and was much lower than the arterial level, in two cases only around 50% of the arterial concentration. It is concluded that early after glucose administration there is a considerable extraction of both glucose and insulin by the forearm. Since the insulin extraction was quite variable venous insulin concentrations cannot be used for the assessment of early insulin response to glucose.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1432-198X
    Keywords: Renal transplantation ; Cadaver donor ; Cyclosporine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract We report the results of 41 consecutive renal transplantations performed on 39 children (median age 2.7 years). Twenty-six recipients were less than 5 years old. Twenty-one recipients (13 under the age of 5 years) received cadaver (CAD) grafts. All grafts except 2 were from adult donors and were placed extraperitoneally. Patients were on triple immunosuppression (cyclosporine plus azathioprine plus methylprednisolone). Mean followup time was 2.3 years. No vascular and only one ureteral complication was seen. Acute tubular necrosis occurred in 3 patients (7.3%). No grafts were lost due to acute rejection. Three-year patient survival and 1-year graft survival were 100%. The overall 3-year actuarial graft survival was 86%. Three-year survival of grafts from living-related donors (LRD) was 92% and that of CAD grafts 75%. In recipients younger than 5 years, 3-year LRD graft survival was 89% and CAD graft survival 73%. No significant differences in graft survival between recipients of different age groups or between LRD and CAD grafts were found. We conclude that results of renal transplantation in children under 5 years of age are comparable to those of older children, even using CAD grafts, when adult donors and triple immunosuppression are used.
    Type of Medium: Electronic Resource
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