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Je něco špatně v tomto záznamu ?
Odlišují se nemocní po transplantaci ledviny od CKD klasifikace?
[Chronic kidney disease in kidney transplant recipients-is it different from chronic native kidney disease?]
Udayaraj UP, Casula A, Ansell D, Dudley CR, Ravanan R.
Jazyk čeština Země Česko
- MeSH
- chronická nemoc epidemiologie MeSH
- dárci tkání statistika a číselné údaje MeSH
- diabetické nefropatie chirurgie MeSH
- dospělí MeSH
- glomerulonefritida chirurgie MeSH
- hodnoty glomerulární filtrace MeSH
- lidé středního věku MeSH
- lidé MeSH
- míra přežití MeSH
- mladiství MeSH
- nemoci ledvin epidemiologie MeSH
- polycystická choroba ledvin chirurgie MeSH
- senioři MeSH
- transplantace ledvin fyziologie mortalita patologie MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladiství MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
BACKGROUND: The rate of change in estimated glomerular filtration rate (?eGFR), factors influencing ?eGFR, and its association with mortality has not been well studied in renal transplant recipients. METHODS.: Adult kidney-only recipients between January 2001 and December 2004, with surviving grafts 1 year after transplantation, from England and Wales were followed up till 31 December 2006, graft failure or death. The four variable modification of diet in renal disease equation was used to estimate GFR and ?eGFR assessed using linear least square regression. ?eGFR of -1 mL/min/1.73m per year and above was considered to be stable or improving function. Linear regression and Cox regression analyses were used to examine factors influencing ?eGFR and its association with mortality, respectively. RESULTS: Of the 2, 927 patients included, ?eGFR was -1.3±6.0 mL/min/1.73 m per year and eGFR remained stable or improved in the majority (54.8%). Baseline graft function at 1 year or live donor status did not influence ?eGFR. Male donor to female recipient transplantation, younger recipients, diabetes, white race, and human leukocyte antigen mismatch were associated with faster decline in eGFR. ?eGFR was not associated with mortality when censored for graft failure. CONCLUSIONS: Majority of renal transplant recipients experienced stable or improved graft function. Specific donor and recipient characteristics influenced the rate of decline in eGFR. The lack of association of ?eGFR with mortality, the stability of eGFR in the majority, and influence of donor characteristics on ?eGFR suggest caution when applying prognosis knowledge from the native kidney disease to the kidney transplant population.
Chronic kidney disease in kidney transplant recipients-is it different from chronic native kidney disease?
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- $a Chronic kidney disease in kidney transplant recipients-is it different from chronic native kidney disease?
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- $a Richard Bright Renal Unit, Southmead Hospital, Southmead Road, Bristol, United Kingdom udaya.udayaraj@nbt.nhs.uk
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- $a BACKGROUND: The rate of change in estimated glomerular filtration rate (?eGFR), factors influencing ?eGFR, and its association with mortality has not been well studied in renal transplant recipients. METHODS.: Adult kidney-only recipients between January 2001 and December 2004, with surviving grafts 1 year after transplantation, from England and Wales were followed up till 31 December 2006, graft failure or death. The four variable modification of diet in renal disease equation was used to estimate GFR and ?eGFR assessed using linear least square regression. ?eGFR of -1 mL/min/1.73m per year and above was considered to be stable or improving function. Linear regression and Cox regression analyses were used to examine factors influencing ?eGFR and its association with mortality, respectively. RESULTS: Of the 2, 927 patients included, ?eGFR was -1.3±6.0 mL/min/1.73 m per year and eGFR remained stable or improved in the majority (54.8%). Baseline graft function at 1 year or live donor status did not influence ?eGFR. Male donor to female recipient transplantation, younger recipients, diabetes, white race, and human leukocyte antigen mismatch were associated with faster decline in eGFR. ?eGFR was not associated with mortality when censored for graft failure. CONCLUSIONS: Majority of renal transplant recipients experienced stable or improved graft function. Specific donor and recipient characteristics influenced the rate of decline in eGFR. The lack of association of ?eGFR with mortality, the stability of eGFR in the majority, and influence of donor characteristics on ?eGFR suggest caution when applying prognosis knowledge from the native kidney disease to the kidney transplant population.
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