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1.
Transplantation ; 65(5): 671-6, 1998 Mar 15.
Article in English | MEDLINE | ID: mdl-9521202

ABSTRACT

BACKGROUND: The aim of the present study was to analyze whether minor differences in recipient body surface area have any predictive value on renal allograft evolution. METHODS: For this study, we considered 236 pairs of recipients who received a kidney from the same donor at our center between March 1985 and December 1995. Pairs in whom at least one patient presented any of the following events were excluded: graft loss during the first year of follow-up, diabetes mellitus, noncompliance with treatment, chronic pyelonephritis, and recurrent or de novo glomerulonephritis. Recipients of each pair were classified as large or small according to their body surface area (BSA). The percentage difference of BSA in each pair was calculated, and two cohorts of pairs were defined: BSA difference < or = 10% (n=76 pairs) and BSA difference >10% (n=70 pairs). RESULTS: The large recipients of the cohort with a BSA difference >10% showed a higher incidence of posttransplant delayed graft function (22/70 vs. 12/70, P=0.075), hypertension at 1 year of follow-up (51/70 vs. 35/70, P=0.006), and a higher serum creatinine level at 1-year follow-up (173 vs. 142 micromol/L, P=0.003), whereas in the cohort with a BSA difference < or = 10%, posttransplant evolution in large and small recipients was not different. Multivariate analysis showed that recipient BSA was an independent predictor of delayed graft function, posttransplant hypertension, and serum creatinine at 1-year follow-up. CONCLUSIONS: Relatively small differences in recipient BSA influence renal allograft evolution. Consequently, our data support that recipient size should be taken into consideration for renal allograft allocation.


Subject(s)
Kidney Transplantation , Kidney/physiology , Adult , Age Factors , Body Mass Index , Creatinine/blood , Female , Graft Survival , Humans , Hypertension/etiology , Kidney Diseases/pathology , Male , Middle Aged , Multivariate Analysis , Organ Size , Surface Properties
2.
Kidney Int Suppl ; 55: S160-2, 1996 Jun.
Article in English | MEDLINE | ID: mdl-8743543

ABSTRACT

Left ventricular hypertrophy (LVH) is associated with an increase in cardiovascular death in essential hypertension (EH). The factors involved in LVH are multiple and complex. We looked for risk factors of LVH in a group of 28 nonobese patients with EH (mean age = 45.3 years). We analyzed the activity of several erythrocyte ion transports (Vmax of NaLi countertransport, NaKCl cotransport and NaK-pump, and the Na-leak Kp Na), the intracellular Na and the insulin sensitivity index. All these parameters were used as independent variables whereas the left ventricular mass index (LVMI) was used as the dependent variable. Variables showing a significant univariate correlation (age, time of EH, mean blood pressure and Vmax of NaLi countertransport) were introduced in a stepwise multiple regression model. Only age (P = 0.014), time of EH (P = 0.038) and Vmax of NaLi countertransport (P = 0.032) were independently associated with LVMI (R2 = 0.581, P = 0.0001). The NaLi CT, an operating mode of the NaH exchanger that facilitates cellular growth, may be a marker of LVH, and consequently a marker of increased cardiovascular risk.


Subject(s)
Antiporters/blood , Hypertension/physiopathology , Hypertrophy, Left Ventricular/physiopathology , Adult , Erythrocytes/metabolism , Female , Humans , Hypertension/epidemiology , Hypertension/metabolism , Hypertrophy, Left Ventricular/epidemiology , Hypertrophy, Left Ventricular/metabolism , Kinetics , Lipids/blood , Male , Middle Aged , Risk Factors , Sodium/blood
5.
Age Ageing ; 23(5): 356-9, 1994 Sep.
Article in English | MEDLINE | ID: mdl-7825479

ABSTRACT

There is in the Western World a progressive ageing of the population, and consequently haemodialysis patients are also getting older. Some ethical questions have been raised as a consequence of the economic issues related to the scarcity of available resources. In this paper we review our experience in the treatment of very old chronic haemodialysis patients. Fifty patients (7.2% of our haemodialysis patients) aged over 80 years at the beginning of dialysis were included (f = 25, m = 26, age = 82.6 +/- 0.3 years). In 42% of the patients the aetiology of renal disease was unknown. In the remainder, the aetiology was: interstitial nephritis 26%, hypertensive nephrosclerosis 14%, chronic glomerulonephritis 8%, diabetes 8% and polycystic disease 2%. There was a great comorbidity: intradialytic hypotension 82%, cardiac disease 74%, gastrointestinal disease 32%, cerebrovascular disease 26%. Vascular access related problems were the main reason for hospitalization. The major cause of death was vascular (cardiac and cerebral disease). Actuarial survival was 89%, 78%, 56% and 48% at 6, 12, 24 and 36 months, respectively. We think that haemodialysis is the best available choice for treating very old chronic renal failure patients. However further studies are needed to improve the quality of life of these patients.


Subject(s)
Kidney Failure, Chronic/therapy , Renal Dialysis , Aged , Aged, 80 and over , Cost Control/trends , Female , Health Care Rationing/economics , Humans , Kidney Failure, Chronic/economics , Kidney Failure, Chronic/etiology , Male , Portugal , Quality of Life , Renal Dialysis/economics , Treatment Outcome
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