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Biomedical subjects

S Alloatti

Publications and source records attributed to S Alloatti.

At least 19 recordsLinked to original sources
PubMed1992

Follow-up of nerve conduction in chronic uremic patients during hemodialysis.

We studied to evolution of nerve conduction during hemodialysis following 21 patients with chronic renal failure. Mean motor nerve conduction velocity (MCV) was significantly different at hemodialysis onset and 3 years later for both common peroneal nerve (44.5 and 41.0 m./sec.) and ulnar nerve (52.5 and 47.1 m./sec.). MCV decreased more in patients with low Kt/V (a depuration index) than in those with high Kt/V.

Adult↗
PubMed1989

Scant reliability of Co/Ct ratio in urea kinetic formulas.

The ratio initial/final urea value is used in urea kinetic formulas. To assess its reliability we employed mass balances and urea clearances to study 15 hemodialysis treatments divided in several parts. The mass balances clearly indicated urea disequilibrium. In the first phases of dialysis, urea extraction, measured by dialysate collection, was lower than the corresponding change in urea pool, whereas in the later phases the opposite occurred. On account of this lack of equilibrium, clearances bases on the Co/Ct ratio (K2) are less reliable than standard clearances derived from total dialysate collection (K1): in the first quarter of dialysis, K2 is greater than K1 (p less than 0.01), while in the 3rd and 4th quarters it is lower. The comparison of clearances in a cumulative way showed a significant fall in K2 (p less than 0.01) while K1 remained stable. From a practical point of view, aberrations induced by non monocompartmental urea behaviour are negligible, and do not invalidate the usefulness of the single-pool Gotch model in clinical practice. However, at least in experimental work, the limits of urea kinetic formulas must be taken into account.

Humans↗
PubMed1982

Clinical significance of the detection of circulating immune complexes in lupus nephritis.

32 patients (22 biopsed) with lupus nephritis (LN) were observed for circulating immune complexes (IC). Solid phase C1q (SPC1q) and polyethylene glycol (PEG) precipitation tests were used. The patients were studied during the clinical follow-up in different phases of disease activity. Comparative studies between each histological class of LN and corresponding forms of idiopathic glomerulonephritis (IGN) were made: no significant differences were found between either mesangial LN and stalk mesangial IGN, or between focal proliferative LN an focal proliferative IGN. However, a significant difference was found for SPC1q data between diffuse proliferative LN and mesangiocapillary IGN, and between membranous LN and membranous IGN. LN, with an acute nephritic syndrome and hypocomplementemia, displayed SPC1q data significantly above the levels of IC found in IGN with similar clinical features. IC serum data would seem an important element for the diagnosis and the clinical management of patients affected by LN.

Adolescent↗
PubMed1982

The immunological state in chronic renal insufficiency.

To evaluate the immunological state in chronic renal insufficiency, the Authors studied cellular and humoral immunity in 292 patients with chronic renal failure. They were divided into 3 groups: 1) 37 with creatinine clearance between 50 and 20 ml/min; 2) 57 with creatinine clearance between 20 and 8 ml/min; 3) 178 treated by hemodialysis. In vivo and in vitro tests, that is DNCB, PPD skin tests, spontaneous, active and EAC rosettes, surface membrane immunoglobulin test, complement (C3, C4) and serum immunoglobulins were taken as markers of the immune response. Cell-mediated immunity was found to be significantly impaired in patients with terminal renal insufficiency or on hemodialysis and also markedly reduced in patients with non-terminal renal insufficiency. Humoral immunity produced less significant results: the B lymphocyte count and serum immunoglobulins were normal; only C3 levels were found below normal range. Thus it would seem that cell-mediated immunodeficiency appears in an early stage of chronic renal failure and that hemodialysis does not improve this deficiency.

Adult↗
PubMed1981

Effects of blood transfusion on cellular immunity.

To evaluate the effect of transfusion on immunity, 14 uraemic patients treated with 3 blood transfusions from a single donor, at weekly intervals, were studied: in 5 cases HLA-A,B were compatible, in 9 cases they were not. As markers of cellular and humoral immunity DNCB, PPD skin tests, spontaneous and active E-rosettes, EAC-rosettes, surface membrane immunoglobulins, C3, C4, C3d, serum immunoglobulins, circulating immune complexes and C-reactive protein were investigated. This protocol was applied before transfusions, 1 week after each transfusion (day +7, +14, +21) and 20 weeks later (day +80). Before transfusions 8/14 patients were DNCB negative; both spontaneous and active E-rosettes were below normal range. The other parameters were normal. On day +7 T and B lymphocytes were increased, while the other parameters were unmodified. On day +21 there was a significant reduction (p less than 0.5) in T lymphocytes in patients treated with compatible transfusions. On day +80 3/3 DNCB positive patients, treated with compatible transfusions, became negative and 1/3 DNCB positive patients, treated with random transfusions, also became negative. Three/fourteen patients showed a decrease in B lymphocytes. The other results were unchanged. Our preliminary results suggest that transfusions, either from an HLA compatible donor or not, can impair lymphocyte function.

Adult↗
PubMed1975

[Use of coil negative pressure in the kidney].

A sealed compartment recycling system has been created for use with Extracorporeal commercial filters in order to exploit the negative pressure of the dialysate for purposes of ultrafiltration. The results of in vivo and in vitro tests regarding ultrafiltration and dialysates of urea, creatinine, Hipaque I125 and vit. B12 Co57 are reported. The tests highlighted improved dehydration characteristics in the system compared with the traditional coil technique, while the dialysates of small and medium molecules showed no decrease. The system can profitably be used as an alternative to the open compartment coil system and is particularly interesting because it can be combined with monitors which provide exclusively for the use of closed circuit dialysate instruments.

Creatinine↗
PubMedDate not supplied

Transcellular disequilibrium and intradialytic catabolism reduce the reliability of urea kinetic formulas.

To elucidate the limits of single-pool models as regard aberrations induced by urea transcompartmental disequilibrium during urea kinetics, mass balances and fractional clearances were studied, and original formulas developed to calculate urea clearance and distribution volume. In the early dialytic phases, aberrations were more evident, with low kinetic volume (VK) values and kinetic clearance (KK) values double those obtained by dialysate collection (KDC). Over the whole session, both VDC and VK were underestimated (9.9 and 8.2%), compared with anthropometric data (VA). In 3 patients, the comparison of VA and VDC, and the behavior of effective body water clearance (KE), agreed with the hypothesis of dialysis-induced catabolism. Both disequilibrium and hypercatabolism can affect the reliability of the single-pool urea kinetic model; because of overlap, their effects are difficult to separate, and became particularly important in high-efficiency dialysis. A modified model, using V and CtET as input is suggested in order to establish the most appropriate dialysis prescription for uremia therapy.

Anthropometry↗
PubMedDate not supplied

[Effect of dialytic treatment and the relation between erythrocyte urea and plasma urea].

The existence of an intraerythrocytic binding between haemoglobin and urea is known; it determines, in normals, a higher erythrocyte than plasma urea concentration; this binding, in vitro, is progressive for an urea concentration range of 10-400 mg/dl. The only data found relating to dialysis patients, are reported by Nolph et al.; they indicate a decrease in the plasma-blood urea ratio during the blood transit through the dialyzer and a different ratio in comparison with normals, but in our opinion the method used to measure urea concentration was unsuitable. We determined urea distribution ratios by measuring, in blood and plasma, water and urea concentration in uremic inflow and outflow blood samples during dialysis. Our data indicate 1) an increase in outflow erythrocyte water (H2Oe inflow: 0.659, H2Oe outflow: 0.671 P less than 0.01) induced by a different erythrocyte osmotic gradient; 2) a not different ratio between urea of erythrocyte water and urea of plasma water in inflow and outflow samples of dialysed patients and in normals (respectively 1.06, 1.16, 1.13 p = n.s.). Our data from normal and uremic patients are like those found by Murdaugh & Doyle and by Colton & Lowrie in normals.

Body Water↗
PubMedDate not supplied

[High-efficiency hemodialysis. Review of the literature and initial clinical experience].

A literature review allows us to distinguish two types of high efficiency therapy: HED (high efficiency dialysis), with low ultrafiltration coefficient membranes, and HFD (high flux dialysis), with high ultrafiltration coefficient membranes. Data reported show an unchanged hematochemical with the same, or better, treatment tolerance, but there are few data on hydrosaline balance (and correlate hypertension) and middle moleculas removal. Finally we report the experience of our centre in 59 months of treatment in four patients.

Evaluation Studies as Topic↗