687 research outputs found

    Acute changes in peritoneal morphology and transport properties with infectious peritonitis and mechanical injury

    Get PDF
    Acute changes in peritoneal morphology and transport properties with infectious peritonitis and mechanical injury. Peritoneal clearance studies were performed in rats undergoing acute peritoneal dialysis. Some of these animals were then exposed to laparotomy and mechanical drying of the peritoneum. Peritoneal clearance studies were repeated at intervals up to 11 days. Another group of rats was placed on daily peritoneal dialysis and allowed to spontaneously develop peritonitis which was not treated. These rats underwent peritoneal transport studies at differing durations of infection. In all groups, animals were sacrificed at the time of the last transport studies for morphological assessment of the peritoneum by light microscopy, scanning electron microscopy, and transmission electron microscopy. The results showed similar decreases in drainage volume and increases in glucose absorption and protein losses with both infection and drying. Both types of injury resulted in extensive mesothelial structural changes. While drying caused mainly denudation of the mesothelial surface, infectious peritonitis was associated with separation of mesothelial cells, and the appearance of numerous white blood cells between and on mesothelial cells. Exposure to peritoneal dialysis alone had no obvious effects on anatomy. Although changes in the peritoneal microcirculation and deeper structures cannot be excluded as contributing to peritoneal transport alterations, the findings suggest that alterations of mesothelium might explain some of the changes in peritoneal transport properties under the conditions of these studies.Modifications aiguĂ«s de la morphologie et des propriĂ©tĂ©s de transport du pĂ©ritoine par pĂ©ritonite infectieuse et lĂ©sion mĂ©canique. Des Ă©tudes de clearance pĂ©ritonĂ©ale ont Ă©tĂ© entreprises chez des rats en dialyse pĂ©ritonĂ©ale aiguĂ«. Certains de ces animaux Ă©taient soumis Ă  une laparotomie et Ă  un sĂ©chage mĂ©canique du pĂ©ritoine. Les Ă©tudes de clearance pĂ©ritonĂ©ale Ă©taient rĂ©pĂ©tĂ©es Ă  des intervalles allant jusqu'Ă  11 jours. Un autre groupe de rat Ă©tait placĂ© en dialyse pĂ©ritonĂ©ale journaliĂšre, et il pouvait dĂ©velopper spontanĂ©ment une pĂ©ritonite qui n'Ă©tait pas traitĂ©e. Chez ces rats ont Ă©tĂ© effectuĂ©es des Ă©tudes de transport pĂ©ritonĂ©al Ă  diffĂ©rents stades d'infection. Dans tous les groupes, les animaux Ă©taient sacrifiĂ©s lors de la derniĂšre Ă©tude de transport afin d'Ă©tudier morphologiquement le pĂ©ritoine par microscopie optique, microscopie Ă©lectronique Ă  balayage, et microscopie Ă©lectronique par transmission. Les rĂ©sultats ont montrĂ© des diminutions du volume de drainage et des augmentations de l'absorption du glucose et des pertes protĂ©iques identiques avec l'infection ou le sĂ©chage. Les deux types de lĂ©sions ont entrainĂ© des modifications structurelles mĂ©sothĂ©liales importantes. Tandis que le sĂ©chage entrainait principalement une dĂ©nudation de la surface mĂ©sothĂ©liale, la pĂ©ritonite infectieuse Ă©tait associĂ©e Ă  une sĂ©paration des cellules mĂ©sothĂ©liales, et Ă  l'apparition de nombreux globules blancs entre et sur les cellules mĂ©sothĂ©liales. L'exposition Ă  la dialyse pĂ©ritonĂ©ale seule n'avait pas d'effets anatomiques Ă©vidents. Bien que la contribution aux altĂ©rations du transport pĂ©ritonĂ©al de modifications de la micro-circulation pĂ©ritonĂ©ale et des structures plus profondes ne puisse ĂȘtre exclue, ces rĂ©sultats suggĂšrent que les altĂ©rations du mĂ©sothĂ©lium pourraient expliquer certaines des modifications des propriĂ©tĂ©s de transport pĂ©ritonĂ©al dans les conditions de ces Ă©tudes

    Blood pressure (BP) measurements in adults

    Get PDF
    The author discusses issues that relate to devices used for measuring blood pressure

    Determinants of low clearances of small solutes during peritoneal dialysis

    Get PDF
    Peritoneal dialysis plasma clearances of large molecular weight solutes such as inulin (5,200 daltons) usually equal or exceed plasma clearances of such solutes seen with extracorporeal dialyzers, [1–4]. Clearances of smaller solutes such as urea (60 daltons), however, are usually 15% or less of urea clearances with extracorporeal dialysis systems. In Table 1, typical values for clearances of urea and inulin, dialysis solution flow rate (QD), blood flow rate (QB), and surface area are compared for peritoneal and extracorporeal (hemodialysis) techniques. Effective peritoneal capillary blood flow rate is unknown. Gross total anatomical peritoneal surface area is estimated to be approximately equal to body surface area [2, 4]

    Role of peritoneal cavity lymphatic absorption in peritoneal dialysis

    Get PDF

    The influence of solution composition on protein loss during peritoneal dialysis

    Get PDF
    A number of recent studies in man [1–3] and rats [1, 4, 5] has investigated the influence of the composition of commercial peritoneal dialysis solutions on the microcirculation and on the removal of solutes during peritoneal dialysis. One of those studies [3] demonstrated that dialysis with a normal osmolality Krebs solution greatly enhanced the concentration of protein in the drainage solution in comparison to that obtained with commercial, 1.5% dextrose solutions. We proposed that these results represented an effect of osmolality on interstitial movement of protein [6]. Since protein movement in the interstitium probably occurs through water channels in the gel-like matrix of the interstitium [7, 8], a change to a high osmolality dialysis solution could dehydrate the interstitium. This would increase the resistance to protein movement and thus decrease the loss of protein in the dialysate. During the first few exchanges, the high osmolality of commercial dialysis solutions could also pull residual protein out of the interstitium because it produced a generalized dehydration of the interstitial tissues. This would lead to large concentrations of protein in the drainage solution during the first few exchanges and then a progressive fall in dialysate protein with subsequent exchanges. An alternative hypothesis to explain such results would be that there is simply a washout of residual protein from the peritoneal cavity or from tissue spaces within the cavity.The following studies were designed to test which of these two hypotheses, an increased resistance to protein movement through dehydration of the interstitial tissue or a washout of residual protein already present in the peritoneal cavity, could explain our previous findings [3]

    An hypothesis to explain the ultrafiltration characteristics of peritoneal dialysis

    Get PDF
    Net removal of fluid and sodium from the body during peritoneal dialysis is accomplished with dialysis solutions that contain high glucose concentrations and are hyperosmolar to body fluid [1]. Commercially available peritoneal dialysis solutions contain glucose concentrations ranging from 1.5 to 4.25 g/dl and have osmolalities ranging from 334 to 490 mOsm/kg H2O. The solutions also contain concentrations of sodium, chloride, magnesium, and calcium that approach those of normal extracellular fluid. Acetate or lactate, rather than bicarbonate, is used as the nonchloride anion. Potassium may be added or, depending on the need for potassium removal, solutions may be potassium-free

    Icodextrin Improves the Serum Potassium Profile with the Enhancement of Nutritional Status in Continuous Ambulatory Peritoneal Dialysis Patients

    Get PDF
    The impact of glucose-free icodextrin (ID) for overnight dwell as compared to conventional glucose-containing dialysate (GD) on potassium (K+) metabolism in continuous ambulatory peritoneal dialysis (CAPD) patients has not yet been investigated. Serum K+ in a total of 255 stable patients (116 on GD and 139 on ID) on CAPD for more than 6 months and in 139 patients on ID before and after ID use (Pre-ID and Post-ID) were observed along with nutritional markers in a 2-year study period (Jan. 2006 to Dec. 2007). The prevalence of hypokalemia was similar between patients on GD and ID (16.7% vs 17.3%), but was lower on Post-ID than Pre-ID (17.3% vs 20.5%) without statistic significance. The mean serum K+ level was higher on ID than on GD (P<0.05) as well as Post-ID than Pre-ID (P<0.001). In the multivariate analysis, serum K+ levels were positively correlated with serum albumin, and creatinine in all patients (P<0.05), and ID-use in younger patients (age≀56, P<0.001). Serum albumin, creatinine, total CO2, and body mass index were significantly higher on Post-ID than Pre-ID. Icodextrin dialysate for chronic overnight dwell could increase serum K+ levels and lower the prevalence of hypokalemia compared to conventional glucose-containing dialysate. The improved chronic K+ balance in CAPD patients on icodextrin could be related to enhanced nutritional status rather than its impact on acute intracellular K+ redistribution
    • 

    corecore