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as well as the normalized protein nitrogen appearance using the Randerson formula<span class="elsevierStyleSup">17</span>&#46; The urine samples were only collected for those with diuresis equal to or greater than 200ml&#47;day&#59; if this was not the case&#44; they were considered anuric&#46; The Department of Nutrition&#44; though the food frequency questionnaire of the Nutritional Habits and Nutrient Consumption Evaluation System<span class="elsevierStyleSup">18</span> determined the average daily phosphorus intake&#46;</p><p class="elsevierStylePara">&#160;</p><p class="elsevierStylePara"><span class="elsevierStyleBold">STATISTICAL ANALYSIS</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara">The results were expressed as means and standard deviations in the case of numeric variables or as proportions for categorical variables&#46; The comparison of means between the two groups was carried out with Student&#8217;s t-test for independent groups or with its non-parametric alternative &#40;U-Mann-Whitney&#41;&#44; in accordance with the distribution of each variable&#46; The comparison of proportions was carried out using the &#967;<span class="elsevierStyleSup">2 </span>test&#46; Variables were associated using Spearman&#8217;s correlation coefficient&#46;</p><p class="elsevierStylePara">We carried out a concordance analysis between two tests &#40;D&#47;P Cr and D&#47;P P&#59; CrCl and PCl&#41; using the Bland and Altman method&#46; We created a graph showing the difference between the two methods against their average&#46; 95&#37; of differences are found in this graph between two limits that define the confidence interval &#40;CI&#41;&#46; The concordance limits are displayed with their respective 95&#37; CI&#46;</p><p class="elsevierStylePara">To compare more than two means&#44; we carried out a one-way ANOVA test with the Bonferroni test&#46; In order to divide up the database in the best way possible with regard to the D&#47;P P variable&#44; we used a classification tree&#44; taking the CHAID &#40;<span class="elsevierStyleItalic">Chi Squared Automatic Interaction Detector</span>&#41; method as the form of growth&#46;</p><p class="elsevierStylePara">Values of <span class="elsevierStyleItalic">P</span>&#60;&#46;05 were considered to be statistically significant&#46; The statistical package SPSS version 15 for Windows was used&#46;</p><p class="elsevierStylePara">&#160;</p><p class="elsevierStylePara"><span class="elsevierStyleBold">RESULTS</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara">We included 60 patients&#44; of which 4 PET were excluded due to having a greater D&#47;P P than the unit and we eliminated 10 solute clearance measurements due to the following&#58; one due to inadequate sample collection&#44; one due to not requiring dialysis after recovery from acute renal damage&#44; four due to a 24-hour ultrafiltration volume lower than the infused volume&#44; two due to being in NAPD mode and two due to not having a stable dialysis dose because of poor adherence to their prescription&#46;</p><p class="elsevierStylePara">The population characteristics and the biochemical and treatment parameters can be observed in Table 1&#46;</p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">Phosphorus</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara">Mean serum phosphorus in our population was 5&#46;3&#177;1&#46;7mg&#47;dl &#40;2&#46;6-9&#46;7mg&#47;dl&#41;&#44; with 21 &#40;31&#46;3&#37;&#41; cases of hyperphosphataemia&#44; with there being a low inverse correlation between phosphorus levels and D&#47;P P&#44; r&#61;&#8722;0&#46;273&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;04 and a statistically significant difference in D&#47;P P in those with normal phosphataemia when we compared them with hyperphosphataemic patients&#44; 0&#46;61&#177;0&#46;13mg&#47;dl versus 0&#46;54&#177;0&#46;10mg&#47;dl &#40;<span class="elsevierStyleItalic">p</span>&#61;&#46;035&#41;&#46; Daily estimated mean phosphorus intake was 1290&#177;472mg&#47;day &#40;522-2794mg&#47;day&#41;&#46; We found that those who consumed a quantity lower than or equal to 1000mg&#47;day &#40;n&#61;18&#44; 32&#37;&#41; had significantly lower serum phosphorus when we compared them with those who consumed more than 1000mg&#47;day &#40;4&#46;8&#177;1&#46;6mg&#47;dl versus 5&#46;6&#177;1&#46;7mg&#47;dl&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;039&#41;&#46;</p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">Dialysate&#47;plasma phosphorus and creatinine ratios</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara">The mean D&#47;P Cr for our population was 0&#46;70&#177;0&#46;10 &#40;0&#46;51-0&#46;92&#41; and the mean D&#47;P P was 0&#46;58&#177;0&#46;12 &#40;0&#46;28-0&#46;85&#41;&#44; and we observed an adequate correlation between the two&#44; with r&#61;0&#46;90&#44; <span class="elsevierStyleItalic">p</span>&#60;&#46;05 &#40;Figure 1&#41;&#46; However&#44; we observed a poor concordance between the two methods with upper and lower limits of D&#47;P Cr with respect to D&#47;P P of &#8722;0&#46;17 &#40;&#8722;0&#46;21 to &#8722;0&#46;13 95&#37; CI&#41; and 0&#46;47 &#40;0&#46;35-0&#46;59 95&#37; CI&#41;&#44; respectively &#40;Figure 2&#41;&#46;</p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">Phosphorus clearance&#44; creatinine clearance and Kt&#47;V of urea</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara">We observed a low correlation between PCl and D&#47;P P &#40;r&#61;0&#46;33&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;02&#41;&#44; and between PCl and D&#47;P Cr &#40;r&#61;0&#46;30&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;03&#41;&#46; However&#44; when we carried out a subanalysis that only included those with a Kt&#47;V of urea &#8805;1&#46;7&#44; we found a correlation between PCl and D&#47;P P &#40;r&#61;0&#46;384&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;04&#41;&#44; but not between PCl and D&#47;P Cr &#40;r&#61;0&#46;348&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;06&#41;&#46; We also explored this association in anuric patients&#44; where we similarly observed that PCl was significantly related to D&#47;P P &#40;r&#61;0&#46;392&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;04&#41;&#44; but not to D&#47;P Cr &#40;r&#61;0&#46;358&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;52&#41;&#46;</p><p class="elsevierStylePara">We attempted to find an association between the Kt&#47;V of urea&#44; CrCl and PCl in their total&#44; peritoneal and renal measurements and we found the following&#58; Kt&#47;V of urea had significant correlations with CrCl in its total&#44; peritoneal and renal measurements &#40;r&#61;0&#46;68&#44; <span class="elsevierStyleItalic">p</span>&#60;&#46;05&#59; r&#61;0&#46;78&#44; <span class="elsevierStyleItalic">p</span>&#60;&#46;05&#59; r&#61;0&#46;47&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;03&#44; respectively&#41;&#59; PCl showed significant correlations with CrCl in its total&#44; peritoneal and renal measurements &#40;r&#61;0&#46;45&#44; <span class="elsevierStyleItalic">p</span>&#60;&#46;05&#44; r&#61;0&#46;59&#44; <span class="elsevierStyleItalic">p</span>&#60;&#46;05 and r&#61;0&#46;67&#44; <span class="elsevierStyleItalic">p</span>&#60;&#46;05&#44; respectively&#41;&#46; However&#44; the concordance analysis showed that it is poor&#44; with lower and upper concordance limits of &#8722;13&#46;54l&#47;week&#47;1&#46;73m<span class="elsevierStyleSup">2</span> BSA &#40;95&#37; CI &#8722;21&#46;68 to &#8722;5&#46;4&#41; and of 58&#46;98l&#47;week&#47;1&#46;73m<span class="elsevierStyleSup">2</span> BSA &#40;95&#37; CI 50&#46;84-67&#46;12&#41;&#44; respectively&#44; of total CrCl with respect to total PCl &#40;Figure 3&#41;&#46; Moreover&#44; renal PCl showed an almost significant association with Kt&#47;V of renal urea &#40;r&#61;0&#46;43&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;05&#41;&#44; while total and peritoneal PCl did not display a significant association with Kt&#47;V of total and peritoneal urea &#40;r&#61;0&#46;18&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;31 for both&#41;&#46;</p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">Phosphorus clearance&#44; serum phosphorus levels and residual renal function</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara">When we divided patients in accordance with diuresis and subdivided each group into normal phosphataemia and hyperphosphataemia &#40;Table 2&#41;&#44; we could observe that mean serum phosphorus for anuric patients with hyperphosphataemia was significantly higher than those with hyperphosphataemia who maintained diuresis &#40;7&#46;4&#177;1&#46;4mg&#47;dl versus 6&#46;3&#177;0&#46;8mg&#47;dl&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;03&#41;&#46; D&#47;P P was significantly lower in anuric patients with hyperphosphataemia&#44; compared with those who had normal serum phosphorus levels &#40;0&#46;51&#177;0&#46;8 versus 0&#46;62&#177;0&#46;14&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;006&#41;&#46; Although total PCl was higher in patients with diuresis compared with the anuric patient subgroup &#40;40&#46;2&#177;10&#46;4l&#47;week&#47;1&#46;73m<span class="elsevierStyleSup">2</span> BSA vs&#46; 35&#46;6&#177;9&#46;6l&#47;week&#47;1&#46;73m<span class="elsevierStyleSup">2</span> BSA&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;12&#41;&#44; it was not significantly different&#46; However&#44; peritoneal PCl in anuric patients was significantly higher when we compared it with patients who maintained diuresis &#40;35&#46;5&#177;9&#46;8l&#47;week&#47;1&#46;73m<span class="elsevierStyleSup">2</span> BSA vs&#46; 28&#46;3&#177;10&#46;25l&#47;week&#47;1&#46;73m<span class="elsevierStyleSup">2</span> BSA&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;01&#41;&#46; Residual renal function was significantly lower in patients with hyperphosphataemia compared with those with normal phosphataemia &#40;3&#46;2&#177;1&#46;2ml&#47;min vs&#46; 4&#46;8&#177;2&#46;0ml&#47;min&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;048&#41;&#46;</p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">Phosphorus excretion</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara">We also evaluated the potential association between total and peritoneal phosphorus excretion with total and peritoneal CrCl and PCl&#44; and we found the following&#58; total phosphorus excretion showed a better correlation with total PCl &#40;r&#61;0&#46;62&#44; <span class="elsevierStyleItalic">p</span>&#60;&#46;05&#41; than with total CrCl &#40;r&#61;0&#46;360&#44; <span class="elsevierStyleItalic">p</span>&#60;&#46;05&#41;&#46; Peritoneal phosphorus excretion also had a better correlation with peritoneal PCl &#40;r&#61;0&#46;687&#44; <span class="elsevierStyleItalic">p</span>&#60;&#46;05&#41; in comparison with peritoneal CrCl &#40;r&#61;0&#46;466&#44; <span class="elsevierStyleItalic">p</span>&#60;&#46;05&#41;&#46; Lastly&#44; in patients with a Kt&#47;V of urea &#8805;1&#46;7 the correlation between total PCl and total phosphorus excretion was significant &#40;r&#61;0&#46;643&#44; <span class="elsevierStyleItalic">p</span>&#60;&#46;05&#41;&#44; but was not between total CrCl and total phosphorus excretion &#40;r&#61;0&#46;222&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;23&#41;&#46;</p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">Categorization of phosphorus transport</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara">On the basis of D&#47;P P distribution using the CHAID method&#44; we created a classification tree and obtained the following nodes with their respective ranges&#58; node 1&#58; &#8804;0&#46;5&#44; node 2&#58; 0&#46;51-0&#46;55&#44; node 3&#58; 0&#46;56-0&#46;66&#44; node 4&#58; 0&#46;67-0&#46;76&#44; node 5&#58; &#62;0&#46;76&#44; and we found statistically significant differences between nodes in terms of serum phosphorus levels&#44; total and peritoneal PCl&#44; and Kt&#47;V of urea &#40;Table 3&#41;&#46;</p><p class="elsevierStylePara">&#160;</p><p class="elsevierStylePara"><span class="elsevierStyleBold">DISCUSSION</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara">Phosphorus clearance is the result of the complex interaction between diffusion&#44; convection&#44; osmotic and chemical factors&#44; electrical gradients&#44; and active transmembrane phosphorus transporters<span class="elsevierStyleSup">19&#44;20</span>&#46; It has been demonstrated that absorption by lymphatic convection has no impact and that solutions with a higher concentration remove a higher quantity of phosphorus and are attributed to the convection factor&#46; However&#44; it was not possible to establish for certain whether ultrafiltration influences clearance<span class="elsevierStyleSup">21</span>&#46; Messa et al&#46; demonstrated in 35 patients that glucose concentration was one of the predictors of phosphorus clearance and this was independent of the ultrafiltration volume<span class="elsevierStyleSup">22</span>&#44; while Granja et al&#46; calculated that 11&#37; of the phosphorus eliminated was due to ultrafiltration<span class="elsevierStyleSup">23</span>&#46;</p><p class="elsevierStylePara">In our population&#44; we found that the frequency of hyperphosphataemia was 31&#46;3&#37;&#44; which is similar to that reported in the literature<span class="elsevierStyleSup">7</span>&#46; In previous studies&#44; an adequate correlation was found between D&#47;P Cr and D&#47;P P&#44; and between CrCl and PCl&#44; suggesting equivalence between them<span class="elsevierStyleSup">12&#44;13</span>&#46; In this study&#44; we demonstrated that although&#44; D&#47;P Cr and D&#47;P P displayed adequate correlation&#44; the concordance was poor&#44; since the concordance limits were very broad&#46; With such great variability of D&#47;P Cr or CrCl with respect to the phosphorus parameters&#44; there would be a very significant impact on clearance&#44; excretion and therefore serum phosphorus levels&#44; and as such&#44; these measurements could not be considered equivalents&#46; For example&#44; a patient with a D&#47;P P of 0&#46;4 may have a D&#47;P Cr from 0&#46;16 to 0&#46;94&#44; values that are very different from the value of D&#47;P P&#46; Likewise&#44; a patient with PCl of 35l&#47;week&#47;1&#46;73m<span class="elsevierStyleSup">2</span> BSA could have CrCl from 13&#46;32l&#47;week&#47;1&#46;73m<span class="elsevierStyleSup">2</span> BSA to 102&#46;12l&#47;week&#47;1&#46;73m<span class="elsevierStyleSup">2</span> BSA&#46; Given the poor concordance that exists between the values studied and that they cannot be taken as replacements&#44; we proposed a phosphorus transport classification tree with five nodes based on its D&#47;P P&#44; amongst which we identified statistically significant differences between groups for total and peritoneal PCl&#46;</p><p class="elsevierStylePara">Our results confirm the role of diuresis in maintaining phosphorus levels at low values compared to anuria&#46; In anuric patients&#44; in whom the peritoneum has an exclusive role in phosphorus clearance&#44; the determination of phosphorus transport indicators is particularly important for two factors&#58; 1&#41; D&#47;P P is significantly lower in hyperphosphataemic patients&#59; 2&#41; Peritoneal PCl is significantly higher compared with those who maintain diuresis &#40;Table 2&#41;&#46;</p><p class="elsevierStylePara">The current recommendations for the prescription of peritoneal dialysis in accordance with the 2006 K&#47;DOQI clinical guidelines<span class="elsevierStyleSup">24</span>&#44; based on the results of three major studies<span class="elsevierStyleSup">25-27</span>&#44; set a Kt&#47;V of urea target of &#8805;1&#46;7&#44; which has not managed to reduce mortality in this population&#46; As such&#44; the search for new markers of targets is vitally important&#46; The current recommendations are to maintain the phosphorus level within the normal limits<span class="elsevierStyleSup">28</span>&#44; although this is an arduous challenge for patients and physicians&#44; since beyond dietary restriction and the adequate use of binders&#44; the doctor must know the role that dialysis exercises on PCl&#46; This study demonstrates the independence of phosphorus transport with respect to urea and creatinine and it leads to a series of questions such as the PCl dose necessary for helping patients achieve the serum phosphorus targets&#44; whether this value is different in patients with diuresis and anuric patients&#44; whether the dialysis adjustment to achieve an established PCl target improves mortality compared with the current Kt&#47;V of urea targets or whether a low D&#47;P P is associated with greater mortality&#44; amongst others&#46; As such&#44; studies must be carried out to determine the benefits of the adjustment of peritoneal dialysis based on D&#47;P P with different PCl doses&#44; establish the mid- and long-term morbidity and mortality&#44; and thus compare them with the current recommendations on dialysis&#46;</p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">CONCLUSIONS</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara">This study shows that D&#47;P P and PCl measurements are not concordant with those of D&#47;P Cr and CrCl&#44; respectively&#44; despite having an adequate correlation&#46; As such&#44; given the current lack of knowledge about phosphorus transport in peritoneal dialysis in clinical practice&#44; in a group of patients in whom phosphataemia control is imperative&#44; it is necessary to give continuity to the research of these indicators&#44; since they are useful tools for physicians and may guide dialysis prescription in search for a better control of serum phosphorus&#46;</p><p class="elsevierStylePara">&#160;</p><p class="elsevierStylePara"><span class="elsevierStyleBold">Conflicts of interest</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara">The authors declare that they have no conflicts of interest related to the contents of this article&#46;</p><p class="elsevierStylePara"><a href="grande&#47;12281&#95;16025&#95;61888&#95;en&#95;t112281&#46;jpg" class="elsevierStyleCrossRefs"><img src="12281_16025_61888_en_t112281.jpg" alt="Population characteristics&#58; medical and dialysis management "></img></a></p><p class="elsevierStylePara">Table 1&#46; Population characteristics&#58; medical and dialysis management </p><p class="elsevierStylePara"><a href="grande&#47;12281&#95;16025&#95;61889&#95;en&#95;t212281&#46;jpg" class="elsevierStyleCrossRefs"><img src="12281_16025_61889_en_t212281.jpg" alt="Transport of solutes&#44; dialysis dose and phosphataemia in accordance with residual uresis"></img></a></p><p class="elsevierStylePara">Table 2&#46; Transport of solutes&#44; dialysis dose and phosphataemia in accordance with residual uresis</p><p class="elsevierStylePara"><a href="grande&#47;12281&#95;16025&#95;61890&#95;en&#95;t312281&#46;jpg" class="elsevierStyleCrossRefs"><img src="12281_16025_61890_en_t312281.jpg" alt="Phosphorus and clearance characteristics between transport nodes "></img></a></p><p class="elsevierStylePara">Table 3&#46; Phosphorus and clearance characteristics between transport nodes </p><p class="elsevierStylePara"><a href="grande&#47;12281&#95;16025&#95;61892&#95;en&#95;f112281&#46;jpg" class="elsevierStyleCrossRefs"><img src="12281_16025_61892_en_f112281.jpg" alt="Correlation between the dialysate&#47;plasma creatinine ratio and the dialysate&#47;plasma phosphorus ratio&#46;"></img></a></p><p class="elsevierStylePara">Figure 1&#46; Correlation between the dialysate&#47;plasma creatinine ratio and the dialysate&#47;plasma phosphorus ratio&#46;</p><p class="elsevierStylePara"><a href="grande&#47;12281&#95;16025&#95;61893&#95;en&#95;f2122813&#46;jpg" class="elsevierStyleCrossRefs"><img src="12281_16025_61893_en_f2122813.jpg" alt="Concordance between the dialysate&#47;plasma creatinine ratio and the dialysate&#47;plasma phosphorus ratio&#46;"></img></a></p><p class="elsevierStylePara">Figure 2&#46; Concordance between the dialysate&#47;plasma creatinine ratio and the dialysate&#47;plasma phosphorus ratio&#46;</p><p class="elsevierStylePara"><a href="grande&#47;12281&#95;16025&#95;61894&#95;en&#95;f3122813&#46;jpg" class="elsevierStyleCrossRefs"><img src="12281_16025_61894_en_f3122813.jpg" alt="Concordance between creatinine clearance and phosphorus clearance&#46;"></img></a></p><p class="elsevierStylePara">Figure 3&#46; Concordance between creatinine clearance and phosphorus clearance&#46;</p>"
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        "resumen" => "<p class="elsevierStylePara"><span class="elsevierStyleBold">Introducci&#243;n&#58;</span> La hiperfosfatemia &#40;f&#243;sforo s&#233;rico &#8805;&#160;5&#44;5&#160;mg&#47;dl&#41; es un factor independiente de mortalidad en la poblaci&#243;n en di&#225;lisis&#46; Comparamos el transporte peritoneal de f&#243;sforo&#44; creatinina y urea para demostrar diferencias y se&#241;alar la relevancia de estos par&#225;metros en el control del f&#243;sforo s&#233;rico&#46; <span class="elsevierStyleBold">Material y m&#233;todos&#58;</span> Se incluyeron 60 pacientes en di&#225;lisis peritoneal y se determin&#243; el &#237;ndice dializante&#47;plasma de f&#243;sforo &#40;D&#47;P P&#41; y creatinina &#40;D&#47;P Cr&#41;&#44; el aclaramiento semanal de f&#243;sforo &#40;AclP&#41; y creatinina &#40;AclCr&#41;&#44; Kt&#47;V de urea semanal y la excreci&#243;n peritoneal de f&#243;sforo &#40;ExP&#41;&#46; <span class="elsevierStyleBold">Resultados&#58;</span> El D&#47;P P fue superior en pacientes con normofosfatemia&#44; comparados con los que presentaron hiperfosfatemia&#44; 0&#44;61&#160;&#177;&#160;0&#44;13 frente a 0&#44;54&#160;&#177;&#160;0&#44;10 &#40;<span class="elsevierStyleItalic">p&#160;</span>&#61;&#160;0&#44;035&#41;&#46; Se observ&#243; una adecuada correlaci&#243;n entre el D&#47;P P y el D&#47;P Cr&#44; r&#160;&#61;&#160;0&#44;90&#44; p&#160;&#60;&#160;0&#44;05&#44; pero una pobre concordancia entre ambos&#44; con un l&#237;mite inferior de &#8722;0&#44;17 &#40;&#8722;0&#44;24 a &#8722;0&#44;09 IC 95&#160;&#37;&#41; y l&#237;mite superior de 0&#44;47 &#40;0&#44;39-0&#44;54 IC 95&#160;&#37;&#41; para el D&#47;P Cr respecto al D&#47;P P&#46; El AclP tuvo una adecuada correlaci&#243;n con el D&#47;P P en pacientes con Kt&#47;V &#8805;&#160;1&#44;7 &#40;r&#160;&#61;&#160;0&#44;384&#44; <span class="elsevierStyleItalic">p</span>&#160;&#61;&#160;0&#44;04&#41; y en an&#250;ricos &#40;r&#160;&#61;&#160;0&#44;392&#44; p&#160;&#61;&#160;0&#44;04&#41;&#44; pero no con el D&#47;P Cr&#46; Hubo una pobre concordancia del AclCr respecto al AclP con l&#237;mite inferior de &#8722;13&#44;54&#160;l&#47;sem&#47;1&#44;73&#160;m<span class="elsevierStyleSup">2</span> SC &#40;&#8722;21&#44;68 a &#8722;5&#44;4 IC 95&#160;&#37;&#41; y l&#237;mite superior de 58&#44;98&#160;l&#47;sem&#47;1&#44;73&#160;m<span class="elsevierStyleSup">2</span> SC &#40;50&#44;84-67&#44;12 IC 95&#160;&#37;&#41;&#46; La ExP total se relacion&#243; con el AclP &#40;r&#160;&#61;&#160;0&#44;643&#44; <span class="elsevierStyleItalic">p</span>&#160;&#60;&#160;0&#44;05&#41;&#44; mientras que no lo hizo con el AclCr &#40;r&#160;&#61;&#160;0&#44;222&#44; <span class="elsevierStyleItalic">p</span>&#160;&#61;&#160;0&#44;23&#41;&#46; Mediante el m&#233;todo CHAID se realiz&#243; un &#225;rbol de clasificaci&#243;n del transporte de f&#243;sforo con base en su D&#47;P&#44; obteniendo 5 nodos &#40;&#8804;&#160;0&#44;5&#44; 0&#44;51-0&#44;55&#44; 0&#44;56-0&#44;66&#44; 0&#44;67-0&#44;76&#44; &#62;&#160;0&#44;76&#41;&#44; mostrando diferencias estad&#237;sticamente significativas entre nodos para niveles s&#233;ricos de f&#243;sforo&#44; AclP total y peritoneal&#44; as&#237; como Kt&#47;V de urea semanal&#46; <span class="elsevierStyleBold">Conclusiones&#58;</span> Las mediciones de D&#47;P P y AclP no concuerdan con las mediciones de D&#47;P Cr y AclCr&#44; respectivamente&#44; por lo que su determinaci&#243;n es una herramienta cl&#237;nica para el control del nivel de f&#243;sforo s&#233;rico&#46;</p>"
      ]
      "en" => array:1 [
        "resumen" => "<p class="elsevierStylePara"><span class="elsevierStyleBold">Background&#58;</span> Hyperphosphataemia &#40;serum phosphorus &#8805;5&#46;5mg&#47;dl&#41; is an independent mortality factor for the dialysis population&#46; We compared phosphorus&#44; creatinine and urea peritoneal transport to demonstrate differences and indicate the relevance of these parameters in the control of serum phosphorus&#46; <span class="elsevierStyleBold">Material and method&#58;</span> We included 60 patients on peritoneal dialysis and determined the dialysate&#47;plasma phosphorus &#40;D&#47;P P&#41; and creatinine &#40;D&#47;P Cr&#41; ratios&#44; weekly creatinine clearance &#40;CrCl&#41; and phosphorus clearance &#40;PCl&#41;&#44; weekly Kt&#47;V of urea&#44; and peritoneal phosphorus excretion &#40;PEx&#41;&#46; <span class="elsevierStyleBold">Results&#58;</span> D&#47;P P was higher in patients with normal phosphataemia&#44; compared with those who were hyperphosphataemic 0&#46;61&#177;0&#46;13 versus 0&#46;54&#177;0&#46;10 &#40;<span class="elsevierStyleItalic">p</span>&#61;&#46;035&#41;&#46; We observed an adequate correlation between D&#47;P P and D&#47;P Cr&#44; r&#61;0&#46;90&#44; <span class="elsevierStyleItalic">p</span>&#60;&#46;05&#44; but poor concordance between both&#44; with a lower limit of &#8722;0&#46;17 &#40;&#8722;0&#46;24 to &#8722;0&#46;09 95&#37; CI&#41; and an upper limit of 0&#46;47 &#40;0&#46;39-0&#46;54 95&#37; CI&#41; for D&#47;P Cr with respect to D&#47;P P&#46; PCl had an adequate correlation with D&#47;P P in patients with a Kt&#47;V &#8805;1&#46;7 &#40;r&#61;0&#46;384&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;04&#41; and in anuric patients &#40;r&#61;0&#46;392&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;04&#41;&#44; but not with D&#47;P Cr&#46; There was poor concordance of the CrCl with respect to PCl with a lower limit of &#8722;13&#46;54l&#47;week&#47;1&#46;73m<span class="elsevierStyleSup">2</span> BSA &#40;&#8722;21&#46;68 to &#8722;5&#46;4 95&#37; CI&#41; and an upper limit of 58&#46;98l&#47;week&#47;1&#46;73m<span class="elsevierStyleSup">2</span> BSA &#40;50&#46;84-67&#46;12 95&#37; CI&#41;&#46; Total PEx was related to PCl &#40;r&#61;0&#46;643&#44; <span class="elsevierStyleItalic">p</span>&#60;&#46;05&#41;&#44; while it was not related to CrCl &#40;r&#61;0&#46;222&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;23&#41;&#46; Using the CHAID method&#44; we created a classification tree for phosphorus transport based on its D&#47;P&#44; obtaining 5 nodes &#40;&#8804;0&#46;5&#44; 0&#46;51-0&#46;55&#44; 0&#46;56-0&#46;66&#44; 0&#46;67-0&#46;76&#44; &#62;0&#46;76&#41;&#44; with statistically significant differences between nodes for serum phosphorus&#44; total and peritoneal PCl and weekly Kt&#47;V of urea&#46; <span class="elsevierStyleBold">Conclusions&#58;</span> D&#47;P P and PCl are not concordant with D&#47;P Cr and CrCl respectively and therefore their determination is a clinical tool to control serum phosphorus levels&#46;</p>"
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            19 => array:3 [
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                  ]
                ]
              ]
            ]
            20 => array:3 [
              "identificador" => "bib21"
              "etiqueta" => "21"
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                0 => array:3 [
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                  ]
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                  ]
                ]
              ]
            ]
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Determination of peritoneal phosphate transport as a tool for controlling serum phosphorus
Determinación del transporte peritoneal de fósforo como herramienta para el control del fósforo sérico
Eduardo A. López-Guerraa, Eduardo A. López-Guerraa, Víctor H. Rodríguez-Garcíab, Francisco E. Rodríguez-Castellanosb
a Servicio de Nefrología, Instituto Nacional de Cardiología Ignacio Chávez Ciudad de México, Distrito Federal, México,
b Servicio de Nefrología, Instituto Nacional de Cardiología Ignacio Chavez Ciudad de México, Distrito Federal, México,
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    "textoCompleto" => "<p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">INTRODUCTION</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara">Cardiovascular disease is the main cause of mortality in population with advanced renal disease&#44; and hyperphosphatemia &#40;serum phosphate &#62; 5&#46;5 mg&#47;dl&#41; is an independent risk factor that can range from 30 to 40&#37; of the population subjected to renal replacement therapy&#44; resulting amongst other complications&#44; calcification of the tunica media of blood vessels&#44; particularly in coronary arteries&#44; which precipitates acute cardiovascular events&#44; with fatal consequences<span class="elsevierStyleSup">1-10</span>&#46; For these reasons&#44; controlling serum phosphorus is imperative in the management of chronic kidney disease patients&#46;</p><p class="elsevierStylePara">There is little information with respect to weekly phosphorus clearance &#40;PCl&#41; and dialysate&#47;plasma phosphorus &#40;D&#47;P P&#41;&#46; Sedlacek et al&#46; found a high correlation between dialysate&#47;plasma creatinine &#40;D&#47;P Cr&#41; and D&#47;P P&#44; as well as their respective clearances&#44; concluding that the clearance of both solutes is closely linked&#44; and as such&#44; the main determinant for weekly creatinine clearance &#40;CrCl&#41; and PCl is D&#47;P Cr<span class="elsevierStyleSup">11</span>&#46; In a study of paediatric patients on automated peritoneal dialysis&#44; they found a good correlation between both D&#47;P&#44; but PCl was related better to D&#47;P P than to D&#47;P Cr&#44; with the conclusion that the former is a better predictor<span class="elsevierStyleSup">12</span>&#46; Bernardo et al&#46; classified phosphorus transport by its D&#47;P based on Twardowski&#8217;s creatinine transport classification<span class="elsevierStyleSup">13 </span>and they observed that the distribution of patients based on D&#47;P P in the different categories was different to that presented for D&#47;P Cr&#44; suggesting that&#44; despite there being a correlation between D&#47;P P and D&#47;P Cr&#44; the latter measure is not adequate enough to classify patients in accordance with the transport of phosphorus<span class="elsevierStyleSup">14</span>&#46; This study evaluates concordance between D&#47;P Cr and D&#47;P P&#44; and between CrCl and PCl&#44; using the Bland and Altman method<span class="elsevierStyleSup">15</span>&#44; with the objective of finding out how much one test may differ from the other and thus determine whether D&#47;P Cr and CrCl can continue to be reliable replacements of peritoneal phosphorus transport&#46; Furthermore&#44; we evaluated peritoneal phosphorus transport in a dialysis population with the aim of highlighting its role in phosphataemia control beyond dietary restriction and the use of phosphate binders&#46;</p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">MATERIALs AND METHODs</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara">We carried out a cross-sectional&#44; observational and comparative study in which we included 60 patients of the peritoneal dialysis outpatient clinic&#46; Inclusion criteria&#58; patients older than 16 years of age who were on renal replacement therapy for at least one month through continuous ambulatory peritoneal dialysis or nocturnal automated peritoneal dialysis &#40;NAPD&#41;&#46; Exclusion criteria&#58; having presented with peritonitis at the time of the study&#44; with this being considered to be the presence of 100 or more leukocytes per field in the cytological study of dialysate&#44; who completed antibiotic treatment within the two previous months or patients who presented or had presented in the previous month with an incapacitating medical condition&#46; For the peritoneal equilibration test &#40;PET&#41;&#44; we included as exclusion criteria ultrafiltration failure&#44; defined as lower than 400ml after the application of a 4&#46;25&#37; 2000ml bag after 4 hours in the peritoneal cavity&#44; catheter mechanical problems&#44; defined as a fluid entry time greater than 10 minutes and an exit time greater than 30 minutes or having greater D&#47;P P than the unit&#46; The following were counted as exclusion criteria in solute clearance measurement&#58; NAPD mode &#40;reasons unrelated to the interests of this study&#41;&#44; peritonitis&#44; the 24-hour dialysate effluent volume being lower than the infused volume and a lack of adherence to the dialysis prescription&#44; confirmed subjectively by the patient&#46;</p><p class="elsevierStylePara">We performed a PET on all patients using a 4&#46;25&#37; solution to determine D&#47;P P and D&#47;P Cr&#46; We carried out a cytology of the dialysate in order to rule out an active infectious condition&#46; We calculated weekly the Kt&#47;V of urea and weekly PCl and CrCl expressed in litres per week adjusted to body surface area &#40;l&#47;week&#47;1&#46;73m<span class="elsevierStyleSup">2</span> BSA&#41;&#44; all in their renal&#44; peritoneal and total forms using standard methods<span class="elsevierStyleSup">16</span>&#44; as well as the normalized protein nitrogen appearance using the Randerson formula<span class="elsevierStyleSup">17</span>&#46; The urine samples were only collected for those with diuresis equal to or greater than 200ml&#47;day&#59; if this was not the case&#44; they were considered anuric&#46; The Department of Nutrition&#44; though the food frequency questionnaire of the Nutritional Habits and Nutrient Consumption Evaluation System<span class="elsevierStyleSup">18</span> determined the average daily phosphorus intake&#46;</p><p class="elsevierStylePara">&#160;</p><p class="elsevierStylePara"><span class="elsevierStyleBold">STATISTICAL ANALYSIS</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara">The results were expressed as means and standard deviations in the case of numeric variables or as proportions for categorical variables&#46; The comparison of means between the two groups was carried out with Student&#8217;s t-test for independent groups or with its non-parametric alternative &#40;U-Mann-Whitney&#41;&#44; in accordance with the distribution of each variable&#46; The comparison of proportions was carried out using the &#967;<span class="elsevierStyleSup">2 </span>test&#46; Variables were associated using Spearman&#8217;s correlation coefficient&#46;</p><p class="elsevierStylePara">We carried out a concordance analysis between two tests &#40;D&#47;P Cr and D&#47;P P&#59; CrCl and PCl&#41; using the Bland and Altman method&#46; We created a graph showing the difference between the two methods against their average&#46; 95&#37; of differences are found in this graph between two limits that define the confidence interval &#40;CI&#41;&#46; The concordance limits are displayed with their respective 95&#37; CI&#46;</p><p class="elsevierStylePara">To compare more than two means&#44; we carried out a one-way ANOVA test with the Bonferroni test&#46; In order to divide up the database in the best way possible with regard to the D&#47;P P variable&#44; we used a classification tree&#44; taking the CHAID &#40;<span class="elsevierStyleItalic">Chi Squared Automatic Interaction Detector</span>&#41; method as the form of growth&#46;</p><p class="elsevierStylePara">Values of <span class="elsevierStyleItalic">P</span>&#60;&#46;05 were considered to be statistically significant&#46; The statistical package SPSS version 15 for Windows was used&#46;</p><p class="elsevierStylePara">&#160;</p><p class="elsevierStylePara"><span class="elsevierStyleBold">RESULTS</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara">We included 60 patients&#44; of which 4 PET were excluded due to having a greater D&#47;P P than the unit and we eliminated 10 solute clearance measurements due to the following&#58; one due to inadequate sample collection&#44; one due to not requiring dialysis after recovery from acute renal damage&#44; four due to a 24-hour ultrafiltration volume lower than the infused volume&#44; two due to being in NAPD mode and two due to not having a stable dialysis dose because of poor adherence to their prescription&#46;</p><p class="elsevierStylePara">The population characteristics and the biochemical and treatment parameters can be observed in Table 1&#46;</p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">Phosphorus</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara">Mean serum phosphorus in our population was 5&#46;3&#177;1&#46;7mg&#47;dl &#40;2&#46;6-9&#46;7mg&#47;dl&#41;&#44; with 21 &#40;31&#46;3&#37;&#41; cases of hyperphosphataemia&#44; with there being a low inverse correlation between phosphorus levels and D&#47;P P&#44; r&#61;&#8722;0&#46;273&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;04 and a statistically significant difference in D&#47;P P in those with normal phosphataemia when we compared them with hyperphosphataemic patients&#44; 0&#46;61&#177;0&#46;13mg&#47;dl versus 0&#46;54&#177;0&#46;10mg&#47;dl &#40;<span class="elsevierStyleItalic">p</span>&#61;&#46;035&#41;&#46; Daily estimated mean phosphorus intake was 1290&#177;472mg&#47;day &#40;522-2794mg&#47;day&#41;&#46; We found that those who consumed a quantity lower than or equal to 1000mg&#47;day &#40;n&#61;18&#44; 32&#37;&#41; had significantly lower serum phosphorus when we compared them with those who consumed more than 1000mg&#47;day &#40;4&#46;8&#177;1&#46;6mg&#47;dl versus 5&#46;6&#177;1&#46;7mg&#47;dl&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;039&#41;&#46;</p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">Dialysate&#47;plasma phosphorus and creatinine ratios</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara">The mean D&#47;P Cr for our population was 0&#46;70&#177;0&#46;10 &#40;0&#46;51-0&#46;92&#41; and the mean D&#47;P P was 0&#46;58&#177;0&#46;12 &#40;0&#46;28-0&#46;85&#41;&#44; and we observed an adequate correlation between the two&#44; with r&#61;0&#46;90&#44; <span class="elsevierStyleItalic">p</span>&#60;&#46;05 &#40;Figure 1&#41;&#46; However&#44; we observed a poor concordance between the two methods with upper and lower limits of D&#47;P Cr with respect to D&#47;P P of &#8722;0&#46;17 &#40;&#8722;0&#46;21 to &#8722;0&#46;13 95&#37; CI&#41; and 0&#46;47 &#40;0&#46;35-0&#46;59 95&#37; CI&#41;&#44; respectively &#40;Figure 2&#41;&#46;</p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">Phosphorus clearance&#44; creatinine clearance and Kt&#47;V of urea</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara">We observed a low correlation between PCl and D&#47;P P &#40;r&#61;0&#46;33&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;02&#41;&#44; and between PCl and D&#47;P Cr &#40;r&#61;0&#46;30&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;03&#41;&#46; However&#44; when we carried out a subanalysis that only included those with a Kt&#47;V of urea &#8805;1&#46;7&#44; we found a correlation between PCl and D&#47;P P &#40;r&#61;0&#46;384&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;04&#41;&#44; but not between PCl and D&#47;P Cr &#40;r&#61;0&#46;348&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;06&#41;&#46; We also explored this association in anuric patients&#44; where we similarly observed that PCl was significantly related to D&#47;P P &#40;r&#61;0&#46;392&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;04&#41;&#44; but not to D&#47;P Cr &#40;r&#61;0&#46;358&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;52&#41;&#46;</p><p class="elsevierStylePara">We attempted to find an association between the Kt&#47;V of urea&#44; CrCl and PCl in their total&#44; peritoneal and renal measurements and we found the following&#58; Kt&#47;V of urea had significant correlations with CrCl in its total&#44; peritoneal and renal measurements &#40;r&#61;0&#46;68&#44; <span class="elsevierStyleItalic">p</span>&#60;&#46;05&#59; r&#61;0&#46;78&#44; <span class="elsevierStyleItalic">p</span>&#60;&#46;05&#59; r&#61;0&#46;47&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;03&#44; respectively&#41;&#59; PCl showed significant correlations with CrCl in its total&#44; peritoneal and renal measurements &#40;r&#61;0&#46;45&#44; <span class="elsevierStyleItalic">p</span>&#60;&#46;05&#44; r&#61;0&#46;59&#44; <span class="elsevierStyleItalic">p</span>&#60;&#46;05 and r&#61;0&#46;67&#44; <span class="elsevierStyleItalic">p</span>&#60;&#46;05&#44; respectively&#41;&#46; However&#44; the concordance analysis showed that it is poor&#44; with lower and upper concordance limits of &#8722;13&#46;54l&#47;week&#47;1&#46;73m<span class="elsevierStyleSup">2</span> BSA &#40;95&#37; CI &#8722;21&#46;68 to &#8722;5&#46;4&#41; and of 58&#46;98l&#47;week&#47;1&#46;73m<span class="elsevierStyleSup">2</span> BSA &#40;95&#37; CI 50&#46;84-67&#46;12&#41;&#44; respectively&#44; of total CrCl with respect to total PCl &#40;Figure 3&#41;&#46; Moreover&#44; renal PCl showed an almost significant association with Kt&#47;V of renal urea &#40;r&#61;0&#46;43&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;05&#41;&#44; while total and peritoneal PCl did not display a significant association with Kt&#47;V of total and peritoneal urea &#40;r&#61;0&#46;18&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;31 for both&#41;&#46;</p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">Phosphorus clearance&#44; serum phosphorus levels and residual renal function</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara">When we divided patients in accordance with diuresis and subdivided each group into normal phosphataemia and hyperphosphataemia &#40;Table 2&#41;&#44; we could observe that mean serum phosphorus for anuric patients with hyperphosphataemia was significantly higher than those with hyperphosphataemia who maintained diuresis &#40;7&#46;4&#177;1&#46;4mg&#47;dl versus 6&#46;3&#177;0&#46;8mg&#47;dl&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;03&#41;&#46; D&#47;P P was significantly lower in anuric patients with hyperphosphataemia&#44; compared with those who had normal serum phosphorus levels &#40;0&#46;51&#177;0&#46;8 versus 0&#46;62&#177;0&#46;14&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;006&#41;&#46; Although total PCl was higher in patients with diuresis compared with the anuric patient subgroup &#40;40&#46;2&#177;10&#46;4l&#47;week&#47;1&#46;73m<span class="elsevierStyleSup">2</span> BSA vs&#46; 35&#46;6&#177;9&#46;6l&#47;week&#47;1&#46;73m<span class="elsevierStyleSup">2</span> BSA&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;12&#41;&#44; it was not significantly different&#46; However&#44; peritoneal PCl in anuric patients was significantly higher when we compared it with patients who maintained diuresis &#40;35&#46;5&#177;9&#46;8l&#47;week&#47;1&#46;73m<span class="elsevierStyleSup">2</span> BSA vs&#46; 28&#46;3&#177;10&#46;25l&#47;week&#47;1&#46;73m<span class="elsevierStyleSup">2</span> BSA&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;01&#41;&#46; Residual renal function was significantly lower in patients with hyperphosphataemia compared with those with normal phosphataemia &#40;3&#46;2&#177;1&#46;2ml&#47;min vs&#46; 4&#46;8&#177;2&#46;0ml&#47;min&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;048&#41;&#46;</p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">Phosphorus excretion</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara">We also evaluated the potential association between total and peritoneal phosphorus excretion with total and peritoneal CrCl and PCl&#44; and we found the following&#58; total phosphorus excretion showed a better correlation with total PCl &#40;r&#61;0&#46;62&#44; <span class="elsevierStyleItalic">p</span>&#60;&#46;05&#41; than with total CrCl &#40;r&#61;0&#46;360&#44; <span class="elsevierStyleItalic">p</span>&#60;&#46;05&#41;&#46; Peritoneal phosphorus excretion also had a better correlation with peritoneal PCl &#40;r&#61;0&#46;687&#44; <span class="elsevierStyleItalic">p</span>&#60;&#46;05&#41; in comparison with peritoneal CrCl &#40;r&#61;0&#46;466&#44; <span class="elsevierStyleItalic">p</span>&#60;&#46;05&#41;&#46; Lastly&#44; in patients with a Kt&#47;V of urea &#8805;1&#46;7 the correlation between total PCl and total phosphorus excretion was significant &#40;r&#61;0&#46;643&#44; <span class="elsevierStyleItalic">p</span>&#60;&#46;05&#41;&#44; but was not between total CrCl and total phosphorus excretion &#40;r&#61;0&#46;222&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;23&#41;&#46;</p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">Categorization of phosphorus transport</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara">On the basis of D&#47;P P distribution using the CHAID method&#44; we created a classification tree and obtained the following nodes with their respective ranges&#58; node 1&#58; &#8804;0&#46;5&#44; node 2&#58; 0&#46;51-0&#46;55&#44; node 3&#58; 0&#46;56-0&#46;66&#44; node 4&#58; 0&#46;67-0&#46;76&#44; node 5&#58; &#62;0&#46;76&#44; and we found statistically significant differences between nodes in terms of serum phosphorus levels&#44; total and peritoneal PCl&#44; and Kt&#47;V of urea &#40;Table 3&#41;&#46;</p><p class="elsevierStylePara">&#160;</p><p class="elsevierStylePara"><span class="elsevierStyleBold">DISCUSSION</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara">Phosphorus clearance is the result of the complex interaction between diffusion&#44; convection&#44; osmotic and chemical factors&#44; electrical gradients&#44; and active transmembrane phosphorus transporters<span class="elsevierStyleSup">19&#44;20</span>&#46; It has been demonstrated that absorption by lymphatic convection has no impact and that solutions with a higher concentration remove a higher quantity of phosphorus and are attributed to the convection factor&#46; However&#44; it was not possible to establish for certain whether ultrafiltration influences clearance<span class="elsevierStyleSup">21</span>&#46; Messa et al&#46; demonstrated in 35 patients that glucose concentration was one of the predictors of phosphorus clearance and this was independent of the ultrafiltration volume<span class="elsevierStyleSup">22</span>&#44; while Granja et al&#46; calculated that 11&#37; of the phosphorus eliminated was due to ultrafiltration<span class="elsevierStyleSup">23</span>&#46;</p><p class="elsevierStylePara">In our population&#44; we found that the frequency of hyperphosphataemia was 31&#46;3&#37;&#44; which is similar to that reported in the literature<span class="elsevierStyleSup">7</span>&#46; In previous studies&#44; an adequate correlation was found between D&#47;P Cr and D&#47;P P&#44; and between CrCl and PCl&#44; suggesting equivalence between them<span class="elsevierStyleSup">12&#44;13</span>&#46; In this study&#44; we demonstrated that although&#44; D&#47;P Cr and D&#47;P P displayed adequate correlation&#44; the concordance was poor&#44; since the concordance limits were very broad&#46; With such great variability of D&#47;P Cr or CrCl with respect to the phosphorus parameters&#44; there would be a very significant impact on clearance&#44; excretion and therefore serum phosphorus levels&#44; and as such&#44; these measurements could not be considered equivalents&#46; For example&#44; a patient with a D&#47;P P of 0&#46;4 may have a D&#47;P Cr from 0&#46;16 to 0&#46;94&#44; values that are very different from the value of D&#47;P P&#46; Likewise&#44; a patient with PCl of 35l&#47;week&#47;1&#46;73m<span class="elsevierStyleSup">2</span> BSA could have CrCl from 13&#46;32l&#47;week&#47;1&#46;73m<span class="elsevierStyleSup">2</span> BSA to 102&#46;12l&#47;week&#47;1&#46;73m<span class="elsevierStyleSup">2</span> BSA&#46; Given the poor concordance that exists between the values studied and that they cannot be taken as replacements&#44; we proposed a phosphorus transport classification tree with five nodes based on its D&#47;P P&#44; amongst which we identified statistically significant differences between groups for total and peritoneal PCl&#46;</p><p class="elsevierStylePara">Our results confirm the role of diuresis in maintaining phosphorus levels at low values compared to anuria&#46; In anuric patients&#44; in whom the peritoneum has an exclusive role in phosphorus clearance&#44; the determination of phosphorus transport indicators is particularly important for two factors&#58; 1&#41; D&#47;P P is significantly lower in hyperphosphataemic patients&#59; 2&#41; Peritoneal PCl is significantly higher compared with those who maintain diuresis &#40;Table 2&#41;&#46;</p><p class="elsevierStylePara">The current recommendations for the prescription of peritoneal dialysis in accordance with the 2006 K&#47;DOQI clinical guidelines<span class="elsevierStyleSup">24</span>&#44; based on the results of three major studies<span class="elsevierStyleSup">25-27</span>&#44; set a Kt&#47;V of urea target of &#8805;1&#46;7&#44; which has not managed to reduce mortality in this population&#46; As such&#44; the search for new markers of targets is vitally important&#46; The current recommendations are to maintain the phosphorus level within the normal limits<span class="elsevierStyleSup">28</span>&#44; although this is an arduous challenge for patients and physicians&#44; since beyond dietary restriction and the adequate use of binders&#44; the doctor must know the role that dialysis exercises on PCl&#46; This study demonstrates the independence of phosphorus transport with respect to urea and creatinine and it leads to a series of questions such as the PCl dose necessary for helping patients achieve the serum phosphorus targets&#44; whether this value is different in patients with diuresis and anuric patients&#44; whether the dialysis adjustment to achieve an established PCl target improves mortality compared with the current Kt&#47;V of urea targets or whether a low D&#47;P P is associated with greater mortality&#44; amongst others&#46; As such&#44; studies must be carried out to determine the benefits of the adjustment of peritoneal dialysis based on D&#47;P P with different PCl doses&#44; establish the mid- and long-term morbidity and mortality&#44; and thus compare them with the current recommendations on dialysis&#46;</p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">CONCLUSIONS</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara">This study shows that D&#47;P P and PCl measurements are not concordant with those of D&#47;P Cr and CrCl&#44; respectively&#44; despite having an adequate correlation&#46; As such&#44; given the current lack of knowledge about phosphorus transport in peritoneal dialysis in clinical practice&#44; in a group of patients in whom phosphataemia control is imperative&#44; it is necessary to give continuity to the research of these indicators&#44; since they are useful tools for physicians and may guide dialysis prescription in search for a better control of serum phosphorus&#46;</p><p class="elsevierStylePara">&#160;</p><p class="elsevierStylePara"><span class="elsevierStyleBold">Conflicts of interest</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara">The authors declare that they have no conflicts of interest related to the contents of this article&#46;</p><p class="elsevierStylePara"><a href="grande&#47;12281&#95;16025&#95;61888&#95;en&#95;t112281&#46;jpg" class="elsevierStyleCrossRefs"><img src="12281_16025_61888_en_t112281.jpg" alt="Population characteristics&#58; medical and dialysis management "></img></a></p><p class="elsevierStylePara">Table 1&#46; Population characteristics&#58; medical and dialysis management </p><p class="elsevierStylePara"><a href="grande&#47;12281&#95;16025&#95;61889&#95;en&#95;t212281&#46;jpg" class="elsevierStyleCrossRefs"><img src="12281_16025_61889_en_t212281.jpg" alt="Transport of solutes&#44; dialysis dose and phosphataemia in accordance with residual uresis"></img></a></p><p class="elsevierStylePara">Table 2&#46; Transport of solutes&#44; dialysis dose and phosphataemia in accordance with residual uresis</p><p class="elsevierStylePara"><a href="grande&#47;12281&#95;16025&#95;61890&#95;en&#95;t312281&#46;jpg" class="elsevierStyleCrossRefs"><img src="12281_16025_61890_en_t312281.jpg" alt="Phosphorus and clearance characteristics between transport nodes "></img></a></p><p class="elsevierStylePara">Table 3&#46; Phosphorus and clearance characteristics between transport nodes </p><p class="elsevierStylePara"><a href="grande&#47;12281&#95;16025&#95;61892&#95;en&#95;f112281&#46;jpg" class="elsevierStyleCrossRefs"><img src="12281_16025_61892_en_f112281.jpg" alt="Correlation between the dialysate&#47;plasma creatinine ratio and the dialysate&#47;plasma phosphorus ratio&#46;"></img></a></p><p class="elsevierStylePara">Figure 1&#46; Correlation between the dialysate&#47;plasma creatinine ratio and the dialysate&#47;plasma phosphorus ratio&#46;</p><p class="elsevierStylePara"><a href="grande&#47;12281&#95;16025&#95;61893&#95;en&#95;f2122813&#46;jpg" class="elsevierStyleCrossRefs"><img src="12281_16025_61893_en_f2122813.jpg" alt="Concordance between the dialysate&#47;plasma creatinine ratio and the dialysate&#47;plasma phosphorus ratio&#46;"></img></a></p><p class="elsevierStylePara">Figure 2&#46; Concordance between the dialysate&#47;plasma creatinine ratio and the dialysate&#47;plasma phosphorus ratio&#46;</p><p class="elsevierStylePara"><a href="grande&#47;12281&#95;16025&#95;61894&#95;en&#95;f3122813&#46;jpg" class="elsevierStyleCrossRefs"><img src="12281_16025_61894_en_f3122813.jpg" alt="Concordance between creatinine clearance and phosphorus clearance&#46;"></img></a></p><p class="elsevierStylePara">Figure 3&#46; Concordance between creatinine clearance and phosphorus clearance&#46;</p>"
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        "resumen" => "<p class="elsevierStylePara"><span class="elsevierStyleBold">Introducci&#243;n&#58;</span> La hiperfosfatemia &#40;f&#243;sforo s&#233;rico &#8805;&#160;5&#44;5&#160;mg&#47;dl&#41; es un factor independiente de mortalidad en la poblaci&#243;n en di&#225;lisis&#46; Comparamos el transporte peritoneal de f&#243;sforo&#44; creatinina y urea para demostrar diferencias y se&#241;alar la relevancia de estos par&#225;metros en el control del f&#243;sforo s&#233;rico&#46; <span class="elsevierStyleBold">Material y m&#233;todos&#58;</span> Se incluyeron 60 pacientes en di&#225;lisis peritoneal y se determin&#243; el &#237;ndice dializante&#47;plasma de f&#243;sforo &#40;D&#47;P P&#41; y creatinina &#40;D&#47;P Cr&#41;&#44; el aclaramiento semanal de f&#243;sforo &#40;AclP&#41; y creatinina &#40;AclCr&#41;&#44; Kt&#47;V de urea semanal y la excreci&#243;n peritoneal de f&#243;sforo &#40;ExP&#41;&#46; <span class="elsevierStyleBold">Resultados&#58;</span> El D&#47;P P fue superior en pacientes con normofosfatemia&#44; comparados con los que presentaron hiperfosfatemia&#44; 0&#44;61&#160;&#177;&#160;0&#44;13 frente a 0&#44;54&#160;&#177;&#160;0&#44;10 &#40;<span class="elsevierStyleItalic">p&#160;</span>&#61;&#160;0&#44;035&#41;&#46; Se observ&#243; una adecuada correlaci&#243;n entre el D&#47;P P y el D&#47;P Cr&#44; r&#160;&#61;&#160;0&#44;90&#44; p&#160;&#60;&#160;0&#44;05&#44; pero una pobre concordancia entre ambos&#44; con un l&#237;mite inferior de &#8722;0&#44;17 &#40;&#8722;0&#44;24 a &#8722;0&#44;09 IC 95&#160;&#37;&#41; y l&#237;mite superior de 0&#44;47 &#40;0&#44;39-0&#44;54 IC 95&#160;&#37;&#41; para el D&#47;P Cr respecto al D&#47;P P&#46; El AclP tuvo una adecuada correlaci&#243;n con el D&#47;P P en pacientes con Kt&#47;V &#8805;&#160;1&#44;7 &#40;r&#160;&#61;&#160;0&#44;384&#44; <span class="elsevierStyleItalic">p</span>&#160;&#61;&#160;0&#44;04&#41; y en an&#250;ricos &#40;r&#160;&#61;&#160;0&#44;392&#44; p&#160;&#61;&#160;0&#44;04&#41;&#44; pero no con el D&#47;P Cr&#46; Hubo una pobre concordancia del AclCr respecto al AclP con l&#237;mite inferior de &#8722;13&#44;54&#160;l&#47;sem&#47;1&#44;73&#160;m<span class="elsevierStyleSup">2</span> SC &#40;&#8722;21&#44;68 a &#8722;5&#44;4 IC 95&#160;&#37;&#41; y l&#237;mite superior de 58&#44;98&#160;l&#47;sem&#47;1&#44;73&#160;m<span class="elsevierStyleSup">2</span> SC &#40;50&#44;84-67&#44;12 IC 95&#160;&#37;&#41;&#46; La ExP total se relacion&#243; con el AclP &#40;r&#160;&#61;&#160;0&#44;643&#44; <span class="elsevierStyleItalic">p</span>&#160;&#60;&#160;0&#44;05&#41;&#44; mientras que no lo hizo con el AclCr &#40;r&#160;&#61;&#160;0&#44;222&#44; <span class="elsevierStyleItalic">p</span>&#160;&#61;&#160;0&#44;23&#41;&#46; Mediante el m&#233;todo CHAID se realiz&#243; un &#225;rbol de clasificaci&#243;n del transporte de f&#243;sforo con base en su D&#47;P&#44; obteniendo 5 nodos &#40;&#8804;&#160;0&#44;5&#44; 0&#44;51-0&#44;55&#44; 0&#44;56-0&#44;66&#44; 0&#44;67-0&#44;76&#44; &#62;&#160;0&#44;76&#41;&#44; mostrando diferencias estad&#237;sticamente significativas entre nodos para niveles s&#233;ricos de f&#243;sforo&#44; AclP total y peritoneal&#44; as&#237; como Kt&#47;V de urea semanal&#46; <span class="elsevierStyleBold">Conclusiones&#58;</span> Las mediciones de D&#47;P P y AclP no concuerdan con las mediciones de D&#47;P Cr y AclCr&#44; respectivamente&#44; por lo que su determinaci&#243;n es una herramienta cl&#237;nica para el control del nivel de f&#243;sforo s&#233;rico&#46;</p>"
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        "resumen" => "<p class="elsevierStylePara"><span class="elsevierStyleBold">Background&#58;</span> Hyperphosphataemia &#40;serum phosphorus &#8805;5&#46;5mg&#47;dl&#41; is an independent mortality factor for the dialysis population&#46; We compared phosphorus&#44; creatinine and urea peritoneal transport to demonstrate differences and indicate the relevance of these parameters in the control of serum phosphorus&#46; <span class="elsevierStyleBold">Material and method&#58;</span> We included 60 patients on peritoneal dialysis and determined the dialysate&#47;plasma phosphorus &#40;D&#47;P P&#41; and creatinine &#40;D&#47;P Cr&#41; ratios&#44; weekly creatinine clearance &#40;CrCl&#41; and phosphorus clearance &#40;PCl&#41;&#44; weekly Kt&#47;V of urea&#44; and peritoneal phosphorus excretion &#40;PEx&#41;&#46; <span class="elsevierStyleBold">Results&#58;</span> D&#47;P P was higher in patients with normal phosphataemia&#44; compared with those who were hyperphosphataemic 0&#46;61&#177;0&#46;13 versus 0&#46;54&#177;0&#46;10 &#40;<span class="elsevierStyleItalic">p</span>&#61;&#46;035&#41;&#46; We observed an adequate correlation between D&#47;P P and D&#47;P Cr&#44; r&#61;0&#46;90&#44; <span class="elsevierStyleItalic">p</span>&#60;&#46;05&#44; but poor concordance between both&#44; with a lower limit of &#8722;0&#46;17 &#40;&#8722;0&#46;24 to &#8722;0&#46;09 95&#37; CI&#41; and an upper limit of 0&#46;47 &#40;0&#46;39-0&#46;54 95&#37; CI&#41; for D&#47;P Cr with respect to D&#47;P P&#46; PCl had an adequate correlation with D&#47;P P in patients with a Kt&#47;V &#8805;1&#46;7 &#40;r&#61;0&#46;384&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;04&#41; and in anuric patients &#40;r&#61;0&#46;392&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;04&#41;&#44; but not with D&#47;P Cr&#46; There was poor concordance of the CrCl with respect to PCl with a lower limit of &#8722;13&#46;54l&#47;week&#47;1&#46;73m<span class="elsevierStyleSup">2</span> BSA &#40;&#8722;21&#46;68 to &#8722;5&#46;4 95&#37; CI&#41; and an upper limit of 58&#46;98l&#47;week&#47;1&#46;73m<span class="elsevierStyleSup">2</span> BSA &#40;50&#46;84-67&#46;12 95&#37; CI&#41;&#46; Total PEx was related to PCl &#40;r&#61;0&#46;643&#44; <span class="elsevierStyleItalic">p</span>&#60;&#46;05&#41;&#44; while it was not related to CrCl &#40;r&#61;0&#46;222&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;23&#41;&#46; Using the CHAID method&#44; we created a classification tree for phosphorus transport based on its D&#47;P&#44; obtaining 5 nodes &#40;&#8804;0&#46;5&#44; 0&#46;51-0&#46;55&#44; 0&#46;56-0&#46;66&#44; 0&#46;67-0&#46;76&#44; &#62;0&#46;76&#41;&#44; with statistically significant differences between nodes for serum phosphorus&#44; total and peritoneal PCl and weekly Kt&#47;V of urea&#46; <span class="elsevierStyleBold">Conclusions&#58;</span> D&#47;P P and PCl are not concordant with D&#47;P Cr and CrCl respectively and therefore their determination is a clinical tool to control serum phosphorus levels&#46;</p>"
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