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What is the contribution of sodium sieving?" 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"tieneTextoCompleto" => true "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "214" "paginaFinal" => "219" ] ] "autores" => array:1 [ 0 => array:3 [ "autoresLista" => "Julio Hernández Jaras, I. Rico Salvador, E. Torregrosa de Juan, R. Pons Prades, A. Rius Peris, M.A. Fenollosa Segarra, J.J. Sánchez Canel, T. Carbajo Mateo" "autores" => array:8 [ 0 => array:4 [ "nombre" => "Julio" "apellidos" => "Hernández Jaras" "email" => array:1 [ 0 => "hernandez_jul@gva.es" ] "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "affa" ] ] ] 1 => array:3 [ "Iniciales" => "I." "apellidos" => "Rico Salvador" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "affa" ] ] ] 2 => array:3 [ "Iniciales" => "E." "apellidos" => "Torregrosa de Juan" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "affa" ] ] ] 3 => array:3 [ "Iniciales" => "R." "apellidos" => "Pons Prades" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "affa" ] ] ] 4 => array:3 [ "Iniciales" => "A." "apellidos" => "Rius Peris" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "affa" ] ] ] 5 => array:3 [ "Iniciales" => "M.A." "apellidos" => "Fenollosa Segarra" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "affa" ] ] ] 6 => array:3 [ "Iniciales" => "J.J." "apellidos" => "Sánchez Canel" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "affa" ] ] ] 7 => array:3 [ "Iniciales" => "T." "apellidos" => "Carbajo Mateo" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "affa" ] ] ] ] "afiliaciones" => array:1 [ 0 => array:3 [ "entidad" => "Servicio de Nefrología, Hospital General de Castellón, Castellón, España, " "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "affa" ] ] ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "¿Mejora la aproximación físico-química de Stewart-Fencl la valoración del equilibrio ácido-base en pacientes estables en hemodiafiltración?" ] ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:8 [ "identificador" => "fig1" "etiqueta" => "Tab. 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "copyright" => "Elsevier España" "figura" => array:1 [ 0 => array:4 [ "imagen" => "10037108_a11_t1.jpg" "Alto" => 292 "Ancho" => 1094 "Tamanyo" => 56692 ] ] "descripcion" => array:1 [ "en" => "Measured parameters of acid-base status pre- and post-HDF" ] ] ] "textoCompleto" => "<p class="elsevierStylePara"><span class="elsevierStyleBold">INTRODUCTION </span></p><p class="elsevierStylePara">Metabolic acidosis is a common disorder in patients suffering renal failure on haemodialysis (HD).<span class="elsevierStyleSup">1 </span>The evaluation of acid-base status is based on Henderson- Hasselbalch equation. With this equation, hydrogen-ion [H<span class="elsevierStyleSup">+</span>] concentration behaviour is explained by variations of other variables such as HCO<span class="elsevierStyleSup">3</span>, OH<span class="elsevierStyleSup">–</span>, CO<span class="elsevierStyleSup">3</span>H<span class="elsevierStyleSup">2</span>, in an independent fashion. In 1983, P. Stewart developed an acid-base status quantitative analysis showing a system of independent variables that are modified independently of the rest.<span class="elsevierStyleSup">2 </span>Amongst these variables included are: pCO<span class="elsevierStyleSup">2 </span>that is regulated mainly through alveolar gas; the strong ion difference (SID), particularly the difference between the sum of strong cations (Na<span class="elsevierStyleSup">+</span>, K<span class="elsevierStyleSup">+</span>, Ca<span class="elsevierStyleSup">++</span>, Mg<span class="elsevierStyleSup">++</span>) and the sum of strong anions (Cl<span class="elsevierStyleSup">–</span>, lactate); and total plasma concentration of non-volatile weak acids, mainly inorganic phosphate and albumin (A.Tot.). There is a second type of dependent variables modified as a group, simultaneously and only if one of the independent variables change. These include H<span class="elsevierStyleSup">+</span>, OH<span class="elsevierStyleSup">– </span>and HCO<span class="elsevierStyleSup">3 –</span>. In 1992 Fencl, Figge et al. developed a mathematical model to estimate SID from pCO<span class="elsevierStyleSup">2</span>, albumin and phosphate (SIDe). The difference between them (SIDm and SIDe) allows us to calculate the SID <span class="elsevierStyleItalic">gap</span>, which includes both metabolisable ions (pyruvate, acetoacetate, citrate, etc.) and nonmetabolisable ions (sulphate, hippurate) that take part in electro-neutrality. The aim of this study is to evaluate acid-base status in stable patients on haemodiafiltration (HDF) from both perspectives: classic (pH, HCO<span class="elsevierStyleSup">3</span>, excess base and <span class="elsevierStyleItalic">anion gap</span>) and physical-chemical (SIDm, SIDe and SID <span class="elsevierStyleItalic">gap</span>). </p><p class="elsevierStylePara"><span class="elsevierStyleBold">MATERIAL AND METHODS </span></p><p class="elsevierStylePara">Thirty-five patients were studied, 24 male and 11 female, mean age of 67.2 ± 15.7 years and dry weight of 72.8 ± 19.8kg. They remained on HD for 68.3 ± 43.3 months. Seventeen patients (48.5%) were on “on-line” HDF and the rest on conventional HDF. The filter used was high-permeability 1.9m<span class="elsevierStyleSup">2 </span>polysulfone. Session length was 253.6 ± 40.5 min. Blood flow (Qb) and dialysis liquid (Qb) were 368 ± 44 and 751 ± 83ml/min, respectively. A mean convection of 15.2 ± 6.4L was performed per session. The dialysis liquid employed had the following theoretical composition: Na 140, K 1.5, Cl 107, Mg 1 and acetate 4mEq/l. Calcium varied from 2.5 to 3.5mEq/l depending on patient’s needs. This same liquid was used as infusion liquid in “on-line” HDF and in conventional HDF a biocarbonate solution of 60mEq/l was used. The study was performed at the weekly intermediate session. Sample tests were taken from the pre-HD and post-HD arterial line (after having Qb at 50ml/min during 1 min.). From the samples, pH, pCO<span class="elsevierStyleSup">2</span>, HCO<span class="elsevierStyleSup">3 –</span>, albumin, Na<span class="elsevierStyleSup">+</span>, K<span class="elsevierStyleSup">+</span>, Cl<span class="elsevierStyleSup">– </span>, Ca<span class="elsevierStyleSup">++</span>, P, Mg and lactate were determined. pH, pCO<span class="elsevierStyleSup">2</span>, HCO<span class="elsevierStyleSup">3 – </span>determination, base excess, Ca<span class="elsevierStyleSup">++ </span>and lactate were carried out in a gas analyser (IL GEM Premier 3000). Determination of Na, K, Cl, P, Mg and albumin was performed by laboratory standard techniques with an automatic auto-analyser (Olympus AV-640). </p><p class="elsevierStylePara"><span class="elsevierStyleBold">Definitions and calculations </span></p><p class="elsevierStylePara">SID measure (SIDm) was calculated as: [Na<span class="elsevierStyleSup">+</span>] + [K<span class="elsevierStyleSup">+</span>] + [Ca<span class="elsevierStyleSup">++</span>] + [Mg<span class="elsevierStyleSup">++</span>] – [Cl<span class="elsevierStyleSup">–</span>] – [lactate]. Mg in mmol/l was converted to mEq/l multiplied by 2 and it was considered that 65% of total Mg corresponded to the ionised form. The estimated SID (SIDe) was determined from albumin by the formula proposed by Figge: 1.000 x 2.46<span class="elsevierStyleSup">–11 </span>x pCO<span class="elsevierStyleSup">2</span>/(10–<span class="elsevierStyleSup">pH</span>) + Albumin g/dl x (0.123 x pH–0.631) + P in mmol/l x (0.309 x pH–0.469)<span class="elsevierStyleSup">3</span>. From this formula albumin anionic (Album<span class="elsevierStyleSup">–</span>) and phosphorus (P<span class="elsevierStyleSup">–</span>) charges were calculated. The <span class="elsevierStyleItalic">anion gap </span>(AGap) was calculated by: (Na + K) – (Cl + HCO3<span class="elsevierStyleSup">–</span>). The SID <span class="elsevierStyleItalic">gap </span>was calculated by: SIDm – SIDe. The variations in the session of base excess, albumin and phosphate charge, Cl and SID <span class="elsevierStyleItalic">gap </span>(ΔExBa, ΔAlbum.<span class="elsevierStyleSup">–</span>, ΔP<span class="elsevierStyleSup">–</span>, ΔCl<span class="elsevierStyleSup">– </span>and Δ<span class="elsevierStyleItalic">gap-</span>SID) were calculated as the difference between pre- and post-HDF values. </p><p class="elsevierStylePara"><span class="elsevierStyleBold">Statistical methods </span></p><p class="elsevierStylePara">The results are expressed as mean ± SD. Normality between variables was corroborated by Kolmogorov–Smirnov test. Student’s T test for paired data was used to analyse the difference between pre- and post HD variables. The correlation coefficients were determined by linear regression analysis by the least square method. Statistical signification was set at an error probability lower than 0.05 (p < 0.05). </p><p class="elsevierStylePara"><span class="elsevierStyleBold">RESULTS </span></p><p class="elsevierStylePara">The values measured are expressed in table 1. pH, HCO<span class="elsevierStyleSup">3 </span>and Ca<span class="elsevierStyleSup">++ </span>increased significantly along the session, while K<span class="elsevierStyleSup">+</span>, Mg<span class="elsevierStyleSup">++ </span>and lactate values decreased. No significant differences were observed between pre- and post-HDF Na<span class="elsevierStyleSup">+ </span>and Cl<span class="elsevierStyleSup">–</span>. The values calculated are shown in table 2. A decrease in SIDm can be appreciated from 46.2 ± 2.9 to 45 ± 2.3mEq/l (p < 0.05), as well as in the <span class="elsevierStyleItalic">anion gap</span>, and SID <span class="elsevierStyleItalic">gap</span>, and in the anionic charge of P. On the contrary, SIDe increases from 38.5 ± 3.8 to 42.9 ± 3.1mEq/l (p < 0.01), as it does the albumin charge and base excess. Maintenance of plasma electro-neutrality between cations and anions pre- and post-HDF can be observed in figure 1. A correlation was observed between the <span class="elsevierStyleItalic">anion gap </span>and SID<span class="elsevierStyleItalic">gap </span>pre- and post HDF, shown in figure 2. Furthermore, a significant correlation was observed between Δbase excess y ΔSID<span class="elsevierStyleItalic">-gap </span>(r = 0.45; p <0.01). No correlation was observed between Δbase excess and ΔAlbum.<span class="elsevierStyleSup">–</span>, ΔP<span class="elsevierStyleSup">– </span>and ΔCl<span class="elsevierStyleSup">–</span>. </p><p class="elsevierStylePara"><span class="elsevierStyleBold">DISCUSSION </span></p><p class="elsevierStylePara">Metabolic acidosis is a common disorder in HD patients with renal failure. The main source of H<span class="elsevierStyleSup">+ </span>in these patients comes from the metabolism of sulphur-containing amino acids, methionine, and cystine. Their oxidation<span class="elsevierStyleSup">4,5 </span>generates sulphuric acid, a strong acid (low pK) that dissociates and increases the levels of sulphate and H<span class="elsevierStyleSup">+</span>. From the classic approach viewpoint, bicarbonate is consumed by the generated H<span class="elsevierStyleSup">+</span>. Therefore, the HD is seen as an alkalinising therapy transferring bicarbonate from the dialysis liquid into the blood to replenish the consumed bicarbonate. This results in an increase of pH, bicarbonate, and base excess at the end of the session.<span class="elsevierStyleSup">6 </span>According to Stewart-Fencl physical-chemical approach, the strong ion difference (SIDm), specifically, i.e. the difference between measured strong cations and measured strong anions, is what controls the metabolic component of the acid-base status. In this way, metabolic acidosis and alkalosis are reflected in a decrease and increase of SID, respectively.<span class="elsevierStyleSup">7 </span>Under this perspective, the patient on periodic HD evidences decreased SID in predialysis situation and the objective of the HD session is to increase reduced SID by the accumulation of other strong anions, such as sulphate, hippurate, etc.<span class="elsevierStyleSup">8 </span>According to the Stewart-Fencl approach, since only independent variables can modify acid-base status, HD would not cause transfer of bicarbonate from dialysis liquid into blood, but it would eliminate the strong anions accumulated, thus normalising serum Cl and restoring SID, which translates into a secondary bicarbonate increase. This way bicarbonate stops being the main factor in the regeneration of acid-base status. In 1992 Fencl, Finge et al. developed a mathematical model to calculate SID when the other independent variables are known (pCO<span class="elsevierStyleSup">2</span>, albumin and phosphate), as well as pH.<span class="elsevierStyleSup">3 </span>This new definition of estimated SID (SIDe) is similar to the concept of <span class="elsevierStyleItalic">buffer </span>base (BB) developed by Singer and Hasting in 1948.<span class="elsevierStyleSup">9 </span>The simplified equation is the one employed in our study, and it is composed of CO<span class="elsevierStyleSup">2</span>T, anion charge of albumin, and anion charge of phosphate. The study by Leblanc et al. stresses the increment of SIDm during the session in patients on chronic HD.<span class="elsevierStyleSup">8 </span>On the contrary, in our study we have observed a significantly slight decrease in SIDm during the HD session, moving from 46.2 to 45mEq/l by the end of the session. All this is in apparent contradiction with an increase of pH, bicarbonate, and base excess, which would increase as expected by the alkalinising effect of HD. We have confirmed similar results in patients on daily “online” HDF during a 1-year-follow-up period.<span class="elsevierStyleSup">10 </span>How is this apparent contradiction possible between these two variables that are supposed to measure the same effect? As those stable patients on periodic HD usually have normal levels of Cl<span class="elsevierStyleSup">–</span>, the not-measured strong anions (sulphate, hippurate, etc.) are the ones that decrease. These anions are not taken into account in the SIDm formula, so that, apparently, this variable will not change. On the contrary, SIDe will take into account that CO<span class="elsevierStyleSup">2</span>T increases throughout the session. In our study we have only appreciated a significant correlation between Δbase excess and ΔSID-<span class="elsevierStyleItalic">gap</span>, but not between the first parameter and that of Δ Cl, Albumin<span class="elsevierStyleSup">– </span>and P<span class="elsevierStyleSup">–</span>, which makes clear that SID-<span class="elsevierStyleItalic">gap </span>is the only element associating with base excess regeneration. The study by Liborio et al.,<span class="elsevierStyleSup">11 </span>with critically ill patients admitted to ICU, shows similar results to ours, but when classifying their patients in groups with high Cl<span class="elsevierStyleSup">– </span>and low Cl<span class="elsevierStyleSup">– </span>with relation to this anion levels in the dialysis fluid, they observed that acid-base status correction (by means of variation of base excess) is significantly higher in the group with high Cl<span class="elsevierStyleSup">– </span>values. Furthermore, these authors observed a correlation between Δ base excess and Δ SID-<span class="elsevierStyleItalic">gap </span>and ΔCl<span class="elsevierStyleSup">–</span>. In other studies the same authors emphasised the importance of Cl<span class="elsevierStyleSup">– </span>serum levels as acidosis components in patients on chronic HD.<span class="elsevierStyleSup">12,13 </span>This would corroborate our results, since, in this situation, the correction of acid-base status during the session would not only be due to the elimination of not-measured strong anions but also to a normalisation of Cl<span class="elsevierStyleSup">– </span>serum levels. SIDm is only able to detect increments, whether when Na<span class="elsevierStyleSup">+ </span>increases without accompanying Cl<span class="elsevierStyleSup">– </span>or when Cl<span class="elsevierStyleSup">– </span>decreases. Neither of these situations occurred in our patients included in the programme of chronic HDF. In HDF the composition of the re-infusion liquid with an increased SID would also accomplish the same objective. It is intended to use liquids with strong cations (Na<span class="elsevierStyleSup">+</span>) with a smaller amount of strong accompanying anion (Cl<span class="elsevierStyleSup">–</span>) in an attempt to restore SID.<span class="elsevierStyleSup">14 </span>Other important aspect is the albumin and phosphate anion charges, included in the expression total weak anions (ATot). This physical-chemical approach considers the possibility that a decrease or an increase in these parameters may cause metabolic alkalosis or acidosis, respectively.<span class="elsevierStyleSup">15 </span>In our study, the ATot as a whole were not modified throughout the session, as the increment of albumin charge post-session (10.9 to 12.1mEq/l) was compensated by the decrease in the phosphate charge (from 2.4 to 1.2mEq/l). The Stewart-Fencl approach allows evaluation of not measured anions much more precisely than the <span class="elsevierStyleItalic">anion gap</span>. This parameter largely used in the classic approach presents remarkable interferences on the part of serum albumin and phosphate, which make difficult the correct evaluation of the type of metabolic acidosis, mostly in situations with important alterations in the ATot components, such as nephrotic syndrome, malnutrition, negative protein catabolism or phosphorus intoxications.<span class="elsevierStyleSup">16,17 </span>In fact, the difference between SIDm and SIDe provides a quantity of not-measured anions (<span class="elsevierStyleItalic">gap</span>-SID) free from the interference of weak acids and, therefore, partially dissociated. The studies of Kellum et al. make reference to a poor correlation scale between <span class="elsevierStyleItalic">anion gap </span>and <span class="elsevierStyleItalic">gap</span>-SID in critical patients at the ICU, with low concentrations of serum albumin.<span class="elsevierStyleSup">18 </span>On the contrary, Gilfix et al. do find this correlation between AG and <span class="elsevierStyleItalic">gap</span>-SID with the same type of patients. Other studies have demonstrated the usefulness of this parameter in critical patients at the ICU.<span class="elsevierStyleSup">19 </span>Our results do show an important correlation between <span class="elsevierStyleItalic">anion gap </span>and <span class="elsevierStyleItalic">gap</span>-SID, pre- and post-HDF, maybe due to the normal albumin figures throughout the session. Therefore the <span class="elsevierStyleItalic">anion gap </span>may be a good not-measured anion marker in stable chronic patients on HD, but its effectiveness is doubtful in patients with acute renal failure. However, it is <span class="elsevierStyleItalic">gap</span>-SID the parameter that best reflects not-measured anion accumulation during the inter-dialysis period. This parameter decreases significantly and, logically enough, it includes anions, especially sulphate, from protein catabolism, which will be adequately eliminated during the HDF session. As opposed to <span class="elsevierStyleItalic">anion gap</span>, <span class="elsevierStyleItalic">gap</span>-SID will not change either with pH or with the albumin and phosphate changes. To conclude, Stewart-Fencl approach does not improve the evaluation of acid-base status in patients on chronic HDF. In the presence of normochloraemia, SIDm does not reflect the alkalinising process of the haemodialysis session. Under this perspective, the HD session is conceived as a nonmetabolisable inorganic anion withdrawal, especially sulphate. The room left by these anions is replaced by OH<span class="elsevierStyleSup">– </span>and secondarily by HCO<span class="elsevierStyleSup">3 –</span>. The only advantage would involve a better evaluation of anions not measured by <span class="elsevierStyleItalic">gap</span>- SID, without the effect of albumin and phosphate.  </p><p class="elsevierStylePara"><a href="grande/10037108_a11_t1.jpg" class="elsevierStyleCrossRefs"><img src="10037108_a11_t1.jpg" alt="Measured parameters of acid-base status pre- and post-HDF"></img></a></p><p class="elsevierStylePara">Table 1. Measured parameters of acid-base status pre- and post-HDF</p><p class="elsevierStylePara"><a href="grande/1003718078_tripav30_n2_2010_t2_pag216_copy1.jpg" class="elsevierStyleCrossRefs"><img src="1003718078_tripav30_n2_2010_t2_pag216_copy1.jpg" alt="Measured parameters of acid-base status pre- and post-HDF"></img></a></p><p class="elsevierStylePara">Table 2. Measured parameters of acid-base status pre- and post-HDF</p><p class="elsevierStylePara"><a href="grande/10037108_a11_f1.jpg" class="elsevierStyleCrossRefs"><img src="10037108_a11_f1.jpg" alt="Plasma electro-neutrality between pre- and post-HDF cations and anions."></img></a></p><p class="elsevierStylePara">Figure 1. Plasma electro-neutrality between pre- and post-HDF cations and anions.</p><p class="elsevierStylePara"><a href="grande/10037108_a11_f2.jpg" class="elsevierStyleCrossRefs"><img src="10037108_a11_f2.jpg" alt="Correlation between the levels of anion gap and SID gap pre- and post-HDF."></img></a></p><p class="elsevierStylePara">Figure 2. Correlation between the levels of anion gap and SID gap pre- and post-HDF.</p>" "pdfFichero" => "P1-E47-S1877-A10037-EN.pdf" "tienePdf" => true "PalabrasClave" => array:2 [ "es" => array:4 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Palabras clave" "identificador" => "xpalclavsec437467" "palabras" => array:1 [ 0 => "Anion gap" ] ] 1 => array:4 [ "clase" => "keyword" "titulo" => "Palabras clave" "identificador" => "xpalclavsec437469" "palabras" => array:1 [ 0 => "Hemodiafiltración" ] ] 2 => array:4 [ "clase" => "keyword" "titulo" => "Palabras clave" "identificador" => "xpalclavsec437471" "palabras" => array:1 [ 0 => "Acidosis" ] ] 3 => array:4 [ "clase" => "keyword" "titulo" => "Palabras clave" "identificador" => "xpalclavsec437473" "palabras" => array:1 [ 0 => "Aproximación de Stewart-Fencl" ] ] ] "en" => array:4 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Keywords" "identificador" => "xpalclavsec437468" "palabras" => array:1 [ 0 => "Gap anion" ] ] 1 => array:4 [ "clase" => "keyword" "titulo" => "Keywords" "identificador" => "xpalclavsec437470" "palabras" => array:1 [ 0 => "Hemodiafiltration" ] ] 2 => array:4 [ "clase" => "keyword" "titulo" => "Keywords" "identificador" => "xpalclavsec437472" "palabras" => array:1 [ 0 => "Acidosis" ] ] 3 => array:4 [ "clase" => "keyword" "titulo" => "Keywords" "identificador" => "xpalclavsec437474" "palabras" => array:1 [ 0 => "Stewart-Fencl approach" ] ] ] ] "tieneResumen" => true "resumen" => array:2 [ "en" => array:1 [ "resumen" => "<p class="elsevierStylePara">Introduction: The traditional evaluation of acid-base status relies on the Henderson-Hasselbach equation. In 1983, an alternative approach, based on physical and chemical principles was proposed by P. Stewart. In this approach, plasma pH is determined by 3 independent variables: pCO2, Strong Ion Difference (SIDm), which is the difference between the strong cations (Na+, K+, Ca++, Mg++) and the strong anions (Cl–, lactate) and total plasma concentration of nonvolatile weak acids (ATot), mainly inorganic phosphate and albumin. Bicarbonate is considered a dependent variable. The aim of this study was to evaluate the acid-base status using both perspectives, physical chemical and traditional approach. Material and methods: we studied 35 patients (24 male; 11 female) on hemodiafiltration, mean age was 67.2 ± 15.7, 8 ± 19.2 kg. We analyzed plasma chemistry including pH, pCO2, HCO3–, base excess and Na+, K+, Cl–, Ca++, Mg++, lactate and SIDm. The SID estimated (SIDe) was calculated by Figge’s formula (1,000 x 2.46–11 x pCO2/[10 – pH] + Album g/dl x [0.123 x pH –0.631] + P in mmol/l0 x [0.309 x pH –0.469]) and Gap of the SID as the difference SIDm-SIDe. Results: pH preHD was 7.36 ± 0.08 and pH post-HD 7.44 ± 0.08 (p <0.001). There was no significant differences between pCO2 pre- and post-HD. HCO3– and base excess increased during the session (p <0.001). SIDm decreased from 46.2 ± 2.9 pre-HD to 45 ± 2.3 mEq/l post-HD (p <0.05). On the opposite, SIDe increased from 38.5 ± 3.8 to 429 ± 3.1 mEq/l (p <0.001). The Gap Anion <br />descended from 18.6 ± 3.8 pre-HD to 12.8 ± 2.8 mEq/l post-HD (p <0.001) and the Gap of the SID 7.6 ± 3 to 2.1 ± 2 (p <0.001). Anion Gap correlated with the Gap-SID so much pre-HDF as pos-HDF. ¿ Base excess correlated only with ¿ of the Gap SID. Conclusion: Stewart-Fencl’s approach does not improve characterization of acid-base status in patients on chronic HDF. In presence of normocloremia the SIDm does not reflect the alkalinizing process of the session of hemodialysis. According this approach, hemodialysis therapy can be viewed as a withdrawal of inorganic anions, especially the sulphate. These anions are replaced by OH– and secondarily for HCO3–. The approach only improves the evaluation of unmeasured anions by the Gap of the SID, without the effect of albumin and phosphate.</p>" ] "es" => array:1 [ "resumen" => "<p class="elsevierStylePara">Introducción: la evaluación del equilibrio ácido-base se basa en la ecuación de Henderson-Hasselbach. En 1983, P. Stewart desarrolló un análisis cuantitativo del equilibrio ácido-base en el que muestra un sistema con unas variables independientes entre las que se incluyen pCO2, diferencia iónica fuerte medida (SIDm), es decir, la diferencia entre la suma de cationes fuertes (Na+, K+, Ca++, Mg++) y la suma de aniones fuertes (Cl–, lactato) y la concentración total de todos los aniones débiles no volátiles (ATot), cuyos principales representantes son el fósforo inorgánico (P–) y la albúmina (Albúm.–). El objetivo de este estudio es evaluar desde ambas perspectivas el equilibrio ácido-base en pacientes en hemodiafiltración (HDF) crónica. Material y métodos: se estudian 35 pacientes (24 hombres y 11 mujeres, con una edad media de 67,2 ± 15,7 años y con un peso seco de 72,8 ± 19,2 kg. La duración media de la hemodiálisis (HD) fue de 253,6 ± 40,5 minutos. Se analizan los parámetros gasométricos (pH, pCO2, HCO3–y exceso de bases) y Na+, K+, Cl–, Ca++, Mg++ y lactato. Se calcularon la SIDm, la SIDe mediante la fórmula de Figge (1.000 x 2,46–11 x pCO2 /[10 – pH] + Albúm. g/dl x [0,123 x pH –0,631] + P en mmol/l x [0,309 x pH –0,469)] y gap del SID (SIDm-SIDe). Resultados: el pH pre-HD fue de 7,36 ± 0,08 y el pH post-HD de 7,44 ± 0,08 (p <0,001). No se apreciaron diferencias significativas entre pCO2 pre y post-HD. El HCO3 – y el exceso de bases se incrementaron durante la sesión (p <0,001). La SIDm descendió de manera significativa de 46,2 ± 2,9 preHD a 45 ± 2,3 post-HD (p <0,05). Por el contrario, la SIDe se elevó de 38,5 ± 3,8 a 42,9 ± 3,1 (p <0,001). El anion gap descendió de 18,6 ± 3,8 pre-HD a 12,8 ± 2,8 Eq/l post-HD (p <0,001) y el gap del SID de 7,6 ± 3 a 2,1 ± 2 (p <0,001). Se apreció una correlación entre el anion gap y el gap-SID tanto antes como después de la HDF. Asimismo, se apreció una correlación significativa entre el ¿ exceso de bases y ¿ del gap-SID. Conclusión: en conclusión, la aproximación físico-química de Stewart-Fencl no mejora la valoración del equilibrio ácido-base en pacientes en HDF crónica. En presencia de normocloremia la SIDm no refleja el proceso alcalinizante de la sesión de hemodiálisis. Bajo esta perspectiva, la sesión de hemodiálisis se concibe como una retirada de aniones inorgánicos no metabolizables, en especial el sulfato. El espacio dejado por estos aniones es reemplazado por OH–y secundariamente por HCO3–. La única ventaja vendría dada por una mejor valoración de los aniones no medidos mediante el gap del SID, sin el efecto de la albúmina y el fosfato.</p>" ] ] "multimedia" => array:4 [ 0 => array:8 [ "identificador" => "fig1" "etiqueta" => "Tab. 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "copyright" => "Elsevier España" "figura" => array:1 [ 0 => array:4 [ "imagen" => "10037108_a11_t1.jpg" "Alto" => 292 "Ancho" => 1094 "Tamanyo" => 56692 ] ] "descripcion" => array:1 [ "en" => "Measured parameters of acid-base status pre- and post-HDF" ] ] 1 => array:8 [ "identificador" => "fig2" "etiqueta" => "Tab. 2" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "copyright" => "Elsevier España" "figura" => array:1 [ 0 => array:4 [ "imagen" => "1003718078_tripav30_n2_2010_t2_pag216_copy1.jpg" "Alto" => 230 "Ancho" => 1082 "Tamanyo" => 47091 ] ] "descripcion" => array:1 [ "en" => "Measured parameters of acid-base status pre- and post-HDF" ] ] 2 => array:8 [ "identificador" => "fig3" "etiqueta" => "Fig. 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "copyright" => "Elsevier España" "figura" => array:1 [ 0 => array:4 [ "imagen" => "10037108_a11_f1.jpg" "Alto" => 336 "Ancho" => 549 "Tamanyo" => 22230 ] ] "descripcion" => array:1 [ "en" => "Plasma electro-neutrality between pre- and post-HDF cations and anions." ] ] 3 => array:8 [ "identificador" => "fig4" "etiqueta" => "Fig. 2" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "copyright" => "Elsevier España" "figura" => array:1 [ 0 => array:4 [ "imagen" => "10037108_a11_f2.jpg" "Alto" => 536 "Ancho" => 529 "Tamanyo" => 32163 ] ] "descripcion" => array:1 [ "en" => "Correlation between the levels of anion gap and SID gap pre- and post-HDF." ] ] ] "bibliografia" => array:2 [ "titulo" => "Bibliography" "seccion" => array:1 [ 0 => array:1 [ "bibliografiaReferencia" => array:19 [ 0 => array:3 [ "identificador" => "bib1" "etiqueta" => "1" "referencia" => array:1 [ 0 => array:3 [ "referenciaCompleta" => "Kraut JA, Kurtz I. 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Year/Month | Html | Total | |
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2024 November | 7 | 5 | 12 |
2024 October | 50 | 48 | 98 |
2024 September | 76 | 37 | 113 |
2024 August | 77 | 62 | 139 |
2024 July | 60 | 35 | 95 |
2024 June | 74 | 43 | 117 |
2024 May | 101 | 59 | 160 |
2024 April | 72 | 49 | 121 |
2024 March | 50 | 24 | 74 |
2024 February | 46 | 43 | 89 |
2024 January | 34 | 24 | 58 |
2023 December | 44 | 35 | 79 |
2023 November | 59 | 38 | 97 |
2023 October | 74 | 37 | 111 |
2023 September | 55 | 36 | 91 |
2023 August | 82 | 18 | 100 |
2023 July | 74 | 24 | 98 |
2023 June | 55 | 19 | 74 |
2023 May | 97 | 45 | 142 |
2023 April | 47 | 22 | 69 |
2023 March | 65 | 19 | 84 |
2023 February | 47 | 20 | 67 |
2023 January | 53 | 18 | 71 |
2022 December | 58 | 41 | 99 |
2022 November | 53 | 32 | 85 |
2022 October | 55 | 49 | 104 |
2022 September | 57 | 28 | 85 |
2022 August | 63 | 52 | 115 |
2022 July | 51 | 49 | 100 |
2022 June | 57 | 50 | 107 |
2022 May | 44 | 40 | 84 |
2022 April | 51 | 78 | 129 |
2022 March | 59 | 60 | 119 |
2022 February | 50 | 54 | 104 |
2022 January | 70 | 58 | 128 |
2021 December | 46 | 60 | 106 |
2021 November | 37 | 35 | 72 |
2021 October | 53 | 50 | 103 |
2021 September | 36 | 36 | 72 |
2021 August | 55 | 34 | 89 |
2021 July | 56 | 46 | 102 |
2021 June | 56 | 61 | 117 |
2021 May | 48 | 30 | 78 |
2021 April | 73 | 68 | 141 |
2021 March | 64 | 22 | 86 |
2021 February | 56 | 25 | 81 |
2021 January | 47 | 28 | 75 |
2020 December | 46 | 15 | 61 |
2020 November | 42 | 13 | 55 |
2020 October | 51 | 15 | 66 |
2020 September | 31 | 5 | 36 |
2020 August | 56 | 14 | 70 |
2020 July | 32 | 8 | 40 |
2020 June | 36 | 7 | 43 |
2020 May | 44 | 16 | 60 |
2020 April | 32 | 16 | 48 |
2020 March | 43 | 12 | 55 |
2020 February | 41 | 20 | 61 |
2020 January | 73 | 34 | 107 |
2019 December | 68 | 22 | 90 |
2019 November | 57 | 22 | 79 |
2019 October | 50 | 15 | 65 |
2019 September | 43 | 28 | 71 |
2019 August | 64 | 17 | 81 |
2019 July | 102 | 25 | 127 |
2019 June | 68 | 21 | 89 |
2019 May | 85 | 23 | 108 |
2019 April | 133 | 38 | 171 |
2019 March | 91 | 28 | 119 |
2019 February | 75 | 20 | 95 |
2019 January | 77 | 23 | 100 |
2018 December | 143 | 44 | 187 |
2018 November | 117 | 8 | 125 |
2018 October | 135 | 10 | 145 |
2018 September | 133 | 11 | 144 |
2018 August | 117 | 19 | 136 |
2018 July | 103 | 17 | 120 |
2018 June | 86 | 11 | 97 |
2018 May | 98 | 14 | 112 |
2018 April | 127 | 10 | 137 |
2018 March | 107 | 7 | 114 |
2018 February | 103 | 7 | 110 |
2018 January | 83 | 8 | 91 |
2017 December | 89 | 7 | 96 |
2017 November | 113 | 20 | 133 |
2017 October | 74 | 12 | 86 |
2017 September | 117 | 12 | 129 |
2017 August | 63 | 15 | 78 |
2017 July | 109 | 13 | 122 |
2017 June | 103 | 12 | 115 |
2017 May | 159 | 13 | 172 |
2017 April | 94 | 13 | 107 |
2017 March | 77 | 9 | 86 |
2017 February | 154 | 15 | 169 |
2017 January | 155 | 12 | 167 |
2016 December | 110 | 8 | 118 |
2016 November | 112 | 11 | 123 |
2016 October | 181 | 8 | 189 |
2016 September | 231 | 7 | 238 |
2016 August | 234 | 8 | 242 |
2016 July | 196 | 9 | 205 |
2016 June | 143 | 0 | 143 |
2016 May | 164 | 0 | 164 |
2016 April | 102 | 0 | 102 |
2016 March | 97 | 0 | 97 |
2016 February | 109 | 0 | 109 |
2016 January | 129 | 0 | 129 |
2015 December | 145 | 0 | 145 |
2015 November | 120 | 0 | 120 |
2015 October | 111 | 0 | 111 |
2015 September | 142 | 0 | 142 |
2015 August | 74 | 0 | 74 |
2015 July | 74 | 0 | 74 |
2015 June | 50 | 0 | 50 |
2015 May | 75 | 0 | 75 |
2015 April | 6 | 0 | 6 |