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we selected patients from our haemodialysis unit who had an adequate control of phosphataemia &#40;serum phosphorus &#60;5mg&#47;dl&#41;&#44; on treatment with Al&#40;OH&#41;<span class="elsevierStyleInf">3</span> binder monotherapy who required continuation of this treatment&#46; We followed the indications on dietary restriction of phosphorus rich foods regularly and without variation&#44; in accordance with the unit&#8217;s standard protocol&#46; Twenty-one patients &#40;66&#46;7&#37; male&#44; aged 56&#46;7&#177;16&#46;4 years&#41; met the inclusion criteria&#46; They all underwent dialysis in three four-hour weekly sessions&#59; 6 received high-flux haemodialysis and 15 received online haemodiafiltration&#46; Both the regimen and dialysate remained unchanged throughout the study&#44; with there being a constant magnesium concentration of 0&#46;5mmol&#47;l&#46; The dialysate calcium concentration did not change and was 1&#46;25mmol&#47;l in eight patients and 1&#46;5mmol&#47;l in the remaining 13&#46; 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parathyroid hormone &#40;PTH&#41; and serum magnesium&#46; Serum aluminium was measured at baseline and after four months&#46; Patients were regularly questioned about their adherence to the treatment with phosphate binders&#46;</p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">Statistical analysis</span></p><p class="elsevierStylePara">&#160;</p><p class="elsevierStylePara">All statistical analyses were performed using the SPSS version 17&#46;0 software &#40;SPSS Inc&#44; Chicago&#44; IL&#41;&#46; The variables were recorded as percentages or as a mean &#177; standard deviation&#46; Qualitative variables were compared using McNemar&#39;s test and quantitative data were analysed using the Wilcoxon signed-rank test for related non-parametric variables&#46; We considered relationships with a <span class="elsevierStyleItalic">P</span> value &#60;&#46;05 to be significant&#46;</p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">RESULTS</span></p><p class="elsevierStylePara">&#160;</p><p class="elsevierStylePara">We observed a statistically significant decrease in serum phosphorus levels four months after the conversion to MgCO<span class="elsevierStyleInf">3</span> &#40;4&#46;52&#177;0&#46;99 versus 4&#46;02&#177;1&#46;07mg&#47;dl&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;027&#41;&#44; and in calcium-phosphorus product levels &#40;40&#46;20&#177;10&#46;44 versus 35&#46;16&#177;11&#46;06mg<span class="elsevierStyleSup">2</span>&#47;dl<span class="elsevierStyleSup">2</span>&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;037&#41;&#46; Despite the additional intake of oral calcium&#44; the change in serum calcium was not significant &#40;8&#46;85&#177;0&#46;65 versus 8&#46;66&#177;0&#46;81mg&#47;dl&#41;&#46; No significant changes were observed in PTH or vitamin D levels&#46; Changes in laboratory results throughout follow-up are summarised in Table 2&#46;</p><p class="elsevierStylePara">The improvement in phosphataemia control was achieved by decreasing the number of MgCO<span class="elsevierStyleInf">3 </span>pills &#40;from 3&#46;33&#177;2&#46;29 to 2&#46;15&#177;2&#46;21 pills per day&#44; <span class="elsevierStyleItalic">P</span>&#61;&#46;020&#41;&#46; There were no significant changes in the rest of the drugs used to treat SHPT &#40;Table 3&#41;&#46;</p><p class="elsevierStylePara">We discontinued treatment with MgCO<span class="elsevierStyleInf">3</span> in six patients &#40;30&#37;&#41;&#44; in five due to hypophosphataemia and in one due to digestive intolerance&#46; We observed a significant increase in magnesaemia from the first month &#40;2&#46;21&#177;0&#46;24 versus 2&#46;43&#177;0&#46;39mg&#47;dl&#44; <span class="elsevierStyleItalic">P</span>&#61;&#46;001&#41;&#44; which remained stable for four months&#46; We recorded just one case of hypermagnesaemia &#40;&#62;3mg&#47;dl&#41;&#44; which was suitably resolved by reducing the dose&#46;</p><p class="elsevierStylePara">Likewise&#44; we found a decrease in serum aluminium levels from 14&#46;91&#177;8&#46;55 to 8&#46;47&#177;3&#46;98&#181;g&#47;l &#40;<span class="elsevierStyleItalic">p</span>&#61;&#46;004&#41;&#44; with levels being within the recommended range &#40;&#60;40&#181;g&#47;l&#41; in all patients&#46;</p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">DISCUSSION</span></p><p class="elsevierStylePara">&#160;</p><p class="elsevierStylePara">The conversion from Al&#40;OH&#41;<span class="elsevierStyleInf">3</span> to MgCO<span class="elsevierStyleInf">3</span> allowed phosphorus to be controlled adequately in this haemodialysis patient cohort&#46; Although we were not able to demonstrate clearly that a decrease in serum phosphorus results in reduced mortality&#44; the obvious pathophysiological role that it plays has led to clear indications in national and international guidelines&#46;<span class="elsevierStyleSup">12</span></p><p class="elsevierStylePara">There are currently a wide variety of binders available&#44; all of which are effective in reducing hyperphosphataemia&#44; but with differences in other aspects that force doctors to make a decision about which binder to prescribe&#46;<span class="elsevierStyleSup">13-15</span> Until recently&#44; aluminium salts were considered the most powerful binder&#44; with a very low cost&#47;benefit ratio&#46;<span class="elsevierStyleSup">11 </span>However&#44; the potential toxicity of aluminium had restricted its use in the literature to settings with fewer economic resources&#46;<span class="elsevierStyleSup">16-18 </span>There has even been a certain concern about aluminium intake from other drugs&#44; both in terms of hidden intake and alongside other indications&#44; especially antacids&#46;<span class="elsevierStyleSup">19 </span>Improvement in the treatment of dialysis water&#44; with the resulting lower aluminium concentration&#44; and its low cost in this period of adjustments has challenged these limitations&#46; Various recent studies in which no long term toxicity was observed have reopened the debate on the potential use of aluminium salts&#46;<span class="elsevierStyleSup">9&#44;10&#44;20&#44;21</span></p><p class="elsevierStylePara">In our study&#44; we found that suppressing aluminium salt-based binders effectively decreases serum levels of this element&#44; although no patient had levels higher than 40&#181;g&#47;l at any given time&#46; For now and until there is more evidence on the use of aluminium salts with the current water controls&#44; the guidelines continue to advise against them&#46; Furthermore&#44; the manufacture and distribution of the aluminium binder available in our setting was recently interrupted&#44; forcing us to seek other therapeutic options&#46;</p><p class="elsevierStylePara">The purpose of our study was to assess the replacement of Al&#40;OH&#41;<span class="elsevierStyleInf">3 </span>with MgCO<span class="elsevierStyleInf">3</span>&#46; The first studies in this line were carried out in the nineteen eighties&#44; in different conditions to the current situation&#46;<span class="elsevierStyleSup">22 </span>Since then&#44; many studies have used magnesium salts as phosphate binders&#46;<span class="elsevierStyleSup">23 </span>Of the many drugs available&#44; MgCO<span class="elsevierStyleInf">3 </span>has advantages in terms of safety and tolerance&#44; with an efficacy that is comparable to that of other more modern binders&#46;<span class="elsevierStyleSup">24</span> In our study&#44; we found a significant reduction in the number of pills&#44; which allowed an improvement in adherence and therefore in hyperphosphataemia control&#46;<span class="elsevierStyleSup">25</span> It also has a lower cost than other non-calcium binders&#44; which is important in the current situation&#46;<span class="elsevierStyleSup">8</span></p><p class="elsevierStylePara">Another advantage of using MgCO<span class="elsevierStyleInf">3</span> is the benefits of magnesium intake&#44; an element that is increasingly important&#46;<span class="elsevierStyleSup">26</span> There is growing evidence of the relationship between lower levels of magnesium in the general population and the occurrence or poor control of diseases such as diabetes&#44; high blood pressure or cardiovascular disease&#46;<span class="elsevierStyleSup">27-31 In chronic kidney disease patients&#44; reduced levels of magnesium have been associated with greater mortality&#44; a worsening of mineral and bone disorder and an increase in vascular calcifications&#46;32-35 </span>An interventional study demonstrated delayed arterial calcification with a reduction in intima-media thickness in relation to magnesium supplements&#46;<span class="elsevierStyleSup">36 </span>At present&#44; there are few studies on the effects of different dialysate concentrations&#46;<span class="elsevierStyleSup">37&#44;38 </span>It seems that there could be certain advantages to using dialysate with a higher magnesium content&#44; such as better haemodynamic tolerance&#46;<span class="elsevierStyleSup">39 </span>It is not clear what levels of serum magnesium are suitable&#44; although there seems to be an increasingly greater consensus that somewhat higher levels could be beneficial for patients on dialysis&#46; Intervention trials&#44; which assess the medium and long term effects of increasing magnesium&#44; whether through oral intake or higher dialysate concentrations&#44; are necessary&#46;</p><p class="elsevierStylePara">In our study&#44; we observed a slight increase in magnesium levels&#44; which&#44; as in the CALMAG study&#44; occurred at the start of treatment and subsequently remained stable&#46;<span class="elsevierStyleSup">24 </span>Only one case of asymptomatic hypermagnesaemia was recorded&#44; which returned to levels below 3mg&#47;dl after dose reduction&#46; Likewise&#44; we only found one case of digestive intolerance due to diarrhoea&#44; which forced us to discontinue treatment&#46;</p><p class="elsevierStylePara">Our study has various limitations&#58; it is a non-controlled observational study&#44; with a small patient sample and without strict control of adherence to a low phosphorus diet and binders&#46; It is possible that due to the &#8220;study effect&#8221; patients will improve their level of adherence&#46; Nevertheless&#44; the changes observed in serum aluminium and magnesium suggest that there was at least partial adherence to treatment&#46;</p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">CONCLUSIONS</span></p><p class="elsevierStylePara">&#160;</p><p class="elsevierStylePara">After the conversion from Al&#40;OH&#41;<span class="elsevierStyleInf">3</span> to MgCO<span class="elsevierStyleInf">3</span>&#44; there was adequate control of serum phosphorus and patients required a lower number of pills&#46; We observed a slight increase in magnesaemia within the normal limits&#44; whose long term clinical significance is as yet unknown&#46; Prospective studies with a longer follow-up period are required for an accurate assessment of the long term effect of high levels of serum magnesium in patients on dialysis&#46;</p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">Conflicts of interest</span></p><p class="elsevierStylePara">&#160;</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;12145&#95;16025&#95;55977&#95;en&#95;t17&#46;12145i&#46;jpg" class="elsevierStyleCrossRefs"><img src="12145_16025_55977_en_t17.12145i.jpg" alt="Patient baseline characteristics&#46;"></img></a></p><p class="elsevierStylePara">Table 1&#46; Patient baseline characteristics&#46;</p><p class="elsevierStylePara"><a href="grande&#47;12145&#95;16025&#95;55978&#95;en&#95;t27&#46;12145i&#46;jpg" class="elsevierStyleCrossRefs"><img src="12145_16025_55978_en_t27.12145i.jpg" alt="Change in laboratory parameters after replacing aluminium hydroxide with calcium acetate&#47;magnesium carbonate&#46;"></img></a></p><p class="elsevierStylePara">Table 2&#46; Change in laboratory parameters after replacing aluminium hydroxide with calcium acetate&#47;magnesium carbonate&#46;</p><p class="elsevierStylePara"><a href="grande&#47;12145&#95;16025&#95;55979&#95;en&#95;t37&#46;12145i&#46;jpg" class="elsevierStyleCrossRefs"><img src="12145_16025_55979_en_t37.12145i.jpg" alt="Other treatments used for phosphorus-calcium metabolism disorders&#46;"></img></a></p><p class="elsevierStylePara">Table 3&#46; Other treatments used for phosphorus-calcium metabolism disorders&#46;</p>"
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        "resumen" => "<p class="elsevierStylePara"><span class="elsevierStyleBold">Introducci&#243;n&#58; </span>El acetato c&#225;lcico&#47;carbonato magn&#233;sico &#40;MgCO<span class="elsevierStyleInf">3</span>&#41; es un quelante de f&#243;sforo con ventajas en cuanto a coste&#44; seguridad y tolerancia&#44; con similar eficacia a la de otros f&#225;rmacos&#46; El objetivo del estudio es evaluar los efectos sobre el metabolismo fosfoc&#225;lcico al sustituir hidr&#243;xido de aluminio &#91;Al&#40;OH<span class="elsevierStyleInf">3</span>&#41;&#93; por MgCO<span class="elsevierStyleInf">3</span> en una cohorte de pacientes en hemodi&#225;lisis&#46; <span class="elsevierStyleBold">Material y m&#233;todos&#58; </span>Se incluyen 21 pacientes con f&#243;sforo &#60;&#160;5 mg&#47;dl&#44; con Al&#40;OH<span class="elsevierStyleInf">3</span>&#41; como &#250;nico quelante&#46; La conversi&#243;n a MgCO<span class="elsevierStyleInf">3</span> se realiz&#243; sin variar el n&#250;mero de comprimidos&#46; Se registraron caracter&#237;sticas cl&#237;nico-demogr&#225;ficas&#44; tratamiento para hiperparatiroidismo secundario y par&#225;metros anal&#237;ticos antes de la conversi&#243;n&#44; y mensualmente durante cuatro meses&#46; <span class="elsevierStyleBold">Resultados&#58; </span>La fosforemia disminuy&#243; de 4&#44;52&#160;&#177;&#160;0&#44;99 a 4&#44;02&#160;&#177;&#160;1&#44;07 mg&#47;dl &#40;p&#160;&#61;&#160;0&#44;027&#41;&#44; con una reducci&#243;n del producto calcio-f&#243;sforo de 40&#44;20&#160;&#177;&#160;10&#44;44 a 35&#44;16&#160;&#177;&#160;11&#44;06 mg<span class="elsevierStyleSup">2</span>&#47;dl<span class="elsevierStyleSup">2</span> &#40;p&#160;&#61;&#160;0&#44;037&#41;&#46; No encontramos variaciones significativas en los niveles de calcio&#44; hormona paratiroidea o 25-OH-vitamina D<span class="elsevierStyleInf">3</span>&#46; El n&#250;mero prescrito de comprimidos diarios se redujo de 3&#44;33&#160;&#177;&#160;2&#44;29 a 2&#44;15&#160;&#177;&#160;2&#44;21 &#40;p&#160;&#61;&#160;0&#44;020&#41;&#46; Los tratamientos concomitantes no variaron&#46; Observamos un aumento significativo inicial de la magnesemia de 2&#44;21&#160;&#177;&#160;0&#44;24 a 2&#44;43&#160;&#177;&#160;0&#44;39 mg&#47;dl &#40;p&#160;&#61;&#160;0&#44;001&#41;&#44; que posteriormente se mantuvo estable&#46; Encontramos una disminuci&#243;n del aluminio s&#233;rico de 14&#44;91&#160;&#177;&#160;8&#44;55 a 8&#44;47&#160;&#177;&#160;3&#44;98 &#181;g&#47;l &#40;p&#160;&#61;&#160;0&#44;004&#41;&#44; con niveles en rango recomendado en todos los pacientes&#46; <span class="elsevierStyleBold">Conclusiones&#58; </span>El MgCO<span class="elsevierStyleInf">3</span> permite un buen control del f&#243;sforo s&#233;rico en pacientes en hemodi&#225;lisis previamente bien controlados con Al&#40;OH&#41;<span class="elsevierStyleInf">3</span>&#44; con menos comprimidos diarios&#46; Se produce un ligero aumento en el magnesio s&#233;rico&#44; sin significado cl&#237;nico a corto plazo&#46; Desconocemos los efectos de este aumento a m&#225;s largo plazo&#46;</p>"
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        "resumen" => "<p class="elsevierStylePara"><span class="elsevierStyleBold">Introduction&#58; </span>Calcium acetate&#47;magnesium carbonate &#40;MgCO<span class="elsevierStyleInf">3</span>&#41; is a phosphorus binder with advantages in terms of cost&#44; safety and tolerance and it has a similar efficacy to other drugs&#46; The objective of the study is to assess the effects of replacing aluminium hydroxide &#91;Al&#40;OH<span class="elsevierStyleInf">3</span>&#41;&#93; with MgCO<span class="elsevierStyleInf">3 </span>on<span class="elsevierStyleInf"> </span>phosphorus and calcium metabolism in a cohort of haemodialysis patients&#46; <span class="elsevierStyleBold">Materials and methods&#58;</span> We included 21 patients with phosphorus &#60;5mg&#47;dl&#44; with Al&#40;OH<span class="elsevierStyleInf">3</span>&#41; as the only binder&#46; The conversion to MgCO<span class="elsevierStyleInf">3 </span>was carried out without changing the number of pills&#46; We recorded clinical-demographic characteristics&#44; treatment for secondary hyperparathyroidism and laboratory parameters before conversion and every month for four months&#46; <span class="elsevierStyleBold">Results&#58; </span>Phosphataemia decreased from 4&#46;52&#177;0&#46;99 to 4&#46;02&#177;1&#46;07mg&#47;dl &#40;<span class="elsevierStyleItalic">p</span>&#61;&#46;027&#41;&#44; and there was a decrease in the calcium-phosphorus product from 40&#46;20&#177;10&#46;44 to 35&#46;16&#177;11&#46;06mg<span class="elsevierStyleSup">2</span>&#47;dl<span class="elsevierStyleSup">2</span> &#40;<span class="elsevierStyleItalic">p</span>&#61;&#46;037&#41;&#46; We did not observe significant changes in levels of calcium&#44; parathyroid hormone or 25-OH-vitamin D<span class="elsevierStyleInf">3</span>&#46; The daily number of pills prescribed was reduced from 3&#46;33&#177;2&#46;29 to 2&#46;15&#177;2&#46;21 &#40;<span class="elsevierStyleItalic">p</span>&#61;&#46;020&#41;&#46; Concomitant treatments were not altered&#46; We observed an initial significant increase in magnesaemia from 2&#46;21&#177;0&#46;24 to 2&#46;43&#177;0&#46;39mg&#47;dl &#40;<span class="elsevierStyleItalic">p</span>&#61;&#46;001&#41;&#44; which subsequently remained stable&#46; We found a decrease in serum aluminium from 14&#46;91&#177;8&#46;55 to 8&#46;47&#177;3&#46;98&#181;g&#47;l &#40;<span class="elsevierStyleItalic">p</span>&#61;&#46;004&#41;&#44; with levels within the recommended range in all patients&#46; <span class="elsevierStyleBold">Conclusions&#58;</span> MgCO<span class="elsevierStyleInf">3 </span>allowed good control of serum phosphorus in haemodialysis patients who were previously well controlled with Al&#40;OH&#41;<span class="elsevierStyleInf">3</span>&#44; using fewer daily pills&#46; There was a slight increase in serum magnesium&#44; without short-term clinical significance&#46; We do not know the effects of this increase in the longer term&#46;</p>"
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                  "referenciaCompleta" => "Collins AJ, Li S, Ma JZ, Herzog C. Cardiovascular disease in end-stage renal disease patients. Am J Kidney Dis 2001;38(4 Suppl 1):S26-9. <a href="http://www.ncbi.nlm.nih.gov/pubmed/11576917" target="_blank">[Pubmed]</a>"
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The effect of replacing aluminium hydroxide with calcium acetate/magnesium carbonate on serum phosphorus control in haemodialysis patients
Efecto en el control del fósforo sérico tras la sustitución de hidróxido de aluminio por acetato cálcico/carbonato magnésico en pacientes en hemodiálisis
David Arroyoa, Nayara Panizoa, Soraya Abada, Almudena Vegaa, Ana Pérez-de Joséa, Juan M. López-Gómeza
a Servicio de Nefrología, Hospital General Universitario Gregorio Marañón, Madrid,
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we selected patients from our haemodialysis unit who had an adequate control of phosphataemia &#40;serum phosphorus &#60;5mg&#47;dl&#41;&#44; on treatment with Al&#40;OH&#41;<span class="elsevierStyleInf">3</span> binder monotherapy who required continuation of this treatment&#46; We followed the indications on dietary restriction of phosphorus rich foods regularly and without variation&#44; in accordance with the unit&#8217;s standard protocol&#46; Twenty-one patients &#40;66&#46;7&#37; male&#44; aged 56&#46;7&#177;16&#46;4 years&#41; met the inclusion criteria&#46; They all underwent dialysis in three four-hour weekly sessions&#59; 6 received high-flux haemodialysis and 15 received online haemodiafiltration&#46; Both the regimen and dialysate remained unchanged throughout the study&#44; with there being a constant magnesium concentration of 0&#46;5mmol&#47;l&#46; The dialysate calcium concentration did not change and was 1&#46;25mmol&#47;l in eight patients and 1&#46;5mmol&#47;l in the remaining 13&#46; 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parathyroid hormone &#40;PTH&#41; and serum magnesium&#46; Serum aluminium was measured at baseline and after four months&#46; Patients were regularly questioned about their adherence to the treatment with phosphate binders&#46;</p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">Statistical analysis</span></p><p class="elsevierStylePara">&#160;</p><p class="elsevierStylePara">All statistical analyses were performed using the SPSS version 17&#46;0 software &#40;SPSS Inc&#44; Chicago&#44; IL&#41;&#46; The variables were recorded as percentages or as a mean &#177; standard deviation&#46; Qualitative variables were compared using McNemar&#39;s test and quantitative data were analysed using the Wilcoxon signed-rank test for related non-parametric variables&#46; We considered relationships with a <span class="elsevierStyleItalic">P</span> value &#60;&#46;05 to be significant&#46;</p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">RESULTS</span></p><p class="elsevierStylePara">&#160;</p><p class="elsevierStylePara">We observed a statistically significant decrease in serum phosphorus levels four months after the conversion to MgCO<span class="elsevierStyleInf">3</span> &#40;4&#46;52&#177;0&#46;99 versus 4&#46;02&#177;1&#46;07mg&#47;dl&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;027&#41;&#44; and in calcium-phosphorus product levels &#40;40&#46;20&#177;10&#46;44 versus 35&#46;16&#177;11&#46;06mg<span class="elsevierStyleSup">2</span>&#47;dl<span class="elsevierStyleSup">2</span>&#44; <span class="elsevierStyleItalic">p</span>&#61;&#46;037&#41;&#46; Despite the additional intake of oral calcium&#44; the change in serum calcium was not significant &#40;8&#46;85&#177;0&#46;65 versus 8&#46;66&#177;0&#46;81mg&#47;dl&#41;&#46; No significant changes were observed in PTH or vitamin D levels&#46; Changes in laboratory results throughout follow-up are summarised in Table 2&#46;</p><p class="elsevierStylePara">The improvement in phosphataemia control was achieved by decreasing the number of MgCO<span class="elsevierStyleInf">3 </span>pills &#40;from 3&#46;33&#177;2&#46;29 to 2&#46;15&#177;2&#46;21 pills per day&#44; <span class="elsevierStyleItalic">P</span>&#61;&#46;020&#41;&#46; There were no significant changes in the rest of the drugs used to treat SHPT &#40;Table 3&#41;&#46;</p><p class="elsevierStylePara">We discontinued treatment with MgCO<span class="elsevierStyleInf">3</span> in six patients &#40;30&#37;&#41;&#44; in five due to hypophosphataemia and in one due to digestive intolerance&#46; We observed a significant increase in magnesaemia from the first month &#40;2&#46;21&#177;0&#46;24 versus 2&#46;43&#177;0&#46;39mg&#47;dl&#44; <span class="elsevierStyleItalic">P</span>&#61;&#46;001&#41;&#44; which remained stable for four months&#46; We recorded just one case of hypermagnesaemia &#40;&#62;3mg&#47;dl&#41;&#44; which was suitably resolved by reducing the dose&#46;</p><p class="elsevierStylePara">Likewise&#44; we found a decrease in serum aluminium levels from 14&#46;91&#177;8&#46;55 to 8&#46;47&#177;3&#46;98&#181;g&#47;l &#40;<span class="elsevierStyleItalic">p</span>&#61;&#46;004&#41;&#44; with levels being within the recommended range &#40;&#60;40&#181;g&#47;l&#41; in all patients&#46;</p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">DISCUSSION</span></p><p class="elsevierStylePara">&#160;</p><p class="elsevierStylePara">The conversion from Al&#40;OH&#41;<span class="elsevierStyleInf">3</span> to MgCO<span class="elsevierStyleInf">3</span> allowed phosphorus to be controlled adequately in this haemodialysis patient cohort&#46; Although we were not able to demonstrate clearly that a decrease in serum phosphorus results in reduced mortality&#44; the obvious pathophysiological role that it plays has led to clear indications in national and international guidelines&#46;<span class="elsevierStyleSup">12</span></p><p class="elsevierStylePara">There are currently a wide variety of binders available&#44; all of which are effective in reducing hyperphosphataemia&#44; but with differences in other aspects that force doctors to make a decision about which binder to prescribe&#46;<span class="elsevierStyleSup">13-15</span> Until recently&#44; aluminium salts were considered the most powerful binder&#44; with a very low cost&#47;benefit ratio&#46;<span class="elsevierStyleSup">11 </span>However&#44; the potential toxicity of aluminium had restricted its use in the literature to settings with fewer economic resources&#46;<span class="elsevierStyleSup">16-18 </span>There has even been a certain concern about aluminium intake from other drugs&#44; both in terms of hidden intake and alongside other indications&#44; especially antacids&#46;<span class="elsevierStyleSup">19 </span>Improvement in the treatment of dialysis water&#44; with the resulting lower aluminium concentration&#44; and its low cost in this period of adjustments has challenged these limitations&#46; Various recent studies in which no long term toxicity was observed have reopened the debate on the potential use of aluminium salts&#46;<span class="elsevierStyleSup">9&#44;10&#44;20&#44;21</span></p><p class="elsevierStylePara">In our study&#44; we found that suppressing aluminium salt-based binders effectively decreases serum levels of this element&#44; although no patient had levels higher than 40&#181;g&#47;l at any given time&#46; For now and until there is more evidence on the use of aluminium salts with the current water controls&#44; the guidelines continue to advise against them&#46; Furthermore&#44; the manufacture and distribution of the aluminium binder available in our setting was recently interrupted&#44; forcing us to seek other therapeutic options&#46;</p><p class="elsevierStylePara">The purpose of our study was to assess the replacement of Al&#40;OH&#41;<span class="elsevierStyleInf">3 </span>with MgCO<span class="elsevierStyleInf">3</span>&#46; The first studies in this line were carried out in the nineteen eighties&#44; in different conditions to the current situation&#46;<span class="elsevierStyleSup">22 </span>Since then&#44; many studies have used magnesium salts as phosphate binders&#46;<span class="elsevierStyleSup">23 </span>Of the many drugs available&#44; MgCO<span class="elsevierStyleInf">3 </span>has advantages in terms of safety and tolerance&#44; with an efficacy that is comparable to that of other more modern binders&#46;<span class="elsevierStyleSup">24</span> In our study&#44; we found a significant reduction in the number of pills&#44; which allowed an improvement in adherence and therefore in hyperphosphataemia control&#46;<span class="elsevierStyleSup">25</span> It also has a lower cost than other non-calcium binders&#44; which is important in the current situation&#46;<span class="elsevierStyleSup">8</span></p><p class="elsevierStylePara">Another advantage of using MgCO<span class="elsevierStyleInf">3</span> is the benefits of magnesium intake&#44; an element that is increasingly important&#46;<span class="elsevierStyleSup">26</span> There is growing evidence of the relationship between lower levels of magnesium in the general population and the occurrence or poor control of diseases such as diabetes&#44; high blood pressure or cardiovascular disease&#46;<span class="elsevierStyleSup">27-31 In chronic kidney disease patients&#44; reduced levels of magnesium have been associated with greater mortality&#44; a worsening of mineral and bone disorder and an increase in vascular calcifications&#46;32-35 </span>An interventional study demonstrated delayed arterial calcification with a reduction in intima-media thickness in relation to magnesium supplements&#46;<span class="elsevierStyleSup">36 </span>At present&#44; there are few studies on the effects of different dialysate concentrations&#46;<span class="elsevierStyleSup">37&#44;38 </span>It seems that there could be certain advantages to using dialysate with a higher magnesium content&#44; such as better haemodynamic tolerance&#46;<span class="elsevierStyleSup">39 </span>It is not clear what levels of serum magnesium are suitable&#44; although there seems to be an increasingly greater consensus that somewhat higher levels could be beneficial for patients on dialysis&#46; Intervention trials&#44; which assess the medium and long term effects of increasing magnesium&#44; whether through oral intake or higher dialysate concentrations&#44; are necessary&#46;</p><p class="elsevierStylePara">In our study&#44; we observed a slight increase in magnesium levels&#44; which&#44; as in the CALMAG study&#44; occurred at the start of treatment and subsequently remained stable&#46;<span class="elsevierStyleSup">24 </span>Only one case of asymptomatic hypermagnesaemia was recorded&#44; which returned to levels below 3mg&#47;dl after dose reduction&#46; Likewise&#44; we only found one case of digestive intolerance due to diarrhoea&#44; which forced us to discontinue treatment&#46;</p><p class="elsevierStylePara">Our study has various limitations&#58; it is a non-controlled observational study&#44; with a small patient sample and without strict control of adherence to a low phosphorus diet and binders&#46; It is possible that due to the &#8220;study effect&#8221; patients will improve their level of adherence&#46; Nevertheless&#44; the changes observed in serum aluminium and magnesium suggest that there was at least partial adherence to treatment&#46;</p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">CONCLUSIONS</span></p><p class="elsevierStylePara">&#160;</p><p class="elsevierStylePara">After the conversion from Al&#40;OH&#41;<span class="elsevierStyleInf">3</span> to MgCO<span class="elsevierStyleInf">3</span>&#44; there was adequate control of serum phosphorus and patients required a lower number of pills&#46; We observed a slight increase in magnesaemia within the normal limits&#44; whose long term clinical significance is as yet unknown&#46; Prospective studies with a longer follow-up period are required for an accurate assessment of the long term effect of high levels of serum magnesium in patients on dialysis&#46;</p><p class="elsevierStylePara"><span class="elsevierStyleBold">&#160;</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">Conflicts of interest</span></p><p class="elsevierStylePara">&#160;</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;12145&#95;16025&#95;55977&#95;en&#95;t17&#46;12145i&#46;jpg" class="elsevierStyleCrossRefs"><img src="12145_16025_55977_en_t17.12145i.jpg" alt="Patient baseline characteristics&#46;"></img></a></p><p class="elsevierStylePara">Table 1&#46; Patient baseline characteristics&#46;</p><p class="elsevierStylePara"><a href="grande&#47;12145&#95;16025&#95;55978&#95;en&#95;t27&#46;12145i&#46;jpg" class="elsevierStyleCrossRefs"><img src="12145_16025_55978_en_t27.12145i.jpg" alt="Change in laboratory parameters after replacing aluminium hydroxide with calcium acetate&#47;magnesium carbonate&#46;"></img></a></p><p class="elsevierStylePara">Table 2&#46; Change in laboratory parameters after replacing aluminium hydroxide with calcium acetate&#47;magnesium carbonate&#46;</p><p class="elsevierStylePara"><a href="grande&#47;12145&#95;16025&#95;55979&#95;en&#95;t37&#46;12145i&#46;jpg" class="elsevierStyleCrossRefs"><img src="12145_16025_55979_en_t37.12145i.jpg" alt="Other treatments used for phosphorus-calcium metabolism disorders&#46;"></img></a></p><p class="elsevierStylePara">Table 3&#46; Other treatments used for phosphorus-calcium metabolism disorders&#46;</p>"
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        "resumen" => "<p class="elsevierStylePara"><span class="elsevierStyleBold">Introducci&#243;n&#58; </span>El acetato c&#225;lcico&#47;carbonato magn&#233;sico &#40;MgCO<span class="elsevierStyleInf">3</span>&#41; es un quelante de f&#243;sforo con ventajas en cuanto a coste&#44; seguridad y tolerancia&#44; con similar eficacia a la de otros f&#225;rmacos&#46; El objetivo del estudio es evaluar los efectos sobre el metabolismo fosfoc&#225;lcico al sustituir hidr&#243;xido de aluminio &#91;Al&#40;OH<span class="elsevierStyleInf">3</span>&#41;&#93; por MgCO<span class="elsevierStyleInf">3</span> en una cohorte de pacientes en hemodi&#225;lisis&#46; <span class="elsevierStyleBold">Material y m&#233;todos&#58; </span>Se incluyen 21 pacientes con f&#243;sforo &#60;&#160;5 mg&#47;dl&#44; con Al&#40;OH<span class="elsevierStyleInf">3</span>&#41; como &#250;nico quelante&#46; La conversi&#243;n a MgCO<span class="elsevierStyleInf">3</span> se realiz&#243; sin variar el n&#250;mero de comprimidos&#46; Se registraron caracter&#237;sticas cl&#237;nico-demogr&#225;ficas&#44; tratamiento para hiperparatiroidismo secundario y par&#225;metros anal&#237;ticos antes de la conversi&#243;n&#44; y mensualmente durante cuatro meses&#46; <span class="elsevierStyleBold">Resultados&#58; </span>La fosforemia disminuy&#243; de 4&#44;52&#160;&#177;&#160;0&#44;99 a 4&#44;02&#160;&#177;&#160;1&#44;07 mg&#47;dl &#40;p&#160;&#61;&#160;0&#44;027&#41;&#44; con una reducci&#243;n del producto calcio-f&#243;sforo de 40&#44;20&#160;&#177;&#160;10&#44;44 a 35&#44;16&#160;&#177;&#160;11&#44;06 mg<span class="elsevierStyleSup">2</span>&#47;dl<span class="elsevierStyleSup">2</span> &#40;p&#160;&#61;&#160;0&#44;037&#41;&#46; No encontramos variaciones significativas en los niveles de calcio&#44; hormona paratiroidea o 25-OH-vitamina D<span class="elsevierStyleInf">3</span>&#46; El n&#250;mero prescrito de comprimidos diarios se redujo de 3&#44;33&#160;&#177;&#160;2&#44;29 a 2&#44;15&#160;&#177;&#160;2&#44;21 &#40;p&#160;&#61;&#160;0&#44;020&#41;&#46; Los tratamientos concomitantes no variaron&#46; Observamos un aumento significativo inicial de la magnesemia de 2&#44;21&#160;&#177;&#160;0&#44;24 a 2&#44;43&#160;&#177;&#160;0&#44;39 mg&#47;dl &#40;p&#160;&#61;&#160;0&#44;001&#41;&#44; que posteriormente se mantuvo estable&#46; Encontramos una disminuci&#243;n del aluminio s&#233;rico de 14&#44;91&#160;&#177;&#160;8&#44;55 a 8&#44;47&#160;&#177;&#160;3&#44;98 &#181;g&#47;l &#40;p&#160;&#61;&#160;0&#44;004&#41;&#44; con niveles en rango recomendado en todos los pacientes&#46; <span class="elsevierStyleBold">Conclusiones&#58; </span>El MgCO<span class="elsevierStyleInf">3</span> permite un buen control del f&#243;sforo s&#233;rico en pacientes en hemodi&#225;lisis previamente bien controlados con Al&#40;OH&#41;<span class="elsevierStyleInf">3</span>&#44; con menos comprimidos diarios&#46; Se produce un ligero aumento en el magnesio s&#233;rico&#44; sin significado cl&#237;nico a corto plazo&#46; Desconocemos los efectos de este aumento a m&#225;s largo plazo&#46;</p>"
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        "resumen" => "<p class="elsevierStylePara"><span class="elsevierStyleBold">Introduction&#58; </span>Calcium acetate&#47;magnesium carbonate &#40;MgCO<span class="elsevierStyleInf">3</span>&#41; is a phosphorus binder with advantages in terms of cost&#44; safety and tolerance and it has a similar efficacy to other drugs&#46; The objective of the study is to assess the effects of replacing aluminium hydroxide &#91;Al&#40;OH<span class="elsevierStyleInf">3</span>&#41;&#93; with MgCO<span class="elsevierStyleInf">3 </span>on<span class="elsevierStyleInf"> </span>phosphorus and calcium metabolism in a cohort of haemodialysis patients&#46; <span class="elsevierStyleBold">Materials and methods&#58;</span> We included 21 patients with phosphorus &#60;5mg&#47;dl&#44; with Al&#40;OH<span class="elsevierStyleInf">3</span>&#41; as the only binder&#46; The conversion to MgCO<span class="elsevierStyleInf">3 </span>was carried out without changing the number of pills&#46; We recorded clinical-demographic characteristics&#44; treatment for secondary hyperparathyroidism and laboratory parameters before conversion and every month for four months&#46; <span class="elsevierStyleBold">Results&#58; </span>Phosphataemia decreased from 4&#46;52&#177;0&#46;99 to 4&#46;02&#177;1&#46;07mg&#47;dl &#40;<span class="elsevierStyleItalic">p</span>&#61;&#46;027&#41;&#44; and there was a decrease in the calcium-phosphorus product from 40&#46;20&#177;10&#46;44 to 35&#46;16&#177;11&#46;06mg<span class="elsevierStyleSup">2</span>&#47;dl<span class="elsevierStyleSup">2</span> &#40;<span class="elsevierStyleItalic">p</span>&#61;&#46;037&#41;&#46; We did not observe significant changes in levels of calcium&#44; parathyroid hormone or 25-OH-vitamin D<span class="elsevierStyleInf">3</span>&#46; The daily number of pills prescribed was reduced from 3&#46;33&#177;2&#46;29 to 2&#46;15&#177;2&#46;21 &#40;<span class="elsevierStyleItalic">p</span>&#61;&#46;020&#41;&#46; Concomitant treatments were not altered&#46; We observed an initial significant increase in magnesaemia from 2&#46;21&#177;0&#46;24 to 2&#46;43&#177;0&#46;39mg&#47;dl &#40;<span class="elsevierStyleItalic">p</span>&#61;&#46;001&#41;&#44; which subsequently remained stable&#46; We found a decrease in serum aluminium from 14&#46;91&#177;8&#46;55 to 8&#46;47&#177;3&#46;98&#181;g&#47;l &#40;<span class="elsevierStyleItalic">p</span>&#61;&#46;004&#41;&#44; with levels within the recommended range in all patients&#46; <span class="elsevierStyleBold">Conclusions&#58;</span> MgCO<span class="elsevierStyleInf">3 </span>allowed good control of serum phosphorus in haemodialysis patients who were previously well controlled with Al&#40;OH&#41;<span class="elsevierStyleInf">3</span>&#44; using fewer daily pills&#46; There was a slight increase in serum magnesium&#44; without short-term clinical significance&#46; We do not know the effects of this increase in the longer term&#46;</p>"
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                  "referenciaCompleta" => "Collins AJ, Li S, Ma JZ, Herzog C. Cardiovascular disease in end-stage renal disease patients. Am J Kidney Dis 2001;38(4 Suppl 1):S26-9. <a href="http://www.ncbi.nlm.nih.gov/pubmed/11576917" target="_blank">[Pubmed]</a>"
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Article information
ISSN: 20132514
Original language: English
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2022 July 59 75 134
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2022 May 89 47 136
2022 April 64 65 129
2022 March 58 66 124
2022 February 49 51 100
2022 January 80 34 114
2021 December 92 49 141
2021 November 96 40 136
2021 October 152 42 194
2021 September 94 41 135
2021 August 64 41 105
2021 July 85 31 116
2021 June 68 29 97
2021 May 63 46 109
2021 April 140 93 233
2021 March 110 35 145
2021 February 105 24 129
2021 January 66 16 82
2020 December 71 19 90
2020 November 85 16 101
2020 October 56 22 78
2020 September 54 8 62
2020 August 66 17 83
2020 July 56 10 66
2020 June 62 17 79
2020 May 74 10 84
2020 April 74 20 94
2020 March 78 15 93
2020 February 88 20 108
2020 January 103 23 126
2019 December 94 22 116
2019 November 95 25 120
2019 October 128 20 148
2019 September 126 16 142
2019 August 70 13 83
2019 July 69 25 94
2019 June 76 31 107
2019 May 101 17 118
2019 April 101 41 142
2019 March 73 31 104
2019 February 51 19 70
2019 January 82 31 113
2018 December 126 54 180
2018 November 123 31 154
2018 October 121 32 153
2018 September 209 22 231
2018 August 114 32 146
2018 July 137 21 158
2018 June 145 19 164
2018 May 129 19 148
2018 April 113 8 121
2018 March 70 11 81
2018 February 92 13 105
2018 January 86 6 92
2017 December 88 15 103
2017 November 88 18 106
2017 October 65 15 80
2017 September 98 17 115
2017 August 92 6 98
2017 July 117 25 142
2017 June 78 13 91
2017 May 95 12 107
2017 April 65 11 76
2017 March 95 15 110
2017 February 120 17 137
2017 January 62 14 76
2016 December 119 8 127
2016 November 157 7 164
2016 October 202 12 214
2016 September 329 6 335
2016 August 408 6 414
2016 July 318 16 334
2016 June 216 0 216
2016 May 174 0 174
2016 April 180 0 180
2016 March 140 0 140
2016 February 160 0 160
2016 January 151 0 151
2015 December 162 0 162
2015 November 137 0 137
2015 October 143 0 143
2015 September 111 0 111
2015 August 91 0 91
2015 July 125 0 125
2015 June 73 0 73
2015 May 87 0 87
2015 April 9 0 9
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¿Es usted profesional sanitario apto para prescribir o dispensar medicamentos?

Are you a health professional able to prescribe or dispense drugs?