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    "textoCompleto" => "<p class="elsevierStylePara">Over the past 15 years&#44; peritoneal dialysis has undergone considerable development from a technological point of view&#46;<span class="elsevierStyleSup">1&#44;2</span> It is currently a fully validated form of dialysis treatment which is cheaper than haemodialysis and comparable in terms of survival rates and the effect on quality of life&#46;<span class="elsevierStyleSup">3-6</span> Nevertheless&#44; haemodialysis continues to be the more commonly used replacement therapy all over the world&#46; In 2001 data pertaining to 1&#44;479&#44;000 renal patients undergoing replacement therapies in 120 countries across 5 continents was published&#59; peritoneal dialysis was only being used by 8&#46;5&#37; of patients while 69&#37; of patients were being treated with haemodialysis&#46;<span class="elsevierStyleSup">7</span> The situation in Spain is similar&#46;<span class="elsevierStyleSup">8</span> There are several reasons behind this&#44; some of which may seem illogical to some&#46; The technique had a disastrous start when it was first introduced &#40;with a high rate of peritonitis and obsolete technology&#41; and this still casts a shadow over its reputation&#46; Another factor is functional exhaustion of the peritoneum which some patients experience over the long-term and at least has some theoretical basis&#46; The deterioration of the peritoneal membrane has been associated with the use of glucose as an osmotic agent&#46; Its well-known deleterious effects on the peritoneum may lead to failure of the peritoneal dialysis treatment in the mid- to long-term&#46;<span class="elsevierStyleSup">9</span> With this in mind&#44; an extensive effort has been made to find dialysis solutions that are more biocompatible&#44; one of these being icodextrin&#46;</p><p class="elsevierStylePara">Icodextrin is a cornstarch-derived glucose polymer and acts as a colloid osmotic agent&#46; Its high molecular weight &#40;16&#44;000 Daltons&#41; makes reabsorption difficult and therefore its ultrafiltration rate is steady for a longer period of time compared with glucose solutions&#46;<span class="elsevierStyleSup">10&#44;11</span> Icodextrin ultrafiltration occurs across the small pores in the peritoneal membrane and is characterised by minimal lymphatic reabsorption&#46; Ultrafiltration with a 7&#46;5&#37; icodextrin solution exchange is similar to that of a 3&#46;86&#37; glucose solution at 8 hours and is higher in dwell times of 12 hours&#46;<span class="elsevierStyleSup">12&#44;13</span> It has been observed that in patients undergoing continuous ambulatory peritoneal dialysis the use of icodextrin during the overnight 8-12 hour dwell resulted in 500ml ultrafiltration&#44; as compared with 300ml during the <span class="elsevierStyleSup">14-16</span> hour long daytime dwell using the automated cycling technique&#46; Neri et al&#46;14 have suggested that this may be due to the increase in lymphatic absorption caused by greater intraperitoneal pressure whilst standing up&#46; Icodextrin solutions have a similar osmolarity to plasma &#40;282mOsm&#47;kg&#41; and fewer glucose degradation products&#44; which at least in theory makes them more biocompatible&#46; The use of icodextrin is linked to improved volaemia in prospective studies&#46;<span class="elsevierStyleSup">15 </span>It maintains residual renal function for longer and achieves better convective solute clearance&#46;<span class="elsevierStyleSup">16</span> In short&#44; icodextrin represents a significant contribution in the management of patients that lose ultrafiltration&#46; This will benefit high or fast transporters&#44; moderate-high transporters<span class="elsevierStyleSup">17&#44;18</span> and possibly diabetics&#46;<span class="elsevierStyleSup">19</span> The increase in ultrafiltration is maintained over time and during episodes of peritonitis&#46;</p><p class="elsevierStylePara">The peritoneum is a dialyzing membrane and as such undergoes functional and structural changes in the long-term that lead to the progressive deterioration of peritoneal transport&#46;<span class="elsevierStyleSup">20&#44;21</span> Peritoneal fibrosis with progressive mesothelial thickening&#44; neoangiogenesis and vasculopathy are some of the changes that can be attributed to the repeated exposure of the peritoneum to solutions that are not physiological or biocompatible&#44; among other causes&#46; These structural changes finally result in the functional failure of the peritoneal membrane for a variable percentage of patients&#46;</p><p class="elsevierStylePara">Peritoneal membrane transport rates can be categorised as low&#44; medium-low&#44; medium-high and high&#44; in accordance with the peritoneal equilibration test devised by Twardowski&#46;<span class="elsevierStyleSup">22</span> The higher the peritoneal transport rate&#44; the lower the ultrafiltration rate and the higher the risk of volume overload&#46; A high peritoneal transport rate is also associated with greater protein losses into the dialysate&#46; The dialysate&#47;plasma ratio of solutes with low molecular weight depends on the peritoneal vascular surface area&#46; The increase in peritoneal vascularisation results in fast transporter status&#46; This has been linked to an increase in mortality of up to 15&#37;&#44; especially in patients undergoing continuous ambulatory peritoneal dialysis and using glucose solution exclusively&#46;<span class="elsevierStyleSup">23-26</span> Other authors have not found any link between the peritoneal transport rate and patient mortality in the long term&#46;<span class="elsevierStyleSup">27</span> This apparent contradiction has prompted many authors to carry out in-depth studies on peritoneal transport rates at different stages during dialysis&#44; in order to determine the influence of transport status on patient progress&#46;</p><p class="elsevierStylePara">To investigate this&#44; patients were divided into high transporter at the initiation of dialysis and those who acquired high transport status during follow-up&#46;<span class="elsevierStyleSup">28-30</span></p><p class="elsevierStylePara">The incidence of fast transporters at the start of dialysis treatment &#40;inherent high transporters&#41; was 15&#37;&#46;<span class="elsevierStyleSup">28&#44;29</span> Similarly&#44; a distinction was made between the two subtypes of high transport from the outset&#58; type 1 is associated with comorbidity and inflammation and is accompanied by high IL-6 and VEGF plasma levels&#46; This condition is associated with males&#44; diabetics&#44; low initial levels of albumin and increased baseline comorbidity&#46; The prognosis for these patients is poor even if they are treated with haemodialysis&#46; Type 2 is associated with high levels of CA125 in the peritoneal effluent&#44; suggesting a large peritoneal surface area and&#44; consequently&#44; a large number of mesothelial cells&#46; Type 2 has good prognosis if the peritoneum is unaffected by complications such as peritonitis and the patient remains euvolaemic&#44; given that fast transport tends to normalise with time&#46;<span class="elsevierStyleSup">31&#44;32</span></p><p class="elsevierStylePara">Acquired high transport &#40;type 3&#41; may be transitory and reversible &#40;for example during peritonitis&#41; or permanent&#46; The latter is developed by 30&#37; of patients who have been undergoing peritoneal dialysis for a period of over 4 years&#46;</p><p class="elsevierStylePara">This is due to peritoneal neoangiogenesis caused by the exposure of the peritoneum to solutions that are not physiological &#40;glucose&#44; glucose degradation products&#44; pH and lactate buffer&#41; and peritoneal damage caused by complications like peritonitis&#46; This is linked to an increased risk of overhydration&#44; especially taking into consideration the loss of residual renal function after several years of peritoneal dialysis&#46;</p><p class="elsevierStylePara">The treatment of high transporter status begins with its prevention&#46; Some of the proposed measures include preserving residual function&#44; preventing peritonitis and using icodextrin solution exchange during long dwell times and a cycler with short cycles to prevent hypervolaemia&#46;<span class="elsevierStyleSup">29</span> The use of ACE inhibitors may also be beneficial in the preservation of residual renal function during the first year of dialysis&#46;<span class="elsevierStyleSup">33</span></p><p class="elsevierStylePara">In this issue&#44; Fern&#225;ndez-Reyes et al&#46;<span class="elsevierStyleSup">34</span> analyse peritoneal transport in the short-term to mid-term in patients that have been using icodextrin from the outset&#46; Their results showed that patients that used an icodextrin solution exchange tended to normalise peritoneal permeability&#46; This finding was particularly evident in patients with high transport from the outset&#44; and normalisation was greater when compared with that of patients who used glucose solution &#40;control group&#41;&#46; The study is particularly interesting since it included incident patients and the results are similar to those recently published in a prevalent population&#46;<span class="elsevierStyleSup">35</span> In this EAPOS substudy&#44; it was evident that the patients treated with icodextrin maintained adequate peritoneal function for at least two years&#44; whereas those who received glucose solution experienced a significant deterioration in solute transport and ultrafiltration capacity with subsequent fluid overload&#46; In the study by Fern&#225;ndez-Reyes et al&#46;<span class="elsevierStyleSup">34</span> the group of patients using icodextrin had suffered less episodes of peritonitis and a higher proportion of them were on ACE inhibitors at the start of the study&#46; There is a need to carry out a randomized control study before any improvement in peritoneal transport can be attributed to icodextrin alone&#46;</p><p class="elsevierStylePara">The way in which icodextrin improves peritoneal permeability in high transporters and the long-term benefits of icodextrin will be the subject of future studies&#46;</p><p class="elsevierStylePara"><span class="elsevierStyleBold">KEY CONCEPTS</span></p><p class="elsevierStylePara">1&#46; Peritoneal transport status is a dynamic concept that varies over time and is influenced by different factors&#46;</p><p class="elsevierStylePara">2&#46; &#34;High transporters&#34; according to the classification system devised by Twardowski are also known as &#34;fast transporters&#46;&#34;</p><p class="elsevierStylePara">3&#46; There are three types of fast transporters&#58; inherent &#40;type 1 and type 2&#41; occurring at the initiation of treatment&#44; and acquired &#40;type 3&#41;&#46;</p><p class="elsevierStylePara">4&#46; The worst prognosis for fast transporters has been associated with the use of glucose solutions and manual technique&#46;</p><p class="elsevierStylePara">5&#46; Fast transporters should undergo automated peritoneal dialysis using icodextrin&#46;</p>"
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Icodextrin as first treatment: reasons to be optimistic
Icodextrina de inicio : Razones para ser optimista
Maite Riveraa
a Servicio de Nefrología, Hospital Ramón y Cajal Madrid, Madrid, España,
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    "textoCompleto" => "<p class="elsevierStylePara">Over the past 15 years&#44; peritoneal dialysis has undergone considerable development from a technological point of view&#46;<span class="elsevierStyleSup">1&#44;2</span> It is currently a fully validated form of dialysis treatment which is cheaper than haemodialysis and comparable in terms of survival rates and the effect on quality of life&#46;<span class="elsevierStyleSup">3-6</span> Nevertheless&#44; haemodialysis continues to be the more commonly used replacement therapy all over the world&#46; In 2001 data pertaining to 1&#44;479&#44;000 renal patients undergoing replacement therapies in 120 countries across 5 continents was published&#59; peritoneal dialysis was only being used by 8&#46;5&#37; of patients while 69&#37; of patients were being treated with haemodialysis&#46;<span class="elsevierStyleSup">7</span> The situation in Spain is similar&#46;<span class="elsevierStyleSup">8</span> There are several reasons behind this&#44; some of which may seem illogical to some&#46; The technique had a disastrous start when it was first introduced &#40;with a high rate of peritonitis and obsolete technology&#41; and this still casts a shadow over its reputation&#46; Another factor is functional exhaustion of the peritoneum which some patients experience over the long-term and at least has some theoretical basis&#46; The deterioration of the peritoneal membrane has been associated with the use of glucose as an osmotic agent&#46; Its well-known deleterious effects on the peritoneum may lead to failure of the peritoneal dialysis treatment in the mid- to long-term&#46;<span class="elsevierStyleSup">9</span> With this in mind&#44; an extensive effort has been made to find dialysis solutions that are more biocompatible&#44; one of these being icodextrin&#46;</p><p class="elsevierStylePara">Icodextrin is a cornstarch-derived glucose polymer and acts as a colloid osmotic agent&#46; Its high molecular weight &#40;16&#44;000 Daltons&#41; makes reabsorption difficult and therefore its ultrafiltration rate is steady for a longer period of time compared with glucose solutions&#46;<span class="elsevierStyleSup">10&#44;11</span> Icodextrin ultrafiltration occurs across the small pores in the peritoneal membrane and is characterised by minimal lymphatic reabsorption&#46; Ultrafiltration with a 7&#46;5&#37; icodextrin solution exchange is similar to that of a 3&#46;86&#37; glucose solution at 8 hours and is higher in dwell times of 12 hours&#46;<span class="elsevierStyleSup">12&#44;13</span> It has been observed that in patients undergoing continuous ambulatory peritoneal dialysis the use of icodextrin during the overnight 8-12 hour dwell resulted in 500ml ultrafiltration&#44; as compared with 300ml during the <span class="elsevierStyleSup">14-16</span> hour long daytime dwell using the automated cycling technique&#46; Neri et al&#46;14 have suggested that this may be due to the increase in lymphatic absorption caused by greater intraperitoneal pressure whilst standing up&#46; Icodextrin solutions have a similar osmolarity to plasma &#40;282mOsm&#47;kg&#41; and fewer glucose degradation products&#44; which at least in theory makes them more biocompatible&#46; The use of icodextrin is linked to improved volaemia in prospective studies&#46;<span class="elsevierStyleSup">15 </span>It maintains residual renal function for longer and achieves better convective solute clearance&#46;<span class="elsevierStyleSup">16</span> In short&#44; icodextrin represents a significant contribution in the management of patients that lose ultrafiltration&#46; This will benefit high or fast transporters&#44; moderate-high transporters<span class="elsevierStyleSup">17&#44;18</span> and possibly diabetics&#46;<span class="elsevierStyleSup">19</span> The increase in ultrafiltration is maintained over time and during episodes of peritonitis&#46;</p><p class="elsevierStylePara">The peritoneum is a dialyzing membrane and as such undergoes functional and structural changes in the long-term that lead to the progressive deterioration of peritoneal transport&#46;<span class="elsevierStyleSup">20&#44;21</span> Peritoneal fibrosis with progressive mesothelial thickening&#44; neoangiogenesis and vasculopathy are some of the changes that can be attributed to the repeated exposure of the peritoneum to solutions that are not physiological or biocompatible&#44; among other causes&#46; These structural changes finally result in the functional failure of the peritoneal membrane for a variable percentage of patients&#46;</p><p class="elsevierStylePara">Peritoneal membrane transport rates can be categorised as low&#44; medium-low&#44; medium-high and high&#44; in accordance with the peritoneal equilibration test devised by Twardowski&#46;<span class="elsevierStyleSup">22</span> The higher the peritoneal transport rate&#44; the lower the ultrafiltration rate and the higher the risk of volume overload&#46; A high peritoneal transport rate is also associated with greater protein losses into the dialysate&#46; The dialysate&#47;plasma ratio of solutes with low molecular weight depends on the peritoneal vascular surface area&#46; The increase in peritoneal vascularisation results in fast transporter status&#46; This has been linked to an increase in mortality of up to 15&#37;&#44; especially in patients undergoing continuous ambulatory peritoneal dialysis and using glucose solution exclusively&#46;<span class="elsevierStyleSup">23-26</span> Other authors have not found any link between the peritoneal transport rate and patient mortality in the long term&#46;<span class="elsevierStyleSup">27</span> This apparent contradiction has prompted many authors to carry out in-depth studies on peritoneal transport rates at different stages during dialysis&#44; in order to determine the influence of transport status on patient progress&#46;</p><p class="elsevierStylePara">To investigate this&#44; patients were divided into high transporter at the initiation of dialysis and those who acquired high transport status during follow-up&#46;<span class="elsevierStyleSup">28-30</span></p><p class="elsevierStylePara">The incidence of fast transporters at the start of dialysis treatment &#40;inherent high transporters&#41; was 15&#37;&#46;<span class="elsevierStyleSup">28&#44;29</span> Similarly&#44; a distinction was made between the two subtypes of high transport from the outset&#58; type 1 is associated with comorbidity and inflammation and is accompanied by high IL-6 and VEGF plasma levels&#46; This condition is associated with males&#44; diabetics&#44; low initial levels of albumin and increased baseline comorbidity&#46; The prognosis for these patients is poor even if they are treated with haemodialysis&#46; Type 2 is associated with high levels of CA125 in the peritoneal effluent&#44; suggesting a large peritoneal surface area and&#44; consequently&#44; a large number of mesothelial cells&#46; Type 2 has good prognosis if the peritoneum is unaffected by complications such as peritonitis and the patient remains euvolaemic&#44; given that fast transport tends to normalise with time&#46;<span class="elsevierStyleSup">31&#44;32</span></p><p class="elsevierStylePara">Acquired high transport &#40;type 3&#41; may be transitory and reversible &#40;for example during peritonitis&#41; or permanent&#46; The latter is developed by 30&#37; of patients who have been undergoing peritoneal dialysis for a period of over 4 years&#46;</p><p class="elsevierStylePara">This is due to peritoneal neoangiogenesis caused by the exposure of the peritoneum to solutions that are not physiological &#40;glucose&#44; glucose degradation products&#44; pH and lactate buffer&#41; and peritoneal damage caused by complications like peritonitis&#46; This is linked to an increased risk of overhydration&#44; especially taking into consideration the loss of residual renal function after several years of peritoneal dialysis&#46;</p><p class="elsevierStylePara">The treatment of high transporter status begins with its prevention&#46; Some of the proposed measures include preserving residual function&#44; preventing peritonitis and using icodextrin solution exchange during long dwell times and a cycler with short cycles to prevent hypervolaemia&#46;<span class="elsevierStyleSup">29</span> The use of ACE inhibitors may also be beneficial in the preservation of residual renal function during the first year of dialysis&#46;<span class="elsevierStyleSup">33</span></p><p class="elsevierStylePara">In this issue&#44; Fern&#225;ndez-Reyes et al&#46;<span class="elsevierStyleSup">34</span> analyse peritoneal transport in the short-term to mid-term in patients that have been using icodextrin from the outset&#46; Their results showed that patients that used an icodextrin solution exchange tended to normalise peritoneal permeability&#46; This finding was particularly evident in patients with high transport from the outset&#44; and normalisation was greater when compared with that of patients who used glucose solution &#40;control group&#41;&#46; The study is particularly interesting since it included incident patients and the results are similar to those recently published in a prevalent population&#46;<span class="elsevierStyleSup">35</span> In this EAPOS substudy&#44; it was evident that the patients treated with icodextrin maintained adequate peritoneal function for at least two years&#44; whereas those who received glucose solution experienced a significant deterioration in solute transport and ultrafiltration capacity with subsequent fluid overload&#46; In the study by Fern&#225;ndez-Reyes et al&#46;<span class="elsevierStyleSup">34</span> the group of patients using icodextrin had suffered less episodes of peritonitis and a higher proportion of them were on ACE inhibitors at the start of the study&#46; There is a need to carry out a randomized control study before any improvement in peritoneal transport can be attributed to icodextrin alone&#46;</p><p class="elsevierStylePara">The way in which icodextrin improves peritoneal permeability in high transporters and the long-term benefits of icodextrin will be the subject of future studies&#46;</p><p class="elsevierStylePara"><span class="elsevierStyleBold">KEY CONCEPTS</span></p><p class="elsevierStylePara">1&#46; Peritoneal transport status is a dynamic concept that varies over time and is influenced by different factors&#46;</p><p class="elsevierStylePara">2&#46; &#34;High transporters&#34; according to the classification system devised by Twardowski are also known as &#34;fast transporters&#46;&#34;</p><p class="elsevierStylePara">3&#46; There are three types of fast transporters&#58; inherent &#40;type 1 and type 2&#41; occurring at the initiation of treatment&#44; and acquired &#40;type 3&#41;&#46;</p><p class="elsevierStylePara">4&#46; The worst prognosis for fast transporters has been associated with the use of glucose solutions and manual technique&#46;</p><p class="elsevierStylePara">5&#46; Fast transporters should undergo automated peritoneal dialysis using icodextrin&#46;</p>"
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Nefrología (English Edition)