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in keeping with the increase in metabolic and obesity problems in the general population&#44; which makes this issue more relevant&#46;<span class="elsevierStyleSup">2</span></p><p class="elsevierStylePara">Studies that attempted to compare the progress of patients on haemodialysis &#40;HD&#41; to those on PD have had ethical and methodological problems&#44; and on some occasions&#44; they even produced contradictory results&#46; There seems to be a consensus that PD outcomes are better than on HD during the first two years&#44; after which this tendency reverses&#46;<span class="elsevierStyleSup">3-5</span> In addition&#44; none of these studies makes any specific recommendations for DM patients&#46;</p><p class="elsevierStylePara">For this reason&#44; we have analysed the outcomes of our patients at the GCDP &#40;Peritoneal Dialysis Centre Group&#41; based on data for patients incident during three years &#40;2003-2006&#41;&#46; In particular&#44; we have concentrated on the characteristics&#44; outcomes and factors determining the prognosis of incident patients with type 2 DM&#46;<span class="elsevierStyleBold"></span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">PATIENTS AND METHODS</span></p><p class="elsevierStylePara">This was a multi-centre prospective observational epidemiologic study with systematic consecutive sampling and a maximum follow-up of three years&#46; The study&#191;s primary objective was to compare the outcomes of patients undergoing PD who have type 2 DM with those who are not diabetic &#40;Non-DM&#41;&#46; Our secondary objective was to examine the management and characteristics of these patients and to identify possible risk factors&#46;</p><p class="elsevierStylePara">The GCDP is made up of 18 public hospitals in the center of Spain which are responsible for the health of 8&#46;8 million inhabitants in that area&#46; During three years &#40;from January 2003 to January 2006&#41;&#44; data was collected from all incident PD patients from the start of PD and during follow-up until the treatment was stopped or death occurred&#46; We recorded demographic parameters&#44; aetiology&#44; comorbidity&#44; origin and whether the technique was freely chosen or imposed&#46; Comorbidity was calculated using the Charlson Comorbidity Index &#40;CCI&#41;&#44; which gives a score based on 16 comorbid conditions and the patient&#191;s age&#44; previously been validated for PD&#46;6 Diagnoses of CV events are based on clinical criteria&#58; stroke&#44; peripheral artery disease&#44; coronary artery disease and heart failure class II or higher using the NYHA classification&#46; At the initiation of dialysis and then on a weekly basis we recorded data such as technique type&#44; adequacy&#44; residual renal function &#40;RRF&#41;&#44; peritoneal transport&#44; treatment for anaemia and control of blood pressure &#40;BP&#41;&#46; Baseline data on adequacy and peritoneal kinetics were obtained between four and six weeks after the start of the treatment&#46; Events such as peritonitis&#44; hospitalisation or leaving the programme were recorded when they occurred&#46; We assessed compliance with the standards recommended for adequacy&#44; anaemia and BP control described in current guidelines&#46;<span class="elsevierStyleSup">7</span></p><p class="elsevierStylePara">Database design&#44; management and analysis were undertaken by the scientific committee with no participation of the companies that provide funding&#46; A Data Manager audited and sorted out the data by ranges and rational practices&#46; Statistical management and analysis were performed using SPSS software version 11&#46;0&#46; The group discussed interim analyses yearly&#46;</p><p class="elsevierStylePara">Numerical variables were shown as mean and standard deviation &#40;SD&#41;&#46; Comparisons were made using the Student&#191;s t-test or the Chi-square test&#44; according to the nature of the variables&#46; Survival data was analysed using the Kaplan-Meier method&#44; considering different events where applicable&#46; In the patient mortality analysis&#44; death is the event&#44; and leaving the programme for any other reason &#40;change of technique&#44; recovery of renal function&#44; transplant or transfer&#41; is censored&#46; For the analysis of PD technique failure&#44; changing to HD is the event&#44; and for the analysis up to first episode of peritonitis&#44; this is considered the event&#46; Survival data are shown as a mean survival probability and 95&#37; confidence interval &#40;CI&#41;&#46; The Cox proportional hazard model was used to establish hazard ratio &#40;HR&#41; values&#46; We included those variables with a p &#60;0&#46;1 for the univariate analysis in a backward stepwise regression model&#44; based on the likelihood ratio statistic and verifying possible confounders&#46; For the final model&#44; we verified that there was proportionality in the risk level throughout the study&#46;</p><p class="elsevierStylePara">All rates obtained &#40;for mortality&#44; hospitalisations and peritonitis&#41; refer to the real time each patient was undergoing treatment and are shown with a CI of 95&#37;&#46;<span class="elsevierStyleBold"></span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">COHORT DESCRIPTION</span></p><p class="elsevierStylePara">The cohort is composed of 469 patients between January 2003 and January 2006&#44; with a mean follow-up period of 13&#46;4 months &#40;ranging from 2 to 36 months&#41;&#46; The most relevant baseline characteristics were as follows&#58; mean age 53&#46;6 years &#40;SD 16&#46;1&#41;&#44; 61&#46;6&#37; male&#44; CCI 5&#46;2 &#40;SD 2&#46;5&#41;&#44; 19&#37; diabetic and 23&#46;7&#37; had history of a previous CV event&#46; Of this cohort&#44; 65 type 2 DM patients and 380 non-DM patients were selected for the analysis&#59; the 24 type 1 DM patients were excluded&#46;</p><p class="elsevierStylePara">Before entering the PD programme&#44; the patients selected have had the following events&#58; 8&#46;4&#37; had an acute myocardial infarction&#44; 12&#46;8&#37; had peripheral artery disease &#40;1&#46;6&#37; with a major amputation&#41;&#44; 4&#46;8&#37; had a stroke&#44; and 7&#46;1&#37; had episodes of heart failure &#40;NYHA class II or above&#41;&#46; 89&#46;9&#37; suffered from high blood pressure&#44; 83&#46;6&#37; were under treatment&#44; 19&#46;2&#37; had haemoglobin levels &#40;Hb&#41; &#60;11g&#47;dl&#46; 90&#46;4&#37; had chosen PD freely&#44; and the rest were following medical advice and 36&#46;9&#37; of the patients were included on the transplant waiting list during the first six months&#46;</p><p class="elsevierStylePara">The most prevalent aetiologies for chronic kidney disease were&#58; glomerular disease 26&#46;8&#37;&#44; diabetic nephropathy&#44; ischaemic or renovascular disease 12&#46;6&#37;&#44; interstitial nephropathy 14&#46;2&#37;&#44; and adult polycystic kidney disease 11&#46;5&#37;&#46; The initial technique was continuous ambulatory PD &#40;CAPD&#41; for 66&#46;9&#37; of the patients&#44; and automatic PD &#40;APD&#41; for the rest&#46; Table 1 shows additional descriptive data&#46; At the end of the follow-up period&#44; 21&#46;0&#37; of the patients had received a transplant&#44; 6&#46;6&#37; had died&#44; 7&#46;5&#37; had changed to HD and 1&#46;5&#37; had recovered renal function&#46; The rest remained on PD&#46; Contact was lost with three patients &#40;0&#46;7&#37;&#41;&#46;<span class="elsevierStyleBold"></span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">RESULTS</span></p><p class="elsevierStylePara">Baseline characteristics and compliance with standards&#58; The clinical characteristics of patients with type 2 DM are significantly different from those from the Non-DM group &#40;table 1&#41;&#46; The type 2 DM group is older&#44; with higher CCI&#44; increased prevalence of previous CV events&#44; and higher systolic BP and pulse pressure&#46; However&#44; they also have higher RRF and Kt&#47;Vurea values and higher total weekly creatinine clearance &#40;CrCl&#41;&#46;</p><p class="elsevierStylePara"> When we examined whether BP targets were achieved&#44; we see that results are poorer among diabetics &#40;table 2&#41;&#46; However&#44; there were no differences in other parameters&#44; such as adequacy of dialysis or correction of anaemia&#46;</p><p class="elsevierStylePara">Mortality&#58; 28 patients died during follow-up&#44; thus the overall annual mortality risk is calculated at 5&#46;2&#37; &#91;95&#37; CI&#44; &#91;3&#46;7-7&#46;8&#37;&#93;&#46; The annual mortality rate for the type 2 DM patients was 12&#46;4&#37; &#91;95&#37; CI&#44; 4&#46;7-20&#46;1&#37; compared with 4&#46;1&#37; &#91;95&#37; CI&#44; 2&#46;1-6-0&#37;&#93; for the non diabetics&#46; The causes of death in type 2 DM patients were 50&#37; cardiac&#44; 10&#37; vascular&#44; 20&#37; infectious&#44; 10&#37; cancer and 10&#37; from other causes&#46; In non-diabetics&#44; the leading cause of death was also CV &#40;33&#37; cardiac and 11&#46;1&#37; vascular&#41;&#46;</p><p class="elsevierStylePara">The survival rate for type 2 DM patients was significantly lower&#44; as shown in figure 1 &#40;log-rank 11&#46;4 p &#61; 0&#46;001&#41;&#46; The probability of surviving two years in non-DM patients is above 90&#37;&#44; while in type 2 DM patients the probability of surviving two years is only 68&#37;&#46; In the Cox proportional hazards model&#44; the presence of type 2 DM indicated a higher risk of death &#40;HR 2&#46;5 &#91;95&#37; CI&#44; 1&#46;1-5&#46;6&#93;&#44; adjusted for age&#41;&#46; When we introduce the history of a previous CV event in the model&#44; DM loses significance within that model&#44; due to the association between type 2 DM and CV disease and the latter&#191;s strong association with mortality&#46; None of the analysed factors &#40;blood pressure&#44; effectiveness of PD&#44; residual renal function or baseline haemoglobin level&#41; were significant in the multivariate model&#46;</p><p class="elsevierStylePara">Morbidity &#40;hospitalisations and peritonitis&#41;&#58; The annual risk of hospitalisation for the whole population was 0&#46;67 &#91;95&#37; CI&#44; 0&#46;60-0&#46;74&#93;&#46;</p><p class="elsevierStylePara">Patients with type 2 DM had an annual risk of hospitalisation of 1&#46;1 &#91;95&#37; CI&#44; 0&#46;9-1&#46;3&#93; compared with 0&#46;6 &#91;95&#37; CI&#44; 0&#46;5-0&#46;7&#93; in non-diabetics&#46;</p><p class="elsevierStylePara">Regarding loss of RRF&#44; the type 2 DM group showed a similar reduction in GRF to that of the non-DM group&#58; 1&#46;6 &#40;SD 6&#46;3&#41; ml&#47;min per year vs&#46; 1&#46;5 &#40;SD 3&#46;4&#41; ml&#47;min per year&#46;</p><p class="elsevierStylePara">Patients with type 2 DM tended to have a higher rate of peritonitis than the non-DM group&#44; but his was not statistically significant&#46; The annual risk of developing peritonitis in type 2 DM patients was 0&#46;53 episodes &#91;95&#37; CI&#44; 0&#46;4-0&#46;7&#93; compared with 0&#46;49 &#91;95&#37; CI&#44; 0&#46;4-0&#46;5&#93; in the Non DM group&#46; The length of time elapsed before the first peritonitis episode was not different between the groups &#40;log-rank 3&#44; 7&#44; p&#61;0&#46;2&#41;&#46;</p><p class="elsevierStylePara">Technique survival&#58; Type 2 DM patients had a lower technique survival rate &#40;log-rank 6&#46;7&#44; p &#61; 0&#46;009&#41;&#44; with an HR of 2&#46;4 &#91;1&#46;2-4&#46;9&#93;&#44; without age&#44; gender&#44; imposed referral to PD or achieving guideline targets acting as confounders&#46;</p><p class="elsevierStylePara">The probability of technique survival at two years was 86&#46;7&#37; in non-DM patients and 75&#46;2&#37; in DM 2 patients&#46;<span class="elsevierStyleBold"></span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">DISCUSSION</span></p><p class="elsevierStylePara">Our study provides current&#44; reliable data on patient characteristics&#44; achievement of guideline targets&#44; hospitalisation and mortality rates in type 2 DM patients who undergo PD in our area&#46; The prognosis for type 2 DM patients is worse than for the non-DM group&#44; and the associated CV morbidity seems to be the most important predictor in our analysis&#46;</p><p class="elsevierStylePara">For many years&#44; DM has been the most common cause for entering dialysis in the United States<span class="elsevierStyleSup">8</span> and since 2007&#44; the same is true in Spain&#46;<span class="elsevierStyleSup">2</span> The progression of DM and its complications are associated with a number of abnormalities and a higher mortality rate&#44; primarily due to CV causes&#44; whether they undergo PD or HD&#46;<span class="elsevierStyleSup">9</span> Therefore&#44; it is not easy to recommend a particular modality of treatment since the prognosis does not seem to be better with HD&#46; Most studies find that patients on PD have a mortality rate that is lower than or similar to mortality for those on HD during the first two years&#44;<span class="elsevierStyleSup">5&#44;10-12</span> with an increase in mortality after the second year&#44;<span class="elsevierStyleSup">3-5</span> particularly for patients older than 65&#46; Studies carried out in our country conclude that the dialysis technique chosen has no prognostic value when we correct for selection criteria and comorbidity&#46;<span class="elsevierStyleSup">13</span> Furthermore&#44; patients with CV disease seem to have a lower survival rate on PD than on HD&#46;<span class="elsevierStyleSup">14-16</span> When sub-analyses are carried out for diabetic patients&#44; some studies show better outcomes for PD1 and others for HD&#46;<span class="elsevierStyleSup">1&#44;17</span></p><p class="elsevierStylePara">Demographic characteristics in the Spanish population are comparable to those of European and Canadian studies than to studies from the United States&#46; In fact&#44; Registry datas how the prevalence of DM in U&#46;S&#46; to be as high as 45&#37;&#44; which makes it difficult to extrapolate their annual results to other cohorts&#46;<span class="elsevierStyleSup">5</span> Unfortunately&#44; the Spanish Registry of renal patients has no available data for detailed analyses of aspects such as comorbidity&#44; achieving the recommended targets hospitalisation&#44; etc&#46; For these reasons&#44; it is important to have studies like the one we are presenting&#44; and they should be updated periodically as a reference for a particular period and geographical area&#46;<span class="elsevierStyleSup">18&#44;19</span></p><p class="elsevierStylePara">The hospitalisation rate in our study is somewhat lower than that cited recently in U&#46;S&#46; studies&#44;<span class="elsevierStyleSup">17</span> and this may be because it only includes incident patients and because of a lower comorbidity&#46; A Canadian study indicates that the hospitalisation rate increases with age and is higher for women and those with DM&#46;<span class="elsevierStyleSup">20</span> In a previous analysis of our entire cohort&#44; higher comorbidity &#40;estimated by the CCI or prevalence of CV events&#41; and lower baseline haemoglobin &#40;Hb&#41; was associated with a higher hospitalisation rate&#44;<span class="elsevierStyleSup">7</span> which is similar to that for patients undergoing HD&#46;<span class="elsevierStyleSup">21</span> The relevance of Hb as a risk marker is due to it being the only modifiable marker&#46;</p><p class="elsevierStylePara">In the previously published report of the entire cohort&#44; mortality was associated with higher comorbidity at the beginning of the treatment&#44; whether using the CCI or the prevalence of DM or previous CV events as the variable&#46;<span class="elsevierStyleSup">7</span> Although conflicting results do exist&#44;<span class="elsevierStyleSup">20</span> most studies report that age and diabetes are independently associated with greater mortality&#46;<span class="elsevierStyleSup">5&#44;12&#44;22-26</span> However&#44; type 1 and 2 DM patients cannot be analysed as a single group&#44; since their epidemiology and clinical presentation are completely different&#46; We therefore decided to analyse the data from type 2 DM patients separately&#46;</p><p class="elsevierStylePara">We did not use the Charlson comorbidity index in the current study because it is calculated using DM as a factor &#40;the principal variable in this study&#41;&#46; If we were to eliminate DM from the Charlson index&#44; it would lose its validity&#46; When we attempt to see which patient management factors make the difference between type 2 DM patients and non-diabetics&#44; we find that the type 2 DM group has poorer pressure control&#44; similar Hb levels and better PD efficiency at the expense of a higher initial RRF&#46; Regarding the compliance with the guidelines recommendations&#44; type 2 DM patients have poorer control of blood pressure&#44; particularly systolic BP&#44; and a non-significant tendency to have better control over anaemia and better PD efficiency&#46; None of these factors&#44; whether they are continuous or categorical variables &#40;achieving objectives&#41;&#44; proved to have prognostic influence in our study&#46; All previous publications showed inconsistent results&#46;<span class="elsevierStyleSup">27-30</span></p><p class="elsevierStylePara">We must recognise that the CCI has significant limitations&#46; Among them&#44; we can highlight the lack of a measure of severity of the illness&#44; the fact that it was designed for the general population&#44; and the time elapsed since it was created&#44; in which drastic changes have occurred in the prognostic value of some illnesses such as AIDS&#46; For these reasons&#44; some authors have proposed adapting the comorbidity index to a patient on PD through a modification in its scoring&#44;<span class="elsevierStyleSup">6</span> or by using specific comorbidity markers with a measure of severity&#46;<span class="elsevierStyleSup">31</span> However&#44; the Charlson comorbidity index is still the most widely used&#44; and it allows us to establish comparisons with other studies on patients whether inside or outside of the field of dialysis&#46; Clinical studies&#44; such as this by our group&#44; have yet to meet the challenge of designing a prognostic indicator that will be sensitive and specific enough for PD patients&#46;</p><p class="elsevierStylePara">The important difference between non-DM patients and type 2 DM patients is the extent of CV damage before the start of PD&#46; For this reason&#44; when adjusting multivariate analyses&#44; we observe that it is not possible to keep type 2 DM and the CV event in the same model&#46; This is due to the association between the two being very pronounced&#59; the prevalence of prior CV events is more than three times higher in type 2 DM patients than in non-diabetics&#46; Baseline CV comorbidity is&#44; therefore&#44; the main factor determining survival for type 2 DM patients on PD&#46;</p><p class="elsevierStylePara">It seems that this study&#191;s conclusions are what would be expected&#44; but it is important to have current&#44; well-founded data to corroborate and establish the importance of each of the risk factors&#46;</p><p class="elsevierStylePara">The main limitation of this study is the number of cumulative deaths&#46; A longer follow-up would enable us to register more events&#44; although the average time undergoing PD treatment does not exceed two years according to other records with a longer follow-up time&#46;<span class="elsevierStyleSup">18</span> Other factors that influence mortality&#44; such as the patient&#191;s nutritional or inflammatory state&#44; could not be evaluated due to the heterogeneity of data collected in different centres&#46; However&#44; we consider this study to be relevant due to its careful design and follow-up and its large sample size &#40;for a PD study&#41;&#46; In fact&#44; most of the PD units in Spain have a low number of patients&#44;<span class="elsevierStyleSup">18</span> which is why it is necessary to launch multi-centre initiatives in order to obtain sufficient statistical power&#46;</p><p class="elsevierStylePara">To sum up&#44; our data seems to confirm that type 2 DM patients have worse outcomes than non-diabetic patients&#46; This is fundamentally due to higher comorbidity&#44; and particularly to a higher prevalence of CV events prior to starting dialysis&#46; Patients with type 2 diabetes start dialysis with a higher RRF&#44; better total adequacy and good correction of anaemia and blood pressure over the course of the followup&#46; All of these factors&#44; which should improve patients&#191; prognosis&#44; cannot compensate for the weight of the CV comorbidity that developed before dialysis&#44; and before the onset of DM itself&#46;</p><p class="elsevierStylePara">We need more studies on the progress of these patients who undergo different modalities of renal replacement therapy in order to improve their prognosis&#46;<br></br></p><p class="elsevierStylePara"><a href="grande&#47;12118078&#95;t1&#95;338&#46;jpg" class="elsevierStyleCrossRefs"><img src="12118078_t1_338.jpg" alt="Characteristics of type 2 DM patients compared with non-diabetics&#46; Shown as mean &#40;standard deviation&#44; SD&#41; or as a percentage&#46; Student&#39;s t-test&#44;&#60;br &#47;&#62; Chi-square test or incidence rate ratio is used depending on the nature of the variables&#46;"></img></a></p><p class="elsevierStylePara">Table 1&#46; Characteristics of type 2 DM patients compared with non-diabetics&#46; Shown as mean &#40;standard deviation&#44; SD&#41; or as a percentage&#46; Student&#39;s t-test&#44;<br></br> Chi-square test or incidence rate ratio is used depending on the nature of the variables&#46;</p><p class="elsevierStylePara"><a href="grande&#47;12118078&#95;f1&#95;338&#46;jpg" class="elsevierStyleCrossRefs"><img src="12118078_f1_338.jpg"></img></a></p><p class="elsevierStylePara">Figure 1&#46; </p><p class="elsevierStylePara"><a href="grande&#47;12118078&#95;t2&#95;339&#46;jpg" class="elsevierStyleCrossRefs"><img src="12118078_t2_339.jpg" alt="Achievement of recommended targets for HT&#44; anaemia and PD adequacy by type 2 DM patients&#60;br &#47;&#62;compared with non-diabetics shown as percentages&#46; Chi-square test applied depending on the nature of the&#60;br &#47;&#62;variables&#46;"></img></a></p><p class="elsevierStylePara">Table 2&#46; Achievement of recommended targets for HT&#44; anaemia and PD adequacy by type 2 DM patients<br></br>compared with non-diabetics shown as percentages&#46; Chi-square test applied depending on the nature of the<br></br>variables&#46;</p>"
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        "resumen" => "<p class="elsevierStylePara">Objetivo&#58; Describir las caracter&#237;sticas y el pron&#243;stico de pacientes con diabetes mellitus &#40;DM&#41; tipo 2 en di&#225;lisis peritoneal &#40;DP&#41; y compararlo con el de los no diab&#233;ticos &#40;NoDM&#41;&#46; M&#233;todos&#58; Estudio de cohorte prospectivo de todos los pacientes incidentes en DP en el registro del Grupo Centro de DP &#40;2003-2006&#41;&#46; Se recogen datos basales&#44; eventos cardiovasculares &#40;CV&#41; previos&#44; ingresos&#44; peritonitis&#44; trasplantes y exitus&#46; Resultados&#58; Los 65 pacientes DM tipo 2 son mayores&#44; con mayor tasa de eventos CV previos &#40;60&#44;9 vs&#46; 17&#44;7&#37;&#41; y peor control de la presi&#243;n arterial al inicio de DP que los 376 pacientes NoDM&#46; Los DM tipo 2 tienen una mayor tasa de hospitalizaci&#243;n &#40;1&#44;1 &#91;0&#44;9-1&#44;4&#93; vs&#46; 0&#44;6 &#91;0&#44;5-0&#44;7&#93; ingresos por a&#241;o en riesgo&#41;&#44; pero similar eficacia de la DP y control de la anemia&#46; Los DM tipo 2 tienen una supervivencia en t&#233;cnica menor que los NoDM &#40;870 vs&#46; 1002 d&#237;as&#59; p &#61; 0&#44;009 seg&#250;n la estimaci&#243;n de Kaplan-Meyer&#41; y una mayor tasa de mortalidad anual &#40;13&#44;7 vs&#46; 4&#44;1&#37;&#59; p &#61; 0&#44;021&#41;&#44; con una HR de mortalidad de 2&#44;5 &#91;1&#44;1-5&#44;6&#93; tras la correcci&#243;n por la edad&#46; La asociaci&#243;n entre DM tipo 2 y eventos CV previos excluye la variable DM tipo 2 del modelo multivariante&#46; La probabilidad de supervivencia a los dos a&#241;os es del 86&#44;7&#37; en NoDM y del 72&#44;5&#37; en DM tipo 2&#46; Conclusi&#243;n&#58; Los DM tipo 2 presentan un mayor porcentaje de eventos CV previos y peor pron&#243;stico vital&#46; Los eventos CV previos pueden explicar gran parte de este riesgo&#46;</p>"
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        "resumen" => "Objective&#58; To describe the characteristics&#44; practice patterns&#44; targets and outcome of the Type 2 diabetic patients &#40;DM 2&#41; in peritoneal dialysis &#40;PD&#41; and to compare them with non-diabeticones&#46; Methods&#58; Prospective cohort study of every incident PD patient in a regional public health care system &#40;2003-2006&#41;&#46; We prospectively collected baseline data&#44; hospital admissions&#44; peritonitis&#44; transplants&#44; CV events and deaths&#46; Every six months PD prescription data and results on efficacy&#44; anaemia&#44; blood pressure &#40;BP&#41; were collected&#46; Results&#58; DM 2 patients &#40;n &#61; 65&#41; were older and presented a higher rate of previous CV events &#40;60&#46;9&#37; vs&#46; 17&#46;7&#37; p <0001 than non-dm patients n="376&#41;" and worse bp control at inclusion on pd there were no differences in dialysis efficacy targets anaemia management hospital admissions: dm 2 present higher hospitalisation rates 1 0 9-1 4 nodm ones 6 5-0 7 admissions per year risk survival: lower pd-technique survival 870 vs 1002 days kaplan-mayer estimation p="0&#46;009&#41;" annual mortality rate 13 p: 021 with a crude hazard ratio hr of 5 1-5 after correction by age however the best predictive model for cox proportional hazards includes existence previous cv events forced excludes association between ruled out from multivariate conclusion: type had prevalence global outcome may explain part this</0001>"
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Patients on peritoneal dialysis with type 2 diabetes have poorer outcomes than non-diabetics due to preceding cardiovascular comorbidity
LOS PACIENTES DIABETICOS TIPO 2 PRESENTAN PEOR EVOLUCION QUE LOS NO DIABETICOS EN DIALISIS PERITONEAL A EXPENSAS DE SU COMORBILIDAD CARDIOVASCULAR.
miembros del GCDP, José Portolésb, Elena Corchetec, Paula López-Sánchezc, Francisco Coroneld, Javier Ocañae, Alberto Ortizf
b Jefe de Servicio, Hospital Universitario Fundación Alcorcón, Madrid, Madrid, España,
c Hospital Universitario Fundación Alcorcón, Madrid, Madrid, España,
d Hospital Universitario San Carlos, Madrid, Madrid, España,
e Hospital General Universitario de Guadalajara, Guadalajara, Madrid, España,
f Fundación Jiménez Díaz, Madrid, Madrid, España,
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    "textoCompleto" => "<p class="elsevierStylePara"><span class="elsevierStyleBold">INTRODUCTION</span></p><p class="elsevierStylePara">Traditionally&#44; it was understood that patients with type 2 DM would benefit from certain advantages offered by PD&#46; Improved control of volaemia and blood pressure&#44; the continuous dialysis and the preservation of residual renal function &#40;RRF&#41; were a few of the advantages cited for PD&#46;<span class="elsevierStyleSup">1</span> In addition&#44; cardiovascular problems &#40;CV&#41;&#44; haemodynamic instability and the need for vascular access creation can make haemodialysis &#40;HD&#41; less suitable for these patients&#46; However&#44; metabolic problems associated with PD may have a harmful effect on patients with type 2 DM&#46;<span class="elsevierStyleSup">1</span></p><p class="elsevierStylePara">The Spanish Society of Nephrology&#191;s &#40;SEN&#41; register of kidney patients reports an increased prevalence of DM in dialysis programmes&#44; in keeping with the increase in metabolic and obesity problems in the general population&#44; which makes this issue more relevant&#46;<span class="elsevierStyleSup">2</span></p><p class="elsevierStylePara">Studies that attempted to compare the progress of patients on haemodialysis &#40;HD&#41; to those on PD have had ethical and methodological problems&#44; and on some occasions&#44; they even produced contradictory results&#46; There seems to be a consensus that PD outcomes are better than on HD during the first two years&#44; after which this tendency reverses&#46;<span class="elsevierStyleSup">3-5</span> In addition&#44; none of these studies makes any specific recommendations for DM patients&#46;</p><p class="elsevierStylePara">For this reason&#44; we have analysed the outcomes of our patients at the GCDP &#40;Peritoneal Dialysis Centre Group&#41; based on data for patients incident during three years &#40;2003-2006&#41;&#46; In particular&#44; we have concentrated on the characteristics&#44; outcomes and factors determining the prognosis of incident patients with type 2 DM&#46;<span class="elsevierStyleBold"></span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">PATIENTS AND METHODS</span></p><p class="elsevierStylePara">This was a multi-centre prospective observational epidemiologic study with systematic consecutive sampling and a maximum follow-up of three years&#46; The study&#191;s primary objective was to compare the outcomes of patients undergoing PD who have type 2 DM with those who are not diabetic &#40;Non-DM&#41;&#46; Our secondary objective was to examine the management and characteristics of these patients and to identify possible risk factors&#46;</p><p class="elsevierStylePara">The GCDP is made up of 18 public hospitals in the center of Spain which are responsible for the health of 8&#46;8 million inhabitants in that area&#46; During three years &#40;from January 2003 to January 2006&#41;&#44; data was collected from all incident PD patients from the start of PD and during follow-up until the treatment was stopped or death occurred&#46; We recorded demographic parameters&#44; aetiology&#44; comorbidity&#44; origin and whether the technique was freely chosen or imposed&#46; Comorbidity was calculated using the Charlson Comorbidity Index &#40;CCI&#41;&#44; which gives a score based on 16 comorbid conditions and the patient&#191;s age&#44; previously been validated for PD&#46;6 Diagnoses of CV events are based on clinical criteria&#58; stroke&#44; peripheral artery disease&#44; coronary artery disease and heart failure class II or higher using the NYHA classification&#46; At the initiation of dialysis and then on a weekly basis we recorded data such as technique type&#44; adequacy&#44; residual renal function &#40;RRF&#41;&#44; peritoneal transport&#44; treatment for anaemia and control of blood pressure &#40;BP&#41;&#46; Baseline data on adequacy and peritoneal kinetics were obtained between four and six weeks after the start of the treatment&#46; Events such as peritonitis&#44; hospitalisation or leaving the programme were recorded when they occurred&#46; We assessed compliance with the standards recommended for adequacy&#44; anaemia and BP control described in current guidelines&#46;<span class="elsevierStyleSup">7</span></p><p class="elsevierStylePara">Database design&#44; management and analysis were undertaken by the scientific committee with no participation of the companies that provide funding&#46; A Data Manager audited and sorted out the data by ranges and rational practices&#46; Statistical management and analysis were performed using SPSS software version 11&#46;0&#46; The group discussed interim analyses yearly&#46;</p><p class="elsevierStylePara">Numerical variables were shown as mean and standard deviation &#40;SD&#41;&#46; Comparisons were made using the Student&#191;s t-test or the Chi-square test&#44; according to the nature of the variables&#46; Survival data was analysed using the Kaplan-Meier method&#44; considering different events where applicable&#46; In the patient mortality analysis&#44; death is the event&#44; and leaving the programme for any other reason &#40;change of technique&#44; recovery of renal function&#44; transplant or transfer&#41; is censored&#46; For the analysis of PD technique failure&#44; changing to HD is the event&#44; and for the analysis up to first episode of peritonitis&#44; this is considered the event&#46; Survival data are shown as a mean survival probability and 95&#37; confidence interval &#40;CI&#41;&#46; The Cox proportional hazard model was used to establish hazard ratio &#40;HR&#41; values&#46; We included those variables with a p &#60;0&#46;1 for the univariate analysis in a backward stepwise regression model&#44; based on the likelihood ratio statistic and verifying possible confounders&#46; For the final model&#44; we verified that there was proportionality in the risk level throughout the study&#46;</p><p class="elsevierStylePara">All rates obtained &#40;for mortality&#44; hospitalisations and peritonitis&#41; refer to the real time each patient was undergoing treatment and are shown with a CI of 95&#37;&#46;<span class="elsevierStyleBold"></span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">COHORT DESCRIPTION</span></p><p class="elsevierStylePara">The cohort is composed of 469 patients between January 2003 and January 2006&#44; with a mean follow-up period of 13&#46;4 months &#40;ranging from 2 to 36 months&#41;&#46; The most relevant baseline characteristics were as follows&#58; mean age 53&#46;6 years &#40;SD 16&#46;1&#41;&#44; 61&#46;6&#37; male&#44; CCI 5&#46;2 &#40;SD 2&#46;5&#41;&#44; 19&#37; diabetic and 23&#46;7&#37; had history of a previous CV event&#46; Of this cohort&#44; 65 type 2 DM patients and 380 non-DM patients were selected for the analysis&#59; the 24 type 1 DM patients were excluded&#46;</p><p class="elsevierStylePara">Before entering the PD programme&#44; the patients selected have had the following events&#58; 8&#46;4&#37; had an acute myocardial infarction&#44; 12&#46;8&#37; had peripheral artery disease &#40;1&#46;6&#37; with a major amputation&#41;&#44; 4&#46;8&#37; had a stroke&#44; and 7&#46;1&#37; had episodes of heart failure &#40;NYHA class II or above&#41;&#46; 89&#46;9&#37; suffered from high blood pressure&#44; 83&#46;6&#37; were under treatment&#44; 19&#46;2&#37; had haemoglobin levels &#40;Hb&#41; &#60;11g&#47;dl&#46; 90&#46;4&#37; had chosen PD freely&#44; and the rest were following medical advice and 36&#46;9&#37; of the patients were included on the transplant waiting list during the first six months&#46;</p><p class="elsevierStylePara">The most prevalent aetiologies for chronic kidney disease were&#58; glomerular disease 26&#46;8&#37;&#44; diabetic nephropathy&#44; ischaemic or renovascular disease 12&#46;6&#37;&#44; interstitial nephropathy 14&#46;2&#37;&#44; and adult polycystic kidney disease 11&#46;5&#37;&#46; The initial technique was continuous ambulatory PD &#40;CAPD&#41; for 66&#46;9&#37; of the patients&#44; and automatic PD &#40;APD&#41; for the rest&#46; Table 1 shows additional descriptive data&#46; At the end of the follow-up period&#44; 21&#46;0&#37; of the patients had received a transplant&#44; 6&#46;6&#37; had died&#44; 7&#46;5&#37; had changed to HD and 1&#46;5&#37; had recovered renal function&#46; The rest remained on PD&#46; Contact was lost with three patients &#40;0&#46;7&#37;&#41;&#46;<span class="elsevierStyleBold"></span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">RESULTS</span></p><p class="elsevierStylePara">Baseline characteristics and compliance with standards&#58; The clinical characteristics of patients with type 2 DM are significantly different from those from the Non-DM group &#40;table 1&#41;&#46; The type 2 DM group is older&#44; with higher CCI&#44; increased prevalence of previous CV events&#44; and higher systolic BP and pulse pressure&#46; However&#44; they also have higher RRF and Kt&#47;Vurea values and higher total weekly creatinine clearance &#40;CrCl&#41;&#46;</p><p class="elsevierStylePara"> When we examined whether BP targets were achieved&#44; we see that results are poorer among diabetics &#40;table 2&#41;&#46; However&#44; there were no differences in other parameters&#44; such as adequacy of dialysis or correction of anaemia&#46;</p><p class="elsevierStylePara">Mortality&#58; 28 patients died during follow-up&#44; thus the overall annual mortality risk is calculated at 5&#46;2&#37; &#91;95&#37; CI&#44; &#91;3&#46;7-7&#46;8&#37;&#93;&#46; The annual mortality rate for the type 2 DM patients was 12&#46;4&#37; &#91;95&#37; CI&#44; 4&#46;7-20&#46;1&#37; compared with 4&#46;1&#37; &#91;95&#37; CI&#44; 2&#46;1-6-0&#37;&#93; for the non diabetics&#46; The causes of death in type 2 DM patients were 50&#37; cardiac&#44; 10&#37; vascular&#44; 20&#37; infectious&#44; 10&#37; cancer and 10&#37; from other causes&#46; In non-diabetics&#44; the leading cause of death was also CV &#40;33&#37; cardiac and 11&#46;1&#37; vascular&#41;&#46;</p><p class="elsevierStylePara">The survival rate for type 2 DM patients was significantly lower&#44; as shown in figure 1 &#40;log-rank 11&#46;4 p &#61; 0&#46;001&#41;&#46; The probability of surviving two years in non-DM patients is above 90&#37;&#44; while in type 2 DM patients the probability of surviving two years is only 68&#37;&#46; In the Cox proportional hazards model&#44; the presence of type 2 DM indicated a higher risk of death &#40;HR 2&#46;5 &#91;95&#37; CI&#44; 1&#46;1-5&#46;6&#93;&#44; adjusted for age&#41;&#46; When we introduce the history of a previous CV event in the model&#44; DM loses significance within that model&#44; due to the association between type 2 DM and CV disease and the latter&#191;s strong association with mortality&#46; None of the analysed factors &#40;blood pressure&#44; effectiveness of PD&#44; residual renal function or baseline haemoglobin level&#41; were significant in the multivariate model&#46;</p><p class="elsevierStylePara">Morbidity &#40;hospitalisations and peritonitis&#41;&#58; The annual risk of hospitalisation for the whole population was 0&#46;67 &#91;95&#37; CI&#44; 0&#46;60-0&#46;74&#93;&#46;</p><p class="elsevierStylePara">Patients with type 2 DM had an annual risk of hospitalisation of 1&#46;1 &#91;95&#37; CI&#44; 0&#46;9-1&#46;3&#93; compared with 0&#46;6 &#91;95&#37; CI&#44; 0&#46;5-0&#46;7&#93; in non-diabetics&#46;</p><p class="elsevierStylePara">Regarding loss of RRF&#44; the type 2 DM group showed a similar reduction in GRF to that of the non-DM group&#58; 1&#46;6 &#40;SD 6&#46;3&#41; ml&#47;min per year vs&#46; 1&#46;5 &#40;SD 3&#46;4&#41; ml&#47;min per year&#46;</p><p class="elsevierStylePara">Patients with type 2 DM tended to have a higher rate of peritonitis than the non-DM group&#44; but his was not statistically significant&#46; The annual risk of developing peritonitis in type 2 DM patients was 0&#46;53 episodes &#91;95&#37; CI&#44; 0&#46;4-0&#46;7&#93; compared with 0&#46;49 &#91;95&#37; CI&#44; 0&#46;4-0&#46;5&#93; in the Non DM group&#46; The length of time elapsed before the first peritonitis episode was not different between the groups &#40;log-rank 3&#44; 7&#44; p&#61;0&#46;2&#41;&#46;</p><p class="elsevierStylePara">Technique survival&#58; Type 2 DM patients had a lower technique survival rate &#40;log-rank 6&#46;7&#44; p &#61; 0&#46;009&#41;&#44; with an HR of 2&#46;4 &#91;1&#46;2-4&#46;9&#93;&#44; without age&#44; gender&#44; imposed referral to PD or achieving guideline targets acting as confounders&#46;</p><p class="elsevierStylePara">The probability of technique survival at two years was 86&#46;7&#37; in non-DM patients and 75&#46;2&#37; in DM 2 patients&#46;<span class="elsevierStyleBold"></span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">DISCUSSION</span></p><p class="elsevierStylePara">Our study provides current&#44; reliable data on patient characteristics&#44; achievement of guideline targets&#44; hospitalisation and mortality rates in type 2 DM patients who undergo PD in our area&#46; The prognosis for type 2 DM patients is worse than for the non-DM group&#44; and the associated CV morbidity seems to be the most important predictor in our analysis&#46;</p><p class="elsevierStylePara">For many years&#44; DM has been the most common cause for entering dialysis in the United States<span class="elsevierStyleSup">8</span> and since 2007&#44; the same is true in Spain&#46;<span class="elsevierStyleSup">2</span> The progression of DM and its complications are associated with a number of abnormalities and a higher mortality rate&#44; primarily due to CV causes&#44; whether they undergo PD or HD&#46;<span class="elsevierStyleSup">9</span> Therefore&#44; it is not easy to recommend a particular modality of treatment since the prognosis does not seem to be better with HD&#46; Most studies find that patients on PD have a mortality rate that is lower than or similar to mortality for those on HD during the first two years&#44;<span class="elsevierStyleSup">5&#44;10-12</span> with an increase in mortality after the second year&#44;<span class="elsevierStyleSup">3-5</span> particularly for patients older than 65&#46; Studies carried out in our country conclude that the dialysis technique chosen has no prognostic value when we correct for selection criteria and comorbidity&#46;<span class="elsevierStyleSup">13</span> Furthermore&#44; patients with CV disease seem to have a lower survival rate on PD than on HD&#46;<span class="elsevierStyleSup">14-16</span> When sub-analyses are carried out for diabetic patients&#44; some studies show better outcomes for PD1 and others for HD&#46;<span class="elsevierStyleSup">1&#44;17</span></p><p class="elsevierStylePara">Demographic characteristics in the Spanish population are comparable to those of European and Canadian studies than to studies from the United States&#46; In fact&#44; Registry datas how the prevalence of DM in U&#46;S&#46; to be as high as 45&#37;&#44; which makes it difficult to extrapolate their annual results to other cohorts&#46;<span class="elsevierStyleSup">5</span> Unfortunately&#44; the Spanish Registry of renal patients has no available data for detailed analyses of aspects such as comorbidity&#44; achieving the recommended targets hospitalisation&#44; etc&#46; For these reasons&#44; it is important to have studies like the one we are presenting&#44; and they should be updated periodically as a reference for a particular period and geographical area&#46;<span class="elsevierStyleSup">18&#44;19</span></p><p class="elsevierStylePara">The hospitalisation rate in our study is somewhat lower than that cited recently in U&#46;S&#46; studies&#44;<span class="elsevierStyleSup">17</span> and this may be because it only includes incident patients and because of a lower comorbidity&#46; A Canadian study indicates that the hospitalisation rate increases with age and is higher for women and those with DM&#46;<span class="elsevierStyleSup">20</span> In a previous analysis of our entire cohort&#44; higher comorbidity &#40;estimated by the CCI or prevalence of CV events&#41; and lower baseline haemoglobin &#40;Hb&#41; was associated with a higher hospitalisation rate&#44;<span class="elsevierStyleSup">7</span> which is similar to that for patients undergoing HD&#46;<span class="elsevierStyleSup">21</span> The relevance of Hb as a risk marker is due to it being the only modifiable marker&#46;</p><p class="elsevierStylePara">In the previously published report of the entire cohort&#44; mortality was associated with higher comorbidity at the beginning of the treatment&#44; whether using the CCI or the prevalence of DM or previous CV events as the variable&#46;<span class="elsevierStyleSup">7</span> Although conflicting results do exist&#44;<span class="elsevierStyleSup">20</span> most studies report that age and diabetes are independently associated with greater mortality&#46;<span class="elsevierStyleSup">5&#44;12&#44;22-26</span> However&#44; type 1 and 2 DM patients cannot be analysed as a single group&#44; since their epidemiology and clinical presentation are completely different&#46; We therefore decided to analyse the data from type 2 DM patients separately&#46;</p><p class="elsevierStylePara">We did not use the Charlson comorbidity index in the current study because it is calculated using DM as a factor &#40;the principal variable in this study&#41;&#46; If we were to eliminate DM from the Charlson index&#44; it would lose its validity&#46; When we attempt to see which patient management factors make the difference between type 2 DM patients and non-diabetics&#44; we find that the type 2 DM group has poorer pressure control&#44; similar Hb levels and better PD efficiency at the expense of a higher initial RRF&#46; Regarding the compliance with the guidelines recommendations&#44; type 2 DM patients have poorer control of blood pressure&#44; particularly systolic BP&#44; and a non-significant tendency to have better control over anaemia and better PD efficiency&#46; None of these factors&#44; whether they are continuous or categorical variables &#40;achieving objectives&#41;&#44; proved to have prognostic influence in our study&#46; All previous publications showed inconsistent results&#46;<span class="elsevierStyleSup">27-30</span></p><p class="elsevierStylePara">We must recognise that the CCI has significant limitations&#46; Among them&#44; we can highlight the lack of a measure of severity of the illness&#44; the fact that it was designed for the general population&#44; and the time elapsed since it was created&#44; in which drastic changes have occurred in the prognostic value of some illnesses such as AIDS&#46; For these reasons&#44; some authors have proposed adapting the comorbidity index to a patient on PD through a modification in its scoring&#44;<span class="elsevierStyleSup">6</span> or by using specific comorbidity markers with a measure of severity&#46;<span class="elsevierStyleSup">31</span> However&#44; the Charlson comorbidity index is still the most widely used&#44; and it allows us to establish comparisons with other studies on patients whether inside or outside of the field of dialysis&#46; Clinical studies&#44; such as this by our group&#44; have yet to meet the challenge of designing a prognostic indicator that will be sensitive and specific enough for PD patients&#46;</p><p class="elsevierStylePara">The important difference between non-DM patients and type 2 DM patients is the extent of CV damage before the start of PD&#46; For this reason&#44; when adjusting multivariate analyses&#44; we observe that it is not possible to keep type 2 DM and the CV event in the same model&#46; This is due to the association between the two being very pronounced&#59; the prevalence of prior CV events is more than three times higher in type 2 DM patients than in non-diabetics&#46; Baseline CV comorbidity is&#44; therefore&#44; the main factor determining survival for type 2 DM patients on PD&#46;</p><p class="elsevierStylePara">It seems that this study&#191;s conclusions are what would be expected&#44; but it is important to have current&#44; well-founded data to corroborate and establish the importance of each of the risk factors&#46;</p><p class="elsevierStylePara">The main limitation of this study is the number of cumulative deaths&#46; A longer follow-up would enable us to register more events&#44; although the average time undergoing PD treatment does not exceed two years according to other records with a longer follow-up time&#46;<span class="elsevierStyleSup">18</span> Other factors that influence mortality&#44; such as the patient&#191;s nutritional or inflammatory state&#44; could not be evaluated due to the heterogeneity of data collected in different centres&#46; However&#44; we consider this study to be relevant due to its careful design and follow-up and its large sample size &#40;for a PD study&#41;&#46; In fact&#44; most of the PD units in Spain have a low number of patients&#44;<span class="elsevierStyleSup">18</span> which is why it is necessary to launch multi-centre initiatives in order to obtain sufficient statistical power&#46;</p><p class="elsevierStylePara">To sum up&#44; our data seems to confirm that type 2 DM patients have worse outcomes than non-diabetic patients&#46; This is fundamentally due to higher comorbidity&#44; and particularly to a higher prevalence of CV events prior to starting dialysis&#46; Patients with type 2 diabetes start dialysis with a higher RRF&#44; better total adequacy and good correction of anaemia and blood pressure over the course of the followup&#46; All of these factors&#44; which should improve patients&#191; prognosis&#44; cannot compensate for the weight of the CV comorbidity that developed before dialysis&#44; and before the onset of DM itself&#46;</p><p class="elsevierStylePara">We need more studies on the progress of these patients who undergo different modalities of renal replacement therapy in order to improve their prognosis&#46;<br></br></p><p class="elsevierStylePara"><a href="grande&#47;12118078&#95;t1&#95;338&#46;jpg" class="elsevierStyleCrossRefs"><img src="12118078_t1_338.jpg" alt="Characteristics of type 2 DM patients compared with non-diabetics&#46; Shown as mean &#40;standard deviation&#44; SD&#41; or as a percentage&#46; Student&#39;s t-test&#44;&#60;br &#47;&#62; Chi-square test or incidence rate ratio is used depending on the nature of the variables&#46;"></img></a></p><p class="elsevierStylePara">Table 1&#46; Characteristics of type 2 DM patients compared with non-diabetics&#46; Shown as mean &#40;standard deviation&#44; SD&#41; or as a percentage&#46; Student&#39;s t-test&#44;<br></br> Chi-square test or incidence rate ratio is used depending on the nature of the variables&#46;</p><p class="elsevierStylePara"><a href="grande&#47;12118078&#95;f1&#95;338&#46;jpg" class="elsevierStyleCrossRefs"><img src="12118078_f1_338.jpg"></img></a></p><p class="elsevierStylePara">Figure 1&#46; </p><p class="elsevierStylePara"><a href="grande&#47;12118078&#95;t2&#95;339&#46;jpg" class="elsevierStyleCrossRefs"><img src="12118078_t2_339.jpg" alt="Achievement of recommended targets for HT&#44; anaemia and PD adequacy by type 2 DM patients&#60;br &#47;&#62;compared with non-diabetics shown as percentages&#46; Chi-square test applied depending on the nature of the&#60;br &#47;&#62;variables&#46;"></img></a></p><p class="elsevierStylePara">Table 2&#46; Achievement of recommended targets for HT&#44; anaemia and PD adequacy by type 2 DM patients<br></br>compared with non-diabetics shown as percentages&#46; Chi-square test applied depending on the nature of the<br></br>variables&#46;</p>"
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        "resumen" => "<p class="elsevierStylePara">Objetivo&#58; Describir las caracter&#237;sticas y el pron&#243;stico de pacientes con diabetes mellitus &#40;DM&#41; tipo 2 en di&#225;lisis peritoneal &#40;DP&#41; y compararlo con el de los no diab&#233;ticos &#40;NoDM&#41;&#46; M&#233;todos&#58; Estudio de cohorte prospectivo de todos los pacientes incidentes en DP en el registro del Grupo Centro de DP &#40;2003-2006&#41;&#46; Se recogen datos basales&#44; eventos cardiovasculares &#40;CV&#41; previos&#44; ingresos&#44; peritonitis&#44; trasplantes y exitus&#46; Resultados&#58; Los 65 pacientes DM tipo 2 son mayores&#44; con mayor tasa de eventos CV previos &#40;60&#44;9 vs&#46; 17&#44;7&#37;&#41; y peor control de la presi&#243;n arterial al inicio de DP que los 376 pacientes NoDM&#46; Los DM tipo 2 tienen una mayor tasa de hospitalizaci&#243;n &#40;1&#44;1 &#91;0&#44;9-1&#44;4&#93; vs&#46; 0&#44;6 &#91;0&#44;5-0&#44;7&#93; ingresos por a&#241;o en riesgo&#41;&#44; pero similar eficacia de la DP y control de la anemia&#46; Los DM tipo 2 tienen una supervivencia en t&#233;cnica menor que los NoDM &#40;870 vs&#46; 1002 d&#237;as&#59; p &#61; 0&#44;009 seg&#250;n la estimaci&#243;n de Kaplan-Meyer&#41; y una mayor tasa de mortalidad anual &#40;13&#44;7 vs&#46; 4&#44;1&#37;&#59; p &#61; 0&#44;021&#41;&#44; con una HR de mortalidad de 2&#44;5 &#91;1&#44;1-5&#44;6&#93; tras la correcci&#243;n por la edad&#46; La asociaci&#243;n entre DM tipo 2 y eventos CV previos excluye la variable DM tipo 2 del modelo multivariante&#46; La probabilidad de supervivencia a los dos a&#241;os es del 86&#44;7&#37; en NoDM y del 72&#44;5&#37; en DM tipo 2&#46; Conclusi&#243;n&#58; Los DM tipo 2 presentan un mayor porcentaje de eventos CV previos y peor pron&#243;stico vital&#46; Los eventos CV previos pueden explicar gran parte de este riesgo&#46;</p>"
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        "resumen" => "Objective&#58; To describe the characteristics&#44; practice patterns&#44; targets and outcome of the Type 2 diabetic patients &#40;DM 2&#41; in peritoneal dialysis &#40;PD&#41; and to compare them with non-diabeticones&#46; Methods&#58; Prospective cohort study of every incident PD patient in a regional public health care system &#40;2003-2006&#41;&#46; We prospectively collected baseline data&#44; hospital admissions&#44; peritonitis&#44; transplants&#44; CV events and deaths&#46; Every six months PD prescription data and results on efficacy&#44; anaemia&#44; blood pressure &#40;BP&#41; were collected&#46; Results&#58; DM 2 patients &#40;n &#61; 65&#41; were older and presented a higher rate of previous CV events &#40;60&#46;9&#37; vs&#46; 17&#46;7&#37; p <0001 than non-dm patients n="376&#41;" and worse bp control at inclusion on pd there were no differences in dialysis efficacy targets anaemia management hospital admissions: dm 2 present higher hospitalisation rates 1 0 9-1 4 nodm ones 6 5-0 7 admissions per year risk survival: lower pd-technique survival 870 vs 1002 days kaplan-mayer estimation p="0&#46;009&#41;" annual mortality rate 13 p: 021 with a crude hazard ratio hr of 5 1-5 after correction by age however the best predictive model for cox proportional hazards includes existence previous cv events forced excludes association between ruled out from multivariate conclusion: type had prevalence global outcome may explain part this</0001>"
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                  "referenciaCompleta" => "Mailloux L. Dialysis in diabetic nephropathy. In: Burton D Rose, ed. UpToDate. Walthan, MA: UpToDate 2008. Disponible en http://www.uptodateonline.com con acceso 21 de enero de 2009."
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                  "referenciaCompleta" => "Jaar BG, Coresh J, Plantinga LC, Fink NE, Klag MJ, Levey AS et al. Comparing the risk for death with peritoneal dialysis and hemodialysis in a national cohort of patients with chronic kidney disease. Ann Intern Med 2005;143:174-83.  <a href="http://www.ncbi.nlm.nih.gov/pubmed/16061915" target="_blank">[Pubmed]</a>"
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