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<title>Clinical Journal of the American Society of Nephrology Dialysis</title>
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<description>Clinical Journal of the American Society of Nephrology RSS feed -- recent Dialysis articles</description>
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<title>Clinical Journal of the American Society of Nephrology</title>
<url>http://cjasn.asnjournals.org/icons/banner/title.gif</url>
<link>http://cjasn.asnjournals.org</link>
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<title><![CDATA[Correlates and Outcomes of Fatigue among Incident Dialysis Patients]]></title>
<link>http://cjasn.asnjournals.org/cgi/content/short/4/11/1779?rss=1</link>
<description><![CDATA[
<p>Background &amp; objectives: Fatigue is a debilitating symptom experienced by patients undergoing dialysis, but there is only limited information on its prevalence and its association with patient outcomes. This study examines the correlates of self-reported fatigue at initiation of dialysis and after 1 yr and assesses the extent to which fatigue was associated with health-related quality of life and survival.</p>
<p>Design, setting, participants, &amp; measurements: A longitudinal cohort of 917 incident hemodialysis and peritoneal dialysis patients who completed the CHOICE Health Experience Questionnaire (CHEQ) participated in the study. Fatigue was assessed using the SF-36 vitality scale. Known predictors of fatigue including sociodemographic and psychosocial factors, dialysis-related factors, biochemical variables including inflammatory markers, comorbidities, and medications were used as covariates.</p>
<p>Results: A low vitality score was independently associated with white race, higher Index of Coexistent Disease score, higher body mass index, lack of physical exercise, antidepressant use, and higher C-reactive protein levels (CRP). A lower vitality score was strongly associated with lower SF-36 physical functioning, mental health, bodily pain scores, and decreased sleep quality (all <I>P</I> &lt; 0.001) at baseline. Among surviving participants, higher serum creatinine at baseline was associated with preserved vitality at 1 yr. Patients with the highest baseline vitality scores were associated with longer survival (hazard ratio 0.75; 95% CI 0.58 to 0.96, <I>P</I> = 0.03).</p>
<p>Conclusions: The findings of this study demonstrate that ESRD patients experience profound levels of fatigue and elucidate its correlates. Also, the association of fatigue with survival may have significant implications for this population.</p>
]]></description>
<dc:creator><![CDATA[Jhamb, M., Argyropoulos, C., Steel, J. L., Plantinga, L., Wu, A. W., Fink, N. E., Powe, N. R., Meyer, K. B., Unruh, M. L., for the Choices for Healthy Outcomes in Caring for End-Stage Renal Disease (CHOICE) Study]]></dc:creator>
<dc:date>Tue, 03 Nov 2009 10:02:23 PST</dc:date>
<dc:identifier>info:doi/10.2215/CJN.00190109</dc:identifier>
<dc:title><![CDATA[Correlates and Outcomes of Fatigue among Incident Dialysis Patients]]></dc:title>
<dc:publisher>American Society of Nephrology</dc:publisher>
<prism:number>11</prism:number>
<prism:volume>4</prism:volume>
<prism:endingPage>1786</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1779</prism:startingPage>
<prism:section>Dialysis</prism:section>
</item>

<item rdf:about="http://cjasn.asnjournals.org/cgi/content/short/4/11/1787?rss=1">
<title><![CDATA[Does Heparin Coating Improve Patency or Reduce Infection of Tunneled Dialysis Catheters?]]></title>
<link>http://cjasn.asnjournals.org/cgi/content/short/4/11/1787?rss=1</link>
<description><![CDATA[
<p>Background and objectives: Tunneled dialysis catheters are prone to frequent malfunction and infection. Catheter thrombosis occurs despite prophylactic anticoagulant locks. Catheter thrombi may also serve as a nidus for catheter infection, thereby increasing the risk of bacteremia. Thus, heparin coating of catheters may reduce thrombosis and infection. This study evaluated whether heparin-coated hemodialysis catheters have fewer infections or greater cumulative survival than noncoated catheters.</p>
<p>Design, setting, participants, &amp; measurements: We retrospectively queried a prospective access database to analyze the outcomes of 175 tunneled dialysis catheters placed in the internal jugular vein, including 89 heparin-coated catheters and 86 noncoated catheters. The primary outcome was cumulative catheter survival, and the secondary outcome was infection-free catheter survival.</p>
<p>Results: The two patient groups were similar in demographics and clinical and catheter features. Catheter-related bacteremia occurred less frequently with heparin-coated catheters than with noncoated catheters (34 <I>versus</I> 60%, <I>P</I> &lt; 0.001). Cumulative catheter survival was similar in heparin-coated and noncoated catheters (hazard ratio, 0.87; 95% confidence interval, 0.55 to 1.36; <I>P</I> = 0.53). On multiple variable survival analysis including catheter type, age, sex, diabetes, coronary artery disease, peripheral vascular disease, cerebrovascular disease, catheter location, and previous catheter, only catheter location predicted cumulative catheter survival (hazard ratio, 2.03; 95% CI, 1.27 to 3.25, with the right internal jugular location being the reference group, <I>P</I> = 0.003). The frequency of thrombolytic instillation was 1.8 per 1000 catheter-days in both groups.</p>
<p>Conclusions: Heparin coating decreases the frequency of catheter-related bacteremia but does not reduce the frequency of catheter malfunction.</p>
]]></description>
<dc:creator><![CDATA[Jain, G., Allon, M., Saddekni, S., Barker, J.-F., Maya, I. D.]]></dc:creator>
<dc:date>Tue, 03 Nov 2009 10:02:23 PST</dc:date>
<dc:identifier>info:doi/10.2215/CJN.03920609</dc:identifier>
<dc:title><![CDATA[Does Heparin Coating Improve Patency or Reduce Infection of Tunneled Dialysis Catheters?]]></dc:title>
<dc:publisher>American Society of Nephrology</dc:publisher>
<prism:number>11</prism:number>
<prism:volume>4</prism:volume>
<prism:endingPage>1790</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1787</prism:startingPage>
<prism:section>Dialysis</prism:section>
</item>

<item rdf:about="http://cjasn.asnjournals.org/cgi/content/short/4/11/1791?rss=1">
<title><![CDATA[Combining Near-Subject Absolute and Relative Measures of Longitudinal Hydration in Hemodialysis]]></title>
<link>http://cjasn.asnjournals.org/cgi/content/short/4/11/1791?rss=1</link>
<description><![CDATA[
<p>Background and objectives: The feasibility and additional value of combining bioimpedance analysis (BIA) with near-subject absolute measurement of total body water using deuterium dilution (TBW<SUB>D</SUB>) in determining longitudinal fluid status was investigated.</p>
<p>Design, setting, participants, &amp; measurements: Fifty-nine hemodialysis patients (17 female; age 58.4 &plusmn; 16.1 yr; body mass index 27.0 &plusmn; 5.4) were enrolled into a 12-mo, two-center, prospective cohort study. Deuterium concentration was measured in breath by flowing-afterglow mass spectrometry using a validated protocol ensuring full equilibration with the TBW; BIA was measured using a multifrequency, multisegmental device. Comorbidity was quantified by the Stoke score. Clinicians were blinded to body composition data.</p>
<p>Results: At baseline and 12 mo, there was an incremental discrepancy between TBW<SUB>BIA</SUB> and TBW<SUB>D</SUB> volumes such that greater comorbidity was associated with increasing overhydration. Forty-three patients who completed the study had no longitudinal differences in the prescribed or achieved postdialysis weights. In contrast, TBW<SUB>D</SUB> increased without a change in TBW<SUB>BIA</SUB> (mean difference &ndash;0.10 L). Changes in TBW and lean body mass differed according to baseline comorbidity; without comorbidity, BIA also identified an increase in TBW and lean body mass, whereas with increasing comorbid burden, BIA failed to demonstrate increases in tissue hydration identified by TBW<SUB>D</SUB>.</p>
<p>Conclusions: Combined near-patient measurements of absolute and BIA-estimated TBW are achievable in a dialysis facility by identifying changes in body composition not fully appreciated by routine assessment. BIA underestimates tissue overhydration that is associated with comorbidity, resulting in reduced sensitivity to longitudinal increases during a 12-mo period.</p>
]]></description>
<dc:creator><![CDATA[Chan, C., McIntyre, C., Smith, D., Spanel, P., Davies, S. J.]]></dc:creator>
<dc:date>Tue, 03 Nov 2009 10:02:23 PST</dc:date>
<dc:identifier>info:doi/10.2215/CJN.02510409</dc:identifier>
<dc:title><![CDATA[Combining Near-Subject Absolute and Relative Measures of Longitudinal Hydration in Hemodialysis]]></dc:title>
<dc:publisher>American Society of Nephrology</dc:publisher>
<prism:number>11</prism:number>
<prism:volume>4</prism:volume>
<prism:endingPage>1798</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1791</prism:startingPage>
<prism:section>Dialysis</prism:section>
</item>

<item rdf:about="http://cjasn.asnjournals.org/cgi/content/short/4/11/1799?rss=1">
<title><![CDATA[Randomized Controlled Trial of Icodextrin versus Glucose Containing Peritoneal Dialysis Fluid]]></title>
<link>http://cjasn.asnjournals.org/cgi/content/short/4/11/1799?rss=1</link>
<description><![CDATA[
<p>Background and objectives: While peritoneal dialysis with icodextrin is commonly used in patients with poor peritoneal membrane characteristics, the data on the usefulness of this solution in patients with lower transport characteristics are limited. The study was designed to compare icodextrin to glucose in Chinese prevalent peritoneal dialysis patients of different peritoneal transport characteristics (PET) categories.</p>
<p>Design, setting, participants, &amp; measurements: This was a randomized, double-blind, perspective control study. Stable prevalent continuous ambulatory peritoneal dialysis (CAPD) patients were randomized to either 7.5% icodextrin (ICO) or 2.5% glucose (GLU) solution for 4 wk. Peritoneal membrane function was measured to define PET category in baseline. Creatinine clearance (Ccr), urea nitrogen clearance (C<SUB>BUN</SUB>), ultrafiltration (UF) during the long night dwell, dialysate, and metabolic biomarkers were measured at baseline, 2, and 4 wk. UF, Ccr, and C<SUB>BUN</SUB> were compared among different PET categories.</p>
<p>Results: A total of 201 CAPD patients were enrolled in the study. There were no baseline differences between the groups. Following 2 and 4 wk of therapy, Ccr, C<SUB>BUN,</SUB> and UF were all significantly higher in the ICO <I>versus</I> the GLU group. Additionally, switching to ICO resulted in a significant increase in UF in high, high-average, and low-average transporters as compared with baseline. The extent of increased UF was more obvious in higher transporters. Blood cholesterol level in the ICO group decreased significantly than that in the GLU group.</p>
<p>Conclusion: Compared with glucose-based solution, 7.5% icodextrin significantly improved UF and small solute clearance, even in patients with low-average peritoneal transport.</p>
]]></description>
<dc:creator><![CDATA[Lin, A., Qian, J., Li, X., Yu, X., Liu, W., Sun, Y., Chen, N., Mei, C., for the Icodextrin National Multi-center Cooperation Group]]></dc:creator>
<dc:date>Tue, 03 Nov 2009 10:02:23 PST</dc:date>
<dc:identifier>info:doi/10.2215/CJN.02950509</dc:identifier>
<dc:title><![CDATA[Randomized Controlled Trial of Icodextrin versus Glucose Containing Peritoneal Dialysis Fluid]]></dc:title>
<dc:publisher>American Society of Nephrology</dc:publisher>
<prism:number>11</prism:number>
<prism:volume>4</prism:volume>
<prism:endingPage>1804</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1799</prism:startingPage>
<prism:section>Dialysis</prism:section>
</item>

<item rdf:about="http://cjasn.asnjournals.org/cgi/content/short/4/10/1601?rss=1">
<title><![CDATA[Bacteremia Associated with Tunneled Hemodialysis Catheters: Outcome after Attempted Salvage]]></title>
<link>http://cjasn.asnjournals.org/cgi/content/short/4/10/1601?rss=1</link>
<description><![CDATA[
<p>Background and objectives: Treatment without catheter replacement (catheter salvage) has been described for bacteremia associated with tunneled venous catheters in hemodialysis patients, but few data are available on which to base an estimation of the likelihood of treatment success.</p>
<p>Design, setting, participants, &amp; measurements: In a prospective cohort study, all cases of catheter-associated bacteremia that occurred in a large dialysis center were identified during a 12-mo period. Catheter salvage was attempted according to a standard protocol in all cases in which a favorable early response to antibiotic therapy was seen, and patients were followed for at least 6 mo. Bacteremias, catheter changes, and all major clinical events were recorded.</p>
<p>Results: During a period covering 252,986 catheter days, 208 episodes were identified involving 133 patients, 74% of which were selected for attempted salvage. Salvage was successful in 66.1% of incident bacteremias with a very low complication risk (0.9%). Some bacteremias, however, recurred as late as 6 mo after the initial infection; salvage was less likely to be successful in treating recurrences.</p>
<p>Conclusions: Appropriately used catheter salvage can be successful in approximately two thirds of cases; however, recurrences continue to occur up to 6 mo later and are unlikely to be cured without catheter replacement.</p>
]]></description>
<dc:creator><![CDATA[Ashby, D. R., Power, A., Singh, S., Choi, P., Taube, D. H., Duncan, N. D., Cairns, T. D.]]></dc:creator>
<dc:date>Mon, 05 Oct 2009 10:02:28 PDT</dc:date>
<dc:identifier>info:doi/10.2215/CJN.01840309</dc:identifier>
<dc:title><![CDATA[Bacteremia Associated with Tunneled Hemodialysis Catheters: Outcome after Attempted Salvage]]></dc:title>
<dc:publisher>American Society of Nephrology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>4</prism:volume>
<prism:endingPage>1605</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>1601</prism:startingPage>
<prism:section>Dialysis</prism:section>
</item>

<item rdf:about="http://cjasn.asnjournals.org/cgi/content/short/4/10/1606?rss=1">
<title><![CDATA[Cystatin C Levels in Functionally Anephric Patients Undergoing Dialysis: The Effect of Different Methods and Intensities]]></title>
<link>http://cjasn.asnjournals.org/cgi/content/short/4/10/1606?rss=1</link>
<description><![CDATA[
<p>Background and objectives: Cystatin C, a low molecular weight protein, is produced by nucleated cells, filtered by glomeruli, and degraded by tubules at a constant rate. Its serum concentration has been proposed as a marker of GFR. Its size should make it dialyzable. It is hypothesized that serum cystatin C levels are influenced by the method and intensity of dialysis received.</p>
<p>Design: This is a cross-sectional pilot study of cystatin C in functionally anephric dialysis patients. It was measured predialysis in 14 patients on conventional (3 to 5 h, 3 <FONT FACE="arial,helvetica">x</FONT> wk) hemodialysis; eight on nocturnal hemodialysis (three to seven nights, 6 to 8 h); three on daily hemodialysis (6 d, 11/2 to 21/2 h); and 10 on automated peritoneal dialysis. All had urea kinetic studies and values for single pool Kt/V (Sp Kt/V), standard weekly Kt/V (Std Kt/V), and protein equivalent of nitrogen appearance (nPNA; g/kg/d). C reactive protein (CRP; mg/L) and thyroid stimulating hormone (TSH; mIU/L) were measured as factors known to influence cystatin C.</p>
<p>Results: There was no correlation between cystatin C and Sp Kt/V, but there was a significant inverse linear correlation with Std Kt/V and there were significant differences between treatment modalities in cystatin C levels and in Std Kt/V. The estimation of cystatin C was reliable and stable over 3 to 6 wk and its levels uninfluenced by nPNA, CRP, or TSH.</p>
<p>Conclusion: Serum cystatin C levels are influenced by the method and intensity of dialysis and may have a role in treatment adequacy monitoring.</p>
]]></description>
<dc:creator><![CDATA[Al-Malki, N., Heidenheim, P. A., Filler, G., Yasin, A., Lindsay, R. M.]]></dc:creator>
<dc:date>Mon, 05 Oct 2009 10:02:28 PDT</dc:date>
<dc:identifier>info:doi/10.2215/CJN.02910509</dc:identifier>
<dc:title><![CDATA[Cystatin C Levels in Functionally Anephric Patients Undergoing Dialysis: The Effect of Different Methods and Intensities]]></dc:title>
<dc:publisher>American Society of Nephrology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>4</prism:volume>
<prism:endingPage>1610</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>1606</prism:startingPage>
<prism:section>Dialysis</prism:section>
</item>

<item rdf:about="http://cjasn.asnjournals.org/cgi/content/short/4/10/1611?rss=1">
<title><![CDATA[Is Maximum Conservative Management an Equivalent Treatment Option to Dialysis for Elderly Patients with Significant Comorbid Disease?]]></title>
<link>http://cjasn.asnjournals.org/cgi/content/short/4/10/1611?rss=1</link>
<description><![CDATA[
<p>Background and objectives: There is ongoing growth of elderly populations with ESRD in Western Europe and North America. In our center, we offer an alternative care pathway of &lsquo;maximum conservative management&rsquo; (MCM) to patients who elect not to start dialysis, often because of a heavy burden of comorbid illness and advanced age. The objective of our study was to compare clinical outcomes for patients who had ESRD and chose either MCM or renal replacement therapy (RRT).</p>
<p>Design, setting, participants, &amp; measurements: This is an observational study of a single-center cohort in the United Kingdom that evaluating 202 elderly (&ge;70 yr) patients who had ESRD and had chosen either MCM (<I>n</I> = 29) or RRT (<I>n</I> = 173). We report survival, hospitalization rates, and location of death for this cohort. Survival was measured from a standardized &lsquo;threshold&rsquo; estimated GFR of 10.8 ml/min per 1.73 m<sup>2</sup>.</p>
<p>Results: Median survival, including the first 90 d, was 37.8 mo (range 0 to 106 mo) for RRT patients and 13.9 mo (range 2 to 44) for MCM patients (<I>P</I> &lt; 0.01). RRT patients had higher rates of hospitalization (0.069 [95% confidence interval (CI) 0.068 to 0.070]) <I>versus</I> 0.043 [95% CI 0.040 to 0.047] hospital days/patient-days survived) compared with MCM patients. MCM patients were significantly more likely to die at home or in a hospice (odds ratio 4.15; 95% CI 1.67 to 10.25). A survey of the literature describing elderly ESRD outcomes is also presented.</p>
<p>Conclusions: Dialysis prolongs survival for elderly patients who have ESRD with significant comorbidity by approximately 2 yr; however, patients who choose MCM can survive a substantial length of time, achieving similar numbers of hospital-free days to patients who choose hemodialysis.</p>
]]></description>
<dc:creator><![CDATA[Carson, R. C., Juszczak, M., Davenport, A., Burns, A.]]></dc:creator>
<dc:date>Mon, 05 Oct 2009 10:02:28 PDT</dc:date>
<dc:identifier>info:doi/10.2215/CJN.00510109</dc:identifier>
<dc:title><![CDATA[Is Maximum Conservative Management an Equivalent Treatment Option to Dialysis for Elderly Patients with Significant Comorbid Disease?]]></dc:title>
<dc:publisher>American Society of Nephrology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>4</prism:volume>
<prism:endingPage>1619</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>1611</prism:startingPage>
<prism:section>Dialysis</prism:section>
</item>

<item rdf:about="http://cjasn.asnjournals.org/cgi/content/short/4/10/1620?rss=1">
<title><![CDATA[Association of Dialysis Modality and Cardiovascular Mortality in Incident Dialysis Patients]]></title>
<link>http://cjasn.asnjournals.org/cgi/content/short/4/10/1620?rss=1</link>
<description><![CDATA[
<p>Background and objectives: The aim of the investigation presented here was to compare the rates, causes, and timing of cardiovascular (CV) death in incident peritoneal dialysis (PD) and hemodialysis (HD) patients.</p>
<p>Design, setting, participants, &amp; measurements: The study included all adult Australian and New Zealand patients commencing dialysis between January 1, 1997 and December 31, 2007. Rates of and times to CV death were compared by incident rate ratios, cumulative incidence, and multivariable Cox proportional hazards model analyses. Dialysis modality was included in the model as a time-varying covariate, and a competing risks approach was used to obtain cause-specific hazard ratios.</p>
<p>Results: Of the 24,587 patients who commenced dialysis (first treatment PD <I>n</I> = 6521; HD <I>n</I> = 18,066) during the study, 5669 (21%) died from CV causes [PD 2044 (28%) <I>versus</I> HD 3625 (21%)]. The incidence rates of CV mortality in PD and HD patients were 9.99 and 7.96 per 100 patient-years, respectively (incidence rate ratio PD <I>versus</I> HD, 1.25; 95% confidence interval 1.12 to 1.32). PD was consistently associated with an increased hazard of CV death compared with HD after 1 yr of treatment. This increased risk in PD patients was largely accounted for by an increased risk of death due to myocardial infarction.</p>
<p>Conclusions: Dialysis modality is significantly associated with the risk, causes, and timing of CV death experienced by ESRD patients in Australia and New Zealand.</p>
]]></description>
<dc:creator><![CDATA[Johnson, D. W., Dent, H., Hawley, C. M., McDonald, S. P., Rosman, J. B., Brown, F. G., Bannister, K., Wiggins, K. J.]]></dc:creator>
<dc:date>Mon, 05 Oct 2009 10:02:28 PDT</dc:date>
<dc:identifier>info:doi/10.2215/CJN.01750309</dc:identifier>
<dc:title><![CDATA[Association of Dialysis Modality and Cardiovascular Mortality in Incident Dialysis Patients]]></dc:title>
<dc:publisher>American Society of Nephrology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>4</prism:volume>
<prism:endingPage>1628</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>1620</prism:startingPage>
<prism:section>Dialysis</prism:section>
</item>

<item rdf:about="http://cjasn.asnjournals.org/cgi/content/short/4/10/1629?rss=1">
<title><![CDATA[Is Valvular Calcification a Part of the Missing Link between Residual Kidney Function and Cardiac Hypertrophy in Peritoneal Dialysis Patients?]]></title>
<link>http://cjasn.asnjournals.org/cgi/content/short/4/10/1629?rss=1</link>
<description><![CDATA[
<p>Background and objectives: Residual renal function (RRF) predicts survival and shows an important inverse relation with cardiac hypertrophy in peritoneal dialysis (PD) patients. We hypothesized that valvular calcification and the calcification milieu may be part of the process linking loss of RRF and cardiac hypertrophy.</p>
<p>Design, setting, participants, &amp; measurements: A cross-sectional study was conducted by performing two-dimensional echocardiography on 230 PD patients to assess valvular calcification and left ventricular (LV) mass and collecting 24-h urine for estimation of RRF.</p>
<p>Results: Patients having valvular calcification had lower RRF than those without. Patients with no RRF showed higher calcium-phosphorus product (Ca <FONT FACE="arial,helvetica">x</FONT> P) and C-reactive protein (CRP). Using multiple logistic regression analysis, every 1-ml/min per 1.73 m<sup>2</sup> increase in residual GFR was associated with a 28% reduction in the risk for valvular calcification. The association was lost after additional adjustment for Ca <FONT FACE="arial,helvetica">x</FONT> P and CRP. Using multiple linear regression analysis, loss of RRF showed significant association with increased LV mass index, but this association was lost after additional adjustment for CRP, Ca <FONT FACE="arial,helvetica">x</FONT> P, and valvular calcification. Patients with all three calcification risk factors, namely inflammation, high Ca<FONT FACE="arial,helvetica">x</FONT>P, and no RRF, showed the highest prevalence of valvular calcification and had the most severe cardiac hypertrophy.</p>
<p>Conclusions: The association among loss of RRF, valvular calcification, and cardiac hypertrophy was closely linked to increased inflammation and high Ca <FONT FACE="arial,helvetica">x</FONT> P in PD patients. These data suggest that valvular calcification and the calcification milieu are part of the processes linking loss of RRF and worsening cardiac hypertrophy in PD.</p>
]]></description>
<dc:creator><![CDATA[Wang, A. Y.-M., Lam, C. W.-K., Wang, M., Chan, I. H.-S., Lui, S.-F., Sanderson, J. E.]]></dc:creator>
<dc:date>Mon, 05 Oct 2009 10:02:28 PDT</dc:date>
<dc:identifier>info:doi/10.2215/CJN.03100509</dc:identifier>
<dc:title><![CDATA[Is Valvular Calcification a Part of the Missing Link between Residual Kidney Function and Cardiac Hypertrophy in Peritoneal Dialysis Patients?]]></dc:title>
<dc:publisher>American Society of Nephrology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>4</prism:volume>
<prism:endingPage>1636</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>1629</prism:startingPage>
<prism:section>Dialysis</prism:section>
</item>

<item rdf:about="http://cjasn.asnjournals.org/cgi/content/short/4/9/1441?rss=1">
<title><![CDATA[Technical Breakthroughs in the Wearable Artificial Kidney (WAK)]]></title>
<link>http://cjasn.asnjournals.org/cgi/content/short/4/9/1441?rss=1</link>
<description><![CDATA[
<p>Background: The wearable artificial kidney (WAK) has been a holy grail in kidney failure for decades. Described herein are the breakthroughs that made possible the creation of the WAK V1.0 and its advanced versions V 1.1 and 1.2.</p>
<p>Design: The battery-powered WAK pump has a double channel pulsatile counter phase flow. This study clarifies the role of pulsatile blood and dialysate flow, a high-flux membrane with a larger surface area, and the optimization of the dialysate pH. Flows and clearances from the WAK pump were compared with conventional pumps and with gravity steady flow.</p>
<p>Results: Raising dialysate pH to 7.4 increased adsorption of ammonia. Clearances were higher with pulsatile flow as compared with steady flow. The light WAK pump, geometrically suitable for wearability, delivered the same clearances as larger and heavier pumps that cannot be battery operated. Beta<SUB>2</SUB> microglobulin (&beta;<SUB>2</SUB>M) was removed from human blood <I>in vitro</I>. Activated charcoal adsorbed most &beta;<SUB>2</SUB>M in the dialysate. The WAK V1.0 delivered an effective creatinine clearance of 18.5 &plusmn; 3.2 ml/min and the WAK V1.1 27.0 &plusmn; 4.0 ml/min in uremic pigs.</p>
<p>Conclusions: Half-cycle differences between blood and dialysate, alternating transmembrane pressures (TMP), higher amplitude pulsations, and a push-pull flow increased convective transport. This creates a yet undescribed type of hemodiafiltration. Further improvements were achieved with a larger surface area high-flux dialyzer and a higher dialysate pH. The data suggest that the WAK might be an efficient way of providing daily dialysis and optimizing end stage renal disease (ESRD) treatment.</p>
]]></description>
<dc:creator><![CDATA[Gura, V., Macy, A. S., Beizai, M., Ezon, C., Golper, T. A.]]></dc:creator>
<dc:date>Thu, 03 Sep 2009 14:47:31 PDT</dc:date>
<dc:identifier>info:doi/10.2215/CJN.02790409</dc:identifier>
<dc:title><![CDATA[Technical Breakthroughs in the Wearable Artificial Kidney (WAK)]]></dc:title>
<dc:publisher>American Society of Nephrology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>4</prism:volume>
<prism:endingPage>1448</prism:endingPage>
<prism:publicationDate>2009-09-01</prism:publicationDate>
<prism:startingPage>1441</prism:startingPage>
<prism:section>Dialysis</prism:section>
</item>

<item rdf:about="http://cjasn.asnjournals.org/cgi/content/short/4/9/1449?rss=1">
<title><![CDATA[Interferon for Hepatitis C Virus in Hemodialysis--an Individual Patient Meta-analysis of Factors Associated with Sustained Virological Response]]></title>
<link>http://cjasn.asnjournals.org/cgi/content/short/4/9/1449?rss=1</link>
<description><![CDATA[
<p>Background and objectives: Hepatitis C virus (HCV) infection is prevalent in hemodialysis patients and causes excess mortality. Interferon (IFN) treatment of chronic HCV infection in hemodialysis patients results in high sustained virological response (SVR) rates 6 mo after treatment. The authors aimed to identify factors associated with SVR in hemodialysis patients through analysis of individual patient data obtained from systematic review of published literature.</p>
<p>Design, setting, participants &amp; measurements: Medline was searched from 1966 through February 2009, and prospective studies describing IFN treatment of hemodialysis patients with chronic HCV infection with published individual patient data were included. To identify factors associated with SVR, logistic regression was applied with adjustment for study.</p>
<p>Results: Twenty studies of IFN treatment provided data on 428 patients. Overall SVR was 45% and in univariate analyses was higher with: 1) three million units or higher three times weekly of IFN; 2) treatment for at least 6 mo; 3) treatment completion; 4) lower baseline HCV RNA; 5) female gender; and 6) early virological negativity. Although limited by missing data, these relationships persisted in multivariate regression.</p>
<p>Conclusions: SVR is more likely with larger IFN dose, longer treatment duration, treatment completion, female gender, lower HCV RNA and early virological negativity. For appropriate treatment candidates, regimens should consist of three million units of IFN three times weekly for at least 6 mo, with patients encouraged to complete the full course.</p>
]]></description>
<dc:creator><![CDATA[Gordon, C. E., Uhlig, K., Lau, J., Schmid, C. H., Levey, A. S., Wong, J. B.]]></dc:creator>
<dc:date>Thu, 03 Sep 2009 14:47:31 PDT</dc:date>
<dc:identifier>info:doi/10.2215/CJN.01850309</dc:identifier>
<dc:title><![CDATA[Interferon for Hepatitis C Virus in Hemodialysis--an Individual Patient Meta-analysis of Factors Associated with Sustained Virological Response]]></dc:title>
<dc:publisher>American Society of Nephrology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>4</prism:volume>
<prism:endingPage>1458</prism:endingPage>
<prism:publicationDate>2009-09-01</prism:publicationDate>
<prism:startingPage>1449</prism:startingPage>
<prism:section>Dialysis</prism:section>
</item>

<item rdf:about="http://cjasn.asnjournals.org/cgi/content/short/4/9/1459?rss=1">
<title><![CDATA[Increased Efficiency of Hemodialysis with Citrate Dialysate: A Prospective Controlled Study]]></title>
<link>http://cjasn.asnjournals.org/cgi/content/short/4/9/1459?rss=1</link>
<description><![CDATA[
<p>Background and objectives: A bicarbonate dialysate acidified with citrate (CD) has been reported to have local anticoagulant effect. This study examines the effect of CD on dialysis efficiency, measured as eKt/Vurea, and predialysis concentrations of BUN, creatinine, phosphate, and &beta;-2 microglobulin in chronic dialysis units.</p>
<p>Design, settings, participants, &amp; measurements: Three outpatient chronic hemodialysis units with 142 patients were switched to CD for 6 mo. Using each patient's prior 6 mo on regular bicarbonate dialysate acidified by acetate (AD) as control, eKt/Vurea was compared with that of CD. Follow-up data for 7 mo after the study were collected from about one-half of the participants remaining on CD and the others returned to AD.</p>
<p>Results: eKt/Vurea, increased (<I>P</I> &lt; 0.0001) from pre-CD value of 1.51 &plusmn; 0.01 to 1.57 &plusmn; 0.01 with CD. During CD use &beta;-2 microglobulin levels declined (<I>P</I> = 0.0001) from 28.1 &plusmn; 10.0 to 25.9 &plusmn; 10.0. Similarly, the concentrations of BUN, creatinine, and phosphate also decreased on CD (<I>P</I> &lt; 0.008). In the poststudy period, eKt/Vurea for the patients staying on CD remained unchanged at 1.60 &plusmn; 0.17 <I>versus</I> 1.59 &plusmn; 0.18 (<I>P</I> = NS), whereas in those returning to AD the eKt/Vurea decreased from 1.55 &plusmn; 0.20 to 1.52 &plusmn; 0.17 (<I>P</I> &lt; 0.0001).</p>
<p>Conclusions: Data suggest that CD use is associated with increased solute removal.</p>
]]></description>
<dc:creator><![CDATA[Kossmann, R. J., Gonzales, A., Callan, R., Ahmad, S.]]></dc:creator>
<dc:date>Thu, 03 Sep 2009 14:47:31 PDT</dc:date>
<dc:identifier>info:doi/10.2215/CJN.02590409</dc:identifier>
<dc:title><![CDATA[Increased Efficiency of Hemodialysis with Citrate Dialysate: A Prospective Controlled Study]]></dc:title>
<dc:publisher>American Society of Nephrology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>4</prism:volume>
<prism:endingPage>1464</prism:endingPage>
<prism:publicationDate>2009-09-01</prism:publicationDate>
<prism:startingPage>1459</prism:startingPage>
<prism:section>Dialysis</prism:section>
</item>

<item rdf:about="http://cjasn.asnjournals.org/cgi/content/short/4/9/1465?rss=1">
<title><![CDATA[Simultaneous Control of PTH and CaxP Is Sustained over Three Years of Treatment with Cinacalcet HCl]]></title>
<link>http://cjasn.asnjournals.org/cgi/content/short/4/9/1465?rss=1</link>
<description><![CDATA[
<p>Background &amp; objectives: Chronic kidney disease (CKD) is commonly complicated by secondary hyperparathyroidism (SHPT), leading to increased risk of morbidity and mortality. SHPT is a progressive disease often requiring long-term therapy to control parathyroid hormone (PTH) and mineral imbalances. Vitamin D sterols and phosphate binders, used as traditional therapies to lower PTH and phosphorus, may provide inadequate long-term control for many dialysis patients. Cinacalcet, by simultaneously lowering PTH, calcium, phosphorus, and calcium-phosphorus levels, may maintain PTH and mineral balance in these individuals. However, as with traditional therapies, long-term data are limited.</p>
<p>Design, setting, participants, &amp; measurement: Dialysis subjects from at least one of five lead-in studies (double-blind placebo-controlled, including one extension trial) completing up to 52 wk of either cinacalcet or placebo were eligible for this open-label extension study, including an 8-wk dose titration (initiated at 30 mg/d), followed by 24-wk maintenance and up to 132 wk of follow-up. Final efficacy analysis was at week 180.</p>
<p>Results: Three hundred thirty-four of 589 enrolled subjects received cinacalcet from the beginning of the lead-in study. Weekly median PTH values were &le;300 pg/ml (weeks 16 through 180) and median Ca<FONT FACE="arial,helvetica">x</FONT>P values were &le;55 mg<sup>2</sup>/dl<sup>2</sup> (weeks 4 through 180). Similar results were exhibited in the 255 subjects who initially received placebo. Among the patients exposed to cinacalcet from the beginning of the lead-in study, 3% of subjects exhibited treatment-related serious adverse events.</p>
<p>Conclusions: Cinacalcet effectively maintained PTH, Ca and P reductions in dialysis subjects for up to 180 wk.</p>
]]></description>
<dc:creator><![CDATA[Sprague, S. M., Evenepoel, P., Curzi, M. P., Gonzalez, M. T., Husserl, F. E., Kopyt, N., Sterling, L. R., Mix, C., Wong, G.]]></dc:creator>
<dc:date>Thu, 03 Sep 2009 14:47:31 PDT</dc:date>
<dc:identifier>info:doi/10.2215/CJN.06141108</dc:identifier>
<dc:title><![CDATA[Simultaneous Control of PTH and CaxP Is Sustained over Three Years of Treatment with Cinacalcet HCl]]></dc:title>
<dc:publisher>American Society of Nephrology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>4</prism:volume>
<prism:endingPage>1476</prism:endingPage>
<prism:publicationDate>2009-09-01</prism:publicationDate>
<prism:startingPage>1465</prism:startingPage>
<prism:section>Dialysis</prism:section>
</item>

<item rdf:about="http://cjasn.asnjournals.org/cgi/content/short/4/9/1477?rss=1">
<title><![CDATA[Determinants of Left Ventricular Mass and Hypertrophy in Hemodialysis Patients Assessed by Cardiac Magnetic Resonance Imaging]]></title>
<link>http://cjasn.asnjournals.org/cgi/content/short/4/9/1477?rss=1</link>
<description><![CDATA[
<p>Background and objectives: Left ventricular hypertrophy (LVH) is an independent risk factor for premature cardiovascular death in hemodialysis (HD) patients and one of the three forms of uremic cardiomyopathy. Cardiovascular magnetic resonance (CMR) is a volume-independent technique to assess cardiac structure. We used CMR to assess the determinants of left ventricular mass (LVM) and LVH in HD patients.</p>
<p>Design, setting, participants, &amp; measurements: A total of 246 HD patients (63.8% male; mean age 51.5 &plusmn; 12.1 yr) underwent CMR on a postdialysis day. LVM was measured from a stack of cine loops and indexed for body surface area (LVM index [LVMI]). Demographic, past biochemical, hematologic, and dialysis data were collected by patient record review. Results up to 180 d before CMR were collected. LVH was defined as LVMI &gt;84.1 g/m<sup>2</sup> (male) or &gt;76.4 g/m<sup>2</sup> (female).</p>
<p>Results: A total of 157 (63.8%) patients had LVH. LVH was more common in patients with higher predialysis systolic BP, predialysis pulse pressure, and calcium-phosphate product (Ca <FONT FACE="arial,helvetica">x</FONT> PO<SUB>4</SUB>). Furthermore, LVH was significantly associated with higher end-diastolic and systolic volumes and lower ejection fraction. There were positive correlations with LVMI and end-diastolic and systolic volumes. There were weak positive correlations among LVMI, mean volume of ultrafiltration, and Ca <FONT FACE="arial,helvetica">x</FONT> PO<SUB>4</SUB>. Using multivariate linear and logistic regression (entering one BP and cardiac variable), the independent predictors of LVMI and LVH were end-diastolic volume, predialysis systolic BP, and Ca <FONT FACE="arial,helvetica">x</FONT> PO<SUB>4</SUB>.</p>
<p>Conclusions: The principal determinants of LVM and LVH in HD patients are end-diastolic LV volume, predialysis BP, and Ca <FONT FACE="arial,helvetica">x</FONT> PO<SUB>4</SUB>.</p>
]]></description>
<dc:creator><![CDATA[Patel, R. K., Oliver, S., Mark, P. B., Powell, J. R., McQuarrie, E. P., Traynor, J. P., Dargie, H. J., Jardine, A. G.]]></dc:creator>
<dc:date>Thu, 03 Sep 2009 14:47:31 PDT</dc:date>
<dc:identifier>info:doi/10.2215/CJN.03350509</dc:identifier>
<dc:title><![CDATA[Determinants of Left Ventricular Mass and Hypertrophy in Hemodialysis Patients Assessed by Cardiac Magnetic Resonance Imaging]]></dc:title>
<dc:publisher>American Society of Nephrology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>4</prism:volume>
<prism:endingPage>1483</prism:endingPage>
<prism:publicationDate>2009-09-01</prism:publicationDate>
<prism:startingPage>1477</prism:startingPage>
<prism:section>Dialysis</prism:section>
</item>

<item rdf:about="http://cjasn.asnjournals.org/cgi/content/short/4/8/1324?rss=1">
<title><![CDATA[Does Timing of Dialysis in Patients with ESRD and Acute Myocardial Infarcts Affect Morbidity or Mortality?]]></title>
<link>http://cjasn.asnjournals.org/cgi/content/short/4/8/1324?rss=1</link>
<description><![CDATA[
<p>Background and objectives: Patients with ESRD have an increased incidence of coronary events with a relatively higher risk for mortality after acute myocardial infarction (AMI). We evaluated whether it is safer to delay dialysis in AMI or if delay poses separate risks.</p>
<p>Design, setting, participants, &amp; measurements: We conducted a retrospective review of 131 long-term hemodialysis patients who had AMI and were admitted between 1997 and 2005 at three New York City municipal hospitals. Patients were separated into three groups on the basis of time between cardiac symptoms and first dialysis (&lt;24 h, 24 to 48 h, and &gt;48 h).</p>
<p>Results: A total of 17 (13%) patients died, 10 (59%) of whom had either hypotension or an arrhythmia during their first cardiac care unit dialysis. Although these groups were comparable in acuity and cardiac status, there were no findings of increased morbidity (26, 36, and 20%, respectively) or mortality (11, 18, and 13%, respectively), despite differences in the timing of each group's dialysis. We found that previous cardiac disease, predialysis K<sup>+</sup>, K<sup>+</sup> after dialysis, and APACHE scores were significantly higher in patients with peridialysis morbidity.</p>
<p>Conclusions: We conclude that there is no increased morbidity with early dialysis in AMI, but rather close attention needs to be paid to the rate of decrease in serum potassium in patients with ESRD and their level of acuity when undergoing dialysis.</p>
]]></description>
<dc:creator><![CDATA[Coritsidis, G., Sutariya, D., Stern, A., Gupta, G., Carvounis, C., Arora, R., Balmir, S., Acharya, A.]]></dc:creator>
<dc:date>Tue, 04 Aug 2009 10:02:00 PDT</dc:date>
<dc:identifier>info:doi/10.2215/CJN.04470908</dc:identifier>
<dc:title><![CDATA[Does Timing of Dialysis in Patients with ESRD and Acute Myocardial Infarcts Affect Morbidity or Mortality?]]></dc:title>
<dc:publisher>American Society of Nephrology</dc:publisher>
<prism:number>8</prism:number>
<prism:volume>4</prism:volume>
<prism:endingPage>1330</prism:endingPage>
<prism:publicationDate>2009-08-01</prism:publicationDate>
<prism:startingPage>1324</prism:startingPage>
<prism:section>Dialysis</prism:section>
</item>

<item rdf:about="http://cjasn.asnjournals.org/cgi/content/short/4/8/1331?rss=1">
<title><![CDATA[HFE Mutations Modulate the Effect of Iron on Serum Hepcidin-25 in Chronic Hemodialysis Patients]]></title>
<link>http://cjasn.asnjournals.org/cgi/content/short/4/8/1331?rss=1</link>
<description><![CDATA[
<p>Background and objectives: Increased serum hepcidin has been reported in patients receiving chronic hemodialysis, and hypothesized to contribute to the alterations of iron metabolism of end-stage renal disease. However, no quantitative assessment is available to date; the clinical determinants are still under definition; and the role of genetic factors, namely HFE mutations, has not yet been evaluated. The aim of this study was to quantitatively assess serum hepcidin-25 in hemodialysis patients <I>versus</I> controls, and analyze the relationship between hepcidin, iron indices, HFE genotype, and erythropoietic parameters.</p>
<p>Design, setting, participants &amp; measurements: Sixty-five hemodialysis patients and 57 healthy controls were considered. Hepcidin-25 was evaluated by surface-enhanced laser desorption/ionization time-of-flight mass spectrometry, HFE genotype by restriction analysis.</p>
<p>Results: Serum hepcidin-25 was higher in hemodialysis patients compared with controls. In patients, hepcidin-25 correlated positively with ferritin and C reactive protein, and negatively with serum iron after adjustment for confounders. Hepcidin/ferritin ratio was lower in patients with (n = 25) than in those without (n = 40) HFE mutations. At multivariate analysis, hepcidin-25 was independently associated with ferritin and HFE status. In a subgroup of 22 "stable" patients, <I>i.e.,</I> with Hb levels on target, normal CRP levels, and absence of complications for at least 1 yr, hepcidin-25 was negatively correlated with Hb levels independently of confounders.</p>
<p>Conclusions: Serum hepcidin-25 is increased in hemodialysis patients, regulated by iron stores and inflammation, and relatively reduced in subjects carrying frequent HFE mutations. Hepcidin-25 may contribute to the pathogenesis of anemia by decreasing iron availability.</p>
]]></description>
<dc:creator><![CDATA[Valenti, L., Girelli, D., Valenti, G. F., Castagna, A., Como, G., Campostrini, N., Rametta, R., Dongiovanni, P., Messa, P., Fargion, S.]]></dc:creator>
<dc:date>Tue, 04 Aug 2009 10:02:00 PDT</dc:date>
<dc:identifier>info:doi/10.2215/CJN.01370209</dc:identifier>
<dc:title><![CDATA[HFE Mutations Modulate the Effect of Iron on Serum Hepcidin-25 in Chronic Hemodialysis Patients]]></dc:title>
<dc:publisher>American Society of Nephrology</dc:publisher>
<prism:number>8</prism:number>
<prism:volume>4</prism:volume>
<prism:endingPage>1337</prism:endingPage>
<prism:publicationDate>2009-08-01</prism:publicationDate>
<prism:startingPage>1331</prism:startingPage>
<prism:section>Dialysis</prism:section>
</item>

<item rdf:about="http://cjasn.asnjournals.org/cgi/content/short/4/8/1338?rss=1">
<title><![CDATA[Sustained Low Efficiency Dialysis in the Continuous Mode (C-SLED): Dialysis Efficacy, Clinical Outcomes, and Survival Predictors in Critically Ill Cancer Patients]]></title>
<link>http://cjasn.asnjournals.org/cgi/content/short/4/8/1338?rss=1</link>
<description><![CDATA[
<p>Background and objectives: Oliguric, hypotensive patients who require large amounts of fluids may benefit from sustained low-efficiency dialysis performed continuously (C-SLED). C-SLED through higher clearance may improve survival, or through greater nutritional loss may worsen survival. No studies have assessed survival on C-SLED. The objective was to examine patient outcomes and survival predictors on C-SLED.</p>
<p>Design, setting, participants, &amp; measurements: The data of 199 consecutive cancer patients treated with C-SLED were analyzed. The median duration of C-SLED was 50 h. With 48 h of C-SLED, the blood urea nitrogen (BUN) and serum creatinine levels had decreased by 80% and 73%, respectively. The mean arterial pressure (MAP) was maintained despite higher ultrafiltration and reduced vasopressor use. The 30-d mortality rate was 65%. Despite excellent dialysis, the sequential organ failure assessment (SOFA) score remained predictive of mortality. In the univariate model, higher SOFA scores and lower values for MAP, blood pH, and serum albumin and creatinine levels were associated with higher mortality. Administration of total parenteral nutrition (TPN) was, however, associated with lower mortality.</p>
<p>Results: In the multivariate model, the higher SOFA score and lower blood pH, MAP and C-SLED duration were associated with higher mortality. In a subset analysis of 129 patients who received C-SLED for at least 48 h, those with higher BUN levels, which were associated with higher TPN infusion, had a lower mortality risk.</p>
<p>Conclusion: This first detailed report on C-SLED indicates that C-SLED can be effective and suggests a link between nutrition and survival.</p>
]]></description>
<dc:creator><![CDATA[Salahudeen, A. K., Kumar, V., Madan, N., Xiao, L., Lahoti, A., Samuels, J., Nates, J., Price, K.]]></dc:creator>
<dc:date>Tue, 04 Aug 2009 10:02:00 PDT</dc:date>
<dc:identifier>info:doi/10.2215/CJN.02130309</dc:identifier>
<dc:title><![CDATA[Sustained Low Efficiency Dialysis in the Continuous Mode (C-SLED): Dialysis Efficacy, Clinical Outcomes, and Survival Predictors in Critically Ill Cancer Patients]]></dc:title>
<dc:publisher>American Society of Nephrology</dc:publisher>
<prism:number>8</prism:number>
<prism:volume>4</prism:volume>
<prism:endingPage>1346</prism:endingPage>
<prism:publicationDate>2009-08-01</prism:publicationDate>
<prism:startingPage>1338</prism:startingPage>
<prism:section>Dialysis</prism:section>
</item>

</rdf:RDF>