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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">ETM</journal-id>
<journal-title-group>
<journal-title>Experimental and Therapeutic Medicine</journal-title>
</journal-title-group>
<issn pub-type="ppub">1792-0981</issn>
<issn pub-type="epub">1792-1015</issn>
<publisher>
<publisher-name>D.A. Spandidos</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="publisher-id">ETM-0-0-8608</article-id>
<article-id pub-id-type="doi">10.3892/etm.2020.8608</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Articles</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Characteristics of patients at initiation of renal replacement therapy - experience of a hemodialysis center</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name><surname>Timofte</surname><given-names>Delia</given-names></name>
<xref rid="af1-etm-0-0-8608" ref-type="aff">1</xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Dragos</surname><given-names>Dorin</given-names></name>
<xref rid="af2-etm-0-0-8608" ref-type="aff">2</xref>
<xref rid="af3-etm-0-0-8608" ref-type="aff">3</xref>
<xref rid="fn1-etm-0-0-8608" ref-type="author-notes">&#x002A;</xref>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name><surname>Balcangiu-Stroescu</surname><given-names>Andra-Elena</given-names></name>
<xref rid="af1-etm-0-0-8608" ref-type="aff">1</xref>
<xref rid="af4-etm-0-0-8608" ref-type="aff">4</xref>
<xref rid="fn1-etm-0-0-8608" ref-type="author-notes">&#x002A;</xref>
<xref rid="c1-etm-0-0-8608" ref-type="corresp"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Tanasescu</surname><given-names>Maria-Daniela</given-names></name>
<xref rid="af2-etm-0-0-8608" ref-type="aff">2</xref>
<xref rid="af3-etm-0-0-8608" ref-type="aff">3</xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Gabriela Balan</surname><given-names>Daniela</given-names></name>
<xref rid="af4-etm-0-0-8608" ref-type="aff">4</xref>
<xref rid="fn1-etm-0-0-8608" ref-type="author-notes">&#x002A;</xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Raducu</surname><given-names>Laura</given-names></name>
<xref rid="af5-etm-0-0-8608" ref-type="aff">5</xref>
<xref rid="af6-etm-0-0-8608" ref-type="aff">6</xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Jecan</surname><given-names>Cristian-Radu</given-names></name>
<xref rid="af5-etm-0-0-8608" ref-type="aff">5</xref>
<xref rid="af6-etm-0-0-8608" ref-type="aff">6</xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Stiru</surname><given-names>Ovidiu</given-names></name>
<xref rid="af7-etm-0-0-8608" ref-type="aff">7</xref>
<xref rid="af8-etm-0-0-8608" ref-type="aff">8</xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Medrihan</surname><given-names>Lavinia</given-names></name>
<xref rid="af9-etm-0-0-8608" ref-type="aff">9</xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Ionescu</surname><given-names>Dorin</given-names></name>
<xref rid="af2-etm-0-0-8608" ref-type="aff">2</xref>
<xref rid="af3-etm-0-0-8608" ref-type="aff">3</xref>
<xref rid="fn1-etm-0-0-8608" ref-type="author-notes">&#x002A;</xref>
</contrib>
</contrib-group>
<aff id="af1-etm-0-0-8608"><label>1</label>Department of Dialysis, Emergency University Hospital, 050098 Bucharest, Romania</aff>
<aff id="af2-etm-0-0-8608"><label>2</label>Discipline of Internal Medicine I and Nephrology, Faculty of Medicine, &#x2018;Carol Davila&#x2019; University of Medicine and Pharmacy, 020021 Bucharest, Romania</aff>
<aff id="af3-etm-0-0-8608"><label>3</label>Department of Nephrology, Emergency University Hospital, 050098 Bucharest, Romania</aff>
<aff id="af4-etm-0-0-8608"><label>4</label>Discipline of Physiology, Faculty of Dental Medicine, &#x2018;Carol Davila&#x2019; University of Medicine and Pharmacy, 020021 Bucharest, Romania</aff>
<aff id="af5-etm-0-0-8608"><label>5</label>Discipline of Plastic and Reconstructive Surgery, Faculty of Medicine, &#x2018;Carol Davila&#x2019; University of Medicine and Pharmacy, 020021 Bucharest, Romania</aff>
<aff id="af6-etm-0-0-8608"><label>6</label>Department of Plastic and Reconstructive Surgery, Clinical Emergency Hospital &#x2018;Prof. Dr. Agrippa Ionescu&#x2019;, 011356 Bucharest, Romania</aff>
<aff id="af7-etm-0-0-8608"><label>7</label>Department of Cardiovascular Surgery, Faculty of Medicine, &#x2018;Carol Davila&#x2019; University of Medicine and Pharmacy, 020021 Bucharest, Romania</aff>
<aff id="af8-etm-0-0-8608"><label>8</label>Department of Cardiovascular Surgery, &#x2018;Prof. Dr. C. C. Iliescu&#x2019; Emergency Institute for Cardiovascular Diseases, 022322 Bucharest, Romania</aff>
<aff id="af9-etm-0-0-8608"><label>9</label>Department of Diabetology-Endocrinology-Nutrition, Lille University, 59019 Lille, France</aff>
<author-notes>
<corresp id="c1-etm-0-0-8608"><italic>Correspondence to:</italic> Dr Andra-Elena Balcangiu-Stroescu, Department of Dialysis, Emergency University Hospital, Splaiul Independen&#x0163;ei 169, 050098 Bucharest, Romania <email>stroescu_andra@yahoo.ro</email></corresp>
<fn><p><italic>Abbreviations:</italic> AF, atrial fibrillation; AVF, arterio-venous fistula; CKD, chronic kidney disease; CVC, central venous catheter; DM, diabetes mellitus; HBP, high blood pressure; HF, heart failure; IHD, ischemic heart disease; LVH, left ventricular hypertrophy; PAD, peripheral arterial disease; RRT, renal replacement treatment</p></fn>
<fn id="fn1-etm-0-0-8608"><p><sup>&#x002A;</sup>Contributed equally</p></fn>
</author-notes>
<pub-date pub-type="ppub">
<month>07</month>
<year>2020</year></pub-date>
<pub-date pub-type="epub">
<day>17</day>
<month>03</month>
<year>2020</year></pub-date>
<volume>20</volume>
<issue>1</issue>
<fpage>103</fpage>
<lpage>108</lpage>
<history>
<date date-type="received">
<day>31</day>
<month>01</month>
<year>2020</year>
</date>
<date date-type="accepted">
<day>03</day>
<month>03</month>
<year>2020</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright: &#x00A9; Timofte et al.</copyright-statement>
<copyright-year>2020</copyright-year>
<license license-type="open-access">
<license-p>This is an open access article distributed under the terms of the <ext-link ext-link-type="uri" xlink:href="https://creativecommons.org/licenses/by-nc-nd/4.0/">Creative Commons Attribution-NonCommercial-NoDerivs License</ext-link>, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.</license-p></license>
</permissions>
<abstract>
<p>The monitoring and care of patients with chronic kidney disease (CKD) before the dialysis initiation contribute to a better survival rate and an improvement in quality of life. The patients who do not benefit from a good predialysis management have a worse short and long-term prognosis. A retrospective, unicentric study was performed to evaluate the status of patients with stage 5 CKD at the time of initiation of renal replacement treatment. A total of 109 patients were included in the study. The evaluation of the patients included the clinical manifestations leading to hemodialysis initiation, the clinical and laboratory data of the patients when the hemodialysis was started. Based on the obtained data, a statistical analysis was performed using the Chi-square test, Fisher&#x0027;s exact test, ANOVA, and Kruskal-Wallis H test. The mean age of the patients was 64.61&#x00B1;13.59 years. Of the patients 51.38&#x0025; were women. Vascular nephropathies and diabetes mellitus dominated the etiology of CKD. The comorbidities were high blood pressure, ischemic heart disease, history of myocardial infarction, heart failure, history of stroke, peripheral artery disease or atrial fibrillation. Only 43 (39.45&#x0025;) of our patients were monitored before the hemodialysis initiation. Hemodialysis was initiated on central venous catheter (in most cases non-tunneled) in 78.90&#x0025; of the patients. Most of the patients had an altered general status, fatigue/tiredness with poor exercise capacity when hemodialysis was initiated. Most of the patients (98.17&#x0025;) had anemia, the average level of hemoglobin being 8.69&#x00B1;1.85 g/dl. In conclusion, careful monitoring of patients in the early stages of CKD would result in lower morbidity and mortality. These objectives can be achieved by implementing screening programs and early interventions.</p>
</abstract>
<kwd-group>
<kwd>chronic kidney disease</kwd>
<kwd>predialysis management</kwd>
<kwd>dialysis initiation</kwd>
<kwd>renal replacement treatment</kwd>
<kwd>arterio-venous fistula</kwd>
<kwd>central venous catheters</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<sec sec-type="intro">
<title>Introduction</title>
<p>Chronic kidney disease (CKD) has a considerable impact on health, by progressive loss of kidney functions up to end-stage renal disease (ESRD) requiring renal replacement treatment (RRT), either by dialysis or by kidney transplant. Moreover, health and survival are endangered by the complications associated with CKD, such as anemia, disturbances of bone and mineral metabolism, high blood pressure (HBP), cardiovascular disease, anxiety or depression and altered quality of life (<xref rid="b1-etm-0-0-8608" ref-type="bibr">1</xref>,<xref rid="b2-etm-0-0-8608" ref-type="bibr">2</xref>).</p>
<p>Therefore, an early diagnosis is important, followed by adequate assessment, monitoring, and treatment of patients with CKD, because proper management may slow down the progression and even prevent the occurrence of ESRD (<xref rid="b1-etm-0-0-8608" ref-type="bibr">1</xref>).</p>
<p>Referring these patients to the nephrologist is one of the mainstays of the correct management of CKD. An early assessment by the nephrologist may unravel the etiology of kidney disease and may lead to prompt initiation of strategies able to delay the progressive decline of kidney function, prevent and treat the complications, and appropriately prepare for and timely initiate RRT (<xref rid="b3-etm-0-0-8608" ref-type="bibr">3</xref>).</p>
</sec>
<sec sec-type="Materials|methods">
<title>Materials and methods</title>
<p>This is a retrospective, unicentric study regarding the status of patients with stage 5 CKD at the time of RRT initiation. The evaluation included the clinical manifestations leading to hemodialysis initiation, as well as the clinical and laboratory features of the patients when hemodialysis was started, including etiology of CKD, associated comorbidities, biological status, previous nephrological monitoring, preparation of patients by vascular access creation prior to the initiation of RRT. The subjects of this study were patients with stage 5 CKD admitted to the Nephrology Clinic of the Emergency University Hospital of Bucharest (Romania), in whom hemodialysis was initiated between January 1st, 2017 and March 31st, 2018. The inclusion criteria were age over 18 years and hemodialysis initiation. The exclusion criteria was acute kidney injury unresponsive to conservatory treatment, but with recovery of the kidney function after several hemodialysis sessions.</p>
<p>A total of 109 patients were included in the study. Information was obtained regarding age, gender, socioeconomic background, etiology and duration of CKD, risk factors, history, including HBP, diabetes mellitus (DM), myocardial infarction, left ventricular hypertrophy, ischemic heart disease (IHD), heart failure (HF), stroke, peripheral arterial disease (PAD), and cardiac arrhythmias. The assessment included also routine laboratory tests. Glomerular filtration rate was calculated by means of 2009 CKD-EPI Creatinine Equation. The statistical analysis was performed by means of Chi-square test, Fisher&#x0027;s exact test, ANOVA, and Kruskal-Wallis H test.</p>
<p>This study was approved by Ethics Committee of the Emergency University Hospital of Bucharest. Written informed consent was obtained from all patients prior to publication.</p>
</sec>
<sec sec-type="Results">
<title>Results</title>
<sec>
<title/>
<sec>
<title>Demographics</title>
<p>In our sample, there were 56 (51.38&#x0025;) women and 53 men (48.62&#x0025;). The mean age of the patients was 64.61&#x00B1;13.59 years, with a minimum age of 25 and a maximum of 91 years. In women, the average age was 66.46&#x00B1;14.09 years and in men 62.66&#x00B1;12.88 years. Of the patients 69.72&#x0025; lived in an urban setting.</p>
</sec>
<sec>
<title>Etiology</title>
<p>In our sample, the etiology of CKD was: i) vascular nephropathies (28&#x0025;); ii) DM (24&#x0025;); iii) glomerular nephropathies (10&#x0025;); iv) obstructive nephropathy (9&#x0025;); v) tubulointerstitial nephropathy (5&#x0025;); vi) other etiology including kidney polycystic disease (6&#x0025;); and vii) unknown etiology in 12&#x0025; of the patients. Gender predominance varied according to CKD etiology, with a female preponderance in diabetic nephropathy, obstructive nephropathy, tubulointerstitial nephropathy, and in kidney disease of unknown cause. By contrast, there was a male preponderance for vascular and glomerular nephropathies, and for polycystic kidney disease.</p>
</sec>
<sec>
<title>Comorbidities</title>
<p>Most of our patients (93 i.e., 85.32&#x0025;) had HBP. There was a mild female preponderance (48 out of 93) among our hypertensive patients. There were 46 patients with left ventricular hypertrophy (LVH), most of these patients being males (31 males vs. 15 females). The higher proportion of males was statistically significant: Chi-squared with Yates correction = 3.87 with a P=0.049, while the P-value yielded by Fisher&#x0027;s exact test was 0.036. HF was present in 41 (37.61&#x0025;) patients. A history of stroke was identified in 15 patients (7 females and 8 males). PAD was present in 27 patients (13 females and 14 males). Atrial fibrillation (AF) was present in 19.27&#x0025; of the patients.</p>
</sec>
<sec>
<title>Duration of CKD</title>
<p>The duration of CKD prior to RRT was not known in 42 of our patients. In the other 67 patients, the mean duration of the known evolution of CKD (from the moment of diagnosis until RRT initiation) was 41.28&#x00B1;35.71 months.</p>
</sec>
<sec>
<title>Pre-dialysis monitoring</title>
<p>Only 43 (39.45&#x0025;) of our patients were monitored prior to hemodialysis initiation. Among these patients followed by a nephrologist, there was a higher proportion of females (<xref rid="tI-etm-0-0-8608" ref-type="table">Table I</xref>; <xref rid="f1-etm-0-0-8608" ref-type="fig">Fig. 1</xref>).</p>
</sec>
<sec>
<title>Vascular access and preparation for hemodialysis</title>
<p>In our study, a low availability of arteriovenous fistula (AVF) was identified for hemodialysis initiation: only 10 of or patients (9.17&#x0025;) presented AVF, and only 5 of them had AVF mature enough to be used for hemodialysis. Consequently, hemodialysis was initiated on central venous catheter (CVC) (in most cases non-tunneled) in 78.90&#x0025; of the patients (<xref rid="f2-etm-0-0-8608" ref-type="fig">Fig. 2</xref>).</p>
<p>For the patients included in our study, hemodialysis was initiated at a GFR of 4 to 5 ml/min/1.73 m<sup>2</sup>. Hemodialysis was initiated at a higher GFR in males (5.32&#x00B1;2.14 ml/min/1.73 m&#x00B2;) than in females (4.25&#x00B1;1.96 ml/min/1.73 m&#x00B2;), a statistically significant difference (P=0.007 on ANOVA, P=0.0013, corresponding to a 10.34 statistic, on Kruskal-Wallis H test). Most of the patients included in our study had an altered general status and fatigue/tiredness with poor exercise capacity when started on hemodialysis (<xref rid="f3-etm-0-0-8608" ref-type="fig">Fig. 3</xref>).</p>
</sec>
<sec>
<title>Pulmonary manifestations</title>
<p>Pulmonary manifestations were present in 39.45&#x0025; of the patients and cardiovascular manifestations in more than half of the cases. Acute pulmonary edema was present in 17.43&#x0025; of the patients, but 33.94&#x0025; had clinical and/or laboratory signs of hyperhydration. Digestive manifestations, such as loss of appetite, nausea and vomiting were encountered in most of the patients (78.90&#x0025;) enrolled in our study. Only a low proportion of patients (7.34&#x0025;) had hemorrhagic events when hemodialysis was initiated, and 5.5&#x0025; had an upper gastrointestinal bleeding.</p>
</sec>
<sec>
<title>Neurological manifestations</title>
<p>A proportion of 37.61&#x0025; of the patients had neurological manifestations, but only 1.83&#x0025; had uremic encephalopathy (<xref rid="tII-etm-0-0-8608" ref-type="table">Table II</xref>).</p>
</sec>
<sec>
<title>Anemia</title>
<p>Most of the patients (98.17&#x0025;) had anemia, the mean level of hemoglobin being 8.69&#x00B1;1.85 g/dl. Dividing the patients in three categories based on the level of hemoglobin (10-12 g/dl, 8-9.9 g/dl, and less than 8 g/dl), the middle category was the most numerous (41.28&#x0025;).</p>
<p>In our study, the hemoglobin level did not differ significantly between the patients monitored by a nephrologist (8.71&#x00B1;1.65 g/dl) and the unmonitored ones (8.67&#x00B1;1.98 g/dl) (<xref rid="f4-etm-0-0-8608" ref-type="fig">Fig. 4</xref>).</p>
</sec>
<sec>
<title>Nutritional status</title>
<p>The mean serum albumin level was 3.35&#x00B1;0.70 g/dl and mean serum uric acid 7.44&#x00B1;2.7 mg/dl, while the mean body mass index was 25.97&#x00B1;6.27 kg/m<sup>2</sup>.</p>
</sec>
<sec>
<title>Bone and mineral metabolism</title>
<p>The mean serum calcium level was 7.70&#x00B1;1.11 mg/dl and mean serum phosphorus 6.55&#x00B1;2.43 mg/dl. Most of the patients had hypocalcemia.</p>
</sec>
</sec>
</sec>
<sec sec-type="Discussion">
<title>Discussion</title>
<p>In our study group there were slightly more females, although most of the currently available studies agree on a higher prevalence of CKD in males than in females, and also on a slower progression of CKD in females than in males (<xref rid="b3-etm-0-0-8608" ref-type="bibr">3</xref>). The fact that most of the patients included in the study lived in an urban setting may be explained by healthcare facilities being more readily available to the urban population. The poor access to medical care in the countryside is a consequence of the low socioeconomic level (<xref rid="b4-etm-0-0-8608" ref-type="bibr">4</xref>,<xref rid="b5-etm-0-0-8608" ref-type="bibr">5</xref>). Vascular nephropathies and DM were the dominant etiology of CKD, in agreement with available data pointing out HBP and DM as the main causes of CKD (<xref rid="b6-etm-0-0-8608" ref-type="bibr">6</xref>,<xref rid="b7-etm-0-0-8608" ref-type="bibr">7</xref>). However, it should be noted that HBP may also be the result of CKD, not only the cause (<xref rid="b8-etm-0-0-8608" ref-type="bibr">8</xref>).</p>
<p>Regarding gender predominance for diabetic nephropathy, a recent study concluded that female gender should be counted among the unmodifiable risk factors for diabetic nephropathy, while male gender is one of the factors incriminated for its progression (<xref rid="b7-etm-0-0-8608" ref-type="bibr">7</xref>). It is common knowledge that HBP is one of the major risk factors for glomerulosclerosis (<xref rid="b9-etm-0-0-8608" ref-type="bibr">9</xref>). Both systolic and diastolic arterial pressure were higher in males (<xref rid="b10-etm-0-0-8608" ref-type="bibr">10</xref>). These observations may explain the higher percentage of male patients in our study, with HBP as etiology for CKD. In our study, the patients with CKD secondary to a glomerular disease were more frequently males. As reported in the literature, the gender predominance differs according to the type of glomerular disease: females in lupus nephritis and males in acute post infectious nephritis, focal segmental glomerulosclerosis and IgA nephropathy (<xref rid="b11-etm-0-0-8608" ref-type="bibr">11</xref>). In our study, information was lacking about the exact type of glomerular disease responsible for ESRD, therefore we could not find an explanation for the higher percentage of males in the subset defined by glomerular disease etiology. The female predominance among the patients with obstructive nephropathy as the cause of ESRD in our sample is at odds with the data in the literature, where male gender dominates this particular etiology of ESRD (<xref rid="b12-etm-0-0-8608" ref-type="bibr">12</xref>). For autosomal dominant polycystic kidney disease, the data in the literature indicate that RRT is initiated in males earlier than in females, which may explain the results of our study (<xref rid="b13-etm-0-0-8608" ref-type="bibr">13</xref>).</p>
<p>Most of our patients had HBP, which is in agreement with the data from the literature indicating a 90&#x0025; prevalence of HBP among ESRD patients at the time when hemodialysis is initiated (<xref rid="b14-etm-0-0-8608" ref-type="bibr">14</xref>). Of our patients 68.81&#x0025; had IHD at the time when hemodialysis was started. IHD is an important comorbidity in patients started on hemodialysis, as it is associated with a higher mortality (<xref rid="b15-etm-0-0-8608" ref-type="bibr">15</xref>). Other identifiable comorbidities were left ventricular hypertrophy (LVH), HF, stroke, PAD and AF. The available studies confirm the presence of LVH in patients with ESRD, and associate it with an increased risk of sudden death, highlighting the need that the practitioners should pay particular attention to therapeutic strategies aimed at reducing LVH (<xref rid="b16-etm-0-0-8608" ref-type="bibr">16</xref>). Like IHD, HF is an important risk factor for death in ESRD patients started on hemodialysis, both on short and long-term (<xref rid="b17-etm-0-0-8608" ref-type="bibr">17</xref>). Stroke seems to occur with increased frequency in the 3 months preceding the onset of chronic hemodialysis, the highest risk being in the month preceding the initiation of RRT. However, after starting hemodialysis, the stroke risk declines (<xref rid="b18-etm-0-0-8608" ref-type="bibr">18</xref>). A history of PAD in patients started on chronic hemodialysis is associated with a higher need of either revascularization or amputation (<xref rid="b19-etm-0-0-8608" ref-type="bibr">19</xref>). Patients with AF are known to have a bad prognosis because of a higher risk of cardiovascular events (<xref rid="b20-etm-0-0-8608 b21-etm-0-0-8608 b22-etm-0-0-8608 b23-etm-0-0-8608" ref-type="bibr">20-23</xref>).</p>
<p>According to literature, the evolution of CKD to more advanced stages is slower in elderly patients (<xref rid="b24-etm-0-0-8608" ref-type="bibr">24</xref>).</p>
<p>The patient with CKD needs specialized care. The guidelines state that specialized nephrological care is preferable for patients with a GFR &#x003C;60 ml/min/1.73 m<sup>2</sup> and mandatory for those with a GFR &#x003C;30 ml/min/1.73 m<sup>2</sup> (<xref rid="b25-etm-0-0-8608" ref-type="bibr">25</xref>). The occurrence of complications typical for CKD (HBP, cardiovascular disease, anemia, bone and mineral metabolism disturbances, anxiety or depression) has an important impact on the health status and on the survival of these patients (<xref rid="b1-etm-0-0-8608" ref-type="bibr">1</xref>). Early monitoring and implementation of therapeutic strategies aimed at slowing down the progressive decline of kidney function, as well as adequate preparation for and timely initiation of RRT, are important for ameliorating the prognosis of these patients (<xref rid="b2-etm-0-0-8608" ref-type="bibr">2</xref>). Delaying the referral to a nephrologist is one of the major issues leading to suboptimal care of a CKD patient. A patient not included soon enough in a monitoring program lead by a nephrologist is more likely to be started on RRT on an emergency basis, which may be deleterious for the outcome of the patient, resulting in lower quality of life and increased morbidity, mortality, and healthcare costs (<xref rid="b26-etm-0-0-8608" ref-type="bibr">26</xref>).</p>
<p>When RRT is required, the clinician together with the patient have to choose between hemodialysis, peritoneal dialysis and kidney transplant. The first option for treatment of choice (in Romania and in most other countries) is hemodialysis (<xref rid="b27-etm-0-0-8608" ref-type="bibr">27</xref>). Performing hemodialysis requires vascular (venous) access. The conclusion of most of the studies and the current recommendation in most of the guidelines is that the preferred vascular access for hemodialysis initiation is an arteriovenous fistula (AVF). However, in most ESRD patients hemodialysis is initiated on a CVC, either untunneled or tunneled (<xref rid="b28-etm-0-0-8608" ref-type="bibr">28</xref>). The data collected in our study are consistent with the literature. Suboptimal preparation of the patients is the result of poor referral to the specialist. Regarding GFR, there is no optimal level for hemodialysis initiation defined by the guidelines. The symptoms and the general lack of well-being of the patient, rather than a certain GFR are major criteria for starting hemodialysis (<xref rid="b27-etm-0-0-8608" ref-type="bibr">27</xref>). However, the occurrence of certain manifestations recommend earlier initiation of hemodialysis, even at a GFR of 15 ml/min/1.73 m<sup>2</sup>, including hyperkalemia, hyper hydration, weight loss and malnutrition, cognitive decline (<xref rid="b29-etm-0-0-8608" ref-type="bibr">29</xref>,<xref rid="b30-etm-0-0-8608" ref-type="bibr">30</xref>). The identified symptomatology of our patients is in line with specialty literature: pulmonary, cardiovascular and digestive manifestations, acute pulmonary edema.</p>
<p>CKD patients are known to have a higher risk of bleeding, gastrointestinal tract being frequently involved (<xref rid="b31-etm-0-0-8608" ref-type="bibr">31</xref>).</p>
<p>However, our study identified an unacceptably high number of patients with a hemoglobin level below 8 g/dl, which is an important issue because a level of hemoglobin below 8 g/dl is associated with higher mortality. This increased death risk persists even if the hemoglobin level is restored to above 10 g/dl after 4 months of dialysis (<xref rid="b32-etm-0-0-8608" ref-type="bibr">32</xref>). The most probable explanation is that among the 43 patients monitored by a nephrologist only a few (23.26&#x0025;) received an erythropoiesis stimulating agent, and none of them reached the targeted level of hemoglobin, a sobering fact that underlines the necessity of improving anemia management in predialysis patients (<xref rid="b32-etm-0-0-8608" ref-type="bibr">32</xref>).</p>
<p>Both in predialysis and in chronically hemodialysis patients there is a close relation between the nutritional status and mortality (<xref rid="b33-etm-0-0-8608" ref-type="bibr">33</xref>). The nutritional status was assessed by means of the body mass index and the serum albumin level, lipid fractions, and uric acid. In most of the subjects the serum cholesterol level was below 150 mg/dl, while the serum triglycerides level was normal, which differs from the results of other studies in which the serum triglycerides level was increased (<xref rid="b34-etm-0-0-8608" ref-type="bibr">34</xref>,<xref rid="b35-etm-0-0-8608" ref-type="bibr">35</xref>). In our study, we evaluated markers of nutritional status (albumin, uric acid, body mass index), as well as bone and mineral metabolism (calcium, phosphorus) markers.</p>
<p>Unfortunately, data regarding the serum PTH level were not available. Assessing for bone and mineral metabolism disorders is of paramount importance for the survival of the patients on chronic hemodialysis, because these complications have a great impact on both morbidity and mortality (<xref rid="b36-etm-0-0-8608" ref-type="bibr">36</xref>,<xref rid="b37-etm-0-0-8608" ref-type="bibr">37</xref>), due to their close association with cardiovascular complications (<xref rid="b38-etm-0-0-8608" ref-type="bibr">38</xref>).</p>
<p>In conclusion, increasing the number of monitored patients in early stages of CKD and improving their management result in lower morbidity and mortality. These objectives may be achieved by implementing screening programs and early interventions. In the advanced stages of the disease, when RRT is needed, choosing the optimal moment and the type of treatment are decisions that should be taken by the physician together with the patient and his/her family members and individually adapted to the needs of each patient.</p>
</sec>
</body>
<back>
<ack>
<title>Acknowledgements</title>
<p>Not applicable.</p>
</ack>
<sec>
<title>Funding</title>
<p>No funding was received.</p>
</sec>
<sec>
<title>Availability of data and materials</title>
<p>Due to confidentiality reasons data generated or analyzed during this study are not included in this published article.</p>
</sec>
<sec>
<title>Authors&#x0027; contributions</title>
<p>DT, DD, AEBS, DGB, OS and DI designed the study, analysed and interpreted datasets and wrote the manuscript. MDT and LM collected the data and analysed the datasets. DT, DD, AEBS, DGB, OS, DI, LR and CRJ performed a literature search and selected the studies to be included. DT, DD, AEBS, DGB, OS and DI critically revised the manuscript. All authors read and approved the final manuscript. The contributions of all the authors on this article are greatly valued and appreciated.</p>
</sec>
<sec>
<title>Ethics approval and consent to participate</title>
<p>This study was approved by Ethics Committee of the Emergency University Hospital of Bucharest (Romania). Written informed consent was obtained from all patients prior to publication.</p>
</sec>
<sec>
<title>Patient consent for publication</title>
<p>Not applicable.</p>
</sec>
<sec>
<title>Competing interests</title>
<p>The authors declare that they have no competing interests.</p>
</sec>
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<floats-group>
<fig id="f1-etm-0-0-8608" position="float">
<label>Figure 1</label>
<caption><p>Distribution of patients as a function of predialysis monitoring. F, female; M, male.</p></caption>
<graphic xlink:href="etm-20-01-0103-g00.tif" />
</fig>
<fig id="f2-etm-0-0-8608" position="float">
<label>Figure 2</label>
<caption><p>Distribution of the patients as a function of FAV existence at the initiation hemodialysis. AVF, arteriovenous fistula.</p></caption>
<graphic xlink:href="etm-20-01-0103-g01.tif" />
</fig>
<fig id="f3-etm-0-0-8608" position="float">
<label>Figure 3</label>
<caption><p>Distribution of the patients as a function of clinical manifestations at hemodialysis initiation.</p></caption>
<graphic xlink:href="etm-20-01-0103-g02.tif" />
</fig>
<fig id="f4-etm-0-0-8608" position="float">
<label>Figure 4</label>
<caption><p>Distribution of the patients as a function of hemoglobin level.</p></caption>
<graphic xlink:href="etm-20-01-0103-g03.tif" />
</fig>
<table-wrap id="tI-etm-0-0-8608" position="float">
<label>Table I</label>
<caption><p>The characteristics of the study group.</p></caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="middle">General characteristics</th>
<th align="center" valign="middle">Values</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="middle">Total number of patients</td>
<td align="center" valign="middle">109</td>
</tr>
<tr>
<td align="left" valign="middle">Sex</td>
<td align="center" valign="middle">F: 51.38&#x0025;; M: 48.62&#x0025;</td>
</tr>
<tr>
<td align="left" valign="middle">Socioeconomic background</td>
<td align="center" valign="middle">Urban: 69.72&#x0025;; Rural: 30.28&#x0025;</td>
</tr>
<tr>
<td align="left" valign="middle">Mean age</td>
<td align="center" valign="middle">64.61&#x00B1;13.59 years</td>
</tr>
<tr>
<td align="left" valign="middle">Duration of CKD</td>
<td align="center" valign="middle">41.28&#x00B1;35.71 months</td>
</tr>
<tr>
<td align="left" valign="middle">Body mass index</td>
<td align="center" valign="middle">25.97&#x00B1;6.27 kg/m<sup>2</sup></td>
</tr>
<tr>
<td align="left" valign="middle" colspan="2">CKD etiology (&#x0025;)</td>
</tr>
<tr>
<td align="left" valign="middle">&#x00A0;&#x00A0;&#x00A0;&#x00A0;&#x00A0;Vascular nephropathies</td>
<td align="center" valign="middle">28.44</td>
</tr>
<tr>
<td align="left" valign="middle">&#x00A0;&#x00A0;&#x00A0;&#x00A0;&#x00A0;Diabetic nephropathy</td>
<td align="center" valign="middle">23.85</td>
</tr>
<tr>
<td align="left" valign="middle">&#x00A0;&#x00A0;&#x00A0;&#x00A0;&#x00A0;Glomerular nephropathy</td>
<td align="center" valign="middle">10.09</td>
</tr>
<tr>
<td align="left" valign="middle">&#x00A0;&#x00A0;&#x00A0;&#x00A0;&#x00A0;Tubulointerstitial nephropathy</td>
<td align="center" valign="middle">4.59</td>
</tr>
<tr>
<td align="left" valign="middle">&#x00A0;&#x00A0;&#x00A0;&#x00A0;&#x00A0;Polycystic kidney disease</td>
<td align="center" valign="middle">6.42</td>
</tr>
<tr>
<td align="left" valign="middle">&#x00A0;&#x00A0;&#x00A0;&#x00A0;&#x00A0;Obstructive nephropathy</td>
<td align="center" valign="middle">9.17</td>
</tr>
<tr>
<td align="left" valign="middle">&#x00A0;&#x00A0;&#x00A0;&#x00A0;&#x00A0;Unknown etiology</td>
<td align="center" valign="middle">11.93</td>
</tr>
<tr>
<td align="left" valign="middle" colspan="2">Comorbidities (&#x0025;)</td>
</tr>
<tr>
<td align="left" valign="middle">&#x00A0;&#x00A0;&#x00A0;&#x00A0;&#x00A0;High blood pressure</td>
<td align="center" valign="middle">85.32</td>
</tr>
<tr>
<td align="left" valign="middle">&#x00A0;&#x00A0;&#x00A0;&#x00A0;&#x00A0;Ischemic heart disease</td>
<td align="center" valign="middle">68.81</td>
</tr>
<tr>
<td align="left" valign="middle">&#x00A0;&#x00A0;&#x00A0;&#x00A0;&#x00A0;Left ventricular hypertrophy</td>
<td align="center" valign="middle">42.20</td>
</tr>
<tr>
<td align="left" valign="middle">&#x00A0;&#x00A0;&#x00A0;&#x00A0;&#x00A0;Cardiac failure</td>
<td align="center" valign="middle">37.61</td>
</tr>
<tr>
<td align="left" valign="middle">&#x00A0;&#x00A0;&#x00A0;&#x00A0;&#x00A0;Stroke</td>
<td align="center" valign="middle">13.76</td>
</tr>
<tr>
<td align="left" valign="middle">&#x00A0;&#x00A0;&#x00A0;&#x00A0;&#x00A0;Peripheral arterial disease</td>
<td align="center" valign="middle">24.77</td>
</tr>
<tr>
<td align="left" valign="middle">&#x00A0;&#x00A0;&#x00A0;&#x00A0;&#x00A0;Atrial fibrillation</td>
<td align="center" valign="middle">19.27</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn><p>F, female; M, male; CKD, chronic kidney disease.</p></fn>
</table-wrap-foot>
</table-wrap>
<table-wrap id="tII-etm-0-0-8608" position="float">
<label>Table II</label>
<caption><p>Biological parameters of the study group.</p></caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="middle">Parameters</th>
<th align="center" valign="middle">Values</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="middle">Hemoglobin</td>
<td align="center" valign="middle">8.6&#x00B1;1.8 g/dl</td>
</tr>
<tr>
<td align="left" valign="middle">Cholesterol</td>
<td align="center" valign="middle">173.14&#x00B1;47.14 mg/dl</td>
</tr>
<tr>
<td align="left" valign="middle">Triglycerides</td>
<td align="center" valign="middle">164.04&#x00B1;91.32 mg/dl</td>
</tr>
<tr>
<td align="left" valign="middle">Calcium</td>
<td align="center" valign="middle">7.7&#x00B1;1.11 mg/dl</td>
</tr>
<tr>
<td align="left" valign="middle">Phosphorus</td>
<td align="center" valign="middle">6.55&#x00B1;2.43 mg/dl</td>
</tr>
<tr>
<td align="left" valign="middle">Calcium x Phosphorus</td>
<td align="center" valign="middle">33.2&#x00B1;27.2 mg/dl</td>
</tr>
<tr>
<td align="left" valign="middle">Potassium</td>
<td align="center" valign="middle">5.06&#x00B1;1.32 mmol/dl</td>
</tr>
<tr>
<td align="left" valign="middle">Uric acid</td>
<td align="center" valign="middle">7.4&#x00B1;2.7 mg/dl</td>
</tr>
<tr>
<td align="left" valign="middle">Albumin</td>
<td align="center" valign="middle">3.35&#x00B1;0.70 g/dl</td>
</tr>
</tbody>
</table>
</table-wrap>
</floats-group>
</article>
