<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.1d1 20130915//EN" "JATS-journalpublishing1.dtd">
<article article-type="research-article" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:mml="http://www.w3.org/1998/Math/MathML" xml:lang="en">
<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">JRENHEP</journal-id>
<journal-title-group>
<journal-title>Journal of Renal and Hepatic Disorders</journal-title>
<abbrev-journal-title>JRENHEP</abbrev-journal-title>
</journal-title-group>
<issn pub-type="epub">2207-3744</issn>
<publisher>
<publisher-name>Codon Publications</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="publisher-id">JRENHEP-5-044</article-id>
<article-id pub-id-type="doi">10.15586/jrenhep.v5i1.98</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>ORIGINAL ARTICLE</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Echocardiographic Changes in Patients with End-Stage Renal Disease at Initiation of Dialysis</article-title>
</title-group>
<contrib-group content-type="authors">
<contrib contrib-type="author"><name><surname>Nazneen</surname> <given-names>Shabana</given-names></name></contrib> 
<contrib contrib-type="author" corresp="yes"><name><surname>Latief</surname> <given-names>Muzamil</given-names></name><xref ref-type="corresp" rid="cor1"/></contrib> 
<contrib contrib-type="author"><name><surname>Yadla</surname> <given-names>Manjusha</given-names></name></contrib>
<aff id="aff1">Department of Nephrology, Gandhi Medical College, Secunderabad, Hyderabad, India</aff>
</contrib-group>
<author-notes>
<corresp id="cor1"><italic>Author for correspondence</italic>: Latief M, Department of Nephrology, Gandhi Medical College, Secunderabad, Hyderabad, India, Email: <email>muzamillatief.b@gmail.com</email></corresp>
</author-notes>
<pub-date pub-type="epub">
<day>08</day>
<month>06</month>
<year>2021</year>
</pub-date>
<pub-date pub-type="collection"><year>2021</year></pub-date>
<volume>5</volume>
<issue>1</issue>
<fpage>44</fpage>
<lpage>48</lpage>
<history>
<date date-type="received"><day>28</day><month>04</month><year>2021</year></date> 
<date date-type="accepted"><day>29</day><month>05</month><year>2021</year></date> 
</history>
<permissions>
<copyright-statement><italic>Copyright</italic>: Nazneen S, et al.</copyright-statement>
<copyright-year>2021</copyright-year>
<license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/4.0/">
<license-p>This open access article is licensed under Creative Commons Attribution 4.0 International (CC BY 4.0). <ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by/4.0">http://creativecommons.org/licenses/by/4.0</ext-link></license-p>
</license>
</permissions>
<abstract>
<sec id="st1">
<title>Introduction</title>
<p>Echocardiography is a simple and established method of evaluating cardiac functions, assessing left ventricle geometry, and systolic and diastolic functions. Patients with chronic kidney disease have a tremendous burden of cardiovascular disease (CVD), and patients with end-stage renal disease (ESRD) are at a greater risk of CVD and deaths.</p>
</sec>
<sec id="st2">
<title>Materials and Methods</title>
<p>In this study, 245 incident dialysis patients were included, and none of the patient was on erythropoietin. All the patients were aged &#x003E;18 years. Patients with ESRD, already on maintenance dialysis, were not included in this study. Patient&#x2019;s data such as demographic details, comorbidities, laboratory values, echocardiographic changes, management, and outcome were recorded.</p>
</sec>
<sec id="st3">
<title>Results</title>
<p>Out of 245 patients, 165 (67.3%) were males and 80 (32.6%) females. The mean age of the patients was 49.7 years. Left ventricular hypertrophy (LVH) was observed in 188 (76.7%), mild left ventricular dysfunction (LVD) in 25.7%, moderate LVD in 23.67%, severe LVD in 8.5%, global hypokinesia in 33.8%, valvular heart disease in 26.5%, regional wall motion abnormality in 4.4%, and pericardial effusion in 1.6% patients. Echocardiographic changes, such as LVD, LVH, and global hypokinesia, were observed in greater number in hypertensive group compared to normotensive group (P &#x003C; 0.05). On regression analysis adjusted for age and gender, we found that hypertension and anemia (&#x003C;10 g/dL) were associated with LVH. Further, hypertension and anemia (Hb &#x003C; 10 g/dL) were associated with LVD. Similarly, anemia (Hb &#x003C; 10 g/dL) was associated with global hypokinesia and valvular heart disease. LVD was associated with death in our study.</p>
</sec>
<sec id="st4">
<title>Conclusion</title>
<p>Echocardiography is a noninvasive diagnostic test which detects early changes in cardiac parameters. All ESRD patients with hypertension and anemia at the time of initiation of renal replacement therapy must undergo echocardiography screening.</p>
</sec>
</abstract>
<kwd-group>
<kwd>echocardiography</kwd>
<kwd>hypertension</kwd>
<kwd>CKD</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<sec id="S1" sec-type="intro">
<title>Introduction</title>
<p>Patients with chronic kidney disease (CKD) have a tremendous burden of cardiovascular disease (CVD), and patients with end-stage renal disease (ESRD) are at a greater risk of CVD and death (<xref ref-type="bibr" rid="ref1">1</xref>,<xref ref-type="bibr" rid="ref2">2</xref>,<xref ref-type="bibr" rid="ref3">3</xref>). CKD is a risk factor for cardiovascular events, and the risk of events increases as CKD progresses to ESRD. Association of CKD with CVD is commonly explained by a typical clustering of several cardiovascular risk factors, including traditional and nontraditional CKD-related factors (<xref ref-type="bibr" rid="ref2">2</xref>,<xref ref-type="bibr" rid="ref3">3</xref>,<xref ref-type="bibr" rid="ref4">4</xref>). Anemia and hypertension are most consistently associated with cardiac failure, a pre-lethal occurrence that leads to two-thirds of deaths in all patients on dialysis (<xref ref-type="bibr" rid="ref5">5</xref>). The risk of cardiovascular mortality is 10- to 20-fold higher than in age- and gender-matched control subjects (<xref ref-type="bibr" rid="ref2">2</xref>,<xref ref-type="bibr" rid="ref5">5</xref>). One of the major structural cardiac abnormalities in patients with CKD is left ventricular hypertrophy (LVH), which is associated with increased risk for cardiac ischemia, congestive heart failure as well as a very strong independent predictor of cardiovascular mortality (<xref ref-type="bibr" rid="ref1">1</xref>,<xref ref-type="bibr" rid="ref6">6</xref>,<xref ref-type="bibr" rid="ref7">7</xref>). LVH is the most common geometric abnormality in CKD and independent prognostic predictor, especially in patients on dialysis (<xref ref-type="bibr" rid="ref8">8</xref>). Left ventricular dysfunction (LVD) on start of hemodialysis is a stratifying risk of CVD and an all-cause mortality in ESRD (<xref ref-type="bibr" rid="ref6">6</xref>,<xref ref-type="bibr" rid="ref9">9</xref>). It is strongly associated with cardiac failure and as one of the independent predictors of cardiovascular death. Echocardiography is a simple and established method of evaluating cardiac functions, assessing left ventricle geometry, and systolic and diastolic functions.</p>
</sec>
<sec id="S2" sec-type="materials|methods">
<title>Materials and Methods</title>
<p>In this prospective observational study conducted in a tertiary care teaching hospital over a period of 1 year, the included patients were incident dialysis patients, and none of the patient was on erythropoietin. All the patients were aged &#x003E;18 years. Patients with ESRD already on maintenance dialysis were not included in this study. Patient data such as demographic details, comorbidities, laboratory values, echocardiographic changes, management, and outcome were recorded. Echocardiography (two-dimensional and M-mode) was done in all patients. A total of 245 patients were included in the study. Data analysis was performed using statistical software SPSS (Version 20.0). Descriptive statistics were used for the analysis. Statistical tests were two-tailed, and P &#x003C; 0.05 was considered to show a statistical difference. Chi-square test for association was performed between different treatment modalities used and the patient outcomes.</p>
</sec>
<sec id="S3" sec-type="results">
<title>Results</title>
<p>Out of the included 245 patients, 165 (67.3%) were males and 80 (32.6%) females. The mean age of the patients was 49.7 years, and the mean serum creatinine was 7.7 mg/dL. The majority of patients were in the age group of 41&#x2013;50 years, as shown in <xref ref-type="table" rid="T1">Table 1</xref>. Hypertension was found in 199 (81%), diabetes in 70 (28.5%), coronary heart disease (CHD) in 18 (7.3%), and anemia in 193 (78.7%) patients. Etiology of the CKD was presumed. Chronic interstitial nephritis (CIN) was established in 189 (77.1%), chronic glomerulonephritis (CGN) in 26 (10.6%), diabetic kidney disease in 23 (9.38%), and polycystic kidney disease in 7 (2.8%) patients. LVH was observed in 188 (76.7%), mild LVD in 25.7%, moderate LVD in 23.67%, severe LVD in 8.5%, global hypokinesia in 33.8%, valvular heart disease in 26.5%, regional wall motion abnormality (RWMA) in 4.4%, and pericardial effusion in 1.6% patients (<xref ref-type="table" rid="T2">Table 2</xref>). Echocardiographic changes, such as LVD, left ventricular hypertrophy (LVH), and global hypokinesia, were found in greater number in hypertensive group compared to normotensive group (P &#x003C; 0.05) (<xref ref-type="table" rid="T3">Table 3</xref>). Patients with hemoglobin (Hb) &#x003C; 10 gm/dL had echocardiographic changes such as LVH in 82%, LVD in 66%, global hypokinesia in 49%, and valvular heart disease in 30% patients, with statistically significant P &#x003C; 0.05, compared with anemic patients with Hb &#x003E;10 gm/dL (<xref ref-type="table" rid="T4">Table 4</xref>). Patients were further analyzed on the basis of ejection fraction (EF), and demographic details, comorbidities, and echocardiographic changes and outcomes were also studied. In reduced EF group, 68.7% were females, 64% had hypertension, 75.8% had LVH, and RWMA was found in 81.8% patients. Among patients who died, 92.3% had reduced EF (<xref ref-type="table" rid="T5">Table 5</xref>). Patients with LVD and global hypokinesia had higher mortality compared with those who had normal left ventricular function with a statistically significant P &#x003C; 0.05 (<xref ref-type="table" rid="T6">Table 6</xref>). On regression analysis adjusted for age and gender, we found that hypertension and anemia (Hb &#x003C; 10 g/dL) was associated with LVH with odds ratio (OR) = 0.06 and 0.29 (P &#x003C; 0.001 and P = 0.003), respectively. Further, hypertension and anemia (Hb &#x003C; 10 g/dL) were associated with LVD with OR = 3.36 and 5.04 (P = 0.001 and P &#x003C; 0.001), respectively. Similarly, anemia (Hb &#x003C; 10 g/dL) was associated with global hypokinesia, OR = 8.44 (P &#x003C; 0.001) and valvular heart disease, OR = 4.02 (P = 0.006). LVD was associated with mortality with OR = 16.9 (P = 0.001).</p>
<table-wrap id="T1" orientation="portrait" position="float">
<label>Table 1:</label><caption><p>Demographic details of patients</p></caption>
<table frame="border" rules="all">
<thead valign="top">
<tr>
<th>Mean age</th>
<th align="center">49.7</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td>Mean serum creatinine</td>
<td align="center">7.7</td>
</tr>
<tr>
<td>Males</td>
<td align="center">165 (67%)</td>
</tr>
<tr>
<td>Females</td>
<td align="center">80</td>
</tr>
</tbody>
</table></table-wrap>
<table-wrap id="T2" orientation="portrait" position="float">
<label>Table 2:</label><caption><p>Echocardiographic changes.</p></caption>
<table frame="border" rules="all">
<thead valign="top">
<tr>
<th>Echocardiographic Changes</th>
<th align="center">Number of Patients<break/>N (%)</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td>LVH</td>
<td>188 (76.7%)</td>
</tr>
<tr>
<td>Mild LVD</td>
<td>63 (25.7%)</td>
</tr>
<tr>
<td>Moderate LVD</td>
<td>58 (23.67%)</td>
</tr>
<tr>
<td>Severe LVD</td>
<td>21 (8.5%)</td>
</tr>
<tr>
<td>Global hypokinesia</td>
<td>83 (33.8%)</td>
</tr>
<tr>
<td>RWMA</td>
<td>11 (4.4%)</td>
</tr>
<tr>
<td>Valvular heart disease</td>
<td>65 (26.5%)</td>
</tr>
<tr>
<td>Pericardial effusion</td>
<td>4 (1.6%)</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn id="TF2-1"><p>RWMA: regional wall motion abnormalities; LVD: left ventricular dysfunction; LVH: left ventricular hypertrophy.</p></fn></table-wrap-foot>
</table-wrap>
<table-wrap id="T3" orientation="portrait" position="float">
<label>Table 3:</label><caption><p>Echocardiographic changes compared in normotensive and hypertensive patients.</p></caption>
<table frame="border" rules="all">
<thead valign="top">
<tr>
<th>&#x00A0;</th>
<th align="center">Hypertensive (N = 199)</th>
<th align="center">Normotensive (N = 46)</th>
<th align="center">P-value</th> 
</tr>
</thead>
<tbody valign="top">
<tr>
<td>LVD</td>
<td>128</td>
<td>14</td>
<td>0.00032</td>
</tr>
<tr>
<td>LVH</td>
<td>174</td>
<td>14</td>
<td>&#x003C;0.001</td>
</tr>
<tr>
<td>Global hypokinesia</td>
<td>74</td>
<td>9</td>
<td>0.02</td>
</tr>
<tr>
<td>RWMA</td>
<td>10</td>
<td>1</td>
<td>0.47</td>
</tr>
<tr>
<td>Valvular heart disease</td>
<td>59</td>
<td>6</td>
<td>0.025</td>
</tr>
<tr>
<td>Pericardial effusion</td>
<td>2</td>
<td>2</td>
<td>0.16</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn id="TF3-1"><p>RWMA: regional wall motion abnormalities; LVD: left ventricular dysfunction; LVH: left ventricular hypertrophy.</p></fn></table-wrap-foot>
</table-wrap>
<table-wrap id="T4" orientation="portrait" position="float">
<label>Table 4:</label><caption><p>Echo changes compared with hemoglobin values.</p></caption>
<table frame="border" rules="all">
<thead valign="top">
<tr>
<th>&#x00A0;</th>
<th align="center">Hb &#x003C; 10 gm/dL (N = 193)</th> 
<th align="center">Hb &#x003E; 10 gm/dL (N = 52)</th>
<th align="center">P-value</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td>LVH</td>
<td>159 (82%)</td>
<td>29 (15%)</td>
<td>0.0003</td>
</tr>
<tr>
<td>LVD</td>
<td>128 (66%)</td>
<td>14 (7.2%)</td>
<td>&#x003C;0.0001</td>
</tr>
<tr>
<td>Global hypokinesia</td>
<td>79 (49%)</td>
<td>4 (2%)</td>
<td>0.000004</td>
</tr>
<tr>
<td>RWMA</td>
<td>10 (5.1%)</td>
<td>1 (0.5%)</td>
<td>0.47</td>
</tr>
<tr>
<td>Valvular heart disease</td>
<td>58 (30%)</td>
<td>7 (3.6%)</td>
<td>0.02</td>
</tr>
<tr>
<td>Pericardial effusion</td>
<td>3 (1.5%)</td>
<td>1 (0.5%)</td>
<td>1</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn id="TF4-1"><p>RWMA: regional wall motion abnormalities; LVD: left ventricular dysfunction; LVH: left ventricular hypertrophy.</p></fn></table-wrap-foot>
</table-wrap>
<table-wrap id="T5" orientation="portrait" position="float">
<label>Table 5:</label><caption><p>Comparison of groups with preserved and reduced ejection fraction</p></caption>
<table frame="border" rules="all">
<thead valign="top">
<tr>
<th>Column 1</th>
<th align="center">Preserved EF (103)</th>
<th align="center">Reduced EF (n = 142)</th>
<th align="center">P value</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td>Male</td>
<td>76 (46.6%)</td>
<td>87 (53.7%)</td>
<td>&#x00A0;</td>
</tr>
<tr>
<td>Female</td>
<td>26 (32.5%)</td>
<td>55 (68.7%)</td>
<td>&#x00A0;</td>
</tr>
<tr>
<td>HTN</td>
<td>71 (35.6%)</td>
<td>128 (64%)</td>
<td>0.00003</td>
</tr>
<tr>
<td>DM</td>
<td>29 (41.4%)</td>
<td>41 (56.9%)</td>
<td>1</td>
</tr>
<tr>
<td>CAD</td>
<td>3 (16.6%)</td>
<td>15 (83%)</td>
<td>0.02</td>
</tr>
<tr>
<td>LVH</td>
<td>43 (24%)</td>
<td>135 (75.8%)</td>
<td>2.6</td>
</tr>
<tr>
<td>RWMA</td>
<td>2 (18%)</td>
<td>9 (81.8%)</td>
<td>0.1</td>
</tr>
<tr>
<td>Valvular heart disease</td>
<td>14 (22.9%)</td>
<td>47 (77%)</td>
<td>0.00052</td>
</tr>
<tr>
<td>PE</td>
<td>2 (40%)</td>
<td>3 (60%)</td>
<td>1</td>
</tr>
<tr>
<td>Global hypokinesia</td>
<td>13 (13.5%)</td>
<td>83 (86.4%)</td>
<td>2.3</td>
</tr>
<tr>
<td>Hb &#x003C; 10 gm/dL</td>
<td>65 (33.6%)</td>
<td>128 (66.3%)</td>
<td>3.7</td>
</tr>
<tr>
<td>Death</td>
<td>2 (7.6%)</td>
<td>24 (92.3%)</td>
<td>0.00021</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn id="TF5-1"><p>HTN: Hypertension; DM : Diabetes Mellitus; CAD: Coronary artery disease; LVH: Left Ventricular Hypertrophy; PE: Pericardial Effusion; Hb: Haemoglobin</p></fn></table-wrap-foot>
</table-wrap>
<table-wrap id="T6" orientation="portrait" position="float">
<label>Table 6:</label><caption><p>Factors associated with mortality.</p></caption>
<table frame="border" rules="all">
<thead valign="top">
<tr>
<th>&#x00A0;</th>
<th align="center">Death<break/>N = 26</th>
<th align="center">Alive</th>
<th align="center">P-value</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td>Hb &#x003C; 10 gm/dL</td>
<td>23</td>
<td>&#x00A0;</td>
<td>0.3</td>
</tr>
<tr>
<td>LVH</td>
<td>23</td>
<td>&#x00A0;</td>
<td>0.2</td>
</tr>
<tr>
<td>LVD</td>
<td>24</td>
<td>&#x00A0;</td>
<td>0.002</td>
</tr>
<tr>
<td>Global hypokinesia</td>
<td>19</td>
<td>&#x00A0;</td>
<td>0.0001</td>
</tr>
<tr>
<td>RWMA</td>
<td>3</td>
<td>&#x00A0;</td>
<td>0.1</td>
</tr>
<tr>
<td>Valvular heart disease</td>
<td>9</td>
<td>&#x00A0;</td>
<td>0.3</td>
</tr>
<tr>
<td>Pericardial effusion</td>
<td>1</td>
<td>&#x00A0;</td>
<td>0.3</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn id="TF6-1"><p>RWMA: regional wall motion abnormalities; LVD: left ventricular dysfunction; LVH: left ventricular hypertrophy.</p></fn></table-wrap-foot>
</table-wrap>
</sec>
<sec id="S4" sec-type="discussion">
<title>Discussion</title>
<p>Cardiovascular disease is very common in patients with CKD, and is by far the leading cause of morbidity and mortality in end-stage renal disease. We observed that majority of the patients were aged 41&#x2013;50 years, with the mean age of 49.7 years, similar to the findings of Singh et al. (<xref ref-type="bibr" rid="ref5">5</xref>) (<xref ref-type="table" rid="T7">Table 7</xref>). In our study, male population (67%) was predominant, similar to Singh et al. (<xref ref-type="bibr" rid="ref5">5</xref>) and Foley et al. (<xref ref-type="bibr" rid="ref7">7</xref>). Hypertension was found in 81.2% patients, correlating with other studies (<xref ref-type="bibr" rid="ref6">6</xref>,<xref ref-type="bibr" rid="ref8">8</xref>). We observed significant echocardiographic changes in hypertensive group compared to normotensive group. LVH was examined in 76% patients, as observed by Laddha et al., who observed LVH in 74% patients in their study (<xref ref-type="bibr" rid="ref10">10</xref>). In a study conducted by Zoccali et al., LVH was found in 77% patients (<xref ref-type="bibr" rid="ref9">9</xref>). Similar observations were made by Singh et al. (<xref ref-type="bibr" rid="ref5">5</xref>). In anemic patients (with Hb &#x003C; 10 gm/dL), echocardiogarphic changes were observed correlating with other studies. In anemic patients, LVH was found in 82% and LVD in 66% cases. It was comparable with the observations made by Singh et al. (<xref ref-type="bibr" rid="ref5">5</xref>), Parfrey et al. (<xref ref-type="bibr" rid="ref8">8</xref>), and Datta et al. (<xref ref-type="bibr" rid="ref11">11</xref>). Patients with reduced EF had higher risk of valvular heart disease and significant mortality, similar to the observations made by Yamada et al. (<xref ref-type="bibr" rid="ref6">6</xref>). Mortality occurred in 26 (10.6%) patients; among these, Hb &#x003C; 10 gm/dL was found in 23 (88.4%), LVH in 23 (88.4%), LVD in 24 (92%), and global hypokinesia in 19 (73%) patients, correlating with the studies carried out by Yamada et al. (<xref ref-type="bibr" rid="ref6">6</xref>) and Zoccali et al. (<xref ref-type="bibr" rid="ref9">9</xref>).</p>
<table-wrap id="T7" orientation="portrait" position="float">
<label>Table 7:</label><caption><p>Comparison with other studies.</p></caption>
<table frame="border" rules="all">
<thead valign="top">
<tr>
<th rowspan="2"></th>
<th rowspan="2">N</th> 
<th colspan="3">LVH</th>
<th rowspan="2">LVD</th> 
</tr>
<tr>
<th>Overall</th>
<th>HTN</th>
<th>Hb (&#x003C;10 gm/dL)</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td>Present study</td>
<td align="center">245</td>
<td>76.7%</td>
<td align="center">87%</td>
<td align="center">82%</td>
<td>57%</td>
</tr>
<tr>
<td>Foley et al. (<xref ref-type="bibr" rid="ref7">7</xref>)</td>
<td align="center">433</td>
<td>75%</td>
<td>&#x00A0;</td>
<td>&#x00A0;</td>
<td>&#x00A0;</td>
</tr>
<tr>
<td>Bansal et al. (<xref ref-type="bibr" rid="ref1">1</xref>)</td>
<td align="center">190</td>
<td>79%</td>
<td>&#x00A0;</td>
<td>&#x00A0;</td>
<td>48%</td>
</tr>
<tr>
<td>Laddha et al. (<xref ref-type="bibr" rid="ref10">10</xref>)</td>
<td align="center">70</td>
<td>74%</td>
<td align="center">74%</td>
<td align="center">82%</td>
<td>23%</td>
</tr>
<tr>
<td>Zoccali et al. (<xref ref-type="bibr" rid="ref9">9</xref>)</td>
<td>&#x00A0;</td>
<td>71%</td>
<td>&#x00A0;</td>
<td>&#x00A0;</td>
<td>46%</td>
</tr>
<tr>
<td>Yamada et al. (<xref ref-type="bibr" rid="ref6">6</xref>)</td>
<td align="center">1254</td>
<td>&#x00A0;</td>
<td>&#x00A0;</td>
<td>&#x00A0;</td>
<td>13%, EF &#x003C; 35 predicts poor outcome</td>
</tr>
<tr>
<td>Datta et al. (<xref ref-type="bibr" rid="ref11">11</xref>)</td>
<td align="center">230</td>
<td>96%</td>
<td>&#x00A0;</td>
<td align="center">89%</td>
<td>51%</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn id="TF7-1"><p>LVD: left ventricular dysfunction; LVH: left ventricular hypertrophy; EF: ejection fraction; HTN:</p></fn></table-wrap-foot>
</table-wrap> 
</sec>
<sec id="S5">
<title>Limitations</title>
<p>This was a 1-year study and no further follow-up took place.</p>
</sec>
<sec id="S6" sec-type="conclusions">
<title>Conclusion</title>
<p>Echocardiohraphy is a noninvasive diagnostic test to detect early changes in cardiac parameters. All ESRD patients with hypertension and anemia at the time of initiation of renal replacement therapy (RRT) should undergo echocardiography screening.</p></sec>
</body>
<back>
<sec id="S7" sec-type="COI-statement">
<title>Conflict of Interest</title>
<p>None. All the authors contributed equally to this study.</p>
</sec>
<sec id="S8">
<title>Funding</title>
<p>No funding was received for this study.</p>
</sec>
<fn-group>
<fn id="fn1"><p><italic>How to cite</italic>: Nazneen S, et al. Echocardiographic Changes in Patients with End-Stage Renal Disease at Initiation of Dialysis. J Ren Hepat Disord. 2021;5(1): 44&#x2013;48.</p></fn></fn-group>
<ref-list>
<ref id="ref1"><label>1.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><string-name><surname>Bansal</surname> <given-names>N</given-names></string-name>, <string-name><surname>Keane</surname> <given-names>M</given-names></string-name>, <string-name><surname>Delafontaine</surname> <given-names>P</given-names></string-name>, <string-name><surname>Dries</surname> <given-names>D</given-names></string-name>, <string-name><surname>Foster</surname> <given-names>E</given-names></string-name>, <string-name><surname>Gadegbeku</surname> <given-names>CA</given-names></string-name>, <etal>et al</etal></person-group>. <article-title>A longitudinal study of left ventricular function and structure from CKD to ESRD: the CRIC study</article-title>. <source>Clin J Am Soc Nephrol</source>. <year>2013</year> <month>Mar</month>;<volume>8</volume>(<issue>3</issue>):<fpage>355</fpage>&#x2013;<lpage>62</lpage>. <pub-id pub-id-type="doi">10.2215/CJN.06020612</pub-id></mixed-citation></ref>
<ref id="ref2"><label>2.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><string-name><surname>Herzog</surname> <given-names>CA</given-names></string-name>, <string-name><surname>Ma</surname> <given-names>JZ</given-names></string-name>, <string-name><surname>Collins</surname> <given-names>AJ</given-names></string-name></person-group>. <article-title>Poor long-term survival after acute myocardial infarction among patients on long-term dialysis</article-title>. <source>N Engl J Med</source>. <year>1998</year> <month>Sep</month> <day>17</day>;<volume>339</volume>(<issue>12</issue>):<fpage>799</fpage>&#x2013;<lpage>805</lpage>. <pub-id pub-id-type="doi">10.1056/NEJM199809173391203</pub-id></mixed-citation></ref>
<ref id="ref3"><label>3.</label><mixed-citation publication-type="book"><person-group person-group-type="author"><string-name><surname>Go</surname> <given-names>AS</given-names></string-name>, <string-name><surname>Chertow</surname> <given-names>GM</given-names></string-name>, <string-name><surname>Fan</surname> <given-names>D</given-names></string-name>, <string-name><surname>McCulloch</surname> <given-names>CE</given-names></string-name>, <string-name><surname>Hsu</surname> <given-names>CY</given-names></string-name></person-group>. <chapter-title>Chronic kidney disease and the risks of death, cardiovascular events, and hospitalization</chapter-title>. <source>N Engl J Med</source>. <year>2004</year> <month>Sep</month> <day>23</day>;<volume>351</volume>(<issue>13</issue>):<fpage>1296</fpage>&#x2013;<lpage>305</lpage>. <pub-id pub-id-type="doi">10.1056/NEJMoa041031</pub-id>. Erratum In: N Engl J Med. 2008;18(4):4. PMid: <pub-id pub-id-type="pmid">15385656</pub-id>.</mixed-citation></ref>
<ref id="ref4"><label>4.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><string-name><surname>Baigent</surname> <given-names>C</given-names></string-name>, <string-name><surname>Burbury</surname> <given-names>K</given-names></string-name>, <string-name><surname>Wheeler</surname> <given-names>D</given-names></string-name></person-group>. <article-title>Premature cardiovascular disease in chronic renal failure</article-title>. <source>Lancet</source>. <year>2000</year> <month>Jul</month> <day>8</day>;<volume>356</volume>(<issue>9224</issue>):<fpage>147</fpage>&#x2013;<lpage>152</lpage>. <pub-id pub-id-type="doi">10.1016/S0140-6736(00)02456-9</pub-id></mixed-citation></ref>
<ref id="ref5"><label>5.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><string-name><surname>Singh</surname> <given-names>Shivendra</given-names></string-name>, <string-name><surname>Doley</surname> <given-names>PK</given-names></string-name>, <string-name><surname>Pragya</surname> <given-names>P</given-names></string-name>, <string-name><surname>Sivasankar</surname> <given-names>M</given-names></string-name>, <string-name><surname>Singh</surname> <given-names>VP</given-names></string-name>, <string-name><surname>Singh</surname> <given-names>Neelam</given-names></string-name></person-group>. <article-title>Echocardiographic changes in pts with ESRD on MHD-A single center study</article-title>. <source>J Cardiovasc Dis Diagn</source>. <year>2014</year>; <volume>2</volume>:<fpage>4</fpage>. <pub-id pub-id-type="doi">10.4172/2329-9517.1000165</pub-id></mixed-citation></ref>
<ref id="ref6"><label>6.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><string-name><surname>Yamada</surname> <given-names>S</given-names></string-name>, <string-name><surname>Ishii</surname> <given-names>H</given-names></string-name>, <string-name><surname>Takahashi</surname> <given-names>H</given-names></string-name>, <string-name><surname>Aoyama</surname> <given-names>T</given-names></string-name>, <string-name><surname>Morita</surname> <given-names>Y</given-names></string-name>, <string-name><surname>Kasuga</surname> <given-names>H</given-names></string-name>, <etal>et al</etal></person-group>. <article-title>Prognostic value of reduced left ventricular ejection fraction at start of hemodialysis therapy on cardiovascular and all-cause mortality in end-stage renal disease patients</article-title>. <source>Clin J Am Soc Nephrol</source>. <year>2010</year> <month>Oct</month>;<volume>5</volume>(<issue>10</issue>):<fpage>1793</fpage>&#x2013;<lpage>1798</lpage>. <pub-id pub-id-type="doi">10.2215/CJN.00050110</pub-id>. Epub 2010 Jul 1.</mixed-citation></ref>
<ref id="ref7"><label>7.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><string-name><surname>Foley</surname> <given-names>RN</given-names></string-name>, <string-name><surname>Parfrey</surname> <given-names>PS</given-names></string-name>, <string-name><surname>Sarnak</surname> <given-names>MJ</given-names></string-name></person-group>. <article-title>Clinical epidemiology of cardiovascular disease in chronic renal disease</article-title>. <source>Am J Kidney Dis</source>. <year>1998</year> <month>Nov</month>;<volume>32</volume>(5 <supplement>Suppl 3</supplement>):<fpage>S112</fpage>&#x2013;<lpage>S119</lpage>. <pub-id pub-id-type="doi">10.1053/ajkd.1998.v32.pm9820470</pub-id></mixed-citation></ref>
<ref id="ref8"><label>8.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><string-name><surname>Parfrey</surname> <given-names>PS</given-names></string-name>, <string-name><surname>Foley</surname> <given-names>RN</given-names></string-name>, <string-name><surname>Harnett</surname> <given-names>JD</given-names></string-name>, <string-name><surname>Kent</surname> <given-names>GM</given-names></string-name>, <string-name><surname>Murray</surname> <given-names>DC</given-names></string-name>, <string-name><surname>Barre</surname> <given-names>PE</given-names></string-name></person-group>. <article-title>Outcome and risk factors for left ventricular disorders in chronic uraemia</article-title>. <source>Nephrol Dial Transplant</source>. <year>1996</year> <month>Jul</month>;<volume>11</volume>(<issue>7</issue>):<fpage>1277</fpage>&#x2013;<lpage>1285</lpage>. <pub-id pub-id-type="doi">10.1093/ndt/11.7.1277</pub-id></mixed-citation></ref>
<ref id="ref9"><label>9.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><string-name><surname>Zoccali</surname> <given-names>C</given-names></string-name>, <string-name><surname>Benedetto</surname> <given-names>FA</given-names></string-name>, <string-name><surname>Mallamaci</surname> <given-names>F</given-names></string-name>, <string-name><surname>Tripepi</surname> <given-names>G</given-names></string-name>, <string-name><surname>Giacone</surname> <given-names>G</given-names></string-name>, <string-name><surname>Cataliotti</surname> <given-names>A</given-names></string-name>, <etal>et al</etal></person-group>. <article-title>Prognostic value of echocardiographic indicators of left ventricular systolic function in asymptomatic dialysis patients</article-title>. <source>J Am Soc Nephrol</source>. <year>2004</year> <month>Apr</month>;<volume>15</volume>(<issue>4</issue>):<fpage>1029</fpage>&#x2013;<lpage>1037</lpage>. <pub-id pub-id-type="doi">10.1097/01.asn.0000117977.14912.91</pub-id></mixed-citation></ref>
<ref id="ref10"><label>10.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><string-name><surname>Laddha</surname> <given-names>M</given-names></string-name>, <string-name><surname>Sachdeva</surname> <given-names>V</given-names></string-name>, <string-name><surname>Diggikar</surname> <given-names>PM</given-names></string-name>, <string-name><surname>Satpathy</surname> <given-names>PK</given-names></string-name>, <string-name><surname>Kakrani</surname> <given-names>AL</given-names></string-name></person-group>. <article-title>Echocardiographic assessment of cardiac dysfunction in patients of end stage renal disease on haemodialysis</article-title>. <source>J Assoc Physicians India</source>. <year>2014</year> <month>Jan</month>;<volume>62</volume>(<issue>1</issue>):<fpage>28</fpage>&#x2013;<lpage>32</lpage>. PMid: <pub-id pub-id-type="pmid">25327089</pub-id>.</mixed-citation></ref>
<ref id="ref11"><label>11.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><string-name><surname>Datta</surname> <given-names>S</given-names></string-name>, <string-name><surname>Abraham</surname> <given-names>G</given-names></string-name>, <string-name><surname>Mathew</surname> <given-names>M</given-names></string-name>, <string-name><surname>Somasundaram</surname> <given-names>H</given-names></string-name>, <string-name><surname>Muralidharan</surname> <given-names>TR</given-names></string-name>, <string-name><surname>Moorthy</surname> <given-names>A</given-names></string-name>, <etal>et al</etal></person-group>. <article-title>Correlation of anemia, secondary hyperparathyroidism with left ventricular hypertrophy in chronic kidney disease patients</article-title>. <source>J Assoc Phys India (JAPI)</source>. <year>2006</year> <month>Sep</month>;<volume>54</volume>:<fpage>699</fpage>&#x2013;<lpage>703</lpage>. PMid: <pub-id pub-id-type="pmid">17212016</pub-id>.</mixed-citation></ref>
</ref-list>
</back>
</article>