<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">OALibJ</journal-id><journal-title-group><journal-title>Open Access Library Journal</journal-title></journal-title-group><issn pub-type="epub">2333-9705</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/oalib.1101818</article-id><article-id pub-id-type="publisher-id">OALibJ-65104</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Biomedical&amp;Life Sciences</subject><subject> Business&amp;Economics</subject><subject> Chemistry&amp;Materials Science</subject><subject> Computer Science&amp;Communications</subject><subject> Earth&amp;Environmental Sciences</subject><subject> Engineering</subject><subject> Medicine&amp;Healthcare</subject><subject> Physics&amp;Mathematics</subject><subject> Social Sciences&amp;Humanities</subject></subj-group></article-categories><title-group><article-title>
 
 
  The Relationship between the Changes of Blood NT-proBNP Levels and Postoperative Atrial Fibrillation Occurance in Coronary Artery By-Pass Grafting Surgery Patients
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Davut</surname><given-names>Azboy</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Erdal</surname><given-names>Simsek</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Burak</surname><given-names>Erdolu</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Zeki</surname><given-names>Temizturk</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Mehmet</surname><given-names>Ali Yilmaz</given-names></name><xref ref-type="aff" rid="aff4"><sup>4</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Kasim</surname><given-names>Karapinar</given-names></name><xref ref-type="aff" rid="aff5"><sup>5</sup></xref></contrib></contrib-group><aff id="aff5"><addr-line>Department of Cardiovascular Surgery, Diskapi Yildirim Beyazit Training and Research Hospital, Ankara, Turkey</addr-line></aff><aff id="aff4"><addr-line>Department of Cardiovascular Surgery, Tarsus Madicalpark Hospital, Mersin, Turkey</addr-line></aff><aff id="aff2"><addr-line>Department of Cardiovascular Surgery, Turkiye Yuksek Ihtisas Training and Research Hospital, Ankara, Turkey</addr-line></aff><aff id="aff1"><addr-line>Department of Cardiovascular Surgery, Elazig Training and Research Hospital, Elazig, Turkey</addr-line></aff><aff id="aff3"><addr-line>Department of Cardiovascular Surgery, Bursa Yuksek Ihtisas Training and Research Hospital, Bursa, Turkey</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>ofdogan@hacettepe.edu.tr(ES)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>29</day><month>01</month><year>2016</year></pub-date><volume>03</volume><issue>01</issue><fpage>1</fpage><lpage>8</lpage><history><date date-type="received"><day>20</day>	<month>December</month>	<year>2015</year></date><date date-type="rev-recd"><day>accepted</day>	<month>3</month>	<year>January</year>	</date><date date-type="accepted"><day>7</day>	<month>January</month>	<year>2016</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Background: The new onset of atrial fibrillation (NOAF) can be occurred after coronary artery bypass grafting (CABG) surgery. NOAF can be occurred because of postoperative severe hemodynamic instability, long duration of ICU and hospital staying time, morbidity and mortality. Our aim of this study was to investigate whether N-terminal pro-brain natriuretic peptide (NT-proBNP) is a cause of NOAF after CABG. Methods: Forty CABG patients were enrolled for this study. Twenty patients operated on cardiopulmonary bypass (Group I; n: 20). The remaining patients have operated using a beating heart technique (Group II; n: 20). The NT-proBNP levels were calculated pre- and postoperatively. Results: High rate of NOAF was detected in group I patients (P &lt; 0.05). In both groups, the NT-proBNP levels were low with sinus rhythm. The NT-proBNP blood levels in different times (T1, T2, T3, T4) among Group I were found higher than Group II. Conclusions: Our research demonstrated that there was a strongly close relationship between blood NT-proBNP levels’ and atrial fibrillation occurrence in CABG patients. According to our results to detect postoperative AF development in early time and its treatment, blood NT-proBNP levels can be calculated in those patients for reducing morbidity and mortality due to AF.
 
</p></abstract><kwd-group><kwd>Atrial Fibrillation</kwd><kwd> Coronary Artery Bypass Surgery</kwd><kwd> NT-proBNP</kwd><kwd> Open Heart Surgery</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Atrial fibrillation is a common arrhytmias associated with not only increased morbidity after coronary artery bypass grafting but also increased healthcare costs. Many factors are associated with atrial fibrillation onset after coronary artery bypass grafting. The prevalence of AF is 6% among 65 years old and over, and 0.5% - 1% among general population [<xref ref-type="bibr" rid="scirp.65104-ref1">1</xref>] . Especially in older patients AF as a postoperative complication can occur because of postoperative morbidity and mortality. The incidence of postoperative AF after CABG has been reported as 20% - 40% of patients [<xref ref-type="bibr" rid="scirp.65104-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.65104-ref3">3</xref>] . The patient’s pre-existing arrhythmia [<xref ref-type="bibr" rid="scirp.65104-ref4">4</xref>] , advanced age [<xref ref-type="bibr" rid="scirp.65104-ref4">4</xref>] , preoperative beta-blocker medication [<xref ref-type="bibr" rid="scirp.65104-ref5">5</xref>] , hypertension, left ventricule dysfunction, angina pectoris, myocard infarction (MI), and right coronary artery stenosis [<xref ref-type="bibr" rid="scirp.65104-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.65104-ref6">6</xref>] are accepted the important factors for postoperative AF risk. Multiple mechanisms may be involved in postoperative atrial fibrillation including myocardial enzyme and/or high brain natriuretic peptid levels postoperatively. Previous reports have showed that the risk for postoperative AF was the highest immediately postoperatively and at 48 hours. The risk declined to approximately zero within 18 hours postoperatively. Current research demonstrated that predominant risk factors were older age, longer cross clamp time, and concomitant mitral valve procedure.</p><p>Natriuretic peptides are vasoactive hormones secreted from various tissues. There are atrial natriuretic peptide (ANP) secreted from atria, brain natriuretic peptide (BNP) secreted more from ventricles, vascular endothelium central nervous system and C-Type natriuretic peptid secreted from the kidney (CNP). ANP is secreted by the increase in atrium wall tension related to the increase in intravascular volume [<xref ref-type="bibr" rid="scirp.65104-ref7">7</xref>] . In chronic and asymptomatic cardiac insufficiency, ANP level increases. Although BNP is secreted from ventricules fundamentally, a little amount is also secreted from atria [<xref ref-type="bibr" rid="scirp.65104-ref8">8</xref>] . BNP level is the susceptible symptom of ventricule overload [<xref ref-type="bibr" rid="scirp.65104-ref9">9</xref>] . Plasma BNP level increases in congestive heart failure, hypertrophic cardiomyopathy, acute MI, hypoxic myocard, primary pulmonary hypertension, and diastolic dysfunction [<xref ref-type="bibr" rid="scirp.65104-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.65104-ref11">11</xref>] . Active BNP, proBNP, and N-terminal natriuretic peptide (NT-proBNP) are found in plasma and can be measured with immunoassay tests. BNP enables diuresis and vasodilatation, inhibiting the hypertrophy of vascular smooth muscles and cardiac muscle by renin aldosterone production. It has been shown that natriuretic hormones help determine ventricle dysfunction and predict the complications occuring in the early postoperative period [<xref ref-type="bibr" rid="scirp.65104-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.65104-ref13">13</xref>] . ANP inhibits the collagen synthesis in fibroblasts and the hypertrophy in myocytes [<xref ref-type="bibr" rid="scirp.65104-ref14">14</xref>] .</p><p>Therefore, in our study, we searched the relationships between new onset AF (NOAF) and NT-proBNP levels in a small number of CABG patients who underwent on-pump or OPCAB procedures.</p></sec><sec id="s2"><title>2. Methods</title><p>This study has been done between November 2015 and April 2015. Fortycoronary artery disease (CAD) patients required CABG were included in this study. This study has been approved by local ethics committee. The patients divided into two groups according to CABG techniques (Cardiopulmonary bypass (CPB) use) (Group I; n: 20), and beating heart coronary artery revascularisation (Group II; n: 20). AF occurrence in the patients constituted the primary end-point of the study. The demographycs of the patients has been summarized in <xref ref-type="table" rid="table1">Table 1</xref>.</p><p>The patients who have left ventricular ejection fraction (LVEF) &lt; 45%, severe heart valve disease, preoperative atrial or ventricular arrhytmia, chronic obstructive lung diseases were exluded from the research. In addition, patients with enlarged left or right atrium, who have used any antiarrhythmic drug were not included in the study. The patients’ age more than 70 y, or with acute coronary syndrome and cardiac failure, emergency operations have also exluded. Patients who had underwent temporary or permanent pacemakers, who required inotropic agents longer than 24 hours postoperatively, intra aortic balloon pumps use requirement, renal function disorders (creatine level &gt; 2 mg/dl) were not included for this study.</p><sec id="s2_1"><title>2.1. Surgery</title><p>After midline sternotomy incision, aortic and single venous cannulation was performed abd CPB was instituted. After aortic X-Clamp, myocardial protection was provided using an ante grade and retrograde cold bloodcar-</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Demographic data of the patients</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >Group I</th><th align="center" valign="middle" >Group II</th><th align="center" valign="middle" >P value</th></tr></thead><tr><td align="center" valign="middle" >Age</td><td align="center" valign="middle" >60.70 &#177; 5.38</td><td align="center" valign="middle" >59.30 &#177; 5.56</td><td align="center" valign="middle" >0.424</td></tr><tr><td align="center" valign="middle" >EF (%)</td><td align="center" valign="middle" >50.25 &#177; 3.54</td><td align="center" valign="middle" >49.20 &#177; 2.61</td><td align="center" valign="middle" >0.292</td></tr><tr><td align="center" valign="middle" >LVESD</td><td align="center" valign="middle" >3.18 &#177; 0.41</td><td align="center" valign="middle" >3.08 &#177; 0.38</td><td align="center" valign="middle" >0.404</td></tr><tr><td align="center" valign="middle" >LVEDD</td><td align="center" valign="middle" >4.79 &#177; 0.62</td><td align="center" valign="middle" >4.85 &#177; 0.55</td><td align="center" valign="middle" >0.726</td></tr><tr><td align="center" valign="middle" >LA diameter</td><td align="center" valign="middle" >3.28 &#177; 0.50</td><td align="center" valign="middle" >3.03 &#177; 0.52</td><td align="center" valign="middle" >0.135</td></tr><tr><td align="center" valign="middle" >RA diameter</td><td align="center" valign="middle" >3.56 &#177; 0.59</td><td align="center" valign="middle" >3.54 &#177; 0.58</td><td align="center" valign="middle" >0.893</td></tr><tr><td align="center" valign="middle" >RV diameter</td><td align="center" valign="middle" >2.13 &#177; 0.21</td><td align="center" valign="middle" >2.20 &#177; 0.18</td><td align="center" valign="middle" >0.273</td></tr><tr><td align="center" valign="middle" >Duration of anesthesia (hour)</td><td align="center" valign="middle" >241.85 &#177; 40.75</td><td align="center" valign="middle" >216.40 &#177; 26.84</td><td align="center" valign="middle" >0.026</td></tr><tr><td align="center" valign="middle" >Number of bypass (≤2)</td><td align="center" valign="middle" >5</td><td align="center" valign="middle" >10</td><td align="center" valign="middle" >0.102</td></tr><tr><td align="center" valign="middle" >Inotropicagents usage</td><td align="center" valign="middle" >12</td><td align="center" valign="middle" >9</td><td align="center" valign="middle" >0.342</td></tr><tr><td align="center" valign="middle" >Hyperlipidemia</td><td align="center" valign="middle" >18</td><td align="center" valign="middle" >18</td><td align="center" valign="middle" >1.000</td></tr><tr><td align="center" valign="middle" >Hypertension</td><td align="center" valign="middle" >18</td><td align="center" valign="middle" >16</td><td align="center" valign="middle" >0.661</td></tr><tr><td align="center" valign="middle" >Diabetesmellitus</td><td align="center" valign="middle" >13</td><td align="center" valign="middle" >10</td><td align="center" valign="middle" >0.523</td></tr></tbody></table></table-wrap><p>LVESD: Left Ventricule End Systolic Diameter, LVEDD: Left Ventricule End Diastolic Diameter, LA: Left Atrium, RA: Right Atrium, RV: Right Ventricule, EF: Ejection fraction.</p><p>dioplegia. Hot-Shot blood delivery was applied via antegradely before aortic cross clamp release. Moderate hypothermia (32˚C - 34˚C) was applied in all patients. In patients who underwent beating heart bypass operations, heparin was administered and activating coagulation time (ACT) was provided.</p></sec><sec id="s2_2"><title>2.2. Blood NT-proBNP Levels</title><p>The blood taken from peripheral venous line and kept under +4 centigrade degrees until decomposed with a 5 min. centrifugation in 3500 rotation. The decomposed serums were kept in 80 centigrade deep freeze. NT- proBNP levels were measured at four stages; preoperatively (T1), 1st day (T2), 3rd day (T3) and 5th day (T4) after the operation. Measurements have been with ELISA Kit Test system.BNP levels have been determined as pg/ml. The lowest NT-proBNP level that the test could verify was determined as 0.312 pg/ml. Starting from the first day after the operation, all the patients were given Acetylsalicylic acid and beta blocker drugs however; they weren’t given any antiaritmic drugs. Their cardiac rhythms were followed by daily 12 lead ECG.AF was defined as the development of irregular ventricular rhythm or P wave deficiency before QRS complex during ECG. Occurrence of AF once created the primary endpoint.</p></sec><sec id="s2_3"><title>2.3. Statistical Analysis</title><p>For both groups, Student’s t-Test was used to compare age, NT-proBNP levels, EF, LVESD, LVEDD, LA, RA and RV diameters, anesthesia durations, cross clamp and CPB times in group I over AF factors. Again in comparing theses variables among the groups―AF taken into consideration―Student’s t-Test was used. Among the categorical variables that took place in our study: distal anastomosis numbers, inotropic agent support, diabetes mellitus, hypertension, hyperlipidemia analysis, Pearson chi square correlation was benefited from. Fisher’s Exact Test and Pearson chi square correlation were practised upon for the relationship between categorical variables and AF. The results’ being P &lt; 0.05 was evaluated at a level of significance.</p></sec></sec><sec id="s3"><title>3. Results</title><p>The clinical and operational information of group I and II patients and also group I’s cross clamp and CPB durations are shown in <xref ref-type="table" rid="table1">Table 1</xref>. In both groups; age, EF, Left Ventricule End Systolic Diameter (LVESD), Left Ventricule End Diastolic Diameter (LVEDD), Left Atrium (LA), right atrium and right ventricule diameters, anesthesia duration, cross clamp and CPB durations were measured. The effects of these parameters on AF occurrence were evaluated. Among Group I patients, AF occurred ones’ ages, LVESD, LVEDD, LA, RA, RV diameters were found significantly higher compared to patients with normal rhythm (P &lt; 0.05). EF value in AF patients was found significantly lower compared to sinus rhythm patients (P &lt; 0.05). There wasn’t found any significant difference between the AF observed patients’ and normal rhythm patients’ ages and anesthesia durations in group II (P &gt; 0.05). However, in AF developed patients in group II, LVESD, LVEDD, LA, RA, and RV diameter averages were noted significantly higher than the patients’ with normal rhythm (P &lt; 0.05). EF values were noted significantly lower in AF developed patients than in patients of normal rhythm (P &lt; 0.05). When both groups were compared in terms of AF developed patients, there was no significant difference between age, EF, LVESD, LVEDD, LA, RA, RV diameters and anesthesia durations (P &gt; 0.05). All phases of NT-proBNP levels of AF developed patients among group I and II that were found significantly higher than the levels of patients with normal rhythm (P &lt; 0.05) (<xref ref-type="table" rid="table2">Table 2</xref>).</p><p>While NT-proBNP levels in T1 weren’t found any significant difference between two groups’ AF developed patients, T2, T3, T4 times were found significantly higher in average of AF developed group I patients (P &lt; 0.05) (<xref ref-type="table" rid="table3">Table 3</xref>). The relationship of anastomosed distal bypass number and inotropic agent usage with AF could not be determined in either group (P &gt; 0.05).</p><p>There wasn’t a significant difference, in terms of cross clamp and CPB periods, between AF patients and normal sinus rhythm patients among group I (P &gt; 0.05).</p></sec><sec id="s4"><title>4. Discussion</title><p>Atrial fibrillation is a common arrhythmia after CABG operations. Many factors are associated with NOAF in CABG patients. AF can be cause postoperative morbidity and mortality especially in older patients. The incidence of postoperative AF in CABG patients has been reported as 20% - 40% of patients [<xref ref-type="bibr" rid="scirp.65104-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.65104-ref3">3</xref>] . The patient’s pre-existing arrhythmia [<xref ref-type="bibr" rid="scirp.65104-ref4">4</xref>] , advanced age [<xref ref-type="bibr" rid="scirp.65104-ref4">4</xref>] , preoperative beta-blocker medication [<xref ref-type="bibr" rid="scirp.65104-ref5">5</xref>] , hypertension, left ventricle dysfunction, angina pectoris, MI, right coronary artery stenosis [<xref ref-type="bibr" rid="scirp.65104-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.65104-ref6">6</xref>] are accepted the main important risk factors for postoperative AF. Multiple mechanisms may be involved in postoperative atrial fibrillation including myocardial enzyme release and/or high brain natriuretic peptid postoperatively. Previous reports have showed that the risk for postoperative AF was highest immediately postoperatively and at 48 hours. The risk declined to approximately zero within 18 hours postoperatively. Current research demonstrated that predominant risk factors were older age, longer cross clamp time, and concomitant mitral valve procedure. A number of risk factors including biochemical changes during the ECC have been researched for new onset of AF; however, there is a limited number of studies the relationships between the NOAF and blood proBNP levels.</p><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> NT-proBNP values in different times</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >Group I</th><th align="center" valign="middle" >Group I with AF</th><th align="center" valign="middle" >P value</th><th align="center" valign="middle" >Group II</th><th align="center" valign="middle" >Group II with AF</th><th align="center" valign="middle" >P value</th></tr></thead><tr><td align="center" valign="middle" >NT proBNP pg/ml (T1)</td><td align="center" valign="middle" >15.56</td><td align="center" valign="middle" >30.28</td><td align="center" valign="middle" >0.014</td><td align="center" valign="middle" >13.14</td><td align="center" valign="middle" >21.35</td><td align="center" valign="middle" >0.003</td></tr><tr><td align="center" valign="middle" >NT proBNP pg/ml (T2)</td><td align="center" valign="middle" >16.11</td><td align="center" valign="middle" >35.34</td><td align="center" valign="middle" >0.008</td><td align="center" valign="middle" >16.84</td><td align="center" valign="middle" >24.92</td><td align="center" valign="middle" >0.002</td></tr><tr><td align="center" valign="middle" >NT proBNP pg/ml (T3)</td><td align="center" valign="middle" >18</td><td align="center" valign="middle" >37.17</td><td align="center" valign="middle" >0.001</td><td align="center" valign="middle" >18.49</td><td align="center" valign="middle" >28</td><td align="center" valign="middle" >0.008</td></tr><tr><td align="center" valign="middle" >NT proBNP pg/ml (T4)</td><td align="center" valign="middle" >22.27</td><td align="center" valign="middle" >40</td><td align="center" valign="middle" >0.007</td><td align="center" valign="middle" >19</td><td align="center" valign="middle" >31.48</td><td align="center" valign="middle" >0.000</td></tr></tbody></table></table-wrap><p>AF: Atrial Fibrillation, NT-proBNP: N-terminal natriuretic peptide, T1: pre-operation time, T2:1st day after the operation, T3: 3rd day after the operation, T4: 5th day after the operation (T4). P &lt; 0.05 was evaluated at a level of significance.</p><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Blood NT proBNP levels (different times) and AF occurrence in Group I and II</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >Group I with AF</th><th align="center" valign="middle" >Group II with AF</th><th align="center" valign="middle" >P value</th></tr></thead><tr><td align="center" valign="middle" >NT proBNP (T1)</td><td align="center" valign="middle" >30.29</td><td align="center" valign="middle" >21.35</td><td align="center" valign="middle" >0.070</td></tr><tr><td align="center" valign="middle" >NT proBNP (T2)</td><td align="center" valign="middle" >35.34</td><td align="center" valign="middle" >24.92</td><td align="center" valign="middle" >0.027</td></tr><tr><td align="center" valign="middle" >NT proBNP (T3)</td><td align="center" valign="middle" >37.17</td><td align="center" valign="middle" >28</td><td align="center" valign="middle" >0.034</td></tr><tr><td align="center" valign="middle" >NT proBNP (T4)</td><td align="center" valign="middle" >40</td><td align="center" valign="middle" >31.48</td><td align="center" valign="middle" >0.036</td></tr></tbody></table></table-wrap><p>NT-proBNP; N-terminal natriuretic peptide; AF: Atrial Fibrillation; T1: pre-operation time, T2: 1st day after the operation, T3: 3rd day after the operation, T4: 5th day after the operation. P &lt; 0.05 was evaluated at a level of significance.</p><p>As we know that natriuretic peptides are vasoactive hormones secreted from various tissues. Such as atrium or brain. This biochemical marker also secreted from ventricles, vascular endothelium, central nervous system. C- type natriuretic peptid secreted from the kidney (CNP). Atrial Natriuretic Peptide is secreted fromthe atrium related to high atrial wall tension and intravascular volume loading [<xref ref-type="bibr" rid="scirp.65104-ref7">7</xref>] . BNP is secreted from the ventricle and is also secreted from atria [<xref ref-type="bibr" rid="scirp.65104-ref8">8</xref>] . But, BNP level is a susceptible for symptom of ventricular overloading [<xref ref-type="bibr" rid="scirp.65104-ref9">9</xref>] . Plasma BNP level increases in congestive heart failure, hypertrophic cardiomyopathy, acute MI, hypoxic myocard, primary pulmonary hypertension, diastolic dysfunction [<xref ref-type="bibr" rid="scirp.65104-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.65104-ref11">11</xref>] . Active BNP, proBNP, N-terminal natriuretic peptide (NT-proBNP) can be measured with immunoassay tests. BNP is a cause of diuresis and vasodilatation, inhibiting the hypertrophy of vascular smooth and cardiac muscle by renin-aldoster one production. It has been shown that natriuretic hormones help determine ventricle dysfunction and predict the complications occuring in the early postoperative period [<xref ref-type="bibr" rid="scirp.65104-ref12">12</xref>] - [<xref ref-type="bibr" rid="scirp.65104-ref14">14</xref>] .</p><p>It has been demonstrated that in patients with enlarged left atrium and ventricle, and low EF are the risk factors of postoperative AF occurrence [<xref ref-type="bibr" rid="scirp.65104-ref17">17</xref>] . To provide confusing of postoperative AF causes in our patients, we selected the patients without the risk factors including age, preoperative arrhytmia, valvular disease, cardiomegaly related to any reason, etc. in both groups. Indeed, preoperative echocardiographyc examinations showed that there was no significant difference between left ventricular end-systolic and end-diastolic diameter, bi-atrial and bi-ventricular enlargement in both groups. A multivariate analysis has been shown that advanced age is a strong postoperative AF development predictor. A multy-variate analyses demonstrated that hypertension, Re- Do CABG were found to be a significant risk factors for NOAF in previous studies. Also, prolonged aortic cross clamping and longer operation [<xref ref-type="bibr" rid="scirp.65104-ref19">19</xref>] , anesthesics, insufficient ventilation [<xref ref-type="bibr" rid="scirp.65104-ref4">4</xref>] , cardioplegic arrest are the risk factors of AF. In our study, if patients’ cross clamp time and CPB durations increased in On-Pump group, these patients were excluded from the study to provide any confusing of the reason of AF occurrence.</p><p>AF incidence has been reported between 20% to 40% in wide series [<xref ref-type="bibr" rid="scirp.65104-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.65104-ref3">3</xref>] . Previous studies exhibited that AF frequency did not change in patients underwent beating heart technique [<xref ref-type="bibr" rid="scirp.65104-ref20">20</xref>] - [<xref ref-type="bibr" rid="scirp.65104-ref22">22</xref>] . However, the authors stated that CPB was a risk factor of NOAF [<xref ref-type="bibr" rid="scirp.65104-ref23">23</xref>] [<xref ref-type="bibr" rid="scirp.65104-ref24">24</xref>] .</p><p>In our study, postoperative AF development rate was found 25% of the patients in “On-Pump” group. AF developed in 15% of OPCAB patients. This was statistically significant. The postoperative AF occurrence was significantly low in terms of statistics, in the patients underwent beating heart bypass technique. In our opinion, proBNP levels can be related this important result.</p><p>In congestive heart failure and acute MI, NT-proBNP levels is increased [<xref ref-type="bibr" rid="scirp.65104-ref25">25</xref>] . It has been shown that NT-proBNP levels and myocardial ischemia, creatine kinase-MB and ventricular function are related to NOAF [<xref ref-type="bibr" rid="scirp.65104-ref26">26</xref>] .</p><p>In the presence of minor perioperative myocardial ischemia, NT-proBNP was brought forward to be a sensitive marker of dysfunction after ischemia [<xref ref-type="bibr" rid="scirp.65104-ref27">27</xref>] . Recently in some studies, it has been put forth that perioperative NT-proBNP levels correlate with complications such as; inotropic agency, intra aortic oballoon pump use, length of hospitalization, postoperative AF and mortality [<xref ref-type="bibr" rid="scirp.65104-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.65104-ref28">28</xref>] .</p><p>It has been stated that postoperative high proBNP levels are independent risk factors for postoperative AF occurrence [<xref ref-type="bibr" rid="scirp.65104-ref29">29</xref>] . In a previous study included patients with and without left ventricular dysfunction in CABG patients has been reported that no correlation has been detected between blood proBNP levels and NOAF. This study demonstrated that there was no statistical significancy NOAF after surgery when compared to two groups’ BNP level changes in post surgery 24t h. However, the same authors stated that 48th h post surgery, there was a significant increment in NOAF in theirs groups who have had high BNP levels [<xref ref-type="bibr" rid="scirp.65104-ref30">30</xref>] .</p><p>The published studies showed the increment of NT-proBNP levels started at 6th h and reached its peak point on 4-6th days, post surgery. This clinical situation may continued during weeks [<xref ref-type="bibr" rid="scirp.65104-ref28">28</xref>] [<xref ref-type="bibr" rid="scirp.65104-ref30">30</xref>] . In our study, postoperative NT-proBNP levels increased gradually in both goups. We detected highest level of NT-proBNP after On-Pump surgery was related preoperative NT-proBNP levels especially in older age in both groups. To the best of our knowledge this clinical situation has been detected in our research.</p><p>Postoperative changes of NT-proBNP levels increased in On-Pump and OPCAB patients. However, we seen that these increament was more common in On-Pump patients. There was a strong relationship between NT- proBNP levels and NOAF in this groups. Also, in our study exhibited that there was a significant correlation in older age patients, number of diseased coronary arteries, cross clamp and CPB duration. Therefore, our study suggested that NT-proBNP may be measured in older CABG patients who underwent CPB. The specifity of NT-proBNP has been reported as 69.7% - 83.3%.</p></sec><sec id="s5"><title>5. Conclusion</title><p>Our research demonstrated a positive correlation between NT-proBNP levels and NOAF. Therefore, we suggested that NT-proBNP values could be used as important risk indexes in terms of postoperative AF occurrence after CABG. Therefore, previous studies indicated the risk factors for NOAF postoperatively; we established that NT-proBNP levels could be used in older patients with high preoperative NT-proBNP level, low EF, atrial and a large atrio-ventricular diameter. NT-proBNP level may be investigated as a routine test prior to open heart surgery, extremely important in terms of decreasing foreseen morbidity and mortality. If we detect high level of NT-proBNP before the CABG operation we can choose beating bypass procedure if it is possible.</p></sec><sec id="s6"><title>6. Limitations of Study</title><p>Our study includes a small number of coronaryartery disease. Therefore, for definition of importance of NT- proBNP levels the study can be designed in a large number of patients. Thus, we continued this research programme in our CABG patients. Rhytm and tension Holter monitoring can be decided in these patients to detect transient atrio-ventricular arrhytmia development.</p></sec><sec id="s7"><title>Acknowledgements</title><p>The authors would like to thanks to Prof. Dr. Omer Faruk Dogan, the chief of cardiovascular surgery, because he helped to prepare and revision processess of our manuscript.</p></sec><sec id="s8"><title>Cite this paper</title><p>Davut Azboy,Erdal Simsek,Burak Erdolu,Zeki Temizturk,Mehmet Ali Yilmaz,Kasim Karapinar, (2016) The Relationship between the Changes of Blood NT-proBNP Levels and Postoperative Atrial Fibrillation Occurance in Coronary Artery By-Pass Grafting Surgery Patients. Open Access Library Journal,03,1-8. doi: 10.4236/oalib.1101818</p></sec><sec id="s9"><title>Abbreviations</title><p>NOAF: new onset of atrial fibrillation</p><p>CABG: coronary artery bypass grafting</p><p>NT-proBNP: N-terminal pro-brain natriuretic peptide</p><p>LVEF: left ventricular ejection fraction</p><p>EF: ejection fraction</p><p>LVESD: left ventricular end-systolic diameter</p><p>LVEDD: left ventricular end-diastolic diameter</p><p>LA: left atrium</p><p>RA: right atrium</p><p>RV: right ventricule</p><p>CPB: cardiopulmonary by-pass</p><p>CNP: C-type natriuretic peptid</p><p>MI: myocardial infarctus</p><p>OPCAB: off-pump coronary artery bypass</p><p>CPB: cardiopulmonary by-pass</p></sec><sec id="s10"><title>NOTES</title></sec></body><back><ref-list><title>References</title><ref id="scirp.65104-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Lloyd-Jones, D.M., Wang, T.J., Leip, E.P., Larson, M.G., Levy, D., Vasan, R.S., et al. 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