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 <!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.0 20120330//EN" "http://jats.nlm.nih.gov/publishing/1.0/JATS-journalpublishing1.dtd"> <article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" article-type="research-article" dtd-version="1.0" xml:lang="en">
  <front>
    <journal-meta>
      <journal-id journal-id-type="publisher-id">JVAT</journal-id>
      <journal-title-group>
        <journal-title>Journal of Current Viruses and Treatment Methodologies</journal-title>
      </journal-title-group>
      <issn pub-type="epub">2691-8862</issn>
      <publisher>
        <publisher-name>Open Access Pub</publisher-name>
        <publisher-loc>United States</publisher-loc>
      </publisher>
    </journal-meta>
    <article-meta>
      <article-id pub-id-type="doi">10.14302/issn.2691-8862.jvat-21-3999</article-id>
      <article-id pub-id-type="publisher-id">JVAT-21-3999</article-id>
      <article-categories>
        <subj-group>
          <subject>research-article</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>Characterization of the Vaccine Abdala</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <name>
            <surname>Katia</surname>
            <given-names>Pino Marrero</given-names>
          </name>
          <xref ref-type="aff" rid="idm1843347812">1</xref>
          <xref ref-type="aff" rid="idm1843344212">*</xref>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Alvaro</surname>
            <given-names>Laurencio Pérez</given-names>
          </name>
          <xref ref-type="aff" rid="idm1843347020">2</xref>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Dania</surname>
            <given-names>Vargas Batista</given-names>
          </name>
          <xref ref-type="aff" rid="idm1843346012">3</xref>
        </contrib>
      </contrib-group>
      <aff id="idm1843347812">
        <label>1</label>
        <addr-line>Holguin's university of medical sciences, Cuba.</addr-line>
      </aff>
      <aff id="idm1843347020">
        <label>2</label>
        <addr-line>Electrical Department, Faculty Engineering, Holguin University, Cuba.</addr-line>
      </aff>
      <aff id="idm1843346012">
        <label>3</label>
        <addr-line>Holguin's university of medical sciences, Cuba.</addr-line>
      </aff>
      <aff id="idm1843344212">
        <label>*</label>
        <addr-line>Corresponding author</addr-line>
      </aff>
      <contrib-group>
        <contrib contrib-type="editor">
          <name>
            <surname>Qianqian</surname>
            <given-names>Song</given-names>
          </name>
          <xref ref-type="aff" rid="idm1843194844">1</xref>
        </contrib>
      </contrib-group>
      <aff id="idm1843194844">
        <label>1</label>
        <addr-line>Wake Forest School of Medicine, Wake Forest Baptist Comprehensive Cancer               Center, Medical Center Boulevard, Winston-Salem, NC 27157.</addr-line>
      </aff>
      <author-notes>
        <corresp>
    
    Alvaro Laurencio Pérez, <addr-line>Electrical Department, Faculty Engineering, Holguin University, Cuba.</addr-line><email>alvarolaurencio040@gmail.com</email></corresp>
        <fn fn-type="conflict" id="idm1842459332">
          <p>The authors have declared that no competing interests exist.</p>
        </fn>
      </author-notes>
      <pub-date pub-type="epub" iso-8601-date="2021-12-25">
        <day>25</day>
        <month>12</month>
        <year>2021</year>
      </pub-date>
      <volume>1</volume>
      <issue>4</issue>
      <fpage>1</fpage>
      <lpage>8</lpage>
      <history>
        <date date-type="received">
          <day>18</day>
          <month>10</month>
          <year>2021</year>
        </date>
        <date date-type="accepted">
          <day>18</day>
          <month>12</month>
          <year>2021</year>
        </date>
        <date date-type="online">
          <day>25</day>
          <month>12</month>
          <year>2021</year>
        </date>
      </history>
      <permissions>
        <copyright-statement>© </copyright-statement>
        <copyright-year>2021</copyright-year>
        <copyright-holder>Katia Pino Marrero, et al.</copyright-holder>
        <license xlink:href="http://creativecommons.org/licenses/by/4.0/" xlink:type="simple">
          <license-p>This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</license-p>
        </license>
      </permissions>
      <self-uri xlink:href="http://openaccesspub.org/jvat/article/1746">This article is available from http://openaccesspub.org/jvat/article/1746</self-uri>
      <abstract>
        <p>Vaccines symbolize the main pandemic control tool in the world, which is why they are the object of study in many investigations. In this work, the Abdala vaccine was characterized in terms of adverse reactions by conducting a survey and statistical processing of the data taken through distribution graphs of the same,                developed in the Minitab software 16. Of the                    people involved, 47.67% presented Symptoms that were mild to moderate with the presence of pain in the area of the injection, drowsiness and decay,                 mainly. Based on the distribution of the data in                    histograms, the duration of these symptoms was                approximately 1 day. Likewise, it was observed that the symptoms occur mainly in females, for 33.72% of the cases in the first dose and 23.26% after the second dose was applied.</p>
      </abstract>
      <kwd-group>
        <kwd>Adverse reactions</kwd>
        <kwd>symptom</kwd>
        <kwd>vaccine.</kwd>
      </kwd-group>
      <counts>
        <fig-count count="9"/>
        <table-count count="1"/>
        <page-count count="8"/>
      </counts>
    </article-meta>
  </front>
  <body>
    <sec id="idm1843192900" sec-type="intro">
      <title> Introduction</title>
      <p>Vaccines are one of the main achievements of biomedical, with which an improvement in the quality of life of human beings is promoted.</p>
      <p>The emergence of the covid 19 pandemic         infection represents a challenge from the                       corresponding authorities and scientists around the world in order to lessen its spread, where some authors suggest a close relationship between               demography and this pandemic <xref ref-type="bibr" rid="ridm1842573892">1</xref>. Early and timely diagnosis and treatment are essential elements, as well as the location of the infected person's contacts. On the other hand, vaccines symbolize the main              control tool in the world, so they are objects of study for many researchers  <xref ref-type="bibr" rid="ridm1842579868">2</xref><xref ref-type="bibr" rid="ridm1842584196">3</xref><xref ref-type="bibr" rid="ridm1842674188">4</xref>.</p>
      <p>In the country, an integrating role is fulfilled with an innovative approach, both at the national level and in the to achieve progress in this order, as an example of this is presented the development of five candidates                      vaccination <xref ref-type="bibr" rid="ridm1842430964">5</xref><xref ref-type="bibr" rid="ridm1842435212">6</xref>. Among these candidates is Abdala, which according to the authors is considered to be 92.28% effective after applying all the established doses <xref ref-type="bibr" rid="ridm1842431756">7</xref><xref ref-type="bibr" rid="ridm1842419972">8</xref>. This vaccine is composed of a small portion of S proteins, whose active principle is the recombinant Receptor              Binding Domain (RBD) protein that allows the interaction of ACE2, its receptor in human cells, a molecule expressed in the yeast Pichia pastoris, adjuvated in aluminum                hydroxide  <xref ref-type="bibr" rid="ridm1842423644">9</xref><xref ref-type="bibr" rid="ridm1842397100">10</xref><xref ref-type="bibr" rid="ridm1842394436">11</xref>. According to researchers, it has been shown to be effective in counteracting different variants of the virus <xref ref-type="bibr" rid="ridm1842431756">7</xref><xref ref-type="bibr" rid="ridm1842398180">12</xref>. However, the literature consulted does not clarify the possible adverse reactions that it could bring with it.</p>
      <p>Almufty et al., 2021 emphasizes revealing the     potential effects after being applied a vaccine against           covid 19, associated with risk factors and comparing the vaccines available in Iraq: Sinopharm, AstraZeneca-Oxford and Pfizer-BioNTech; where 84% of the cases were                 symptomatic after vaccination. The major symptoms were mild to moderate in terms of severity, most notably               fatigue, fever, myalgia, headache, and chills <xref ref-type="bibr" rid="ridm1842383116">13</xref>. While Abu et al., 2021, in their comparison of the Pfizer – BioNTech and Sinopharm vaccines, states that 46.3% of the participants present adverse reactions in the first dose. For the second dose, the number of symptomatic people reached 48.6%, mainly with the presence of pain in the injection area. Adverse effects were mostly mild to                   moderate <xref ref-type="bibr" rid="ridm1842379372">14</xref>.</p>
      <p>On the other hand, a study carried out in Saudi Arabia related to the ChAdOx1-S vaccine reports 34.7% of the cases where adverse reactions occurred during the first dose, the main symptoms being pain at the injection site, muscle aches, rash. on the skin, gastrointestinal                symptoms and fever <xref ref-type="bibr" rid="ridm1842584196">3</xref>.</p>
      <p>Likewise, the work of Worafi et al., 2021 suggests that all participants experienced to a lesser degree at least one of the adverse reactions taken into account: pain in the injection site, fatigue, headache and fever. These               adverse effects, for the most part, were described as                moderate to mild lasting between one day and one                 week <xref ref-type="bibr" rid="ridm1842376204">15</xref>.</p>
      <p>A study carried out by Jeet et al., 2021 in which the adverse reactions of 11 vaccines against covid 19               applied in the world are exposed, as well as the duration of the symptoms, suggests that most of those involved       present an intensity of mild to moderate vaccine reactions lasting 3 to 4 days. The most common reactions that occur are pain, swelling, and redness at the injection site. In            addition, fever, fatigue, myalgia, and headache were               reported <xref ref-type="bibr" rid="ridm1842388732">16</xref>.</p>
      <p>The aversion to uncertainty, the population's      concerns about the virus containment measures (quarantines and social distancing) and the new massive vaccination programs are elements that encourage both the interest of the population in science and the trust in it of authorities and decision makers. All of this emphasizes the importance of achieving adequate communication of health-related risks, as well as making informed and              well-founded decisions to contain the spread of the virus. The World Health Organization (WHO) recommends that risk communication be transparent, timely, easy to               understand, that it recognizes uncertainty in the                       information, and that it be disseminated through different platforms <xref ref-type="bibr" rid="ridm1842385276">17</xref>. Hence the need to know, among other             elements, the fundamental reactions that vaccinates                present for characterization and decision-making.  </p>
      <p>The literature consulted in relation to the               characteristic adverse reactions of the Abdala vaccine is limited due to its recent application. In this work, it is                 proposed to characterize the Abdala vaccine in terms of adverse reactions, through a statistical analysis of cases in the Edecio Rey Pérez ＃ 4 vaccination center, belonging to the Alcides Pino polyclinic, located in the municipality of Holguín, Holguín province, Cuba, With the help of the              Minitab 16 software, it is possible to establish the main symptoms and the duration of the symptoms arising after the administration of the vaccine. For this, surveys were carried out and the information taken by means of data distribution graphs was statistically processed.</p>
    </sec>
    <sec id="idm1843190812" sec-type="materials">
      <title>Materials and Methods</title>
      <p>A descriptive study is carried out, in which the random sample is 86 patients older than 18 years, who had acquired at least two doses of the Abdala vaccine so far. Informed consent was obtained from the surveyed patients, as well as from the health personnel in charge of the vaccination process.</p>
      <p>This section aims to present the elements and methods taken into account for the development of the research.</p>
      <sec id="idm1843197508">
        <title>Collection of Data and Statistical Analysis</title>
        <p>For data collection, the survey is applied as an instrument. The variables used during it were: sex, age, personal medical history, acquired dose, and the most  frequent adverse reactions. In addition, the duration of these symptoms is considered.</p>
        <p>The survey was carried out at the ＃ 4 Edecio Rey Pérez center in the town of Alcides Pino in the                               municipality of Holguín.</p>
        <p>The statistical method to apply for the analysis of the data is fundamentally the graphical method. For this, the Minitab 16 software is used, which is considered an effective statistical tool by several authors <xref ref-type="bibr" rid="ridm1842362932">18</xref><xref ref-type="bibr" rid="ridm1842360484">19</xref><xref ref-type="bibr" rid="ridm1842358180">20</xref>.</p>
      </sec>
    </sec>
    <sec id="idm1843196932" sec-type="results">
      <title>Results and Discussion</title>
      <p>A total of 86 people participated in the study, where approximately 32.55% had one or more underlying diseases. <xref ref-type="table" rid="idm1841960292">Table 1</xref> shows the pathological antecedents found and the number of patients who suffer from it.</p>
      <table-wrap id="idm1841960292">
        <label>Table 1.</label>
        <caption>
          <title> Chronic diseases and number of people who suffer from it</title>
        </caption>
        <table rules="all" frame="box">
          <tbody>
            <tr>
              <td>
                <bold>Base </bold>
                <bold>diseases</bold>
              </td>
              <td>
                <bold>Patients</bold>
                <bold>quantity</bold>
              </td>
            </tr>
            <tr>
              <td>Hypertension</td>
              <td>14</td>
            </tr>
            <tr>
              <td>Mellitus diabetes</td>
              <td>2</td>
            </tr>
            <tr>
              <td>Spasmodic asthma</td>
              <td>6</td>
            </tr>
            <tr>
              <td>Cardiopathy</td>
              <td>1</td>
            </tr>
            <tr>
              <td>Hipotiroidismo</td>
              <td>5</td>
            </tr>
          </tbody>
        </table>
      </table-wrap>
      <sec id="idm1843178876">
        <title>Main Symptoms and Duration</title>
        <p>The results are divided into two groups based on the first and second doses received of the Abdala vaccine.</p>
        <p>47.67 % of the cases presented symptoms of some kind after the first dose of the vaccine. <xref ref-type="fig" rid="idm1841913804">Figure 1</xref> shows the              distribution of these perceived symptoms in the                         participants, in percentage terms.</p>
        <fig id="idm1841913804">
          <label>Figure 1.</label>
          <caption>
            <title> Percentage distribution of symptoms in patients after the first dose</title>
          </caption>
          <graphic xlink:href="images/image1.jpg" mime-subtype="jpg"/>
        </fig>
        <p>The existence of several conditions can be seen in this first dose, where pain in the injection area and drowsiness prevail with a representativeness of 25.58 and 20.93% of the cases involved, respectively. Chills, runny nose, and sore throat were not present at this dose.</p>
        <p>On the other hand, the second dose caused                  adverse reactions in around 26.75% of the patients, whose distribution is shown in <xref ref-type="fig" rid="idm1841914164">Figure 2</xref>.</p>
        <fig id="idm1841914164">
          <label>Figure 2.</label>
          <caption>
            <title> Percentage distribution of symptoms in patients after the second dose</title>
          </caption>
          <graphic xlink:href="images/image2.jpg" mime-subtype="jpg"/>
        </fig>
        <p>The duration of symptoms in the first dose was 1.4 days on average. <xref ref-type="fig" rid="idm1841911140">Figure 3</xref> shows a histogram with the distribution of the duration of the symptoms in the                     patients.</p>
        <p>Note that most people suffer for a day, with 82.5% of cases.</p>
        <fig id="idm1841911140">
          <label>Figure 3.</label>
          <caption>
            <title> Histogram of the duration of symptoms in the first dose</title>
          </caption>
          <graphic xlink:href="images/image3.jpg" mime-subtype="jpg"/>
        </fig>
        <p>With the application of the second dose, the               duration of the symptoms was given for an average of 1.24 days. In 85.71 % of the cases the symptoms persisted for only one day. The distribution graph of the duration of the adverse reactions during the second dose is shown in             <xref ref-type="fig" rid="idm1841909844">Figure 4</xref>.</p>
        <fig id="idm1841909844">
          <label>Figure 4.</label>
          <caption>
            <title> Histogram of the duration of symptoms in the second dose</title>
          </caption>
          <graphic xlink:href="images/image4.jpg" mime-subtype="jpg"/>
        </fig>
        <p>Age in this type of study constitutes a                         considerable element, since the organism's reaction to a foreign agent behaves differently for different stages of life.</p>
        <p>The distribution of people by age groups with symptoms after the application of the vaccine is shown in <xref ref-type="fig" rid="idm1841909628">Figure 5</xref>.</p>
        <fig id="idm1841909628">
          <label>Figure 5.</label>
          <caption>
            <title> Symptomatic people by age group.</title>
          </caption>
          <graphic xlink:href="images/image5.jpg" mime-subtype="jpg"/>
        </fig>
        <p>Note that the age group 40 -59 is considered the most representative in terms of symptoms with                       approximately 50% of cases.</p>
      </sec>
      <sec id="idm1843148412">
        <title>Symptoms by Gender</title>
        <p>The survey considers 61.3% female versus 38.37% male.</p>
        <p>Of the total number of patients, there were                  adverse reactions described in 33.72 and 13.95% for the female and male gender, respectively, with the application of a first dose of the vaccine. The distribution of symptoms is presented in <xref ref-type="fig" rid="idm1841904588">figure 6</xref> and <xref ref-type="fig" rid="idm1841904876">figure 7</xref>, for women and men,                     respectively.</p>
        <fig id="idm1841904588">
          <label>Figure 6.</label>
          <caption>
            <title> Symptoms in women during the first dose</title>
          </caption>
          <graphic xlink:href="images/image6.jpg" mime-subtype="jpg"/>
        </fig>
        <fig id="idm1841904876">
          <label>Figure 7.</label>
          <caption>
            <title> Symptoms in men during the first dose</title>
          </caption>
          <graphic xlink:href="images/image7.jpg" mime-subtype="jpg"/>
        </fig>
        <p>In both cases, pain at the injection site and drowsiness stand out as the main symptoms during the first dose.</p>
        <p>In the second dose, for females, the most                    prominent pain symptoms remained in the injection area, as shown in <xref ref-type="fig" rid="idm1841902860">figure 8</xref>.</p>
        <fig id="idm1841902860">
          <label>Figure 8.</label>
          <caption>
            <title> Symptoms in women during the second dose</title>
          </caption>
          <graphic xlink:href="images/image8.jpg" mime-subtype="jpg"/>
        </fig>
        <p>Headache remained second, followed by decline, drowsiness and other symptoms.</p>
        <p>In men, drowsiness was mainly present with the application of the second dose, as shown in <xref ref-type="fig" rid="idm1841903796">Figure 9</xref>.</p>
        <fig id="idm1841903796">
          <label>Figure 9.</label>
          <caption>
            <title> Symptoms in men during the second dose</title>
          </caption>
          <graphic xlink:href="images/image9.jpg" mime-subtype="jpg"/>
        </fig>
        <p>Symptoms were mild to moderate in all involved cases, both in the first and second doses.</p>
      </sec>
    </sec>
    <sec id="idm1843132956" sec-type="conclusions">
      <title>Conclusions</title>
      <p>The application of the vaccine produces adverse reactions in 47.67 % of the patients, in which pain in the injection area, drowsiness and decay, which were mild to moderate, is mainly appreciated. In more isolated cases it can cause headache and myalgia. In this way, the Abdala vaccine is characterized in terms of adverse reactions.</p>
      <p>The duration of symptoms is approximately 1 day, present in 82.5 and 85.71 % of cases for the first and               second dose respectively.</p>
      <p>The symptoms are more frequent in the female gender and pain in the injection area stands out.</p>
    </sec>
  </body>
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