<?xml version="1.0" encoding="ISO-8859-1"?><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">
<front>
<journal-meta>
<journal-id>0034-7531</journal-id>
<journal-title><![CDATA[Revista Cubana de Pediatría]]></journal-title>
<abbrev-journal-title><![CDATA[Rev Cubana Pediatr]]></abbrev-journal-title>
<issn>0034-7531</issn>
<publisher>
<publisher-name><![CDATA[Centro Nacional de Información de Ciencias MédicasEditorial Ciencias Médicas]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0034-75312017000100012</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Appropriate indicated use for IVIG in neonatal infections]]></article-title>
<article-title xml:lang="es"><![CDATA[Uso indicado y apropiado de la inmunoglobulina G intravenosa para el tratamiento de infecciones neonatales]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Wang]]></surname>
<given-names><![CDATA[Ying]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Ping Liu]]></surname>
<given-names><![CDATA[Yi]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Yan Yuan]]></surname>
<given-names><![CDATA[Hai]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Wen Xiao]]></surname>
<given-names><![CDATA[Yi]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Ping]]></surname>
<given-names><![CDATA[Xu]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Bo]]></surname>
<given-names><![CDATA[Tao]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,The second Xiangya Hospital of Central-South University Department of Pharmacy Clinical Pharmacist Office]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>China</country>
</aff>
<aff id="A02">
<institution><![CDATA[,The second Xiangya Hospital of Central-South University Neonatal Department Nonatal Intensive Care Unit]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>China</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>03</month>
<year>2017</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>03</month>
<year>2017</year>
</pub-date>
<volume>89</volume>
<numero>1</numero>
<fpage>92</fpage>
<lpage>97</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_arttext&amp;pid=S0034-75312017000100012&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_abstract&amp;pid=S0034-75312017000100012&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_pdf&amp;pid=S0034-75312017000100012&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[Infection is a leading cause of mortality and morbidity in the newborn and preterm neonates due to immuno-incompetence in these patients. Administration of intravenous immunoglobulin (IVIG) provides immunoglobulin G (IgG) that can protect the body from infection. In theory, morbidity and mortality due to infections in newborns and preterm infants could be reduced by the administration of IVIG. Two meta-analyses were evaluated comparing IVIG to treat various infection versus conventional treatments. The results showed that IVIG is not effective as an adjunctive treatment for suspected or proven infections in neonates.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[La infección es la causa principal de la mortalidad y de la morbilidad entre los recién nacidos y los neonatos prematuros debido a la incompetencia inmunológica de estos pacientes. El suministro de inmunoglobulina por vía intravenosa brinda la inmunoglobulina G que protege al cuerpo humano de las infecciones. En términos teóricos, la morbilidad y la mortalidad por infecciones en recién nacidos y en bebés prematuros, podrían reducirse si se administra inmunoglobulina G intravenosa. Se evaluaron dos meta-análisis que comparaban el uso de la inmunoglobulina G intravenosa para tratar diversas infecciones con los tratamientos convencionales. Los resultados demostraron que dicha inmunoglobulina no es eficaz como tratamiento adyuvante para combatir sospechas de infección o infecciones comprobadas en los recién nacidos.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[intravenous immunoglobulin]]></kwd>
<kwd lng="en"><![CDATA[newborn]]></kwd>
<kwd lng="en"><![CDATA[preterm neonates]]></kwd>
<kwd lng="en"><![CDATA[infection]]></kwd>
<kwd lng="en"><![CDATA[meta-analyses]]></kwd>
<kwd lng="es"><![CDATA[inmunoglobulina intravenosa]]></kwd>
<kwd lng="es"><![CDATA[recién nacido]]></kwd>
<kwd lng="es"><![CDATA[neonatos prematuros]]></kwd>
<kwd lng="es"><![CDATA[infección]]></kwd>
<kwd lng="es"><![CDATA[meta-análisis]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[ <p align="right"> <font face="Verdana" size="2"><a></a><b>Rev Cubana Pediatr.    2017;89(1)</b></font></p>     <p align="right"><font face="Verdana" size="2"><a><b>    <br>   SPECIAL COLLABORATION</b></a></font></p>     <p align="left">&nbsp;</p>     <p align="left"><font face="Verdana" size="2"><b><font size="4">Appropriate indicated    use for IVIG in neonatal infections</font></b></font></p>     <p align="left">&nbsp;</p>     <p align="left"><b><font face="Verdana" size="3">Uso indicado y apropiado de la    inmunoglobulina G intravenosa para el tratamiento de infecciones neonatales</font></b></p>     <p align="left">&nbsp;</p>     <p align="left">&nbsp;</p>     <p> <font face="Verdana" size="2"><b>Ying Wang,<sup>I</sup> Yi Ping Liu,<sup>I    </sup>Hai Yan Yuan,<sup>I</sup> Yi Wen Xiao,<sup>I</sup> Xu Ping,<sup>I</sup>    Tao Bo<sup>II</sup></b> </font></p>     ]]></body>
<body><![CDATA[<p> <font face="Verdana" size="2"><a><sup>I</sup></a>Clinical Pharmacist Office.    Department of Pharmacy. The second Xiangya Hospital of Central-South University.    China. </font>    <br>   <font face="Verdana" size="2"><sup>II</sup>Nonatal Intensive Care Unit. Neonatal    Department. The second Xiangya Hospital of Central-South University. China.</font></p>     <p>&nbsp;</p>     <p>&nbsp;</p> <hr>     <p><font face="Verdana" size="2"><b>ABSTRACT</b> </font></p>     <p><font face="Verdana" size="2"> Infection is a leading cause of mortality and    morbidity in the newborn and preterm neonates due to immuno-incompetence in    these patients. Administration of intravenous immunoglobulin (IVIG) provides    immunoglobulin G (IgG) that can protect the body from infection. In theory,    morbidity and mortality due to infections in newborns and preterm infants could    be reduced by the administration of IVIG. Two meta-analyses were evaluated comparing    IVIG to treat various infection <i>versus</i> conventional treatments. The results    showed that IVIG is not effective as an adjunctive treatment for suspected or    proven infections in neonates. </font></p>     <p><font face="Verdana" size="2"><b>Key words:<a> </a></b> intravenous immunoglobulin;    newborn; preterm neonates; infection; meta-analyses.</font></p> <hr>     <p><font face="Verdana" size="2"><b>RESUMEN</b></font></p>     <p><font face="Verdana" size="2">La infecci&oacute;n es la causa principal de    la mortalidad y de la morbilidad entre los reci&eacute;n nacidos y los neonatos    prematuros debido a la incompetencia inmunol&oacute;gica de estos pacientes.    El suministro de inmunoglobulina por v&iacute;a intravenosa brinda la inmunoglobulina    G que protege al cuerpo humano de las infecciones. En t&eacute;rminos te&oacute;ricos,    la morbilidad y la mortalidad por infecciones en reci&eacute;n nacidos y en    beb&eacute;s prematuros, podr&iacute;an reducirse si se administra inmunoglobulina    G intravenosa. Se evaluaron dos meta-an&aacute;lisis que comparaban el uso de    la inmunoglobulina G intravenosa para tratar diversas infecciones con los tratamientos    convencionales. Los resultados demostraron que dicha inmunoglobulina no es eficaz    como tratamiento adyuvante para combatir sospechas de infecci&oacute;n o infecciones    comprobadas en los reci&eacute;n nacidos.</font></p>     <p><font face="Verdana" size="2"><b>Palabras clave:</b> inmunoglobulina intravenosa;    reci&eacute;n nacido; neonatos prematuros; infecci&oacute;n; meta-an&aacute;lisis.</font></p> <hr>     ]]></body>
<body><![CDATA[<p>&nbsp; </p>     <p>    <br> </p>     <p> <font face="Verdana" size="2"><b><font size="3">INTRODUCTION</font></b> </font></p>     <p><font face="Verdana" size="2"> Neonatal systemic infection is a major cause    of morbidity and mortality in the world.<sup>1</sup> In particular, the preterm    neonates are at high risk because their organs and tissues are not fully developed.    Symptoms may be subtle and clinical signs may be non-specific. Common signs    and symptoms of infection are tachypnea, apnea or other respiratory distress,    which may lead quickly result in permanent neurological impairment or death.<sup>2</sup>    </font></p>     <p><font face="Verdana" size="2"> Approximately 10-20 % of very low birth weight    (&lt; 1 500 mg) infants suffer from proven infection and 10-20 % die from infection    despite antimicrobial treatment during their neonatal period.<sup>3</sup> The    exact causes of infection in neonates are not well understood. It is hypothesized    that the B-lymphocytes are produced shortly before 12th week of gestation. As    a result, maternal IgG are actively translocated into the fetal bloodstream    via the placenta.<sup>4</sup> Endogenous immunoglobulin synthesis does not begin    until 24 weeks of life: thus, young infants rely on in-utero maternally acquired    immunoglobulins for protection against systemic infection.<sup>5</sup> Premature    interruption of transplacental IgG transfer contributes to weakened defense    capacity of the fetus during gestational-age.<sup>6</sup> Since maternal IgG    are generally cleared from the neonatal circulation after birth, it has been    proposed the use of intravenous immunoglobulins (IVIG) to prevent and treat    neonatal sepsis.<sup>7</sup> </font></p>     <p><font face="Verdana" size="2"> The objective of this article is to evaluate    two meta-analyses in order to know if IVIG is effective as an adjunctive treatment    for suspected or proven infections in neonates. </font></p>     <p>    <br>   <font face="Verdana" size="2"><b>PHARMACOLOGIC TREATMENT</b></font></p>     <p><font face="Verdana" size="2"><b>Antimicrobial</b> </font></p>     ]]></body>
<body><![CDATA[<p><font face="Verdana" size="2"><i>Coagulase-negative staphylococci</i> are the    prevalent organisms followed by E. coli and multidrug resistant Gram-negative    organisms including Klebsiella, Pseudomonas and fungi.<sup>8</sup> Misuse or    inappropriate use or broad-spectrum antimicrobial therapy could result in super-infections    and multi-drug resistance.<sup>8</sup> This is becoming a clinical and financial    burden in China. </font></p>     <p><font face="Verdana" size="2"><b>    <br>   IVIG</b> </font></p>     <p><font face="Verdana" size="2">IVIG is a therapeutic preparation that mainly    includes human IgG collected from a large number of healthy donors that is commonly    used for replacement therapy in patients with primary or secondary antibody    deficiencies. IgG is a type of antibody, which be created and released by plasma    B-cells and consists of approximately 75 % of serum antibodies in humans IgG.<sup>9</sup>    They can bind to pathogens such as viruses, bacteria, and fungi. In theory,    the contribution from IgG is to protect the body from infection. The mechanism    of actions for IgG is unclear but it is thought to: </font></p> <ul>       <li> <font face="Verdana" size="2">Mediate the binding of pathogens causes the      immobilization of pathogens.    <br>         <br>     </font></li>       <li> <font face="Verdana" size="2">Coating of pathogen surfaces allows their      recognition and ingestion by phagocytic immune cells.    <br>         <br>     </font></li>       ]]></body>
<body><![CDATA[<li> <font face="Verdana" size="2">Activates the classical pathway of the complement      systems.    <br>         <br>     </font></li>       <li> <font face="Verdana" size="2">Binds and neutralizes toxins associated with      type II and type III hypersensitivity reactions. </font></li>     </ul>     <p><font face="Verdana" size="2">     <br>   In clinical studies,<sup>10</sup> it has been shown that polyvalent IVIG can    <a></a> <a> provide opsonic activity, activate complement, promote antibody-dependent    cytotoxicity and improve neutrophilic chemo-luminescence. So theoretically IVIG    are being evaluated as an adjunctive treatment for suspected or proven infection,    to reduce morbidity and mortality. </a> </font></p>     <p><font face="Verdana" size="2"> As indicated in <a href="c0112117.gif">chart</a>,    the key difference among three countries is the definition of <a>secondary immunodeficiency</a>.    The Chinese guidelines include infection and neonatal sepsis as secondary immunodeficiency.<sup>11</sup>    However the international definition of secondary immunodeficiencies<sup>5,8    </sup>due to leukemia, lymphomas, various tumors, chemotherapy, other immunosuppressive    therapy and human immunodeficiency virus infection is accepted by many countries.    Perhaps, the Chinese indications for secondary immunodeficiency should be re-examined    through evidence-based medicine. </font></p>     <p>&nbsp;</p>     <p><font face="Verdana" size="2"><b>EVIDENCE-BASED REVIEW</b> </font></p>     ]]></body>
<body><![CDATA[<p><font face="Verdana" size="2">A systematic review included randomized controlled    trials (RCT) or quasi-RCT to evaluate the use of IVIG for children with pneumonia    in China.<sup>10</sup> This study was one of the references in China Food and    Drug Administration (CFDA) product package insert. The study compared IVIG plus    conventional treatment such as antimicrobial use versus conventional treatment.    The study did not conduct a thorough literature to include all databases. The    sample size for the systematic review was over 3 602 children. The investigators    used clinical surrogate markers such as rales, fever, and cough to diagnose    pneumonia. The clinical outcome measures were length of hospital stay, and resolution    of the surrogate symptoms. The results showed the mean difference for fever    was -1.73 (-2.06, -1.39), for rales -2.09 (-2.34,-1.83), cough -1.85 (-2.17,-1.53),    length of hospital stay -2.53 (-2.86,-2.21). The investigators stated that the    results showed that IVIG used, as an adjunctive therapy is more effective than    conventional treatments for children with severe pneumonia. However, there are    many limitations to the systematic review. First, the population cannot be applied    to neonate since it was studied in children. There was no indication of attempt    to prove that there was no selection bias in the studies. Also, none of the    study mentioned about allocation concealment. Most importantly, the study did    not examine clinical outcome measures such as death cause, death from infections,    complication of infections, or follow-up after patients were discharged from    hospital. </font></p>     <p><font face="Verdana" size="2"> The second systematic review is a Cochrane Review,<sup>12    </sup>which included all RCT, and quasi-RCT evaluating the use of IVIG with    conventional treatment <i>versus</i> conventional treatment alone in proven    or suspected infections in neonates. The Cochrane review was very cleared with    their literature search using all possible databases. The review included over    3973 neonates. The studies defined neonates as newborns &lt; 28 days old. Suspected    infection was defined as having clinical signs and symptoms (temperature instability,    feeding intolerance, prolonged jaundice) consistent without culture. Proven    infection was defined as clinical signs and symptoms consistent with infection    in association with isolation of a causative organism (bacteria or fungi) from    the blood, cerebrospinal fluid culture, urine culture or a normally sterile    site such as liver, spleen, or lung. </font></p>     <p><font face="Verdana" size="2"> The strengths of the Cochrane review are: </font></p>     <p><font face="Verdana" size="2"> 1. Large sample size. </font></p>     <p><font face="Verdana" size="2"> 2. Most studies disclosed allocation concealment.    </font></p>     <p><font face="Verdana" size="2"> 3. The primary outcomes are clinical outcome    measures such as death, complications and length of hospital stay. </font></p>     <p><font face="Verdana" size="2"> 4. There was a follow-up on death and complications    after patients were discharged. </font></p>     <p><font face="Verdana" size="2"> 5. The population is applicable to neonates.    </font></p>     <p><font face="Verdana" size="2">     <br>   The results from Cochrane review show that <a>IVIG is not effective as an adjunctive    treatment of suspected or proven infections in neonates</a>. As for the other    systematic review, the patient population studies do not applied to neonates.    Therefore, clinicians should take caution when interpreting results from this    review and attempt to apply to their practice. </font></p>     ]]></body>
<body><![CDATA[<p>    <br>   <font face="Verdana" size="2"><b>CONFLICTS OF INTEREST</b> </font></p>     <p><font face="Verdana" size="2">The authors declare no conflicts or financial    interest in any product or service mentioned in the manuscript. </font></p>     <p>&nbsp; </p>     <p> <font face="Verdana" size="2"><b>REFERENCE</b> </font></p>     <!-- ref --><p><font face="Verdana" size="2">1. Alison R. Bedford Russell. <a></a><a>Neonatal    Sepsis</a>. Paediatrics and Child Health. 2010;21(6):265-69.     </font></p>     <!-- ref --><p><font face="Verdana" size="2"> 2. Raimondi F, Ferrara T, Maffucci R, Milite    P, Del Buono D, Santoro P, et al. Neonatal Sepsis: A Difficult Diagnostic Challenge.    Clinical Biochemistry. 2011;44:463-4.     </font></p>     <!-- ref --><p><font face="Verdana" size="2"> 3. Di Rosa R, Pietrosanti M, Luzi G, Salemi    S, D'Amelio R. Polyclonal intravenous immunoglobulin: An important additional    strategy in sepsis? European Journal of Internal Medicine. 2014;25:511-6.     </font></p>     <!-- ref --><p><font face="Verdana" size="2"> 4. Capasso L, Borrelli AC, Cerullo J, Pisanti    R, Figliuolo C, Izzo F, et al. Role of immunoglobulins in neonatal sepsis. Transl    Med UniSa. 2015;11(5):28-33.     </font></p>     <!-- ref --><p><font face="Verdana" size="2"> 5. Cohen-Wolkowiez M, Benjamin DK Jr., Capparelli    E. Immunotherapy in neonatal sepsis: advances in treatment and prophylaxis.    Curr Opin Pediatr. 2009;21(2):177-81.     </font></p>     <!-- ref --><p><font face="Verdana" size="2"> 6. Wynn JL, Seed PC, Cotten CM. Does IVIg administration    yield improved immune function in very premature neonates? Journal of Perinatology.    2010;30(10):635-42.     </font></p>     <!-- ref --><p><font face="Verdana" size="2"> 7. Laguna P, Golebiowska-Staroszcayk S, Trzaska    M, Grabarczyk M, Matysiak M. Immunoglobulins and their use in children. Adv    Clin Exp Med. 2015;24(1):153-9.     </font></p>     <!-- ref --><p><font face="Verdana" size="2"> 8. Tarnow-Mordi WO, Cruz M. Evidence-based <a></a><a>neonatal</a>    medicine in Latin America: What can we learn from the International Neonatal    Immunotherapy Study and Trials of IVIg? Jornal de Pediatria. 2012;88(5):369-71.        </font></p>     <!-- ref --><p><font face="Verdana" size="2"> 9. Capasso L, Borrelli AC, Ferrara T, Coppola    C, Cerullo J, Izzo F, et al. <a></a><a>Immunoglobulins in Neonatal Sepsis: Has    the Final Word Been Said?</a> Early Human Development. 2014;90(S2):S47-S49.        </font></p>     <!-- ref --><p><font face="Verdana" size="2"> 10. Bing H, Junmei B, Yushu J, Ying F. Intravenous    immunoglobulin therapy in the treatment of children's severe pneumonia: A systematic    review. Medical Journal of Wuhan University. 2013;34(4):588-95.     </font></p>     <!-- ref --><p><font face="Verdana" size="2"> 11. China Food and Drug Administration [Internet];    updated 2007 Jan 25 [cited 2016 Jul 8]. Available from: <a href="http://www.sda.gov.cn/WS01/CL0449/23699.html" target="_blank">http://www.sda.gov.cn/WS01/CL0449/23699.html</a>    </font><!-- ref --><p><font face="Verdana" size="2"> 12. Ohlsson A, Lacy JB. Intravenous immunoglobulin    for suspected or proven infection in neonates (Reviews). Cochrane Database Syst    Rev. 2015 Mar 27;3:CD001239. doi: 10.1002/14651858.CD001239.pub5.     </font></p>     <p>&nbsp;</p>     <p>&nbsp;</p>     ]]></body>
<body><![CDATA[<p><font face="Verdana" size="2">Recibido: 12 de mayo de 2016. <br/>   Aprobado: 28 de junio de 2016. </font></p>     <p>&nbsp;</p>     <p>&nbsp; </p>     <p> <font face="Verdana" size="2"><i>Ying Wang</i><i>.</i> Clinical Pharmacist    Office. Department of Pharmacy. The Second Xiangya Hospital of Central-South    University. China. E-mail: </font><font face="Verdana" size="2"><a href="mailto:yyzz1314@hotmail.com">yyzz1314@hotmail.com</a>    </font></p>      ]]></body><back>
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