<?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>0873-2159</journal-id>
<journal-title><![CDATA[Revista Portuguesa de Pneumologia]]></journal-title>
<abbrev-journal-title><![CDATA[Rev Port Pneumol]]></abbrev-journal-title>
<issn>0873-2159</issn>
<publisher>
<publisher-name><![CDATA[Sociedade Portuguesa de Pneumologia]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0873-21592006000100001</article-id>
<title-group>
<article-title xml:lang="pt"><![CDATA[Estudo Viriato: Actualização de dados de susceptibilidade aos antimicrobianos de bactérias responsáveis por infecções respiratórias adquiridas na comunidade em Portugal em 2003 e 2004]]></article-title>
<article-title xml:lang="en"><![CDATA[The Viriato Study: Update of antimicrobial susceptibility data of bacterial pathogens from community-acquired respiratory tract infections in Portugal in 2003 and 2004]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Melo-Cristino]]></surname>
<given-names><![CDATA[J.]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Santos]]></surname>
<given-names><![CDATA[Letícia]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Ramirez]]></surname>
<given-names><![CDATA[Mário]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Faculdade de Medicina de Lisboa Instituto de Medicina Molecular Instituto de Microbiologia]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>01</month>
<year>2006</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>01</month>
<year>2006</year>
</pub-date>
<volume>12</volume>
<numero>1</numero>
<fpage>09</fpage>
<lpage>30</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_arttext&amp;pid=S0873-21592006000100001&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_abstract&amp;pid=S0873-21592006000100001&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_pdf&amp;pid=S0873-21592006000100001&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="pt"><p><![CDATA[O Estudo Viriato é um estudo nacional, prospectivo e multicêntrico, de vigilância da susceptibilidade aos antimicrobianos de bactérias frequentemente responsáveis por infecções do aparelho respiratório adquiridas na comunidade. Nos anos de 2003 e 2004 participaram 29 laboratórios de todo o país. Isolaram-se 2945 microrganismos que foram estudados num laboratório coordenador. Das 513 estirpes de Streptococcus pyogenes de doentes com amigdalo-faringite aguda, todas eram susceptíveis à penicilina e outros antibióticos beta-lactâmicos, mas 18,9% eram resistentes à eritromicina, claritromicina e azitromicina. Nas estirpes resistentes foi mais frequente o fenótipo M (67,0%) que confere resistência à eritromicina (CIM90=16 mg/L), claritromicina e azitromicina, mas susceptibilidade à clindamicina (CIM90=0,094 mg/L). De doentes com infecção do aparelho respiratório inferior estudaram-se 1300 estirpes de Streptococcus pneumoniae (pneumococos), 829 de Haemophilus influenzae e 303 de Moraxella catarrhalis. Em S. pneumoniae, 18,4% das estirpes eram resistentes à penicilina (3,5% com resistência elevada), 7,1% à cefuroxima, 0,5% à amoxicilina, 0,5% à amoxicilina/clavulanato, 18,8% à eritromicina, claritromicina e azitromicina, 14,5 % à tetraciclina, 16,5% ao co-trimoxazol e 0,4% à levofloxacina. Nas estirpes resistentes aos macrólidos, dominou o fenótipo MLS B (83,7%), caracterizado por resistência elevada (CIM90>256 mg/L) à eritromicina, claritromicina, azitromicina e clindamicina. Produziam beta-lactamase 10,0% de H. influenzae e 96,4% de M. catarrhalis. Em H. influenzae demonstrou-se 5,5% de resistência à claritromicina e 13,4% ao co-trimoxazol. A quase totalidade das estirpes era susceptível à amoxicilina / clavulanato, cefuroxima, azitromicina, tetraciclina e ciprofloxacina. Em M. catarrhalis a resistência ao co-trimoxazol foi de 27,1% e à tetraciclina de 1,0%. Todas as estirpes eram susceptíveis à amoxicilina / clavulanato, cefuroxima, claritromicina, azitromicina e ciprofloxacina. De entre o conjunto de antibióticos ensaiado, a penicilina continua a ser o mais activo contra S. pyogenes e a amoxicilina / clavulanato e as quinolonas os mais activos simultaneamente contra S. pneumoniae, H. influenzae e M. catarrhalis.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[The Viriato Study is a nationwide, prospective, multicenter surveillance study of the antimicrobial susceptibility of bacterial pathogens commonly associated with community-acquired respiratory tract infections in Portugal. In 2003 and 2004 a total of 2945 isolates was recovered in the 29 laboratories that participated in the study. Testing was undertaken in a central laboratory. Of the 513 Streptococcus pyogenes strains isolated from patients with acute tonsillitis all were susceptible to penicillin and other beta-lactams but 18.9% were resistant to erythromycin, clarithromycin and azithromycin. The M phenotype dominated (67%), conferring resistance to erythromycin (MIC90=16mg/L), clarythromycin and azithromycin, but susceptibility to clindamycin (MIC90=0.094 mg/L). From patients with lower respiratory tract infection 1,300 strains of Streptococcus pneumoniae, 829 of Haemophilus influenzae, and 303 of Moraxella catarrhalis were studied. Among S. pneumoniae isolates 18.4% were resistant to penicillin (3.5% showing high-level resistance), 7.1% to cefuroxime, 0.5% to amoxicillin and amoxicillin/clavulanate, 18.8% to erythromycin, clarithromycin and azithromycin, 14.9% to tetracycline, 16.5% to co-trimoxazol, and 0.4% to levofloxacin. Beta-lactamases were produced by 10.0% of H. influenzae and 96.4% of M. catarrhalis. In H. influenzae resistance to clarithromycin was 5.5% and to co-trimoxazole was 13.4%. Most strains were susceptible to amoxicillin/clavulanate, cefuroxime, azithromycin, tetracycline and ciprofloxacin. In M. catarrhalis resistance to co-trimoxazole was 27.1% and to tetracycline 1.0%. All strains were susceptible to amoxicillin/clavulanate, cefuroxime, clarithromycin, azithromycin and ciprofloxacin. Penicillin was the most active antimicrobial agent against S. pyogenes and amoxycillin / clavulanate and the quinolones the most active in vitro simultaneously against S. pneumoniae, H. influenza and M. catarrhalis.]]></p></abstract>
<kwd-group>
<kwd lng="pt"><![CDATA[Portugal]]></kwd>
<kwd lng="pt"><![CDATA[Estudo Viriato]]></kwd>
<kwd lng="pt"><![CDATA[infecção respiratória]]></kwd>
<kwd lng="pt"><![CDATA[comunidade]]></kwd>
<kwd lng="pt"><![CDATA[2003]]></kwd>
<kwd lng="pt"><![CDATA[2004]]></kwd>
<kwd lng="pt"><![CDATA[susceptibilidade aos antimicrobianos]]></kwd>
<kwd lng="pt"><![CDATA[Streptococcus pyogenes]]></kwd>
<kwd lng="pt"><![CDATA[Streptococcus pneumoniae]]></kwd>
<kwd lng="pt"><![CDATA[Haemophilus influenzae]]></kwd>
<kwd lng="pt"><![CDATA[Moraxella catarrhalis]]></kwd>
<kwd lng="en"><![CDATA[Portugal]]></kwd>
<kwd lng="en"><![CDATA[Viriato Study]]></kwd>
<kwd lng="en"><![CDATA[respiratory tract infections]]></kwd>
<kwd lng="en"><![CDATA[community]]></kwd>
<kwd lng="en"><![CDATA[2003]]></kwd>
<kwd lng="en"><![CDATA[2004]]></kwd>
<kwd lng="en"><![CDATA[antimicrobial resistance]]></kwd>
<kwd lng="en"><![CDATA[Streptococcus pyogenes]]></kwd>
<kwd lng="en"><![CDATA[Streptococcus pneumoniae]]></kwd>
<kwd lng="en"><![CDATA[Haemophilus influenzae]]></kwd>
<kwd lng="en"><![CDATA[Moraxella catarrhalis]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[ <P align="justify"><B>Estudo Viriato: Actualiza&ccedil;&atilde;o de dados de susceptibilidade    aos antimicrobianos de bact&eacute;rias respons&aacute;veis por infec&ccedil;&otilde;es    respirat&oacute;rias adquiridas na comunidade em Portugal em 2003 e 2004</b></P>      <P align="justify"><I>The Viriato Study: Update of antimicrobial susceptibility    data of bacterial pathogens from community-acquired respiratory tract infections    in Portugal in 2003 and 2004</I></P>      <p>&nbsp;</p>     <p>&nbsp;</p>      <P align="right"><B>J. Melo-Cristino<SUP><a href="#1">1</a><a name="top1"></a>    </SUP></B></P>     <P align="right"><B>Let&iacute;cia Santos<SUP><a href="#1">1</a><a name="top1"></a></SUP></B></P>      <P align="right"><B>M&aacute;rio Ramirez<SUP><a href="#1">1</a><a name="top1"></a></SUP></B></P>      <P align="right"><B>Grupo de Estudo Portugu&ecirc;s de Bact&eacute;rias Patog&eacute;nicas    Respirat&oacute;rias<SUP><a href="#2">2</a><a name="top2"></a></SUP></B></P>      <p>&nbsp;</p>     <p>&nbsp;</p>      ]]></body>
<body><![CDATA[<P align="center"><B>Resumo</B></P>      <P align="justify">O Estudo Viriato &eacute; um estudo nacional, prospectivo e    multic&ecirc;ntrico, de vigil&acirc;ncia da susceptibilidade aos antimicrobianos    de bact&eacute;rias frequentemente respons&aacute;veis por infec&ccedil;&otilde;es    do aparelho respirat&oacute;rio adquiridas na comunidade. Nos anos de 2003 e    2004 participaram 29 laborat&oacute;rios de todo o pa&iacute;s. Isolaram-se    2945 microrganismos que foram estudados num laborat&oacute;rio coordenador.    Das 513 estirpes de <I>Streptococcus pyogenes</I> de doentes com amigdalo-faringite    aguda, todas eram suscept&iacute;veis &agrave; penicilina e outros antibi&oacute;ticos    beta-lact&acirc;micos, mas 18,9% eram resistentes &agrave; eritromicina, claritromicina    e azitromicina<I>. </I>Nas estirpes resistentes foi mais frequente o fen&oacute;tipo    <I>M</I> (67,0%) que confere resist&ecirc;ncia &agrave; eritromicina (CIM<SUB>90</SUB>=16    mg/L), claritromicina e azitromicina, mas susceptibilidade &agrave; clindamicina    (CIM<SUB>90</SUB>=0,094 mg/L). De doentes com infec&ccedil;&atilde;o do aparelho    respirat&oacute;rio inferior estudaram-se 1300 estirpes de <I>Streptococcus    pneumoniae</I> (pneumococos), 829 de <I>Haemophilus influenzae</I> e 303 de    <I>Moraxella catarrhalis</I>. Em <I>S. pneumoniae, </I>18,4% das estirpes eram    resistentes &agrave; penicilina (3,5% com resist&ecirc;ncia elevada), 7,1% &agrave;    cefuroxima, 0,5% &agrave; amoxicilina, 0,5% &agrave; amoxicilina/clavulanato,    18,8% &agrave; eritromicina, claritromicina e azitromicina, 14,5 % &agrave;    tetraciclina, 16,5% ao co-trimoxazol e 0,4% &agrave; levofloxacina. Nas estirpes    resistentes aos macr&oacute;lidos, dominou o fen&oacute;tipo MLS<SUB>B</SUB>    (83,7%), caracterizado por resist&ecirc;ncia elevada (CIM<SUB>90</SUB>&gt;256    mg/L) &agrave; eritromicina, claritromicina, azitromicina e clindamicina. Produziam    beta-lactamase 10,0% de <I>H. influenzae </I>e 96,4% de <I>M. catarrhalis</I>.    Em <I>H. influenzae</I> demonstrou-se 5,5% de resist&ecirc;ncia &agrave; claritromicina    e 13,4% ao co-trimoxazol. A quase totalidade das estirpes era suscept&iacute;vel    &agrave; amoxicilina / clavulanato, cefuroxima, azitromicina, tetraciclina e    ciprofloxacina. Em <I>M. catarrhalis </I>a resist&ecirc;ncia ao co-trimoxazol    foi de 27,1% e &agrave; tetraciclina de 1,0%. Todas as estirpes eram suscept&iacute;veis    &agrave; amoxicilina / clavulanato, cefuroxima, claritromicina, azitromicina    e ciprofloxacina. De entre o conjunto de antibi&oacute;ticos ensaiado, a penicilina    continua a ser o mais activo contra <I>S. pyogenes </I>e a amoxicilina / clavulanato    e as quinolonas os mais activos simultaneamente contra <I>S. pneumoniae, </I>    <I>H. influenzae</I> e <I>M. catarrhalis</I>.       <P align="justify"><B>Palavras-chave</B>: Portugal, Estudo Viriato, infec&ccedil;&atilde;o    respirat&oacute;ria, comunidade, 2003, 2004, susceptibilidade aos antimicrobianos,    <I>Streptococcus pyogenes, Streptococcus pneumoniae, Haemophilus influenzae,    Moraxella catarrhalis.</I></P>      <p>&nbsp;</p>      <P align="center"><B>Abstract</B></P>       <P align="justify">The Viriato Study is a nationwide, prospective, multicenter    surveillance study of the antimicrobial susceptibility of bacterial pathogens    commonly associated with community-acquired respiratory tract infections in    Portugal. In 2003 and 2004 a total of 2945 isolates was recovered in the 29    laboratories that participated in the study. Testing was undertaken in a central    laboratory. Of the <I>513 Streptococcus pyogenes</I> strains isolated from patients    with acute tonsillitis all were susceptible to penicillin and other beta-lactams    but 18.9% were resistant to erythromycin, clarithromycin and azithromycin. The    M phenotype dominated (67%), conferring resistance to erythromycin (MIC<sub>90</sub>=16mg/L),    clarythromycin and azithromycin, but susceptibility to clindamycin (MIC<sub>90</sub>=0.094    mg/L). From patients with lower respiratory tract infection 1,300 strains of    <I>Streptococcus pneumoniae</I>, 829 of <I>Haemophilus influenzae</I>, and 303    of <I>Moraxella catarrhalis</I> were studied. Among <I>S. pneumoniae</I> isolates    18.4% were resistant to penicillin (3.5% showing high-level resistance), 7.1%    to cefuroxime, 0.5% to amoxicillin and amoxicillin/clavulanate, 18.8% to erythromycin,    clarithromycin and azithromycin, 14.9% to tetracycline, 16.5% to co-trimoxazol,    and 0.4% to levofloxacin. Beta-lactamases were produced by 10.0% of <I>H. influenzae</I>    and 96.4% of <I>M. catarrhalis</I>. In <I>H. influenzae</I> resistance to clarithromycin    was 5.5% and to co-trimoxazole was 13.4%. Most strains were susceptible to amoxicillin/clavulanate,    cefuroxime, azithromycin, tetracycline and ciprofloxacin. In <I>M. catarrhalis</I>    resistance to co-trimoxazole was 27.1% and to tetracycline 1.0%. All strains    were susceptible to amoxicillin/clavulanate, cefuroxime, clarithromycin, azithromycin    and ciprofloxacin. Penicillin was the most active antimicrobial agent against    <I>S. pyogenes</I> and amoxycillin / clavulanate and the quinolones the most    active <I>in vitro</I> simultaneously against <I>S. pneumoniae, H. influenza</I>    and <I>M. catarrhalis</I>.</P>       <P><B>Key-words</B>: Portugal, Viriato Study, respiratory tract infections,  community, 2003, 2004, antimicrobial resistance, <I>Streptococcus pyogenes,  Streptococcus pneumoniae, Haemophilus influenzae, Moraxella catarrhalis</I>.</P>      <p>&nbsp;</p>     <p>&nbsp;</p>      <p>Texto completo disponível apenas em PDF.</p>     ]]></body>
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Archives of  Internal Medicine 2000; 160: 1399-1408.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000040&pid=S0873-2159200600010000100014&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><P>15. Melo-Cristino J, Ramirez M, Serrano N, H&auml;nscheid T, and  The Portuguese Surveillance Group for the Study of Respiratory Pathogens.  Macrolide resistance in <I>Streptococcus pneumoniae</I> isolated from  patients with community-acquired lower respiratory tract infections  in Portugal: Results of a 3-year (1999-2001) multicenter surveillance  study. Microbial Drug Resistance 2003; 9: 73-80.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000041&pid=S0873-2159200600010000100015&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><P>16. Bajanca-Lavado Mp, Casin I, Vaz Pato Mv and The Multicentre  Study Group. Antimicrobial resistance and epidemiological study of  <I>Haemophilus influenzae</I> strains isolated in Portugal. Journal  of Antimicrobial Chemotherapy 1996; 38: 615-625.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000042&pid=S0873-2159200600010000100016&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><P>17. Verduin Cm, Hol C, Fleer A, Van Dijk H, Van Belkum A.  <I>Moraxella catarrhalis</I>: from emerging to established  pathogen. Clinical Microbiology Reviews 2002; 15: 125-144.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000043&pid=S0873-2159200600010000100017&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><p>&nbsp;</p>     <p>&nbsp;</p>      <P align="justify"><SUP><a href="#top1">1</a><a name="1"></a> </SUP>Instituto    de Microbiologia. Instituto de Medicina Molecular. Faculdade de Medicina de    Lisboa/<I>Microbiology Institute. Molecular Medicine Institute Lisbon Medical    School.</I>      <P align="justify">Av. Prof Egas Moniz 1649-028 Lisboa. Tel. 217999458. Fax. 217999459.</P>      <P align="justify"><SUP><a href="#top2">2</a><a name="2"></a></SUP> Grupo de Estudo    Portugu&ecirc;s de Bact&eacute;rias Patog&eacute;nicas Respirat&oacute;rias/<I>Portuguese    Respiratory Bacterial Pathogens Research Group</I>: Centro Hospitalar do Alto    Minho, Viana do Castelo: S&iacute;lvia Lozano; Centro Hospitalar de Cascais:    Ana Fonseca, Adriana Coutinho; Centro Hospitalar de Coimbra: Ana Florinda Alves,    Lu&iacute;s Albuquerque; Centro Hospitalar da P&oacute;voa do Varzim/Vila do    Conde: Fernando Fonseca; Centro Hospitalar de Vila Nova de Gaia: Paulo Lopes,    Ism&aacute;lia Calheiros, Lu&iacute;sa Fel&iacute;cio, Lourdes Sobral; Hospital    do Barlavento Algarvio: Teresa Vaz, Mar&iacute;lia Gi&atilde;o; Hospital Central    do Funchal: Teresa Afonso; Hospital Curry Cabral, Lisboa: Maria Jos&eacute;    Silvestre, Helena Peres, Teresa Pina; Hospital Distrital de Abrantes: Clotilde    Rold&atilde;o; Hospital do Divino Esp&iacute;rito Santo, Ponta Delgada: Eul&aacute;lia    Carvalho; Hospital Infante D. Pedro, Aveiro: Elmano Ramalheira, Ana Margarida    Paradela; Hospital D. Estef&acirc;nia, Lisboa: Rosa M. Barros, Maria Isabel    Peres; Hospital Garcia de Orta, Almada: Jos&eacute; Diogo, Ana Rodrigues, Isabel    Nascimento; Hospital Pedro Hispano, Matosinhos: Valqu&iacute;ria Alves, Ant&oacute;nia    Read, Margarida Monteiro; Hospital de Pulido Valente, Lisboa: Margarida Abecassis,    Isilda Alves, Rita Pinto; Hospital dos S.A.M.S., Lisboa: Lu&iacute;sa Cabral,    Olga Neto; Filipa Antunes; Hospital de Santa Luzia, Elvas: Ilse Fontes; Hospital    de Santa Maria, Lisboa: Lu&iacute;s Lito, Maria Lu&iacute;s Fernandes, Maria    Jos&eacute; Salgado; Hospital de Santa Marta, Lisboa: Margarida Pinto, Herm&iacute;nia    Choon; Hospital de Santo Ant&oacute;nio, Porto: Ana Paula Castro, Maria Helena    Ramos, Jos&eacute; Manuel Amorim; Hospital de S&atilde;o Francisco Xavier, Lisboa:    Filomena Martins, Maria Ana Pessanha, Elsa Gon&ccedil;alves; Hospital de S&atilde;o    Jo&atilde;o, Porto: Fernanda Cotta, J. Correia da Fonseca; Hospital de S&atilde;o    Jos&eacute;, Lisboa: Maria Odete Spencer, Jo&atilde;o Marques; Hospital de S&atilde;o    Marcos, Braga: Maria Alberta Faustino, Adelaide Alves; Hospital de S&atilde;o    Teot&oacute;nio, Viseu: Isabel Marques, Jos&eacute; Miguel Ribeiro; Hospital    Senhora da Oliveira, Guimar&atilde;es: Ana Paula M. Vieira, Francisco B. Moniz;    Hospitais da Universidade de Coimbra: Rosa Velho, Rui Tom&eacute;, Celeste Pontes;    Hospital de Vila Real: Ana Paula Castro; Instituto Nacional de Sa&uacute;de    Dr. Ricardo Jorge, Porto: M&#170;. Olinda Bas&iacute;lio, M&#170; da Gra&ccedil;a    Martins, Cristiana Pereira, Engr&aacute;cia Raposo, Maria de Lurdes Magalh&atilde;es,    Helena Rocha.</P>      <p>&nbsp;</p>      <p>Recebido para publicação/received for publication: 05.12.13 </p>     <p>Aceite para publicação/accepted for publication: 06.01.04       ]]></body><back>
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