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  <front>
    <journal-meta><journal-id journal-id-type="publisher">JBJI</journal-id><journal-title-group>
    <journal-title>Journal of Bone and Joint Infection</journal-title>
    <abbrev-journal-title abbrev-type="publisher">JBJI</abbrev-journal-title><abbrev-journal-title abbrev-type="nlm-ta">J. Bone Joint Infect.</abbrev-journal-title>
  </journal-title-group><issn pub-type="epub">2206-3552</issn><publisher>
    <publisher-name>Copernicus Publications</publisher-name>
    <publisher-loc>Göttingen, Germany</publisher-loc>
  </publisher></journal-meta>
    <article-meta>
      <article-id pub-id-type="doi">10.5194/jbji-6-91-2021</article-id><title-group><article-title>One-year infection control rates of a DAIR (debridement, antibiotics and implant retention) procedure after primary and prosthetic-joint-infection-related revision arthroplasty – a retrospective cohort study</article-title><alt-title>One-year infection control rates of a DAIR procedure</alt-title>
      </title-group><?xmltex \runningtitle{One-year infection control rates of a DAIR procedure}?><?xmltex \runningauthor{F.~R.~H.~A.~Nurmohamed et al.}?>
      <contrib-group>
        <contrib contrib-type="author" corresp="yes" rid="aff1">
          <name><surname>Nurmohamed</surname><given-names>F. Ruben H. A.</given-names></name>
          <email>f.r.h.a.nurmohamed-2@umcutrecht.nl</email>
        <ext-link>https://orcid.org/0000-0001-5369-9853</ext-link></contrib>
        <contrib contrib-type="author" corresp="no" rid="aff1">
          <name><surname>van Dijk</surname><given-names>Bruce</given-names></name>
          
        </contrib>
        <contrib contrib-type="author" corresp="no" rid="aff1">
          <name><surname>Veltman</surname><given-names>Ewout S.</given-names></name>
          
        </contrib>
        <contrib contrib-type="author" corresp="no" rid="aff1">
          <name><surname>Hoekstra</surname><given-names>Marrit</given-names></name>
          
        </contrib>
        <contrib contrib-type="author" corresp="no" rid="aff2">
          <name><surname>Rentenaar</surname><given-names>Rob J.</given-names></name>
          
        </contrib>
        <contrib contrib-type="author" corresp="no" rid="aff1 aff3">
          <name><surname>Weinans</surname><given-names>Harrie H.</given-names></name>
          
        </contrib>
        <contrib contrib-type="author" corresp="no" rid="aff1">
          <name><surname>Vogely</surname><given-names>H. Charles</given-names></name>
          
        <ext-link>https://orcid.org/0000-0002-0934-2985</ext-link></contrib>
        <contrib contrib-type="author" corresp="no" rid="aff1">
          <name><surname>van der Wal</surname><given-names>Bart C. H.</given-names></name>
          
        </contrib>
        <aff id="aff1"><label>1</label><institution>Department of Orthopedics, University Medical Center Utrecht,
Utrecht, the Netherlands</institution>
        </aff>
        <aff id="aff2"><label>2</label><institution>Department of Microbiology, University Medical Center Utrecht,
Utrecht, the Netherlands</institution>
        </aff>
        <aff id="aff3"><label>3</label><institution>Department of BioMechanical Engineering, Delft University of Technology, Delft, the
Netherlands</institution>
        </aff>
      </contrib-group>
      <author-notes><corresp id="corr1">F. Ruben H. A. Nurmohamed (f.r.h.a.nurmohamed-2@umcutrecht.nl)</corresp></author-notes><pub-date><day>27</day><month>January</month><year>2021</year></pub-date>
      
      <volume>6</volume>
      <issue>4</issue>
      <fpage>91</fpage><lpage>97</lpage>
      <history>
        <date date-type="received"><day>13</day><month>October</month><year>2020</year></date>
           <date date-type="rev-recd"><day>30</day><month>December</month><year>2020</year></date>
           <date date-type="accepted"><day>10</day><month>January</month><year>2021</year></date>
      </history>
      <permissions>
        <copyright-statement>Copyright: © 2021 F. Ruben H. A. Nurmohamed et al.</copyright-statement>
        <copyright-year>2021</copyright-year>
      <license license-type="open-access"><license-p>This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this licence, visit <ext-link ext-link-type="uri" xlink:href="https://creativecommons.org/licenses/by/4.0/">https://creativecommons.org/licenses/by/4.0/</ext-link></license-p></license></permissions><self-uri xlink:href="https://jbji.copernicus.org/articles/6/91/2021/jbji-6-91-2021.html">This article is available from https://jbji.copernicus.org/articles/6/91/2021/jbji-6-91-2021.html</self-uri><self-uri xlink:href="https://jbji.copernicus.org/articles/6/91/2021/jbji-6-91-2021.pdf">The full text article is available as a PDF file from https://jbji.copernicus.org/articles/6/91/2021/jbji-6-91-2021.pdf</self-uri>
      <abstract><title>Abstract</title>
    <p id="d1e156"><bold>Introduction</bold>: Debridement, antibiotics and implant retention (DAIR)
procedures are effective treatments for acute postoperative or acute
hematogenous periprosthetic joint infections. However, literature reporting
on the effectiveness of DAIR procedures performed after a one- or two-stage
revision because of a prosthetic joint infection (PJI) (PJI-related revision arthroplasty) is scarce. The
aim of this study is to retrospectively evaluate the infection control after
1 year of a DAIR procedure in the case of an early postoperative infection
either after primary arthroplasty or after PJI-related revision
arthroplasty.
<bold>Materials and methods</bold>: All patients treated with a DAIR procedure within 3
months after onset of PJI between 2009 and 2017 were retrospectively
included. Data were collected on patient and infection characteristics. All
infections were confirmed by applying the Musculoskeletal Infection Society (MSIS) 2014 criteria. The primary
outcome was successful control of infection at 1 year after a DAIR
procedure, which was defined as the absence of clinical signs, such as pain,
swelling, and erythema; radiological signs, such as protheses loosening; or
laboratory signs, such as C-reactive protein (CRP) (<inline-formula><mml:math id="M1" display="inline"><mml:mrow><mml:mo>&lt;</mml:mo><mml:mn mathvariant="normal">10</mml:mn></mml:mrow></mml:math></inline-formula>) with no use of antibiotic therapy.
<bold>Results</bold>: Sixty-seven patients were treated with a DAIR procedure (41 hips and 26
knees). Successful infection control rates of a DAIR procedure after primary
arthroplasty (<inline-formula><mml:math id="M2" display="inline"><mml:mrow><mml:mi>n</mml:mi><mml:mo>=</mml:mo><mml:mn mathvariant="normal">51</mml:mn></mml:mrow></mml:math></inline-formula>) and after prior PJI-related revision arthroplasty
(<inline-formula><mml:math id="M3" display="inline"><mml:mrow><mml:mi>n</mml:mi><mml:mo>=</mml:mo><mml:mn mathvariant="normal">16</mml:mn></mml:mrow></mml:math></inline-formula>) were 69 % and 56 %, respectively (<inline-formula><mml:math id="M4" display="inline"><mml:mrow><mml:mi>p</mml:mi><mml:mo>=</mml:mo><mml:mn mathvariant="normal">0.38</mml:mn></mml:mrow></mml:math></inline-formula>). The successful infection control rates of a DAIR procedure after an early acute infection
(<inline-formula><mml:math id="M5" display="inline"><mml:mrow><mml:mi>n</mml:mi><mml:mo>=</mml:mo><mml:mn mathvariant="normal">35</mml:mn></mml:mrow></mml:math></inline-formula>) and after a hematogenous infection (<inline-formula><mml:math id="M6" display="inline"><mml:mrow><mml:mi>n</mml:mi><mml:mo>=</mml:mo><mml:mn mathvariant="normal">16</mml:mn></mml:mrow></mml:math></inline-formula>) following primary
arthroplasty were both 69 % (<inline-formula><mml:math id="M7" display="inline"><mml:mrow><mml:mi>p</mml:mi><mml:mo>=</mml:mo><mml:mn mathvariant="normal">1.00</mml:mn></mml:mrow></mml:math></inline-formula>).
<bold>Conclusion</bold>: In this limited study population, no statistically significant
difference is found in infection control after 1 year between DAIR
procedures after primary arthroplasty and PJI-related revision arthroplasty.</p>
  </abstract>
    </article-meta>
  </front>
<body>
      

<sec id="Ch1.S1" sec-type="intro">
  <label>1</label><title>Introduction</title>
      <p id="d1e262">Prosthetic joint infection (PJI) is a devastating complication following
total hip and knee arthroplasty. The incidences of PJI in the Western
countries are reported to range up to 4 % for primary total hip and knee
arthroplasty and even as high as 20 % following revision arthroplasty
(Ahmed et al., 2020; Hosny and
Keenan, 2020).</p>
      <p id="d1e265">The most common clinical signs of acute and hematogenous PJI include acute
pain, erythema and fever (Barrett and
Atkins, 2014; Zimmerli, 2006). A debridement, antibiotics and implant
retention (DAIR) procedure is the treatment of choice for acute PJI of the
hip and knee
(Chotanaphuti
et al., 2019; Sukeik and Haddad, 2019; Wouthuyzen-Bakker et al., 2020). A
recent systematic review and meta-analysis reported a wide range of success
percentages for DAIR procedures from 11 % to 100 %
(Kunutsor
et al., 2018; Tsang et<?pagebreak page92?> al., 2017). Several studies have shown that the time
between onset of symptoms and the DAIR procedure is strongly associated with
the success rate of treatment
(Karczewski
et al., 2019; Kuiper et al., 2013; Kunutsor et al., 2018; Sendi et al.,
2017). Nonetheless, even more than 6 weeks after the index arthroplasty an
eradication rate of 60 % can be achieved when performing DAIR
(Löwik et al., 2019). The
success rate of DAIR for early postoperative infection is better than for
hematogenous infections
(Volpin
et al., 2016; Wouthuyzen-Bakker et al., 2020). There is no place for DAIR in
the treatment of chronic infections (Sukeik and Haddad,
2019). Prior infection in another prosthetic joint and prior two-stage
exchange for PJI of the same joint are both reported to worsen the infection
eradication rate of a repeated revision procedure compared to a first
revision
(Chalmers
et al., 2019; Khan et al., 2019). However, the effectiveness of DAIR
procedures after prior PJI-related revision arthroplasty is still up for
debate.</p>
      <p id="d1e268">The primary aim of this study is to retrospectively evaluate the infection
control rate of DAIR procedures performed after a one- or two-stage revision
because of a PJI (PJI-related revision arthroplasty) in comparison to DAIR
procedures performed after primary arthroplasty. The secondary aim of this
study is to evaluate if the infection control rate of a DAIR procedure after
primary arthroplasty depends on whether an infection is early postoperative
or hematogenous. We hypothesize that previous PJI-related revision
arthroplasty procedures have a negative effect on the infection control rate of
subsequently performed DAIR procedures.</p>
</sec>
<sec id="Ch1.S2">
  <label>2</label><title>Methods</title>
      <p id="d1e279">In this observational study, we reviewed the records of all patients in our prospectively collected database who had an infection treatment of the hip or knee in our hospital between 2009 and 2017. After approval, we
reviewed the records of all patients in our prospectively collected database
who had an infection treatment of the hip or knee in our hospital between
2009 and 2017. We included all patients with one periprosthetic joint
infection. All DAIR procedures were performed after placing a primary hip or
knee prothesis or after full reimplantation of a hip or knee prothesis for
infection revision surgery. In all patients, diagnosis of infection was
affirmed according to the Musculoskeletal Infection Society criteria
(Parvizi and Gehrke, 2014). In our institution, DAIR
procedures are only performed within 3 months after the onset of
symptoms.</p>
      <p id="d1e282">We retrieved general patient and infection characteristics, complications
during treatment, and final outcomes from patients' records. Primary outcome
was tier 1 infection control after DAIR treatment, based on the
outcome-reporting tool suggested by the Musculoskeletal Infection Society
workgroup (Fillingham et al., 2019). The absence
of clinical signs, such as pain, swelling, and erythema; radiological signs,
such as protheses loosening; or laboratory signs, such as CRP (<inline-formula><mml:math id="M8" display="inline"><mml:mrow><mml:mo>&lt;</mml:mo><mml:mn mathvariant="normal">10</mml:mn></mml:mrow></mml:math></inline-formula>),
with no use of antibiotic therapy at the final follow-up 1 year after the
first subsequently performed DAIR procedure was seen as a successful outcome.
We used the presence of a prior PJI-related revision procedure and type of
infection (acute early or hematogenous) as variables to separately analyze
whether the infection control rate was affected (McPherson
et al., 2002).</p>
      <p id="d1e295">Failure of treatment was defined as failed control of the periprosthetic
infection. This includes tier 2 or higher based on the aforementioned
outcome-reporting tool. Specifically, additional surgeries, such as resection
arthroplasty, arthrodesis or amputation of the limb, or the administration
of suppressive antibiotics prior to the final 1-year
postoperative follow-up was seen as a failed outcome. Only a third repeated DAIR procedure was
considered failure of treatment.</p>
<sec id="Ch1.S2.SS1">
  <label>2.1</label><title>Patient characteristics</title>
      <p id="d1e305">Characteristics such as age, sex, BMI (body mass index), ASA class (American Society of Anesthesiologists), smoking or alcohol use,
co-morbidities, and previous infection treatment were extracted from the
medical charts. Previous PJI-related procedures were subdivided into
(multiple) DAIR procedures and (one- or two-stage) revision procedures.</p>
</sec>
<sec id="Ch1.S2.SS2">
  <label>2.2</label><title>Prosthetic joint infection characteristics</title>
      <p id="d1e317">PJI characteristics included location of infection, type of infection and
involvement of soft tissue. To determine the degree of compromise of the
host and the infection site, the McPherson staging system was used
(McPherson et al., 2002). For early acute infections,
defined as onset of infection within 3 months after surgery, the time
between primary or PJI-related revision arthroplasty and the DAIR procedure
was used as the infection period. For acute hematogenous infections, defined
as infections spread from a distant infectious focus, the time from onset of
symptoms until the DAIR procedure was calculated as the infection period.</p>
</sec>
<sec id="Ch1.S2.SS3">
  <label>2.3</label><title>The DAIR procedure</title>
      <p id="d1e328">A debridement, antibiotics and implant retention procedure consists of
several steps in consecutive order. First, six synovial fluid or tissue
samples are collected for culture and a meticulous debridement of the joint
is performed to remove all infected tissue. The interchangeable parts
(insert of the knee and inlay and head of the hip) are removed to facilitate
posterior joint debridement and are then replaced. During surgery, the joint
is extensively lavaged with 6 L of NaCl 0.9 %.</p>
      <p id="d1e331">All patients were treated with cefazolin until culture results were
available. When culture results were available, the definite antibiotic
strategy was determined according to the found pathogen and antibiotic
susceptibility test<?pagebreak page93?> results in close consultation with a medical
microbiologist and an infectious disease specialist. Patients generally
received 3 months of antibiotic treatment following DAIR.</p>
</sec>
<sec id="Ch1.S2.SS4">
  <label>2.4</label><title>Statistical analysis</title>
      <p id="d1e342">Descriptive statistics, mean and range are used to represent the
demographics of the patients. Fisher's exact test was used to assess the
level of significance for differences between the infection control rates of
the groups. A <inline-formula><mml:math id="M9" display="inline"><mml:mi>P</mml:mi></mml:math></inline-formula> value <inline-formula><mml:math id="M10" display="inline"><mml:mrow><mml:mo>&lt;</mml:mo><mml:mn mathvariant="normal">0.05</mml:mn></mml:mrow></mml:math></inline-formula> was considered to be statistically
significant. Calculations and statistical analyses were performed using
Excel and SPSS software (version 27).</p>

      <?xmltex \floatpos{p}?><fig id="Ch1.F1" specific-use="star"><?xmltex \currentcnt{1}?><?xmltex \def\figurename{Figure}?><label>Figure 1</label><caption><p id="d1e364">Flow diagram showing the infection characteristics, previous PJI procedures and number of successfully controlled infections.</p></caption>
          <?xmltex \igopts{width=483.69685pt}?><graphic xlink:href="https://jbji.copernicus.org/articles/6/91/2021/jbji-6-91-2021-f01.png"/>

        </fig>

      <?xmltex \floatpos{t}?><fig id="Ch1.F2"><?xmltex \currentcnt{2}?><?xmltex \def\figurename{Figure}?><label>Figure 2</label><caption><p id="d1e375">Flow diagram showing the numbers of patients with successfully controlled infections according to the frequency of previous PJI-related revision arthroplasty.</p></caption>
          <?xmltex \igopts{width=170.716535pt}?><graphic xlink:href="https://jbji.copernicus.org/articles/6/91/2021/jbji-6-91-2021-f02.png"/>

        </fig>

<?xmltex \floatpos{p}?><table-wrap id="Ch1.T1" specific-use="star"><?xmltex \currentcnt{1}?><label>Table 1</label><caption><p id="d1e388">Baseline patient characteristics.</p></caption><oasis:table frame="topbot"><oasis:tgroup cols="4">
     <oasis:colspec colnum="1" colname="col1" align="left"/>
     <oasis:colspec colnum="2" colname="col2" align="right"/>
     <oasis:colspec colnum="3" colname="col3" align="right"/>
     <oasis:colspec colnum="4" colname="col4" align="right"/>
     <oasis:thead>
       <oasis:row rowsep="1">
         <oasis:entry colname="col1"/>
         <oasis:entry colname="col2">Total (<inline-formula><mml:math id="M11" display="inline"><mml:mi>n</mml:mi></mml:math></inline-formula>)</oasis:entry>
         <oasis:entry colname="col3">Successful infection control (<inline-formula><mml:math id="M12" display="inline"><mml:mi>n</mml:mi></mml:math></inline-formula>)</oasis:entry>
         <oasis:entry colname="col4">Failed infection control (<inline-formula><mml:math id="M13" display="inline"><mml:mi>n</mml:mi></mml:math></inline-formula>)</oasis:entry>
       </oasis:row>
     </oasis:thead>
     <oasis:tbody>
       <oasis:row>
         <oasis:entry colname="col1">Number of patients</oasis:entry>
         <oasis:entry colname="col2">67</oasis:entry>
         <oasis:entry colname="col3">44 (66 %)</oasis:entry>
         <oasis:entry colname="col4">23 (34 %)</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1">Hip</oasis:entry>
         <oasis:entry colname="col2">41</oasis:entry>
         <oasis:entry colname="col3">29 (71 %)</oasis:entry>
         <oasis:entry colname="col4">12 (29 %)</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1">Knee</oasis:entry>
         <oasis:entry colname="col2">26</oasis:entry>
         <oasis:entry colname="col3">15 (58 %)</oasis:entry>
         <oasis:entry colname="col4">11 (42 %)</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1">Mean age (range)</oasis:entry>
         <oasis:entry colname="col2">67 (18–92)</oasis:entry>
         <oasis:entry colname="col3">68 (18–92)</oasis:entry>
         <oasis:entry colname="col4">63 (35–78)</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1">Gender M/F</oasis:entry>
         <oasis:entry colname="col2">29/38</oasis:entry>
         <oasis:entry colname="col3">16 (55 %)/28 (74 %)</oasis:entry>
         <oasis:entry colname="col4">13 (45 %)/10 (26 %)</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1">Mean BMI (range)</oasis:entry>
         <oasis:entry colname="col2">27 (19–45)</oasis:entry>
         <oasis:entry colname="col3">27 (19–44)</oasis:entry>
         <oasis:entry colname="col4">28 (19–45)</oasis:entry>
       </oasis:row>
       <oasis:row rowsep="1">
         <oasis:entry colname="col1">Mean duration of infection (days)</oasis:entry>
         <oasis:entry colname="col2">20</oasis:entry>
         <oasis:entry colname="col3">22</oasis:entry>
         <oasis:entry colname="col4">16</oasis:entry>
       </oasis:row>
       <oasis:row rowsep="1">
         <oasis:entry namest="col1" nameend="col4">Risk factors </oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1">Smoking</oasis:entry>
         <oasis:entry colname="col2">12</oasis:entry>
         <oasis:entry colname="col3">7 (58 %)</oasis:entry>
         <oasis:entry colname="col4">5 (42 %)</oasis:entry>
       </oasis:row>
       <oasis:row rowsep="1">
         <oasis:entry colname="col1">Alcohol abuse</oasis:entry>
         <oasis:entry colname="col2">7</oasis:entry>
         <oasis:entry colname="col3">6 (86 %)</oasis:entry>
         <oasis:entry colname="col4">1 (14 %)</oasis:entry>
       </oasis:row>
       <oasis:row rowsep="1">
         <oasis:entry colname="col1">ASA 1/2/3</oasis:entry>
         <oasis:entry colname="col2">6/37/24</oasis:entry>
         <oasis:entry colname="col3">4/23/17</oasis:entry>
         <oasis:entry colname="col4">2/14/7</oasis:entry>
       </oasis:row>
       <oasis:row rowsep="1">
         <oasis:entry namest="col1" nameend="col4">Host score (according to McPherson) </oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1">Uncompromised</oasis:entry>
         <oasis:entry colname="col2">19</oasis:entry>
         <oasis:entry colname="col3">9 (47 %)</oasis:entry>
         <oasis:entry colname="col4">10 (53 %)</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1">Compromised</oasis:entry>
         <oasis:entry colname="col2">44</oasis:entry>
         <oasis:entry colname="col3">32 (73 %)</oasis:entry>
         <oasis:entry colname="col4">12 (27 %)</oasis:entry>
       </oasis:row>
       <oasis:row rowsep="1">
         <oasis:entry colname="col1">Significantly compromised</oasis:entry>
         <oasis:entry colname="col2">4</oasis:entry>
         <oasis:entry colname="col3">3 (75 %)</oasis:entry>
         <oasis:entry colname="col4">1 (25 %)</oasis:entry>
       </oasis:row>
       <oasis:row rowsep="1">
         <oasis:entry namest="col1" nameend="col4">Local extremity grade (according to McPherson) </oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1">Uncompromised</oasis:entry>
         <oasis:entry colname="col2">58</oasis:entry>
         <oasis:entry colname="col3">41 (71 %)</oasis:entry>
         <oasis:entry colname="col4">17 (29 %)</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1">Compromised</oasis:entry>
         <oasis:entry colname="col2">9</oasis:entry>
         <oasis:entry colname="col3">3 (33 %)</oasis:entry>
         <oasis:entry colname="col4">6 (67 %)</oasis:entry>
       </oasis:row>
     </oasis:tbody>
   </oasis:tgroup></oasis:table></table-wrap>

<?xmltex \floatpos{t}?><table-wrap id="Ch1.T2" specific-use="star"><?xmltex \currentcnt{2}?><label>Table 2</label><caption><p id="d1e695">Microbiology findings.</p></caption><oasis:table frame="topbot"><oasis:tgroup cols="3">
     <oasis:colspec colnum="1" colname="col1" align="left"/>
     <oasis:colspec colnum="2" colname="col2" align="right"/>
     <oasis:colspec colnum="3" colname="col3" align="right"/>
     <oasis:thead>
       <oasis:row rowsep="1">
         <oasis:entry colname="col1"/>
         <oasis:entry colname="col2">Cases (<inline-formula><mml:math id="M36" display="inline"><mml:mi>n</mml:mi></mml:math></inline-formula>)</oasis:entry>
         <oasis:entry colname="col3">Successful infection control (<inline-formula><mml:math id="M37" display="inline"><mml:mi>n</mml:mi></mml:math></inline-formula>)</oasis:entry>
       </oasis:row>
     </oasis:thead>
     <oasis:tbody>
       <oasis:row>
         <oasis:entry colname="col1"><italic>Staphylococcus aureus</italic></oasis:entry>
         <oasis:entry colname="col2">13</oasis:entry>
         <oasis:entry colname="col3">8</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1"><italic>Staphylococcus epidermidis</italic></oasis:entry>
         <oasis:entry colname="col2">14</oasis:entry>
         <oasis:entry colname="col3">10</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1">Other staphylococci<inline-formula><mml:math id="M38" display="inline"><mml:msup><mml:mi/><mml:mi mathvariant="normal">a</mml:mi></mml:msup></mml:math></inline-formula></oasis:entry>
         <oasis:entry colname="col2">5</oasis:entry>
         <oasis:entry colname="col3">5</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1">Beta-hemolytic streptococci<inline-formula><mml:math id="M39" display="inline"><mml:msup><mml:mi/><mml:mi mathvariant="normal">b</mml:mi></mml:msup></mml:math></inline-formula></oasis:entry>
         <oasis:entry colname="col2">4</oasis:entry>
         <oasis:entry colname="col3">3</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1">Enterococci<inline-formula><mml:math id="M40" display="inline"><mml:msup><mml:mi/><mml:mi mathvariant="normal">c</mml:mi></mml:msup></mml:math></inline-formula></oasis:entry>
         <oasis:entry colname="col2">6</oasis:entry>
         <oasis:entry colname="col3">2</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1">Enterobacterales<inline-formula><mml:math id="M41" display="inline"><mml:msup><mml:mi/><mml:mi mathvariant="normal">d</mml:mi></mml:msup></mml:math></inline-formula></oasis:entry>
         <oasis:entry colname="col2">6</oasis:entry>
         <oasis:entry colname="col3">5</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1"><italic>Pseudomonas aeruginosa</italic></oasis:entry>
         <oasis:entry colname="col2">2</oasis:entry>
         <oasis:entry colname="col3">2</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1">Other pathogens<inline-formula><mml:math id="M42" display="inline"><mml:msup><mml:mi/><mml:mi mathvariant="normal">e</mml:mi></mml:msup></mml:math></inline-formula></oasis:entry>
         <oasis:entry colname="col2">7</oasis:entry>
         <oasis:entry colname="col3">4</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1">Polymicrobial</oasis:entry>
         <oasis:entry colname="col2">6</oasis:entry>
         <oasis:entry colname="col3">2</oasis:entry>
       </oasis:row>
       <oasis:row rowsep="1">
         <oasis:entry colname="col1">No organism identified</oasis:entry>
         <oasis:entry colname="col2">4</oasis:entry>
         <oasis:entry colname="col3">3</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1">Total</oasis:entry>
         <oasis:entry colname="col2">67</oasis:entry>
         <oasis:entry colname="col3">44</oasis:entry>
       </oasis:row>
     </oasis:tbody>
   </oasis:tgroup></oasis:table><table-wrap-foot><p id="d1e698"><inline-formula><mml:math id="M14" display="inline"><mml:msup><mml:mi/><mml:mi mathvariant="normal">a</mml:mi></mml:msup></mml:math></inline-formula> <italic>S. capitis</italic> (<inline-formula><mml:math id="M15" display="inline"><mml:mrow><mml:mi>n</mml:mi><mml:mo>=</mml:mo><mml:mn mathvariant="normal">2</mml:mn></mml:mrow></mml:math></inline-formula>), <italic>S. warneri</italic> (<inline-formula><mml:math id="M16" display="inline"><mml:mrow><mml:mi>n</mml:mi><mml:mo>=</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:math></inline-formula>), <italic>S. haemolyticus</italic> (<inline-formula><mml:math id="M17" display="inline"><mml:mrow><mml:mi>n</mml:mi><mml:mo>=</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:math></inline-formula>) and <italic>S. pseudintermedius</italic> (<inline-formula><mml:math id="M18" display="inline"><mml:mrow><mml:mi>n</mml:mi><mml:mo>=</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:math></inline-formula>).<?xmltex \hack{\\}?><inline-formula><mml:math id="M19" display="inline"><mml:msup><mml:mi/><mml:mi mathvariant="normal">b</mml:mi></mml:msup></mml:math></inline-formula> <italic>S. dysgalactiae</italic> (<inline-formula><mml:math id="M20" display="inline"><mml:mrow><mml:mi>n</mml:mi><mml:mo>=</mml:mo><mml:mn mathvariant="normal">3</mml:mn></mml:mrow></mml:math></inline-formula>) and <italic>S. agalactiae</italic> (<inline-formula><mml:math id="M21" display="inline"><mml:mrow><mml:mi>n</mml:mi><mml:mo>=</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:math></inline-formula>).<?xmltex \hack{\\}?><inline-formula><mml:math id="M22" display="inline"><mml:msup><mml:mi/><mml:mi mathvariant="normal">c</mml:mi></mml:msup></mml:math></inline-formula> <italic>Enterococcus faecalis</italic> (<inline-formula><mml:math id="M23" display="inline"><mml:mrow><mml:mi>n</mml:mi><mml:mo>=</mml:mo><mml:mn mathvariant="normal">3</mml:mn></mml:mrow></mml:math></inline-formula>) and <italic>E. faecium</italic> (<inline-formula><mml:math id="M24" display="inline"><mml:mrow><mml:mi>n</mml:mi><mml:mo>=</mml:mo><mml:mn mathvariant="normal">3</mml:mn></mml:mrow></mml:math></inline-formula>).<?xmltex \hack{\\}?><inline-formula><mml:math id="M25" display="inline"><mml:msup><mml:mi/><mml:mi mathvariant="normal">d</mml:mi></mml:msup></mml:math></inline-formula> <italic>Escherichia coli</italic> (<inline-formula><mml:math id="M26" display="inline"><mml:mrow><mml:mi>n</mml:mi><mml:mo>=</mml:mo><mml:mn mathvariant="normal">2</mml:mn></mml:mrow></mml:math></inline-formula>), <italic>Klebsiella pneumoniae</italic> (<inline-formula><mml:math id="M27" display="inline"><mml:mrow><mml:mi>n</mml:mi><mml:mo>=</mml:mo><mml:mn mathvariant="normal">2</mml:mn></mml:mrow></mml:math></inline-formula>), <italic>Enterobacter cloacae</italic> complex (<inline-formula><mml:math id="M28" display="inline"><mml:mrow><mml:mi>n</mml:mi><mml:mo>=</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:math></inline-formula>) and
<italic>Serratia marcescens</italic> (<inline-formula><mml:math id="M29" display="inline"><mml:mrow><mml:mi>n</mml:mi><mml:mo>=</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:math></inline-formula>).<?xmltex \hack{\\}?><inline-formula><mml:math id="M30" display="inline"><mml:msup><mml:mi/><mml:mi mathvariant="normal">e</mml:mi></mml:msup></mml:math></inline-formula> <italic>Corynebacterium striatum</italic> (<inline-formula><mml:math id="M31" display="inline"><mml:mrow><mml:mi>n</mml:mi><mml:mo>=</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:math></inline-formula>), <italic>Corynebacterium tuberculostearicum</italic> (<inline-formula><mml:math id="M32" display="inline"><mml:mrow><mml:mi>n</mml:mi><mml:mo>=</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:math></inline-formula>),
<italic>Anaerococcus hydrogenalis</italic> (<inline-formula><mml:math id="M33" display="inline"><mml:mrow><mml:mi>n</mml:mi><mml:mo>=</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:math></inline-formula>), <italic>Cutibacterium acnes</italic> (<inline-formula><mml:math id="M34" display="inline"><mml:mrow><mml:mi>n</mml:mi><mml:mo>=</mml:mo><mml:mn mathvariant="normal">3</mml:mn></mml:mrow></mml:math></inline-formula>) and <italic>Ureaplasma parvum</italic> (<inline-formula><mml:math id="M35" display="inline"><mml:mrow><mml:mi>n</mml:mi><mml:mo>=</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:math></inline-formula>).</p></table-wrap-foot></table-wrap>

</sec>
</sec>
<sec id="Ch1.S3">
  <label>3</label><title>Results</title>
      <p id="d1e1238">Between 2009 and 2017, sixty-seven patients were treated for acute PJI with a DAIR
procedure. Forty-one hip and 26 knee surgeries were performed. General
patient and infection characteristics are shown in Figs. 1 and 2 and
Tables 1 and 2. All patients had a follow-up 1 year after the first
DAIR procedure. Overall, the infection was eradicated in 44 out of 67
patients.</p>
<sec id="Ch1.S3.SS1">
  <label>3.1</label><title>DAIR procedure after primary arthroplasty versus after previous PJI-related revision arthroplasty</title>
      <p id="d1e1248">In 51 patients a DAIR procedure was performed after primary arthroplasty. In
16 patients a DAIR procedure was performed after a previous PJI-related
revision procedure. A flow diagram of included patients and type of
PJI-related revision arthroplasty can be found in Fig. 1. For the two
patients with a hematogenous infection after previous PJI-related revision
arthroplasty, the interval between revision surgery and the onset of
hematogenous infection were 215 and 722 d. The infection control rate of
DAIR procedures performed after primary arthroplasty was 69 % (35 out of
51 cases). For hip and knee cases, the infection control rate was 72 % (21
out of 29 cases) and 64 % (14 out of 22 cases), respectively. The infection
control rate of DAIR procedures performed after PJI-related revision
arthroplasty was 56 % (9 out of 16 cases). For hip and knee cases, the
infection control rate was 67 % (8 out of 12 cases) and 25 % (1 out of 4
cases), respectively. There was no statistically significant difference in
the infection control rate between DAIR procedures performed after primary
arthroplasty and after PJI-related revision arthroplasty (<inline-formula><mml:math id="M43" display="inline"><mml:mrow><mml:mi>p</mml:mi><mml:mo>=</mml:mo><mml:mn mathvariant="normal">0.38</mml:mn></mml:mrow></mml:math></inline-formula>).</p>
</sec>
<sec id="Ch1.S3.SS2">
  <label>3.2</label><title>DAIR after early acute versus hematogenous infections after primary arthroplasty</title>
      <p id="d1e1271">In 35 patients a DAIR procedure was performed for an early acute infection
following primary arthroplasty. In 16 patients a DAIR procedure was
performed for an acute hematogenous infection (Fig. 1). The mean duration
of symptoms was 12 d (0–83 d) for hematogenous infections. The
infection control rate of DAIR procedures for early acute infections was
69 % (24 out of 35 cases). For hip and knee cases, infection control rate
was 74 % (17 out of 23 cases) and 58 % (7 out of 12 cases), respectively.
The infection control rate of DAIR procedures performed for hematogenous
infections was 69 % (11 out of 16 cases). For hip and knee cases, the
infection control rate was 67 % (4 out of 6 cases) and 70 % (7 out of 10
cases), respectively. There was no statistically significant difference in
the infection control rate between these two groups (<inline-formula><mml:math id="M44" display="inline"><mml:mrow><mml:mi>p</mml:mi><mml:mo>=</mml:mo><mml:mn mathvariant="normal">1.00</mml:mn></mml:mrow></mml:math></inline-formula>).</p>
</sec>
<sec id="Ch1.S3.SS3">
  <label>3.3</label><title>Microbiology findings</title>
      <p id="d1e1294">The microbiology culture results of the tissue cultures taken during DAIR
treatment can be found in Table 2. Sixty-three cases had positive
perioperative findings. No pathogen was identified in four cases. In two of
these cases, preoperative antibiotic treatment was administered by the
referring physician prior to surgery.</p>
</sec>
</sec>
<sec id="Ch1.S4" sec-type="conclusions">
  <label>4</label><title>Discussion</title>
      <p id="d1e1306">This study retrospectively evaluated the infection control rate of DAIR
procedures performed for PJI after primary arthroplasty or after previous
PJI-related revision arthroplasty of the hip and knee in a tertiary referral
center. The infection control rate of DAIR procedures after primary
arthroplasty was 69 % (35 out of 51 cases) compared to 56 % (9 out of 16
cases) for DAIR procedures after previous PJI-related revision arthroplasty.
Our study population is too small to draw definite conclusions; however,
these results show a trend that previous PJI treatment could have a negative
effect on the infection control rate of DAIR procedures.</p>
      <p id="d1e1309">There seems to be a contrast between the infection control rates of DAIR
performed after primary arthroplasty and DAIR after PJI-related revision
arthroplasty. Even though the infection control rate for DAIR procedures
after previous PJI-related revision arthroplasty is reduced, our data show
that about 6 out of 10 infections can still be controlled without further
major revision surgery. Furthermore, only 2 out of 6 DAIR procedures after
multiple PJI-related revision arthroplasty procedures were successful, whereas the
infection was controlled in 7 out of 10 DAIR procedures after a single
PJI-related revision procedure (<inline-formula><mml:math id="M45" display="inline"><mml:mrow><mml:mi>p</mml:mi><mml:mo>=</mml:mo><mml:mn mathvariant="normal">0.30</mml:mn></mml:mrow></mml:math></inline-formula>) (Fig. 2). The infection control
rate of DAIR treatment seems to further decline as the number of previously
performed PJI-related revision arthroplasty procedures increases.</p>
      <?pagebreak page95?><p id="d1e1324">Most of our infection control rates of DAIR procedures are comparable to the
overall pooled success rate of 61.4 % reported in a recent meta-analysis
(Kunutsor et al., 2018). However,
some other retrospective studies have reported higher infection control
rates for DAIR procedures
(Byren
et al., 2009; Sendi et al., 2017; Volpin et al., 2016; Wouthuyzen-Bakker et
al., 2020). The relatively large number of patients with ASA 3 and McPherson
compromised host score (Table 1) may cause a lower successful control rate
in our population.</p>
      <p id="d1e1327">Literature on the results of DAIR procedures after revision surgery is
scarce. Byren and colleagues reported a failure rate of 35 % and a 3.1
times increase in hazard ratio for failure of DAIR if it is performed after
revision arthroplasty compared to after primary arthroplasty
(Byren et al., 2009). Shohat and colleagues found no
significant difference in the success rate if DAIR was performed after
primary or revision arthroplasty (<inline-formula><mml:math id="M46" display="inline"><mml:mrow><mml:mi>p</mml:mi><mml:mo>=</mml:mo><mml:mn mathvariant="normal">0.182</mml:mn></mml:mrow></mml:math></inline-formula>)
(Shohat et al., 2020).
Lastly, Wouthuyzen-Bakker and colleagues found unadjusted and adjusted
odds ratios of 1.65 (<inline-formula><mml:math id="M47" display="inline"><mml:mrow><mml:mi>p</mml:mi><mml:mo>=</mml:mo><mml:mn mathvariant="normal">0.04</mml:mn></mml:mrow></mml:math></inline-formula>) and 0.96 (<inline-formula><mml:math id="M48" display="inline"><mml:mrow><mml:mi>p</mml:mi><mml:mo>=</mml:mo><mml:mn mathvariant="normal">0.90</mml:mn></mml:mrow></mml:math></inline-formula>), respectively, for failure of a DAIR
performed on revised prostheses with late prosthetic joint infections
(Wouthuyzen-Bakker
et al., 2019). Considering that no significant difference is found in the
infection control rate of DAIR procedures after PJI-related revision
arthroplasty in two studies and that this study found an infection control
rate of 56 %, a DAIR procedure should still be a treatment option for PJI
after revision arthroplasty. Nonetheless, the aforementioned studies show
the same trend as reported in this study.</p>
      <p id="d1e1367">A limitation of this study is reflected by the retrospective design. The
number of patients included in this study was relatively low, which was
caused by the scarcity of PJI cases requiring DAIR. Logically, especially the
number of patients with DAIR after revision surgery was low. Moreover,
misclassification bias and risk factors that were present but not measured
should also be accounted for. Heterogeneity of the groups can cause bias.</p>
      <p id="d1e1370">Our results show that even though the infection control rate may decrease
after prior PJI-related revision arthroplasty, a subsequently performed DAIR
procedure can retain the prosthesis in about 60 % of the patients. These
findings should be confirmed prospectively in a larger group of patients. We
recommend performing a prospective multicenter evaluation of DAIR treatment
to give a conclusive answer. Moreover, for patients with an infection after
primary arthroplasty, we found no difference in infection control rate
between early postoperative and acute hematogenous infections.</p>
</sec>

      
      </body>
    <back><notes notes-type="specialsection"><title>Ethical statement</title>
    

      <?pagebreak page96?><p id="d1e1380">This study was conducted in a tertiary referral healthcare center. Ethical
approval was waived by the local Medical Ethics Review Committee (METC) (no. 17-284/C).</p>
  </notes><notes notes-type="codeavailability"><title>Code availability</title>

      <p id="d1e1386">The data underlying the results presented in the study are available in the supporting SPSS information file.</p>
  </notes><notes notes-type="dataavailability"><title>Data availability</title>

      <p id="d1e1392">Raw data were generated at the University Medical Center Utrecht. Derived data
supporting the findings of this study are available from the corresponding
author, F. Ruben H. A. Nurmohamed, on request.</p>
  </notes><app-group>
        <supplementary-material position="anchor"><p id="d1e1395">The supplement related to this article is available online at: <inline-supplementary-material xlink:href="https://doi.org/10.5194/jbji-6-91-2021-supplement" xlink:title="zip">https://doi.org/10.5194/jbji-6-91-2021-supplement</inline-supplementary-material>.</p></supplementary-material>
        </app-group><notes notes-type="authorcontribution"><title>Author contributions</title>

      <p id="d1e1404">FRHAN contributed to data collection, analysis and drafting of the article. ESV and
RRR contributed to analysis and revision of the article. BvD, MH and HHW
contributed to the conception and design of the article. HCV performed surgery and
provided data. BCHvdW performed surgery; provided data; and contributed to
the conception, design, and revision of the article. All authors approved the final
article.</p>
  </notes><notes notes-type="competinginterests"><title>Competing interests</title>

      <p id="d1e1410">The authors declare that they have no conflict of interest.</p>
  </notes><notes notes-type="reviewstatement"><title>Review statement</title>

      <p id="d1e1416">This paper was edited by Parham Sendi and reviewed by three anonymous referees.</p>
  </notes><ref-list>
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Martínez-Pastor, J. C., Soriano, A., and Wouthuyzen-Bakker, M.:
Debridement, antibiotics and implant retention is a viable treatment option
for early periprosthetic joint infection presenting more than four weeks
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Clauss, M.: Debridement and implant retention in the management of hip
periprosthetic joint infection, Bone Jt. J., 99B, 330–336,
<ext-link xlink:href="https://doi.org/10.1302/0301-620X.99B3.BJJ-2016-0609.R1" ext-link-type="DOI">10.1302/0301-620X.99B3.BJJ-2016-0609.R1</ext-link>, 2017.</mixed-citation></ref>
      <?pagebreak page97?><ref id="bib1.bib16"><label>16</label><?label 1?><mixed-citation>Shohat, N., Goswami, K., Tan, T. L., Yayac, M., Soriano, A., Sousa, R.,
Wouthuyzen-Bakker, M., and Parvizi, J.: 2020 Frank Stinchfield Award:
Identifying who will fail following irrigation and debridement for
prosthetic joint infection, Bone Joint J., 102-B, 11–19,
<ext-link xlink:href="https://doi.org/10.1302/0301-620X.102B7.BJJ-2019-1628.R1" ext-link-type="DOI">10.1302/0301-620X.102B7.BJJ-2019-1628.R1</ext-link>, 2020.</mixed-citation></ref>
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hip replacement: an algorithmic approach, Sicot-J, 5, 5,
<ext-link xlink:href="https://doi.org/10.1051/sicotj/2019004" ext-link-type="DOI">10.1051/sicotj/2019004</ext-link>, 2019.</mixed-citation></ref>
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following debridement, antibiotics and implant retention in the management
of periprosthetic infections of the hip: A review of cohort studies, Bone
Jt. J., 99B, 1458–1466,
<ext-link xlink:href="https://doi.org/10.1302/0301-620X.99B11.BJJ-2017-0088.R1" ext-link-type="DOI">10.1302/0301-620X.99B11.BJJ-2017-0088.R1</ext-link>, 2017.</mixed-citation></ref>
      <ref id="bib1.bib19"><label>19</label><?label 1?><mixed-citation>Volpin, A., Sukeik, M., Alazzawi, S., and Haddad, F. S.: Aggressive Early
Debridement in Treatment of Acute Periprosthetic Joint Infections After Hip
and Knee Replacements, Open Orthop. J., 10, 669–678,
<ext-link xlink:href="https://doi.org/10.2174/1874325001610010669" ext-link-type="DOI">10.2174/1874325001610010669</ext-link>, 2016.</mixed-citation></ref>
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B., Murillo, O., Parvizi, J., Shohat, N., Reinoso, J. C., Sánchez, R.
E., Fernandez-Sampedro, M., Senneville, E., Huotari, K., Barbero, J. M.,
Garcia-Cañete, J., Lora-Tamayo, J., Ferrari, M. C., Vaznaisiene, D.,
Yusuf, E., Aboltins, C., Trebse, R., Salles, M. J., Benito, N., Vila, A.,
Toro, M. D. Del, Kramer, T. S., Petersdorf, S., Diaz-Brito, V., Tufan, Z.
K., Sanchez, M., Arvieux, C., and Soriano, A.: Clinical outcome and risk
factors for failure in late acute prosthetic joint infections treated with
debridement and implant retention, J. Infect., 78, 40–47,
<ext-link xlink:href="https://doi.org/10.1016/j.jinf.2018.07.014" ext-link-type="DOI">10.1016/j.jinf.2018.07.014</ext-link>, 2019.
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R., Benavent, E., Parvizi, J., Fernandez-Sampedro, M., Barbero, J. M.,
Garcia-Cañete, J., Trebse, R., Del Toro, M., Diaz-Brito, V., Sanchez,
M., Scarborough, M., Soriano, A., Taylor, A., Arvieux, C., Cobo, J.,
Murillo, O., Senneville, E., Lora-Tamayo, J., Vaznaisiene, D., Aboltins, C.,
Salles, M. J., Benito, N., Vila, A., and Tufan, Z. K.: Lower Success Rate of
Débridement and Implant Retention in Late Acute versus Early Acute
Periprosthetic Joint Infection Caused by Staphylococcus spp. Results from a
Matched Cohort Study, Clin. Orthop. Relat. Res., 478, 1348–1355,
<ext-link xlink:href="https://doi.org/10.1097/CORR.0000000000001171" ext-link-type="DOI">10.1097/CORR.0000000000001171</ext-link>, 2020.</mixed-citation></ref>
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Rheumatol., 20, 1045–1063, <ext-link xlink:href="https://doi.org/10.1016/j.berh.2006.08.003" ext-link-type="DOI">10.1016/j.berh.2006.08.003</ext-link>,
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  </ref-list></back>
    <!--<article-title-html>One-year infection control rates of a DAIR (debridement, antibiotics and implant retention) procedure after primary and prosthetic-joint-infection-related revision arthroplasty – a retrospective cohort study</article-title-html>
<abstract-html><p><strong>Introduction</strong>: Debridement, antibiotics and implant retention (DAIR)
procedures are effective treatments for acute postoperative or acute
hematogenous periprosthetic joint infections. However, literature reporting
on the effectiveness of DAIR procedures performed after a one- or two-stage
revision because of a prosthetic joint infection (PJI) (PJI-related revision arthroplasty) is scarce. The
aim of this study is to retrospectively evaluate the infection control after
1 year of a DAIR procedure in the case of an early postoperative infection
either after primary arthroplasty or after PJI-related revision
arthroplasty.
<strong>Materials and methods</strong>: All patients treated with a DAIR procedure within 3
months after onset of PJI between 2009 and 2017 were retrospectively
included. Data were collected on patient and infection characteristics. All
infections were confirmed by applying the Musculoskeletal Infection Society (MSIS) 2014 criteria. The primary
outcome was successful control of infection at 1 year after a DAIR
procedure, which was defined as the absence of clinical signs, such as pain,
swelling, and erythema; radiological signs, such as protheses loosening; or
laboratory signs, such as C-reactive protein (CRP) ( &lt; 10) with no use of antibiotic therapy.
<strong>Results</strong>: Sixty-seven patients were treated with a DAIR procedure (41 hips and 26
knees). Successful infection control rates of a DAIR procedure after primary
arthroplasty (<i>n</i> = 51) and after prior PJI-related revision arthroplasty
(<i>n</i> = 16) were 69&thinsp;% and 56&thinsp;%, respectively (<i>p</i> = 0.38). The successful infection control rates of a DAIR procedure after an early acute infection
(<i>n</i> = 35) and after a hematogenous infection (<i>n</i> = 16) following primary
arthroplasty were both 69&thinsp;% (<i>p</i> = 1.00).
<strong>Conclusion</strong>: In this limited study population, no statistically significant
difference is found in infection control after 1 year between DAIR
procedures after primary arthroplasty and PJI-related revision arthroplasty.</p></abstract-html>
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