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  <title>Welcome to IDSA Practice Guideline Discussion Forums : IDSA Practice Guideline for the Treatment of Diabetic Foot Infections : Practice Guideline for the Diagnosis and Treatment of Diabetic Foot Infections</title>
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  <description><![CDATA[<p><span class="search-term-highlight">Foot </span><span class="search-term-highlight">infections</span> are a common <span class="search-term-highlight">and</span> serious problem in persons with diabetes. <span class="search-term-highlight">Diabetic </span><span class="search-term-highlight">foot </span><span class="search-term-highlight">infections</span> (DFIs) typically begin in a wound, most <span class="search-term-highlight">of</span>ten a neuropathic ulceration. While all wounds are colonized with microorganisms, the presence <span class="search-term-highlight">of</span> infection is defined by ≥2 classic findings <span class="search-term-highlight">of</span> inflammation or purulence. <span class="search-term-highlight">Infections</span> are then classified into mild (superficial <span class="search-term-highlight">and</span> limited in size <span class="search-term-highlight">and</span> depth), moderate (deeper or more extensive), or severe (accompanied by systemic signs or metabolic perturbations). This classification system, along with a vascular assessment, helps determine which patients should be hospitalized, which may require special imaging procedures or surgical interventions, <span class="search-term-highlight">and</span> which will require amputation. <a title="Read full text guideline " href="http://cid.oxfordjournals.org/content/54/12/e132.full?sid=54d872f6-fe76-4e81-b7ce-0133a3fb4e96" target="_blank">Read full text guideline </a> </p>
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  <pubDate>Tue, 28 Aug 2012 19:29:38 GMT</pubDate>
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  <description><![CDATA[These guidelines have been viewed 560 times but to date there are no comments or questions. The guideline panel members would like to hear what you think about what we've written, especially if you think we're left out something important or you disagree with one of our recommendations. Perhaps we can get a discussion going. Thanks!
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  <pubDate>Tue, 19 Feb 2013 21:06:14 GMT</pubDate>
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  <description><![CDATA[<p> D<span lang="EN-US">r Lipsky,
could you provide some clarification on empiric antiobiotic choice?</span></p>
<p><span lang="EN-US">In table 8,
under moderate or severe DFIs, we have the following probable pathogens
groups:</span></p>
<p><span lang="EN-US">1) MSSA;
Streptococcus spp; Enterobacteriaceae; obligate anaerobes</span></p>
<p><span lang="EN-US">So far,
everything clear; these are the pts with no risk for MRSA or Pseudomonas; treat
them with “usual” antibiotics</span></p>
<p><span lang="EN-US">2) MRSA –
treat with linezolid, daptomycin, or vancomycin</span></p>
<p><span lang="EN-US">Obvious</span></p>
<p><span lang="EN-US">3)
Pseudomonas - piperacillin-tazobactam</span></p>
<p><span lang="EN-US">OK</span></p>
<p><span lang="EN-US">4) MRSA, Enterobacteriacae,
Pseudomonas, and obligate anaerobes; suggested antibiotics: vancomycin,
ceftazidime, cefepime, piperacillin-tazobactam, aztreonam, or a carbapenem.</span></p>
<p><span lang="EN-US">Now I have
trouble – what clinical scenario is it? Did you mean patients with risk factors
for both MRSA and Pseudomonas, and hence the need for very broad-spectrum
antibiotics? If so, then we should probably use vancomycin (linezolid,
daptomycin) <strong>AND </strong>one of the remaining (or, maybe more specifically, vancomycin
plus piperacillin-tazobactam, because the latter is preferred for Pseudomonas).
Why this list is longer, if required spectrum is broader?</span></p>
<p>Thank you.</p>
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  <pubDate>Mon, 25 Feb 2013 00:22:57 GMT</pubDate>
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