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Antimicrobial management of diabetic foot infection<br />
with more extensive ulceration requiring<br />
surgery. Resection of infected bone will treat<br />
osteomyelitis but increases the risk of altered<br />
foot biomechanics and transfer ulceration.<br />
Surgical intervention should be considered in<br />
cases of osteomyelitis accompanied by: spreading<br />
soft tissue infection; destroyed soft tissue<br />
envelope; progressive bone destruction on X-ray;<br />
or bone protruding through the ulcer (Bakker<br />
et al, 2015). The decision to institute either a<br />
primary medical or surgical approach based on<br />
randomised clinical trial data is difficult, as the<br />
diagnosis of osteomyelitis in some trials was not<br />
based on bone culture and histology.<br />
The IWGDF guideline recommends 6 weeks<br />
of antibiotic therapy for patients who do not<br />
undergo resection of infected bone and no<br />
more than a week of antibiotic treatment if all<br />
infected bone is resected. Similar guidance<br />
is provided with the IDSA guidelines, which<br />
advise 4–6 weeks of antibiotics if there is<br />
residual infected, but viable, bone. However,<br />
the IDSA guidelines recommend greater than<br />
3 months, of antibiotic therapy if there is no<br />
surgery or residual dead bone postoperatively<br />
(Table 2 [Lipsky et al, 2012; Bakker et al,<br />
2015). There is variance in the recommendation<br />
between the two guidelines, and the decision<br />
to extend antibiotic treatment beyond 6 weeks<br />
to 3 months should be made in consultation<br />
with an infectious diseases or clinical<br />
microbiological specialist.<br />
The optimal treatment of DFI with DFO will<br />
be based on clinical severity, likely or proven<br />
causative agents and clinical progression. A<br />
consultation with an infectious diseases or<br />
clinical microbiological specialist and the wider<br />
MDT is recommended.<br />
Conclusion<br />
DFIs are a common and serious complication<br />
of diabetes (present in up to 60% of DFUs;<br />
Markakis et al, 2016). DFIs can spread rapidly<br />
to underlying tissues, including bone, and<br />
DFO is a frequent outcome. Early diagnosis<br />
of DFI and rapid initiation of antimicrobial<br />
therapy is vital to minimise the adverse patient<br />
outcomes associated with foot infections, such as<br />
amputation. The Australian guidelines, IDSA,<br />
IWGDF and NICE all offer clear guidance on<br />
appropriate antimicrobial therapy dependent on<br />
the severity of the infection, clinical situation<br />
and efficacy of the agents. <br />
n<br />
Acknowledgement<br />
This article has been modified from one<br />
previously published in The Diabetic Foot Journal<br />
(2016, 3: 132–7).<br />
Akkus G, Evran M, Gungor D et al (2016) Tinea pedis and<br />
onychomycosis frequency in diabetes mellitus patients and<br />
diabetic foot ulcers: A cross sectional-observational study.<br />
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Prevention, Identification and Management of Foot<br />
Complications in Diabetes (Part of the Guidelines on<br />
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Diabetes Metab Res Rev 32(Supp 1): 254–60<br />
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Guidance for Daily Practice 2015, based on the IWGDF<br />
Guidance Documents. Diabetes Metab Res Rev 32(Suppl 1):<br />
7–15<br />
“Early diagnosis of<br />
diabetic foot infections<br />
and rapid initiation of<br />
antimicrobial therapy<br />
is vital to minimise<br />
the adverse patient<br />
outcomes associated<br />
with foot infections,<br />
such as amputation.”<br />
Diabetes & Primary Care Australia Vol 2 No 1 2017 29