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nfection is a major impediment to healing of diabetic For this to happen, silver has to be bioavailable and should
foot ulcers. Before wounds become infected, most are be in the ionic form. In the past, silver nitrate (0.5% or 3,176
colonized. When the wound burden increases to >105 mg/L) and silver sulfadiazine (1%) were the primary sources
organisms, it is said to be critically colonized and clini- of silver. In the last few years, a number of silver-containing
cal infection can then occur.1 In more virulent organisms, dressings have been developed. Silver ions (ionic silver,
however, this critical wound burden is not always crucial. nanocrystalline silver) have been incorporated in hydro-
Optimal management of the wound bacterial load is fiber, foam, hydrocolloid, and alginate dressings,3 and have
important in achieving healing of diabetic foot ulcers. Most been used to treat acute and chronic wounds.4
often, antibiotics are necessary to treat infection and
reduce the bacterial load on the wound. Dressings also play FEW STUDIE S AVAIL ABLE
an important role in managing diabetic foot ulcers. Using Very few studies have been published regarding the use of
antimicrobials can reduce the number of organisms in the silver-containing dressings in the treatment of diabetic foot
wound and therefore not only treat the infection but also ulcers. In a small study of 27 patients, the healing of diabetic
prevent colonized wounds from becoming critically colo- foot ulcers using Contreet foam, silver-releasing foam dress-
nized. ing, (Coloplast; Humlebaek, Denmark) was investigated. In
this open-label study of the 18 patients who completed it,
TOPICAL ANTIMICROBIAL AGENTS four healed (22.2%) in the 4-week treatment period with
Various topical antimicrobials, antiseptics, and antibi- reduced infection in the ulcer and with good exudate man-
otics have been used in treating diabetic foot ulcer infec- agement.5 There was a 56% reduction in ulcer area during
tion.2 Topical antibiotics such as neomycin, bacitracin, follow-up. A progressive decrease in incidence and severity of
polymyxin B, gentamycin, fusidic acid, mupirocin, and topi- maceration from the first week of treatment with the overall
cal antiseptics including hexachlorophene, povidone incidence declining from 52.8% to 30% was observed.
iodine, and chlorhexidine have been tried in various set- In the first randomized controlled trial of silver dressings in
tings. Although these have their advantages, topical antibi- diabetic foot ulcers, 134 patients with neuropathic foot
otics have not been very popular. Iodine is probably one of ulcers were randomly assigned to either Aquacel Ag (AQAg;
the most common topical antiseptics used in infected foot ConvaTec, Chester, UK) or Algosteril calcium alginate (CA)
ulcers. Although antiseptics and antibiotics are widely used, (Smith & Nephew, Hull, UK) dressings and secondary foam
there is insufficient evidence for their use in diabetic foot dressings.6 Patients were treated for 8 weeks or until healing,
ulcers.2 whichever occurred first. The mean time to healing was 53
days in the AQAg-treated ulcers and 58 days for the CA-
SILVER A S AN ANTIMICROBIAL treated ulcers (P=.34). Ulcers treated with AQAg, however,
Silver has been shown to have bactericidal properties showed greater depth reduction than CA-treated ulcers
and has been used in wounds as an antimicrobial for more (P=.04). Greater improvement in the ulcer was seen in the
than a century. It acts by impairing the bacterial electron AQAg group. Patients were also stratified according to those
transport system and some of its DNA function. It kills the requiring antibiotic treatment (ie, clinically infected ulcers),
microbes on contact through multiple mechanisms of and patients treated with AQAg primary dressing showed
action, such as inhibiting cellular respiration, denaturing improved healing and more overall ulcer improvement with
nucleic acids, and altering cellular membrane permeability. less deterioration in the ulcer (P=.02).
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ized controlled study of hydrofiber dressing containing ionic silver or calcium alginate dressings in non-
ischaemic diabetic foot ulcers. Diabet Med. 2007;24:280-288.
7. Newman GR, Walker M, Hobot JA, Bowler PG. Visualisation of bacterial sequestration and bacterici-
dal activity within hydrating hydrofiber wound dressings. Biomaterials. 2006;27:1129-1139.
8. Bowler PG, Jones SA, Davies BJ, Coyne E. Infection control properties of some wound dressings. J
Wound Care. 1999;8:499-502.
9. Piagessi A, Vaccetti F, Rizzo L, et al. Sodium carboxy-methyl-cellulose dressings in the management
of deep ulcerations of diabetic foot. Diabet Med. 2001;18:320-324.
10. Jude EB, Unsworth PF. Optimal Treatment of Infected Diabetic Foot Ulcers. Drugs Aging.
2004;21:833-850.
11. Tentolouris N, Jude E B, Smirnof I, et al. Methicillin-resistant Staphylococcus aureus: Increasing
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problem in a diabetic foot clinic. Diabet Med. 1999;16:767-771.
12. Jones SA, Bowler PG, Walker M, Parsons D. Controlling wound bioburden with a novel silver-con-
taining hydrofiber dressing. Wound Rep Reg. 2004;12:288-294.
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