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Effectiveness of measures to prevent needlestick injuries among ...

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4 Intervention program evaluation<br />

all used gloves were tested for perforation, a surrogate measure <strong>of</strong> risk <strong>of</strong> NSI. In<br />

addition <strong>to</strong> reducing likelihood <strong>of</strong> confounding by random allocation <strong>to</strong> the blunt<br />

versus traditional needle groups, the authors evaluated potential confounding by<br />

time <strong>of</strong> day, operation length, and surgeon experience.<br />

Overall, 14 NSI were observed, all due <strong>to</strong> sharp needles. Seventy-six perforations<br />

were detected in 69 pairs <strong>of</strong> gloves, and 58 <strong>of</strong> them (76 %) were from sharp needles.<br />

Glove perforations during abdominal fascia closure were found <strong>to</strong> be mostly related<br />

<strong>to</strong> use <strong>of</strong> sharp needles (50 % due <strong>to</strong> sharp needles versus 7 % due <strong>to</strong> blunt needles;<br />

p < 0.0006). Surgeon experience and duration <strong>of</strong> procedure were not associated with<br />

the likelihood <strong>of</strong> NSI or glove perforation, but skin contamination was more likely <strong>to</strong><br />

occur during procedures carried out during the night shift.<br />

� Intermediate quality<br />

The remaining five evaluations <strong>of</strong> blunt suture needles were rated “intermediate”<br />

quality [61 <strong>to</strong> 65]. Three <strong>of</strong> these articles described evaluations <strong>of</strong> the Ethigard<br />

(Ethicon) blunt suture needle: Hartley et al. reported a decrease in the rate <strong>of</strong> glove<br />

perforation from 14/39 sharp needles used <strong>to</strong> 3/46 when the Ethigard was used,<br />

p < 0.001 [62]. Wright et al. noted 31 perforations in 16 out <strong>of</strong> 62 gloves worn while<br />

using a “cutting needle” and 18 perforations in ten out <strong>of</strong> 76 gloves worn while using<br />

a “taperpoint needle” (p = 0.049). In addition, three NSI were reported, two from<br />

cutting needles and one from a wound-drain introducer, but none from the Ethigard<br />

[64]. The final study in this group reported a reduction from 5.9 NSI/100 procedures<br />

prior <strong>to</strong> introduction <strong>of</strong> the Ethigard <strong>to</strong> 1.1 NSI/100 procedures after the Ethigard was<br />

adopted [61]. Rice et al. evaluated the Maxon Protec blunt suture needle (Davis and<br />

Geck, Inc.), and found that 16 % <strong>of</strong> outer and 6 % <strong>of</strong> inner gloves were perforated<br />

when traditional sharp needles were used, but there were no perforations <strong>among</strong><br />

gloves worn by surgeons using the Maxon Protec (p = 0.026) [63]. Meyer et al. found<br />

that 39 % <strong>of</strong> surgical gloves were perforated when standard sharp needles were used,<br />

compared <strong>to</strong> 23 % <strong>of</strong> gloves perforated with use <strong>of</strong> the Protect Point (Maxon-Faden)<br />

blunt suture needle [65].<br />

Report „Needlestick <strong>injuries</strong>“ 43

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