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Standards for assessing, measuring and monitoring vital signs in ...

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S T A N D A R D S F O R A S S E S S I N G , M E A S U R I N G A N D M O N I T O R I N G V I T A L S I G N S I N I N F A N T S<br />

4<br />

Medical devices <strong>and</strong> equipment<br />

<strong>St<strong>and</strong>ards</strong><br />

Medical devices have a CE mark<strong>in</strong>g (product that meets<br />

the requirements of the applicable European Directive)<br />

<strong>and</strong> are suitable <strong>for</strong> use with <strong>in</strong>fants, children <strong>and</strong> young<br />

people <strong>and</strong> are appropriate <strong>for</strong> the sett<strong>in</strong>g where they<br />

are to be used i.e. hospital, community or home.<br />

All medical devices <strong>and</strong> equipment are regularly<br />

cleaned dur<strong>in</strong>g on-go<strong>in</strong>g use by one patient <strong>and</strong><br />

between different patients, <strong>in</strong> accordance with <strong>in</strong>fection<br />

control policies <strong>and</strong> guidel<strong>in</strong>es.<br />

All probe sites are changed regularly <strong>in</strong> rotation to<br />

prevent tissue damage.<br />

Alarms on medical devices are set to quickly alert staff<br />

to changes <strong>in</strong> <strong>vital</strong> <strong>signs</strong>.<br />

All disposable or s<strong>in</strong>gle use equipment is identified <strong>and</strong><br />

used as such.<br />

All medical devices are serviced <strong>and</strong> calibrated regularly<br />

<strong>in</strong> accordance with manufacturers’ <strong>in</strong>structions.<br />

There are clear policies <strong>and</strong> procedures concern<strong>in</strong>g the<br />

hazards associated with all medical devices <strong>and</strong> <strong>in</strong><br />

particular those conta<strong>in</strong><strong>in</strong>g mercury.<br />

The accuracy of data from cardiac <strong>and</strong> other monitors is<br />

checked, as a m<strong>in</strong>imum, at the start of each shift.<br />

✦<br />

Medical device errors <strong>and</strong> failures should be<br />

reported <strong>in</strong> accordance with NPSA (National Patient<br />

Safety Agency) <strong>and</strong> MHRA (Medic<strong>in</strong>es <strong>and</strong><br />

Healthcare Regulatory Authority) guidance.<br />

Practice criteria<br />

✦<br />

✦<br />

✦<br />

✦<br />

✦<br />

Tra<strong>in</strong><strong>in</strong>g <strong>in</strong> the use of medical devices should<br />

comply with CNST (Cl<strong>in</strong>ical Negligence Scheme <strong>for</strong><br />

Trusts) requirements.<br />

Tra<strong>in</strong><strong>in</strong>g should <strong>in</strong>clude the correct sett<strong>in</strong>g <strong>and</strong> use<br />

of alarms.<br />

Cables should be kept tidy to prevent damage <strong>and</strong><br />

risk to others.<br />

Battery-operated equipment should be charged<br />

when not <strong>in</strong> use.<br />

When not <strong>in</strong> use, all equipment should be stored <strong>in</strong> a<br />

safe place, with use by unauthorised personnel<br />

restricted.<br />

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