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