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Pediatric Informatics: Computer Applications in Child Health (Health ...

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27 Dispens<strong>in</strong>g: Pharmacy Information Systems 351<br />

be missed). Rules and data across the cl<strong>in</strong>ical systems with<strong>in</strong> an <strong>in</strong>stitution (such as<br />

CPOE and PharmIS) should be as consistent as possible. Differences <strong>in</strong> tolerances<br />

for errors or flexibility may lead to conflict<strong>in</strong>g alerts (such as a situation where a<br />

CPOE system that does not display a dosage warn<strong>in</strong>g to a prescriber, but for which<br />

the l<strong>in</strong>ked PharmIS provides a dosage error to the pharmacist.<br />

Example of dose range check:<br />

Drug “X” has the follow<strong>in</strong>g dose limits<br />

<strong>Pediatric</strong> limits:<br />

Per Dose: 25–50 mg/kg<br />

Per Day: 50–100 mg/kg [daily dose usually divided twice per day (every 12 h)]<br />

Adult limits:<br />

Per Dose: 1,000–2,000 mg<br />

Per Day: 2,000–4,000 mg [daily dose usually divided twice per day<br />

(every 12 h)]<br />

In a 12 kg pediatric patient – if the prescriber orders 300 mg per dose every<br />

12 h, the 300 mg value is the one needed by most PharmIS, as it reflect the<br />

f<strong>in</strong>al dose to be compounded, labeled, dispensed, and adm<strong>in</strong>istered. For Dose<br />

Screen<strong>in</strong>g, however, the 300 mg value must be divided by the weight <strong>in</strong> order<br />

to check it aga<strong>in</strong>st the above parameters (i.e. 300 mg per dose/12 kg = 25<br />

mg/kg/dose; 25 mg/kg/dose × 2 doses per day = 50 mg/kg/day). It should also be<br />

checked aga<strong>in</strong>st maximum adult doses to assure that, <strong>in</strong> an example of a larger<br />

adolescent pediatric patient, the correct mg/kg dose is not <strong>in</strong> excess of the adult<br />

maximum doses.<br />

27.3.3.2 Detect<strong>in</strong>g Known Allergy and Drug Interactions<br />

Another essential PharmIS CDS function is allergy check<strong>in</strong>g/screen<strong>in</strong>g, 8 which<br />

requires l<strong>in</strong>kage to an accurate and current patient allergy profile (which must be<br />

ma<strong>in</strong>ta<strong>in</strong>ed and available to the PharmIS). Although drug allergy checks should<br />

be comprehensive and <strong>in</strong>clude chemically related drugs with known cross-reactive<br />

potential (such as is known penicill<strong>in</strong> with piperacill<strong>in</strong> or cefotaxime), this is challeng<strong>in</strong>g<br />

because of the lack of an available evidence-based standard cod<strong>in</strong>g scheme<br />

of cross-reactivity potentials and an effective method to dist<strong>in</strong>guish (or notate a<br />

dist<strong>in</strong>ction) between true allergy (such as anaphylaxis) and <strong>in</strong>dividual <strong>in</strong>tolerance<br />

(such as nausea to narcotics) to a medication. Most systems do not differentiate<br />

these two phenomena, and it is unknown if do<strong>in</strong>g so would improve safety <strong>in</strong> this<br />

area.<br />

As with automated dose check<strong>in</strong>g, allergy screen<strong>in</strong>g rules may be provided by<br />

an <strong>in</strong>terfaced third party CDS system or may be configured locally. Allergy check<strong>in</strong>g<br />

functionality is currently available on many PharmIS. The same advantages and

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