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UTMB DEPARTMENT OF PHARMACY POLICY AND PROCEDURES

Section 07.68 Page 1 of 2


Policy PRN Analgesic Range Orders Effective Date: 08/12/04
Last Review/Revision Date: 07/14/05
Next Review Date: 07/14/08
Author: Department of Pharmacy

AUDIENCE All Healthcare providers ordering and/or administering analgesic range orders

POLICY Range orders


§ may allow for a dosage range (example: Morphine 2 – 6 mg)
§ may not specify a frequency range

PROCEDURES DOSE:
§ All doses including the initial dose should be based on the assessment of
the patient’s pain severity using the 0-10 pain scale, age-appropriate
scale, desired outcomes, history of previous doses, or other indicators.
§ Initial dose selection
• for the analgesic naïve patient, the first dose administered should be
the lowest dose in the range;
• if the patient is analgesic tolerant, or has received recent doses with
inadequate pain relief and tolerable side effects , a dose on the
higher end of the range can be administered.
§ Dose escalation
• for moderate to severe pain increase the dose by 50 – 100%;
• for mild pain (fine tuning) increase by 25%
• Do not increase dose by more than 100%
• Doses of short acting analgesics can be increased at subsequent
dosing intervals, while longer acting products should be increased
less frequently
§ A nurse may determine that the higher dose of the range order is
necessary to adequately manage the patient’s pain, but this rationale must
be clearly stated in the patient record.
§ Notify the physician if the maximum dose ordered is ineffective.

FREQUENCY/DOSING INTERVAL:
§ The frequency of analgesics should be based on the patient’s pain level;
therefore if pain returns before the prescribed interval, the physician
should be notified. The patient may need a change in drug, dose or
interval or consider continuous schedule.

DOCUMENTATION:
§ The initial pain assessment must include pain location, severity,
description, aggravating/relieving factors, examination of pain site, and
patient’s pain goal e.g., get pain from an 8 to a 2. Subsequent
assessment of same site pain must include pain severity.
§ Pain severity must be included in all notations about pain.
§ The effect of the analgesic on patient must be recorded. Was the
medication or nonpharmacologic intervention successful? Are there any
side effects?
§ Document drug, amount, time, per routine on the medication
administration record.
UTMB DEPARTMENT OF PHARMACY POLICY AND PROCEDURES
Section 07.68 Page 2 of 2
Policy PRN Analgesic Range Orders Effective Date: 08/12/04
Last Review/Revision Date: 07/14/05
Next Review Date: 07/14/08
Author: Department of Pharmacy

Considerations:
§ Pain relief. The main goal for pain medication orders is to obtain relief of
pain.
§ Reasonable range. A range order should be two to three times the
lowest base dose so that it is large enough to provide appropriate options
for dose titration, but small enough so that appropriate reassessment is
done in a timely manner (e.g., if the lowest dose is 2 mg the higher dose
should be x2 (4mg) or x3 (6mg).
§ Patient’s prior drug exposure. If the patient is opioid-naïve, the first
dose administered should be the lowest dose in the range; if the patient is
opioid tolerant, or has received a recent dose with inadequate pain relief
and tolerable side effects, a dose on the higher end of the range should
be administered.
§ Prior response. Inquire about this patient’s response to previous doses
to determine how much relief was provided, how long the relief lasted and
if the patient experienced any side effects.
§ Age. For very young or elderly patients, “start low and go slow” – begin
with a low dose and titrate up slowly and carefully.
§ Liver and renal function. If your patient has hepatic or renal
insufficiency, anticipate a more pronounced peak effect and a longer
duration of action.
§ Pain severity. As a general rule, for moderate to severe pain increase the
dose by 50-100%; do not increase by >100% at one time; to “fine-tune” the
dose once pain is at a mild level, increase or decrease by 25%.
§ Anticipated pain duration. Is the pain acute, chronic, or progressive
(likely to worsen)?
§ Pharmacokinetics. Know the onset, peak, and duration of action for the
specific drug ordered. Doses of short-acting opioids can be increased at
each specified dosing interval, unlike scheduled long-acting opioid
formulations.
§ Comorbidities that may affect patient response. Example:
Debilitated patients, or those with respiratory insufficiency, may be at more
risk for hypoxia if oversedated.
§ Concomitant administration of other sedating drugs. When other
CNS depressants are administered in combination with opioids, the dose
of each medication required to achieve the desired effect may be 30-50%
less than if either drug was administered alone.
§ Combination drugs. Limit doses of combination drugs, e.g., opioids with
acetaminophen or a nonsteroidal anti-inflammatory. Average adults should
not receive more than 4000mg of acetaminophen in 24 hours.
Combinations drugs may contain as much as 750mg of acetaminophen
per tablet. If substantial upward dose titration is required or anticipated,
use opioid-only preparations.

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