HYDROMORPHONE

(Dilaudid)

Standard Prescription

hydromorphone__mcg IV{PO} Q__H PRN pain ( __ mcg/kg/dose)

hydromorphone controlled release__mg PO Q__H

hydromorphone__mcg/kg/hr continuous IV infusion

Note: continuous infusion to be ordered by APS only.

Dosages

Analgesia: titrate to effect.
Intermittent Dosing:
Children <= 50 kg:
Oral:
0.04-0.08 mg/kg/dose PO every 3-4 hr PRN

IV:
15 mcg/kg/dose IV every 2-4 hr PRN  

Continuous IV Infusion:
1-8 mcg/kg/hr continuous IV infusion.  Higher doses may be required, especially in opioid tolerant patients.

Children >50 kg:
Oral:
1-2 mg PO every 3-4 hr PRN

IV:
0.2-0.5 mg IV every 2-4 hr PRN

Usual Adult dose:
2-4 mg PO every 3-4 hr

Epidural Infusion (with ropivacaine)
0.3-1.5 mcg/kg/hour

Mechanism of Action

Opioid analgesic

Forms Supplied

injection: 2 mg/mL; 10 mg/mL 20 mg/100 mL PCA bag

Immediate release tablet: 1 mg, 4 mg,

liquid: 1 mg/mL

Standard concentrations for IV infusions:
40 mcg/mL (pts up to 6 kg)
80 mcg/mL (pts 6-30 kg)
200 mcg/mL (pts > 30 kg)

controlled release capsules: 3 mg, 6 mg, 12 mg, 24 mg 30 mg

Comments

CAUTION: Hydromorphone is 5x more potent than morphine (eg. Hydromorphone 2 mg IV ≈ morphine 10 mg IV).

Should not be used in patients with a true allergic reaction to morphine.

Antidote for opioid overdose is naloxone.

Peak analgesic effect: 10-20 min. after IV and immediate release oral doses.

Duration of analgesia: 3-4 hr.

See also Opioid Administration Guidelines (white pages of print copy).

Opioid tolerant patients may require higher doses

Hydromorphone considered safer for use in renal impairment.

Use extreme caution when converting from one opioid to another. Consult with APS/Palliative Care when converting opioids. Cross-tolerance at the opioid receptor may not occur and equianalgesic opioid dosing tables may overestimate opioid requirements.

Controlled release capsules are NOT suitable for PRN dosing. Daily hydromorphone requirements should be established using immediate release formulations before converting to long acting formulations.  Controlled release formulations are usually dosed Q12H.

Controlled release tablets should generally be swallowed whole. Consult individual product monograph prior to manipulating the formulation.


References

44, 389

Last Edited

2024-02-22 07:18:43