Normal Oral Dosage of Dilaudid (Hydromorphone) for Severe Pain
For opioid-naïve patients with severe pain, start with hydromorphone 2-4 mg orally every 4-6 hours, with breakthrough doses of 10-20% of the total daily dose available as needed. 1
Initial Dosing for Opioid-Naïve Patients
The FDA-approved starting dose for immediate-release oral hydromorphone is 2-4 mg every 4-6 hours. 1 This conservative approach minimizes the risk of respiratory depression while providing effective analgesia for severe pain.
- For patients without prior opioid exposure, the 2 mg starting dose is generally safer, as it is better to underestimate initial requirements than risk overdose 1
- The dosing interval of 4-6 hours aligns with hydromorphone's elimination half-life of 2-4 hours, allowing steady-state to be reached within 24 hours 2
Breakthrough Pain Dosing
Provide breakthrough doses equivalent to 10-20% of the total 24-hour opioid dose for transient pain exacerbations. 3, 2
- For a patient taking 2 mg every 4 hours (12 mg daily), the breakthrough dose would be 1.2-2.4 mg 2
- If more than 3-4 breakthrough doses per day are required, increase the scheduled baseline dose rather than shortening the dosing interval 3, 2
- Assess efficacy and side effects every 60 minutes after oral breakthrough dosing 2
Dose Titration Strategy
When pain control is inadequate, increase the dose rather than the frequency of administration. 2
- There is no advantage to dosing more frequently than every 4 hours, and doing so creates non-standard schedules that increase medication errors 2
- If pain returns before the next scheduled dose, this indicates underdosing, not a need for more frequent administration 2
- Titrate upward using small increments until adequate analgesia is achieved without unacceptable side effects 1
Conversion from Other Opioids
When converting from other opioids, calculate the equianalgesic dose and reduce by 25-50% to account for incomplete cross-tolerance. 2, 4
- Oral hydromorphone is approximately 5-7 times more potent than oral morphine 3, 4
- The CDC conversion factor is 1 mg hydromorphone = 4 mg morphine for calculating morphine milligram equivalents 4
- Always start conservatively when switching opioids, as individual variability in opioid potency is significant 1
Special Population Considerations
In patients with renal or hepatic impairment, start with one-fourth to one-half the usual dose. 1, 2
- Hydromorphone exposure increases 2-fold in moderate renal impairment and 3-fold in severe renal impairment 2
- In hepatic impairment, exposure increases 4-fold in moderate disease 2
- Despite being safer than morphine in renal failure, active metabolites can still accumulate between dialysis treatments 2
Around-the-Clock Dosing for Chronic Severe Pain
For chronic severe pain, administer scheduled doses around-the-clock rather than as-needed. 1
- A supplemental dose of 5-15% of total daily usage may be given every 2 hours on an as-needed basis 1
- This approach maintains steady analgesia and prevents pain breakthrough 3
Critical Safety Considerations
Monitor patients closely for respiratory depression, especially within the first 24-72 hours of initiating therapy or following dose increases. 1
- Institute prophylactic bowel regimen with stimulant laxatives in all patients, as constipation is universal with opioid therapy 2
- Monitor for myoclonus, particularly with chronic use, renal failure, or electrolyte disturbances 2, 5
- If myoclonus occurs, decrease the dose or rotate to a different opioid structure at a lower equianalgesic dose 2
Common Pitfalls to Avoid
- Do not increase dosing frequency to every 3 hours - this creates non-standard schedules without pharmacologic advantage 2
- Do not use smaller breakthrough doses than regular doses - the full scheduled dose is more likely to be effective for breakthrough pain 2
- Do not combine with mixed agonist-antagonist opioids (like nalbuphine or butorphanol), as this can precipitate withdrawal in opioid-dependent patients 2
- Do not give 2 mg IV hydromorphone as a routine initial dose - this has been associated with oxygen desaturation in about one-third of patients 6