From the Guidelines
For a patient with chronic low back pain and bone cancer currently on Dilaudid and Tramadol/Acetaminophen with pain levels of 6-8/10 and normal renal function (GFR 75 mL/min), a recommended PCA morphine regimen would be: 1-2 mg morphine demand dose with a 6-10 minute lockout interval, no continuous basal infusion initially, and a 4-hour limit of 30-40 mg. The patient's current pain regimen, which includes Dilaudid (Hydromorphone) and Tramadol (Tramadol)/Paracetamol (Acetaminophen), indicates a need for potent opioid analgesia, as supported by the ESMO clinical practice guidelines for the management of cancer pain in adult patients 1. Given the patient's opioid exposure, they will have some tolerance, so higher initial doses within this range may be appropriate. The regimen should be reassessed after 24 hours, with adjustments based on the number of demands, successful deliveries, and pain control. If pain remains inadequately controlled, consider adding a basal rate of 0.5-1 mg/hour. The patient should be monitored for side effects including respiratory depression, sedation, nausea, and constipation, with prophylactic bowel regimen initiated. Key considerations in this regimen include the average relative potency ratio of oral to i.v. morphine, which is between 1:2 and 1:3 1, and the potential for opioid switching if the patient experiences inadequate pain control or significant side effects. The choice of opioid is important to achieve an optimum balance between analgesia and unwanted adverse effects, and morphine is considered the opioid of first choice for moderate to severe cancer pain 1. Breakthrough pain medication, typically 5-10 mg oral morphine every 2-4 hours as needed, should also be provided to the patient. This regimen balances effective pain control with safety for a patient with cancer pain who has some opioid tolerance but normal organ function. Some points to consider when converting the patient's current regimen to PCA morphine include:
- The patient's current opioid regimen and potential for opioid tolerance
- The need for potent opioid analgesia to manage the patient's cancer pain
- The importance of monitoring for side effects and adjusting the regimen as needed
- The potential for opioid switching if the patient experiences inadequate pain control or significant side effects.
From the Research
Patient Background
- The patient is a 45-year-old woman with chronic low back pain and bone cancer.
- She is currently taking:
- Dilaudid 10 mg qid
- Dilaudid 2 mg PO Q 2 hours (4 per day on average)
- Tramadol 75mg / Paracetamol 650 mg, 1 tablet qid
- Her current pain level is ranging from 6-8/10 all day long.
- Labs are WNL, GFR=75 mL/minute.
Conversion to PCA Morphine
- To convert the patient's current pain regimen to PCA Morphine, we need to consider the equivalent doses of morphine to her current medications.
- According to the study 2, hydromorphone (Dilaudid) and morphine have similar analgesic efficacy, but morphine may have less adverse effects on cognitive function.
- The study 3 suggests that a hydromorphone titration protocol can be effective in managing acute severe pain, but it does not provide direct guidance on converting to PCA Morphine.
- The study 4 recommends a "sub-analgesic" background infusion rate of morphine (0.01 mg/kg/h) plus low-dose PCA bolus for effective pain control.
Recommended PCA Morphine Regimen
- Based on the patient's current pain level and medication regimen, a possible PCA Morphine regimen could be:
- Background infusion rate: 0.5-1.0 mg/h (considering the patient's GFR and current medication regimen)
- PCA bolus dose: 0.5-1.0 mg (considering the patient's current pain level and medication regimen)
- Lockout interval: 7-10 minutes (to prevent overdose and allow for adequate pain control)
- The study 5 suggests that patients receiving morphine PCA should be monitored closely from 8 to 24 hours postoperatively for signs of respiratory depression.
- The study 6 compares tramadol and morphine via subcutaneous PCA following major orthopaedic surgery, but it does not provide direct guidance on converting to PCA Morphine in this patient's scenario.
Monitoring and Adjustments
- The patient's pain level, vital signs, and respiratory status should be closely monitored during the first 24-48 hours after initiating PCA Morphine.
- Adjustments to the PCA Morphine regimen may be necessary based on the patient's response to treatment and any adverse effects that may occur 4, 3, 2, 5, 6.