- Chang AK et al.; Ann Emerg Med 2013:
- This was a prospective study that evaluated the safety and efficacy of administering an initial dose of hydromorphone 2 mg IV compared to an initial dose of hydromorphone 1 mg IV followed by a second optional dose of hydromorphone 1 mg administered 15 minutes later (“1 + 1” protocol).
- Patients in both groups were assessed at 60 minutes to determine the level of analgesia on a standard pain scale ranging from 0 to 10 and if additional pain medication was needed.
- Patients were included in the study if between 21 and 64 years of age at the time of presentation and presented with acute pain (less than or equal to seven days in duration) to the emergency department with a systolic blood pressure (SBP) greater than 90 mmHg and oxygen saturation greater than 95%.
- Excluded patients included those with a history of chronic pain, use of opioid analgesics within the previous seven days of presentation, and those who weighed less than 150 pounds.
- Nearly 70% of the 334 patients enrolled in the study had an initial pain score of 9 or 10, with most of the pain localized to the abdomen. Weight of patients in both treatment groups ranged from 165 to 220 pounds (75 to 100 kg).
- For those patients who received an initial dose of hydromorphone 2 mg IV, 67.5% declined additional analgesic medication at 60 minutes.
- 61% of patients who received an initial dose of hydromorphone 1 mg IV did not require an additional dose at 15 minutes, with 67.3% of patients in this group declining additional analgesic medication at 60 minutes.
- Only 1 patient in the “1 + 1 protocol” group experienced oxygen desaturation to less than 95% with the initial bolus; the incidence of all other adverse events were similar between both treatment groups.
- J Opioid Manag 2009; 5:75-80.
A single dose of hydromorphone 2 mg IV was associated with rapid analgesia, with one-third of patients experiencing oxygen desaturation to less than 95%.
- Ann Emerg Med 2011; 58:352-359.
- The use of a “1 + 1” protocol of hydromorphone as described above was found to achieve superior pain control in both intent to treat and per protocol analyses with a difference of greater than 10% in pain control compared to those patients who received usual standard care with any dose, interval, and frequency of an intravenous opioid analgesic administered at the discretion of the emergency medicine physician.
- Acad Emerg Med 2013; 20:185-192.
- A single dose of hydromorphone 2 mg IV was found to be decrease the need of additional analgesic medication at 30 minutes post-administration in 77.4% of patients compared to 65.8% with the same outcome who received usual care with any dose, interval, and frequency of an intravenous opioid analgesic administered at the discretion of the emergency medicine physician.
- Ann Emerg Med 2005; 46:362-367.
- The aim of this study was to evaluate the proportion of patients who achieved less than a 50% reduction in the level of pain using a pain scale ranging from 0 to 10 following the administration of a single, weight-based dose of morphine 0.1 mg/kg IV.
- Patients were included if between the ages of 21 and 65 at the time of presentation to the emergency department with acute pain lasting for no more than seven days in duration.
- In the 119 patients, two-thirds experienced less than a 50% decrease in pain following administration of this weight-based dose of morphine.
- The authors concluded that this dose of IV morphine does not provide adequate analgesia in the majority of patients who present to the emergency department, which may potentially suggests the need for evaluation of higher doses to be used in this setting.
- Follow up study: Ann Emerg Med 2007; 49:445-453.
- A double-blind, placebo controlled study was conducted in 280 patients presenting to the emergency department with acute pain who were randomized to receive intravenous morphine at a dose of 0.10 mg/kg or 0.10 mg/kg followed by an additional 0.05 mg/kg at 30 minutes for a total dose of 0.15 mg/kg.
- The primary outcome was to determine the mean difference in pain score from baseline to 60 minutes following administration of the agent.
- At 60 minutes, patients in the morphine 0.10 mg/kg IV group had a mean pain score of 4.5 versus 5.3 in those patients who received morphine 0.15 mg/kg IV (difference of 0.8), with similar rates of adverse events between both treatment groups.
- Although this was found to be statistically significant in favoring a higher analgesic dose of morphine at 0.15 mg/kg IV, this difference was not found to be clinically significant, according to the authors threshold of at least 1.3 units on the pain scale.
- The authors do suggest that there is a potential to evaluate higher doses of morphine (suggested at 0.2 mg/kg IV divided into two doses of 0.1 mg/kg given five minutes apart). Interestingly enough, the maximum single dose of morphine used in this study in both treatment groups was 10 mg, which reflects that there is some hesitancy of administering relatively high doses of morphine.
Selected References for Nurse-Driven Titration Protocols:
1. Emerg Med (Fremantle) 2002; 14:249-254. [PMID: 12487041]
2. Can J Emerg Med 2005; 7:149-154. [PMID: 17355670]
3. Contemp Nurse 2012; 43:29-37. [PMID: 23343230]
4. Emerg Med J 2005; 22:30-32. [PMID: 15611538]
5. Emerg Med Australas 2013; 25:316-323. [PMID: 23911022]