Annals of Emergency Medicine
Volume 46, Issue 4 , Pages 362-367, October 2005

Intravenous Morphine at 0.1 mg/kg Is Not Effective for Controlling Severe Acute Pain In the Majority of Patients

  • Polly E. Bijur, PhD

      Affiliations

    • Corresponding Author InformationAddress for correspondence: Polly E. Bijur, PhD, Albert Einstein College of Medicine, Rose F. Kennedy Center, 1410 Pelham Parkway South, Bronx, NY 10461; 718-430-4217, fax 718-430-8821
  • ,
  • Mark K. Kenny, PhD
  • ,
  • E. John Gallagher, MD

From the Department of Emergency Medicine, Albert Einstein College of Medicine, Bronx, NY

Received 15 December 2004; received in revised form 7 February 2005 and 15 February 2005; accepted 10 March 2005.

Study objective

The objective was to quantify the analgesic effect of a dose of intravenous morphine, 0.1 mg/kg, to emergency department (ED) patients presenting in acute, severe pain.

Methods

This was a prospective convenience cohort of patients aged 21 to 65 years and presenting to an academic urban ED with acute, severe pain. Patients rated their pain intensity on a validated 11-point verbal numeric rating scale ranging from 0, “no pain,” to 10, “worst possible pain,” immediately before they received 0.1 mg of intravenous morphine per kilogram of body weight and 30 minutes later. The main outcome was proportion of patients whose pain decreased by less than 50% during the 30-minute interval.

Results

Of 119 patients who received intravenous morphine at 0.1 mg/kg, the average age was 42 years (SD=11 years), 55% were female patients, 65% were Hispanic, 28% were black, and 7% were classified as other. The median numeric rating scale pain score at baseline was 10 (interquartile range 9 to 10). Sixty-seven percent (95% confidence interval 58% to 76%) of the patients receiving intravenous morphine at 0.1 mg/kg reported a less than 50% decrease in pain. No patient required an opioid antagonist at any time during or after the study period.

Conclusion

The data suggest that a 0.1 mg/kg dose of morphine may be too low to adequately control acute severe pain.

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  •  Shaded area indicates number and percentage of patients whose pain scores decreased <50%.

 Supervising editors: Knox H. Todd, MD, MPH; Michael L. Callaham, MDAuthor contributions: PEB, MKK, and EJG contributed to the concept, design, and writing. MKK was responsible for editing. PEB and EJG incorporated revisions. PEB conducted the analysis. PEB takes responsibility for the paper as a whole.Funding and support: This study was supported in part by a grant from the Agency for Healthcare Research and Quality 1 R01 HS13924.Reprints not available from the authors.

PII: S0196-0644(05)00334-3

doi:10.1016/j.annemergmed.2005.03.010

Annals of Emergency Medicine
Volume 46, Issue 4 , Pages 362-367, October 2005