Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comparative Study
. 2018 Jan;36(1):88-92.
doi: 10.1016/j.ajem.2017.07.037. Epub 2017 Jul 13.

Opioid doses and acute care utilization outcomes for adults with sickle cell disease: ED versus acute care unit

Affiliations
Comparative Study

Opioid doses and acute care utilization outcomes for adults with sickle cell disease: ED versus acute care unit

Robert E Molokie et al. Am J Emerg Med. 2018 Jan.

Abstract

Background: Acute care units (ACUs) with focused sickle cell disease (SCD) care have been shown to effectively address pain and limit hospitalizations compared to emergency departments (ED), the reason for differences in admission rates is understudied. Our aim was compare effects of usual care for adult SCD pain in ACU and ED on opioid doses and discharge pain ratings, hospital admission rates and lengths of stay.

Methods: In a retrospective, comparative cohort, single academic tertiary center study, 148 adults with sickle cell pain received care in the ED, ACU or both. From the medical records we documented opioid doses, unit discharge pain ratings, hospital admission rates, and lengths of stay.

Findings: Pain on admission to the ED averaged 8.7±1.5 and to the ACU averaged 8.0±1.6. The average pain on discharge from the ED was 6.4±3.0 and for the ACU was 4.5±2.5. 70% of the 144 ED visits resulted in hospital admissions as compared to 37% of the 73 ACU visits. Admissions from the ED or ACU had similar inpatient lengths of stay. Significant differences between ED and ACU in first opioid dose and hourly opioid dose were noted.

Conclusions: Applying guidelines for higher dosing of opioids for acute painful episodes in adults with SCD in ACU was associated with improved pain outcomes and decreased hospitalizations, compared to ED. Adoption of this approach for SCD pain in ED may result in improved outcomes, including a decrease in hospital admissions.

Keywords: Acute care unit; Emergency department; Hospital admission; Opioid; Pain; Sickle cell disease.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflicts of interest.

Figures

Fig. 1.
Fig. 1.
Initial and discharge pain ratings in two settings: emergency department (ED) and acute care unit (AC).

Similar articles

Cited by

References

    1. Yusuf HR, Atrash HK, Grosse SD, Parker CS, Grant AM. Emergency department visits made by patients with sickle cell disease: a descriptive study, 1999–2007.Am J Prev Med 2010;38 (S536-41). - PMC - PubMed
    1. Shankar SM, Arbogast PG, Mitchel E, Cooper WO, Wang WC, Griffin MR. Medical care utilization and mortality in sickle cell disease: a population-based study. Am J Hematol 2005;80:262–70. - PubMed
    1. Raphael JL, Dietrich CL, Whitmire D, Mahoney DH, Mueller BU, Giardino AP. Healthcare utilization and expenditures for low income children with sickle cell disease. Pediatr Blood Cancer 2009;52:263–7. - PubMed
    1. Benjamin LJ, Swinson GI, Nagel RL Sickle Cell Anemia Day Hospital: An approach for the management of uncomplicated painful crisis. Blood 2000;95:1130–6. - PubMed
    1. Ballas SK. Sickle cell pain. 1 edition ed. Seattle: IASP Press; 1998.

Publication types

Substances