None listed
Conditions
Brief summary
Despite pain being the primary reason most patients present to emergency departments (EDs), current methods of pain management in EDs are suboptimal. Patient controlled analgesia (PCA) involves the patient self-administering intravenous analgesia via a pre-set medication administration pump. Although PCAs have being rigorously evaluated and widely used in other clinical areas, they are not routinely used in EDs. This study will identify and describe ED clinicians’ perceptions of the use of PCA in EDs. In phase one, semi-structured interviews will be conducted in a private and a public ED in Western Australia (WA) to identify the perceptions of ED clinicians of using PCAs in EDs. In phase two, a survey will be developed based on findings in the previous phase. This survey will be distributed to ED doctors and nurses across Australia and New Zealand in phase three. This research will add to a limited body of knowledge in the area of pain management in EDs and potentially enhance pain management in the ED through the use of PCAs.
Interventions
Patient controlled analgesia (PCA) is a method widely used in surgical, obstetric, orthopaedic, and palliative care units to manage pain. PCA pumps are loaded with pre-filled syringes of an opioid analgesic, connected to a patient’s intravenous (IV) line, and analgesia is administered in set doses when the patient activates a button on the PCA. Lockout periods are pre-programed to prevent patients from receiving unsafe doses of the medication. Research in the post-operative environment has identified several advantages of PCAs including increased patient autonomy, decreased nursing workload, decreased time to receive analgesia, and improved patient satisfaction (McNicol et al., 2015). Due to these benefits, PCAs are used extensively in other settings however their use in Emergency Departments (EDs) is minimal or non-existent. Interviews will be conducted with ED clinicians in nursing, medicine, and pharmacy disciplines at two participating sites. This purposeful sample will have direct experience and involvement with opioid prescribing or preparation in an ED and thus are an important component of the multidisciplinary team; it is anticipated they will provide useful insight and expertise from different perspectives. A single interview will be conducted with each participant. Interviews will be approximately fifteen minutes long and digitally recorded. The researcher will use an interview guide while conducting the interview. References McNicol, E. D., Ferguson, M. C., & Hudcova, J. (2015). Patient controlled opioid analgesia versus non-patient controlled opioid analgesia for postoperative pain. Cochrane Database of Systematic Reviews, 2015(6), 1–129.
Sponsors
Eligibility
Inclusion criteria
Interviews will be conducted with ED clinicians in nursing, medicine, and pharmacy disciplines at two participating EDs. This purposeful sample will have direct experience and involvement with opioid prescribing or preparation in an ED and thus are an important component of the multidisciplinary team; it is anticipated they will provide useful insight and expertise from different perspectives. Phase three: surveys will be distributed to ED doctors and nurses in Australia and New Zealand via the peak professional colleges and associations of ED doctors and nurses.
Exclusion criteria
No experience in pain management (prescribing analgesia, assessing pain, dispensing analgesia and/or administering analgesia)