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Reducing time to analgesia in the emergency department using a nurse-initiated pain protocol: a before-and-after study.

In adult patients presenting to the Emergency Department in pain does a nurse-initiated pain protocol compared to usual practice reduce time to analgesia

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12611000953932
Enrollment
889
Registered
2011-09-05
Start date
2009-04-04
Completion date
2009-06-25
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

We sought to introduce and evaluate the practice of ‘nurse-initiated analgesia’ in the emergency department of a busy tertiary hospital in Western Australia, whereby the ED triage nurse (or other specifically trained ED nurse) administered analgesic medications according to a pre-defined protocol, without the patient being first assessed by a medical officer.

Interventions

Nurse-initiated pain protocol in emergency department - involved the administration of various oral analgesic medications (type of drug and dose specified) depending on the patient's pain score (0-10). For example, 2 x paracetamol 500mg oral (or 2 x Ibuprofen 200mg ) for mild pain (pain score 1-3); 2 x paracetamol 500mg with codeine 30mg (or 3 x Ibuprofen 200mg/Codeine 12.8mg) for moderate pain (pain score 4-6), and oxycodone 5mg for severe pain (pain score 7+). The nurse-initiated analgesia p

Nurse-initiated pain protocol in emergency department - involved the administration of various oral analgesic medications (type of drug and dose specified) depending on the patient's pain score (0-10). For example, 2 x paracetamol 500mg oral (or 2 x Ibuprofen 200mg ) for mild pain (pain score 1-3); 2 x paracetamol 500mg with codeine 30mg (or 3 x Ibuprofen 200mg/Codeine 12.8mg) for moderate pain (pain score 4-6), and oxycodone 5mg for severe pain (pain score 7+). The nurse-initiated analgesia protocol could only be used once for each patient without further consultation with a medical officer, ie the duration was for initial pain relief in the Emergency Department only. The nurse-initiated protocol was trialled between 4 April 2009 and 25 June 2009.

Sponsors

Professor Judith Finn
Lead SponsorIndividual

Study design

Allocation
Non-randomised trial
Intervention model
Single group
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

All adult patients presenting to the ED with pain

Exclusion criteria

Patients meeting the following conditions were excluded: presented with chest pain of presumed cardiac origin or headache; were triaged as emergency or urgent (Australasian Triage Score 1 & 2)[12]; exhibited unstable vital signs; were pregnant or lactating; had known contraindications to one of the study drugs; declined analgesia; or already had an analgesia related management plan in place.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026