Skip to content

An observational study of discharge analgesia and analgesic outcomes after discharge following surgery in Southern Adelaide Local Health Network: A prospective pilot study

Observational study investigating appropriateness of discharge analgesia prescribing and analgesic outcomes in elective and emergency surgical patients after discharge in Southern Adelaide Local Health Network: A prospective pilot study

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ANZCTR
Registry ID
ACTRN12620000882921
Enrollment
400
Registered
2020-09-04
Start date
2020-09-18
Completion date
2020-10-29
Last updated
2020-09-14

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

Conditions

None listed

Brief summary

Many patients experience pain after surgery, but this can vary significantly between individuals. With patients being discharged from hospital following surgery earlier than in previous generations, managing pain after discharge has become an important part caring for surgical patients. Frequently, this includes the prescription of opioid medications on discharge. While opioid medications are widely used to treat pain after surgery, there is now a large amount of evidence demonstrating that when prescribed on discharge opioids can contribute to a range of adverse outcomes for patients and the community more broadly. This presents a challenge to clinicians, who need to balance these risks while meeting the pain relief needs of patients. The purpose of this study is to capture accurate data on the nature of opioid prescribing and usage on discharge within Southern Adelaide Local Health Network, data which has previously never been captured or reported. We are aiming to assess if; 1. Opioid analgesia prescribed on discharge following surgery undertaken in SALHN is undertaken in accordance with current clinical guidelines. 2. Opioid analgesia prescribed on discharge following surgery undertaken in Southern Adelaide Local Health Network (SALHN) is adequate for patient analgesia requirements. 3. Opioid analgesia prescribed on discharge following surgery undertaken in SALHN results in unused prescription opioid in the community. 4. The volume of opioid prescribed on discharge could be reduced without increasing rates of patients needing to return to hospital as a consequence of pain OR patients experiencing pain limiting function when they are unable to access care.

Interventions

A non-interventional, prospective observational cohort study with post-hoc survey will be undertaken. Participants will be recruited from patients undergoing surgery at Flinders Medical Centre and Noarlunga Health Service and will be surveyed on analgesia usage and outcome at time points of two weeks and six months post discharge. Participants will also be surveyed on analgesia education received prior to discharge, which is incorporated into the follow up survey at two weeks post discharge. As

A non-interventional, prospective observational cohort study with post-hoc survey will be undertaken. Participants will be recruited from patients undergoing surgery at Flinders Medical Centre and Noarlunga Health Service and will be surveyed on analgesia usage and outcome at time points of two weeks and six months post discharge. Participants will also be surveyed on analgesia education received prior to discharge, which is incorporated into the follow up survey at two weeks post discharge. As no appropriate validated survey was available to capture the outcomes of interest, surveys were designed specifically for this study. Both surveys should take participants less then 5 minutes to complete.

Sponsors

Flinders Medical Centre - Department of Anaesthesia
Lead SponsorHospital

Eligibility

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

Inclusion criteria

- Undergoing elective or emergency surgery at Flinders Medical Centre or Noarlunga Health Service. - Aged 18 years or greater at time of consent.

Exclusion criteria

- Unable to provide informed consent for self (as per consent to surgery). - Self identifies as being unable to complete an online survey on their smart phone. - Non-English speaking. - Declines participation.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026