ELF: Emergency Laparotomy and Frailty Study

Sponsor
North Western Research Collaborative (Other)
Overall Status
Unknown status
CT.gov ID
NCT02952430
Collaborator
Older persons Surgical Outcomes Collaboration (Other)
500
5

Study Details

Study Description

Brief Summary

Patients aged over 65 comprise more than half the emergency general surgical workload, however, available risk-prediction tools for such patients are extrapolated from younger cohorts. Research suggests that high pre-operative frailty scores correlate with increased post-operative mortality and morbidity. Validated frailty assessments may help identify high risk older emergency surgical patients, facilitating decision-making and informing patient choice.

We propose the first prospective UK observational study assessing frailty as an independent predictor of outcome in the older surgical patient undergoing emergency laparotomy.

Prospective data collection of patients over 65 undergoing emergency laparotomy will be performed in 20 NHS Trusts. Pre-operative frailty scores will be evaluated using the Rockwood Frailty Scale. Primary outcome measure is 30-day mortality. Secondary outcome measures are post-operative complications, altered independence status and length of stay.

Results will be disseminated at national/international surgical meetings and published in a peer-reviewed journal.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Emergency laparotomy

Detailed Description

The ELF steering committee will run this project as part of the North West Research Collaborative(NWRC), consisting of surgical trainees with a successful record of publishing credible research and establishing clinical trials.

Following ethical approval, data will be collected from NHS Trusts throughout the UK. Trained leads will facilitate data collection adhering to a study protocol and local clinical governance.

Patients over 65 undergoing emergency laparotomy will be identified prospectively over 3 months. Demographics, time to surgical intervention, length of stay(LOS), pre- and post-admission independence, intermediate care stay, Clavien-Dindo post-operative complications, 30-day mortality and 30-day re-admission data will be collected on a secure database. Pre-operative frailty will be assessed using the Rockwood Frailty Scale.

500 patients are required for a statistically significant difference in primary outcome (30 day mortality). Secondary outcome measures are complications, change in independence status and LOS. Outcomes will be analysed to compare the impact of frailty.

Study Design

Study Type:
Observational
Anticipated Enrollment :
500 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Emergency Laparotomy and Frailty; a National Multicentre Prospective Cohort Study of Older Surgical Patients (ELF Study)
Study Start Date :
Dec 1, 2016
Anticipated Primary Completion Date :
Mar 1, 2017
Anticipated Study Completion Date :
May 1, 2017

Arms and Interventions

Arm Intervention/Treatment
Frail

Patients over 65 year old having emergency laparotomy with a Frailty score (Modified Rockwood score) of greater than or equal to five. This group will then be observed after intervention to review outcomes.

Procedure: Emergency laparotomy
Patients already undergoing emergency laparotomy - groups divided pre-operatively into frail and not frail based on modified Rockwood score. Then outcomes observed.

Not frail

Patients over 65 year old having emergency laparotomy with a Frailty score (Modified Rockwood score) of less than five. This group will then be observed after intervention to review outcomes.

Procedure: Emergency laparotomy
Patients already undergoing emergency laparotomy - groups divided pre-operatively into frail and not frail based on modified Rockwood score. Then outcomes observed.

Outcome Measures

Primary Outcome Measures

  1. Mortality [90 days]

    Patient alive at 90 days (rounded up to the nearest whole day) post operatively

Secondary Outcome Measures

  1. Post-operative complications [30 days]

    Evidence of post-operative complications at 30 days (rounded up to the nearest whole day) post operatively. Measured using the Clavein Dindo classification

  2. Lowering of independence status post-operatively [30 days]

    Change in living status from pre to post operatively. Including increased care required at home and discharge to increased care (such as residential or nursing home care).

  3. Length of stay [30 days]

    Length of hospital admission - rounded up to whole days

  4. Readmission [30 days]

    All cause readmission to hospital for emergency care - within 30 days post-operatively (rounded up to the nearest whole day).

Eligibility Criteria

Criteria

Ages Eligible for Study:
65 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients aged 65 years and older

  • Admitted to emergency surgical departments

  • Requiring an emergency laparotomy

Exclusion Criteria:
  • Patients less than 65 years old

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • North Western Research Collaborative
  • Older persons Surgical Outcomes Collaboration

Investigators

  • Principal Investigator: Susan Moug, MBChB, PhD,

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
North Western Research Collaborative
ClinicalTrials.gov Identifier:
NCT02952430
Other Study ID Numbers:
  • NWRC- ELF
First Posted:
Nov 2, 2016
Last Update Posted:
Nov 2, 2016
Last Verified:
Oct 1, 2016
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 2, 2016