Geographic Influences on Emergency Laparotomy Outcomes

Introduction

'Emergency Laparotomy' is an umbrella term for a set of commonly performed procedures which are known to carry a significant risk of mortality and morbidity. Previous work has shown considerable inter-hospital variation in emergency laparotomy outcomes within the United Kingdom. It is unknown whether there are significant differences in outcomes following laparotomy which may be explained by geographic factors.

Aims

The aim of this study is to describe emergency laparotomy outcomes in Scotland as they vary by the urban-rural nature of the patient's home location and travel time from hospital.

Methods

This research study is a retrospective observational enquiry which will utilise administrative data from the Information Services Division (ISD) of NHS National Services Scotland. Patient episodes will be identified by a set of procedure codes for emergency laparotomy, and the urban-rural classification of patients will be derived from postcode data. Travel time from hospital will also be derived from postcode data. The investigators will study a 10 year period from January 2001 to December 2010.

The primary outcome measure will be risk-adjusted 30 day/inpatient mortality, and secondary outcome measures will be 30 day readmission rate, 30 day re-operation rate and post-operative length of stay.

Study Overview

• Status: Completed
• Conditions: Abdomen, Acute

Detailed Description

The aim of this study is to explore the possibility that outcomes from emergency laparotomy may vary according to:

1. the urban-rural nature of the patient's home location and
2. travel time from hospital.

This is a retrospective study of all emergency laparotomies performed in Scotland during the period from 1st January 2001 - 31st December 2010. It will use routinely collected administrative data from the Information Services Division (ISD) of NHS National Services Scotland.

Emergency laparotomy will be defined as a non-elective abdominal procedure primarily on the gut tube; and such cases will be identified by the use of a set of procedural codes, which will be validated against local records.

Potentially significant confounding variables such as age, gender, and co-morbidity will be studied for their predictive value in a univariate model and included in a multivariate model if they remain significant. The primary outcome measure will be risk-adjusted 30 day/inpatient mortality, and secondary outcome measures will be 30 day readmission rate, 30 day re-operation rate, and post-operative length of stay.

The registry which will supply the data for this study is the Scottish Morbidity Record 01 (SMR01), the full title of which is the "General / Acute Inpatient and Day Case dataset" (see http://www.adls.ac.uk/nhs-scotland/general-acute-inpatient-day-case-smr01/?detail). SMR01 is collated and administered by ISD, and data submission is mandatory for all Scottish NHS providers of in-patient or day-case care. Approximately 1.4 million records are added each year. Diagnoses are coded according to International Classification of Diseases (ICD)-10 standards and procedures are coded according to the United Kingdom's Office of Population Census Statistics (OPCS) standards, the most recent of which is version 4.5.

The data quality in SMR01 is high and is assured by regular internal audits. In the 2010 audit of accuracy, Main Condition was recorded with an accuracy of 88% and Main Procedure was recorded with an accuracy of 94%. Where data inconsistencies are identified in the extract supplied for this study, further clarification will be obtained where possible with ISD's data retrieval support team. Data completeness is very high in SMR01. However, where significant volumes of data are missing or unusable, the need for data imputation will be explored.

The study period was decided on pragmatically by a desire to provide an assessment of contemporary practice, fully within the era of wide-spread laparoscopic surgery.

A power calculation also suggested that this would provide an adequate sample size to demonstrate mortality differences. A recent paper showed 30 day mortality for emergency laparotomy to be 14.9% (Saunders DI, Murray D, Pichel AC, Varley S, Peden CJ. Variations in mortality after emergency laparotomy: the first report of the UK Emergency Laparotomy Network. Br J Anaesth. 2012 Sep 1;109(3):368-75.)

It was decided that we wanted to be able to detect a mortality difference (absolute) of 2%. Alpha was specified as 0.05 and power 0.9. Using a chi-2 test in G Power 3.1.7, it was determined that a total N of 5221 was required to show this difference. In the study already cited, 35 hospitals submitted data on 3 months of practice, giving a total of 1853 patients. We extrapolated to estimate that one hospital completes 212 laparotomies per year. There are currently 31 adult surgical centres in Scotland, resulting in an estimate of 6,565 laparotomies per year. Even accepting the smaller size of Scottish hospitals, this demonstrates that a 10 year cohort should be more than adequate to detect a clinically significant difference in length of stay.

The investigators will use the Scottish government's own 8-fold urban-rural classification system (see http://www.scotland.gov.uk/Topics/Statistics/About/Methodology/UrbanRuralClassification) to investigate the possible relationship between patient geographical location and outcome. Urban-rural categories may be grouped for analysis, according to initial exploratory work.

The investigators will further calculate the approximate travelling time from patient home location (using postcode) to the treating hospital, by constructing isocrones at time/distance intervals from hospitals. Travel time will be analysed as a continuous and discrete variable.

• Study Type: Observational
• Enrollment (Anticipated): 40000

Contacts and Locations

Study Locations

• United Kingdom
  • All Scottish surgical units, United Kingdom
    • All Scottish NHS Hospitals

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (ADULT, OLDER_ADULT)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

• Sampling Method: Probability Sample

Study Population

All Scottish adult residents undergoing emergency laparotomy during the study period

Description

Inclusion Criteria:

• All patients aged 18 years or older who undergo emergency laparotomy within the study period

Exclusion Criteria:

• Patients who are non-resident in Scotland
• Multiple laparotomies on a single patient will not be counted as separate index events unless ≥6 months have passed between previous discharge and new hospital admission.

Study Plan

How is the study designed?

Number of groups / cohorts

9

Cohorts and Interventions

Group / Cohort
Urban-Rural Classification 1: Large Urban Areas; Settlements of over 125,000 people
Urban-Rural Classification 2: Other Urban Areas; Settlements of 10,000 to 125,000 people
Urban-Rural Classification 3: Accessible Small Towns; Settlements of between 3,000 and 10,000 people and within 30 minutes drive of a settlement of 10,000 or more.
Urban-Rural Classification 4: Remote Small Towns; Settlements of between 3,000 and 10,000 people and with a drive time of over 30 minutes to a settlement of 10,000 or more.
Urban-Rural Classification 5: Very Remote Small Towns; Settlements of between 3,000 and 10,000 people and with a drive time of over 60 minutes to a settlement of 10,000 or more
Urban-Rural Classification 6: Accessible Rural; Areas with a population of less than 3,000 people, and within a 30 minute drive time of a settlement of 10,000 or more
Urban-Rural Classification 7: Remote Rural; Areas with a population of less than 3,000 people, and with a drive time of over 30 minutes to a settlement of 10,000 or more
Urban-Rural Classification 8: Very Remote Rural; Areas with a population of less than 3,000 people, and with a drive time of over 60 minutes to a settlement of 10,000 or more
Travel Time - see below; Travel time will be analysed as a continuous and discrete variable.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Mortality	Death as an in-patient or ≤30 days of procedure. Deaths will be recognised from SMR01 which is linked to the Registrar General's database of deaths.	Either within 30 days of procedure, or during continuous in-patient stay

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Re-admission	Re-admission to any hospital specialty ≤30 days have elapsed since date of discharge.	Within 30 days of index discharge
Post-operative length of stay	(Whole) days from date of laparotomy to date of discharge. Because this is a retrospective study using a complete national data set, with the last admission 2.5 years distant from the time of data collection, we will use actual time period rather than censoring length of stay at a set point.	From date of laparotomy to date of discharge (whole days) - see below
Re-operation	The occurrence of an abdominal procedure either subsequent to laparotomy and within the index admission, or ≤30 days of discharge.	Within the index admission or within 30 days of discharge

Collaborators and Investigators

• Sponsor: University of Edinburgh

Study record dates

Study Major Dates

• Study Start: January 1, 2001
• Primary Completion (ACTUAL): December 1, 2010
• Study Completion (ACTUAL): August 1, 2013

Study Registration Dates

• First Submitted: November 21, 2013
• First Submitted That Met QC Criteria: December 16, 2013
• First Posted (ESTIMATE): December 23, 2013

Study Record Updates

• Last Update Posted (ESTIMATE): December 23, 2013
• Last Update Submitted That Met QC Criteria: December 16, 2013
• Last Verified: December 1, 2013

More Information

Terms related to this study

• Keywords: General Surgery; Laparotomy; Outcome Assessment (Health Care); Hospitals,General; Hospitals,Rural; Hospitals,Urban; Rural Health Services; Geography, Medical
• Additional Relevant MeSH Terms: Pathologic Processes; Pain; Neurologic Manifestations; Disease Attributes; Signs and Symptoms, Digestive; Abdominal Pain; Emergencies; Abdomen, Acute
• Other Study ID Numbers: XRB13069-GEL