Royal Infirmary of Edinburgh
Edinburgh, EH16 4SA, United Kingdom
NCT Number: NCT02179112
A multicentre, international evaluation of emergency abdominal surgery to establish surgical outcomes and identify common, modifiable best practice processes.
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Observational
Edinburgh, EH16 4SA, United Kingdom
Background: With over 200 million surgical operations per year worldwide and with nearly every acute hospital providing surgical services, outcomes from emergency general surgery represent internationally important healthcare markers. Best practice and modifiable processes that are relevant to good patient outcomes around the world require validation using patient-level data.
Aim: The primary aim of this study is to identify internationally relevant, modifiable surgical practices (in terms of modifiable equipment and clinical management) associated with best care. These factors will include use of imaging, supplementary oxygen, pulse oximetry, critical care, and safety checklists.
Method: This is a multicentre, international, prospective cohort study. Any hospital in the world performing acute surgery will be eligible to enter. Any patient undergoing emergency surgery with an incision entering the peritoneal cavity is eligible. Routine, anonymised clinical data on consecutive patients will be collected over a two week period in each surgical centre, with up to 30 days follow-up data collected. The primary outcome is 24-hour post-operative mortality rate. Secondary outcomes include 30-day inpatient post-operative mortality rate, and 30-day serious complication rate. Participating centres will also be asked to complete a survey that will collect data on hospital structural and resource characteristics.
Data will be entered and stored securely via the University of Edinburgh's REDCap system. This pragmatic protocol (which will delivered across many low-resource settings) does not allow for independent verification of data entry. Data collection norms are laid out in the protocol, where data definitions are also clearly provided. Sample size is not relevant to this exploratory audit. Centres will only be included where there is at least 95% data completeness.
Potential explanatory variables that will be explored in subsequent analysis include country Human Developmental Index, and resource differences.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Centre Inclusion Criteria:
Inclusion criteria
Exclusion criteria
Emergency intra-peritoneal surgery (only exclusion: Caesarian section).
Time frame: At 24 hours following conclusion of the operation
Number of deaths during operation or within 24 hours of operation conclusion, divided by number of operations undertaken.
Time frame: Up to 30 days from the operation (or point of discharge- see definition)
Number of deaths during operation or within 30 days of operation, or at the point of final discharge if out-patient mortality status unknown.
Please see reference for justification of our use of this definition in our global cohort.
Watters DA, Hollands MJ, Gruen RL, Maoate K, Perndt H, McDougall RJ, et al. Perioperative Mortality Rate (POMR): A Global Indicator of Access to Safe Surgery and Anaesthesia. World J Surg. 2014 May 20;1-9.
Time frame: Up to 30 days from the operation (or point of final discharge - see below)
Number of serious complications occurring, divided by number of operations. Measured at operation or within 30 days of operation, or point of final discharge if out-patient information unavailable. (See definition of POMR-30 above for justification).
Serious complications defined as Grade III or V within the Clavien-Dindo classification (Grade III = complications requiring surgical, endoscopic or radiological intervention; Grade V = death).
Dindo D, Demartines N, Clavien P-A. Classification of Surgical Complications. Ann Surg. 2004 Aug;240(2):205-13.
University of Edinburgh
Other
Acronym: GlobalSurg-1
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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