The Hospital Volume Relationship in 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 differences in hospital procedural volume.
Aims
The aim of this study is to compare emergency laparotomy outcomes in Scotland as they vary by hospital procedural volume.
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.
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 length of stay.
Visão geral do estudo
Status
Condições
Descrição detalhada
The aim of this study is to explore the possibility of a hospital procedural volume-outcome relationship in Scottish emergency laparotomy outcomes.
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.
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 current 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 current practice, fully within the era of widely practised 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.)
We 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.
Hospitals will be placed into tertiles of high, medium and low volume, according to the number of procedures performed over the study period.
The study will compare risk-adjusted 30 day/in-patient mortality as the primary outcome, with secondary outcomes of 30 day re-admission rate, 30 day re-operation rate and post-operative length of stay. 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.
Tipo de estudo
Inscrição (Antecipado)
Contactos e Locais
Locais de estudo
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All Scottish Surgical Centres, Reino Unido
- All Scottish NHS Hospitals
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Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
Aceita Voluntários Saudáveis
Gêneros Elegíveis para o Estudo
Método de amostragem
População do estudo
Descrição
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.
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
Coortes e Intervenções
Grupo / Coorte |
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High volume hospitals
The hospitals in the upper tertile for procedural volume
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Medium volume hospitals
The hospitals in the middle tertile for procedural volume
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Low volume hospitals
The hospitals in the lowest tertile for procedural volume.
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O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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Mortality
Prazo: Either within 30 days of procedure, or during continuous in-patient stay (up to 12.5 years)
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Death as an in-patient or ≤30 days of procedure. This is a retrospective study using a complete national data set, with the first admission 12.5 years distant from the time of data collection, and the last admission 2.5 years prior to the time of data collection. The theoretical maximal length of stay is 12.5 years. 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 (up to 12.5 years)
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Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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Readmissão
Prazo: Dentro de 30 dias após a alta do índice
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Re-admissão em qualquer especialidade hospitalar ≤ 30 dias decorridos desde a data da alta.
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Dentro de 30 dias após a alta do índice
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Post-operative length of stay
Prazo: From date of laparotomy to date of discharge (whole days) - up to 12.5 years
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(Whole) days from date of laparotomy to date of discharge. B This is a retrospective study using a complete national data set, with the first admission 12.5 years distant from the time of data collection, and the last admission 2.5 years prior to the time of data collection. The theoretical maximal length of stay is 12.5 years. |
From date of laparotomy to date of discharge (whole days) - up to 12.5 years
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Re-operation
Prazo: Within the index admission (theoretically, up to a maximum of 12.5 years) or within 30 days of discharge
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The occurrence of an abdominal procedure either subsequent to laparotomy and within the index admission, or ≤30 days of discharge. As above, this is a retrospective study using a complete national data set, with the first admission 12.5 years distant from the time of data collection, and the last admission 2.5 years prior to the time of data collection. The theoretical maximal length of stay for the index admission is 12.5 years. |
Within the index admission (theoretically, up to a maximum of 12.5 years) or within 30 days of discharge
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Colaboradores e Investigadores
Patrocinador
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo
Conclusão Primária (Real)
Conclusão do estudo (Real)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Estimativa)
Atualizações de registro de estudo
Última Atualização Postada (Estimativa)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- XRB13069-VEL
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