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The Hospital Volume Relationship in Emergency Laparotomy Outcomes

2014年1月24日 更新者:University of Edinburgh

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.

研究概览

地位

完全的

详细说明

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.

研究类型

观察性的

注册 (预期的)

40000

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

      • All Scottish Surgical Centres、英国
        • All Scottish NHS Hospitals

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

有资格学习的性别

全部

取样方法

概率样本

研究人群

All Scottish adult residents undergoing emergency laparotomy during the study period

描述

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.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

队列和干预

团体/队列
High volume hospitals
The hospitals in the upper tertile for procedural volume
Medium volume hospitals
The hospitals in the middle tertile for procedural volume
Low volume hospitals
The hospitals in the lowest tertile for procedural volume.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Mortality
大体时间:Either within 30 days of procedure, or during continuous in-patient stay (up to 12.5 years)

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)

次要结果测量

结果测量
措施说明
大体时间
重新入场
大体时间:指数发布后 30 天内
自出院之日起 ≤ 30 天后再次入院任何医院专科。
指数发布后 30 天内
Post-operative length of stay
大体时间:From date of laparotomy to date of discharge (whole days) - up to 12.5 years

(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
Re-operation
大体时间:Within the index admission (theoretically, up to a maximum of 12.5 years) or within 30 days of discharge

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

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2001年1月1日

初级完成 (实际的)

2010年12月1日

研究完成 (实际的)

2013年8月1日

研究注册日期

首次提交

2013年12月16日

首先提交符合 QC 标准的

2014年1月24日

首次发布 (估计)

2014年1月28日

研究记录更新

最后更新发布 (估计)

2014年1月28日

上次提交的符合 QC 标准的更新

2014年1月24日

最后验证

2014年1月1日

更多信息

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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