Risk of Atrial Fibrillation and Association With Other Diseases: Protocol of the Derivation and International External Validation of a Prediction Model Using Nationwide Population-based Electronic Health Records
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 2,159,663
- 试验地点
- 1
- 主要终点
- 1. To develop and validate a model for predicting the risk of new onset AF within the next 6 months
研究概览
简要总结
Atrial fibrillation (AF) is a major public health issue: it is increasingly common, incurs substantial healthcare expenditure, and is associated with a range of adverse outcomes. There is rationale for the early diagnosis of AF, before the first complication occurs. Previous AF screening research is limited by low yields of new cases and strokes prevented in the screened populations. For AF screening to be clinically and cost-effective, the efficiency of identification of newly diagnosed AF needs to be improved and the intervention offered may have to extend beyond oral anticoagulation for stroke prophylaxis. Previous prediction models for incident AF have been limited by their data sources and methodologies. An accurate model that utilises existing routinely-collected data is needed to inform clinicians of patient-level risk of AF, inform national screening policy and highlight opportunities to improve patient outcomes from AF screening beyond that of only stroke prevention. The investigators will use routinely-collected hospital-linked primary care data to develop and validate a model for prediction of incident AF within a short prediction horizon, incorporating both a machine learning and traditional regression method. They will also investigate how atrial fibrillation risk is associated with other diseases and death. Using only clinical factors readily accessible in the community, the investigators will provide a method for the identification of individuals in the community who are at risk of AF, thus accelerating research assessing whether atrial fibrillation screening is clinically effective when targeted to high-risk individuals.
详细描述
Atrial fibrillation (AF) is a major public health issue: it is increasingly common, incurs substantial healthcare expenditure, and is associated with a range of adverse outcomes. There is rationale for the early diagnosis of AF, before the first complication occurs. Previous AF screening research is limited by low yields of new cases and strokes prevented in the screened populations. For AF screening to be clinically and cost-effective, the efficiency of identification of newly diagnosed AF needs to be improved and the intervention offered may have to extend beyond oral anticoagulation for stroke prophylaxis. Previous prediction models for incident AF have been limited by their data sources and methodologies. An accurate model that utilises existing routinely-collected data is needed to inform clinicians of patient-level risk of AF, inform national screening policy and highlight opportunities to improve patient outcomes from AF screening beyond that of only stroke prevention.
The application of Random Forest will be investigated and multivariable logistic regression to predict incident AF within a 6 months prediction horizon, that is a time-window consistent with conducting investigation for AF. The Clinical Practice Research Datalink (CPRD)-GOLD dataset will be used for derivation, and the Clalit Health Services dataset will be used for international external geographical validation. Both comprise a large representative population and include clinical outcomes across primary and secondary care. Analyses will include metrics of prediction performance and clinical utility. Only risk factors accessible in the community will be used and the model could thus enable passive screening for high-risk individuals in electronic health records that is updated with presentation of new data. The study aims to create a calculator from a parsimonious model. Kaplan-Meier plots for individuals identified as higher and lower predicted risk of AF will be calculated and derive the cumulative incidence rate for non-AF cardio-renal-metabolic diseases and death over the longer term to establish how predicted AF risk is associated with a range of new non-AF disease states.
To ascertain whether the prediction model is transportable to geographies outside of the UK, the model's performance will be externally validated in the Clalit Health Services database in Israel. The validation will include participants insured by Clalit with continuous membership for at least 1 year before 01/01/2019: 2,159,663 patients with 4,330 of them having a new incident of AF (Atrial fibrillation and/or atrial flutter) in the first half of 2019. The study population will comprise all available patients who have at least 1-year follow up. The outcome of interest is the first diagnosed AF after baseline and will be identified using Read codes and ICD-9/10 codes. Patients with less than one year of registration, who are under thirty years of age at point of study entry, or have a preceding diagnosis of atrial fibrillation, will be excluded.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Retrospective
入排标准
- 年龄范围
- 30 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •A least 1 year follow-up
排除标准
- •Diagnosed AF before study entry
结局指标
主要结局
1. To develop and validate a model for predicting the risk of new onset AF within the next 6 months
时间窗: Between 1st Jan 1998 and 31st December 2018
a. Predictive factors will be identified using Read codes and ICD-9/10 codes (diagnoses) Variables considered as potential predictors may include sociodemographic variables (age, sex, ethnicity) and morbidities.
1. To quantify the association between risk of new-onset AF and the hazard of other cardio-renal-metabolic diseases and death
时间窗: Between 1st Jan 1998 and 31st December 2018
a. All patients categorized as lower or higher predicted AF risk by the developed prediction model will be included. The initial presentation of a cardiovascular, renal, or metabolic disease or death will be considered because AF is associated with a high risk of adverse clinical outcomes. The occurrence of death by any cause will be quantified. Incident diagnoses will be defined as the first record of that condition in primary or secondary care records from any diagnostic position. Kaplan-Meier plots will be created for individuals identified as higher and lower predicted risk of AF and derive the cumulative incidence rate for each outcome at 1, 5 and 10 years considering the competing risk of death, as well as death at 5 and 10 years. For each specified outcome, the hazard ratio (HR) will be calculated between higher and lower predicted risk of AF using the Fine and Gray's model with adjustment for the competing risk of death.
次要结局
未报告次要终点
研究者
Dr Christopher Gale
Professor of Cardiovascular Medicine
University of Leeds
