Robson John, Ayerbe Luis, Mathur Rohini, Addo Juliet, Wragg Andrew
Centre for Primary Care and Public Health, Queen Mary University of London, London, UK.
Department of Non-communicable Disease Epidemiology, London School of Hygiene and Tropical Medicine, London, UK.
BMJ Open. 2015 Apr 15;5(4):e007251. doi: 10.1136/bmjopen-2014-007251.
The recognition of coronary artery disease (CAD) among patients who report chest pain remains difficult in primary care. This study investigates the association between chest pain (specified, unspecified or musculoskeletal) and prodromes (dyspepsia, fatigue or dyspnoea), with first-ever acute CAD, and increased longer term cardiovascular risk.
Cohort study.
Anonymised clinical data recorded electronically by general practitioners from 140 primary care surgeries in London (UK) between April 2008 and April 2013.
Data were extracted for all patients aged 30 years and over at the beginning of the study period, registered in the surgeries.
Clinical data included chest pain, dyspepsia, dyspnoea and fatigue, first-ever CAD and long-term cardiovascular risk (QRisk2). Regression models were used to analyse the association between chest pain together with prodromes and CAD and QRisk2≥20%.
354,052 patients were included in the study. 4842 patients had first-ever CAD of which 270 reported chest pain in the year before the acute event. 257,019 patients had QRisk2 estimations. Chest pain was associated with a higher risk of CAD. HRs: 21.12 (16.68 to 26.76), p<0.001; 7.51 (6.49 to 8.68), p<0.001; and 1.84 (1.14 to 3.00), p<0.001 for specified, unspecified and musculoskeletal chest pain. Dyspepsia, dyspnoea or fatigue was also associated with a higher risk of CAD. Chest pain of all subtypes, dyspepsia and dyspnoea were also associated with an increased 10-year cardiovascular risk of 20% or more.
All patients with chest pain, including those with atypical symptoms, require careful assessment for acute and longer term cardiovascular risk. Prodromes may have independent diagnostic value in the estimation of cardiovascular disease risk.
在初级医疗保健中,识别报告胸痛的患者是否患有冠状动脉疾病(CAD)仍然困难。本研究调查胸痛(特定、非特定或肌肉骨骼性)和前驱症状(消化不良、疲劳或呼吸困难)与首次急性CAD以及长期心血管风险增加之间的关联。
队列研究。
2008年4月至2013年4月期间,英国伦敦140家初级医疗保健机构的全科医生以电子方式记录的匿名临床数据。
提取研究开始时年龄在30岁及以上且在这些机构注册的所有患者的数据。
临床数据包括胸痛、消化不良、呼吸困难和疲劳、首次CAD以及长期心血管风险(QRisk2)。使用回归模型分析胸痛与前驱症状一起与CAD以及QRisk2≥20%之间酌关联。
354,052名患者纳入研究。4842名患者首次发生CAD,其中270名在急性事件发生前一年报告有胸痛。257,019名患者有QRisk2估计值。胸痛与CAD风险较高相关。特定、非特定和肌肉骨骼性胸痛的风险比分别为:21.12(16.68至26.76),p<0.001;7.51(6.49至8.68),p<0.001;1.84(1.14至3.00),p<0.001。消化不良、呼吸困难或疲劳也与CAD风险较高相关。所有亚型的胸痛、消化不良和呼吸困难也与10年心血管风险增加20%或更多相关。
所有胸痛患者,包括那些有非典型症状的患者,都需要仔细评估急性和长期心血管风险。前驱症状在估计心血管疾病风险方面可能具有独立的诊断价值。