TY - JOUR
T1 - Assessing the severity of cardiovascular disease in 213 088 patients with coronary heart disease
T2 - a retrospective cohort study
AU - Zghebi, Salwa S
AU - Mamas, Mamas A
AU - Ashcroft, Darren M
AU - Rutter, Martin K
AU - VanMarwijk, Harm
AU - Salisbury, Chris
AU - Mallen, Christian D
AU - Chew-Graham, Caroline A
AU - Qureshi, Nadeem
AU - Weng, Stephen F
AU - Holt, Tim
AU - Buchan, Iain
AU - Peek, Niels
AU - Giles, Sally
AU - Reeves, David
AU - Kontopantelis, Evangelos
N1 - Funding Information:
those of the NIHR or the Department of Health and Social Care. The funder of the study had no role in study design, data collection, data analysis, data interpretation or writing of the report. The lead author had full access to the data in the study, takes responsibility for its integrity and the data analysis and had final responsibility for the decision to submit for publication. Competing interests DMA reports research grants from Abbvie, Almirall, Celgene, Eli Lilly, Novartis, UCB and the Leo Foundation and is funded by the NIHR Greater Manchester Patient Safety Translational Research Centre, the NIHR School for Primary Care Research, and the NIHR Manchester Biomedical Research Centre. MKR has received educational grant support from MSD and Novo Nordisk; has modest stock ownership in GSK; and has consulted for Roche. CS reports grants from NIHR School for Primary Care Research during the conduct of the study, is partially supported by NHS ARC West and is an NIHR Senior Investigator. CDM is funded by the NIHR Collaborations for Leadership in Applied Health Research and Care West Midlands, the NIHR School for Primary Care Research and a NIHR Research Professorship in General Practice (NIHR-RP-2014-04-026). He has provided support for a Bristol Myer Squibb non-pharmacological Atrial Fibrillation study (funding to School). NQ reports grants from the NIHR SPCR and NIHR HTA, during the conduct of the study. SFW is an employee of Janssen R NIHR Senior Investigator grant. NP’s time was partially funded by the NIHR Manchester Biomedical Research Centre. Other coauthors have no disclosures.
Funding Information:
CS reports grants from NIHR School for Primary Care Research during the conduct of the study, is partially supported by NHS ARC West and is an NIHR Senior Investigator. CDM is funded by the NIHR Collaborations for Leadership in Applied Health Research and Care West Midlands, the NIHR School for Primary Care Research and a NIHR Research Professorship in General Practice (NIHR-RP-2014-04-026). He has provided support for a Bristol Myer Squibb non-pharmacological Atrial Fibrillation study (funding to School). NQ reports grants from the NIHR SPCR and NIHR HTA, during the conduct of the study. SFW is an employee of Janssen R NIHR Senior Investigator grant. NP's time was partially funded by the NIHR Manchester Biomedical Research Centre. Other coauthors have no disclosures.
Funding Information:
Funding This study is funded by the National Institute for Health Research (NIHR) School for Primary Care Research (NIHR SPCR – grant number 331).
Publisher Copyright:
© 2021 Author(s) (or their employer(s). Re-use permitted under CC BY. Published by BMJ.
PY - 2021/4/20
Y1 - 2021/4/20
N2 - OBJECTIVE: Most current cardiovascular disease (CVD) risk stratification tools are for people without CVD, but very few are for prevalent CVD. In this study, we developed and validated a CVD severity score in people with coronary heart disease (CHD) and evaluated the association between severity and adverse outcomes.METHODS: Primary and secondary care data for 213 088 people with CHD in 398 practices in England between 2007 and 2017 were used. The cohort was randomly divided into training and validation datasets (80%/20%) for the severity model. Using 20 clinical severity indicators (each assigned a weight=1), baseline and longitudinal CVD severity scores were calculated as the sum of indicators. Adjusted Cox and competing-risk regression models were used to estimate risks for all-cause and cause-specific hospitalisation and mortality.RESULTS: Mean age was 64.5±12.7 years, 46% women, 16% from deprived areas, baseline severity score 1.5±1.2, with higher scores indicating a higher burden of disease. In the training dataset, 138 510 (81%) patients were hospitalised at least once, and 39 944 (23%) patients died. Each 1-unit increase in baseline severity was associated with 41% (95% CI 37% to 45%, area under the receiver operating characteristics (AUROC) curve=0.79) risk for 1 year for all-cause mortality; 59% (95% CI 52% to 67%, AUROC=0.80) for cardiovascular (CV)/diabetes mortality; 27% (95% CI 26% to 28%) for any-cause hospitalisation and 37% (95% CI 36% to 38%) for CV/diabetes hospitalisation. Findings were consistent in the validation dataset.CONCLUSIONS: Higher CVD severity score is associated with higher risks for any-cause and cause-specific hospital admissions and mortality in people with CHD. Our reproducible score based on routinely collected data can help practitioners better prioritise management of people with CHD in primary care.
AB - OBJECTIVE: Most current cardiovascular disease (CVD) risk stratification tools are for people without CVD, but very few are for prevalent CVD. In this study, we developed and validated a CVD severity score in people with coronary heart disease (CHD) and evaluated the association between severity and adverse outcomes.METHODS: Primary and secondary care data for 213 088 people with CHD in 398 practices in England between 2007 and 2017 were used. The cohort was randomly divided into training and validation datasets (80%/20%) for the severity model. Using 20 clinical severity indicators (each assigned a weight=1), baseline and longitudinal CVD severity scores were calculated as the sum of indicators. Adjusted Cox and competing-risk regression models were used to estimate risks for all-cause and cause-specific hospitalisation and mortality.RESULTS: Mean age was 64.5±12.7 years, 46% women, 16% from deprived areas, baseline severity score 1.5±1.2, with higher scores indicating a higher burden of disease. In the training dataset, 138 510 (81%) patients were hospitalised at least once, and 39 944 (23%) patients died. Each 1-unit increase in baseline severity was associated with 41% (95% CI 37% to 45%, area under the receiver operating characteristics (AUROC) curve=0.79) risk for 1 year for all-cause mortality; 59% (95% CI 52% to 67%, AUROC=0.80) for cardiovascular (CV)/diabetes mortality; 27% (95% CI 26% to 28%) for any-cause hospitalisation and 37% (95% CI 36% to 38%) for CV/diabetes hospitalisation. Findings were consistent in the validation dataset.CONCLUSIONS: Higher CVD severity score is associated with higher risks for any-cause and cause-specific hospital admissions and mortality in people with CHD. Our reproducible score based on routinely collected data can help practitioners better prioritise management of people with CHD in primary care.
KW - Cardiovascular Diseases/diagnosis
KW - Cause of Death/trends
KW - Coronary Angiography
KW - Coronary Disease/diagnosis
KW - England/epidemiology
KW - Female
KW - Follow-Up Studies
KW - Humans
KW - Male
KW - Middle Aged
KW - Morbidity/trends
KW - Retrospective Studies
KW - Risk Assessment/methods
KW - Risk Factors
KW - Survival Rate/trends
U2 - 10.1136/openhrt-2020-001498
DO - 10.1136/openhrt-2020-001498
M3 - Article
C2 - 33879507
SN - 2053-3624
VL - 8
JO - Open Heart
JF - Open Heart
IS - 1
M1 - e001498
ER -