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dc.contributor.author
Gaziano, Thomas A.
dc.contributor.author
Abrahams Gessel, Shafika
dc.contributor.author
Alam, Sartaj
dc.contributor.author
Alam, Dewan
dc.contributor.author
Ali, Mohammed
dc.contributor.author
Bloomfield, Gerald
dc.contributor.author
Carrillo Larco, Rodrigo M.
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Dorairaj, Prabhakaran
dc.contributor.author
Gutierrez, Laura
dc.contributor.author
Irazola, Vilma
dc.contributor.author
Levitt, Naomi S.
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Miranda, J. Jaime
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Bernabe Ortiz, Antonio
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Pandya, Ankur
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Rubinstein, Adolfo Luis
dc.contributor.author
Steyn, Krisela
dc.contributor.author
Xavier, Denis
dc.contributor.author
Yan, Lijing L.
dc.date.available
2020-01-27T19:21:07Z
dc.date.issued
2016-03
dc.identifier.citation
Gaziano, Thomas A.; Abrahams Gessel, Shafika; Alam, Sartaj; Alam, Dewan; Ali, Mohammed; et al.; Comparison of Nonblood-Based and Blood-Based Total CV Risk Scores in Global Populations; Elsevier; Global Heart; 11; 1; 3-2016; 37-46.e2
dc.identifier.issn
2211-8160
dc.identifier.uri
http://hdl.handle.net/11336/95880
dc.description.abstract
Background Cost-effective primary prevention of cardiovascular disease (CVD) in low- and middle-income countries requires accurate risk assessment. Laboratory-based risk tools currently used in high-income countries are relatively expensive and impractical in many settings due to lack of facilities. Objectives This study sought to assess the correlation between a non-laboratory-based risk tool and 4 commonly used, laboratory-based risk scores in 7 countries representing nearly one-half of the world's population. Methods We calculated 10-year CVD risk scores for 47,466 persons with cross-sectional data collected from 16 different cohorts in 9 countries. The performance of the non-laboratory-based risk score was compared with 4 laboratory-based risk scores: Pooled Cohort Risk Equations (ASCVD [Atherosclerotic Cardiovascular Disease]), Framingham, and SCORE (Systematic Coronary Risk Evaluation) for high- and low-risk countries. Rankings of each score were compared using Spearman rank correlations. Based on these correlations, we measured concordance between individual absolute CVD risk as measured by the Harvard NHANES (National Health and Nutrition Examination Survey) risk score, and the 4 laboratory-based risk scores, using both the conventional Framingham risk thresholds of >20% and the recent ASCVD guideline threshold of >7.5%. Results The aggregate Spearman rank correlations between the non-laboratory-based risk score and the laboratory-based scores ranged from 0.915 to 0.979 for women and from 0.923 to 0.970 for men. When applying the conventional Framingham risk threshold of >20% over 10 years, 92.7% to 96.0% of women and 88.3% to 92.8% of men were equivalently characterized as "high" or "low" risk. Applying the recent ASCVD guidelines risk threshold of >7.5% resulted in risk characterization agreement for women ranging from 88.1% to 94.4% and from 89.0% to 93.7% for men. Conclusions The correlation between non-laboratory-based and laboratory-based risk scores is very high for both men and women. Potentially large numbers of high-risk individuals could be detected with relatively simple tools.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
Elsevier
dc.rights
info:eu-repo/semantics/openAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subject
CARDIOVASCULAR
dc.subject
RISK
dc.subject
SCORES
dc.subject
GLOBAL
dc.subject.classification
Epidemiología
dc.subject.classification
Ciencias de la Salud
dc.subject.classification
CIENCIAS MÉDICAS Y DE LA SALUD
dc.title
Comparison of Nonblood-Based and Blood-Based Total CV Risk Scores in Global Populations
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2019-11-26T19:56:13Z
dc.identifier.eissn
2211-8179
dc.journal.volume
11
dc.journal.number
1
dc.journal.pagination
37-46.e2
dc.journal.pais
Estados Unidos
dc.description.fil
Fil: Gaziano, Thomas A.. Brigham And Women's Hospital; . Harvard T.h. Chan School Of Public Boston;
dc.description.fil
Fil: Abrahams-Gessel, Shafika. Harvard T.h. Chan School Of Public Boston;
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Fil: Alam, Sartaj. Harvard T.h. Chan School Of Public Boston;
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Fil: Alam, Dewan. Saint Michael's Hospital University Of Toronto; Canadá
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Fil: Ali, Mohammed. Centre For Chronic Disease Control; India
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Fil: Bloomfield, Gerald. Duke Clinical Research Institute;
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Fil: Carrillo-Larco, Rodrigo M.. Cronicas Centro de Excelencia En Enfermedades Crónicas; Perú
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Fil: Dorairaj, Prabhakaran. Public Health Foundation Of India; India. Centre For Chronic Disease Control; India
dc.description.fil
Fil: Gutierrez, Laura. Institute For Clinical Effectiveness And Health Policy, Ciudad Autonoma de Buenos Aires; Argentina
dc.description.fil
Fil: Irazola, Vilma. Institute For Clinical Effectiveness And Health Policy, Ciudad Autonoma de Buenos Aires; Argentina
dc.description.fil
Fil: Levitt, Naomi S.. University Of Cape Town, Faculty Of Health Sciences;
dc.description.fil
Fil: Miranda, J. Jaime. Cronicas Centro de Excelencia En Enfermedades Crónicas; Perú. Universidad Peruana Cayetano Heredia; Perú
dc.description.fil
Fil: Bernabe-Ortiz, Antonio. Cronicas Centro de Excelencia En Enfermedades Crónicas; Perú
dc.description.fil
Fil: Pandya, Ankur. Harvard T.h. Chan School Of Public Boston;
dc.description.fil
Fil: Rubinstein, Adolfo Luis. Instituto de Efectividad Clínica y Sanitaria; Argentina
dc.description.fil
Fil: Steyn, Krisela. University Of Cape Town, Faculty Of Health Sciences;
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Fil: Xavier, Denis. St. John's Medical College; India
dc.description.fil
Fil: Yan, Lijing L.. Peking University Health Science Center; China. Duke Kunshan University; China
dc.journal.title
Global Heart
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S2211816015003087
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.gheart.2015.12.003
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