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dc.contributor.author
Gaziano, Thomas A.  
dc.contributor.author
Abrahams Gessel, Shafika  
dc.contributor.author
Alam, Sartaj  
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Alam, Dewan  
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Ali, Mohammed  
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Bloomfield, Gerald  
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Carrillo Larco, Rodrigo M.  
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Dorairaj, Prabhakaran  
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Gutierrez, Laura  
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Irazola, Vilma  
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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  
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Steyn, Krisela  
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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  
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RISK  
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SCORES  
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GLOBAL  
dc.subject.classification
Epidemiología  
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Ciencias de la Salud  
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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;  
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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  
dc.description.fil
Fil: Dorairaj, Prabhakaran. Public Health Foundation Of India; India. Centre For Chronic Disease Control; India  
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Fil: Gutierrez, Laura. Institute For Clinical Effectiveness And Health Policy, Ciudad Autonoma de Buenos Aires; Argentina  
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Fil: Irazola, Vilma. Institute For Clinical Effectiveness And Health Policy, Ciudad Autonoma de Buenos Aires; Argentina  
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Fil: Levitt, Naomi S.. University Of Cape Town, Faculty Of Health Sciences;  
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Fil: Miranda, J. Jaime. Cronicas Centro de Excelencia En Enfermedades Crónicas; Perú. Universidad Peruana Cayetano Heredia; Perú  
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Fil: Bernabe-Ortiz, Antonio. Cronicas Centro de Excelencia En Enfermedades Crónicas; Perú  
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Fil: Pandya, Ankur. Harvard T.h. Chan School Of Public Boston;  
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Fil: Rubinstein, Adolfo Luis. Instituto de Efectividad Clínica y Sanitaria; Argentina  
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Fil: Steyn, Krisela. University Of Cape Town, Faculty Of Health Sciences;  
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Fil: Xavier, Denis. St. John's Medical College; India  
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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