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Development of a risk score for early saphenous vein graft failure: An individual patient data meta-analysis

OBJECTIVES: Early saphenous vein graft (SVG) occlusion is typically attributed to technical factors. We aimed at exploring clinical, anatomical, and operative factors associated with the risk of early SVG occlusion (within 12 months postsurgery). METHODS: Published literature in MEDLINE was searched...

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Autores principales: Antonopoulos, Alexios S., Odutayo, Ayodele, Oikonomou, Evangelos K., Trivella, Marialena, Petrou, Mario, Collins, Gary S., Antoniades, Charalambos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mosby 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7322547/
https://www.ncbi.nlm.nih.gov/pubmed/31606176
http://dx.doi.org/10.1016/j.jtcvs.2019.07.086
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author Antonopoulos, Alexios S.
Odutayo, Ayodele
Oikonomou, Evangelos K.
Trivella, Marialena
Petrou, Mario
Collins, Gary S.
Antoniades, Charalambos
author_facet Antonopoulos, Alexios S.
Odutayo, Ayodele
Oikonomou, Evangelos K.
Trivella, Marialena
Petrou, Mario
Collins, Gary S.
Antoniades, Charalambos
author_sort Antonopoulos, Alexios S.
collection PubMed
description OBJECTIVES: Early saphenous vein graft (SVG) occlusion is typically attributed to technical factors. We aimed at exploring clinical, anatomical, and operative factors associated with the risk of early SVG occlusion (within 12 months postsurgery). METHODS: Published literature in MEDLINE was searched for studies reporting the incidence of early SVG occlusion. Individual patient data (IPD) on early SVG occlusion were used from the SAFINOUS-CABG Consortium. A derivation (n = 1492 patients) and validation (n = 372 patients) cohort were used for model training (with 10-fold cross-validation) and external validation respectively. RESULTS: In aggregate data meta-analysis (48 studies, 41,530 SVGs) the pooled estimate for early SVG occlusion was 11%. The developed IPD model for early SVG occlusion, which included clinical, anatomical, and operative characteristics (age, sex, dyslipidemia, diabetes mellitus, smoking, serum creatinine, endoscopic vein harvesting, use of complex grafts, grafted target vessel, and number of SVGs), had good performance in the derivation (c-index = 0.744; 95% confidence interval [CI], 0.701-0.774) and validation cohort (c-index = 0.734; 95% CI, 0.659-0.809). Based on this model. we constructed a simplified 12-variable risk score system (SAFINOUS score) with good performance for early SVG occlusion (c-index = 0.700, 95% CI, 0.684-0.716). CONCLUSIONS: From a large international IPD collaboration, we developed a novel risk score to assess the individualized risk for early SVG occlusion. The SAFINOUS risk score could be used to identify patients that are more likely to benefit from aggressive treatment strategies.
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spelling pubmed-73225472020-07-01 Development of a risk score for early saphenous vein graft failure: An individual patient data meta-analysis Antonopoulos, Alexios S. Odutayo, Ayodele Oikonomou, Evangelos K. Trivella, Marialena Petrou, Mario Collins, Gary S. Antoniades, Charalambos J Thorac Cardiovasc Surg Article OBJECTIVES: Early saphenous vein graft (SVG) occlusion is typically attributed to technical factors. We aimed at exploring clinical, anatomical, and operative factors associated with the risk of early SVG occlusion (within 12 months postsurgery). METHODS: Published literature in MEDLINE was searched for studies reporting the incidence of early SVG occlusion. Individual patient data (IPD) on early SVG occlusion were used from the SAFINOUS-CABG Consortium. A derivation (n = 1492 patients) and validation (n = 372 patients) cohort were used for model training (with 10-fold cross-validation) and external validation respectively. RESULTS: In aggregate data meta-analysis (48 studies, 41,530 SVGs) the pooled estimate for early SVG occlusion was 11%. The developed IPD model for early SVG occlusion, which included clinical, anatomical, and operative characteristics (age, sex, dyslipidemia, diabetes mellitus, smoking, serum creatinine, endoscopic vein harvesting, use of complex grafts, grafted target vessel, and number of SVGs), had good performance in the derivation (c-index = 0.744; 95% confidence interval [CI], 0.701-0.774) and validation cohort (c-index = 0.734; 95% CI, 0.659-0.809). Based on this model. we constructed a simplified 12-variable risk score system (SAFINOUS score) with good performance for early SVG occlusion (c-index = 0.700, 95% CI, 0.684-0.716). CONCLUSIONS: From a large international IPD collaboration, we developed a novel risk score to assess the individualized risk for early SVG occlusion. The SAFINOUS risk score could be used to identify patients that are more likely to benefit from aggressive treatment strategies. Mosby 2020-07 /pmc/articles/PMC7322547/ /pubmed/31606176 http://dx.doi.org/10.1016/j.jtcvs.2019.07.086 Text en © 2019 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Antonopoulos, Alexios S.
Odutayo, Ayodele
Oikonomou, Evangelos K.
Trivella, Marialena
Petrou, Mario
Collins, Gary S.
Antoniades, Charalambos
Development of a risk score for early saphenous vein graft failure: An individual patient data meta-analysis
title Development of a risk score for early saphenous vein graft failure: An individual patient data meta-analysis
title_full Development of a risk score for early saphenous vein graft failure: An individual patient data meta-analysis
title_fullStr Development of a risk score for early saphenous vein graft failure: An individual patient data meta-analysis
title_full_unstemmed Development of a risk score for early saphenous vein graft failure: An individual patient data meta-analysis
title_short Development of a risk score for early saphenous vein graft failure: An individual patient data meta-analysis
title_sort development of a risk score for early saphenous vein graft failure: an individual patient data meta-analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7322547/
https://www.ncbi.nlm.nih.gov/pubmed/31606176
http://dx.doi.org/10.1016/j.jtcvs.2019.07.086
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