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Statin therapy and postoperative short‐term mortality after rectal cancer surgery

AIM: This study aimed to assess the correlation between regular statin therapy and postoperative mortality following surgical resection for rectal cancer. METHOD: This retrospective cohort study included all adult patients undergoing abdominal rectal cancer surgery in Sweden between January 2007 and...

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Autores principales: Pourlotfi, Arvid, Ahl, Rebecka, Sjolin, Gabriel, Forssten, Maximilian Peter, Bass, Gary A., Cao, Yang, Matthiessen, Peter, Mohseni, Shahin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8246857/
https://www.ncbi.nlm.nih.gov/pubmed/33305498
http://dx.doi.org/10.1111/codi.15481
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author Pourlotfi, Arvid
Ahl, Rebecka
Sjolin, Gabriel
Forssten, Maximilian Peter
Bass, Gary A.
Cao, Yang
Matthiessen, Peter
Mohseni, Shahin
author_facet Pourlotfi, Arvid
Ahl, Rebecka
Sjolin, Gabriel
Forssten, Maximilian Peter
Bass, Gary A.
Cao, Yang
Matthiessen, Peter
Mohseni, Shahin
author_sort Pourlotfi, Arvid
collection PubMed
description AIM: This study aimed to assess the correlation between regular statin therapy and postoperative mortality following surgical resection for rectal cancer. METHOD: This retrospective cohort study included all adult patients undergoing abdominal rectal cancer surgery in Sweden between January 2007 and September 2016. Data were gathered from the Swedish Colorectal Cancer Registry, a large population‐based prospectively collected registry. Statin users were defined as patients with one or more collected prescriptions of a statin within 12 months before the date of surgery. The statin‐positive and statin‐negative cohorts were matched by propensity scores based on baseline demographics. RESULTS: A total of 11 966 patients underwent surgical resection for rectal cancer, of whom 3019 (25%) were identified as statin users. After applying propensity score matching (1:1), 3017 pairs were available for comparison. In the matched groups, statin users demonstrated reduced 90‐day all‐cause mortality (0.7% vs. 5.5%, p < 0.001) and also showed significantly reduced cause‐specific mortality due to cardiovascular and respiratory events, as well as sepsis and multiorgan failure. The significant postoperative survival benefit of statin users was seen despite a higher rate of cardiovascular comorbidity. CONCLUSION: Preoperative statin therapy displays a strong association with reduced postoperative mortality following surgical resection for rectal cancer. The results from the current study warrant further investigation to determine whether a causal relationship exists.
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spelling pubmed-82468572021-07-02 Statin therapy and postoperative short‐term mortality after rectal cancer surgery Pourlotfi, Arvid Ahl, Rebecka Sjolin, Gabriel Forssten, Maximilian Peter Bass, Gary A. Cao, Yang Matthiessen, Peter Mohseni, Shahin Colorectal Dis Original Articles AIM: This study aimed to assess the correlation between regular statin therapy and postoperative mortality following surgical resection for rectal cancer. METHOD: This retrospective cohort study included all adult patients undergoing abdominal rectal cancer surgery in Sweden between January 2007 and September 2016. Data were gathered from the Swedish Colorectal Cancer Registry, a large population‐based prospectively collected registry. Statin users were defined as patients with one or more collected prescriptions of a statin within 12 months before the date of surgery. The statin‐positive and statin‐negative cohorts were matched by propensity scores based on baseline demographics. RESULTS: A total of 11 966 patients underwent surgical resection for rectal cancer, of whom 3019 (25%) were identified as statin users. After applying propensity score matching (1:1), 3017 pairs were available for comparison. In the matched groups, statin users demonstrated reduced 90‐day all‐cause mortality (0.7% vs. 5.5%, p < 0.001) and also showed significantly reduced cause‐specific mortality due to cardiovascular and respiratory events, as well as sepsis and multiorgan failure. The significant postoperative survival benefit of statin users was seen despite a higher rate of cardiovascular comorbidity. CONCLUSION: Preoperative statin therapy displays a strong association with reduced postoperative mortality following surgical resection for rectal cancer. The results from the current study warrant further investigation to determine whether a causal relationship exists. John Wiley and Sons Inc. 2020-12-23 2021-04 /pmc/articles/PMC8246857/ /pubmed/33305498 http://dx.doi.org/10.1111/codi.15481 Text en © 2020 The Authors. Colorectal Disease published by John Wiley & Sons Ltd on behalf of Association of Coloproctology of Great Britain and Ireland. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Pourlotfi, Arvid
Ahl, Rebecka
Sjolin, Gabriel
Forssten, Maximilian Peter
Bass, Gary A.
Cao, Yang
Matthiessen, Peter
Mohseni, Shahin
Statin therapy and postoperative short‐term mortality after rectal cancer surgery
title Statin therapy and postoperative short‐term mortality after rectal cancer surgery
title_full Statin therapy and postoperative short‐term mortality after rectal cancer surgery
title_fullStr Statin therapy and postoperative short‐term mortality after rectal cancer surgery
title_full_unstemmed Statin therapy and postoperative short‐term mortality after rectal cancer surgery
title_short Statin therapy and postoperative short‐term mortality after rectal cancer surgery
title_sort statin therapy and postoperative short‐term mortality after rectal cancer surgery
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8246857/
https://www.ncbi.nlm.nih.gov/pubmed/33305498
http://dx.doi.org/10.1111/codi.15481
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