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Serum creatinine elevation after renin-angiotensin system blockade and long term cardiorenal risks: cohort study

Objective To examine long term cardiorenal outcomes associated with increased concentrations of creatinine after the start of angiotensin converting enzyme inhibitor/angiotensin receptor blocker treatment. Design Population based cohort study using electronic health records from the Clinical Practic...

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Autores principales: Schmidt, Morten, Mansfield, Kathryn E, Bhaskaran, Krishnan, Nitsch, Dorothea, Sørensen, Henrik Toft, Smeeth, Liam, Tomlinson, Laurie A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group Ltd. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5421447/
https://www.ncbi.nlm.nih.gov/pubmed/28279964
http://dx.doi.org/10.1136/bmj.j791
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author Schmidt, Morten
Mansfield, Kathryn E
Bhaskaran, Krishnan
Nitsch, Dorothea
Sørensen, Henrik Toft
Smeeth, Liam
Tomlinson, Laurie A
author_facet Schmidt, Morten
Mansfield, Kathryn E
Bhaskaran, Krishnan
Nitsch, Dorothea
Sørensen, Henrik Toft
Smeeth, Liam
Tomlinson, Laurie A
author_sort Schmidt, Morten
collection PubMed
description Objective To examine long term cardiorenal outcomes associated with increased concentrations of creatinine after the start of angiotensin converting enzyme inhibitor/angiotensin receptor blocker treatment. Design Population based cohort study using electronic health records from the Clinical Practice Research Datalink and Hospital Episode Statistics. Setting UK primary care, 1997-2014. Participants Patients starting treatment with angiotensin converting enzyme inhibitors or angiotensin receptor blockers (n=122 363). Main outcome measures Poisson regression was used to compare rates of end stage renal disease, myocardial infarction, heart failure, and death among patients with creatinine increases of 30% or more after starting treatment against those without such increases, and for each 10% increase in creatinine. Analyses were adjusted for age, sex, calendar period, socioeconomic status, lifestyle factors, chronic kidney disease, diabetes, cardiovascular comorbidities, and use of other antihypertensive drugs and non-steroidal anti-inflammatory drugs. Results Among the 2078 (1.7%) patients with creatinine increases of 30% or more, a higher proportion were female, were elderly, had cardiorenal comorbidity, and used non-steroidal anti-inflammatory drugs, loop diuretics, or potassium sparing diuretics. Creatinine increases of 30% or more were associated with an increased adjusted incidence rate ratio for all outcomes, compared with increases of less than 30%: 3.43 (95% confidence interval 2.40 to 4.91) for end stage renal disease, 1.46 (1.16 to 1.84) for myocardial infarction, 1.37 (1.14 to 1.65) for heart failure, and 1.84 (1.65 to 2.05) for death. The detailed categorisation of increases in creatinine concentrations (<10%, 10-19%, 20-29%, 30-39%, and ≥40%) showed a graduated relation for all outcomes (all P values for trends <0.001). Notably, creatinine increases of less than 30% were also associated with increased incidence rate ratios for all outcomes, including death (1.15 (1.09 to 1.22) for increases of 10-19% and 1.35 (1.23 to 1.49) for increases of 20-29%, using <10% as reference). Results were consistent across calendar periods, across subgroups of patients, and among continuing users. Conclusions Increases in creatinine after the start of angiotensin converting enzyme inhibitor/angiotensin receptor blocker treatment were associated with adverse cardiorenal outcomes in a graduated relation, even below the guideline recommended threshold of a 30% increase for stopping treatment.
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spelling pubmed-54214472017-05-12 Serum creatinine elevation after renin-angiotensin system blockade and long term cardiorenal risks: cohort study Schmidt, Morten Mansfield, Kathryn E Bhaskaran, Krishnan Nitsch, Dorothea Sørensen, Henrik Toft Smeeth, Liam Tomlinson, Laurie A BMJ Research Objective To examine long term cardiorenal outcomes associated with increased concentrations of creatinine after the start of angiotensin converting enzyme inhibitor/angiotensin receptor blocker treatment. Design Population based cohort study using electronic health records from the Clinical Practice Research Datalink and Hospital Episode Statistics. Setting UK primary care, 1997-2014. Participants Patients starting treatment with angiotensin converting enzyme inhibitors or angiotensin receptor blockers (n=122 363). Main outcome measures Poisson regression was used to compare rates of end stage renal disease, myocardial infarction, heart failure, and death among patients with creatinine increases of 30% or more after starting treatment against those without such increases, and for each 10% increase in creatinine. Analyses were adjusted for age, sex, calendar period, socioeconomic status, lifestyle factors, chronic kidney disease, diabetes, cardiovascular comorbidities, and use of other antihypertensive drugs and non-steroidal anti-inflammatory drugs. Results Among the 2078 (1.7%) patients with creatinine increases of 30% or more, a higher proportion were female, were elderly, had cardiorenal comorbidity, and used non-steroidal anti-inflammatory drugs, loop diuretics, or potassium sparing diuretics. Creatinine increases of 30% or more were associated with an increased adjusted incidence rate ratio for all outcomes, compared with increases of less than 30%: 3.43 (95% confidence interval 2.40 to 4.91) for end stage renal disease, 1.46 (1.16 to 1.84) for myocardial infarction, 1.37 (1.14 to 1.65) for heart failure, and 1.84 (1.65 to 2.05) for death. The detailed categorisation of increases in creatinine concentrations (<10%, 10-19%, 20-29%, 30-39%, and ≥40%) showed a graduated relation for all outcomes (all P values for trends <0.001). Notably, creatinine increases of less than 30% were also associated with increased incidence rate ratios for all outcomes, including death (1.15 (1.09 to 1.22) for increases of 10-19% and 1.35 (1.23 to 1.49) for increases of 20-29%, using <10% as reference). Results were consistent across calendar periods, across subgroups of patients, and among continuing users. Conclusions Increases in creatinine after the start of angiotensin converting enzyme inhibitor/angiotensin receptor blocker treatment were associated with adverse cardiorenal outcomes in a graduated relation, even below the guideline recommended threshold of a 30% increase for stopping treatment. BMJ Publishing Group Ltd. 2017-03-09 /pmc/articles/PMC5421447/ /pubmed/28279964 http://dx.doi.org/10.1136/bmj.j791 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/4.0/.
spellingShingle Research
Schmidt, Morten
Mansfield, Kathryn E
Bhaskaran, Krishnan
Nitsch, Dorothea
Sørensen, Henrik Toft
Smeeth, Liam
Tomlinson, Laurie A
Serum creatinine elevation after renin-angiotensin system blockade and long term cardiorenal risks: cohort study
title Serum creatinine elevation after renin-angiotensin system blockade and long term cardiorenal risks: cohort study
title_full Serum creatinine elevation after renin-angiotensin system blockade and long term cardiorenal risks: cohort study
title_fullStr Serum creatinine elevation after renin-angiotensin system blockade and long term cardiorenal risks: cohort study
title_full_unstemmed Serum creatinine elevation after renin-angiotensin system blockade and long term cardiorenal risks: cohort study
title_short Serum creatinine elevation after renin-angiotensin system blockade and long term cardiorenal risks: cohort study
title_sort serum creatinine elevation after renin-angiotensin system blockade and long term cardiorenal risks: cohort study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5421447/
https://www.ncbi.nlm.nih.gov/pubmed/28279964
http://dx.doi.org/10.1136/bmj.j791
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