Selective serotonin re‐uptake inhibiting antidepressants and the risk of overanticoagulation during acenocoumarol maintenance treatment

WHAT IS ALREADY KNOWN ABOUT THIS SUBJECT • Coumarin anticoagulants and selective serotonin re‐uptake inhibitors (SSRIs) have been reported to cause bleeding. Combination of these drug groups might enhance this risk. Case reports showed an increase of prothrombin time for the combination of warfarin...

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Published inBritish journal of clinical pharmacology Vol. 72; no. 5; pp. 798 - 805
Main Authors Teichert, Martina, Visser, Loes E., Uitterlinden, Andrė G., Hofman, Albert, Buhre, Peter J., Straus, Sabine, De Smet, Peter A. G. M., Stricker, Bruno HCh
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Publishing Ltd 01.11.2011
Blackwell
Blackwell Science Inc
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ISSN0306-5251
1365-2125
1365-2125
DOI10.1111/j.1365-2125.2011.04004.x

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Abstract WHAT IS ALREADY KNOWN ABOUT THIS SUBJECT • Coumarin anticoagulants and selective serotonin re‐uptake inhibitors (SSRIs) have been reported to cause bleeding. Combination of these drug groups might enhance this risk. Case reports showed an increase of prothrombin time for the combination of warfarin with fluvoxamine and fluoxetine. This has not yet been confirmed by population based studies. WHAT THIS STUDY ADDS • Fluvoxamine and venlafaxine increased prothrombin time in users of acenocoumarol above a critical value which is associated with an increased bleeding risk. The other SSRIs had no influence on acenocoumarol effectiveness, however numbers of drug users were low. The combination of fluvoxamine and venlafaxine with acenocoumarol should be monitored by measurements of the international normalized ratio to avoid overanticoagulation. AIM The aim of this study was to investigate the effects of co‐medication with selective serotonin re‐uptake inhibitors (SSRIs) on overanticoagulation during acenocoumarol maintenance treatment. METHODS All subjects from The Rotterdam Study who received acenocoumarol maintenance treatment between April 1 1991 and September 9 2009 were followed for the event of an international normalized ratio (INR) ≥6, until death, end of treatment or end of the study period. With the Andersen‐Gill extension of the Cox proportional hazards model, risks for repeated events of overanticoagulation in relation to concomitant SSRI use were calculated. RESULTS The risk for overanticoagulation during acenocoumarol maintenance treatment was increased in combination with fluvoxamine (HR 2.63, 95% CI 1.49, 4.66) and venlafaxine (HR 2.19, 95% CI 1.21, 3.99). There was no increase in risk for the other SSRIs, but numbers of exposed cases were low for all SSRIs except paroxetine. CONCLUSION Fluvoxamine and venlafaxine were associated with a more than double risk of INR values ≥6 in acenocoumarol treated subjects.
AbstractList WHAT IS ALREADY KNOWN ABOUT THIS SUBJECT • Coumarin anticoagulants and selective serotonin re‐uptake inhibitors (SSRIs) have been reported to cause bleeding. Combination of these drug groups might enhance this risk. Case reports showed an increase of prothrombin time for the combination of warfarin with fluvoxamine and fluoxetine. This has not yet been confirmed by population based studies. WHAT THIS STUDY ADDS • Fluvoxamine and venlafaxine increased prothrombin time in users of acenocoumarol above a critical value which is associated with an increased bleeding risk. The other SSRIs had no influence on acenocoumarol effectiveness, however numbers of drug users were low. The combination of fluvoxamine and venlafaxine with acenocoumarol should be monitored by measurements of the international normalized ratio to avoid overanticoagulation. AIM The aim of this study was to investigate the effects of co‐medication with selective serotonin re‐uptake inhibitors (SSRIs) on overanticoagulation during acenocoumarol maintenance treatment. METHODS All subjects from The Rotterdam Study who received acenocoumarol maintenance treatment between April 1 1991 and September 9 2009 were followed for the event of an international normalized ratio (INR) ≥6, until death, end of treatment or end of the study period. With the Andersen‐Gill extension of the Cox proportional hazards model, risks for repeated events of overanticoagulation in relation to concomitant SSRI use were calculated. RESULTS The risk for overanticoagulation during acenocoumarol maintenance treatment was increased in combination with fluvoxamine (HR 2.63, 95% CI 1.49, 4.66) and venlafaxine (HR 2.19, 95% CI 1.21, 3.99). There was no increase in risk for the other SSRIs, but numbers of exposed cases were low for all SSRIs except paroxetine. CONCLUSION Fluvoxamine and venlafaxine were associated with a more than double risk of INR values ≥6 in acenocoumarol treated subjects.
WHAT IS ALREADY KNOWN ABOUT THIS SUBJECT • Coumarin anticoagulants and selective serotonin re‐uptake inhibitors (SSRIs) have been reported to cause bleeding. Combination of these drug groups might enhance this risk. Case reports showed an increase of prothrombin time for the combination of warfarin with fluvoxamine and fluoxetine. This has not yet been confirmed by population based studies. WHAT THIS STUDY ADDS • Fluvoxamine and venlafaxine increased prothrombin time in users of acenocoumarol above a critical value which is associated with an increased bleeding risk. The other SSRIs had no influence on acenocoumarol effectiveness, however numbers of drug users were low. The combination of fluvoxamine and venlafaxine with acenocoumarol should be monitored by measurements of the international normalized ratio to avoid overanticoagulation. AIM The aim of this study was to investigate the effects of co‐medication with selective serotonin re‐uptake inhibitors (SSRIs) on overanticoagulation during acenocoumarol maintenance treatment. METHODS All subjects from The Rotterdam Study who received acenocoumarol maintenance treatment between April 1 1991 and September 9 2009 were followed for the event of an international normalized ratio (INR) ≥6, until death, end of treatment or end of the study period. With the Andersen‐Gill extension of the Cox proportional hazards model, risks for repeated events of overanticoagulation in relation to concomitant SSRI use were calculated. RESULTS The risk for overanticoagulation during acenocoumarol maintenance treatment was increased in combination with fluvoxamine (HR 2.63, 95% CI 1.49, 4.66) and venlafaxine (HR 2.19, 95% CI 1.21, 3.99). There was no increase in risk for the other SSRIs, but numbers of exposed cases were low for all SSRIs except paroxetine. CONCLUSION Fluvoxamine and venlafaxine were associated with a more than double risk of INR values ≥6 in acenocoumarol treated subjects.
The aim of this study was to investigate the effects of co-medication with selective serotonin re-uptake inhibitors (SSRIs) on overanticoagulation during acenocoumarol maintenance treatment.AIMThe aim of this study was to investigate the effects of co-medication with selective serotonin re-uptake inhibitors (SSRIs) on overanticoagulation during acenocoumarol maintenance treatment.All subjects from The Rotterdam Study who received acenocoumarol maintenance treatment between April 1 1991 and September 9 2009 were followed for the event of an international normalized ratio (INR) ≥6, until death, end of treatment or end of the study period. With the Andersen-Gill extension of the Cox proportional hazards model, risks for repeated events of overanticoagulation in relation to concomitant SSRI use were calculated.METHODSAll subjects from The Rotterdam Study who received acenocoumarol maintenance treatment between April 1 1991 and September 9 2009 were followed for the event of an international normalized ratio (INR) ≥6, until death, end of treatment or end of the study period. With the Andersen-Gill extension of the Cox proportional hazards model, risks for repeated events of overanticoagulation in relation to concomitant SSRI use were calculated.The risk for overanticoagulation during acenocoumarol maintenance treatment was increased in combination with fluvoxamine (HR 2.63, 95% CI 1.49, 4.66) and venlafaxine (HR 2.19, 95% CI 1.21, 3.99). There was no increase in risk for the other SSRIs, but numbers of exposed cases were low for all SSRIs except paroxetine.RESULTSThe risk for overanticoagulation during acenocoumarol maintenance treatment was increased in combination with fluvoxamine (HR 2.63, 95% CI 1.49, 4.66) and venlafaxine (HR 2.19, 95% CI 1.21, 3.99). There was no increase in risk for the other SSRIs, but numbers of exposed cases were low for all SSRIs except paroxetine.Fluvoxamine and venlafaxine were associated with a more than double risk of INR values ≥6 in acenocoumarol treated subjects.CONCLUSIONFluvoxamine and venlafaxine were associated with a more than double risk of INR values ≥6 in acenocoumarol treated subjects.
The aim of this study was to investigate the effects of co-medication with selective serotonin re-uptake inhibitors (SSRIs) on overanticoagulation during acenocoumarol maintenance treatment. All subjects from The Rotterdam Study who received acenocoumarol maintenance treatment between April 1 1991 and September 9 2009 were followed for the event of an international normalized ratio (INR) ≥6, until death, end of treatment or end of the study period. With the Andersen-Gill extension of the Cox proportional hazards model, risks for repeated events of overanticoagulation in relation to concomitant SSRI use were calculated. The risk for overanticoagulation during acenocoumarol maintenance treatment was increased in combination with fluvoxamine (HR 2.63, 95% CI 1.49, 4.66) and venlafaxine (HR 2.19, 95% CI 1.21, 3.99). There was no increase in risk for the other SSRIs, but numbers of exposed cases were low for all SSRIs except paroxetine. Fluvoxamine and venlafaxine were associated with a more than double risk of INR values ≥6 in acenocoumarol treated subjects.
times Coumarin anticoagulants and selective serotonin re-uptake inhibitors (SSRIs) have been reported to cause bleeding. Combination of these drug groups might enhance this risk. Case reports showed an increase of prothrombin time for the combination of warfarin with fluvoxamine and fluoxetine. This has not yet been confirmed by population based studies. WHAT THIS STUDY ADDS times Fluvoxamine and venlafaxine increased prothrombin time in users of acenocoumarol above a critical value which is associated with an increased bleeding risk. The other SSRIs had no influence on acenocoumarol effectiveness, however numbers of drug users were low. The combination of fluvoxamine and venlafaxine with acenocoumarol should be monitored by measurements of the international normalized ratio to avoid overanticoagulation. AIM The aim of this study was to investigate the effects of co-medication with selective serotonin re-uptake inhibitors (SSRIs) on overanticoagulation during acenocoumarol maintenance treatment. METHODS All subjects from The Rotterdam Study who received acenocoumarol maintenance treatment between April 1 1991 and September 9 2009 were followed for the event of an international normalized ratio (INR) greater than or equal to 6, until death, end of treatment or end of the study period. With the Andersen-Gill extension of the Cox proportional hazards model, risks for repeated events of overanticoagulation in relation to concomitant SSRI use were calculated. RESULTS The risk for overanticoagulation during acenocoumarol maintenance treatment was increased in combination with fluvoxamine (HR 2.63, 95% CI 1.49, 4.66) and venlafaxine (HR 2.19, 95% CI 1.21, 3.99). There was no increase in risk for the other SSRIs, but numbers of exposed cases were low for all SSRIs except paroxetine. CONCLUSION Fluvoxamine and venlafaxine were associated with a more than double risk of INR values greater than or equal to 6 in acenocoumarol treated subjects.Original Abstract: WHAT IS ALREADY KNOWN ABOUT THIS SUBJECT
Author Teichert, Martina
Visser, Loes E.
Buhre, Peter J.
Hofman, Albert
Straus, Sabine
Uitterlinden, Andrė G.
De Smet, Peter A. G. M.
Stricker, Bruno HCh
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Issue 5
Keywords Serotonin
Psychotropic
Coumarine derivatives
Overdosing
selective serotonin re-uptake inhibitors
Phénéthylamine derivatives
Anticoagulant
Catecholamine
Reuptake inhibitor
Uptake
Selective serotonin reuptake inhibitor
Antivitamin K
Maintenance treatment
Risk factor
Neurotransmitter
Antidepressant agent
Venlafaxine
Norepinephrine
Fluvoxamine
Acenocoumarol
Language English
License http://onlinelibrary.wiley.com/termsAndConditions#vor
CC BY 4.0
2011 The Authors. British Journal of Clinical Pharmacology © 2011 The British Pharmacological Society.
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SSID ssj0013165
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Snippet WHAT IS ALREADY KNOWN ABOUT THIS SUBJECT • Coumarin anticoagulants and selective serotonin re‐uptake inhibitors (SSRIs) have been reported to cause bleeding....
The aim of this study was to investigate the effects of co-medication with selective serotonin re-uptake inhibitors (SSRIs) on overanticoagulation during...
times Coumarin anticoagulants and selective serotonin re-uptake inhibitors (SSRIs) have been reported to cause bleeding. Combination of these drug groups might...
SourceID pubmedcentral
proquest
pubmed
pascalfrancis
crossref
wiley
SourceType Open Access Repository
Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 798
SubjectTerms acenocoumarol
Acenocoumarol - therapeutic use
Aged
Aged, 80 and over
Anticoagulants
Anticoagulants - therapeutic use
Antidepressants
Antidepressive Agents - pharmacology
Biological and medical sciences
Bleeding
Blood Coagulation - drug effects
Case reports
Cohort Studies
Coumarin
Cyclohexanols - pharmacology
Drug abuse
Drug Interactions
Drugs
Fluoxetine
fluvoxamine
Fluvoxamine - pharmacology
Hemorrhage - chemically induced
Humans
Medical sciences
Middle Aged
paroxetine
Pharmacology. Drug treatments
Population studies
Proportional Hazards Models
prothrombin
Risk Factors
selective serotonin re‐uptake inhibitors
Serotonin - pharmacology
Serotonin uptake inhibitors
Serotonin Uptake Inhibitors - pharmacology
Venlafaxine
Venlafaxine Hydrochloride
Warfarin
Title Selective serotonin re‐uptake inhibiting antidepressants and the risk of overanticoagulation during acenocoumarol maintenance treatment
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fj.1365-2125.2011.04004.x
https://www.ncbi.nlm.nih.gov/pubmed/21545482
https://www.proquest.com/docview/1093429144
https://www.proquest.com/docview/904012438
https://pubmed.ncbi.nlm.nih.gov/PMC3243014
Volume 72
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