SNFGE SNFGE
 
Thématique :
- Endoscopie/Imagerie
Originalité :
Réexamen
Solidité :
A confirmer
Doit faire évoluer notre pratique :
Dans certains cas
 
 
Nom du veilleur :
Docteur Florian ROSTAIN
Coup de coeur :
 
 
Gastroenterology
  2016/09  
 
  2016 Sep 14. pii: S0016-5085(16)35034-X  
  doi: 10.1053/j.gastro.2016.08.054  
 
  Association of Proton Pump Inhibitors with Reduced Risk of Warfarin-related Serious Upper Gastrointestinal Bleeding  
 
  Ray WA, Chung CP, Murray KT, Smalley WE, Daugherty JR, Dupont WD, Stein CM  
  http://www.sciencedirect.com/science/article/pii/S001650851635034X  
 
 

Background & Aims

Proton-pump inhibitors (PPIs) might reduce the risk of serious warfarin-related upper gastrointestinal bleeding, but the evidence of their efficacy for this indication is limited. A gastroprotective effect of PPIs would be particularly important for patients who take warfarin with antiplatelet drugs or nonselective non-steroidal anti-inflammatory drugs (NSAIDs), which further increase the risk of gastrointestinal bleeding.

Methods

This retrospective cohort study of patients beginning warfarin treatment in Tennessee Medicaid and the 5% National Medicare Sample identified 97,430 new episodes of warfarin treatment with 75,720 person-years of follow up. The study endpoints were hospitalizations for upper gastrointestinal bleeding potentially preventable by PPIs and for bleeding at other sites.

Results

Patients who took warfarin without PPI co-therapy had 119 hospitalizations for upper gastrointestinal bleeding per 10,000 person-years of treatment. The risk decreased by 24% among patients who received PPI co-therapy (adjusted hazard ratio [HR], 0.76; 95% CI, 0.63–0.91). There was no significant reduction in the risk of other gastrointestinal bleeding hospitalizations (HR, 1.07; 95% CI, 0.94–1.22) or non-gastrointestinal bleeding hospitalizations (HR, 0.98; 95% CI, 0.84–1.15) in this group. Among patients concurrently using antiplatelet drugs or NSAIDs, those without PPI co-therapy had 284 upper gastrointestinal bleeding hospitalizations per 10,000 person-years of warfarin treatment. The risk decreased by 45% (HR, 0.55; 95% CI, 0.39–0.77) with PPI co-therapy. PPI co-therapy had no significant protective effect for warfarin patients not using antiplatelet drugs or NSAIDs (HR, 0.86; 95% CI, 0.70-1.06). Findings were similar in both study populations.

Conclusions

In an analysis of patients beginning warfarin treatment in Tennessee Medicaid and the 5% National Medicare Sample, PPI co-therapy was associated with reduced risk of warfarin-related upper gastrointestinal bleeding; the greatest reduction occurred in patients also taking antiplatelet drugs or NSAIDs.

 
Question posée
 
Un traitement par IPP diminue-t-il le risque d’hémorragie digestive haute chez les patients traités par warfarine ?
 
Question posée
 
Etude de cohorte américaine : Le traitement par IPP diminuait de 24 % le risque d’hémorragie digestive haute chez les patients traités par warfarine (ratio [HR], 0.76; 95% CI, 0.63-0.91). Le traitement par IPP diminuait de 45% le risque d’hémorragie digestive haute chez les patients traités par warfarine associé à un anti-agrégant plaquettaire ou un AINS (HR, 0.55; 95% CI, 0.39-0.77).
 
Commentaires

Cette étude incite à associer à la warfarine un traitement préventif par IPP d’autant plus si les patients ont un traitement anti-agrégant ou AINS associé.

 
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