2011
DOI: 10.1016/j.gie.2011.03.1258
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Bleeding after percutaneous endoscopic gastrostomy is linked to serotonin reuptake inhibitors, not aspirin or clopidogrel

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Cited by 63 publications
(52 citation statements)
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“…Overall, the incidence of post-PEG bleeding in this study (3.3%) was very close to that previously reported in the literature (2.5-2.8%) [6,17,18]. Bleeding directly attributed to PEG placement (excluding unrelated peptic ulcer disease and other lesions) was very low (0.3%).…”
Section: Discussionsupporting
confidence: 87%
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“…Overall, the incidence of post-PEG bleeding in this study (3.3%) was very close to that previously reported in the literature (2.5-2.8%) [6,17,18]. Bleeding directly attributed to PEG placement (excluding unrelated peptic ulcer disease and other lesions) was very low (0.3%).…”
Section: Discussionsupporting
confidence: 87%
“…Furthermore, premature discontinuation of aspirin and clopidogrel in the setting of a drug-eluting coronary stent is associated with high incidence of stent thrombosis [37]. There is sufficient evidence to show that there is no statistically significant association of aspirin and bleeding after PEG [18] and after colonoscopy with polypectomy [3,38,39]. Data on clopidogrel in high-risk endoscopic procedures is more limited, but three studies [18,40,41] have demonstrated that clopidogrel alone was not an independent risk factor for post PEG and postpolypectomy bleeding.…”
Section: Discussionmentioning
confidence: 99%
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“…192 Continued administration of aspirin for PEG placement has not been associated with an increased risk of haemorrhage. 193 Additionally, there was no increased risk of haemorhage on clopidogrel in a retrospective single-centre casecontrol study of 990 patients, 194 although this study was statistically underpowered to demonstrate an effect due to this drug. There have been no studies examining the risk of PEG placement in patients on prasugrel, ticagrelor or DOAC.…”
Section: Percutaneous Endoscopic Gastrostomymentioning
confidence: 84%
“…Anticoagulants are categorized as either warfarins or novel oral anticoagulants (NOACs; eg, dabigatran, apixaban, rivaroxaban, or edoxaban); the former are indirect inhibitors, whereas the latter are direct inhibitors of the coagulation system. 31) Because of the difference in the mechanisms of action, patients receiving warfarin require longer time for the recovery of the coagulation system compared with those receiving NOACs. Therefore, transient heparinization (heparin bridge) has become a common practice for patients receiving warfarin.…”
Section: Percutaneous Endoscopic Gastrostomymentioning
confidence: 99%