This article is protected by copyright.
All rights reserved
score matching procedures. Since it could not be included in the propensity score model, it was
controlled for in analyses using Firth’s penalized method.
GI bleed characteristics were first summarized descriptively for all patients with GI bleed. Next, the
variable balance for propensity score matching was assessed. Frequencies and percentages were
presented for categorical variables and means, medians, standard deviations, and interquartile ranges
were presented for continuous variables. Variable balance was assessed using the absolute
standardized difference, with an absolute difference smaller than 0.25 considered acceptable[23].
To assess the association between hospital medication use with GI bleed during hospitalization,
hospital medication use was summarized descriptively across GI bleed groups (frequencies,
percentages, means, medians). Conditional logistic regression was then used to account for the
propensity score matched data. Hospital medication use for each medication type was considered as a
potential risk factor. For the medications antiplatelets, anticoagulants, steroids, and NSAIDs, hospital
medication use was considered to occur for patients with GI bleed only if the medication was ordered
prior to the GI bleed. Antiplatelet agents searched for included: aspirin, dipyridamole, cilostazol,
thienopyridines (clopidogrel, prasugrel, ticlodipine, ticagrelor), GPllb/llla inhibitors (tirofiban,
abcixab, eptifibatide), PAR-1 inhibitor (vorapaxar). Anticoagulants searched for included: warfarin,
unfractionated heparin, low molecular weight heparin, dalteparin, fondaparinux, rivaroxaban,
apixaban, edoxaban, dabigatran, and desirudin.
For the medications proton pump inhibitors (PPIs) and histamine receptor blocker (H2R blockers),
hospital medication use for all patients was considered to occur for patients if prescribed
prophylactically within the first 24 hours of admission, and additionally only for patients with GI
bleed if the medication was ordered prior to the GI bleed.
Interaction between home and hospital
medication use was assessed for each medication type in the multivariable models but none
were found to be significant. All models were assessed for multicollinearity. Timing and
adherence to home medications could not be verified and thus we did not look at medication
risk factors for GI bleed on admission.
Do'stlaringiz bilan baham: