2.2. Statistical Analysis

RP Riccardo Proietti
JR José Miguel Rivera-Caravaca
RL Raquel López-Gálvez
SH Stephanie L. Harrison
FM Francisco Marín
PU Paula Underhill
ES Eduard Shantsila
GM Garry McDowell
MV Manlio Vinciguerra
RD Rhys Davies
CG Clarissa Giebel
DL Deirdre A. Lane
GL Gregory Y. H. Lip
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Continuous variables (age) were expressed as mean and standard deviation (SD), and tested for differences with independent-sample t test. Categorical variables (sex, ethnicity, comorbidities, and pharmacological therapy) were expressed as absolute frequencies and percentages, and tested for differences with chi-squared test. The TriNetX platform was used to run 1:1 propensity score matching (PSM) using logistic regression. The platform uses ‘greedy nearest-neighbour matching’ with a caliper of 0.1 pooled standard deviations and difference between propensity scores ≤0.1. Covariate balance between groups was assessed using standardised mean differences (SMDs). Any baseline characteristic with a SMD between cohorts <0.1 is considered well-matched [9].

HR and 95% CI were calculated following PSM, and displayed as Kaplan-Meier survival curves with log-rank tests. No imputations were made for missing data. Two-sided p-values < 0.05 were accepted as statistically significant. Statistical analysis was performed using the TriNetX Analytics function in the online research platform.

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