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Future studies should take age at Parkinson's disease onset into account.
We sorted pre-TMS α-phase (100 ms prior to TMS onset) into six equidistant bins.
The mean age of onset into BZD use was around 31 years old.
We classified PTD by mode of onset into 'spontaneous PTD' or 'non-spontaneous PTD.' Non-spontaneous PTD included births that required medically induced labor or a cesarean section before labor.
The association remained non-significant when the analysis was restricted to cases divided by age of onset into those diagnosed ⩽55 years (OR=1.50, 95% CI 0.79 2.85) or to patients diagnosed >55 years (OR=1.27, 95% CI 0.59 2.74).
When bleeding was classified according to the timing of onset into two types, i.e., early bleeding (defined as bleeding within 3 post-operative days) and late bleeding (defined as bleeding from post-operative day 4 to 14), early bleeding accounted for 33%% and late bleeding for 67%%, showing that late bleeding was more common (Fig. 2).
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On the other hand, the same proportion of patients with CCH at onset turns into episodic within 10 years later while nearly the half with CCH at onset still has CCH after 20 or more years [4].
This study adds further support for the classification of community onset BSI into separate CA and HCA categories.
Then, within each TLE group, we categorized patients based on their age of seizure onset (SO) into two subgroups: early/childhood or late/adult age of seizure onset.
Therefore, we expect to see two different kinds of arrows: Besides unidirectional information out-flow from the seizure onset zone into the surrounding areas we will typically observe arrows pointing from one electrode to another within the seizure onset zone.
These data add further support for the classification of community onset BSI into CA-BSI and HCA-BSI in infectious diseases surveillance and inclusion in guidelines guiding empiric antimicrobial therapies in patients presenting to hospital with infectious diseases.
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Justyna Jupowicz-Kozak
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