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We found no such effect for any other trimester of gestation.
The participants with a higher trimester yielded significantly more tooth sites with bleeding and PPD ≥ 4 mm than those in other trimester (all p < 0.05).> The severity, extent and prevalence of impacts accordin to the individual OHIP-14 items are summaried in Table 2.
Similar(57)
Controlling for depression symptom levels in other trimesters, only second trimester depression symptoms predicted higher infant negative affectivity (β = .44).44
This may have minimized the measurement error in exposure assessment during the third trimester, and as such, the third-trimester specific resulthird-trimester specificss eresultsaredo the other trimester-specific resulikely
Adjustment for season had a greater influence on the trimester-specific estimates: After adjustment for season, the PR of birth weight < 3,000 g associated with an increase of 1 μg/m in third-trimester PM2.5 levels simultaneously adjusted for other trimester-specific variables increased to 1.25 (95% CI, 1.04 to 1.50).
**Any use of antihypertensives in first trimester regardless of use in other trimesters.
No information was available about fatty acid concentrations in other trimesters.
Trimester exposures were autocorrelated, but adjustment of trimester effects for exposure in other trimesters minimally influenced results and thus were not considered further.
The results among those who used ACE inhibitors in the first trimester regardless of use during other trimesters showed a similar pattern of the association.
We are not aware of a biologic mechanism that would explain stronger associations with exposures during the first trimester than exposures during other trimesters.
In Table 2, crude and adjusted ORs for all CBT by trimester of ultrasound exposure are shown, including exposure exclusively in one trimester and for combinations with other trimesters.
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