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Clinical features identified in these studies were weight loss, fever or night sweats, hemoptysis, age >45 years old, productive cough, and upper-lobe infiltrate on chest radiograph or cavities.
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The main outcome that was reported in all studies was weight change.
25 27 However, the main outcome of many of those studies was weight reduction, not development of diabetes.
The primary outcomes in this non-blinded study were weight and HbA1c.
The primary outcomes of the study were weight loss and waist circumference reduction.
The primary measures in this study were weight, BMI, and body fat percentage; however, heart rate and blood pressure taken at each visit were also analyzed.
The exposures evaluated in this study were weight gain during weeks 0 15, 15 30, 30 delivery, and 0 delivery; weight gain from week 0 of pregnancy to 6 months postpartum; and weight loss from delivery to 6 months postpartum.
The 4 groups used in this study were weight stable (WS; n = 5), initial (≤5%; n = 6), moderate (6 19%; n = 4), and severe (≥20%; n = 6) degrees of body weight loss, when compared to peak body weight.
The primary outcome of this study was weight status.
Another factor related to health system delay in our study was weight loss.
The principal objective of the nizatidine study was weight prevention when initiating olanzapine treatment.
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