23 research outputs found

    Adjusted Hazard Ratios for Predictors of Initiation of Antidepressants within 6 months of Bereavement.

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    a<p>Hazard ratios adjusted for all determinants in table, UK Region and Year.</p>b<p>Comparing Association in Bereaved and Non-Bereaved Groups.</p>c<p>Quintiles of annual practice prescribing to non-bereaved couples (% of patients in receipt of this drug class).</p>*<p>Full data on non-bereaved analysis is presented in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0077734#pone.0077734.s001" target="_blank">table S1</a>.</p

    Probability of Initiation (%) of Psychotropic Drugs in the Year after Bereavement in Bereaved (B) and Non Bereaved (NB) Patients.

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    <p>Initiation probabilities during the first year after bereavement are derived from Kaplan Meier estimates and divided into the following periods Light Grey: 6–12 months Medium Grey: 2–6 months Dark Grey: 0–2 months.</p

    Proportion of Patients in Receipt of Psychotropic Medication in the Year Before and After Bereavement.

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    <p>Blue: All Bereaved (n = 29,548) Green: All Non-Bereaved (n = 80,471) Red: Bereaved without psychotropic medication in year before bereavement (n = 21,122) Purple: Non-Bereaved without psychotropic medication in year before bereavement (n = 59,280) Daily percentages are based on a denominator of patients still registered on that day.</p

    One Year Continuation of Psychotropic Medication Initiated in the First Two Months after Bereavement.

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    *<p>Alive and registered with practice on first anniversary of bereavement date.</p>†<p>Received same class of medication within 90 days of anniversary of bereavement.</p

    Baseline characteristics of 298 randomised participants.

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    <p><sup>a</sup>National quintiles of Index of Multiple Deprivation rank [<a href="http://www.plosmedicine.org/article/info:doi/10.1371/journal.pmed.1001783#pmed.1001783.ref021" target="_blank">21</a>].</p><p><sup>b</sup>Full references for general health, chronic disease score, limiting long-standing illness, self-reported pain, Falls Risk Assessment Tool (FRAT), Geriatric Depression Score (GDS-15), FEAR anxiety score, Townsend Disability Score, Self-Efficacy Score, difficulty in paying bills, are given in the trial protocol [<a href="http://www.plosmedicine.org/article/info:doi/10.1371/journal.pmed.1001783#pmed.1001783.ref013" target="_blank">13</a>].</p><p><sup>c</sup>For fat mass, waist circumference, and all accelerometry data, numbers presented are mean (standard deviation [SD]).</p><p>Baseline characteristics of 298 randomised participants.</p

    PACE-UP and PACE-Lift studies.

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    <p><b>Effect estimates and 95% confidence intervals for change in (a) average daily steps and (b) total weekly minutes of MVPA in bouts at 3 months, 12 months, and 3 years (PACE-UP) and 4 years (PACE-Lift).</b> Effect sizes, 95% confidence intervals, and <i>p-</i>values were obtained from multilevel linear regression models (see <a href="http://www.plosmedicine.org/article/info:doi/10.1371/journal.pmed.1002526#sec009" target="_blank">Methods</a>). 3 months: <i>p</i> < 0.001 for all PACE-UP and PACE-Lift steps and MVPA intervention effects. 12 months: <i>p</i> < 0.001 for PACE-UP steps and PACE-UP MVPA; <i>p</i> = 0.02 for PACE-Lift steps and <i>p</i> < 0.001 for PACE-Lift MVPA. 3 years: <i>p</i> < 0.01 for PACE-UP steps and PACE-UP MVPA postal group; <i>p</i> = 0.03 for PACE-UP MVPA nurse group. 4 years: <i>p</i> = 0.17 for PACE-Lift steps and <i>p</i> = 0.02 for PACE-Lift MVPA. MVPA, moderate-to-vigorous physical activity; PACE-Lift, Pedometer Accelerometer Consultation Evaluation-Lift; PACE-UP, Pedometer And Consultation Evaluation-UP.</p

    Other outcome measures.

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    <p><sup><b>a</b></sup>The treatment effect is the difference between groups (intervention-control) in change from baseline at 3 months and 12 months. The differences at 3 and 12 months are adjusted for baseline measure, practice, age, gender, and month of baseline accelerometry in a multi-level model with household as a random effect.</p><p><sup><b>b</b></sup>Fat mass was missing for six and three participants in the control group and for five and seven participants in the intervention group at baseline and 3 months, respectively.</p><p><sup><b>c</b></sup>Geriatric depression scores, fear anxiety scores, and self-reported pain were missing for varying numbers of participants (maximum 15) at each time-point.</p><p>Other outcome measures.</p
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