15 research outputs found

    Association between PDE5 inhibitor use and malignant melanoma, by cumulative number of prescriptions received and time since first prescription (index date).

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    <p>Cumulative number of prescriptions received (top panel) and time since index date (bottom panel). From a Cox model with age timescale, stratified by matched set and adjusted for number of consultations in year before index date, BMI category, alcohol use, and smoking status.</p

    Effect of PDE5 inhibitor use on malignant melanoma risk, stratified by individual-level factors.

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    <p>From Cox models containing interaction terms between individual-level factors and exposure (interactions fitted one at a time), with age timescale, stratified by matched set and adjusted for number of consultations in year before index date, BMI category, alcohol use, and smoking status.</p

    Crude rate for malignant melanoma and control outcomes by exposure to PDE5 inhibitors, and unadjusted and adjusted hazard ratios.

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    <p>Crude rate for malignant melanoma and control outcomes by exposure to PDE5 inhibitors, and unadjusted and adjusted hazard ratios.</p

    Graphical representation of the three different treatment stages: Users of GTZ drugs and other antidiabetic drugs classified according to first- or second-line mono- or combination therapy at the index date.

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    <p>For instance, to be a glitazone user in category (2), first-line non-GTZ treatment for diabetes was discontinued after 1999 when a GTZ was prescribed as second-line monotherapy. A patient could be matched to a GTZ user in category (2) if they had received an antidiabetic drug other than a GTZ (for example: Metformin) but stopped using their first-line antidiabetic treatment after 1999 and began taking another drug (for example: Sulfonylurea) as monotherapy after at least 12 months of registered follow-up.</p

    IRR of PD adjusted for potential confounders.

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    <p>* Main analysis: IRR for the association between GTZ use and incident PD using conditional Poisson regression to control for gender, age, practice, and treatment stage</p><p>IRR of PD adjusted for potential confounders.</p
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