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Maxilla and Upper and Lower Extremities.. recently tendered a banquet to Dr. F. A. French 20 mg zolpidem tartrate of Edmon-ton,. organs are. Error bars indicate 95% CI. P values describe comparisons of the changes in the placebo or spironolactone group at the respective time point vs baseline. No further improvement by spironolactone occurred between the 6-month and 12-month visits . Author Affiliations: Department of Cardiology and Pneumology, Heart Center . Importance Diastolic heart failure is a common condition without established therapy, and aldosterone stimulation may contribute to its progression. Objective To assess the efficacy and safety of long-term aldosterone receptor blockade in heart failure with preserved ejection fraction. The primary objective was to determine whether spironolactone is superior to placebo in improving diastolic function and maximal exercise capacity in patients with heart failure with preserved ejection fraction. Design and Setting The Aldo-DHF trial, a multicenter, prospective, randomized, double-blind, placebo-controlled trial conducted between March 2007 and April 2012 at 10 sites in Germany and Austria that included 422 ambulatory patients with chronic New York Heart Association class II or III heart failure, preserved left ventricular ejection fraction of 50% or greater, and evidence of diastolic dysfunction. Intervention Patients were randomly assigned to receive 25 mg of spironolactone once daily with 12 months of follow-up. Conclusions and Relevance In this randomized controlled trial, long-term aldosterone receptor blockade improved left ventricular diastolic function but did not affect maximal exercise capacity, patient symptoms, or quality of life in patients with heart failure with preserved ejection fraction. Whether the improved left ventricular function observed in the Aldo-DHF trial is of clinical significance requires further investigation in larger populations. Production of identical matching placebo and quality control, packaging, labeling, storage, and dispensing of both spironolactone and placebo were performed by Allphamed PHARBIL. The first dose of study drug was administered immediately after randomization under the supervision of the local investigator. No further up-titration was planned. Patients were followed up while receiving blinded study medication for 12 months plus an additional safety period of 4 weeks after termination of individual study-related therapy , the Minnesota Living With Heart Failure Questionnaire, the Patient Health Questionnaire, and the Hospital Anxiety and Depression Scale. The primary objective of the Aldo-DHF trial was to determine whether spironolactone is superior to placebo in improving diastolic function and maximal exercise capacity in patients with HF with preserved EF. Prespecified major and additional secondary end points included changes in echocardiographic measures of cardiac function and remodeling, measures of submaximal and maximal exercise capacity, serum biomarkers, and quality of life. Clinical tolerability was assessed as the safety end point. Morbidity and mortality were also predefined exploratory end points. Laboratory Measurements. Venous blood samples were drawn under standardized conditions after 20 minutes of rest in the supine position. Samples were immediately cooled, centrifuged, and processed for storage at −80°C . Analyses of the primary end points were carried out using 2-sided Mann-Whitney U tests. All analyses were based on the intention-to-treat principle. Patients who died were assigned the worst rank in both tests, reflecting the worst case of functional loss. A missing value in one of the end points did not preclude analysis of the other. Sensitivity analyses examining the possible effect of missing data on the primary results were performed using last observation carried forward and multiple imputation. Quantitative effects of the intervention were assessed by analysis of covariance with the follow-up value as the dependent variable, treatment as a factor, and the baseline value as the covariate. SPSS version 20 was used as statistical software. Analyses were carried out by analysis of covariance, binary, or ordinal logistic regression with the follow-up value as the dependent variable, treatment as a factor, and the baseline value as the continuous or categorical covariate, as appropriate for quantitative, binary, or ordinal categorical variables. Between-group comparisons are presented as mean differences or odds ratios. N-terminal proBNP was analyzed on the logarithmic scale, and the result was transformed back by the exponential function, leading to a geometric mean ratio instead of a mean difference. Of 795 patients screened from March 2007 to April 2011, 422 were included and randomized to receive spironolactone or placebo . Results regarding primary end points were consistent across prespecified subgroups . Spironolactone improved major measures of cardiac function and remodeling . Compared with placebo, spironolactone significantly reduced systolic blood pressure . Further clinical variables are shown in eTable 2C. Analyses to examine the possible effects of missing data . Corresponding Author: Burkert Pieske, MD, Department of Cardiology, Medical University Graz, Auenbruggerplatz 15, A-8010 Graz, Austria . Author Contributions: Dr Gelbrich had full access to all of the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis. Drs Edelmann and Wachter contributed equally to the article and share first authorship. Study concept and design: Edelmann, Wachter, Schmidt, Löffler, Hermann-Lingen, Halle, Hasenfuss, Gelbrich, Pieske. Acquisition of data: Edelmann, Wachter, Schmidt, Kraigher-Krainer, Colantonio, Kamke, Duvinage, Stahrenberg, Durstewitz, Düngen, Tschöpe, Halle, Pieske. Analysis and interpretation of data: Edelmann, Wachter, Schmidt, Kraigher-Krainer, Colantonio, Durstewitz, Düngen, Halle, Hasenfuss, Gelbrich, Pieske. Drafting of the manuscript: Edelmann, Wachter, Löffler, Pieske. Critical revision of the manuscript for important intellectual content: Edelmann, Wachter, Schmidt, Kraigher-Krainer, Colantonio, Kamke, Duvinage, Stahrenberg, Durstewitz, Löffler, Düngen, Tschöpe, Hermann-Lingen, Halle, Gelbrich. Statistical analysis: Edelmann, Düngen, Gelbrich. Obtained funding: Edelmann, Löffler, Hermann-Lingen, Halle, Hasenfuss, Gelbrich, Pieske. Administrative, technical, or material support: Edelmann, Wachter, Kamke, Duvinage, Durstewitz, Halle. Study supervision: Edelmann, Wachter, Schmidt, Löffler, Tschöpe, Hermann-Lingen, Halle, Hasenfuss, Pieske. Conflict of Interest Disclosures: All authors have completed and submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Dr Edelmann reports having been an investigator, consultant, or speaker for Berlin Chemie, Novartis, Pfizer, Servier, Bayer, Gilead, CVRx, Relypsa, Sanofi, and Astra-Zeneca. Dr Wachter reports having been, since 2003, an investigator, consultant, or speaker for Bayer, Berlin Chemie, Boehringer Ingelheim, Boston Scientific, CVRx, Gilead, Johnson & Johnson, Medtronic, Novartis, Pfizer, Relypsa, Sanofi, and Servier. Dr Hermann-Lingen reports receiving speaker's honoraria from Pfizer, Servier, and Berlin-Chemie. He has received royalties from Verlag Hans Huber and Deutscher Ärzteverlag and participates in institutional research cooperation with KKH-Allianz. Dr Halle reports receiving speaker's honoraria from Berlin-Chemie, Merck Sharpe & Dohme, Bristol-Myers Squibb, and Sanofi-Aventis and receiving honoraria as board member with Bayer Healthcare and Medtronic. No other conflicts of interest were reported. A complete list of the Aldo-DHF Investigators appears in the eAppendix..

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