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Browsing by Author "Janković, Slobodan M. (7101906319)"

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    Effects of treatment adherence on clinical and economic outcomes in patients with psoriasis; [Uticaj pridržavanja pacijenata s psorijazom propisanog terapijskog režima na kliničke ishode i troškove lečenja]
    (2013)
    Jevtić, Tatjana (26423088500)
    ;
    Bukumirić, Zoran (36600111200)
    ;
    Janković, Slobodan M. (7101906319)
    Aim To compare clinical and cost outcomes of psoriasis in non-biological treatment of adherent and non-adherent patients in a developing Balkans country going through socio-economic transition. Methods The study was designed as a retrospective cohort study involving patients with psoriasis adherent and non-adherent to the prescribed treatment regimen. The patients were followed for a period of one year, through four visits with intervals of three months. The adherence to the prescribed regimen was measured at the end of the follow-up period by the medication possession ratio. Clinical outcomes of the treatment were estimated by the Psoriasis Area Severity Index (PASI) at each visit and the treatment costs were collected from patients' iles at each visit. Results The study enrolled 108 patients, 61 (56.5%) were adherent to the prescribed treatment, and 47 (43.5%) were non-adherent. A signiicant decrease of PASI score was noted in the patients adherent to prescribed therapy (p<0.001). The costs also decreased signiicantly in the group of adherent patients (p=0.001), and the drop of costs was the highest from the visit 3. The decrease in PASI score and costs were less rapid in non-adherent patients. Conclusion Better treatment adherence leads to faster clinical improvement and a more rapid decrease in costs of treatment, which diminish overall expenditure of the health system and society, leaving room for treatment of other diseases more eficiently. Therefore, health systems of developing countries should support additional research of causes of treatment non-adherence in patients with psoriasis, in order to minimize this fenomenon more eficiently, and make signiicant savings.
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    Results of the trycort: Cohort study of add-on antihypertensives for treatment of resistant hypertension
    (2023)
    Janković, Slobodan M. (7101906319)
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    Stojković, Siniša (6603759580)
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    Petrović, Milovan (16234216100)
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    Kostić, Tomislav (26023450500)
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    Zdravković, Marija (24924016800)
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    Radovanović, Slavica (24492602300)
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    Cvjetan, Radosava (56866434200)
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    Ratković, Nenad (6506233469)
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    Rihor, Branislav (57190662754)
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    Spiroski, Dejan (57190161724)
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    Stanković, Aleksandar (57208351458)
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    Andelković, Branko (58300622000)
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    Gocić Petrović, Renata (58300359900)
    Although true treatment resistant hypertension is relatively rare (about 7.3% of all patients with hypertension), optimal control of blood pressure is not achieved in every other patient due to suboptimal treatment or nonadherence. The aim of this study was to compare effectiveness, safety and tolerability of various add-on treatment options in adult patients with treatment resistant hypertension The study was designed as multi-center, prospective observational cohort study, which compared effectiveness and safety of various add-on treatment options in adult patients with treatment resistant hypertension. Both office and home blood pressure measures were recorded at baseline and then every month for 6 visits. The study cohort was composed of 515 patients (268 females and 247 males), with average age of 64.7 ± 10.8 years. The patients were switched from initial add-on therapy to more effective ones at each study visit. The blood pressure measured both at office and home below 140/90 mm Hg was achieved in 80% of patients with add-on spironolactone, while 88% of patients taking this drug also achieved decrease of systolic blood pressure for more than 10 mm Hg from baseline, and diastolic blood pressure for more than 5 mm Hg from baseline. Effectiveness of centrally acting antihypertensives as add-on therapy was inferior, achieving the study endpoints in <70% of patients. Adverse drug reactions were reported in 9 patients (1.7%), none of them serious. Incidence rate of hyperkalemia with spironolactone was 0.44%, and gynecomastia was found in 1 patient (0.22%). In conclusion, the most effective and safe add-on therapy of resistant hypertension were spironolactone alone and combination of spironolactone and a centrally acting antihypertensive drug. © 2023 Lippincott Williams and Wilkins. All rights reserved.
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    Risk factors for potential drug–drug interactions in patients with myasthenia gravis
    (2021)
    Aleksić, Dejan Z. (56893486100)
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    Milosavljević, Miloš N. (57199185758)
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    Stefanović, Srđan M. (57200608544)
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    Bukonjić, Andriana (56698333700)
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    Milosavljević, Jovana Z. (57221731974)
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    Janković, Slobodan M. (7101906319)
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    Božović, Ivo (57194468421)
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    Perić, Stojan (35750481700)
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    Lavrnić, Dragana (6602473221)
    Objectives: Our aim was to determine risk factors for and frequency of potential drug-drug interactions (pDDIs) among hospitalized patients with myasthenia gravis (MG). Methods: This was a retrospective cross-sectional study of the-first time hospitalized MG patients or patients hospitalized because of the exacerbation of MG at the Neurology Clinic of the Clinical Center of Serbia, Belgrade. Medical records and discharge summaries of hospitalized MG patients over a 10-year period were reviewed. The pDDIs were identified by means of Micromedex, and multivariate regression methods were used to reveal potential predictors of number of pDDIs per patient. Results: The study included 687 patients with MG. In total, 2041 pDDIs were detected in 608 (88.5%) patients. Among the discovered pDDIs, 329 different pDDIs were observed. The most frequent pDDIs were pyridostigmine-prednisone (487patients/70.9%) and aspirin-prednisone (90 patients/13.1%) classified as moderate, and enalapril-potassium chloride (71patients/10.3%) classified as major pDDI. Five drugs (aspirin, insulin, prednisone, cyclosporine, metformin) were responsible for 22.6% of different pDDIs. Dyspnea, generalized form of MG, diabetes mellitus, hypertension, total number of drugs-used, use of antiplatelets were identified as the relevant risk factors for total number of pDDIs (R2 = 0.626,F = 73.797, p < 0.001), while age of patients and history of cancer were inversely correlated with such an outcome. Conclusion: The frequency of the pDDIs in hospitalized MG patients is high, and adversely influenced by dyspnea, generalized MG, diabetes mellitus, hypertension, total number of drugs-used and use of antiplatelets. © 2021 Informa UK Limited, trading as Taylor & Francis Group.
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    Risk factors for potential drug–drug interactions in patients with myasthenia gravis
    (2021)
    Aleksić, Dejan Z. (56893486100)
    ;
    Milosavljević, Miloš N. (57199185758)
    ;
    Stefanović, Srđan M. (57200608544)
    ;
    Bukonjić, Andriana (56698333700)
    ;
    Milosavljević, Jovana Z. (57221731974)
    ;
    Janković, Slobodan M. (7101906319)
    ;
    Božović, Ivo (57194468421)
    ;
    Perić, Stojan (35750481700)
    ;
    Lavrnić, Dragana (6602473221)
    Objectives: Our aim was to determine risk factors for and frequency of potential drug-drug interactions (pDDIs) among hospitalized patients with myasthenia gravis (MG). Methods: This was a retrospective cross-sectional study of the-first time hospitalized MG patients or patients hospitalized because of the exacerbation of MG at the Neurology Clinic of the Clinical Center of Serbia, Belgrade. Medical records and discharge summaries of hospitalized MG patients over a 10-year period were reviewed. The pDDIs were identified by means of Micromedex, and multivariate regression methods were used to reveal potential predictors of number of pDDIs per patient. Results: The study included 687 patients with MG. In total, 2041 pDDIs were detected in 608 (88.5%) patients. Among the discovered pDDIs, 329 different pDDIs were observed. The most frequent pDDIs were pyridostigmine-prednisone (487patients/70.9%) and aspirin-prednisone (90 patients/13.1%) classified as moderate, and enalapril-potassium chloride (71patients/10.3%) classified as major pDDI. Five drugs (aspirin, insulin, prednisone, cyclosporine, metformin) were responsible for 22.6% of different pDDIs. Dyspnea, generalized form of MG, diabetes mellitus, hypertension, total number of drugs-used, use of antiplatelets were identified as the relevant risk factors for total number of pDDIs (R2 = 0.626,F = 73.797, p < 0.001), while age of patients and history of cancer were inversely correlated with such an outcome. Conclusion: The frequency of the pDDIs in hospitalized MG patients is high, and adversely influenced by dyspnea, generalized MG, diabetes mellitus, hypertension, total number of drugs-used and use of antiplatelets. © 2021 Informa UK Limited, trading as Taylor & Francis Group.

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