383 research outputs found

    Collegii medici hoc tempore decanus Rudolfus Guilielmus Crausius, phil. + med. D. prax. + chim. profess. publ. collegii laudati senior, lectori benevolo S. D. P.

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    Elektronische Reproduktion von: Collegii Medici hoc tempore Decanus Rvdolfvs Gvilielmvs Cravsivs, Phil. + Med. D. Prax. + Chim. Profess. Publ. Collegii laudati Senior, Lectori benevolo S. D. P. - [1713]. - [Jena] : Literis Krebsianis. - 8 Seiten. - Standort: Universität Marburg, Universitätsbibliothek. - Signatur: VIII B 331 db, 22. - Fingerprint: e.i- u-r- u-ut n-a- C 1713Q. - Werktitel: Collegii medici hoc tempore decanus Rudolfus Guilielmus Crausius, phil. + med. D. prax. + chim. profess. publ. collegii laudati senior, lectori benevolo S. D. P. - Anmerkung: Einladungsschrift zur Disputation des Johann Ludwig Schmid. - Erscheinungsjahr nach Datierung am Textende: "Anno M DC CXIII. d. 9. April." . - (Hassiaca) Digitalisiert 202

    Transfer of manualized CBT for social phobia into clinical practice (SOPHO-PRAX) : a study protocol for a cluster-randomized controlled trial

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    Background: Cognitive-behavioral therapy (CBT) is generally known to be efficacious in the treatment of social phobia when applied in RCT's, namely when the treatment manual is based on the Clark-Wells approach. However, little is known about the efficacy of manualized treatments in routine clinical practice (Phase IV of psychotherapy research). The present study (SOPHO-PRAX) is a continuation of a large multi-centre randomized clinical trial (SOPHO-NET) and analyses the extent to which additional training practitioners in manualized procedures enhances treatment effect. Methods: N = 36 private practitioners will be included in three treatment centres and randomly designated to either training in manualized CBT or no specific training. The treatment effects of the therapies conducted by both groups of therapists will be compared. A total of 162 patients (N = 116 completers; N = 58 per condition) will be enrolled. Liebowitz Social Anxiety Scale (LSAS) will serve as primary outcome measure. Remission from social phobia is defined as LSAS total [less than or equal to] 30 points. Data will be collected at treatment begin, after 8, 15, and 25 sessions (50 mins. each), at treatment completion, as well at 6 and 12 months post-treatment. Discussion: The present CBT trial combines elements of randomized-controlled trials and naturalistic studies in an innovative way. It will directly inform about the incremental effects of procedures established in a controlled trial into clinical practice. Study results are relevant to health care decisions and policy. They may serve to improve quality of treatment, and shorten the timeframe between the development and widespread dissemination of effective methods, thereby reducing health cost expenditures. The results of this study will not only inform about the degree to which the new methods lead to an improvement of treatment course and outcome, but also about whether the effects of routine psychotherapeutic treatment are comparable to those of the controlled, strictly manualized treatments of the SOPHO-NET study. Trial Registration: ClinicalTrials.gov identifier: NCT01388231. This study was funded by the German Federal Ministry of Education and Research (SOPHO-NET: BMBF 01GV0607; SOPHO-PRAX: BMBF 01GV1001)

    Do different subjective evaluation criteria reflect distinct constructs?

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    This is not the published version. Published version available from: http://journals.lww.com/jonmd/pages/default.asp

    Potential risk factors for adverse drug reactions in elderly patients : contribution to safer drug prescribing

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    Because of demographic aging the proportion of elderly persons in the population is increasing, especially in industrialized countries. Increasing age is associated with a higher prevalence of comorbidities possibly necessitating pharmacotherapy. Elderly persons are not only treated with more drugs than younger ones, but they are also more vulnerable to adverse drug reactions (ADRs). The aim of the thesis was to elucidate potential risk factors that increase the risk for ADRs in the elderly with the purpose to improve safety of medical treatment. First, the literature was reviewed in order to get an overview on the potential risk factors already known. It has been shown that not only physiological changes that affect pharmacokinetic and/or pharmacodynamic effects of drugs, but also specific drugs and drug classes may increase the risk for ADRs. Two studies were then performed to evaluate specific aspects of drug prescribing, which may enhance the risk for ADRs. In the first study age-specific differences in the prevalence of clinically relevant potential drug-drug interactions (pDDIs) in ambulatory dyslipidemic patients treated with a statin were evaluated. Practitioners from different parts of Switzerland collected data for a total of 2’742 patients treated with a statin which attended their practice. Medical treatment was screened for clinically relevant pDDIs, defined as a DDI that could have had a potential serious outcome, using an interactive electronic drug interaction program. The prevalence of clinically relevant pDDIs was significantly higher in patients aged ³75 years than in patients aged £54 years (18.4% versus 7.9%; p < 0.001). This was ascribed to a higher number of diseases (3.5 versus 2.8; p < 0.001) and pharmacologically active substances prescribed (5.8 versus 3.8; p < 0.001). Beside polypharmacy, also heart failure and arrhythmia have been identified as risk factors for pDDIs in elderly patients. The more frequent prescription of cardiovascular drugs with a high potential for drug interactions (e.g. amiodarone and digoxin) was mainly responsible for the observed increase in statin and non statin pDDIs. The aim of the second study was to retrospectively evaluate and compare the prevalence of potentially inappropriate medication (PIM) use and prescription of drugs with strong anticholinergic properties in 800 elderly patients hospitalized on general medical or geriatric wards throughout hospital stay. PIMs as defined by the Beers criteria and anticholinergic drugs have been associated with a higher risk for ADRs in patients aged ³65 years. At hospital discharge, geriatric patients had a lower prevalence of use of PIMs that should generally be avoided than at admission (15.9% versus 22.1%; p < 0.05), whereas no difference was observed in medical patients. Overall, the three most prevalent inappropriate drugs/drug classes were amiodarone, long-acting benzodiazepines and anticholinergic antispasmodics. On the other hand, geriatric patients were discharged with a higher prevalence of use of PIMs that should be avoided in the presence of specific underlying diseases compared to medical patients (23.7% versus 11.7%; p < 0.001). The main reason was the higher prescription rate of benzodiazepines to patients with a history of falls and syncope. There was neither a difference in the prevalence of patients with anticholinergic drugs at admission nor at discharge between medical and geriatric patients. Compared with internists, geriatricians appeared to be more aware of PIMs that should generally be avoided. However, the results of this study should be interpreted with caution, because some of the drugs identified as potentially inappropriate may in fact be beneficial when the patient’s individual clinical condition is taken into consideration. Finally, a patient with lithium intoxication as a result of a drug-drug interaction (DDI) with rofecoxib is presented. This 68-year-old woman had several risk factors that finally resulted in the clinical manifestation of the DDI, illustrating well the problems of pharmacotherapy in the elderly. The already impaired renal function (calculated creatinine clearance 40 mL/min) deteriorated after the addition of rofecoxib, a selective cyclooxygenase 2 (COX-2) inhibitor. As a consequence, renal clearance of lithium was impaired, leading to an accumulation of the drug and symptoms of lithium intoxication such as vomiting, hypokinesia and tremor. Selective COX-2 inhibitors seem therefore not to be safer than conventional nonsteroidal anti-inflammatory drugs concerning their effect on renal function, especially in patients with renal insufficiency. Depending on the underlying disease, medical treatment with drugs associated with a high potential for DDIs and/or ADRs may not always be avoided. Knowledge of the potential risk can help to take appropriate measures to lower the probability for an adverse outcome, e.g. close monitoring of the patient, dose adjustment or selection of an alternative drug

    Did female prisoners with mental disorders receive psychiatric treatment before imprisonment?

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    © 2015 Mundt et al.; licensee BioMed Central. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.BackgroundThroughout the world, high prevalence rates of mental disorders have been found in prison populations, especially in females. It has been suggested that these populations do not access psychiatric treatment. The aim of this study was to establish rates of psychiatric in- and outpatient treatments prior to imprisonment in female prisoners and to explore reasons for discontinuation of such treatments.Methods150 consecutively admitted female prisoners were interviewed in Berlin, Germany. Socio-demographic characteristics, mental disorders, and previous psychiatric in- and outpatient treatments were assessed by trained researchers. Open questions were used to explore reasons for ending previous psychiatric treatment.ResultsA vast majority of 99 prisoners (66%; 95% CI: 58¿73) of the total sample reported that they had previously been in psychiatric treatment, 80 (53%; 95 CI: 45¿61) in inpatient treatment, 62 (41%; 95 CI: 34¿49) in outpatient treatment and 42 (29%; 21¿39) in both in- and outpatient treatments. All prisoners with psychosis and 72% of the ones with any lifetime mental health disorder had been in previous treatment. The number of inpatient treatments and imprisonments were positively correlated (rho¿=¿0.27; p¿<¿0.01). Inpatient treatment was described as successfully completed by 56% (N¿=¿41) of those having given reasons for ending such treatment, whilst various reasons were reported for prematurely ending outpatient treatments.ConclusionThe data do not support the notion of a general `mental health treatment gap¿ in female prisoners. Although inpatient care is often successfully completed, repeated inpatient treatments are not linked with fewer imprisonments. Improved transition from inpatient to outpatient treatment and services that engage female prisoners to sustained outpatient treatments are needed

    Myslenie a konanie, filozofia a životná prax (Thinking and Acting, Philosophy and Life Practice)

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    The author of the article is concerned with metaphilosophical problem of defining philosophy in the context of life practice. He investigates terms “thinking” and “acting” in ordinary language. He is pointing out that dichotomy of thinking and acting, or rather philosophy and life practice, is not strictly and clearly defined. The content of this dichotomy is in fact bound to intent, which determines its formulation

    Avaliação clínica da fluorescência de dentes naturais

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    Tese (doutorado) - Universidade Federal de Santa Catarina, Centro de Ciências da Saúde, Programa de Pós-Graduação em Odontologia, Florianópolis, 2006.Esta pesquisa teve como objetivo avaliar clinicamente a fluorescência presente nos dentes naturais e a sua relação com a faixa etária. 40 voluntários foram selecionados de acordo com critérios pré-estabelecidos e divididos de acordo com sua faixa etária em 4 grupos (n=10): Grupo 1; de 06 à 14 anos; Grupo 2; de 15 à 29 anos; Grupo 3; de 30 à 44 anos e Grupo 4; de 45 à 59 anos. A refletância espectral e as coordenadas de cor foram mensuradas de acordo com a escala de cor CIELAB da Comissão internacional de Luminosidade (CIE) relativa ao iluminante padrão D65. Foi utilizada a geometria de medição D/8°, com iluminação difusa a 10°, comprimento de onda de 360 a 740nm, com a componente especular exclusa e com a luz ultravioleta excluída e incluída. A fluorescência foi calculada pela diferença na reflectância pela exclusão e inclusão da luz ultra-violeta. A intensidade da fluorescência não foi influenciada pela faixa etária (p>0,05). Apesar do grupo 1 ter apresentado valores de luminosidade estatisticamente maiores (p=0,005), não foi observada relação entre a cor dos dentes e a intensidade de emissão fluorescente. Concluímos que, quando avaliada clinicamente, a fluorescência dos dentes naturais não foi afetada pela idade dos pacientes.The objective of this study was to analyze the fluorescence of natural teeth and its relation with age. 40 volunteers were selected in view of pre- established criteria, and divided in 4 groups according to their age (n=10): Group 1; from 06 to 14 years; Group 2; from 15 to 29 years; Group 3; from 30 to 44 years and Group 4; from 45 to 59 years. Spectral reflectance and color coordinates were measured according to the Commission Internationale de l'Eclairage (CIE) CIELAB color scale relative to the standard illuminant D65. The measurement geometry used was D/8°, with 10° diffuse illumination, 360 to 740nm wavelengths, specular component excluded and ultraviolet light excluded or included. Fluorescence was calculated from the subtraction of the reflectance values by the inclusion and exclusion of the ultraviolet component. The fluorescence intensity was not influenced by the age (p>0.05). Even tough group 1 presented luminosity values statistically higher (p=0.005), no relation was observed between teeth color and intensity of fluorescent emission. We conclude that, when measured in a clinical environment, the fluorescence of natural teeth was not related with patients' age

    Genotyping of Cryptosporidium spp. isolated from human stool samples in Switzerland

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    In a study to estimate the frequency of Cryptosporidium infections in Switzerland, stool samples from patients found to be positive for Cryptosporidium spp. by modified Ziehl-Neelson staining and fluorescence microscopy were used for genotyping experiments. With 9 of 12 samples, DNA extraction and subsequent genotyping was successful. All Cryptosporidium-isolates belonged to the bovine genotype. In one stool sample, two strains of Cryptosporidium were demonstrated, suggesting a mixed infection. In comparison with reference strains from calves, one of the isolates showed a full sequence identity and the other a similarity of 97.5%. The fact that only bovine genotypes were detected suggests, that cryptosporidiosis must primarily be considered as a zoonotic disease in Switzerland. This is in contrast to other countries, where the human genotype of C. parvum was shown to dominate the epidemiological situation. The results of our study are supported by the previous finding, that two of the analysed strains originated from patients who used to consume raw milk or raw cream, a known risk factor for cryptosporidiosis
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