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Dive into the research topics where Tobias Weberschock is active.

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Featured researches published by Tobias Weberschock.


Journal Der Deutschen Dermatologischen Gesellschaft | 2012

S3 – Guidelines on the treatment of psoriasis vulgaris (English version). Update

Alexander Nast; Wolf-Henning Boehncke; Ulrich Mrowietz; Hans-Michael Ockenfels; Sandra Philipp; Kristian Reich; Thomas Rosenbach; Adel Sammain; Martin Schlaeger; Michael Sebastian; Wolfram Sterry; Volker Streit; Matthias Augustin; Ricardo Erdmann; Joachim Klaus; Joachim Koza; Siegrid Muller; Hans-Dieter Orzechowski; Stefanie Rosumeck; Gerhard Schmid-Ott; Tobias Weberschock; Berthold Rzany

Psoriasis vulgaris is a common and often chronic inflammatory skin disease. The incidence of psoriasis in Western industrialized countries ranges from 1.5% to 2%. Patients afflicted with severe psoriasis vulgaris may experience a significant reduction in quality of life. Despite the large variety of treatment options available, surveys have shown that patients still do not received optimal treatments. To optimize the treatment of psoriasis in Germany, the Deutsche Dermatologi sche Gesellschaft (DDG) and the Berufsverband Deutscher Dermatologen (BVDD) have initiated a project to develop evidence‐based guidelines for the management of psoriasis. They were first published in 2006 and updated in 2011. The Guidelines focus on induction therapy in cases of mild, moderate and severe plaque‐type psoriasis in adults including systemic therapy, UV therapy and topical therapies.


Archives of Dermatological Research | 2007

German evidence-based guidelines for the treatment of Psoriasis vulgaris (short version)

Alexander Nast; Ina Kopp; Matthias Augustin; Kirstin-Benita Banditt; Wolf-Henning Boehncke; Markus Follmann; Markus Friedrich; Matthias Huber; Christina Kahl; Joachim Klaus; Joachim Koza; Inga Kreiselmaier; Johannes Mohr; Ulrich Mrowietz; Hans-Michael Ockenfels; Hans-Dieter Orzechowski; Jörg C. Prinz; Kristian Reich; Thomas Rosenbach; Stefanie Rosumeck; Martin Schlaeger; Gerhard Schmid-Ott; Michael Sebastian; Volker Streit; Tobias Weberschock; Berthold Rzany

Psoriasis vulgaris is a common and chronic inflammatory skin disease which has the potential to significantly reduce the quality of life in severely affected patients. The incidence of psoriasis in Western industrialized countries ranges from 1.5 to 2%. Despite the large variety of treatment options available, patient surveys have revealed insufficient satisfaction with the efficacy of available treatments and a high rate of medication non-compliance. To optimize the treatment of psoriasis in Germany, the Deutsche Dermatologische Gesellschaft and the Berufsverband Deutscher Dermatologen (BVDD) have initiated a project to develop evidence-based guidelines for the management of psoriasis. The guidelines focus on induction therapy in cases of mild, moderate, and severe plaque-type psoriasis in adults. The short version of the guidelines reported here consist of a series of therapeutic recommendations that are based on a systematic literature search and subsequent discussion with experts in the field; they have been approved by a team of dermatology experts. In addition to the therapeutic recommendations provided in this short version, the full version of the guidelines includes information on contraindications, adverse events, drug interactions, practicality, and costs as well as detailed information on how best to apply the treatments described (for full version, please see Nast et al., JDDG, Suppl 2:S1–S126, 2006; or http://www.psoriasis-leitlinie.de).


Archives of Dermatological Research | 2012

German S3-guidelines on the treatment of psoriasis vulgaris (short version)

Alexander Nast; Wolf-Henning Boehncke; Ulrich Mrowietz; Hans-Michael Ockenfels; Sandra Philipp; Kristian Reich; Thomas Rosenbach; Adel Sammain; Martin Schlaeger; Michael Sebastian; Wolfram Sterry; Volker Streit; Matthias Augustin; Ricardo Erdmann; Joachim Klaus; Joachim Koza; S. Müller; Hans-Dieter Orzechowski; Stefanie Rosumeck; Gerhard Schmid-Ott; Tobias Weberschock; Berthold Rzany

Psoriasis vulgaris is a common and often chronic inflammatory skin disease. The incidence of psoriasis in Western industrialized countries ranges from 1.5 to 2%. Patients afflicted with severe psoriasis vulgaris may experience a significant reduction in quality of life. Despite the large variety of treatment options available, patient surveys have revealed insufficient satisfaction with the efficacy of available treatments and a high rate of medication non-compliance (Richards et al. in J Am Acad Dermatol 41(4):581–583, 1999). To optimize the treatment of psoriasis in Germany, the Deutsche Dermatologische Gesellschaft (DDG) and the Berufsverband Deutscher Dermatologen (BVDD) have initiated a project to develop evidence-based guidelines for the management of psoriasis first published in 2006 and now updated in 2011. The Guidelines focus on induction therapy in cases of mild, moderate, and severe plaque-type psoriasis in adults. This short version of the guidelines presents the resulting series of therapeutic recommendations, which were based on a systematic literature search and discussed and approved by a team of dermatology experts. In addition to the therapeutic recommendations provided in this short version, the full version of the guidelines includes information on contraindications, adverse events, drug interactions, practicality, and costs, as well as detailed information on how best to apply the treatments described (for full version please see Nast et al. in JDDG Suppl 2:S1–S104, 2011 or http://www.psoriasis-leitlinie.de).


Medical Education | 2005

Change in knowledge and skills of Year 3 undergraduates in evidence-based medicine seminars

Tobias Weberschock; Timothy Charles Ginn; Johannes Reinhold; Reinhard Strametz; Daniel Krug; Martin Bergold; Johannes Schulze

Purpose  To evaluate the effect of a compulsory evidence‐based medicine (EBM) seminar in critical appraisal skills and the overall acceptance of compulsory EBM seminars for Year 3 medical undergraduate students.


Archives of Dermatological Research | 2007

Tolerance to coxibs in patients with intolerance to non-steroidal anti-inflammatory drugs (NSAIDs): a systematic structured review of the literature

Tobias Weberschock; Sylke-Monina Muller; Sandra Boehncke; Wolf-Henning Boehncke

Adverse events triggered by non-steroidal anti-inflammatory drugs (NSAIDs) are among the most common drug-related intolerance reactions in medicine; they are possibly related to inhibition of cyclooxygenase-1. Coxibs, preferentially inhibiting cyclooxygenase-2, may therefore represent safe alternatives in patients with NSAID intolerance. We reviewed the literature in a systematic and structured manner to identify and evaluate studies on the tolerance of coxibs in patients with NSAID intolerance. We searched MEDLINE (1966–2006), the COCHRANE LIBRARY (4th Issue 2006) and EMBASE (1966–2006) up to December 9, 2006, and analysed all publications included using a predefined evaluation sheet. Symptoms and severity of adverse events to coxibs were analysed based on all articles comprising such information. Subsequently, the probability for adverse events triggered by coxibs was determined on analyses of double-blind prospective trials only. Among 3,304 patients with NSAID intolerance, 119 adverse events occurred under coxib medication. All adverse events, except two, have been allergic/urticarial in nature; none was lethal, but two were graded as life-threatening (grade 4). The two non-allergic adverse events were described as a grade 1 upper respiratory tract haemorrhage, and a grade 1 gastrointestinal symptom, respectively. In 13 double-blind prospective studies comprising a total of 591 patients with NSAID intolerance, only 13 adverse reactions to coxib provocations were observed. The triggering coxibs were rofecoxib (2/286), celecoxib (6/208), etoricoxib (4/56), and valdecoxib (1/41). This review documents the good tolerability of coxibs in patients with NSAID intolerance, for whom access to this class of drugs for short-term treatment of pain and inflammation is advantageous.


Journal Der Deutschen Dermatologischen Gesellschaft | 2016

German guidelines for the diagnosis and therapy of localized scleroderma.

Alexander Kreuter; Thomas Krieg; Margitta Worm; Jörg Wenzel; Pia Moinzadeh; Annegret Kuhn; Elisabeth Aberer; Karin Scharffetter-Kochanek; Gerd Horneff; Emma Reil; Tobias Weberschock; Nicolas Hunzelmann

Localized scleroderma designates a heterogeneous group of sclerotic skin disorders. Depending on the subtype, severity, and site affected, adjacent structures such as adipose tissue, muscles, joints, and bones may be involved. This is an update of the existing German AWMF (Association of the Scientific Medical Societies in Germany) guidelines (classification: S2k). These guidelines provide an overview of the definition, epidemiology, classification, pathogenesis, laboratory workup, histopathology, clinical scoring systems, as well as imaging and device‐based workup of localized scleroderma. Moreover, consensus‐based recommendations are given on the management of localized scleroderma depending on its clinical subtype. Treatment recommendations are presented in a therapeutic algorithm. No financial support was given by any pharmaceutical company. The guidelines are valid until July 2019.


Journal Der Deutschen Dermatologischen Gesellschaft | 2011

S3-Leitlinie zur Therapie der Psoriasis vulgaris Update 2011

Alexander Nast; Wolf-Henning Boehncke; Ulrich Mrowietz; Hans-Michael Ockenfels; Sandra Philipp; Kristian Reich; Thomas Rosenbach; Adel Sammain; Martin Schlaeger; Michael Sebastian; Wolfram Sterry; Volker Streit; Matthias Augustin; Ricardo Erdmann; Joachim Klaus; Joachim Koza; Siegrid Muller; Hans-Dieter Orzechowski; Stefanie Rosumeck; Gerhard Schmid-Ott; Tobias Weberschock; Berthold Rzany

Alexander Nast, Wolf-Henning Boehncke, Ulrich Mrowietz, Hans-Michael Ockenfels, Sandra Philipp, Kristian Reich, Thomas Rosenbach, Adel Sammain, Martin Schlaeger, Michael Sebastian, Wolfram Sterry, Volker Streit, Matthias Augustin, Ricardo Erdmann, Joachim Klaus, Joachim Koza, Siegrid Müller, Hans-Dieter Orzechowski, Stefanie Rosumeck, Gerhard Schmid-Ott, Tobias Weberschock, Berthold Rzany (1) Division of Evidence Based Medicine (dEBM), Klinik für Dermatologie, Venerologie und Allergologie, Charité – Universitätsmedizin Berlin (2) Zentrum der Dermatologie und Venerologie, Klinikum der Johann Wolfgang Goethe Universität, Frankfurt/M. (3) Klinik für Dermatologie, Venerologie, Allergologie, Universitätsklinikum Schleswig-Holstein, Campus Kiel (4) Hautund Allergieklinik, Klinikum Hanau (5) Psoriasisstudienzentrum, Klinik für Dermatologie, Venerologie und Allergologie, Charité – Universitätsmedizin Berlin (6) Dermatologikum Hamburg (7) Niedergelassener Dermatologe, Osnabrück (8) Niedergelassener Dermatologe, Oldenburg (9) Niedergelassener Dermatologe, Mahlow (10) Klinik für Dermatologie, Venerologie und Allergologie, Charité – Universitätsmedizin Berlin (11) Niedergelassener Dermatologe, Buchholz (12) Universitätsklinikum Hamburg-Eppendorf, Klinik und Poliklinik für Dermatologie und Venerologie, Hamburg (13) Deutscher Psoriasis Bund e.V. (14) Pflegevertreterin, Ravenstein (15) Institut für Klinische Pharmakologie und Toxikologie, Charité – Universitätsmedizin Berlin (16) Berolina Klinik, Löhne


Journal Der Deutschen Dermatologischen Gesellschaft | 2011

Diagnosis and treatment of Staphylococcus aureus infections of the skin and mucous membranes.

Helmut Schöfer; Roswitha Bruns; Isaak Effendy; Martin Hartmann; Uta Jappe; Andreas Plettenberg; Holger Reimann; Harald Seifert; Pramod M. Shah; Cord Sunderkötter; Tobias Weberschock; Thomas A. Wichelhaus; Alexander Nast

© Deutsche Dermatologische Gesellschaft u. a. • Journal compilation


British Journal of Dermatology | 2016

Report from the kick-off meeting of the Cochrane Skin Group Core Outcome Set Initiative (CSG-COUSIN).

Jochen Schmitt; Stefanie Deckert; Murad Alam; Christian Apfelbacher; J. Barbaric; Andrea Bauer; Joanne R. Chalmers; O. Chosidow; Finola M Delamere; Elizabeth Doney; Viktoria Eleftheriadou; Matthew J. Grainge; L. Johannsen; Jan Kottner; L. Le Cleach; Anke Mayer; M. Pinart; L. Prescott; Cecilia A.C. Prinsen; Sonia Ratib; J. G. Schlager; M. Sharma; Kim S Thomas; Tobias Weberschock; K. Weller; Ricardo Niklas Werner; Thomas Wild; Sally R. Wilkes; Hywel C. Williams

A major obstacle of evidence‐based clinical decision making is the use of nonstandardized, partly untested outcome measurement instruments. Core Outcome Sets (COSs) are currently developed in different medical fields to standardize and improve the selection of outcomes and outcome measurement instruments in clinical trials, in order to pool results of trials or to allow indirect comparison between interventions. A COS is an agreed minimum set of outcomes that should be measured and reported in all clinical trials of a specific disease or trial population. The international, multidisciplinary Cochrane Skin Group Core Outcome Set Initiative (CSG‐COUSIN) aims to develop and implement COSs in dermatology, thus making trial evidence comparable and, herewith, more useful for clinical decision making. The inaugural meeting of CSG‐COUSIN was held on 17–18 March 2015 in Dresden, Germany, as the exclusive theme of the Annual Cochrane Skin Group Meeting. In total, 29 individuals representing a broad mix of different stakeholder groups, professions, skills and perspectives attended. This report provides a description of existing COS initiatives in dermatology, highlights current methodological challenges in COS development, and presents the concept, aims and structure of CSG‐COUSIN.


Contact Dermatitis | 2011

The risk for cross-reactions after a cutaneous delayed-type hypersensitivity reaction to heparin preparations is independent of their molecular weight: a systematic review

Tobias Weberschock; Anna Christina Meister; Kevin Bohrt; Jochen Schmitt; Wolf-Henning Boehncke; Ralf J. Ludwig

Background. Heparins are a widely used class of drugs known to cause delayed‐type hypersensitivity (DTH) reactions. Recent publications indicate that the incidence of these may be higher than previously thought. To date, patient‐related but no drug‐related risk factors for the development of DTH reactions to heparins have been identified, although molecular weight is discussed as a potentially relevant parameter.

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Reinhard Strametz

Goethe University Frankfurt

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Kristian Reich

University of Göttingen

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Thomas Rosenbach

Humboldt University of Berlin

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