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  1. Book ; Thesis: Etablierung einer immunhistochemischen Methode zur Darstellung von CD25 am Paraffinschnitt und dessen Expression beim Hodgkin-Lymphom

    Rothfuß, Katja Simone

    2000  

    Author's details vorgelegt von Katja Simone Rothfuß
    Language German
    Size 94 S. : Ill., graph. Darst.
    Publishing country Germany
    Document type Book ; Thesis
    Thesis / German Habilitation thesis Köln, Univ., Diss., 2000
    HBZ-ID HT012794407
    Database Catalogue ZB MED Medicine, Health

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  2. Article ; Online: CED in Zeiten von COVID-19

    Rothfuss, Katja / Stange, Eduard

    Gastro-News

    2020  Volume 7, Issue 3, Page(s) 50–53

    Keywords covid19
    Language German
    Publisher Springer Science and Business Media LLC
    Publishing country us
    Document type Article ; Online
    ZDB-ID 2914098-5
    ISSN 2520-8667 ; 1869-1005
    ISSN (online) 2520-8667
    ISSN 1869-1005
    DOI 10.1007/s15036-020-1342-5
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  3. Article ; Conference proceedings: Behandlungssteuerung bei Patienten mit post-pankreatitischen Flüssigkeitsansammlungen: die Endosonographie als diagnostisches und therapeutisches Schlüsselinstrument

    Widmann, Annina / Meisner, Christoph / Grün, Kira / Rothfuss, Katja / Peveling-Oberhag, Jan / Lubomierski, Nikolaus / Albert, Jörg

    Ultraschall in der Medizin - European Journal of Ultrasound

    2022  Volume 43, Issue S 01

    Event/congress Interdisziplinärer Kongress | Ultraschall 2022, Zürich, 2022-06-29
    Language German
    Publishing date 2022-06-01
    Publisher Georg Thieme Verlag
    Publishing place Stuttgart ; New York
    Document type Article ; Conference proceedings
    ZDB-ID 801064-x
    ISSN 1438-8782 ; 0172-4614 ; 1439-0914 ; 1431-4894
    ISSN (online) 1438-8782
    ISSN 0172-4614 ; 1439-0914 ; 1431-4894
    DOI 10.1055/s-0042-1749487
    Database Thieme publisher's database

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  4. Article ; Online: Pneumocystis jirovecii Pneumonia in Patients with Inflammatory Bowel Disease-a Case Series.

    Vieujean, Sophie / Moens, Annick / Hassid, Deborah / Rothfuss, Katja / Savarino, Edoardo Vincenzo / Vavricka, Stephan R / Reenaers, Catherine / Jacobsen, Bent Ascanius / Allez, Matthieu / Ferrante, Marc / Rahier, Jean-Francois

    Journal of Crohn's & colitis

    2022  Volume 17, Issue 4, Page(s) 472–479

    Abstract: Background and aim: Pneumocystis jirovecii pneumonia [PJP] is a very rare, potentially life-threatening pulmonary fungal infection that occurs in immunocompromised individuals including patients with inflammatory bowel disease [IBD]. Our aim was to ... ...

    Abstract Background and aim: Pneumocystis jirovecii pneumonia [PJP] is a very rare, potentially life-threatening pulmonary fungal infection that occurs in immunocompromised individuals including patients with inflammatory bowel disease [IBD]. Our aim was to describe immunosuppressive treatment exposure as well as the outcome in IBD patients with PJP.
    Methods: PJP cases were retrospectively collected through the COllaborative Network For Exceptionally Rare case reports of the European Crohn's and Colitis Organisation. Clinical data were provided through a case report form.
    Results: In all, 18 PJP episodes were reported in 17 IBD patients [10 ulcerative colitis and seven Crohn's disease]. The median age at PJP diagnosis was 55 years (interquartile range [IQR], 40-68 years]. Two PJP [11.1%] occurred in patients on triple immunosuppression, 10 patients [55.6%] had double immunosuppressive treatment, four patients [22.2%] had monotherapy and two PJP occurred in absence of immunosuppressive treatment [one in a human immunodeficiency virus patient and one in a patient with a history of autologous stem cell transplantation]. Immunosuppressive therapies included steroids [n = 12], thiopurines [n = 10], infliximab [n = 4], ciclosporin [n = 2], methotrexate [n = 1], and tacrolimus [n = 1]. None of the patients diagnosed with PJP had received prophylaxis. All patients were treated by trimethoprim/sulphamethoxazole or atovaquone and an intensive care unit [ICU] stay was required in seven cases. Two patients [aged 71 and 32 years] died, and one patient had a recurrent episode 16 months after initial treatment. Evolution was favourable for the others.
    Conclusion: This case series reporting potentially fatal PJP highlights the need for adjusted prophylactic therapy in patients with IBD on immunosuppressive therapy.
    MeSH term(s) Humans ; Adult ; Middle Aged ; Aged ; Pneumonia, Pneumocystis/diagnosis ; Pneumonia, Pneumocystis/etiology ; Pneumonia, Pneumocystis/drug therapy ; Retrospective Studies ; Hematopoietic Stem Cell Transplantation/adverse effects ; Pneumocystis carinii ; Transplantation, Autologous/adverse effects ; Immunosuppressive Agents/adverse effects ; Inflammatory Bowel Diseases/drug therapy ; Crohn Disease/drug therapy
    Chemical Substances Immunosuppressive Agents
    Language English
    Publishing date 2022-10-11
    Publishing country England
    Document type Journal Article
    ZDB-ID 2390120-2
    ISSN 1876-4479 ; 1873-9946
    ISSN (online) 1876-4479
    ISSN 1873-9946
    DOI 10.1093/ecco-jcc/jjac153
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Book ; Thesis: Etablierung einer immunhistochemischen Methode zur Darstellung von CD25 am Paraffinschnitt und dessen Expression beim Hodgkin-Lymphom

    Rothfuß, Katja Simone

    2000  

    Author's details vorgelegt von Katja Simone Rothfuß
    Language German
    Size 94 S, Ill., graph. Darst, 21 cm
    Document type Book ; Thesis
    Thesis / German Habilitation thesis Univ., Diss--Köln, 2000
    Database Former special subject collection: coastal and deep sea fishing

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  6. Article ; Online: A urinary peptidomic profile predicts outcome in SARS-CoV-2-infected patients.

    Wendt, Ralph / Thijs, Lutgarde / Kalbitz, Sven / Mischak, Harald / Siwy, Justyna / Raad, Julia / Metzger, Jochen / Neuhaus, Barbara / Leyen, Heiko von der / Dudoignon, Emmanuel / Mebazaa, Alexandre / Spasovski, Goce / Milenkova, Mimoza / Canevska-Talevska, Aleksandra / Czerwieńska, Beata / Wiecek, Andrzej / Peters, Björn / Nilsson, Åsa / Schwab, Matthias /
    Rothfuss, Katja / Lübbert, Christoph / Staessen, Jan A / Beige, Joachim

    EClinicalMedicine

    2021  Volume 36, Page(s) 100883

    Abstract: Background: COVID-19 prediction models based on clinical characteristics, routine biochemistry and imaging, have been developed, but little is known on proteomic markers reflecting the molecular pathophysiology of disease progression.: Methods: The ... ...

    Abstract Background: COVID-19 prediction models based on clinical characteristics, routine biochemistry and imaging, have been developed, but little is known on proteomic markers reflecting the molecular pathophysiology of disease progression.
    Methods: The multicentre (six European study sites) Prospective Validation of a Proteomic Urine Test for Early and Accurate Prognosis of Critical Course Complications in Patients with SARS-CoV-2 Infection Study (Crit-COV-U) is recruiting consecutive patients (≥ 18 years) with PCR-confirmed SARS-CoV-2 infection. A urinary proteomic biomarker (COV50) developed by capillary-electrophoresis-mass spectrometry (CE-MS) technology, comprising 50 sequenced peptides and identifying the parental proteins, was evaluated in 228 patients (derivation cohort) with replication in 99 patients (validation cohort). Death and progression along the World Health Organization (WHO) Clinical Progression Scale were assessed up to 21 days after the initial PCR test. Statistical methods included logistic regression, receiver operating curve (ROC) analysis and comparison of the area under the curve (AUC).
    Findings: In the derivation cohort, 23 patients died, and 48 developed worse WHO scores. The odds ratios (OR) for death per 1 standard deviation (SD) increment in COV50 were 3·52 (95% CI, 2·02-6·13,
    Interpretation: This first CRIT-COV-U report proves the concept that urinary proteomic profiling generates biomarkers indicating adverse COVID-19 outcomes, even at an early disease stage, including WHO stages 1-3. These findings need to be consolidated in an upcoming final dataset.
    Funding: The German Federal Ministry of Health funded the study.
    Language English
    Publishing date 2021-05-03
    Publishing country England
    Document type Journal Article
    ISSN 2589-5370
    ISSN (online) 2589-5370
    DOI 10.1016/j.eclinm.2021.100883
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: Extraintestinal manifestations and complications in inflammatory bowel diseases.

    Rothfuss, Katja S / Stange, Eduard F / Herrlinger, Klaus R

    World journal of gastroenterology

    2005  Volume 12, Issue 30, Page(s) 4819–4831

    Abstract: Crohn's disease (CD) and ulcerative colitis (UC) are chronic inflammatory bowel diseases (IBD) that often involve organs other than those of the gastrointestinal tract. These nonintestinal affections are termed extraintestinal symptoms. Differentiating ... ...

    Abstract Crohn's disease (CD) and ulcerative colitis (UC) are chronic inflammatory bowel diseases (IBD) that often involve organs other than those of the gastrointestinal tract. These nonintestinal affections are termed extraintestinal symptoms. Differentiating the true extraintestinal manifestations of inflammatory bowel diseases from secondary extraintestinal complications, caused by malnutrition, chronic inflammation or side effects of therapy, may be difficult. This review concentrates on frequency, clinical presentation and therapeutic implications of extraintestinal symptoms in inflammatory bowel diseases. If possible, extraintestinal manifestations are differentiated from extraintestinal complications. Special attention is given to the more recently described sites of involvement; i.e. thromboembolic events, osteoporosis, pulmonary involvement and affection of the central nervous system.
    MeSH term(s) Biliary Tract Diseases/etiology ; Eye Diseases/etiology ; Heart Diseases/etiology ; Humans ; Inflammatory Bowel Diseases/complications ; Inflammatory Bowel Diseases/pathology ; Kidney Diseases/etiology ; Liver Diseases/etiology ; Lung Diseases/etiology ; Musculoskeletal Diseases/etiology ; Musculoskeletal Diseases/pathology ; Nervous System Diseases/etiology ; Pancreatic Diseases/etiology ; Skin Diseases/etiology ; Skin Diseases/pathology ; Thromboembolism/etiology ; Urologic Diseases/etiology
    Language English
    Publishing date 2005-07-20
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 2185929-2
    ISSN 2219-2840 ; 1007-9327
    ISSN (online) 2219-2840
    ISSN 1007-9327
    DOI 10.3748/wjg.v12.i30.4819
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Predictive performance and clinical application of COV50, a urinary proteomic biomarker in early COVID-19 infection: a cohort study

    Staessen, Jan A / Wendt, Ralph / Yu, Yu-Ling / Thijs, Lutgarde / Siwy, Justyna / Raad, Julia / Metzger, Jochen / Neuhaus, Barbara / Papkalla, Armin / von der Leyen, Heiko / Mebazaa, Alexandre / Dudoignon, Emmanual / Spasovski, Goce / Milenkova, Mimoza / Canevska-Taneska, Aleksandra / Psichogiou, Mina / Rajzer, Marke W / Fulawka, Lukasz / Dzitkowska-Zabielska, Magdalena /
    Weiss, Guenter / Feldt, Torsten / Stegemann, Miriam / Normark, Johan / Zoufaly, Alexander / Schmiedel, Stefan / Seilmaier, Michael / Rumpf, Benedikt / Banasik, Miroslaw / Krajewska, Magdalena / Catanese, Lorenzo / Rupprecht, Harald / Czerwienska, Beata / Peters, Bjoern / Nilsson, Asa / Rothfuss, Katja / Luebbert, Christoph / Mischak, Harald / Beige, Joachim

    medRxiv

    Abstract: Background The SARS CoV-2 pandemic remains a worldwide challenge. The CRIT Cov U pilot study generated a urinary proteomic biomarker consisting of 50 peptides (COV50), which predicted death and disease progression. Following the interim analysis demanded ...

    Abstract Background The SARS CoV-2 pandemic remains a worldwide challenge. The CRIT Cov U pilot study generated a urinary proteomic biomarker consisting of 50 peptides (COV50), which predicted death and disease progression. Following the interim analysis demanded by the German government, the full dataset was analysed to consolidate findings and propose clinical applications. Methods In eight European countries, 1012 adults with PCR-confirmed COVID-19 were followed up for death and progression along the 8 point WHO scale. Capillary electrophoresis coupled with mass spectrometry was used for urinary proteomic profiling. Statistical methods included logistic regression, receiver operating curve analysis with comparison of the area under curve (AUC) between nested models. Hospitalisation costs were derived from the care facility corresponding with the Markov chain probability of reaching WHO scores ranging from 3 to 8 and flat-rate hospitalistion costs standardised across countries. Findings The entry WHO scores were 1-3, 4-5 and 6 in 445 (44,0%), 529 (52,3%), and 38 (3,8%) patients, of whom 119 died and 271 progressed. The standardised odds ratios associated with COV50 for death were 2,44 (95% CI, 2,05-2,92) unadjusted and 1,67 (1,34-2,07) if adjusted for sex, age, body mass index, comorbidities and baseline WHO score, and 1,79 (1,60-2,01) and 1,63 (1,40-1,90), respectively, for disease progression (p<0,0001 for all). The predictive accuracy of optimised COV50 thresholds were 74,4% (95% CI, 71,6-77,1) for mortality (threshold 0,47) and 67,4% (64,1-70,3) for disease progression (threshold 0,04). On top of covariables and the baseline WHO score, these thresholds improved AUCs from 0,835 to 0,853 (p=0,0331) and from 0,697 to 0,730 (p=0,0008) for death and progression, respectively. Of 196 ambulatory patients, 194 (99,0%) did not reach the 0,04 threshold. Earlier intervention guided by high-risk COV50 levels should reduce hospital days with cost reductions expressed per 1000 patient-days ranging from MEuro 1,208 (95% percentile interval, 1,035-1,406) at low risk (COV50 <0,04) to MEuro 4,503 (4,107-4,864) at high risk (COV50 above 0,04 and age above 65 years). Interpretation The urinary proteomic COV50 marker is accurate in predicting adverse COVID-19 outcomes. Even in mild-to-moderate PCR-confirmed infections (WHO scores 1-5), the 0,04 threshold justifies earlier drug treatment, thereby reducing hospitalisation days and costs.
    Keywords covid19
    Language English
    Publishing date 2022-01-23
    Publisher Cold Spring Harbor Laboratory Press
    Document type Article ; Online
    DOI 10.1101/2022.01.20.22269599
    Database COVID19

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  9. Article ; Online: Predictive performance and clinical application of COV50, a urinary proteomic biomarker in early COVID-19 infection: a prospective multicentre cohort study.

    Staessen, Jan A / Wendt, Ralph / Yu, Yu-Ling / Kalbitz, Sven / Thijs, Lutgarde / Siwy, Justyna / Raad, Julia / Metzger, Jochen / Neuhaus, Barbara / Papkalla, Armin / von der Leyen, Heiko / Mebazaa, Alexandre / Dudoignon, Emmanuel / Spasovski, Goce / Milenkova, Mimoza / Canevska-Taneska, Aleksandra / Salgueira Lazo, Mercedes / Psichogiou, Mina / Rajzer, Marek W /
    Fuławka, Łukasz / Dzitkowska-Zabielska, Magdalena / Weiss, Guenter / Feldt, Torsten / Stegemann, Miriam / Normark, Johan / Zoufaly, Alexander / Schmiedel, Stefan / Seilmaier, Michael / Rumpf, Benedikt / Banasik, Mirosław / Krajewska, Magdalena / Catanese, Lorenzo / Rupprecht, Harald D / Czerwieńska, Beata / Peters, Björn / Nilsson, Åsa / Rothfuss, Katja / Lübbert, Christoph / Mischak, Harald / Beige, Joachim

    The Lancet. Digital health

    2022  Volume 4, Issue 10, Page(s) e727–e737

    Abstract: Background: The SARS-CoV-2 pandemic is a worldwide challenge. The CRIT-CoV-U pilot study generated a urinary proteomic biomarker consisting of 50 peptides (COV50), which predicted death and disease progression from SARS-CoV-2. After the interim analysis ...

    Abstract Background: The SARS-CoV-2 pandemic is a worldwide challenge. The CRIT-CoV-U pilot study generated a urinary proteomic biomarker consisting of 50 peptides (COV50), which predicted death and disease progression from SARS-CoV-2. After the interim analysis presented for the German Government, here, we aimed to analyse the full dataset to consolidate the findings and propose potential clinical applications of this biomarker.
    Methods: CRIT-CoV-U was a prospective multicentre cohort study. In eight European countries (Austria, France, Germany, Greece, North Macedonia, Poland, Spain, and Sweden), 1012 adults with PCR-confirmed COVID-19 were followed up for death and progression along the 8-point WHO scale. Capillary electrophoresis coupled with mass spectrometry was used for urinary proteomic profiling. Statistical methods included logistic regression and receiver operating characteristic curve analysis with a comparison of the area under curve (AUC) between nested models. Hospitalisation costs were derived from the care facility corresponding with the Markov chain probability of reaching WHO scores ranging from 3 to 8 and flat-rate hospitalisation costs adjusted for the gross per capita domestic product of each country.
    Findings: From June 30 to Nov 19, 2020, 228 participants were recruited, and from April 30, 2020, to April 14, 2021, 784 participants were recruited, resulting in a total of 1012 participants. The entry WHO scores were 1-3 in 445 (44%) participants, 4-5 in 529 (52%) participants, and 6 in 38 (4%) participants; and of all participants, 119 died and 271 had disease progression. The odds ratio (OR) associated with COV50 in all 1012 participants for death was 2·44 (95% CI 2·05-2·92) unadjusted and 1·67 (1·34-2·07) when adjusted for sex, age, BMI, comorbidities, and baseline WHO score; and for disease progression, the OR was 1·79 (1·60-2·01) when unadjusted and 1·63 (1·41-1·91) when adjusted (p<0·0001 for all). The predictive accuracy of the optimised COV50 thresholds was 74·4% (71·6-77·1%) for mortality (threshold 0·47) and 67·4% (64·4-70·3%) for disease progression (threshold 0·04). When adjusted for covariables and the baseline WHO score, these thresholds improved AUCs from 0·835 to 0·853 (p=0·033) for death and from 0·697 to 0·730 (p=0·0008) for progression. Of 196 participants who received ambulatory care, 194 (99%) did not reach the 0·04 threshold. The cost reductions associated with 1 day less hospitalisation per 1000 participants were million Euro (M€) 0·887 (5-95% percentile interval 0·730-1·039) in participants at a low risk (COV50 <0·04) and M€2·098 (1·839-2·365) in participants at a high risk (COV50 ≥0·04).
    Interpretation: The urinary proteomic COV50 marker might be predictive of adverse COVID-19 outcomes. Even in people with mild-to-moderate PCR-confirmed infections (WHO scores 1-4), the 0·04 COV50 threshold justifies earlier drug treatment, thereby potentially reducing the number of days in hospital and associated costs.
    Funding: German Federal Ministry of Health.
    MeSH term(s) Adult ; Biomarkers ; COVID-19/diagnosis ; Cohort Studies ; Disease Progression ; Humans ; Pilot Projects ; Prospective Studies ; Proteomics ; SARS-CoV-2
    Chemical Substances Biomarkers
    Language English
    Publishing date 2022-08-31
    Publishing country England
    Document type Journal Article ; Multicenter Study ; Research Support, Non-U.S. Gov't
    ISSN 2589-7500
    ISSN (online) 2589-7500
    DOI 10.1016/S2589-7500(22)00150-9
    Database MEDical Literature Analysis and Retrieval System OnLINE

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