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  1. AU="Koch, Cornelia"
  2. AU="Białecki, Piotr"
  3. AU="Taylor, Maureen E"
  4. AU="Karpov, M."
  5. AU="Vogel Gonzalez, M"
  6. AU="Montevecchi, William A"
  7. AU="Vanhoni, Laura Rassi"
  8. AU="Atkins, Kristen A"
  9. AU="Sun, Zhenyu J"
  10. AU="Boton, Noah H"
  11. AU=Anderson Claire
  12. AU="Pielmus, Alexandru-Gabriel"
  13. AU="Neacsu, Ionela Andreea"
  14. AU=Keller Ray
  15. AU="Gopas, Jacob"
  16. AU="Berthelson, P R"
  17. AU="Rivera-Torres, Juan J"
  18. AU="Henriquez, Javier"
  19. AU="Adele N Burgess"
  20. AU="Spencer T. Plumb"

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  1. Buch ; Online ; Dissertation / Habilitation: Etablierung eines Verfahrens zur Kryokonservierung einzelner Spermatozoen

    Koch, Cornelia [Verfasser]

    2016  

    Verfasserangabe Cornelia Koch
    Schlagwörter Medizin, Gesundheit ; Medicine, Health
    Thema/Rubrik (Code) sg610
    Sprache Deutsch
    Verlag Universitäts- und Landesbibliothek Bonn
    Erscheinungsort Bonn
    Dokumenttyp Buch ; Online ; Dissertation / Habilitation
    Datenquelle Digitale Dissertationen im Internet

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  2. Buch ; Online ; Dissertation / Habilitation: Annahmeverzug des Arbeitgebers während des Kündigungsschutzprozesses

    Koch, Cornelia

    Möglichkeiten zur Risikominimierung

    2007  

    Verfasserangabe vorgelegt von Cornelia Koch
    Sprache Englisch
    Umfang Online-Ressource (PDF-Datei: XXVI, 168 S., 1.750 KB)
    Verlag Universitätsbibliothek
    Erscheinungsort Konstanz
    Dokumenttyp Buch ; Online ; Dissertation / Habilitation
    Dissertation / Habilitation Univ. , Diss.--Konstanz, 2007
    Datenquelle Ehemaliges Sondersammelgebiet Küsten- und Hochseefischerei

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  3. Artikel ; Online: Outcomes with sacubitril/valsartan in outpatients with heart failure and reduced ejection fraction: The ARIADNE registry.

    Maggioni, Aldo P / Clark, Andrew L / Barrios, Vivencio / Damy, Thibaud / Drozdz, Jaroslaw / Fonseca, Candida / Lund, Lars H / Kalus, Stefanie / Ferber, Philippe C / Hussain, Rizwan I / Koch, Cornelia / Zeymer, Uwe

    ESC heart failure

    2022  

    Abstract: Aims: ARIADNE aimed to assess the association between effects of sacubitril/valsartan and no sacubitril/valsartan treatment and clinical characteristics, functional capacity, and clinical outcomes (cause-specific mortality and hospitalizations) in ... ...

    Abstract Aims: ARIADNE aimed to assess the association between effects of sacubitril/valsartan and no sacubitril/valsartan treatment and clinical characteristics, functional capacity, and clinical outcomes (cause-specific mortality and hospitalizations) in outpatients with heart failure (HF) with reduced ejection fraction (HFrEF).
    Methods: ARIADNE was a prospective European registry of 9069 patients with HFrEF treated by office-based cardiologists or selected primary care physicians. Of the 8787 eligible for analysis, 4173 patients were on conventional HF treatment (non-S/V group), whereas 4614 patients were either on sacubitril/valsartan treatment at enrolment or started sacubitril/valsartan within 1 month of enrolment (S/V group). We also generated a restricted analysis set (rS/V) including only those 2108 patients who started sacubitril/valsartan treatment within the month prior to or after enrolment.
    Results: At the baseline, average age of patients enrolled in the study was 68 years, and 23.9% (2099/8787) were female. At the baseline, the proportions of patients with New York Heart Association (NYHA) Class III symptoms were 30.9 (1288/4173), 42.8 (1974/4614), and 48.2% (1015/2108), in non-S/V, S/V, and rS/V groups, respectively. After 12 months of treatment, the proportion of patients with NYHA Class III at baseline who improved to Class II was 32.0% (290/907) in the non-S/V group vs. 46.3% (648/1399) in S/V group and 48.7% (349/717) in rS/V group. The overall mortality rate was 5.0 per 100 patient-years. Rates of HF hospitalizations were high (20.9, 20.3, and 21.2 per 100 patient-years in the non-S/V, S/V, and rS/V groups, respectively). Emergency room visits without hospitalization occurred in 3.9, 3.2, and 3.9% of patients in the non-S/V, S/V, and rS/V groups, respectively.
    Conclusions: This large HFrEF European registry provides a contemporary outcome profile of outpatients with HFrEF treated with or without sacubitril/valsartan. In a real-world setting, sacubitril/valsartan was associated with an improvement of symptoms in patients with HFrEF compared with the conventional HFrEF treatment.
    Sprache Englisch
    Erscheinungsdatum 2022-09-15
    Erscheinungsland England
    Dokumenttyp Journal Article
    ZDB-ID 2814355-3
    ISSN 2055-5822 ; 2055-5822
    ISSN (online) 2055-5822
    ISSN 2055-5822
    DOI 10.1002/ehf2.14014
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  4. Artikel ; Online: Association between sacubitril/valsartan initiation and changes in left ventricular ejection fraction: Insights from ARIADNE registry.

    Lund, Lars H / Zeymer, Uwe / Clark, Andrew L / Barrios, Vivencio / Damy, Thibaud / Drożdż, Jaroslaw / Fonseca, Candida / Kalus, Stefanie / Ferber, Philippe C / Koch, Cornelia / Maggioni, Aldo P

    International journal of cardiology

    2022  Band 370, Seite(n) 279–286

    Abstract: Aims: We tested the hypothesis that initiation versus non-initiation of sacubitril/valsartan is associated with a more favorable subsequent change in left ventricular ejection fraction (LVEF) in a real-world setting.: Methods: A prospective, non- ... ...

    Abstract Aims: We tested the hypothesis that initiation versus non-initiation of sacubitril/valsartan is associated with a more favorable subsequent change in left ventricular ejection fraction (LVEF) in a real-world setting.
    Methods: A prospective, non-randomized, double-arm, open-label, cohort study had been conducted across 687 centers in 17 European countries enrolling HFrEF patients aged ≥18 years with symptoms of HF (New York Heart Association [NYHA] II-IV) and "reduced LVEF". For the current analysis, 2602 patients with LVEF measured at baseline and follow-up were chosen, of which 860 (33%, mean age 67 years, 26% women) were started on sacubitril/valsartan at baseline and 1742 (67%, 68 years, 23% women) were not. Patients started on sacubitril/valsartan had higher NYHA class and lower LVEF.
    Results: LVEF increased from mean 32.7% to 38.1% in the sacubitril/valsartan group versus from 35.9% to 38.7% in the non-sacubitril/valsartan group (mean difference in increase 2.6%, p < 0.001). LVEF increased from baseline in 64% versus 53% of patients and increased by ≥5% (absolute %) in 50% versus 35% of patients in the sacubitril/valsartan versus non-sacubitril/valsartan groups, respectively. In the overall cohort, initiation of sacubitril/valsartan was independently associated with any increase in LVEF (adjusted odds ratio [OR] 1.49 [1.26-1.75]) and with increase by ≥5% (OR 1.65 [1.39-1.95]).
    Conclusion: Initiating versus not initiating sacubitril/valsartan was independently associated with a greater subsequent increase in LVEF in this real-world setting. Reverse cardiac remodeling may be one mechanism of benefit of sacubitril/valsartan.
    Sprache Englisch
    Erscheinungsdatum 2022-10-07
    Erscheinungsland Netherlands
    Dokumenttyp Journal Article
    ZDB-ID 779519-1
    ISSN 1874-1754 ; 0167-5273
    ISSN (online) 1874-1754
    ISSN 0167-5273
    DOI 10.1016/j.ijcard.2022.10.012
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  5. Artikel ; Online: Vildagliptin versus insulin in patients with type 2 diabetes mellitus inadequately controlled with sulfonylurea: results from a randomized, 24 week study.

    Forst, Thomas / Koch, Cornelia / Dworak, Markus

    Current medical research and opinion

    2015  Band 31, Heft 6, Seite(n) 1079–1084

    Abstract: Objective: There is limited evidence to guide the selection of second-line anti-hyperglycemic agents in patients with type 2 diabetes mellitus (T2DM) who are inadequately controlled with sulfonylurea monotherapy and are intolerant to metformin. We ... ...

    Abstract Objective: There is limited evidence to guide the selection of second-line anti-hyperglycemic agents in patients with type 2 diabetes mellitus (T2DM) who are inadequately controlled with sulfonylurea monotherapy and are intolerant to metformin. We compared the efficacy and safety of vildagliptin 50 mg qd and Neutral Protamine Hagedorn (NPH) insulin qd in such patients.
    Methods: This was a 24 week, multicenter, randomized, open-label study. The co-primary endpoints were (i) proportion of patients achieving HbA1c <7.0% without any confirmed hypoglycemic events (HEs) or weight gain ≥3% (composite endpoint); (ii) rate of confirmed HEs. Treatment satisfaction was assessed using the TSQM-9 questionnaire at study end.
    Results: A total of 162 patients were randomly assigned to vildagliptin (n = 83) and NPH insulin (n = 79). Similar proportion of patients achieved the composite endpoint in vildagliptin versus NPH insulin group (35.4% versus 34.2%; OR 0.985; 95% CI 0.507, 1.915; p = 0.96). After 24 weeks, 48.8% of patients in the vildagliptin group and 60.8% in the NPH insulin group achieved HbA1c <7.0%; 13.4% in the vildagliptin group and 29.1% in the insulin group had at least one confirmed HE; while 11.0% in the vildagliptin group and 22.8% in the insulin group experienced weight gain. The rate of confirmed HEs was significantly lower in patients receiving vildagliptin versus NPH insulin (1.3 versus 5.1 events per year). The TSQM-9 score for 'convenience' at week 24 increased significantly more with vildagliptin than with NPH insulin.
    Conclusions: Addition of vildagliptin and NPH insulin resulted in a similar number of patients reaching HbA1c target without HEs or weight gain in T2DM patients inadequately controlled with sulfonylurea. The addition of vildagliptin to sulfonylurea could be considered as a treatment option prior to intensification with insulin, with the advantages of a lower HE rate and greater patient convenience. Study results are limited by a higher drop-out rate in the vildagliptin arm.
    Mesh-Begriff(e) Adamantane/analogs & derivatives ; Adamantane/therapeutic use ; Adult ; Diabetes Mellitus, Type 2/drug therapy ; Female ; Humans ; Hypoglycemic Agents/therapeutic use ; Insulin, Isophane/therapeutic use ; Male ; Middle Aged ; Nitriles/therapeutic use ; Pyrrolidines/therapeutic use ; Sulfonylurea Compounds/therapeutic use ; Weight Gain/drug effects
    Chemische Substanzen Hypoglycemic Agents ; Nitriles ; Pyrrolidines ; Sulfonylurea Compounds ; Insulin, Isophane (53027-39-7) ; vildagliptin (I6B4B2U96P) ; Adamantane (PJY633525U)
    Sprache Englisch
    Erscheinungsdatum 2015-06
    Erscheinungsland England
    Dokumenttyp Comparative Study ; Journal Article ; Multicenter Study ; Randomized Controlled Trial ; Research Support, Non-U.S. Gov't
    ZDB-ID 80296-7
    ISSN 1473-4877 ; 0300-7995
    ISSN (online) 1473-4877
    ISSN 0300-7995
    DOI 10.1185/03007995.2015.1039936
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  6. Artikel ; Online: Individualised treatment targets in patients with type-2 diabetes and hypertension.

    Schmieder, Roland E / Tschöpe, Diethelm / Koch, Cornelia / Ouarrak, Taoufik / Gitt, Anselm K

    Cardiovascular diabetology

    2018  Band 17, Heft 1, Seite(n) 18

    Abstract: Aim: Patients with type-2 diabetes mellitus (T2DM) are at high risk of cardiovascular events, accentuated in the presence of hypertension. At present, it is unclear to what extent the guidelines for the management of T2DM, advocating reduction in HbA1c ... ...

    Abstract Aim: Patients with type-2 diabetes mellitus (T2DM) are at high risk of cardiovascular events, accentuated in the presence of hypertension. At present, it is unclear to what extent the guidelines for the management of T2DM, advocating reduction in HbA1c levels to below target levels, are being adhered to in clinical practice.
    Methods: DIALOGUE was a prospective, observational, non-interventional registry performed across multiple centres in Germany. Patients aged 18 years or older who had T2DM and hypertension for whom the treating physician considered blood glucose lowering medication as inadequate and/or not safe/tolerable and chose to add a further oral drug or switch drug treatment were included. Patients were assigned a treatment target HbA1c value (≤ 6.5% [strict]; > 6.5 to ≤ 7.0% [intermediate]; > 7.0 to ≤ 7.5% [lenient]).
    Results: 8568 patients with T2DM and hypertension were enrolled. 6691 (78.1%) had 12-month follow-up. Patients who were assigned a strict HbA1c treatment target (n = 2644) were younger, had shorter diabetes duration, and less comorbidity in comparison to those with intermediate (n = 2912) or lenient targets (n = 1135). Only 53.1% of patients achieved their HbA1c treatment target (46.2% [strict], 56.8% [intermediate], 59.4% [lenient]). There was little sign of treatment intensification for patients that had not achieved their HbA1c target.
    Conclusions: Achievement of treatment targets was poor, leaving many patients with sub-optimal blood glucose levels. The apparent reluctance of physicians to intensify antidiabetic drug therapy is alarming, especially considering the evidence pointing to an association of hyperglycaemia and microvascular complications in patients with T2DM.
    Mesh-Begriff(e) Aged ; Biomarkers/blood ; Blood Glucose/drug effects ; Blood Glucose/metabolism ; Blood Pressure ; Clinical Decision-Making ; Comorbidity ; Diabetes Mellitus, Type 2/blood ; Diabetes Mellitus, Type 2/diagnosis ; Diabetes Mellitus, Type 2/drug therapy ; Diabetes Mellitus, Type 2/epidemiology ; Drug Substitution ; Drug Therapy, Combination ; Female ; Germany/epidemiology ; Glycated Hemoglobin A/metabolism ; Guideline Adherence ; Humans ; Hypertension/diagnosis ; Hypertension/epidemiology ; Hypertension/physiopathology ; Hypoglycemic Agents/administration & dosage ; Hypoglycemic Agents/adverse effects ; Male ; Middle Aged ; Practice Guidelines as Topic ; Practice Patterns, Physicians' ; Prospective Studies ; Registries ; Risk Factors ; Time Factors ; Treatment Outcome
    Chemische Substanzen Biomarkers ; Blood Glucose ; Glycated Hemoglobin A ; Hypoglycemic Agents ; hemoglobin A1c protein, human
    Sprache Englisch
    Erscheinungsdatum 2018-01-22
    Erscheinungsland England
    Dokumenttyp Journal Article ; Multicenter Study ; Observational Study ; Research Support, Non-U.S. Gov't
    ISSN 1475-2840
    ISSN (online) 1475-2840
    DOI 10.1186/s12933-018-0661-8
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  7. Buch ; Online ; Dissertation / Habilitation: Annahmeverzug des Arbeitgebers während des Kündigungsschutzprozesses

    Koch, Cornelia [Verfasser]

    Möglichkeiten zur Risikominimierung

    2007  

    Verfasserangabe vorgelegt von Cornelia Koch
    Schlagwörter Recht ; Law
    Thema/Rubrik (Code) sg340
    Sprache Englisch
    Dokumenttyp Buch ; Online ; Dissertation / Habilitation
    Datenquelle Digitale Dissertationen im Internet

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  8. Artikel ; Online: Utilization of sacubitril/valsartan in patients with heart failure with reduced ejection fraction: real-world data from the ARIADNE registry.

    Zeymer, Uwe / Clark, Andrew L / Barrios, Vivencio / Damy, Thibaud / Drożdż, Jaroslaw / Fonseca, Candida / Lund, Lars H / Kalus, Stefanie / Ferber, Philippe C / Hussain, Rizwan I / Koch, Cornelia / Maggioni, Aldo P

    European heart journal. Quality of care & clinical outcomes

    2021  Band 8, Heft 4, Seite(n) 469–477

    Abstract: Aims: To compare baseline characteristics of patients with heart failure with reduced ejection fraction (HFrEF) initiated on sacubitril/valsartan compared with patients continued on conventional heart failure (HF)-treatment in a European out-patient ... ...

    Abstract Aims: To compare baseline characteristics of patients with heart failure with reduced ejection fraction (HFrEF) initiated on sacubitril/valsartan compared with patients continued on conventional heart failure (HF)-treatment in a European out-patient setting.
    Methods and results: Between July 2016 and July 2019, ARIADNE enrolled 8787 outpatients aged ≥18 years with HFrEF from 17 European countries. Choice of therapy was solely at the investigators' discretion. In total, 4173 patients were on conventional HF-treatment (non-S/V group), while 4614 patients were on sacubitril/valsartan either at enrolment or started sacubitril/valsartan within 1 month of enrolment (S/V group). Of these, 2108 patients started sacubitril/valsartan treatment ±1 month around enrolment [restricted S/V (rS/V) group]. The average age of the patients was 68 years. Patients on S/V were more likely to have New York Heart Association (NYHA) class III or IV symptoms (50.3%, 44.6%, 32.1% in rS/V, S/V, and non-S/V, respectively) and had lower left ventricular ejection fraction (LVEF; 32.3%, 32.7%, and 35.4% in rS/V, S/V, and non-S/V, respectively; P < 0.0001). The most frequently received HF treatments were angiotensin-converting enzyme inhibitor/angiotensin receptor blocker (ACEI/ARB; ∼84% in non-S/V), followed by β-blockers (∼80%) and mineralocorticoid receptor antagonists (MRAs; 53%). The use of triple HF therapy (ACEI/ARB/angiotensin receptor neprilysin inhibitor with β-blockers and MRA) was higher in the S/V groups than non-S/V group (48.2%, 48.2%, and 40.2% in rS/V, S/V, and non-S/V, respectively).
    Conclusion: In this large multinational HFrEF registry, patients receiving sacubitril/valsartan tended to be younger with lower LVEF and higher NYHA class. Fewer than half of the patients received triple HF therapy.
    Mesh-Begriff(e) Adolescent ; Adult ; Aged ; Aminobutyrates/therapeutic use ; Angiotensin Receptor Antagonists/therapeutic use ; Angiotensin-Converting Enzyme Inhibitors ; Biphenyl Compounds ; Heart Failure/drug therapy ; Heart Failure/epidemiology ; Humans ; Registries ; Stroke Volume ; Tetrazoles/therapeutic use ; Treatment Outcome ; Valsartan ; Ventricular Dysfunction, Left ; Ventricular Function, Left
    Chemische Substanzen Aminobutyrates ; Angiotensin Receptor Antagonists ; Angiotensin-Converting Enzyme Inhibitors ; Biphenyl Compounds ; Tetrazoles ; sacubitril (17ERJ0MKGI) ; Valsartan (80M03YXJ7I)
    Sprache Englisch
    Erscheinungsdatum 2021-03-15
    Erscheinungsland England
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2823451-0
    ISSN 2058-1742 ; 2058-5225
    ISSN (online) 2058-1742
    ISSN 2058-5225
    DOI 10.1093/ehjqcco/qcab019
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  9. Buch ; Dissertation / Habilitation: Untersuchungen zur prognostischen Aussage der Serumproteinfraktionen erkrankter junger Kälber

    Koch, Cornelia Christina

    2005  

    Verfasserangabe von Cornelia Christina Koch
    Sprache Deutsch
    Umfang 101 S, graph. Darst, 21 cm
    Dokumenttyp Buch ; Dissertation / Habilitation
    Dissertation / Habilitation Univ., Diss.--München, 2005
    Anmerkung Zusfassung in dt. und engl. Sprache
    Datenquelle Friedrich Loeffler-Institut, Bundesforschungsinstitut für Tiergesundheit

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  10. Buch ; Dissertation / Habilitation: Untersuchungen zur prognostischen Aussage der Serumproteinfraktionen erkrankter junger Kälber

    Koch, Cornelia Christina

    2005  

    Verfasserangabe von Cornelia Christina Koch
    Sprache Deutsch
    Umfang 101 S, graph. Darst, 21 cm
    Dokumenttyp Buch ; Dissertation / Habilitation
    Dissertation / Habilitation Univ., Diss.--München, 2005
    Anmerkung Zusfassung in dt. und engl. Sprache
    Datenquelle Ehemaliges Sondersammelgebiet Küsten- und Hochseefischerei

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