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2022

Associations between health literacy and shared decision making for psoriasis systemic treatment: Patients’ and physicians’ perspectives

N. da Silva, M. Augustin, S. Pohl, J. Traxler, R. Sommer (2022, October)

Poster presented at the DKVF Conference, Potsdam, Germany 

Parents with Asthmatic Children, Quality of Life

C. Crespo1, N. da Silva1,2 

1Faculty of Psychology and Educational Sciences, University of Coimbra, Coimbra, Portugal

2 University Medical Center Hamburg-Eppendorf (UKE), Hamburg, Germany

Encyclopedia entry: Encyclopedia of Quality of Life and Well-Being Research

Psychological (co)morbidity in patients with psoriasis: the impact of pruritus and anogenital involvement on symptoms of depression and anxiety and on body dysmorphic concerns – a cross-sectional study

N. da Silva1, M. Augustin1, C. Hilbring1, C.C. Braren-von Stülpnagel1, R. Sommer1

1 Institute for Health Services Research in Dermatology and Nursing (IVDP), University Medical Center Hamburg-Eppendorf (UKE), Hamburg, Germany

Objectives While stress plays a paramount role on the onset/exacerbation of psoriasis, via overactivation of the hypothalamic–pituitary–adrenal axis and increased release of pro-inflammatory cytokines, cutaneous inflammatory response induces, in turn, anxiety/depression symptoms, via body disfigurement and stigmatisation. The intensity of pruritus and anogenital involvement are additional risk factors for psychological comorbidity.Aims were to (1) examine the effects of intensity of pruritus and anogenital psoriasis on disease burden and psychological comorbidity and (2) identify the variables associated with the presence of clinically significant depression, anxiety, and dysmorphic concerns.

Design Cross-sectional study.

Setting Conducted at the University Medical Center Hamburg-Eppendorf (UKE).

Participants 107 patients with psoriasis (mean age = 46.3, SD = 14.6 years; 53.3% male): 64 with none/mild pruritus; 43 with moderate/severe pruritus; 31 with anogenital psoriasis; 76 not affected in the anogenital area.

Primary/secondary outcomes measures Disease severity was assessed with Psoriasis Area and Severity Index and intensity of pruritus was rated by patients. Patient-reported outcomes included the Dermatology Life Quality Index, ItchyQoL, Patient Benefit Index, Perceived Stigmatisation Questionnaire, and Relationship and Sexuality Scale. Psychological morbidity was assessed with the Patient Health Questionnaire, Generalised Anxiety Disorder, and Dysmorphic Concern Questionnaire.

Results Patients with moderate/severe pruritus reported more quality of life impairments, depression, anxiety and dysmorphic concerns, and less treatment benefits than those with none/mild pruritus. Moderate/severe pruritus had a deleterious effect on depression and stigmatisation for patients without anogenital involvement. Less patient benefits were associated with a higher likelihood of clinically significant depression/anxiety.

Conclusion Pruritus induces significant burden and psychological morbidity, particularly for patients without anogenital involvement. However, coping strategies used by patients with anogenital psoriasis might be dysfunctional for overall psychosocial adaptation. Patient-centred healthcare might be the best way to prevent psychological comorbidity.

Measuring wellbeing in psoriasis: Psychometric properties of the WHO-5 questionnaire

R. Sommer, L. Westphal, U. Mrowietz, S. Gerdes, M. Augustin (2022, September)

ePoster presented at 31st European Academy of Dermatology and Venereology (EADV) Congress

Is Social Stigma Responsible for the Poor Psychological Adjustment of People with Visible Skin Disease? A Meta-Analysis

CFZ. Stuhlmann, S. Lysakova, C. Jordan, TA. Revenson (2022, April)

Poster preseted at the Society of Behavioral Medicine, Baltimore, MD.

Developments in quality of life assessment in children with dermatological conditions: Validation protocol for the German version of the InToDermQoL

J. Traxler, N. da Silva, M. Augustin, R. Fölster-Holst, R. Sommer (2022, October)

Poster presented at the DKVF Conference, Potsdam, Germany 

Development and validation of an outcome instrument measuring dry skin - the Xerosis Area and Severity Index (XASI).

R. Sommer1, M. Augustin1, N. da Silva1, C.C. von Stülpnagel1

1Institute for Health Services Research in Dermatology and Nursing (IVDP), University Medical Center Hamburg-Eppendorf (UKE), Hamburg, Germany

J Eur Acad Dermatol Venereol. 2022 Jan;36(1):e70-e72

 

The aim of this study was the development and validation of a composite measuring instrument for the assessment of the extent (surface area affected) and severity of xerosis in clinical practice and research.

Psychometric properties of the short version of the Freiburg Life Quality Assessment for chronic venous disease

T.M. Klein1, B. Bal2, A.L. Newi2, G. Bruning3, R. Sommer2, M. Augustin2, C. Blome2

1Institute for Health Services Research in Dermatology and Nursing, University Medical Center Hamburg-Eppendorf, Hamburg, Germany. Electronic address: t.klein@uke.de

2Institute for Health Services Research in Dermatology and Nursing, University Medical Center Hamburg-Eppendorf, Hamburg, Germany

3Institute for Scientific Phlebology, Krankenhaus Tabea, Hamburg, Germany

J Vasc Surg Venous Lymphat Disord. 2022 Jan;10(1):139-145.e1

 

Chronic venous disease is a frequent vascular condition. International societies have recommended the use of health-related quality of life (HRQoL) instruments in the assessment of patients with vascular diseases. Thus, the Freiburg Life Quality Assessment for chronic venous disease, 10-item questionnaire (FLQA-VS-10) was developed. The aim of the present study was to validate the FLQA-VS-10 in a prospective study.

Measuring Well-being in Psoriasis: Psychometric Properties of the WHO-5 Questionnaire

R. Sommer1, L. Westphal1, U. Mrowietz2, S. Gerdes2, M. Augustin1

Institute for Health Services Research in Dermatology and Nursing (IVDP), University Medical Center Hamburg-Eppendorf (UKE), Hamburg, Germany

Psoriasis-Center Kiel, Department of Dermatology, University Medical Center Schleswig-Holstein, Kiel, Germany

According to the definition of the World Health Organization, health is not only understood as the absence of disease, but also as the restoration of full physical, mental and social well-being. Therefore, in the management of psoriatic disease, well-being should be included as an important endpoint. So far, primarily burden-focused patient-reported outcome instruments such as the Dermatology Life Quality Index (DLQI) are used in practice and research, many showing marked limitations. Thus, the aim of this study was to test the psychometric properties of the generic WHO-5 questionnaire for the assessment of well-being in people with psoriasis.

Destigmatization of people with skin diseases in body care professions – a study protocol

J. Traxler, M. Augustin, M. Grosser, R. Sommer (2022, October)

Poster presented at the DKVF Conference, Potsdam, Germany