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    <subfield code="a">10.3390/jcm10225446</subfield>
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  <datafield tag="100" ind1=" " ind2=" ">
    <subfield code="a">Krajewski, P.K.</subfield>
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  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">The use of HSQoL-24 in an assessment of quality-of-life impairment among hidradenitis suppurativa patients: First look at real-life data</subfield>
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    <subfield code="c">2021</subfield>
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    <subfield code="a">Hidradenitis suppurativa (HS) is a chronic inflammatory skin disorder with well-documented effects on patients’ quality of life (QoL). The aim of this study was to evaluate the QoL of patients with HS via the use of a newly developed questionnaire: Hidradenitis Suppurativa Quality of Life-24 (HSQoL-24). This study was performed on a population of 342 HS patients. Their QoL was assessed via the HSQoL-24 questionnaire. The perceived impairment of QoL due to HS in the studied group was considered to be serious (mean HSQoL-24 score: 58.3 ± 21.0 points). Women tended to experience a significantly higher impact from the disease than men (61.6 ± 19.2 points vs. 51.1 ± 23.1 points, p &lt; 0.001). The HS severity had an effect on the perceived QoL, with statistically significant differences being evident between the self-assessed HS severity groups. The level of QoL impairment correlated positively with the number of affected body areas (r = 0.285, p &lt; 0.001) and the duration of the disease (r = 0.173, p = 0.001), while the patients’ age at disease onset correlated negatively with the HSQoL-24 global score (r = -0.182, p = 0.001). Patients living in their family house scored higher than other groups. The least affected were patients who lived alone. The study shows that the HSQoL-24 questionnaire is a reliable, HS-specific tool for measuring the QoL among patients with HS in real-life clinical settings. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.</subfield>
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    <subfield code="a">Medicine (miscellaneous)</subfield>
    <subfield code="c">2021</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Marrón, S.E.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0001-5632-0351</subfield>
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    <subfield code="a">Gomez-Barrera, M.</subfield>
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    <subfield code="a">Tomas-Aragones, L.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0003-1917-6906</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Gilaberte-Calzada, Y.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0001-8034-3617</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Szepietowski, J.C.</subfield>
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  <datafield tag="710" ind1="2" ind2=" ">
    <subfield code="1">4009</subfield>
    <subfield code="2">735</subfield>
    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Psicología y Sociología</subfield>
    <subfield code="c">Área Psicolog.Evolut.Educac</subfield>
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    <subfield code="1">1007</subfield>
    <subfield code="2">183</subfield>
    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Medicina, Psiqu. y Derm.</subfield>
    <subfield code="c">Área Dermatología</subfield>
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    <subfield code="g">10, 22 (2021), 5446 [9 pp]</subfield>
    <subfield code="p">J. clin.med.</subfield>
    <subfield code="t">Journal of Clinical Medicine</subfield>
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