Skip to main content
Top
Gepubliceerd in: Quality of Life Research 11/2016

03-06-2016

Health-related quality of life in patients with psoriasis: a systematic review of the European literature

Auteurs: Montse Obradors, Carles Blanch, Marta Comellas, Montse Figueras, Luis Lizan

Gepubliceerd in: Quality of Life Research | Uitgave 11/2016

Log in om toegang te krijgen
share
DELEN

Deel dit onderdeel of sectie (kopieer de link)

  • Optie A:
    Klik op de rechtermuisknop op de link en selecteer de optie “linkadres kopiëren”
  • Optie B:
    Deel de link per e-mail

Abstract

Purpose

To summarize the data published over the last 5 years in the European Union related to the health-related quality of life (HRQoL) of patients with psoriasis and its conditioning factors.

Methods

International electronic databases and gray literature were searched to identify studies conducted on patient-reported outcomes in patients with psoriasis, published in Europe between January 1, 2009 and December 31, 2013. Bibliographic references were hand-searched. Editorials, letters, commentaries, opinion papers, and studies related to specific treatments were excluded.

Results

A total of 46 studies met the inclusion criteria, 27 of them reporting data related to HRQoL or its conditioning factors. The publications reviewed highlighted the substantial negative impact of psoriasis on patients’ HRQoL. Most of the studies that analyzed the relationship between HRQoL and sociodemographic characteristics described a relation between gender (female) and age (young patients) and poorer HRQoL. An association between HRQoL impairment and visibility of skin lesions and disease activity and severity was also established. Skin discomfort and pruritus were identified as elements that negatively influenced HRQoL. Use of biological agents had a positive impact on HRQoL and on treatment satisfaction, a better HRQoL being seen in patients treated with systemic therapies and biologics.

Conclusions

HRQoL has been broadly addressed in patients with psoriasis in Europe. Several disease- and patient-related factors contributed to its deterioration. Therapeutic measures with proven effectiveness in controlling disease symptoms and reducing PASI should be considered in patients with a severe disease who have a poorer HRQoL.
Bijlagen
Alleen toegankelijk voor geautoriseerde gebruikers
Literatuur
1.
go back to reference Langley, R. G. B., Krueger, G. G., & Griffiths, C. E. M. (2005). Psoriasis: Epidemiology, clinical features, and quality of life. Annals of the Rheumatic Diseases, 64(suppl 2), ii18–ii23.PubMedPubMedCentral Langley, R. G. B., Krueger, G. G., & Griffiths, C. E. M. (2005). Psoriasis: Epidemiology, clinical features, and quality of life. Annals of the Rheumatic Diseases, 64(suppl 2), ii18–ii23.PubMedPubMedCentral
2.
go back to reference Perera, G. K., Di Meglio, P., Frank, O., & Nestle, F. O. (2012). Psoriasis. Annual Review of Pathology: Mechanisms of Disease, 7, 385–422.CrossRef Perera, G. K., Di Meglio, P., Frank, O., & Nestle, F. O. (2012). Psoriasis. Annual Review of Pathology: Mechanisms of Disease, 7, 385–422.CrossRef
3.
go back to reference Ortonne, J. P., & Prinz, J. C. (2004). Alefacept: A novel and selective biologic agent for the treatment of chronic plaque psoriasis. The European Journal of Dermatology, 14, 41–45.PubMed Ortonne, J. P., & Prinz, J. C. (2004). Alefacept: A novel and selective biologic agent for the treatment of chronic plaque psoriasis. The European Journal of Dermatology, 14, 41–45.PubMed
4.
go back to reference Lebwohl, M. G., Bachelez, H., Barker, J., Girolomoni, G., Kavanaugh, A., Langley, R. G., et al. (2014). Patient perspectives in the management of psoriasis: Results from the population-based Multinational Assessment of Psoriasis and Psoriatic Arthritis Survey. Journal of the American Academy of Dermatology, 70(5), 871–881.CrossRefPubMed Lebwohl, M. G., Bachelez, H., Barker, J., Girolomoni, G., Kavanaugh, A., Langley, R. G., et al. (2014). Patient perspectives in the management of psoriasis: Results from the population-based Multinational Assessment of Psoriasis and Psoriatic Arthritis Survey. Journal of the American Academy of Dermatology, 70(5), 871–881.CrossRefPubMed
5.
go back to reference Tan, X., Feldman, S. R., & Balkrishnan, R. (2012). Quality of life issues and measurement in patients with psoriasis. Psoriasis: Targets and Therapy, 2(1), 13–23. Tan, X., Feldman, S. R., & Balkrishnan, R. (2012). Quality of life issues and measurement in patients with psoriasis. Psoriasis: Targets and Therapy, 2(1), 13–23.
6.
go back to reference Rapp, S. R., Feldman, S. R., Exum, M. L., Fleischer, A. B, Jr., & Reboussin, D. M. (1999). Psoriasis causes as much disability as other major medical disease. Journal of the American Academy of Dermatology, 41(3 Ot 1), 401–407.CrossRefPubMed Rapp, S. R., Feldman, S. R., Exum, M. L., Fleischer, A. B, Jr., & Reboussin, D. M. (1999). Psoriasis causes as much disability as other major medical disease. Journal of the American Academy of Dermatology, 41(3 Ot 1), 401–407.CrossRefPubMed
7.
go back to reference Fowler, J. F., Duh, M. S., Rovba, L., Buteau, S., Pinheiro, L., Lobo, F., et al. (2008). The impact of psoriasis on health care costs and patient work loss. Journal of the American Academy of Dermatology, 59(5), 772–780.CrossRefPubMed Fowler, J. F., Duh, M. S., Rovba, L., Buteau, S., Pinheiro, L., Lobo, F., et al. (2008). The impact of psoriasis on health care costs and patient work loss. Journal of the American Academy of Dermatology, 59(5), 772–780.CrossRefPubMed
8.
go back to reference Bhosle, M. J., Kulkarni, A., Feldman, S. R., & Balkrishnan, R. (2006). Quality of life in patients with psoriasis. Health and Quality of Life Outcomes, 4(1), 35–37.CrossRefPubMedPubMedCentral Bhosle, M. J., Kulkarni, A., Feldman, S. R., & Balkrishnan, R. (2006). Quality of life in patients with psoriasis. Health and Quality of Life Outcomes, 4(1), 35–37.CrossRefPubMedPubMedCentral
9.
go back to reference Both, H., Essink-Bot, M. L., Busschbach, J., & Nijsten, T. (2007). Critical review of generic and dermatology-specific health-related quality of life instruments. Journal of Investigative Dermatology, 127(12), 2726–2739.CrossRefPubMed Both, H., Essink-Bot, M. L., Busschbach, J., & Nijsten, T. (2007). Critical review of generic and dermatology-specific health-related quality of life instruments. Journal of Investigative Dermatology, 127(12), 2726–2739.CrossRefPubMed
10.
go back to reference Higgins, J. P. (Ed.). (2008). Cochrane handbook for systematic reviews of interventions (Vol. 5). Chichester: Wiley. Higgins, J. P. (Ed.). (2008). Cochrane handbook for systematic reviews of interventions (Vol. 5). Chichester: Wiley.
13.
go back to reference Norlin, J. M., Steen Carlsson, K., Persson, U., & Schmitt-Egenolf, M. (2012). Analysis of three outcome measures in moderate to severe psoriasis: A registry-based study of 2450 patients. British Journal of Dermatology, 166(4), 797–802.CrossRefPubMed Norlin, J. M., Steen Carlsson, K., Persson, U., & Schmitt-Egenolf, M. (2012). Analysis of three outcome measures in moderate to severe psoriasis: A registry-based study of 2450 patients. British Journal of Dermatology, 166(4), 797–802.CrossRefPubMed
14.
go back to reference Daudén, E., Conejo, J., & García-Calvo, C. (2011). Percepción del médico y paciente de la gravedad de la psoriasis, su impacto en la calidad de vida y satisfacción con la atención y el tratamiento recibido. Estudio observacional en España. Actas Dermo-Sifiliográficas, 102(4), 270–276.CrossRef Daudén, E., Conejo, J., & García-Calvo, C. (2011). Percepción del médico y paciente de la gravedad de la psoriasis, su impacto en la calidad de vida y satisfacción con la atención y el tratamiento recibido. Estudio observacional en España. Actas Dermo-Sifiliográficas, 102(4), 270–276.CrossRef
15.
go back to reference Anstey, A., McAteer, H., Kamath, N., & Percival, F. (2012). Extending psychosocial assessment of patients with psoriasis in the UK, using a self-rated, web-based survey. Clinical and Experimental Dermatology, 37, 735–740.CrossRefPubMed Anstey, A., McAteer, H., Kamath, N., & Percival, F. (2012). Extending psychosocial assessment of patients with psoriasis in the UK, using a self-rated, web-based survey. Clinical and Experimental Dermatology, 37, 735–740.CrossRefPubMed
16.
go back to reference Sampogna, F., Tabolli, S., & Abeni, D. (2012). Living with psoriasis: Prevalence of shame, anger, worry, and problems in daily activities and social life. Acta Dermato-Venereologica, 92, 299–303.CrossRefPubMed Sampogna, F., Tabolli, S., & Abeni, D. (2012). Living with psoriasis: Prevalence of shame, anger, worry, and problems in daily activities and social life. Acta Dermato-Venereologica, 92, 299–303.CrossRefPubMed
17.
go back to reference Tadros, A., Vergou, T., Stratigos, A., Tzavara, C., Hletsos, M., Katsambas, A., et al. (2011). Psoriasis: Is it the tip of the iceberg for the quality of life of patients and their families? Journal of the European Academy of Dermatology and Venereology, 25, 1282–1287.CrossRefPubMed Tadros, A., Vergou, T., Stratigos, A., Tzavara, C., Hletsos, M., Katsambas, A., et al. (2011). Psoriasis: Is it the tip of the iceberg for the quality of life of patients and their families? Journal of the European Academy of Dermatology and Venereology, 25, 1282–1287.CrossRefPubMed
18.
go back to reference Böhm, D., Stock Gissendanner, S., Bangemann, K., Snitjer, I., Werfel, T., Weyergraf, A., et al. (2013). Perceived relationships between severity of psoriasis symptoms, gender, stigmatization and quality of life. Journal of the European Academy of Dermatology and Venereology, 27, 220–226.CrossRefPubMed Böhm, D., Stock Gissendanner, S., Bangemann, K., Snitjer, I., Werfel, T., Weyergraf, A., et al. (2013). Perceived relationships between severity of psoriasis symptoms, gender, stigmatization and quality of life. Journal of the European Academy of Dermatology and Venereology, 27, 220–226.CrossRefPubMed
19.
go back to reference Daudén, E., Herrera, E., Puig, L., Sánchez-Carazo, J. L., Toribio, J., & Perulero, N. (2013). Impact of active and stable psoriasis on health-related quality of life: The PSO-LIFE study. Actas Dermo-Sifiliográficas, 104(8), 685–693.CrossRefPubMed Daudén, E., Herrera, E., Puig, L., Sánchez-Carazo, J. L., Toribio, J., & Perulero, N. (2013). Impact of active and stable psoriasis on health-related quality of life: The PSO-LIFE study. Actas Dermo-Sifiliográficas, 104(8), 685–693.CrossRefPubMed
20.
go back to reference Lindberg, M., Isacson, D., & Bingefors, K. (2013). Self-reported skin diseases, quality of life and medication use: A nationwide pharmaco-epidemiological survey in Sweden. Acta Dermato-Venereologica, 94(2), 188–191.CrossRef Lindberg, M., Isacson, D., & Bingefors, K. (2013). Self-reported skin diseases, quality of life and medication use: A nationwide pharmaco-epidemiological survey in Sweden. Acta Dermato-Venereologica, 94(2), 188–191.CrossRef
21.
go back to reference Blome, C., Simianer, S., Purwins, S., Laass, A., Rustenbach, S. J., Schaefer, I., et al. (2010). Time needed for treatment is the major predictor of quality of life in psoriasis. Dermatology, 221, 154–159.CrossRefPubMed Blome, C., Simianer, S., Purwins, S., Laass, A., Rustenbach, S. J., Schaefer, I., et al. (2010). Time needed for treatment is the major predictor of quality of life in psoriasis. Dermatology, 221, 154–159.CrossRefPubMed
22.
go back to reference Daudén, E., Pujol, R. M., Sánchez-Carazo, J. L., Toribio, J., Vanaclocha, F., Puig, L., et al. (2013). Demographic characteristics and health-related quality of life of patients with moderate-to-severe psoriasis: The VACAP study. Actas Dermo-Sifiliográficas, 104, 807–814.PubMed Daudén, E., Pujol, R. M., Sánchez-Carazo, J. L., Toribio, J., Vanaclocha, F., Puig, L., et al. (2013). Demographic characteristics and health-related quality of life of patients with moderate-to-severe psoriasis: The VACAP study. Actas Dermo-Sifiliográficas, 104, 807–814.PubMed
23.
go back to reference Miniszewska, J., Chodkiewicz, J., Ograczyk, A., & Zalewska-Janowska, A. (2013). Optimism as a predictor of health-related quality of life in psoriatics. Postępy Dermatologii i Alergologii, 30(2), 91–95.PubMedPubMedCentral Miniszewska, J., Chodkiewicz, J., Ograczyk, A., & Zalewska-Janowska, A. (2013). Optimism as a predictor of health-related quality of life in psoriatics. Postępy Dermatologii i Alergologii, 30(2), 91–95.PubMedPubMedCentral
24.
go back to reference Miniszewska, J., Juczyski, Z., Ograczyk, A., & Zalewska, A. (2013). Health-related quality of life in psoriasis: Important role of personal resources. Acta Dermato-Venereologica, 93(5), 551–556.CrossRefPubMed Miniszewska, J., Juczyski, Z., Ograczyk, A., & Zalewska, A. (2013). Health-related quality of life in psoriasis: Important role of personal resources. Acta Dermato-Venereologica, 93(5), 551–556.CrossRefPubMed
25.
go back to reference Fernandez-Torres, R. M., Paradela, S., & Fonseca, E. (2012). Psoriasis in patients older than 65 years. A comparative study with younger adult psoriatic patients. The Journal of Nutrition, Health & Aging, 16, 586–589.CrossRef Fernandez-Torres, R. M., Paradela, S., & Fonseca, E. (2012). Psoriasis in patients older than 65 years. A comparative study with younger adult psoriatic patients. The Journal of Nutrition, Health & Aging, 16, 586–589.CrossRef
26.
go back to reference Hernánz, J. M., Sánchez-Regaña, M., Izu, R., Mendiola, V., & García-Calvo, C. (2012). Clinical and therapeutic evaluation of patients with moderate to severe psoriasis in Spain: The Secuence Study. Actas Dermo-Sifiliográficas, 103(10), 897–904.CrossRef Hernánz, J. M., Sánchez-Regaña, M., Izu, R., Mendiola, V., & García-Calvo, C. (2012). Clinical and therapeutic evaluation of patients with moderate to severe psoriasis in Spain: The Secuence Study. Actas Dermo-Sifiliográficas, 103(10), 897–904.CrossRef
27.
go back to reference Cozzani, E., Borrini, V., Pennella, A., Burlando, M., Cardo, P., Rebora, A., et al. (2010). The quality of life in Italian psoriatic patients treated with biological drugs. Giornale italiano di dermatologia e venereologia: organo ufficiale, Societa italiana di dermatologia e sifilografia, 145(6), 709–712. Cozzani, E., Borrini, V., Pennella, A., Burlando, M., Cardo, P., Rebora, A., et al. (2010). The quality of life in Italian psoriatic patients treated with biological drugs. Giornale italiano di dermatologia e venereologia: organo ufficiale, Societa italiana di dermatologia e sifilografia, 145(6), 709–712.
28.
go back to reference Pereira, M. G., Brito, L., & Smith, T. (2012). Dyadic adjustment, family coping, body image, quality of life and psychological morbidity in patients with psoriasis and their partners. The International Journal of Behavioral Medicine, 9(3), 260–269.CrossRef Pereira, M. G., Brito, L., & Smith, T. (2012). Dyadic adjustment, family coping, body image, quality of life and psychological morbidity in patients with psoriasis and their partners. The International Journal of Behavioral Medicine, 9(3), 260–269.CrossRef
29.
go back to reference Richards, H. L., Fortune, D. G., Griffiths, C. E., & Main, C. J. (2001). The contribution of perceptions of stigmatization to disability in patients with psoriasis. The Journal of Psychosomatic Research, 50, 11–15.CrossRefPubMed Richards, H. L., Fortune, D. G., Griffiths, C. E., & Main, C. J. (2001). The contribution of perceptions of stigmatization to disability in patients with psoriasis. The Journal of Psychosomatic Research, 50, 11–15.CrossRefPubMed
30.
go back to reference Gupta, M. A., Gupta, A. K., & Watteel, G. N. (1998). Perceived deprivation of social touch in psoriasis is associated with greater psychologic morbidity: An index of the stigma experience in dermatologic disorder. Cutis, 61, 339–342.PubMed Gupta, M. A., Gupta, A. K., & Watteel, G. N. (1998). Perceived deprivation of social touch in psoriasis is associated with greater psychologic morbidity: An index of the stigma experience in dermatologic disorder. Cutis, 61, 339–342.PubMed
31.
go back to reference Palotai, T., Szepietowski, J. C., Pec, J., Arenberger, P., Giurcaneanu, C., Gyulai, R., et al. (2010). A survey of disease severity, quality of life, and treatment patterns of biologically naïve patients with psoriasis in Central and Eastern Europe. Acta Dermatovenerologica Croatica, 18(3), 151–162. Palotai, T., Szepietowski, J. C., Pec, J., Arenberger, P., Giurcaneanu, C., Gyulai, R., et al. (2010). A survey of disease severity, quality of life, and treatment patterns of biologically naïve patients with psoriasis in Central and Eastern Europe. Acta Dermatovenerologica Croatica, 18(3), 151–162.
32.
go back to reference Panigalli, S., Coccarielli, D., Germi, L., Trevisan, G. P., & Veller-Fornasa, C. (2009). Non-randomized pilot study on the evaluation of the quality of life and psychosocial stress before and after systemic therapy in patients affected by moderate to severe psoriasis. Journal of Biological Regulators and Homeostatic Agents, 23(2), 111–117.PubMed Panigalli, S., Coccarielli, D., Germi, L., Trevisan, G. P., & Veller-Fornasa, C. (2009). Non-randomized pilot study on the evaluation of the quality of life and psychosocial stress before and after systemic therapy in patients affected by moderate to severe psoriasis. Journal of Biological Regulators and Homeostatic Agents, 23(2), 111–117.PubMed
33.
go back to reference Ghatnekar, O., Ljungberg, A., Wirestrand, L. E., & Svensson, A. (2012). Cost and quality of life for psoriatic patients at different degrees of severity in southern Sweden—A cross-sectional study. The European Journal of Dermatology, 22(2), 238–2345.PubMed Ghatnekar, O., Ljungberg, A., Wirestrand, L. E., & Svensson, A. (2012). Cost and quality of life for psoriatic patients at different degrees of severity in southern Sweden—A cross-sectional study. The European Journal of Dermatology, 22(2), 238–2345.PubMed
34.
go back to reference Jacobi, A., Kupke, C., Behzad, M., & Hertl, M. (2013). Comorbidities, metabolic risk profile and health-related quality of life in German patients with plaque-type psoriasis: A cross-sectional prospective study. International Journal of Dermatology, 52, 1081–1087.CrossRefPubMed Jacobi, A., Kupke, C., Behzad, M., & Hertl, M. (2013). Comorbidities, metabolic risk profile and health-related quality of life in German patients with plaque-type psoriasis: A cross-sectional prospective study. International Journal of Dermatology, 52, 1081–1087.CrossRefPubMed
35.
go back to reference Ljosaa, T. M., Mork, C., Stubhaug, A., Moum, T., & Wahl, A. K. (2012). Skin pain and skin discomfort is associated with quality of life in patients with psoriasis. Journal of the European Academy of Dermatology and Venereology, 26, 29–35.CrossRefPubMed Ljosaa, T. M., Mork, C., Stubhaug, A., Moum, T., & Wahl, A. K. (2012). Skin pain and skin discomfort is associated with quality of life in patients with psoriasis. Journal of the European Academy of Dermatology and Venereology, 26, 29–35.CrossRefPubMed
36.
go back to reference Reich, A., Hrehorow, E., & Szepietowski, J. C. (2010). Pruritus is an important factor negatively influencing the well-being of psoriatic patients. Acta Dermato-Venereologica, 90(3), 257–263.CrossRefPubMed Reich, A., Hrehorow, E., & Szepietowski, J. C. (2010). Pruritus is an important factor negatively influencing the well-being of psoriatic patients. Acta Dermato-Venereologica, 90(3), 257–263.CrossRefPubMed
37.
go back to reference Finlay, A. Y., & Khan, G. K. (1994). Dermatology Life Quality Index (DLQI)—A simple practical measure for routine clinical use. Clinical and Experimental Dermatology, 19(3), 210–216.CrossRefPubMed Finlay, A. Y., & Khan, G. K. (1994). Dermatology Life Quality Index (DLQI)—A simple practical measure for routine clinical use. Clinical and Experimental Dermatology, 19(3), 210–216.CrossRefPubMed
38.
go back to reference Ghajarzadeh, M., Ghiasi, M., & Kheirkhah, S. (2012). Associations between skin disease and quality of life: A comparision of psoriasis, vitiligo, and alopecia areata. Acta Medica Iranica, 50(7), 511–515.PubMed Ghajarzadeh, M., Ghiasi, M., & Kheirkhah, S. (2012). Associations between skin disease and quality of life: A comparision of psoriasis, vitiligo, and alopecia areata. Acta Medica Iranica, 50(7), 511–515.PubMed
39.
go back to reference Pärna, E., Aluoja, A., & Kingo, K. (2015). Quality of life and emotional state in chornic skin disease. Acta Dermato-Venereologica, 95(3), 312–316.CrossRefPubMed Pärna, E., Aluoja, A., & Kingo, K. (2015). Quality of life and emotional state in chornic skin disease. Acta Dermato-Venereologica, 95(3), 312–316.CrossRefPubMed
40.
go back to reference Martínez-García, E., Arias-Santiago, S., Valenzuela-Salas, I., Garrido-Colmenero, C., García-Mellado, V., & Buendía-Eisman, A. (2014). Quality of life in persons living with psoriasis patients. Journal of the American Academy of Dermatology, 71, 302–307.CrossRefPubMed Martínez-García, E., Arias-Santiago, S., Valenzuela-Salas, I., Garrido-Colmenero, C., García-Mellado, V., & Buendía-Eisman, A. (2014). Quality of life in persons living with psoriasis patients. Journal of the American Academy of Dermatology, 71, 302–307.CrossRefPubMed
41.
go back to reference Takeshita, J., Duffin, K. C., Shin, D. B., Krueger, G. G., Robertson, A. D., Troxel, A. B., et al. (2014). Patient-reported outcomes for psoriasis patients with clear versus almost clear skin in the clinical setting. Journal of the American Academy of Dermatology, 71(4), 633–641.CrossRefPubMedPubMedCentral Takeshita, J., Duffin, K. C., Shin, D. B., Krueger, G. G., Robertson, A. D., Troxel, A. B., et al. (2014). Patient-reported outcomes for psoriasis patients with clear versus almost clear skin in the clinical setting. Journal of the American Academy of Dermatology, 71(4), 633–641.CrossRefPubMedPubMedCentral
42.
go back to reference Viswanathan, H. N., Chau, D., Milmont, C. E., Yang, W., Erondu, N., Revicki, D. A., et al. (2014). Total Skin clearance results in improvements in health-related quality of life and reduced symptom severity among patients with moderate to severe psoriasis. Journal of Dermatological Treatment, 31, 1–5. Viswanathan, H. N., Chau, D., Milmont, C. E., Yang, W., Erondu, N., Revicki, D. A., et al. (2014). Total Skin clearance results in improvements in health-related quality of life and reduced symptom severity among patients with moderate to severe psoriasis. Journal of Dermatological Treatment, 31, 1–5.
43.
go back to reference Mattei, P. L., Corey, K. C., & Kimball, A. B. (2014). Psoriasis Area Severity Index (PASI) and the Dermatology Life Quality Index (DLQI): The correlation between disease severity and psychological burden in patients treated with biological therapies. Journal of the European Academy of Dermatology and Venereology, 28, 333–337.CrossRefPubMed Mattei, P. L., Corey, K. C., & Kimball, A. B. (2014). Psoriasis Area Severity Index (PASI) and the Dermatology Life Quality Index (DLQI): The correlation between disease severity and psychological burden in patients treated with biological therapies. Journal of the European Academy of Dermatology and Venereology, 28, 333–337.CrossRefPubMed
44.
go back to reference Moreno-Ramírez, D., Fonseca, E., Herranz, P., & Ara, M. (2010). Realidad terapéutica de la psoriasis moderada-grave en España. Encuesta de opinión. Actas Dermo-Sifiliográficas, 101(10), 858–865.CrossRef Moreno-Ramírez, D., Fonseca, E., Herranz, P., & Ara, M. (2010). Realidad terapéutica de la psoriasis moderada-grave en España. Encuesta de opinión. Actas Dermo-Sifiliográficas, 101(10), 858–865.CrossRef
45.
go back to reference Hägg, D., Sundström, A., Eriksson, M., & Schimitt-Egenolf, M. (2015). Decision for biological treatment in real life is more strongly associated with the Psoriasis Area and Severity Index (PASI) than with the Dermatology Life Quality Index (DLQI). Journal of the European Academy of Dermatology and Venereology, 9(3), 452–456.CrossRef Hägg, D., Sundström, A., Eriksson, M., & Schimitt-Egenolf, M. (2015). Decision for biological treatment in real life is more strongly associated with the Psoriasis Area and Severity Index (PASI) than with the Dermatology Life Quality Index (DLQI). Journal of the European Academy of Dermatology and Venereology, 9(3), 452–456.CrossRef
46.
go back to reference Mrowietz, U., Kragballe, K., Reich, K., Spuls, P., Griffiths, C. E., Nast, A., et al. (2011). Definition of treatment goals for moderate to severe psoriasis: A European consensus. Archives of Dermatological Research, 303, 1–10.CrossRefPubMed Mrowietz, U., Kragballe, K., Reich, K., Spuls, P., Griffiths, C. E., Nast, A., et al. (2011). Definition of treatment goals for moderate to severe psoriasis: A European consensus. Archives of Dermatological Research, 303, 1–10.CrossRefPubMed
47.
go back to reference Melero, R., Ibánez, D., Tiemblo, C., Díez, B., del Arco, J., García, M. Á., & Castro, M. B. (2011). [Estudio Psoriafarm Bizkaia: características más relevantes]. Pharmaceutical Care España, 13(2), 74–90. Melero, R., Ibánez, D., Tiemblo, C., Díez, B., del Arco, J., García, M. Á., & Castro, M. B. (2011). [Estudio Psoriafarm Bizkaia: características más relevantes]. Pharmaceutical Care España, 13(2), 74–90.
48.
go back to reference Norlin, J. M., Carlsson K. S., Persson, U., & Schmitt-Egenolf, M. (2012b). Switch to biological agent in psoriasis significantly improved clinical and patient-reported outcomes in real-word practice. Dermatology, 225(4), 326–332.CrossRefPubMed Norlin, J. M., Carlsson K. S., Persson, U., & Schmitt-Egenolf, M. (2012b). Switch to biological agent in psoriasis significantly improved clinical and patient-reported outcomes in real-word practice. Dermatology, 225(4), 326–332.CrossRefPubMed
49.
go back to reference Palijan, T. Z., Kovacevic, D., Koic, E., Ruzic, K., & Dervinja, F. (2011). The impact of psoriasis on the quality of life and psychological characteristics of persons suffering from psoriasis. Collegium Antropologicum, 35(2), 81–85.PubMed Palijan, T. Z., Kovacevic, D., Koic, E., Ruzic, K., & Dervinja, F. (2011). The impact of psoriasis on the quality of life and psychological characteristics of persons suffering from psoriasis. Collegium Antropologicum, 35(2), 81–85.PubMed
50.
go back to reference Zeljko-Penavic, J., Situm, M., Simic, D., & Vurnek-Zivkovic., M. (2010). Quality of life in psoriatic patients and the relationship between type I and type II psoriasis. Collegium Antropologicum, 34(1), 195–198.PubMed Zeljko-Penavic, J., Situm, M., Simic, D., & Vurnek-Zivkovic., M. (2010). Quality of life in psoriatic patients and the relationship between type I and type II psoriasis. Collegium Antropologicum, 34(1), 195–198.PubMed
51.
go back to reference Tennvall, G., Hjortsberg, C., Bjarnason, A., Gniadecki, R., Heikkila, H., & Jemec, G. B. et al. (2013). Treatment patterns, treatment satisfaction, severity of disease problems, and quality of life in patients with psoriasis in three nordic countries. Acta Dermato-Venereologica, 93, 442–445.CrossRef Tennvall, G., Hjortsberg, C., Bjarnason, A., Gniadecki, R., Heikkila, H., & Jemec, G. B. et al. (2013). Treatment patterns, treatment satisfaction, severity of disease problems, and quality of life in patients with psoriasis in three nordic countries. Acta Dermato-Venereologica, 93, 442–445.CrossRef
Metagegevens
Titel
Health-related quality of life in patients with psoriasis: a systematic review of the European literature
Auteurs
Montse Obradors
Carles Blanch
Marta Comellas
Montse Figueras
Luis Lizan
Publicatiedatum
03-06-2016
Uitgeverij
Springer International Publishing
Gepubliceerd in
Quality of Life Research / Uitgave 11/2016
Print ISSN: 0962-9343
Elektronisch ISSN: 1573-2649
DOI
https://doi.org/10.1007/s11136-016-1321-7

Andere artikelen Uitgave 11/2016

Quality of Life Research 11/2016 Naar de uitgave