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The role of beliefs: lessons from a pilot study on illness perception, psychological distress and quality of life in patients with primary cicatricial alopecia
Author(s) -
Chiang Y.Z.,
Bundy C.,
Griffiths C.E.M.,
Paus R.,
Harries M.J.
Publication year - 2015
Publication title -
british journal of dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.304
H-Index - 179
eISSN - 1365-2133
pISSN - 0007-0963
DOI - 10.1111/bjd.13259
Subject(s) - quality of life (healthcare) , medicine , anxiety , depression (economics) , hospital anxiety and depression scale , dermatology life quality index , distress , disease , psychological distress , clinical psychology , psychiatry , nursing , economics , macroeconomics
Summary Background While alopecia has been shown to have substantial psychological consequences, previous studies have not explicitly explored the key beliefs of patients with primary cicatricial alopecia ( PCA ) and the relationship between clinical and psychological measures. Objectives To identify the key psychological factors and quality of life ( Q o L ) of patients with PCA and the relationship between these factors and established clinical measures. Methods In total 105 patients with PCA were recruited from a specialist hair research clinic in M anchester, U . K . Patients completed the revised I llness P erception Q uestionnaire, H ospital A nxiety and D epression S cale ( HADS ) and D ermatology L ife Q uality I ndex. These psychological measures were correlated with disease activity in patients with lichen planopilaris ( LPP ) and frontal fibrosing alopecia, using the LPP A ctivity I ndex ( LPPAI ). Results Patients perceived PCA as a chronic condition with significant personal consequences and emotional impact, and reported that they had low levels of control over the condition and its treatment. Considerable levels of psychological distress were observed (mean HADS total score 11·3 ± 8·1). Impaired Q o L was associated with strong beliefs that the symptoms were attributed to their disease ( P < 0·001), and that alopecia had serious consequences ( P < 0·001) and was distressing ( P < 0·001). Disease activity ( LPPAI ) showed a significant positive correlation with HADS ‐Depression ( r = 0·343, P = 0·026). Conclusions Patients with PCA experience significant psychological distress and impaired Q o L , both of which are associated with key beliefs about illness. Management of PCA should involve assessment of the beliefs and emotions that drive patients' psychological distress, as well as giving access to psychological therapy.