Literature DB >> 21664737

Culture, gender and health care stigma: Practitioners' response to facial masking experienced by people with Parkinson's disease.

Linda Tickle-Degnen1, Leslie A Zebrowitz, Hui-ing Ma.   

Abstract

Facial masking in Parkinson's disease is the reduction of automatic and controlled expressive movement of facial musculature, creating an appearance of apathy, social disengagement or compromised cognitive status. Research in western cultures demonstrates that practitioners form negatively biased impressions associated with patient masking. Socio-cultural norms about facial expressivity vary according to culture and gender, yet little research has studied the effect of these factors on practitioners' responses toward patients who vary in facial expressivity. This study evaluated the effect of masking, culture and gender on practitioners' impressions of patient psychological attributes. Practitioners (N = 284) in the United States and Taiwan judged 12 Caucasian American and 12 Asian Taiwanese women and men patients in video clips from interviews. Half of each patient group had a moderate degree of facial masking and the other half had near-normal expressivity. Practitioners in both countries judged patients with higher masking to be more depressed and less sociable, less socially supportive, and less cognitively competent than patients with lower masking. Practitioners were more biased by masking when judging the sociability of the American patients, and American practitioners' judgments of patient sociability were more negatively biased in response to masking than were those of Taiwanese practitioners. Practitioners were more biased by masking when judging the cognitive competence and social supportiveness of the Taiwanese patients, and Taiwanese practitioners' judgments of patient cognitive competence were more negatively biased in response to masking than were those of American practitioners. The negative response to higher masking was stronger in practitioner judgments of women than men patients, particularly American patients. The findings suggest local cultural values as well as ethnic and gender stereotypes operate on practitioners' use of facial expressivity in clinical impression formation.
Copyright © 2011 Elsevier Ltd. All rights reserved.

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Year:  2011        PMID: 21664737      PMCID: PMC3142938          DOI: 10.1016/j.socscimed.2011.05.008

Source DB:  PubMed          Journal:  Soc Sci Med        ISSN: 0277-9536            Impact factor:   4.634


  43 in total

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Authors:  T K Pitcairn; S Clemie; J M Gray; B Pentland
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  23 in total

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6.  Stigma as a key determinant of health-related quality of life in Parkinson's disease.

Authors:  Hui-Ing Ma; Marie Saint-Hilaire; Cathi A Thomas; Linda Tickle-Degnen
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7.  The Relationship between the Experience of Hypomimia and Social Wellbeing in People with Parkinson's Disease and their Care Partners.

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8.  Predictors of self-perceived stigma in Parkinson's disease.

Authors:  Robert D Salazar; Emma Weizenbaum; Terry D Ellis; Gammon M Earhart; Matthew P Ford; Leland E Dibble; Alice Cronin-Golomb
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9.  Profile of social self-management practices in daily life with Parkinson's disease is associated with symptom severity and health quality of life.

Authors:  Linda Tickle-Degnen; Michael T Stevenson; Sarah D Gunnery; Marie Saint-Hilaire; Cathi A Thomas; Linda Sprague Martinez; Barbara Habermann; Elena N Naumova
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Review 10.  Integrating psychosocial care into neuro-oncology: challenges and strategies.

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