Restorative Neurology and Neuroscience 33 (2015) 335–345
DOI 10.3233/RNN-140484
IOS Press
335
Theory of mind impairment after severe
traumatic brain injury and its relationship
with caregivers’ quality of life
Umberto Bivona
a,∗
, Rita Formisano
a
, Sara De Laurentiis
a
, Natascia Accetta
a
, Maria Rita Di Cosimo
a
,
Roberta Massicci
a
, Paola Ciurli
a
, Eva Azicnuda
a
, Daniela Silvestro
a
, Umberto Sabatini
a
,
Chiara Falletta Caravasso
a
, Giovanni Augusto Carlesimo
a,b
, Carlo Caltagirone
a,b
and Alberto Costa
a
a
Fondazione Santa Lucia – Rome, Italy
b
Universit` a di Roma Tor Vergata – Rome, Italy
Abstract.
Purpose: Theory of mind (ToM) deficits are common consequences of severe Traumatic Brain Injury (sTBI), but little is known
about their impact on patients’ and their caregivers’ quality of life. This study aimed (i) to examine the presence of ToM difficulties
in individuals with sTBI and adequate levels of self-awareness (SA); (ii) to investigate their relationship with perceived Health
Related Quality of Life (HRQoL) in patients and their caregivers.
Methods: Twenty individuals with sTBI and adequate levels of SA, and 20 healthy controls (HCs) were recruited. ToM was
examined by the Faux-pas Recognition paradigm. The QOLIBRI questionnaire was administered to patients and their caregivers
to assess their HRQoL. Cognitive functioning and psychopathology were evaluated.
Results: Individuals with sTBI were less accurate than HCs on the Faux-pas Recognition paradigm. Patients’ satisfaction of
HRQoL was related to their performance on the Wisconsin Card Sorting Test. Caregivers’ satisfaction was significantly predicted
by patients’ score on the Faux-pas paradigm.
Conclusions: ToM is impaired in individuals with sTBI and adequate levels of SA. Moreover, their ToM performance predicted
HRQoL in the caregivers. From a clinical perspective, these results provide understanding of the potential impact of ToM
impairment in subjects with sTBI and their social system.
Keywords: Traumatic brain injury, theory of mind, self-awareness, quality of life, psychological support, neuropsychotherapeutic
approach
1. Introduction
Cognitive and emotional deficits are common seque-
lae of severe traumatic brain injury (sTBI) that can
negatively affect both patients’(Soberg et al., 2013) and
their caregivers (Marsh et al., 1998; Ponsford et al.,
2003; Wells et al., 1987). Indeed, it has long been
∗
Corresponding author: Umberto Bivona, IRCCS Fondazione
Santa Lucia, Via Ardeatina 306, 00100 – Rome, Italy. Tel.:
+39 0651501749; Fax: +39 0651501752; E-mail: u.bivona@
hsantalucia.it.
known that in patients with sTBI decreased cogni-
tive functioning (i.e., disorders of attention, executive
functioning, memory and information processing) and
personality changes (e.g., disinhibition, irritability,
egocentrism, low sensitivity to relatives’ needs) are
strongly associated with poor social outcome (Pons-
ford et al., 2003; Elsass & Kinsella, 1987). Moreover,
many studies have pointed out the role of the neurobe-
havioural deficits associated with TBI as significant
predictors of caregivers’ distress (Marsh et al., 1998;
Ponsford et al., 2003; Wells et al., 1987) and quality of
life (Wells et al., 1987; Bullinger et al., 2002).
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