ANDREA BOVERO

Dr. ANDREA BOVERO


Research Focus & Metrics

Academic Career Length

24Years (2003-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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27 July 2015 in European Journal of Cancer Care
Verified
Journal Article
Closed access
PDF file
ABANDREA BOVERO
ANDREA BOVERO
PLPaolo Leombruni
Paolo Leombruni
MMMarco Miniotti
Marco Miniotti
GRG. Rocca
G. Rocca
RTR. Torta
R. Torta
The purpose of this study was to show the different components of spirituality in the last few weeks of life for advanced cancer patients admitted to hospice and to evaluate quality of life (QoL), pain, anxiety, depression and psychological adjustment to cancer. One hundred and fifteen patients were interviewed with a series of rating scales: the Functional Assessment of Chronic Illness Therapy – Spiritual Well-Being Scale, the Hospital Anxiety and Depression Scale, the Visual Analogue Scale for pain, the Brief Coping Orientation to Problem Experienced and the Functional Assessment of Cancer Therapy Scale – General Measure. Workers and single patients with higher education level showed a worse QoL. Moreover, anxiety and pain were negatively associated with QoL, while spirituality and ‘Instrumental Support’ coping style were positively associated with QoL. In the Italian sample, it was observed that when patients are close to death, faith is a more important component of spirituality than meaning/peace. This study confirms that QoL could be related to physical and psychological symptoms, and this reiterates the importance of faith in end-of-life care.

6 September 2018 in Psycho-Oncology
Verified
Journal Article
Closed access
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ABANDREA BOVERO
ANDREA BOVERO
NSNader Alessandro Sedghi
Nader Alessandro Sedghi
MOMarta Opezzo
Marta Opezzo
RBRossana Botto
Rossana Botto
MPManuela Pinto
Manuela Pinto
RTRiccardo Torta
Riccardo Torta

14 June 2019 in Palliative and Supportive Care
Verified
Journal Article
Open access
PDF file
ABANDREA BOVERO
ANDREA BOVERO
RBRossana Botto
Rossana Botto
BABeatrice Adriano
Beatrice Adriano
MOMarta Opezzo
Marta Opezzo
VTValentina Tesio
Valentina Tesio
RTRiccardo Torta
Riccardo Torta
Objective: Demoralization is an existential distress syndrome that consists of an incapacity of coping, helplessness, hopelessness, loss of meaning and purpose, and impaired self-esteem. It can affect cancer patients, and the Demoralization Scale is a valid instrument to assess it. The present study aimed to investigate the prevalence of demoralization in end-of-life cancer patients and its associations with the medical and psychosocial variables. In addition, the latent dimensions of demoralization emerging in this distinctive population were explored.Method: The study is cross-sectional. The sample consisted of 235 end-of-life cancer patients with a Karnofsky performance status (KPS) lower than 50 and a life expectancy of a few weeks. For each patient, personal and medical data was gathered by a palliative physician and a set of validated rating scales, assessing demoralization, anxiety, depression, physical symptoms, pain, spiritual well-being, and dignity, was administered by a psychologist during the first consultation.Result: Sixty-four participants (27.2%) had low demoralization, 50.2% (n = 118) had medium demoralization, and 22.6% (n = 53) had high demoralization. Factor analysis evidenced a five-factor solution that identified the following demoralization factors: Emotional Distress and Inability to Cope, Loss of Purpose and Meaning, Worthlessness, Sense of Failure, and Dysphoria. All the considered variables were associated with demoralization, except for pain, nausea, breathing problems, and sociodemographic and clinical variables.Significance of results: End-of-life cancer patients showed higher levels of demoralization than has been reported in other studies with advanced cancer. These data could suggest that demoralization could increase in proximity to death and with impaired clinical condition. In particular, the five demoralization dimensions that emerged could represent the typical concerns around which the syndrome evolves in end-of-life cancer patients. Finally, spiritual well-being could play a protective role with respect to demoralization.

4 June 2019 in Journal of Religion and Health
Verified
Journal Article
Closed access
PDF file
ABANDREA BOVERO
ANDREA BOVERO
CTChiara Tosi
Chiara Tosi
RBRossana Botto
Rossana Botto
MOMarta Opezzo
Marta Opezzo
FGFederica Giono-Calvetto
Federica Giono-Calvetto
RTRiccardo Torta
Riccardo Torta

11 January 2023 in Psycho-Oncology
Verified
Journal Article
Open access
ABANDREA BOVERO
ANDREA BOVERO
MOMarta Opezzo
Marta Opezzo
VTValentina Tesio
Valentina Tesio
Objective: To examine the relationship between demoralization and health‐related quality of life (HRQoL) in a sample of end‐of‐life cancer patients with a life expectancy of 4 months or less undergoing palliative care, controlling for sociodemographic, clinical, and psychological variables.Methods: Sociodemographic, clinical, and psychological data from 170 end‐of‐life cancer patients were collected using the following scales: Edmonton Symptom Assessment System for palliative care patients' symptoms; Patient Health Questionnaire‐9 (PHQ‐9) for depressive symptoms; Functional Assessment of Cancer Therapy Scale ‐ General Measure (FACT‐G) for HRQoL; Functional Assessment of Chronic Illness Therapy ‐ Spiritual Well‐Being for spirituality (FACIT‐Sp); Demoralization Scale ‐ Italian Version (DS‐IT) for demoralization.Results: The DS‐IT showed that 51.8% of cancer patients were severely demoralized. In addition, 36.5% of the sample had clinically significant depressive symptoms and QoL was severely impaired (FACT‐G). The result of regression analysis showed that demoralization (especially “Disheartenment” and “Sense of failure”) was the strongest contributor for HRQoL, followed by ESAS_Lack of Well‐Being and depression (PHQ‐9), with the final model explaining 66% of the variance of the FACT‐G.Conclusions: The results highlight a very high prevalence of severe demoralization in end‐of life cancer patients. Moreover, demoralization was not only associated with patients' HRQoL, but it was also the most important contributing factor. This finding underscores the need to identify preventive or therapeutic psychological interventions that focus on preventing existential distress, and thus improve the QoL of dying patients in their last days of life.

24 October 2019 in American Journal of Hospice and Palliative Medicine®
Verified
Journal Article
Closed access
PDF file
ABANDREA BOVERO
ANDREA BOVERO
FGFrancesco Gottardo
Francesco Gottardo
RBRossana Botto
Rossana Botto
CTChiara Tosi
Chiara Tosi
MSMarta Selvatico
Marta Selvatico
RTRiccardo Torta
Riccardo Torta
The concept of a good death is crucial in palliative care, but its relationship with attitudes toward death and feelings of interconnectedness needs to be further deepened. The first aim of this study was to explore the concept of good death, attitudes toward death, and feelings of interconnectedness among family caregivers (FCs) and health-care providers (HCPs) of terminally ill patients with cancer. The second aim was to analyze associations of good death concept with attitudes toward death and feelings of interconnectedness. Participants were asked to assess the importance of features that characterize a good death. To explore each person’s attitude toward death and feelings of interconnectedness, 3 open questions were used. The sample consisted of 49 participants: 24 (48.98%) FCs and 25 (51.02%) HCPs. Nine good death features were considered essential by more than 70% of participants. These referred to the physical (eg, symptoms control), social (eg, loved ones’ presence), emotional (eg, sharing emotions), and spiritual (eg, inner peace) dimensions. Importance attributed to components of a good death such as patient’s awareness and acceptance of death, meaning, respect for the patient’s wishes, and inner peace were found to be associated with lack of avoidance and acceptance toward death and feelings of interconnectedness. Given the importance of FCs and HCPs in providing care and their impact on the patients’ dying process, it is necessary to reflect upon how their personal attitudes and previous experiences influence the care of dying patients.