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  1. Article: A multiple criteria approach to map ecological-inclusive business models for sustainable development

    Norese, Maria Franca / Corazza, Laura / Bruschi, Fabio / Cisi, Maurizio

    international journal of sustainable development and world ecology. 2021 Jan. 02, v. 28, no. 1

    2021  

    Abstract: The paper presents the first attempt to apply a multiple criteria approach to map ecological-inclusive business models and to structure their main features, in terms of sustainable development. Ecological-inclusive business models are presented in this ... ...

    Abstract The paper presents the first attempt to apply a multiple criteria approach to map ecological-inclusive business models and to structure their main features, in terms of sustainable development. Ecological-inclusive business models are presented in this study, and 15 cases pertaining to agro-food organisations located in Sub-Saharan Africa are considered. These companies simultaneously deliver positive social and environmental value, and confirm a well-established market presence. As far as social value is concerned, the companies included in the sample use a Bottom-of-Pyramid approach, involving low-income customers and/or low-income business partners. As for environmental value, all the analysed companies implement frugal innovation or sustainable exploitation of natural resources in the afro-food sector. One of the results that has been achieved is that of disentangling the complexity behind a triple bottom-line business model through a multidimensional analysis framework that identifies the aspects that play a fundamental role in ecological-inclusive business models. An evaluation model and the application of a multiple criteria outranking method are proposed as examples of how some criteria, such as the extent of socio-environmental concerns, strategy orientation and value of partnerships can be used to compare, rank and/or select business models to facilitate decision makers. This work presents the results of an interdisciplinary study on the social entrepreneurship field of knowledge.
    Keywords business enterprises ; business partnerships ; consumers (people) ; decision making ; ecological value ; ecology ; econometric models ; entrepreneurship ; knowledge ; markets ; natural resources ; organizations ; paper ; social benefit ; sustainable development ; Sub-Saharan Africa
    Language English
    Dates of publication 2021-0102
    Size p. 75-91.
    Publishing place Taylor & Francis
    Document type Article
    Note NAL-light
    ISSN 1745-2627
    DOI 10.1080/13504509.2020.1800531
    Database NAL-Catalogue (AGRICOLA)

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  2. Article ; Online: Parent-proxy pediatric CMT quality of life outcome measure: Validation of the Italian version.

    Danti, Federica Rachele / Pagliano, Emanuela / Pareyson, Davide / Foscan, Maria / Marchi, Alessia / Feoli, Alessia / Bruschi, Fabio / Piscosquito, Giuseppe / Shy, Micheal E / Ramchandren, Sindhu / Moroni, Isabella / Wu, Tong Tong

    Journal of the peripheral nervous system : JPNS

    2024  Volume 29, Issue 1, Page(s) 107–110

    Abstract: Background and aims: The parent-proxy reports can offer complementary informations or be the only source of Quality of Life measurement in young children. The aim of this study was to provide and validate the Italian version of the recently published ... ...

    Abstract Background and aims: The parent-proxy reports can offer complementary informations or be the only source of Quality of Life measurement in young children. The aim of this study was to provide and validate the Italian version of the recently published parent-proxy pCMT-QOL for patients aged 8-18 years old, making it available for possible trials in Italian speaking children.
    Methods: The English-language instrument was translated and adapted into the Italian language using standard procedures: translation, transcultural adaptation, and back-translation. Parent-proxy pCMT-QOL was administered to parents of patients with a genetic diagnosis of CMT, aged 8-18 years old. All parents were retested 2 weeks later to assess reliability.
    Results: A total of 21 parents of CMT patients (18 CMT1A, 2 CMT2A, 1 CMT2K) were assessed during their children clinical appointments. The Italian-pCMT-QOL showed a high test-retest reliability; none of the parents had any difficulties with the completion of the questionnaire and no further revisions were necessary after completion.
    Interpretation: The Italian parent-proxy pCMT-QOL is a reliable, culturally adapted, and comparable version of the original English instrument. This questionnaire will improve the quality of the follow-up and will make it possible to monitor more accurately the severity of the disease in Italian-speaking families.
    MeSH term(s) Humans ; Child ; Child, Preschool ; Adolescent ; Quality of Life ; Reproducibility of Results ; Surveys and Questionnaires ; Parents ; Language ; Italy ; Psychometrics
    Language English
    Publishing date 2024-02-08
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1364009-4
    ISSN 1529-8027 ; 1085-9489
    ISSN (online) 1529-8027
    ISSN 1085-9489
    DOI 10.1111/jns.12615
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Book ; Online: La portée pratique de la phénoménologie

    Popa, Délia / Bruschi, Fabio / Kanabus, Benoît

    Normativité, critique sociale et psychopathologie

    2015  

    Abstract: Cet ouvrage cible la pratique qui est solidaire de la fondation de la connaissance réalisée par la phénoménologie, en voyant dans cette pratique la condition même de la formulation positive de son projet. Dans cette perspective, la critique sociale et la ...

    Abstract Cet ouvrage cible la pratique qui est solidaire de la fondation de la connaissance réalisée par la phénoménologie, en voyant dans cette pratique la condition même de la formulation positive de son projet. Dans cette perspective, la critique sociale et la psychopathologie sont notamment les deux champs pratiques où la phénoménologie se trouve investie, par-delà son premier élan de critique théorique, pour intervenir sur les formes de normativité qui y sont à l'œuvre. En abordant ces champs à travers les différentes contributions qui le composent, l'ouvrage ambitionne d'analyser la portée pratiq
    Language French
    Size Online-Ressource (292 p)
    Publisher P.I.E.-Peter Lang S.A
    Publishing place Brssel
    Document type Book ; Online
    Note Description based upon print version of record
    ISBN 9782875742148 ; 2875742140
    Database Library catalogue of the German National Library of Science and Technology (TIB), Hannover

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  4. Article ; Online: Evidence of SARS-CoV-2 in nasal brushings and olfactory mucosa biopsies of COVID-19 patients.

    Pipolo, Carlotta / Bottai, Daniele / Fuccillo, Emanuela / Aronica, Eleonora / Bruschi, Fabio / Bulfamante, Antonio Mario / Castellani, Luca / Canevini, Maria Paola / Chiumello, Davide / Ferrari, Sergio / Martinelli, Carla / Muttini, Stefano / Priori, Alberto / Saibene, Alberto Maria / Spoldi, Chiara / Tosi, Delfina / Zanusso, Gianluigi / Bulfamante, Gaetano Pietro / Felisati, Giovanni

    PloS one

    2022  Volume 17, Issue 4, Page(s) e0266740

    Abstract: The aim of the present study is to detect the presence of SARS-CoV-2 of patients affected by COVID-19 in olfactory mucosa (OM), sampled with nasal brushing (NB) and biopsy, and to assess whether a non-invasive procedure, such as NB, might be used as a ... ...

    Abstract The aim of the present study is to detect the presence of SARS-CoV-2 of patients affected by COVID-19 in olfactory mucosa (OM), sampled with nasal brushing (NB) and biopsy, and to assess whether a non-invasive procedure, such as NB, might be used as a large-scale procedure for demonstrating SARS-CoV-2 presence in olfactory neuroepithelium. Nasal brushings obtained from all the COVID-19 patients resulted positive to SARS-CoV-2 immunocytochemistry while controls were negative. Double immunofluorescence showed that SARS-CoV-2 positive cells included supporting cells as well as olfactory neurons and basal cells. OM biopsies showed an uneven distribution of SARS-CoV-2 positivity along the olfactory neuroepithelium, while OM from controls were negative. SARS-CoV-2 was distinctively found in sustentacular cells, olfactory neurons, and basal cells, supporting what was observed in NB. Ultrastructural analysis of OM biopsies showed SARS-CoV-2 viral particles in the cytoplasm of sustentacular cells. This study shows the presence of SARS-CoV-2 at the level of the olfactory neuroepithelium in patients affected by COVID-19. For the first time, we used NB as a rapid non-invasive tool for assessing a potential neuroinvasion by SARS-CoV-2 infection.
    MeSH term(s) Biopsy ; COVID-19/diagnosis ; Humans ; Olfactory Mucosa/pathology ; SARS-CoV-2
    Language English
    Publishing date 2022-04-12
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2267670-3
    ISSN 1932-6203 ; 1932-6203
    ISSN (online) 1932-6203
    ISSN 1932-6203
    DOI 10.1371/journal.pone.0266740
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Epilepsy in adult patients with tuberous sclerosis complex.

    Vignoli, Aglaia / La Briola, Francesca / Turner, Katherine / Peron, Angela / Vannicola, Chiara / Chiesa, Valentina / Zambrelli, Elena / Bruschi, Fabio / Viganò, Ilaria / Canevini, Maria Paola

    Acta neurologica Scandinavica

    2021  Volume 144, Issue 1, Page(s) 29–40

    Abstract: Objectives: Little is known about the evolution of epilepsy in individuals with tuberous sclerosis complex (TSC) in adulthood. This study aims at describing the characteristics of epilepsy in adult TSC patients attending a single multidisciplinary ... ...

    Abstract Objectives: Little is known about the evolution of epilepsy in individuals with tuberous sclerosis complex (TSC) in adulthood. This study aims at describing the characteristics of epilepsy in adult TSC patients attending a single multidisciplinary clinic.
    Materials and methods: We collected data about epilepsy (age at onset, seizure types, history of infantile spasms (IS), epilepsy diagnosis and outcome), genetic and neuroradiological findings, cognitive outcome and psychiatric comorbidities.
    Results: Out of 257 adults with TSC, 183 (71.2%) had epilepsy: 121 (67.2%) were drug-resistant; 59 (32.8%) seizure-free, at a median age of 18 years. 22% of the seizure-free patients (13/59) discontinued medication. Median age at seizure onset was 9 months. Seventy-six patients (41.5%) had a history of IS. TSC2 pathogenic variants (p = 0.018), cortical tubers (p < 0.001) and subependymal nodules (SENs) (p < 0.001) were more frequent in those who developed epilepsy. Cognitive functioning was lower (p < 0.001) and psychiatric disorders more frequent (p = 0.001). We did not find significant differences regarding age, gender, mutation and tubers/SENs in seizure-free vs drug-resistant individuals. Intellectual disability (p < 0.001) and psychiatric disorders (p = 0.004) were more common among drug-resistant patients.
    Conclusions: Epilepsy in TSC can be a lifelong disorder, but one-third of individuals reach seizure freedom by early adulthood. In the long term, age at epilepsy onset has a crucial role in drug resistance and in developing intellectual disability, both in drug-resistant and drug-sensible patients. Patients with drug-refractory seizures tend to develop psychiatric issues, which should be recognized and adequately treated.
    MeSH term(s) Adolescent ; Adult ; Child ; Child, Preschool ; Drug Resistant Epilepsy/diagnosis ; Drug Resistant Epilepsy/epidemiology ; Drug Resistant Epilepsy/psychology ; Epilepsy/diagnosis ; Epilepsy/epidemiology ; Epilepsy/psychology ; Follow-Up Studies ; Humans ; Infant ; Intellectual Disability/diagnosis ; Intellectual Disability/epidemiology ; Intellectual Disability/psychology ; Male ; Retrospective Studies ; Spasms, Infantile/diagnosis ; Spasms, Infantile/epidemiology ; Spasms, Infantile/psychology ; Tuberous Sclerosis/diagnosis ; Tuberous Sclerosis/epidemiology ; Tuberous Sclerosis/psychology
    Language English
    Publishing date 2021-03-22
    Publishing country Denmark
    Document type Journal Article
    ZDB-ID 90-5
    ISSN 1600-0404 ; 0001-6314
    ISSN (online) 1600-0404
    ISSN 0001-6314
    DOI 10.1111/ane.13416
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Tuberous sclerosis complex (TSC), lymphangioleiomyomatosis, and COVID-19: The experience of a TSC clinic in Italy.

    Peron, Angela / La Briola, Francesca / Bruschi, Fabio / Terraneo, Silvia / Vannicola, Chiara / Previtali, Roberto / Perazzoli, Sabrina / Morenghi, Emanuela / Bulfamante, Gaetano / Vignoli, Aglaia / Canevini, Maria Paola

    American journal of medical genetics. Part A

    2020  Volume 182, Issue 11, Page(s) 2479–2485

    Abstract: Individuals with comorbidities are at higher risk of coronavirus disease 2019 (COVID-19) and worse outcome, but little information has been available about patients with genetic diseases and COVID-19. This study aims at evaluating the presence and ... ...

    Abstract Individuals with comorbidities are at higher risk of coronavirus disease 2019 (COVID-19) and worse outcome, but little information has been available about patients with genetic diseases and COVID-19. This study aims at evaluating the presence and outcome of COVID-19 in a cohort of Italian patients with tuberous sclerosis complex (TSC) and/or lymphangioleiomyomatosis (LAM), and at reviewing the possible effects of mTOR inhibitors on SARS-CoV-2 infection. We included 102 unselected individuals with a diagnosis of TSC and/or LAM assessed between January 1, 2020 and April 24, 2020 (29% children, 71% adults). Twenty-six patients were on mTOR inhibitors. Demographic data, TSC manifestations, presence, and outcomes in individuals with confirmed or suspected SARS-CoV-2 infection were evaluated. Health status and outcomes of all patients on mTOR inhibitors were assessed. One patient with severe TSC had polymerase chain reaction (PCR)-confirmed SARS-CoV-2 infection, was admitted to ICU, and died. Nine additional patients either met the definition of suspect case or presented with at least two of the most common symptoms of SARS-CoV-2 infection. All recovered fully. None of the patients treated with mTOR inhibitors for their underlying comorbidities was diagnosed with COVID-19, and those who showed suspicious respiratory symptoms recovered fully. This cohort study provides preliminary information on COVID-19 in people with TSC in Italy and suggests feasibility to systematically evaluate the role of mTOR inhibitors in SARS-CoV-2 infection.
    MeSH term(s) Adolescent ; Adult ; Aged ; Betacoronavirus/genetics ; Betacoronavirus/isolation & purification ; COVID-19 ; Child ; Child, Preschool ; Cohort Studies ; Comorbidity ; Coronavirus Infections/epidemiology ; Coronavirus Infections/virology ; Female ; Hospitalization ; Humans ; Infant ; Italy/epidemiology ; Lymphangioleiomyomatosis/epidemiology ; Male ; Middle Aged ; Pandemics ; Pneumonia, Viral/epidemiology ; Pneumonia, Viral/virology ; Retrospective Studies ; SARS-CoV-2 ; Tuberous Sclerosis/epidemiology ; Young Adult
    Keywords covid19
    Language English
    Publishing date 2020-08-17
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2108614-X
    ISSN 1552-4833 ; 0148-7299 ; 1552-4825
    ISSN (online) 1552-4833
    ISSN 0148-7299 ; 1552-4825
    DOI 10.1002/ajmg.a.61810
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: Tuberous sclerosis complex (TSC), lymphangioleiomyomatosis, and COVID-19: The experience of a TSC clinic in Italy

    Peron, Angela / La Briola, Francesca / Bruschi, Fabio / Terraneo, Silvia / Vannicola, Chiara / Previtali, Roberto / Perazzoli, Sabrina / Morenghi, Emanuela / Bulfamante, Gaetano / Vignoli, Aglaia / Canevini, Maria Paola

    Am J Med Genet A

    Abstract: Individuals with comorbidities are at higher risk of coronavirus disease 2019 (COVID-19) and worse outcome, but little information has been available about patients with genetic diseases and COVID-19. This study aims at evaluating the presence and ... ...

    Abstract Individuals with comorbidities are at higher risk of coronavirus disease 2019 (COVID-19) and worse outcome, but little information has been available about patients with genetic diseases and COVID-19. This study aims at evaluating the presence and outcome of COVID-19 in a cohort of Italian patients with tuberous sclerosis complex (TSC) and/or lymphangioleiomyomatosis (LAM), and at reviewing the possible effects of mTOR inhibitors on SARS-CoV-2 infection. We included 102 unselected individuals with a diagnosis of TSC and/or LAM assessed between January 1, 2020 and April 24, 2020 (29% children, 71% adults). Twenty-six patients were on mTOR inhibitors. Demographic data, TSC manifestations, presence, and outcomes in individuals with confirmed or suspected SARS-CoV-2 infection were evaluated. Health status and outcomes of all patients on mTOR inhibitors were assessed. One patient with severe TSC had polymerase chain reaction (PCR)-confirmed SARS-CoV-2 infection, was admitted to ICU, and died. Nine additional patients either met the definition of suspect case or presented with at least two of the most common symptoms of SARS-CoV-2 infection. All recovered fully. None of the patients treated with mTOR inhibitors for their underlying comorbidities was diagnosed with COVID-19, and those who showed suspicious respiratory symptoms recovered fully. This cohort study provides preliminary information on COVID-19 in people with TSC in Italy and suggests feasibility to systematically evaluate the role of mTOR inhibitors in SARS-CoV-2 infection.
    Keywords covid19
    Publisher WHO
    Document type Article
    Note WHO #Covidence: #716196
    Database COVID19

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  8. Article ; Online: Tuberous sclerosis complex (TSC), lymphangioleiomyomatosis, and COVID ‐19

    Peron, Angela / La Briola, Francesca / Bruschi, Fabio / Terraneo, Silvia / Vannicola, Chiara / Previtali, Roberto / Perazzoli, Sabrina / Morenghi, Emanuela / Bulfamante, Gaetano / Vignoli, Aglaia / Canevini, Maria Paola

    American Journal of Medical Genetics Part A ; ISSN 1552-4825 1552-4833

    The experience of a TSC clinic in Italy

    2020  

    Keywords Genetics(clinical) ; Genetics ; covid19
    Language English
    Publisher Wiley
    Publishing country us
    Document type Article ; Online
    DOI 10.1002/ajmg.a.61810
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  9. Article ; Online: Validation of the Italian version of the PSP Quality of Life questionnaire.

    Picillo, Marina / Cuoco, Sofia / Amboni, Marianna / Bonifacio, Francesco Paolo / Bruschi, Fabio / Carotenuto, Immacolata / De Micco, Rosa / De Rosa, Anna / Del Prete, Eleonora / Di Biasio, Francesca / Elifani, Francesca / Erro, Roberto / Fabbri, Margherita / Falla, Marika / Franco, Giulia / Frosini, Daniela / Galantucci, Sebastiano / Lazzeri, Giulia / Magistrelli, Luca /
    Malaguti, Maria Chiara / Milner, Anna Vera / Minafra, Brigida / Olivola, Enrica / Pilotto, Andrea / Rascunà, Cristina / Rizzetti, Maria Cristina / Schirinzi, Tommaso / Borroni, Barbara / Ceravolo, Roberto / Di Fonzo, Alessio / Marchese, Roberta / Mercuri, Nicola B / Modugno, Nicola / Nicoletti, Alessandra / Padovani, Alessandro / Santangelo, Gabriella / Stefani, Alessandro / Tessitore, Alessandro / Volontè, Maria Antonietta / Zangaglia, Roberta / Zappia, Mario / Zibetti, Maurizio / Barone, Paolo

    Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

    2019  Volume 40, Issue 12, Page(s) 2587–2594

    Abstract: Background: Progressive supranuclear palsy (PSP) is a rare rapidly progressive, neurodegenerative disease characterized by falls and ocular movement disturbances. The use of health-related quality of life (HR-QoL) measures allows assessing changes in ... ...

    Abstract Background: Progressive supranuclear palsy (PSP) is a rare rapidly progressive, neurodegenerative disease characterized by falls and ocular movement disturbances. The use of health-related quality of life (HR-QoL) measures allows assessing changes in health status induced by therapeutic interventions or disease progress in neurodegenerative diseases. The PSP-QoL is a 45-item, self-administered questionnaire designed to evaluate HR-QoL in PSP.
    Methods and results: Here, the PSP-QoL was translated into Italian and validated in 190 PSP (96 women and 94 men; mean age ± standard deviation, 72 ± 6.5; mean disease duration, 4.2 ± 2.3) patients diagnosed according to the Movement Disorder Society criteria and recruited in 16 third level movement disorders centers participating in the Neurecanet project. The mean PSP-QoL total score was 77.8 ± 37 (physical subscore, 46.5 ± 18.7; mental subscore, 33.6 ± 19.2). The internal consistency was high (Cronbach's alpha = 0.954); corrected item-total correlation was > 0.40 for the majority of items. The significant and moderate correlation of the PSP-QoL with other HR-QoL measures as well as with motor and disability assessments indicated adequate convergent validity of the scale. Gender and geographic location presented a significant impact on the PSP-QoL in our sample with women and patients from the South of Italy scoring higher than their counterparts.
    Conclusion: In conclusion, the Italian version of the PSP-QoL is an easy, reliable and valid tool for assessment of HR-QoL in PSP.
    MeSH term(s) Aged ; Aged, 80 and over ; Female ; Humans ; Italy ; Male ; Psychometrics/instrumentation ; Psychometrics/standards ; Quality of Life ; Reproducibility of Results ; Self Report ; Supranuclear Palsy, Progressive/diagnosis
    Language English
    Publishing date 2019-07-26
    Publishing country Italy
    Document type Journal Article ; Validation Study
    ZDB-ID 2016546-8
    ISSN 1590-3478 ; 1590-1874
    ISSN (online) 1590-3478
    ISSN 1590-1874
    DOI 10.1007/s10072-019-04010-2
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Validation of the Italian version of carers' quality-of-life questionnaire for parkinsonism (PQoL Carer) in progressive supranuclear palsy.

    Picillo, Marina / Cuoco, Sofia / Amboni, Marianna / Bonifacio, Francesco Paolo / Bruno, Antonino / Bruschi, Fabio / Cappiello, Arianna / De Micco, Rosa / De Rosa, Anna / Di Biasio, Francesca / Elifani, Francesca / Erro, Roberto / Fabbri, Margherita / Falla, Marika / Franco, Giulia / Frosini, Daniela / Galantucci, Sebastiano / Lazzeri, Giulia / Magistrelli, Luca /
    Malaguti, Maria Chiara / Milner, Anna Vera / Minafra, Brigida / Olivola, Enrica / Pilotto, Andrea / Rascunà, Cristina / Rizzetti, Maria Cristina / Schirinzi, Tommaso / Borroni, Barbara / Ceravolo, Roberto / Di Fonzo, Alessio / Lopiano, Leonardo / Marchese, Roberta / Mercuri, Nicola B / Modugno, Nicola / Nicoletti, Alessandra / Padovani, Alessandro / Santangelo, Gabriella / Stefani, Alessandro / Tessitore, Alessandro / Volontè, Maria Antonietta / Zangaglia, Roberta / Zappia, Mario / Barone, Paolo

    Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

    2019  Volume 40, Issue 10, Page(s) 2163–2169

    Abstract: Progressive supranuclear palsy (PSP) is a rare, rapidly progressive, neurodegenerative disease characterized by falls and ocular movement disturbances. Caring for a partner or relative who suffers from PSP entails a strenuous and demanding task, usually ... ...

    Abstract Progressive supranuclear palsy (PSP) is a rare, rapidly progressive, neurodegenerative disease characterized by falls and ocular movement disturbances. Caring for a partner or relative who suffers from PSP entails a strenuous and demanding task, usually lasting for years that affects carers' everyday life routines and emotional and social well-being. The 26-item Parkinsonism Carers QoL (PQoL Carer) is a self-administered, concise instrument evaluating the quality of life of caregivers of patients with atypical parkinsonism (both PSP and multiple system atrophy). Here, the PQoL Carer was translated into Italian and validated in 162 carers of PSP patients (54.3% women; mean age (standard deviation), 62.4 (15.4)) diagnosed according to the Movement Disorder Society criteria and recruited in 16 third-level movement disorders centers participating in the Neurecanet project. The mean PQoL total score was 40.66 ± 19.46. The internal consistency was excellent (Cronbach's alpha = 0.941); corrected item-total correlation was > 0.40 for all the items. A correlation with other health-related quality of life measures as well as with behavioral assessments was shown suggesting adequate convergent validity of the scale. PQoL also correlated with patients' severity of disease. The discriminant validity of the scale was evidenced by its capacity to differentiate between carers with varying levels of self-reported health (p < 0.001). In conclusion, the Italian version of the PQoL Carer is an easy, consistent, and valid tool for the assessment of the quality of life in carers of PSP patients.
    MeSH term(s) Adult ; Aged ; Caregivers/psychology ; Female ; Humans ; Italy ; Male ; Middle Aged ; Parkinsonian Disorders/etiology ; Psychometrics/instrumentation ; Quality of Life/psychology ; Supranuclear Palsy, Progressive/complications ; Surveys and Questionnaires ; Translating
    Language English
    Publishing date 2019-06-12
    Publishing country Italy
    Document type Journal Article ; Validation Study
    ZDB-ID 2016546-8
    ISSN 1590-3478 ; 1590-1874
    ISSN (online) 1590-3478
    ISSN 1590-1874
    DOI 10.1007/s10072-019-03944-x
    Database MEDical Literature Analysis and Retrieval System OnLINE

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