痴呆症患者及其护理人员的管理和护理:意大利全国护理人员和服务使用调查结果。

IF 1.7
Alice Paggetti, Patrizia Lorenzini, Elisa Fabrizi, Annachiara Di Nolfi, Francesca Zambri, Angela Giusti, Vittorio Palermo, Ilaria Palazzesi, Serena Passoni, Flaminia Camilli, Guido Bellomo, Nicoletta Locuratolo, Francesco Sciancalepore, Antonio Ancidoni, Susanna Cipollari, Manuela Berardinelli, Luisa Bartorelli, Nicola Vanacore, Francesco Della Gatta
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引用次数: 0

摘要

背景:预期寿命的延长将导致更多的人患有痴呆症(PLwD),因此,更多的照顾者将面临负担。护理人员负担受PLwD和护理人员自身特征以及医疗服务组织的影响。新冠肺炎大流行和意大利实施的封锁措施使残疾人及其照顾者的健康状况恶化。认识到了解PLwD及其护理人员的概况和护理需求的重要性,意大利阿尔茨海默氏症和痴呆症基金开展了一项全国性调查,调查意大利PLwD护理人员及其护理对象的社会人口统计学特征。本研究旨在描述意大利PLwD护理人员的特点,他们对服务的使用,以及对后者的满意度。方法:采用全国横断面调查方法。一份自我管理的问卷主要由多项选择题组成。结果:共有2369名护理人员参与调查。其中大多数居住在意大利北部(60.1%),为女性(73.4%)和照顾者的子女(74.1%)。诊断延迟的中位数为7至36个月。诊断主要是由认知障碍和痴呆中心的一名医生制定的。护理人员培训报告不足(34.1%)。大流行期间,PLwD临床状况恶化。对痴呆症服务的平均满意度是“可以接受的”。消极/非常消极的满意程度与以下因素有关:不在北方生活、照顾者年龄增加、未接受培训、疾病严重、从私人医生那里得到怀疑诊断、未使用日托中心或认知障碍和痴呆症中心。结论:意大利出现了护理人员的社会人口特征差异和服务差异。需要在疾病进展的所有阶段建立一个全面、可获得和整合良好的服务网络。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Management and Care for People Living With Dementia and Their Caregivers: Findings From an Italian National Survey on Caregivers and Services Use.

Management and Care for People Living With Dementia and Their Caregivers: Findings From an Italian National Survey on Caregivers and Services Use.

Management and Care for People Living With Dementia and Their Caregivers: Findings From an Italian National Survey on Caregivers and Services Use.

Management and Care for People Living With Dementia and Their Caregivers: Findings From an Italian National Survey on Caregivers and Services Use.

Background: Increasing life expectancy will lead to more people living with dementia (PLwD) and, consequently, more caregivers experiencing burden. Caregivers burden is influenced by characteristics of both PLwD and caregivers themselves, as well as healthcare services organisation. The COVID-19 pandemic and lockdown measures implemented in Italy worsened PLwD and their caregivers' well-being. Recognising the importance of understanding the profiles and care needs of PLwD and their caregivers, a national survey was conducted within the Italian Fund for Alzheimer's and Dementias to investigate the sociodemographic characteristics of PLwD caregivers and their care recipients in Italy. This study aimed to describe the characteristics of Italian caregivers of PLwD, their use of services, and satisfaction with the latter.

Methods: A cross-sectional national survey was conducted. A self-administered questionnaire was developed consisting mainly of multiple-choice questions.

Results: A total of 2369 caregivers participated in the survey. Most of them resided in Northern Italy (60.1%), were females (73.4%) and care recipients' children (74.1%). Median diagnostic delay ranged from 7 to 36 months. Diagnosis was formulated mainly by a physician from a Centre for Cognitive Disorders and Dementia. Caregiver training was poorly reported (34.1%). PLwD clinical condition worsened during the pandemic. The mean degree of satisfaction with services dedicated to dementia was "acceptable". Negative/very negative degree of satisfaction was associated with not living in the North, increased caregiver's age, not having received training, severe degree of disease, having received the diagnosis suspicion from a private doctor, and not having used day care centres or Centres for Cognitive Disorders and Dementia.

Conclusions: Differences in the sociodemographic profile of caregivers and disparity in services across Italy emerged. The establishment of a comprehensive, accessible, and well-integrated network of services across all stages of the disease progression is needed.

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