Department of Family Medicine, McGill University, Montreal, Quebec, Canada.
ICES, Toronto, Ontario, Canada.
J Am Geriatr Soc. 2020 May;68(5):1056-1063. doi: 10.1111/jgs.16347. Epub 2020 Feb 5.
Growing evidence points to underlying sex differences in the risk factors and clinical presentation of dementia. It is unclear, however, whether sex differences also exist in the management and healthcare utilization of persons with dementia. We compared primary care performance and health service use indicators for newly identified men and women with dementia in Ontario, Canada, over a 12-year period.
Population-based, repeated cohort study between 2002 and 2014.
Ontario, Canada.
A total of 318 350 community-dwelling adults, aged 65 years and older, newly identified with dementia, followed for up to 1 year.
Eighteen indicators of primary care performance and health service use were assessed.
Approximately 60% of the study population were women. Few differences in the indicators were observed between sexes, although men had fewer diagnoses first recorded by the family physician, more visits to noncognition specialists, less use of home care, more hospitalizations and readmissions, and longer discharge delays. Most indicators remained relatively stable over time for both men (median relative change = 13.7%; interquartile range [IQR] = 4.5%-29.7%) and women (median relative change = 15.7%; IQR = 5.9%-31.5%). Notable improvements over time for both sexes included access to an interprofessional primary care team, use of home care, and decreased use of long-term care. Areas of worsening included a higher occurrence of emergency department visits, lower continuity of care, and longer discharge delays.
These findings raise awareness on the similarities and differences in management and health system use for men and women newly diagnosed with dementia, particularly the imbalance in hospital and home care use. As health systems continue to adapt to meet the needs of the growing dementia population, policy makers and clinicians should be mindful to develop care plans and interventions that consider the influence of sex on the need for services. J Am Geriatr Soc 68:1056-1063, 2020.
越来越多的证据表明,痴呆的风险因素和临床表现存在潜在的性别差异。然而,在痴呆患者的管理和医疗保健利用方面是否存在性别差异尚不清楚。我们比较了加拿大安大略省在 12 年内新确诊的男性和女性痴呆患者的初级保健绩效和卫生服务使用指标。
2002 年至 2014 年期间进行的基于人群的重复队列研究。
加拿大安大略省。
共有 318350 名年龄在 65 岁及以上、新确诊为痴呆的社区居住成年人,随访时间长达 1 年。
评估了 18 项初级保健绩效和卫生服务使用指标。
研究人群中约有 60%为女性。尽管男性首次由家庭医生记录的诊断较少,就诊于非认知专家的次数更多,使用家庭护理的次数更少,住院和再入院次数更多,出院延迟时间更长,但在这些指标上男女之间几乎没有差异。对于男性(中位数相对变化=13.7%;四分位距[IQR]=4.5%-29.7%)和女性(中位数相对变化=15.7%;IQR=5.9%-31.5%),大多数指标在一段时间内相对稳定。两性都有显著改善的领域包括获得多学科初级保健团队、使用家庭护理和减少长期护理的使用。恶化的领域包括急诊就诊次数增加、连续性护理降低和出院延迟时间延长。
这些发现使人们意识到新诊断为痴呆的男性和女性在管理和卫生系统使用方面的相似之处和不同之处,特别是在医院和家庭护理使用方面的不平衡。随着卫生系统继续适应不断增长的痴呆人口的需求,政策制定者和临床医生应该注意制定考虑到性别对服务需求的影响的护理计划和干预措施。美国老年医学会杂志 68:1056-1063,2020。