King's College London, London, UK.
King's College London, London, UK.
Lancet. 2015 Feb 26;385 Suppl 1:S93. doi: 10.1016/S0140-6736(15)60408-1.
The provision of good quality and equitable end-of-life care is high on the public and political agenda. Hospice is second only to home in terms of preference for place of death and scores higher than any other setting for quality of care. However, hospices have been criticised for inequality of access with respect to age, diagnosis, and socioeconomic status. We aimed to describe the demographic characteristics associated with hospice death in England, and assessed how these characteristics have changed over time.
In this population-based study (part of the GUIDE_Care project), we included all adults older than 25 years who had died in inpatient hospices in England from 1993 to 2002. We compared deaths in 1998-2002, 2003-07, and 2008-12, with those in 1993-97 using multivariable Poisson regression. Explanatory variables included individual factors (age, sex, marital status, underlying cause of death) and measures of deprivation based on area of residence.
446 615 deaths were included. The annual number of hospice deaths increased from 17 440 in 1993 to 26 032 in 2012, accounting for 3·4% of 519 313 deaths in England in 1993, and 6·0% of 434 105 deaths in 2012. 226 188 hospice decedents (50·6%) were men (mean age 69·9 years, SD 12·4). The likelihood of hospice decedents being in the oldest age group (>85 years) increased from 1993-97 to 2008-12 (Poisson ratio 1·43, 95% CI 1·39-1·48). Only 23 258 hospice decedents (5·2%) had non-cancer diagnoses, though the likelihood of non-cancer conditions increased during the same time period (1·41, 1·37-1·46). The likelihood of hospice decedents being resident in the least deprived quintile also increased (1·25, 1·22-1·29).
Inequalities among hospice decedents by diagnosis have decreased, although the absolute numbers of non-cancer diagnoses remain very small. Trends in deprivation are concerning, and require further exploration.
The GUIDE_Care project was funded by the National Institute for Health Research (NIHR) Health Services and Delivery Research programme (project number 09/2000/58).
提供高质量和公平的临终关怀是公众和政治议程的重中之重。临终关怀在临终地点的选择方面仅次于家庭,在护理质量方面的得分高于任何其他环境。然而,临终关怀机构因其在年龄、诊断和社会经济地位方面的准入不平等而受到批评。我们旨在描述与英格兰临终关怀死亡相关的人口统计学特征,并评估这些特征随时间的变化情况。
在这项基于人群的研究(GUIDE_Care 项目的一部分)中,我们纳入了所有年龄在 25 岁以上、1993 年至 2002 年期间在英格兰住院临终关怀机构去世的成年人。我们将 1998-2002 年、2003-07 年和 2008-12 年的死亡情况与 1993-97 年进行了比较,使用多变量泊松回归进行比较。解释变量包括个体因素(年龄、性别、婚姻状况、死亡的根本原因)和基于居住地区的贫困程度指标。
共纳入 446615 例死亡。临终关怀死亡人数从 1993 年的 17440 人增加到 2012 年的 26032 人,占 1993 年英格兰 519313 例死亡人数的 3.4%和 2012 年 434105 例死亡人数的 6.0%。226188 名(50.6%)临终关怀死者为男性(平均年龄 69.9 岁,标准差 12.4)。年龄最大(>85 岁)组的临终关怀死者比例从 1993-97 年增加到 2008-12 年(泊松比 1.43,95%CI 1.39-1.48)。尽管同期非癌症疾病的可能性增加(1.41,1.37-1.46),但仅有 23258 名(5.2%)临终关怀死者有非癌症诊断。临终关怀死者居住在最贫困五分位数的比例也有所增加(1.25,1.22-1.29)。
尽管非癌症诊断的绝对数量仍然很小,但在诊断方面,临终关怀死者的不平等情况有所减少。贫困趋势令人担忧,需要进一步探讨。
GUIDE_Care 项目由英国国家卫生研究所(NIHR)健康服务和交付研究计划(项目编号 09/2000/58)资助。