Flieger Signe Peterson, Chui Kenneth, Koch-Weser Susan
Tufts University School of Medicine, Boston, MA, USA.
J Gen Intern Med. 2020 Jul;35(7):2059-2064. doi: 10.1007/s11606-020-05730-4. Epub 2020 Mar 10.
Despite recent growth in palliative care programs palliative care remains underutilized. Studies suggest that patients and providers commonly associate palliative care with end of life, often leading to misconceptions and late referrals.
To characterize self-reported palliative care knowledge and misconceptions about palliative care among US adults and demographic, health, and social role factors associated with knowledge and misconceptions.
We conducted secondary data analysis of nationally representative, self-reported data from the 2018 Health Information National Trends Survey (HINTS) 5, Cycle 2. We examined associations between knowledge and misconceptions about palliative care together with demographics, health care access, health status, and social roles.
3504 US adults. 2594 included in the first analysis after omitting missing cases; 683 who reported knowing about palliative care were included in the second analysis.
Palliative care knowledge was self-reported in response to: "How would you describe your level of knowledge about palliative care?" Level of misconceptions was based on a series of factual and attitudinal statements about palliative care.
Among US adults, 28.8% report knowing about palliative care, but only 12.6% report knowing what palliative care is and hold no misconceptions. Those most likely to report knowing about palliative care are female, college-educated, higher income, have a primary health care provider, or are a caregiver. Among those who report knowing about palliative care, misconceptions were common: 44.4% automatically think of death, 38.0% equate palliative care with hospice, 17.8% believe you must stop other treatments, and 15.9% see palliative care as giving up.
US adults who have some knowledge of palliative care are most likely to confuse it with hospice but are less likely to see it as requiring forgoing treatment or as giving up. Primary care clinicians should be encouraged to communicate about palliative care with patients.
尽管姑息治疗项目近期有所增加,但姑息治疗的利用率仍然较低。研究表明,患者和医护人员通常将姑息治疗与生命末期联系在一起,这往往会导致误解和转诊延迟。
描述美国成年人自我报告的姑息治疗知识、对姑息治疗的误解,以及与知识和误解相关的人口统计学、健康和社会角色因素。
我们对2018年健康信息国家趋势调查(HINTS)5周期2的全国代表性自我报告数据进行了二次数据分析。我们研究了对姑息治疗的知识和误解与人口统计学、医疗保健可及性、健康状况和社会角色之间的关联。
3504名美国成年人。在剔除缺失病例后,2594人纳入首次分析;683名报告了解姑息治疗的人纳入二次分析。
姑息治疗知识通过回答“你如何描述自己对姑息治疗的了解程度?”进行自我报告。误解程度基于一系列关于姑息治疗的事实性和态度性陈述。
在美国成年人中,28.8%的人报告了解姑息治疗,但只有12.6%的人报告知道姑息治疗是什么且没有误解。最有可能报告了解姑息治疗的人是女性、受过大学教育、收入较高、有初级医疗保健提供者或为护理人员。在报告了解姑息治疗的人中,误解很常见:44.4%的人自动联想到死亡,38.0%的人将姑息治疗等同于临终关怀,17.8%的人认为必须停止其他治疗,15.9%的人将姑息治疗视为放弃。
对姑息治疗有一定了解的美国成年人最有可能将其与临终关怀混淆,但不太可能认为它需要放弃治疗或等同于放弃。应鼓励初级保健临床医生与患者就姑息治疗进行沟通。