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一项针对心力衰竭患者医疗决策角色及其与患者特征和患者报告结局之间关联的前瞻性队列研究。

A Prospective Cohort Study of Medical Decision-Making Roles and Their Associations with Patient Characteristics and Patient-Reported Outcomes among Patients with Heart Failure.

机构信息

Signature Program in Health Services and Systems Research, Lien Centre for Palliative Care, Duke-NUS Medical School, Singapore.

Department of Population Health Sciences, Duke Clinical Research Institute, Duke University, USA.

出版信息

Med Decis Making. 2023 Oct-Nov;43(7-8):863-874. doi: 10.1177/0272989X231201609. Epub 2023 Sep 28.

Abstract

OBJECTIVE

Among patients with heart failure (HF), we examined 1) the evolution of patient involvement in decision making over 2 y, 2) the association of patient characteristics with decision-making roles, and 3) the association of decision-making roles with distress, spiritual well-being, and quality of physician communication.

METHODS

We administered the survey every 4 mo over 24 mo to patients with New York Heart Association class 3/4 symptoms recruited from inpatient clinics. The decision-making roles were categorized as no patient involvement, physician/family-led, joint (with family and/or physicians), patient-led, or patient-alone decision making. The associations between patient characteristics and decision-making roles were assessed using a mixed-effects ordered logistic regression, whereas those between patient outcomes and decision-making roles were investigated using mixed-effects linear regressions.

RESULTS

Of the 557 patients invited, 251 participated in the study. The most common roles in decision making at baseline assessment were "no involvement" (27.53%) and "patient-alone decision making" (25.10%). The proportions of different decision-making roles did not change over 2 y ( = 0.37). Older age (odds ratio [OR] = 0.97;  = 0.003) and being married (OR = 0.63;  = 0.035) were associated with lower involvement in decision making. Chinese ethnicity (OR = 1.91;  = 0.003), higher education (OR = 1.87;  = 0.003), awareness of terminal condition (OR = 2.00;  < 0.001), and adequate self-care confidence (OR = 1.74;  < 0.001) were associated with greater involvement. Compared with no patient involvement, joint (β = -0.58;  = 0.026) and patient-led (β = -0.59;  = 0.014) decision making were associated with lower distress, while family/physician-led (β = 4.37;  = 0.001), joint (β = 3.86;  < 0.001), patient-led (β = 3.46;  < 0.001), and patient-alone (β = 3.99;  < 0.001) decision making were associated with better spiritual well-being.

CONCLUSION

A substantial proportion of patients was not involved in decision making. Patients should be encouraged to participate in decision making since it is associated with lower distress and better spiritual well-being.

HIGHLIGHTS

The level of involvement in medical decision making did not change over time among patients with heart failure. A substantial proportion of patients were not involved in decision making throughout the 24-mo study period.Patients' involvement in decision making varied by age, ethnicity, education level, marital status, awareness of the terminal condition, and confidence in self-care.Compared with no patient involvement in decision making, joint and patient-led decision making were associated with lower distress, and any level of patient involvement in decision making was associated with better spiritual well-being.

摘要

目的

在心力衰竭(HF)患者中,我们检验了 1)患者在 2 年内参与决策的演变,2)患者特征与决策角色的关联,以及 3)决策角色与痛苦、精神健康和医生沟通质量的关联。

方法

我们每 4 个月向从住院诊所招募的纽约心脏协会 3/4 级症状的患者进行一次问卷调查,持续 24 个月。决策角色分为无患者参与、医生/家庭主导、共同(与家庭和/或医生)、患者主导或患者独自决策。使用混合效应有序逻辑回归评估患者特征与决策角色之间的关联,而使用混合效应线性回归评估患者结局与决策角色之间的关联。

结果

在邀请的 557 名患者中,有 251 名参加了研究。基线评估中最常见的决策角色是“无参与”(27.53%)和“患者独自决策”(25.10%)。2 年内不同决策角色的比例没有变化(=0.37)。年龄较大(比值比[OR] = 0.97;=0.003)和已婚(OR = 0.63;=0.035)与决策参与度较低相关。华裔(OR = 1.91;=0.003)、受教育程度较高(OR = 1.87;=0.003)、对终末期疾病的认识(OR = 2.00;<0.001)和适当的自我护理信心(OR = 1.74;<0.001)与更高的参与度相关。与无患者参与相比,共同(β=−0.58;=0.026)和患者主导(β=−0.59;=0.014)决策与较低的痛苦相关,而家庭/医生主导(β=4.37;=0.001)、共同(β=3.86;<0.001)、患者主导(β=3.46;<0.001)和患者独自(β=3.99;<0.001)决策与更好的精神健康相关。

结论

相当一部分患者没有参与决策。应鼓励患者参与决策,因为这与较低的痛苦和更好的精神健康有关。

重点

心力衰竭患者的医疗决策参与度在 2 年内没有随时间变化。在整个 24 个月的研究期间,相当一部分患者没有参与决策。

患者参与决策的程度因年龄、种族、教育水平、婚姻状况、对终末期疾病的认识和自我护理信心而异。

与无患者参与决策相比,共同和患者主导的决策与较低的痛苦相关,任何程度的患者参与决策都与更好的精神健康相关。

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