Lau R R, Williams H S, Williams L C, Ware J E, Brook R H
J Community Health. 1982 Summer;7(4):250-61. doi: 10.1007/BF01318958.
This study concerns the psychosocial aspects of treatment for chronically ill children. The English-speaking parents of 44 children 5-13 years of age being seen at five specialty clinics at a large county hospital in Los Angeles, and their attending physicians, were the subjects in this study. The parents were interviewed concerning their expectations for the current visit, and the doctor-patient interaction was tape-recorded. Identical categories of information were abstracted from the tape recording and from a chart review of the patients' medical records. Although parents expected 76% of the psychosocial aspects of care to be covered by the doctor, only one fourth were actually discussed in the visit. These unfulfilled expectations were associated with lower satisfaction with medical care received (r = .47, p less than 0.01). Finally, while doctors recorded about 80% of discussions of symptoms and physical examinations in the patient's medical record, they recorded only 25% of discussion of psychosocial problems.
本研究关注慢性病患儿治疗中的社会心理方面。在洛杉矶一家大型县医院的五个专科诊所就诊的44名5至13岁儿童的讲英语的家长及其主治医生是本研究的对象。就家长对此次就诊的期望对他们进行了访谈,并对医患互动进行了录音。从录音以及对患者病历的图表审查中提取了相同类别的信息。尽管家长期望医生能涵盖76%的社会心理护理方面,但就诊时实际讨论的仅占四分之一。这些未得到满足的期望与对所接受医疗护理的较低满意度相关(r = 0.47,p < 0.01)。最后,虽然医生在患者病历中记录了约80%的症状讨论和体格检查,但他们仅记录了25%的社会心理问题讨论。