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The use of patient-reported outcomes becomes standard practice in the routine clinical care of lung–heart transplant patients

机译:在肺心移植患者的常规临床护理中,使用患者报告的结果已成为标准做法

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Objective: To assess the use of patient-reported outcome (PROs) measures in the routine clinical care of lung–heart transplant patients. We assessed whether the addition of PROs in routine clinical care affected the duration of the consultation and patient’s and clinician’s views. Method: Consecutive lung–heart transplant patients visiting the outpatient clinic, University of Alberta Hospital, completed the Chronic Respiratory Questionnaire (CRQ) and the Health Utilities Index (HUI) on touchscreen computers. Information on the patient’s responses was made available to the members of the transplant team prior to the encounter with the patient. The duration of clinical encounters was noted. At the end of every visit, clinicians completed a questionnaire on the usefulness of having PRO information available. After 6 months patients completed a survey of their experiences. Results: The final patient sample consisted of 172 patients with a mean (SD) age of 52 (13.3) years old; 47% were female; 68% were organ recipients and 32% candidates. The transplant team, comprising four pulmunologists, two nurses, and one pharmacist had an average of 9 years of practical experience in pulmunology. The mean duration of patient–clinician encounters in minutes was 15.15 (4.52). Ninety-eight percent of patients indicated that they would be happy to complete the CRQ and HUI at every clinic visit. Ninety-one percent of the assessments completed by clinicians showed complete satisfaction with the use of PROs in routine practice. Further, the clinicians developed guidelines for the use of PRO information in clinical practice. Conclusions: The incorporation of PRO measures in the routine clinical care of lung–heart transplant patients resulted in a reduction of the duration of patient–clinician encounters. The experience was well accepted by patients and clinicians. We conclude that the routine use of PROs in lung–heart transplant patients has become standard practice.
机译:目的:评估患者报告的结局(PROs)措施在肺心移植患者的常规临床护理中的使用。我们评估了常规临床护理中增加PRO的使用是否会影响咨询的持续时间以及患者和临床医生的意见。方法:连续的肺心移植患者前往阿尔伯塔大学医院门诊就诊,并在触摸屏计算机上完成了慢性呼吸调查问卷(CRQ)和健康公用事业指数(HUI)。在与患者会面之前,已将有关患者反应的信息提供给移植小组的成员。记录了临床遭遇的持续时间。在每次拜访结束时,临床医生填写了有关提供PRO信息的有用性的问卷。 6个月后,患者完成了对其经历的调查。结果:最终的患者样本包括172名平均(SD)年龄为52(13.3)岁的患者。女性占47%; 68%是器官接受者,32%是候选人。移植团队由四名肺病学家,两名护士和一名药剂师组成,平均拥有9年的肺病实践经验。病人与临床医生的平均持续时间(分钟)为15.15(4.52)。 98%的患者表示,他们愿意在每次门诊就诊时完成CRQ和HUI。临床医生完成的评估中有91%对常规实践中使用PRO表示完全满意。此外,临床医生制定了在临床实践中使用PRO信息的指南。结论:在肺心移植患者的常规临床护理中纳入PRO措施可缩短患者与临床医生的接触时间。经验被患者和临床医生所接受。我们得出的结论是,在肺心移植患者中常规使用PRO已成为标准做法。

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