Wiener Renda Soylemez, Clark Jack A, Koppelman Elisa, Bolton Rendelle, Fix Gemmae M, Slatore Christopher G, Kathuria Hasmeena
Center for Healthcare Organization & Implementation Research, Edith Nourse Rogers Memorial Veterans Hospital, Bedford, MA; The Pulmonary Center, Boston University School of Medicine, Boston, MA.
Boston University School of Public Health Boston, MA.
Chest. 2020 Sep;158(3):1240-1249. doi: 10.1016/j.chest.2020.03.081. Epub 2020 May 7.
In the incidental pulmonary nodule and breast cancer screening settings, high-quality patient-centered communication can improve adherence to evaluation and mitigate patient distress. Although guidelines emphasize shared decision-making before lung cancer screening, little is known about patient-clinician communication after lung cancer screening.
How do patients and clinicians perceive communication and results notification after lung cancer screening, and are there approaches that may mitigate or exacerbate distress?
We conducted interviews and focus groups with 49 patients who underwent lung cancer screening in the prior year and 36 clinicians who communicate screening results (primary care providers, pulmonologists, nurses), recruited from lung cancer screening programs at 4 hospitals. We analyzed transcripts using conventional content analysis.
Clinicians and patients diverged in their impressions of the quality of communication after lung cancer screening. Clinicians recognized the potential for patient distress and tailored their approach to disclosure based on how clinically concerning they perceived results to be. Disclosure of normal or low-risk findings usually occurred by letter; clinicians believed this process was efficient and well received by patients. Yet many patients were dissatisfied: several could not recall receiving results at all, and others reported that receiving results by letter left them confused and concerned, with little opportunity to ask questions. By contrast, patients with larger nodules typically received results during an immediate phone call or clinic visit, and both patients and clinicians agreed that these conversations represented high-quality communication that met patient needs. Regardless of their cancer risk, patients who learned their results in a conversation appreciated the opportunity to discuss both the meaning of the nodule and the evaluation plan, and to have their concerns addressed, preempting distress.
Tension exists between clinicians' interest in efficiency of results notification by letter in low-risk cases and patients' need to understand and be reassured about screening results, their implications, and the plan for subsequent screening or nodule evaluation-even when clinicians did not perceive results as concerning. Brief conversations to discuss lung cancer screening results may improve patient understanding and satisfaction while reducing distress.
在偶发性肺结节和乳腺癌筛查中,高质量的以患者为中心的沟通可以提高对评估的依从性并减轻患者的痛苦。尽管指南强调在肺癌筛查前进行共同决策,但对于肺癌筛查后的医患沟通情况却知之甚少。
患者和临床医生如何看待肺癌筛查后的沟通及结果告知,是否存在可能减轻或加剧痛苦的方式?
我们对49名去年接受过肺癌筛查的患者以及36名传达筛查结果的临床医生(初级保健医生、肺科医生、护士)进行了访谈和焦点小组讨论,这些人员均来自4家医院的肺癌筛查项目。我们使用常规内容分析法对访谈记录进行了分析。
临床医生和患者对肺癌筛查后沟通质量的印象存在差异。临床医生认识到患者可能会感到痛苦,并根据他们对结果临床关注度的认知来调整告知方式。正常或低风险结果通常通过信件告知;临床医生认为这个过程效率高且患者易于接受。然而,许多患者并不满意:一些患者根本记不起收到过结果,另一些患者则表示通过信件收到结果让他们感到困惑和担忧,几乎没有机会提问。相比之下,结节较大的患者通常会在立即接到的电话或门诊就诊时收到结果,患者和临床医生都认为这些沟通代表了满足患者需求的高质量沟通。无论癌症风险如何,通过对话得知结果的患者都很感激有机会讨论结节的意义和评估计划,并解决他们的担忧,从而避免痛苦。
在低风险情况下临床医生倾向于通过信件高效告知结果的意愿与患者理解并确信筛查结果、其含义以及后续筛查或结节评估计划的需求之间存在矛盾——即使临床医生认为结果并无大碍。简短的对话来讨论肺癌筛查结果可能会提高患者的理解度和满意度,同时减轻痛苦。