Department of General Medicine, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA
Department of Medicine, Harvard Medical School, Boston, Massachusetts, USA.
BMJ Qual Saf. 2024 Aug 16;33(9):597-608. doi: 10.1136/bmjqs-2022-015793.
Accurate and timely diagnosis relies on sharing perspectives among team members and avoiding information asymmetries. Patients/Families hold unique diagnostic process (DxP) information, including knowledge of diagnostic safety blindspots-information that patients/families know, but may be invisible to clinicians. To improve information sharing, we co-developed with patients/families an online tool called 'Our Diagnosis (OurDX)'. We aimed to characterise patient/family contributions in OurDX and how they differed between individuals with and without diagnostic concerns.
We implemented OurDX in two academic organisations serving patients/families living with chronic conditions in three subspecialty clinics and one primary care clinic. Prior to each visit, patients/families were invited to contribute visit priorities, recent histories and potential diagnostic concerns. Responses were available in the electronic health record and could be incorporated by clinicians into visit notes. We randomly sampled OurDX reports with and without diagnostic concerns for chart review and used inductive and deductive qualitative analysis to assess patient/family contributions.
7075 (39%) OurDX reports were submitted at 18 129 paediatric subspecialty clinic visits and 460 (65%) reports were submitted among 706 eligible adult primary care visits. Qualitative analysis of OurDX reports in the chart review sample (n=450) revealed that participants contributed DxP information across 10 categories, most commonly: clinical symptoms/medical history (82%), tests/referrals (54%) and diagnosis/next steps (51%). Participants with diagnostic concerns were more likely to contribute information on DxP risks including access barriers, recent visits for the same problem, problems with tests/referrals or care coordination and communication breakdowns, some of which may represent diagnostic blindspots.
Partnering with patients and families living with chronic conditions through OurDX may help clinicians gain a broader perspective of the DxP, including unique information to coproduce diagnostic safety.
准确、及时的诊断依赖于团队成员之间的观点共享,避免信息不对称。患者/家属拥有独特的诊断过程(DxP)信息,包括诊断安全盲点的知识——患者/家属知道但可能不为临床医生所察觉的信息。为了改善信息共享,我们与患者/家属共同开发了一个名为“我们的诊断(OurDX)”的在线工具。我们旨在描述患者/家属在 OurDX 中的贡献,以及他们在有无诊断问题的个体之间的差异。
我们在两个为患有慢性病的患者/家属提供服务的学术机构中实施了 OurDX,这两个机构位于三个亚专科诊所和一个初级保健诊所。在每次就诊前,患者/家属被邀请为就诊重点、近期病史和潜在诊断问题做出贡献。这些回复在电子健康记录中可用,临床医生可以将其纳入就诊记录。我们随机抽取了有和无诊断问题的 OurDX 报告进行图表审查,并使用归纳和演绎的定性分析方法评估患者/家属的贡献。
在 18129 次儿科亚专科诊所就诊和 706 次符合条件的成人初级保健就诊中,共提交了 7075 份(39%)的 OurDX 报告,其中 460 份(65%)报告是在 706 份成人初级保健就诊中的 65 份报告中提交的。在图表审查样本(n=450)中对 OurDX 报告的定性分析显示,参与者在 10 个类别中提供了 DxP 信息,最常见的是:临床症状/病史(82%)、检查/转介(54%)和诊断/下一步(51%)。有诊断问题的参与者更有可能提供 DxP 风险方面的信息,包括获取障碍、因同一问题最近就诊、检查/转介或医疗协调以及沟通障碍的问题,其中一些可能代表诊断盲点。
通过 OurDX 与患有慢性病的患者和家属合作,可能有助于临床医生更全面地了解 DxP,包括共同生成诊断安全性所需的独特信息。