Etchegaray Jason M, Ottosen Madelene J, Aigbe Aitebureme, Sedlock Emily, Sage William M, Bell Sigall K, Gallagher Thomas H, Thomas Eric J
RAND Corporation, Santa Monica, CA.
UT-MH Center for Healthcare Quality and Safety, McGovern Medical School, Department of Family Health, School of Nursing, University of Texas Health Science Center at Houston, Houston, TX.
Health Serv Res. 2016 Dec;51 Suppl 3(Suppl 3):2600-2614. doi: 10.1111/1475-6773.12593. Epub 2016 Oct 24.
Patient safety experts believe that patients/family members should be involved in adverse event review. However, it is unclear how aware patients/family members are about the causes of adverse events they experienced.
To determine whether patients/family members interviewed could identify at least one contributing factor for the event they experienced. Secondary objectives included understanding the way patients/family members became aware of adverse events, the types of contributing factors patients/family members identified for different types of adverse events, and recommendations provided by patients/family members to address the contributing factors.
We interviewed patients/family members using semistructured interviews to understand their perceptions about why these adverse events occurred. The adverse events occurred between 1991 and 2014.
Participants described adverse events that occurred in various types of health care organizations (i.e., hospitals, ambulatory facilities/clinics, and dental clinics).
We interviewed 72 patients and family members who each described a unique adverse event. Eligibility requirements were that patients/family members spoke English or Spanish and were aware of an adverse event that happened to them or a loved one. INTERVENTION(S) FOR CLINICAL TRIALS OR EXPOSURE(S) FOR OBSERVATIONAL STUDIES: N/A.
MAIN OUTCOME(S) AND MEASURE(S): The main outcome was determining whether patients/family members could identify at least one contributing factor they perceived as related to the adverse event they described.
Each participant identified at least one contributing factor and on average identified 3.67 contributing factors for their event. The most frequently mentioned contributing factors were Staff Qualifications/Knowledge (79 percent), Safety Policies/Procedures (74 percent), and Communication (64 percent). Participants knew about the contributing factors from personal observation only (32 percent), personal reasoning (11 percent), personal research (7 percent), record review (either their own medical records or reports they received in their own investigation; 6 percent), and being told by a physician (5 percent). Finally, patients/family members were able to provide recommendations that address each of the nine contributing factors we examined.
Patients/family members identified contributing factors related to their adverse event. Given that these contributing factors might not be known to health care organizations because most participants stated that they were not involved in the analysis process, opportunities for organizational learning from patients are potentially being missed. Health care organizations should interview patients/family about the event that harmed them to help ensure a full understanding of the causes of the event.
患者安全专家认为患者/家庭成员应参与不良事件审查。然而,尚不清楚患者/家庭成员对其经历的不良事件的原因了解程度如何。
确定接受访谈的患者/家庭成员是否能够识别出至少一个与其经历的事件相关的促成因素。次要目标包括了解患者/家庭成员知晓不良事件的方式、患者/家庭成员为不同类型不良事件识别出的促成因素类型,以及患者/家庭成员为解决促成因素而提出的建议。
我们采用半结构化访谈对患者/家庭成员进行访谈,以了解他们对这些不良事件发生原因的看法。这些不良事件发生在1991年至2014年期间。
参与者描述了在各类医疗保健机构(即医院、门诊设施/诊所和牙科诊所)发生的不良事件。
我们访谈了72名患者和家庭成员,他们每人都描述了一个独特的不良事件。入选要求是患者/家庭成员会说英语或西班牙语,并且知晓他们自己或亲人所遭遇的不良事件。临床试验的干预措施或观察性研究的暴露因素:无。
主要结局是确定患者/家庭成员是否能够识别出至少一个他们认为与所描述的不良事件相关的促成因素。
每位参与者都识别出了至少一个促成因素,平均为其事件识别出3.67个促成因素。最常被提及的促成因素是员工资质/知识(79%)、安全政策/程序(74%)和沟通(64%)。参与者知晓促成因素的途径仅为个人观察(32%)、个人推理(11%)、个人研究(7%)、记录审查(他们自己的病历或他们在自身调查中收到报告;6%)以及医生告知(5%)。最后,患者/家庭成员能够针对我们所研究的九个促成因素中的每一个提供建议。
患者/家庭成员识别出了与其不良事件相关的促成因素。鉴于大多数参与者表示他们未参与分析过程,医疗保健机构可能并不知晓这些促成因素,因而错失了从患者身上进行组织学习的机会。医疗保健机构应就伤害患者的事件对患者/家庭成员进行访谈,以帮助确保全面了解事件原因。