Cook Nicole, Hollar T Lucas, Zunker Christie, Peterson Michael, Phillips Teina, De Lucca Michael
Master of Public Health Program, College of Osteopathic Medicine, Nova Southeastern University, Fort Lauderdale, Florida (Drs Cook, Hollar, and Peterson); ICF International, Atlanta, Georgia (Dr Zunker); and Broward Regional Health Planning Council, Hollywood, Florida (Ms Phillips and Mr De Lucca).
J Public Health Manag Pract. 2016 May-Jun;22(3):265-74. doi: 10.1097/PHH.0000000000000263.
The prevalence of chronic disease in the United States is rapidly increasing, with a disproportionate number of underserved, vulnerable patients sharing the burden. The Patient-Centered Medical Home (PCMH) is a care delivery model that has shown promise to improve primary care and address the burden of chronic illness.
The purpose of this study was to (1) understand patient characteristics that might influence perceived patient experience in a large primary care safety net undergoing PCMH transformation; (2) identify community-level quality improvement opportunities to support ongoing transformation activities; and (3) establish a baseline of patient experience across the primary care safety net that could be used in repeated evaluations over the course of transformation.
A cross-sectional study design was used to conduct this research.
A total of 351 racially and ethnically diverse patients of 4 primary care safety net organizations in Broward County, Florida, were surveyed regarding their experience with access to care and coordination of care.
Reported access to care and coordination of care.
Patients with chronic disease who reported having visited the clinic 3 or more times in the past 12 months reported a better coordination of care experience than patients who had fewer than 3 visits in the past 12 months (odds ratio = 3.57; 95% confidence interval, 1.76-7.24). Patients without chronic disease who had been receiving care at the clinic for 2 or more years of care reported worse experience with access to care than patients with less than 2 years of care (odds ratio = 0.26; 95% confidence interval, 0.11-0.60.) Race, ethnicity, language, and education were not significant predictors of patient experience.
Findings support ongoing efforts to improve patient engagement among all patients and to enhance resources to manage chronic disease, including community-based self-management programs, in primary care safety nets undergoing PCMH transformation.
美国慢性病的患病率正在迅速上升,大量未得到充分服务的弱势群体承受着不成比例的负担。以患者为中心的医疗之家(PCMH)是一种医疗服务提供模式,已显示出有望改善初级医疗并应对慢性病负担。
本研究的目的是:(1)了解在经历PCMH转型的大型初级医疗安全网中,可能影响患者感知体验的患者特征;(2)确定社区层面的质量改进机会,以支持正在进行的转型活动;(3)建立初级医疗安全网中患者体验的基线,可在转型过程中用于重复评估。
采用横断面研究设计进行本研究。
对佛罗里达州布劳沃德县4个初级医疗安全网组织的351名种族和族裔各异的患者进行了调查,询问他们在获得医疗服务和医疗协调方面的体验。
报告的获得医疗服务和医疗协调情况。
报告在过去12个月内就诊3次或更多次的慢性病患者,其医疗协调体验比过去12个月内就诊次数少于3次的患者更好(优势比=3.57;95%置信区间,1.76 - 7.24)。在诊所接受2年或更长时间治疗的无慢性病患者,其获得医疗服务的体验比治疗时间少于2年的患者更差(优势比=0.26;95%置信区间,0.11 - 0.60)。种族、族裔、语言和教育程度不是患者体验的显著预测因素。
研究结果支持持续努力提高所有患者的参与度,并加强资源以管理慢性病,包括在经历PCMH转型的初级医疗安全网中开展基于社区的自我管理项目。