Redulla Rhoda R, Reddy K Rajender, Faust Thomas W, Dudley-Brown Sharon
Rhoda R. Redulla, DNP, RN, is Director of Education, Memorial Hospital of Salem County, New Jersey; and Adjunct Faculty, Drexel University, Philadelphia, Pennsylvania. Dr. Redulla is also a SGNA Scholar. K. Rajender Reddy, MD, is Ruimy Family President's Distinguished Professor, Director of Hepatology, Medical Director of Liver Transplantation, Hospital of the University of Pennsylvania, Philadelphia. Thomas W. Faust, MD, MBE, is Transplant Hepatologist, Medstar Georgetown Transplant Institute, Medstar Georgetown University Hospital, Washington, DC. Sharon Dudley-Brown, PhD, FNP-BC, FAAN, is Assistant Professor of Medicine, Johns Hopkins University, Baltimore, Maryland. Dr. Dudley-Brown is also a SGNA Scholar.
Gastroenterol Nurs. 2015 Sep-Oct;38(5):369-78. doi: 10.1097/SGA.0000000000000166.
Chronic hepatitis C virus (HCV) remains a major healthcare concern. The 24-48 week treatment of pegylated interferon and ribavirin therapy requires a tremendous amount of commitment from patients and providers. Thus, there has been a huge focus on health-related quality of life and various measures to support patient adherence and completion of the recommended HCV treatment regimen. This quality improvement project aimed to develop and test a nurse-driven evidence-based pathway that supports the care of patients receiving hepatitis C medication therapy in a tertiary, academic hepatology practice. All adult patients, 18 years and older, who were started on HCV treatment from January 20 to February 15, 2011, were included in the testing of a nurse-driven HCV pathway for the first 12 weeks of treatment. The majority of the patients treated were male (71.8% prepathway and 83.3% postpathway), of White ethnic background (61.5% prepathway and 58.3% postpathway), genotype 1 (69% prepathway and 91.7% postpathway), and had comorbid conditions classified as "other" (38.5% prepathway and 33.3% postpathway). As for treatment status, the majority of the patients were "treatment naive" in prepathway or had never received prior HCV treatment (59.0%) or "had recurrent HCV after liver transplantation" (41.7%). The 4-week treatment completion rate was 94.9% for the prepathway group and 100.0% for the postpathway group; 12-week completion rate was 87.2% (prepathway) and 58.3% for the postpathway group. The mean 4-week adherence score for the prepathway group was 2.46 and the postpathway group was 2.92. Mean lag time to treatment was decreased with 26 days in the postpathway and 43 in the prepathway. Providers and nurses expressed overall satisfaction with the nurse-driven pathway.
慢性丙型肝炎病毒(HCV)仍然是医疗保健领域的一个主要关注点。聚乙二醇化干扰素和利巴韦林疗法进行24至48周的治疗需要患者和医护人员付出巨大努力。因此,人们高度关注与健康相关的生活质量以及各种支持患者坚持并完成推荐的HCV治疗方案的措施。这个质量改进项目旨在开发并测试一条由护士主导的循证路径,以支持在三级学术肝病科实践中接受丙型肝炎药物治疗的患者的护理。所有年龄在18岁及以上、于2011年1月20日至2月15日开始接受HCV治疗的成年患者,在治疗的前12周被纳入由护士主导的HCV路径测试。接受治疗的患者大多数为男性(路径实施前占71.8%,路径实施后占83.3%),白人种族背景(路径实施前占61.5%,路径实施后占58.3%),基因型1(路径实施前占69%,路径实施后占91.7%),并且患有归类为“其他”的合并症(路径实施前占38.5%,路径实施后占33.3%)。至于治疗状态,大多数患者在路径实施前“未接受过治疗”或从未接受过先前的HCV治疗(59. 0%),或“肝移植后复发性HCV”(41.7%)。路径实施前组的4周治疗完成率为94.9%,路径实施后组为100.0%;12周完成率分别为87.2%(路径实施前)和58.3%(路径实施后)。路径实施前组的平均4周依从性得分为2.46,路径实施后组为2.92。路径实施后治疗的平均延迟时间减少至26天,路径实施前为43天。医护人员对由护士主导的路径总体表示满意。