It may take many villages, but progress can be made toward HCV elimination among people who inject drugs.
It may take many villages, but progress can be made toward HCV elimination among people who inject drugs.
复制标题
DOI:
10.1016/j.lana.2023.100510
复制
发表时间:
2023-06
期刊:
影响因子:
--
通讯作者:
Page, Kimberly
中科院分区:
文献类型:
--
作者:
Page, Kimberly
Treatment barriers continue to limit provision and uptake of highly effective treatment for many people with chronic hepatitis C virus (HCV) infection. In the United States, notable barriers include both patient level (for example, poor access to healthcare, lack of health insurance, low diagnosis and treatment uptake rates, and fear of discrimination), and system level (such as costs and administrative rules, including requirements for prior authorizations, abstinence from substance use and alcohol, and prescriber restrictions, among others 1). The high prevalence of HCV infection among PWID (People Who Inject Drugs), globally, warrants novel approaches to HCV treatment to reduce prevalence and ongoing transmission. 2 The cascade of care, or sequence of steps that individuals must go through to receive HCV treatment, from diagnosis to sustained virologic response is not promising, 3–5 despite studies showing that PWID with HCV can be engaged and successfully treated for HCV. 6–8 Notwithstanding the lack of concerted population level approaches to, progress is being made in small increments by dedicated and creative groups to test and provide models of care for PWID. In this issue of Lancet Regional Health-Americas, Lettner et al., 9 present results from a novel program in Toronto, Canada, that brings together many of the elements proposed as needed to improve HCV treatment uptake and completion among PWID: access to testing and medication, integrated care, trust, and community support. 10 The authors describe the program as low barrier-and although patients did actually face many barriers, the program provides essential strategies for successful HCV treatment programs for PWID. In this study, which was conducted at a Supervised Consumption Service called “keepSIX”, an HCV treatment program was implemented that offered point-ofcare (POC) HCV RNA testing, on-site providers including nurses and physicians who could conduct pretreatment assessments and prescribe and dispense medications. Overall, among 64 participants who were HCV RNA positive, 89%(57/64) were eligible for treatment, 67.2%(43/64) were linked to co-located HCV care (intake with the health center’s HCV Treatment Nurse).Of those linked to onsite HCV treatment, 67.4%(29/43) initiated treatment, and 86.2%(25/29) achieved SVR. Overall, a substantial proportion-43.9%(25/57) of those eligible were cured of HCV infection, demonstrating a successful HCV treatment model. This success is notable since the participants faced many of the same barriers-especially at the system-level-extant in healthcare systems. The term" low barrier" is used to describe programs or services that are designed to be easily accessible and available to individuals who may face obstacles to receiving healthcare, such as financial or logistical barriers. However, there are situations where a program or service that is marketed as" low barrier" may not actually be low barrier in practice. Participants with HCV in this study were still required to have confirmatory HCV RNA testing from a reference laboratory, and to have two consecutive positive HCV RNA tests six months apart for confirmation of chronic HCV viremia. Further, the study was impacted by the COVID-19 pandemic, which challenged healthcare delivery everywhere. The median time from first positive HCV RNA test to linkage to care was 63 days (IQR: 6–230 days), and the median time between first positive HCV RNA test and treatment initiation was 265 days (IQR: 177–503 days). Despite these drawbacks, the program offered key factors necessary for low-barrier HCV treatment access which need to be highlighted.(1 …
登录
查看更多内容
影响因子:
11.8
作者:
Facente, Shelley N.;Patel, Sheena;Morris, Meghan D.
通讯作者:
Morris, Meghan D.
影响因子:
6.4
作者:
Trooskin, Stacey B.;Dore, Gregory;Kostman, Jay
通讯作者:
Kostman, Jay
影响因子:
11.8
作者:
Grebely, Jason;Mauss, Stefan;Dore, Gregory J.
通讯作者:
Dore, Gregory J.
影响因子:
5.1
作者:
Feld JJ;Ward JW
通讯作者:
Ward JW
影响因子:
6
作者:
Iversen, Jenny;Wand, Handan;Maher, Lisa
通讯作者:
Maher, Lisa