Ward Zoe, Platt Lucy, Sweeney Sedona, Hope Vivian D, Maher Lisa, Hutchinson Sharon, Palmateer Norah, Smith Josie, Craine Noel, Taylor Avril, Martin Natasha, Ayres Rachel, Dillon John, Hickman Matthew, Vickerman Peter
Bristol Medical School, Population Health Sciences, University of Bristol, Bristol, UK.
Faculty of Public Health and Policy, London School of Hygiene and Tropical Medicine, London, UK.
Addiction. 2018 May 17;113(9):1727-38. doi: 10.1111/add.14217.
To estimate the impact of existing high-coverage needle and syringe provision (HCNSP, defined as obtaining more than one sterile needle and syringe per injection reported) and opioid substitution therapy (OST) on hepatitis C virus (HCV) transmission among people who inject drugs (PWID) in three UK settings and to determine required scale-up of interventions, including HCV treatment, needed to reach the World Health Organization (WHO) target of reducing HCV incidence by 90% by 2030.
HCV transmission modelling using UK empirical estimates for effect of OST and/or HCNSP on individual risk of HCV acquisition.
Three UK cities with varying chronic HCV prevalence (Bristol 45%, Dundee 26%, Walsall 19%), OST (72-81%) and HCNSP coverage (28-56%).
Relative change in new HCV infections throughout 2016-30 if current interventions were stopped. Scale-up of HCNSP, OST and HCV treatment required to achieve the WHO elimination target.
Removing HCNSP or OST would increase the number of new HCV infections throughout 2016 to 2030 by 23-64 and 92-483%, respectively. Conversely, scaling-up these interventions to 80% coverage could achieve a 29 or 49% reduction in Bristol and Walsall, respectively, whereas Dundee may achieve a 90% decrease in incidence with current levels of intervention because of existing high levels of HCV treatment (47-58 treatments per 1000 PWID). If OST and HCNSP are scaled-up, Walsall and Bristol can achieve the same impact by treating 14 or 40 per 1000 PWID annually, respectively (currently two and nine treatments per 1000 PWID), while 18 and 43 treatments per 1000 PWID would be required if OST and HCNSP are not scaled-up.
Current opioid substitution therapy and high-coverage needle and syringe provision coverage is averting substantial hepatitis C transmission in the United Kingdom. Maintaining this coverage while getting current drug injectors onto treatment can reduce incidence by 90% by 2030.
评估现有的高覆盖率针头和注射器供应(HCNSP,定义为报告的每次注射获得超过一个无菌针头和注射器)以及阿片类药物替代疗法(OST)对英国三个地区注射毒品者(PWID)中丙型肝炎病毒(HCV)传播的影响,并确定为实现世界卫生组织(WHO)到2030年将HCV发病率降低90%的目标所需扩大的干预措施规模,包括HCV治疗。
使用英国关于OST和/或HCNSP对个体感染HCV风险影响的实证估计进行HCV传播建模。
英国三个慢性HCV流行率不同的城市(布里斯托尔45%,邓迪26%,沃尔索尔19%),OST覆盖率(72 - 81%)和HCNSP覆盖率(28 - 56%)。
如果停止当前干预措施,2016 - 2030年期间新HCV感染的相对变化。实现WHO消除目标所需扩大的HCNSP、OST和HCV治疗规模。
取消HCNSP或OST将分别使2016年至2030年期间新HCV感染数量增加23 - 64%和92 - 483%。相反,将这些干预措施的覆盖率扩大到80%,在布里斯托尔和沃尔索尔分别可使感染率降低29%或49%,而由于现有的高水平HCV治疗(每1000名PWID中有47 - 58例治疗),邓迪在当前干预水平下可能使发病率降低90%。如果扩大OST和HCNSP,沃尔索尔和布里斯托尔分别通过每年每1000名PWID治疗14例或40例(目前每1000名PWID分别为2例和9例治疗)可实现相同的影响,而如果不扩大OST和HCNSP,则每1000名PWID分别需要18例和43例治疗。
目前的阿片类药物替代疗法和高覆盖率针头和注射器供应正在避免英国大量的丙型肝炎传播。在让当前的药物注射者接受治疗的同时维持这种覆盖率,到2030年可将发病率降低90%。