Carver Alicia B, Edmonds Cori, Whelchel Kristen, Moore Ryan, Choi Leena, Gillis Lynette A
Specialty Pharmacy Services, Vanderbilt University Medical Center, Nashville, TN, United States.
Department of Biostatistics, Vanderbilt University Medical Center, Nashville, TN, United States.
J Pediatric Infect Dis Soc. 2025 May 13;14(5). doi: 10.1093/jpids/piaf042.
This study evaluated the Cascade of Care (CoC) and real-world efficacy of direct-acting antivirals (DAAs) for hepatitis C treatment in pediatric and adolescent patients utilizing an integrated health system specialty pharmacy (HSSP) to assist with medication selection, insurance approval, swallowing practice, initiation, and monitoring.
This single-center, retrospective, observational cohort study included chronic hepatitis C patients <18 years old evaluated by pediatric hepatologists at an academic health system between January 1, 2017 and September 30, 2022. The primary endpoint was sustained virologic response (SVR) ≥12 weeks following treatment completion in patients initiating DAAs. Secondary endpoints were CoC advancement, variables impacting DAA initiation, patient-reported side effects, and adherence. An ordinal logistic regression model assessed whether initiation time was associated with a patient's ability to swallow, prior authorization outcome, and medication availability to HSSP at referral. The odds ratio reflects the likelihood of a shift in time to initiation for a given group relative to its respective reference group.
Of 98 patients evaluated by a hepatologist, 73 (75%) were referred to the HSSP. Loss to follow-up was the primary reason (88%; 22/25) for nonreferral, most commonly (73%; 16/22) in those aged ≤5 years. Following HSSP referral, 88% (64/73) initiated DAA and 92% (59/64) of those achieved SVR. Time from HSSP referral to medication initiation was impacted by DAA availability (OR = 41.47; 95% CI, 9.51-180.87; P <.001) and inability to swallow the dosage form at evaluation (OR = 3.94; 95% CI, 1.56-9.98; P =.004). Over half (53%; 34/64) of patients initiating DAA reported ≥1 adverse event; none discontinued treatment. Most (69%; 44/64) reported no missed doses.
The largest CoC drop-off occurred following initial clinic evaluation, primarily in children aged ≤5 years. Enhanced linkage to care efforts is needed in these patients. Conversely, nearly all patients referred to the HSSP were initiated on DAA, completed therapy, and achieved SVR.
本研究利用综合医疗系统专科药房(HSSP)协助进行药物选择、保险审批、吞咽练习、起始治疗及监测,评估了儿童和青少年丙型肝炎患者的治疗级联(CoC)及直接抗病毒药物(DAA)治疗丙型肝炎的真实疗效。
这项单中心、回顾性观察队列研究纳入了2017年1月1日至2022年9月30日期间在一所学术医疗系统由儿科肝病专家评估的18岁以下慢性丙型肝炎患者。主要终点是开始使用DAA治疗的患者在治疗完成后持续病毒学应答(SVR)≥12周。次要终点包括CoC进展、影响DAA起始治疗的变量、患者报告的副作用及依从性。一个有序逻辑回归模型评估了起始治疗时间是否与患者的吞咽能力、事先批准结果以及转诊时HSSP的药物可获得性相关。优势比反映了给定组相对于其各自参照组起始治疗时间变化的可能性。
在98名由肝病专家评估的患者中,73名(75%)被转诊至HSSP。失访是未转诊的主要原因(88%;22/25),最常见于5岁及以下儿童(73%;16/22)。在转诊至HSSP后,88%(64/73)开始使用DAA,其中92%(59/64)实现了SVR。从HSSP转诊到开始用药的时间受DAA可获得性(优势比=41.47;95%置信区间,9.51 - 180.87;P<0.001)以及评估时无法吞咽剂型(优势比=3.94;95%置信区间,1.56 - 9.98;P = 0.004)的影响。开始使用DAA的患者中超过一半(53%;34/64)报告了≥1次不良事件;无人停止治疗。大多数(69%;44/64)报告无漏服剂量。
最大的CoC下降发生在初始门诊评估之后,主要发生在5岁及以下儿童中。这些患者需要加强与护理工作的联系。相反,几乎所有转诊至HSSP的患者都开始使用了DAA,完成了治疗,并实现了SVR。