From the Department of Pharmacy, Children's Hospital of Orange County, Orange, California.
Biostatistics, Epidemiology and Research Design, Institute for Clinical and Translational Science, University of California, Irvine, California.
Pediatr Infect Dis J. 2018 Nov;37(11):1124-1129. doi: 10.1097/INF.0000000000001999.
Palivizumab provides passive immunity for respiratory syncytial virus (RSV), but poor adherence compromises protection. A hospital initiative promoted administration of first palivizumab doses at an outpatient clinic immediately after discharge. The objectives of this study were to evaluate the impact of the initiative on location and timing of first palivizumab dose, patient adherence, reimbursement, acquisition cost and RSV-positive hospital readmissions.
This retrospective cohort study included pediatric patients who received palivizumab from 2012 to 2016. Three groups were compared: "before initiative," "transition" and "after initiative." Patients who did not qualify for palivizumab or who were eligible for palivizumab in previous RSV seasons were excluded. Multivariable logistic and linear regressions adjusted for patients' characteristics were used in outcome analysis.
After adjusting for patients' characteristics, there was a 13.5-fold (95% confidence interval: 5.9-30.5, P < 0.0001) increase in odds that patients would receive outpatient administration of palivizumab and 2.7-fold (95% confidence interval: 1.3-5.7, P = 0.0103) increase in odds of receiving the second dose within 35 days after initiative implementation compared with before. Although there was no significant difference in reimbursement percentage after initiative implementation (32% ± 30% after initiative and 31% ± 22% before), calculated palivizumab acquisition costs were 20.8% lower. RSV readmissions were not significantly different.
Implementation of an initiative with defined workflow, multidisciplinary collaboration, and early case management efforts to obtain insurance authorization increased outpatient administration of first palivizumab doses. Patient adherence improved as demonstrated by more timely receipt of the second palivizumab dose. There was no difference in reimbursement; however, acquisition cost decreased which is valuable considering low reimbursement rates. RSV-positive readmissions did not change significantly.
帕利珠单抗为呼吸道合胞病毒(RSV)提供被动免疫,但低依从性会影响保护效果。一项医院发起的计划,提倡在患儿出院后立即于门诊为其首次注射帕利珠单抗。本研究的目的是评估该计划对首次帕利珠单抗剂量的给药地点和时间、患者依从性、报销、购置成本和 RSV 阳性患儿再入院的影响。
本回顾性队列研究纳入了 2012 年至 2016 年接受帕利珠单抗治疗的儿科患者。比较了三组:“计划前”、“过渡期”和“计划后”。排除了不符合帕利珠单抗使用条件或在前一个 RSV 季节有资格使用帕利珠单抗的患者。采用多变量逻辑回归和线性回归对患者特征进行调整,并用于结果分析。
在调整了患者特征后,患者在门诊接受帕利珠单抗治疗的可能性增加了 13.5 倍(95%置信区间:5.9-30.5,P<0.0001),并且在计划实施后 35 天内接受第二剂帕利珠单抗治疗的可能性增加了 2.7 倍(95%置信区间:1.3-5.7,P=0.0103)。虽然计划实施后报销比例没有显著差异(计划后 32%±30%,计划前 31%±22%),但计算出的帕利珠单抗购置成本降低了 20.8%。RSV 再入院率无显著差异。
实施一项具有明确工作流程、多学科合作和早期管理努力以获得保险授权的计划,增加了首次帕利珠单抗的门诊给药。正如第二剂帕利珠单抗更及时地接受所表明的那样,患者的依从性得到了改善。报销没有差异;然而,考虑到低报销率,购置成本的降低是有价值的。RSV 阳性再入院率没有显著变化。