Ong Wan Chee, Lim Miao Shan, Chan Elaine, Lim Thomson Chong Teik, Lim Teong Guan, Chan Webber
Department of Pharmacy Singapore General Hospital Singapore.
Department of Gastroenterology and Hepatology Singapore General Hospital Singapore.
JGH Open. 2022 Jun 1;6(7):470-476. doi: 10.1002/jgh3.12776. eCollection 2022 Jul.
Patients with inflammatory bowel disease (IBD) requiring infliximab frequently spend hours to attend treatment. Through quality improvement (QI) methodology, we aimed to shorten the time spent in the biologics infusion center using the accelerated infusion protocol and describe patient outcomes, safety, and associated cost savings.
From September 2018 through December 2019, eligible IBD patients receiving infliximab were recruited. We implemented interventions including the accelerated infusion protocol, and modifying collection location of infliximab. Statistical process control charts were created. Patients' clinical outcome and cost savings data were analyzed using descriptive statistics and Pearson's chi-square.
During the study period, a total of 60 patients with IBD receiving infliximab were recruited. A total of 315 infusions were administered-152 were under accelerated infusion protocol and 163 under standard protocol. The mean infliximab infusion time was reduced by 47%, from 2.4 h (142 ± 14 min) to 1.2 h (75 ± 10 min) (142 min 75 min, < 0.001), with total time spent in the infusion center reduced by 52%, from 3.6 h (214 ± 25 min) to 1.7 h (102 ± 14 min) (214 106 min, < 0.001). Three mild infusion-related reactions (3/152 = 1.97%) were recorded. Estimated cost savings over the 16-month project period was SGD $6721.4 (nursing) and SGD $23 560 (patients). A high level of satisfaction (4.84 out of 5) with the protocol was reported.
Our QI project shortened the infliximab infusion time and total time spent in the infusion center, without compromising patient safety. Estimated cost savings were substantial. The protocol helps reduce work productivity loss.
需要使用英夫利昔单抗治疗的炎症性肠病(IBD)患者常常要花费数小时接受治疗。通过质量改进(QI)方法,我们旨在采用加速输注方案缩短在生物制剂输注中心的治疗时间,并描述患者的治疗结果、安全性及相关成本节约情况。
从2018年9月至2019年12月,招募符合条件的接受英夫利昔单抗治疗的IBD患者。我们实施了包括加速输注方案及改变英夫利昔单抗采集地点在内的干预措施。创建了统计过程控制图。使用描述性统计和Pearson卡方检验分析患者的临床结果和成本节约数据。
在研究期间,共招募了60例接受英夫利昔单抗治疗的IBD患者。共进行了315次输注,其中152次采用加速输注方案,163次采用标准方案。英夫利昔单抗的平均输注时间减少了47%,从2.4小时(142±14分钟)降至1.2小时(75±10分钟)(142分钟对75分钟,P<0.001),输注中心的总花费时间减少了52%,从3.6小时(214±25分钟)降至1.7小时(102±14分钟)(214分钟对106分钟,P<0.001)。记录到3例轻度输注相关反应(3/152 = 1.97%)。在16个月的项目期间,估计节约成本为护理方面6721.4新元,患者方面23560新元。据报告,患者对该方案的满意度较高(5分制中为4.84分)。
我们的QI项目缩短了英夫利昔单抗的输注时间和在输注中心的总花费时间,且未影响患者安全。估计成本节约显著。该方案有助于减少工作效率损失。