Buono Jessica L, Tourkodimitris Stavros, Sarocco Phil, Johnston Jeffrey M, Carson Robyn T
Manager, Health Economics and Outcomes Research, Forest Research Institute, LLC, a subsidiary of Actavis plc, Jersey City, NJ.
Director, Biostatistics, Forest Research Institute, LLC, a subsidiary of Actavis plc, Jersey City, NJ.
Am Health Drug Benefits. 2014 Aug;7(5):289-97.
Irritable bowel syndrome with constipation (IBS-C), a chronic functional gastrointestinal disorder, has been shown to negatively affect work productivity and impair daily activity, resulting in a substantial burden for patients and employers. Linaclotide is a first-in-class guanylate cyclase-C agonist approved for the treatment of adults with IBS-C and chronic idiopathic constipation in the United States.
To analyze the impact of treatment with linaclotide on work productivity and daily activity impairment in adults with IBS-C and estimate the indirect costs associated with this condition.
This was a post-hoc analysis of data on IBS-C-related work time missed and work and activity impairment from 2 phase 3 clinical trials that assessed the efficacy and safety of linaclotide therapy in adults with IBS-C. The Work Productivity and Activity Impairment Questionnaire for IBS-C (WPAI:IBS-C) was self-administered at baseline and at weeks 4, 8, and 12 during the 12-week treatment periods in Trials 1 and 2 and at weeks 16, 20, and 26 during the extended treatment period in Trial 2. An analysis of covariance was conducted to assess changes from baseline to all study weeks for each WPAI:IBS-C measure. Indirect costs were calculated by converting overall work productivity losses into monetary values using the human capital cost approach.
Of the 1602 patients with IBS-C who were randomized in the 2 clinical trials, 1555 (97.1%) completed a baseline and at least 1 postbaseline WPAI:IBS-C assessment and were included in the analysis cohort; 1148 (71.7%) of these patients were employed. Once-daily treatment with linaclotide significantly reduced overall work productivity loss and daily activity impairment among patients with IBS-C at all study weeks. From baseline to week 12, compared with placebo, linaclotide significantly reduced presenteeism by 5.2%, overall work productivity loss by 6.1%, and daily activity impairment by 4.7% (all P <.01) and led to a numerically greater decrease in absenteeism. From baseline to week 26, compared with placebo, reductions with linaclotide were 5.9% for presenteeism, 7.5% for overall work productivity loss, and 6.7% for daily activity impairment (all P <.05). Reductions in overall work productivity loss from baseline to week 26 translate to 103 hours to 156 hours annually and correspond to an avoided overall work loss of $3209 to $4861 annually for an employee with IBS-C.
The results of this analysis indicate that appropriate treatment of IBS-C with medications such as linaclotide can reduce work-related impairment associated with IBS-C. In addition, IBS-C therapies that effectively manage this chronic condition and improve employees' quality of life and work productivity may represent significant cost-savings for employers in the form of avoided work productivity losses.
便秘型肠易激综合征(IBS-C)是一种慢性功能性胃肠疾病,已被证明会对工作效率产生负面影响并损害日常活动,给患者和雇主带来沉重负担。利那洛肽是美国批准用于治疗成人IBS-C和慢性特发性便秘的首个鸟苷酸环化酶-C激动剂。
分析利那洛肽治疗对IBS-C成人患者工作效率和日常活动损害的影响,并估计与该疾病相关的间接成本。
这是一项对两项3期临床试验中与IBS-C相关的工作时间缺勤以及工作和活动损害数据的事后分析,这两项试验评估了利那洛肽治疗IBS-C成人患者的疗效和安全性。在试验1和试验2的12周治疗期的基线以及第4、8和12周,以及试验2延长治疗期的第16、20和26周,由患者自行填写IBS-C工作效率和活动损害问卷(WPAI:IBS-C)。进行协方差分析以评估每个WPAI:IBS-C指标从基线到所有研究周的变化。使用人力资本成本方法将总体工作效率损失转化为货币价值来计算间接成本。
在两项临床试验中随机分组的1602例IBS-C患者中,1555例(97.1%)完成了基线和至少1次基线后WPAI:IBS-C评估,并被纳入分析队列;其中1148例(71.7%)患者受雇。利那洛肽每日一次治疗在所有研究周均显著降低了IBS-C患者的总体工作效率损失和日常活动损害。从基线到第12周,与安慰剂相比,利那洛肽显著降低出勤主义5.2%、总体工作效率损失6.1%、日常活动损害4.7%(均P<.01),并导致缺勤率在数值上有更大下降。从基线到第26周,与安慰剂相比,利那洛肽使出勤主义降低5.9%、总体工作效率损失降低7.5%、日常活动损害降低6.7%(均P<.05)。从基线到第26周总体工作效率损失的降低转化为每年103小时至156小时,对于患有IBS-C的员工而言,相当于每年避免了3209美元至4861美元的总体工作损失。
该分析结果表明,使用利那洛肽等药物对IBS-C进行适当治疗可减少与IBS-C相关的工作损害。此外,有效管理这种慢性疾病并提高员工生活质量和工作效率的IBS-C治疗方法可能会为雇主带来显著的成本节约,形式为避免工作效率损失。