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Economic evaluation of the NET intervention versus guideline dissemination for management of mild head injury in hospital emergency departments

机译:医院急诊部门净干预净干预与指南传播的经济评价

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Evidence-based guidelines for the management of mild traumatic brain injury (mTBI) in the emergency department (ED) are now widely available, and yet, clinical practice remains inconsistent with the guidelines. The Neurotrauma Evidence Translation (NET) intervention was developed to increase the uptake of guideline recommendations and improve the management of minor head injury in Australian emergency departments (EDs). However, the adoption of this type of intervention typically entails an upfront investment that may or may not be fully offset by improvements in clinical practice, health outcomes and/or reductions in health service utilisation. The present study estimates the cost and cost-effectiveness of the NET intervention, as compared to the passive dissemination of the guideline, to evaluate whether any improvements in clinical practice or health outcomes due to the NET intervention can be obtained at an acceptable cost. Study setting: The NET cluster randomised controlled trial [ACTRN12612001286831]. Study sample: Seventeen EDs were randomised to the control condition and 14 to the intervention. One thousand nine hundred forty-three patients were included in the analysis of clinical practice outcomes (NET sample). A total of 343 patients from 14 control and 10 intervention EDs participated in follow-up interviews and were included in the analysis of patient-reported health outcomes (NET-Plus sample). Outcome measures: Appropriate post-traumatic amnesia (PTA) screening in the ED (primary outcome). Secondary clinical practice outcomes: provision of written information on discharge (INFO) and safe discharge (defined as CT scan appropriately provided plus PTA plus INFO). Secondary patient-reported, post-discharge health outcomes: anxiety (Hospital Anxiety and Depression Scale), post-concussive symptoms (Rivermead), and preference-based health-related quality of life (SF6D). Methods: Trial-based economic evaluations from a health sector perspective, with time horizons set to coincide with the final follow-up for the NET sample (2?months post-intervention) and to 1-month post-discharge for the NET-Plus sample. Results: Intervention and control groups were not significantly different in health service utilisation received in the ED/inpatient ward following the initial mTBI presentation (adjusted mean difference $23.86 per patient; 95%CI ??$106, $153; p?=?0.719) or over the longer follow-up in the NET-plus sample (adjusted mean difference $341.78 per patient; 95%CI ??$58, $742; p?=?0.094). Savings from lower health service utilisation are therefore unlikely to offset the significantly higher upfront cost of the intervention (mean difference $138.20 per patient; 95%CI $135, $141; p??0.000). Estimates of the net effect of the intervention on total cost (intervention cost net of health service utilisation) suggest that the intervention entails significantly higher costs than the control condition (adjusted mean difference $169.89 per patient; 95%CI $43, $297, p?=?0.009). This effect is larger in absolute magnitude over the longer follow-up in the NET-plus sample (adjusted mean difference $505.06; 95%CI $96, $915; p?=?0.016), mostly due to additional health service utilisation. For the primary outcome, the NET intervention is more costly and more effective than passive dissemination; entailing an additional cost of $1246 per additional patient appropriately screened for PTA ($169.89/0.1363; Fieller’s 95%CI $525, $2055). For NET to be considered cost-effective with 95% confidence, decision-makers would need to be willing to trade one quality-adjusted life year (QALY) for 25 additional patients appropriately screened for PTA. While these results reflect our best estimate of cost-effectiveness given the data, it is possible that a NET intervention that has been scaled and streamlined ready for wider roll-out may be more or less cost-effective than the NET intervention as delivered in the trial. While the NET intervention does improve the management of mTBI in the ED, it also entails a significant increase in cost and—as delivered in the trial—is unlikely to be cost-effective at currently accepted funding thresholds. There may be a scope for a scaled-up and streamlined NET intervention to achieve a better balance between costs and outcomes. Australian New Zealand Clinical Trials Registry ACTRN12612001286831 , date registered 12 December 2012.
机译:急诊部门(ED)中的轻度创伤性脑损伤(MTBI)管理的基于循证指南现在广泛可用,但临床实践与指南不一致。作者:制定了神经统计证据翻译(净)干预,以增加对澳大利亚急诊部门(EDS)的轻微脑部损伤管理的增加。然而,通过这种类型的干预措施通常需要提前投资,这些投资可能或可能不会通过改善临床实践,健康结果和/或减少卫生服务利用率而完全抵消。本研究估计与指南的被动传播相比,净干预的成本和成本效益,以评估是否可以以可接受的成本获得临床实践或健康结果的任何改进。研究环境:网络集群随机控制试验[ACTRN12612001286831]。研究样本:将17个EDS随机化为控制​​条件和14到干预。一千九百四十三名患者被纳入临床实践结果(净样品)。共有343名来自14名控制和10名干预EDS参与后续访谈的患者,并纳入患者报告的健康结果(NET-Plus样品)分析。结果措施:在ED(主要结果)中适当的创伤后胃癌(PTA)筛选。次要临床实践结果:提供有关放电(信息)和安全放电的书面信息(定义为适当提供的CT扫描加上PTA Plus Info)。次要患者报告,出院后健康结果:焦虑(医院焦虑和抑郁症),震荡症状(Rivermead),以及基于偏好的健康相关的生活质量(SF6D)。方法:从卫生部门的角度来看,基于审判的经济评估,时间范围与净样品(干预后2个月)的最终随访恰逢其时的视野,并为NET-Plus排放1个月样本。结果:在初始MTBI介绍后,干预和对照组在ED / Inpatient病房中收到的健康服务利用率没有显着差异(调整后平均差异为每位患者23.86美元; 95%CI $ 106,153美元; P?= 0.719)或在Net-Plus样品中的更长的随访中(调整平均差异为341.78美元; 95%CI ?? $ 58,742美元; p?= 0.094)。因此,较低的健康服务利用率的节省不太可能抵消干预的显着提高成本(平均差异为每位患者138.20美元; 95%CI $ 135,141美元; P?<?0.000)。估计干预总成本的净效应(卫生服务利用的干预成本净净)表明,干预的成本明显高于控制条件(调整后平均差异为每位患者169.89美元; 95%CI $ 43,$ 297,P?= ?0.009)。在Net-Plus样品中的较长随后(调整平均值505.06美元,95%CI $ 96,915美元; P?0.016),这种效果在较长的时间内较大,主要是由于额外的健康服务利用率。对于主要结果,净干预比被动传播更昂贵,更有效;为PTA筛选每额外患者的额外费用为1246美元($ 169.89 / 0.1363; Fieller的95%CI $ 525,2055美元)。对于净被认为具有95%信心的成本效益,决策者需要愿意为PTA适当筛选的25例患者进行一项质量调整的寿命年份(QALY)。虽然这些结果反映了对数据的最佳成本效益的最佳估计,但在数据中,已经进行了缩放和简化的净干预,准备好更广泛的推出可能比净干预更加成本或多或少审判。虽然净干预确实改善了MTBI的管理层,但它也需要在试验中的成本显着增加 - 在目前接受的资金门槛上不太可能具有成本效益。扩大率和简化的净干预可能存在范围,以在成本和结果之间实现更好的平衡。澳大利亚新西兰临床试验登记架ACTRN12612001286831 2012年12月12日注册。

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