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肺动脉导管在重症监护患者管理中的临床及成本效益评估:系统评价与随机对照试验

An evaluation of the clinical and cost-effectiveness of pulmonary artery catheters in patient management in intensive care: a systematic review and a randomised controlled trial.

作者信息

Harvey S, Stevens K, Harrison D, Young D, Brampton W, McCabe C, Singer M, Rowan K

机构信息

Intensive Care National Audit and Research Centre, London, UK.

出版信息

Health Technol Assess. 2006 Aug;10(29):iii-iv, ix-xi, 1-133. doi: 10.3310/hta10290.

DOI:10.3310/hta10290
PMID:16904048
Abstract

OBJECTIVES

To evaluate the clinical and cost-effectiveness of managing critically ill patients in adult, general intensive care with or without pulmonary artery catheters (PACs).

DESIGN

An open, multi-centre, randomised controlled trial with economic evaluation (cost-utility and cost-effectiveness analysis).

SETTING

The setting was general (mixed medical/surgical) intensive care units (ICUs) in the UK admitting adults.

PARTICIPANTS

Adult patients in participating ICUs deemed by the responsible treating clinician to require management with a PAC.

INTERVENTIONS

These were insertion of a PAC and subsequent clinical management, at the discretion of the responsible treating clinicians, using data derived from the PAC. The control group were managed without a PAC but with the option of using alternative cardiac output monitoring devices.

MAIN OUTCOME MEASURES

The main outcome measure was hospital mortality. Secondary outcome measures were length of stay in the ICU, length of stay in an acute hospital and organ-days of support in the ICU. For the economic evaluation, the main outcome measure was quality-adjusted life-years (QALYs) and the secondary outcome measure was hospital mortality.

RESULTS

Sixty-five ICUs in the UK participated. Of these, 43 (66%) used alternative cardiac output monitoring devices in control group patients. A total of 1263 patients were identified as being eligible for the trial. Of these, 1041 (82.4%) were randomised and allocated to management with (n = 519) or without (n = 522) a PAC. There were no losses to follow-up. However, 27 patients (13 in the PAC group and 14 in the control group) were withdrawn from the trial because either the patient withdrew consent on recovering mental competency or the relatives withdrew agreement following randomisation. Data on 1014 patients were included in the analysis. Participants in the two groups had similar baseline characteristics. There was no difference in hospital mortality for patients managed with (68.4%) or without (65.7%) a PAC. The adjusted hazard ratio (PAC versus no PAC) was 1.09 [95% confidence interval (CI) 0.94 to 1.27]. There was no difference in the median length of stay in ICU, the median length of stay in an acute hospital or mean organ-days of support in ICU between the two groups. The economic evaluation found that the expected cost per QALY gained from the withdrawal of PAC was 2985 pounds. The expected cost per life gained from the withdrawal of PAC was 22,038 pounds.

CONCLUSIONS

Clinical management of critically ill patients with a PAC, as currently practised in the UK, neither improves hospital survival for adult, general intensive care patients nor reduces length of stay in hospital. The lack of demonstrable benefit from a device previously believed to be beneficial could be explained by statistical chance, by misinterpretation of PAC-derived data, by ineffective treatment strategies based on data correctly interpreted using the current paradigm or by subsequent inaction following insertion of the device. It is also possible that detailed data on haemodynamics, however used, cannot modify the disease process sufficiently to influence disease outcome. The economic evaluation, using decision analysis techniques rather than conventional hypothesis testing, suggests that the withdrawal of the PAC from routine clinical practice in the NHS would be considered cost-effective in the current decision-making climate, and might result in lives or life-years being saved at modest cost. With the declining use of PACs in the UK and the findings of this report indicating no overall benefit from management with a PAC, it should now be possible to examine protocolised management with a PAC in selected groups of critically ill patients against appropriate controls, something that was difficult while PACs were the considered standard of care.

摘要

目的

评估在成人综合重症监护中使用或不使用肺动脉导管(PAC)管理重症患者的临床效果和成本效益。

设计

一项开放、多中心、随机对照试验,并进行经济评估(成本效用和成本效益分析)。

设置

研究地点为英国收治成人患者的综合(内科/外科混合)重症监护病房(ICU)。

参与者

参与研究的ICU中,经负责治疗的临床医生判定需要使用PAC进行管理的成年患者。

干预措施

干预措施为插入PAC并随后由负责治疗的临床医生根据PAC获得的数据自行决定进行临床管理。对照组不使用PAC,但可选择使用其他心输出量监测设备。

主要结局指标

主要结局指标为医院死亡率。次要结局指标为ICU住院时间、急性医院住院时间以及ICU中器官支持天数。对于经济评估,主要结局指标为质量调整生命年(QALY),次要结局指标为医院死亡率。

结果

英国65家ICU参与了研究。其中,43家(66%)在对照组患者中使用了其他心输出量监测设备。共确定1263例患者符合试验条件。其中,1041例(82.4%)被随机分组,分配至使用PAC管理组(n = 519)或不使用PAC管理组(n = 522)。无失访情况。然而,27例患者(PAC组13例,对照组14例)退出试验,原因是患者恢复精神能力后撤回同意或亲属在随机分组后撤回同意。1014例患者的数据纳入分析。两组参与者的基线特征相似。使用PAC管理的患者与未使用PAC管理的患者在医院死亡率方面无差异。调整后的风险比(PAC组与无PAC组)为1.09[95%置信区间(CI)0.94至1.27]。两组在ICU中位住院时间、急性医院中位住院时间或ICU中平均器官支持天数方面无差异。经济评估发现,停用PAC每获得一个QALY的预期成本为2985英镑。停用PAC每挽救一条生命的预期成本为22,038英镑。

结论

目前在英国,使用PAC对重症患者进行临床管理,既不能提高成人综合重症监护患者的医院生存率,也不能缩短住院时间。此前认为有益的设备却未显示出明显益处,这可能是由于统计机遇、对PAC衍生数据的错误解读、基于当前范式正确解读的数据所采用的无效治疗策略,或者是在插入设备后随后的不作为。也有可能无论如何使用血流动力学详细数据,都无法充分改变疾病进程以影响疾病结局。经济评估采用决策分析技术而非传统假设检验,表明在当前决策环境下,在英国国家医疗服务体系(NHS)的常规临床实践中停用PAC将被视为具有成本效益,并且可能以适度成本挽救生命或生命年。鉴于英国PAC的使用逐渐减少,且本报告结果表明使用PAC管理并无总体益处,现在应该可以针对特定重症患者群体,对照适当的对照组,研究使用PAC的规范化管理方法,而在PAC被视为标准治疗方法时这是难以做到的。

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