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Cost/Utility Ratio in the Management of Patients With Acquired Severe Brain Injury

2012年12月5日 更新者:Soccorso Capomolla, MD、Fondazione Don Carlo Gnocchi Onlus

Cost/Utility Ratio in the Management of Patients With Acquired Severe Brain Injury: Comparison Between a Programme of In-hospital Graded Intensity Rehabilitation and Usual Care.

The aim of this study was to compare the cost/utility ratio of a management model of integrated, graded, intensive rehabilitation (GIR) versus usual care (UC) for patients with acquired Severe Brain Injury (SBI).

研究概览

详细说明

Materials and methods Study design This study was an organizational assessment of an integrated system of care (GIR) for patients with SBI and was designed as a prospective, randomised trial. An individual record was created for each patient with SBI; this record contained the patient's personal data, information prior to admission to intensive care or neurosurgery, clinical characteristics, the presence of devices, complications, time of hospitalisation in an Intensive Care Unit, and cognitive conditions. Once it had been determined that the study entry criteria were met, the patients were entered in the register and prospectively in parallel-group randomised to two different management strategies.

The concealment of allocation was guaranteed by the availability of beds in the ward. Patients and health care providers and assessors were blinded to the study designed to compare the strategies management. Data analysts were blinded to treatment.

Sample size The sample size requirements for this study are intended to provide adequate power for the analysis of the primary objective ( decrease event-related mortality). The simulation were run in statsoft six sigma software according to the following hypotheses: the mortality of severe brain injury used as a Null hypothesis was 58%. This percent value is expected to decrease at 40% in the study arm. The target type-I error(α) was 0.05. A sample size of 119 patients per group would allow a power of 80% to detect an individual risk score ratio of 0.70 with a type -I error of 0.05.

Based on the availability of beds in the ward, two groups were formed:

(i) the UC patients who, while meeting the criteria for access into the Graded Intensity of Rehabilitation Unit for patients with SBI (SBI-GIRU), did not enter the department because no beds were free and were, therefore, discharged from the Intensive Care Unit into the management models available, such as acute care, Intensive Brain Injury rehabilitation ( cod 75) brain injury rehabilitation (code 56) ( hospital admission, lasting on average 60 days, in which intensive rehabilitation care is delivered prior to transfer to another structure), long-term care, home.

(ii) The GIR patients who met the criteria for access into the SBI-GIRU and for whom a bed was available in the Unit, where an individualised programme of intensive rehabilitation care was structured.

The primary outcome for assessing the effectiveness of the two different forms of management was mortality; secondary outcomes included the improvement of quality of life evaluated using a classification system based on the Health Utilities Index Mark 2 (8) and the number of days of hospitalisation.

Patients Patients with acquired SBI referred to our unit between January 2007 and January 2010 were considered for this study. The diagnosis of acquired SBI was made on the basis of the clinical history, physical examination, clinical symptoms, Glasgow Coma Scale score <8 and neuro-radiological investigations.

After having been entered into the register, patients in the UC group began the monitoring phase, while the patients in the GIR group were submitted to clinical evaluation, prognostic stratification, and clinical and instrumental investigations, after which an individualised rehabilitation plan was made, characterized by structured multidisciplinary interventions that were periodically reviewed. The alternative management strategies are described in greater detail below.

Usual care In this case patients were managed according to the organization of the management model which took on the care of the patient. The organization of these models is characterized by one or two professional figures (physiatrists, neurologist), with hierarchical relationships, in spaces limited to a specific pathology; access is determined by clinical stability; the instruments of governance are guidelines and consensus and the rehabilitation programme is focused on functional and cognitive areas; the medical care process is governed by hierarchy. The technology in this model is limited to a specific specialty.

Graded intensive rehabilitation This is a result-oriented management model; it is multidisciplinary and has the purpose of determining the appropriateness of hospitalization and the patients' needs through the use of a ranking; the management is "disease-based", and the instruments of governance are the diagnostic-therapeutic rehabilitation pathways (DTRP), the quality system and product standards; the medical care process has separate strands with result-oriented autonomy; the technology present in this model is identified on the basis of health needs and support of vital signs.

Classifying patients In relation to their clinical conditions and complexity of care needs, three profiles of patients with SBI have been identified: the critically patient, the complex patient and the frail patient. The critically ill patient is a patient with abnormal vital parameters who requires constant monitoring and may need immediate therapeutic interventions. The complex patient is an individual with significant comorbidities who requires complicated, expensive and often invasive diagnostic investigations and/or numerous therapies sometimes conflicting with each other with a strong risk of interactions. The complexity of care increases in "frail patients". Frail patients have: (i) a marked susceptibility to develop acute illnesses that are manifested by atypical clinical pictures;(ii) rapid fluctuations of health, even in the same day, with a strong tendency to develop complications (failure cascade); (iii) a high risk of adverse events and iatrogenic events; (iv) slow and, almost always, only partial recovery; (v) continued requirements for medical interventions, need for ongoing assistance; and (vi) a high risk of mortality.

Levels of intensity of care On the basis of the above-described evaluation, the patient is assigned to the most appropriate of the following settings.

Level 1 (intensive): the patient is critical and unstable, dependent or potentially dependent on technological aids and at high risk of complications. Area of competence - red: monitored beds, single rooms, infusion pumps, telemetry, daily medical round, and intensive nursing activities 24 hours a day.

Level 2 (medium): the patient is clinically unstable and requires constant monitoring of vital parameters. Highly complex medical activities and intensive nursing care are prevalent. Area of competence - yellow: rooms with two beds, infusion pumps, telemetry, daily medical round, intensive, structured nursing activities, physiotherapy and speech therapy.

Level 3 (low): the patient is clinically stable and does not require constant monitoring of vital signs or the continuous presence of a doctor. Activities are prevalently physiotherapy and nursing care. Area of competence - green.

Level 4 (minimum): the patient is clinically stable and requires only social and nursing care for discharge. Area of competence - white.

The transition between different levels is determined by clinical criteria that define the area of competence required.

Staff The staff of the SBI-GIRU consists of a neurologist, an internist, a physiatrist, a cardiologist, a speech physician, twelve nurses with specific skills, a chief nurse, a nutritionist, two speech therapists, three physiotherapists, a psychologist and a social worker. The aim of the multidisciplinary approach is to facilitate recovery from disability caused by SBI.

Each member of the team has the duty to control, analyse and redesign the organization that supports the activities and processes set out in the individual rehabilitation plan. Three types of intervention - medical, nursing and physiotherapeutic - can be identified in the rehabilitation plan and are strongly integrated in order to achieve the rehabilitation objectives. The healthcare and rehabilitation processes are founded on guidelines and the criteria of evidence-based medicine.

The rehabilitation process The treatment plan is discussed in collaboration with the whole multidisciplinary team. An individual rehabilitation plan is drawn up which outlines: (i) the appropriateness of access; (ii) the type of access (SBI of traumatic, anoxic one, ischaemic or haemorrhagic nature); (iii) the objectives of the rehabilitation process (prognostic stratification, therapy optimization, prevention of secondary injury, management of devices, management of cognitive impairment, prevention of damage by immobility, recovery of motor function); (iv) use of the instruments to implement the plan (multi-disciplinary meeting, electroencephalogram, physiotherapy briefings, diagnostic radiology, consultancy, monitoring systems, infusion systems); (v) time-course of the plan; (vi) result indicators in the short to medium term; (vii) results indicators in the long-term; (viii) the method of discharge; and (ix) management counselling.

Follow-up A monitoring form was used for each patient to record the following information: personal data, outcome measures, employment issues, degree of socialisation, commitment of caregivers and the results of the Health Utilities Index Mark 2 questionnaire.

Outcomes Three types of outcomes were considered: management outcomes, functional results and a hard end-point (survival).

Management outcomes. The management outcomes considered were: access time, number of structures involved in the management of the patient, the healthcare path, the number of days spent in hospital, the type of management to which the patient was subsequently addressed.

Functional results. These included the number of devices at discharge, the Glasgow Outcome Scale (GOS) score, the Barthel Index score and any change in quality of life, assessed using the classification system based on the Health Utilities Index Mark 2 Survival. The patient's death related to the event index was considered as a hard event. In the survival analysis the two management models were considered as predictors of mortality. These predictors were adjusted for confounding variables (age, sex, aetiology, GOS score, Level of Cognitive Functioning score and indices of organ function). The association between independent predictors and outcome was assessed by comparing the follow-up data with a Cox proportional hazards regression model. The end-point of the study was event-related mortality. The distribution of the time function of the events was analysed with the Kaplan-Meier method

Cost analysis The cost/utility analysis was performed from the payer's prospective (the health authority). Hospital admissions for the implementation of the process and for health care - in particular, admissions to intensive care, acute care, rehabilitation and the social welfare sector - were considered. Management costs incurred at home were excluded. The prices used for calculations were those of the average daily cost of hospitalisation per type of management as listed in the Interregional Tariff Agreement [Tariffa Unica Convenzionale, TUC] 2009 for hospital healthcare services. The QALY was determined by calculating the years of life gained in management models adjusted for the quality of life. The difference in QALYs between the two models was obtained by considering the average increase of life derived from the survival curves (difference between the areas of the survival curves) adjusted for the quality of life.

Sensitivity analysis The sensitivity analysis was performed by calculating the cost/utility ratio using the extremes; in particular, changes in QALY and costs were evaluated by considering the extremes (confidence limits of the variations of the mean).

Statistical analysis To compare the clinical and functional parameters between the two groups we used the one-way analysis of variance for continuous variables and chi-square tests for categorical variables. For the analysis of prognostic indicators, the two management strategies were considered as independent predictors of outcome. The analysis was adjusted for confounding factors. event-related mortality was considered as an end-point of the study.

The association between independent predictors and outcome was assessed by comparing the follow-up data with a Cox proportional hazards regression model. The assumption of the proportionality of risk during the observation time, has been evaluated using the analysis of residues of Schoenfeld. Deaths from causes unrelated to the SBI were treated as censored observations. The distribution of the time function of the events was analysed using the method of Kaplan-Meier. The prognostic information is presented as relative risk with 95% confidence limits. Descriptive statistics are expressed as the mean value ± standard deviation. Probability values <0.05 are considered statistically significant.

研究类型

介入性

注册 (实际的)

249

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Avellino
      • Sant'Angelo dei lombardi、Avellino、意大利、83054
        • Intenstive brain injury rehabilitation Unit of Polo Specialistico Riabilitativo

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Patients with acquired Severe brain injury
  • patients with Glasgow Coma Scale score <8
  • patients with Focal ischaemic lesion, cerebral contusion or hemorrhage on computed tomography or magnetic resonance imaging

Exclusion Criteria:

  • patient with age< 18 years
  • patients with previous degenerative nervous disease
  • oncological patients with reduce life expectancy
  • patients with impaired vital signs

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:卫生服务研究
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:三倍

武器和干预

参与者组/臂
干预/治疗
有源比较器:usual care
In this arm patients were managed according to the organization of the management model which took on the care of the patient. The organization of these models is characterized by one or two professional figures (physiatrists, neurologist), with hierarchical relationships, in spaces limited to a specific pathology; access is determined by clinical stability; the instruments of governance are guidelines and consensus and the rehabilitation programme is focused on functional and cognitive areas; the medical care process is governed by hierarchy. The technology in this model is limited to a specific specialty.

specific pathology. access is determined by clinical stability. the instruments of governance are guidelines and consensus and the rehabilitation programme is focused on functional and cognitive areas.

the medical care process is governed by hierarchy. The technology in this model is limited to a specific specialty

实验性的:Graded intensive rehabilitation

Instruments of governance are the diagnostic-therapeutic rehabilitation. pathways (DTRP), the Quality system and product standards.

Medical care process with result-oriented autonomy. Technology support of vital signs. Multidisciplinary intervention

Multidisciplinary intervention Instruments of governance are the diagnostic-therapeutic rehabilitation pathways (DTRP), the Quality system and product standards; Medical care process with result-oriented autonomy Technology support of vital signs.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
cost/utility ratio
大体时间:up to 1 year

Management outcomes. The management outcomes considered were: access time, number of structures involved in the management of the patient, the healthcare path, the number of days spent in hospital, the type of management to which the patient was subsequently addressed.

Functional results. These included the number of devices at discharge, the Glasgow Outcome Scale (GOS) score, the Barthel Index score and any change in quality of life, assessed using the classification system based on the Health Utilities Index Mark 2 Survival. The patient's death related to the event index was considered as a hard event. In the survival analysis the two management models were considered as predictors of mortality. The association between independent predictors and outcome was assessed by comparing the follow-up data with a Cox proportional hazards regression model. The end-point of the study was event-related mortality

up to 1 year

次要结果测量

结果测量
措施说明
大体时间
quality of live
大体时间:up to 1 year
quality of life, assessed using the classification system based on the Health Utilities Index Mark 2
up to 1 year

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Antonio S Capomolla, MD、Fondazione Don Carlo Gnocchi Onlus

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2007年1月1日

初级完成 (实际的)

2010年1月1日

研究完成 (实际的)

2012年1月1日

研究注册日期

首次提交

2012年9月5日

首先提交符合 QC 标准的

2012年12月5日

首次发布 (估计)

2012年12月6日

研究记录更新

最后更新发布 (估计)

2012年12月6日

上次提交的符合 QC 标准的更新

2012年12月5日

最后验证

2012年12月1日

更多信息

与本研究相关的术语

其他研究编号

  • 270360
  • FDCGPLCPSR01012007 (其他标识符:FDCGPLCPSR01012007)

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

usual care的临床试验

3
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