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临床试验/NCT03902028
NCT03902028已完成不适用

Interest of an Optimized Medico-pharmaceutical Collaboration in the Drug Management of Patients With Heart Failure: Controlled, Randomized, Multicentric Study

University Hospital, Montpellier2 个研究点 分布在 1 个国家目标入组 229 人开始时间: 2019年8月2日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
229
试验地点
2
主要终点
Rehospitalisation for heart failure

研究概览

简要总结

This is a controlled, randomized, open-label, multicentric study evaluating the value of coordinated medico-pharmaceutical management compared to standard management in patients with heart failure. The aim of this study is to evaluate the impact of these optimized activities on the re-hospitalization of the patient with cardiac insufficiency for a disease-related event within three months of the initial hospitalization.

详细描述

Heart failure (FH) is a public health problem with an estimated prevalence of about 1.5% in developed countries. In 2013, the number of patients hospitalized in France for heart failure amounted to 165 231 and 20% of them were re-hospitalized at least once for the same reason during this year. Several factors contribute to the occurrence of cardiac decompensation (DC) : some modifiable (age, severity of IC, etiology ...) and others modifiable, such as therapeutics. Various elements could reduce the frequency of re-hospitalizations and the mortality due to this disease :

  • a better knowledge of treatments by patients and consequently a better therapeutic compliance
  • a better knowledge of the factors and signs of DC (low-sodium diet, weighing...)
  • a better implementation of prescribing recommendations : less than 50% of patients have optimal treatment compared to ESC recommendations
  • a better communication at the transition points of the patient pathway. The creation of a binomial cardiologist-clinical pharmacist during hospitalization and the maintenance of this optimized multidisciplinary follow-up within 3 months post-hospitalization is a proposal to intervene on these factors. Indeed, the clinical pharmacist (present in the care unit) works in collaboration with the medical and paramedical teams and can improve the care of patients. In the experimental group, a specific multidisciplinary consultation is planned for one month after the end of the hospitalization. A 3-month follow-up visit will be carried out by phone call to meet the criteria for readmission, mortality, quality of life, adherence and persistence of treatments.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patient aged more than 18 years
  • Adult patient admitted in cardiology department (full hospitalisation or intensive care) for heart failure no matter the type and the stage of the disease
  • Person affiliated or beneficiary of a social security system
  • Collection of a free, informed, express and written consent

排除标准

  • Non autonomous drug management patients and not disposing
  • a present caregiver during hospitalisation
  • Patients living in an institution
  • Person participating in another clinical trial with an exclusion period still ongoing
  • Person whose physical and/or psychological health is severely altered, and which, in the opinion of the investigator, may affect the participation's to the study
  • Person deprived of his rights, person under tutorship or guardianship
  • Refusal to sign the consent

研究组 & 干预措施

Reinforced multidisciplinary follow-up

Experimental

Entrance medication reconciliation performed by a pharmacist

  • Patient compliance evaluation
  • Patient quality of life evaluation
  • Pharmaceutical analysis with focus on medication optimization with a specific check-list (according to ESC 2016 recommendations)
  • Hospitalisation discharge medication reconciliation
  • Patient pharmaceutic interview at the hospitalisation discharge
  • Transmission of informations to the general practitioner and the pharmacist's patient
  • Multidisciplinary consult at 1 month after hospitalisation discharge

干预措施: Reinforced multidisciplinary follow-up (Other)

Standard care

No Intervention
  • Drug review by a paramedic or a pharmacist
  • Pharmaceutical analysis
  • Therapeutic optimisation based on the usual practices care of the cardiologic department
  • Writing of the prescription given on leaving hospital based on the usual care of the department
  • Treatments explanations and support to the patient on the usual care
  • Transmission of the hospitalisation report to the patient general practitioner as the usual practice
  • Medical consult in usual time frames (an average of 1 month after hospitalisation discharge) at the patient location of choice

结局指标

主要结局

Rehospitalisation for heart failure

时间窗: Call at 3 months after hospitalisation discharge

At least one rehospitalisation with heart failure related cause

次要结局

  • Prescriptions conformity rates compared to heart failure recommendations edited by the European Society of Cardiology in 2016(At hospitalisation discharge (Day 0))
  • Compliance level(At hospitalisation discharge (Day 0))
  • Compliance level(At 1 month after hospitalisation discharge for the experimental group only)
  • Compliance level(Call at 3 months after hospitalisation discharge)
  • Satisfaction of the patient(Call at 3 months after hospitalisation discharge)
  • Incremental cost-effectiveness ratio(3 months after hospitalisation discharge)
  • Prescriptions conformity rates compared to heart failure recommendations edited by the European Society of Cardiology in 2016(Call at 3 months after hospitalisation discharge)
  • Time before death(Call at 3 months after hospitalisation discharge)
  • Time of occurrence of a potential rehospitalisation related to the disease(Call at 3 months after hospitalisation discharge)
  • Treatment persistence rates(Call at 3 months after hospitalisation discharge)
  • Death rate(Call at 3 months after hospitalisation discharge)
  • Quality of life score(Call at 3 months after hospitalisation discharge)
  • Satisfaction of health professionals(online questionnaire at 3 months after hospitalisation discharge)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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