Strategy to Recognize and Initiate Treatment of Chronic Heart Failure

Not Applicable

Completed

• Conditions: Heart Failure
• Interventions: Other: Training of general practitioners in an uptitration protocol.

• Registration Number: NCT01202006
• Lead Sponsor: UMC Utrecht

Brief Summary

The purpose of this study is to determine whether a structured diagnostic-therapeutic strategy to detect and treat previously unrecognized (or unestablished) heart failure in primary care will improve the functional capacity, quality of care, the quality of life, and eventually the prognosis of these patients.

Detailed Description

Heart failure is an emerging epidemic in especially the elderly, with high mortality rates, substantial loss in quality of life, and high healthcare costs, mainly due to hospitalizations. The majority of (usually elderly) patients with heart failure are diagnosed and managed in primary care. However underdiagnosis and undertreatment of patients with heart failure in primary care are common. Implementation of a standardized diagnostic protocol together with educating general practitioners in a pragmatic treatment strategy in which the focus lays on uptitration of heartfailure medication, would fill the gap of underdiagnosis and undertreatment that nowadays exists in primary care.

All participants will undergo a standardized diagnostic work-up to establish or rule out heart failure. In those participants with an abnormal ECG and/or elevated natriuretic peptide level additional echocardiography will be performed at the outpatient clinic of the Diakonessenhuis in Zeist. The definite diagnosis of heart failure ('systolic' or 'diastolic') will be established by an expert panel consisting of two cardiologists and a general practitioner. The panel will apply the criteria of the updated heart failure guidelines (2008) of the European Society of Cardiology (ESC). Patients with heart failure will subsequently be treated by their own general practitioner. The participating general practitioners will be randomly divided into either care as usual (control group) or special uptitration (intervention group). Both groups will be using medication as recommended in the Dutch heart failure standard. However, general practitioners in the intervention group will be especially trained in the practical appliance of this guideline: the initiation of diuretics and ACE-inhibitors and structured uptitration of ACE-inhibitors and beta-blockers. In the training, practical examples will be used concerning barriers the general practitioners themselves encountered when using this medication. In the intervention group, patients with 'systolic' heart failure will receive the recommended maximal dose or the highest tolerated dose. Patients with 'diastolic' heart failure will receive optimal blood pressure and heart rate control with the preferred cardiovascular drugs. At baseline and six months after heart failure is established or ruled out, participants are asked to perform the six-minute walk test and fill out quality of life questionnaires. During those six months, only participants with heart failure will additionally fill out one of these questionnaires every three weeks. Also after six months, electronical files of the general practitioners will be scrutinized to assess the (dosage of) prescribed medication and visits to general practice and cardiology department.

Study Timeline

• Study First Submitted: 2010-09-14
• Study First Submitted QC: 2010-09-14
• Study First Posted: 2010-09-15
• Study Start: 2010-10
• Primary Completion: 2012-12
• Study Completion: 2012-12
• Status Verified: 2015-07
• Last Update Submitted: 2015-07-07
• Last Update Posted: 2015-07-08

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 585

Inclusion Criteria

• Age 65 years or over
• Shortness of breath as reason for GP contact in the previous 12 months

Exclusion Criteria

• Already established heart failure, that is a diagnosis of heart failure confirmed by the cardiologist with echocardiography
• A life expectancy shorter than 6 months
• Not being able to give informed consent

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Intervention	Training of general practitioners in an uptitration protocol.	General practitioners of patients in the intervention group will receive detailed instructions on uptitration of ACE-inhibitors and beta-blockers before the inclusion of participants.

Primary Outcome Measures

Name	Time	Method
Differences in prescription of heart failure medication between the intervention and control group.	6 months
Differences in quality of life between the intervention and control group.	6 months
Prevalence of heart failure in elderly who presented to the general practitioner with shortness of breath on exertion.	one year
Differences in walking distance between the intervention and control group.	6 months	This outcome was added because of its relevance for patients with heart failure in April 2011. The change in study protocol was communicated to and approved by the Medical Ethics Committee of the UMC Utrecht.
Differences in (heart failure related) doctor-appointments and hospitalization rates between the intervention and control group.	6 months

Secondary Outcome Measures

Name	Time	Method
Cost-effectiveness of the implemented diagnostic-therapeutic strategy.	6 months

Trial Locations

Locations (1)

Julius Center for Health Sciences and Primary care; 🇳🇱 Utrecht, Netherlands