Skip to main content
Clinical Trials/NCT01801722
NCT01801722
Completed
Not Applicable

Using NT-proBNP to Detect Chronic Heart Failure in Patients With Chronic Obstructive Pulmonary Disease.

Lund University1 site in 1 country75 target enrollmentApril 2008

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Chronic Obstructive Pulmonary Disease
Sponsor
Lund University
Enrollment
75
Locations
1
Primary Endpoint
Percentage of patients with elevated NT-proBNP.
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

The aim of the present study was to evaluate if the analysis of NT-proBNP might be used as an initial step for the diagnosis of chronic heart failure in patients with COPD in primary health care, and to select patients for a further examination by echocardiography.

Detailed Description

Patients with a confirmed diagnosis of COPD were examined regarding chronic heart failure. 1. An interview regarding symptoms: breathlessness, orthopnoea, night cough, nocturia, walking distance. 2. Physical examination: weight and height, heart and lung auscultation, blood pressure measurement after 5 minutes' rest in the sitting position and the presence of peripheral oedema. 3. Electrocardiography. 4. Natriuretic peptide- NT-proBNP (Immulite 2500, Siemens Healthcare Diagnostics AB Sweden). 5. Patients with the NT-proBNP level of \> 1200 pg/ml were referred for echocardiography to assess left ventricular function.

Registry
clinicaltrials.gov
Start Date
April 2008
End Date
June 2008
Last Updated
8 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Elzbieta Kaszuba

PhD student

Lund University

Eligibility Criteria

Inclusion Criteria

  • Patients aged 65 years and older with the following diagnosis codes according to International Statistical Classification of Diseases and Related Health Problems - Tenth Revision:J44 (COPD) and J41, J42 (chronic bronchitis) registered during the period 1 January 2008-16 April 2008 according to the electronic patient record.

Exclusion Criteria

  • Impaired cognitive function and/or anticipated difficulties in carrying out spirometry due to immobility,
  • psychiatric disorders or terminal illness.

Outcomes

Primary Outcomes

Percentage of patients with elevated NT-proBNP.

Time Frame: 3 months

NT-proBNP has taken only once in each patient without follow up follow up. Three months was a period when we collected data from all participants.

Secondary Outcomes

  • Percentage of patients with abnormal left ventricular function assessed by echocardiography. Association between elevated NT-proBNP and symptoms, signs and electrocardiography.(3 months)

Study Sites (1)

Loading locations...

Similar Trials