Heart Failure Clinical Trial
Official title:
NT-proBNP Testing in Patients Presenting to the Emergency Department With Acute Dyspnea: Evaluation of Effects on Treatment, Hospitalisation Rate and Costs
Diagnostic uncertainty in patients with complaints of shortness of breath presenting to the
Emergency Department of a hospital may delay treatment and proper care. In patients with
shortness of breath due to heart failure increased plasma levels of NT-pro-B-type
natriuretic peptide (NT-proBNP) can be demonstrated. The use of NT-proBNP as a biomarker for
heart failure in patients presenting to the emergency department with dyspnea might improve
care and reduce length of hospital stay.
To investigate the effect of NT-proBNP testing on patient care and time to discharge the
NT-proBNP test will be randomized. In patients in the study group, the NT-proBNP plasma
level is determined at admission and the physician in charge will immediately receive the
result of the test. In patients in the control group blood will be sampled but the physician
will recieve no information on the NT-proBNP plasma level.
In our study we will investigate the effect of introduction of NT-proBNP as biomarker for
heart failure on treatment, time to discharge and costs.
n/a
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Single Blind, Primary Purpose: Diagnostic
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