B-type natriuretic peptide in the evaluation and management of dyspnoea in primary care

E Burri, K Hochholzer, N Arenja, H Martin-Braschler, L Kaestner, H Gekeler, T Hatziisaak, M Büttiker, A Fräulin, M Potocki, T Breidthardt, T Reichlin, T Socrates, R Twerenbold, C Mueller, E Burri, K Hochholzer, N Arenja, H Martin-Braschler, L Kaestner, H Gekeler, T Hatziisaak, M Büttiker, A Fräulin, M Potocki, T Breidthardt, T Reichlin, T Socrates, R Twerenbold, C Mueller

Abstract

Objectives: The rapid and accurate diagnosis of heart failure in primary care is a major unmet clinical need. We evaluated the additional use of B-type natriuretic peptide (BNP) levels.

Design: A randomized controlled trial.

Setting: Twenty-nine primary care physicians in Switzerland and Germany coordinated by the University Hospital Basel, Switzerland.

Subjects: A total of 323 consecutive patients presenting with dyspnoea.

Interventions: Assignment in a 1 : 1 ratio to a diagnostic strategy including point-of-care measurement of BNP (n = 163) or standard assessment without BNP (n = 160). The total medical cost at 3 months was the primary end-point. Secondary end-points were diagnostic certainty, time to appropriate therapy, functional capacity, hospitalization and mortality. The final diagnosis was adjudicated by a physician blinded to the BNP levels.

Results: Heart failure was the final diagnosis in 34% of patients. The number of hospitalizations, functional status and total medical cost at 3 months [median $1655, interquartile range (IQR), 850-3331 vs. $1541, IQR 859-2827; P = 0.68] were similar in both groups. BNP increased diagnostic certainty as defined by the need for further diagnostic work-up (33% vs. 45%; P = 0.02) and accelerated the initiation of the appropriate treatment (13 days vs. 25 days; P = 0.01). The area under the receiver-operating characteristics curve for BNP to identify heart failure was 0.87 (95% confidence interval, 0.81-0.93).

Conclusions: The use of BNP levels in primary care did not reduce total medical cost, but improved some of the secondary end-points including diagnostic certainty and time to initiation of appropriate treatment.

Trial registration: ClinicalTrials.gov NCT00130611.

© 2012 The Association for the Publication of the Journal of Internal Medicine.

Source: PubMed

3
Sottoscrivi