Key result
In adults with congenital heart disease and elevated baseline NT-proBNP, repeated NT-proBNP measurements were significantly associated with adverse cardiovascular events (HR per 2-fold higher value 2.08).
Why the study?
Do serial NT-proBNP measurements provide additional prognostic value for cardiovascular events in adults with congenital heart disease?
Cohort (n=602)
No
Do serial NT-proBNP measurements provide additional prognostic value for cardiovascular events in adults with congenital heart disease?
Hazard Ratio: 2.08 (95% CI 1.31–3.87)
p-value: p=<0.001
Serial NT-proBNP measurements provide additional prognostic value over a single baseline measurement in adults with congenital heart disease and elevated baseline NT-proBNP.
May support serial NT-proBNP monitoring for risk stratification in ACHD; leaves open impact on management or outcomes.
Background A single NT ‐pro BNP (N‐terminal pro‐B‐type natriuretic peptide) measurement is a strong prognostic factor in adult congenital heart disease. This study investigates NT ‐pro BNP profiles within patients with adult congenital heart disease and relates these to cardiovascular events. Methods and Results In this prospective cohort, 602 patients with adult congenital heart disease were enrolled at the outpatient clinic (years 2011–2013). NT ‐pro BNP was measured at study inclusion in 595 patients (median age 33 [ IQR 25–41] years, 58% male, 90% NYHA I) and at subsequent annual visits. The primary end point was defined as death, heart failure, hospitalization, arrhythmia, thromboembolic event, or cardiac intervention; the secondary end point as death or heart failure. Repeated measurements were analyzed using linear mixed models and joint models. During a median follow‐up of 4.4 [ IQR 3.8–4.8] years, a total of 2424 repeated measurements were collected. Average NT ‐pro BNP increase was 2.9 pmol/L the year before the primary end point (n=199, 34%) and 18.2 pmol/L before the secondary end point (n=58, 10%), compared with 0.3 pmol/L in patients who remained end point‐free ( P ‐value for difference in slope 0.006 and <0.001, respectively). In patients with elevated baseline NT ‐pro BNP (>14 pmol/L, n=315, 53%), repeated measurements were associated with the primary end point ( HR per 2‐fold higher value 2.08; 95% CI 1.31–3.87; P <0.001) and secondary end point ( HR 2.47; 95% CI 1.13–5.70; P =0.017), when adjusted for the baseline measurement. Conclusions NT ‐pro BNP increased before the occurrence of events, especially in patients who died or developed heart failure. Serial NT ‐pro BNP measurements could be of additional prognostic value in the annual follow‐up of patients with adult congenitive heart disease with an elevated NT ‐pro BNP .
No takes yet. Share an insight, caveat, or question.
Baggen et al. (2018) conducted a cohort in Adult congenital heart disease (n=602). Repeated NT-proBNP measurements vs. Baseline NT-proBNP measurement alone was evaluated on Composite of death, heart failure, hospitalization, arrhythmia, thromboembolic event, or cardiac intervention (HR 2.08, 95% CI 1.31-3.87, p=<0.001). In adults with congenital heart disease and elevated baseline NT-proBNP, repeated NT-proBNP measurements were significantly associated with adverse cardiovascular events (HR per 2-fold higher value 2.08).
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: