Key result
Combining NT-proBNP, capnometry, and clinical assessment (AUROC 0.97; 95% CI 0.90-0.99) was superior to NT-proBNP and clinical assessment (AUROC 0.94) for diagnosing HF-related dyspnea (P=0.006).
Why the study?
Does the combination of quantitative capnometry, NT-proBNP, and clinical assessment improve diagnostic accuracy compared to NT-proBNP alone or with clinical assessment in differentiating acute heart failure from pulmonary disease in pre-hospital acute dyspnea?
Observational (n=441)
No
Does the combination of quantitative capnometry, NT-proBNP, and clinical assessment improve diagnostic accuracy compared to NT-proBNP alone or with clinical assessment in differentiating acute heart failure from pulmonary disease in pre-hospital acute dyspnea?
Effect estimate: AUROC 0.97 (95% CI 0.90-0.99)
Absolute Event Rate: 0.97% vs 0.94%
p-value: p=0.006
Adding quantitative capnometry to NT-proBNP and clinical assessment significantly improves the diagnostic accuracy for differentiating acute heart failure from pulmonary causes of dyspnea in the pre-hospital setting.
May enhance prehospital HF dyspnea diagnosis; hypothesis-generating, requires prospective validation before practice change.
AIM: To determine the diagnostic accuracy of the combination of quantitative capnometry (QC), N-terminal pro-brain natriuretic peptide (NT-proBNP), and clinical assessment in differentiating heart failure (HF)-related acute dyspnea from pulmonary-related acute dyspnea in a pre-hospital setting. METHODS: This prospective study was performed in the Center for Emergency Medicine Maribor, Slovenia, January 2005-June 2007. Two groups of patients with acute dyspnea apnea were compared: HF-related acute dyspnea group (n = 238) vs pulmonary-related acute dyspnea (asthma/COPD) group (n = 203). The primary outcome was the comparison of combination of QC, NT-proBNP, and clinical assessment vs NT-proBNP alone or NT-proBNP in combination with clinical assessment, in differentiating HF-related acute dyspnea from pulmonary-related acute dyspnea (asthma/COPD) in pre-hospital emergency setting, using the area under the receiver operating characteristic curve (AUROC). The secondary outcomes end points were identification of independent predictors for final diagnosis of acute dyspnea (caused by acute HF or pulmonary diseases), and determination of NT-proBNP levels, as well as capnometry, in the subgroup of patients with a previous history of HF and in the subgroup of patients with a previous history of pulmonary disease. RESULTS: In differentiating between cardiac and respiratory causes of acute dyspnea in pre-hospital emergency setting, NT-proBNP in combination with PetCO2 and clinical assessment (AUROC, 0.97; 95% confidence interval [CI], 0.90-0.99) was superior to combination of NT-proBNP and clinical assessment (AUROC, 0.94; 95% CI, 0.88-0.96; P = 0.006) or NT-proBNP alone (AUROC, 0.90; 95% CI, 0.85-0.94; P = 0.005). The values of NT-proBNP> or = 2000 pg/mL and PetCO2 < or = 4 kPa were strong independent predictors for acute HF. In the group of acute HF dyspneic patients, subgroup of patients with previous COPD/asthma had significantly higher PetCO2 (3.8 +/- 1.2 vs 5.8 +/- 1.3 kPa, P = 0.009). In the group of COPD/asthma dyspneic patients, NT-proBNP was significantly higher in the subgroup of patients with previous HF (1453.3 +/- 552.3 vs 741.5 +/- 435.5 pg/mL, P = 0.010). CONCLUSION: In differentiating between cardiac and respiratory causes of acute dyspnea in pre-hospital emergency setting, NT-proBNP in combination with capnometry and clinical assessment was superior to NT-proBNP alone or NT-proBNP in combination with clinical assessment.
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Klemen et al. (2009) conducted an observational in Acute dyspnea (n=441). Combination of quantitative capnometry, NT-proBNP, and clinical assessment vs. NT-proBNP alone or NT-proBNP in combination with clinical assessment was evaluated on Differentiating HF-related acute dyspnea from pulmonary-related acute dyspnea using AUROC (AUROC 0.97, 95% CI 0.90-0.99, p=0.006). Combining NT-proBNP, capnometry, and clinical assessment (AUROC 0.97; 95% CI 0.90-0.99) was superior to NT-proBNP and clinical assessment (AUROC 0.94) for diagnosing HF-related dyspnea (P=0.006).
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