PMID- 12422152 OWN - NLM STAT- MEDLINE DCOM- 20021230 LR - 20190626 IS - 1097-6744 (Electronic) IS - 0002-8703 (Linking) VI - 144 IP - 5 DP - 2002 Nov TI - A rapid B-type natriuretic peptide assay accurately diagnoses left ventricular dysfunction and heart failure: a multicenter evaluation. PG - 834-9 AB - BACKGROUND: B-Type natriuretic peptide (BNP), a protein released from the left ventricle in response to volume expansion and pressure overload, has emerged as the first whole blood marker for the identification of individuals with congestive heart failure (CHF). OBJECTIVE: The purpose of this study was to assess the performance of a point-of-care assay to diagnose and evaluate the severity of CHF on the basis of the New York Heart Association (NYHA) classification system. METHODS: Through a prospective, multicenter trial, whole blood samples were collected from a total of 1050 inpatients, outpatients, and healthy control patients. Participants were divided into subgroups for BNP analysis: patients without cardiovascular CHF (n = 473), patients with hypertension and no cardiovascular disease (n = 168), NYHA class I CHF (n = 73), class II CHF (n = 135), class III CHF (n = 141), and class IV CHF (n = 60). RESULTS: Circulating BNP concentrations determined from the bedside assay increased with CHF severity, as determined by the NYHA classification system, but were only statistically significant (P <.001) between individuals with and without CHF. Individuals without CHF had a median BNP concentration of 9.29 pg/mL. Median BNP values, with their corresponding interquartile ranges, for NYHA classification I through IV were 83.1 pg/mL (49.4-137 pg/mL), 235 pg/mL (137-391 pg/mL), 459 pg/mL (200-871 pg/mL), and 1119 pg/mL (728->1300 pg/mL), respectively. With the use of a decision threshold of 100 pg/mL, the assay demonstrated 82% sensitivity and 99% specificity for distinguishing control patients and patients with CHF. CONCLUSIONS: BNP concentrations obtained from whole blood samples are useful in the diagnosis of CHF and staging the severity of the disease. FAU - Wieczorek, Stacey J AU - Wieczorek SJ AD - Department of Pathology and Laboratory Medicine, Hartford Hospital, Hartford, Conn, USA. FAU - Wu, Alan H B AU - Wu AH FAU - Christenson, Robert AU - Christenson R FAU - Krishnaswamy, Padma AU - Krishnaswamy P FAU - Gottlieb, Stephen AU - Gottlieb S FAU - Rosano, Thomas AU - Rosano T FAU - Hager, David AU - Hager D FAU - Gardetto, Nancy AU - Gardetto N FAU - Chiu, Albert AU - Chiu A FAU - Bailly, Kathryn R AU - Bailly KR FAU - Maisel, Alan AU - Maisel A LA - eng PT - Clinical Trial PT - Controlled Clinical Trial PT - Journal Article PT - Multicenter Study PT - Research Support, Non-U.S. Gov't PL - United States TA - Am Heart J JT - American heart journal JID - 0370465 RN - 0 (Biomarkers) RN - 114471-18-0 (Natriuretic Peptide, Brain) RN - 85637-73-6 (Atrial Natriuretic Factor) SB - IM MH - Adult MH - Aged MH - Atrial Natriuretic Factor/*blood MH - Biomarkers/blood MH - Female MH - Heart Failure/blood/*diagnosis MH - Humans MH - Male MH - Middle Aged MH - Natriuretic Peptide, Brain MH - *Point-of-Care Systems MH - Prospective Studies MH - ROC Curve MH - Sensitivity and Specificity MH - Severity of Illness Index MH - Ventricular Dysfunction, Left/blood/*diagnosis EDAT- 2002/11/08 04:00 MHDA- 2002/12/31 04:00 CRDT- 2002/11/08 04:00 PHST- 2002/11/08 04:00 [pubmed] PHST- 2002/12/31 04:00 [medline] PHST- 2002/11/08 04:00 [entrez] AID - S0002870302001941 [pii] AID - 10.1067/mhj.2002.125623 [doi] PST - ppublish SO - Am Heart J. 2002 Nov;144(5):834-9. doi: 10.1067/mhj.2002.125623.