Testing for BNP and NT-proBNP in the diagnosis and prognosis of heart failure.

C Balion, P L Santaguida, S Hill, A Worster, M McQueen, M Oremus, R McKelvie, L Booker, J Fagbemi, S Reichert, P Raina
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引用次数: 0

Abstract

Objectives: The purpose of this systematic review was to evaluate BNP and NT-proBNP to: (a) identify determinants, (b) establish their diagnostic performance in heart failure (HF) patients, (c) determine their predictive ability with respect to mortality and other cardiac endpoints, and (d) determine their value in monitoring HF treatment.

Data sources: MEDLINE, EMBASE, CINAHL, Cochrane Central, and AMED from 1989 to February 2005 were searched for primary studies.

Review methods: Standard systematic review methodology, including meta-analysis, was employed. All study designs were included. Eligibility criteria included English-only studies and restricted the number of test methods to maximize generalizability. Outcomes for prognosis were limited to mortality and specific cardiac events. Further specific criteria were developed for each research question.

Results: Determinants: There were 103 determinants identified including age, gender, disease, treatment, as well as biochemical and physiological measures. Few studies reported independent associations and of those that did age, female gender and creatinine levels were positively associated with BNP and NT-proBNP.

Diagnosis: Pooled sensitivity and specificity values were 94 and 66 percent for BNP and 92 and 65 percent for NT-proBNP; there was minimal difference among settings (emergency, specialized clinics, and primary care). B-type natriuretic peptides also added independent diagnostic information above traditional measures for HF.

Prognosis: Both BNP and NT-proBNP were found to be independent predictors of mortality and other cardiac composite endpoints in patients with risk of coronary artery disease (CAD) (risk estimate range = 1.10 to 5.40), diagnosed CAD (risk estimate range = 1.50 to 3.00), and diagnosed HF patients (risk estimate range = 2.11 to 9.35). With respect to screening, the AUC values (range = 0.57 to 0.88) suggested poor performance. Monitoring Treatment: Studies showed therapy reduced BNP and NT-proBNP, however, relationship to outcome was limited and not consistent.

Conclusions: Determinants: The importance of the identified determinants for clinical use is not clear.

Diagnosis: In all settings both BNP and NT-proBNP show good diagnostic properties as a rule out test for HF.

Prognosis: BNP and NT-proBNP are consistent independent predictors of mortality and other cardiac composite endpoints for populations with risk of CAD, diagnosed CAD, and diagnosed HF. There is insufficient evidence to determine the value of B-type natriuretic peptides for screening of HF. Monitoring Treatment: There is insufficient evidence to demonstrate that BNP and NT-proBNP levels show change in response to therapies to manage stable chronic HF patients.

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BNP和NT-proBNP检测在心衰诊断和预后中的价值。
目的:本系统综述的目的是评估BNP和NT-proBNP以:(a)确定决定因素,(b)确定其在心力衰竭(HF)患者中的诊断性能,(c)确定其对死亡率和其他心脏终点的预测能力,以及(d)确定其在监测HF治疗中的价值。资料来源:MEDLINE, EMBASE, CINAHL, Cochrane Central和AMED从1989年至2005年2月检索主要研究。评价方法:采用标准的系统评价方法,包括meta分析。所有的研究设计都包括在内。入选标准包括纯英语研究,并限制测试方法的数量,以最大限度地推广。预后结果仅限于死亡率和特定心脏事件。为每个研究问题制定了进一步的具体标准。结果:决定因素:确定了103个决定因素,包括年龄、性别、疾病、治疗以及生化和生理措施。很少有研究报告了BNP和NT-proBNP之间的独立关联,而年龄、女性性别和肌酐水平与BNP和NT-proBNP呈正相关。诊断:BNP的敏感性和特异性分别为94%和66%,NT-proBNP的敏感性和特异性分别为92%和65%;不同环境(急诊、专科诊所和初级保健)之间的差异很小。b型利钠肽也比传统的心衰检测方法增加了独立的诊断信息。预后:我们发现BNP和NT-proBNP是有冠心病(CAD)风险(风险估计范围= 1.10 ~ 5.40)、诊断为CAD(风险估计范围= 1.50 ~ 3.00)和诊断为HF(风险估计范围= 2.11 ~ 9.35)患者死亡率和其他心脏复合终点的独立预测因子。在筛选方面,AUC值(范围为0.57 ~ 0.88)表明表现不佳。监测治疗:研究显示治疗降低了BNP和NT-proBNP,然而,与结果的关系有限且不一致。结论:决定因素:确定的决定因素对临床应用的重要性尚不清楚。诊断:在所有情况下,BNP和NT-proBNP作为HF的排除试验显示出良好的诊断特性。预后:BNP和NT-proBNP是冠心病、诊断为冠心病和诊断为心衰人群死亡率和其他心脏复合终点的一致独立预测因子。没有足够的证据来确定b型利钠肽在筛选心衰方面的价值。监测治疗:没有足够的证据表明BNP和NT-proBNP水平对稳定型慢性心衰患者的治疗反应有变化。
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