Balion C, Santaguida P L, Hill S, Worster A, McQueen M, Oremus M, McKelvie R, Booker L, Fagbemi J, Reichert S, Raina P
Evid Rep Technol Assess (Full Rep). 2006 Sep(142):1-147.
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.
MEDLINE, EMBASE, CINAHL, Cochrane Central, and AMED from 1989 to February 2005 were searched for primary studies.
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.
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.
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.
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.
Determinants: The importance of the identified determinants for clinical use is not clear.
In all settings both BNP and NT-proBNP show good diagnostic properties as a rule out test for HF.
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.
本系统评价旨在评估B型利钠肽(BNP)和N末端B型利钠肽原(NT-proBNP),以:(a)确定决定因素;(b)确定它们在心力衰竭(HF)患者中的诊断性能;(c)确定它们对死亡率和其他心脏终点的预测能力;(d)确定它们在监测HF治疗中的价值。
检索1989年至2005年2月期间的MEDLINE、EMBASE、护理学与健康领域数据库(CINAHL)、Cochrane中心对照试验注册库及澳大利亚和新西兰医学文摘数据库(AMED),查找相关的原始研究。
采用包括荟萃分析在内的标准系统评价方法。纳入所有研究设计。纳入标准包括仅英文研究,并限制检测方法数量以提高可推广性。预后结局限于死亡率和特定心脏事件。针对每个研究问题制定了进一步的具体标准。
决定因素:共确定了103个决定因素,包括年龄、性别、疾病、治疗以及生化和生理指标。很少有研究报告独立关联,其中年龄、女性性别和肌酐水平与BNP和NT-proBNP呈正相关。
BNP的合并敏感性和特异性值分别为94%和66%,NT-proBNP为92%和65%;不同场景(急诊科、专科诊所和初级保健)之间差异极小。B型利钠肽在传统HF检测指标之外还增加了独立的诊断信息。
在有冠状动脉疾病(CAD)风险的患者(风险估计范围=1.10至5.40)、已诊断CAD的患者(风险估计范围=1.50至3.00)和已诊断HF的患者(风险估计范围=2.11至9.35)中,BNP和NT-proBNP均被发现是死亡率和其他心脏复合终点的独立预测因子。关于筛查,曲线下面积(AUC)值(范围=0.57至0.88)表明性能不佳。监测治疗:研究表明治疗可降低BNP和NT-proBNP,但与结局的关系有限且不一致。
决定因素:已确定的决定因素在临床应用中的重要性尚不清楚。
在所有场景中,BNP和NT-proBNP作为HF的排除试验均显示出良好的诊断特性。
BNP和NT-proBNP是有CAD风险人群、已诊断CAD人群和已诊断HF人群死亡率和其他心脏复合终点的一致独立预测因子。尚无足够证据确定B型利钠肽在HF筛查中的价值。监测治疗:尚无足够证据表明BNP和NT-proBNP水平会因治疗稳定慢性HF患者而发生变化。