Greub Gilbert, Lepidi Hubert, Rovery Clarisse, Casalta Jean-Paul, Habib Gilbert, Collard Frédéric, Fournier Pierre-Edouard, Raoult Didier
Unité des Rickettsies, Faculté de Médecine, Université de la Méditerranée, Marseille, France.
Am J Med. 2005 Mar;118(3):230-8. doi: 10.1016/j.amjmed.2004.12.014.
Histologic examination of valve samples is considered as the gold standard for the diagnosis of infectious endocarditis. Molecular tools are also very promising for patients with negative-culture endocarditis. Thus, we studied the contribution of valvular histology, culture, and 16S rRNA PCR amplification plus sequencing to the diagnosis of infectious endocarditis in patients undergoing valve surgery.
We performed culture, histological examination, and broad-range PCR amplification plus sequencing on valve samples taken from 127 patients with infectious endocarditis and from 118 patients without endocarditis. The sensitivity and specificity of these tests for the diagnosis of endocarditis in patients undergoing valve surgery were studied.
The sensitivity of PCR was of 61% (64/105) whereas that of histological examination was of 63% (62/98) and that of valve culture was of only 13% (14/105). All 68 positive PCR results considered reliable according to an interpretation scheme were from patients with infectious endocarditis, resulting in a 100% (118/118) specificity of the interpreted molecular approach. The specificity of histology was also of 100% (118/118) when using stringent criteria (ie, presence of vegetation, microorganisms, and/or valvular inflammation with mainly polymorphonuclear cells). PCR identified an etiological agent in 38% (5/13) of definite blood culture-negative infectious endocarditis.
We show that valvular histology with stringent criteria is the gold standard for the diagnosis of infectious endocarditis. Broad-range amplification of 16S rRNA gene is indicated for infectious endocarditis of unknown etiology, whereas valve culture is of limited sensitivity.
瓣膜样本的组织学检查被认为是感染性心内膜炎诊断的金标准。分子工具对于培养结果阴性的心内膜炎患者也很有前景。因此,我们研究了瓣膜组织学、培养以及16S rRNA聚合酶链反应(PCR)扩增加测序在瓣膜手术患者感染性心内膜炎诊断中的作用。
我们对取自127例感染性心内膜炎患者和118例无心内膜炎患者的瓣膜样本进行了培养、组织学检查以及广谱PCR扩增加测序。研究了这些检测方法在瓣膜手术患者心内膜炎诊断中的敏感性和特异性。
PCR的敏感性为61%(64/105),而组织学检查的敏感性为63%(62/98),瓣膜培养的敏感性仅为13%(14/105)。根据一种解读方案,所有68个被认为可靠的阳性PCR结果均来自感染性心内膜炎患者,由此得出所解读分子方法的特异性为100%(118/118)。当使用严格标准(即存在赘生物、微生物和/或主要为多形核细胞的瓣膜炎症)时,组织学检查的特异性也为100%(118/118)。PCR在38%(5/13)的明确血培养阴性的感染性心内膜炎中鉴定出了病原体。
我们表明,采用严格标准的瓣膜组织学检查是感染性心内膜炎诊断的金标准。16S rRNA基因的广谱扩增适用于病因不明的感染性心内膜炎,而瓣膜培养的敏感性有限。