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Molecular detection of Coxiella burnetii in heart valve tissue from patients with culture-negative infective endocarditisopen access

Authors
Jang, Young-RockSong, Joon SeonJin, Choong EunRyu, Byung-HanPark, Se YoonLee, Sang-OhChoi, Sang-HoKim, Yang SooWoo, Jun HeeSong, Jae-KwanShin, YongKim, Sung-Han
Issue Date
Aug-2018
Publisher
Lippincott Williams & Wilkins Ltd.
Keywords
diagnosis; endocarditis; polymerase chain reaction; Q fever
Citation
Medicine, v.97, no.34
Journal Title
Medicine
Volume
97
Number
34
URI
https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/5767
DOI
10.1097/MD.0000000000011881
ISSN
0025-7974
1536-5964
Abstract
Coxiella burnetii is a common cause of blood culture-negative infective endocarditis (IE). Molecular detection of C burnetii DNA in clinical specimens is a promising method of diagnosing Q fever endocarditis. Here, we examined the diagnostic utility of Q fever polymerase chain reaction (PCR) of formalin-fixed heart valve tissue from patients with blood culture-negative IE who underwent heart valve surgery. Clinical and laboratory data of patients with blood culture-negative IE who underwent heart valve surgery during a 6-year period and for whom biopsy tissues were available were reviewed retrospectively. Blood culture-positive IE patients who underwent heart valve surgery within the last 3 years were used as controls. Heart valve samples were cultured and also subjected to histological examination and PCR for Q fever, brucellosis, and bartonellosis. Data from 20 patients with blood culture-negative IE and 20 with blood culture-positive IE were analyzed. Eight cases of blood culture-negative IE were PCR-positive for C burnetii (40%; 95% confidence interval, 19-64). No specimen was PCR-positive for brucellosis or bartonellosis. Histologically, 4 of 8 specimens with a positive Q fever PCR result were characterized by clusters of multinucleated giant cells without a fibrin ring. None of 20 patients with blood culture-negative IE received anti-Coxiella antibiotic therapy due to lack of clinical suspicion. Six-month mortality was higher in the Q fever PCR-positive group than in the Q fever PCR-negative group [38% (3/8) vs 0% (0/12), P = .049). Of the 20 patients with blood culture-positive IE, none yielded a positive Q fever PCR result for valve tissue. Approximately 40% of patients with culture-negative IE who received heart valve surgery were PCR-positive for Q fever; patients without clinical suspicion suffered high mortality. These data suggest that Q fever IE in patients with culture-negative IE is often missed in routine clinical practice.
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