دورية أكاديمية

Microbiological challenges in the diagnosis of chronic Q fever.

التفاصيل البيبلوغرافية
العنوان: Microbiological challenges in the diagnosis of chronic Q fever.
المؤلفون: Kampschreur LM; Division of Medicine, Dept. of Internal Medicine and Infectious Diseases, University Medical Center Utrecht, Utrecht, the Netherlands. l.m.kampschreur@umcutrecht.nl, Oosterheert JJ, Koop AM, Wegdam-Blans MC, Delsing CE, Bleeker-Rovers CP, De Jager-Leclercq MG, Groot CA, Sprong T, Nabuurs-Franssen MH, Renders NH, van Kasteren ME, Soethoudt Y, Blank SN, Pronk MJ, Groenwold RH, Hoepelman AI, Wever PC
المصدر: Clinical and vaccine immunology : CVI [Clin Vaccine Immunol] 2012 May; Vol. 19 (5), pp. 787-90. Date of Electronic Publication: 2012 Mar 21.
نوع المنشور: Evaluation Study; Journal Article
اللغة: English
بيانات الدورية: Publisher: American Society for Microbiology Country of Publication: United States NLM ID: 101252125 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1556-679X (Electronic) Linking ISSN: 1556679X NLM ISO Abbreviation: Clin Vaccine Immunol Subsets: MEDLINE
أسماء مطبوعة: Original Publication: Washington, D.C. : American Society for Microbiology, [2006]-
مواضيع طبية MeSH: Antibodies, Bacterial/*blood , Clinical Laboratory Techniques/*methods , Coxiella burnetii/*immunology , Q Fever/*diagnosis, Adult ; Aged ; Aged, 80 and over ; Coxiella burnetii/genetics ; Coxiella burnetii/isolation & purification ; DNA, Bacterial/blood ; Female ; Humans ; Immunoglobulin G/blood ; Male ; Middle Aged ; Polymerase Chain Reaction ; Predictive Value of Tests ; Sensitivity and Specificity
مستخلص: Diagnosis of chronic Q fever is difficult. PCR and culture lack sensitivity; hence, diagnosis relies mainly on serologic tests using an immunofluorescence assay (IFA). Optimal phase I IgG cutoff titers are debated but are estimated to be between 1:800 and 1:1,600. In patients with proven, probable, or possible chronic Q fever, we studied phase I IgG antibody titers at the time of positive blood PCR, at diagnosis, and at peak levels during chronic Q fever. We evaluated 200 patients, of whom 93 (46.5%) had proven, 51 (25.5%) had probable, and 56 (28.0%) had possible chronic Q fever. Sixty-five percent of proven cases had positive Coxiella burnetii PCR results for blood, which was associated with high phase I IgG. Median phase I IgG titers at diagnosis and peak titers in patients with proven chronic Q fever were significantly higher than those for patients with probable and possible chronic Q fever. The positive predictive values for proven chronic Q fever, compared to possible chronic Q fever, at titers 1:1,024, 1:2,048, 1:4,096, and ≥1:8,192 were 62.2%, 66.7%, 76.5%, and ≥86.2%, respectively. However, sensitivity dropped to <60% when cutoff titers of ≥1:8,192 were used. Although our study demonstrated a strong association between high phase I IgG titers and proven chronic Q fever, increasing the current diagnostic phase I IgG cutoff to >1:1,024 is not recommended due to increased false-negative findings (sensitivity < 60%) and the high morbidity and mortality of untreated chronic Q fever. Our study emphasizes that serologic results are not diagnostic on their own but should always be interpreted in combination with clinical parameters.
References: Clin Infect Dis. 2001 Aug 1;33(3):312-6. (PMID: 11438895)
Clin Infect Dis. 2011 Jun 15;52(12):1431-6. (PMID: 21628483)
Clin Infect Dis. 2007 May 15;44(10):1337-40. (PMID: 17443471)
Eur J Clin Microbiol Infect Dis. 2007 Sep;26(9):635-40. (PMID: 17629755)
Clin Infect Dis. 2011 Oct;53(7):749-50. (PMID: 21890784)
Euro Surveill. 2010 Mar 25;15(12):. (PMID: 20350500)
J Clin Microbiol. 2011 Apr;49(4):1692-4. (PMID: 21289146)
Clin Microbiol Rev. 1999 Oct;12(4):518-53. (PMID: 10515901)
Ann N Y Acad Sci. 1990;590:51-60. (PMID: 2378473)
Medicine (Baltimore). 2000 Mar;79(2):109-23. (PMID: 10771709)
J Infect. 2011 Jan;62(1):39-44. (PMID: 21034771)
Lancet Infect Dis. 2010 Aug;10(8):527-35. (PMID: 20637694)
J Clin Microbiol. 1995 Dec;33(12):3129-32. (PMID: 8586687)
Clin Diagn Lab Immunol. 1994 Mar;1(2):189-96. (PMID: 7496944)
J Clin Microbiol. 2004 Nov;42(11):4919-24. (PMID: 15528674)
Clin Vaccine Immunol. 2010 Feb;17(2):286-90. (PMID: 20032219)
J Infect. 2012 Mar;64(3):247-59. (PMID: 22226692)
Emerg Infect Dis. 2011 Mar;17(3):350-6. (PMID: 21392423)
Neth J Med. 2010 Dec;68(12):382-7. (PMID: 21209463)
Clin Infect Dis. 2011 Apr 15;52(8):1013-9. (PMID: 21460316)
Lancet Infect Dis. 2005 Apr;5(4):219-26. (PMID: 15792739)
Clin Infect Dis. 2007 Jan 15;44(2):232-7. (PMID: 17173223)
المشرفين على المادة: 0 (Antibodies, Bacterial)
0 (DNA, Bacterial)
0 (Immunoglobulin G)
تواريخ الأحداث: Date Created: 20120324 Date Completed: 20120815 Latest Revision: 20211021
رمز التحديث: 20240829
مُعرف محوري في PubMed: PMC3346333
DOI: 10.1128/CVI.05724-11
PMID: 22441385
قاعدة البيانات: MEDLINE
الوصف
تدمد:1556-679X
DOI:10.1128/CVI.05724-11