Plasma Microbial Cell-Free DNA Sequencing in Immunocompromised Patients With Pneumonia: A Prospective Observational Study

被引:32
作者
Bergin, Stephen P. [1 ,2 ,20 ]
Chemaly, Roy F. [3 ]
Dadwal, Sanjeet S. [4 ]
Hill, Joshua A. [5 ,6 ]
Lee, Yeon Joo [7 ,8 ]
Haidar, Ghady [9 ]
Luk, Alfred [10 ]
Drelick, Alexander [8 ,11 ]
Chin-Hong, Peter, V
Benamu, Esther
Khawaja, Fareed [3 ]
Nanayakkara, Deepa [4 ]
Papanicolaou, Genovefa A. [7 ,8 ]
Small, Catherine Butkus [8 ,11 ]
Fung, Monica [12 ]
Barron, Michelle A. [13 ]
Davis, Thomas [14 ]
Mcclain, Micah T. [15 ]
Maziarz, Eileen K. [15 ]
Madut, Deng B. [15 ]
Bedoya, Armando D. [1 ]
Gilstrap, Daniel L. [1 ]
Todd, Jamie L. [1 ,2 ]
Barkauskas, Christina E. [1 ]
Bigelow, Robert [2 ]
Leimberger, Jeffrey D. [2 ]
Tsalik, Ephraim L. [15 ,16 ,17 ]
Wolf, Olivia [2 ]
Mughar, Mona
Hollemon, Desiree
Duttagupta, Radha
Lupu, Daniel S. [18 ]
Bercovici, Sivan [18 ]
Perkins, Bradley A. [18 ]
Blauwkamp, Timothy A. [18 ]
Fowler, Vance G. [2 ,15 ]
Holland, Thomas L. [2 ,15 ,19 ]
机构
[1] Duke Univ, Sch Med, Div Pulm Allergy & Crit Care Med, Dept Med, Durham, NC USA
[2] Duke Clin Res Inst, Durham, NC USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Infect Dis Infect Control & Employee Hlth, Houston, TX USA
[4] City Hope Natl Med Ctr, Dept Med, Div Infect Dis, Duarte, CA USA
[5] Fred Hutchinson Canc Ctr, Vaccine & Infect Dis Div, Seattle, WA USA
[6] Univ Washington Sch Med, Dept Med, Seattle, WA USA
[7] Mem Sloan Kettering Canc Ctr, Infect Dis Serv, New York, NY USA
[8] Weill Cornell Med, Dept Med, New York, NY USA
[9] Univ Pittsburgh, Med Ctr, Dept Med, Div Infect Dis, Pittsburgh, PA USA
[10] Tulane Univ Sch Med, John W Deming Dept Med, Sect Infect Dis, New Orleans, LA USA
[11] New York Presbyterian Hosp, Dept Med, New York, NY USA
[12] Univ Calif San Francisco, Div Infect Dis, San Francisco, CA USA
[13] Univ Colorado, Div Infect Dis, Aurora, CO USA
[14] Indiana Univ Sch Med, Dept Pathol & Lab Med, Indianapolis, IN USA
[15] Duke Univ Sch Med, Dept Med, Div Infect Dis, Durham, NC USA
[16] Emergency Med Serv, Durham Vet Affairs Hlth Care Syst, Durham, NC USA
[17] Infect Dis Danaher Diagnost, Washington, DC USA
[18] Karius Inc, Redwood City, CA USA
[19] Duke Univ, Med Ctr, Dept Med, Div Infect Dis, DUMC 102359, Durham, NC 27710 USA
[20] Duke Univ, Med Ctr, Div Pulm Allergy & Crit Care Med, Dept Med, DUMC 2629, Durham, NC 27710 USA
关键词
immunocompromised pneumonia; bronchoscopy; hematologic malignancy; hematopoietic cell transplant; microbial cell-free DNA sequencing; FUNGAL-INFECTIONS; PULMONARY;
D O I
10.1093/cid/ciad599
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Pneumonia is a common cause of morbidity and mortality, yet a causative pathogen is identified in a minority of cases. Plasma microbial cell-free DNA sequencing may improve diagnostic yield in immunocompromised patients with pneumonia.Methods. In this prospective, multicenter, observational study of immunocompromised adults undergoing bronchoscopy to establish a pneumonia etiology, plasma microbial cell-free DNA sequencing was compared to standardized usual care testing. Pneumonia etiology was adjudicated by a blinded independent committee. The primary outcome, additive diagnostic value, was assessed in the Per Protocol population (patients with complete testing results and no major protocol deviations) and defined as the percent of patients with an etiology of pneumonia exclusively identified by plasma microbial cell-free DNA sequencing. Clinical additive diagnostic value was assessed in the Per Protocol subgroup with negative usual care testing.Results. Of 257 patients, 173 met Per Protocol criteria. A pneumonia etiology was identified by usual care in 52/173 (30.1%), plasma microbial cell-free DNA sequencing in 49/173 (28.3%) and the combination of both in 73/173 (42.2%) patients. Plasma microbial cell-free DNA sequencing exclusively identified an etiology of pneumonia in 21/173 patients (additive diagnostic value 12.1%, 95% confidence interval [CI], 7.7% to 18.0%, P < .001). In the Per Protocol subgroup with negative usual care testing, plasma microbial cell-free DNA sequencing identified a pneumonia etiology in 21/121 patients (clinical additive diagnostic value 17.4%, 95% CI, 11.1% to 25.3%).Conclusions. Non-invasive plasma microbial cell-free DNA sequencing significantly increased diagnostic yield in immunocompromised patients with pneumonia undergoing bronchoscopy and extensive microbiologic and molecular testing.
引用
收藏
页码:775 / 784
页数:10
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