Publications by Year: 2009

2009

Kirby, James E, Meghan Delaney, Qinfang Qian, and Howard S Gold. (2009) 2009. “Optimal Use of Myco/F Lytic and Standard BACTEC Blood Culture Bottles for Detection of Yeast and Mycobacteria.”. Archives of Pathology & Laboratory Medicine 133 (1): 93-6.

CONTEXT: The optimal use of dedicated fungal and mycobacterial blood culture bottles, such as the BACTEC Myco/F Lytic bottle, has not been well defined in clinical practice.

OBJECTIVES: To compare the performance of Myco/F Lytic and standard blood culture in clinical practice in an urban tertiary care hospital setting and to implement a strategy for optimal use of Myco/F Lytic culture.

DATA SOURCES: Retrospective review of laboratory records.

RESULTS: Myco/F Lytic culture did not increase detection of yeasts. Nor did it decrease time to detection except for Candida glabrata, where mean time to positivity dropped from 2.6 +/- 1.1 days in standard to 1.8 +/- 0.8 days in Myco/F Lytic culture. Therefore, an algorithm was developed in which Myco/F Lytic culture was reserved primarily for detection of mycobacteria in patients with severely depressed CD4 counts. Implementation of this algorithm led to a sustained 3-fold reduction in Myco/F Lytic blood culture usage.

CONCLUSIONS: Retrospective analysis suggests substantial clinical equivalence of standard blood and Myco/F Lytic culture for detection of yeast. A multifaceted educational approach based on this data led to a sustained change in physician ordering practices and more cost-effective use of resources.

Wang, Yihong, James E Kirby, and Qinfang Qian. (2009) 2009. “Effective Use of JC Virus PCR for Diagnosis of Progressive Multifocal Leukoencephalopathy.”. Journal of Medical Microbiology 58 (Pt 2): 253-55. https://doi.org/10.1099/jmm.0.004432-0.

In a retrospective review of data from 168 patients with suspected progressive multifocal leukoencephalopathy (PML) between 1996 and 2006, JC virus (JCV) PCR on cerebrospinal fluid (CSF) samples was positive only in human immunodeficiency virus (HIV)-infected patients with low CD4 cell counts and in severely immunocompromised patients with radiographic lesions consistent with PML or infectious processes generally. Of note, one HIV patient with a very low CD4 cell count had a positive JCV PCR despite a normal magnetic resonance imaging exam. We concluded that JCV PCR testing on CSF specimens should therefore be targeted to these high-risk patients.

Pollock, Nira R, Scott Duong, Annie Cheng, Linda L Han, Sandra Smole, and James E Kirby. (2009) 2009. “Ruling Out Novel H1N1 Influenza Virus Infection With Direct Fluorescent Antigen Testing.”. Clinical Infectious Diseases : An Official Publication of the Infectious Diseases Society of America 49 (6): e66-8. https://doi.org/10.1086/644502.

We evaluated the ability of direct fluorescent antigen (DFA) influenza tests to identify novel H1N1 influenza virus. DFA results were compared with polymerase chain reaction results. The negative predictive value of DFA testing was at least 96%. Therefore, when performed on specimens of adequate quality, DFA tests can effectively rule out infection due to novel H1N1 virus.