Mrinal Sircar1, Prashant Ranjan2, Rajesh Gupta3, Onkar Kumar Jha4, Amit Gupta5, Ravneet Kaur6, Neela Chavhan7, Mukta Singh8, Sujeet Kumar Singh9. 1. Department of Pulmonology and Critical Care Medicine, Fortis Hospital, Noida, Uttar Pradesh, India. Electronic address: mrinal.sircar@fortishealthcare.com. 2. Department of Pulmonology and Critical Care Medicine, Fortis Hospital, Noida, Uttar Pradesh, India. Electronic address: docranjan@gmail.com. 3. Department of Pulmonology and Critical Care Medicine, Fortis Hospital, Noida, Uttar Pradesh, India. Electronic address: drrajeshgupta2387@gmail.com. 4. Department of Pulmonology and Critical Care Medicine, Fortis Hospital, Noida, Uttar Pradesh, India. 5. Department of Pulmonology and Critical Care Medicine, Fortis Hospital, Noida, Uttar Pradesh, India. Electronic address: amitguptaicu@gmail.com. 6. SRL Diagnostics, Fortis Hospital, Noida, India. Electronic address: ravneetkaur168@gmail.com. 7. Department of Pulmonology and Critical Care Medicine, Fortis Hospital, Noida, Uttar Pradesh, India. Electronic address: dr_neela_c@yahoo.com. 8. Department of Pulmonology and Critical Care Medicine, Fortis Hospital, Noida, Uttar Pradesh, India. Electronic address: dr_mukta@rediffmail.com. 9. Department of Pulmonology and Critical Care Medicine, Fortis Hospital, Noida, Uttar Pradesh, India. Electronic address: sujeetsinghfortis@gmail.com.
Abstract
PURPOSE: The purpose of the study is to evaluate the impact of adding bronchoalveolar lavage multiplex polymerase chain reaction (M-PCR) to conventional cultures (CC) on microbiological yield and therapeutic decisions in adult intensive care unit patients with pneumonia and severe sepsis or septic shock. MATERIAL AND METHODS: In this retrospective case-control study, bronchoalveolar lavage cultures were taken for control (58 patients, 58 admissions) and study arms (57 patients, 58 admissions). Bronchoalveolar lavage M-PCR was sent simultaneously for the latter. RESULTS: A total of 267 microorganisms were identified (M-PCR alone, 211; CC alone, 15; both, 41) in the study arm vs 64 in controls. Concordance between M-PCR and culture was complete in 32 (55.17%), partial in 4 (6.9%), and discordant in 22 (37.93%) including 17 with positive M-PCR but negative CC. Time to antibiotic therapy modification was significantly less (P < .001) in M-PCR group compared to controls (32.40 ± 14.41 vs 41.74 ± 45.61 hours). There was no significant difference in index episode resolution (48.3% vs 50%; P = 1), intensive care unit mortality (57.4% vs 51.2%; P = .67), and hospital mortality (59.6% vs 61.5%; P = 1) in study and control arms, respectively, despite more septic shock patients in the study arm (89.7% vs 75.9%; P = .05). CONCLUSION: Bronchoalveolar lavage M-PCR with culture leads to higher microbiological yield and earlier modification of antibiotics compared to conventional culture.
PURPOSE: The purpose of the study is to evaluate the impact of adding bronchoalveolar lavage multiplex polymerase chain reaction (M-PCR) to conventional cultures (CC) on microbiological yield and therapeutic decisions in adult intensive care unit patients with pneumonia and severe sepsis or septic shock. MATERIAL AND METHODS: In this retrospective case-control study, bronchoalveolar lavage cultures were taken for control (58 patients, 58 admissions) and study arms (57 patients, 58 admissions). Bronchoalveolar lavage M-PCR was sent simultaneously for the latter. RESULTS: A total of 267 microorganisms were identified (M-PCR alone, 211; CC alone, 15; both, 41) in the study arm vs 64 in controls. Concordance between M-PCR and culture was complete in 32 (55.17%), partial in 4 (6.9%), and discordant in 22 (37.93%) including 17 with positive M-PCR but negative CC. Time to antibiotic therapy modification was significantly less (P < .001) in M-PCR group compared to controls (32.40 ± 14.41 vs 41.74 ± 45.61 hours). There was no significant difference in index episode resolution (48.3% vs 50%; P = 1), intensive care unit mortality (57.4% vs 51.2%; P = .67), and hospital mortality (59.6% vs 61.5%; P = 1) in study and control arms, respectively, despite more septic shockpatients in the study arm (89.7% vs 75.9%; P = .05). CONCLUSION: Bronchoalveolar lavage M-PCR with culture leads to higher microbiological yield and earlier modification of antibiotics compared to conventional culture.
Authors: Naomi J Gadsby; Martin P McHugh; Callum Forbes; Laura MacKenzie; Stephen K D Hamilton; David M Griffith; Kate E Templeton Journal: Eur J Clin Microbiol Infect Dis Date: 2019-03-11 Impact factor: 3.267
Authors: Kenneth H Rand; Stacy G Beal; Kartikeya Cherabuddi; Brianne Couturier; Beth Lingenfelter; Cory Rindlisbacher; Jay Jones; Herbert J Houck; Kylie J Lessard; Elizabeth E Tremblay Journal: Open Forum Infect Dis Date: 2020-11-29 Impact factor: 3.835
Authors: Scott E Evans; Ann L Jennerich; Marwan M Azar; Bin Cao; Kristina Crothers; Robert P Dickson; Susanne Herold; Seema Jain; Ann Madhavan; Mark L Metersky; Laura C Myers; Eyal Oren; Marcos I Restrepo; Makeda Semret; Ajay Sheshadri; Richard G Wunderink; Charles S Dela Cruz Journal: Am J Respir Crit Care Med Date: 2021-05-01 Impact factor: 30.528