Spinal Manipulation and Biopsychosocial Self-Management for Back Pain
Summary
Fast Antimicrobial Susceptibility Testing for Gram-Negative Bacteremia: The FAST Randomized Clinical Trial. Banerjee R(1), Komarow L(2), Li Y(2), Mau D(3), Dodd A(3), Geres H(3), Greenwood-Quaintance K(4), Adler A(5), Baliga S(6), Chowers M(7)(8), Chrysos G(9), Zarkotou O(9), Paul M(10), Pournaras S(11), Regueiro DS(12), Evans S(2), Chambers H(13), Fowler VG Jr(3), Patel R(4); Antibacterial Resistance Leadership Group. Collaborators: Chambers HF, Evans SR, Fowler VG Jr, Hamasaki T, Patel R, Cros
Content
# Spinal Manipulation and Biopsychosocial Self-Management for Back Pain
*Published: 2026 May 26*
Fast Antimicrobial Susceptibility Testing for Gram-Negative Bacteremia: The FAST Randomized Clinical Trial. Banerjee R(1), Komarow L(2), Li Y(2), Mau D(3), Dodd A(3), Geres H(3), Greenwood-Quaintance K(4), Adler A(5), Baliga S(6), Chowers M(7)(8), Chrysos G(9), Zarkotou O(9), Paul M(10), Pournaras S(11), Regueiro DS(12), Evans S(2), Chambers H(13), Fowler VG Jr(3), Patel R(4); Antibacterial Resistance Leadership Group. Collaborators: Chambers HF, Evans SR, Fowler VG Jr, Hamasaki T, Patel R, Cross H, Harris AD, Pettigrew MM, van Duin D, Boucher HW, Huntley C, Raterman E, Samuel T, Moon K, Hanson KE, Doi Y, Holland TL, Lodise T, Shelburne SA, Banerjee R, Cosgrove SE, Paterson DL, Lautenbach E, Mehigan M, Doernberg SB, Perdue S, Singh TA, Wickward CA, Souto DA, Waller JE. Author information: (1)Department of Pediatrics, Vanderbilt University Medical Center, Nashville, Tennessee. (2)The Biostatistics Center and Department of Biostatistics and Bioinformatics, Milken Institute School of Public Health, The George Washington University, Bethesda, Maryland. (3)Duke Clinical Research Institute, Duke University Medical Center, Durham, North Carolina. (4)Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota. (5)Tel Aviv Sourasky Medical Center, Tel Aviv, Israel. (6)Department of Microbiology, Kasturba Medical College, Mangalore, Manipal Academy of Higher Education, Manipal, India. (7)Meir Medical Center, Kfar Saba, Israel. (8)Gray Faculty of Medical and Health Sciences, Tel Aviv University, Tel Aviv, Israel. (9)Tzaneio General Hospital, Piraeus, Greece. (10)Rambam Health Care Campus, Haifa, Israel. (11)Attikon General University Hospital, Athens, Greece. (12)University Hospital Complex of La Coruna, A Coruña, Spain. (13)University of California, San Francisco. Comment in JAMA. 2026 May 26;335(20):1760-1761. doi: 10.1001/jama.2026.5504.
## IMPORTANCE
Novel blood culture diagnostics provide rapid antimicrobial susceptibility testing (AST) results for bacteria causing bloodstream infections (BSIs) but have unclear clinical impact.
## OBJECTIVE
To evaluate clinical outcomes of blood culture testing using a rapid AST method compared with standard AST in patients with BSIs caused by gram-negative bacilli in regions with high prevalence of antimicrobial resistance. DESIGN, SETTING, AND PARTICIPANTS
Open-label randomized clinical trial that enrolled participants from December 2023 to May 2025 (final follow-up, June 18, 2025) at 7 medical centers in Greece (n = 2), India (n = 1), Israel (n = 3), and Spain (n = 1). Hospitalized patients (adults and children) with BSIs caused by gram-negative bacilli were eligible. Statistical analysis was conducted from August 2025 to January 2026. INTERVENTION: Patients were randomized to undergo blood culture evaluation using rapid, phenotypic AST directly from positive blood cultures plus standard susceptibility testing (n = 413) vs standard susceptibility testing alone (n = 437). Local antimicrobial stewardship teams reviewed all patients and provided treatment recommendations. MAIN OUTCOMES AND MEASURES
The primary outcome was a desirability of outcome ranking (DOOR) at day 30, with 3 categories (alive without deleterious events, alive with deleterious events, and death). The difference between rapid and standard testing was summarized as the probability that the DOOR outcomes were more desirable in the rapid testing group. Superiority was concluded if the lower limit of the 95% CI exceeded 50%. Secondary outcomes included 30-day mortality, length of hospitalization, intensive care unit admission, acquisition of hospital-acquired infections, time to effective antibiotic therapy within 3 days, and time to antibiotic escalation or deescalation within 3 days.
## RESULTS
Of the 899 patients randomized, 850 were included in the primary outcome analysis (median [IQR] age, 72 [21] years; 43% female). The probability that DOOR outcomes were more favorable in the rapid testing group was 48.8% (95% CI, 45.3%-52.4%). Median time to effective antibiotic therapy was not different between the groups in the as-randomized population. Median time to antibiotic escalation or deescalation was faster in the rapid testing group by 14 hours (95% CI, 6-22) in the as-randomized population. There were no differences between the groups in other secondary outcomes. In the prespecified subgroup with carbapenem-resistant infections, median time to effective therapy was 9.5 hours in the rapid testing group vs 28 hours in the standard testing group (difference, -18 hours [95% CI, -42 to 6]). CONCLUSIONS AND RELEVANCE
Among patients with gram-negative bacilli BSIs, rapid blood culture AST was not superior to standard testing by DOOR. When considered with other efficacy and safety outcomes, these findings may help inform the use of rapid susceptibility testing in clinical practice.
## TRIAL REGISTRATION
ClinicalTrials.gov Identifier: NCT06174649. DOI: 10.1001/jama.2026.5487 PMCID: PMC13092117
DOI: 10.1001/jama.2026.2707