Abstract

BackgroundThe clinical usefulness of follow-up blood cultures (FUBCs) in gram-negative bloodstream infections (GN-BSIs) represents a debated issue. ObjectiveTo assess the impact on the clinical outcome of FUBCs in patients with GN-BSI and to predict risk factors for persistent bacteraemia. Data sourcesPubMed-MEDLINE, Scopus, and the Cochrane Library Database were independently searched until 24 June, 2022. Study eligibility criteriaRandomized controlled trials, prospective, or retrospective observational studies, including patients affected by GN-BSIs. Primary endpoints were in-hospital mortality rate, and persistent blood stream infections were defined as FUBC-positive for the same pathogen isolated from index blood cultures (BCs). ParticipantsHospitalized patients with documented GN-BSIs. InterventionPerformance of FUBCs (defined as subsequent BCs collected at least 24 hours after index BCs). Assessment of risk of biasQuality of included studies was independently assessed according to the Cochrane Risk of Bias Tool and the Risk Of Bias In Non-randomized Studies of Interventions. Methods of data synthesisMeta-analysis was performed by pooling odds ratio (OR) retrieved from studies providing adjustment for confounders using random-effect model with the inverse variance method. Risk factors for persistent blood stream infections were also assessed. ResultsA total of 3747 articles were screened, and 11 observational studies (6 assessing impact on outcome (N = 4631), and 5 investigating risk factors for persistent GN-BSI (N = 2566)), conducted between 2002 and 2020 were included. The execution of FUBCs was associated with a significantly lower risk of mortality (OR, 0.58; 95% CI, 0.49–0.70; I2 = 0.0%). The presence of end-stage renal disease (OR, 2.99; 95% CI, 1.77–5.05), central venous catheter (OR, 3.30; 95% CI, 1.82–5.95), infections due to extended-spectrum β-lactamase-producing strains (OR, 2.25; 95% CI, 1.18–4.28), resistance to empirical treatment (OR, 2.70; 95% CI, 1.65–4.41), and unfavourable response at 48 hours (OR, 2.99; 95% CI, 1.44–6.24) emerged as independent risk factors for persistent bacteraemia. ConclusionsThe execution of FUBCs is associated with a significantly low risk of mortality in patients with GN-BSIs. Our analysis could be useful to stratify patients at a high risk of persistent bacteraemia to optimize the use of FUBCs.

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