Matrix‐assisted laser desorption/ionization time‐of‐flight mass spectrometry ( MALDI ‐ TOF ) directly from positive blood culture flasks allows rapid identification of bloodstream infections in immunosuppressed hosts

In immunosuppressed hosts, rapid identification of microorganisms of bloodstream infections is crucial to ensuring effective antimicrobial therapy. Conventional culture requires up to 72 h from sample collection to pathogen identification. Methods We used the SepsiTyper Kit and matrix‐assisted laser desorption/ionization time‐of‐flight mass spectrometry ( MALDI ‐ TOF ; Microflex, Bruker) directly from positive blood culture (BacT/ ALERT 3D, FN / FA vials; bioMérieux) in comparison to standard culture methodology ( VITEK 2; bioMérieux) for species identification. Results A total of 62 consecutive positive blood cultures from immunosuppressed patients (solid organ or hematopoietic transplant recipients, or with febrile neutropenia) were analyzed. Culture yielded gram‐negative bacteria ( GNB ) in 27/62 (43.5%) and gram‐positive ( GPB ) in 35/62 (56.5%) vials. For GNB , the predominant species identified by MALDI ‐ TOF and confirmed by VITEK were E scherichia coli (16/16 correctly identified) and E nterobacter cloacae (4/4), with a sensitivity and specificity of 92.6% and 100%, respectively. For GPB , predominant species were S taphylococcus aureus (3/3), coagulase‐negative staphylococci (12/24), and E nterococcus faecium (6/6) with a sensitivity of 100%, 60%, and 100%, respectively. The median time from blood collection to species identification was 27.4 h with MALDI ‐ TOF identification and 46.6 h with conventional methodology. Conclusion Using MALDI ‐ TOF directly from positive blood cultures allowed a shorter time to identification with high sensitivity and specificity in immunosuppressed patients.