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EBJIS-2024 Poster-Karolinska-final

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IMPROVED METHOD FOR BIOPSY INTRODUCTION Microbial infections in prosthetic joint infections(PJIs) present HOMOGENISATION AND RAPID significant diagnostic challenges. This study explores two homogenization techniques combined with isothermal microcalorimetry (IMC), for detecting microbial infections. DETECTION OF INFECTIONS »› OBJECTIVE • To evaluate the impact of homogenisation technique on recovery rate and detection speed depending on homogenisation techniques combined with an IMC readout. JOSEFIN LARSSON1,2, KARIN LIDEROT3, MARTA VESES GARCIA1, • To assess the potential of these methods in a clinical CHAITANYA TELLAPRAGADA2, WILHELM PAULANDER1, CHRISTIAN GISKE2 workflow, compared to standa

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otential of these methods in a clinical CHAITANYA TELLAPRAGADA2, WILHELM PAULANDER1, CHRISTIAN GISKE2 workflow, compared to standard hospital techniques. 1 Symcel AB, Stockholm, Sweden 2 Karolinska Institute, Sweden 3 Karolinska University Hospital METHODS 1 2 IN VIVO EXPERIMENT IN VITRO EXPERIMENT Standard Bead-based microbiology homogenisation methods volume 100-500ul rapid infection detection and estimation of bacterial load Bead-based/stone-milling IMC and plating homogenisation Alternative Method RESULTS COMPARING THE IMPACT ON DETECTION TIME AND MICROBIAL APPLYING OUR WORKFLOW (HOMOGENISATION + IMC READOUT) RECOVERY OF HOMOGENISATION TECHNIQUE DIRECTLY ON LIQUID

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ROBIAL APPLYING OUR WORKFLOW (HOMOGENISATION + IMC READOUT) RECOVERY OF HOMOGENISATION TECHNIQUE DIRECTLY ON LIQUID TO CLINICAL SAMPLES COMPARED TO STANDARD WORKFLOW S. aureus CULTURES 50% faster detection of S. aureus (<2 h) after 5 times higher microbial recovery using alternative 48 patient samples from 22 PJI patients. Two homogenisation homogenisation Rapid withof detection alternative S.aureus homogenisation homogenisation methods (2 min interval) than the standard methods with IMC based readout and hospital standard method method with IMC infection compared directly on to standard method. homogenate homogenisation method. were compared. Metabolic 150 Recovery (%) alternative homogeniser activity alternative homogeniser standard homogeniser (uW) (hospital) Heat flow (µW) 100 hospital homogeniser Majority of sample goes for hospital 50 workflow leaving less biopsy Time to material for the tested workflow. Detection Creating a bias, possibly leading to

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Creating a bias, possibly leading to false negatives.* 0 Time (h) 4 6 8 10 Homogenisation interval Time (h) RECOVERY OF OXYGEN SENSITIVE C. acnes FROM SPIKED PIG In two polymicrobial samples the standard TISSUE AFTER HOMOGENISATION homogenisation + IMC missed detection of S. aureus or E. cloacae complex, respectively. Two to 2.5 x higher In three polymicrobial recovery of C. acnes (6.15 to samples E. faecalis 7.6*104 cells) depending on and C. acnes were not homogenisation interval with detected in standard alternative method compared

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detected in standard alternative method compared workflow. standard method in the clinics (2.75 – 3.3*104 cells). WHAT´S % of 105 C. acnes cells that were used to spike NEXT? *Four samples (not shown) of the homegenisation+IMC procedure were false negative the tissue. compared to hospital procedure which can be explained using less biopsy material. In an ongoing study we expand the study group to 120 PJI patients allowing to

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patients allowing to determine infection detection speed with CONCLUSION SIGNIFICANCE the use of IMC. The alternative homogenisation method (SpinAX/ProbeAX Evolution, A semiautomated workflow combining an improved Axonlab AG, Germany) shows to be less harsh on bacteria homogenisation technique, for higher recovery rates and speed in compared to standard homogenisation method (Bullet Blender combination with a sensitive IMC-based readout, are promising as a 50DX. Next Advance, USA), allowing for faster and higher recovery, less invasive and more efficient alternative to the current ultimately increasing accuracy and speed. clinical standard. Using IMC for semi-automated readout, provides microbial detection within hours as compared to days with standard microbiology methods. CONTACT With funding from: Increased detection of sensitive C. acnes with the alternative homogenization method is promising. Confirmation of these findings in a larger study group is necessary wilhelm.paulander@symcel.com

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wilhelm.paulander@symcel.com