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Development of VRE meningitis due to haematogenous spread while on high-dose daptomycin therapy
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Abstract
Introduction
Vancomycin-resistant Enterococcus faecium (VRE) meningitis accounts for only 0.3%–4.0% of bacterial meningitis cases and typically occurs following neurosurgical intervention. We describe a rare case of a patient without neurological devices in situ or a recent neurological procedure who developed VRE meningitis via haematogenous spread. Optimal treatment for VRE meningitis is unknown.
Case presentation
A 67-year-old male with end-stage liver failure underwent liver transplantation complicated by VRE bacteraemia and subsequently developed VRE meningitis while on high-dose daptomycin therapy (12 mg/kg/day). Due to clinical and microbiological failure with daptomycin, he was switched to linezolid and symptoms resolved rapidly. He completed 2 weeks of linezolid, fully recovered, and continued to do well without complications at the 5 month follow-up.
Conclusions
This case highlights the severity of VRE infections in solid organ transplant recipients and raises concerns about daptomycin penetration into the CNS. Linezolid could be considered the preferred treatment for VRE CNS infections rather than high-dose daptomycin.
Oxford University Press (OUP)
Title: Development of VRE meningitis due to haematogenous spread while on high-dose daptomycin therapy
Description:
Abstract
Introduction
Vancomycin-resistant Enterococcus faecium (VRE) meningitis accounts for only 0.
3%–4.
0% of bacterial meningitis cases and typically occurs following neurosurgical intervention.
We describe a rare case of a patient without neurological devices in situ or a recent neurological procedure who developed VRE meningitis via haematogenous spread.
Optimal treatment for VRE meningitis is unknown.
Case presentation
A 67-year-old male with end-stage liver failure underwent liver transplantation complicated by VRE bacteraemia and subsequently developed VRE meningitis while on high-dose daptomycin therapy (12 mg/kg/day).
Due to clinical and microbiological failure with daptomycin, he was switched to linezolid and symptoms resolved rapidly.
He completed 2 weeks of linezolid, fully recovered, and continued to do well without complications at the 5 month follow-up.
Conclusions
This case highlights the severity of VRE infections in solid organ transplant recipients and raises concerns about daptomycin penetration into the CNS.
Linezolid could be considered the preferred treatment for VRE CNS infections rather than high-dose daptomycin.
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