Pleocytosis is not fully responsible for low CSFglucose in meningitis The mechanism of hypoglycorrhachia-low CSFglucose-in meningitis remains unknown. We sought to evaluate the relative contribution of CSF inflammation vs microorganisms (bacteria and fungi) in lowering CSFglucose levels. We retrospectively categorized CSF profiles into microbial and aseptic meningitis and analyzed CSF leukocyte count, glucose, and protein concentrations. We assessed the relationship between these markers using multivariate and stratified linear regression analysis for initial and repeated CSF sampling. We also calculated the receiver operating characteristics of CSFglucose and CSF-to-serum glucose ratios to presumptively diagnose microbial meningitis. We found that increasing levels of CSF
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Pearls & Oy-sters: Chronic mumps meningoencephalitis with low CSFglucose and acute hydrocephalus in an adult. Chronic lymphocytic meningoencephalitis with low glucose and increased adenosine deaminase (ADA) levels in the CSF together with hydrocephalus represents a diagnostic challenge of varied etiology and only seldom is due to a viral (mumps) infection.
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Child Neurology: Differential diagnosis of a low CSFglucose in children and young adults. Analysis of CSF is daily routine in patients with acute neurologic disorders like CNS infections. In those patients, the finding of a low CSFglucose may influence further diagnostic workup and therapeutic choices. The interpretation of a low CSFglucose in patients with a chronic neurologic disorder , however, is a less common practice. We present a practical overview on the differential diagnosis of a low CSFglucose and stress the importance of recognizing a low CSFglucose as the diagnostic marker for GLUT1 deficiency syndrome, a treatable neurometabolic disorder.
protein levels, and decreased CSFglucose levels. Imaging findings more common in GFAP-IgG than in AQP4-IgG myelitis were longer diseased segments, central canal enhancement, and gadolinium-enhancing brain lesions. Higher EDSS scores at discharge distinguished GFAP-IgG from MOG-IgG. Clinical, laboratory, imaging, and outcome variables facilitate differential diagnosis of myelitis subtypes.
administered intranasally) or I-40 group (n = 42, 1ml 40U/ml insulin administered intranasally). POD incidence within postoperative days 1-3 was recorded. Fingertip blood glucose levels were recorded 40 min after insulin or saline administration the day before surgery, operating room entry and immediately after the procedure. Cerebrospinal fluid (CSF) glucose and lactate levels were also measured. Compared with the Control group, the I-20 and I-40 groups showed significantly lower POD incidence (39.5% versus 11.4% versus 14.3%, p = 0.002). Furthermore, no significant difference in POD incidence was observed between the I-20 and I-40 groups. CSFglucose levels were significantly higher in the I-40 group than in the Control group (p <0.0167). CSF lactate and fingertip blood glucose levels were not significantly
concentration * CSFglucose concentration * CSF microscopy, Gram stain, culture and sensitivities * CSF lactate (adults) * throat swab for cultureFull detailsInvestigations to consider * cranial CT * complement deficiency (children) * serum HIV (adults)Full detailsLog in or subscribe to access all of BMJ Best PracticeTreatment algorithmINITIALsuspected bacterial meningitis: presenting in hospitalsuspected
concentration * CSFglucose concentration * CSF microscopy, Gram stain, culture and sensitivities * CSF lactate (adults) * throat swab for cultureFull detailsInvestigations to consider * cranial CT * complement deficiency (children) * serum HIV (adults)Full detailsLog in or subscribe to access all of BMJ Best PracticeTreatment algorithmINITIALsuspected bacterial meningitis: presenting in hospitalsuspected
infection: duration of postoperative external drainage (odds ratio [OR] 1.19, P = 0.005), continued fever (OR 2.11, P = 0.036), CSF turbidity (OR 2.73, P = 0.014), CSF pressure (OR 1.01, P = 0.018), CSF total protein level (OR 1.26, P = 0.026), CSFglucose concentration (OR 0.74, P = 0.029), and postoperative serum albumin level (OR 0.84, P < 0.001). Using these variables to construct the final model
puncture was performed, which revealed cloudy cerebrospinal fluid (CSF), with an elevated CSF protein level (78 mg/dL; reference range, 7.0-35.0 mg/dL) and a low CSFglucose level (37 mg/dL [2.05 mmol/L]; reference range, 45-70 mg/dL [2.50-3.89 mmol/L]); otherwise, CSF encephalopathy, an autoimmune panel, and cultures were negative. CT and MRI of the brain with paranasal sinus were performed. Nasal
, and another CBC revealed progressive cytopenia. A bone marrow study showed hypocellularity and active hemophagocytic activity, and intravenous immunoglobulin was additionally given due to the diagnosis of HLH. Cerebrospinal fluid (CSF) analysis showed 60/mm white blood cells (N 55%, L 45%), 141 mg/dL glucose (0.7 blood-CSFglucose ratio), < 4 mg/dL protein; results of Gram stain and bacterial culture were
based on a sustained reduction in cerebrospinal fluid (CSF) glucose levels. Multiple CSF cultures were sterile. We confirmed infection by Ureaplasma species using the melting temperature mapping method. Treatment with erythromycin and ciprofloxacin resulted in a gradual decrease in the bacterial count in the CSF to 0. Our study highlights the potential utility of the melting temperature mapping method