Cerebrospinal fluid cell count variability is a major confounding factor in external ventricular drain-associated infection surveillance diagnostics: a prospective observational study

被引:8
|
作者
Badholm, Marcus [1 ,2 ]
Blixt, Jonas [1 ,2 ]
Glimaker, Martin [3 ]
Ternhag, Anders [3 ,4 ]
Hedlund, Jonas [3 ,4 ]
Nelson, David W. [1 ,2 ]
机构
[1] Karolinska Univ Hosp, Funct Perioperat Med & Intens Care, Stockholm, Sweden
[2] Karolinska Inst, Dept Physiol & Pharmacol, Stockholm, Sweden
[3] Karolinska Univ Hosp, Dept Infect Dis, Stockholm, Sweden
[4] Karolinska Inst, Dept Med, Div Infect Dis, Stockholm, Sweden
关键词
External ventricular drain; External ventricular drain associated infections; Infection diagnostics; Cerebrospinal fluid; Cell counts; GRAVITY SEDIMENTATION; LUMBAR; LEUKOCYTES; MENINGITIS; INDEX;
D O I
10.1186/s13054-021-03715-1
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Background External ventricular drain (EVD)-related infections (EVDIs) are feared complications that are difficult to rapidly and correctly diagnose, which can lead to unnecessary treatment with broad-spectrum antibiotics. No readily available diagnostic parameters have been identified to reliably predict or identify EVDIs. Moreover, intraventricular hemorrhage is common and affect cerebrospinal fluid (CSF) cellularity. The relationship between leukocytes and erythrocytes is often used to identify suspected infection and triggers the use of antibiotics pending results of cultures, which may take days. Cell count based surveillance diagnostics assumes a homogeneous distribution of cells in the CSF. Given the intraventricular sedimentation of erythrocytes on computed tomography scans this assumption may be erroneous and could affect diagnostics. Aims To evaluate the consistency of cell counts in serially sampled CSF from EVDs, with and without patient repositioning, to assess the effect on infection diagnostics. Methods We performed a prospective single-center study where routine CSF sampling was followed by a second sample after 10 min, allocated around a standard patient repositioning, or not. Changes in absolute and pairwise cell counts and ratios were analyzed, including mixed regression models. Results Data from 51 patients and 162 paired samples were analyzed. We observed substantial changes in CSF cellularity as the result of both resampling and repositioning, with repositioning found to be an independent predictor of bidirectional cellular change. Glucose and lactate levels were affected, however clinically non-significant. No positive CSF cultures were seen during the study. Thirty percent (30%) of patients changed suspected EVDI status, as defined by the cell component of local and national guidelines, when resampling after repositioning. Conclusions CSF cell counts are not consistent and are affected by patient movement suggesting a heterogeneity in the intraventricular space. The relationship between leukocytes and erythrocytes was less affected than absolute changes. Importantly, cell changes are found to increase with increased cellularity, often leading to changes in suspected EVDI status. Faster and more precise diagnostics are needed, and methods such as emerging next generation sequencing techniques my provide tools to more timely and accurately guide antibiotic treatment. Trial Registration NCT04736407, Clinicaltrials.gov, retrospectively registered 2nd February 2021.
引用
收藏
页数:14
相关论文
共 7 条
  • [1] Cerebrospinal fluid cell count variability is a major confounding factor in external ventricular drain-associated infection surveillance diagnostics: a prospective observational study
    Marcus Bådholm
    Jonas Blixt
    Martin Glimåker
    Anders Ternhag
    Jonas Hedlund
    David W. Nelson
    Critical Care, 25
  • [2] Reduction of drain-associated cerebrospinal fluid infections in neurosurgical inpatients: a prospective study
    Zakaria, R.
    Tripathy, S.
    Srikandarajah, N.
    Rothburn, M. M.
    Lawson, D. D. A.
    JOURNAL OF HOSPITAL INFECTION, 2013, 84 (03) : 215 - 221
  • [3] Performance of routine surveillance diagnostics of external ventricular drain-associated infections in a critical care setting: a retrospective cohort study
    Stahlberg, Marcus
    Blixt, Jonas
    Mehle, Christer
    Hellkvist, Viveca Hambaeck
    Giske, Christian G.
    Weitzberg, Eddie
    Nelson, David W.
    BMC INFECTIOUS DISEASES, 2025, 25 (01)
  • [4] Significance of cerebrospinal fluid inflammatory markers for diagnosing external ventricular drain-associated ventriculitis in patients with severe traumatic brain injury
    Lenski, Markus
    Biczok, Annamaria
    Neufischer, Katrin
    Tonn, Joerg-Christian
    Briegel, Josef
    Thon, Niklas
    NEUROSURGICAL FOCUS, 2019, 47 (05)
  • [5] Inflammatory Markers in Serum and Cerebrospinal Fluid for Early Detection of External Ventricular Drain-associated Ventriculitis in Patients With Subarachnoid Hemorrhage
    Lenski, Markus
    Huge, Volker
    Schmutzer, Michael
    Ueberschaer, Moritz
    Briegel, Josef
    Tonn, Joerg-Christian
    Schichor, Christian
    Thon, Niklas
    JOURNAL OF NEUROSURGICAL ANESTHESIOLOGY, 2019, 31 (02) : 227 - 233
  • [6] From the Skin to the Brain: Pathophysiology of Colonization and Infection of External Ventricular Drain, a Prospective Observational Study
    Mounier, Roman
    Lobo, David
    Cook, Fabrice
    Martin, Mathieu
    Attias, Arie
    Ait-Mamar, Bouziane
    Gabriel, Inanna
    Bekaert, Olivier
    Bardon, Jean
    Nebbad, Biba
    Plaud, Benoit
    Dhonneur, Gilles
    PLoS One, 2015, 10 (11):
  • [7] Effectiveness of a Chlorhexidine Dressing on Silver-coated External Ventricular Drain-associated Colonization and Infection: A Prospective Single-blinded Randomized Controlled Clinical Trial
    Roethlisberger, Michel
    Moffa, Giusi
    Fisch, Urs
    Wiggli, Benedikt
    Schoen, Stephan
    Kelly, Christopher
    Leu, Severina
    Croci, Davide
    Zumofen, Daniel W.
    Cueni, Nadine
    Nogarth, Danica
    Schulz, Marianne
    Bucher, Heiner C.
    Weisser-Rohacek, Maja
    Wasner, Morten-Goetz
    Widmer, Andreas F.
    Mariani, Luigi
    CLINICAL INFECTIOUS DISEASES, 2018, 67 (12) : 1868 - 1877