Evidence map›Paper›PMID 41054788›Full record

ArticleSurgical infections2026

Infection of Cerebrospinal Fluid Drainage Devices.

Kathryn B Whitlock, Christopher E Pope, Paul Hodor, David L Limbrick, Patrick J McDonald, Jason S Hauptman, Lucas R Hoffman, Tamara D Simon, Cerebrospinal FLuId MicroBiota in Shunts (CLIMB) Study Group*

Abstract read
In one paragraph

Article in Surgical infections, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Kathryn B WhitlockNew Harmony Statistical Consulting LLC, Clinton, Washington, USA.
Christopher E PopeDepartment of Pediatrics, University of Washington, Seattle, Washington, USA.
Paul HodorAurynia LLC, Seattle, Washington, USA.
David L LimbrickDepartment of Neurosurgery, Washington University in St. Louis, St. Louis, Missouri, USA.
Patrick J McDonaldDivision of Neurosurgery, University of British Columbia, Vancouver, Canada.
Jason S HauptmanDepartment of Neurosurgery, University of Washington, Seattle, Washington, USA.
Lucas R HoffmanDepartment of Pediatrics, University of Washington, Seattle, Washington, USA.
Tamara D SimonDepartment of Pediatrics, University of Southern California, Los Angeles, California, USA.
Cerebrospinal FLuId MicroBiota in Shunts (CLIMB) Study Group*

Funding

Southern California Clinical and Translational Science InstituteUL1TR001855 · NCATS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Thomas A Buchanan, Michele D. Kipke · 2016 to 2026
$81.3M
Translational Research Center to Expedite Novel Therapies in Cystic FibrosisP30DK089507 · NIDDK · SEATTLE CHILDREN'S HOSPITAL · PI Sonya Heltshe · 2010 to 2026
$21.4M
Targeting the CSF microbiota to optimize CSF shunt infection treatmentR01NS095979 · NINDS · SEATTLE CHILDREN'S HOSPITAL · PI SIMON, TAMARA DANIELLE · 2016 to 2020
$2.0M
Patient-oriented microbiome and advanced culture approaches to identifying the microbial determinants of chronic pediatric diseaseK24HL141669 · NHLBI · UNIVERSITY OF WASHINGTON · PI Lucas R Hoffman · 2018 to 2026
$929k
NCATS NIH HHS UL1 TR001855NHLBI NIH HHS K24 HL141669NIDDK NIH HHS P30 DK089507NINDS NIH HHS R01 NS095979
6 · The paper itself

Abstract

backgroundVentricular reservoir infections and cerebrospinal fluid (CSF) shunt infections are diagnosed when bacteria are recovered from microbiological cultures of CSF samples from these devices. We applied high throughput sequencing (HTS) to understand the course of changes in ventricular reservoir and shunt infection microbiota.

objectivesEvaluate the utility of monitoring microbiota in CSF (1) from ventricular reservoirs to detect development of an infection and (2) during treatment of CSF shunt infections to assess treatment response.

methodsStudy populations included (1) neonates with temporizing ventricular reservoirs who developed reservoir infection and (2) children undergoing treatment for conventional culture-confirmed CSF shunt infection. The V4 region of the 16S ribosomal RNA gene was amplified and sequenced. Comparison of taxonomic results of HTS with standard microbiological culture results (when available) was described for each CSF sample. A robust HTS signal was defined by a microbial load of ≥1e5 microbial genome equivalents/mL.

resultsIn none of the five ventricular reservoir infection cases was there a robust HTS signal for the responsible bacteria immediately prior to infection. In six of the seven CSF shunt infection cases, there was a robust HTS signal for the genus of the responsible bacteria in the sample at the time of positive CSF culture. The proportion of sequences from the genus associated with the responsible bacteria decreased during infection treatment.

conclusionsThese pilot data suggest limited utility in using HTS for surveillance for ventricular reservoir infections, as they emerge abruptly. In CSF shunt infection, HTS demonstrates a return to heterogeneous microbiota when bacterial cultures become negative.

Indexed as

BacteriaCerebrospinal FluidCerebrospinal Fluid ShuntsDrainageChildChild, PreschoolFemaleHigh-Throughput Nucleotide SequencingHumansInfantInfant, NewbornMaleRNA, Ribosomal, 16SRNA, Ribosomal, 16Scerebrospinal fluiddrainagehigh throughput sequencinginfectionshuntventricular reservoir

Identifiers

PMID41054788
PMCPMC13220980

What OpenQuestion holds

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.