Evidence map›Paper›PMID 42005930›Full record

ArticleEClinicalMedicine2026

Effect of different management strategies on outcomes in subarachnoid neurocysticercosis: a descriptive, multicentre, retrospective cohort study in the USA.

Janitzio J Guzmán, Megan M Duffey, Jill Weatherhead, Eva H Clark, Jesica Herrick, Senate Amusu, Felicia C Chow, Paul R Allyn, Noah Wald-Dickler, J Martin Rodriguez and 18 more

Abstract read
In one paragraph

Article in EClinicalMedicine, 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

28 authors.

Janitzio J GuzmánLaboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, Bethesda, MD, USA.
Megan M DuffeySection of Infectious Diseases, Baylor College of Medicine, Houston, TX, USA.
Jill WeatherheadSection of Infectious Diseases, Baylor College of Medicine, Houston, TX, USA.
Eva H ClarkSection of Infectious Diseases, Baylor College of Medicine, Houston, TX, USA.
Jesica HerrickDivision of Infectious Diseases, University of Illinois at Chicago, Chicago, IL, USA.
Senate AmusuDivision of Infectious Diseases, University of Illinois at Chicago, Chicago, IL, USA.
Felicia C ChowWeill Institute for Neurosciences, Department of Neurology, University of California, San Francisco, CA, USA.
Paul R AllynDivision of Infectious Diseases, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
Noah Wald-DicklerDivision of Infectious Diseases, Los Angeles General Medical Center, Los Angeles, CA, USA.
J Martin RodriguezDivision of Infectious Diseases, UAB Heersink School of Medicine, Birmingham, AL, USA.
Natalie M BowmanDivision of Infectious Diseases, University of North Carolina School of Medicine, Chapel Hill, NC, USA.
Timothy J HatlenDepartment of Medicine, The Lundquist Institute at Harbor-UCLA Medical Center, Torrance, CA, USA.
Dannae MartinDepartment of Medicine, The Lundquist Institute at Harbor-UCLA Medical Center, Torrance, CA, USA.
Travis LarsenDivision of Infectious Diseases, Los Angeles General Medical Center, Los Angeles, CA, USA.
Anna M Cervantes-ArslanianDepartment of Neurology, Boston University Medical Center School of Medicine + Boston Medical Center, Boston, MA, USA.
Christina CoyleDepartment of Infectious Diseases, Albert Einstein College of Medicine, Bronx, NY, USA.
A Clinton WhiteInfectious Disease Division, Department of Internal Medicine, University of Texas Medical Branch, Galveston, TX, USA.
Elliott WelfordSchool of Medicine, University of California San Diego, La Jolla, CA, USA.
Annie N CowellSchool of Medicine, University of California San Diego, La Jolla, CA, USA.
Jeffrey D JenksDivision of Infectious Diseases, Department of Medicine, Duke University Medical Center, Durham, NC, USA.
Andrés F Henao-MartinezDivision of Infectious Diseases, Department of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Carlos Franco-ParedesHospital Infantil de México, Federico Gὁmez, México City, México.
Glenn MathisenDepartment of Infectious Diseases, Olive View-UCLA Medical Center, Sylmar, CA, USA.
Paola LichtenbergerUniversity of Miami Miller School of Medicine, Miami, FL, USA.
Jose A SerpaDepartment of Medicine, University of Texas at Tyler, Tyler, TX, USA.
Rory BouzigardDivision of Infectious Diseases and Geographic Medicine, Department of Internal Medicine, University of Texas Southwestern Medical Center + Parkland Health, Dallas, TX, USA.
Laila M CastellinoDivision of Infectious Diseases and Geographic Medicine, Department of Internal Medicine, University of Texas Southwestern Medical Center + Parkland Health, Dallas, TX, USA.
Elise M O'ConnellLaboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, Bethesda, MD, USA.

Funding

HOPE Training GrantT32AI007384 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Sara Gianella Weibel, Scott L Letendre · 1990 to 2026
$9.7M
NIAID NIH HHS T32 AI007384
6 · The paper itself

Abstract

Background: Subarachnoid neurocysticercosis (SANCC) is an uncommon but severe form of Methods: We performed a multicentre retrospective cohort study with patients from 15 medical centres across nine states in the USA. SANCC was defined based on histopathology; the presence of cysts in the basilar subarachnoid spaces/sylvian fissures/spine with antibody positivity to Findings: Data were collected on 75 patients with neurocysticercosis. Of whom, six patients were determined to not meet the definition of SANCC and were excluded; ultimately, 69 (40 male, 29 female) met the definition of SANCC. The year of case-defining SANCC hospitalisation ranged from 2009 to 2022, with a median year of 2016. Median 2.5 years, interquartile range (IQR) 0.94-4.0 years. SANCC was a new diagnosis in 59 patients. Of these, 18 (31%) had prior medical visits for SANCC manifestations (i.e. hydrocephalus [17%], stroke [5%], and/or meningitis [7%], brain mass [3.3%], TIA [1.6%], or intracranial hypertension without hydrocephalus [1.6%]) but SANCC was not considered. At the time of discharge, 9 (13%) patients were not given albendazole and/or praziquantel due to cost or availability. 52 patients had >60 of post-hospitalisation follow-up and completed the intended course of therapy. Use of CSF Interpretation: SANCC is commonly misdiagnosed and diagnostic and therapeutic delays may lead to more subsequent hospital encounters for SANCC-related problems. Use of CSF Ts biomarkers to guide anthelmintic therapy may decrease SANCC recurrence. However, given the small sample size, adjustment for confounders with regression analysis was not performed and we cannot exclude confounding as responsible for differences seen. Larger, prospective studies are needed to confirm these findings. Funding: Division of Intramural Research, National Institute of Allergy and Infectious Diseases.

Indexed as

CysticercosisMeningitisNeurocysticercosisRacemoseSubarachnoid neurocysticercosis

Identifiers

PMID42005930
PMCPMC13087451

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.