Evidence map›Paper›PMID 21674195›Full record

ReviewJournal of neurology2012

Neuroschistosomiasis.

Allen G Ross, Donald P McManus, Jeremy Farrar, Richard J Hunstman, Darren J Gray, Yue-Sheng Li

Abstract readReview
PubMed Publisher
In one paragraph

Review in Journal of neurology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 1 pooled it
4.9field-weighted citation impact, top 4% of its field
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

47 citing papers in PubMed, 1 synthesis or guideline pooled it, 138 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. In Vitro and In Vivo Models of Neuroschistosomiasis.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Neuroschistosomiasis in Young Filipino Patient Presenting with Seizure.European journal of case reports in internal medicine · 2024
    Article
  15. Review
  16. Article
  17. Mansonic neuroschistosomiasis in the childhood: an undiagnosed pathology?Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2023
    Review
  18. Article
  19. Article
  20. From the immune system to mood disorders especially induced byFrontiers in cellular and infection microbiology · 2023
    Review
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

6 authors at 4 institutions in 4 countries.

Allen G RossSchool of Public Health, Griffith University, Meadowbrook, QLD, Australia. a.ross@griffith.edu.au
Donald P McManus
Jeremy Farrar
Richard J Hunstman
Darren J Gray
Yue-Sheng Li
QIMR Berghofer Medical Research Institute · AUGriffith University · AUOxford University Clinical Research Unit · VNUniversity of Saskatchewan · CA

Funding

Howard Hughes Medical InstituteWellcome Trust
6 · The paper itself

Abstract

Schistosomiasis (bilharzia) is a neglected tropical disease caused by digenetic trematode platyhelminths of the genus Schistosoma. Neuroschistosomiasis is one of the most severe clinical outcomes associated with schistosome infection. Neurological complications early during the course of infection are thought to occur through in situ egg deposition following aberrant migration of adult worms to the brain or spinal cord. The presence of eggs in the CNS induces a cell-mediated Th2-driven periovular granulomatous reaction. The mass effect of thousands of eggs and the large granulomas concentrated within the brain or spinal cord explain the signs and symptoms of increased intracranial pressure, myelopathy, radiculopathy and subsequent clinical sequelae. Myelopathy (acute transverse myelitis and subacute myeloradiculopathy) of the lumbosacral region is the most common neurological manifestation of S. mansoni or S. haematobium infection, whereas acute encephalitis of the cortex, subcortical white matter, basal ganglia or internal capsule is typical of S. japonicum infection. Cerebral complications include encephalopathy with headache, visual impairment, delirium, seizures, motor deficits and ataxia, whereas spinal symptoms include lumbar pain, lower limb radicular pain, muscle weakness, sensory loss and bladder dysfunction. The finding of eggs in the stool or a positive serology, provides supportive but not direct evidence of neuroschistosomiasis. A definitive diagnosis can only be made with histopathological study showing Schistosoma eggs and granulomas. Schistosomicidal drugs (notably praziquantel), steroids and surgery are currently used for the treatment of neuroschistosomiasis. During the 'acute phase' of the disease, neuroschistosomiasis is treated with corticosteroids which are augmented with a course of praziquantel once female worm ovipositioning commences. Surgery should be reserved for special cases such as in those with evidence of medullary compression and in those who deteriorate despite clinical management.

Indexed as

Adrenal Cortex HormonesAnimalsArtemetherArtemisininsHumansImmunologic TestsLife Cycle StagesMagnetic Resonance ImagingNeuroschistosomiasisPraziquantelSchistosomaSchistosomicidesTomography, X-Ray ComputedAdrenal Cortex HormonesArtemetherArtemisininsPraziquantelSchistosomicides

Identifiers

PMID21674195
OpenAlexW3191086964

What OpenQuestion holds

Textmetadata
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.