Evidence map›Paper›PMID 32318922›Full record

ReviewNeurosurgical review2021

Surgical treatment of hypothalamic hamartomas.

Pierre Bourdillon, S Ferrand-Sorbet, C Apra, M Chipaux, E Raffo, S Rosenberg, C Bulteau, N Dorison, O Bekaert, V Dinkelacker and 3 more

Abstract readReview
PubMed Publisher
In one paragraph

Review in Neurosurgical review, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
–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

22 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Endoscopic endonasal resection of olfactory tract hamartoma for pediatric epilepsy.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2024
    Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Multimodal Approach for the Treatment of Complex Hypothalamic Hamartomas.Advances and technical standards in neurosurgery · 2024
    Review
  16. Advances in epileptic network findings of hypothalamic hamartomas.Journal of central nervous system disease · 2024
    Review
  17. Review
  18. Article
  19. Article
  20. 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

13 authors.

Pierre Bourdillon *Department of Neurosurgery, Rothschild Foundation Hospital, 29 Rue Manin, 75019, Paris, France. pierre.bourdillon@neurochirurgie.fr.
S Ferrand-Sorbet *Department of Pediatric Neurosurgery, Rothschild Foundation Hospital, Paris, France.
C ApraSorbonne Université, Paris, France.
M ChipauxDepartment of Pediatric Neurosurgery, Rothschild Foundation Hospital, Paris, France.
E RaffoDepartment of Pediatric Neurosurgery, Rothschild Foundation Hospital, Paris, France.
S RosenbergDepartment of Pediatric Neurosurgery, Rothschild Foundation Hospital, Paris, France.
C BulteauDepartment of Pediatric Neurosurgery, Rothschild Foundation Hospital, Paris, France.
N DorisonDepartment of Pediatric Neurosurgery, Rothschild Foundation Hospital, Paris, France.
O BekaertDepartment of Pediatric Neurosurgery, Rothschild Foundation Hospital, Paris, France.
V DinkelackerDepartment of Neurology, Rothschild Foundation Hospital, Paris, France.
C Le GuérinelDepartment of Neurosurgery, Rothschild Foundation Hospital, 29 Rue Manin, 75019, Paris, France.
M FohlenDepartment of Pediatric Neurosurgery, Rothschild Foundation Hospital, Paris, France.
G DorfmüllerDepartment of Pediatric Neurosurgery, Rothschild Foundation Hospital, Paris, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hypothalamic hamartomas are aberrant masses, composed of abnormally distributed neurons and glia. Along endocrine and cognitive symptoms, they may cause epileptic seizures, including the specific gelastic and dacrystic seizures. Surgery is the treatment of drug-resistant hamartoma epilepsy, with associated positive results on endocrine, psychiatric, and cognitive symptoms. Recently, alternatives to open microsurgical treatment have been proposed. We review these techniques and compare their efficacy and safety. Open resection or disconnection of the hamartoma, either through pterional, transcallosal, or transventricular approach, leads to good epileptological control, but its high complication rate, up to 30%, limits its indications. The purely cisternal peduncular forms remain the only indication of open, pterional approach, while other strategies have been developed to overcome the neurological, endocrine, behavioral, or cognitive complications. Laser and radiofrequency thermocoagulation-based disconnection through robot-guided stereo-endoscopy has been proposed as an alternative to open microsurgical resection and stereotactic destruction. The goal is to allow safe and complete disconnection of a possibly complex attachment zone, through a single intraparenchymal trajectory which allows multiple laser or radiofrequency probe trajectory inside the ventricle. The efficacy was high, with 78% of favorable outcome, and the overall complication rate was 8%. It was especially effective in patients with isolated gelastic seizures and pure intraventricular hamartomas. Stereotactic radiosurgery has proved as efficacious and safer than open microsurgery, with around 60% of seizure control and a very low complication rate. Multiple stereotactic thermocoagulation showed very interesting results with 71% of seizure freedom and 2% of permanent complications. Stereotactic laser interstitial thermotherapy (LiTT) seems as effective as open microsurgery (from 76 to 81% of seizure freedom) but causes up to 20% of permanent complications. This technique has however been highly improved by targeting only the epileptogenic onset zone in the hamartoma, as shown on preoperative functional MRI, leading to an improvement of epilepsy control by 45% (92% of seizure freedom) with no postoperative morbidity. All these results suggest that the impact of the surgical procedure does not depend on purely technical matters (laser vs radiofrequency thermocoagulation or stereotactic vs robot-guided stereo-endoscopy) but relies on the understanding of the epileptic network, including inside the hamartoma, the aim being to plan an effective disconnection or lesion of the epileptogenic part while sparing the adjacent functional structures.

Indexed as

Cerebral VentriclesDrug Resistant EpilepsyFemaleHamartomaHumansHypothalamic DiseasesImaging, Three-DimensionalMagnetic Resonance ImagingMaleNeuroendoscopyNeurosurgical ProceduresRadiosurgerySeizuresTreatment OutcomeCoagulationDisconnectionEpilepsyGelasticLaserLiTTRadiofrequencyStereotactic

Identifiers

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.