Evidence map›Paper›PMID 33665678›Full record

ArticleChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2021

Endoscopic extended transsphenoidal surgery for newly diagnosed paediatric craniopharyngiomas.

Mohsen Javadpour, Michael Amoo, Darach Crimmins, John Caird, Patricia Daly, Jane Pears, Cormac Owens, Michael Capra, Declan Cody

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Article in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

11 citing papers in PubMed, 23 citations in OpenAlex.

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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 at 3 institutions in 1 country.

Mohsen JavadpourNational Neurosurgical Centre, Beaumont Hospital, Dublin, Ireland. mjavadpour@rcsi.ie.
Michael AmooNational Neurosurgical Centre, Beaumont Hospital, Dublin, Ireland.ORCID http://orcid.org/0000-0001-6886-6714
Darach CrimminsNational Neurosurgical Centre, Beaumont Hospital, Dublin, Ireland.
John CairdNational Neurosurgical Centre, Beaumont Hospital, Dublin, Ireland.
Patricia DalyTrinity College Dublin, Dublin, Ireland.
Jane PearsDepartments of Paediatric Oncology, Children's Health Ireland at Crumlin, Dublin, Ireland.
Cormac OwensDepartments of Paediatric Oncology, Children's Health Ireland at Crumlin, Dublin, Ireland.
Michael CapraDepartments of Paediatric Oncology, Children's Health Ireland at Crumlin, Dublin, Ireland.
Declan CodyDepartments of Paediatric Endocrinology, Children's Health Ireland at Crumlin, Dublin, Ireland.
Children's Health Ireland at Crumlin · IERoyal College of Surgeons in Ireland · IETrinity College Dublin · IE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeEndoscopic extended transsphenoidal surgery (EETSS) has gained popularity for treatment of craniopharyngiomas. The aim of this study is to assess the outcome of endoscopic extended transsphenoidal surgery (EETSS) for newly diagnosed paediatric craniopharyngiomas.

methodsPatient details were obtained from a prospective database of all endoscopic transnasal operations performed by a single surgeon. Outcomes including visual function, pituitary function, body mass index (BMI), postoperative neurological deficit, extent of resection and recurrence on follow-up were obtained. Obesity was defined as BMI percentile of equal to or greater than 95%.

resultsBetween January 2011 and January 2020, 15 of 16 children (5-18 years old) with newly diagnosed craniopharyngiomas underwent EETSS. Four patients had a conchal-type sphenoid sinus. Gross total resection (GTR) was achieved in 4 patients and near total resection (NTR) in 5 patients. The remaining 6 had subtotal resection (STR). Postoperative radiotherapy was used in 6 patients (4 with STR, 2 with NTR). There were no postoperative deaths, strokes or CSF leaks. Normalisation of visual fields (VF) occurred in 9/13 patients with preoperative VF defects. One patient developed a new visual field defect. During a median follow-up period of 74 (8-104) months, 2 patients have required further surgery for tumour progression following initial STR, where a tumour remnant was left in situ to preserve the pituitary stalk. 6/11 patients developed new anterior pituitary dysfunction as a result of surgery and 9/12 developed new diabetes insipidus (DI). At the time of last follow-up, 14/15 children had anterior panhypopituitarism, 13/15 had DI and 1 patient developed new onset obesity. Two patients, who were obese preoperatively, were no longer obese at last follow-up.

conclusionsEETSS can be performed as the first option in the majority of children with newly diagnosed craniopharyngioma, despite factors such as small nose, non-pneumatised sphenoid sinus, small sella or purely suprasellar tumour location. Preservation of the pituitary stalk at the expense of leaving residual tumour may not be in the best interests of the patient.

Indexed as

CraniopharyngiomaNeuroendoscopyPituitary NeoplasmsAdolescentChildChild, PreschoolHumansNeoplasm Recurrence, LocalPostoperative ComplicationsRetrospective StudiesTreatment OutcomeBrain tumourCraniopharyngiomaEndoscopicExtended transsphenoidalPaediatricPituitarySuprasellarSurgeryTransnasalTranssphenoidal

Identifiers

PMID33665678
OpenAlexW3135103440

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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.