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Peer-reviewedCC BYActa neurochirurgica

Sonolucent cranial windows for bedside ultrasound identification of MRI-concordant glioblastoma recurrence during outpatient surveillance: an imaging correlation pilot study.

2 more authors
6 affiliations
  1. 1Northwell, New Hyde Park, NY, USA.
  2. 2Department of Neurosurgery, Lenox Hill Hospital, New York, NY, USA.
  3. 3Northwell, New Hyde Park, NY, USA. [email protected].
  4. 4Department of Neurosurgery, Lenox Hill Hospital, New York, NY, USA. [email protected].
  5. 5New York Medical College School of Medicine, 40 Sunshine Cottage Rd, Valhalla, NY, 10595, USA. [email protected].
  6. 6Division of Neurology, Department of Neurosurgery, University of São Paulo, São Paulo, SP, Brazil.

Abstract

Background and objective

Glioblastoma (GBM) is characterized by near-universal recurrence after surgical resection, necessitating close postoperative surveillance. Although MRI remains the gold standard for detecting tumor progression, fixed imaging intervals may delay recognition of recurrence. Sonolucent cranial implants enable transcranioplasty ultrasound (TCUS), offering a potential point-of-care adjunct for interval monitoring between scheduled MRI studies. We evaluated the feasibility of identifying sonographic findings concordant with MRI-confirmed GBM recurrence during routine outpatient follow-up.Methods

We conducted a retrospective review of prospectively registered consecutive GBM patients who underwent tumor resection with placement of a sonolucent cranial implant (ClearFit®, Longeviti Inc., Baltimore, MD) at a single tertiary center (February 2023-November 2025). Patients were included if they developed MRI-confirmed recurrence and underwent TCUS within 6 weeks before or after the recurrence-detecting MRI. TCUS examinations were performed during routine outpatient visits and interpreted by a clinician blinded to MRI findings. MRIs were independently reviewed by board-certified neuroradiologists. TCUS findings were qualitatively compared with MRI-defined recurrence.Results

Of 13 patients with sonolucent implants, 8 developed MRI-confirmed recurrence within 13 months of resection, with a range of 1 to 13 months. Four underwent TCUS within six weeks of the recurrence-detecting MRI. In all four cases, TCUS demonstrated hyperechoic abnormalities spatially concordant with MRI-defined recurrence. Examinations were safely performed (n = 4) in the outpatient setting.Conclusion

TCUS through sonolucent cranial implants may demonstrate concordant findings with MRI-confirmed GBM recurrence. This preliminary series supports its spatial correlation to inform future studies that evaluate TCUS as a point-of-care adjunct for interval surveillance. Prospective studies are warranted to define standardized protocols and diagnostic performance.

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BibTeX
@article{thomas2026sonolucent,
  title = {{Sonolucent cranial windows for bedside ultrasound identification of MRI-concordant glioblastoma recurrence during outpatient surveillance: an imaging correlation pilot study.}},
  author = {Griffin Thomas and Shoaib A Syed and Samuel Latzman and Marcio Yuri Ferreira and Seth Mejia and Artur Shlifer and Vadim Zhigin and Tamika Wong and Sanskruti Sana Bokil and Sara Massimo and Raphael Bertani and John A Boockvar and Netanel Ben-Shalom and Randy S D'Amico},
  journal = {Acta neurochirurgica},
  year = {2026},
  month = aug,
  doi = {10.1007/s00701-026-06999-w},
  url = {https://europepmc.org/article/MED/42902051},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - Sonolucent cranial windows for bedside ultrasound identification of MRI-concordant glioblastoma recurrence during outpatient surveillance: an imaging correlation pilot study.
AU  - Griffin Thomas
AU  - Shoaib A Syed
AU  - Samuel Latzman
AU  - Marcio Yuri Ferreira
AU  - Seth Mejia
AU  - Artur Shlifer
AU  - Vadim Zhigin
AU  - Tamika Wong
AU  - Sanskruti Sana Bokil
AU  - Sara Massimo
AU  - Raphael Bertani
AU  - John A Boockvar
AU  - Netanel Ben-Shalom
AU  - Randy S D'Amico
PY  - 2026
DA  - 2026/08/01
JO  - Acta neurochirurgica
DO  - 10.1007/s00701-026-06999-w
UR  - https://europepmc.org/article/MED/42902051
AB  - Background and objective  Glioblastoma (GBM) is characterized by near-universal recurrence after surgical resection, necessitating close postoperative surveillance. Although MRI remains the gold standard for detecting tumor progression, fixed imaging intervals may delay recognition of recurrence. Sonolucent cranial implants enable transcranioplasty ultrasound (TCUS), offering a potential point-of-care adjunct for interval monitoring between scheduled MRI studies. We evaluated the feasibility of identifying sonographic findings concordant with MRI-confirmed GBM recurrence during routine outpatient follow-up.Methods  We conducted a retrospective review of prospectively registered consecutive GBM patients who underwent tumor resection with placement of a sonolucent cranial implant (ClearFit®, Longeviti Inc., Baltimore, MD) at a single tertiary center (February 2023-November 2025). Patients were included if they developed MRI-confirmed recurrence and underwent TCUS within 6 weeks before or after the recurrence-detecting MRI. TCUS examinations were performed during routine outpatient visits and interpreted by a clinician blinded to MRI findings. MRIs were independently reviewed by board-certified neuroradiologists. TCUS findings were qualitatively compared with MRI-defined recurrence.Results  Of 13 patients with sonolucent implants, 8 developed MRI-confirmed recurrence within 13 months of resection, with a range of 1 to 13 months. Four underwent TCUS within six weeks of the recurrence-detecting MRI. In all four cases, TCUS demonstrated hyperechoic abnormalities spatially concordant with MRI-defined recurrence. Examinations were safely performed (n = 4) in the outpatient setting.Conclusion  TCUS through sonolucent cranial implants may demonstrate concordant findings with MRI-confirmed GBM recurrence. This preliminary series supports its spatial correlation to inform future studies that evaluate TCUS as a point-of-care adjunct for interval surveillance. Prospective studies are warranted to define standardized protocols and diagnostic performance.
SN  - 0001-6268
SN  - 0942-0940
ER  -