PMID- 31299743 OWN - NLM STAT- MEDLINE DCOM- 20191028 LR - 20240329 IS - 1536-3732 (Electronic) IS - 1049-2275 (Print) IS - 1049-2275 (Linking) VI - 30 IP - 5 DP - 2019 Jul TI - Sonolucent Cranial Implants: Cadaveric Study and Clinical Findings Supporting Diagnostic and Therapeutic Transcranioplasty Ultrasound. PG - 1456-1461 LID - 10.1097/SCS.0000000000005454 [doi] AB - BACKGROUND: Previously, sonographic evaluation of the intracranial contents was limited to intraoperative use following bone flap removal, with placement of the probe directly on the cortical surface or through a transsulcal tubular retractor. Cranioplasty with sonolucent implants may represent a postoperative window into the brain by allowing ultrasound to serve as a novel bedside imaging modality. The potential sonolucency of various commonly used cranial implant types was examined in this study. METHODS: A 3-phase study was comprised of cadaveric evaluation of transcranioplasty ultrasound (TCU) with cranioplasty implants of varying materials, intraoperative TCU during right-sided cranioplasty with clear implant made of poly-methyl-methacrylate (PMMA), and bedside TCU on postoperative day 5 after cranioplasty. RESULTS: The TCU through clear PMMA, polyether-ether-ketone, and opaque PMMA cranial implants revealed implant sonoluceny, in contrast to autologous bone and porous-polyethylene. Intraoperative ultrasound via the clear PMMA implant in a single patient revealed recognizable ventricular anatomy. Furthermore, postoperative bedside ultrasound in the same patient revealed comparable ventricular anatomy and a small epidural fluid collection corresponding to that visualized on an axial computed tomography scan. CONCLUSION: Sonolucent cranial implants, such as those made of clear PMMA, hold great promise for enhanced diagnostic and therapeutic applications previously limited by cranial bone. Furthermore, as functional cranial implants are manufactured with implantable devices housed within clear PMMA, the possibility of utilizing ultrasound for real-time surveillance of intracranial pathology becomes much more feasible. FAU - Belzberg, Micah AU - Belzberg M AD - Department of Plastic and Reconstructive Surgery, Johns Hopkins University School of Medicine, Baltimore, MD. FAU - Shalom, Netanel Ben AU - Shalom NB AD - Department of Neurosurgery, Johns Hopkins University School of Medicine, Baltimore, MD. FAU - Yuhanna, Edward AU - Yuhanna E AD - Department of Radiology, Johns Hopkins Hospital, Baltimore, MD. FAU - Manbachi, Amir AU - Manbachi A AD - Department of Radiology, Johns Hopkins Hospital, Baltimore, MD. AD - Department of Biomedical Engineering, Johns Hopkins University, Baltimore, MD. FAU - Tekes, Aylin AU - Tekes A AD - Division of Pediatric Radiology and Pediatric Neuroradiology, The Russell H. Morgan Department of Radiology and Radiological Science, Johns Hopkins University School of Medicine, Baltimore, MD. FAU - Huang, Judy AU - Huang J AD - Department of Neurosurgery, Johns Hopkins University School of Medicine, Baltimore, MD. FAU - Brem, Henry AU - Brem H AD - Department of Neurosurgery, Johns Hopkins University School of Medicine, Baltimore, MD. FAU - Gordon, Chad R AU - Gordon CR AD - Department of Plastic and Reconstructive Surgery, Johns Hopkins University School of Medicine, Baltimore, MD. AD - Department of Neurosurgery, Johns Hopkins University School of Medicine, Baltimore, MD. LA - eng PT - Journal Article PL - United States TA - J Craniofac Surg JT - The Journal of craniofacial surgery JID - 9010410 RN - 9011-14-7 (Polymethyl Methacrylate) MH - Adult MH - Cadaver MH - Humans MH - Male MH - Polymethyl Methacrylate/therapeutic use MH - Porosity MH - Postoperative Period MH - *Prostheses and Implants MH - Skull/surgery MH - Tomography, X-Ray Computed MH - Ultrasonic Therapy PMC - PMC7329202 COIS- CG is a consultant for Stryker and Longeviti Neuro Solutions. JH and CG are stockholders of Longeviti Neuro Solutions. The remaining authors report no conflicts of interest. EDAT- 2019/07/14 06:00 MHDA- 2019/10/29 06:00 PMCR- 2020/07/01 CRDT- 2019/07/14 06:00 PHST- 2019/07/14 06:00 [entrez] PHST- 2019/07/14 06:00 [pubmed] PHST- 2019/10/29 06:00 [medline] PHST- 2020/07/01 00:00 [pmc-release] AID - 00001665-201907000-00035 [pii] AID - SCS-18-01857 [pii] AID - 10.1097/SCS.0000000000005454 [doi] PST - ppublish SO - J Craniofac Surg. 2019 Jul;30(5):1456-1461. doi: 10.1097/SCS.0000000000005454.