36 research outputs found
Randomized Clinical Trials and Observational Tribulations: Providing Clinical Evidence for Personalized Surgical Pain Management Care Models
Proving clinical superiority of personalized care models in interventional and surgical pain
management is challenging. The apparent difficulties may arise from the inability to standardize
complex surgical procedures that often involve multiple steps. Ensuring the surgery is performed
the same way every time is nearly impossible. Confounding factors, such as the variability of the
patient population and selection bias regarding comorbidities and anatomical variations are also
difficult to control for. Small sample sizes in study groups comparing iterations of a surgical protocol
may amplify bias. It is essentially impossible to conceal the surgical treatment from the surgeon and
the operating team. Restrictive inclusion and exclusion criteria may distort the study population
to no longer reflect patients seen in daily practice. Hindsight bias is introduced by the inability to
effectively blind patient group allocation, which affects clinical result interpretation, particularly if
the outcome is already known to the investigators when the outcome analysis is performed (often a
long time after the intervention). Randomization is equally problematic, as many patients want to
avoid being randomly assigned to a study group, particularly if they perceive their surgeon to be
unsure of which treatment will likely render the best clinical outcome for them. Ethical concerns
may also exist if the study involves additional and unnecessary risks. Lastly, surgical trials are costly,
especially if the tested interventions are complex and require long-term follow-up to assess their
benefit. Traditional clinical testing of personalized surgical pain management treatments may be
more challenging because individualized solutions tailored to each patient’s pain generator can vary
extensively. However, high-grade evidence is needed to prompt a protocol change and break with
traditional image-based criteria for treatment. In this article, the authors review issues in surgical
trials and offer practical solutions
The Changing Environment in Postgraduate Education in Orthopedic Surgery and Neurosurgery and Its Impact on Technology-Driven Targeted Interventional and Surgical Pain Management : Perspectives from Europe, Latin America, Asia, and The United States
Personalized care models are dominating modern medicine. These models are rooted in
teaching future physicians the skill set to keep up with innovation. In orthopedic surgery and neurosurgery, education is increasingly influenced by augmented reality, simulation, navigation, robotics,
and in some cases, artificial intelligence. The postpandemic learning environment has also changed,
emphasizing online learning and skill- and competency-based teaching models incorporating clinical
and bench-top research. Attempts to improve work–life balance and minimize physician burnout
have led to work-hour restrictions in postgraduate training programs. These restrictions have made it
particularly challenging for orthopedic and neurosurgery residents to acquire the knowledge and skill
set to meet the requirements for certification. The fast-paced flow of information and the rapid implementation of innovation require higher efficiencies in the modern postgraduate training environment.
However, what is taught typically lags several years behind. Examples include minimally invasive
tissue-sparing techniques through tubular small-bladed retractor systems, robotic and navigation,
endoscopic, patient-specific implants made possible by advances in imaging technology and 3D
printing, and regenerative strategies. Currently, the traditional roles of mentee and mentor are being
redefined. The future orthopedic surgeons and neurosurgeons involved in personalized surgical pain
management will need to be versed in several disciplines ranging from bioengineering, basic research,
computer, social and health sciences, clinical study, trial design, public health policy development,
and economic accountability. Solutions to the fast-paced innovation cycle in orthopedic surgery and
neurosurgery include adaptive learning skills to seize opportunities for innovation with execution
and implementation by facilitating translational research and clinical program development across
traditional boundaries between clinical and nonclinical specialties. Preparing the future generation
of surgeons to have the aptitude to keep up with the rapid technological advances is challenging
for postgraduate residency programs and accreditation agencies. However, implementing clinical
protocol change when the entrepreneur–investigator surgeon substantiates it with high-grade clinical
evidence is at the heart of personalized surgical pain management
AOSpine Consensus Paper on Nomenclature for Working-Channel Endoscopic Spinal Procedures
Study Design: International consensus paper on a unified nomenclature for full-endoscopic spine surgery.
Objectives: Minimally invasive endoscopic spinal procedures have undergone rapid development during the past decade. Evolution of working-channel endoscopes and surgical instruments as well as innovation in surgical techniques have expanded the types of spinal pathology that can be addressed. However, there is in the literature a heterogeneous nomenclature defining approach corridors and procedures, and this lack of common language has hampered communication between endoscopic spine surgeons, patients, hospitals, and insurance providers.
Methods: The current report summarizes the nomenclature reported for working-channel endoscopic procedures that address cervical, thoracic, and lumbar spinal pathology.
Results: We propose a uniform system that defines the working-channel endoscope (full-endoscopic), approach corridor (anterior, posterior, interlaminar, transforaminal), spinal segment (cervical, thoracic, lumbar), and procedure performed (eg, discectomy, foraminotomy). We suggest the following nomenclature for the most common full-endoscopic procedures: posterior endoscopic cervical foraminotomy (PECF), transforaminal endoscopic thoracic discectomy (TETD), transforaminal endoscopic lumbar discectomy (TELD), transforaminal lumbar foraminotomy (TELF), interlaminar endoscopic lumbar discectomy (IELD), interlaminar endoscopic lateral recess decompression (IE-LRD), and lumbar endoscopic unilateral laminotomy for bilateral decompression (LE-ULBD).
Conclusions: We believe that it is critical to delineate a consensus nomenclature to facilitate uniformity of working-channel endoscopic procedures within academic scholarship. This will hopefully facilitate development, standardization of procedures, teaching, and widespread acceptance of full-endoscopic spinal procedures
Molecular and functional interactions between tumor necrosis factor-alpha receptors and the glutamatergic system in the mouse hippocampus : implications for seizure susceptibility
Tumor necrosis factor (TNF)-alpha is a proinflammatory cytokine acting on two distinct receptor subtypes, namely p55 and p75 receptors. TNF-alpha p55 and p75 receptor knockout mice were previously shown to display a decreased or enhanced susceptibility to seizures, respectively, suggesting intrinsic modifications in neuronal excitability. We investigated whether alterations in glutamate system function occur in these naive knockout mice with perturbed cytokine signaling that could explain their different propensity to develop seizures. Using Western blot analysis of hippocampal homogenates, we found that p55(-/-) mice have decreased levels of membrane GluR3 and NR1 glutamate receptor subunits while GluR1, GluR2, GluR6/7 and NR2A/B were unchanged as compared to wild-type mice. In p75(-/-) mice, GluR2, GluR3, GluR6/7 and NR2A/B glutamate receptor subunits were increased in the hippocampus while GluR1 and NR1 did not change. Extracellular single-cell recordings of the electrical activity of hippocampal neurons were carried out in anesthetized mice by standard electrophysiological techniques. Microiontophoretic application of glutamate increased the basal firing rate of hippocampal neurons in p75(-/-) mice versus wild-type mice, and this effect was blocked by 2-amino-5-phosphopentanoic acid and 6-nitro-7-sulfamoyl-benzo(f)quinoxaline-2,3-dione denoting the involvement of N-methyl-D-aspartic acid and AMPA receptors. In p55(-/-) mice, hippocampal neurons responses to glutamate were similar to wild-type mice. Spontaneous glutamate release measured by in vivo hippocampal microdialysis was significantly decreased only in p55(-/-) mice. No changes were observed in KCl-induced glutamate release in both receptor knockout mice strains versus wild-type mice. These findings highlight specific molecular and functional interactions between p55 and p75 receptor-mediated signaling and the glutamate system. These interactions may be relevant for controlling neuronal excitability in physiological and pathological conditions.peer-reviewe
Odontoid screw fixation of a type II odontoid fracture in a patient with autofused C2–C3 vertebral bodies
Background: Anterior odontoid screw fixation for the treatment of type II odontoid fractures, in contrast to posterior C1–2 fusion, allows for maintenance of cervical rotatory motion at C1–2. The approach requires an accessible C2–3 disc space from which a screw can be inserted into the vertebral body and odontoid process across the fracture. Less is known about the potential use of this technique in patients with inaccessible C2–3 disc spaces. Case description: A 20 year-old female presented to the emergency department following a motor vehicle accident with diffuse neck pain in the absence of weakness or paresthesias. A CT of the patient's C-spine revealed a type II dens fracture with 3 mm of posterior displacement and congenital fusion of the C2 and C3 vertebral bodies. She was initially treated conservatively with a halo brace for 3 months, but experienced persistent neck pain and a CT of the C-spine at that time showed incomplete healing. The patient was counseled and elected to undergo anterior odontoid screw fixation. During the procedure, due to the autofusion of the C2–3 vertebral bodies, the C3–4 disc space was accessed and a screw was placed through the C2–C3 fusion block into the odontoid process. The patient tolerated the procedure well and postoperative imaging demonstrated healing of the fracture fragments. Conclusion: This case demonstrates that patients with inaccessible C2–3 disc spaces can still undergo anterior fixation. In younger patients, this may be particularly valuable as the rotatory potential of their cervical spine is preserved. Keywords: Type II odontoid fracture, Autofusion, Anterior fusio
Chordoma—Current Understanding and Modern Treatment Paradigms
Chordoma is a low-grade notochordal tumor of the skull base, mobile spine and sacrum which behaves malignantly and confers a poor prognosis despite indolent growth patterns. These tumors often present late in the disease course, tend to encapsulate adjacent neurovascular anatomy, seed resection cavities, recur locally and respond poorly to radiotherapy and conventional chemotherapy, all of which make chordomas challenging to treat. Extent of surgical resection and adequacy of surgical margins are the most important prognostic factors and thus patients with chordoma should be cared for by a highly experienced, multi-disciplinary surgical team in a quaternary center. Ongoing research into the molecular pathophysiology of chordoma has led to the discovery of several pathways that may serve as potential targets for molecular therapy, including a multitude of receptor tyrosine kinases (e.g., platelet-derived growth factor receptor [PDGFR], epidermal growth factor receptor [EGFR]), downstream cascades (e.g., phosphoinositide 3-kinase [PI3K]/protein kinase B [Akt]/mechanistic target of rapamycin [mTOR]), brachyury—a transcription factor expressed ubiquitously in chordoma but not in other tissues—and the fibroblast growth factor [FGF]/mitogen-activated protein kinase kinase [MEK]/extracellular signal-regulated kinase [ERK] pathway. In this review article, the pathophysiology, diagnosis and modern treatment paradigms of chordoma will be discussed with an emphasis on the ongoing research and advances in the field that may lead to improved outcomes for patients with this challenging disease
Natural language processing augments comorbidity documentation in neurosurgical inpatient admissions.
ObjectiveTo establish whether or not a natural language processing technique could identify two common inpatient neurosurgical comorbidities using only text reports of inpatient head imaging.Materials and methodsA training and testing dataset of reports of 979 CT or MRI scans of the brain for patients admitted to the neurosurgery service of a single hospital in June 2021 or to the Emergency Department between July 1-8, 2021, was identified. A variety of machine learning and deep learning algorithms utilizing natural language processing were trained on the training set (84% of the total cohort) and tested on the remaining images. A subset comparison cohort (n = 76) was then assessed to compare output of the best algorithm against real-life inpatient documentation.ResultsFor "brain compression", a random forest classifier outperformed other candidate algorithms with an accuracy of 0.81 and area under the curve of 0.90 in the testing dataset. For "brain edema", a random forest classifier again outperformed other candidate algorithms with an accuracy of 0.92 and AUC of 0.94 in the testing dataset. In the provider comparison dataset, for "brain compression," the random forest algorithm demonstrated better accuracy (0.76 vs 0.70) and sensitivity (0.73 vs 0.43) than provider documentation. For "brain edema," the algorithm again demonstrated better accuracy (0.92 vs 0.84) and AUC (0.45 vs 0.09) than provider documentation.DiscussionA natural language processing-based machine learning algorithm can reliably and reproducibly identify selected common neurosurgical comorbidities from radiology reports.ConclusionThis result may justify the use of machine learning-based decision support to augment provider documentation