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Dive into the research topics where Frederick F. Marciano is active.

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Featured researches published by Frederick F. Marciano.


Spine | 1997

Acute axis fractures. Analysis of management and outcome in 340 consecutive cases.

Karl A. Greene; Curtis A. Dickman; Frederick F. Marciano; Janine Drabier; Mark N. Hadley; Volker K. H. Sonntag

Study Design. Retrospective review of acute axis fractures treated at a tertiary referral center. Objective. To determine the optimal treatment of axis fractures based on 340 cases from a single institution. Summary of Background Data. Axis fractures account for almost 20% of acute cervical spine fractures. However, their management and the clinical criteria predictive of nonoperative failure remain unclear. Methods. Admission imaging studies and clinical variables were obtained for 340 consecutive axis fracture patients. Fractures were classified as odontoid Type I, II, or III with dens displacement on admission roentgenograms; hangmans fractures of Francis grade and Effendi type; and miscellaneous fractures. Treatment methods were documented, and outcomes were based on dynamic lateral roentgenograms, clinical examination, or telephone interviews at last follow‐up. Results. Follow‐up data were available in 92% of cases. Type II odontoid fractures comprised 35% of all axis fractures, were the most difficult to treat, and had the highest nonunion rate (28.4%). Odontoid displacement of 6 mm or more was associated with Type II nonunion (chi‐square = 33.74, P < 0.0001). Patients underwent surgical fusion if fracture alignment could not be maintained by an external orthosis, or if they had odontoid fractures with transverse ligament disruption, Type II odontoid fractures with dens displacement of at least 6 mm, or hangmans fractures of severe Francis grade or Effendi type. Conclusions. Type II odontoid fractures have the highest nonunion rate and were associated with dens displacement of 6 mm or greater. Early surgical fusion is recommended for acute fracture instability despite external immobilization, transverse ligament disruption, Type II odontoid fractures with dens displacement of at least 6 mm on admission, or severe Francis grade or Effendi‐type hangmans fractures. Otherwise, nonoperative management is sufficient.


Spine | 1994

Transverse atlantal ligament disruption associated with odontoid fractures.

Karl A. Greene; Curtis A. Dickman; Frederick F. Marciano; Janine Drabier; Burton P. Drayer; Volker K. H. Sonntag

Objectives. The authors evaluated transverse atlantal ligament integrity in patients with fractures of the odontoid process of the axis. Summary of Background Data. Injuries of the transverse atlantal ligament can result in atlantoaxial instability after fractures of the atlas or axis, even if osseous healing occurs. Methods. The clinical histories and follow‐up examinations and radiographic data of 30 patients with odontoid fractures were reviewed, using a combination of magnetic resonance (MR) imaging, thin‐cut computed tomography (CT), and plain radiographs to evaluate osseous and ligamentous injuries. Results and Conclusions. Osteoperiosteal ligamentous avulsion injuries were identified on MR imaging in three patients and were associated with acute and delayed instability and nonunion. The combination of MR imaging, CT, and plain radiographs is useful in evaluating unstable odontoid fractures to facilitate rational treatment planning. Odontoid fractures with transverse ligament injuries should be considered for early surgical stabilization because this combination of injuries is unlikely to heal nonoperatively. Anterior odontoid screw fixation should be avoided when the ligament is injured. [Key words: cervical spine injury, magnetic resonance imaging, odontoid fracture, transverse atlantal ligament] Spine 1994;19:2307‐2314


Spine | 2009

A new stand-alone cervical anterior interbody fusion device: biomechanical comparison with established anterior cervical fixation devices.

Matti Scholz; Phillip M. Reyes; Philipp Schleicher; Anna G.U. Sawa; Seungwon Baek; Frank Kandziora; Frederick F. Marciano; Neil R. Crawford

Study Design. A new anchored spacer—a low-profile cervical interbody fusion cage with integrated anterior fixation—was compared biomechanically to established anterior cervical devices. Objective. To evaluate the fixation properties of the new stand-alone device and compare these properties with established fixation methods. The hypothesis is that the new device will provide stability comparable to that provided by an anterior cervical cage when supplemented with an anterior plate. Summary of Background Data. It is accepted that the use of anterior cervical plating increases the chance of achieving a solid fusion. However, its use may be associated with an increase in operation time and a higher postoperative morbidity caused by a larger anterior approach and disruption of the anterior musculature. This dilemma has led to the development of a new, low profile stand-alone cervical anterior cage device with integrated screw fixation. Methods. Twenty-four human cadaveric C4–C7 cervical spines were loaded nondestructively with pure moments in a nonconstraining testing apparatus to induce flexion, extension, lateral bending, and axial rotation while angular motion was measured optoelectronically. The specimens were tested:1. Intact (N = 24).2. After discectomy and anterior stabilization.a. Interbody cage + locking plate (N = 8).b. Interbody cage + dynamic plate (N = 8).c. Anchored spacer (N = 8).3. After ventral plate removal of group 2a and 2b (N = 16). Results. All fixation techniques decreased range of motion (ROM) and lax zone (LZ) (P < 0.05) in all test modes compared with the intact motion segment and cage-only group. There were no significant differences between the anchored spacer and cage + locking plate or cage + dynamic plate. Conclusion. The anchored spacer provided a similar biomechanical stability to that of the established anterior fusion technique using an anterior plate plus cage and has a potentially lower perioperative and postoperative morbidity. These results support progression to clinical trials using the cervical anchored spacer as a stand-alone implant.


Neurosurgery | 2000

Extreme lateral supracerebellar infratentorial approach to the posterolateral mesencephalon: technique and clinical experience.

Vishteh Ag; David Ca; Frederick F. Marciano; Coscarella E; Robert F. Spetzler

OBJECTIVE Lesions situated posterolaterally along the mesencephalon present neurosurgeons with a special challenge. The midline and paramedian variations of the supracerebellar infratentorial approaches do not adequately expose this region. The subtemporal approach risks injury to the vein of Labbé. An extreme lateral supracerebellar infratentorial approach with more radical resection of bone superiorly and laterally, and skeletonization of the sigmoid and transverse sinuses, was used to approach lesions at this location in eight METHODS Five cavernous malformations, two juvenile pilocytic astrocytomas, and one peripheral superior cerebellar artery aneurysm located in this region were approached in eight patients. In this extreme lateral approach, the sigmoid sinus is unroofed more superiorly and the bone flap includes not only a posterior fossa craniotomy but also a portion that extends just above the transverse sinus. The dural opening is based along the transverse and sigmoid sinuses. After the cerebrospinal fluid has been drained, the lateral aspect of the brainstem is approached via the cerebellar surface. A proximal tentorial incision offers additional rostral exposure where needed. RESULTS Seven patients in this series underwent successful resection of their lesion. The remaining patients aneurysm was clipped successfully with no major complications. CONCLUSION The extreme lateral supracerebellar infratentorial approach differs from the midline and paramedian supracerebellar infratentorial variants in the area of exposure, patient positioning, and location of the craniotomy. The technique is effective for approaching the posterolateral mesencephalon.


Journal of Trauma-injury Infection and Critical Care | 1996

Impact of traumatic subarachnoid hemorrhage on outcome in nonpenetrating head injury. Part II: Relationship to clinical course and outcome variables during acute hospitalization.

Karl A. Greene; Ronald Jacobowitz; Frederick F. Marciano; Blake A. Johnson; Robert F. Spetzler; Timothy R. Harrington

Patients with a nonpenetrating head injury and traumatic subarachnoid hemorrhage (tSAH) on admission head computed tomography scan (n = 240) were compared with patients without tSAH matched in terms of admission postresuscitation Glasgow Coma Scale (GCS) values, age, sex, and the presence of one or more types of intracranial mass lesions. Admission Injury Severity Score was higher only in tSAH patients with admission GCS scores between 13 and 15; GCS values at 6, 24, and 48 hours were lower for tSAH patients. Patients with tSAH underwent fewer craniotomies, but more than twice as many tSAH patients had high intracranial pressure at the time of ventriculostomy placement and 6 hours after admission. tSAH patients underwent more chest procedures and their incidence of hypoxia and hypotension was greater. tSAH patients spent more days in intensive care unit, more total days hospitalized, and had worse Glasgow Outcome Scale scores at acute hospital discharge. Fewer tSAH patients were discharged home, and almost 1.5 times as many tSAH patients died during hospitalization. Given a similar overall degree of injury at admission, patients with tSAH associated with a nonpenetrating head injury had a worse outcome than similar patients without tSAH.


Progress in Neuro-psychopharmacology & Biological Psychiatry | 2002

Physiology and pathophysiology of cortico-basal ganglia-thalamocortical loops: theoretical and practical aspects.

Konstantin V. Baev; Karl A. Greene; Frederick F. Marciano; Johan E.S Samanta; Andrew G. Shetter; Kris A. Smith; Mark Stacy; Robert F. Spetzler

A new theoretical framework is used to analyze functions and pathophysiological processes of cortico-basal ganglia-thalamocortical loops and to demonstrate the hierarchical relationships between various loops. All hierarchical levels are built according to the same functional principle: Each loop is a neural optimal control system (NOCS) and includes a model of object behavior and an error distribution system. The latter includes dopaminergic neurons and is necessary to tune the model to a controlled object (CO). The regularities of pathophysiological processes in NOCSs are analyzed. Mechanisms of current functional neurosurgical procedures like lesioning and deep brain stimulation (DBS) of various basal ganglia structures and neurotransplantation are described based on proposed theoretical ideas. Parkinsons disease (PD) is used to exemplify clinical applications of the proposed theory. Within the proposed theoretical framework, PD must be considered as a disease of the error distribution system. The proposed theoretical views have broad fundamental and clinical applications.


Pediatric Neurosurgery | 1994

Cardiopulmonary Bypass, Hypothermic Circulatory Arrest and Barbiturate Cerebral Protection for the Treatment of Giant Vertebrobasilar Aneurysms in Children

Karl A. Greene; Frederick F. Marciano; Mark G. Hamilton; James M. Herman; Harold L. Rekate; Robert F. Spetzler

Intracranial aneurysms in the pediatric population are rare lesions with a significant proportion occurring as giant aneurysms involving the vertebrobasilar system. The complex anatomy of these lesions frequently creates an extremely difficult management dilemma. We present two patients, a 9-year-old and a 13-year-old, with giant fusiform vertebrobasilar aneurysms, to illustrate the utility of cardiopulmonary bypass, hypothermic circulatory arrest and barbiturate cerebral protection for successful surgical treatment of these complex intracranial vascular lesions in children.


Neurosurgery | 2011

Results of the Prospective, Randomized, Multicenter Clinical Trial Evaluating a Biosynthesized Cellulose Graft for Repair of Dural Defects

Charles L. Rosen; Gary K. Steinberg; Franco DeMonte; Johnny B. Delashaw; Stephen B. Lewis; Mark E. Shaffrey; Khaled M. Aziz; Johanna Hantel; Frederick F. Marciano

BACKGROUND After intradural cranial surgery, a dural substitute is often required for dural closure. Although preferred, limitations of autograft include local availability and additional surgical site morbidity. Thus, allografts, xenografts, and synthetics are frequently used. OBJECTIVE To report 6-month results of a randomized, controlled trial of a biosynthesized cellulose (BSC) composed duraplasty device compared with commercially available dural replacements. METHODS A total of 99 patients (62 BSC; 37 control) were treated on protocol, using a 2:1 (BSC:control) blocked randomization schedule. Physical examinations were performed pre- and postoperatively within 10 days and at 1, 3, and 6 months. Magnetic resonance imaging was performed preoperatively and at 6 months. The primary study endpoint was the absence of pseudomeningocele and extracerebral fluid collection confirmed radiographically and the absence of cerebrospinal fluid fistula at 6 months. RESULTS At 6 months, the primary hypothesis, noninferiority of the BSC implant compared with the control group, was confirmed (P = .0206). Overall success was achieved by 96.6% of BSC and 97.1% of control patients. No significant difference was revealed between treatment groups for surgical site infection (P = 1.0000) or wound healing assessment (P ≥ .3685) outcomes, or radiologic endpoints (P ≥ .4061). Device strength and seal quality favored BSC. CONCLUSION This randomized, controlled trial establishes BSC as noninferior to commercially available dural replacement devices. BSC offers a hypothetical advantage concerning prion and other infectious agent exposure; superior handling qualities are evident. Longer term data are necessary to identify limitations of BSC and its potential equivalence to the gold standard of pericranium. ABBREVIATIONS BSC: biosynthesized cellulose


Journal of Spinal Disorders | 1996

Pharmacological management of spinal cord injury : Current status of drugs designed to augment functional recovery of the injured human spinal cord

Karl A. Greene; Frederick F. Marciano; Volker K. H. Sonntag

Spinal cord injury often results in devastating physical, psychological, and economic disabilities. Research efforts are directed toward providing prognostic outcome data and animal models that parallel the human disorder, thereby elucidating the mechanisms responsible for its dismal clinical prognosis. Investigators continue to search for pharmacological agents that halt the cascade of events that lead to loss of function after cord injury. The scientific and federal regulatory processes by which new drugs are discovered and implemented clinically permit clinicians to evaluate the potential benefits of any new agent, and provide an estimate of the duration required for promising new agents to be made clinically available. Understanding these processes makes the task of classifying the availability status of new drugs much simpler, allowing rational dissemination of realistic information to patients and their families frequently made desperate for viable alternatives to the prospect of permanent paralysis. In this review, we describe the scientific and regulatory processes necessary for the clinical introduction of new drugs using spinal cord injury as an example. A classification scheme based on current Food and Drug Administration regulations is presented that provides drug availability status at a glance. It is hoped that such an organizational scheme will be of practical benefit to clinicians involved in the management of spinal cord-injured patients.


Neurosurgical Focus | 2013

Minimally invasive transforaminal lumbar interbody fusions and fluoroscopy: a low-dose protocol to minimize ionizing radiation

Justin C. Clark; Gary Jasmer; Frederick F. Marciano; Luis M. Tumialán

OBJECT There is an increasing awareness of radiation exposure to surgeons and the lifelong implications of such exposure. One of the main criticisms of minimally invasive transforaminal lumbar interbody fusion (MIS TLIF) is the amount of ionizing radiation required to perform the procedure. The goal in this study was to develop a protocol that would minimize the fluoroscopy time and radiation exposure needed to perform an MIS TLIF without compromising visualization of the anatomy or efficiency of the procedure. METHODS A retrospective review of a prospectively collected database was performed to review the development of a low-dose protocol for MIS TLIFs in which a combination of low-dose pulsed fluoroscopy and digital spot images was used. Total fluoroscopy time and radiation dose were reviewed for 50 patients who underwent single-level MIS TLIFs. RESULTS Fifty patients underwent single-level MIS TLIFs, resulting in the placement of 200 pedicle screws and 57 interbody spacers. There were 28 women and 22 men with an average age of 58.3 years (range 32-78 years). The mean body mass index was 26.2 kg/m(2) (range 17.1-37.6 kg/m(2)). Indications for surgery included spondylolisthesis (32 patients), degenerative disc disease with radiculopathy (12 patients), and recurrent disc herniation (6 patients). Operative levels included 7 at L3-4, 40 at L4-5, and 3 at L5-S1. The mean operative time was 177 minutes (range 139-241 minutes). The mean fluoroscopic time was 18.72 seconds (range 7-29 seconds). The mean radiation dose was 0.247 mGy*m(2) (range 0.06046-0.84054 mGy*m(2)). No revision surgery was required for any of the patients in this series. CONCLUSIONS Altering the fluoroscopic technique to low-dose pulse images or digital spot images can dramatically decrease fluoroscopy times and radiation doses in patients undergoing MIS TLIFs, without compromising image quality, accuracy of pedicle screw placement, or efficiency of the procedure.

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Karl A. Greene

St. Joseph's Hospital and Medical Center

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Nicholas Theodore

St. Joseph's Hospital and Medical Center

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Randall W. Porter

St. Joseph's Hospital and Medical Center

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Robert F. Spetzler

St. Joseph's Hospital and Medical Center

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Volker K. H. Sonntag

St. Joseph's Hospital and Medical Center

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Luis M. Tumialán

St. Joseph's Hospital and Medical Center

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Neil R. Crawford

St. Joseph's Hospital and Medical Center

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Anna G.U. Sawa

St. Joseph's Hospital and Medical Center

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Justin C. Clark

St. Joseph's Hospital and Medical Center

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Seungwon Baek

St. Joseph's Hospital and Medical Center

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