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1907 citation(s) found for "Györi, Georg".

Rivaroxaban for Preventing Venous Thromboembolism in High-Risk Ambulatory Patients with Cancer: Rationale and Design of the CASSINI Trial
Khorana, Alok A. , Vadhan‐Raj, Saroj , Kuderer, Nicole M. , Wun, Ted , Liebman, Howard A. , Soff, Gerald A. , O’Reilly, Eileen M. , McBane, Robert D. , Damaraju, C. V. , Beyers, Karen, Dietrich, Flavia, Kakkar, Ajay K. , Riess, Hanno, McBane, Robert , O'Reilly, Eileen M , Wun, Ted , Belani, Chandra P. , Eikelboom, John W. , Peixoto, Renata D’Alpino , Lyman, Gary H

Thrombosis and Haemostasis | September 21, 2017 | Volume: 117 | Issue: 11 | Pages: 2135-2145

10.1160/th17-03-0171 | PMID 28933799 Get It

AbstractVenous thromboembolism (VTE) is a frequent complication of cancer associated with morbidity, mortality, increased hospitalizations and higher health care costs. Cancer patients at increased risk for VTE can be identified using a validated risk assessment score, and the incidence of VTE can be reduced in high-risk settings using anticoagulation. Rivaroxaban is a potent, oral, direct, factor Xa inhibitor approved for the prevention and treatment of thromboembolic events, including VTE. CASSINI is a double-blind, randomized, parallel-group, multicentre study comparing rivaroxaban with placebo in adult ambulatory patients with various cancers who are initiating systemic cancer therapy and are at high risk of VTE (Khorana score ≥ 2). Patients with primary brain tumours or those at risk for bleeding are excluded. Approximately 700 patients will be randomized 1:1 to rivaroxaban 10 mg daily or placebo for up to 6 months if there is no evidence of VTE from compression ultrasonography (CU) during screening or from routine care imaging within 30 days prior to randomization. Mandatory CU will also be performed at weeks 8 and 16 (±7 days), and at study end (±3 days). The primary efficacy hypothesis is that anticoagulation with rivaroxaban reduces the composite of objectively confirmed symptomatic or asymptomatic, lower-extremity, proximal deep-vein thrombosis (DVT); symptomatic, upper-extremity DVT; symptomatic or incidental pulmonary embolism; and VTE-related death compared with placebo. The primary safety objective is to assess major bleeding events (Clinical trial information: NCT02555878).
Factor IX Gene (F9) Genotyping Trends and Spectrum of Mutations Identified: A Reference Laboratory Experience
Botero, Juliana Perez , Coon, Lea M., Majerus, Julie A. , Chen, Dong , Pruthi, Rajiv K. , Perez Botero, Juliana , Chen, Dong

Seminars in Thrombosis and Hemostasis | September 14, 2017 | Volume: 44 | Issue: 03 | Pages: 287-292

10.1055/s-0037-1605567 | PMID 28905352 Get It

AbstractIn hemophilia B (HB), factor IX gene (F9) genotyping is used for molecular confirmation of affected individuals, for carrier testing, to facilitate the identification of those at risk for anaphylaxis/inhibitors (associated with large deletions), and to assist in assigning disease severity. Owing to test costs, optimal test utilization involves pre/post-test counseling and appropriate patient and test selection (e.g., mutation screening [F9MS] vs. known mutation [F9KM] testing). This article aims to review the trends and outcomes of F9-genotyping orders and describe the spectrum of variants identified in a sample of individuals in our reference laboratory. We performed a retrospective review of consecutive orders submitted to the Special Coagulation DNA Diagnostic Laboratory, Mayo Clinic, between 2012 and 2015. A total of 133 orders (38%) were identified for men: 118 (88%) were F9MS and 15 (12%) were F9KM. Thirteen orders (10%) were cancelled. A total of 209 orders were identified for women: 178 (85%) were F9MS and 31 (15%) were F9KM. Thirty-seven orders (18%) were cancelled and 30% of the tests performed yielded negative results. A total of 164 samples (47%) were received without clinical information. Seventeen previously unreported variants were identified. F9 genotyping provides useful information for HB management; however, 18% of our orders were cancelled and almost half were received without relevant clinical information, thus reaffirming the need for ongoing scrutiny of submitted orders. Optimal patient and test selection is important as is the accurate interpretation of variants identified. Most of the pathogenic variants identified were point mutations, with very few large deletions, consistent with the literature.
Safety and efficacy of coaxial lumen-apposing metal stents in the management of refractory gastrointestinal luminal strictures: a multicenter study
Heffley, Jason D. , Dayyeh, Barham Abu, Nieto, José , Sawas, Tarek , Zaghlol, Raja , Buttar, Navtej , Topazian, Mark , Song, Louis Wong Kee, Levy, Michael J. , Keilin, Steve, Cai, Qiang , Bazerbachi, Fateh , Abu Dayyeh, Barham K, Vargas, Eric J. , Buttar, Navtej S, Wong Kee Song, Louis M, Levy, Michael J. , Willingham, Field F.

Endoscopy International Open | September 12, 2017 | Volume: 05 | Issue: 09 | Pages: E861-E867

10.1055/s-0043-114665 | PMID 28924591 Get It

Abstract Background and aims Benign gastrointestinal (GI) strictures are often refractory to standard endoscopic interventions. Fully covered coaxial lumen-apposing metal stents (LAMS) have emerged as a novel therapy for these strictures. The aim of this study was to evaluate the safety and efficacy of LAMS for refractory GI strictures. Patients and methods A retrospective analysis was performed for patients who underwent LAMS placement for benign luminal strictures in three US centers between January 2014 and December 2016. The primary outcomes were technical success and initial clinical success of LAMS placement. Secondary outcomes were stent migration, rate of re-intervention, and adverse events. Results A total of 49 patients underwent 56 LAMS placement procedures. Previous treatment had failed in 39 patients (79.6 %), and anastomotic strictures were the indication in 77.6 % (38/49), with the most common site being gastrojejunal (34.7 % [17/49]). Technical success was achieved in all procedures and initial clinical success was achieved in 96.4 % of all procedures (54/56). Patient initial clinical success was 95.9 % (47/49). Stent migration occurred in 17.9 % of procedures, and was more likely to occur at sites in the lower GI tract (P = 0.02). The mean stent dwell time was 100.6 days, and the mean follow-up was 169.8 days. Minor adverse events, not requiring hospitalization, occurred in 33.9 % of procedures, including subsequent stricture progression (10.7 %). In cases where LAMS were removed, mean follow-up time was 102.2 days. The re-intervention rate was 75 % at 300 days follow-up after stent removal. Of the LAMS placed at anastomotic strictures, 36.4 % required re-intervention, with approximately two-thirds of these re-interventions requiring placement of a new stent or surgery. Conclusion LAMS placement was successful for the management of refractory GI strictures, with good technical and initial clinical success rates. However, re-intervention rates after LAMS removal were high, and many strictures were not resolved by an extended period of stenting with these coaxial stents. LAMS placement offers additional therapeutic options and in selected cases might be considered a destination therapy for patients with recalcitrant benign strictures.
Esthesioneuroblastoma and Olfactory Preservation: Is it Reasonable to Attempt Smell Preservation?
Janus, Jeffrey R. , Hughes, Joshua , Stokken, Janalee K., Moore, Eric J. , Ryan, Tarek, Link, Michael J. , Hughes, Joshua D, Gompel, Jamie J. Van , Price, Daniel L.

Journal of Neurological Surgery Part B: Skull Base | August 28, 2017 | Volume: 79 | Issue: 02 | Pages: 184-188

10.1055/s-0037-1606307 | PMID 29868325 Get It

Objective Olfactory preservation after resection of esthesioneuroblastoma (ENB) has been reported, however, the ability to predict tumor involvement of the olfactory system is critical to this surgical strategy. This study aims to answer the question: Can a surgeon predict, based on preoperative imaging, whether there is unilateral involvement of the olfactory system allowing for safe attempt of olfactory preservation? Methods This is a retrospective review of post-resection ENB meeting inclusion criteria of having bilateral olfactory tracts and bulbs submitted at the time of primary resection for pathologic margins. Five board-certified skull base surgeons blinded to the pathology individually reviewed the preoperative MRI scans to predict degree of tumor involvement. Results Olfactory bulb involvement occurred in both bulbs in 35% of cases and unilateral in 39% of cases, and there was no involvement in 26% of cases sampled. When comparing physician prediction of involved tracts or bulbs, involvement was appropriate or over-called (i.e., called positive when pathology was in fact negative) in 96% of cases. Conclusion This study demonstrates unilateral or no pathologic olfactory involvement of the olfactory system in 65% of cases. Our ability to predict this involvement, which may allow for a management strategy that attempts to preserve olfactory function, was accurate at 96%. Therefore, interpretation of imaging and proceeding with smell preservation in ENB appears reasonable in this cohort.Level of Evidence: Level 2b.
Neurotization of the Superficial Sensory Branch of Ulnar Nerve by the Distal Posterior Interosseous Nerve: Cadaveric Feasibility Study
Decaestecker, Laurent, Delclaux, Stépahnie, Aprédoaei, C., Tibbo, Meagan E. , Courtade-Saïdi, Monique , Mansat, Pierre , Laumonerie, Pierre , Laumonerie, Pierre

Journal of Reconstructive Microsurgery | August 25, 2017 | Volume: 33 | Issue: 09 | Pages: 636-640

10.1055/s-0037-1605365 | PMID 28841737 Get It

Background In 2014, Delclaux et al described a case wherein the Battiston and Lanzetta's technique, modified by utilization of the posterior interosseus nerve (PIN), was used to perform double neurotization of the ulnar nerve (UN). This study evaluates the feasibility of transfer of proprioceptive fascicles of the PIN to the superficial sensory branch of the UN (SSBUN). Methods The surgeries were performed on 16 fresh cadaveric wrist specimens. PIN transfer was performed through the interosseous membrane and sutured to the SSBUN. The diameter for each nerve, number of fascicles, and the percentage of fascicles without axons, under ×10, ×40, and ×100 magnifications were performed by two observers. Results Neurotization of the SSBUN by the PIN was successful in all cases. The median diameter of the SSBUN and PIN was 3.5 (3–4) and 2.3 mm (1.6–3), respectively. The SSBUN contained 5.5 fascicles (4–7), while the PIN contained 2 fascicles (0–4). The 16 PIN had limited (10 cases) or no axonal reserve (6 cases). Conclusion This study supports the surgical and anatomical feasibility of neurotization of the SSBUN by the PIN. However, the PIN's limited axonal reserve may partially or totally compromise recovery.
Sleep Disturbance, Cognitive Decline, and Dementia: A Review
Wu, Mark N. , Rosenberg, Paul B. , Spira, Adam P. , Wennberg, Alexandra , Wennberg, Alexandra M V, Wennberg, Alexandra M V

Seminars in Neurology | August 24, 2017 | Volume: 37 | Issue: 04 | Pages: 395-406

10.1055/s-0037-1604351 | PMID 28837986 Get It

Abstract Approximately half of older people report sleep disturbances, which are associated with various health conditions, including neurodegenerative disease and dementia. Indeed, 60 to 70% of people with cognitive impairment or dementia have sleep disturbances, which are linked to poorer disease prognosis. Sleep disturbances in people with dementia have long been recognized and studied; however, in the past 10 years, researchers have begun to study disturbed sleep, including sleep fragmentation, abnormal sleep duration, and sleep disorders, as risk factors for dementia. In this review the authors summarize evidence linking sleep disturbance and dementia. They describe how specific aspects of sleep (e.g., quality, duration) and the prevalence of clinical sleep disorders (e.g., sleep-disordered breathing, rapid eye movement sleep behavior disorder) change with age; how sleep parameters and sleep disorders are associated with the risk of dementia; how sleep can be disturbed in dementia; and how disturbed sleep affects dementia prognosis. These findings highlight the potential importance of identifying and treating sleep problems and disorders in middle-aged and older adults as a strategy to prevent cognitive decline and dementia. The authors also review recent evidence linking sleep disturbances to the pathophysiology underlying dementing conditions, and briefly summarize available treatments for sleep disorders in people with dementia.
Langzeitnutzen der Enzymersatztherapie (EET) mit Sebelipase alfa (SebA) über 76 Wochen bei Kindern und Erwachsenen mit lysosomaler saurer Lipase Defizienz (LAL-D) (ARISE)
Furuya, KN, Marulkar, S, Friedman, M, Bk, Burton, Abel, F, Marulkar, Sachin

Zeitschrift für Gastroenterologie | August 22, 2017 | Volume: No volume available | Issue: No issue available | Pages: No page available

10.1055/s-0037-1604983 Get It

Computational Fluid Dynamics of a Fatal Ruptured Anterior Communicating Artery Aneurysm
Švihlová, Helena , Sejkorová, Alena , Radovnický, Tomáš , Adámek, Daniel, Hron, J. , Dragomir‐Daescu, Dan , Málek, Josef , Sameš, Martin, Hejčl, Aleš , Dragomir-Daescu, Dan, Sejkorová, Alena , Hejčl, Aleš , Hron, Jaroslav , Švihlová, Helena

Journal of Neurological Surgery Part A: Central European Neurosurgery | August 11, 2017 | Volume: 78 | Issue: 06 | Pages: 610-616

10.1055/s-0037-1604286 | PMID 28800663 Get It

AbstractComputational fluid dynamics (CFD) has been studied as a tool for the stratification of aneurysm rupture risk. We performed CFD analysis in a patient operated on for a ruptured anterior communicating artery aneurysm. The point of rupture was identified during surgery. The aneurysm and blood vessels were segmented from computed tomography angiography to prepare a model for simulations. We found that the streamlines showed a concentrated inflow jet directed straight at the rupture point, and high wall shear stress was found at the point of rupture in the aneurysm sac. Thus specific local hemodynamics may be indicative of the aneurysm rupture site.
The Protruding Ear: Cosmetic and Reconstruction
Ali, Kausar , Meaike, Jesse D. , Maricevich, Renata S. , Olshinka, Asaf

Seminars in Plastic Surgery | August 9, 2017 | Volume: 31 | Issue: 03 | Pages: 152-160

10.1055/s-0037-1604241 | PMID 28798550 Get It

AbstractEar prominence is a relatively common cosmetic deformity with no associated functional deficits, but with profound psychosocial impact, especially in young patients. Protruding ears in children have propagated surgical advances that incorporate reconstructive techniques. Here we outline a systematic framework to evaluate the protruding ear and present various reconstructive surgical options for correction. Both cosmetic and reconstructive perspectives should be entertained when addressing this anatomical deformity.
Comparative Cost Analysis of Endoscopic versus Microscopic Endonasal Transsphenoidal Surgery for Pituitary Adenomas
Eseonu, Chikezie I. , ReFaey, Karim , García, Óscar , Salvatori, Roberto , Quiñones‐Hinojosa, Alfredo , ReFaey, Karim

Journal of Neurological Surgery Part B: Skull Base | August 8, 2017 | Volume: 79 | Issue: 02 | Pages: 131-138

10.1055/s-0037-1604484 | PMID 29868317 Get It

Objective This study presents a comparative analysis of cost efficacy between the microscopic and endoscopic transsphenoidal approaches, evaluating neurological outcome, extent of resection (EOR), and inpatient hospital costs. Design This study was a retrospective chart review. Setting This study was conducted at a tertiary care center. Participants The study group consisted of 68 patients with transsphenoidal surgeries between January 2007 and January 2014. Main Outcome Measures Two-sample t-tests and Pearson's chi-square test evaluated inpatient costs, quality-adjusted life years (QALYs), volumetric EOR, and neurological outcomes. Results Total inpatient costs per patient was $22,853 in the microscopic group and less ($19,736) in the endoscopic group (p = 0.049). Operating room costs were $5,974 in the microscopic group and lower in the endoscopic group ($5,045; p = 0.038). Operative time was 203.6 minutes in the microscopic group and 166.3 minutes in the endoscopic group (p = 0.032). The QALY score, length of hospital stay, and postoperative outcomes were found to be similar between the two cohorts. Multivariate linear regression modeling suggested that length of stay (p < 0.001) and operative time (p = 0.008) were important factors that influenced total inpatient costs following transsphenoidal surgery. Conclusion This study shows that transsphenoidal surgery is more cost effective with the endoscopic approach than with the microscopic approach and depends on efficiency in the operating room as well as reduction in the length of hospitalization.