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848 citation(s) found for "Erasmus, D".

Real-Time Ultrasound Imaging of the Tear Trough: Lessons Learned From Functional Anatomy
Calomeni, Mariana, Alfertshofer, Michael , Frank, Konstantin , Dennison, Rebekah, Bravo, Bruna Felix, Velthuis, Peter J. , Cotofana, Sebastian , Bihun, Rebekah , Elias, Mariana Calomeni , Alfertshofer, Michael , Bravo, Bruna , Cotofana, Sebastian , Frank, Konstantin , Moellhoff, Nicholas , Schelke, Leonie , Green, Jeremy B. , Bihun, Rebekah J.

Mayo Clinic

Aesthetic Surgery Journal | October 6, 2021 | Volume: 42 | Issue: 5 | Pages: 518-526

10.1093/asj/sjab351 | PMID 34610093 Get It

AbstractBackgroundThe tear trough is one of the most challenging facial regions for soft-tissue filler injections. A thorough understanding of the underlying facial, muscular, and vascular anatomy is crucial to perform safe and effective tear trough injectable treatments.ObjectivesThe authors sought to evaluate the location and function of the angular vein in the tear trough in 3 different facial expressions: repose, smiling, and max. orbicularis oculi contraction.MethodsTwenty study participants with a mean age of 48.3 years and mean BMI of 24.5 kg/m2 were investigated via functional ultrasound imaging. The diameter of the angular vein and the velocity and direction of venous blood flow were analyzed in repose, smiling, and during max. orbicularis oculi contraction.ResultsThe angular vein was identified in 100% of the cases to travel inside the orbicularis oculi muscle (intra-muscular course) within the tear trough, whereas the angular artery was not identified in this location. The distance between the angular vein and the inferior orbital rim was (lateral to medial): 4.6 mm, 4.5 mm, 3.9 mm, and 3.8 mm. The caudally directed blood flow was in repose 10.2 cm/s and was 7.3 cm/s at max. orbicularis oculi muscle contraction; however, no blood flow was detectable during smiling.ConclusionsThe diameter and the venous blood flow of the angular vein varied between the 3 tested facial expressions. Based on these anatomical findings, the deep injection approach to the tear trough is recommended due to the intramuscular course of the angular vein.
Filler Anatomy
Cotofana, Sebastian , Cotofana, Sebastian , Velthuis, Peter J. , Schelke, Leonie

Mayo Clinic

Aesthetic Surgery Journal | October 1, 2021 | Volume: 42 | Issue: 1 | Pages: NP89-NP90

10.1093/asj/sjab348 | PMID 34597360 Get It

Critical appraisal of technologies to assess electrical activity during atrial fibrillation: a position paper from the European Heart Rhythm Association and European Society of Cardiology Working Group on eCardiology in collaboration with the Heart Rhythm
Groot, Natasja M.S. de , Shah, Dipen , Boyle, Patrick M. , Clifford, Gari D. , Dessel, Pascal van, Heinzel, Frank R. , Lambiase, Pier D. , Lumens, Joost , Platonov, Pyotr G. , Ngarmukos, Tachapong , Martí­nez, Juan Pablo , Sánchez, Alejandro Olaya, Takahashi, Yoshihide , Valdigem, Bruno Pereira , Veen, Alle-Jan van der, Vernooy, Kevin , Casado-Arroyo, Rubén , Group, ESC Scientific Document, Linz, Dominik , Svennberg, Emma , Kim, Young‐Hoon , López-Cabanillas, Néstor , Locati, Emanuela T, MacFarlane, Peter, Locati, Emanuela H. , Lambiase, Pier D , de Groot, Natasja M S , Linz, Dominik , Anter, Elad , Deisenhofer, Isabel , Deneke, Thomas , Dessel, Pascal F.H.M. van , Doessel, Olaf , Dilaveris, Polychronis E , Kapa, Suraj , Veen, Alle-Jan van der , Group, ESC Scientific Document, Potter, Tom J. R. De , Dinov, Borislav , Kosiuk, Jędrzej , Neubeck, Lis , Wan, Elaine Y. , Casado-Arroyo, Rubén

Mayo Clinic

EP Europace | September 21, 2021 | Volume: 24 | Issue: 2 | Pages: 313-330

10.1093/europace/euab254 | PMID 34878119 Get It

Abstract We aim to provide a critical appraisal of basic concepts underlying signal recording and processing technologies applied for (i) atrial fibrillation (AF) mapping to unravel AF mechanisms and/or identifying target sites for AF therapy and (ii) AF detection, to optimize usage of technologies, stimulate research aimed at closing knowledge gaps, and developing ideal AF recording and processing technologies. Recording and processing techniques for assessment of electrical activity during AF essential for diagnosis and guiding ablative therapy including body surface electrocardiograms (ECG) and endo- or epicardial electrograms (EGM) are evaluated. Discussion of (i) differences in uni-, bi-, and multi-polar (omnipolar/Laplacian) recording modes, (ii) impact of recording technologies on EGM morphology, (iii) global or local mapping using various types of EGM involving signal processing techniques including isochronal-, voltage- fractionation-, dipole density-, and rotor mapping, enabling derivation of parameters like atrial rate, entropy, conduction velocity/direction, (iv) value of epicardial and optical mapping, (v) AF detection by cardiac implantable electronic devices containing various detection algorithms applicable to stored EGMs, (vi) contribution of machine learning (ML) to further improvement of signals processing technologies. Recording and processing of EGM (or ECG) are the cornerstones of (body surface) mapping of AF. Currently available AF recording and processing technologies are mainly restricted to specific applications or have technological limitations. Improvements in AF mapping by obtaining highest fidelity source signals (e.g. catheter–electrode combinations) for signal processing (e.g. filtering, digitization, and noise elimination) is of utmost importance. Novel acquisition instruments (multi-polar catheters combined with improved physical modelling and ML techniques) will enable enhanced and automated interpretation of EGM recordings in the near future.
Population screening for liver fibrosis: Toward early diagnosis and intervention for chronic liver diseases
Ginès, Pere , Lammert, Frank , Graupera, Isabel , Serra‐Burriel, Miquel , Allen, Alina M. , Wong, Vincent Wai‐Sun , Thiele, Maja , Grgurević, Ivica , Augustín, Salvador , Tsochatzis, Emmanuel , Schattenberg, Jörn M. , Guha, Indra Neil , Martini, Andréa , Morillas, Rosa M. , Koning, Harry J. de , Pich, Judit, T., Ann , Díaz, M. A. Cruz , Newsome, Philip N. , Manns, Michael P. , Kamath, Patrick S. , Krag, Aleksander , Cervera, Marta , Allen, Alina M , Wong, Vincent Wai-Sun , de Knegt, Robert J , Tsochatzis, Emmanuel A , Schattenberg, Jörn M , Guha, Indra Neil , de Koning, Harry J , Fabrellas, Núria , Ma, Ann T , Newsome, Philip N , Krag, Aleksander , Gines, Pere , Thiele, Maja , Castera, Laurent , Hartmann, Phillipp , Caballería, Llorenç , Garcı́a-Retortillo, Montserrat , Fabrellas, Núria , Diaz, M. Alba, Roulot, Dominique M.

Mayo Clinic

Hepatology | September 19, 2021 | Volume: 75 | Issue: 1 | Pages: 219-228

10.1002/hep.32163 | PMID 34537988 Get It

Abstract Cirrhosis, highly prevalent worldwide, develops after years of hepatic inflammation triggering progressive fibrosis. Currently, the main etiologies of cirrhosis are non‐alcoholic fatty liver disease and alcohol‐related liver disease, although chronic hepatitis B and C infections are still major etiological factors in some areas of the world. Recent studies have shown that liver fibrosis can be assessed with relatively high accuracy noninvasively by serological tests, transient elastography, and radiological methods. These modalities may be utilized for screening for liver fibrosis in at‐risk populations. Thus far, a limited number of population‐based studies using noninvasive tests in different areas of the world indicate that a significant percentage of subjects without known liver disease (around 5% in general populations and a higher rate −18% to 27%‐in populations with risk factors for liver disease) have significant undetected liver fibrosis or established cirrhosis. Larger international studies are required to show the harms and benefits before concluding that screening for liver fibrosis should be applied to populations at risk for chronic liver diseases. Screening for liver fibrosis has the potential for changing the current approach from diagnosing chronic liver diseases late when patients have already developed complications of cirrhosis to diagnosing liver fibrosis in asymptomatic subjects providing the opportunity of preventing disease progression.
P03.06 Boolean logic puzzles as a neurosurgical mapping tool to preserve programming skill
Donders-Kamphuis, Marike , Miller, Karl, Kallen, Bas F.W. van der, Broekman, Marike L. D. , Miller, K J

Mayo Clinic

Neuro-Oncology | September 9, 2021 | Volume: 23 | Issue: Supplement_2 | Pages: ii18-ii18

10.1093/neuonc/noab180.058 Get It

Abstract BACKGROUND In glioma surgery, awake craniotomy with Direct Electrical Stimulation (DES) is increasingly becoming the gold standard treatment to preserve language, cognition and motor function and to optimize extent of resection. Computer programming is historically seen as an integration of cognition, language, and mathematics but an intraoperative task to monitor computer programming does not exist yet. In this study we describe a new task for intraoperative monitoring, using visual Boolean Logic Puzzles. MATERIAL AND METHODS We describe a computer programmer who underwent awake craniotomy to resect an anaplastic astrocytoma in the left superior frontal gyrus. At the request of the patient we tested programming language. We developed a new task and set of logic puzzle visual stimuli to monitor underlying cognitive function used for programming language. This test was used during preoperative functional MRI (fMRI), direct electrical stimulation (DES) and ongoing monitoring during resection. RESULTS In fMRI this task showed bilateral activation in Brodmann area 6 and 8 and for left hemisphere in Brodmann area 10. These areas are below and lateral of the tumor. Monitoring of language, motor skills and Boolean mapping was performed during DES and while resection was performed. No deficits in programming ability could be identified intra- and postoperatively. CONCLUSION Boolean Logic Puzzles may be a useful intraoperative task to preserve programming skills.
Morbidity and Function Loss After Resection of Malignant Peripheral Nerve Sheath Tumors
Martin, Enrico , Pendleton, Courtney , Verhoef, Cornelis , Spinner, Robert J. , Coert, J. Henk , Verhoef, Cornelis

Mayo Clinic

Neurosurgery | September 8, 2021 | Volume: 90 | Issue: 3 | Pages: 354-364

10.1093/neuros/nyab342 | PMID 34528095 Get It

BACKGROUND: Malignant peripheral nerve sheath tumors (MPNSTs) are aggressive soft tissue sarcomas. Their resection may lead to serious morbidity. Incidence of postoperative motor and sensory deficits is unknown, and reconstruction aimed at restoring such deficits is infrequently carried out. OBJECTIVE: To identify the incidence and risk factors of postoperative morbidity in MPNST as well as the use and outcomes of functional reconstructions in these patients. METHODS: Postoperative function and treatment of MPNSTs diagnosed from 1988 to 2019 in 10 cancer centers was obtained. Two models were constructed evaluating factors independently associated with postoperative motor (<M3) or critical sensory loss. Critical sensation was defined as partial or complete loss of hand, foot, or buttocks sensation. RESULTS: A total of 756 patients (33.4% neurofibromatosis type 1, NF1) were included. MPNSTs originated in 34.4% from a major nerve. Of 658 surgically treated patients, 27.2% had <M3 muscle power and 24.3% critical sensory loss. Amputations were carried out in 61 patients. Independent risk factors for motor and sensory loss included patients with NF1, symptomatic, deep-seated, extremity, or plexus tumors originating from major nerves (all P < .05). A total of 26 patients underwent functional reconstructions. The majority (64%) of these patients regained at least M3 muscle power and 33% M4 despite 86% receiving multimodal therapy. CONCLUSION: Resection of MPNSTs commonly results in motor and sensory deficits. Patients with NF1, symptomatic, deep-seated tumors, arising from major nerves were associated with a higher risk for developing postoperative morbidity. Functional reconstructions are infrequently performed but can improve functional outcomes.
Expanding the phenotype of ASXL3‐related syndrome: A comprehensive description of 45 unpublished individuals with inherited and de novo pathogenic variants in ASXL3
Schirwani, Schaida , Albaba, Shadi , Carere, Deanna Alexis , Sacoto, María J. Guillen , Zamora, Francisca Milan, Si, Yue , Rabin, Rachel , Renaud, Deborah L. , Hauser, Natalie , Blanchet, Patricia, Foulds, Nichola, Dixit, Abhijit , Fisher, Richard, Armstrong, Ruth, Isidor, Bertrand , Demirdas, Serwet , Dykzeul, Natalie, Cohen, Julie S. , Grand, Katheryn , Swols, Dayna Morel , Albassam, Hessa F., Naik, Swati , Ragge, Nicola , Tedesco, Maria Giovanna , Harrison, Rachel , Bouman, Arjan , Palen, Emily, Challman, Thomas D. , Willemsen, Marjolein H. , Vogt, Julie , Cunniff, Christopher , Bergstrom, Katherine , Bruel, Ange‐Line , Kini, Usha , Alkuraya, Fowzan S. , Slegesky, Valerie, Meeks, Naomi, Girotto, Paula Natale , Johnson, Diana , Study, DDD, Newbury‐Ecob, Ruth , Lynch, Sally Ann , Graham, John M. , Balasubramanian, Meena , Hauser, Natalie , Schrier Vergano, Samantha , Bouman, Arjan , Cunniff, Christopher , Bergstrom, Katherine , Bruel, Ange-Line , Alkuraya, Fowzan S , Prontera, Paolo , Li, Dong , Graham, John M , Zamora, Francisca Millan, Pappas, John , Reid, Evan , Cogné, Benjamin , Vergano, Samantha A. Schrier , Slavotinek, Anne , Naik, Swati, Dean, John , Costa, Cinzia , Walia, Jagdeep Singh , Study, DDD, Ockeloen, Charlotte W. , Li, Dong , Pierson, Tyler Mark

Mayo Clinic

American Journal of Medical Genetics Part A | August 26, 2021 | Volume: 185 | Issue: 11 | Pages: 3446-3458

10.1002/ajmg.a.62465 | PMID 34436830 Get It

AbstractThe study aimed at widening the clinical and genetic spectrum of ASXL3‐related syndrome, a neurodevelopmental disorder, caused by truncating variants in the ASXL3 gene. In this international collaborative study, we have undertaken a detailed clinical and molecular analysis of 45 previously unpublished individuals with ASXL3‐related syndrome, as well as a review of all previously published individuals. We have reviewed the rather limited functional characterization of pathogenic variants in ASXL3 and discuss current understanding of the consequences of the different ASXL3 variants. In this comprehensive analysis of ASXL3‐related syndrome, we define its natural history and clinical evolution occurring with age. We report familial ASXL3 pathogenic variants, characterize the phenotype in mildly affected individuals and discuss nonpenetrance. We also discuss the role of missense variants in ASXL3. We delineate a variable but consistent phenotype. The most characteristic features are neurodevelopmental delay with consistently limited speech, significant neuro‐behavioral issues, hypotonia, and feeding difficulties. Distinctive features include downslanting palpebral fissures, hypertelorism, tubular nose with a prominent nasal bridge, and low‐hanging columella. The presented data will inform clinical management of individuals with ASXL3‐related syndrome and improve interpretation of new ASXL3 sequence variants.
Ten-year all-cause death after percutaneous or surgical revascularization in diabetic patients with complex coronary artery disease
Wang, Rutao , Serruys, Patrick W. , Gao, Chao , Hara, Hironori , Takahashi, Kuniaki , Ono, Masafumi , Kawashima, Hideyuki , O’Leary, Neil , Holmes, David R. , Curzen, Nick , Geuns, Robert‐Jan van , Morel, Marie‐Angèle , Head, Stuart J., Thuijs, Daniel J.F.M. , Davierwala, Piroze , O’Brien, Timothy , Garg, Scot , Onuma, Yoshinobu , Witkowski, Adam , Curzen, Nick , Burzotta, Francesco , Kappetein, Arie Pieter , Thuijs, Daniel J F M , Garg, Scot , Serruys, Patrick W , Onuma, Yoshinobu , Witkowski, Adam , James, Stefan Karl , Kappetein, A. Pieter , Fuster, Valentı́n

Mayo Clinic

European Heart Journal | August 13, 2021 | Volume: 43 | Issue: 1 | Pages: 56-67

10.1093/eurheartj/ehab441 | PMID 34405232 Get It

Abstract Aims The aim of this article was to compare rates of all-cause death at 10 years following coronary artery bypass grafting (CABG) or percutaneous coronary intervention (PCI) in patients with or without diabetes. Methods and results The SYNTAXES study evaluated up to 10-year survival of 1800 patients with three-vessel disease (3VD) and/or left main coronary artery disease (LMCAD) randomized to receive either PCI or CABG in the SYNTAX trial. Ten-year all-cause death according to diabetic status and revascularization strategy was examined. In diabetics (n = 452), the risk of mortality was numerically higher with PCI compared with CABG at 5 years [19.6% vs. 13.3%, hazard ratio (HR): 1.53, 95% confidence interval (CI): 0.96, 2.43, P = 0.075], with the opposite seen between 5 and 10 years (PCI vs. CABG: 20.8% vs. 24.4%, HR: 0.82, 95% CI: 0.52, 1.27, P = 0.366). Irrespective of diabetic status, there was no significant difference in all-cause death at 10 years between patients receiving PCI or CABG, the absolute treatment difference was 1.9% in diabetics (PCI vs. CABG: 36.4% vs. 34.5%, difference: 1.9%, 95% CI: −7.6%, 11.1%, P = 0.551). Among insulin-treated patients (n = 182), all-cause death at 10 years was numerically higher with PCI (47.9% vs. 39.6%, difference: 8.2%, 95% CI: −6.5%, 22.5%, P = 0.227). Conclusions The treatment effects of PCI vs. CABG on all-cause death at 10 years in patients with 3VD and/or LMCAD were similar irrespective of the presence of diabetes. There may, however, be a survival benefit with CABG in patients with insulin-treated diabetes. The association between revascularization strategy and very long-term ischaemic and safety outcomes for patients with diabetes needs further investigation in dedicated trials. Trial registration SYNTAX: ClinicalTrials.gov reference: NCT00114972 and SYNTAX Extended Survival: ClinicalTrials.gov reference: NCT03417050.
Long-term survival after coronary bypass surgery with multiple versus single arterial grafts
Thuijs, Daniel J.F.M. , Davierwala, Piroze , Milojevic, Milan , Noack, Thilo , Kappetein, A. Pieter , Mohr, Friedrich‐Wilhelm, Morice, Marie‐Claude, Mack, Michael J. , Ståhle, Elisabeth , Verberkmoes, Niels , Holmes, David R. , Head, Stuart J., Investigators, for the SYNTAX Extended Survival, Noack, Thilo , Kappetein, Arie Pieter , Ståhle, L Elisabeth G E , Serruys, Patrick W , Milojevic, Milan , Deo, Salil V. , Serruys, Patrick W. , Investigators, for the SYNTAX Extended Survival

Mayo Clinic

European Journal of Cardio-Thoracic Surgery | August 8, 2021 | Volume: 61 | Issue: 4 | Pages: 925-933

10.1093/ejcts/ezab392 | PMID 34618017 Get It

Abstract OBJECTIVES This study sought to evaluate the long-term differences in survival between multiple arterial grafts (MAG) and single arterial grafts (SAG) in patients who underwent coronary artery bypass grafting (CABG) in the SYNTAX study. METHODS The present analysis included the randomized and registry-treated CABG patients (n = 1509) from the SYNTAX Extended Survival study (SYNTAXES). Patients with only venous (n = 42) or synthetic grafts (n = 1) were excluded. The primary end point was all-cause death at the longest follow-up. Multivariable Cox regression was used to adjust for differences in baseline characteristics. Sensitivity analysis using propensity matching with inverse probability for treatment weights was performed. RESULTS Of the 1466 included patients, 465 (31.7%) received MAG and 1001 (68.3%) SAG. Patients receiving MAG were younger and at lower risk. At the longest follow-up of 12.6 years, all-cause death occurred in 23.6% of MAG and 40.0% of SAG patients [adjusted hazard ratio (HR) 0.74, 95% confidence interval (CI) (0.55–0.98); P = 0.038], which was confirmed by sensitivity analysis. MAG in patients with the three-vessel disease was associated with significant lower unadjusted and adjusted all-cause death at 12.6 years [adjusted HR 0.65, 95% CI (0.44–0.97); P = 0.033]. In contrast, no significance was observed after risk adjustment in patients with the left main disease, with and without diabetes, or among SYNTAX score tertiles. CONCLUSIONS In the present post hoc analysis of all-comers patients from the SYNTAX trial, MAG resulted in markedly lower all-cause death at 12.6-year follow-up compared to a SAG strategy. Hence, this striking long-term survival benefit of MAG over SAG encourages more extensive use of multiple arterial grafting in selected patients with reasonable life expectancy. Trial registration SYNTAXES ClinicalTrials.gov reference: NCT03417050; SYNTAX ClinicalTrials.gov reference: NCT00114972.