6 results on '"Efstathios Detorakis"'
Search Results
2. Ocular trauma, visual acuity related to time of referral and psychosocial determinants, during COVID‑19 pandemic: A prospective study
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Elli Kyriakaki, Efstathios Detorakis, Antonios Bertsias, Georgios Markakis, Nikolaos Tsakalis, Panagiotis Volkos, Demetrios Spandidos, and Emmanouil Symvoulakis
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Cancer Research ,Immunology and Microbiology (miscellaneous) ,General Medicine - Published
- 2023
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3. Role of Smoking in the Evolution of Cardiovascular Magnetic Resonance and Laboratory Findings of Acute Myocarditis
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Ismini Lasithiotaki, Efstathios Detorakis, Emmanouil Foukarakis, Rowland Illing, and Maria Raissaki
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Cardiac function curve ,medicine.medical_specialty ,lcsh:Diseases of the circulatory (Cardiovascular) system ,cigarette smoking ,030204 cardiovascular system & hematology ,cardiac magnetic resonance ,03 medical and health sciences ,0302 clinical medicine ,Internal medicine ,Troponin I ,medicine ,follow-up ,troponin I ,Ejection fraction ,medicine.diagnostic_test ,business.industry ,Incidence (epidemiology) ,Magnetic resonance imaging ,030229 sport sciences ,Acute myocarditis ,late gadolinium enhancement ,lcsh:RC666-701 ,Erythrocyte sedimentation rate ,Cardiology ,Original Article ,business ,Electrocardiography - Abstract
Purpose: The purpose is to investigate cardiac magnetic resonance and laboratory findings in patients with clinically suspected acute myocarditis and re-assess the evolution of findings in relation to clinical parameters and smoking habits. Methods: We prospectively analyzed 68 consecutive patients (4 females, 64 males, median age 25 years) at baseline and 51 patients 12 months later with regard to age, symptoms, and signs, smoking history, cardiac troponin I, erythrocyte sedimentation rate, c-reactive protein blood levels, electrocardiography changes, and cardiac magnetic resonance findings. Statistical analysis included group comparisons and linear regression between clinical parameters and the obtained data. Results: A statistically significant correlation was recorded between smoking and late gadolinium enhancement extent, both at baseline and follow-up study. Late gadolinium enhancement extent was positively associated with cardiac troponin I serum levels and c-reactive protein and negatively with left ventricular ejection fraction at baseline study. Myocardial segments 4 and 5 were most frequently involved. Late gadolinium enhancement persisted in 96% of patients with no significant extent change at 12-month follow-up, while improved. Conclusions: A strong correlation was recorded between smoking patients with acute myocarditis and extent both at baseline and follow-up cardiac magnetic resonance. Myocardial segments 4 and 5 involvement was most prevalent. Late gadolinium enhancement persisted at follow-up, its incidence was higher than that reported in other studies and did not have an impact on the patient's clinical status or cardiac function. However, longer-term follow-up is highly recommended in these patients.
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- 2019
4. Air trapping in Wegener’s granulomatosis: an additional finding on expiratory chest HRCT
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Eleftherios Magkanas, Nicholas Gourtsoyiannis, Efstathios Detorakis, Sofia Gourtsoyianni, Michalis Linardakis, Prodromos Sidiropoulos, Dimitrios T. Boumpas, and I. Nikolakopoulos
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Adult ,Male ,medicine.medical_specialty ,Adolescent ,Air bronchogram ,Air trapping ,Statistics, Nonparametric ,Humans ,Medicine ,Radiology, Nuclear Medicine and imaging ,In patient ,Expiration ,Aged ,Retrospective Studies ,Neuroradiology ,Wegener s ,Lung ,business.industry ,Air ,Granulomatosis with Polyangiitis ,General Medicine ,Middle Aged ,respiratory system ,Bronchiectasis ,respiratory tract diseases ,medicine.anatomical_structure ,Female ,Radiology ,medicine.symptom ,Tomography, X-Ray Computed ,business ,Airway ,Nuclear medicine - Abstract
This study was undertaken to assess the presence and extent of air trapping (AT) on high-resolution computed tomography (HRCT) in patients with Wegener’s granulomatosis (WG) and to correlate the finding with the inspiratory pattern and bronchial/bronchiolar involvement. Twenty-one patients (7 M/14 F) with WG underwent inspiratory and expiratory HRCT. Images were evaluated for the presence and extent of AT and for airway involvement (bronchi/bronchioles); the predominant HRCT pattern was also documented. The attenuation difference was measured between the areas of AT on expiration and the same areas on inspiration in order to verify the finding of AT. The extent of AT was calculated by visual scoring and correlated with the predominant inspiratory patterns and bronchial/bronchiolar involvement. AT was found in seven patients (33.3%) and its extent ranged between 3% and 70% (mean 15.8±7). Two patients showed no lesions on inspiratory HRCT, and the only finding was AT on expiration. The attenuation difference between areas of AT on expiration and the same areas on inspiration ranged between 32 and 89 HU. Inspiratory HRCT was pathological in 19 patients (90.4%), and the principal lung patterns were nodular, cavitary or noncavitary (n=7, 38.9%); ground-glass opacities (n=5, 26.3%); masses (n=3, 15.8%); fibrotic (n=3, 15.8%); and consolidation with air bronchogram (n=1, 5.3%). Bronchial and bronchiolar involvement was found in 14 and five patients, respectively. No statistically significant correlation was found between AT extent and the findings on inspiration. In addition, there were no specific patterns that caused higher or lower scores of AT. Moreover, when bronchial or bronchiolar involvement was absent, the mean AT score was statistically significantly higher. Areas of AT represent a new and indirect HRCT finding, — and in rare cases the only finding — of pulmonary WG. The nonsignificant correlation between AT extent and inspiratory findings may suggest AT as an additional HRCT finding in patients with WG.
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- 2011
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5. Cardiovascular magnetic resonance and computed tomography in the evaluation of aneurysmal coronary-cameral fistula
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Emmanouil Foukarakis, Efstathios Detorakis, George Karavolias, and Alkiviades Dermitzakis
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Adult ,Male ,medicine.medical_specialty ,Fistula ,Coronary Angiography ,Magnetic resonance angiography ,Diagnosis, Differential ,Angina ,Electrocardiography ,Internal medicine ,medicine ,Humans ,Radiology, Nuclear Medicine and imaging ,Cardiac Imaging ,Coronary sinus ,Ultrasonography ,Vascular Fistula ,medicine.diagnostic_test ,business.industry ,Coronary Aneurysm ,medicine.disease ,Coronary Vessels ,Treatment Outcome ,medicine.anatomical_structure ,Heart failure ,Cardiology ,Radiology ,Venae cavae ,Tomography, X-Ray Computed ,business ,Magnetic Resonance Angiography ,Artery - Abstract
Coronary artery fistulas represent abnormal communications between a coronary artery and a major vessel like venae cavae, pulmonary arteries or veins, the coronary sinus, or a cardiac chamber. The latter is called coronary cameral fistula is a rare condition and is most of the times congenital but can be also post traumatic or post surgical, especially after cardiovascular interventional procedures. Most patients are asymptomatic and coronary-cameral fistulae are discovered incidentally during angiographic evaluation for coronary vascular disorders, while other patients have a clinical presentation ranging from angina pectoris to heart failure. In this article, we report a rare case of an aneurysmal right coronary cameral fistula draining into the left ventricle. Echocardiography usually represents the first diagnostic imaging approach, but often due to a poor acoustic window may not show the entire course of the fistula which is crucial for the final diagnosis. ECG-gated cardiovascular CT may play an important role in the evaluation of the origin, course, termination and morphology of the fistula, its relation to the adjacent anatomical structures as well as the morphology and contractility of the heart. Cardiac MRI instead plays an additional crucial role regarding not only the above mentioned factors but also in estimating the blood flow within the fistula, providing more detailed information about the cardiac function but also about myocardial wall viability.
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- 2015
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6. A 1-year study to compare the efficacy and safety of once-daily travoprost 0.004%/timolol 0.5% to once-daily latanoprost 0.005%/timolol 0.5% in patients with open-angle glaucoma or ocular hypertension
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Topouzis1, F., Melamed2, S., DANESH MEYER3, H., Wells4, A. P., Kozobolis5, V., Wieland6, H., Andrew6, R., Wells6, D., THE INTERNATIONAL TRAVOPROST/TIMOLOL STUDY GROUP University Hospital of Alexandroupolis, Ophthalmic, Department, Kozobolis*, Greece: Vassilios P., George, Maskaleris, Efstathios Detorakis, • II Department of Ophthalmology, Aristotle University of Thessaloniki, Thessaloniki, Greece: Fotis Topouzis, Eleftherios, Anastasopoulos, Theofanis Pappas, • Ophthalmiatrio Hospital of Athens, Greece: Artemios Kandarakis, John Koutroumanos, • Associate Professor of Ophthalmology, Eye Clinic of the General University Hospital of Ioannina, Greece: Miltiadis Aspiotis, Chrisavgi Pappa, • General Hospital of Nikaia 'AG, Panteleimon, Pireous, ', Greece: Emmanuel Vaikoussis, Thrassyvoulos, Paschalidis, Panagiotis, Bournas, Nikos Kazatzis, • Eye Associates, Sydney, Nsw, Australia: Ivan Goldberg, Stuart, Graham, Paul Healey, • Eye Surgery Associates, East Melbourne VIC, • Suite 8, Australia: Julian Lockhart Rait, Lindfield, Nsw, Australia: Allan Bank*, • Western Sydney Eye Hospital, University, Clinic, Westmead, Hospital, Westmead, Nsw, Healey*, Australia: Paul R., Jonathan, Crowston, Magdalena, Guzowski, Ranier, Covar, Anne, Lee, Jen, Wan, Domit Azar, • Quai des Tanneries 26, • Marktplatz 3, Belgium: Paul Stadion, Eupen, Belgium: François Lizin*, • University Hospital Antwerp, Service of Ophthalmology, Belgium: Veva De Groot, Patrick, Schraepen, Bruno Reyntjens, • University Hospital Ghent, Ghent, Belgium: Anna Maria Kestelyn Stevens, Fien Witters, • Department of Ophthalmology, University of Tartu, Estonia: Pait Teesalu, Imbi, Kuus, Maris Oll, • Ida Tallinna Keskhaigla Silmakliinik, Tallinn, Estonia: Ulle Aamer, Elo, Alas, Marko Pastak, • Hopital Jean Minjoz, Service, D’Ophtalmologie, Besancon, Cedex, Delbosc* • Augenarzt, France: Bernard Y. C., Goeppingen, Germany: Albrecht Gerstenberger*, • Augenarzt, Mannheim, Germany: Peter Jungmann*, • Facharzt fuer Augenheilkunde, Starnberg, Hamacher*, Germany: Ludwig T., Ursula Hellmair •, M. u. e. n. c. h. e. n. e. r. s. t. r. 3., Weilheim, Bayer*, Germany: Andreas U. M., Wolfgang Foerster, • Marktplatz 34 36, Schorndorf, Germany: Thomas Christ*, • Dipartimento di Specialità Medico Chirurgiche dell’Università di Catania, Marta, Azienda Ospedaliera '. S., Emanuele, V., Ferrarotto, Catania, ', Italy: Alfredo Reibaldi, Maurizio, Uva, Antonio, Longo, Daniela Lombardo, • Policlinico San Matteo, Clinica, Oculistica, Pavia, Italy: Fernando Trimarchi, Giovanni, Milano, Antonella, Clemente, Gemma Rossi, M., Ilaria, Scatassi, Francesca Montemurro, • Clinica Oculistica, Università di Torino, Grignolo, Federico, Beatrice, Brogliatti, Rolle, Teresa, Cristina, Favero, Elisabetta, Giacosa, Angela Fornero, • Goldschleger Eye Institute, Sheba Medical Center, Tel, Hashomer, Israel: Shlomo Melamed, Mordehai, Goldenfeld, Hani, Verbin, Zohar, Vilner, Ran, Knaan, Iris Moroz, • Department of Ophthalmology, Carmel Medical Center, Haifa, Israel: Orna Geyer, Eitan Segev, • Department of Ophthalmology, Tel Aviv Sourasky Medical Center, Tel, Aviv, Israel: Shimon Kurtz, Meira, Neudorfer, Gabi, Shemesh, Shiri Zayit, • Glaucoma Service, Outpatient, Department, Clinical Hospital 'Gailezers, Riga, ', Latvia: Lasma Volksone, Lija Karlsone, • Department of Ophthalmology, Riga Stradins University Hospital, Riga, Latvia: Guna Laganovska, Kristine, Baumane, Ilze Egite, • Eye Clinic, Kaunas University of Medicine, Kaunas, Lithuania: Ingrida Januleviciene, Loreta Kuzmiene, • Eye Institute, Remuera, Auckland, New Zealand: Helen Danesh Meyer*, • Eye Department, Wellington, Hospital, Wellington, Wells*, New Zealand: Anthony P., Andrew, Riley, Anthony, Bedggood, Helen, Long, Nina Ashraff, • Hospital Sao Jose, Servico de Oftalmologia, Lisbon, Abrantes*, Portugal: Pedro A. L., Maria, Reina, Jose Pedro Silva, Joao Ilharco, • Department of Ophthalmology, National University Hospital, Singapore: Paul Tec Kwan Chew, Lennard, Thean, Lim Boon Ang, Joseph, Manuel, Loon Seng Chee, Clement, Tan, Yeong Suet Ming, • Singapore National Eye Centre, Singapore: Steve Kah Leng Seah, Francis, Oen, Rahat, Husain, Hoh Sek Tian, Aung Tin, • Hospital Clinico San Carlos, Madrid, Spain: Julián Garcia Sánchez, Julián García Feijoo, José María Martínez de La Casa, Alfredo Castillo Gómez, • Hospital Universitario Miguel Servet, Consulta de Ojos, Zaragoza, Spain: Francisco Manuel Honrubia López, Vicente Polo Llorens, Luis Pablo Júlvez, Maria Luisa Gómez Martínez, José Manuel Larrosa Póvez, • Fundación Hospital Alcorcón, Servicio de Oftalmología, Universidad Rey Juan Carlos, Alcorcon, Madrid, Spain: Alfonso Arias Puente, Carmen, Carrasco, Maria del Carmen, García, Yolanda, Andrés Alba, • Hospital Universitario La Princesa, Spain: Elena Gurdiel, Emilio, Dorronzoro, Maria Jesús Muniesa, • Department of Ophthalmology, Tri Service General Hospital, Taipei, Taiwan: Da Wen Lu*, • Consultant Ophthalmologist, Arrowe Park Hospital, Wirral, Merseyside, Clearkin*, UK: Louis G., and Yogesh, Patwala
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Male ,medicine.medical_specialty ,Intraocular pressure ,genetic structures ,Ocular hypertension ,Timolol ,law.invention ,03 medical and health sciences ,chemistry.chemical_compound ,Tonometry, Ocular ,0302 clinical medicine ,Travoprost ,Randomized controlled trial ,Double-Blind Method ,law ,Ophthalmology ,medicine ,Humans ,Prospective Studies ,Latanoprost ,Antihypertensive Agents ,Intraocular Pressure ,Aged ,business.industry ,Repeated measures design ,Cloprostenol ,General Medicine ,medicine.disease ,eye diseases ,Confidence interval ,Treatment Outcome ,chemistry ,Anesthesia ,Prostaglandins F, Synthetic ,030221 ophthalmology & optometry ,Drug Therapy, Combination ,Female ,Ocular Hypertension ,Ophthalmic Solutions ,business ,030217 neurology & neurosurgery ,Glaucoma, Open-Angle ,medicine.drug - Abstract
Purpose The objective of the study was to compare the intraocular pressure (IOP)-lowering efficacy and safety of travoprost 0.004%/timolol 0.5% ophthalmic solution (Trav/Tim) to latanoprost 0.005%/timolol 0.5% ophthalmic solution (Lat/Tim), dosed once daily in the morning, in patients with open-angle glaucoma (OAG) or ocular hypertension (OH). Methods This was a randomized, double-masked, multicenter, parallel group, active-controlled study conducted at 41 sites. At the eligibility visit the patients were randomized (1:1) to the assigned masked medication if they met inclusion/exclusion criteria, and the mean IOP values in the eligible eyes were ≥24 mmHg at 9 AM and ≥21 mmHg at 11 AM and 4 PM. Patients were excluded if the mean IOP in either eye was >36 mmHg. Patients were instructed to administer the assigned medication each morning at 9 AM. During the treatment phase of the study, IOP was measured at 9 AM at week 2, week 6, month 3, and month 9. At the month 6 and month 12 visits, IOP was measured at 9 AM, 11 AM, and 4 PM. Statistical methods included a repeated measures analysis of variance (ANOVA); to test for noninferiority, a 95% confidence interval for the treatment group difference was constructed based on the ANOVA results for each time point at month 12. Results Patients (n=408) with OAG or OH were enrolled at 41 sites. One patient withdrew prior to receiving medication so 207 in the Trav/Tim group and 200 in the Lat/Tim group were evaluable for safety. Baseline demographic characteristics as well as IOP values showed no statistical differences between the two groups. Trav/Tim provided lower mean IOP values than Lat/Tim that were statistically significant at the week 2 9 AM (p=0.0081), month 6 9 AM (p=0.0056), and month 6 11 AM (p=0.0128) time points and at 9 AM time point pooled across all visits (p=0.0235) when mean IOP was 0.6 mmHg lower in the Trav/Tim group. Treatment-related adverse events were mild in both groups. Although hyperemia was reported from a higher percentage of patients in Trav/Tim group, differences in average hyperemia scores between the two groups were not considered clinically relevant. Conclusions Travoprost 0.004%/timolol 0.5% ophthalmic solution produced mean IOP levels that are statistically noninferior to latanoprost 0.005%/timolol 0.5% ophthalmic solution. Furthermore, at 9:00 AM, 24 hours after dosing, IOP was statistically lower for travoprost 0.004%/timolol 0.5% pooled across all visits. Travoprost 0.004%/timolol 0.5% fixed combination ophthalmic solution is an effective treatment for reducing IOP and it is safe and well-tolerated in patients with OAG or OH. (Eur J Ophthalmol 2007; 17: 183–90)
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- 2007
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