80 results on '"Sacchetti, Ml"'
Search Results
2. The Barthel index: italian translation, adaptation and validation
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A. Lauta, Castiglia Sf, Valter Santilli, Giovanni Galeoto, Roberta Mollica, Sacchetti Ml, and A. Palumbo
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validation ,functional disability ,business.industry ,Barthel index ,barthel index ,cultural adaptation ,italian ,Translation (geometry) ,computer.software_genre ,Medicine ,Artificial intelligence ,business ,Adaptation (computer science) ,computer ,Natural language processing - Published
- 2015
3. Agenzia sanitaria e sociale regionale. Servizio Sanitario Regionale Emilia-Romagna. G-PAC. Guida formativa per la PREVENZIONE SECONDARIA degli accidenti cerebrovascolari
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Ferro S, Petetti F, Terri F, Biocca M, Polizzi BM, Basaglia N, Cerrato P, CAvazzuti M, D'Argenio P, Di Pasquale G, Fontana S, Gensini GF, Guidetti D, Lanza G, Liberati A, Malferrari G, MArcello N, Pedrini N, Provinciali L, Rasi S, Ricci S, Sacchetti ML, Sacquegna T, Sterzi R, Tola MR, Tortorici G, Zampolini M, Zaninelli A., BORGHI, CLAUDIO, Ferro S, Petetti F, Terri F, Biocca M, Polizzi BM, Basaglia N, Borghi C, Cerrato P, CAvazzuti M, D'Argenio P, Di Pasquale G, Fontana S, Gensini GF, Guidetti D, Lanza G, Liberati A, Malferrari G, MArcello N, Pedrini N, Provinciali L, Rasi S, Ricci S, Sacchetti ML, Sacquegna T, Sterzi R, Tola MR, Tortorici G, Zampolini M, and Zaninelli A.
- Abstract
progettare e valutare la fattibilità di un piano di formazione per la prevenzione secondaria degli accidenti cerebrovascolari.
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- 2009
4. Nutritional recommendations for the prevention of ischemic stroke
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Rotilio G, Berni Canani R, Barba G, Branca F, Cairella G, Dilaghi B, Fieschi C, Garbagnati F, Gentile MG, Gensini GF, Gualtieri A, Inzitari D, La Massa M, Luisi ML, Mancia G, Marcelli M, Masini ML, Mastrilli F, Paolucci S, Pratesi L, Sacchetti ML, Salvia A, Scalfi L, Scognamiglio U, Siani A, Strazzullo P, Italian Working Group on Nutrition, Stroke P.r.e.v.e.n.t.i.o.n., RUBBA, PAOLO OSVALDO FEDERICO, Rotilio, G, Berni Canani, R, Barba, G, Branca, F, Cairella, G, Dilaghi, B, Fieschi, C, Garbagnati, F, Gentile, Mg, Gensini, Gf, Gualtieri, A, Inzitari, D, La Massa, M, Luisi, Ml, Mancia, G, Marcelli, M, Masini, Ml, Mastrilli, F, Paolucci, S, Pratesi, L, Rubba, PAOLO OSVALDO FEDERICO, Sacchetti, Ml, Salvia, A, Scalfi, L, Scognamiglio, U, Siani, A, Strazzullo, P, Italian Working Group on, Nutrition, and Stroke, P. r. e. v. e. n. t. i. o. n.
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Surgical critical care ,medicine.medical_specialty ,Nutrition and Dietetics ,food ,ischemic stroke ,nutrients ,nutrition ,prevention ,recommendations ,Endocrinology, Diabetes and Metabolism ,Medicine (miscellaneous) ,Brain Ischemia ,Nutrition Policy ,Stroke ,Italy ,Risk Factors ,Stroke prevention ,Family medicine ,Ischemic stroke ,Practice Guidelines as Topic ,medicine ,Physical therapy ,Humans ,Nutritional Physiological Phenomena ,Cardiology and Cardiovascular Medicine ,Nutrition - Abstract
The Italian Working Group on Nutrition and Stroke Prevention G. Rotilio 1,2, R. Berni Canani 2, G. Barba 3, E Branca 4,17, G. Cairella 5,17, B. Dilaghi 6, C. Fieschi 7, E Garbagnati 2, M.G. Gentile 8,17, G.E Gensini 6, A. Gualtieri 7, D. Inzitari 9, M. La Massa 9, M.L.E. Luisi 1°, 17, G. Mancia n, M. Marcelli 12,17, M.L. Masini 13, E Mastrilli 14, S. Paolucci 14 , L. Pratesi 14, P. Rubba 15 , M.L. Sacchetti 7 , A. Salvia 14 , L. Scalfi 16,17, U. Scognamiglio 2, A. Siani 3,17, p. Strazzul1015 1Department of Biology, Tor Vergata University of Rome, 2Centre of Research on Nutrition and Rehabilitation (CeSAR), IRCCS Fondazione S. Lucia, Rome, 3Institute of Food Sciences, CNR, Avellino, 4National Institute for Research on Food and Nutrition (1NRAN), Rome, 5Department of Prevention Nutrition Unit ASL RMB, Rome, 6Department of Medical and Surgical Critical Care, Section of Clinical Medicine and Cardiology, A.O.U. Careggi, Florence, 7Department of Neurology, University "La Sapienza", Rome, 8Clincal Nutrition Unit, Niguarda Hospital, Milan, 9Department of Neurological and Psychiatric Sciences, University of Florence, 1°Don Carlo Gnocchi Foundation, IRCCS Florence, 11Department of Clinical Medicine, Prevention and Applied Biotechnologies, University of Milano-Bicocca, Monza, 12Clinical Nutrition Unit A.O.S. Giovanni Addolorata, Rome, 13Dietetic Unit A.O.U. Careggi, Florence, 14IRCCS Fondazione S. Lucia, Rome, 15Department of Clinical and Experimental Medicine, Federico 1I University of Naples, 16Department of Food Science, Federico II University of Naples, and 17Italian Society of Human Nutrition (SINU)
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- 2004
5. Nutrizione e Ictus
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ROTILIO G, BERNI CANANI, ROBERTO, BRANCA F, CAIRELLA G, FIESCHI C, GARBAGNATI F, GENTILE MG, GENSINI GF, GUALTIERI A, LUISI MLE, MARCELLI M, MASINI ML, MASTRILLI F, PAOLUCCI S, PRATESI L, SACCHETTI ML, SALVIA A, SCALFI, LUCA, SCOGNAMIGLIO U, STRAZZULLO, PASQUALE, GENSINI F CCORDINATORE, Rotilio, G, BERNI CANANI, Roberto, Branca, F, Cairella, G, Fieschi, C, Garbagnati, F, Gentile, Mg, Gensini, Gf, Gualtieri, A, Luisi, Mle, Marcelli, M, Masini, Ml, Mastrilli, F, Paolucci, S, Pratesi, L, Sacchetti, Ml, Salvia, A, Scalfi, Luca, Scognamiglio, U, and Strazzullo, Pasquale
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- 2003
6. SPREAD: Stroke Prevention and Educational Awareness Diffusion (IV Edizione); Ictus cerebrale:linee guida italiane di prevenzione e trattamento ,Cap. 7- Prevenzione primaria
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Rotilio G, Barba G, Berni Canani R, Branca F, Cairella G, Garbagnati F, Gensini GF, Sacchetti ML, Salvia A, Sandri G, Scalfi L, Scognamiglio U, Siani A, and Strazzullo P
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- 2007
7. SPREAD: Stroke Prevention and Educational Awareness Diffusion (IV Edizione); Ictus cerebrale:linee guida italiane di prevenzione e trattamento. Cap. 7
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Garbagnati F, Gentile MG, Gensini GF, Luisi MLE, Marcelli M, Masini ML, Muscaritoli M, Paolucci S, Pratesi L, Sacchetti ML, Salvia A, Scalfi L, Siani A, Scognamiglio U, and Strazzullo P
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- 2006
8. Efficacy of acute stroke patients management in an Emergency Departement Stroke Unit (EDSU)
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Durastanti, L, Puca, E, Di Angelantonio, E, Lorenzano, S, Falcou, A, Gori, Mc, Sacchetti, Ml, Fiorelli, M, Cavalletti, C, Colosimo, C, Prencipe, M, and Toni, D
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- 2005
9. Caratteristiche cliniche, criteri diagnostici e fattori di rischio nella depressione post-stroke (PSD). Preliminare di studio in aperto controllato per il trattamento della PSD con sertralina
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Ricciardi, A, Ruberto, A, Cavallo, A, Dassiè, F, Travisi, M, Ferrari, M, Lorenzano, S, Sacchetti, Ml, Rasura, M, Fieschi, C, Girardi, P, and Tatarelli, R
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- 2004
10. Elevated troponin levels on Emergency Department admission independently predict short and long-term mortality in ischemic stroke patients
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Di Angelantonio, E, Bonanni, L, Suppa, M, Toni, D, Sacchetti, Ml, Cavalletti, C, Lorenzano, S, Ciarla, Mv, Argentino, C, and Fiorelli, M
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- 2003
11. Circadian variation in the time of stroke onset. The experience of the Emergency Department Stroke Unit of Rome
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Lorenzano, S, Toni, D, Anzini, A, Cavalletti, C, Colosimo, C, De Michele, M, Fausti, S, Fiorelli, M, Morino, S, Sacchetti, Ml, and Argentino
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- 2002
12. How many patients in a stroke population may receive thrombolysis? The experience of a stroke unit located in an emergency department
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Lorenzano, S, Toni, D, Falcou, A, Di Angelantonio, E, Colosimo, C, Fiorelli, M, Cavalletti, C, Sacchetti, Ml, Romano, A, Anzini, A, Argentino, C, and Fieschi, C
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- 2001
13. A randomized double blind clinical trial will be run to assess efficacy and safety of sertraline vs placebo in PSD (post stroke depression) within 6 months after the cerebrovascular event
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Ricciardi, A, Ruberto, A, Girardi, P, Gallo, V, Lorenzano, S, Soscia, F, Sacchetti, Ml, Argentino, C, and Tatarelli, R
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- 2001
14. Psychiatric disorders: prevalence and evolution after stroke in the ‘La Sapienza’ University Emergency Department Stroke Unit
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Lorenzano, S, Gallo, V, Sacchetti, Ml, Ruberto, A, Ricciardi, A, Soscia, F, Paolucci, S, and Argentino, C
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- 2001
15. Admission screening for ischemic heart disease in a stroke unit located in an emergency department. The East Rome Stroke Study (EROSS)
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Di Angelantonio, E, Cavalletti, C, Toni, D, Lorenzano, S, Falcou, A, Sacchetti, Ml, De Michele, M, Colosimo, C, Fiorelli, M, Argentino, C, and Fieschi, C
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- 2001
16. Stupor e coma all'esordio di un stroke cerebrale acuto: Risultati dal registro della Stroke Unit del Policlinico Universitario Umberto I di Roma
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Argentino, C, Di Angelantonio, E, Falcou, A, Fiorelli, M, Sacchetti, Ml, Toni, D, Rasura, M, Lorenzano, S, and Fieschi, C
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- 1999
17. The Rome Emergency Departments Network for Acute Stroke: pilot study on incidence, referral pathways, and eligibility for thrombolytic therapy in Rome urban area
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Fiorelli, M, Falcou, A, Sacchetti, Ml, Toni, D, Di Angelantonio, E, Ferrari, M, Lorenzano, S, Tomassini, V, Argentino, C, and on behalf of the Coordinamento degli Ospedali Romani per l’ictus
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- 1999
18. Early parenchymal hypodensity at CT scan heralds a subsequent territorial infarction in patients with acute ischemic stroke
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Fiorelli, Marco, Bastianello, Stefano, Danilo Toni, Sacchetti Ml Montinaro, E., Falcou, A., and Argentino, Corrado
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- 1995
19. Neuropsychiatric treatments in medieval Rome
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Sacchetti Ml, Lucchi N, and Fieschi C
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History ,History and Philosophy of Science ,Traditional medicine ,Italy ,General Neuroscience ,Mental Disorders ,Humans ,Neurology (clinical) ,Therapeutics ,Ancient history ,Nervous System Diseases ,History, Medieval - Published
- 1993
20. Acute ischemic strokes improving during the first 48 hours of onset: predictability, outcome, and possible mechanisms. A comparison with early deteriorating strokes.
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Toni D, Fiorelli M, Bastianello S, Falcou A, Sette G, Ceschin V, Sacchetti ML, Argentino C, Toni, D, Fiorelli, M, Bastianello, S, Falcou, A, Sette, G, Ceschin, V, Sacchetti, M L, and Argentino, C
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- 1997
- Full Text
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21. Is it time to definitely abandon neuroprotection in acute ischemic stroke?
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Sacchetti ML and Sacchetti, Maria Luisa
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- 2008
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22. An emergency clinical pathway for stroke patients--results of a cluster randomised trial (isrctn41456865).
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De Luca A, Toni D, Lauria L, Sacchetti ML, Giorgi Rossi P, Ferri M, Puca E, Prencipe M, Guasticchi G, IMPLementazione Percorso Clinico Assistenziale ICtus Acuto (IMPLICA) Study Group, De Luca, Assunta, Toni, Danilo, Lauria, Laura, Sacchetti, Maria Luisa, Giorgi Rossi, Paolo, Ferri, Marica, Puca, Emanuele, Prencipe, Massimiliano, and Guasticchi, Gabriella
- Abstract
Background: Emergency Clinical Pathways (ECP) for stroke have never been tested in randomized controlled trials (RCTs).Objective: To evaluate the effectiveness of an ECP for stroke patients in Latium (Italy) emergency system.Methods: cluster-RCT designed to compare stroke patient referrals by Emergency Medical Service (EMS) and Emergency Room (ER) health professionals trained in the ECP, with those of non-trained EMS and ER controls. Primary outcome measure was the proportion of eligible (aged = 80 and symptom onset = 6 hours) stroke patients referred to a stroke unit (SU). Intention to treat (ITT) and per-protocol (PP) analyses were performed, and risk ratios (RR) adjusted by age, gender and area, were calculated.Results: 2656 patients in the intervention arm and 2239 in the control arm required assistance; 78.3% of the former and 80.6% of the latter were admitted to hospitals, and respectively 74.8% and 78.3% were confirmed strokes. Of the eligible confirmed strokes, 106/434 (24.4%) in the intervention arm and 43/328 (13.1%) in the control arm were referred to the SU in the ITT analysis (RR = 2.01; 95% CI: 0.79-4.00), and respectively 105/243 (43.2%) and 43/311 (13.8%) in the PP analysis (RR = 3.21; 95%CI: 1.62-4.98). Of patients suitable for i.v. thrombolysis, 15/175 (8.6%) in the intervention arm and 2/115 (1.7%) in the control arm received thrombolysis (p = 0.02) in the ITT analysis, and respectively 15/99 (15.1%) and 2/107 (1.9%)(p = 0.001) in the PP analysis.Conclusion: Our data suggest potenti efficiency and feasibility of an ECP. The integration of EMS and ERs with SU networks for organised acute stroke care is feasible and may ameliorate the quality of care for stroke patients.Trial Registration: Current Controlled Trials (ISRCTN41456865). [ABSTRACT FROM AUTHOR]- Published
- 2009
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23. Transforming guidelines in routine practice.
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Sacchetti ML, Toni D, Prencipe M, Sacchetti, Maria Luisa, Toni, Danilo, and Prencipe, Massimiliano
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- 2008
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24. Targeting stroke awareness public campaigns.
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Sacchetti ML, Di Mascio MT, Pelone G, Gallo V, Prencipe M, Sacchetti, Maria Luisa, Di Mascio, Maria Teresa, Pelone, Giordana, Gallo, Valentina, and Prencipe, Massimiliano
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- 2008
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25. Major adverse cardiovascular events in non-valvular atrial fibrillation with chronic obstructive pulmonary disease: the ARAPACIS study
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Raparelli, Valeria, Pastori, Daniele, Pignataro, Serena Francesca, Vestri, Anna Rita, Pignatelli, Pasquale, Cangemi, Roberto, Proietti, Marco, Davì, Giovanni, Hiatt, William Robert, Lip, Gregory Yoke Hong, Corazza, Gino Roberto, Perticone, Francesco, Violi, Francesco, Basili, Stefania, Alessandri, C., Serviddio, G., Palange, P., Greco, E., Bruno, G., Averna, M., Giammanco, A., Sposito, P., de Cristofaro, R., Carulli, L., de Gennaro, L., Pellegrini, E., Cominacini, L., Mozzini, C., Pasini, A. F., Sprovieri, M., Spagnuolo, V., Cerqua, G., Cerasola, G., Mulé, G., Barbagallo, M., Lo Sciuto, S., Monteverde, A., Saitta, A., Lo Gullo, A., Malatino, L., Cilia, C., Terranova, V., Pisano, M., Pinto, A., Di Raimondo, D., Tuttolomondo, A., Conigliaro, R., Signorelli, S., de Palma, D., Galderisi, M., Cudemo, G., Galletti, F., Fazio, V., de Luca, N., Meccariello, A., Caputo, D., de Donato, M. T., Iannuzi, A., Bresciani, A., Giunta, R., Utili, R., Iorio, V., Adinolfi, L. E., Sellitto, C., Iuliano, N., Bellis, P., Tirelli, P., Sacerdoti, D., Vanni, D., Iuliano, L., Ciacciarelli, M., Pacelli, A., Palazzuoli, A., Cacciafesta, M., Gueli, N., Lo Iacono, C., Brusco, S., Verrusio, W., Nobili, L., Tarquinio, N., Pellegrini, F., Vincentelli, G. M., Ravallese, F., Santini, C., Letizia, C., Petramala, L., Zinnamosca, L., Minisola, S., Cilli, M., Colangelo, L., Falaschi, P., Martocchia, A., Pastore, F., Bertazzoni, G., Attalla El Halabieh, E., Paradiso, M., Lizzi, E. M., Timmi, S., Battisti, P., Cerci, S., Ciavolella, M., Di Veroli, C., Malci, F., de Ciocchis, A., Abate, D., Castellino, P., Zanoli, L., Fidone, F., Mannarino, E., Pasqualini, L., Oliverio, G., Pende, A., Artom, N., Ricchio, R., Fimognari, F. L., Alletto, M., Messina, S., Sesti, G., Arturi, F., Succurro, E., Fiorentino, T. V., Pedace, E., Scarpino, P. E., Carullo, G., Maio, R., Sciacqua, A., Frugiuele, P., Battaglia, G., Atzori, S., Delitala, G., Angelucci, E., Sestili, S., Traisci, G., de Feudis, L., Di Michele, D., Fava, A., Balsano, C., de Ciantis, P., Desideri, G., Camerota, A., Mezzetti, M., Gresele, P., Vedovati, C., Fierro, T., Puccetti, L., Bertolotti, M., Mussi, C., Boddi, M., Savino, A., Contri, S., Degl’Innocenti, G., Saller, A., Fabris, F., Pesavento, R., Filippi, L., Vedovetto, V., Puato, M., Treleani, M., de Luca, E., de Zaiacomo, F., Giantin, V., Semplicini, A., Minuz, P., Romano, S., Fantin, F., Manica, A., Stockner, I., Pattis, P., Gutmann, B., Catena, C., Colussi, G., Sechi, L. A., Annoni, G., Bruni, A. A., Castagna, A., Spinelli, D., Miceli, E., Padula, D., Schinco, G., Spreafico, S., Secchi, B., Vanoli, M., Casella, G., Pulixi, E. A., Sansone, L., Serra, M. G., Longo, S., Antonaci, S., Belfiore, A., Frualdo, M., Palasciano, G., Ricci, L., Ventrella, F., Bianco, C., Santovito, D., Cipollone, F., Nicolai, S., Salvati, F., Rini, G. B., Scozzari, F., Muiesan, M. L., Salvetti, M., Bazza, A., Picardi, A., Vespasiani-Gentilucci, U., de Vincentis, A., Cosio, P., Terzolo, M., Madaffari, B., Parasporo, B., Fenoglio, L., Bracco, C., Melchio, R., Gentili, T., Salvi, A., Nitti, C., Gabrielli, A., Martino, G. P., Capucci, A., Brambatti, M., Sparagna, A., Tirotta, D., Andreozzi, P., Ettorre, E., Viscogliosi, G., Servello, A., Musumeci, M., Delfino, M., Giorgi, A., Glorioso, N., Melis, G., Marras, G., Matta, M., Sacco, A., Stellitano, E., Scordo, A., Russo, F., Caruso, A. A., Porreca, E., Tana, M., Ferri, C., Cheli, P., Portincasa, P., Muscianisi, G., Giordani, S., Stanghellini, V., Sabbà, C., Mancuso, G., Bartone, M., Calipari, D., Arcidiacono, G., Bellanuova, I., Ferraro, M., Marigliano, G., Cozzolino, D., Lampitella, A., Acri, V., Galasso, D., Mazzei, F., Buratti, A., Galasso, S., Porta, M., Brizzi, M. F., Fattorini, A., Sampietro, F., D’Angelo, A., Manfredini, R., Pala, M., Fabbian, F., Moroni, C., Valente, L., Lopreiato, F., Parente, F., Granata, M., Moia, M., Braham, S., Rossi, M., Pesce, M., Gentile, A., Catozzo, V., Baciarello, G., Cosimati, A., Ageno, W., Rancan, E., Guasti, L., Ciccaglioni, A., Negri, S., Polselli, M., Prisco, D., Marcucci, R., Ferro, D., Perri, L., Cangemi, R., Saliola, M., Del Ben, M., Angelico, F., Baratta, F., Migliacci, R., Porciello, G., Corrao, S., Proietti, M., Raparelli, V., Napoleone, L., Talerico, G., Amoroso, D., Romiti, G. F., Ruscio, E., Toriello, F., Sperduti, N., Todisco, T., Di Tanna, G., Sacchetti, M. L., Puddu, P. E., Farcomeni, A., Anzaldi, M., Bazzini, C., Bianchi, P. I., Boari, B., Buonauro, A., Buttà, C., Buzzetti, E., Calabria, S., Capeci, W., Caradio, F., Carleo, P., Carrabba, M. D., Castorani, L., Cecchetto, L., Cicco, S., Cimini, C., Colombo, B. M., de Giorgi, A., de Vuono, S., Del Corso, L., Denegri, A., Di Giosia, P., Durante Mangoni, E., Falsetti, L., Forgione, A., Giorgini, P., Grassi, D., Grembiale, A., Hijazi, D., Iamele, L., Lorusso, G., Marchese, A., Marra, A. M., Masala, M., Miceli, G., Montebianco Abenavoli, L., Murgia, G., Naccarato, P., Pattoneri, P., Perego, F., Pesce, P., Piano, S., Pinna, M., Pinto, D., Pretti, V., Pucci, G., Salinaro, F., Salzano, A., Santilli, F., Scarpini, F., Scicali, R., Sirico, D., Suppressa, P., Talia, M., Tassone, E. J., Torres, D., Vazzana, N., Vecchio, C. R., Vidili, G., Vitale, F., Zaccone, V., ARAPACIS Study Collaborators, Raparelli, V, Pastori, D, Pignataro, S, Vestri, A, Pignatelli, P, Cangemi, R, Proietti, M, Davi, G, Hiatt, W, Lip, G, Corazza, G, Perticone, F, Violi, F, Basili, S, Alessandri, C, Serviddio, G, Palange, P, Greco, E, Bruno, G, Averna, M, Giammanco, A, Sposito, P, Decristofaro, R, Carulli, L, Degennaro, L, Pellegrini, E, Cominacini, L, Mozzini, C, Pasini, A, Sprovieri, M, Spagnuolo, V, Cerqua, G, Cerasola, G, Mule, G, Barbagallo, M, Lo Sciuto, S, Monteverde, A, Saitta, A, Lo Gullo, A, Malatino, L, Cilia, C, Terranova, V, Pisano, M, Pinto, A, Diraimondo, D, Tuttolomondo, A, Conigliaro, R, Signorelli, S, Depalma, D, Galderisi, M, Cudemo, G, Galletti, F, Fazio, V, Deluca, N, Meccariello, A, Caputo, D, Dedonato, M, Iannuzi, A, Bresciani, A, Giunta, R, Utili, R, Iorio, V, Adinolfi, L, Sellitto, C, Iuliano, N, Bellis, P, Tirelli, P, Sacerdoti, D, Vanni, D, Iuliano, L, Ciacciarelli, M, Pacelli, A, Palazzuoli, A, Cacciafesta, M, Gueli, N, Lo Iacono, C, Brusco, S, Verrusio, W, Nobili, L, Tarquinio, N, Pellegrini, F, Vincentelli, G, Ravallese, F, Santini, C, Letizia, C, Petramala, L, Zinnamosca, L, Minisola, S, Cilli, M, Colangelo, L, Falaschi, P, Martocchia, A, Pastore, F, Bertazzoni, G, Attalla El Halabieh, E, Paradiso, M, Lizzi, E, Timmi, S, Battisti, P, Cerci, S, Ciavolella, M, Diveroli, C, Malci, F, Deciocchis, A, Abate, D, Castellino, P, Zanoli, L, Fidone, F, Mannarino, E, Pasqualini, L, Oliverio, G, Pende, A, Artom, N, Ricchio, R, Fimognari, F, Alletto, M, Messina, S, Sesti, G, Arturi, F, Succurro, E, Fiorentino, T, Pedace, E, Scarpino, P, Carullo, G, Maio, R, Sciacqua, A, Frugiuele, P, Battaglia, G, Atzori, S, Delitala, G, Angelucci, E, Sestili, S, Traisci, G, Defeudis, L, Dimichele, D, Fava, A, Balsano, C, Deciantis, P, Desideri, G, Camerota, A, Mezzetti, M, Gresele, P, Vedovati, C, Fierro, T, Puccetti, L, Bertolotti, M, Mussi, C, Boddi, M, Savino, A, Contri, S, Degl'Innocenti, G, Saller, A, Fabris, F, Pesavento, R, Filippi, L, Vedovetto, V, Puato, M, Treleani, M, Deluca, E, Dezaiacomo, F, Giantin, V, Semplicini, A, Minuz, P, Romano, S, Fantin, F, Manica, A, Stockner, I, Pattis, P, Gutmann, B, Catena, C, Colussi, G, Sechi, L, Annoni, G, Bruni, A, Castagna, A, Spinelli, D, Miceli, E, Padula, D, Schinco, G, Spreafico, S, Secchi, B, Vanoli, M, Casella, G, Pulixi, E, Sansone, L, Serra, M, Longo, S, Antonaci, S, Belfiore, A, Frualdo, M, Palasciano, G, Ricci, L, Ventrella, F, Bianco, C, Santovito, D, Cipollone, F, Nicolai, S, Salvati, F, Rini, G, Scozzari, F, Muiesan, M, Salvetti, M, Bazza, A, Picardi, A, Vespasiani-Gentilucci, U, Devincentis, A, Cosio, P, Terzolo, M, Madaffari, B, Parasporo, B, Fenoglio, L, Bracco, C, Melchio, R, Gentili, T, Salvi, A, Nitti, C, Gabrielli, A, Martino, G, Capucci, A, Brambatti, M, Sparagna, A, Tirotta, D, Andreozzi, P, Ettorre, E, Viscogliosi, G, Servello, A, Musumeci, M, Delfino, M, Giorgi, A, Glorioso, N, Melis, G, Marras, G, Matta, M, Sacco, A, Stellitano, E, Scordo, A, Russo, F, Caruso, A, Porreca, E, Tana, M, Ferri, C, Cheli, P, Portincasa, P, Muscianisi, G, Giordani, S, Stanghellini, V, Sabba, C, Mancuso, G, Bartone, M, Calipari, D, Arcidiacono, G, Bellanuova, I, Ferraro, M, Marigliano, G, Cozzolino, D, Lampitella, A, Acri, V, Galasso, D, Mazzei, F, Buratti, A, Galasso, S, Porta, M, Brizzi, M, Fattorini, A, Sampietro, F, D'Angelo, A, Manfredini, R, Pala, M, Fabbian, F, Moroni, C, Valente, L, Lopreiato, F, Parente, F, Granata, M, Moia, M, Braham, S, Rossi, M, Pesce, M, Gentile, A, Catozzo, V, Baciarello, G, Cosimati, A, Ageno, W, Rancan, E, Guasti, L, Ciccaglioni, A, Negri, S, Polselli, M, Prisco, D, Marcucci, R, Ferro, D, Perri, L, Saliola, M, Delben, M, Angelico, F, Baratta, F, Migliacci, R, Porciello, G, Corrao, S, Napoleone, L, Talerico, G, Amoroso, D, Romiti, G, Ruscio, E, Toriello, F, Sperduti, N, Todisco, T, Ditanna, G, Sacchetti, M, Puddu, P, Farcomeni, A, Anzaldi, M, Bazzini, C, Bianchi, P, Boari, B, Buonauro, A, Butta, C, Buzzetti, E, Calabria, S, Capeci, W, Caradio, F, Carleo, P, Carrabba, M, Castorani, L, Cecchetto, L, Cicco, S, Cimini, C, Colombo, B, De Giorgi, A, Devuono, S, Delcorso, L, Denegri, A, Digiosia, P, Durante Mangoni, E, Falsetti, L, Forgione, A, Giorgini, P, Grassi, D, Grembiale, A, Hijazi, D, Iamele, L, Lorusso, G, Marchese, A, Marra, A, Masala, M, Miceli, G, Montebianco Abenavoli, L, Murgia, G, Naccarato, P, Pattoneri, P, Perego, F, Pesce, P, Piano, S, Pinna, M, Pinto, D, Pretti, V, Pucci, G, Salinaro, F, Salzano, A, Santilli, F, Scarpini, F, Scicali, R, Sirico, D, Suppressa, P, Talia, M, Tassone, E, Torres, D, Vazzana, N, Vecchio, C, Vidili, G, Vitale, F, Zaccone, V, Raparelli, V1, Pastori, D1, Pignataro, Sf1, Vestri, Ar2, Pignatelli, P1, Cangemi, R1, Proietti, M3, Davì, G4, Hiatt, Wr5, Lip, Gyh3, Corazza, Gr6, Perticone, F7, Violi, F8, Basili, S1, De Cristofaro, R, De Gennaro, L, Pasini, Af, Mulé, G, Di Raimondo, D, De Palma, D, De Luca, N, De Donato, Mt, Adinolfi, Le, Vincentelli, Gm, Lizzi, Em, Di Veroli, C, De Ciocchis, A, Fimognari, Fl, Fiorentino, Tv, Scarpino, Pe, De Feudis, L, Di Michele, D, De Ciantis, P, De Luca, E, De Zaiacomo, F, Sechi, La, Bruni, Aa, Pulixi, Ea, Serra, Mg, Rini, Gb, Muiesan, Ml, De Vincentis, A, Martino, Gp, Caruso, Aa, Sabbà, C, Brizzi, Mf, Del Ben, M, Romiti, Gf, Di Tanna, G, Sacchetti, Ml, Puddu, Pe, Bianchi, Pi, Buttà, C, Carrabba, Md, Colombo, Bm, De Vuono, S, Del Corso, L, Di Giosia, P, Marra, Am, Tassone, Ej, Vecchio, Cr, Zaccone, V., Pignataro, Sf, Vestri, Ar, Davì, G, Hiatt, Wr, Lip, Gyh, Corazza, Gr, Raparelli, Valeria, Pastori, Daniele, Pignataro, Serena Francesca, Vestri, Anna Rita, Pignatelli, Pasquale, Cangemi, Roberto, Proietti, Marco, Davì, Giovanni, Hiatt, William Robert, Lip, Gregory Yoke Hong, Corazza, Gino Roberto, Perticone, Francesco, Violi, Francesco, Basili, Stefania, Alessandri C., Serviddio G., Palange P., Greco E., Bruno G., Averna M., Giammanco A., Sposito P., De Cristofaro R., Carulli L., De Gennaro L., Pellegrini E. Cominacini L., Mozzini C., Pasini A.F., Sprovieri M., Spagnuolo V., Cerqua G., Cerasola G., Mulé G., Barbagallo M., Lo Sciuto S., Monteverde A., Saitta A., Lo Gullo A., Malatino L., Cilia C., Terranova V., Pisano M., Pinto A., Di Raimondo D., Tuttolomondo A., Conigliaro R., Signorelli S., De Palma D., Galderisi M., Cudemo G., Galletti F., Fazio V., De Luca N., Meccariello A., Caputo D., De Donato M. T., Iannuzi A., Bresciani A., Giunta R., Utili R., Iorio V., Adinolfi L.E., Sellitto C., Iuliano N., Bellis P., Tirelli P., Sacerdoti D., Vanni D., Iuliano L., Ciacciarelli M., Pacelli A., Palazzuoli A., Cacciafesta M., Gueli N., Lo Iacono C., Brusco S., Verrusio W., Nobili L., Tarquinio N., Pellegrini F., Vincentelli G.M., Ravallese F., Santini C., Letizia C., Petramala L., Zinnamosca L., Minisola S., Cilli M., Colangelo L., Falaschi P., Martocchia A., Pastore F., Bertazzoni G., Attalla El Halabieh E., Paradiso M., Lizzi E.M., Timmi S., Battisti P., Cerci S., Ciavolella M., Di Veroli C., Malci F., De Ciocchis A., Abate D., Castellino P., Zanoli L., Fidone F., Mannarino E., Pasqualini L., Oliverio G., Pende A., Artom N., Ricchio R., Fimognari F.L., Alletto M., Messina S., Sesti G., Arturi F., Succurro E, Fiorentino T.V., Pedace E., Scarpino P.E., Carullo G., Maio R., Sciacqua A., Frugiuele P., Spagnuolo V., Battaglia G., Atzori S., Delitala G., Angelucci E., Sestili S., Traisci G., De Feudis L., Di Michele D., Fava A., Balsano C., De Ciantis P., Desideri G., Camerota A., Mezzetti M., Gresele P., Vedovati C., Fierro T., Puccetti L., Bertolotti M., Mussi C., Boddi M., Savino A., Contri S., Degl’Innocenti G., Saller A., Fabris F., Pesavento R., Filippi L., Vedovetto V., Puato M., Fabris F., Treleani M., De Luca E., De Zaiacomo F., Giantin V., Semplicini A., Minuz P., Romano S., Fantin F., Manica A., Stockner I., Pattis P., Gutmann B., Catena C., Colussi G., Sechi L.A., Annoni G., Bruni A.A., Castagna A., Spinelli D., Miceli E., Padula D., Schinco G., Spreafico S., Secchi B., Vanoli M., Casella G., Pulixi E.A., Sansone L., Serra M.G., Longo S., Antonaci S., Belfiore A., Frualdo M., Palasciano G., Ricci L., Ventrella F., Bianco C., Santovito D., Cipollone F., Nicolai S., Salvati F., Rini G. B., Scozzari F., Muiesan M.L., Salvetti M., Bazza A., Picardi A., Vespasiani-Gentilucci U., De Vincentis A., Cosio P., Terzolo M., Madaffari B., Parasporo B., Fenoglio L., Bracco C., Melchio R., Gentili T., Salvi A., Nitti C., Gabrielli A., Martino G.P., Capucci A., Brambatti M., Sparagna A., Tirotta D., Andreozzi P., Ettorre E., Viscogliosi G., Servello A., Musumeci M., Delfino M., Giorgi A., Glorioso N., Melis G., Marras G., Matta M., Sacco A., Stellitano E., Scordo A., Russo F., Caruso A.A., Porreca E., Tana M., Ferri C., Cheli P., Portincasa P., Muscianisi G., Giordani S., Stanghellini V., Sabbà C., Mancuso G., Bartone M., Calipari D., Arcidiacono G., Bellanuova I., Ferraro M., Marigliano G., Cozzolino D., Lampitella A., Acri V., Galasso D., Mazzei F., Buratti A., Galasso S., Porta M., Brizzi M.F., Fattorini A., Sampietro F., D’Angelo A., Manfredini R., Pala M., Fabbian F., Moroni C., Valente L., Lopreiato F., Parente F., Granata M., Moia M., Braham S., Rossi M., Pesce M., Gentile A., Catozzo V., Baciarello G., Cosimati A., Ageno W., Rancan E., Guasti L., Ciccaglioni A., Negri S., Polselli M., Prisco D., Marcucci R., Ferro D., Perri L., Cangemi R., Saliola M., Del Ben M., Angelico F., Baratta F., Migliacci R., Porciello G., Corrao S. Data entry and Safety Monitoring Board: Proietti M., Raparelli V., Napoleone L., Talerico G., Amoroso D., Romiti G.F., Ruscio E., Toriello F., Sperduti N., Todisco T., Di Tanna G., Sacchetti M.L., Puddu P.E., Farcomeni A. Simi Young Internists Group: Anzaldi M., Bazzini C., Bianchi P.I., Boari B., Bracco C., Buonauro A., Buttà C., Buzzetti E., Calabria S., Capeci W., Caradio F., Carleo P., Carrabba M.D., Castorani L., Cecchetto L., Cicco S., Cimini C., Colombo B.M., De Giorgi A., De Vuono S., Del Corso L., Denegri A., Di Giosia P., Durante Mangoni E., Falsetti L., Forgione A., Giorgini P., Grassi D., Grembiale A., Hijazi D., Iamele L., Lorusso G., Marchese A., Marra A.M., Masala M., Miceli G., Montebianco Abenavoli L., Murgia G., Naccarato P., Padula D., Pattoneri P., Perego F., Pesce P., Piano S., Pinna M., Pinto D., Pretti V., Pucci G., Salinaro F., Salzano A., Santilli F., Scarpini F., Scicali R., Sirico D., Suppressa P., Talia M., Tassone E.J., Torres D., Vazzana N., Vecchio C.R., Vidili G., Vitale F., Zaccone V., Raparelli Valeria, Pastori Daniele, Pignataro Serena Francesca, Vestri Anna Rita, Pignatelli Pasquale, Cangemi Roberto, Proietti Marco, Davì Giovanni, Hiatt William Robert, Lip Gregory Yoke Hong, Corazza Gino Roberto, Perticone Francesco, Violi Francesco, Basili Stefania, Alessandri C, Serviddio G, Palange P, Greco E, Bruno G, Averna M, Giammanco A, Sposito P, De Cristofaro R, Carulli L, De Gennaro L, Pellegrini E, Cominacini L, Mozzini C, Pasini AF, Sprovieri M, Spagnuolo V, Cerqua G, Cerasola G, Mulé G, Barbagallo M, Lo Sciuto S, Monteverde A, Saitta A, Lo Gullo A, Malatino L, Cilia C, Terranova V, Pisano M, Pinto A, Di Raimondo D, Tuttolomondo A, Conigliaro R, Signorelli S, De Palma D, Galderisi M, Cudemo G, Galletti F, Fazio V, De Luca N, Meccariello A, Caputo D, De Donato MT, Iannuzi A, Bresciani A, Giunta R, Utili R, Iorio V, Adinolfi LE, Sellitto C, Iuliano N, Bellis P, Tirelli P, Sacerdoti D, Vanni D, Iuliano L, Ciacciarelli M, Pacelli A, Palazzuoli A, Cacciafesta M, Gueli N, Lo Iacono C, Brusco S, Verrusio W, Nobili L, Tarquinio N, Pellegrini F, Vincentelli GM, Ravallese F, Santini C, Letizia C, Petramala L, Zinnamosca L, Minisola S, Cilli M, Colangelo L, Falaschi P, Martocchia A, Pastore F, Bertazzoni G, Attalla El Halabieh E, Paradiso M, Lizzi EM, Timmi S, Battisti P, Cerci S, Ciavolella M, Di Veroli C, Malci F, De Ciocchis A, Abate D, Castellino P, Zanoli L, Fidone F, Mannarino E, Pasqualini L, Oliverio G, Pende A, Artom N, Ricchio R, Fimognari FL, Alletto M, Messina S, Sesti G, Arturi F, Succurro E, Fiorentino TV, Pedace E, Scarpino PE, Carullo G, Maio R, Sciacqua A, Frugiuele P, Battaglia G, Atzori S, Delitala G, Angelucci E, Sestili S, Traisci G, De Feudis L, Di Michele D, Fava A, Balsano C, De Ciantis P, Desideri G, Camerota A, Mezzetti M, Gresele P, Vedovati C, Fierro T, Puccetti L, Bertolotti M, Mussi C, Boddi M, Savino A, Contri S, Degl’Innocenti G, Saller A, Fabris F, Pesavento R, Filippi L, Vedovetto V, Puato M, Treleani M, De Luca E, De Zaiacomo F, Giantin V, Semplicini A, Minuz P, Romano S, Fantin F, Manica A, Stockner I, Pattis P, Gutmann B, Catena C, Colussi G, Sechi LA, Annoni G, Bruni AA, Castagna A, Spinelli D, Miceli E, Padula D, Schinco G, Spreafico S, Secchi B, Vanoli M, Casella G, Pulixi EA, Sansone L, Serra MG, Longo S, Antonaci S, Belfiore A, Frualdo M, Palasciano G, Ricci L, Ventrella F, Bianco C, Santovito D, Cipollone F, Nicolai S, Salvati F, Rini GB, Scozzari F, Muiesan ML, Salvetti M, Bazza A, Picardi A, Vespasiani-Gentilucci U, De Vincentis A, Cosio P, Terzolo M, Madaffari B, Parasporo B, Fenoglio L, Bracco C, Melchio R, Gentili T, Salvi A, Nitti C, Gabrielli A, Martino GP, Capucci A, Brambatti M, Sparagna A, Tirotta D, Andreozzi P, Ettorre E, Viscogliosi G, Servello A, Musumeci M, Delfino M, Giorgi A, Glorioso N, Melis G, Marras G, Matta M, Sacco A, Stellitano E, Scordo A, Russo F, Caruso AA, Porreca E, Tana M, Ferri C, Cheli P, Portincasa P, Muscianisi G, Giordani S, Stanghellini V, Sabbà C, Mancuso G, Bartone M, Calipari D, Arcidiacono G, Bellanuova I, Ferraro M, Marigliano G, Cozzolino D, Lampitella A, Acri V, Galasso D, Mazzei F, Buratti A, Galasso S, Porta M, Brizzi MF, Fattorini A, Sampietro F, D’Angelo A, Manfredini R, Pala M, Fabbian F, Moroni C, Valente L, Lopreiato F, Parente F, Granata M, Moia M, Braham S, Rossi M, Pesce M, Gentile A, Catozzo V, Baciarello G, Cosimati A, Ageno W, Rancan E, Guasti L, Ciccaglioni A, Negri S, Polselli M, Prisco D, Marcucci R, Ferro D, Perri L, Cangemi R, Saliola M, Del Ben M, Angelico F, Baratta F, Migliacci R, Porciello G, Corrao S, Proietti M, Raparelli V, Napoleone L, Talerico G, Amoroso D, Romiti GF, Ruscio E, Toriello F, Sperduti N, Todisco T, Di Tanna G, Sacchetti ML, Puddu PE, Farcomeni A, Anzaldi M, Bazzini C, Bianchi PI, Boari B, Buonauro A, Buttà C, Buzzetti E, Calabria S, Capeci W, Caradio F, Carleo P, Carrabba MD, Castorani L, Cecchetto L, Cicco S, Cimini C, Colombo BM, De Giorgi A, De Vuono S, Del Corso L, Denegri A, Di Giosia P, Durante Mangoni E, Falsetti L, Forgione A, Giorgini P, Grassi D, Grembiale A, Hijazi D, Iamele L, Lorusso G, Marchese A, Marra AM, Masala M, Miceli G, Montebianco Abenavoli L, Murgia G, Naccarato P, Pattoneri P, Perego F, Pesce P, Piano S, Pinna M, Pinto D, Pretti V, Pucci G, Salinaro F, Salzano A, Santilli F, Scarpini F, Scicali R, Sirico D, Suppressa P, Talia M, Tassone EJ, Torres D, Vazzana N, Vecchio CR, Vidili G, Vitale F, and Zaccone V
- Subjects
Male ,Settore MED/09 - Medicina Interna ,030204 cardiovascular system & hematology ,Pulmonary Disease, Chronic Obstructive ,0302 clinical medicine ,Risk Factors ,Major cardiovascular event ,Cause of Death ,Risk of mortality ,Prevalence ,Medicine ,030212 general & internal medicine ,Prospective Studies ,Registries ,Prospective cohort study ,Stroke ,Cause of death ,COPD ,Chronic obstructive pulmonary disease ,Incidence ,Hazard ratio ,Atrial fibrillation ,Cardiovascular mortality ,Major cardiovascular events ,Aged ,Atrial Fibrillation ,Cardiovascular Diseases ,Endpoint Determination ,Female ,Follow-Up Studies ,Humans ,Italy ,Predictive Value of Tests ,Internal Medicine ,Emergency Medicine ,Atrial fibrillation, Cardiovascular mortality, Chronic obstructive pulmonary disease, Major cardiovascular events ,Cardiology ,Settore SECS-S/01 - Statistica ,medicine.medical_specialty ,Chronic Obstructive ,Socio-culturale ,Pulmonary Disease ,03 medical and health sciences ,Internal medicine ,cardiovascular diseases ,business.industry ,medicine.disease ,business ,Mace - Abstract
Chronic obstructive pulmonary disease (COPD) increases the risk of mortality in non-valvular atrial fibrillation (NVAF) patients. Data on the relationship of COPD to major cardiovascular events (MACE) in AF have not been defined. The aim of the study is to assess the predictive value of COPD on incident MACE in NVAF patients over a 3-year follow-up. In the Atrial Fibrillation Registry for Ankle-Brachial Index Prevalence Assessment-Collaborative Italian Study (ARAPACIS) cohort, we evaluate the impact of COPD on the following clinical endpoints: MACE (including vascular death, fatal/non-fatal MI and stroke/TIA), cardiovascular (CV) death and all-cause mortality. Among 2027 NVAF patients, patients with COPD (9%) are more commonly male, elderly and at higher thromboembolic risk. During a median 36.0months follow-up, 186 patients experienced MACE: vascular death (n = 72), MI (n = 57), stroke/TIA (n = 57). All major outcomes (including stroke/TIA, MI, vascular death, and all-cause death) are centrally adjudicated. Kaplan–Meier curves show that NVAF patients with COPD are at higher risk for MACE (p < 0.001), CV death (p < 0.001) and all-cause death (p < 0.001). On Cox proportional hazard analysis, COPD is an independent predictor of MACE (Hazard ratio [HR] 1.77, 95% Confidence Intervals [CI] 1.20–2.61; p = 0.004), CV death (HR 2.73, 95% CI 1.76–4.23; p < 0.0001) and all-cause death (HR 2.16, 95% CI 1.48–3.16; p < 0.0001). COPD is an independent predictor of MACE, CV death and all-cause death during a long-term follow-up of NVAF patients.
- Published
- 2018
26. Cognitive Training in Patients with Alzheimer's Disease: Findings of a 12-month Randomized Controlled Trial.
- Author
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Trebbastoni A, Imbriano L, Podda L, Rendace L, Sacchetti ML, Campanelli A, D'Antonio F, and de Lena C
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- Aged, Aged, 80 and over, Alzheimer Disease psychology, Cognition, Cognitive Dysfunction prevention & control, Female, Follow-Up Studies, Humans, Longitudinal Studies, Male, Middle Aged, Neuropsychological Tests, Single-Blind Method, Treatment Outcome, Alzheimer Disease therapy, Cognitive Behavioral Therapy methods
- Abstract
Background: Cognitive training (CT) is a non-pharmacological intervention based on a set of tasks that reflect specific cognitive functions. CT is aimed at improving cognition in patients with cognitive impairment, though no definitive conclusions have yet been drawn on its efficacy in Alzheimer's disease (AD)., Objective: To assess the effectiveness of a CT program designed to improve cognition in AD patients., Method: This is a randomized, controlled, single-blind, longitudinal trial with a no-treatment control condition in mild-to-moderate AD. Treated patients received in-group CT twice a week for six months, whereas controls did not. CT consisted of tasks ranging from paper-and-pencil to verbal-learning exercises. Participants' cognitive levels were assessed at baseline, post-intervention and 6 months later by means of a complete neuropsychological test battery. Repeated measures ANOVA was used to analyze the effect of time on the outcome measures, as well as to compare treated and untreated patients over time, with demographic data considered as covariates., Results: Of the 140 patients enrolled, 45 in the treated group and 85 controls concluded the study. The CT significantly improved treated subjects' cognitive functions immediately after the CT. Six months later, some test scores remained stable when compared with those obtained at baseline. The control group performed significantly worse than the treated group at each time-point, displaying a progressive cognitive decline over time., Conclusion: Our results suggest that CT may improve cognitive functions in patients with AD and may help to temporarily slow their cognitive decline., (Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.org.)
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- 2018
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27. Dysphagia and Obstructive Sleep Apnea in Acute, First-Ever, Ischemic Stroke.
- Author
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Losurdo A, Brunetti V, Broccolini A, Caliandro P, Frisullo G, Morosetti R, Pilato F, Profice P, Giannantoni NM, Sacchetti ML, Testani E, Vollono C, and Della Marca G
- Subjects
- Adult, Aged, Aged, 80 and over, Brain Ischemia diagnosis, Comorbidity, Deglutition, Deglutition Disorders diagnosis, Deglutition Disorders physiopathology, Disability Evaluation, Female, Humans, Lung physiopathology, Magnetic Resonance Imaging, Male, Middle Aged, Prevalence, Prognosis, Respiration, Risk Factors, Rome epidemiology, Sleep, Sleep Apnea, Obstructive diagnosis, Sleep Apnea, Obstructive physiopathology, Stroke diagnosis, Time Factors, Tomography, X-Ray Computed, Young Adult, Brain Ischemia epidemiology, Deglutition Disorders epidemiology, Sleep Apnea, Obstructive epidemiology, Stroke epidemiology
- Abstract
Background: Obstructive sleep apnea (OSA) and dysphagia are common in acute stroke and are both associated with increased risk of complications and worse prognosis. The aims of the present study were (1) to evaluate the prevalence of OSA and dysphagia in patients with acute, first-ever, ischemic stroke; (2) to investigate their clinical correlates; and (3) to verify if these conditions are associated in acute ischemic stroke., Methods: We enrolled a cohort of 140 consecutive patients with acute-onset (<48 hours), first-ever ischemic stroke. Computed tomography (CT) and magnetic resonance imaging scans confirmed the diagnosis. Neurological deficit was measured using the National Institutes of Health Stroke Scale (NIHSS) by examiners trained and certified in the use of this scale. Patients underwent a clinical evaluation of dysphagia (Gugging Swallowing Screen) and a cardiorespiratory sleep study to evaluate the presence of OSA., Results: There are 72 patients (51.4%) with obstructive sleep apnea (OSA+), and there are 81 patients (57.8%) with dysphagia (Dys+). OSA+ patients were significantly older (P = .046) and had greater body mass index (BMI) (P = .002), neck circumference (P = .001), presence of diabetes (P = .013), and hypertension (P < .001). Dys+ patients had greater NIHSS (P < .001), lower Alberta Stroke Programme Early CT Score (P < .001), with greater BMI (P = .030). The association of OSA and dysphagia was greater than that expected based on the prevalence of each condition in acute stroke (P < .001)., Conclusions: OSA and dysphagia are associated in first-ever, acute ischemic stroke., (Copyright © 2018 National Stroke Association. Published by Elsevier Inc. All rights reserved.)
- Published
- 2018
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28. The culturally adapted Italian version of the Barthel Index (IcaBI): assessment of structural validity, inter-rater reliability and responsiveness to clinically relevant improvements in patients admitted to inpatient rehabilitation centers.
- Author
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Castiglia SF, Galeoto G, Lauta A, Palumbo A, Tirinelli F, Viselli F, Santilli V, and Sacchetti ML
- Subjects
- Adult, Aged, Aged, 80 and over, Female, Humans, Inpatients, Italy, Male, Middle Aged, Rehabilitation Centers statistics & numerical data, Reproducibility of Results, Severity of Illness Index, Surveys and Questionnaires, Young Adult, Culture, Disability Evaluation, Movement Disorders rehabilitation, Outcome Assessment, Health Care methods, Translating
- Abstract
The Barthel Index (BI) is widely used to determine eligibility criteria for inpatient rehabilitation and to monitor patients' recovery, irrespective of the illnesses that affect them. The culturally adapted Italian version of the Barthel Index (IcaBI) was recently validated. This paper reports the structural validity and inter-rater reliability of the IcaBI and its responsiveness to the results of inpatient rehabilitation. The IcaBI was administered to a cohort of 264 patients hospitalized in two rehabilitation centers in Rome, Italy. Factor analysis using principal component analysis revealed a monofactorial structure for neurological patients and, after removal of item 1 "feeding", also for orthopedic patients. Substantial to optimal inter-rater reliability was found (0.74 > intraclass correlation coefficient < 0.96). The IcaBI was found to be accurate (area under the curve= 0.72) with a minimal clinically important change score of 35 points. This work confirms that IcaBI is a useful tool for measuring disability in health and social care settings along the continuum of care. Further studies are needed to assess its criterion validity, interpretability and responsiveness in other specific disease conditions.
- Published
- 2017
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29. Resting state functional thalamic connectivity abnormalities in patients with post-stroke sleep apnoea: a pilot case-control study.
- Author
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Sacchetti ML, Di Mascio MT, Tinelli E, Mainero C, Russo G, Fiorelli M, Calistri V, de Lena C, Minni A, and Caramia F
- Subjects
- Adult, Brain Mapping, Case-Control Studies, Female, Humans, Magnetic Resonance Imaging, Male, Middle Aged, Pilot Projects, Polysomnography, Sleep Apnea Syndromes etiology, Stroke complications, Thalamus diagnostic imaging, Sleep Apnea Syndromes physiopathology, Stroke physiopathology, Thalamus physiopathology
- Abstract
Objective: Sleep apnoea is common after stroke, and has adverse effects on the clinical outcome of affected cases. Its pathophysiological mechanisms are only partially known. Increases in brain connectivity after stroke might influence networks involved in arousal modulation and breathing control. The aim of this study was to investigate the resting state functional MRI thalamic hyper-connectivity of stroke patients affected by sleep apnoea (SA) with respect to cases not affected, and to healthy controls (HC)., Patients and Methods: A series of stabilized strokes were submitted to 3T resting state functional MRI imaging and full polysomnography. The ventral-posterior-lateral thalamic nucleus was used as seed., Results: At the between groups comparison analysis, in SA cases versus HC, the regions significantly hyper-connected with the seed were those encoding noxious threats (frontal eye field, somatosensory association, secondary visual cortices). Comparisons between SA cases versus those without SA revealed in the former group significantly increased connectivity with regions modulating the response to stimuli independently to their potentiality of threat (prefrontal, primary and somatosensory association, superolateral and medial-inferior temporal, associative and secondary occipital ones). Further significantly functionally hyper-connections were documented with regions involved also in the modulation of breathing during sleep (pons, midbrain, cerebellum, posterior cingulate cortices), and in the modulation of breathing response to chemical variations (anterior, posterior and para-hippocampal cingulate cortices)., Conclusions: Our preliminary data support the presence of functional hyper connectivity in thalamic circuits modulating sensorial stimuli, in patients with post-stroke sleep apnoea, possibly influencing both their arousal ability and breathing modulation during sleep.
- Published
- 2017
30. Are stroke cases affected by sleep disordered breathings all the same?
- Author
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Sacchetti ML and Della Marca G
- Subjects
- Humans, Patient Outcome Assessment, Stroke classification, Continuous Positive Airway Pressure methods, Models, Biological, Sleep physiology, Sleep Apnea Syndromes classification, Sleep Apnea Syndromes etiology, Sleep Apnea Syndromes therapy, Stroke complications
- Abstract
Sleep disordered breathings (SDB) worsens the clinical prognosis of stroke patients. Continuous positive airway pressure (CPAP) is a promising effective treatment. Unfortunately, not all patients are compliant with CPAP, suggesting that it is not appropriate for all patients with obstructive sleep apnoea (OSA) after stroke. People with the highest likelihood of benefiting have to be identified. We present a classification of cases with stroke and SDB to be adopted in order to identify the best responders to CPAP treatment. We propose to classify patients in four subgroups: (1) patients who terminate the apnoea by arousing from sleep; these cases are those affected either by an anatomical or a functional obstruction of upper airways that may precede or are the consequence of stroke; (2) cases that alternate OSA to central sleep apnoea (CSA) cause of an altered loop gain; (3) cases in whom ischemic damages have altered the sleep microstructure (CAP); (4) cases that manifest a CSA as the direct consequence of stroke on the central neuronal drive to breath. So far, no study has investigated the consequences of stroke on sleep microstructure. In order to better elucidate these relationships, when reviewing the PSG tracings of stroke patients, the microstructure of sleep should be systematically analysed., (Copyright © 2014 Elsevier Ltd. All rights reserved.)
- Published
- 2014
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31. May stroke cause a Complex Sleep Apnea-CompSA?
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Sacchetti ML, Di Mascio MT, Ottaviani S, Faedda TM, Fiorelli M, Toni D, and Roukos R
- Subjects
- Humans, Male, Brain Ischemia physiopathology, Sleep Apnea, Central physiopathology, Sleep Apnea, Obstructive physiopathology, Stroke physiopathology
- Published
- 2013
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32. Post stroke sleep apnea hypopnea syndrome: a series of 12 consecutive stable stroke cases.
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Sacchetti ML, Di Mascio MT, Fiorelli M, Toni D, Roukos R, Minni A, and Saponara M
- Subjects
- Aged, Female, Humans, Male, Middle Aged, Risk Factors, Sleep Apnea, Obstructive etiology, Sleep Apnea, Obstructive epidemiology, Stroke complications
- Abstract
Objectives: Sleep Disordered Breathing (SDB) is a negative prognostic factor for stroke patients. In order to reveal: (1) the frequency of Sleep Apnea-Hypopnea Syndrome (SAHS) in the stable phase of the illness; (2) the type of SAHS, either obstructive (OSAHS) or central (CSAHS); (3) the possible association between SAHS and daily sleepiness, cardiac arrhythmias, stroke / TIA recurrence and location of the brain lesion, an observational study is on-going at Sapienza University of Rome. We report here the results of cases included in the feasibility study., Patients and Methods: clinical evaluations, brain images and polisomnographic study were performed at discharge and after 4 and 9 months of stroke., Results: Eleven out of the 12 patients included (91.6%) had an Apnea/Hypopnea Index-AHI >= 5. In 5 cases, the majority of total respiratory events were purely central in origin. In 3 of these 5 cases, a concomitant obstruction of the upper airways was revealed; the 2 remaining had risk factors for OSAHS (smoke, hypertension, BMI > 25). A significant association was found between central apnea/hypopnea events and cardiac arrhythmias (p value 0.017)., Conclusions: These findings confirm the high prevalence of SDB, either obstructive or/and central, even in the stable phase of the illness, which in those patients who had accumulated risk factors for OSAHS result in Complex-sleep apnea/hypopnea syndrome (CompSAHS). As patients with CompSAHS are left with very disrupted breathing on continuous positive airway pressure, in order to select cases with stable stroke who benefit from continuos-positive airway pressure (C-PAP) treatment, further and more detailed clinical studies are needed to better distinguish CompSAHS from mixed SAHS.
- Published
- 2012
33. Time of action of neuroprotectors plays a role?
- Author
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Sacchetti ML
- Subjects
- Humans, Fibrinolytic Agents adverse effects, Stroke drug therapy, Tissue Plasminogen Activator adverse effects
- Published
- 2012
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- View/download PDF
34. Relevance of prehospital stroke code activation for acute treatment measures in stroke care: a review.
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Baldereschi M, Piccardi B, Di Carlo A, Lucente G, Guidetti D, Consoli D, Provinciali L, Toni D, Sacchetti ML, Polizzi BM, and Inzitari D
- Subjects
- Disease Management, Fibrinolytic Agents therapeutic use, Humans, Stroke diagnosis, Time Factors, Tissue Plasminogen Activator therapeutic use, Clinical Coding, Emergency Medical Services trends, Stroke drug therapy, Thrombolytic Therapy statistics & numerical data
- Abstract
Background: The use of emergency services with prehospital stroke assessment and early notification to the treatment hospital (stroke code) is a crucial determinant of delay time for acute stroke treatment. We reviewed and summarized the literature on prehospital stroke code system implementation., Methods: Two databases were explored (last update June 20, 2011) with 3 key words (stroke code, stroke prehospital management and stroke prehospital services). Inclusion criteria were: randomized and quasirandomized controlled trials, cohort and case-control studies, and hospital- and emergency-based registers, with no year or language restrictions. We examined the reference lists of all included articles. All potentially relevant reports and abstracts were transcribed into a specifically designed data abstraction form., Results: Only 19 of the 680 studies which were initially retrieved, published from 1999 to 2011, fulfilled our inclusion criteria. One clinical trial was identified. Large differences in stroke code procedures and study designs within and across countries prohibited the pooling of the data. Most studies were carried out in urban areas. Assuming the rate of tissue-plasminogen activator treatment as the performance measure, most studies report a significant increase in the rate of treatment (increase between 3.2 and 16%) with only 1 study not reporting any increase., Conclusions: Despite its limitations, this review suggests that the use of prehospital stroke code is an important intervention to improve the accessibility of the benefits of thrombolysis, especially when implemented together with educational campaigns to optimize the awareness and behavior of patients and bystanders., (Copyright © 2012 S. Karger AG, Basel.)
- Published
- 2012
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35. Autophagy and VMP1 expression are early cellular events in experimental diabetes.
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Grasso D, Sacchetti ML, Bruno L, Lo Ré A, Iovanna JL, Gonzalez CD, and Vaccaro MI
- Subjects
- Animals, Gene Expression drug effects, Islets of Langerhans drug effects, Islets of Langerhans physiopathology, Male, Rats, Rats, Wistar, Streptozocin, Autophagy, Diabetes Mellitus, Experimental physiopathology, Membrane Proteins biosynthesis
- Abstract
Background/aims: We have described VMP1 as a new protein which expression triggers autophagy in mammalian cells. Here we show that experimental diabetes activates VMP1 expression and autophagy in pancreas beta cells as a direct response to streptozotocin (STZ)., Methods: Male Wistar rats were treated with 65 mg/kg STZ and pancreas islets from untreated rats were incubated with 1 mM STZ., Results: RT-PCR analysis shows early VMP1 induction after STZ treatment. In situ hybridization reveals VMP1 mRNA in islet beta cells. Electron microscopy shows chromatin aggregation and autophagy morphology that was confirmed by LC3 expression and LC3-VMP1 co-localization. Apoptotic cell death and the reduction of beta cell pool are evident after 24 h treatment, while VMP1 is still expressed in the remaining cells. VMP1-Beclin1 colocalization in pancreas tissue from STZ-treated rats suggests that VMP1-Beclin1 interaction is involved in the autophagic process activation during experimental diabetes. Results were confirmed using pancreas islets, showing VMP1 expression and autophagy in beta cells as a direct effect of STZ treatment., Conclusion: Pancreas beta cells trigger VMP1 expression and autophagy during the early cellular events in response to experimental diabetes., (Copyright 2008 S. Karger AG, Basel and IAP.)
- Published
- 2009
- Full Text
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36. Early clinical diagnosis of lacunar strokes.
- Author
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Toni D, Sacchetti ML, and Prencipe M
- Subjects
- Early Diagnosis, Humans, Brain Infarction classification, Brain Infarction diagnosis
- Published
- 2008
- Full Text
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37. The pancreatitis-induced vacuole membrane protein 1 triggers autophagy in mammalian cells.
- Author
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Ropolo A, Grasso D, Pardo R, Sacchetti ML, Archange C, Lo Re A, Seux M, Nowak J, Gonzalez CD, Iovanna JL, and Vaccaro MI
- Subjects
- Adenine analogs & derivatives, Adenine pharmacology, Animals, Antibiotics, Antineoplastic pharmacology, Apoptosis Regulatory Proteins genetics, Apoptosis Regulatory Proteins metabolism, Beclin-1, HeLa Cells, Humans, Membrane Proteins genetics, Membrane Proteins metabolism, Mice, Microtubule-Associated Proteins genetics, Microtubule-Associated Proteins metabolism, NIH 3T3 Cells, Neoplasms genetics, Neoplasms metabolism, Neoplasms pathology, Neurodegenerative Diseases genetics, Neurodegenerative Diseases metabolism, Neurodegenerative Diseases pathology, Pancreatitis, Acute Necrotizing genetics, Pancreatitis, Acute Necrotizing pathology, Phagosomes genetics, Phagosomes ultrastructure, Protein Binding drug effects, Protein Binding genetics, Proteins genetics, Proteins metabolism, RNA, Small Interfering pharmacology, Sirolimus pharmacology, Autophagy drug effects, Autophagy genetics, Membrane Proteins biosynthesis, Pancreatitis, Acute Necrotizing metabolism, Phagosomes metabolism
- Abstract
Autophagy is a degradation process of cytoplasmic cellular constituents, which serves as a survival mechanism in starving cells, and it is characterized by sequestration of bulk cytoplasm and organelles in double-membrane vesicles called autophagosomes. Autophagy has been linked to a variety of pathological processes such as neurodegenerative diseases and tumorigenesis, which highlights its biological and medical importance. We have previously characterized the vacuole membrane protein 1 (VMP1) gene, which is highly activated in acute pancreatitis, a disease associated with morphological changes resembling autophagy. Here we show that VMP1 expression triggers autophagy in mammalian cells. VMP1 expression induces the formation of ultrastructural features of autophagy and recruitment of the microtubule-associated protein 1 light-chain 3 (LC3), which is inhibited after treatment with the autophagy inhibitor 3-methiladenine. VMP1 is induced by starvation and rapamycin treatments. Its expression is necessary for autophagy, because VMP1 small interfering RNA inhibits autophagosome formation under both autophagic stimuli. VMP1 is a transmembrane protein that co-localizes with LC3, a marker of the autophagosomes. It interacts with Beclin 1, a mammalian autophagy initiator, through the VMP1-Atg domain, which is essential for autophagosome formation. VMP1 endogenous expression co-localizes with LC3 in pancreas tissue undergoing pancreatitis-induced autophagy. Finally, VMP1 stable expression targeted to pancreas acinar cell in transgenic mice induces autophagosome formation. Our results identify VMP1 as a novel autophagy-related membrane protein involved in the initial steps of the mammalian cell autophagic process.
- Published
- 2007
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38. Determinants of plasma levels of brain natriuretic peptide after acute ischemic stroke or TIA.
- Author
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Di Angelantonio E, De Castro S, Toni D, Sacchetti ML, Biraschi F, Prencipe M, and Fiorelli M
- Subjects
- Acute Disease, Aged, Aged, 80 and over, Atrial Fibrillation complications, Atrial Fibrillation diagnostic imaging, Atrial Fibrillation physiopathology, Biomarkers analysis, Biomarkers blood, Brain blood supply, Brain metabolism, Brain physiopathology, Brain Ischemia physiopathology, Echocardiography, Female, Heart physiopathology, Heart Failure diagnostic imaging, Heart Failure physiopathology, Humans, Intracranial Embolism blood, Intracranial Embolism etiology, Intracranial Embolism physiopathology, Ischemic Attack, Transient physiopathology, Male, Middle Aged, Natriuretic Peptide, Brain analysis, Prognosis, Risk Factors, Stroke physiopathology, Up-Regulation physiology, Brain Ischemia blood, Heart Failure complications, Ischemic Attack, Transient blood, Natriuretic Peptide, Brain blood, Stroke blood
- Abstract
Plasma levels of brain natriuretic peptide (BNP) are frequently elevated after an acute stroke and have been shown to be an independent predictor of mortality. However, the relationships between stroke and BNP concentrations have not yet been systematically investigated. Plasma BNP assay and echocardiography were performed in 48 patients with ischemic stroke or TIA with a mean delay of 12.7 h after onset. Median BNP concentration was 88.6 pg/mL (range 5-1270). Older age, chronic heart failure, atrial fibrillation, stroke severity, lower hemoglobin levels, lower left ventricular ejection fraction, and abnormalities of left atrium or appendage (LA/LAA) were univariately associated with increased BNP levels. At multivariable analysis, the presence of at least one LA/LAA abnormality (atrial dilatation, low flow velocity, spontaneous echocontrast or thrombus) had the strongest association with BNP, explaining 38.9% of the variance in the whole sample and 28.5% in patients without atrial fibrillation. In acute ischemic stroke patients, elevated plasma BNP levels have multiple determinants, among which left atrial disease appears to be the stronger, even in patients without atrial fibrillation. These results encourage further investigation of plasma BNP concentration as a potential marker of the presence of left atrial sources of emboli.
- Published
- 2007
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39. Which model of stroke unit is better for stroke patient management?
- Author
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Lorenzano S, Anzini A, de Michele M, Falcou A, Fausti S, Gori C, Mancini A, Cavalletti C, Colosimo C, Fiorelli M, Sacchetti ML, Argentino C, and Toni D
- Subjects
- Acute Disease, Humans, Fibrinolytic Agents therapeutic use, Intensive Care Units standards, Outcome Assessment, Health Care, Stroke drug therapy, Thrombolytic Therapy methods
- Abstract
The increasing prevalence of cerebrovascular diseases has made urgent the need to develop timely and effective treatment strategies to tackle this health problem. Stroke units (SUs) appear to be the ideal setting where the management of acute stroke patients, including specific treatments as thrombolysis, may be optimized. Which model of SU gives the best results is still an unsettled issue. The more intensive and timely multidisciplinary approach to the acute phase of stroke, the management of medical complications, and the earlier and more focused rehabilitation, are likely the most qualifying aspects of our Neurovascular treatment unit.
- Published
- 2006
- Full Text
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40. Specific therapies for ischaemic stroke: rTPA and others.
- Author
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Toni D, Lorenzano S, Sacchetti ML, Fiorelli M, De Michele M, and Principe M
- Subjects
- Clinical Trials as Topic, Humans, Time Factors, Brain Ischemia drug therapy, Fibrinolytic Agents therapeutic use, Thrombolytic Therapy methods, Tissue Plasminogen Activator therapeutic use
- Abstract
In the last few years there have been several important advances in the understanding of cerebrovascular disorder pathophysiology that have impacted on stroke management. The development of timely and effective treatment strategies was and is still considered a high priority issue. Therapeutic options dramatically increased both in the prevention and overall in the treatment of acute ischaemic stroke (AIS). At present, whereas neuroprotection remains experimental, intravenous (i.v.) thrombolysis is the only specific therapy effective in reducing mortality and disability associated with stroke. The efficacy and safety of the antithrombotic therapy in AIS treatment are not well established, and few issues in clinical stroke management are more controversial. However, some studies have brought new light and new doubts on the roles of these traditional therapies.
- Published
- 2005
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41. Prognostic significance of admission levels of troponin I in patients with acute ischaemic stroke.
- Author
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Di Angelantonio E, Fiorelli M, Toni D, Sacchetti ML, Lorenzano S, Falcou A, Ciarla MV, Suppa M, Bonanni L, Bertazzoni G, Aguglia F, and Argentino C
- Subjects
- Acute Disease, Aged, Aged, 80 and over, Biomarkers blood, Brain Ischemia complications, Creatine Kinase blood, Creatine Kinase, MB Form, Electrocardiography, Female, Follow-Up Studies, Heart Diseases diagnosis, Heart Diseases etiology, Humans, Isoenzymes blood, Male, Middle Aged, Myoglobin blood, Patient Admission, Predictive Value of Tests, Prognosis, Prospective Studies, Stroke etiology, Brain Ischemia blood, Stroke blood, Troponin I blood
- Abstract
Objectives: Successful prediction of cardiac complications early in the course of acute ischaemic stroke could have an impact on the clinical management. Markers of myocardial injury on admission deserve investigation as potential predictors of poor outcome from stroke., Methods: We prospectively investigated 330 consecutive patients with acute ischaemic stroke admitted to our emergency department based stroke unit. We analysed the association of baseline levels of cardiac troponin I (cTnI) with (a) all-cause mortality over a six month follow up, and (b) in-hospital death or major non-fatal cardiac event (angina, myocardial infarction, or heart failure)., Results: cTnI levels on admission were normal (lower than 0.10 ng/ml) in 277 patients (83.9%), low positive (0.10-0.39 ng/ml) in 35 (10.6%), and high positive (0.40 ng/ml or higher) in 18 (5.5%). Six month survival decreased significantly across the three groups (p<0.0001, log rank test for trend). On multivariate analysis, cTnI level was an independent predictor of mortality (low positive cTnI, hazard ratio (HR) 2.14; 95% CI 1.13 to 4.05; p = 0.01; and high positive cTnI, HR 2.47; 95% CI 1.22 to 5.02; p = 0.01), together with age and stroke severity. cTnI also predicted a higher risk of the combined endpoint "in-hospital death or non-fatal cardiac event". Neither the adjustment for other potential confounders nor the adjustment for ECG changes and levels of CK-MB and myoglobin on admission altered these results., Conclusions: cTnI positivity on admission is an independent prognostic predictor in acute ischaemic stroke. Whether further evaluation and treatment of cTnI positive patients can reduce cardiac morbidity and mortality should be the focus of future research.
- Published
- 2005
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42. Stroke is best managed by neurologists.
- Author
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Sacchetti ML
- Subjects
- Curriculum, Disease Management, Education, Medical, Graduate, Humans, Neurology education, Stroke therapy
- Published
- 2004
- Full Text
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43. Emergency and early carotid endarterectomy in patients with acute ischemic stroke selected with a predefined protocol. A prospective pilot study.
- Author
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Sbarigia E, Toni D, Speziale F, Falcou A, Sacchetti ML, Panico MA, Fiorelli M, Argentino C, Ducasse E, and Fiorani P
- Subjects
- Acute Disease, Aged, Aged, 80 and over, Brain Ischemia etiology, Carotid Stenosis complications, Emergency Treatment, Female, Humans, Male, Middle Aged, Pilot Projects, Prospective Studies, Stroke etiology, Brain Ischemia surgery, Carotid Stenosis surgery, Endarterectomy, Carotid, Stroke surgery
- Abstract
Aim: The appropriateness of early carotid endarterectomy (CEA) in patients with acute ischemic stroke is still unsettled. The aim of this study was to verify the safety and feasibility of early CEA in a consecutive series of patients with acute ischemic stroke observed in an emergency Department Stroke Unit., Methods: During a 24-month study, out of 756 patients with acute ischemic stroke 33 (4.4%) were scheduled for early CEA. Endarterectomy procedures were distinguished according to the time between the onset of stroke and operation as emergency (within 8 hours), early CEA (1-18 days). Patients with impaired consciousness or an infarct larger than 2.5 cm on computed tomographic (CT) or magnetic resonance (MR) scans or both were excluded from surgery. All patients underwent spiral CT, echo-color-Doppler (ECD) sonography, transcranial Doppler (TCD) sonography and, when necessary, MR angiography within 6 hours of admission. No patient underwent conventional angiography. Most patients were operated on under cervical block (CB) anesthesia; general anesthesia (GA) was used only for those with an unstable neurological deficit. Selective shunting was used on the basis of intra-operative transcranial Doppler in patients under GA and the onset or worsening of neurological deficit under CB anesthesia., Results: Of the 6 patients operated on within a median 6 hours after the onset of stroke, 1 (16.5%) had a fatal hemorrhagic transformation of the infarct, while the remaining 5 (83.5%) stopped fluctuating or progressing and had a favourable neurological outcome. Of the 16 patients operated on within a median 36 hours and of the 11 patients operated on within 7 days, none deteriorated after operation., Conclusion: Emergency CEA is feasible for acute ischaemic stroke provided that strict selection criteria are applied and the door-to-surgery interval is kept short (within 8 hours). Early CEA for secondary prevention is feasible and safe, confirming that a delayed operation is in most cases unwarranted. Large randomized trials are warranted before implementing emergent and early CEA in routine clinical practice.
- Published
- 2003
44. Implementation of a surveillance system for stroke based on administrative and clinical data in the Lazio region (Italy): methodological aspects.
- Author
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De Luca A, Agabiti N, Fiorelli M, Sacchetti ML, Tancioni V, Picconi O, Cardo S, and Guasticchi G
- Subjects
- Aged, Catchment Area, Health, Female, Humans, Italy epidemiology, Male, Population Surveillance methods, Stroke epidemiology
- Abstract
Stroke is the third leading cause of death and the most important cause of long-term disability in Italy and other developed countries, heavily influencing quality of life and costs of health care. In spite of the widespread occurrence of the disease and its relevant impact in Italy, there is neither a national nor a regional surveillance system of cerebrovascular diseases. A regional surveillance system for stroke has two important aims: to help to interpret the geographical and temporal trends of the disease for health care planning and resource allocation and to allow close monitoring of the quality of stroke services. Age-standardized mortality rates for cerebrovascular diseases in the Lazio region (5,242,709 inhabitants) in the period 1998-99 were 69.4 for males and 59.4 for females per 100,000 inhabitants. In the year 2000, about 3% of all hospital discharges were for cerebrovascular diseases with a hospitalisation rate of 4.36 per 1000 inhabitants. The mean length of stay is 12 days (median of 9 days) and in-hospital death is 15.4%. The admission rate for cerebrovascular diseases to emergency departments is 3.40 per 1000 inhabitants. The goal of the Lazio Regional Health Authority is to implement a surveillance system for stroke based both on current data (mortality and discharge data) and on information collected in a registry for quality assessment of stroke care. The first step of the study is to develop a regional register of acute stroke using an 'ad hoc' data sheet integrated in the computer-based patient record system of clinical and administrative data (GIPSE) operating in all emergency departments in the region.
- Published
- 2003
45. Acute stroke trials: the problems of local investigators?
- Author
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Toni D, Sacchetti ML, and Chamorro A
- Subjects
- Acute Disease, Humans, Research organization & administration, Anticoagulants therapeutic use, Clinical Trials as Topic standards, Neuroprotective Agents therapeutic use, Stroke drug therapy
- Abstract
During stroke trials local investigators have to face many practical problems and time consuming procedures (filling in huge case report forms, performing repeat blood sample drawings for pharmacokinetic studies etc.) which, however, simply require organizational structures which is understood to be necessary to be able to conduct such kind of studies. Other, and most worrisome problems, are indeed to be solved when a sponsored research may rise potential ethical issues, or when academic research proposals clash with the interest of pharmaceutical companies or find difficulties in being funded by public institutions. It is just a greater involvement of these latter, possibly free from bureaucratic laces, which might help a balance to be struck between academic and industrial aims., (Copyright 2003 S. Karger AG, Basel)
- Published
- 2003
- Full Text
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46. Computed tomography findings in the first few hours of ischemic stroke: implications for the clinician.
- Author
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Fiorelli M, Toni D, Bastianello S, Sacchetti ML, Sette G, Falcou A, Argentino C, Lorenzano S, Di Angelantonio E, and Bozzao L
- Subjects
- Adult, Aged, Aged, 80 and over, Brain diagnostic imaging, Brain physiopathology, Female, Humans, Male, Middle Aged, Middle Cerebral Artery diagnostic imaging, Middle Cerebral Artery physiopathology, Prognosis, Time Factors, Tomography, X-Ray Computed, Hypoxia-Ischemia, Brain diagnostic imaging, Stroke diagnostic imaging
- Abstract
In order to evaluate the clinical usefulness of emergency computed tomography (CT) in acute ischemic stroke, we assessed whether CT findings within the first few hours of stroke onset reliably predict type, site and size of the index infarction, and risk of death or disability. For this reason we reviewed clinical and CT findings in a cohort of unselected consecutive patients referred to the stroke unit of a large urban hospital because of a presumed ischemic stroke in the anterior circulation (AC), and submitted to CT within 5 h from onset. Out of 158 total patients, emergency CT revealed parenchymal changes compatible with AC focal ischemia in 77 (49%) and a hyperdense middle cerebral artery (MCA) in 41 (26%). Parenchymal changes and hyperdense MCA predicted an AC territorial infarction respectively in 97% of cases (95% C.I. 93% to 100%) and in 95% of cases (95% C.I. 88% to 100%). Site and size of early changes coincided with those of final lesions in 79% of patients with cortical changes and in 95% of patients with cortico-subcortical changes, but only in 37% of patients with initial subcortical changes, the remainder of whom developed a cortico-subcortical infarction. At logistic regression parenchymal changes were the only independent predictor of an AC territorial infarction. Negative predictive power, however, was only 40% (95% C. I. 29% to 51%) for parenchymal changes, and 35% for hyperdense MCA (95% C.I. 26% to 44%). The odds for death or disability at 1 month associated with parenchymal changes were thrice as high as with negative CT, even after adjustment for clinical severity on admission. These results indicate that CT scan adds significantly to the prediction of outcome made on clinical grounds. The frequent development of a territorial infarction in patients with initially negative CT and the subsequent recruitment of the cortex in those initially exhibiting only subcortical changes suggest that the transition from ischemia to infarction often occurs after the first five h following stroke.
- Published
- 2000
- Full Text
- View/download PDF
47. Dichotomized efficacy end points and global end-point analysis applied to the ECASS intention-to-treat data set: post hoc analysis of ECASS I.
- Author
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Hacke W, Bluhmki E, Steiner T, Tatlisumak T, Mahagne MH, Sacchetti ML, and Meier D
- Subjects
- Humans, National Institutes of Health (U.S.), Recombinant Proteins, Retrospective Studies, United States, Cerebrovascular Disorders drug therapy, Outcome Assessment, Health Care statistics & numerical data, Plasminogen Activators therapeutic use, Tissue Plasminogen Activator therapeutic use
- Abstract
Background and Purpose: It is not yet known which end points are the most suitable for evaluation of the effects of acute stroke intervention. The European Cooperative Acute Stroke Study (ECASS) I study used 2 primary end points. The study was powered to detect a 15% improvement of the median of each primary end point. The study failed to show this effect and was negative in the intention-to-treat analysis. The National Institute of Neurological Disorders and Stroke (NINDS) study used 4 dichotomized end points and applied a global end-point analysis. This study was positive and led to FDA approval of thrombolytic therapy for acute ischemic stroke. This study was undertaken to answer the question of whether a different statistical design may have shown a positive results of the ECASS I trial., Methods: We performed a retrospective analysis of the ECASS I intention-to-treat data set (615 randomized and treated patients, rtPA treatment versus placebo) and post hoc application of the NINDS trial statistical methodology (global end-point analysis). The scores of the modified Rankin Scale (mRS), Barthel Index (BI), and the National Institutes of Health Stroke Scale (NIHSS) were dichotomized according to the criteria used in the NINDS trial. Favorable outcome was defined as a score of 0 or 1 on mRS, a score of 95 or 100 on BI, and a score of 0 or 1 on NIHSS., Results: The number of patients reaching favorable outcome were higher in all 3 end points in the rtPA-treated group. The effect sizes were 8% for mRS, 6% for BI, and 14% for NIHSS, respectively. The differences are statistically significant for the mRS (P=0.044; odds ratio [OR], 1. 4; 95% confidence interval [CI], 1.0 to 2.0) and the NIHSS (P=0.001; OR, 1.9; 95% CI, 1.4 to 2.8), while for the BI significance was missed (P=0.102; OR, 1.3; 95% CI, 0.9 to 1.8). The global end-point statistics, however, shows a significant increase (P=0.008; OR, 1.5; 95% CI, 1.1 to 2.0) of favorable outcome in the rtPA-treated patient group., Conclusions: Using the global end-point analysis, ECASS is positive in the intention-to-treat analysis. This may indicate that the time window for thrombolysis may be as long as 6 hours. Looking at the 3 dichotomized end points, the effect sizes for 2 end points, mRS and BI, are smaller in the ECASS 6-hour intention-to-treat population compared with the NINDS trial, whereas the effect size for the NIHSS is larger. While in the NINDS trial all 3 end points reveal statistically significant results, in ECASS only 2 of the 3 corresponding end points, mRS and NIHSS, were statistically significant. This finding underlines an important difference of a global end-point approach: it may show a positive overall result although one of the end points is not positive.
- Published
- 1998
- Full Text
- View/download PDF
48. Early spontaneous improvement and deterioration of ischemic stroke patients. A serial study with transcranial Doppler ultrasonography.
- Author
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Toni D, Fiorelli M, Zanette EM, Sacchetti ML, Salerno A, Argentino C, Solaro M, and Fieschi C
- Subjects
- Acute Disease, Aged, Brain Ischemia complications, Cerebrovascular Disorders etiology, Cerebrovascular Disorders mortality, Disease Progression, Female, Humans, Male, Middle Aged, Predictive Value of Tests, Prognosis, Sensitivity and Specificity, Brain Ischemia diagnostic imaging, Cerebrovascular Disorders diagnostic imaging, Ultrasonography, Doppler, Transcranial standards
- Abstract
Background and Purpose: The purpose of our study was to investigate whether emergency transcranial Doppler (TCD) findings and their modifications over the first 48 hours are related to early neurological changes in acute ischemic stroke patients., Methods: Ninety-three patients underwent CT scan within 5 hours of a first-ever ischemic hemispheric stroke, and TCD serial examinations at 6, 24, and 48 hours after stroke onset. We classified TCD findings as follows: normal; middle cerebral artery (MCA) asymmetry (asymmetry index between affected and contralateral MCAs below -21%); and MCA no-flow (absence of flow signal from the affected MCA in the presence of ipsilateral anterior and posterior cerebral artery signals through the same acoustic window). We considered early deterioration and early improvement to be a decrease or an increase of 1 or more points, respectively, in the Canadian Neurological Scale score over the same period., Results: At 6-hour TCD examination, MCA asymmetry and MCA no-flow were present in 6 (22%) and 2 (7%), respectively, of 27 improving patients; in 20 (43%) and 10 (22%) of 46 stable patients, and in 9 (45%) and 8 (40%) of 20 deteriorating patients. TCD findings were normal in the remaining patients (P = 0.001). At serial TCD, we detected early (within 24 hours) recanalization (from no-flow to asymmetry or normal and from asymmetry to normal) in 2 (25%) improving patients, in 7 (23%) stable patients, and in 5 (29%) deteriorating patients and late (between 24 and 48 hours) recanalization in 4 (50%) improving patients, in 6 (20%) stable patients, and in none of the deteriorating patients (P = 0.03, chi 2 for trend, improving versus nonimproving irrespective of the timing of recanalization). One deteriorating patient (5%) developed a non-flow from an initial MCA asymmetry. Logistic regression selected normal TCD (odds ratio [OR], 0.17; 95% confidence interval [CI], 0.06 to 0.46) as an independent predictor of early improvement and abnormal TCD (asymmetry plus no-flow) (OR, 5.02; 95% CI, 1.31 to 19.3) as an independent predictor of early deterioration., Conclusions: TCD examination within 6 hours after stroke can help to predict both early deterioration and early improvement. Serial TCD shows that propagation of arterial occlusion is rarely related to early deterioration, whereas the fact that it can detect early recanalization (within 24 hours) in deteriorating patients and both early and late recanalization (after 24 hours) in improving patients suggests the existence of individual time frames for tissue recovery.
- Published
- 1998
- Full Text
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49. The concept of combination therapy in acute ischemic stroke.
- Author
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Sacchetti ML, Toni D, Fiorelli M, Argentino C, and Fieschi C
- Subjects
- Acute Disease, Brain Ischemia complications, Cerebrovascular Disorders etiology, Drug Therapy, Combination, Humans, Brain Ischemia drug therapy, Cerebrovascular Disorders drug therapy, Excitatory Amino Acid Antagonists therapeutic use, Fibrinolytic Agents therapeutic use, Plasminogen Activators therapeutic use
- Published
- 1997
- Full Text
- View/download PDF
50. Posterior circulation infarcts simulating anterior circulation stroke. Perspective of the acute phase.
- Author
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Argentino C, De Michele M, Fiorelli M, Toni D, Sacchetti ML, Cavalletti C, Sette G, Falcou A, Bastianello S, and Bozzao L
- Subjects
- Acute Disease, Aged, Brain Ischemia mortality, Brain Ischemia physiopathology, Cerebral Infarction mortality, Cerebral Infarction physiopathology, Cerebrovascular Disorders mortality, Cerebrovascular Disorders physiopathology, Diagnosis, Differential, Female, Humans, Male, Middle Aged, Risk Factors, Tomography, X-Ray Computed, Brain Ischemia diagnosis, Cerebral Infarction diagnosis, Cerebrovascular Circulation physiology, Cerebrovascular Disorders diagnosis
- Abstract
Background and Purpose: Ischemic stroke patients whose initial clinical presentation suggests an involvement of the anterior circulation (AC) are sometimes found to have a posterior circulation (PC) infarct, a fact that may generate erroneous decisions in clinical management. We investigated the prevalence of this misdiagnosis in the first few hours after stroke onset., Methods: We performed a cohort study of 158 patients hospitalized within 5 hours of onset of a presumed AC ischemic stroke, as diagnosed on clinical grounds., Results: Final CT or pathology diagnosis was AC infarct in 128 patients (81%), a repeatedly negative CT in 14 (9%), PC infarct (5 pons, 1 midbrain and cerebellum, 6 supratentorial territory of the posterior cerebral artery) in 12 (8%), and other or undiagnosed lesions in 4 (3%). AC and PC stroke patients did not differ in terms of age, vascular risk factors, and initial severity, but the latter were more frequently men (83% versus 53%; P = .04), were hospitalized later (mean +/- SD, 168 +/- 86 versus 109 +/- 55 minutes; P = .001), and presented a pure motor hemiparesis or a sensorimotor stroke (50% versus 33%) more often than their counterparts. At baseline CT, PC stroke patients never exhibited an early parenchymal hypodensity in the carotid territory or a hyperdense middle cerebral artery, which were instead found in 59% (P = .0003) and 31% (P = .02) of AC stroke patients, respectively. Early neurological deterioration, 1 month case-fatality rate, and disablement in survivors were comparable in the two groups., Conclusions: Shortly after onset the clinical discrimination between AC and nontypical PC infarcts is not reliable, which explains the frequent occurrence of this misdiagnosis. Emergency CT scan helps in the differential diagnosis only when it demonstrates an early focal hypodensity within the carotid territory.
- Published
- 1996
- Full Text
- View/download PDF
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