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Pulmonary Aspergilloma: a rational approach to treatment. Am J Med 1976; 61: 626–31.",{"doi":490},"10.1016\u002F0002-9343(76)90140-6",{"id":20,"text":492,"url":20,"identifiers":493},"Fahey PJ, Utell MH, Hyde RW. Spontaneous lysis of mycetomas after acute cavitating lung disease. Am Rev Respir Dis 1981; 23: 336–9.",{},{"id":20,"text":495,"url":20,"identifiers":496},"Butz RO, Acetina JR, Leininger BJ. Ten-year experience with mycetomas in patients with pulmonary tuberculosis. Chest 1985; 87: 356–8.",{"doi":497},"10.1378\u002Fchest.87.3.356",{"id":20,"text":499,"url":20,"identifiers":500},"Blyth W, Hardy JC. Mutagenic and tumorigenic properties of the spores ofAspergillus clavatus. Br J Cancer 1982; 45: 105–17.",{"doi":501},"10.1038\u002Fbjc.1982.13",{"id":20,"text":503,"url":20,"identifiers":504},"Fengrung W, Zhendong Z, Bingzhong J, Zhaoyi W. Experimental studies of lung adenocarcinoma in mice induced by corn flour inoculated with Aspergillus flavus. Chung Hua Chung Liu Tsa Chih 1981; 3: 91–3.",{},{"id":20,"text":506,"url":20,"identifiers":507},"Tomioka H, Iwasaki H, Okumura N, Aoki M, Hashimoto K, Ohbayashi C. Undiagnosed lung cancer complicated by intracavitary Aspergillosis. J Jpn Resp Soc 1999; 37: 78–82.",{},{"id":20,"text":509,"url":20,"identifiers":510},"Fujimoto K, Meno S, Nishimura H, Hayabuchi N, Hayashi A. Aspergilloma within cavitary lung cancer: MR imaging findings. Am J Roentgenol 1994; 163: 565–7.",{"doi":511},"10.2214\u002Fajr.163.3.8079845",{"id":20,"text":513,"url":20,"identifiers":514},"McGregor DH, Papasian CJ, Pierce PD. Aspergilloma within cavitating pulmonary adenocarcinoma. Am J Clin Pathol 1989; 91: 100–3.",{"doi":515},"10.1093\u002Fajcp\u002F91.1.100",{"id":20,"text":517,"url":20,"identifiers":518},"Vuyst PD, Troyer AD, Yernault JC, Verhest A, Vanderhoeft P. Aspergilloma in a necrotic bronchial adenocarcinoma. Eur J Respir Dis 1980; 61: 213–7.",{},{"id":520,"createTime":521,"updateTime":522,"relativeEntities":523,"slug":524,"properties":525,"entityType":123,"verifyStatus":124,"verifyTime":536,"verifyNote":126,"languages":20,"translateLanguages":20,"viewCount":21,"primaryUrl":537,"fullTextUrl":20,"authors":538,"publicationType":219,"publisherRelationship":621,"citationCount":21,"citationInfo":675,"publishDate":279,"publishYear":277,"citationAnalyzeStatus":677,"lastCitationAnalyze":678,"indexDatabases":679,"openAccess":20,"references":20,"isForceReanalyzing":302},"af1cdeef-fab8-4d5a-8157-95ef9ae179cd","2024-02-12T09:50:25.844+00:00","2026-07-27T02:31:57.689+00:00",[],"Evaluation-of-an-internal-thoracic-artery-as-a-coronary-artery-bypass-graft-by-intercostal-duplex-scanning-ultrasonography",{"abstract":526,"title":528,"gsPaper":530,"references":532,"doi":534},{"EN":527},"\n                        Objectives: Although angiography is often used to determine whether the internal thoracic artery is appropriate as a coronary bypass graft, but use of duplex scanning ultrasonography for this purpose is not yet widespread.Methods: The internal diameter and flow of the internal thoracic artery were measured using intercostal duplex scanning in 100 patients during April 1995. The ultrasonographic device (sonos 2000, Hewlett Packard) used had a linear probe delivering a frequency of 7.5 MHz. Bilateral internal thoracic arteries and their blood flow were imaged clearly in all subjects. Diameter was compared by angiography and duplex scanning ultrasonography in 20 patients.Results: The average internal diameter of internal thoracic artery was 2.19±0.46 mm (right) or 2.13±0.32 mm (left) in men and 2.05±0.44 mm (right) or 2.09±0.42 mm (left) in women. The gender difference was statistically significant (p=0.05). The maximum systolic blood flow velocity through the internal thoracic artery was 0.85±0.34 m\u002Fs (right) or 0.84±0.36 m\u002Fs (left) in men and 0.87±0.28 m\u002Fs (right) or 0.82±0.28 m\u002Fs (left) in women. The average internal thoracic arterial blood flow (F) was 54.6±29.0 ml\u002Fmin (right) or 50.9±28.8 ml\u002Fmin (left) in men and 56.8±38.2 ml\u002Fmin (right) or 58.2±33.4 ml\u002Fmin (left) in women. Duplex scanning ultrasonography using an intercostal approach enables easy imaging of bilateral internal thoracic arteries and visualizes entire internal thoracic artery structure by simply changing the probe position.Conclusion: Intercostal duplex scanning ultrasonography is thus recommended for reliable evaluation of the internal diameter and blood flow of the internal thoracic artery.",{"EN":529},"Evaluation of an internal thoracic artery as a coronary artery bypass graft by intercostal duplex scanning ultrasonography",{"VOID":531},"[\"8263949713825382407\"]",{"VOID":533},"Green GE, Stertzer SH, Reppert EH. Coronary arterial bypass grafts. Ann Thorac Surg 1968; 5: 443–50.\nKitamura S, Kawachi K, Taniguchi S, Kawata T, Kobayashi S, Nishioka H, et al. Long-term benefits of internal thoracic artery-coronary artery bypass in Japanese patients. Jpn J Thorac Cardiovasc Surg 1998; 46: 1–10.\nSons HJ, Marx R, Godehardt, Losse B, Kunert J, Birks W. Duplex sonography of the internal thoracic artery. J Thorac Cardiovasc Surg 1994; 108: 549–55.\nTakemura H, Kawasuji M, Sakakibara N, Matsumoto Y, Fujii S, Ushijima T, et al. Quantitative hemodynamic assessment of internal thoracic artery grafts using transthoracic duplex imaging (Eng abstr). J Jpn Assn Thorac Surg 1994; 42: 2171–77.\nKawaue Y, Hayashi S. Description of arterial grafts from the aspect of preoperative angiography (Eng abstr). J Jpn Assn Thorac Surg 1994; 42: 13–17.\nFurutani Y, Takahashi T, Imagawa H, Taniguchi K, Kadoba K, Matsuda H, et al. Noninvasive hemodynamic assessment of internal thoracic artery grafts using duplex echocardiography from supraclavicular fossa-a comparison with Doppler catheter method- (Eng abstr). J Jpn Assn Thorac Surg 1997, 45: 1803–09.\nGoto Y, Atsumi H, Kadowaki K, Sato T, Abe Y, Nakakome A, et al. Noninvasive assessment of left internal thoracic artery graft patency using transthoracic echocardiography (Eng abstr). J Jpn Assn Thorac Surg 1993; 41: 2013–18.\nSungun M, Duran E, Cebeci BS, Us MH, Saba D, Saygin G. The assessment of internal mammary artery grafts by color Doppler in coronary artery surgery. J Cardiovasc Surg 1998; 39: 75–78.\nSingh RN, Sosa JA. Internal mammary artery: a “live” conduit for coronary bypass. J Thorac Cardiovasc Surg 1984; 87: 936–38.\nTakemura H, Kawasuji M, Sakakibara N, Tedoriya T, Ushijima T, Watanabe Y. Internal thoracic artery graft function during exercise assessed by transthoracic Doppler echography. Ann Thorac Surg 1996; 61: 914–19.\nKobayashi H, Kitamura S, Oyama C, Kawachi K, Koh Y, Morita R, et al. A histologic study of atherosclerosis of the internal mammary artery utilized for coronary artery bypass surgery (Eng abstr). J Jpn Assn Thorac Surg 1987; 34: 1671–76.",{"VOID":535},"10.1007\u002FBF02913147","2024-06-25T00:10:33.848+00:00","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002FBF02913147",[539,554,567,580,593,608],{"id":540,"sortIndex":21,"researcher":20,"roles":541,"affiliations":542,"properties":551,"displayName":553,"givenName":20,"familyName":20},"7b78958a-2235-4767-a645-9b6d0c8ca7e7",[132],[543],{"id":544,"sortIndex":21,"affiliation":545,"properties":20},"83faeb77-6e71-4b1c-8c0a-923bd85d98c6",{"id":544,"createTime":20,"updateTime":20,"relativeEntities":546,"slug":20,"properties":547,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":550,"statistic":20},[],{"title":548},{"EN":549},"Department of Cardiovascular Surgery, Shin-Nittetsu Muroran General Hospital, Hokkaido, Japan",[],{"title":552},{"VI":553},"Norifumi 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SH. The problem of valve prosthesis-patient mismatch. Circulation. 1978;58:20–4.",{"doi":804},"10.1161\u002F01.CIR.58.1.20",{"id":20,"text":806,"url":20,"identifiers":807},"Rao V, Jamieson WR, Ivanov J, Armstrong S, David TE. Prosthesis-patient mismatch affects survival after aortic valve replacement. Circulation 2000;102(19 Suppl 3):III5–9.",{"doi":808},"10.1161\u002F01.CIR.102.suppl_3.III-5",{"id":20,"text":810,"url":20,"identifiers":811},"Blais C, Dumesnil JG, Baillot R, Simard S, Doyle D, Pibarot P. Impact of valve prosthesis-patient mismatch on short-term mortality after aortic valve replacement. Circulation. 2003;108:983–8.",{"doi":812},"10.1161\u002F01.CIR.0000085167.67105.32",{"id":20,"text":814,"url":20,"identifiers":815},"Tasca G, Brunelli F, Cirillo M, DallaTomba M, Mhagna Z, Troise G, et al. Impact of valve prosthesis-patient mismatch on left ventricular mass regression following aortic valve replacement. 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Eur J of Cardiothoracic Surg. 2006;30(1):10–4.",{"doi":863},"10.1016\u002Fj.ejcts.2006.03.046",{"id":20,"text":865,"url":20,"identifiers":866},"Kato Y, Suehiro S, Shibata T, Sasaki Y, Hirai H. Impact of valve prosthesis-patient mismatch on long-term survival and left ventricular mass regression after aortic valve replacement for aortic stenosis. J Card Surg. 2007;22:314–9.",{"doi":867},"10.1111\u002Fj.1540-8191.2007.00414.x",{"id":20,"text":869,"url":20,"identifiers":870},"Monin JL, Monchi M, Kirsch ME, Petit-Eisenmann H, Baleynaud S, Chauvel C, et al. Low-gradient aortic stenosis: impact of prosthesis-patient mismatch on survival. Eur Heart J. 2007;28:2620–6.",{"doi":871},"10.1093\u002Feurheartj\u002Fehm393",{"id":20,"text":873,"url":20,"identifiers":874},"Nozohoor S, Nilsson J, Luhrs C, Roijer A, Sjogren J. The influence of patient-prosthesis mismatch on in-hospital complications and early mortality after aortic valve replacement. J Heart Valve Dis. 2007;16:475–82.",{},{"id":20,"text":876,"url":20,"identifiers":877},"Ryomoto M, Mitsuno M, Yamamura M, Tanaka H, Kobayashi Y, Fukui S, et al. Patient-prosthesis mismatch after aortic valve replacement in the elderly. Gen Thorac Cardiovasc Surg. 2008;56:330–4.",{"doi":878},"10.1007\u002Fs11748-008-0255-6",{"id":20,"text":880,"url":20,"identifiers":881},"Tsutsumi K, Nagumo M, Nishikawa K, Takahashi R. Effect of prosthesis-patient mismatch on survival after aortic valve replacement using mechanical prostheses in patients with aortic stenosis. Gen Thorac Cardiovasc Surg. 2008;56:577–83.",{"doi":882},"10.1007\u002Fs11748-008-0317-9",{"id":20,"text":884,"url":20,"identifiers":885},"Vicchio M, Della Corte A, De Santo LS, De Feo M, Caianiello G, Scardone M, et al. Prosthesis-patient mismatch in the elderly: survival, ventricular mass regression, and quality of life. Ann Thoracic Surg. 2008;86:1791–7.",{"doi":886},"10.1016\u002Fj.athoracsur.2008.09.005",{"id":20,"text":888,"url":20,"identifiers":889},"Mannacio VA, De Amicis V, Di Tommaso L, Iorio F, Vosa C. Influence of prosthesis-patient mismatch on exercise-induced arrhythmias: a further aspect after aortic valve replacement. J Thorac Cardiovasc Surg. 2009;138:632–8.",{"doi":890},"10.1016\u002Fj.jtcvs.2009.01.009",{"id":20,"text":892,"url":20,"identifiers":893},"Mascherbauer J, Rosenhek R, Fuchs C, Pernicka E, Klaar U, Scholten C, et al. Moderate patient-prosthesis mismatch after valve replacement for severe aortic stenosis has no impact on short-term and long-term mortality. Heart. 2008;94:1639–45.",{"doi":894},"10.1136\u002Fhrt.2008.142596",{"id":20,"text":896,"url":20,"identifiers":897},"Mohty D, Dumesnil JG, Echahidi N, Mathieu P, Dagenais F, Voisine P, et al. Impact of prosthesis-patient mismatch on long-term survival after aortic valve replacement: influence of age, obesity, and left ventricular dysfunction. J Am Coll Cardiol. 2009;53:39–47.",{"doi":898},"10.1016\u002Fj.jacc.2008.09.022",{"id":20,"text":900,"url":20,"identifiers":901},"Pibarot P, Dumesnil JG, Cartier PC, Metras J, Lemieux M. Patient-prosthesis mismatch can be predicted at the time of operation. Ann Thoracic Surg. 2001;71:S265–8.",{"doi":902},"10.1016\u002FS0003-4975(01)02509-7",{"id":20,"text":904,"url":20,"identifiers":905},"Sakamoto Y, Hashimoto K, Okuyama H, Takakura H, Ishii S, Taguchi S, et al. Prevalence and avoidance of patient-prosthesis mismatch in aortic valve replacement in small adults. Ann Thoracic Surg. 2006;81:1305–9.",{"doi":906},"10.1016\u002Fj.athoracsur.2005.10.013",{"id":20,"text":908,"url":20,"identifiers":909},"Bleiziffer S, Echinger WB, Hettich I, Guenzinger R, Ruzicka D, Bauernschmitt R, Lange R. Prediction of valve prosthesis–patient mismatch prior to aortic valve replacement: which is the best method? Heart. 2007;93:615–20.",{"doi":910},"10.1136\u002Fhrt.2006.102764",{"id":20,"text":912,"url":20,"identifiers":913},"Zoghbi WA, Chambers JB, Dumesnil JG, Foster E, Gottdiener JS, Grayburn PA, et al. Recommendations for evaluation of prosthetic valves with echocardiography and doppler ultrasound: a report From the American Society of Echocardiography’s Guidelines and Standards Committee and the Task Force on Prosthetic Valves, developed in conjunction with the American College of Cardiology Cardiovascular Imaging Committee, Cardiac Imaging Committee of the American Heart Association, the European Association of Echocardiography, a registered branch of the European Society of Cardiology, the Japanese Society of Echocardiography and the Canadian Society of Echocardiography, endorsed by the American College of Cardiology Foundation, American Heart Association, European Association of Echocardiography, a registered branch of the European Society of Cardiology, the Japanese Society of Echocardiography, and Canadian Society of Echocardiography. J Am Soc Echocardiogr. 2009;22:975–1014; quiz 1082–4.",{"doi":914},"10.1016\u002Fj.echo.2009.07.013",{"id":20,"text":916,"url":20,"identifiers":917},"Pibarot P, Dumesnil JG. Hemodynamic and clinical impact of prosthesis-patient mismatch in the aortic valve position and its prevention. J Am Coll Cardiol. 2000;36:1131–41.",{"doi":918},"10.1016\u002FS0735-1097(00)00859-7",{"id":20,"text":920,"url":20,"identifiers":921},"Takakura H, Sasaki T, Hashimoto K, Hachiya T, Onoguchi K, Oshiumi M, et al. Hemodynamic evaluation of 19-mm Carpentier-Edwards pericardial bioprosthesis in aortic position. Ann Thoracic Surg. 2010;71:609–13.",{"doi":922},"10.1016\u002FS0003-4975(00)02210-4",{"id":20,"text":924,"url":20,"identifiers":925},"Sakamoto Y, Yoshitake M, Naganuma H, Kawada N, Kinouchi K, Hashimoto K. Reconsideration of patient-prosthesis mismatch definition from the valve indexed effective orifice area. Ann Thoracic Surg. 2010;89:1951–5.",{"doi":926},"10.1016\u002Fj.athoracsur.2010.03.011",{"id":20,"text":928,"url":20,"identifiers":929},"Dumesnil JG, Honos GN, Lemieux M, Beauchemin J. Validation and applications of indexed aortic prosthetic valve areas calculated by Doppler echocardiography. J Am Coll Cardiol. 1990;16:637–43.",{"doi":930},"10.1016\u002F0735-1097(90)90355-S",{"id":20,"text":932,"url":20,"identifiers":933},"Pibarot P, Dumesnil JG, Cartier PC, Metras J, Durand LG. Impact of prosthesis-patient mismatch on hemodynamics and symptomatic status, morbidity and mortality after aortic valve replacement with a bioprosthetic heart valve. J Heart Valve Dis. 1998;7:211–8.",{},{"id":20,"text":935,"url":20,"identifiers":936},"Rahimtoola SH. Determining that aortic valve stenosis is severe: back-to-the future: physical examination and aortic valve area index\u002Fenergy loss index ≤0.6 cm2\u002Fm2. J Am Coll Cardiol. 2010;3:563–6.",{"doi":937},"10.1016\u002Fj.jcmg.2010.02.006",{"id":20,"text":939,"url":20,"identifiers":940},"Daneshvar SA, Rahimtoola SH. Valve prosthesis-patient mismatch (VP-PM): a long-term perspective. J Am Coll Cardiol. 2012;60:1123–35.",{"doi":941},"10.1016\u002Fj.jacc.2012.05.035",{"id":20,"text":943,"url":20,"identifiers":944},"Kobayashi Y, Fukushima Y, Hayase T, Kojima K, Endo G. Clinical outcome of aortic valve replacement with 16-mm ATS-advanced performance valve for small aortic annulus. Ann Thoracic Surg. 2010;89:1195–9.",{"doi":945},"10.1016\u002Fj.athoracsur.2009.12.074",{"id":20,"text":947,"url":20,"identifiers":948},"Okamura H, Yamaguchi A, Yoshizaki T, Nagano H, Itoh S, Morita H, et al. Clinical outcomes and hemodynamics of the 19-mm Perimount Magna bioprosthesis in an aortic position: comparison with the 19-mm Medtronic Mosaic Ultra Valve. Circ J. 2012;76:102–8.",{"doi":949},"10.1253\u002Fcircj.CJ-11-0728",{"id":20,"text":951,"url":20,"identifiers":952},"Hashimoto K. Patient-prosthesis mismatch: the Japanese experience. Ann Thorac Cardiovasc Surg. 2006;12:159–65.",{},{"id":20,"text":954,"url":20,"identifiers":955},"ATS Medical, Inc.; Pre-Market approval application-Food and Drug Administration; 2000. P990046.",{},{"id":20,"text":957,"url":20,"identifiers":958},"Hashimoto K, Mashiko K, Nakano M, Horikoshi S, Kurosawa H, Arai T. Use of the 21 mm Bjork-Shiley Monostrut valve in patients with a narrow aortic root. Cardiovasc Surg. 1994;2:456–9.",{},{"id":20,"text":960,"url":20,"identifiers":961},"Manouguian S, Seybold-Epting W. Patch enlargement of the aortic valve ring by extending the aortic incision into the anterior mitral leaflet. New operative technique. J Thorac Cardiovasc Surg. 1979;78:402–12.",{"doi":962},"10.1016\u002FS0022-5223(19)38105-X",{"id":20,"text":964,"url":20,"identifiers":965},"Nicks R, Cartmill T, Bernstein L. Hypoplasia of the aortic root. The problem of aortic valve replacement. Thorax. 1970;25:339–46.",{"doi":966},"10.1136\u002Fthx.25.3.339",{"id":20,"text":968,"url":20,"identifiers":969},"Okuyama H, Hashimoto K, Kurosawa H, Tanaka K, Sakamoto Y, Shiratori K. Midterm results of Manouguian double valve replacement: comparison with standard double valve replacement. J Thorac Cardiovasc Surg. 2005;129:869–74.",{"doi":970},"10.1016\u002Fj.jtcvs.2004.10.026",{"id":20,"text":972,"url":20,"identifiers":973},"Moon MR, Lawton JS, Moazami N, Munfakh NA, Pasque MK, Damiano RJ Jr. POINT: prosthesis-patient mismatch does not affect survival for patients greater than 70 years of age undergoing bioprosthetic aortic valve replacement. J Thorac Cardiovasc Surg. 2009;137:278–83.",{"doi":974},"10.1016\u002Fj.jtcvs.2008.09.059",{"id":20,"text":976,"url":20,"identifiers":977},"Vicchio M, De Feo M, Cotrufo M. Prosthesis-patient mismatch does not affect survival and quality of life in the elderly having bileaflet prostheses implant. J Thorac Cardiovasc Surg. 2009;138:787–8.",{"doi":978},"10.1016\u002Fj.jtcvs.2009.03.065",{"id":20,"text":980,"url":20,"identifiers":981},"Urso S, Sadaba R, Vives M, Trujillo J, Beltrame S, Soriano B, et al. Patient-prosthesis mismatch in elderly patients undergoing aortic valve replacement: impact on quality of life and survival. J Heart Valve Dis. 2009;18:248–55.",{},{"id":20,"text":983,"url":20,"identifiers":984},"Tao K, Sakata R, Iguro Y, Ueno M, Tanaka Y, Otsuji Y, et al. Impact of valve prosthesis-patient mismatch on intermediate-term outcome and regression of left ventricular mass following aortic valve replacement with mechanical prosthesis. J Card Surg. 2007;22:486–92.",{"doi":985},"10.1111\u002Fj.1540-8191.2007.00465.x",{"id":20,"text":987,"url":20,"identifiers":988},"Ruel M, Al-Faleh H, Kulik A, Chan KL, Mesana TG, Burwash IG. Prosthesis-patient mismatch after aortic valve replacement predominantly affects patients with preexisting left ventricular dysfunction: effect on survival, freedom from heart failure, and left ventricular mass regression. J Thorac Cardiovasc Surg. 2006;131:1036–44.",{"doi":989},"10.1016\u002Fj.jtcvs.2005.10.028",{"id":20,"text":991,"url":20,"identifiers":992},"Head SJ, Mokhles MM, Osnabrugge RL, Pibarot P, Mack MJ, Takkenberg JJ, et al. The impact of prosthesis-patient mismatch on long-term survival after aortic valve replacement: a systematic review and meta-analysis of 34 observational studies comprising 27 186 patients with 133 141 patient-years. Eur Heart J. 2012;33:1518–29.",{"doi":993},"10.1093\u002Feurheartj\u002Fehs003",{"id":20,"text":995,"url":20,"identifiers":996},"Takagi H, Yamamoto H, Iwata K, Goto SN, Umemoto T. A meta-analysis of effects of prosthesis-patient mismatch after aortic valve replacement on late mortality. Int J Cardiol. 2012;159:150–4.",{"doi":997},"10.1016\u002Fj.ijcard.2012.04.084",{"id":20,"text":999,"url":20,"identifiers":1000},"Misawa Y, Miyata H, Konishi H, Uenishi U, Motomura N, Kobayashi J, et al. Patient-prosthesis mismatch in Patient with aortic valve replacement (abstract). Gen Thorac Cardiovasc Surg. 2011;59(Suppl):194.",{},{"id":20,"text":1002,"url":20,"identifiers":1003},"Pibarot P, Dumesnil JG. Valve prosthesis-patient mismatch, 1978 to 2011: from original concept to compelling evidence. J Am Coll Cardiol. 2012;60:1136–9.",{"doi":1004},"10.1016\u002Fj.jacc.2012.07.005",{"id":1006,"createTime":1007,"updateTime":1008,"relativeEntities":1009,"slug":1010,"properties":1011,"entityType":123,"verifyStatus":124,"verifyTime":1020,"verifyNote":126,"languages":20,"translateLanguages":20,"viewCount":21,"primaryUrl":1021,"fullTextUrl":20,"authors":1022,"publicationType":219,"publisherRelationship":1103,"citationCount":479,"citationInfo":1158,"publishDate":1161,"publishYear":1159,"citationAnalyzeStatus":677,"lastCitationAnalyze":1162,"indexDatabases":1163,"openAccess":20,"references":1164,"isForceReanalyzing":302},"cd0d4f83-f0a2-4aab-800b-f7ab6675d053","2024-01-04T11:12:45.599+00:00","2026-07-24T06:14:33.404+00:00",[],"Is-conservative-therapy-acceptable-for-thrombosed-type-A-acute-aortic-dissection-",{"abstract":1012,"title":1014,"gsPaper":1016,"doi":1018},{"EN":1013},"\n                Objectives: The surgical treatment for thrombosed type A dissection is controversial because it has a better prognosis than with conservative therapy. We discuss the validity of conservative therapy for thrombosed type A dissection and examine the relationship between the morphology of the dissecting aorta and its operative indications. Methods: Subjects were 28 patients with acute type A aortic dissection in which the false lumen was totally thrombosed who were transferred to our hospital in the acute phase between 1990 and 2002. We performed medical therapy on all of them at first. We calculated the ratio of the false lumen and the true lumen (F\u002FT) by enhanced computed tomography scan at the onset. The maximum aneurysmal size was measured approximately every week. Results: Fifteen of them needed surgical repair; six in the acute phase and nine in chronic. One-year and 5-year survival rate for the operative and the non-operative group are 93.3, 80.0 and 92.3, 92.3% respectively. The mean F\u002FT was 30% in the operative group and 50% in the non-operative group (p=0.04). There was almost no reduction in size in the operative group during the follow up (−0.5±1.2 mm). Conclusions: Conservative therapy with frequent imaging follow-up can be a rational option for thrombosed type A acute aortic dissection. A low ratio of the false lumen and the true lumen at the onset and no reduction in the aneurysmal size are the predictive factors by which we should consider surgical repair.",{"EN":1015},"Is conservative therapy acceptable for thrombosed type A acute aortic dissection?",{"VOID":1017},"[\"13856224835404901212\"]",{"VOID":1019},"10.1007\u002Fs11748-003-0109-1","2024-04-29T12:38:06.530+00:00","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs11748-003-0109-1",[1023,1038,1051,1064,1077,1090],{"id":1024,"sortIndex":21,"researcher":20,"roles":1025,"affiliations":1026,"properties":1035,"displayName":1037,"givenName":20,"familyName":20},"147adbef-4494-4135-8ffd-a58dad839fee",[132],[1027],{"id":1028,"sortIndex":21,"affiliation":1029,"properties":20},"5358d176-7ee7-467e-98fe-0da30911e00f",{"id":1028,"createTime":20,"updateTime":20,"relativeEntities":1030,"slug":20,"properties":1031,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":1034,"statistic":20},[],{"title":1032},{"VI":1033},"Division of Cardiovascular Surgery, National Sapporo Hospital, Sapporo, Japan",[],{"title":1036},{"VI":1037},"Yasushige Shingu",{"id":1039,"sortIndex":149,"researcher":20,"roles":1040,"affiliations":1041,"properties":1048,"displayName":1050,"givenName":20,"familyName":20},"acc6cdb1-4d4e-4e2f-b561-91d6f74cc535",[132],[1042],{"id":1028,"sortIndex":21,"affiliation":1043,"properties":20},{"id":1028,"createTime":20,"updateTime":20,"relativeEntities":1044,"slug":20,"properties":1045,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":1047,"statistic":20},[],{"title":1046},{"VI":1033},[],{"title":1049},{"VI":1050},"Kazuhiro Myojin",{"id":1052,"sortIndex":163,"researcher":20,"roles":1053,"affiliations":1054,"properties":1061,"displayName":1063,"givenName":20,"familyName":20},"1119c1db-a594-4fee-9bd1-567dda02212e",[132],[1055],{"id":1028,"sortIndex":21,"affiliation":1056,"properties":20},{"id":1028,"createTime":20,"updateTime":20,"relativeEntities":1057,"slug":20,"properties":1058,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":1060,"statistic":20},[],{"title":1059},{"VI":1033},[],{"title":1062},{"VI":1063},"Yoshimitsu Ishibashi",{"id":1065,"sortIndex":177,"researcher":20,"roles":1066,"affiliations":1067,"properties":1074,"displayName":1076,"givenName":20,"familyName":20},"e89eaff0-1b9f-4e4a-a765-d1a76c90f9e2",[132],[1068],{"id":1028,"sortIndex":21,"affiliation":1069,"properties":20},{"id":1028,"createTime":20,"updateTime":20,"relativeEntities":1070,"slug":20,"properties":1071,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":1073,"statistic":20},[],{"title":1072},{"VI":1033},[],{"title":1075},{"VI":1076},"Koji Ishii",{"id":1078,"sortIndex":193,"researcher":20,"roles":1079,"affiliations":1080,"properties":1087,"displayName":1089,"givenName":20,"familyName":20},"a3a30753-228c-4ee2-89b7-8c5baeae23e2",[132],[1081],{"id":1028,"sortIndex":21,"affiliation":1082,"properties":20},{"id":1028,"createTime":20,"updateTime":20,"relativeEntities":1083,"slug":20,"properties":1084,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":1086,"statistic":20},[],{"title":1085},{"VI":1033},[],{"title":1088},{"VI":1089},"Masakazu Kawasaki",{"id":1091,"sortIndex":207,"researcher":20,"roles":1092,"affiliations":1093,"properties":1100,"displayName":1102,"givenName":20,"familyName":20},"8a3c10b8-e438-47b9-860e-bec675a39d42",[132],[1094],{"id":1028,"sortIndex":21,"affiliation":1095,"properties":20},{"id":1028,"createTime":20,"updateTime":20,"relativeEntities":1096,"slug":20,"properties":1097,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":1099,"statistic":20},[],{"title":1098},{"VI":1033},[],{"title":1101},{"VI":1102},"Keitaro 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Y, Watanabe S, Yonezawa M, Itani Y, Inoue T, Takasu J, et al. Long-term prognosis of acute aortic dissection with medical treatment: A survey of 263 unoperated patients. Jpn Circ J. 2001; 65: 359–63.",{"doi":292},{"id":20,"text":1169,"url":20,"identifiers":1170},"Saitoh Y, Nakayama K, Yamauchi M, Gu K, Sasaki T, Nosaka S, et al. Acute thrombosed aortic dissection: Its clinical manifestation and treatment for Stanford A type (Eng abstr). Nippon Kyobu Geka Gakkai Zasshi 1995; 43: 1789–94.",{},{"id":20,"text":1172,"url":20,"identifiers":1173},"Matsuo H, Inoue K, Uchida H, Kazui K, Kawata S, Kumazaki T, et al. Management of patients with thrombosed Stanford type A aortic dissection: Long-term results from 20 hospitals. The Journal of Japanese College of Angiology, 2002; 42: 67–71.",{},{"id":288,"text":1175,"url":290,"identifiers":1176},"Choi SH, Choi SJ, Kim JH, Bae SJ, Lee JS, Song KS, et al. Useful CT finding for predicting the progression of aortic intramural hematoma to overt aortic dissection. Journal of Computer Assisted Tomography 2001; 25: 295–9.",{"doi":292},{"id":288,"text":1178,"url":290,"identifiers":1179},"Hayashi H, Kawamata H, Takagi R, Kumazaki T. Late phase contrast enhanced-CT analysis of thrombosed type aortic dissection. Nippon Acta Radiologica 1995; 55: 845–54.",{"doi":292},{"id":20,"text":1181,"url":20,"identifiers":1182},"Ochi R. Seirigaku text, 4th ed., chapter 14, 272.",{},{"id":1184,"createTime":1185,"updateTime":1186,"relativeEntities":1187,"slug":1188,"properties":1189,"entityType":123,"verifyStatus":124,"verifyTime":1200,"verifyNote":126,"languages":20,"translateLanguages":20,"viewCount":21,"primaryUrl":1201,"fullTextUrl":20,"authors":1202,"publicationType":219,"publisherRelationship":1244,"citationCount":21,"citationInfo":1299,"publishDate":1302,"publishYear":1300,"citationAnalyzeStatus":19,"lastCitationAnalyze":1303,"indexDatabases":1304,"openAccess":20,"references":20,"isForceReanalyzing":302},"cc71a22f-68cc-4a13-80ed-bd347d811156","2024-02-10T21:47:11.088+00:00","2026-07-23T01:00:37.848+00:00",[],"Retained-foreign-body-following-pleural-drainage-with-a-small-bore-catheter",{"abstract":1190,"title":1192,"gsPaper":1194,"references":1196,"doi":1198},{"EN":1191},"Small-bore radiopaque drains can be used to drain pleural effusions. They offer reliable drainage of simple pleural effusions and provide a safe, less-invasive, more comfortable alternative to the standard tube thoracostomy. Importantly, removal of such drains does not require purse-string sutures and hence can be removed without assistance. We report here the cautionary tale of a retained foreign body related to drainage of a pleural effusion with a Pleurocath in a patient following cardiac surgery to raise awareness of this potential complication. Emphasized is the need for all staff to be familiar with the normal appearance of equipment being utilized in the ward and to report when incomplete removal of drain equipment is suspected. In addition, amendments to insertion techniques for such small-bore drains are proposed to avoid similar undue complications.",{"EN":1193},"Retained foreign body following pleural drainage with a small-bore catheter",{"VOID":1195},"[\"16657369629192926994\"]",{"VOID":1197},"Chetty GK, Elahi MM, Siddagangaiah V, Leverment JN. Bonanno’s catheter: a less invasive and cost-effective alternative for drainage of pleural effusion. J Thorac Cardiovasc Surg 2005;129:219–220.\nRoberts JS, Bratton SL, Brogan TV. Efficacy and complications of percutaneous pigtail catheters for thoracostomy in pediatric patients. Chest 1998;114:1116–1121.\nLegrand M, Lecuyer L, Van De Louw A, Thierry S. Pleural drain malposition. Intensive Care Med 2006;32:941–942.\nGrodzin CJ, Balk RA. Indwelling small pleural catheter needle thoracentesis in the management of large pleural effusions. Chest 1997;111:981–988.\nGammie JS, Banks MC, Fuhrman CR, Pham SM, Griffith BP, Keenan RJ, et al. The pigtail catheter for pleural drainage: a less invasive alternative to tube thoracostomy. JSLS 1999;3: 57–61.\nMoe M, Hussain A. Broken chest tube: a rare complication from use of Bonanno catheter for drainage of a malignant pleural effusion. Clin Oncol 2003;15:220.",{"VOID":1199},"10.1007\u002Fs11748-009-0469-2","2024-05-16T02:32:57.984+00:00","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs11748-009-0469-2",[1203,1218,1231],{"id":1204,"sortIndex":21,"researcher":20,"roles":1205,"affiliations":1206,"properties":1215,"displayName":1217,"givenName":20,"familyName":20},"0f9b22d2-26c2-4a5b-84a6-1aacbeed122f",[132],[1207],{"id":1208,"sortIndex":21,"affiliation":1209,"properties":20},"3e4669d1-93ed-4da8-82ee-e93a656ddf45",{"id":1208,"createTime":20,"updateTime":20,"relativeEntities":1210,"slug":20,"properties":1211,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":1214,"statistic":20},[],{"title":1212},{"VI":1213},"Department of Cardiothoracic Surgery, St. Vincent’s Hospital, Fitzroy, Australia",[],{"title":1216},{"VI":1217},"Alenka 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               Objectives: Preoperative chemotherapy is frequently used for advanced lung cancer. As a valid alternative to pneumonectomy, bronchoplasty has the advantage of enabling lung parenchyma function to be preserved. The effects of antineoplastic agents on healing bronchial anastomosis remain unclear. We studied the effects of preoperative chemotherapy on wound healing in bronchial anastomoses and clarified causes of wound healing impairment in rats. Methods: In experiment I, at 3 days before surgery, rats were injected with cyclophosphamide, doxorubicin, and vincristine (CAV group) or cisplatin and etoposide (PVP treated rats). In experiment II, at 48 hrs before surgery, rats were treated with rabbit antirat macrophage serum and antirat monocyte chemoattractant protein-1 antibody to inhibit macrophage infiltration. On days 3, 5, and 7 after bronchus anastomosis, wound healing was assessed by examining bursting strength and hydroxyproline tissue content. Results: CAV-treated rats showed significant impaired wound healing, marked severe leucopenia, and reduced macrophage infiltration. The PVP group showed no significant changes. In experiment II, rats exhibited inhibited macrophage infiltration, which is associated with significantly impaired of wound healing. Conclusions: Our study suggests that induction chemotherapy, associated with leukopenia in the early phase of wound healing, increases the risk of bronchial anastomosis leakage. Postoperative macrophage depletion is one of the most important causes of impaired wound healing.",{"EN":1315},"Effects of induction therapy on wound healing at bronchial anastomosis sites in rats",{"VOID":1317},"[\"3196669993457401510\"]",{"VOID":1319},"Elias AD, Skarin AT, Leong T, Mentzer S, Strauss G, Lynch T, et al. Neoadjuvant therapy for surgically staged IIIA N2 non-small-cell lung cancer (NSCLC). Lung Cancer 1997; 17: 147–61.\nGaissert HA, Mathisen DJ, Moncure AC, Hilgenberg AD, Grillo HC, Wain JC. Survival and function after sleeve lobectomy for lung cancer. J Thorac Cardiovasc Surg 1996; 111: 948–53.\nDevereux DF, Triche TJ, Webber BL, Thibault LE, Brennan MF. A study of adriamycin-reduced wound breaking strenght in rats: An evaluation by light and electron microscopy, induction of collagen maturation, and hydroxyproline content. Cancer 1980; 45: 2811–5.\nSalm R, Wullich B, Kiefer G, Fiebig HH, Farthmann EH. Effects of a three-drug antineoplastic protocol of wound healing in rats: A biomechanical and histologic study on gastrointestinal anastomoses and laparotomy wounds. J Surg Oncol 1991; 47: 5–11.\nShirafuji T, Oka T, Sawada T, Tamura K, Kishimoto K, Ayabe H, et al. The importance of peripheral blood leukocytes and macrophage infiltration on bronchial wall wound healing in rats treated preoperatively with anticancer agents. Surg Today 2001; 31: 308–16.\nFukuoka M, Furuse K, Saijo N, Nishiwaki Y, Ikegami H, Suemasu K, et al. Randomized trial of cyclophosphamide, doxorubicin, and vincristine versus cisplatin and etoposide versus alternation of these regimens in small-cell lung cancer. J Natl Cancer Inst 1991; 83: 855–61.\nJohnson DH, Hainsworth JD, Hande KR, Greco FA. Current status of etoposide in the management of small-cell lung cancer. Cancer 1991; 67 (Suppl I): 231–44.\nArmitage P, Berry G. Statistical methods in medical research. 3ed edition, Oxford: Blackwell Scientific Publications, 1994: 392–550.\nSensaki K, Arai T, Takemiya K, Kase K, Ogata T, Kikuchi M, et al. Effect of low-power laser on wound healing at the site of tracheal anastomosis in rat. J Natl Def Med Coll 1993; 18: 152–3.\nDiPietro LA, Polverini PJ, Rahbe SM, Kovacs EJ. Modulation of JE\u002FMCP-1 expression in dermal wound repair. Am J Pathol 1995; 146: 868–75.\nLeibovich SJ, Ross R. The role of the macrophage in wound repair: A study with hydrocortisone and antimacrophage serum. Am J Pathol 1975; 78: 71–100.\nOgata H, Takeya M, Yoshimura T, Takagi K, Takahashi K. The role of monocyte chemoattractant protein-1 (MCP-1) in the pathogenesis of collagen-induced arthritis in rats. J Pathol 1997; 182: 106–14.\nHananel N, Gordon PH. Effect of 5-fluorouracil and leucovorin on the integrity of colonic anastomoses in the rat. Dis Colon Rectum 1995; 38: 886–90.\nRoss R. The pathogenesis of atherosclerosis: A perspective for the 1990s. Nature 1993; 362: 801–9.\nBennett NT, Schultz GS. Growth factors and wound healing: Biochemical properties of growth factors and their receptors. Am J Surg 1993; 165: 728–37.\nBlotnick S, Peoples GE, Freeman MR, Eberlein TJ, Klagsbrun M. T lymphocytes synthesize and export heparin-binding epidermal growth factor-like growth factor and basic fibroblast growth factor, mitogens for vascular cells and fibroblasts. Differential production and release by CD4+ and CD8+ T cells. Proc Natl Acad Sci USA 1994; 91: 2890–4.\nRappolee DA, Mark D, Banda MJ, Werb Z. Wound macrophages express TGF-alpha and other growth factors in vivo: Analysis by mRNA phenotyping. Science 1988; 241: 708–12.\nFukasawa M, Campeau JD, Yanagihara DL, Rodgers KE, Dizerega GS. Mitogenic and protein synthetic activity of tissue repair cells: Control by the postsurgical macrophage. J Invest Surg 1989; 2: 169–80.\nMiller JD, DeHoyos A. An evaluation of the role of omentopexy and of early perioperative corticosteroid administration in clinical lung transplantation: The University of Toronto and Washington University Lung Transplant Programs. J Thorac Cardiovasc Surg 1993; 105: 247–52.\nNagayasu T, Kawahara K, Takahashi T, Ide S, Sasaki N, Ayabe H, et al. Prolongation of lung xenograft survival in rats with a short course of deoxyspergualin and cyclosporin A. Transpl Int 1996; 9: 184–93.",{"VOID":1321},"10.1007\u002Fs11748-003-0017-4","2024-09-04T20:36:08.339+00:00","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs11748-003-0017-4",[1325,1340,1353,1366,1379,1392,1407,1422],{"id":1326,"sortIndex":21,"researcher":20,"roles":1327,"affiliations":1328,"properties":1337,"displayName":1339,"givenName":20,"familyName":20},"aa7b0ebf-de94-4912-a9fe-9db63c07ecf7",[132],[1329],{"id":1330,"sortIndex":21,"affiliation":1331,"properties":20},"62eff2ab-be3e-4200-b52c-02da60694ee4",{"id":1330,"createTime":20,"updateTime":20,"relativeEntities":1332,"slug":20,"properties":1333,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":1336,"statistic":20},[],{"title":1334},{"VI":1335},"First Department of Surgery, Nagasaki University School of Medicine, Nagasaki, Japan",[],{"title":1338},{"VI":1339},"Tomoyuki 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EE. Spontaneous pneumothorax in two siblings. Hospitalstid 1921; 64: 573–4.",{},{"id":20,"text":1648,"url":20,"identifiers":1649},"Sharpe IK, Ahmad M, Braun W. Familial spontaneous pneumothorax and HLA antigen. Chest 1980; 78: 264–8.",{"doi":1650},"10.1378\u002Fchest.78.2.264",{"id":20,"text":1652,"url":20,"identifiers":1653},"Terasaki PI. Microdroplet testing for HLA-A,-B,-C, and-D antigens. Am J Clin Path 1978; 69: 103–220.",{"doi":1654},"10.1093\u002Fajcp\u002F69.2.103",{"id":20,"text":1656,"url":20,"identifiers":1657},"Mitsuo A, Hiroyuki M. Clinic of spontaneous pneumothorax. Jpn J Chest Dis 1980; 39: 102–10.",{},{"id":20,"text":1659,"url":20,"identifiers":1660},"Wilson WG, Aylsworth AS. Familial spontaneous pneumothorax. Pediatrics 1979; 64: 172–5.",{"doi":1661},"10.1542\u002Fpeds.64.2.172",{"id":20,"text":1663,"url":20,"identifiers":1664},"Taku I, Mitsunori S, Jyoichi K, Akihiko I, Kenji S, Gyo Y. Familial spontaneous pneumothorax involving three sisters and a son of one af-fected sister. Jpn J Chest Dis 1990; 49: 912–5.",{},{"id":20,"text":1666,"url":20,"identifiers":1667},"Satoshi N, Yasumasa O, Naoki T, Tetsuya Y, Katsuhiro A. Case of spontaneous pneumothorax in twins. Jpn J Chest Dis 1985; 44: 1040–3.",{},{"id":20,"text":1669,"url":20,"identifiers":1670},"Leuler-Petersen P, Grunnet N, Jespersen TW, Jaeger P. Familial spontaneous pneumothorax. Eur Respir J 1990; 3: 342–5.",{"doi":1671},"10.1183\u002F09031936.93.03030342",{"id":20,"text":1673,"url":20,"identifiers":1674},"Cheng YJ, Chou SH, Kao EL. Familial spontaneous pneumothorax-report of seven cases in two families. Kaohsiung J Med Sci 1992; 8: 390–4.",{},{"id":20,"text":1676,"url":20,"identifiers":1677},"Abolnik IZ, Lossos IS, Zlotogora J, Brauer R. On the inheritance of primary spontaneous pneumothorax. Am J Med Genet 1991; 40: 155–8.",{"doi":1678},"10.1002\u002Fajmg.1320400207",{"id":1680,"createTime":1681,"updateTime":1682,"relativeEntities":1683,"slug":1684,"properties":1685,"entityType":123,"verifyStatus":124,"verifyTime":1696,"verifyNote":126,"languages":20,"translateLanguages":20,"viewCount":21,"primaryUrl":1697,"fullTextUrl":20,"authors":1698,"publicationType":219,"publisherRelationship":1750,"citationCount":21,"citationInfo":1805,"publishDate":1808,"publishYear":1806,"citationAnalyzeStatus":19,"lastCitationAnalyze":1682,"indexDatabases":1809,"openAccess":20,"references":20,"isForceReanalyzing":302},"f11ad002-6878-407e-80c1-b661e77984ca","2023-12-28T12:30:44.243+00:00","2026-07-22T01:59:58.842+00:00",[],"Sentinel-lymph-node-biopsy-for-lung-cancer",{"abstract":1686,"title":1688,"gsPaper":1690,"references":1692,"doi":1694},{"EN":1687},"Sentinel lymph node biopsy is a technique to identify the first lymph node (or nodes) draining a tumor. The underlying principle is that as the first site of cancer spread, evaluation of the sentinel node will be most predictive for wider nodal involvement. The introduction of sentinel node biopsy revolutionized the surgical management of cutaneous melanoma and breast cancer, becoming a key component in the management of such patients. For over 20 years, thoracic surgeons have similarly worked to apply this technique to lung cancer but have thus far not had the same impact on lung surgery. In this review, we will summarize the ongoing discussions on the role of sentinel node biopsy in lung cancer, the methods for identifying the sentinel node, and the techniques for evaluating the sentinel node specimen. We will also highlight some of the pressing questions investigators should consider when designing a trial for sentinel node mapping. This will clarify the current status of sentinel node biopsy in lung cancer and thus highlight important future directions for research.",{"EN":1689},"Sentinel lymph node biopsy for lung cancer",{"VOID":1691},"[\"14360294447736594129\"]",{"VOID":1693},"Gao SJ, Kim AW, Puchalski JT, Bramley K, Detterbeck FC, Boffa DJ, et al. Indications for invasive mediastinal staging in patients with early non-small cell lung cancer staged with PET-CT. Lung Cancer. 2017;109(April):36–41.\nMorton DL, Wen DR, Wong JH, Economou JS, Cagle LA, Storm FK, et al. Technical details of intraoperative lymphatic mapping for early stage melanoma. Arch Surg. 1992;127(4):392–9.\nNomori H, Iwatani K, Kobayashi H, Mori A, Yoshioka S. Omission of mediastinal lymph node dissection in lung cancer: its techniques and diagnostic procedures. Ann Thorac Cardiovasc Surg. 2006;12(2):83–8.\nAllen MS, Darling GE, Pechet TTV, Mitchell JD, Herndon JE, Landreneau RJ, et al. Morbidity and mortality of major pulmonary resections in patients with early-stage lung cancer: initial results of the randomized, prospective ACOSOG Z0030 trial. Ann Thorac Surg. 2006;81(3):1013–20.\nDarling GE, Allen MS, Decker PA, Ballman K, Malthaner RA, Inculet RI, et al. Randomized trial of mediastinal lymph node sampling versus complete lymphadenectomy during pulmonary resection in the patient with N0 or N1 (less than hilar) non-small cell carcinoma: results of the American College of Surgery Oncology Group Z0030 Trial. J Thorac Cardiovasc Surg. 2011;141(3):662–8.\nNomori H, Mori T, Ikeda K, Yoshimoto K, Iyama K, Suzuki M. Segmentectomy for selected cT1N0M0 non-small cell lung cancer: a prospective study at a single institute. J Thorac Cardiovasc Surg. 2012;144(1):87–93.\nNomori H, Ohba Y, Shibata H, Shiraishi K, Mori T, Shiraishi S. Required area of lymph node sampling during segmentectomy for clinical stage IA non-small cell lung cancer. J Thorac Cardiovasc Surg. 2010;139(1):38–42.\nMoroga T, Yamashita SI, Tokuishi K, Miyawaki M, Anami K, Yamamoto S, et al. Thoracoscopic segmentectomy with intraoperative evaluation of sentinel nodes for stage I non-small cell lung cancer. Ann Thorac Cardiovasc Surg. 2012;18(2):89–94.\nDigesu CS, Hachey KJ, Gilmore DM, Khullar OV, Tsukada H, Whang B, et al. Long-term outcomes after near-infrared sentinel lymph node mapping in non-small cell lung cancer. J Thorac Cardiovasc Surg. 2018;155(3):1280–91.\nLittle AG, DeHoyos A, Kirgan DM, Arcomano TR, Murray KD, Wood D, et al. Intraoperative lymphatic mapping for non-small cell lung cancer: the sentinel node technique. J Thorac Cardiovasc Surg. 1999;117(2):220–4.\nSugi K, Fukuda M, Nakamura H, Kaneda Y. Comparison of three tracers for detecting sentinel lymph nodes in patients with clinical N0 lung cancer. Lung Cancer. 2003;39(1):37–40.\nRzyman W, Hagen OM, Dziadziuszko R, Kobierska-Gulida G, Karmolinski A, Lothe MI, et al. Blue-dye intraoperative sentinel lymph node mapping in early non-small cell lung cancer. Eur J Surg Oncol. 2006;32(4):462–5.\nSchmidt FE, Woltering EA, Webb WR, Garcia OM, Cohen JE, Rozans MH. Sentinel nodal assessment in patients with carcinoma of the lung. Ann Thorac Surg. 2002;74(3):870–5.\nFaries MB, Bleicher RJ, Ye X, Essner R, Morton DL, Grannis FW, et al. Lymphatic mapping and sentinel lymphadenectomy for primary and metastatic pulmonary malignant neoplasms. Arch Surg. 2004;139(8):870–7.\nTiffet O, Nicholson AG, Khaddage A, Prévot N, Ladas G, Dubois F, et al. Feasibility of the detection of the sentinel lymph node in peripheral non-small cell lung cancer with radio isotopic and blue dye techniques. Chest. 2005;127(2):443–8.\nMeyer A, Cheng C, Antonescu C, Pezzetta E, Bischof-Delaloye A, Ris H-B. Successful migration of three tracers without identification of sentinel nodes during intraoperative lymphatic mapping for non-small cell lung cancer. Interact Cardiovasc Thorac Surg. 2006;6(2):214–8.\nRzyman W, Hagen OM, Dziadziuszko R, Kobierska-Gulida G, Karmolinski A, Lothe IM, et al. Intraoperative, radio-guided sentinel lymph node mapping in 110 nonsmall cell lung cancer patients. Ann Thorac Surg. 2006;82(1):237–42.\nNomori H, Ohba Y, Yoshimoto K, Shibata H, Mori T, Shiraishi S, et al. Difference of sentinel lymph node identification between tin colloid and phytate in patients with non-small cell lung cancer. Ann Thorac Surg. 2009;87(3):906–10.\nAbele JT, Allred K, Clare T, Bédard ELR. Lymphoscintigraphy in early-stage non-small cell lung cancer with technetium-99 m nanocolloids and hybrid SPECT\u002FCT: a pilot project. Ann Nucl Med. 2014;28(5):477–83.\nKim S, Kim HK, Kang DY, Jeong JM, Choi YH. Intra-operative sentinel lymph node identification using a novel receptor-binding agent (technetium-99 m neomannosyl human serum albumin, 99mTc-MSA) in stage I non-small cell lung cancer. Eur J Cardio-thorac Surg. 2010;37(6):1450–6.\nLiptay MJ, Masters GA, Winchester DJ, Edelman BL, Garrido BJ, Hirschtritt TR, et al. Intraoperative radioisotope sentinel lymph node mapping in non-small cell lung cancer. Ann Thorac Surg. 2000;70(2):384–9.\nNomori H, Horio H, Naruke T, Orikasa H, Yamazaki K, Suemasu K. Use of technetium-99m tin colloid for sentinel lymph node identification in non-small cell lung cancer. J Thorac Cardiovasc Surg. 2002;124(3):486–92.\nLiptay MJ, Grondin SC, Fry WA, Pozdol C, Carson D, Knop C, et al. Intraoperative sentinel lymph node mapping in non-small-cell lung cancer improves detection of micrometastases. J Clin Oncol. 2002;20(8):1984–8.\nKaramustafaoglu YA, Yoruk Y, Yanik F, Sarikaya A. Sentinel lymph node mapping in patients with operable non-small cell lung cancer. J Thorac Dis. 2013;5(3):317–20.\nKim HK, Kim S, Sung HK, Lee YS, Jeong JM, Choi YH. Comparison between preoperative versus intraoperative injection of technetium-99 m neomannosyl human serum albumin for sentinel lymph node identification in early stage lung cancer. Ann Surg Oncol. 2012;19(4):1343–9.\nLiptay MJ, D’amico TA, Nwogu C, Demmy TL, Wang XF, Gu L, et al. Intraoperative sentinel node mapping with technitium-99 in lung cancer: results of CALGB 140203 Multicenter Phase II Trial. J Thorac Oncol. 2009;4(2):198–202.\nNakagawa T, Minamiya Y, Katayose Y, Saito H, Taguchi K, Imano H, et al. A novel method for sentinel lymph node mapping using magnetite in patients with non-small cell lung cancer. J Thorac Cardiovasc Surg. 2003;126(2):563–7.\nMinamiya Y, Ito M, Hosono Y, Kawai H, Saito H, Katayose Y, et al. Subpleural injection of tracer improves detection of mediastinal sentinel lymph nodes in non-small cell lung cancer. Eur J Cardio-thorac Surg. 2007;32(5):770–5.\nMinamiya Y, Ito M, Katayose Y, Saito H, Imai K, Sato Y, et al. Intraoperative sentinel lymph node mapping using a new sterilizable magnetometer in patients with nonsmall cell lung cancer. Ann Thorac Surg. 2006;81(1):327–30.\nOno T, Minamiya Y, Ito M, Saito H, Motoyama S, Nanjo H, et al. Sentinel node mapping and micrometastasis in patients with clinical stage IA non-small cell lung cancer. Interact Cardiovasc Thorac Surg. 2009;9(4):659–61.\nImai K, Kawaharada Y, Ogawa JI, Saito H, Kudo S, Takashima S, et al. Development of a new magnetometer for sentinel lymph node mapping designed for video-assisted thoracic surgery in non-small cell lung cancer. Surg Innov. 2015;22(4):401–5.\nSuga K, Yuan Y, Ueda K, Kaneda Y, Kawakami Y, Zaki M, et al. Computed tomography lymphography with intrapulmonary injection of iopamidol for sentinel lymph node localization. Invest Radiol. 2004;39(6):313–24.\nUeda K, Suga K, Kaneda Y, Li T-S, Ueda K, Hamano K. Preoperative imaging of the lung sentinel lymphatic basin with computed tomographic lymphography: a preliminary study. Ann Thorac Surg. 2004;77(3):1033–7.\nSugi K, Kitada K, Yoshino M, Hirazawa K, Matsuda E, Azuma T, et al. New method of visualizing lymphatics in lung cancer patients by multidetector computed tomography. J Comput Assist Tomogr. 2005;29(2):210–4.\nTakizawa H, Kondo K, Toba H, Kajiura K, Ali AHK, Sakiyama S, et al. Computed tomography lymphography by transbronchial injection of iopamidol to identify sentinel nodes in preoperative patients with non-small cell lung cancer: a pilot study. J Thorac Cardiovasc Surg. 2012;144(1):94–9.\nMiwa M. The principle of ICG fluorescence method. Open Surg Oncol J. 2010;2:26–8.\nFerrari-Light D, Geraci TC, Sasankan P, Cerfolio RJ. The utility of near-infrared fluorescence and indocyanine green during robotic pulmonary resection. Front Surg. 2019;6(August):1–7.\nGilmore DM, Khullar OV, Jaklitsch MT, Chirieac LR, Frangioni JV, Colson YL. Identification of metastatic nodal disease in a phase 1 dose-escalation trial of intraoperative sentinel lymph node mapping in non-small cell lung cancer using near-infrared imaging. J Thorac Cardiovasc Surg. 2013;146(3):562–9.\nWada H, Hirohashi K, Anayama T, Nakajima T, Kato T, Chan HHL, et al. Minimally invasive electro-magnetic navigational bronchoscopy-integrated near-infrared-guided sentinel lymph node mapping in the porcine lung. PLoS ONE. 2015;10(5):e0126945.\nHachey KJ, Digesu CS, Armstrong KW, Gilmore DM, Khullar OV, Whang B, et al. A novel technique for tumor localization and targeted lymphatic mapping in early-stage lung cancer. J Thorac Cardiovasc Surg. 2017;154(3):1110–8.\nOh Y, Quan YH, Choi Y, Kim CK, Kim H, Kim HK, et al. Intraoperative combined color and fluorescent images-based sentinel node mapping in the porcine lung: comparison of indocyanine green with or without albumin premixing. J Thorac Cardiovasc Surg. 2013;146(6):1509–15.\nYamashita SI, Tokuishi K, Miyawaki M, Anami K, Moroga T, Takeno S, et al. Sentinel node navigation surgery by thoracoscopic fluorescence imaging system and molecular examination in non-small cell lung cancer. Ann Surg Oncol. 2012;19(3):728–33.\nNomori H, Cong Y, Sugimura H. Utility and pitfalls of sentinel node identification using indocyanine green during segmentectomy for cT1N0M0 non-small cell lung cancer. Surg Today. 2016;46(8):908–13.\nLafuente-Sanchis A, Estors-Guerrero M, Zúñiga Á, Martínez-Hernández NJ, Cremades A, Aparisi-Aparisi F, et al. Clinical significance of molecular micrometastasis in the sentinel lymph node of early-stage non-small cell lung cancer patients. Am J Clin Oncol Cancer Clin Trials. 2018;41(11):1106–12.\nLafuente-Sanchis A, Olmo A, Carretero J, Alcacer Fernandez-Coronado J, Estors-Guerrero M, Martínez-Hernández NJ, et al. Clinical significance of epithelial–mesenchymal transition-related markers expression in the micrometastatic sentinel lymph node of NSCLC. Clin Transl Oncol. 2020;22:381–91.\nHayama M, Chida M, Karube Y, Tamura M, Kobayashi S, Oyaizu T, et al. One-step nucleic acid amplification for detection of lymph node metastasis in lung cancer. Ann Thorac Cardiovasc Surg. 2014;20(3):181–4.\nNakagawa K, Asamura H, Tsuta K, Nagai K, Yamada E, Ishii G, et al. The novel one-step nucleic acid amplification (OSNA) assay for the diagnosis of lymph node metastasis in patients with non-small cell lung cancer (NSCLC): results of a multicenter prospective study. Lung Cancer. 2016;97:1–7.\nWenholz A, Xu XM, Nawgiri R, Okereke I. A prospective analysis of touch preparation cytology for intraoperative detection of mediastinal lymph node metastases. J Am Soc Cytopathol. 2019;8(2):84–8.\nAkopov A, Papayan G, Chistiakov I, Dvorecky S, Ilyin A. P3.04-001 Near-infrared fluorescent identification of lymphatic flow in non-small cell lung cancer. J Thorac Oncol. 2017;12(S1):S1385.\nGilmore DM, Khullar OV, Colson YL. Developing intrathoracic sentinel lymph node mapping with near-infrared fluorescent imaging in non-small cell lung cancer. J Thorac Cardiovasc Surg. 2012;144(3):S80–4.\nYamashita SI, Tokuishi K, Anami K, Miyawaki M, Moroga T, Kamei M, et al. Video-assisted thoracoscopic indocyanine green fluorescence imaging system shows sentinel lymph nodes in non-small-cell lung cancer. J Thorac Cardiovasc Surg. 2011;141(1):141–4.\nRiquet M. Bronchial arteries and lymphatics of the lung. Thorac Surg Clin. 2007;17(4):619–38.\nAsamura H, Chansky K, Crowley J, Goldstraw P, Rusch VW, Vansteenkiste JF, et al. The international association for the study of lung cancer lung cancer staging project: proposals for the revision of the N descriptors in the forthcoming 8th edition of the TNM classification for lung cancer. J Thorac Oncol. 2015;10(12):1675–84.\nKim AW. Lymph node drainage patterns and micrometastasis in lung cancer. Semin Thorac Cardiovasc Surg. 2009;21(4):298–308.\nKang HG, Song SH, Han YB, Lee H-Y, Kim KM, Hong SJ. Proof-of-concept of a multimodal laparoscope for simultaneous NIR\u002Fgamma\u002Fvisible imaging using wavelength division multiplexing. Opt Express. 2018;26(7):8325.\nWada H, Zheng J, Gregor A, Hirohashi K, Hu H-P, Patel P, et al. Intraoperative near-infrared fluorescence-guided peripheral lung tumor localization in rabbit models. Ann Thorac Surg. 2019;107(1):248–56.\nIto N, Fukuta M, Tokushima T, Nakai K, Ohgi S. Sentinel node navigation surgery using indocyanine green in patients with lung cancer. Surg Today. 2004;34(7):581–5.\nPulte D, Li E, Crawford BK, Newman E, Alexander A, Mustalish DC, et al. Sentinel lymph node mapping and molecular staging in nonsmall cell lung carcinoma. Cancer. 2005;104(7):1453–61.\nLardinois D, Brack T, Gaspert A, Spahr T, Schneiter D, Steinert HC, et al. Bronchoscopic radioisotope injection for sentinel lymph-node mapping in potentially resectable non-small-cell lung cancer. Eur J Cardio-thorac Surg. 2003;23(5):824–7.\nMelfi FMA, Chella A, Menconi GF, Givigliano F, Boni G, Mariani G, et al. Intraoperative radioguided sentinel lymph node biopsy in non-small cell lung cancer. Eur J Cardio-thorac Surg. 2003;23(2):214–20.\nSugi K, Kaneda Y, Sudoh M, Sakano H, Hamano K. Effect of radioisotope sentinel node mapping in patients with cT1 NO MO lung cancer. J Thorac Cardiovasc Surg. 2003;126(2):568–73.\nLiptay MJ. Sentinel node mapping in lung cancer. Ann Surg Oncol. 2004;11(3 Suppl):271–4.\nNomori H, Watanabe K, Ohtsuka T, Naruke T, Suemasu K. In vivo identification of sentinel lymph nodes for clinical stage I non-small cell lung cancer for abbreviation of mediastinal lymph node dissection. Lung Cancer. 2004;46(1):49–55.\nUeda K, Suga K, Kaneda Y, Sakano H, Tanaka T, Hayashi M, et al. Radioisotope lymph node mapping in nonsmall cell lung cancer: can it be applicable for sentinel node biopsy? Ann Thorac Surg. 2004;77(2):426–30.\nAtinkaya C, Özlem Küçük N, Koparal H, Aras G, Sak SD, Özdemir N. Mediastinal intraoperative radioisotope sentinel lymph node mapping in non-small-cell lung cancer. Nucl Med Commun. 2005;26(8):717–20.\nLucchi M, Melfi F, Baldini E, Fontanini G, Boni G, Viti A, et al. Sentinel lymph node mapping: detection of micrometastases by polymerase chain reaction in non-small cell lung cancer. J Thorac Oncol. 2007;2(5 SUPPL.1):S37.\nNomori H, Ikeda K, Mori T, Kobayashi H, Iwatani K, Kawanaka K, et al. Sentinel node navigation segmentectomy for clinical stage IA non-small cell lung cancer. J Thorac Cardiovasc Surg. 2007;133(3):780–5.\nNomori H, Ikeda K, Mori T, Shiraishi S, Kobayashi H, Iwatani K, et al. Sentinel node identification in clinical stage Ia non-small cell lung cancer by a combined single photon emission computed tomography\u002Fcomputed tomography system. J Thorac Cardiovasc Surg. 2007;134(1):182–7.\nSugi K, Kobayashi S, Yagi R, Matsuoka T. Usefulness of sentinel lymph node biopsy for the detection of lymph node micrometastasis in early lung cancer. Interact Cardiovasc Thorac Surg. 2008;7(5):913–5.\nMelfi FMA, Lucchi M, Davini F, Viti A, Fontanini G, Boldrini L, et al. Intraoperative sentinel lymph node mapping in stage I non-small cell lung cancer: detection of micrometastases by polymerase chain reaction. Eur J Cardio-thorac Surg. 2008;34(1):181–6.\nEo JS, Kim HK, Kim S, Lee YS, Jeong JM, Choi YH. Gallium-68 neomannosylated human serum albumin-based PET\u002FCT lymphoscintigraphy for sentinel lymph node mapping in non-small cell lung cancer. Ann Surg Oncol. 2015;22(2):636–41.\nBagheri Sr R, Sadeghi R, Shafiei S, Basiri R. P51. Sentinel node mapping in non-small-cell lung cancer by radiotracer. Innov Technol Tech Cardiothorac Vasc Surg. 2017;12(S4):S157.\nOršulić D, Šimundža I. P217. The power of sentinl node in non-small cell lung cancer uniport video-assisted thoracoscopic surgery. Interact Cardiovasc Thorac Surg. 2017;25(S1):57.\nIlic N, Juricic J, Krnic D, Orsulic D, Simundza I, Uric M, et al. P501. VATS sentinel node biopsy reduces the need for systematic mediastinal lymphadenectomy in stage IA NSCLC. Surg Endosc. 2017;31(Supplement 1):S185.\nUribe-Etxebarria Lugariza-Aresti N, Barceló Galíndez R, Pac Ferrer J, Méndez Martín J, Genollá Subirats J, Casanova Viudez J. Biopsy of the sentinel node in lung cancer. Med Clín. 2017;148(6):257–9.\nGalbis-Caravajal JM, Lafuente-Sanchis A, Estors-Guerrero M, Martinez-Hernández N, Fuster-Diana C, Cremades A, et al. Topography of the sentinel node according to the affected lobe in lung cancer. Clin Transl Oncol. 2017;19(7):858–64.\nImai K, Minamiya Y, Saito H, Nakagawa T, Ito M, Ono T, et al. Detection of pleural lymph flow using indocyanine green fluorescence imaging in non-small cell lung cancer surgery: a preliminary study. Surg Today. 2013;43(3):249–54.",{"VOID":1695},"10.1007\u002Fs11748-020-01432-0","2024-05-12T17:18:30.972+00:00","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs11748-020-01432-0",[1699,1714,1737],{"id":1700,"sortIndex":21,"researcher":20,"roles":1701,"affiliations":1702,"properties":1711,"displayName":1713,"givenName":20,"familyName":20},"8f84637e-c638-4165-8643-db6ebcb9cda9",[132],[1703],{"id":1704,"sortIndex":21,"affiliation":1705,"properties":20},"6c229883-9ff1-413b-b1b5-67a150971d49",{"id":1704,"createTime":20,"updateTime":20,"relativeEntities":1706,"slug":20,"properties":1707,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":1710,"statistic":20},[],{"title":1708},{"VI":1709},"Division of Thoracic Surgery, Toronto General Hospital, University Health Network, University of Toronto, Toronto, Canada",[],{"title":1712},{"VI":1713},"Alexander 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Surgery, Hokkaido University Graduate School of Medicine, Sapporo, Japan",[],{"title":1733,"gsAuthor":1735},{"VI":1734},"Hideki Ujiie",{"VOID":1736},"[\"vAE6PuMAAAAJ\"]",{"id":1738,"sortIndex":163,"researcher":20,"roles":1739,"affiliations":1740,"properties":1747,"displayName":1749,"givenName":20,"familyName":20},"546ed626-c01f-4203-9e1f-f49d342aaf55",[132],[1741],{"id":1704,"sortIndex":21,"affiliation":1742,"properties":20},{"id":1704,"createTime":20,"updateTime":20,"relativeEntities":1743,"slug":20,"properties":1744,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":1746,"statistic":20},[],{"title":1745},{"VI":1709},[],{"title":1748},{"VI":1749},"Kazuhiro 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                       Objective: We studied immediate and mid-term results after aortic valve repair.Methods: Immediate and mid-term results were studied in 63 patients undergoing aortic valve repair, calculating survival and reoperation free rates.Results: Subjects were 49 men and 14 women aged 15 to 76 years (mean: 53±17 years). Mean preoperative aortic regurgitation grading of 1 to 4 was 3.2±0.7. Mean preoperative New York Heart Association functional class was 1.9±0.8. Two in-hospital deaths occurred. (3.2%) Mean aortic regurgitation grade at discharge was 1.3±0.8(p\u003C0.0001; vs preoperative grade) and functional class was 1.1±0.2 (p\u003C0.0001; vs preoperative class),—significantly improved. Overall follow-up was 98.4%, and mean follow-up continued 41.4±22.1 months. Mean functional class at follow-up was 1.2±0.4 (n=49), improved from preoperative class (p\u003C0.0001). Mean aortic regurgitation grading at follow-up was 1.8±0.8 (n=41), improved from preoperative grading (p\u003C0.0001). Five-year survival was 95.1±2.8%. One-year reoperation freedom was 96.6±2.4% and 5-year 77.9±6.9%.Conclusions: Survival after surgery was good, while reoperation was comparable to other reports but less satisfactory compared to reoperation freedom after aortic valve replacement. Based on reoperative findings, a change in indication was made. We believe technical refinements could improve postoperative results.",{"EN":1820},"Aortic valve repair in dominant aortic regurgitation",{"VOID":1822},"[\"14003938733715008280\"]",{"VOID":1824},"10.1007\u002FBF02913149","2024-04-23T21:06:52.957+00:00","http:\u002F\u002Flink.springer.com\u002F10.1007\u002FBF02913149",[1828,1851,1870,1889,1908,1927,1946,1965,1984,2003],{"id":1829,"sortIndex":21,"researcher":20,"roles":1830,"affiliations":1831,"properties":1848,"displayName":1850,"givenName":20,"familyName":20},"6da582a2-ac2a-439c-bfdc-a30a6a4c50dc",[132],[1832,1840],{"id":1833,"sortIndex":21,"affiliation":1834,"properties":20},"018c0d13-a64d-4f2d-80db-f199b89caef2",{"id":1833,"createTime":20,"updateTime":20,"relativeEntities":1835,"slug":20,"properties":1836,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":1839,"statistic":20},[],{"title":1837},{"VI":1838},"Department of Cardiovascular Surgery, Iwate Medical University, Morioka, Japan",[],{"id":1841,"sortIndex":149,"affiliation":1842,"properties":20},"4ed6cc96-f09d-41b9-80cd-874c5d927713",{"id":1841,"createTime":20,"updateTime":20,"relativeEntities":1843,"slug":20,"properties":1844,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":1847,"statistic":20},[],{"title":1845},{"VI":1846},"Department of Cardiology, Iwate Medical University Memorial Heart Center, Iwate Medical University, Morioka, Japan",[],{"title":1849},{"VI":1850},"Hiroshi 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