38 results on '"Vander Laenen M."'
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2. Correction to: The Intensive Care Global Study on Severe Acute Respiratory Infection (IC-GLOSSARI): a multicenter, multinational, 14-day inception cohort study
- Author
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Sakr, Yasser, Ferrer, Ricard, Reinhart, Konrad, Beale, Richard, Rhodes, Andrew, Moreno, Rui, Timsit, Jean Francois, Brochard, Laurent, Thompson, B. Taylor, Rezende, Ederlon, Chiche, Jean Daniel, Auer, J., Schatzl, G., Mach, K., Gruber, H., Schreurs, E., Vander Laenen, M., Ceunen, H., Wauters, J., Francois, G., Deschamps, P., Castanares, D., Debels, D., Pierrakos, C., Vincent, J. L., Taccone, F., Vymazal, T., Gornik, I., Vujiaklija Brajkovic, A., Medici, R., Nielsen, J., Bendtsen, A., Siegel, H., Suonsyrjä, T., Hraech, S., Daviaux, F., Guillot, M., Castelain, V., Losser, R-R., Novy, E., Bouadma, L., Misset, B., Philippart, F., Mallat, J., Zogheib, E., Miclo, M., Teboul, J-L., Anguel, N., Darmon, M., Pham, T., Barberet, G., Plantefeve, G., Floccard, B., Kheladze, Z., Bloos, F., Faltlhauser, A., Helmes, T., Zacharowski, K., Meybohm, P., Schwarzkopf, K., Christ, M., Baumgaertel, M., John, S., Nentwich, J., Deja, M., Goldmann, A., Gottschalk, A., Honig, F., Siepe, B., Goebel, U., Lehmke, J., Behrens, S., Fiedler, K., Sagoschen, I., Riessen, R., Haap, M., Simon, Ph., Kaisers, U., Behrens, S., Niesen, M., Jaschinski, U., Hoersch, S., Jung, A., Allgaeuer, S., Haake, H., Lange, A., Papanikolaou, M., Balla, M., Giannakou, M., Soultati, I., Nikos, G., Koulouras, V., Kyriazopoulos, G., Gkika, D., Vlachogianni, G., Psaroulis, K., Mouloudi, E., Massa, E., Nichol, A., Meany, E., Motherway, C., Bellani, G., Pota, V., Schiavone, V., Girardis, M., Busani, S., Petrucci, N., Di Pasquale, R., Mazzini, P., Molin, A., Pellerano, G., Volta, C., Spadaro, S., Guarracino, F., Savioli, M., Pellis, T., Chinellato, N., Gatta, A., Cecchini, F., Raineri, S. M., Cortegiani, A., Kekstas, G., Karosas, V., Anguseva, T., Mitrev, Z., Beck, O., Cimic, N., Janssen, G., Bormans, L., Kuiper, M., Koopmans, K., Den Boer, S., de Groot, M., Dennesen, P., van den Bosch, J., Kluge, G., Mikaszewska-Sokolewicz, M., Lazowski, T., Chruscikowski, M., Machon, J., Adamik, B., Kübler, A., Wieczorek, A., Afonso, S., Matos, R., Catorze, N., Araujo, A., Costa, Z., Pais-de-Lacerda, A., Martins, I., Cardiga, R., Fernandes, L., Serra, I., Martinho, A., Tomescu, D., Popescu, M., Scarlatescu, E., Stoica, R., Macri, A., Filipescu, D., Rupnik, E., Tomic, V., Sifrer, F., Sole Violan, J., Ferrer Agüero, J. M., Izura, J., Monedero, P., de Cabo, C. Muños, Aguilar, G., Belda, F. J., Blanquer, J., Nives Carbonell, E., Lopez-Delgado, J-C., Aragon, C., Joya, C., Ortiz-Leyba, C., Fernandez Gonzalez, C. J., de la Torre-Prados, M-V., Puerto-Morlan, A., Araujo Aguilar, P., Tomás Marsilla, J. I., Vera Aratcoz, P., Olmo, A., Ferrer Roca, R., Catalan, R. M., Garcia Olivares, P., Albis, A., Alvarez, M., Corcoles Gonzalez, V., Gutierrez Rubio, J. M., Montoiro Allue, R., Rubio Mateo-Sidron, J., Hobrok, M., Cecconi, M., Di Tomasso, N., Raj, A., Szakmany, T., Srinivasa, L., Mathew, S., Ferguson, A., Blahut-Zugaj, M., Watters, M., Henderson, S., Sim, M., Csabi, P., O’Neill, O., Nutt, C., Humphreys, S., Bhowmick, K., Donnelly, A., O’Kane, S., Garfield, M., Jha, R., Unni, N., Gordon, A., Rubulotta, F., Ravi, K., Lunch, G., Franco, F., Higgs, D., Strandvik, G., Jonas, A., Hopkins, Ph., Hurst, T., Bellini, A., Balogun, O., Srinivasan, R., Ostermann, M., Alexander, P., McCalman, K., Bedford, J., Fulop, M., Brescia, G., Strachan, J., Meyer, J., Stotz, M., Brett, S., Zand, F., Nikandish, R., Hashemian, S., Jamaati, H., Alsheikhly, A. S., Almekhlafi, G., Albarrak, M., Maghrabi, A., Salahuddin, N., Aisa, T., Atalan, H. K., Sungur, M., Hegazi, M., Bauer, P., Mukkera, S., Fried, J., Barger, M., Gueret, R., Gonzalez, C., Lovesio, C., Dellera, Ch., Barrios, D., Leite Mendes, C., Gottardo, P., Caser, E., Santos, C., Carvalho, A., Teixeira, C., Samaniego, W., Whittle, S., Molano, D., Rojas, A., Guerra, K., Villamagua, B., Salgado-Yepez, E., Morocho, D., Remache-Vargas, N., Ñamendys-Silva, S., Rodriguez, D., Dominguez, G., Barraza, G., Bermudez-Aceves, E., Sanchez-Hurtado, L. A., Baltazar-Torres, J. A., Quispe Sierra, R., Chavez, C., von Osten, I., Van Haren, C., Smalley, N., Kol, M., Wong, H., Smith, R., Yu, L., Wu, X., Chao, L., Zhai, Q., Wu, D., Zhang, X., Jing, X., Bigornia, R., Ikeda-Maquiling, Y., Robles, J., Palo, J. E., Nguyen, T., Dao, C., Dixit, S., Gurjar, M., Reddy, P., Pravin, A., Simran, S., Ramakrishnan, N., Shetty, R., Udwadia, F., Faraz, M., Indraratna, K., Rajasinhe, J., and IC-GLOSSARI Investigators and ESICM Trials Group
- Published
- 2017
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3. Survival of elderly COVID-19 intensive care patients in the first and second Belgian wave: a retrospective single center analysis
- Author
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Vermeiren, G, Willaert, X, Vervloessem, H, Thiessen, S, Boer, W, Fivez, T, Engelen, K, Vander Laenen, M, Van De Velde, M, and Mesotten, D
- Subjects
critical care ,aged ,Science & Technology ,Anesthesiology ,SARS-CoV-2 ,COVID-19 ,CORONAVIRUS DISEASE 2019 ,Life Sciences & Biomedicine ,elderly - Abstract
ispartof: ACTA ANAESTHESIOLOGICA BELGICA vol:72 pages:203-210 status: published
- Published
- 2021
4. Risk factors of Intensive Care Unit-Acquired Weakness: a single center retrospective analysis
- Author
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Hilderson, C, Schramme, D, Naveau, B, Vander Laenen, M, Boer, W, Engelen, K, Fivez, T, Willaert, X, Pierlet, N, Rex, S, Eertmans, W, and Mesotten, D
- Subjects
sepsis ,Science & Technology ,poly-neuropathies ,Anesthesiology ,PREDICTION ,Critical illness ,Life Sciences & Biomedicine ,muscle weakness - Abstract
ispartof: ACTA ANAESTHESIOLOGICA BELGICA vol:72 pages:55-61 status: published
- Published
- 2021
5. Erratum to: The Intensive Care Global Study on Severe Acute Respiratory Infection (IC‐GLOSSARI): a multicenter, multinational, 14-day inception cohort study (Intensive Care Medicine, (2016), 42, 5, (953), 10.1007/s00134-016-4317-4)
- Author
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Auer J., Auer, J, Schatzl, G, Mach, K, Gruber, H, Schreurs, E, Vander Laenen, M, Ceunen, H, Wauters, J, Francois, G, Deschamps, P, Castanares, D, Debels, D, Pierrakos, C, Vincent, J, Taccone, F, Vymazal, T, Gornik, I, Vujiaklija Brajkovic, A, Medici, R, Nielsen, J, Bendtsen, A, Siegel, H, Suonsyrja, T, Hraech, S, Chiche, J, Daviaux, F, Guillot, M, Castelain, V, Losser, R, Novy, E, Timsit, J, Bouadma, L, Misset, B, Philippart, F, Mallat, J, Zogheib, E, Miclo, M, Teboul, J, Anguel, N, Darmon, M, Pham, T, Barberet, G, Plantefeve, G, Floccard, B, Kheladze, Z, Reinhart, K, Sakr, Y, Bloos, F, Faltlhauser, A, Helmes, T, Zacharowski, K, Meybohm, P, Schwarzkopf, K, Christ, M, Baumgaertel, M, John, S, Nentwich, J, Deja, M, Goldmann, A, Gottschalk, A, Honig, F, Siepe, B, Goebel, U, Lehmke, J, Behrens, S, Fiedler, K, Sagoschen, I, Riessen, R, Haap, M, Simon, P, Kaisers, U, Niesen, M, Jaschinski, U, Hoersch, S, Jung, A, Allgaeuer, S, Haake, H, Lange, A, Papanikolaou, M, Balla, M, Giannakou, M, Soultati, I, Nikos, G, Koulouras, V, Kyriazopoulos, G, Gkika, D, Vlachogianni, G, Psaroulis, K, Mouloudi, E, Massa, E, Nichol, A, Meany, E, Motherway, C, Bellani, G, Pota, V, Schiavone, V, Girardis, M, Busani, S, Petrucci, N, Di Pasquale, R, Mazzini, P, Molin, A, Pellerano, G, Volta, C, Spadaro, S, Guarracino, F, Savioli, M, Pellis, T, Chinellato, N, Gatta, A, Cecchini, F, Raineri, S, Cortegiani, A, Kekstas, G, Karosas, V, Anguseva, T, Mitrev, Z, Beck, O, Cimic, N, Janssen, G, Bormans, L, Kuiper, M, Koopmans, K, Den Boer, S, de Groot, M, Dennesen, P, van den Bosch, J, Kluge, G, Mikaszewska-Sokolewicz, M, Lazowski, T, Chruscikowski, M, Machon, J, Adamik, B, Kubler, A, Wieczorek, A, Afonso, S, Matos, R, Catorze, N, Araujo, A, Costa, Z, Pais-de-Lacerda, A, Martins, I, Cardiga, R, Fernandes, L, Serra, I, Martinho, A, Tomescu, D, Popescu, M, Scarlatescu, E, Stoica, R, Macri, A, Filipescu, D, Rupnik, E, Tomic, V, Sifrer, F, Sole Violan, J, Ferrer Aguero, J, Izura, B, Monedero, P, Munos de Cabo, C, Aguilar, G, Belda, F, Blanquer, J, Nives Carbonell, E, Lopez-Delgado, J, Aragon, C, Joya, C, Ortiz-Leyba, C, Fernandez Gonzalez, C, de la Torre-Prados, M, Puerto-Morlan, A, Araujo Aguilar, P, Tomas Marsilla, J, Vera Aratcoz, P, Olmo, A, Ferrer Roca, R, Catalan, R, Garcia Olivares, P, Albis, A, Alvarez, M, Corcoles Gonzalez, V, Gutierrez Rubio, J, Montoiro Allue, R, Rubio Mateo-Sidron, J, Hobrok, M, Cecconi, M, Di Tomasso, N, Raj, A, Szakmany, T, Srinivasa, L, Mathew, S, Ferguson, A, Blahut-Zugaj, M, Watters, M, Henderson, S, Sim, M, Csabi, P, O'Neill, O, Nutt, C, Humphreys, S, Bhowmick, K, Donnelly, A, O'Kane, S, Garfield, M, Jha, R, Unni, N, Gordon, A, Rubulotta, F, Ravi, K, Lunch, G, Franco, F, Higgs, D, Strandvik, G, Jonas, A, Hopkins, P, Hurst, T, Bellini, A, Balogun, O, Srinivasan, R, Ostermann, M, Alexander, P, Mccalman, K, Bedford, J, Fulop, M, Brescia, G, Strachan, J, Meyer, J, Stotz, M, Brett, S, Zand, F, Nikandish, R, Hashemian, S, Jamaati, H, Alsheikhly, A, Almekhlafi, G, Albarrak, M, Maghrabi, A, Salahuddin, N, Aisa, T, Atalan, H, Sungur, M, Hegazi, M, Bauer, P, Mukkera, S, Fried, J, Barger, M, Gueret, R, Gonzalez, C, Lovesio, C, Dellera, C, Barrios, D, Leite Mendes, C, Gottardo, P, Caser, E, Santos, C, Carvalho, A, Teixeira, C, Samaniego, W, Whittle, S, Molano, D, Rojas, A, Guerra, K, Villamagua, B, Salgado-Yepez, E, Morocho, D, Remache-Vargas, N, Namendys-Silva, S, Rodriguez, D, Dominguez, G, Barraza, G, Bermudez-Aceves, E, Sanchez-Hurtado, L, Baltazar-Torres, J, Quispe Sierra, R, Chavez, C, von Osten, I, Van Haren, C, Smalley, N, Kol, M, Wong, H, Smith, R, Yu, L, Wu, X, Chao, L, Zhai, Q, Wu, D, Zhang, X, Jing, X, Bigornia, R, Ikeda-Maquiling, Y, Robles, J, Palo, J, Nguyen, T, Dao, C, Dixit, S, Gurjar, M, Reddy, P, Pravin, A, Simran, S, Ramakrishnan, N, Shetty, R, Udwadia, F, Faraz, M, Indraratna, K, Rajasinhe, J, Auer J., Schatzl G., Mach K., Gruber H., Schreurs E., Vander Laenen M., Ceunen H., Wauters J., Francois G., Deschamps P., Castanares D., Debels D., Pierrakos C., Vincent J. L., Taccone F., Vymazal T., Gornik I., Vujiaklija Brajkovic A., Medici R., Nielsen J., Bendtsen A., Siegel H., Suonsyrja T., Hraech S., Chiche J. -D., Daviaux F., Guillot M., Castelain V., Losser R. -R., Novy E., Timsit J. -F., Bouadma L., Misset B., Philippart F., Mallat J., Zogheib E., Miclo M., Teboul J. -L., Anguel N., Darmon M., Pham T., Barberet G., Plantefeve G., Floccard B., Kheladze Z., Reinhart K., Sakr Y., Bloos F., Faltlhauser A., Helmes T., Zacharowski K., Meybohm P., Schwarzkopf K., Christ M., Baumgaertel M., John S., Nentwich J., Deja M., Goldmann A., Gottschalk A., Honig F., Siepe B., Goebel U., Lehmke J., Behrens S., Fiedler K., Sagoschen I., Riessen R., Haap M., Simon P., Kaisers U., Niesen M., Jaschinski U., Hoersch S., Jung A., Allgaeuer S., Haake H., Lange A., Papanikolaou M., Balla M., Giannakou M., Soultati I., Nikos G., Koulouras V., Kyriazopoulos G., Gkika D., Vlachogianni G., Psaroulis K., Mouloudi E., Massa E., Nichol A., Meany E., Motherway C., Bellani G., Pota V., Schiavone V., Girardis M., Busani S., Petrucci N., Di Pasquale R., Mazzini P., Molin A., Pellerano G., Volta C., Spadaro S., Guarracino F., Savioli M., Pellis T., Chinellato N., Gatta A., Cecchini F., Raineri S. M., Cortegiani A., Kekstas G., Karosas V., Anguseva T., Mitrev Z., Beck O., Cimic N., Janssen G., Bormans L., Kuiper M., Koopmans K., Den Boer S., de Groot M., Dennesen P., van den Bosch J., Kluge G., Mikaszewska-Sokolewicz M., Lazowski T., Chruscikowski M., Machon J., Adamik B., Kubler A., Wieczorek A., Afonso S., Matos R., Catorze N., Araujo A., Costa Z., Pais-de-Lacerda A., Martins I., Cardiga R., Fernandes L., Serra I., Martinho A., Tomescu D., Popescu M., Scarlatescu E., Stoica R., Macri A., Filipescu D., Rupnik E., Tomic V., Sifrer F., Sole Violan J., Ferrer Aguero J. M., Izura B. J., Monedero P., Munos de Cabo C., Aguilar G., Belda F. J., Blanquer J., Nives Carbonell E., Lopez-Delgado J. -C., Aragon C., Joya C., Ortiz-Leyba C., Fernandez Gonzalez C. J., de la Torre-Prados M. -V., Puerto-Morlan A., Araujo Aguilar P., Tomas Marsilla J. I., Vera Aratcoz P., Olmo A., Ferrer Roca R., Catalan R. M., Garcia Olivares P., Albis A., Alvarez M., Corcoles Gonzalez V., Gutierrez Rubio J. M., Montoiro Allue R., Rubio Mateo-Sidron J., Hobrok M., Cecconi M., Di Tomasso N., Raj A., Szakmany T., Srinivasa L., Mathew S., Ferguson A., Blahut-Zugaj M., Watters M., Henderson S., Sim M., Csabi P., O'Neill O., Nutt C., Humphreys S., Bhowmick K., Donnelly A., O'Kane S., Garfield M., Jha R., Unni N., Gordon A., Rubulotta F., Ravi K., Lunch G., Franco F., Higgs D., Strandvik G., Jonas A., Hopkins P., Hurst T., Bellini A., Balogun O., Srinivasan R., Ostermann M., Alexander P., McCalman K., Bedford J., Fulop M., Brescia G., Strachan J., Meyer J., Stotz M., Brett S., Zand F., Nikandish R., Hashemian S., Jamaati H., Alsheikhly A. S., Almekhlafi G., Albarrak M., Maghrabi A., Salahuddin N., Aisa T., Atalan H. K., Sungur M., Hegazi M., Bauer P., Mukkera S., Fried J., Barger M., Gueret R., Gonzalez C., Lovesio C., Dellera C., Barrios D., Leite Mendes C., Gottardo P., Caser E., Santos C., Carvalho A., Teixeira C., Samaniego W., Whittle S., Molano D., Rojas A., Guerra K., Villamagua B., Salgado-Yepez E., Morocho D., Remache-Vargas N., Namendys-Silva S., Rodriguez D., Dominguez G., Barraza G., Bermudez-Aceves E., Sanchez-Hurtado L. A., Baltazar-Torres J. A., Quispe Sierra R., Chavez C., von Osten I., Van Haren C., Smalley N., Kol M., Wong H., Smith R., Yu L., Wu X., Chao L., Zhai Q., Wu D., Zhang X., Jing X., Bigornia R., Ikeda-Maquiling Y., Robles J., Palo J. E., Nguyen T., Dao C., Dixit S., Gurjar M., Reddy P., Pravin A., Simran S., Ramakrishnan N., Shetty R., Udwadia F., Faraz M., Indraratna K., Rajasinhe J., Auer J., Auer, J, Schatzl, G, Mach, K, Gruber, H, Schreurs, E, Vander Laenen, M, Ceunen, H, Wauters, J, Francois, G, Deschamps, P, Castanares, D, Debels, D, Pierrakos, C, Vincent, J, Taccone, F, Vymazal, T, Gornik, I, Vujiaklija Brajkovic, A, Medici, R, Nielsen, J, Bendtsen, A, Siegel, H, Suonsyrja, T, Hraech, S, Chiche, J, Daviaux, F, Guillot, M, Castelain, V, Losser, R, Novy, E, Timsit, J, Bouadma, L, Misset, B, Philippart, F, Mallat, J, Zogheib, E, Miclo, M, Teboul, J, Anguel, N, Darmon, M, Pham, T, Barberet, G, Plantefeve, G, Floccard, B, Kheladze, Z, Reinhart, K, Sakr, Y, Bloos, F, Faltlhauser, A, Helmes, T, Zacharowski, K, Meybohm, P, Schwarzkopf, K, Christ, M, Baumgaertel, M, John, S, Nentwich, J, Deja, M, Goldmann, A, Gottschalk, A, Honig, F, Siepe, B, Goebel, U, Lehmke, J, Behrens, S, Fiedler, K, Sagoschen, I, Riessen, R, Haap, M, Simon, P, Kaisers, U, Niesen, M, Jaschinski, U, Hoersch, S, Jung, A, Allgaeuer, S, Haake, H, Lange, A, Papanikolaou, M, Balla, M, Giannakou, M, Soultati, I, Nikos, G, Koulouras, V, Kyriazopoulos, G, Gkika, D, Vlachogianni, G, Psaroulis, K, Mouloudi, E, Massa, E, Nichol, A, Meany, E, Motherway, C, Bellani, G, Pota, V, Schiavone, V, Girardis, M, Busani, S, Petrucci, N, Di Pasquale, R, Mazzini, P, Molin, A, Pellerano, G, Volta, C, Spadaro, S, Guarracino, F, Savioli, M, Pellis, T, Chinellato, N, Gatta, A, Cecchini, F, Raineri, S, Cortegiani, A, Kekstas, G, Karosas, V, Anguseva, T, Mitrev, Z, Beck, O, Cimic, N, Janssen, G, Bormans, L, Kuiper, M, Koopmans, K, Den Boer, S, de Groot, M, Dennesen, P, van den Bosch, J, Kluge, G, Mikaszewska-Sokolewicz, M, Lazowski, T, Chruscikowski, M, Machon, J, Adamik, B, Kubler, A, Wieczorek, A, Afonso, S, Matos, R, Catorze, N, Araujo, A, Costa, Z, Pais-de-Lacerda, A, Martins, I, Cardiga, R, Fernandes, L, Serra, I, Martinho, A, Tomescu, D, Popescu, M, Scarlatescu, E, Stoica, R, Macri, A, Filipescu, D, Rupnik, E, Tomic, V, Sifrer, F, Sole Violan, J, Ferrer Aguero, J, Izura, B, Monedero, P, Munos de Cabo, C, Aguilar, G, Belda, F, Blanquer, J, Nives Carbonell, E, Lopez-Delgado, J, Aragon, C, Joya, C, Ortiz-Leyba, C, Fernandez Gonzalez, C, de la Torre-Prados, M, Puerto-Morlan, A, Araujo Aguilar, P, Tomas Marsilla, J, Vera Aratcoz, P, Olmo, A, Ferrer Roca, R, Catalan, R, Garcia Olivares, P, Albis, A, Alvarez, M, Corcoles Gonzalez, V, Gutierrez Rubio, J, Montoiro Allue, R, Rubio Mateo-Sidron, J, Hobrok, M, Cecconi, M, Di Tomasso, N, Raj, A, Szakmany, T, Srinivasa, L, Mathew, S, Ferguson, A, Blahut-Zugaj, M, Watters, M, Henderson, S, Sim, M, Csabi, P, O'Neill, O, Nutt, C, Humphreys, S, Bhowmick, K, Donnelly, A, O'Kane, S, Garfield, M, Jha, R, Unni, N, Gordon, A, Rubulotta, F, Ravi, K, Lunch, G, Franco, F, Higgs, D, Strandvik, G, Jonas, A, Hopkins, P, Hurst, T, Bellini, A, Balogun, O, Srinivasan, R, Ostermann, M, Alexander, P, Mccalman, K, Bedford, J, Fulop, M, Brescia, G, Strachan, J, Meyer, J, Stotz, M, Brett, S, Zand, F, Nikandish, R, Hashemian, S, Jamaati, H, Alsheikhly, A, Almekhlafi, G, Albarrak, M, Maghrabi, A, Salahuddin, N, Aisa, T, Atalan, H, Sungur, M, Hegazi, M, Bauer, P, Mukkera, S, Fried, J, Barger, M, Gueret, R, Gonzalez, C, Lovesio, C, Dellera, C, Barrios, D, Leite Mendes, C, Gottardo, P, Caser, E, Santos, C, Carvalho, A, Teixeira, C, Samaniego, W, Whittle, S, Molano, D, Rojas, A, Guerra, K, Villamagua, B, Salgado-Yepez, E, Morocho, D, Remache-Vargas, N, Namendys-Silva, S, Rodriguez, D, Dominguez, G, Barraza, G, Bermudez-Aceves, E, Sanchez-Hurtado, L, Baltazar-Torres, J, Quispe Sierra, R, Chavez, C, von Osten, I, Van Haren, C, Smalley, N, Kol, M, Wong, H, Smith, R, Yu, L, Wu, X, Chao, L, Zhai, Q, Wu, D, Zhang, X, Jing, X, Bigornia, R, Ikeda-Maquiling, Y, Robles, J, Palo, J, Nguyen, T, Dao, C, Dixit, S, Gurjar, M, Reddy, P, Pravin, A, Simran, S, Ramakrishnan, N, Shetty, R, Udwadia, F, Faraz, M, Indraratna, K, Rajasinhe, J, Auer J., Schatzl G., Mach K., Gruber H., Schreurs E., Vander Laenen M., Ceunen H., Wauters J., Francois G., Deschamps P., Castanares D., Debels D., Pierrakos C., Vincent J. L., Taccone F., Vymazal T., Gornik I., Vujiaklija Brajkovic A., Medici R., Nielsen J., Bendtsen A., Siegel H., Suonsyrja T., Hraech S., Chiche J. -D., Daviaux F., Guillot M., Castelain V., Losser R. -R., Novy E., Timsit J. -F., Bouadma L., Misset B., Philippart F., Mallat J., Zogheib E., Miclo M., Teboul J. -L., Anguel N., Darmon M., Pham T., Barberet G., Plantefeve G., Floccard B., Kheladze Z., Reinhart K., Sakr Y., Bloos F., Faltlhauser A., Helmes T., Zacharowski K., Meybohm P., Schwarzkopf K., Christ M., Baumgaertel M., John S., Nentwich J., Deja M., Goldmann A., Gottschalk A., Honig F., Siepe B., Goebel U., Lehmke J., Behrens S., Fiedler K., Sagoschen I., Riessen R., Haap M., Simon P., Kaisers U., Niesen M., Jaschinski U., Hoersch S., Jung A., Allgaeuer S., Haake H., Lange A., Papanikolaou M., Balla M., Giannakou M., Soultati I., Nikos G., Koulouras V., Kyriazopoulos G., Gkika D., Vlachogianni G., Psaroulis K., Mouloudi E., Massa E., Nichol A., Meany E., Motherway C., Bellani G., Pota V., Schiavone V., Girardis M., Busani S., Petrucci N., Di Pasquale R., Mazzini P., Molin A., Pellerano G., Volta C., Spadaro S., Guarracino F., Savioli M., Pellis T., Chinellato N., Gatta A., Cecchini F., Raineri S. M., Cortegiani A., Kekstas G., Karosas V., Anguseva T., Mitrev Z., Beck O., Cimic N., Janssen G., Bormans L., Kuiper M., Koopmans K., Den Boer S., de Groot M., Dennesen P., van den Bosch J., Kluge G., Mikaszewska-Sokolewicz M., Lazowski T., Chruscikowski M., Machon J., Adamik B., Kubler A., Wieczorek A., Afonso S., Matos R., Catorze N., Araujo A., Costa Z., Pais-de-Lacerda A., Martins I., Cardiga R., Fernandes L., Serra I., Martinho A., Tomescu D., Popescu M., Scarlatescu E., Stoica R., Macri A., Filipescu D., Rupnik E., Tomic V., Sifrer F., Sole Violan J., Ferrer Aguero J. M., Izura B. J., Monedero P., Munos de Cabo C., Aguilar G., Belda F. J., Blanquer J., Nives Carbonell E., Lopez-Delgado J. -C., Aragon C., Joya C., Ortiz-Leyba C., Fernandez Gonzalez C. J., de la Torre-Prados M. -V., Puerto-Morlan A., Araujo Aguilar P., Tomas Marsilla J. I., Vera Aratcoz P., Olmo A., Ferrer Roca R., Catalan R. M., Garcia Olivares P., Albis A., Alvarez M., Corcoles Gonzalez V., Gutierrez Rubio J. M., Montoiro Allue R., Rubio Mateo-Sidron J., Hobrok M., Cecconi M., Di Tomasso N., Raj A., Szakmany T., Srinivasa L., Mathew S., Ferguson A., Blahut-Zugaj M., Watters M., Henderson S., Sim M., Csabi P., O'Neill O., Nutt C., Humphreys S., Bhowmick K., Donnelly A., O'Kane S., Garfield M., Jha R., Unni N., Gordon A., Rubulotta F., Ravi K., Lunch G., Franco F., Higgs D., Strandvik G., Jonas A., Hopkins P., Hurst T., Bellini A., Balogun O., Srinivasan R., Ostermann M., Alexander P., McCalman K., Bedford J., Fulop M., Brescia G., Strachan J., Meyer J., Stotz M., Brett S., Zand F., Nikandish R., Hashemian S., Jamaati H., Alsheikhly A. S., Almekhlafi G., Albarrak M., Maghrabi A., Salahuddin N., Aisa T., Atalan H. K., Sungur M., Hegazi M., Bauer P., Mukkera S., Fried J., Barger M., Gueret R., Gonzalez C., Lovesio C., Dellera C., Barrios D., Leite Mendes C., Gottardo P., Caser E., Santos C., Carvalho A., Teixeira C., Samaniego W., Whittle S., Molano D., Rojas A., Guerra K., Villamagua B., Salgado-Yepez E., Morocho D., Remache-Vargas N., Namendys-Silva S., Rodriguez D., Dominguez G., Barraza G., Bermudez-Aceves E., Sanchez-Hurtado L. A., Baltazar-Torres J. A., Quispe Sierra R., Chavez C., von Osten I., Van Haren C., Smalley N., Kol M., Wong H., Smith R., Yu L., Wu X., Chao L., Zhai Q., Wu D., Zhang X., Jing X., Bigornia R., Ikeda-Maquiling Y., Robles J., Palo J. E., Nguyen T., Dao C., Dixit S., Gurjar M., Reddy P., Pravin A., Simran S., Ramakrishnan N., Shetty R., Udwadia F., Faraz M., Indraratna K., and Rajasinhe J.
- Abstract
In both the original publication (DOI 10.1007/s00134-015-4206-2) and the first erratum (DOI 10.1007/s00134-016-4317-4), the members of the IC-GLOSSARI Investigators and the ESICM Trials Group were provided in such a way that they could not be indexed as collaborators on PubMed. The publisher apologizes for these errors and is pleased to list the members of the groups here: (Table presented.).
- Published
- 2018
6. Perioperative measurement of urinary oxygen tension as a tool in the prevention of acute kidney injury?
- Author
-
Desteghe, L, Boer, W, Swennen, Q, Pennemans, V, Vander Laenen, M, Engelen, K, De Deyne, C, and Jans, F
- Published
- 2014
- Full Text
- View/download PDF
7. Erratum to: The Intensive Care Global Study on Severe Acute Respiratory Infection (ICâGLOSSARI): a multicenter, multinational, 14-day inception cohort study (Intensive Care Medicine, (2016), 42, 5, (953), 10.1007/s00134-016-4317-4)
- Author
-
Sakr, Yasser, Ferrer, Ricard, Reinhart, Konrad, Beale, Richard, Rhodes, Andrew, Moreno, Rui, Timsit, Jean Francois, Brochard, Laurent, Thompson, B. Taylor, Rezende, Ederlon, Chiche, Jean Daniel, Auer, J., Schatzl, G., Mach, K., Gruber, H., Schreurs, E., Vander Laenen, M., Ceunen, H., Wauters, J., Francois, G., Deschamps, P., Castanares, D., Debels, D., Pierrakos, C., Vincent, J. L., Taccone, F., Vymazal, T., Gornik, I., Vujiaklija Brajkovic, A., Medici, R., Nielsen, J., Bendtsen, A., Siegel, H., Suonsyrjä, T., Hraech, S., Daviaux, F., Guillot, M., Castelain, V., Losser, R. -R., Novy, E., Bouadma, L., Misset, B., Philippart, F., Mallat, J., Zogheib, E., Miclo, M., Teboul, J. -L., Anguel, N., Darmon, M., Pham, T., Barberet, G., Plantefeve, G., Floccard, B., Kheladze, Z., Bloos, F., Faltlhauser, A., Helmes, T., Zacharowski, K., Meybohm, P., Schwarzkopf, K., Christ, M., Baumgaertel, M., John, S., Nentwich, J., Deja, M., Goldmann, A., Gottschalk, A., Honig, F., Siepe, B., Goebel, U., Lehmke, J., Behrens, S., Fiedler, K., Sagoschen, I., Riessen, R., Haap, M., Simon, Ph., Kaisers, U., Niesen, M., Jaschinski, U., Hoersch, S., Jung, A., Allgaeuer, S., Haake, H., Lange, A., Papanikolaou, M., Balla, M., Giannakou, M., Soultati, I., Nikos, G., Koulouras, V., Kyriazopoulos, G., Gkika, D., Vlachogianni, G., Psaroulis, K., Mouloudi, E., Massa, E., Nichol, A., Meany, E., Motherway, C., Bellani, G., Pota, V., Schiavone, V., Girardis, M., Busani, S., Petrucci, N., Di Pasquale, R., Mazzini, P., Molin, A., Pellerano, G., Volta, C., Spadaro, S., Guarracino, F., Savioli, M., Pellis, T., Chinellato, N., Gatta, A., Cecchini, F., Raineri, S. M., Cortegiani, A., Kekstas, G., Karosas, V., Anguseva, T., Mitrev, Z., Beck, O., Cimic, N., Janssen, G., Bormans, L., Kuiper, M., Koopmans, K., Den Boer, S., de Groot, M., Dennesen, P., van den Bosch, J., Kluge, G., Mikaszewska-Sokolewicz, M., Lazowski, T., Chruscikowski, M., Machon, J., Adamik, B., Kübler, A., Wieczorek, A., Afonso, S., Matos, R., Catorze, N., Araujo, A., Costa, Z., Pais-de-Lacerda, A., Martins, I., Cardiga, R., Fernandes, L., Serra, I., Martinho, A., Tomescu, D., Popescu, M., Scarlatescu, E., Stoica, R., Macri, A., Filipescu, D., Rupnik, E., Tomic, V., Sifrer, F., Sole Violan, J., Ferrer Agüero, J. M., Izura, J., Monedero, P., de Cabo, C. Muños, Aguilar, G., Belda, F. J., Blanquer, J., Nives Carbonell, E., Lopez-Delgado, J. -C., Aragon, C., Joya, C., Ortiz-Leyba, C., Fernandez Gonzalez, C. J., de la Torre-Prados, M. -V., Puerto-Morlan, A., Araujo Aguilar, P., Tomás Marsilla, J. I., Vera Aratcoz, P., Olmo, A., Ferrer Roca, R., Catalan, R. M., Garcia Olivares, P., Albis, A., Alvarez, M., Corcoles Gonzalez, V., Gutierrez Rubio, J. M., Montoiro Allue, R., Rubio Mateo-Sidron, J., Hobrok, M., Cecconi, M., Di Tomasso, N., Raj, A., Szakmany, T., Srinivasa, L., Mathew, S., Ferguson, A., Blahut-Zugaj, M., Watters, M., Henderson, S., Sim, M., Csabi, P., O’Neill, O., Nutt, C., Humphreys, S., Bhowmick, K., Donnelly, A., O’Kane, S., Garfield, M., Jha, R., Unni, N., Gordon, A., Rubulotta, F., Ravi, K., Lunch, G., Franco, F., Higgs, D., Strandvik, G., Jonas, A., Hopkins, Ph., Hurst, T., Bellini, A., Balogun, O., Srinivasan, R., Ostermann, M., Alexander, P., McCalman, K., Bedford, J., Fulop, M., Brescia, G., Strachan, J., Meyer, J., Stotz, M., Brett, S., Zand, F., Nikandish, R., Hashemian, S., Jamaati, H., Alsheikhly, A. S., Almekhlafi, G., Albarrak, M., Maghrabi, A., Salahuddin, N., Aisa, T., Atalan, H. K., Sungur, M., Hegazi, M., Bauer, P., Mukkera, S., Fried, J., Barger, M., Gueret, R., Gonzalez, C., Lovesio, C., Dellera, Ch., Barrios, D., Leite Mendes, C., Gottardo, P., Caser, E., Santos, C., Carvalho, A., Teixeira, C., Samaniego, W., Whittle, S., Molano, D., Rojas, A., Guerra, K., Villamagua, B., Salgado-Yepez, E., Morocho, D., Remache-Vargas, N., Ñamendys-Silva, S., Rodriguez, D., Dominguez, G., Barraza, G., Bermudez-Aceves, E., Sanchez-Hurtado, L. A., Baltazar-Torres, J. A., Quispe Sierra, R., Chavez, C., von Osten, I., Van Haren, C., Smalley, N., Kol, M., Wong, H., Smith, R., Yu, L., Wu, X., Chao, L., Zhai, Q., Wu, D., Zhang, X., Jing, X., Bigornia, R., Ikeda-Maquiling, Y., Robles, J., Palo, J. E., Nguyen, T., Dao, C., Dixit, S., Gurjar, M., Reddy, P., Pravin, A., Simran, S., Ramakrishnan, N., Shetty, R., Udwadia, F., Faraz, M., Indraratna, K., Rajasinhe, J., Sakr, Yasser, Ferrer, Ricard, Reinhart, Konrad, Beale, Richard, Rhodes, Andrew, Moreno, Rui, Timsit, Jean Francoi, Brochard, Laurent, Thompson, B. Taylor, Rezende, Ederlon, Chiche, Jean Daniel, Auer, J., Schatzl, G., Mach, K., Gruber, H., Schreurs, E., Vander Laenen, M., Ceunen, H., Wauters, J., Francois, G., Deschamps, P., Castanares, D., Debels, D., Pierrakos, C., Vincent, J.L., Taccone, F., Vymazal, T., Gornik, I., Vujiaklija Brajkovic, A., Medici, R., Nielsen, J., Bendtsen, A., Siegel, H., Suonsyrjä, T., Hraech, S., Daviaux, F., Guillot, M., Castelain, V., Losser, R.-R., Novy, E., Bouadma, L., Misset, B., Philippart, F., Mallat, J., Zogheib, E., Miclo, M., Teboul, J.-L., Anguel, N., Darmon, M., Pham, T., Barberet, G., Plantefeve, G., Floccard, B., Kheladze, Z., Bloos, F., Faltlhauser, A., Helmes, T., Zacharowski, K., Meybohm, P., Schwarzkopf, K., Christ, M., Baumgaertel, M., John, S., Nentwich, J., Deja, M., Goldmann, A., Gottschalk, A., Honig, F., Siepe, B., Goebel, U., Lehmke, J., Behrens, S., Fiedler, K., Sagoschen, I., Riessen, R., Haap, M., Simon, Ph., Kaisers, U., Niesen, M., Jaschinski, U., Hoersch, S., Jung, A., Allgaeuer, S., Haake, H., Lange, A., Papanikolaou, M., Balla, M., Giannakou, M., Soultati, I., Nikos, G., Koulouras, V., Kyriazopoulos, G., Gkika, D., Vlachogianni, G., Psaroulis, K., Mouloudi, E., Massa, E., Nichol, A., Meany, E., Motherway, C., Bellani, G., Pota, V., Schiavone, V., Girardis, M., Busani, S., Petrucci, N., Di Pasquale, R., Mazzini, P., Molin, A., Pellerano, G., Volta, C., Spadaro, S., Guarracino, F., Savioli, M., Pellis, T., Chinellato, N., Gatta, A., Cecchini, F., Raineri, S.M., Cortegiani, A., Kekstas, G., Karosas, V., Anguseva, T., Mitrev, Z., Beck, O., Cimic, N., Janssen, G., Bormans, L., Kuiper, M., Koopmans, K., Den Boer, S., de Groot, M., Dennesen, P., van den Bosch, J., Kluge, G., Mikaszewska-Sokolewicz, M., Lazowski, T., Chruscikowski, M., Machon, J., Adamik, B., Kübler, A., Wieczorek, A., Afonso, S., Matos, R., Catorze, N., Araujo, A., Costa, Z., Pais-de-Lacerda, A., Martins, I., Cardiga, R., Fernandes, L., Serra, I., Martinho, A., Tomescu, D., Popescu, M., Scarlatescu, E., Stoica, R., Macri, A., Filipescu, D., Rupnik, E., Tomic, V., Sifrer, F., Sole Violan, J., Ferrer Agüero, J.M., Izura, J., Monedero, P., de Cabo, C. Muño, Aguilar, G., Belda, F.J., Blanquer, J., Nives Carbonell, E., Lopez-Delgado, J.-C., Aragon, C., Joya, C., Ortiz-Leyba, C., Fernandez Gonzalez, C.J., de la Torre-Prados, M.-V., Puerto-Morlan, A., Araujo Aguilar, P., Tomás Marsilla, J.I., Vera Aratcoz, P., Olmo, A., Ferrer Roca, R., Catalan, R.M., Garcia Olivares, P., Albis, A., Alvarez, M., Corcoles Gonzalez, V., Gutierrez Rubio, J.M., Montoiro Allue, R., Rubio Mateo-Sidron, J., Hobrok, M., Cecconi, M., Di Tomasso, N., Raj, A., Szakmany, T., Srinivasa, L., Mathew, S., Ferguson, A., Blahut-Zugaj, M., Watters, M., Henderson, S., Sim, M., Csabi, P., O’Neill, O., Nutt, C., Humphreys, S., Bhowmick, K., Donnelly, A., O’Kane, S., Garfield, M., Jha, R., Unni, N., Gordon, A., Rubulotta, F., Ravi, K., Lunch, G., Franco, F., Higgs, D., Strandvik, G., Jonas, A., Hopkins, Ph., Hurst, T., Bellini, A., Balogun, O., Srinivasan, R., Ostermann, M., Alexander, P., McCalman, K., Bedford, J., Fulop, M., Brescia, G., Strachan, J., Meyer, J., Stotz, M., Brett, S., Zand, F., Nikandish, R., Hashemian, S., Jamaati, H., Alsheikhly, A.S., Almekhlafi, G., Albarrak, M., Maghrabi, A., Salahuddin, N., Aisa, T., Atalan, H.K., Sungur, M., Hegazi, M., Bauer, P., Mukkera, S., Fried, J., Barger, M., Gueret, R., Gonzalez, C., Lovesio, C., Dellera, Ch., Barrios, D., Leite Mendes, C., Gottardo, P., Caser, E., Santos, C., Carvalho, A., Teixeira, C., Samaniego, W., Whittle, S., Molano, D., Rojas, A., Guerra, K., Villamagua, B., Salgado-Yepez, E., Morocho, D., Remache-Vargas, N., Ñamendys-Silva, S., Rodriguez, D., Dominguez, G., Barraza, G., Bermudez-Aceves, E., Sanchez-Hurtado, L.A., Baltazar-Torres, J.A., Quispe Sierra, R., Chavez, C., von Osten, I., Van Haren, C., Smalley, N., Kol, M., Wong, H., Smith, R., Yu, L., Wu, X., Chao, L., Zhai, Q., Wu, D., Zhang, X., Jing, X., Bigornia, R., Ikeda-Maquiling, Y., Robles, J., Palo, J.E., Nguyen, T., Dao, C., Dixit, S., Gurjar, M., Reddy, P., Pravin, A., Simran, S., Ramakrishnan, N., Shetty, R., Udwadia, F., Faraz, M., Indraratna, K., and Rajasinhe, J.
- Subjects
Critical Care and Intensive Care Medicine - Abstract
In both the original publication (DOI 10.1007/s00134-015-4206-2) and the first erratum (DOI 10.1007/s00134-016-4317-4), the members of the IC-GLOSSARI Investigators and the ESICM Trials Group were provided in such a way that they could not be indexed as collaborators on PubMed. The publisher apologizes for these errors and is pleased to list the members of the groups here: (Table presented.).
- Published
- 2018
8. Quality of life after COVID-19 induced critical illness: do the old survivors suffer more?
- Author
-
CONINGS, J., VERMEIREN, G., BOER, W., FIVEZ, T., MESOTTEN, D., VANDER LAENEN, M., THIESSEN, S., ENGELEN, K., and WILLAERT, X.
- Published
- 2021
9. An alternative strategy for COVID-pneumonitis: a retrospective analysis from a tertiary center in Belgium.
- Author
-
FIVEZ, T., BRUGGEN, J., MESOTTEN, D., WILLAERT, X., ENGELEN, K., MERCKX, L., VANDER LAENEN, M., PIERLET, N., GOETHUYS, B., HEYLEN, R., and BOER, W.
- Published
- 2021
10. Survival of elderly COVID-19 intensive care patients in the first and second Belgian wave: a retrospective single center analysis.
- Author
-
VERMEIREN, G., WILLAERT, X., VERVLOESSEM, H., THIESSEN, S., BOER, W., FIVEZ, T., ENGELEN, K., VANDER LAENEN, M., VAN DE VELDE, M., and MESOTTEN, D.
- Published
- 2021
11. Risk factors of Intensive Care Unit-Acquired Weakness: a single center retrospective analysis.
- Author
-
HILDERSON, C., SCHRAMME, D., NAVEAU, B., VANDER LAENEN, M., BOER, W., ENGELEN, K., FIVEZ, T., WILLAERT, X., PIERLET, N., REX, S., EERTMANS, W., and MESOTTEN, D.
- Published
- 2021
12. Predictors for aki in a cardiac surgery population undergoing cardio-pulmonary bypass
- Author
-
Ramakers, F, Swennen, Q, Pennemans, V, Penders, J, Vander Laenen, M, and Boer, W
- Published
- 2015
- Full Text
- View/download PDF
13. Neuropathic pain in humans is associated with elevated TNF-α concentrations in blood and cerebrospinal fluid
- Author
-
Beckers, K., primary, Vander, Laenen M., additional, Penders, J., additional, Heylen, R., additional, Van Zundert, J., additional, and Vanelderen, P., additional
- Published
- 2013
- Full Text
- View/download PDF
14. Patients with neuropathic pain exhibit higher concentrations of neuropeptide Y in their blood
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Loos, N., primary, Vander, Laenen M., additional, Penders, J., additional, Heylen, R., additional, Van Zundert, J., additional, and Vanelderen, P., additional
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- 2013
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15. Serum brain-derived neurotrophic factor levels are decreased in patients suffering from neuropathic pain
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Cox, E., primary, Vander, Laenen M., additional, Penders, J., additional, Heylen, R., additional, Van Zundert, J., additional, and Vanelderen, P., additional
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- 2013
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16. Implementation of an emergency department infomation system resulted in significantly reduced waiting times
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Bohy, B., primary, De Deyne, C., additional, Vundelinckx, G., additional, Vander Laenen, M., additional, and Heylen, R., additional
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- 2007
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17. Early leukocytosis occurring after subarachnoid hemorrhage could be used as a predictor of later cerebral vasospasm
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Van Assche, E., primary, De Deyne, C., additional, Schneider, I., additional, Vander Laenen, M., additional, and Heylen, R., additional
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- 2006
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18. Critical care glycemia control in patients suffering from severe subarachnoid hemorrhage
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Cochet, K., primary, De Deyne, C., additional, Mesotten, D., additional, Van Assche, E., additional, Schneider, I., additional, Vander Laenen, M., additional, and Heylen, R., additional
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- 2006
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19. Respiratory complications in patients suffering from severe subarachnoid hemorrhage seem not directly related to hypervolemic therapy
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Schneider, I., primary, De Deyne, C., additional, Van Assche, E., additional, Vander Laenen, M., additional, and Heylen, R., additional
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- 2006
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20. Influence of intravenous clonidine pretreatment on anesthetic requirements during bispectral EEG-guided sevoflurane anesthesia
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De Deyne, C, primary, Struys, M, additional, Heylen, R, additional, De Jongh, R, additional, Vander Laenen, M, additional, Buyse, L, additional, Deghislage, J, additional, and Rolly, G, additional
- Published
- 2000
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21. Boosting the accuracy of existing models by updating and extending: using a multicenter COVID-19 ICU cohort as a proxy.
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Meijs DAM, Wynants L, van Kuijk SMJ, Scheeren CIE, Hana A, Mehagnoul-Schipper J, Stessel B, Vander Laenen M, Cox EGM, Sels JEM, Smits LJM, Bickenbach J, Mesotten D, van der Horst ICC, Marx G, and van Bussel BCT
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- Humans, Male, Female, Middle Aged, Aged, SARS-CoV-2 isolation & purification, Prognosis, Cohort Studies, ROC Curve, COVID-19 mortality, COVID-19 epidemiology, COVID-19 virology, Intensive Care Units
- Abstract
Most published prediction models for Coronavirus Disease 2019 (COVID-19) were poorly reported, at high risk of bias, and heterogeneous in model performance. To tackle methodological challenges faced in previous prediction studies, we investigated whether model updating and extending improves mortality prediction, using the Intensive Care Unit (ICU) as a proxy. All COVID-19 patients admitted to seven ICUs in the Euregio-Meuse Rhine during the first pandemic wave were included. The 4C Mortality and SEIMC scores were selected as promising prognostic models from an external validation study. Five predictors could be estimated based on cohort size. TRIPOD guidelines were followed and logistic regression analyses with the linear predictor, APACHE II score, and country were performed. Bootstrapping with backward selection was applied to select variables for the final model. Additionally, shrinkage was performed. Model discrimination was displayed as optimism-corrected areas under the ROC curve and calibration by calibration slopes and plots. The mortality rate of the 551 included patients was 36%. Discrimination of the 4C Mortality and SEIMC scores increased from 0.70 to 0.74 and 0.70 to 0.73 and calibration plots improved compared to the original models after updating and extending. Mortality prediction can be improved after updating and extending of promising models., (© 2024. The Author(s).)
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- 2024
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22. The effects of differing anticoagulant regimes on blood quality after cell salvage in coronary artery bypass grafting (CABG): a pilot study.
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Boer W, van Tornout M, Brusseleers M, Strauven M, de Vooght P, Vander Laenen M, Hoste E, and Jorens PG
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- Adult, Humans, Pilot Projects, Heparin, Citric Acid, Anticoagulants pharmacology, Anticoagulants therapeutic use, Coronary Artery Bypass methods
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Background: Cell salvage reduces allogenic blood transfusion requirements in surgery. We present a pilot study exploring the impact of anticoagulant choice, citrate or heparin, on the quality of cell salvaged blood in adults undergoing coronary artery bypass grafting (CABG)., Materials and Methods: Elective on pump CABG patients were randomly allocated to citrate or heparin anticoagulation. We measured red blood cell characteristics and inflammation in both the blood collection reservoir and the washed red blood cell concentrate. Postoperatively, the level of biomarkers and the coagulation profile in the peripheral blood as well as the transfusion requirements of allogenic blood products were studied., Results: Thirty eight patients were included, 19 in the citrate group and 19 in the heparin group. Baseline characteristics were similar. In the washed red blood cell concentrate, Mean Hb (g/dl) and Ht (%) were lower in the citrate group [Hb: 18.1 g/dL (SD 1.3) vs. 21.1 (1.6), p < 0.001; Ht: 59.9% (54.7-60.9) vs. 63.7% (62.3-64.8); p < 0.001]; Mean corpuscular volume (MCV, μm 3) was higher [99.1fL (9.4) vs. 88 (4.2), p < 0.001] and mean corpuscular hemoglobin concentration (MCHC, g/dl) lower in the citrate group [31.9 g/dl (29.6-32.4) vs. 33.6 (33.1-34.0) p < 0.001]. Thrombocyte count (1000/μl) was higher in the citrate group [31.0 (26.0-77.0) vs. 13.0 (10.0-39.0); p = 0.006]. There were no differences in the requirement for allogenic blood products' transfusion (intraoperatively and postoperatively) or in the coagulation parameters after washed red blood cell concentrate infusion. Higher IL-10 was found in the citrate group in the blood collection reservoir, higher neutrophil-derived myeloperoxidase (MPO) in the heparin group after washed red blood cell concentrate infusion., Conclusion: Though red blood cells in washed red blood cell concentrate were more swollen and diluted in the citrate group with more residual thrombocytes, published quality guidelines were met in both groups. Our pilot study suggests that differences in inflammatory markers in the blood collection reservoir and after infusion of washed red blood cell concentrate indicate a possible pro-inflammatory effect of heparin compared to citrate. A larger study is warranted to confirm these results and their possible clinical consequences. Trial registration ClinicalTrials.gov : NCT02674906. Registered 5 February 2016., (© 2023. The Author(s).)
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- 2023
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23. Predicting COVID-19 prognosis in the ICU remained challenging: external validation in a multinational regional cohort.
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Meijs DAM, van Kuijk SMJ, Wynants L, Stessel B, Mehagnoul-Schipper J, Hana A, Scheeren CIE, Bergmans DCJJ, Bickenbach J, Vander Laenen M, Smits LJM, van der Horst ICC, Marx G, Mesotten D, and van Bussel BCT
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- Humans, Female, Middle Aged, Aged, Male, Cohort Studies, Intensive Care Units, Prognosis, Critical Care, Hospital Mortality, Retrospective Studies, COVID-19 epidemiology, COVID-19 therapy
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Objectives: Many prediction models for coronavirus disease 2019 (COVID-19) have been developed. External validation is mandatory before implementation in the intensive care unit (ICU). We selected and validated prognostic models in the Euregio Intensive Care COVID (EICC) cohort., Study Design and Setting: In this multinational cohort study, routine data from COVID-19 patients admitted to ICUs within the Euregio Meuse-Rhine were collected from March to August 2020. COVID-19 models were selected based on model type, predictors, outcomes, and reporting. Furthermore, general ICU scores were assessed. Discrimination was assessed by area under the receiver operating characteristic curves (AUCs) and calibration by calibration-in-the-large and calibration plots. A random-effects meta-analysis was used to pool results., Results: 551 patients were admitted. Mean age was 65.4 ± 11.2 years, 29% were female, and ICU mortality was 36%. Nine out of 238 published models were externally validated. Pooled AUCs were between 0.53 and 0.70 and calibration-in-the-large between -9% and 6%. Calibration plots showed generally poor but, for the 4C Mortality score and Spanish Society of Infectious Diseases and Clinical Microbiology (SEIMC) score, moderate calibration., Conclusion: Of the nine prognostic models that were externally validated in the EICC cohort, only two showed reasonable discrimination and moderate calibration. For future pandemics, better models based on routine data are needed to support admission decision-making., (Copyright © 2022 The Author(s). Published by Elsevier Inc. All rights reserved.)
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- 2022
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24. Differences and Similarities Among COVID-19 Patients Treated in Seven ICUs in Three Countries Within One Region: An Observational Cohort Study.
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Mesotten D, Meijs DAM, van Bussel BCT, Stessel B, Mehagnoul-Schipper J, Hana A, Scheeren CIE, Strauch U, van de Poll MCG, Ghossein-Doha C, Buhre WFFA, Bickenbach J, Vander Laenen M, Marx G, and van der Horst ICC
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- APACHE, Aged, COVID-19 mortality, Cohort Studies, Europe epidemiology, Female, Humans, Logistic Models, Male, Middle Aged, Patient Acuity, Patient Transfer, Treatment Outcome, COVID-19 therapy, Critical Care methods, Intensive Care Units organization & administration, Intensive Care Units statistics & numerical data
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Objectives: To investigate healthcare system-driven variation in general characteristics, interventions, and outcomes in coronavirus disease 2019 (COVID-19) patients admitted to the ICU within one Western European region across three countries., Design: Multicenter observational cohort study., Setting: Seven ICUs in the Euregio Meuse-Rhine, one region across Belgium, The Netherlands, and Germany., Patients: Consecutive COVID-19 patients supported in the ICU during the first pandemic wave., Interventions: None., Measurements and Main Results: Baseline demographic and clinical characteristics, laboratory values, and outcome data were retrieved after ethical approval and data-sharing agreements. Descriptive statistics were performed to investigate country-related practice variation. From March 2, 2020, to August 12, 2020, 551 patients were admitted. Mean age was 65.4 ± 11.2 years, and 29% were female. At admission, Acute Physiology and Chronic Health Evaluation II scores were 15.0 ± 5.5, 16.8 ± 5.5, and 15.8 ± 5.3 (p = 0.002), and Sequential Organ Failure Assessment scores were 4.4 ± 2.7, 7.4 ± 2.2, and 7.7 ± 3.2 (p < 0.001) in the Belgian, Dutch, and German parts of Euregio, respectively. The ICU mortality rate was 22%, 42%, and 44%, respectively (p < 0.001). Large differences were observed in the frequency of organ support, antimicrobial/inflammatory therapy application, and ICU capacity. Mixed-multivariable logistic regression analyses showed that differences in ICU mortality were independent of age, sex, disease severity, comorbidities, support strategies, therapies, and complications., Conclusions: COVID-19 patients admitted to ICUs within one region, the Euregio Meuse-Rhine, differed significantly in general characteristics, applied interventions, and outcomes despite presumed genetic and socioeconomic background, admission diagnosis, access to international literature, and data collection are similar. Variances in healthcare systems' organization, particularly ICU capacity and admission criteria, combined with a rapidly spreading pandemic might be important drivers for the observed differences. Heterogeneity between patient groups but also healthcare systems should be presumed to interfere with outcomes in coronavirus disease 2019., Competing Interests: The authors have disclosed that they do not have any potential conflicts of interest., (Copyright © 2022 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the Society of Critical Care Medicine and Wolters Kluwer Health, Inc.)
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- 2022
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25. Citrate dose for continuous hemofiltration: effect on calcium and magnesium balance, parathormone and vitamin D status, a randomized controlled trial.
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Boer W, Fivez T, Vander Laenen M, Bruckers L, Grön HJ, Schetz M, and Oudemans-van Straaten H
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- Aged, Female, Humans, Male, Middle Aged, Prospective Studies, Anticoagulants administration & dosage, Calcium metabolism, Citric Acid administration & dosage, Continuous Renal Replacement Therapy, Magnesium metabolism, Parathyroid Hormone blood, Vitamin D blood
- Abstract
Background: Regional citrate anticoagulation may cause a negative calcium balance, systemic hypocalcemia and parathormone (PTH) activation but randomzed studies are not available. Aim was to determine the effect of citrate dose on calcium (Ca) and magnesium (Mg) balance, PTH and Vitamin D., Methods: Single center prospective randomized study. Patients, requiring continuous venovenous hemofiltration (CVVH) with citrate, randomized to low dose citrate (2.5 mmol/L) vs. high dose (4.5 mmol/L) for 24 h, targeting post-filter ionized calcium (pfiCa) of 0.325-0.4 mmol/L vs. 0.2-0.275 mmol/L, using the Prismaflex® algorithm with 100% postfilter calcium replacement. Extra physician-ordered Ca and Mg supplementation was performed aiming at systemic iCa > 1.0 mmol/L. Arterial blood, effluent and post-filter aliquots were taken for balance calculations (area under the curve), intact (i), oxidized (ox) and non-oxidized (nox) PTH, 25-hydroxy-Vitamin D (25D) and 1,25-dihydroxy-Vitamin D (1,25D)., Results: 35 patients were analyzed, 17 to high, 18 to low citrate. Mean 24-h Ca balance was - 9.72 mmol/d (standard error 1.70) in the high vs - 1.18 mmol/d (se 1.70)) (p = 0.002) in the low citrate group and 24-h Mg-balance was - 25.99 (se 2.10) mmol/d vs. -17.63 (se 2.10) mmol/d (p = 0.008) respectively. Physician-ordered Ca supplementation, higher in the high citrate group, resulted in a positive Ca-balance in both groups. iPTH, oxPTH or noxPTH were not different between groups. Over 24 h, median PTH decreased from 222 (25th-75th percentile 140-384) to 162 (111-265) pg/ml (p = 0.002); oxPTH from 192 (124-353) to 154 pg/ml (87-231), p = 0.002. NoxPTH did not change significantly. Mean 25 D (standard deviation), decreased from 36.5 (11.8) to 33.3 (11.2) nmol/l (p = 0.003), 1,25D rose from 40.9 pg/ml (30.7) to 43.2 (30.7) pg/ml (p = 0.046), without differences between groups., Conclusions: A higher citrate dose caused a more negative CVVH Ca balance than a lower dose, due to a higher effluent Calcium loss. Physician-ordered Ca supplementation, targeting a systemic iCa > 1.0 mmol/L, higher in the high citrate group, resulted in a positive Ca-balance in both groups. iPTH and oxPTH declined, suggesting decreased oxidative stress, while noxPTH did not change. 25D decreased while 1,25-D rose. Mg balance was negative in both groups, more so in the high citrate group., Trial Registration: ClinicalTrials.gov : NCT02194569. Registered 18 July 2014., (© 2021. The Author(s).)
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- 2021
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26. Catheter Port Reversal in Citrate Continuous Veno-Venous Hemofiltration.
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Boer W, Van Tornout M, Vander Laenen M, Engelen K, Meex I, and Jorens P
- Abstract
Introduction: Knowledge of effects of catheter port reversal (CathPR), when blood is withdrawn from the venous port and returned via the arterial port, often used in dysfunctional catheters in renal replacement therapy, is limited in the setting of citrate continuous veno-venous hemofiltration (CVVH)., Methods: In this open trial, post-filter ionized calcium (PfiCa), post-filter citrate concentration (PfCC), catheter recirculation, and solute clearance were measured before, during, and after 6 hours of CathPR, in well-functioning catheters. All other settings, including citrate settings, were left constant during the study., Results: Twenty-three patients were included. Mean PfiCa before CathPR of 0.36 mmol/L (SD 0.06) decreased to 0.31 (0.04) after 2 hours ( P = 0.002), 0.31 (0.04) ( P = 0.002) at 4 hours, and 0.31 (0.04) at 6 hours ( P = 0.001). Return to normal increased mean PfiCa to 0.34 (0.06) ( P = 0.006). Mean PfCC rose from 592 mg/L (SD 164) before CathPR to 649 mg/L (190) after 2 hours ( P = 0.045), to 696 mg/L (192) after 4 hours ( P < 0.001), and to 657 mg/L (214) after 6 hours ( P = 0.018). Return to normal decreased mean PfCC to 598 mg/L (184) ( P = 0.024). Mean recirculation increased during CathPR (from 4.3% [0-8.7] before to 13.8% [9.7-22.2], P < 0.001). Urea, potassium, and creatinine clearances dropped significantly, but calcium clearance was unaffected., Conclusion: CathPR caused a significant decrease in PfiCA and increase in PfCC. Calcium handling differs from other solutes because of increases caused in citrate concentration and subsequent effects on calcium chelation. In citrate CVVH, CathPR in dysfunctional catheters should be limited in time, with intensive follow-up. Trial registration: ClinicalTrials.gov: NCT024600416. Registered 9 November 2015., (© 2021 International Society of Nephrology. Published by Elsevier Inc.)
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- 2021
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27. Venous thromboembolism in SARS-CoV-2 patients: only a problem in ventilated ICU patients, or is there more to it?
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Criel M, Falter M, Jaeken J, Van Kerrebroeck M, Lefere I, Meylaerts L, Mesotten D, Vander Laenen M, Fivez T, Thomeer M, and Ruttens D
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- Aged, Betacoronavirus, Body Mass Index, COVID-19, Cohort Studies, Critical Care, Female, Humans, Intensive Care Units, Male, Middle Aged, Pandemics, Risk Factors, SARS-CoV-2, Treatment Outcome, Coronavirus Infections complications, Pneumonia, Viral complications, Respiration, Artificial adverse effects, Venous Thromboembolism complications, Venous Thromboembolism prevention & control
- Abstract
Competing Interests: Conflict of interest: M. Criel has nothing to disclose. Conflict of interest: M. Falter has nothing to disclose. Conflict of interest: J. Jaeken has nothing to disclose. Conflict of interest: M. Van Kerrebroeck has nothing to disclose. Conflict of interest: I. Lefere has nothing to disclose. Conflict of interest: L. Meylaerts has nothing to disclose. Conflict of interest: D. Mesotten has nothing to disclose. Conflict of interest: M. vander Laenen has nothing to disclose. Conflict of interest: T. Fivez has nothing to disclose. Conflict of interest: M. Thomeer has nothing to disclose. Conflict of interest: D. Ruttens has nothing to disclose.
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- 2020
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28. Association between postoperative delirium and postoperative cerebral oxygen desaturation in older patients after cardiac surgery.
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Eertmans W, De Deyne C, Genbrugge C, Marcus B, Bouneb S, Beran M, Fret T, Gutermann H, Boer W, Vander Laenen M, Heylen R, Mesotten D, Vanelderen P, and Jans F
- Subjects
- Aged, Aged, 80 and over, Belgium, Delirium metabolism, Female, Humans, Male, Postoperative Complications metabolism, Prospective Studies, Spectroscopy, Near-Infrared, Brain metabolism, Cardiac Surgical Procedures, Delirium etiology, Geriatric Assessment methods, Oxygen metabolism, Postoperative Complications etiology
- Abstract
Background: Near-infrared spectroscopy non-invasively measures regional cerebral oxygen saturation. Intraoperative cerebral desaturations have been associated with worse neurological outcomes. We investigated whether perioperative cerebral desaturations are associated with postoperative delirium in older patients after cardiac surgery., Methods: Patients aged 70 yr and older scheduled for on-pump cardiac surgery were included between 2015 and 2017 in a single-centre, prospective, observational study. Baseline cerebral oxygen saturation was measured 1 day before surgery. Throughout surgery and after ICU admission, cerebral oxygen saturation was monitored continuously up to 72 h after operation. The presence of delirium was assessed using the confusion assessment method for the ICU. Association with delirium was evaluated with unadjusted analyses and multivariable logistic regression., Results: Ninety-six of 103 patients were included, and 29 (30%) became delirious. Intraoperative cerebral oxygen saturation was not significantly associated with postoperative delirium. The lowest postoperative cerebral oxygen saturation was lower in patients who became delirious (P=0.001). The absolute and relative postoperative cerebral oxygen saturation decreases were more marked in patients with delirium (13 [6]% and 19 [9]%, respectively) compared with patients without delirium (9 [4]% and 14 [5]%; P=0.002 and P=0.001, respectively). These differences in cerebral oxygen saturation were no longer present after excluding cerebral oxygen saturation values after patients became delirious. Older age, previous stroke, higher EuroSCORE II, lower preoperative Mini-Mental Status Examination, and more substantial absolute postoperative cerebral oxygen saturation decreases were independently associated with postoperative delirium incidence., Conclusions: Postoperative delirium in older patients undergoing cardiac surgery is associated with absolute decreases in postoperative cerebral oxygen saturation. These differences appear most detectable after the onset of delirium., Clinical Trial Registration: NCT02532530., (Copyright © 2019 British Journal of Anaesthesia. Published by Elsevier Ltd. All rights reserved.)
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- 2020
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29. Effect of Selepressin vs Placebo on Ventilator- and Vasopressor-Free Days in Patients With Septic Shock: The SEPSIS-ACT Randomized Clinical Trial.
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Laterre PF, Berry SM, Blemings A, Carlsen JE, François B, Graves T, Jacobsen K, Lewis RJ, Opal SM, Perner A, Pickkers P, Russell JA, Windeløv NA, Yealy DM, Asfar P, Bestle MH, Muller G, Bruel C, Brulé N, Decruyenaere J, Dive AM, Dugernier T, Krell K, Lefrant JY, Megarbane B, Mercier E, Mira JP, Quenot JP, Rasmussen BS, Thorsen-Meyer HC, Vander Laenen M, Vang ML, Vignon P, Vinatier I, Wichmann S, Wittebole X, Kjølbye AL, and Angus DC
- Abstract
Importance: Norepinephrine, the first-line vasopressor for septic shock, is not always effective and has important catecholaminergic adverse effects. Selepressin, a selective vasopressin V1a receptor agonist, is a noncatecholaminergic vasopressor that may mitigate sepsis-induced vasodilatation, vascular leakage, and edema, with fewer adverse effects., Objective: To test whether selepressin improves outcome in septic shock., Design, Setting, and Participants: An adaptive phase 2b/3 randomized clinical trial comprising 2 parts that included adult patients (n = 868) with septic shock requiring more than 5 μg/min of norepinephrine. Part 1 used a Bayesian algorithm to adjust randomization probabilities to alternative selepressin dosing regimens and to trigger transition to part 2, which would compare the best-performing regimen with placebo. The trial was conducted between July 2015 and August 2017 in 63 hospitals in Belgium, Denmark, France, the Netherlands, and the United States, and follow-up was completed by May 2018., Interventions: Random assignment to 1 of 3 dosing regimens of selepressin (starting infusion rates of 1.7, 2.5, and 3.5 ng/kg/min; n = 585) or to placebo (n = 283), all administered as continuous infusions titrated according to hemodynamic parameters., Main Outcomes and Measures: Primary end point was ventilator- and vasopressor-free days within 30 days (deaths assigned zero days) of commencing study drug. Key secondary end points were 90-day mortality, kidney replacement therapy-free days, and ICU-free days., Results: Among 868 randomized patients, 828 received study drug (mean age, 66.3 years; 341 [41.2%] women) and comprised the primary analysis cohort, of whom 562 received 1 of 3 selepressin regimens, 266 received placebo, and 817 (98.7%) completed the trial. The trial was stopped for futility at the end of part 1. Median study drug duration was 37.8 hours (IQR, 17.8-72.4). There were no significant differences in the primary end point (ventilator- and vasopressor-free days: 15.0 vs 14.5 in the selepressin and placebo groups; difference, 0.6 [95% CI, -1.3 to 2.4]; P = .30) or key secondary end points (90-day mortality, 40.6% vs 39.4%; difference, 1.1% [95% CI, -6.5% to 8.8%]; P = .77; kidney replacement therapy-free days: 18.5 vs 18.2; difference, 0.3 [95% CI, -2.1 to 2.6]; P = .85; ICU-free days: 12.6 vs 12.2; difference, 0.5 [95% CI, -1.2 to 2.2]; P = .41). Adverse event rates included cardiac arrhythmias (27.9% vs 25.2% of patients), cardiac ischemia (6.6% vs 5.6%), mesenteric ischemia (3.2% vs 2.6%), and peripheral ischemia (2.3% vs 2.3%)., Conclusions and Relevance: Among patients with septic shock receiving norepinephrine, administration of selepressin, compared with placebo, did not result in improvement in vasopressor- and ventilator-free days within 30 days. Further research would be needed to evaluate the potential role of selepressin for other patient-centered outcomes in septic shock., Trial Registration: ClinicalTrials.gov Identifier: NCT02508649.
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- 2019
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30. The Prognostic Value of Simplified EEG in Out-of-Hospital Cardiac Arrest Patients.
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Eertmans W, Genbrugge C, Haesen J, Drieskens C, Demeestere J, Vander Laenen M, Boer W, Mesotten D, Dens J, Ernon L, Jans F, and De Deyne C
- Subjects
- Aged, Aged, 80 and over, Cardiopulmonary Resuscitation, Electroencephalography methods, Female, Humans, Hypothermia, Induced, Male, Middle Aged, Neurophysiological Monitoring methods, Out-of-Hospital Cardiac Arrest therapy, Predictive Value of Tests, Prognosis, Retrospective Studies, Coma diagnosis, Coma etiology, Electroencephalography standards, Neurophysiological Monitoring standards, Out-of-Hospital Cardiac Arrest complications, Outcome Assessment, Health Care, Seizures diagnosis, Seizures etiology
- Abstract
Background: We previously validated simplified electroencephalogram (EEG) tracings obtained by a bispectral index (BIS) device against standard EEG. This retrospective study now investigated whether BIS EEG tracings can predict neurological outcome after cardiac arrest (CA)., Methods: Bilateral BIS monitoring (BIS VISTA™, Aspect Medical Systems, Inc. Norwood, USA) was started following intensive care unit admission. Six, 12, 18, 24, 36 and 48 h after targeted temperature management (TTM) at 33 °C was started, BIS EEG tracings were extracted and reviewed by two neurophysiologists for the presence of slow diffuse rhythm, burst suppression, cerebral inactivity and epileptic activity (defined as continuous, monomorphic, > 2 Hz generalized sharp activity or continuous, monomorphic, < 2 Hz generalized blunt activity). At 180 days post-CA, neurological outcome was determined using cerebral performance category (CPC) classification (CPC1-2: good and CPC3-5: poor neurological outcome)., Results: Sixty-three out-of-hospital cardiac arrest patients were enrolled for data analysis of whom 32 had a good and 31 a poor neurological outcome. Epileptic activity within 6-12 h predicted CPC3-5 with a positive predictive value (PPV) of 100%. Epileptic activity within time frames 18-24 and 36-48 h showed a PPV for CPC3-5 of 90 and 93%, respectively. Cerebral inactivity within 6-12 h predicted CPC3-5 with a PPV of 57%. In contrast, cerebral inactivity between 36 and 48 h predicted CPC3-5 with a PPV of 100%. The pattern with the worst predictive power at any time point was burst suppression with PPV of 44, 57 and 40% at 6-12 h, at 18-24 h and at 36-48 h, respectively. Slow diffuse rhythms at 6-12 h, at 18-24 h and at 36-48 h predicted CPC1-2 with PPV of 74, 76 and 80%, respectively., Conclusion: Based on simplified BIS EEG, the presence of epileptic activity at any time and cerebral inactivity after the end of TTM may assist poor outcome prognostication in successfully resuscitated CA patients. A slow diffuse rhythm at any time after CA was indicative for a good neurological outcome.
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- 2019
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31. Impact of a VAP bundle in Belgian intensive care units.
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Jadot L, Huyghens L, De Jaeger A, Bourgeois M, Biarent D, Higuet A, de Decker K, Vander Laenen M, Oosterlynck B, Ferdinande P, Reper P, Brimioulle S, Van Cromphaut S, De Clety SC, Sottiaux T, and Damas P
- Abstract
Background: In order to decrease the incidence of ventilator-associated pneumonia (VAP) in Belgium, a national campaign for implementing a VAP bundle involving assessment of sedation, cuff pressure control, oral care with chlorhexidine and semirecumbent position, was launched in 2011-2012. This report will document the impact of this campaign., Methods: On 1 day, once a year from 2010 till 2016, except in 2012, Belgian ICUs were questioned about their ventilated patients. For each of these, data about the application of the bundle and the possible treatment for VAP were recorded., Results: Between 36.6 and 54.8% of the 120 Belgian ICUs participated in the successive surveys. While the characteristics of ventilated patients remained similar throughout the years, the percentage of ventilated patients and especially the duration of ventilation significantly decreased before and after the national VAP bundle campaign. Ventilator care also profoundly changed: Controlling cuff pressure, head positioning above 30° were obtained in more than 90% of cases. Oral care was more frequently performed within a day, using more concentrated solutions of chlorhexidine. Subglottic suctioning also was used but in only 24.7% of the cases in the last years. Regarding the prevalence of VAP, it significantly decreased from 28% of ventilated patients in 2010 to 10.1% in 2016 (p ≤ 0.0001)., Conclusion: Although a causal relationship cannot be inferred from these data, the successive surveys revealed a potential impact of the VAP bundle campaign on both the respiratory care of ventilated patients and the prevalence of VAP in Belgian ICUs encouraging them to follow the guidelines.
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- 2018
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32. The validation of simplified EEG derived from the bispectral index monitor in post-cardiac arrest patients.
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Haesen J, Eertmans W, Genbrugge C, Meex I, Demeestere J, Vander Laenen M, Boer W, Mesotten D, Dens J, Jans F, Ernon L, and De Deyne C
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- Aged, Heart Arrest therapy, Humans, Middle Aged, Monitoring, Physiologic methods, Observer Variation, Retrospective Studies, Sensitivity and Specificity, Consciousness Monitors, Electroencephalography, Status Epilepticus diagnosis
- Abstract
Aims: We aimed to validate retrospectively the accuracy of simplified electroencephalography (EEG) monitoring derived from the bispectral index (BIS) monitor in post-cardiac arrest (CA) patients., Methods: Successfully resuscitated CA patients were transferred to the Catherization Lab followed by percutaneous coronary intervention when indicated. On arrival at the coronary care unit, bilateral BIS monitoring was started and continued up to 72 h. Raw simplified EEG tracings were extracted from the BIS monitor at a time point coinciding with the registration of standard EEG monitoring. BIS EEG tracings were reviewed by two neurophysiologists, who were asked to indicate the presence of following patterns: diffuse slowing rhythm, burst suppression pattern, cerebral inactivity, periodic epileptiform discharges and status epilepticus (SE). Additionally, these simplified BIS EEG tracings were analysed by two inexperienced investigators, who were asked to indicate the presence of SE only., Results: Thirty-two simplified BIS EEG samples were analysed. Compared to standard EEG, neurophysiologists interpreted all simplified EEG samples with a sensitivity of 86%, a specificity of 100% and an interobserver variability of 0.843. Furthermore, SE was identified with a sensitivity of 80% and a specificity of 94% by two unexperienced physicians., Conclusion: Using a simple classification system, raw simplified EEG derived from a BIS monitoring device is comparable to standard EEG monitoring. Moreover, investigators without EEG experience were capable to identify SE in post-CA patients. Future studies will be warranted to confirm our results and to determine the added value of using simplified BIS EEG in terms of prognostic and therapeutic implications., (Copyright © 2018 Elsevier B.V. All rights reserved.)
- Published
- 2018
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33. The prognostic value of bispectral index and suppression ratio monitoring after out-of-hospital cardiac arrest: a prospective observational study.
- Author
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Eertmans W, Genbrugge C, Vander Laenen M, Boer W, Mesotten D, Dens J, Jans F, and De Deyne C
- Abstract
Background: We investigated the ability of bispectral index (BIS) monitoring to predict poor neurological outcome in out-of-hospital cardiac arrest (OHCA) patients fully treated according to guidelines., Results: In this prospective, observational study, 77 successfully resuscitated OHCA patients were enrolled in whom BIS, suppression ratio (SR) and electromyographic (EMG) values were continuously monitored during the first 36 h after the initiation of targeted temperature management at 33 °C. The Cerebral Performance Category (CPC) scale was used to define patients' outcome at 180 days after OHCA (CPC 1-2: good-CPC 3-5: poor neurological outcome). Using mean BIS and SR values calculated per hour, receiver operator characteristics curves were constructed to determine the optimal time point and threshold to predict poor neurological outcome. At 180 days post-cardiac arrest, 39 patients (51%) had a poor neurological outcome. A mean BIS value ≤ 25 at hour 12 predicted poor neurological outcome with a sensitivity of 49% (95% CI 30-65%), a specificity of 97% (95% CI 85-100%) and false positive rate (FPR) of 6% (95% CI 0-29%) [AUC: 0.722 (0.570-0.875); p = 0.006]. A mean SR value ≥ 3 at hour 23 predicted poor neurological with a sensitivity of 74% (95% CI 56-87%), a specificity of 92% (95% CI 78-98%) and FPR of 11% (95% CI 3-29%) [AUC: 0.836 (0.717-0.955); p < 0.001]. No relationship was found between mean EMG and BIS < 25 (R
2 = 0.004; p = 0.209)., Conclusion: This study found that mean BIS ≤ 25 at hour 12 and mean SR ≥ 3 at hour 23 might be used to predict poor neurological outcome in an OHCA population with a presumed cardiac cause. Since no correlation was observed between EMG and BIS < 25, our calculated BIS threshold might assist with poor outcome prognostication following OHCA.- Published
- 2018
- Full Text
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34. Influence of continuously evolving transcatheter aortic valve implantation technology on cerebral oxygenation.
- Author
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Eertmans W, Genbrugge C, Fret T, Beran M, Engelen K, Gutermann H, Vander Laenen M, Boer W, Ferdinande B, Jans F, Dens J, and De Deyne C
- Subjects
- Aged, Aged, 80 and over, Aortic Valve Stenosis physiopathology, Balloon Valvuloplasty, Cardiac Catheterization, Female, Humans, Incidence, Male, Perfusion, Retrospective Studies, Spectroscopy, Near-Infrared, Treatment Outcome, Aortic Valve surgery, Aortic Valve Stenosis surgery, Cerebrovascular Circulation, Heart Valve Prosthesis, Oxygen analysis, Transcatheter Aortic Valve Replacement methods
- Abstract
This study assessed the influence of the evolution in Transcatheter Aortic Valve Implantation technology on cerebral oxygenation. Cerebral oxygenation was measured continuously with Near-Infrared Spectroscopy and compared retrospectively between balloon-expandable, self-expandable and differential deployment valves which were implanted in 12 (34%), 17 (49%) and 6 patients (17%), respectively. Left and right SctO
2 values were averaged at four time points and used for analysis (i.e. at baseline, balloon-aortic valvuloplasty, valve deployment, and at the end of the procedure). During balloon-aortic valvuloplasty and valve deployment, cerebral oxygenation decreased in patients treated with balloon or self-expandable valves (balloon-expandable: p = 0.003 and p = 0.002; self-expandable: p < 0.001 and p = 0.003, respectively). The incidence of cerebral desaturations below 80% of baseline was significantly larger in patients treated with balloon-expandable valves (p = 0.001). In contrast, patients who received differential deployment valves never experienced a cerebral desaturation below 80% of baseline. Furthermore, both the incidence and duration below a cerebral oxygenation of 55% was significantly different between balloon and self-expandable valves (p = 0.038 and p = 0.018, respectively). This study demonstrated that Transcatheter Aortic Valve Implantation procedures are associated with significant cerebral desaturations, especially during balloon-aortic valvuloplasty and valve deployment. Moreover, our results showed that latest innovations in Transcatheter Aortic Valve Implantation technology beneficially influenced the adequacy of cerebral perfusion.- Published
- 2017
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35. The Effect of Deep Versus Moderate Neuromuscular Block on Surgical Conditions and Postoperative Respiratory Function in Bariatric Laparoscopic Surgery: A Randomized, Double Blind Clinical Trial.
- Author
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Baete S, Vercruysse G, Vander Laenen M, De Vooght P, Van Melkebeek J, Dylst D, Beran M, Van Zundert J, Heylen R, Boer W, Van Boxstael S, Fret T, Verhelst H, De Deyne C, Jans F, and Vanelderen P
- Subjects
- Adult, Double-Blind Method, Female, Humans, Intra-Abdominal Hypertension epidemiology, Intra-Abdominal Hypertension physiopathology, Male, Middle Aged, Obesity, Morbid surgery, Postoperative Period, Respiration, Artificial statistics & numerical data, Surgeons, Treatment Outcome, Bariatric Surgery methods, Laparoscopy methods, Neuromuscular Blockade methods, Respiratory Function Tests
- Abstract
Background: In recent literature, it has been suggested that deep neuromuscular block (NMB) improves surgical conditions during laparoscopy; however, the evidence supporting this statement is limited, and this was not investigated in laparoscopic bariatric surgery. Moreover, residual NMB could impair postoperative respiratory function. We tested the hypotheses that deep NMB could improve the quality of surgical conditions for laparoscopic bariatric surgery compared with moderate NMB and investigated whether deep NMB puts patients at risk for postoperative respiratory impairment compared with moderate NMB., Methods: Sixty patients were evenly randomized over a deep NMB group (rocuronium bolus and infusion maintaining a posttetanic count of 1-2) and a moderate NMB group (rocuronium bolus and top-ups maintaining a train-of-four count of 1-2). Anesthesia was induced and maintained with propofol and remifentanil. The primary outcome measures were the quality of surgical conditions assessed by a single surgeon using a 5-point rating scale (1 = extremely poor, 5 = optimal), the number of intra-abdominal pressure increases >18 cmH2O and the duration of surgery. Secondary outcome measure was the postoperative pulmonary function assessed by peak expiratory flow, forced expiratory volume in 1 second, and forced vital capacity, and by the need for postoperative respiratory support. Data are presented as mean ± standard deviation with estimated treatment effect (ETE: mean difference [95% confidence interval]) for group comparisons., Results: There was no statistically significant difference in the surgeon's rating regarding the quality of the surgical field between the deep and moderate NMB group (4.2 ± 1.0 vs 3.9 ± 1.1; P = .16, respectively; ETE: 0.4 [-0.1, 0.9]). There was no difference in the proportional rating of surgical conditions over the 5-point rating scale between both groups (P = .91). The number of intra-abdominal pressure increases >18 cmH2O and the duration of surgery were not statistically different between the deep and moderate NMB group (0.2 ± 0.9 vs 0.3 ± 1.0; P = .69; ETE: -0.1 [-0.5, 0.4] and 61.3 ± 15.1 minutes vs 70.6 ± 20.8 minutes; P = .07, ETE: -9.3 [-18.8, 0.1], respectively). All the pulmonary function tests were considerably impaired in both groups when compared with baseline (P < .001). There was no statistically significant difference in the decrease in peak expiratory flow, forced expiratory volume in 1 second, and forced vital capacity (expressed as % change from baseline) between the deep and the moderate NMB group., Conclusions: Compared with a moderate NMB, there was insufficient evidence to conclude that deep NMB improves surgical conditions during laparoscopic bariatric surgery. Postoperative pulmonary function was substantially decreased after laparoscopic bariatric surgery independently of the NMB regime that was used. The study is limited by a small sample size.
- Published
- 2017
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36. Cerebral tissue oxygen saturation values in volunteers and patients in the lateral decubitus and beach chair positions: a prospective observational study.
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Meex I, Vundelinckx J, Buyse K, Deburggraeve F, De Naeyer S, Desloovere V, Anné L, Truijen J, Vander Laenen M, Heylen R, De Deyne C, and Jans F
- Subjects
- Adult, Aged, Anesthesia, General methods, Blood Pressure physiology, Case-Control Studies, Female, Heart Rate physiology, Humans, Male, Middle Aged, Posture, Prospective Studies, Supine Position, Young Adult, Arthroscopy methods, Oxygen blood, Patient Positioning, Shoulder Joint surgery
- Abstract
Background: The objective of this study was to describe changes in cerebral tissue oxygen saturation (SctO2) due to changes in body position in healthy volunteers and in patients undergoing surgery under general anesthesia in the beach chair position (BCP) and lateral decubitus position (LDP)., Methods: In this prospective observational study, SctO2 was measured in 85 awake volunteers serially positioned every 15 min, beginning with the supine position (SP) and followed by the beach chair, supine, and lateral decubitus positions. Cerebral tissue oxygen saturation was also measured supine and in either the BCP or the LDP in 195 patients (according to surgical preference) undergoing elective arthroscopic shoulder surgery. We measured the lowest stable SctO2 values in each position as well as changes in blood pressure and heart rate., Results: In healthy volunteers, the median (interquartile range [IQR]) lowest stable SctO2 value in the SP was 69 [66-71] %. A change in position to the BCP caused a small but statistically significant decrease in the median [IQR] lowest SctO2 value to 67 [65-70] % (P = 0.028 compared with baseline). This decrease was associated with an increase in median [IQR] arterial pressure from 83 [78-88] mmHg in the SP to 85 [81-93] mmHg in the BCP (P < 0.001 compared with baseline). In patients undergoing surgery in the BCP, the median [IQR] lowest stable SctO2 value was 55 [51-59] %, which was significantly lower (P < 0.001) than the median [IQR] lowest SctO2 value in patients in the LDP (66 [62-69] %). More patients in the BCP group (57%) showed SctO2 values ≤ 55% and/or a decrease of ≥ 20% from baseline (57%) compared with the LDP group (5% and 6%, respectively; P < 0.001 for each comparison)., Conclusions: More than 55% of patients undergoing arthroscopic shoulder surgery in the BCP experience cerebral desaturation events. In volunteers without anesthesia, no desaturation events were observed. The clinical importance of these findings needs further investigation.
- Published
- 2016
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37. Late onset of Strongyloides stercoralis meningitis in a retired Belgian miner.
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Pypen Y, Oris E, Meeuwissen J, Vander Laenen M, Van Gompel F, and Coppens G
- Subjects
- Animals, Belgium, Humans, Immunocompromised Host, Male, Middle Aged, Mining, Meningitis parasitology, Strongyloides stercoralis isolation & purification, Strongyloidiasis diagnosis
- Abstract
We report a rare case of Strongyloides stercoralis meningitis in an immunocompromised patient treated for a lung carcinoma. Despite his Belgian origin, he was infected with S. stercoralis due to his former work as a miner. Although mostly prevalent in (sub)tropical areas, there are temperate regions where this nematode can occur.
- Published
- 2015
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38. Myectomy and mitral repair through the left atrium in hypertrophic obstructive cardiomyopathy: the preferred approach for contemporary surgical candidates?
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Gutermann H, Pettinari M, Van Kerrebroeck C, Vander Laenen M, Engelen K, Fret T, and Dion RA
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- Adult, Cardiomyopathy, Hypertrophic complications, Cardiomyopathy, Hypertrophic diagnosis, Cardiomyopathy, Hypertrophic mortality, Cardiomyopathy, Hypertrophic physiopathology, Echocardiography, Transesophageal, Female, Heart Atria surgery, Humans, Male, Middle Aged, Mitral Valve physiopathology, Mitral Valve Insufficiency diagnosis, Mitral Valve Insufficiency etiology, Mitral Valve Insufficiency mortality, Mitral Valve Insufficiency physiopathology, Papillary Muscles physiopathology, Patient Selection, Recovery of Function, Risk Factors, Treatment Outcome, Ventricular Outflow Obstruction diagnosis, Ventricular Outflow Obstruction etiology, Ventricular Outflow Obstruction mortality, Ventricular Outflow Obstruction physiopathology, Cardiomyopathy, Hypertrophic surgery, Mitral Valve surgery, Mitral Valve Annuloplasty adverse effects, Mitral Valve Annuloplasty mortality, Mitral Valve Insufficiency surgery, Papillary Muscles surgery, Pericardium transplantation, Ventricular Outflow Obstruction surgery
- Abstract
Objective: Patients with hypertrophic obstructive cardiomyopathy due to diffuse hypertrophy extending to or below the papillary muscles are poor candidates for alcohol septal ablation and suboptimal candidates for transaortic septal myectomy. In addition, the outflow obstruction is often aggravated by an abnormal mitral valve and subvalvular apparatus., Methods: We performed transatrial myectomy in 12 patients with diffuse hypertrophy, who were highly symptomatic despite maximal medical therapy. All had at least moderate mitral regurgitation and systolic anterior motion. The anterior mitral leaflet (AML) was detached from commissure to commissure, allowing an easy myectomy through this AML toward the base of the anterior papillary muscle, with mobility fully restored. The abnormal chordae from the septum to the anterior papillary muscle and AML were divided. The continuity of this AML was restored with augmentation using an autologous pericardial patch. The height of the posterior mitral leaflet was reduced and the repair completed using an oversized annuloplasty ring., Results: The peak intraventricular gradients decreased spectacularly from 98.8 ± 6.29 to 19.2 ± 13.4 mm Hg (P < .001), and the systolic anterior motion and mitral regurgitation disappeared. One patient died of left ventricular diastolic dysfunction. All other patients left the hospital in New York Heart Association class I or II., Conclusions: We believe that this technique is preferable for patients with hypertrophic obstructive cardiomyopathy and diffuse hypertrophy extending to the midportion of the left ventricle or beyond. It results in disappearance of outflow tract gradients and allows correction of the mitral valve abnormality., (Copyright © 2014 The American Association for Thoracic Surgery. Published by Mosby, Inc. All rights reserved.)
- Published
- 2014
- Full Text
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