44 results on '"MacCallum, G"'
Search Results
2. Studies in helminthology
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Maccallum, G A and BioStor
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- 1921
3. Notes on the genus Microcotyle. III
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Maccallum, G A and BioStor
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- 1915
4. Four species of Microcotyle, M. pyragraphorus, macroura, eueides and acanthophallus
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Maccallum, G A, Maccallum, W G, and BioStor
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- 1913
5. On the structure of Taenia gigantea (Peters)
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Maccallum, G A, Maccallum, W G, and BioStor
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- 1912
6. The family Koellikeriadae (Didymozoidae Mont.)
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Maccallum, G A, Maccallum, W G, and BioStor
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- 1916
7. Further notes on the genus Microcotyle
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Maccallum, G A and BioStor
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- 1913
8. On Aspidogaster ringens (Linton) and A. kemostoma n.sp
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Maccallum, G A, Maccallum, W G, and BioStor
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- 1913
9. Traffic related pollution and heart rate variability in a panel of elderly subjects
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Schwartz, J, Litonjua, A, Suh, H, Verrier, M, Zanobetti, A, Syring, M, Nearing, B, Verrier, R, Stone, P, MacCallum, G, Speizer, F E, and Gold, D R
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- 2005
10. Epidemic Pneumonia in Reptiles
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MacCallum, G. A.
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- 1921
11. Nematode eggs from the gill region of a shark, Carcharhinus milberti
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Maccallum, G A and BioStor
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- 1926
12. Fertilization and Egg-Laying in Microcotyle Stenotomi
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MacCallum, G. A.
- Published
- 1913
13. Field and laboratory transmission studies of haemic neoplasia in the soft-shell clam, Mya arenaria , from Atlantic Canada
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Mateo, D R, primary, MacCallum, G S, additional, and Davidson, J, additional
- Published
- 2015
- Full Text
- View/download PDF
14. Distribution of haemic neoplasia of soft-shelled clams in Prince Edward Island: an examination of anthropogenic factors and effects of experimental fungicide exposure
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Mateo, D R, primary, MacCallum, G S, additional, McGladdery, S E, additional, and Davidson, J, additional
- Published
- 2015
- Full Text
- View/download PDF
15. Field and laboratory transmission studies of haemic neoplasia in the soft-shell clam, Mya arenaria, from Atlantic Canada.
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Mateo, D R, MacCallum, G S, and Davidson, J
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CLAMS , *MYA arenaria , *FISH kills , *MYTILUS edulis , *ULVA - Abstract
A two-year laboratory and field study was initiated in 2001 in response to mass mortalities associated with haemic neoplasia ( HN) in 1999 in Prince Edward Island ( PEI) soft-shell clams, Mya arenaria. A laboratory proximity experiment (cohabitation) and an inoculation challenge were conducted with clams and mussels ( Mytilus edulis). Three field exposure experiments were also conducted, in which naive clams were held in sediment (in trays) or out of sediment (in mesh bags) at three high HN prevalence sites on PEI. There was a conversion to HN positive in clams in the proximity experiment and in clams injected with whole blood and cell-free homogenate, but not at statistically significant levels. No mussels or control clams became HN positive. There was a significant conversion to HN positive in as little as 24 and 58 days after transfer with clams held out of sediment and in sediment, respectively. The laboratory and field experiments' results suggest that HN-infected clams are spreading the disease through water from infected clams to naïve individuals and via transplantation from affected to unaffected sites. Some environmental conditions (e.g. abnormally high water temperature and hypoxia-induced sea lettuce [ Ulva lacteus] invasion) may make clams susceptible to infections or exacerbate the proliferation of HN. [ABSTRACT FROM AUTHOR]
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- 2016
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16. Distribution of haemic neoplasia of soft-shelled clams in Prince Edward Island: an examination of anthropogenic factors and effects of experimental fungicide exposure.
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Mateo, D R, MacCallum, G S, McGladdery, S E, and Davidson, J
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CLAMS , *HEMATOLOGIC malignancies , *FUNGICIDES , *ANTHROPOGENIC effects on nature , *DISEASES - Abstract
Haemic neoplasia was first considered a disease of concern for soft-shell clams in Prince Edward Island (PEI) when it was diagnosed as the cause of mass mortalities in 1999. The aetiology of the disease remains elusive, but has been associated with environmental degradation. In this study, a 2-year (2001-2002) geographic and seasonal survey was conducted for haemic neoplasia, using histology, in soft-shell clams from PEI. In addition, using geographic information system, the association between anthropogenic factors in the watersheds at sites affected by haemic neoplasia and the prevalence of the disease was investigated. Finally, histopathological changes were assessed in soft-shell clams experimentally exposed to four concentrations of chlorothalonil for 27 days. Haemic neoplasia could not be induced at any concentration of chlorothalonil. Clams exposed to a concentration of 1000 1g L_ 1 of the fungicide, however, exhibited an LC50 of 17 days. Although this information provides additional toxicity information (LC50) for soft-shell clams, further experiments are required to assess longer term exposure to the fungicide. The highest prevalences of haemic neoplasia in PEI were found in North River Correspondence D R Mateo, Department of Pathology and Microbiology, Atlantic Veterinary College, University of Prince Edward Island, 550 University Ave., Charlottetown, PE, Canada C1A 4P3 (e-mail: dmateo@upei.ca) and Miscouche (28.3-50.9% and 33.0-77.8%, respectively). No clear seasonal patterns were found. There was a correlation between haemic neoplasia prevalence and watersheds with a high percentage of potato acreage and forest coverage (P = 0.026 and P = 0.045, respectively), suggesting a link between anthropogenic activity and the prevalence of the disease. [ABSTRACT FROM AUTHOR]
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- 2016
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17. Autopsy of a Black Fish
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MacCallum, G. A.
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- 1920
18. ST-SEGMENT LEVEL ASSOCIATED WITH BLACK CARBON IN ELDERLY BOSTON RESIDENTS.
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Gold, D, primary, Litonjua, A, additional, Zanobetti, A, additional, Schwartz, J, additional, Coull, B F, additional, MacCallum, G, additional, Verrier, R, additional, Jacobson, Canner M, additional, Stone, P, additional, and Nearing, B, additional
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- 2003
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19. Subsets of ambulatory myocardial ischemia based on heart rate activity. Circadian distribution and response to anti-ischemic medication. The Angina and Silent Ischemia Study Group (ASIS)
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Andrews, T C, primary, Fenton, T, additional, Toyosaki, N, additional, Glasser, S P, additional, Young, P M, additional, MacCallum, G, additional, Gibson, R S, additional, Shook, T L, additional, and Stone, P H, additional
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- 1993
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20. Circadian variations in heart rate spectrums.
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Feldman, C.L., Hubelbank, M., Shook, T.L., Polan, B.A., MacCallum, G., and Stone, P.H.
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- 1991
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21. Glucose-6-Phosphate Dehydrogenase Deficiency in a Community with a High Incidence of the Mutant Gene.
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TODD, F. R., MACCALLUM, G. C., BISHOP, A. J., and LANGLEY, G. R.
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- 1969
22. On Some Diseases of Fishes.
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MacCallum, G. A.
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- 1915
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23. Comparison of the standard ECG with the EASIcardiogram for ischemia detection during exercise monitoring.
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Feldman, C.L., MacCallum, G., and Hartley, L.H.
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- 1997
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24. Natural history notes
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Wampler, J., Nilsson, J., Camper, J. D., Herman, J. E., Brosse, W., Stone, Z. S., Wolok, M., Whelan, C. U., Whelan, K. R. T., Clem, S., Rumbach, M., Zhou, J., Hernandez, A., Yuan, Z., Wang, K., Thompson, M. E., Donnelly, M. A., Mendoza, M. S., Blais, B., Ryan, M. J., Latella, I. M., Gustafson, G., Giermakowski, J. T., Snell, H., Mcallister, C. T., Durden, L. A., Kiryu, Y., Landsberg, J. H., Stabile, J., Cárdenas-Ortega, M. S., Herrera-Lopera, J. M., Tice, A. K., Matthew Brown, Altig, R., Carlson, B. E., Nikolakis, Z. L., Westfall, A. K., Goetz, S. M., Laurencio, D., Miller, M. A., Shahrudin, S., Wizen, G., Rueda, J. A. G., Mendoza, J. S., Tortorelli, C. M., Gannon, D. G., Stynoski, J. L., Trama, F. A., Lodge, T. M., Elliott, T. F., Henkel, T. W., Dutra-Araújo, D., Moser, C. F., Ansolch, M., Müller, J., Schünemann, H. E., Hartzell, S. M., Soe, M. M., Nwe, S. S., Platt, S. G., Rainwater, T. R., Hughes, G. N., Monck-Whipp, L., Litzgus, J. D., Henderson, R. A., Puffer, S. R., Lovich, J. E., Rautsaw, R. M., Yanick, C., Medina, S., Parkinson, C. L., Martin, S., Bolt, M. R., Campinhos, E. C., Mônico, A. T., Lauvers, W. D., Clemente-Carvalho, R. B. G., Coombs, G., Franklin, C. J., Oyervides, M. G., Keenan, S. W., Tellez, M., Hartzell, M. B., Tetzlaff, S. J., Schiltz, N. G., Diggins, C. A., Higdon, S. D., Ford, W. M., Mccoy, L., Ponder, J. R., Lasalle, M., Smith, R., Birkhead, R. D., Munscher, E., Butterfield, B. P., Cline, E. A., Dreschel, T. W., Schonhoff, B. R., Mccann, F., Escobedo-Galván, A. H., Cupul-Magaña, F. G., Goldberg, S. R., Bursey, C. R., Grismer, L. L., Nino, K. S., Dos Santos, I. Y. G. S., Dos Santos, E. M., Ljustina, O., Stroud, J. T., White, B. C., Cove, M. V., Marrero, R., Rodríguez-Cabrera, T. M., Torres, J., Paulissen, M. A., Walker, J. M., Carpenter, G. C., Fitzgerald, A. L., Kamees, L. K., Friers, J., Fitzsimons, J., Thomas, J., Dissanayake, D. S. B., Jayasinghe, H. D., Wellappuliarachchi, S., Kartje, M. E., Corneil, J. P., Montgomery, C. E., Reynoso, V. H., Ariano-Sánchez, D., Gil-Escobedo, J., Vicente, N. S., Halloy, M., Paluh, D. J., Bauer, A. M., Adams, A. A. Y., Adams, R. D., Skagen, S. K., Martin, D. J., Lambert, M. R., Goldfarb, B. A., Watkins-Colwell, G. J., Donihue, C. M., Luna-González, J. M., Solís-Rojas, C., Lazcano, D., Ellis, R., Hawkeswood, T. J., Metcalfe, D. C., Vogrinc, P. N., Mccleary, R. J. R., Benel, T. Y., Meneses-Pelayo, E., Aximoff, I., Queiroz, F., Freitas, L., Rhoads, D. D., Moldowan, P. D., Muscat, E., Entiauspe-Neto, O. M., Baptista, G. M., Gonzalez, R. C., Castro, T. M., Silva-Sorares, T., Bello-Sánchez, E. A., Vaca-León, O. I. M., Morales-Mávil, J. E., Brattstrom, B. H., Dieterich, J. K., Dieterich, R., Shipman, M. E., Benício, R. A., Christman, B. L., Barkalow, A., Jennings, R. D., Hamilton, G. L., Bain, J., Palis, J. G., Crnobrna, B., Armes, M., Williams, H. F., Prado, P. C., Koski, D. A., Koski, A. P. V., Doody, J. S., Elmore, K., Meier, A., Kain, P., Tank, C., Sharma, V., Enge, K. M., Mays, J. D., Perkins, M. W., Eason, P. K., Lee, J. L., Duarte, M. R., Fantuzzi, J. A., Jamieson, K., Pollack, K., Zarate, B., Mori, A., Jono, T., Takeuchi, H., Das, I., Donini, J. T., Ussa, M., Desantis, D. L., Mata-Silva, V., Johnson, J. D., Durso, A. M., Rosenthal, B., Lethaby, M., Gray, B. S., Suárez-Varón, G., Suárez-Rodríguez, O., Chávez-Siles, D., Pérez-Arriaga, F., Andrade-Soto, G., Aguilar-Isaac, L., Cancino-Quezadas, N., Hernández-Gallegos, O., Emmons, I. D., Nowak, E. M., Theimer, T. C., Dixon-Maccallum, G. P., Bell, K. A. H., O Connor, B. J., Forrester, A. J., and Geluso, K.
25. Comparison of fondaparinux and enoxaparin in acute coronary syndromes
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Yusuf, S., Mehta, S. R., Bassand, J. P., Budaj, A., Chrolavicius, S., Fox, K. A. A., Granger, C. B., Joyner, C., Peters, R. J. G., Wallentin, L., Avezum, A., Boden, W., Cardona, E., Ceremuzynski, L., Col, J., Commerford, P. J., Diaz, R., Faxon, D., Flather, M., Fodor, G., Franzosi, M. G., Granger, C., Halon, D., Hunt, D., Karatzas, N., Keltai, M., Kenda, M., Kim, J. H., Lanas, F., Lau, C. P., Lewis, B. S., Morais, J., Moccetti, T., Pais, P., Paolasso, E., Parkhomenko, A., Petrauskiene, B., Piegas, L., Pipilis, A., Robaayah, D., Ruda, M., Rumboldt, Z., Rupprecht, H. J., Sitkei, E., Steg, P. G., Swahn, E., Theroux, P., Valentin, V., Varigos, J., Weitz, J., White, H., Widimsky, P., Xavier, D., Zhu, J. R., Ameriso, S., Bonilla, C., Braekken, S., Chan, Y. K., Chen, W., Chenniappan, M., Cohen, E., Cottin, Y., Csiba, L., Czepiel, A., Raedt, H., Finet, G., Gardinale, E., Gaxiola, E., Gorecki, A., Gregor, P., Happola, O., Heras, M., Himbert, D., Irkin, O., Isaaz, K., Iyengar, S. S., Kalvach, P., Kevers, L., Klosiewicz-Wasek, B., Laine, M., Leys, D., Lundstrom, E., Lusic, I., Lutay, Y., Maggioni, A., Massaro, A., Mayosi, B. M., Moulin, T., Narendra, J., Naslund, U., Peeters, A., Penicka, M., Perakis, A., Petersen, P., Polic, S., Radhakrishnan, S., Renkin, J., Stockins, B., Sundararajan, R., Thygesen, K., Turazza, F., Belle, E., Vik-Mo, H., Zaborski, J., Sleight, P., Anderson, J. L., Johnstone, D. E., Hirsh, J., Demets, D., Holmes, D. R., Meeks, B., Afzal, R., Pogue, J., Boccalon, S., Chrysler, K., Cracknell, B., Horsman, C., Hoskin, T., Jedrzejowski, B., Johnson, J., Kotlan, S., Lawrence, M., Smiley, M., Stevens, C., Yallup, R., Connolly, S., Demers, C., Devereaux, P. J., Healey, J., Lonn, E., Magloire, P., Mckelvie, R., Morillo, C., Natarajan, M., Rokoss, M., Teo, K., Valettas, N., Velianou, J., Albisu, J. P., Amuchastegui, M., Bello, F. A., Bluguermann, J. J., Bono, J. O., Caccavo, A., Carlevaro, O. O., Cassettari, A., Cuneo, C., Farras, H. A., Fuselli, J., Garrido, M., Guerrero, R., Hasbani, E., Hominal, M. A., Hrabar, A., Marquez, L. L., Luciardi, H. L., Riera, L. M., Marzetti, E. M., Memoli, R., Nordaby, R., Orlandini, A. D., Perez, M., Piasentin, J. A., Ramos, H. R., Risolo, A. M., Sala, J., Salomone, O., Schygiel, P. O., Ubaldini, J., Vico, M., Amerena, J., Arnolda, L., Aroney, G., Boyd, P., Cahill, P., Chew, D., Counsell, J. T., Cross, D., Edington, J., Fitzpatrick, D., Hicks, P., Horowitz, J. D., Horrigan, M. C. G., New, G., Owensby, D., Schoeman, M., Thompson, P., Tulloch, G., Waites, J., Whelan, A., Ziffer, R., Huber, K., Jordanova, N., Al Shawafi, K., Convens, C., Coussement, P., Meester, A., El Allaf, D., Janssens, L., Marcovitch, O., Muyldermans, L., Roosen, J., Soeur, F., Lierde, J., Vrolix, M., Leaes, P., Carvalho, A. C., Schramm, E. C., Mora, R. D., Amino, J. D., Dutra, O., Manenti, E. R. F., Gun, C., Saraiva, J. F. K., Hayashi, E. K., Lichter, A., Lima, A., Marin-Neto, J. A., Teixeira, S. P. M., Abrantes, J. A. M., Baracioli, L. M., Nicolau, J. C., Maia, L. N., Jaeger, C. P., Esteves, J. P., Rabelo, A., Ramos, R. F., Reis, G., Rossi, P., Dos Santos, F. R., Teixeira, M. S., Silveira, D. S., Lemos, Mabt, Timerman, A., Greque, G. V., Vaz, R., Bhargava, R., Brons, S., Colclough, M., Constance, C., Costi, P., Dacyk, A., Davies, T., Diodati, J., Dupuis, R., Elliott, H., Fell, D. A., Fung, A. Y., Gladstone, P. J. S., Gosselin, G., Grondin, F., Huynh, T., Janzen, I., Kalaparambath, T., Kornder, J., Kouz, S., Kuritzky, R., Labelle-Stimac, S., Lamothe, M., Lauzon, C., Lemay, M., Ma, P., Maccallum, G. C., Mccallum, A., Mitchell, D., Montigny, M., Nguyen, N., Pearce, M., Pistawka, K. J., Rebane, T., Roy, M., Senaratne, M., Smith, J., Stimac, J., Traboulsi, M., Vizel, S., Weeks, A., Zadra, R., Zimmerman, R. H., Alcaino, M. E., Castro, P., Chen, J., Chen, J. L., Fan, W., Ge, J., Hu, D., Huang, J., Jingxuan, G., Ke, Y., Ma, H., Wu, Y., Yingxian, S., Yu, B., Zhu, W., Bakula, M., Bergovec, M., Lukin, A., Milicevic, G., Padovan, M., Raguz, M., Aschermann, M., Belohlavek, J., Bocek, P., Branny, M., Budesinsky, T., Groch, L., Holm, F., Jansky, P., Jelinek, P., Jirka, V., Kaislerova, M., Konecny, P., Lisa, L., Maly, M., Marcinek, G., Oscipovsky, M., Stumar, J., Vacha, M., Nielsen, T., Vigholt, E., Laanmets, P., Soopold, U., Voitk, J., Naveri, H., Niemela, M., Peuhkurinen, K., Tuomainen, P., Ylitalo, A., Py, A., Amat, G., Bessede, G., Boschat, J., Carrie, D., Charbonnier, B., Coliet, J. P., Dambrine, P., Dubois-Rande, J. L., Ferrari, E., Fouche, R., Grollier, G., Jaboureck, O., Ketelers, R., Khalife, K., Leroy, F., Lognone, T., Macquin-Mavier, I., Montalescot, G., Pacouret, G., Poulard, J. E., Puel, J., Richard, M., Schiele, F., Bischoff, K. O., Buerke, M., Buerke, U., Dominick, K., Drexler, H., Feiler, A., Guelker, H., Haltern, G., Katus, H. A., Klauss, V., Klutmann, M., Koeth, O., Meinhardt, G., Muenzel, T. M., Nitschke, T., Offterdinger, M., Rieber, J., Schieffer, B., Stangl, K., Stangl, V., Vom Dahl, J., Witzenbichler, B., Zeymer, U., Alexopoulos, D., Blassopoulou, N., Christon, A., Fotiadis, I., Foussas, S., Grapsas, N., Moschos, N., Papasteriadis, E., Symeonidis, D., Tyrologos, A., Leung, W. S., Li, S. K., Arabadzisz, H., Csikazs, J., Dancs, T., Davidovits, Z., Edes, I., Farkas, E., Herczeg, B., Janos, S., Janosi, A., Kadar, A., Kis, E., Kristof, E., Lupkovics, G., Mark, L., Nagy, A., Nagy, L., Poor, F., Regos, L., Sebo, J., Tomcsanyi, J., Toth, K., Bharani, A., Chidambaram, N., Haridas, K. K., Jain, A., Jain, P. R. K., Jaison, T. M., Kerkar, P. G., Naik, S., Nambiar, A., Panwar, R. B., Parikh, K., Puri, V. K., Rajesh, T., Ramesh, M., Singh, B., Thanikachalam, S., Tongia, R. K., Varma, S., Barbiero, M., Bardelli, G., Bernardi, D., Bolognese, L., Capponi, L., Ferrari, G., Fanelli, R., Frediani, L., Galli, M., Izzo, A., Lombardi, A., Maresta, A., Martinoni, A., Melloni, C., Meneghetti, P., Mennuni, M., Moretti, L., Orlandi, M., Pancaldi, L. G., Petronzelli, S., Piovaccari, G., Salvioni, A., Severini, D., Terrosu, P., Zanini, R., Erglis, A., Kalnins, U., Verboenko, J., Zakke, I., Kugiene, R., Zaliunas, R., Bin Othman, A., Chee, K. H., Hian, S. K., Gutierrez, A. C., Diaz, A. C., Garcia-Castillo, A., Guerrero, M. C., Morales, C. L., Ramos-Lopez, G., Baldew, S. C., Basart, D. C. G., Clappers, N., Daniels, M. C. G., Weerd, G. J., Den Hartog, F. R., Hendriks, Ihgm, Herrman, J. P. R., Kofflard, M., Krasznai, K., Michels, H. R., Stoel, I., Ten Berg, J. M., Umans, Vawn, Beek, G. J., Daele, Merm, Den Berg, B. J., Hessen, M. W. J., Kalmthout, P. M., Rossum, P., Verheugt, F. W. A., Viergever, E. P., Withagen, Ajam, Achremczyk, P., Arasimowicz, P., Baranowska, T., Biegayto, J., Bronisz, M., Buszman, P., Dalkowski, M., Dluzniewski, M., Gessek, J., Goch, J. H., Janik, K., Janion, M., Kawecki, D., Kleinrok, A., Komorowski, P., Krasowski, W., Krauze-Wielicka, M., Malinowski, S., Nowak, T., Nowakowski, P., Ogorek, M., Piepiorka, M., Pluta, W., Puzio, E., Puzniak, M., Rekosz, J., Rybka, P., Sendrowski, D., Siminiak, T., Skura, M., Stopinski, M., Szetemej, R., Szolkiewicz, M., Szpajer, M., Trusz-Gluza, M., Waszyrowski, T., Wita, K., Wodniecki, J., Wojewoda, P., Zambrzycki, J., Zielinski, Z., Cardoso, P., Carrageta, D. M., Ferreira, D., Gomes, M. V., Santos, L., Arkhipov, M., Belousov, Y., Charchoglyan, R., Gordeev, I. G., Gratsiansky, N. A., Grinshtein, Y., Khrustalev, O., Kokorin, V. A., Komarov, A., Kozulin, V., Minushkina, L. O., Panchenko, E., Panov, A., Petrik, E. S., Shakhnovich, R. M., Shalaev, S. V., Sukhinina, T. S., Trifonov, I. R., Zateyshchikov, D. A., Khoo, B. C. H., Tan, H. C., Tan, R. S., Hricak, V., Motovska, Z., Poliacik, P., Kanic, V., Kovacic, D., Kranjec, I., Voga, G., Bayat, J., Essop, M. R., Maritz, F., Marx, J. D., Ntsekhe, M., Pretorius, M. P., Ranjith, N., Theron, H., Chae, I. H., Chae, S. C., Choe, K. H., Chung, N. S., Jeong, M. H., Kim, C. J., Kim, H. S., Kim, W., Rhim, C. Y., Shin, E. K., Shin, G. J., Alameda, M., Alonso-Orcajo, N., Bethencourt, A., Calvo, F., Avellaneda, J. L. C., Delgado, V., Diaz-Castro, O., Esplugas, E., Faus, R., Antonio Fernandez-Ortiz, Frutos, A., Goirena, P., Iglesias, F. C., Llorian, A. R., Macaya, C., Mancisidor, X., Melgares, R., Pascual, C., Ruiz-Nodar, J. M., Simon, J. M., Agewall, S., Ahlstrom, P., Ali, M., Andersson, L., Bandh, S., Digerfeldt, C., Ericsson, H., Forsgren, M., Jabro, J., Janzon, M., Joborn, H., Johnston, N., Karlsson, J. E., Larsson, L. E., Linderfalk, C., Lonnberg, I., Mooe, T., Oldgren, J., Pihl, E., Risenfors, M., Sjolund, E., Soderberg, I., Stjerna, A., Svennberg, L., Wodlin, P., Pagnamenta, A., Pieper, M., Rossi, M. G., Weber, K., Peng, M. C., Cheng, J. J., Chiang, F. T., Kuo, C. T., Tseng, C. D., Andreyeshcheva, I., Dzyak, G. V., Fedtchouk, L., Gontar, A., Karpenko, O., Kononenko, L., Koval, E. A., Kovalsky, I., Kraitz, I., Netiazhenko, V., Polyvoda, S., Prokopenko, Y., Prudkiy, I., Rudenko, L., Serediuk, N., Zolotaykina, V., Adgey, J., Ahsan, A., Brack, M., Bridges, A. B., Burton, J., Findlay, I., Fluck, D. S., Radford, L., Robson, R. H., Senior, R., Starkey, I. R., Alexander, J., Baber, Z., Campbell, M., Caputo, R., Chandna, H., Chandrashekhar, Y., Chu, A., Deraad, R. E., Druken, B., Goyal, A., Holly, D., Kemp, A., Kotlaba, D., Levine, M. J., Miller, G. P., Nygaard, T., Parikh, D. K., Ramos, C., Rivera, E., Rodriguez, R., Sangani, B., Walder, J. S., and Oasis
26. Eggs of a new species of nematoid worm from a shark
- Author
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MacCallum, G. A., primary
- Published
- 1925
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27. Nematode eggs from the gill region of a shark, Carcharhinus milberti
- Author
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MacCallum, G. A., primary
- Published
- 1926
- Full Text
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28. Further notes on the genus Microcotyle
- Author
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Maccallum, G A, primary
- Published
- 1913
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29. Four new species of trematode worms of the subfamily Onchocotylinae
- Author
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MacCallum, G. A., primary
- Published
- 1931
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30. SANITATION IN ASYLUMS FOR THE INSANE WITH ESPECIAL REFERENCE TO TUBERCULOSIS
- Author
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MacCallum, G. A., primary
- Published
- 1902
- Full Text
- View/download PDF
31. Comparison of the standard ECG with the EASIcardiogram for ischemia detection during exercise monitoring
- Author
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Feldman, C.L., primary, MacCallum, G., additional, and Hartley, L.H., additional
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- View/download PDF
32. STSEGMENT LEVEL ASSOCIATED WITH BLACK CARBON IN ELDERLY BOSTON RESIDENTS
- Author
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Gold, D, Litonjua, A, Zanobetti, A, Schwartz, J, Coull, B F, MacCallum, G, Verrier, R, Jacobson, Canner M, Stone, P, and Nearing, B
- Abstract
We investigated associations between ambient pollution levels and between-session ST-segment depression in a repeated measures study on 22 older Boston residents observed up to 12 times in the summer of 1999. The protocol involved 25 minutes of continuous Holter monitoring including 5 minutes of rest, 5 minutes of standing, 5 minutes of exercise outdoors, 5 minutes of recovery and 20 cycles of slow, paced breathing. ST-segment level was averaged for each portion of the protocol. Black carbon levels ranged from 0.23 mg/m3 to 4.34, with a mean of 1.39 mg/m3. Black carbon in the 3rd to 8th hour prior to testing was associated with ST-segment depression. Mixed effects and logistic models were adjusted for the individual, time trend, and temperature. In continuous models all participants who had at least 2 observations where ST mean level was below 0 were included. Depending on the model variable numbers of participants could be included. During the recovery period after exercise, 1 mg/m3 of black carbon in the 5th hour prior to testing predicted a 0.07 mm decrement in ST-segment level. During this period, 1 mg/m3 of black carbon predicted an increased risk (OR: 5.8, 95 C.I.: 1.8–18.3) of having an absolute ST-segment level in the lowest 25th percentile of ST segment levels and an increase risk of having an absolute ST-segment level lower than-0.5 mm (OR: 4.4, 95 C.I.: 1.47–12.9). Black carbon, representing predominantly local traffic in Boston, may lead to ST-segment changes and possible ischemia. This study was funded by Program Project grant 1P01ES09825-01 Star grant number (EPA Cooperative Agreement CR81762; NIEHS Center Grant ES0639 and ES 0002)
- Published
- 2003
33. Randomized trial of a medical food for the dietary management of chronic, stable angina.
- Author
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Maxwell AJ, Zapien MP, Pearce GL, MacCallum G, Stone PH, Maxwell, Andrew J, Zapien, Michael P, Pearce, Greg L, MacCallum, Gail, and Stone, Peter H
- Abstract
Objectives: We determined the electrocardiographic, vascular and clinical effects of a medical food bar enriched with L-arginine and a combination of other nutrients known to enhance endothelium-derived nitric oxide (NO) in patients with stable angina.Background: Enhancement of vascular NO by supplementation with L-arginine and other nutrients has been shown to have clinical benefits in patients with angina secondary to atherosclerotic coronary artery disease (CAD). However, the amounts and combinations of these nutrients required to achieve a clinical effect make traditional delivery by capsules and pills less suitable than alternative delivery methods such as a specially formulated nutrition bar.Methods: Thirty-six stable outpatients with CAD and class II or III angina participated in a randomized, double-blind, placebo-controlled, crossover trial with two treatment periods each of two weeks' duration (two active bars or two placebo bars per day). Flow-mediated brachial artery dilation was measured by ultrasound. Electrocardiographic measures of ischemia, exercise capacity and angina onset time were measured by treadmill exercise testing and by Holter monitor during routine daily activities. Quality of life was assessed by SF-36 and Seattle Angina Questionnaires and by diary.Results: The medical food improved flow-mediated vasodilation (from 5.5 +/- 4.5 to 8.0 +/- 4.9, p = 0.004), treadmill exercise time (by 20% over placebo, p = 0.05) and quality-of-life scores (SF-36 summary score; 68 +/- 13 vs. 63 +/- 21 after placebo, p = 0.04, Seattle Angina Questionnaire summary score; 67 +/- 10 vs. 62 +/- 18, p = 0.04) without affecting electrocardiographic manifestations of ischemia or angina onset time.Conclusions: These findings reveal that this arginine-rich medical food, when used as an adjunct to traditional therapy, improves vascular function, exercise capacity and aspects of quality of life in patients with stable angina. [ABSTRACT FROM AUTHOR]- Published
- 2002
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34. Thoracic CTA in infants and young children: Image quality of dual-source CT (DSCT) with high-pitch spiral scan mode (turbo flash spiral mode) with or without general anesthesia with free-breathing technique.
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Tivnan P, Winant AJ, Johnston PR, Plut D, Smith K, MacCallum G, and Lee EY
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- Anesthesia, General, Child, Child, Preschool, Female, Humans, Infant, Male, Radiation Dosage, Thorax, Artifacts, Tomography, X-Ray Computed
- Abstract
Purpose: To determine whether diagnostic quality thoracic computed tomography angiography (CTA) studies can be obtained without general anesthesia (GA) in infants and young children using dual-source computed tomography (DSCT) with turbo flash spiral mode (TFSM) and free-breathing technique., Materials and Methods: All consecutive infants and young children (≤ 6 years old) who underwent thoracic CTA studies from January 2018 to October 2020 for suspected congenital thoracic disorders were categorized into two groups: with GA (Group 1) and without GA (Group 2). All thoracic CTA studies were performed on a DSCT scanner using TFSM and free-breathing technique. Two pediatric thoracic radiologists independently evaluated motion artifact in three lung zones (upper, mid, and lower). Degree of motion artifact was graded 0-3 (0, none; 1, mild; 2, moderate; and 3, severe). Logistic models adjusted for age and gender were used to compare the degree of motion artifact between lung zones. Interobserver agreement between reviewers was evaluated with kappa statistics., Results: There were a total of 73 pediatric patients (43 males (59%) and 30 females (41%); mean age, 1.4 years; range, 0-5.9 years). Among these 73 patients, 42 patients (58%) underwent thoracic CTA studies with GA (Group 1) and the remaining 31 patients (42%) underwent thoracic CTA studies without GA (Group 2). Overall, the degree of motion artifact was higher for Group 2 (without GA). However, only a very small minority (1/31, 3%) of Group 2 (without GA) thoracic CTA studies had severe motion artifact. There was no significant difference between the two groups with respect to the presence of severe motion artifact (odds ratio [OR] = 6, p = .222). When two groups were compared with respect to the presence of motion artifact for individual lung zones, motion artifact was significantly higher in the upper lung zone for Group 2 (without GA) (OR = 20, p = .043). Interobserver agreement for motion artifact was high, the average Kappa being 0.81 for Group 1 and 0.95 for Group 2., Conclusion: Although the degree of motion artifact was higher in the group without GA, only a small minority (3%) of thoracic CTA studies performed without GA had severe motion artifact, rendering the study nondiagnostic. Therefore, the results of this study support the use of thoracic CTA without GA using DSCT with TFSM and free-breathing in infants and young children. In addition, given that motion artifact was significantly higher in the upper lung zone without GA, increased stabilization in the upper chest and extremities should be considered., (© 2021 Wiley Periodicals LLC.)
- Published
- 2021
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35. Percutaneous sclerotherapy for spongiform venous malformations - analysis of patient-evaluated outcome and satisfaction.
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Clemens RK, Baumann F, Husmann M, Meier TO, Thalhammer C, MacCallum G, Amann-Vesti BR, and Alomari AI
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- Adolescent, Adult, Child, Child, Preschool, Female, Humans, Infant, Male, Recovery of Function, Retreatment, Retrospective Studies, Sclerosing Solutions adverse effects, Sclerotherapy adverse effects, Surveys and Questionnaires, Time Factors, Treatment Outcome, Vascular Malformations diagnostic imaging, Veins diagnostic imaging, Young Adult, Patient Satisfaction, Sclerosing Solutions administration & dosage, Sclerotherapy methods, Vascular Malformations therapy, Veins abnormalities
- Abstract
Background: Congenital venous malformations are frequently treated with sclerotherapy. Primary treatment goal is to control the often size-related symptoms. Functional impairment and aesthetical aspects as well as satisfaction have rarely been evaluated., Patients and Methods: Medical records of patients who underwent sclerotherapy of spongiform venous malformations were reviewed and included in this retrospective study. The outcome of sclerotherapy as self-reported by patients was assessed in a 21 item questionnaire., Results: Questionnaires were sent to 166 patients with a total of 327 procedures. Seventy-seven patients (48 %) with a total of 159 procedures (50 %) responded to the survey. Fifty-seven percent of patients were male. The age ranged from 1 to 38.1 years with a median age of 16.4 years. The lower extremities were the most common treated area. Limitations caused by the venous malformation improved in the majority of patients (e.g. pain improvement 87 %, improvement of swelling 83 %) but also worsening of symptoms occurred in a minority of cases. Seventy-seven per cent would undergo sclerotherapy again., Conclusions: Sclerotherapy for treatment of venous malformations results in significant reduction of symptoms. Multiple treatments are often needed, but patients are willing to undergo them.
- Published
- 2017
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36. Personal coronary risk profiles modify autonomic nervous system responses to air pollution.
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Chen JC, Stone PH, Verrier RL, Nearing BD, MacCallum G, Kim JY, Herrick RF, You J, Zhou H, and Christiani DC
- Subjects
- Adult, Cohort Studies, Electrocardiography, Ambulatory, Health Surveys, Humans, Male, Risk Factors, Welding, Air Pollutants, Occupational adverse effects, Autonomic Nervous System physiology, Cardiovascular Diseases, Heart Rate, Occupational Exposure adverse effects, Particulate Matter adverse effects
- Abstract
Objective: We investigated whether PM2.5-mediated autonomic modulation depends on individual coronary risk profiles., Methods: Five-minute average heart rate (HR) and heart rate variability (HRV, including standard deviation of normal-to-normal intervals [SDNN], square root of the mean squared differences of successive NN intervals [rMSSD], high frequency [HF]) were measured from 24-hour ambulatory electrocardiograms, and personal PM(2.5) exposures were monitored in a prospective study of 10 male boilermakers (aged 34.3 +/- 8.1 years). We used the Framingham score to classify individuals into low (score = 1-3) and high (score = 5-6) risk categories. Mixed-effect models were used for statistical analyses., Results: Each 1-mg/m(3) increase in the preceding 4-hour moving average PM(2.5) was associated with HR increase (5.3 beats/min) and HRV reduction (11.7%, confidence interval [CI] = 6.2-17.1% for SDNN; 11.1%, CI = 3.1-19.1% for rMSSD; 16.6%, CI = 1.5-31.7% for HF). Greater responses (2- to 4-fold differences) were observed in high-risk subjects than in low-risk subjects., Conclusions: Our study suggests that adverse autonomic responses to metal particulate are aggravated in workers with higher coronary risk profiles.
- Published
- 2006
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37. Air pollution and ST-segment depression in elderly subjects.
- Author
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Gold DR, Litonjua AA, Zanobetti A, Coull BA, Schwartz J, MacCallum G, Verrier RL, Nearing BD, Canner MJ, Suh H, and Stone PH
- Subjects
- Aged, Aged, 80 and over, Air Pollutants adverse effects, Air Pollutants analysis, Carbon analysis, Carbon Monoxide adverse effects, Carbon Monoxide analysis, Dust analysis, Environmental Monitoring, Female, Heart Rate, Humans, Male, Air Pollution adverse effects, Carbon adverse effects, Electrocardiography, Ambulatory, Exercise Test, Vehicle Emissions adverse effects
- Abstract
Increased levels of daily ambient particle pollution have been associated with increased risk of cardiovascular morbidity. Black carbon (BC) is a measure of the traffic-related component of particles. We investigated associations between ambient pollution and ST-segment levels in a repeated-measures study including 269 observations on 24 active Boston residents 61-88 years of age, each observed up to 12 times from June through September 1999. The protocol involved continuous Holter electrocardiogram monitoring including 5 min of rest, 5 min of standing, 5 min of exercise outdoors, 5 min of recovery, and 20 cycles of paced breathing. Pollution-associated ST-depression was estimated for a 10th- to 90th-percentile change in BC. We calculated the average ST-segment level, referenced to the P-R isoelectric values, for each portion of the protocol. The mean BC level in the previous 12 hr, and the BC level 5 hr before testing, predicted ST-segment depression in most portions of the protocol, but the effect was strongest in the postexercise periods. During postexercise rest, an elevated BC level was associated with -0.1 mm ST-segment depression (p = 0.02 for 12-hr mean BC; p = 0.001 for 5-hr BC) in continuous models. Elevated BC also predicted increased risk of ST-segment depression > or = 0.5 mm among those with at least one episode of that level of ST-segment depression. Carbon monoxide was not a confounder of this association. ST-segment depression, possibly representing myocardial ischemia or inflammation, is associated with increased exposure to particles whose predominant source is traffic.
- Published
- 2005
- Full Text
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38. Vascular basis for the treatment of myocardial ischemia study: trial design and baseline characteristics.
- Author
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Stone PH, Lloyd-Jones DM, Johnstone M, Carlson W, Rubenstein J, Creager M, Frei B, Sopko G, Clark ME, Maccallum G, Kinlay S, Orav J, and Selwyn AP
- Subjects
- Adult, Aged, Aged, 80 and over, Atorvastatin, Brachial Artery diagnostic imaging, Double-Blind Method, Female, Humans, Male, Middle Aged, Regional Blood Flow, Ultrasonography, Vasodilation, Anticholesteremic Agents therapeutic use, Antioxidants therapeutic use, Ascorbic Acid therapeutic use, Cholesterol, LDL blood, Heptanoic Acids therapeutic use, Myocardial Ischemia blood, Myocardial Ischemia drug therapy, Pyrroles therapeutic use, Vitamin E therapeutic use
- Abstract
Background: Increased low-density lipoprotein (LDL) and oxidized LDL cholesterol levels adversely affect endothelial function in patients with stable coronary artery disease (CAD). Statin drugs are efficacious in primary and secondary prevention of clinical CAD events, but they have not been extensively studied as a treatment for ischemia during routine daily activities or during exercise, indicators of high-risk in patients with stable CAD. The purpose of the Vascular Basis for the Treatment of Myocardial Ischemia study is to determine whether aggressive lowering of LDL cholesterol level with atorvastatin, with or without supplemental antioxidant vitamins C and E, can improve endothelial function and ischemia during ambulatory electrocardiogram (AECG) monitoring and exercise treadmill testing (ETT)., Methods: Patients are eligible when they have ischemia during an ETT and AECG monitoring and when their fasting total cholesterol level is < or =250 mg/dL. Eligible patients are randomized to receive 1 of 3 treatments: intensive atorvastatin to reduce LDL cholesterol level to < or =80 mg/dL, intensive atorvastatin to reduce LDL cholesterol level to < or =80 mg/dL plus antioxidant vitamins C and E, and control of diet and low-dose lovastatin, when needed, to reduce LDL cholesterol level < or = to 130 mg/dL. Patients undergo endothelial function testing, 48-hour AECG monitoring, and ETT at randomization and at 6 and 12 months., Results: A total of 300 patients have been randomized: 101 to receive atorvastatin alone, 103 to receive atorvastatin plus antioxidant vitamins, and 96 to receive placebo. Baseline characteristics are similar across treatment groups., Conclusions: The Vascular Basis study will provide important insight on the effects of aggressive management of dyslipidemia with statin drugs and antioxidant vitamins in patients with stable but high-risk CAD.
- Published
- 2004
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39. Need for coronary artery bypass grafting in Newfoundland and Labrador: the impact of increased demand.
- Author
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Kent GM, Power L, Gregory DM, Barrett BJ, MacCallum GC, Stone EW, and Parfrey PS
- Subjects
- Adult, Age Factors, Aged, Angina Pectoris diagnosis, Angina Pectoris physiopathology, Angina Pectoris therapy, Angioplasty, Balloon, Coronary, Cardiac Catheterization, Cohort Studies, Coronary Angiography statistics & numerical data, Coronary Artery Disease diagnosis, Coronary Artery Disease physiopathology, Exercise Test, Female, Humans, Incidence, Male, Middle Aged, Newfoundland and Labrador epidemiology, Referral and Consultation, Stroke Volume physiology, Time Factors, Coronary Artery Bypass, Coronary Artery Disease therapy, Health Services Needs and Demand
- Abstract
Background: In the past decade, growth of coronary revascularization in Canada has been substantial. It was hypothesized that as coronary angiography (CA) rates increased, referral for necessary coronary artery bypass grafting (CABG) would also increase, and include patients with multivessel disease and class I to III angina who required elective surgery. Furthermore, it was proposed that the number of CABG surgeries needed would increase at a similar rate to that of CA., Methods: An incident cohort of patients who received CA in 1998/1999 was identified, and the group referred for CABG was followed. Clinical characteristics, appropriateness and necessity scores using specific criteria, and waiting times were evaluated and compared with a similar cohort from 1994/1995. Utilization data for coronary revascularization procedures from 1994 to 2002 were reviewed., Results: Between 1994/1995 and 1998/1999, the number of CAs per year increased by 37%. The inappropriateness rate for CA was 4% in 1998/1999. The proportion of patients diagnosed with critical coronary artery disease increased from 68% in 1994/1995 to 74% in 1998/1999. The number referred for CABG increased by 48%, and the number for percutaneous transluminal coronary angioplasty (PTCA) increased by 137%. The increase in the number referred for CABG was attributable to the increase in the number of patients with less severe symptoms who required delayed elective CABG. The necessity rate for CABG in the referred group was 94% in 1994/1995 and 95% in 1998/1999. A further 91 patients were identified who needed CABG but did not receive it, 86% of whom had PTCA. From 1999 to 2002, the annual growth rate in those referred for CABG was higher than the growth rate for CA., Conclusions: With the growth in CA, the rate of discovery of high risk coronary anatomy actually increased. Growth in CABG volume was attributable to growth in the need for elective surgery in patients with class I to III angina. The rate of CABG increased disproportionately to the rate of CA, despite higher rates of PTCA with stenting. It is likely that the demand for CABG will continue to rise steadily, as expansion of angiography occurs, and may be higher than expected from the growth in CA.
- Published
- 2004
40. Protistan parasite QPX of hard-shell clam Mercenaria mercenaria is a member of Labyrinthulomycota.
- Author
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Ragan MA, MacCallum GS, Murphy CA, Cannone JJ, Gutell RR, and McGladdery SE
- Subjects
- Animals, Base Sequence, DNA, Protozoan chemistry, DNA, Protozoan isolation & purification, Electrophoresis, Agar Gel veterinary, Eukaryota chemistry, Eukaryota classification, Molecular Sequence Data, New Brunswick, Polymerase Chain Reaction veterinary, RNA, Ribosomal, 18S chemistry, Sequence Alignment, Sequence Analysis, DNA, Bivalvia parasitology, Eukaryota genetics, Phylogeny
- Abstract
Biomass of the protistan parasite QPX (quahaug parasite X) of hard-shell clam Mercenaria mercenaria was enriched from in vitro culture. The nuclear gene encoding the 18S RNA of the small-subunit ribosomal (ssu-rDNA) was recovered using the polymerase chain reaction (PCR) and sequenced. Phylogenetic analysis clearly showed that QPX is a member of phylum Labyrinthulomycota, within which it appears as a specific relative of Thraustochytrium pachydermum. These results confirm the provisional assignment of QPX to the Labyrinthulomycota made previously on the basis of morphological and ultrastructural characters found in some, but not all, geographic isolates.
- Published
- 2000
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- View/download PDF
41. Effects of therapy with nifedipine GITS or atenolol on mental stress-induced ischemic left ventricular dysfunction.
- Author
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Andrews TC, Parker JD, Jacobs S, Friedman R, Cummings N, MacCallum G, Mannting F, Tofler GH, Carlson W, Muller JE, and Stone PH
- Subjects
- Adult, Aged, Cross-Over Studies, Diastole, Double-Blind Method, Female, Humans, Male, Middle Aged, Nifedipine therapeutic use, Systole, Vasodilator Agents therapeutic use, Ventricular Dysfunction, Left physiopathology, Adrenergic beta-Antagonists therapeutic use, Atenolol therapeutic use, Myocardial Ischemia etiology, Nifedipine administration & dosage, Stress, Psychological complications, Vasodilator Agents administration & dosage, Ventricular Dysfunction, Left drug therapy, Ventricular Dysfunction, Left etiology
- Abstract
Objectives: We sought to determine the effect of nifedipine gastrointestinal therapeutic system (GITS) or atenolol on ischemic left ventricular dysfunction induced by mental stress., Background: The efficacy of conventional antianginal therapy in preventing myocardial ischemia induced by mental stress is unknown., Methods: Nifedipine GITS, atenolol and placebo were administered to 15 subjects with stable angina in a double-blind crossover trial. Subjects underwent a series of mental stressors at the end of each treatment. Radionuclide ventriculography was performed at baseline and at peak mental stress. Other measured variables included time to ischemia on exercise treadmill testing, ischemia on 48-h ambulatory electrocardiogram (ECG) monitoring, and resting and mental stress-induced levels of plasma catecholamines, tissue plasminogen activator antigen, plasminogen activator inhibitor-1 and platelet aggregability., Results: Mental stress resulted in a significant increase in plasma epinephrine and norepinephrine levels during each treatment phase. Atenolol therapy was associated with lower baseline and postmental stress rate-pressure product compared with nifedipine or placebo. Therapy with either nifedipine GITS or atenolol prevented the development of wall-motion abnormalities and the decline in regional ejection fraction (EF) in the segment with the largest deterioration in wall motion during placebo therapy. Both medications prevented the decrease in global EF in subjects who demonstrated at least a 5% fall in global EF on placebo therapy. No therapy exerted a statistically significant benefit on exercise performance or frequency of ischemia during ambulatory ECG monitoring., Conclusions: Both nifedipine GITS and atenolol are effective at preventing mental stress-induced wall-motion abnormalities, although the mechanisms may be different.
- Published
- 1998
- Full Text
- View/download PDF
42. Prognostic significance of myocardial ischemia detected by ambulatory electrocardiography, exercise treadmill testing, and electrocardiogram at rest to predict cardiac events by one year (the Asymptomatic Cardiac Ischemia Pilot [ACIP] study)
- Author
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Stone PH, Chaitman BR, Forman S, Andrews TC, Bittner V, Bourassa MG, Davies RF, Deanfield JE, Frishman W, Goldberg AD, MacCallum G, Ouyang P, Pepine CJ, Pratt CM, Sharaf B, Steingart R, Knatterud GL, Sopko G, and Conti CR
- Subjects
- Exercise Test, Female, Follow-Up Studies, Humans, Male, Middle Aged, Multivariate Analysis, Myocardial Ischemia physiopathology, Myocardial Ischemia therapy, Myocardial Revascularization, Pilot Projects, Predictive Value of Tests, Prognosis, Vasodilator Agents therapeutic use, Electrocardiography, Electrocardiography, Ambulatory methods, Myocardial Ischemia diagnosis, Rest physiology
- Abstract
Myocardial ischemia identified by ambulatory electrocardiography (AECG), exercising treadmill testing, (ETT), or 12-lead electrocardiogram at rest is associated with an adverse prognosis, but the effect of improving these ischemic manifestations by treatment on outcome is unknown. The Asymptomatic Cardiac Ischemia Pilot (ACIP) study was a National Heart, Lung, and Blood Institute funded study to determine the feasibility of conducting a large-scale prognosis study and to assess the effect of 3 treatment strategies (angina-guided strategy, AECG ischemia-guided strategy, and revascularization strategy) in reducing the manifestations of ischemia as indicated by AECG and ETT. The study cohort for this database study consisted of 496 randomized patients who performed the AECG, ETT, and 12-lead electrocardiogram at rest at both the qualifying and week 12 visits. The effect of modifying ischemia by treatment on the incidence of cardiac events (death, myocardial infarction, coronary revascularization procedure, or hospitalization for an ischemic event) at 1 year was examined. In the 2 medical treatment groups (n = 328) there was an association between the number of ambulatory electrocardiographic ischemic episodes at the qualifying visit and combined cardiac events at 1 year (p = 0.003). In the AECG ischemia-guided patients there was a trend associating greater reduction in the number of ambulatory electrocardiographic ischemia episodes with a reduced incidence of combined cardiac events (r = -0.15, p = 0.06). In the revascularization strategy patients this association was absent. In the medical treatment patients the exercise duration on the baseline ETT was inversely associated with an adverse prognosis (p = 0.02). The medical treatment strategies only slightly improved the exercise time and the exercise duration remained of prognostic significance. In the revascularization group strategy patients this association was absent. Thus, myocardial ischemia detected by AECG and an abnormal ETT are each independently associated with an adverse cardiac outcome in patients subsequently treated medically.
- Published
- 1997
- Full Text
- View/download PDF
43. Asymptomatic Cardiac Ischemia Pilot (ACIP) Study. Relationship between exercise-induced and ambulatory ischemia in patients with stable coronary disease.
- Author
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Stone PH, Chaitman BR, McMahon RP, Andrews TC, MacCallum G, Sharaf B, Frishman W, Deanfield JE, Sopko G, Pratt C, Goldberg AD, Rogers WJ, Hill J, Proschan M, Pepine CJ, Bourassa MG, and Conti CR
- Subjects
- Exercise Test, Humans, Myocardial Ischemia etiology, Pilot Projects, Time Factors, Coronary Disease physiopathology, Electrocardiography, Ambulatory, Myocardial Ischemia physiopathology, Physical Exertion
- Abstract
Background: We investigated whether the presence and frequency of asymptomatic ischemic episodes recorded during ambulatory ECG (AECG) monitoring could be predicted on the basis of clinical characteristics or exercise treadmill test (ETT) performance in patients with stable coronary disease and whether the estimate of ischemia severity was similar between the AECG and ETT., Methods and Results: Patients screened for the Asymptomatic Cardiac Ischemia Pilot (ACIP) study were selected for the current analysis if data were available from 48-hour AECG monitoring as well as from an ETT during which the patient developed > or = 1-mm ST-segment depression. Exercise ECG data were available for 143 of the 910 patients without ischemic episodes and for 659 of the 910 patients with ischemic episodes during AECG monitoring. Angina was more frequent among patients with ambulatory ischemic episodes than among patients without such ischemia (P < .001). Patients with AECG ischemia had a consistently more marked ischemic response on the ETT than patients without AECG ischemia; patients likely to have AECG ischemia could be predicted on the basis of ETT performance characteristics. However, the correlation coefficients between the severity of ischemia estimated by ETT and by AECG were small., Conclusions: There are significant relations between ischemia detected by AECG monitoring and by ETT, but the relations are limited, indicating that the two tests are not redundant to characterize coronary patients. A larger study investigating the prognostic significance of the ischemia identified by each modality, with follow-up for clinical events, will be necessary to determine the most appropriate methods to evaluate patients with stable coronary disease.
- Published
- 1996
- Full Text
- View/download PDF
44. Discordance between effects of anti-ischemic therapy on ambulatory ischemia, exercise performance and anginal symptoms in patients with stable angina pectoris. The Angina and Silent Ischemia Study Group (ASIS).
- Author
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Borzak S, Fenton T, Glasser SP, Shook TL, MacCallum G, Young PM, and Stone PH
- Subjects
- Aged, Angina Pectoris physiopathology, Diltiazem pharmacology, Diltiazem therapeutic use, Double-Blind Method, Female, Humans, Male, Middle Aged, Myocardial Ischemia physiopathology, Nifedipine pharmacology, Nifedipine therapeutic use, Predictive Value of Tests, Propranolol pharmacology, Propranolol therapeutic use, Treatment Outcome, Vasodilator Agents pharmacology, Angina Pectoris drug therapy, Electrocardiography, Ambulatory drug effects, Exercise Test drug effects, Myocardial Ischemia drug therapy, Vasodilator Agents therapeutic use
- Abstract
Objectives: We sought to define the extent to which the therapeutic efficacy of three single-drug regimens on ambulatory ischemia paralleled efficacy on other clinical manifestations of ischemia, specifically exercise test performance and anginal symptoms., Background: Some studies have shown that the presence and severity of ambulatory ischemia are predictive of anginal symptoms and exercise test performance, whereas other studies have not. Less is known about effects of antianginal treatment and whether response to therapy for one clinical manifestation reflects therapeutic responses for other clinical manifestations., Methods: We studied 50 patients in the Angina and Silent Ischemia Study who had documented coronary disease, an exercise test positive for ischemia, the presence of ambulatory and asymptomatic ischemia on ambulatory electrocardiographic (ECG) Holter monitoring and stable anginal symptoms. Patients received maximally tolerated doses of sustained release propranolol (mean 293 mg/day), sustained release diltiazem (mean 350 mg/day), nifedipine (mean 79 mg/day) and placebo, each for 2-week periods in a double-blind, crossover fashion. Patients' responses to treatment were assessed by 48-h ambulatory ECG monitoring, exercise test (standard Bruce protocol) and diaries of angina. Levels of efficacy for each agent and for each clinical measure were compared using Spearman correlation analysis., Results: With placebo there was no correlation among the frequency of ischemic episodes by ambulatory ECG monitoring, exercise time to 1.0-mm ST segment depression or frequency of anginal episodes. Furthermore, for a given patient the efficacy of each active medication in reducing ambulatory ischemia was not correlated with response in anginal symptoms or exercise test performance (r = -0.21 to 0.24, p = NS). Within each of these clinical measures, efficacy of one drug was more strongly correlated with efficacy of another drug (r = 0.64 to 0.81 for ambulatory ischemia, 0.48 to 0.56 for exercise test performance and 0.16 to 0.54 for anginal symptoms)., Conclusions: Different measures of ischemia, specifically ambulatory ischemia assessed by ambulatory ECG monitoring, exercise performance on exercise test and anginal symptoms, are independent. Efficacy for each clinical end point must be assessed separately when considering response to drug treatment.
- Published
- 1993
- Full Text
- View/download PDF
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