395 results on '"Spelman D."'
Search Results
102. Phenotypic variation of Staphylococcus epidermidis isolated from a patient with native valve endocarditis
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Deighton, M, primary, Pearson, S, additional, Capstick, J, additional, Spelman, D, additional, and Borland, R, additional
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- 1992
- Full Text
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103. Postsplenectomy infection - strategies for prevention in general practice.
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Jones P, Woolley I, Leder K, Spelman D, Cameron P, and Cheng A
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- 2010
104. Analysis of the impact of early surgery on in-hospital mortality of native valve endocarditis: use of propensity score and instrumental variable methods to adjust for treatment-selection bias.
- Author
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Lalani T, Cabell CH, Benjamin DK, Lasca O, Naber C, Fowler VG Jr, Corey GR, Chu VH, Fenely M, Pachirat O, Tan RS, Watkin R, Ionac A, Moreno A, Mestres CA, Casabé J, Chipigina N, Eisen DP, Spelman D, and Delahaye F
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- 2010
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105. Ross River virus.
- Author
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Barber B, Denholm JT, and Spelman D
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- 2009
106. Current features of infective endocarditis in elderly patients: results of the International Collaboration on Endocarditis Prospective Cohort Study.
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Durante-Mangoni E, Bradley S, Selton-Suty C, Tripodi M, Barsic B, Bouza E, Cabell CH, Ramos AIO, Fowler V Jr., Hoen B, Koneçny P, Moreno A, Murdoch D, Pappas P, Sexton DJ, Spelman D, Tattevin P, Miró JM, van der Meer JTM, and Utili R
- Published
- 2008
- Full Text
- View/download PDF
107. Nocardia Infection in Heart-Lung Transplant Recipients at Alfred Hospital, Melbourne, Australia...
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Roberts, S. A., Franklin, J. C., and Spelman, D.
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COMPLICATIONS from organ transplantation ,NOCARDIA - Abstract
Reports on Nocardia infections or nocardiosis in patients undergoing lung-heart transplantations at Alfred Hospital in Melbourne, Victoria. Factors that increase the risk of Nocardia infection in the group; Frequency of occurrence on infection; Susceptibility of all isolates to trimethoprim-sulfamethoxazole, amikacin and imipenem.
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- 2000
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- View/download PDF
108. Dosage adjustment and clinical outcomes of long-term use of high-dose tobramycin in adult cystic fibrosis patients.
- Author
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Li, Shu C., Bowes, Glenn, Ioannides-Demos, Lisa L., Spicer, W. John, Hooper, Robin E., Spelman, Denis W., Tong, Nicholas, McLean, Allan J., Li, S C, Bowes, G, Ioannides-Demos, L L, Spicer, W J, Hooper, R E, Spelman, D W, Tong, N, and McLean, A J
- Abstract
A two-phase study was undertaken designed to investigate the impact of computer-aided drug monitoring on tobramycin concentrations and clinical outcomes in adult patients with cystic fibrosis. In phase one, a baseline (historical control) study of drug use patterns was performed. During the second phase, patients admitted for intravenous treatment with tobramycin for acute exacerbations of pseudomonal pulmonary infections were randomly allocated to one of two schedules. Group A patients had tobramycin dosage regimens decided by clinicians based on pre-existing protocols using serum tobramycin assay data determined three times weekly. Group B patients had dosage regimens determined by a computerized pharmacokinetic predictive program using both population-based pharmacokinetic parameter estimation and fitting of serum concentration-time data using Bayesian regression. The agreed therapeutic target was a peak serum tobramycin concentration of 8–10 mg/L and a trough concentration of 1–2 mg/L. There was a major difference between the two groups comparing the number of paired trough and peak concentrations within the target concentration ranges (group A–14%; group B–34·7%, χ test, < 0001). Average peak tobramycin level was higher in group A patients (A = 8·2±2·2 mg/L; B = 7·5± 1·9 mg/L; < 0·005) while average trough level was higher in group B patients (A = 0·78±0·44 mg/L; B = 1·01±0·42 mg/L; < 0·05). Average dosage was higher in group B patients (A = 8·56±2·36 mg/kg/day; B = 9·56±1·83 mg/kg/day; < 0·05) and average dosing interval was shorter in group B patients (A = 8·05±1·01 h: B = 6·57±0·82 h; < 0·05). No difference in clinical outcome or mortality was observed and mean hospital stay was not different between the two groups. No case of aminoglycoside-induced nephrotoxicity or ototoxicity was observed. We conclude that the use of a computerized predictive programme can improve the control of aminoglycoside concentration-time profiles and allow targeted dosing without toxicity. The system allows for the possibility of tailoring dosage regimens aimed at optimizing efficacy and quality of life with minimal toxicity. [ABSTRACT FROM PUBLISHER]
- Published
- 1991
109. Costs associated with Needlestick iniuries
- Author
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Harrington, G.A, Russo, P.L, and Spelman, D.
- Abstract
Five different needlestick scenarios were costed to include the cost of blood collection, blood testing, consultation, follow up, vaccination and drug administration. Using the hospital protocols for the management of needlestick incidents as a guide, the final costs ranged from $116 to $1515. The calculated costs depended on several factors including the recipients vaccination status, the ability to identify the donor and the antibody status of the donor.
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- 1995
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110. Cryptosporidiosis in patients with AIDS.
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Stuart, Rhonda L., Hellard, Margaret E., Jolley, Damien, Spelman, Denis, Hoy, Jennifer, Stevenson, Elaine M., Yates, Maria T., Ryan, Norbert J., Fairley, Christopher K., Stuart, R L, Hellard, M E, Jolley, D, Spelman, D, Hoy, J, Stevenson, E M, Yates, M T, Ryan, N J, and Fairley, C K
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CRYPTOSPORIDIOSIS ,AIDS patients ,DIAGNOSIS ,DISEASE risk factors ,ANIMALS ,SEASONS ,AIDS-related opportunistic infections ,DISEASE complications - Abstract
Cases of cryptosporidiosis in patients with the acquired immunodeficiency syndrome (AIDS) residing in Melbourne over a 6-year period (1990-1995) are described. During this period 85 cases occurred, while 979 new AIDS diagnoses were notified. Over this period temporal clustering in cryptosporidial detection was evident (P=0.007), but the pattern was not statistically associated with the season, rainfall (P=0.88), mean average maximal temperature (P=0.15) or mean average minimal temperature. Further studies should identify these risk factors and provide an opportunity to prevent this devastating disease. [ABSTRACT FROM AUTHOR]
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- 1997
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111. Spleen registry may help reduce the incidence of overwhelming postsplenectomy infection in Victoria
- Author
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Denholm, J. T., Jones, P. A., Spelman, D. W., Paul Urquhart Cameron, and Woolley, I. J.
112. An analysis of factors associated with HIV-related peripheral neuropathy
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Ian John Woolley, Faragher, M. W., Ugoni, A., and Spelman, D.
113. Methicillin-resistant Staphylococcus aureus in the Australian community: An evolving epidemic
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Nimmo, G. R., Coombs, G. W., Pearson, J. C., O Brien, F. G., Christiansen, K. J., Turnidge, J. D., Gosbell, I. B., Peter Collignon, Mclaws, M. -L, Faoagali, J., George, N., Harper, J., Schooneveldt, J., Bradbury, S., Tiley, S., Gottlieb, T., Funnell, G., Fernandes, C., Benn, R., Yan, B., Ziochos, H., Vickery, A., Mitchell, D., Ryder, S., Branley, J., Spelman, D., Franklin, C., Garland, S., Gonis, G., Waters, M. J., Joyce, L., Ward, P., Andrew, J., Mcgregor, A., Peterson, R., Bell, J., Lim, I., Pratt, R., Pruul, H., Mulgrave, L., Mcgechie, D., Francis, G., Lurn, G., Paul, M., Robson, J., Lee, P. C., and Benson, S.
114. The epidemiology of candidaemia and mould infections in Australia
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Monica Slavin, Marriott, D., Gottlieb, T., Chen, S., Sorrell, T., Spelman, D., Shaw, D., Franklin, C., Rowland, K., Looke, D., Whitby, M., Nimmo, G., Cooley, L., Mayall, B., Speed, B., Sheorey, H., Joyce, L., Byrnes, G., and Ellis, D.
115. Ross river virus
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Barber, B., Justin Denholm, and Spelman, D.
116. Active surveillance for candidemia, Australia
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Chen, S., Slavin, M., Nguyen, Q., Marriott, D., Playford, E. G., Ellis, D., Tania Sorrell, Mcbride, J., Coulter, C., Mccormack, J., Walmsley, K., Looke, D., Johnson, B., Nimmo, G., Drummond, D., Forgan-Smith, R., Preston, E., Allworth, A., Faoagali, J., Gerns, N., Botes, J., Cherian, S., Robson, J., Vohra, R., Norton, R., O Kane, G., Robb, D., Gottlieb, T., Chambers, I., Dewit, D., Carroll, M., Dobson, P., Ferguson, J., Graves, S., Tierney, L., Jozwiak, F., Munro, R., Tomasotos, V., Pickles, R., Holland, J., Groenwald, F., Hale, K., Watson, M., Vaz, R., Hardiman, R., Baleriola, C., Ryan, S., Pritchard, R., Weeks, K., Benn, R., Adams, N., Lawrence, R., Taylor, P., Lindstrom, S., Harkness, J., Palasanthrian, P., Grant, R., Mcpetrie, R., Johnson, R., Halliday, C., Maszewska, K., Lee, O. C., Meyer, W., Dennis, N., Newton, P., Franklin, C., Morrisey, O., Spelman, D., Wesselingh, S., Speed, B., Hellsten, J., Mayall, B., Russell, J., Broughton, S., Woolley, I., Coloe, S., Sherman, A., Korman, T., Huysmans, M., Gordon, D., Rowlands, K., Shaw, D., Ferguson, W., Ritchie, B., Handke, R., Beaman, M., Chiam, A., Mccarthy, J., Heath, C., Altmann, S., Arthur, I., Speers, D., Cox, E., Cooley, L., Mcgregor, A., Currie, B., Lum, G., and Fisher, D.
117. Non-HACEK gram-negative bacillus endocarditis
- Author
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Morpeth, S, Murdoch, D, Cabell, Ch, Karchmer, Aw, Pappas, P, Levine, D, Nacinovich, F, Tattevin, P, Fernández Hidalgo, N, Dickerman, S, Bouza, E, del Río, A, Lejko Zupanc, T, de Oliveira Ramos, A, Iarussi, D, Klein, J, Chirouze, C, Bedimo, R, Corey, Gr, Fowler VG Jr, Collaborators: Gordon D, International Collaboration on Endocarditis Prospective Cohort Study I. n. v. e. s. t. i. g. a. t. o. r. s., Devi, U, Spelman, D, van der Meer JT, Kauffman, C, Bradley, S, Armstrong, W, Giannitsioti, E, Giamarellou, H, Lerakis, S, del Rio, A, Moreno, A, Mestres, Ca, Paré, C, Garcia de la Maria, C, De Lazzario, E, Marco, F, Gatell, Jm, Miró, Jm, Almela, M, Azqueta, M, Jiménez Expósito MJ, de Benito, N, Perez, N, Almirante, B, Fernandez Hidalgo, N, Rodriguez de Vera, P, Tornos, P, Falcó, V, Claramonte, X, Armero, Y, Sidani, N, Kanj Sharara, S, Kanafani, Z, Raglio, A, Goglio, A, Gnecchi, F, Suter, F, Valsecchi, G, Rizzi, M, Ravasio, V, Hoen, B, Leroy, J, Plesiat, P, Bernard, Y, Casey, A, Lambert, P, Watkin, R, Elliott, T, Patel, M, Dismukes, W, Pan, A, Caros, G, Tribouilloy, Ab, Goissen, T, Delahaye, A, Delahaye, F, Vandenesch, F, Vizzotti, C, Nacinovich, Fm, Marin, M, Trivi, M, Lombardero, M, Cortes, C, Horacio Casabe, J, Altclas, J, Kogan, S, Clara, L, Sanchez, M, Commerford, A, Hansa, C, Deetlefs, E, Ntsekhe, M, Commerford, P, Wray, D, Steed, Ll, Church, P, Cantey, R, Morris, A, Read, K, Raymond, N, Lang, S, Chambers, S, Kotsanas, D, Korman, Tm, Peterson, G, Purcell, J, Southern PM Jr, Shah, M, Reddy, A, Dhar, G, Hanlon Feeney, A, Hannan, M, Kelly, S, Wang, A, Woods, Cw, Sexton, Dj, Benjamin D., Jr, Mcdonald, Jr, Federspiel, J, Engemann, Jj, Reller, Lb, Drew, L, Caram, Lb, Stryjewski, M, Lalani, T, Fowler V., Jr, Chu, V, Mazaheri, B, Neuerburg, C, Naber, C, Athan, E, Henry, M, Harris, O, Alestig, E, Olaison, L, Wikstrom, L, Snygg Martin, U, Francis, J, Venugopal, K, Nair, L, Thomas, V, Chaiworramukkun, J, Pachirat, O, Chetchotisakd, P, Suwanich, T, Kamarulzaman, A, Tamin, Ss, Premru, Mm, Logar, M, Orezzi, C, Moreno, M, Rodríguez Créixems, M, Fernández, M, Muñoz, P, Fernández, R, Ramallo, V, Raoult, D, Thuny, F, Habib, G, Casalta, Jp, Fournier, Pe, Chipigina, N, Kirill, O, Vinogradova, T, Kulichenko, Vp, Butkevich, Om, Lion, C, Alla, F, Coyard, H, Doco Lecompte, T, Durante Mangoni, E, Ragone, E, Dialetto, G, Tripodi, Mf, Utili, R, Casillo, R, Kumar, As, Sharma, G, Dickerman, Sa, Street, A, Eisen, Dp, Mcbryde, Es, Grigg, L, Abrutyn, E, Michelet, C, Donnio, Py, Fortes, Cq, Edathodu, J, Al Hegelan, M, Font, B, Anguera, I, Raimon Guma, J, Cereceda, M, Oyonarte, Mj, Montagna Mella, R, Garcia, P, Braun Jones, S, de Oliveira Ramos AI, Paiva, Mg, de Medeiros RA, Woon, Ll, Lum, Ln, Tan, Rs, Rees, D, Koneçny, P, Lawrence, R, Dever, R, Post, J, Jones, P, Ryan, S, Harkness, J, Feneley, M, Rubinstein, E, Strahilewitz, J, Ionac, A, Mornos, C, Dragulescu, S, Forno, D, Cecchi, E, DE ROSA, Francesco Giuseppe, Imazio, M, Trinchero, R, Wiesbauer, F, Gattringer, R, Deans, G, Andrasevic, At, Barsic, B, Klinar, I, Vincelj, J, Bukovski, S, Krajinovic, V, Cabell, C, Stafford, J, Baloch, K, Redick, T, Harding, T, Bayer, A, Durack, Dt, Corey, R, Moreillon, P, Eykynm, S, and Chu, V.
- Subjects
Eikenella corrodens ,Microbiology ,stomatognathic system ,Haemophilus ,Gram-Negative Bacteria ,Internal Medicine ,medicine ,Endocarditis ,Humans ,Prospective Studies ,Cardiac Surgical Procedures ,Substance Abuse, Intravenous ,Cross Infection ,biology ,business.industry ,Gram Negative Bacillus ,General Medicine ,Endocarditis, Bacterial ,Prostheses and Implants ,biology.organism_classification ,medicine.disease ,Anti-Bacterial Agents ,Community-Acquired Infections ,stomatognathic diseases ,Treatment Outcome ,Infective endocarditis ,Bacteremia ,Actinobacillus ,bacteria ,Cardiobacterium hominis ,business ,Gram-Negative Bacterial Infections - Abstract
Infective endocarditis caused by non-HACEK (species other than Haemophilus species, Actinobacillus actinomycetemcomitans, Cardiobacterium hominis, Eikenella corrodens, or Kingella species) gram-negative bacilli is rare, is poorly characterized, and is commonly considered to be primarily a disease of injection drug users.To describe the clinical characteristics and outcomes of patients with non-HACEK gram-negative bacillus endocarditis in a large, international, contemporary cohort of patients.Observations from the International Collaboration on Infective Endocarditis Prospective Cohort Study (ICE-PCS) database.61 hospitals in 28 countries.Hospitalized patients with definite endocarditis.Characteristics of non-HACEK gram-negative bacillus endocarditis cases were described and compared with those due to other pathogens.Among the 2761 case-patients with definite endocarditis enrolled in ICE-PCS, 49 (1.8%) had endocarditis (20 native valve, 29 prosthetic valve or device) due to non-HACEK, gram-negative bacilli. Escherichia coli (14 patients [29%]) and Pseudomonas aeruginosa (11 patients [22%]) were the most common pathogens. Most patients (57%) with non-HACEK gram-negative bacillus endocarditis had health care-associated infection, whereas injection drug use was rare (4%). Implanted endovascular devices were frequently associated with non-HACEK gram-negative bacillus endocarditis compared with other causes of endocarditis (29% vs. 11%; P0.001). The in-hospital mortality rate of patients with endocarditis due to non-HACEK gram-negative bacilli was high (24%) despite high rates of cardiac surgery (51%).Because of the small number of patients with non-HACEK gram-negative bacillus endocarditis in each treatment group and the lack of long-term follow-up, strong treatment recommendations are difficult to make.In this large, prospective, multinational cohort, more than one half of all cases of non-HACEK gram-negative bacillus endocarditis were associated with health care contact. Non-HACEK gram-negative bacillus endocarditis is not primarily a disease of injection drug users.
118. Molecular typing of Australian Scedosporium isolates showing genetic variability and numerous S. aurantiacum
- Author
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Delhaes, L., Harun, A., Chen, S. C. A., Nguyen, Q., Slavin, M., Heath, C. H., Maszewska, K., Halliday, C., Robert, V., Sorrell, T. C., Meyer, W., Collignon, P., Benn, R., Chambers, I., Chen, S., Dennis, N., Dewit, D., Ferguson, J., Iain Gosbell, Gottlieb, T., Holland, J., Kesson, A., Lawrence, R., Marriott, D., Newton, P., Palasanthrian, P., Pickles, R., Pritchard, R., Sorrell, T., Tierney, L., Tomasotos, V., Vaz, R., Weeks, K., Allworth, A., Coulter, C., Faoagali, J., Johnson, B., Looke, D., Mccormack, J., Nimmo, G., O Kane, G., Playford, E. G., Robson, J., Ellis, D., Handke, R., Rowlands, K., Shaw, D., Cooley, L., Cox, E., Mcgregor, A., Franklin, C., Joseph, C., Korman, T., Morrissey, O., Spelman, D., Speed, B., Sheorey, H., Boan, P., Dyer, J., Heath, C., Gardam, D., Mclennan, D., Murray, R., and Pryce, T.
119. Anaerobic meningitis due to Peptostreptococcus species: Case report and review
- Author
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Tony Korman, Athan, E., and Spelman, D. W.
120. Pancreatic tuberculosis: two cases
- Author
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Jenney, A., Pickles, R., Hellard, M., Spelman, D., Fuller, A., and Spicer, W.J.
- Subjects
Pancreatic diseases -- Diagnosis ,Tuberculosis -- Diagnosis - Abstract
According to an abstract submitted by the authors to the Annual Scientific Meeting of The Australasian Society for Infectious Diseases, held May 21-24, 1995, in Darwin, Northern Territory, "Pancreatic tuberculosis [...]
- Published
- 1995
121. Men Students in "Women in Management" Courses: Learnings and Dilemmas
- Author
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Spelman, D., primary, Crary, M., additional, Weathersby, R., additional, and Bocialetti, G., additional
- Published
- 1986
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122. Correlation of serum cefotaxime levels by HPLC with serum bacteriostatic and bactericidal levels
- Author
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Spicer, W. J., primary, Franklin, J. C., additional, and Spelman, D. W., additional
- Published
- 1984
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123. Intraurethral immunoglobulin in the treatment of non-specific urethritis.
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Spelman, D W, primary and Bradford, D, additional
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- 1984
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124. Lessons From Teaching Ob in an Uncommon Setting
- Author
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Spelman, D., primary
- Published
- 1986
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125. Sialadenitis and Systemic Reaction Associated with Phenylbutazone
- Author
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Speed, B. R., primary and Spelman, D. W., additional
- Published
- 1982
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126. Intimacy or Distance? a Case On Male-Female Attraction At Work1_
- Author
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Spelman, D., primary and Crary, M., additional
- Published
- 1984
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127. CONTINUOUS PANCURONIUM INFUSION IN SEVERE TETANUS
- Author
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Newton-John H and Spelman D
- Subjects
Adult ,Tetanus ,business.industry ,General Medicine ,Middle Aged ,medicine.disease ,Anesthesia ,medicine ,Humans ,Infusions, Parenteral ,Pancuronium ,business ,Aged - Published
- 1980
128. Intraurethral immunoglobulin in the treatment of non-specific urethritis.
- Author
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Spelman, D W and Bradford, D
- Abstract
We report on a 25 year old man with agammaglobulinaemia and refractory non-specific urethritis. After seven months of unsuccessful antibiotic treatment, his symptoms responded to the administration of intraurethral immunoglobulin. [ABSTRACT FROM PUBLISHER]
- Published
- 1984
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129. Enterococcus durans vanB.
- Author
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Jenney, A., Franklin, C., Liolios, L., and Spelman, D.
- Published
- 2000
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130. Methicillin resistant Staphylococcus aureus endocarditis in an Australian tertiary hospital: 1991-2006.
- Author
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Rogers BA, Drake AK, and Spelman D
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- 2009
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131. Infective Endocarditis in Patients on Chronic Hemodialysis
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Juan M. Pericàs, Jaume Llopis, Maria Jesús Jiménez-Exposito, Wissam M. Kourany, Benito Almirante, Giampiero Carosi, Emanuele Durante-Mangoni, Claudio Querido Fortes, Efthymia Giannitsioti, Stamatios Lerakis, Rodrigo Montagna-Mella, Juan Ambrosioni, Ru-San Tan, Carlos A. Mestres, Dannah Wray, Orathai Pachirat, Asuncion Moreno, Vivian H. Chu, Elisa de Lazzari, Vance G. Fowler, Jose M. Miró, Liliana Clara, Marisa Sanchez, José Casabé, Claudia Cortes, Francisco Nacinovich, Pablo Fernandez Oses, Ricardo Ronderos, Adriana Sucari, Jorge Thierer, Javier Altclas, Silvia Kogan, Denis Spelman, Eugene Athan, Owen Harris, Karina Kennedy, Ren Tan, David Gordon, Lito Papanicolas, Tony Korman, Despina Kotsanas, Robyn Dever, Phillip Jones, Pam Konecny, Richard Lawrence, David Rees, Suzanne Ryan, Michael P. Feneley, John Harkness, Jeffrey Post, Porl Reinbott, Rainer Gattringer, Franz Wiesbauer, Adriana Ribas Andrade, Ana Cláudia Passos de Brito, Armenio Costa Guimarães, Max Grinberg, Alfredo José Mansur, Rinaldo Focaccia Siciliano, Tania Mara Varejao Strabelli, Marcelo Luiz Campos Vieira, Regina Aparecida de Medeiros Tranchesi, Marcelo Goulart Paiva, Auristela de Oliveira Ramos, Clara Weksler, Giovanna Ferraiuoli, Wilma Golebiovski, Cristiane Lamas, James A. Karlowsky, Yoav Keynan, Andrew M. Morris, Ethan Rubinstein, Sandra Braun Jones, Patricia Garcia, M. Cereceda, Alberto Fica, Rodrigo Montagna Mella, Ricardo Fernandez, Liliana Franco, Javier Gonzalez, Astrid Natalia Jaramillo, Bruno Barsic, Suzana Bukovski, Vladimir Krajinovic, Ana Pangercic, Igor Rudez, Josip Vincelj, Tomas Freiberger, Jiri Pol, Barbora Zaloudikova, Zainab Ashour, Amani El Kholy, Marwa Mishaal, Dina Osama, Hussien Rizk, Neijla Aissa, Corentine Alauzet, Francois Alla, CHU Catherine Campagnac, Thanh Doco-Lecompte, Christine Selton-Suty, Jean-Paul Casalta, Pierre-Edouard Fournier, Gilbert Habib, Didier Raoult, Franck Thuny, Francois Delahaye, Armelle Delahaye, Francois Vandenesch, Erwan Donal, Pierre Yves Donnio, Erwan Flecher, Christian Michelet, Matthieu Revest, Pierre Tattevin, Florent Chevalier, Antoine Jeu, Jean Paul Rémadi, Dan Rusinaru, Christophe Tribouilloy, Yvette Bernard, Catherine Chirouze, Bruno Hoen, Joel Leroy, Patrick Plesiat, Christoph Naber, Carl Neuerburg, Bahram Mazaheri, Carl Neuerburg Sophia Athanasia, Ioannis Deliolanis, Helen Giamarellou, Tsaganos Thomas, Elena Mylona, Olga Paniara, Konstantinos Papanicolaou, John Pyros, Athanasios Skoutelis, Konstantinos Papanikolaou, Gautam Sharma, Johnson Francis, Lathi Nair, Vinod Thomas, Krishnan Venugopal, Margaret M. Hannan, John P. Hurley, Maor Wanounou, Dan Gilon, Sarah Israel, Maya Korem, Jacob Strahilevitz, Domenico Iossa, Serena Orlando, Maria Paola Ursi, Pia Clara Pafundi, Fabiana D’Amico, Mariano Bernardo, Susanna Cuccurullo, Giovanni Dialetto, Franco Enrico Covino, Sabrina Manduca, Alessandro Della Corte, Marisa De Feo, Marie Françoise Tripodi, Enrico Cecchi, Francesco De Rosa, Davide Forno, Massimo Imazio, Rita Trinchero, Paolo Grossi, Mariangela Lattanzio, Antonio Toniolo, Antonio Goglio, Annibale Raglio, Veronica Ravasio, Marco Rizzi, Fredy Suter, Silvia Magri, Liana Signorini, Zeina Kanafani, Souha S. Kanj, Ahmad Sharif-Yakan, Imran Abidin, Syahidah Syed Tamin, Eduardo Rivera Martínez, Gabriel Israel Soto Nieto, Jan T.M. van der Meer, Stephen Chambers, David Holland, Arthur Morris, Nigel Raymond, Kerry Read, David R. Murdoch, Stefan Dragulescu, Adina Ionac, Cristian Mornos, O.M. Butkevich, Natalia Chipigina, Ozerecky Kirill, Kulichenko Vadim, Tatiana Vinogradova, Jameela Edathodu, Magid Halim, Yee-Yun Liew, Tatjana Lejko-Zupanc, Mateja Logar, Manica Mueller-Premru, Patrick Commerford, Anita Commerford, Eduan Deetlefs, Cass Hansa, Mpiko Ntsekhe, Manel Almela, Manuel Azqueta, Merce Brunet, Pedro Castro, Elisa De Lazzari, Carlos Falces, David Fuster, Guillermina Fita, Cristina Garcia- de- la- Maria, Javier Garcia-Gonzalez, Jose M. Gatell, Francesc Marco, José M. Miró, José Ortiz, Salvador Ninot, J. Carlos Paré, Juan M. Pericas, Eduard Quintana, Jose Ramirez, Irene Rovira, Elena Sandoval, Marta Sitges, Adrian Tellez, José M. Tolosana, Barbara Vidal, Jordi Vila, Ignasi Anguera, Bernat Font, Joan Raimon Guma, Javier Bermejo, Emilio Bouza, Miguel Angel Garcia Fernández, Victor Gonzalez-Ramallo, Mercedes Marín, Patricia Muñoz, Miguel Pedromingo, Jorge Roda, Marta Rodríguez-Créixems, Jorge Solis, Nuria Fernandez-Hidalgo, Pilar Tornos, Arístides de Alarcón, Ricardo Parra, Eric Alestig, Magnus Johansson, Lars Olaison, Ulrika Snygg-Martin, Pimchitra Pachirat, Burabha Pussadhamma, Vichai Senthong, Anna Casey, Tom Elliott, Peter Lambert, Richard Watkin, Christina Eyton, John L. Klein, Suzanne Bradley, Carol Kauffman, Roger Bedimo, G. Ralph Corey, Anna Lisa Crowley, Pamela Douglas, Laura Drew, Thomas Holland, Tahaniyat Lalani, Daniel Mudrick, Zaniab Samad, Daniel Sexton, Martin Stryjewski, Andrew Wang, Christopher W. Woods, Robert Cantey, Lisa Steed, Stuart A. Dickerman, Hector Bonilla, Joseph DiPersio, Sara-Jane Salstrom, John Baddley, Mukesh Patel, Gail Peterson, Amy Stancoven, Donald Levine, Jonathan Riddle, Michael Rybak, Christopher H. Cabell, Pericas, J. M., Llopis, J., Jimenez-Exposito, M. J., Kourany, W. M., Almirante, B., Carosi, G., Durante-Mangoni, E., Fortes, C. Q., Giannitsioti, E., Lerakis, S., Montagna-Mella, R., Ambrosioni, J., Tan, R. -S., Mestres, C. A., Wray, D., Pachirat, O., Moreno, A., Chu, V. H., de Lazzari, E., Fowler, V. G., Miro, J. M., Clara, L., Sanchez, M., Casabe, J., Cortes, C., Nacinovich, F., Oses, P. F., Ronderos, R., Sucari, A., Thierer, J., Altclas, J., Kogan, S., Spelman, D., Athan, E., Harris, O., Kennedy, K., Tan, R., Gordon, D., Papanicolas, L., Korman, T., Kotsanas, D., Dever, R., Jones, P., Konecny, P., Lawrence, R., Rees, D., Ryan, S., Feneley, M. P., Harkness, J., Post, J., Reinbott, P., Gattringer, R., Wiesbauer, F., Andrade, A. R., Passos de Brito, A. C., Guimaraes, A. C., Grinberg, M., Mansur, A. J., Siciliano, R. F., Varejao Strabelli, T. M., Campos Vieira, M. L., de Medeiros Tranchesi, R. A., Paiva, M. G., de Oliveira Ramos, A., Weksler, C., Ferraiuoli, G., Golebiovski, W., Lamas, C., Karlowsky, J. A., Keynan, Y., Morris, A. M., Rubinstein, E., Jones, S. B., Garcia, P., Cereceda, M., Fica, A., Mella, R. M., Fernandez, R., Franco, L., Gonzalez, J., Jaramillo, A. N., Barsic, B., Bukovski, S., Krajinovic, V., Pangercic, A., Rudez, I., Vincelj, J., Freiberger, T., Pol, J., Zaloudikova, B., Ashour, Z., El Kholy, A., Mishaal, M., Osama, D., Rizk, H., Aissa, N., Alauzet, C., Alla, F., Campagnac, C. C., Doco-Lecompte, T., Selton-Suty, C., Casalta, J. -P., Fournier, P. -E., Habib, G., Raoult, D., Thuny, F., Delahaye, F., Delahaye, A., Vandenesch, F., Donal, E., Donnio, P. Y., Flecher, E., Michelet, C., Revest, M., Tattevin, P., Chevalier, F., Jeu, A., Remadi, J. P., Rusinaru, D., Tribouilloy, C., Bernard, Y., Chirouze, C., Hoen, B., Leroy, J., Plesiat, P., Naber, C., Neuerburg, C., Mazaheri, B., Sophia Athanasia, C. N., Deliolanis, I., Giamarellou, H., Thomas, T., Mylona, E., Paniara, O., Papanicolaou, K., Pyros, J., Skoutelis, A., Papanikolaou, K., Sharma, G., Francis, J., Nair, L., Thomas, V., Venugopal, K., Hannan, M. M., Hurley, J. P., Wanounou, M., Gilon, D., Israel, S., Korem, M., Strahilevitz, J., Iossa, D., Orlando, S., Ursi, M. P., Pafundi, P. C., D'Amico, F., Bernardo, M., Cuccurullo, S., Dialetto, G., Covino, F. E., Manduca, S., Della Corte, A., De Feo, M., Tripodi, M. F., Cecchi, E., De Rosa, F., Forno, D., Imazio, M., Trinchero, R., Grossi, P., Lattanzio, M., Toniolo, A., Goglio, A., Raglio, A., Ravasio, V., Rizzi, M., Suter, F., Magri, S., Signorini, L., Kanafani, Z., Kanj, S. S., Sharif-Yakan, A., Abidin, I., Tamin, S. S., Martinez, E. R., Soto Nieto, G. I., van der Meer, J. T. M., Chambers, S., Holland, D., Morris, A., Raymond, N., Read, K., Murdoch, D. R., Dragulescu, S., Ionac, A., Mornos, C., Butkevich, O. M., Chipigina, N., Kirill, O., Vadim, K., Vinogradova, T., Edathodu, J., Halim, M., Liew, Y. -Y., Lejko-Zupanc, T., Logar, M., Mueller-Premru, M., Commerford, P., Commerford, A., Deetlefs, E., Hansa, C., Ntsekhe, M., Almela, M., Azqueta, M., Brunet, M., Castro, P., Falces, C., Fuster, D., Fita, G., Garcia- de- la- Maria, C., Garcia-Gonzalez, J., Gatell, J. M., Marco, F., Ortiz, J., Ninot, S., Pare, J. C., Quintana, E., Ramirez, J., Rovira, I., Sandoval, E., Sitges, M., Tellez, A., Tolosana, J. M., Vidal, B., Vila, J., Anguera, I., Font, B., Guma, J. R., Bermejo, J., Bouza, E., Garcia Fernandez, M. A., Gonzalez-Ramallo, V., Marin, M., Munoz, P., Pedromingo, M., Roda, J., Rodriguez-Creixems, M., Solis, J., Fernandez-Hidalgo, N., Tornos, P., de Alarcon, A., Parra, R., Alestig, E., Johansson, M., Olaison, L., Snygg-Martin, U., Pachirat, P., Pussadhamma, B., Senthong, V., Casey, A., Elliott, T., Lambert, P., Watkin, R., Eyton, C., Klein, J. L., Bradley, S., Kauffman, C., Bedimo, R., Corey, G. R., Crowley, A. L., Douglas, P., Drew, L., Holland, T., Lalani, T., Mudrick, D., Samad, Z., Sexton, D., Stryjewski, M., Wang, A., Woods, C. W., Cantey, R., Steed, L., Dickerman, S. A., Bonilla, H., Dipersio, J., Salstrom, S. -J., Baddley, J., Patel, M., Peterson, G., Stancoven, A., Levine, D., Riddle, J., Rybak, M., Cabell, C. H., Bristol-Myers Squibb Company, Vall d'Hebron University Hospital [Barcelona], Laboratoire Chrono-environnement - CNRS - UBFC (UMR 6249) (LCE), Centre National de la Recherche Scientifique (CNRS)-Université de Franche-Comté (UFC), Université Bourgogne Franche-Comté [COMUE] (UBFC)-Université Bourgogne Franche-Comté [COMUE] (UBFC), Centre Hospitalier Régional Universitaire de Besançon (CHRU Besançon), Centre recherche en CardioVasculaire et Nutrition = Center for CardioVascular and Nutrition research (C2VN), Aix Marseille Université (AMU)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE), CHU Pontchaillou [Rennes], ARN régulateurs bactériens et médecine (BRM), Université de Rennes (UR)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Structure Fédérative de Recherche en Biologie et Santé de Rennes ( Biosit : Biologie - Santé - Innovation Technologique ), and Laboratoire Chrono-environnement (UMR 6249) (LCE)
- Subjects
Male ,relapses ,medicine.medical_treatment ,infective endocarditi ,030204 cardiovascular system & hematology ,Kidney Failure ,Cohort Studies ,Catheters, Indwelling ,0302 clinical medicine ,Surgical ,Epidemiology ,cardiac surgery ,enterococci ,hemodialysis ,infective endocarditis ,Staphylococcus aureus ,Aged ,Anti-Bacterial Agents ,Arteriovenous Shunt, Surgical ,Cardiac Surgical Procedures ,Endocarditis ,Female ,Humans ,Kidney Failure, Chronic ,Methicillin-Resistant Staphylococcus aureus ,Middle Aged ,Renal Dialysis ,Staphylococcal Infections ,030212 general & internal medicine ,Chronic ,Prospective cohort study ,health care economics and organizations ,relapse ,Arteriovenous Shunt ,3. Good health ,Cardiac surgery ,[SDV.MP]Life Sciences [q-bio]/Microbiology and Parasitology ,Indwelling ,Infective endocarditis ,Hemodialysis ,Cardiology and Cardiovascular Medicine ,medicine.medical_specialty ,Catheters ,education ,03 medical and health sciences ,Internal medicine ,medicine ,business.industry ,medicine.disease ,hemodialysi ,Etiology ,Complication ,business ,[SDV.MHEP]Life Sciences [q-bio]/Human health and pathology - Abstract
International audience; Background - Infective endocarditis (IE) is a common and serious complication in patients receiving chronic hemodialysis (HD). Objectives - This study sought to investigate whether there are significant differences in complications, cardiac surgery, relapses, and mortality between IE cases in HD and non-HD patients. Methods - Prospective cohort study (International Collaboration on Endocarditis databases, encompassing 7,715 IE episodes from 2000 to 2006 and from 2008 to 2012). Descriptive analysis of baseline characteristics, epidemiological and etiological features, complications and outcomes, and their comparison between HD and non-HD patients was performed. Risk factors for major embolic events, cardiac surgery, relapses, and in-hospital and 6-month mortality were investigated in HD-patients using multivariable logistic regression. Results - A total of 6,691 patients were included and 553 (8.3%) received HD. North America had a higher HD-IE proportion than the other regions. The predominant microorganism was Staphylococcus aureus (47.8%), followed by enterococci (15.4%). Both in-hospital and 6-month mortality were significantly higher in HD versus non-HD-IE patients (30.4% vs. 17% and 39.8% vs. 20.7%, respectively; p
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- 2021
132. Candida infective endocarditis.
- Author
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Baddley, J. W., Benjamin, D. K., Patel, M., Miró, J., Athan, E., Barsic, B., Bouza, E., Clara, L., Elliott, T., Kanafani, Z., Klein, J., Lerakis, S., Levine, D., Spelman, D., Rubinstein, E., Tornos, P., Morris, A. J., Pappas, P., Fowler, V. G., and Chu, V. H.
- Subjects
- *
CANDIDA , *INFECTIVE endocarditis , *EPIDEMIOLOGY , *ANTIFUNGAL agents , *MORTALITY , *MICROBIOLOGY , *PROSTHETIC heart valves , *THERAPEUTICS - Abstract
Candida infective endocarditis (IE) is uncommon but often fatal. Most epidemiologic data are derived from small case series or case reports. This study was conducted to explore the epidemiology, treatment patterns, and outcomes of patients with Candida IE. We compared 33 Candida IE cases to 2,716 patients with non-fungal IE in the International Collaboration on Endocarditis—Prospective Cohort Study (ICE-PCS). Patients were enrolled and the data collected from June 2000 until August 2005. We noted that patients with Candida IE were more likely to have prosthetic valves ( p < 0.001), short-term indwelling catheters ( p < 0.0001), and have healthcare-associated infections ( p < 0.001). The reasons for surgery differed between the two groups: myocardial abscess (46.7% vs. 22.2%, p = 0.026) and persistent positive blood cultures (33.3% vs. 9.9%, p = 0.003) were more common among those with Candida IE. Mortality at discharge was higher in patients with Candida IE (30.3%) when compared to non-fungal cases (17%, p = 0.046). Among Candida patients, mortality was similar in patients who received combination surgical and antifungal therapy versus antifungal therapy alone (33.3% vs. 27.8%, p = 0.26). New antifungal drugs, particularly echinocandins, were used frequently. These multi-center data suggest distinct epidemiologic features of Candida IE when compared to non-fungal cases. Indications for surgical intervention are different and mortality is increased. Newer antifungal treatment options are increasingly used. Large, multi-center studies are needed to help better define Candida IE. [ABSTRACT FROM AUTHOR]
- Published
- 2008
- Full Text
- View/download PDF
133. Rate of nosocomial transmission of vancomycin-resistant enterococci from isolated patients.
- Author
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Cheng, A. C., Harrington, G., Russo, P., Liolios, L., and Spelman, D.
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- *
NOSOCOMIAL infections , *VANCOMYCIN resistance , *ENTEROCOCCUS , *INFECTIOUS disease transmission , *ISOLATION (Hospital care) - Abstract
To evaluate an isolation policy for patients colonised with vancomycin-resistant enterococci (VRE), we instituted active surveillance for transmission to uncolonised patients. Surveillance rectal swabs were taken and pulsed-field gel electrophoresis was performed on positive isolates. VRE transmission with an identical genotype occurred in 5 patients, giving a transmission rate of 3.7 per 1000 patient days, or 1 patient per ward each week. The present study provides a baseline for assessment of VRE transmission and will be useful in evaluation of the effectiveness of infection control interventions. (Intern Med J 2004; 34: 510−512) [ABSTRACT FROM AUTHOR]
- Published
- 2004
- Full Text
- View/download PDF
134. Clinical presentation, etiology, and outcome of infective endocarditis in the 21st century: the International Collaboration on Endocarditis-Prospective Cohort Study
- Author
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Murdoch , David R, Corey , G Ralph, Hoen , Bruno, Miró , José M, Fowler , Vance G, Bayer , Arnold S, Karchmer , Adolf W, Olaison , Lars, Pappas , Paul A, Moreillon , Philippe, Chambers , Stephen T, Chu , Vivian H, Falcó , Vicenç, Holland , David J, Jones , Philip, Klein , John L, Raymond , Nigel J, Read , Kerry M, Tripodi , Marie Francoise, Utili , Riccardo, Wang , Andrew, Woods , Christopher W, Cabell , Christopher H, Renseigné , Non, International Collaboration on Endocarditis-Prospective Cohort Study (ICE-PCS) Investigators, Gordon, D., Devi, U., Spelman, D., van der Meer, J.T., Kauffman, C., Bradley, S., Armstrong, W., Giannitsioti, E., Giamarellou, H., Lerakis, S., del Rio, A., Moreno, A., Mestres, C.A., Ninot, C.A., Pare, C., de la Maria, C.G., Armero, Y., de Lazzari, E., Marco, F., Gatell, J.M., Almela, M., Azqueta, M., Sitges, M., Claramonte, X., Jiménez-Expósito, M.J., de Benito, N., Ramirez, J., Perez, N., Miro, J.M., Almirante, B., Fernandez-Hidalgo, N., de Vera, P.R., Tornos, P., Falco, V., Sidani, N., Kanj-Sharara, S., Kanafani, Z., Raglio, A., Goglio, A., Gnecchi, F., Suter, F., Valsecchi, G., Rizzi, M., Ravasio, V., Hoen, B., Chirouze, C., Leroy, J., Plesiat, P., Bernard, Y., Casey, A., Lambert, P., Watkin, R., Elliott, T., Patel, M., Dismukes, W., Pan, A., Caros, G., Mathiron, A.B., Tribouilloy, C., Goissen, T., Delahaye, A., Delahaye, F., Vandenesch, F., Vizzotti, C., Nacinovich, F.M., Marin, M., Trivi, M., Lombardero, M., Cortes, C., Casabé, J.H., Altclas, J., Kogan, S., Clara, L., Sanchez, M., Commerford, A., Hansa, C., Deetlefs, E., Ntsekhe, M., Commerford, P., Wray, D., Steed, L.L., Church, P., Cantey, R., Morris, A., Holland, D.J., Murdoch, D.R., Chambers, S.T., Read, K.M., Raymond, N.J., Lang, S., Kotsanas, D., Korman, T.M., Peterson, G., Purcell, J., Southern, P.M., Shah, M., Bedimo, R., Reddy, A., Levine, D., Dhar, G., Hanlon-Feeney, A., Hannan, M., Kelly, S., Wang, A., Cabell, C.H., Woods, C.W., Sexton, D.J., Benjamin, D.J., McDonald, J.R., Federspiel, J., Engemann, J.J., Reller, B., Drew, L., Caram, L.B., Stryjewski, M., Morpeth, S., Lalani, T., Fowler, V.G., Chu, V.H., Mazaheri, B., Neuerburg, C., Naber, C., Athan, E., Henry, M., Harris, O., Alestig, E., Olaison, L., Wikstrom, L., Snygg-Martin, U., Francis, J., Venugopal, K., Nair, L., Thomas, V., Chaiworramukkun, J., Pachirat, O., Chetchotisakd, P., Suwanich, T., Kamarulzaman, A., Tamin, S.S., Premru, M.M., Logar, M., Lejko-Zupanc, T., Orezzi, C., Klein, J.L., Bouz, E., Rodríguez-Créixems, M., Marín, M., Fernández, M., Muñoz, P., Fernández, R., Ramallo, V., Raoult, D., Thuny, F., Habib, G., Casalta, J.P., Fournier, P.E., Chipigina, N., Kirill, O., Vinogradova, T., Kulichenko, V.P., Butkevich, O.M., Lion, C., Selton-Suty, C., Coyard, H., Doco-Lecompte, T., Iarussi, D., Durante-Mangoni, E., Ragone, E., Dialetto, G., Tripodi, M.F., Utili, R., Casillo, R., Kumar, A.S., Sharma, G., Dickerman, S.A., Street, A., Eisen, D.P., McBryde, E.S., Grigg, L., Abrutyn, E., Michelet, C., Tattevin, P., Donnio, P.Y., Fortes, C.Q., Edathodu, J., Al-Hegelan, M., Font, B., Anguera, I., Guma, J.R., Cereceda, M., Oyonarte, M.J., Mella, R.M., Garcia, P., Jones, S.B., Ramos, A.I., Paiva, M.G., Tranchesi, R.A., Woon, L.L., Lum, L.N., Tan, R.S., Rees, D., Kornecny, P., Lawrence, R., Dever, R., Post, J., Jones, P., Ryan, S., Harkness, J., Feneley, M., Rubinstein, E., Strahilewitz, J., Ionac, A., Mornos, C., Dragulescu, S., Forno, D., Cecchi, E., De Rosa, F., Imazio, M., Trinchero, R., Wiesbauer, F., Gattringer, R., Deans, G., Andrasevic, A.T., Barsic, B., Klinar, I., Vincelj, J., Bukovski, S., Krajinovic, V., Stafford, J., Baloch, K., Pappas, P.A., Redick, T., Harding, T., Karchmer, A.W., Bayer, A.S., Corey, R., Moreillon, P., Durack, D.T., Eykyn, S., Service des maladies infectieuses et tropicales, Centre Hospitalier Régional Universitaire [Besançon] ( CHRU Besançon ) -Hôpital Saint-Jacques, Laboratoire Chrono-environnement ( LCE ), Université Bourgogne Franche-Comté ( UBFC ) -Centre National de la Recherche Scientifique ( CNRS ) -Université de Franche-Comté ( UFC ), Centre Hospitalier Régional Universitaire de Besançon (CHRU Besançon)-Hôpital Saint-Jacques, Murdoch, D., Corey, G., Miro', J., Fowler, V. J., Bayer, A., Karchmer, A., Pappas, P., Chambers, S., Chu, V., Falco', V., Holland, D., Klein, J., Raymond, N., Read, K., Tripodi, M. F., Utili, Riccardo, Woods, C., Cabell, C., AII - Amsterdam institute for Infection and Immunity, Infectious diseases, Laboratoire Chrono-environnement - CNRS - UBFC (UMR 6249) (LCE), Centre National de la Recherche Scientifique (CNRS)-Université de Franche-Comté (UFC), and Université Bourgogne Franche-Comté [COMUE] (UBFC)-Université Bourgogne Franche-Comté [COMUE] (UBFC)
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Male ,MESH: Endocarditis ,MESH : Aged ,MESH : Prospective Studies ,030204 cardiovascular system & hematology ,endocarditi ,0302 clinical medicine ,[SDV.MHEP.MI]Life Sciences [q-bio]/Human health and pathology/Infectious diseases ,Mitral valve ,MESH: Staphylococcus aureus ,MESH : Female ,Prospective Studies ,Prospective cohort study ,Abscess ,MESH: Aged ,Adult ,Aged ,Endocarditis/microbiology ,Endocarditis/mortality ,Endocarditis/therapy ,Female ,Humans ,Middle Aged ,Staphylococcal Infections/microbiology ,Staphylococcus aureus/isolation & purification ,endocarditis ,hospital mortality ,0303 health sciences ,MESH: Middle Aged ,Endocarditis ,MESH : Staphylococcus aureus ,Staphylococcal Infections ,MESH : Adult ,MESH : Endocarditis ,3. Good health ,[ SDV.MHEP.MI ] Life Sciences [q-bio]/Human health and pathology/Infectious diseases ,medicine.anatomical_structure ,Infective endocarditis ,epidemiology ,Staphylococcus aureus ,medicine.medical_specialty ,complications ,MESH : Male ,MESH: Staphylococcal Infections ,Staphylococcal infections ,Article ,03 medical and health sciences ,Endocarditis, clinical presentattion, S. aureus ,Internal medicine ,Internal Medicine ,medicine ,MESH : Middle Aged ,staphylococci ,MESH: Humans ,030306 microbiology ,business.industry ,clinical presentattion ,MESH : Humans ,MESH: Adult ,Odds ratio ,S. aureus ,medicine.disease ,[SDV.MP.BAC]Life Sciences [q-bio]/Microbiology and Parasitology/Bacteriology ,MESH: Male ,MESH: Prospective Studies ,Surgery ,Etiology ,MESH : Staphylococcal Infections ,business ,MESH: Female - Abstract
International audience; BACKGROUND: We sought to provide a contemporary picture of the presentation, etiology, and outcome of infective endocarditis (IE) in a large patient cohort from multiple locations worldwide. METHODS: Prospective cohort study of 2781 adults with definite IE who were admitted to 58 hospitals in 25 countries from June 1, 2000, through September 1, 2005. RESULTS: The median age of the cohort was 57.9 (interquartile range, 43.2-71.8) years, and 72.1% had native valve IE. Most patients (77.0%) presented early in the disease (
- Published
- 2009
135. Candida infective endocarditis
- Author
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Pilar Tornos, Denis Spelman, Donald P. Levine, Paul A. Pappas, Tom S.J. Elliott, John L Klein, Liliana Clara, Stamatios Lerakis, José M. Miró, Emilio Bouza, John W. Baddley, Vance G. Fowler, Ethan Rubinstein, Daniel K. Benjamin, Bruno Baršić, Christopher H. Cabell, Eugene Athan, Arthur J. Morris, Mukesh Patel, Zeina A. Kanafani, Vivian H. Chu, Baddley, Jw, Benjamin DK, Jr, Patel, M, Miró, J, Athan, E, Barsic, B, Bouza, E, Clara, L, Elliott, T, Kanafani, Z, Klein, J, Lerakis, S, Levine, D, Spelman, D, Rubinstein, E, Tornos, P, Morris, Aj, Pappas, P, Fowler VG, Jr, Chu, Vh, Cabell, C, among International Collaboration on Endocarditis Prospective Cohort Study, Group, Utili, Riccardo, AII - Amsterdam institute for Infection and Immunity, Infectious diseases, Hewlett-Packard Laboratories [Bangalore], Hewlett-Packard, Institut de médecine moléculaire de Rangueil (I2MR), Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-IFR150-Institut National de la Santé et de la Recherche Médicale (INSERM), and Université Fédérale Toulouse Midi-Pyrénées
- Subjects
Male ,MESH: Endocarditis ,Antifungal Agents ,chemistry.chemical_compound ,0302 clinical medicine ,Catheters, Indwelling ,MESH: Risk Factors ,Risk Factors ,Amphotericin B ,Epidemiology ,030212 general & internal medicine ,Candida ,MESH: Aged ,0303 health sciences ,Cross Infection ,MESH: Middle Aged ,Endocarditis ,Candidiasis ,General Medicine ,Prostheses and Implants ,Middle Aged ,MESH: Candidiasis ,3. Good health ,Infectious Diseases ,Infective endocarditis ,Female ,medicine.drug ,Microbiology (medical) ,Adult ,medicine.medical_specialty ,MESH: Prostheses and Implants ,MESH: Catheters, Indwelling ,Article ,03 medical and health sciences ,MESH: Candida ,Internal medicine ,medicine ,infective endocarditis ,Candida spp ,Humans ,Mycosis ,Aged ,Voriconazole ,MESH: Humans ,030306 microbiology ,business.industry ,MESH: Cross Infection ,MESH: Adult ,MESH: Antifungal Agents ,medicine.disease ,[SDV.MP.BAC]Life Sciences [q-bio]/Microbiology and Parasitology/Bacteriology ,MESH: Male ,Surgery ,chemistry ,Caspofungin ,business ,MESH: Female ,Fluconazole - Abstract
International audience; Candida infective endocarditis (IE) is uncommon but often fatal. Most epidemiologic data are derived from small case series or case reports. This study was conducted to explore the epidemiology, treatment patterns, and outcomes of patients with Candida IE. We compared 33 Candida IE cases to 2,716 patients with non-fungal IE in the International Collaboration on Endocarditis-Prospective Cohort Study (ICE-PCS). Patients were enrolled and the data collected from June 2000 until August 2005. We noted that patients with Candida IE were more likely to have prosthetic valves (p < 0.001), short-term indwelling catheters (p < 0.0001), and have healthcare-associated infections (p < 0.001). The reasons for surgery differed between the two groups: myocardial abscess (46.7% vs. 22.2%, p = 0.026) and persistent positive blood cultures (33.3% vs. 9.9%, p = 0.003) were more common among those with Candida IE. Mortality at discharge was higher in patients with Candida IE (30.3%) when compared to non-fungal cases (17%, p = 0.046). Among Candida patients, mortality was similar in patients who received combination surgical and antifungal therapy versus antifungal therapy alone (33.3% vs. 27.8%, p = 0.26). New antifungal drugs, particularly echinocandins, were used frequently. These multi-center data suggest distinct epidemiologic features of Candida IE when compared to non-fungal cases. Indications for surgical intervention are different and mortality is increased. Newer antifungal treatment options are increasingly used. Large, multi-center studies are needed to help better define Candida IE.
- Published
- 2008
136. Impact of COVID-19 on people with non-functioning spleens in Australia.
- Author
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Barlow M, Jones P, Weerasuria M, O'Bryan J, Spelman D, and Woolley I
- Subjects
- Adult, Child, Female, Humans, Male, Middle Aged, Aged, Adolescent, Australia epidemiology, COVID-19 Vaccines, Pandemics, Spleen, COVID-19 epidemiology
- Abstract
Background: COVID-19 has had enormous impact on health and social systems, with stringent public health measures enacted across Australia. The virus itself disproportionately affects immunocompromised individuals including people without functioning spleens. We thus sought to characterise the psychological and physical impact of COVID-19 and such measures upon this oft-neglected patient group., Methods: Adults ≥ 18 years old identified from the Spleen Australia (SA) database were invited to participate in an online survey in November to December 2021 to assess the impact of the COVID-19 pandemic. Stata (v17, StataCorps, Texas, USA) was used to conduct descriptive and frequency analyses., Results: 2864 respondents were surveyed. The majority were female (1473/2838, 51.9%), Australian-born (2257/2835, 79.6%), and living in Victoria (1755/2822, 62.2%). The largest age group was 61-70 years-old (841/2858, 29.4%). Trauma was the commonest reason for asplenia (826/2724, 30.3%). Respondents reported the pandemic reduced their ability to visit a GP (753/2864, 26.3%), access food (153/2864, 5.3%), medications (179/2864, 6.3%) or spleen-specific vaccines (120/2864, 4.2%), maintain relationships (503/2864, 17.6%), or care for children (127/2864, 4.4%). 84.8% of participants reported at least one impact of COVID, including negative physical health (1463/2864, 51.1%), mental health (733/2864, 25.6%) and financial repercussions (509/2864, 17.8%). 96.9% (2743/2831) had received at least one dose of COVID-19 vaccines., Conclusions: Overall, we found detailed evidence of the negative psychological and physical impacts of the pandemic upon this cohort. We recommend that providers consider people without functioning spleens as requiring extra social and psychological support in circumstances such as the COVID-19 pandemic., Competing Interests: Declaration of Competing Interest The authors have no conflict of interest to declare., (Copyright © 2024 The Author(s). Published by Elsevier Ltd.. All rights reserved.)
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- 2024
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137. Congenital asplenia study: clinical and laboratory characterisation of adults with congenital asplenia.
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Butel-Simoes GI, Jones P, Wood EM, Spelman D, Woolley IJ, and Ojaimi S
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- Anti-Bacterial Agents therapeutic use, Humans, Syndrome, Vaccination, Splenic Diseases
- Abstract
Congenital asplenia is a rare disorder commonly associated with other visceral and cardiac congenital anomalies. Isolated congenital asplenia is even less common than syndromic forms. The risk of severe bacterial infections associated with asplenia is the most concerning clinical implication and carries a significant mortality risk. Prophylactic measures against the clinical syndrome known as overwhelming postsplenectomy infections (OPSI) include vaccination, prophylactic and emergency antibiotics and health education including fever management and travel advice. This case series describes fourteen adults with congenital asplenia and polysplenia syndrome, most of whom were diagnosed incidentally as adults, and outlines the nature of their diagnosis, clinical phenotype, family history and key pathology findings., (© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)
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- 2022
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138. Genomic characterisation of CC398 MRSA causing severe disease in Australia.
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Coombs GW, Daley D, Shoby P, Yee NWT, Robinson JO, Murray R, Korman TM, Warner MS, Papanaoum K, Derrington P, Horvath R, Jenney A, Spelman D, and Mowlaboccus S
- Subjects
- Animals, Anti-Bacterial Agents pharmacology, Anti-Bacterial Agents therapeutic use, Australia epidemiology, Genomics, Livestock, Phylogeny, Staphylococcus aureus genetics, Bacteremia drug therapy, Bacteremia epidemiology, Methicillin-Resistant Staphylococcus aureus, Staphylococcal Infections drug therapy, Staphylococcal Infections epidemiology
- Abstract
Clonal complex 398 (CC398) livestock-associated methicillin-resistant Staphylococcus aureus (LA-MRSA) has been reported worldwide in a variety of food-animal species. Although CC398 is synonymous with LA-MRSA, community-associated MRSA (CA-MRSA) variants have emerged, including the Panton-Valentine leukocidin (PVL)-positive ST398-V and ST398 single-locus variant ST1232-V, and the PVL-negative ST398-V clones. Using comparative genomic analysis, we determined whether ten CC398 MRSA bacteraemia episodes recently identified in Australia were due to LA-MRSA or CA-MRSA CC398. Isolates were sourced from the Australian Group on Antimicrobial Resistance S. aureus surveillance programme and episodes occurred across Australia. Whole-genome sequencing (WGS) and phylogenetic comparison of the ten CC398 bacteraemia isolates with previously published CC398 MRSA whole-genome sequences identified that the Australian CC398 isolates were closely related to the human-associated II-GOI clade and the livestock-associated IIa clade. The identified CC398 MRSA clones were: PVL-positive ST1232-V (5C2&5), PVL-negative community-associated ST398-V (5C2&5) and livestock-associated ST398-V (5C2&5). Our findings demonstrate the importance of using WGS and comparing the sequences with international sequences to distinguish between CC398 CA-MRSA and LA-MRSA and to determine the isolates' origin. Furthermore, our findings suggest that CC398 CA-MRSA has become established in the Australian community and that ST398-V (5C2&5) LA-MRSA is now widespread in Australian piggeries. Our study emphasises the need for national One Health antimicrobial resistance surveillance programmes to assist in monitoring the ongoing epidemiology of MRSA and other clinically significant antimicrobial-resistant organisms., (Copyright © 2022. Published by Elsevier Ltd.)
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- 2022
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139. Development and piloting of a prevention assessment and response tool for healthcare-associated Staphylococcus aureus bloodstream infection (the SAB-PART Study) using a Delphi method.
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Karanfilovska D, Cheng AC, Spelman D, and Worth LJ
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- Delivery of Health Care, Humans, Retrospective Studies, Staphylococcus aureus, Bacteremia epidemiology, Bacteremia prevention & control, Cross Infection epidemiology, Cross Infection prevention & control, Staphylococcal Infections epidemiology, Staphylococcal Infections prevention & control
- Abstract
Background: Healthcare-associated Staphylococcus aureus bloodstream infection (HA-SAB) causes preventable harm in hospitalized patients. Currently, there is no standardized method available to review HA-SAB events in order to identify and target preventable risks requiring action at an organizational level., Aim: To develop a tool to classify SAB events, and the necessary response actions, according to the degree of preventability., Methods: Following a literature review, a tool was developed. Consensus feedback and development of the tool was sought from experts (N = 11) in healthcare-associated infection surveillance using a Delphi technique. The completed tool was retrospectively applied to HA-SAB events (N = 43) that occurred at a large healthcare organization., Findings: Survey completion rates were high (91-100%). Clinicians' poor adherence to infection prevention practices and lack of engagement with feedback processes was established as the key modifiable element. A second key theme was the need for structured and detailed response actions. This feedback was incorporated into the tool and refined until consensus on all elements was achieved. Pilot application of the tool found that 56% of HA-SAB events were highly or possibly preventable; modifiable factors for HA-SAB prevention were not present in the remainder of cases., Conclusion: A prevention assessment and response tool was successfully developed via a consensus method to assist organizations in investigating and responding to individual cases of HA-SAB and identify future priority areas for SAB reduction strategies. Wider use of the tool with routine surveillance activities is required to evaluate impact upon infection prevention programmes and patient outcomes., (Copyright © 2021 The Healthcare Infection Society. Published by Elsevier Ltd. All rights reserved.)
- Published
- 2021
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140. Group A streptococcal bacteraemia at a tertiary hospital in Melbourne: concern of an under-reported risk group in Australia.
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Attwood LO and Spelman D
- Subjects
- Adolescent, Adult, Aged, Aged, 80 and over, Child, Female, Humans, Incidence, Male, Middle Aged, Pregnancy, Retrospective Studies, Streptococcus pyogenes, Tertiary Care Centers, Victoria epidemiology, Young Adult, Bacteremia diagnosis, Bacteremia epidemiology, Streptococcal Infections diagnosis, Streptococcal Infections epidemiology
- Abstract
Background: Invasive group A streptococcal (iGAS) infections are increasing worldwide with at-risk groups being children, pregnant women and the elderly. In 2017, there was a rise in iGAS cases in Victoria, prompting a Chief Health Officer advisory., Aims: To describe the characteristics of patients with GAS bacteraemia admitted to a tertiary hospital. To compare at-risk groups in our population with those identified in the Victorian Government health alert., Methods: Retrospective review of patients with GAS bacteraemia admitted between June 2014 and December 2017 at a tertiary hospital in Melbourne, Victoria., Results: Forty-three cases of GAS bacteraemia occurred. Average age was 52 years (range 15-88 years) with 63% male. Average length of stay was 14 days (range 0-72 days) and all-cause mortality occurred in two (5%) cases. Twelve (28%) patients presented with shock, 11 (26%) required intensive care unit admission and 13 (30%) surgical intervention. A history of intravenous drug use was documented in 18 (42%) cases and was commonly complicated by bone or joint involvement or thrombosis. Typing of GAS samples identified 22 different emm-types., Conclusion: GAS bacteraemia resulted in significant morbidity and prolonged hospitalisation. In contrast to the at-risk groups identified in the Victorian Government health advisory, the commonest risk group in this series were people who inject drugs and most commonly middle-aged men. Invasive GAS should be considered if a person who injects drugs presents with acute severe sepsis., (© 2020 Royal Australasian College of Physicians.)
- Published
- 2021
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141. Successful treatment of disseminated Mycobacterium simiae infection in a patient with advanced HIV.
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Ashok A, Hoy J, Spelman D, McMahon J, and Pai Mangalore R
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- HIV Infections complications, Humans, Mycobacterium Infections, Nontuberculous complications, Mycobacterium Infections, Nontuberculous drug therapy, HIV Infections microbiology, Mycobacterium, Mycobacterium Infections
- Published
- 2021
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142. Splenic autotransplantation: a systematic review.
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Surendran A, Smith M, Houli N, Usatoff V, Spelman D, and Choi J
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- Humans, Postoperative Complications epidemiology, Splenectomy, Transplantation, Autologous, Sepsis, Spleen surgery
- Abstract
Background: Splenectomy is a surgical procedure indicated in a variety of medical conditions including trauma. Post-operatively, there is a lifelong risk of developing overwhelming sepsis from encapsulated bacteria, most commonly due to Streptococcus pneumoniae. Splenic autotransplantation has been proposed as a method to recover splenic function in patients requiring splenectomy with otherwise normal spleens. This study aims to systematically review the literature to determine the efficacy of spleen autotransplantation., Methods: MEDLINE, PubMed and the Cochrane Library were searched for all studies assessing splenic autotransplantation (January 1947 to July 2018). Data were extracted on study characteristics, outcomes assessed, including spleen scintigraphy results, blood film counts and serum immunoglobulin (Ig) levels., Results: Data were obtained from 18 primary studies. All studies demonstrated return of regenerated spleen tissue in the majority of their patients (95.3%) on spleen scintigraphy. In 12 studies, 90.2% of patients had blood films return to normal following transplantation. Ig levels were shown to return to normal in all 12 studies where it was assessed. In 11 studies, 3.7% of patients had post-operative complications. In five studies, 1.3% of patients had post-operative infections in the follow-up period., Conclusion: Splenic autotransplantation is a safe procedure with minimal complications that can return splenic filtration function and Ig levels to normal ranges. It has not been confirmed whether autotransplantation provides meaningful protection against overwhelming post-splenectomy infections., (© 2019 Royal Australasian College of Surgeons.)
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- 2020
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143. Post-splenectomy sepsis: preventative strategies, challenges, and solutions.
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Luu S, Spelman D, and Woolley IJ
- Abstract
Removal of the spleen had already been established as a routine technique to treat splenic trauma and other diseases affecting the spleen before the anatomy, physiology, and function of the spleen were known in the mid-twentieth century. It is now widely accepted that the splenectomized individual is at increased risk for infection, in particular, overwhelming post-splenectomy infection (OPSI). OPSI is a syndrome of fulminant sepsis occurring in splenectomized (asplenic) or hyposplenic individuals that is associated with high mortality and morbidity. Poorly opsonized bacteria such as encapsulated bacteria, in particular, Streptococcus pneumoniae , are often implicated in sepsis. The spleen is a reticuloendothelial organ that facilitates opsonization and phagocytosis of pathogens, in addition to cellular maintenance. Splenectomy is associated with an impairment in immunoglobulin production, antibody-mediated clearance, and phagocytosis, leading to an increased risk of infection and sepsis. Early identification of the at-risk patient, early blood cultures prior to antibiotic administration, urgent blood smears and fast pathogen-detection tests, and sepsis bundles should be utilized in these patients. Prompt management and aggressive treatment can alter the course of disease in the at-risk splenectomized patient. Overwhelming post-splenectomy infection can be prevented through vaccination, chemoprophylaxis, and patient education. This article evaluates post-splenectomy sepsis by summarizing the anatomy and function of the spleen, physiological changes after splenectomy that predispose the splenectomized patient to infection, and current management and prevention strategies., Competing Interests: Dr Sarah Luu reports grants from The Royal College of Pathologists of Australasia, outside the submitted work. The authors report no other conflicts of interest in this work., (© 2019 Luu et al.)
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- 2019
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144. Mortality impact of empirical antimicrobial therapy in ESBL- and AmpC-producing Enterobacteriaceae bacteremia in an Australian tertiary hospital.
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Lim CL and Spelman D
- Subjects
- Aged, Bacteremia complications, Bacteremia microbiology, Bacteremia mortality, Drug Resistance, Bacterial, Enterobacteriaceae drug effects, Enterobacteriaceae Infections complications, Enterobacteriaceae Infections microbiology, Enterobacteriaceae Infections mortality, Female, Humans, Male, Middle Aged, Retrospective Studies, Anti-Bacterial Agents therapeutic use, Bacteremia drug therapy, Bacterial Proteins metabolism, Enterobacteriaceae metabolism, Enterobacteriaceae Infections drug therapy, beta-Lactamases metabolism
- Abstract
Background: Treatment of ESBL- and AmpC-producing Enterobacteriaceae bacteremia is often complicated by lack of appropriate antibiotics. We aimed to determine the predictors of mortality and impact of empirical antibiotics., Methods: A retrospective observational study was performed on consecutive adult cases of ESBL and AmpC bacteremia at the Alfred Hospital from 2014 through April 2018., Results: Among 110 patients with ESBL (88.2%) and AmpC (14.5%) bacteremia episodes, 96.4% had comorbidities such as hematological malignancy (30%). Approximately 45% were on immunosuppressive drugs, while 69% had recent antibiotic exposure. Over 84% of bacteremias were hospital acquired or healthcare associated. Urinary tract was the main source of infection (40%) with E. coli being the commonest organism (66.4%). The isolates were least resistant to gentamicin (21.8%), which was often appropriately used in empirical therapy. About 34% of patients presented with severe sepsis or shock. The 30-day mortality rate was 20% with no correlation with inappropriate empirical antibiotics (52%). There was no significant mortality difference between carbapenem use in empirical and definitive therapy. Respiratory source [OR 11.77, 95% CI 1.30-106.85; p = 0.03], severe sepsis or shock [OR 5.17, 95% CI 1.37-19.55; p = 0.02] and inappropriate definitive therapy [OR 27.93, 95%CI 3.69-211.35; p = 0.001] were independent predictors for mortality., Conclusion: The choice and appropriateness of empirical therapy were not associated with mortality in ESBL and AmpC bacteremia. Prudent use of carbapenem is reasonable with gentamicin as alternative. Emphasis should be on prompt resuscitation in severe sepsis and early detection of ESBL and AmpC to facilitate appropriate switch to definitive therapy., (Copyright © 2019 Australasian College for Infection Prevention and Control. Published by Elsevier B.V. All rights reserved.)
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- 2019
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145. Neurosyphilis: Concordance between cerebrospinal fluid analysis and subsequent antibiotic strategy for patients undergoing evaluation of a diagnosis of neurosyphilis.
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Smibert OC, Abbinga S, Spelman DW, and Jenney AWJ
- Subjects
- Adult, Aged, Cohort Studies, Coinfection, Female, Fluorescent Treponemal Antibody-Absorption Test, Hospitals, Humans, Male, Middle Aged, Neurosyphilis cerebrospinal fluid, Neurosyphilis complications, Neurosyphilis diet therapy, Spinal Puncture, Syphilis Serodiagnosis, Anti-Bacterial Agents therapeutic use, HIV Infections complications, Neurosyphilis diagnosis, Treponema pallidum immunology
- Abstract
Introduction: The confirmation or analysis and exclusion of a diagnosis of neurosyphilis has long presented a challenge for infectious diseases clinicians. The authors reviewed the concordance between cerebrospinal fluid (CSF) analysis and the subsequent antibiotic strategy for patients undergoing evaluation of a diagnosis of neurosyphilis., Methods: All patients with positive serum syphilis serology referred for CSF analysis between January 2009 and May 2016 were included. Indications for CSF analysis were determined by review of the hospital electronic medical records. CSF parameters were determined from the hospital pathology database. Cases were defined as either 'confirmed', 'supportive' of, or 'not supportive' of a diagnosis of neurosyphilis based on existing definitions. Subsequent therapy was defined as for neurosyphilis, late latent primary syphilis or no therapy based on existing guidelines., Results: Of 131 patients reviewed, 95.4% were male and HIV co-infected (74%). A confirmed diagnosis of neurosyphilis was met by fourteen patients (10.7%). All but two of these were treated with a neurosyphilis-directed regimen. Of the 58 patients treated with neurosyphilis antibiotics, 17.2% had no CSF findings suggestive of the diagnosis. Seventy-three patients were not treated for neurosyphilis; however 35 of these met the CSF criteria for a diagnosis supportive of neurosyphilis., Conclusions: The results of routine CSF analysis in patients with a possible diagnosis of neurosyphilis are inconsistently applied in the clinical setting, calling into question the value of routine CSF. Empirical neurosyphilis treatment should be considered up front in patients with high pre-test probability of the diagnosis., (Copyright © 2019 The Authors. Published by Elsevier Ltd.. All rights reserved.)
- Published
- 2019
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146. Nocardiosis: 7-year experience at an Australian tertiary hospital.
- Author
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Paige EK and Spelman D
- Subjects
- Adolescent, Adult, Aged, Aged, 80 and over, Australia, Female, Humans, Lung Diseases complications, Lung Diseases microbiology, Male, Middle Aged, Neoplasms complications, Neoplasms microbiology, Nocardia, Retrospective Studies, Risk Factors, Tertiary Care Centers, Young Adult, Anti-Bacterial Agents therapeutic use, Nocardia Infections drug therapy, Nocardia Infections epidemiology, Trimethoprim, Sulfamethoxazole Drug Combination therapeutic use
- Abstract
Background: Nocardiosis has historically been reported in immunocompromised patients, but Australian epidemiological and antimicrobial susceptibility data are limited., Aim: To describe the epidemiology, diagnosis and initial treatment of nocardiosis in an Australian tertiary hospital over 7 years., Methods: In this retrospective study, all positive cultures for Nocardia species from any site isolated at the Alfred Hospital, Melbourne, between 1 January 2010 and 31 December 2016 were identified, and corresponding laboratory data and medical records reviewed., Results: Sixty-eight non-duplicate isolates were identified from 67 patients. Common predisposing factors were chronic lung disease (38/67; 57%), organ, particularly lung, transplantation (13/67; 19%) and solid organ malignancy (6/67; 9%); 12% (8/67) of patients had no identifiable systemic risk factors. Seventy-nine percent (53/67) of patients had pulmonary nocardiosis only. Nocardia nova was the most commonly isolated species (20/68; 29%). In 48% (32/67) of patients, Nocardia species were isolated only on specific mycobacterial media. All tested species were susceptible to sulfamethoxazole-trimethoprim and amikacin, with the majority (58/63; 92%) susceptible to imipenem. All-cause mortality rates at 6 and 12 months where data were available were 15% (10/66 patients) and 22% (14/64 patients) respectively., Conclusion: In the largest Australian series in 25 years, nocardiosis predominantly affected patients with chronic lung disease or impaired cell-mediated immunity. A significant proportion of organisms from pulmonary sites were isolated on mycobacterial culture media only, suggesting that its use may improve yield. Isolates remain highly susceptible to sulfamethoxazole-trimethoprim, amikacin and imipenem, while other agents should be used only after confirmation of in vitro susceptibility., (© 2018 Royal Australasian College of Physicians.)
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- 2019
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147. Mathematical modelling of vancomycin-resistant enterococci transmission during passive surveillance and active surveillance with contact isolation highlights the need to identify and address the source of acquisition.
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Cheah ALY, Cheng AC, Spelman D, Nation RL, Kong DCM, and McBryde ES
- Subjects
- Bayes Theorem, Gram-Positive Bacterial Infections epidemiology, Gram-Positive Bacterial Infections microbiology, Humans, Markov Chains, Vancomycin-Resistant Enterococci pathogenicity, Gram-Positive Bacterial Infections transmission, Models, Theoretical, Vancomycin-Resistant Enterococci isolation & purification
- Abstract
Background: Clinical studies and mathematical simulation suggest that active surveillance with contact isolation is associated with reduced vancomycin-resistant enterococci (VRE) prevalence compared to passive surveillance. Models using pre- and post-intervention data that account for the imperfect observation and serial dependence of VRE transmission events can better estimate the effectiveness of active surveillance and subsequent contact isolation; however, such analyses have not been performed., Methods: A mathematical model was fitted to surveillance data collected pre- and post-implementation of active surveillance with contact isolation in the haematology-oncology ward. We developed a Hidden Markov Model to describe undetected and observed VRE colonisation/infection status based on the detection activities in the ward. Bayesian inference was used to estimate transmission rates. The effectiveness of active surveillance was assumed to be via increased detection and subsequent contact isolation of VRE positive patients., Results: We estimated that 31% (95% credible interval: 0.33-85%) of the VRE transmissions were due to cross-transmission between patients. The ratio of transmission rates from patients with contact isolation versus those without contact isolation was 0.33 (95% credible interval: 0.050-1.22)., Conclusions: The majority of the VRE acquisitions in the haematology-oncology ward was estimated to be due to background rates of VRE, rather than within ward patient to patient acquisition. The credible interval for cross-transmission was wide which results in a large degree of uncertainty in the estimates. Factors that could account for background VRE acquisition include endogenous acquisition from antibiotic selection pressure and VRE in the environment. Contact isolation was not significantly associated with reduced VRE transmission in settings where the majority of VRE acquisition was due to background acquisition, emphasising the need to identify and address the source of acquisition. As the credible interval for the ratio of VRE transmission in contact isolated versus non-contact isolated patients crossed 1, there is a probability that the transmission rate in contact isolation was not lower. Our finding highlights the need to optimise infection control measures other than active surveillance for VRE and subsequent contact isolation to reduce VRE transmission. Such measures could include antimicrobial stewardship, environmental cleaning, and hand hygiene.
- Published
- 2018
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148. Initial modelling and updates on cost effectiveness from the first 10 years of a spleen registry.
- Author
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Luu S, Jones P, Woolley I, Spelman D, and Gold L
- Subjects
- Australia, Humans, Cost-Benefit Analysis, Registries, Spleen
- Abstract
Objective: To validate our estimates from our original model and re-evaluate the cost-effectiveness of Spleen Australia, the Australian post-splenectomy registry, using our original model with updated model parameters based on advances in the literature and experience of the registry over the past decade., Methods: We revisited a decision model from 2005, comparing 1,000 hypothetical registered patients with asplenia or hyposplenism against 1,000 who were not registered, and updated the model parameters. The cost-effectiveness of the registry was evaluated from a healthcare perspective in terms of additional cost per case of overwhelming post-splenectomy infection (OPSI) avoided and as additional cost per life year gained., Results: Over a cohort lifetime the registry was associated with an additional cost of $125,724 per case of OPSI avoided or $19,286 per life year gained., Conclusions: Despite our initial over-estimation of immunisation and chemoprophylaxis uptake and increases in unit costs, our re-evaluation confirmed use of the registry to be cost-effective. Implications for public health: Improved outcomes for patients with asplenia or hyposplenism can be achieved by a cost-effective registry. Additional research into effectiveness of interventions, OPSI prevalence associated with varying intervention use, and compliance rates over time after registration would provide improved accuracy of cost-effectiveness estimates., (© 2018 The Authors.)
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- 2018
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149. A Registry for Patients With Asplenia/Hyposplenism Reduces the Risk of Infections With Encapsulated Organisms.
- Author
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Arnott A, Jones P, Franklin LJ, Spelman D, Leder K, and Cheng AC
- Subjects
- Adult, Female, Haemophilus Infections prevention & control, Haemophilus influenzae type b, Humans, Incidence, Male, Meningococcal Infections prevention & control, Middle Aged, Neisseria meningitidis, Pneumococcal Infections prevention & control, Postoperative Complications, Retrospective Studies, Risk Factors, Spleen microbiology, Streptococcus pneumoniae, Victoria, Young Adult, Bacterial Infections prevention & control, Registries, Spleen abnormalities, Splenectomy adverse effects
- Abstract
Background: Overwhelming post-splenectomy infection (OPSI) is a serious complication of asplenia. Clinical guidelines recommend numerous measures to reduce the risk of OPSI, but awareness and adherence to preventative measures are generally poor. We aimed to determine whether a registry for asplenic/hyposplenic patients was associated with a reduction in the incidence of infection with encapsulated bacteria., Methods: We performed a retrospective cohort study of asplenic/hyposplenic patients in the state of Victoria, Australia, who registered with Spleen Australia from 2003 through 2014. Spleen Australia provides education, clinical guidance, and annual vaccination reminders to registrants and their healthcare providers. We compared the incidence of infection with Streptococcus pneumoniae, Haemophilus influenzae type B (Hib), and Neisseria meningitidis before and after registration. Registry data were linked with Victorian notifiable disease data on invasive pneumococcal disease (IPD), invasive meningococcal disease (IMD), and Hib between 2000 and 2014., Results: Twenty-seven cases of IPD and 1 of IMD occurred among 3221 registrants. No cases of Hib were reported. The rate of IPD/IMD was 150 per 100000 patient-years prior to registration and 36 per 100000 patient-years after registration; registration was associated with a 69% reduction in the risk of infection (incidence rate ratio, 0.31; 95% confidence interval, 0.12 to 0.83; P = .019). Based on the absolute reduction in incidence, we estimate that Spleen Australia prevents 5-6 invasive infections with encapsulated organisms annually among registrants., Conclusions: Systematic, long-term approaches to post-splenectomy care can significantly reduce the risk of infection with encapsulated organisms among individuals with asplenia/hyposplenism.
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- 2018
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150. Mobile phones and computer keyboards: unlikely reservoirs of multidrug-resistant organisms in the tertiary intensive care unit.
- Author
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Smibert OC, Aung AK, Woolnough E, Carter GP, Schultz MB, Howden BP, Seemann T, Spelman D, McGloughlin S, and Peleg AY
- Subjects
- Cross Infection epidemiology, Disease Transmission, Infectious, Genotype, Gram-Negative Bacteria classification, Gram-Negative Bacteria genetics, Humans, Intensive Care Units, Methicillin-Resistant Staphylococcus aureus classification, Methicillin-Resistant Staphylococcus aureus genetics, Molecular Epidemiology, Polymorphism, Single Nucleotide, Tertiary Care Centers, Vancomycin-Resistant Enterococci classification, Vancomycin-Resistant Enterococci genetics, Whole Genome Sequencing, Cell Phone, Computers, Cross Infection microbiology, Environmental Microbiology, Gram-Negative Bacteria isolation & purification, Methicillin-Resistant Staphylococcus aureus isolation & purification, Vancomycin-Resistant Enterococci isolation & purification
- Abstract
Few studies have used molecular epidemiological methods to study transmission links to clinical isolates in intensive care units. Ninety-four multidrug-resistant organisms (MDROs) cultured from routine specimens from intensive care unit (ICU) patients over 13 weeks were stored (11 meticillin-resistant Staphylococcus aureus (MRSA), two vancomycin-resistant enterococci and 81 Gram-negative bacteria). Medical staff personal mobile phones, departmental phones, and ICU keyboards were swabbed and cultured for MDROs; MRSA was isolated from two phones. Environmental and patient isolates of the same genus were selected for whole genome sequencing. On whole genome sequencing, the mobile phone isolates had a pairwise single nucleotide polymorphism (SNP) distance of 183. However, >15,000 core genome SNPs separated the mobile phone and clinical isolates. In a low-endemic setting, mobile phones and keyboards appear unlikely to contribute to hospital-acquired MDROs., (Copyright © 2018 The Healthcare Infection Society. Published by Elsevier Ltd. All rights reserved.)
- Published
- 2018
- Full Text
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