121 results on '"Sharron, M."'
Search Results
2. Ethnic Identity and Propensity for Practice among African-Descended MSW Students
- Author
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Pierce, Walter J., Singleton, Sharron M., and Hudson, Rhonda E.
- Abstract
This article explores the difference between ethnic identity scores for African-descended MSW students who are native to this country, who are first generation born of immigrant parents, and who are foreign-born Black immigrants. The research further explores whether ethnic identity is associated with the students' commitment to work with their own ethnic groups. Results indicate that all three groups of students demonstrate high ethnic identity, and variability in group means was not statistically significant. However, statistically significant difference existed among the 3 groups on 1 of the measures of propensity for practice. Also determined was a significant relationship between ethnic identity and the propensity for practice items. Implications for social work education and additional research are highlighted. (Contains 3 tables.)
- Published
- 2011
- Full Text
- View/download PDF
3. Role of patient and family engagement in quality improvement for pediatric surgery
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Salva N. Balbale, Maria Cho, Mehul V. Raval, and Sharron M. Close
- Subjects
Pediatrics, Perinatology and Child Health ,Surgery - Published
- 2023
4. The Effect of Mental Health Practioners' Racial Sensitivity on African Americans' Perceptions of Service.
- Author
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Singleton-Bowie, Sharron M.
- Abstract
Client-case manager matches (n=75) from the outpatient services of an urban mental health department were selected to examine case managers' perceived racial sensitivity and its effect on African American clients. Findings demonstrated that case managers were more likely to be perceived as sensitive if they were a minority, female, and a degreed social worker. (JPS)
- Published
- 1995
5. Faculty Personal Comfort and the Teaching of Content on Racial Oppression.
- Author
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Singleton, Sharron M.
- Abstract
Interviews with 11 white and black faculty members in 4 social work schools examined strategies used to ease personal discomfort when teaching about racial oppression, extent to which content and terminology about racial oppression were used, student attitudes, and reactions of other faculty and administrators. (SV)
- Published
- 1994
6. Contributors
- Author
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Alderton, Beverley Ann, primary, Ball, Jonathan W., additional, Barbon, Alberto Rodriguez, additional, Batchelder, Margaret, additional, Beaufrère, Hugues, additional, Bingley, Michelle, additional, Blanco, Michael C., additional, Bays, Teresa Bradley, additional, Brown, Cynthia J., additional, Burgdorf-Moisuk, Anne, additional, Campagna, Michael V., additional, Campbell-Ward, Michelle L., additional, Carmel, Brendan, additional, Chan, Cathy T.T., additional, Chin, Jaime, additional, Chitty, John, additional, Cottrell, Deborah, additional, Crum, David A., additional, DeCubellis, Julie, additional, Divers, Stephen J., additional, Donnelly, Thomas M., additional, Dutton, Michael, additional, Easson, Will, additional, Eshar, David, additional, Evans, Brian A., additional, Fischer, Peter G., additional, Fox, James G., additional, Funk, Amy J., additional, García, Alexis, additional, Graham, Jennifer, additional, Hahn, Caroline, additional, Hermans, Katleen, additional, Hersey-Benner, Candace, additional, Howard, Gretta, additional, Jankowski, Gwendolyn R., additional, Keeble, Emma, additional, Keller, Dominique L., additional, Kerr, Peter, additional, Kirchain, Sharron M., additional, Kirchgessner, Megan, additional, Latney, La'Toya, additional, Lewington, John Henry, additional, Lock, Brad A., additional, Malakoff, Rebecca L., additional, Manley, Caralee, additional, Mans, Christoph, additional, Marini, Robert P., additional, Martínez, Jorge, additional, Mayer, Jörg, additional, Meredith, Anna, additional, Minh, Huynh, additional, Mitchell, Mark A., additional, Mullen, Holly S., additional, Norman, Jason, additional, Palmeiro, Brian S., additional, Paré, Jean A., additional, Patterson, Mary M., additional, Perpiñán, David, additional, Phelps, Carrie A., additional, Pignon, Charly, additional, Pilny, Anthony A., additional, Pinard, Chantale L., additional, Pizzi, Romain, additional, Pollock, Christal, additional, Powers, Lauren V., additional, Raftery, Aidan, additional, Raymundo, Viviane Silva, additional, Reavill, Drury R., additional, Richardson, Virgina C.G., additional, Robat, Cecilia, additional, Roberts, Helen E., additional, Rosenblad, William, additional, Guzman, David Sanchez-Migallon, additional, Saunders, Richard A., additional, Shaw, Shannon N., additional, Shelton, James L. (Jay), additional, Shrubsole-Cockwill, Alana, additional, Schoemaker, Nico J., additional, Smith, Jeffrey, additional, Stahl, Scott J., additional, Starkey, Simon R., additional, Taylor, W. Michael, additional, Tully, Thomas N., additional, Varga, Molly, additional, Vella, David, additional, von Bomhard, Wolf, additional, Walter, Narelle, additional, Wellehan, James F.X., additional, Whittaker, Cameron J.G., additional, Whitwell, Katherine E., additional, Williams, Bruce H., additional, Wojick, Kimberlee B., additional, Wright, Kevin M., additional, Wyre, Nicole R., additional, and Zachariah, Trevor T., additional
- Published
- 2013
- Full Text
- View/download PDF
7. Is fraud a problem in governmental entities?
- Author
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Graves, Sharron M., Lilley, Treba, and Lozano, Marsh Miguel, III.
- Subjects
Business ,Association of Certified Fraud Examiners - Abstract
ABSTRACT The Association of Certified Fraud Examiners estimates the loss from occupational fraud and abuse at approximately $600 billion per year, or about $4,500 per employee. The FBI has labeled [...]
- Published
- 2004
8. Count With Me! : Numbers 1 to 10
- Author
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Sharron M. Johnson and Sharron M. Johnson
- Abstract
I was inspired to take up painting as a complete beginner during the 2020 pandemic. The arrival of my first grandchild, Naarah, presented me with the perfect opportunity to channel my efforts into something that I could share with her as she grew. I painted a series of images for a number counting book, some of which have deep meaning within my family. The book can be used as a first number primer for adults and young children to read together. Enjoy.
- Published
- 2021
9. New or Progressive Multiple Organ Dysfunction Syndrome in Pediatric Severe Sepsis: A Sepsis Phenotype With Higher Morbidity and Mortality
- Author
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Lin, John C, Spinella, Philip C., Fitzgerald, Julie C., Tucci, Marisa, Bush, Jenny L., Nadkarni, Vinay M., Thomas, Neal J., Weiss, Scott L., Fontela, P., Tucci, M., Dumistrascu, M., Skippen, P., Krahn, G., Bezares, E., Puig, G., Puig Ramos, A., Garcia, R., Villar, M., Bigham, M., Polanski, T., Latifi, S., Giebner, D., Anthony, H., Hume, J., Galster, A., Linnerud, L., Sanders, R., Hefley, G., Madden, K., Thompson, A., Shein, S., Gertz, S., Han, Y., Williams, T., Hughes Schalk, A., Chandler, H., Orioles, A., Zielinski, E., Doucette, A., Zebuhr, C., Wilson, T., Dimitriades, C., Ascani, J., Layburn, S., Valley, S., Markowitz, B., Terry, J., Morzov, R., Mcinnes, A., Mcarthur, J., Woods, K., Murkowski, K., Spaeder, M., Sharron, M., Wheeler, D., Beckman, E., Frank, E., Howard, K., Carroll, C., Nett, S., Jarvis, D., Patel, V., Higgerson, R., Christie, L., Typpo, K., Deschenes, J., Kirby, A., Uhl, T., Rehder, K., Cheifetz, I., Wrenn, S., Kypuros, K., Ackerman, K., Maffei, F., Bloomquist, G., Rizkalla, N., Kimura, D., Shah, S., Tigges, C., Su, F., Barlow, C., Michelson, K., Wolfe, K., Goodman, D., Campbell, L., Sorce, L., Bysani, K., Monjure, T., Evans, M., Totapally, B., Chegondi, M., Rodriguez, C., Frazier, J., Steele, L., Viteri, S., Costarino, A., Thomas, N., Spear, D., Hirshberg, E., Lilley, J., Rowan, C., Rider, C., Kane, J., Zimmerman, J., Greeley, C., Lin, J., Jacobs, R., Parker, M., Culver, K., Loftis, L., Jaimon, N., Goldsworthy, M., Diliberto, M., Alen, C., Gessouroun, M., Sapru, A., Lang, T., Alkhouli, M., Kamath, S., Friel, D., Daufeldt, J., Hsing, D., Carlo, C., Pon, S., Scimeme, J., Shaheen, A., Hassinger, A., Qiao, H., Giuliano, J., Tala, J., Vinciguerra, D., Fernandez, A., Carrero, R., Hoyos, P., Jaramillo, J., Posada, A., Izquiierdo, L., Pineres Olave, B. E., Donado, J., Dalmazzo, R., Rendich, S., Palma, L., Lapadula, M., Acuna, C., Cruces, P., De Clety, S. Clement, Dujardin, M., Berghe, C., Renard, S., Zurek, J., Steinherr, H., Mougkou, K., Critselis, E., Di Nardo, M., Picardo, S., Tortora, F., Rossetti, E., Fragasso, T., Cogo, Paola, Netto, R., Dagys, A., Gurskis, V., Kevalas, R., Neeleman, C., Lemson, J., Luijten, C., Wojciech, K., Pagowska Klimek, I., Szczepanska, M., Karpe, J., Nunes, P., Almeida, H., Rios, J., Vieira, M., Garcia Iniguez, J. P., Revilla, P., Urbano, J., Lopez Herce, J., Bustinza, A., Cuesta, A., Hofheinz, S., Rodriguez Nunez, A., Sanagustin, S., Gonzalez, E., Riaza, M., Piaya, R., Soler, P., Esteban, E., Laraudogoitia, J., Monge, C., Herrera, V., Granados, J., Gonzalez, C., Koroglu, T., Ozcelik, E., Baines, P., Plunkett, A., Davis, P., George, S., Tibby, S., Harris, J., Agbeko, R., Lampitt, R., Brierley, J., Peters, M., Jones, A., Dominguez, T., Thiruchelvam, T., Deep, A., Ridley, L., Bowen, W., Levin, R., Macleod, I., Gray, M., Hemat, N., Alexander, J., Ali, S., Pappachan, J., Mccorkell, J., Fortune, P., Macdonald, M., Hudnott, P., Suyun, Q., Singhi, S., Nallasamy, K., Lodha, R., Shime, N., Tabata, Y., Saito, O., Ikeyama, T., Kawasaki, T., Lum, L., Abidin, A., Kee, S., Tang, S., Jalil, R., Guan, Y., Yao, L., Lin, K., Ong, J., Salloo, A., Doedens, L., Mathivha, L., Reubenson, G., Moaisi, S., Pentz, A., Green, R., Schibler, A., Erickson, S., Mceneiry, J., Long, D., Dorofaeff, T., Coulthard, M., Millar, J., Delzoppo, C., Williams, G., Morritt, M., Watts, N., Beca, J., Sherring, C., and Bushell, T.
- Subjects
Male ,medicine.medical_specialty ,Adolescent ,Cross-sectional study ,Multiple Organ Failure ,Vascular damage Radboud Institute for Health Sciences [Radboudumc 16] ,Prevalence ,children ,epidemiology ,multiple organ dysfunction syndrome ,severe sepsis ,Pediatrics, Perinatology and Child Health ,Critical Care and Intensive Care Medicine ,030204 cardiovascular system & hematology ,Global Health ,Intensive Care Units, Pediatric ,Pediatrics ,Article ,Sepsis ,03 medical and health sciences ,0302 clinical medicine ,Internal medicine ,Epidemiology ,medicine ,Humans ,Hospital Mortality ,Prospective Studies ,030212 general & internal medicine ,Child ,Intensive care medicine ,Prospective cohort study ,Septic shock ,business.industry ,Infant, Newborn ,Infant ,Perinatology and Child Health ,Prognosis ,medicine.disease ,Clinical trial ,Cross-Sectional Studies ,Phenotype ,Child, Preschool ,Disease Progression ,Female ,Multiple organ dysfunction syndrome ,business - Abstract
Copyright © 2016 by the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies.Objectives: To describe the epidemiology, morbidity, and mortality of new or progressive multiple organ dysfunction syndrome in children with severe sepsis. Design: Secondary analysis of a prospective, cross-sectional, point prevalence study. Setting: International, multicenter PICUs. Patients: Pediatric patients with severe sepsis identified on five separate days over a 1-year period. Interventions: None. Measurements and Main Results: Of 567 patients from 128 PICUs in 26 countries enrolled, 384 (68%) developed multiple organ dysfunction syndrome within 7 days of severe sepsis recognition. Three hundred twenty-seven had multiple organ dysfunction syndrome on the day of sepsis recognition. Ninety-one of these patients developed progressive multiple organ dysfunction syndrome, whereas an additional 57 patients subsequently developed new multiple organ dysfunction syndrome, yielding a total proportion with severe sepsis-associated new or progressive multiple organ dysfunction syndrome of 26%. Hospital mortality in patients with progressive multiple organ dysfunction syndrome was 51% compared with patients with new multiple organ dysfunction syndrome (28%) and those with single-organ dysfunction without multiple organ dysfunction syndrome (10%) (p < 0.001). Survivors of new or progressive multiple organ dysfunction syndrome also had a higher frequency of moderate to severe disability defined as a Pediatric Overall Performance Category score of greater than or equal to 3 and an increase of greater than or equal to 1 from baseline: 22% versus 29% versus 11% for progressive, new, and no multiple organ dysfunction syndrome, respectively (p < 0.001). Conclusions: Development of new or progressive multiple organ dysfunction syndrome is common (26%) in severe sepsis and is associated with a higher risk of morbidity and mortality than severe sepsis without new or progressive multiple organ dysfunction syndrome. Our data support the use of new or progressive multiple organ dysfunction syndrome as an important outcome in trials of pediatric severe sepsis although efforts are needed to validate whether reducing new or progressive multiple organ dysfunction syndrome leads to improvements in more definitive morbidity and mortality endpoints.
- Published
- 2017
10. Dating Violence Prevention in Middle School and High School Youth
- Author
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Close, Sharron M.
- Published
- 2005
11. Improvisation as a concept for understanding and treating violent behavior among African American youth
- Author
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Pierce, Walter J. and Singleton, Sharron M.
- Subjects
Improvisation (Acting) -- Health aspects ,Violence in children -- Care and treatment ,African American youth -- Psychological aspects ,Family and marriage ,Sociology and social work - Published
- 1995
12. Evaluating internal controls: control self-assessment in government
- Author
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Graves, Sharron M., Longenecker, Bill, Marsh, Treba L., and Milstead, Heidi
- Subjects
Public finance -- Management ,Banking, finance and accounting industries ,Business ,Government ,Company business management ,Management - Abstract
A system of internal control is a tool for ensuring that an organization realizes its mission and objectives. While internal controls are often thought to be the domain of accountants [...]
- Published
- 2003
13. Risk Factors for Mortality in Pediatric Postsurgical versus Medical Severe Sepsis
- Author
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Thakkar, Rajan K., primary, Weiss, Scott L., additional, Fitzgerald, Julie C., additional, Keele, Luke, additional, Thomas, Neal J., additional, Nadkarni, Vinay M., additional, Muszynski, Jennifer A., additional, Hall, Mark W., additional, Fontela, P., additional, Tucci, M., additional, Dumistrascu, M., additional, Skippen, P., additional, Krahn, G., additional, Bezares, E., additional, Puig, G., additional, Puig-Ramos, A., additional, Garcia, R., additional, Villar, M., additional, Bigham, M., additional, Polanski, T., additional, Latifi, S., additional, Giebner, D., additional, Anthony, H., additional, Hume, J., additional, Galster, A., additional, Linnerud, L., additional, Sanders, R., additional, Hefley, G., additional, Madden, K., additional, Thompson, A., additional, Shein, S., additional, Gertz, S., additional, Han, Y., additional, Williams, T., additional, Hughes-Schalk, A., additional, Chandler, H., additional, Orioles, A., additional, Zielinski, E., additional, Doucette, A., additional, Zebuhr, C., additional, Wilson, T., additional, Dimitriades, C., additional, Ascani, J., additional, Layburn, S., additional, Valley, S., additional, Markowitz, B., additional, Terry, J., additional, Morzov, R., additional, Mcinnes, A., additional, McArthur, J., additional, Woods, K., additional, Murkowski, K., additional, Spaeder, M., additional, Sharron, M., additional, Wheeler, D., additional, Beckman, E., additional, Frank, E., additional, Howard, K., additional, Carroll, C., additional, Nett, S., additional, Jarvis, D., additional, Patel, V., additional, Higgerson, R., additional, Christie, L., additional, Typpo, K., additional, Deschenes, J., additional, Kirby, A., additional, Uhl, T., additional, Rehder, K., additional, Cheifetz, I., additional, Wrenn, S., additional, Kypuros, K., additional, Ackerman, K., additional, Maffei, F., additional, Bloomquist, G., additional, Rizkalla, N., additional, Kimura, D., additional, Shah, S., additional, Tigges, C., additional, Su, F., additional, Barlow, C., additional, Michelson, K., additional, Wolfe, K., additional, Goodman, D., additional, Campbell, L., additional, Sorce, L., additional, Bysani, K., additional, Monjure, T., additional, Evans, M., additional, Totapally, B., additional, Chegondi, M., additional, Rodriguez, C., additional, Frazier, J., additional, Steele, L., additional, Viteri, S., additional, Costarino, A., additional, Thomas, N., additional, Spear, D., additional, Hirshberg, E., additional, Lilley, J., additional, Rowan, C., additional, Rider, C., additional, Kane, J., additional, Zimmerman, J., additional, Greeley, C., additional, Lin, J., additional, Jacobs, R., additional, Parker, M., additional, Culver, K., additional, Loftis, L., additional, Jaimon, N., additional, Goldsworthy, M., additional, Fitzgerald, J., additional, Weiss, S., additional, Nadkarni, V., additional, Bush, J., additional, Diliberto, M., additional, Allen, C., additional, Gessouroun, M., additional, Sapru, A., additional, Lang, T., additional, Alkhouli, M., additional, Kamath, S., additional, Friel, D., additional, Daufeldt, J., additional, Hsing, D., additional, Carlo, C., additional, Pon, S., additional, Scimeme, J., additional, Shaheen, A., additional, Hassinger, A., additional, Qiao, H., additional, Giuliano, J., additional, Tala, J., additional, Vinciguerra, D., additional, Fernandez, A., additional, Carrero, R., additional, Hoyos, P., additional, Jaramillo, J., additional, Posada, A., additional, Izquiierdo, L., additional, Olave, B.E. Piñeres, additional, Donado, J., additional, Dalmazzo, R., additional, Rendich, S., additional, Palma, L., additional, Lapadula, M., additional, Acuna, C., additional, Cruces, P., additional, De Clety, S. Clement, additional, Dujardin, M., additional, Berghe, C., additional, Renard, S., additional, Zurek, J., additional, Steinherr, H., additional, Mougkou, K., additional, Critselis, E., additional, Di Nardo, M., additional, Picardo, S., additional, Tortora, F., additional, Rossetti, E., additional, Fragasso, T., additional, Cogo, P., additional, Netto, R., additional, Dagys, A., additional, Gurskis, V., additional, Kevalas, R., additional, Neeleman, C., additional, Lemson, J., additional, Luijten, C., additional, Wojciech, K., additional, Pagowska-Klimek, I., additional, Szczepanska, M., additional, Karpe, J., additional, Nunes, P., additional, Almeida, H., additional, Rios, J., additional, Vieira, M., additional, Iniguez, J. P. Garcia, additional, Revilla, P., additional, Urbano, J., additional, Lopez-Herce, J., additional, Bustinza, A., additional, Palacios, A., additional, Hofheinz, S., additional, Rodriguez-Nunez, A., additional, Sanagustin, S., additional, Gonzalez, E., additional, Riaza, M., additional, Piaya, R., additional, Soler, P., additional, Esteban, E., additional, Laraudogoitia, J., additional, Monge, C., additional, Herrera, V., additional, Granados, J., additional, Gonzalez, C., additional, Koroglu, T., additional, Ozcelik, E., additional, Baines, P., additional, Plunkett, A., additional, Davis, P., additional, George, S., additional, Tibby, S., additional, Harris, J., additional, Agbeko, R., additional, Lampitt, R., additional, Brierley, J., additional, Peters, M., additional, Jones, A., additional, Dominguez, T., additional, Thiruchelvam, T., additional, Deep, A., additional, Ridley, L., additional, Bowen, W., additional, Levin, R., additional, Macleod, I., additional, Gray, M., additional, Hemat, N., additional, Alexander, J., additional, Ali, S., additional, Pappachan, J., additional, McCorkell, J., additional, Fortune, P., additional, MacDonald, M., additional, Hudnott, P., additional, Suyun, Q., additional, Singhi, S., additional, Nallasamy, K., additional, Lodha, R., additional, Shime, N., additional, Tabata, Y., additional, Saito, O., additional, Ikeyama, T., additional, Kawasaki, T., additional, Lum, L., additional, Abidin, A., additional, Kee, S., additional, Tang, S., additional, Jalil, R., additional, Guan, Y., additional, Yao, L., additional, Lin, K., additional, Ong, J., additional, Salloo, A., additional, Doedens, L., additional, Mathivha, L., additional, Reubenson, G., additional, Moaisi, S., additional, Pentz, A., additional, Green, R., additional, Schibler, A., additional, Erickson, S., additional, McEneiry, J., additional, Long, D., additional, Dorofaeff, T., additional, Coulthard, M., additional, Millar, J., additional, Delzoppo, C., additional, Williams, G., additional, Morritt, M., additional, Watts, N., additional, Beca, J., additional, Sherring, C., additional, and Bushell, T., additional
- Published
- 2019
- Full Text
- View/download PDF
14. Comparison of Pediatric Severe Sepsis Managed in U.S. and European ICUs
- Author
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Giuliano, John S, Markovitz, Barry P., Brierley, Joe, Levin, Richard, Williams, Gary, Lum, Lucy Chai See, Dorofaeff, Tavey, Cruces, Pablo, Bush, Jenny L., Keele, Luke, Nadkarni, Vinay M., Thomas, Neal J., Fitzgerald, Julie C., Weiss, Scott L., Fontela, P., Tucci, M., Dumistrascu, M., Skippen, P., Krahn, G., Bezares, E., Puig, G., Puig Ramos, A., Garcia, R., Villar, M., Bigham, M., Polanski, T., Latifi, S., Giebner, D., Anthony, H., Hume, J., Galster, A., Linnerud, L., Sanders, R., Hefley, G., Madden, K., Thompson, A., Shein, S., Gertz, S., Han, Y., Williams, T., Hughes Schalk, A., Chandler, H., Orioles, A., Zielinski, E., Doucette, A., Zebuhr, C., Wilson, T., Dimitriades, C., Ascani, J., Layburn, S., Valley, S., Markowitz, B., Terry, J., Morzov, R., Mcinnes, A., Mcarthur, J., Woods, K., Murkowski, K., Spaeder, M., Sharron, M., Wheeler, D., Beckman, E., Frank, E., Howard, K., Carroll, C., Nett, S., Jarvis, D., Patel, V., Higgerson, R., Christie, L., Typpo, K., Deschenes, J., Kirby, A., Uhl, T., Rehder, K., Cheifetz, I., Wrenn, S., Kypuros, K., Ackerman, K., Maffei, F., Bloomquist, G., Rizkalla, N., Kimura, D., Shah, S., Tigges, C., Su, F., Barlow, C., Michelson, K., Wolfe, K., Goodman, D., Campbell, L., Sorce, L., Bysani, K., Monjure, T., Evans, M., Totapally, B., Chegondi, M., Rodriguez, C., Frazier, J., Steele, L., Viteri, S., Costarino, A., Thomas, N., Spear, D., Hirshberg, E., Lilley, J., Rowan, C., Rider, C., Kane, J., Zimmerman, J., Greeley, C., Lin, J., Jacobs, R., Parker, M., Culver, K., Loftis, L., Jaimon, N., Goldsworthy, M., Fitzgerald, J., Weiss, S., Nadkarni, V., Bush, J., Diliberto, M., Alen, C., Gessouroun, M., Sapru, A., Lang, T., Alkhouli, M., Kamath, S., Friel, D., Daufeldt, J., Hsing, D., Carlo, C., Pon, S., Scimeme, J., Shaheen, A., Hassinger, A., Qiao, H., Giuliano, J., Tala, J., Vinciguerra, D., Fernandez, A., Carrero, R., Hoyos, P., Jaramillo, J., Posada, A., Izquiierdo, L., Piñeres Olave, B. E., Donado, J., Dalmazzo, R., Rendich, S., Palma, L., Lapadula, M., Acuna, C., Cruces, P., Clement De Clety, S., Dujardin, M., Berghe, C., Renard, S., Zurek, J., Steinherr, H., Mougkou, K., Critselis, E., Di Nardo, M., Picardo, S., Tortora, F., Rossetti, E., Fragasso, T., Cogo, Paola, Netto, R., Dagys, A., Gurskis, V., Kevalas, R., Neeleman, C., Lemson, J., Luijten, C., Wojciech, K., Pagowska Klimek, I., Szczepanska, M., Karpe, J., Nunes, P., Almeida, H., Rios, J., Vieira, M., Revilla, P., Urbano, J., Lopez Herce, J., Bustinza, A., Cuesta, A., Hofheinz, S., Rodriguez Nunez, A., Sanagustin, S., Gonzalez, E., Riaza, M., Piaya, R., Soler, P., Esteban, E., Laraudogoitia, J., Monge, C., Herrera, V., Granados, J., Gonzalez, C., Koroglu, T., Ozcelik, E., Baines, P., Plunkett, A., Davis, P., George, S., Tibby, S., Harris, J., Agbeko, R., Lampitt, R., Brierley, J., Peters, M., Jones, A., Dominguez, T., Thiruchelvam, T., Deep, A., Ridley, L., Bowen, W., Levin, R., Macleod, I., Gray, M., Hemat, N., Alexander, J., Ali, S., Pappachan, J., Mccorkell, J., Fortune, P., Macdonald, M., Hudnott, P., Suyun, Q., Singhi, S., Nallasamy, K., Lodha, R., Shime, N., Tabata, Y., Saito, O., Ikeyama, T., Kawasaki, T., Lum, L., Abidin, A., Kee, S., Tang, S., Jalil, R., Guan, Y., Yao, L., Lin, K., Ong, J., Salloo, A., Doedens, L., Mathivha, L., Reubenson, G., Moaisi, S., Pentz, A., Green, R., Schibler, A., Erickson, S., Mceneiry, J., Long, D., Dorofaeff, T., Coulthard, M., Millar, J., Delzoppo, C., Williams, G., Morritt, M., Watts, N., Beca, J., Sherring, C., and Bushell, T.
- Subjects
Male ,Pediatrics ,Cross-sectional study ,shock ,Critical Care and Intensive Care Medicine ,Severity of Illness Index ,0302 clinical medicine ,Prevalence ,Hospital Mortality ,Prospective Studies ,030212 general & internal medicine ,Practice Patterns, Physicians' ,Child ,Prospective cohort study ,Pediatric intensive care unit ,Perinatology and Child Health ,Europe ,Treatment Outcome ,Child, Preschool ,outcome ,children ,management ,pediatric intensive care unit ,Pediatrics, Perinatology and Child Health ,Female ,medicine.symptom ,medicine.medical_specialty ,Adolescent ,Critical Care ,Intensive Care Units, Pediatric ,Sepsis ,03 medical and health sciences ,Intensive care ,Severity of illness ,medicine ,Humans ,Healthcare Disparities ,business.industry ,Organ dysfunction ,Infant, Newborn ,Infant ,030208 emergency & critical care medicine ,Health Status Disparities ,medicine.disease ,United States ,Clinical trial ,Cross-Sectional Studies ,Multivariate Analysis ,Emergency medicine ,business - Abstract
Copyright © 2016 by the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies.Objectives: Pediatric severe sepsis remains a significant global health problem without new therapies despite many multicenter clinical trials. We compared children managed with severe sepsis in European and U.S. PICUs to identify geographic variation, which may improve the design of future international studies. Design: We conducted a secondary analysis of the Sepsis PRevalence, OUtcomes, and Therapies study. Data about PICU characteristics, patient demographics, therapies, and outcomes were compared. Multivariable regression models were used to determine adjusted differences in morbidity and mortality. Setting: European and U.S. PICUs. Patients: Children with severe sepsis managed in European and U.S. PICUs enrolled in the Sepsis PRevalence, OUtcomes, and Therapies study. Interventions: None. Measurements and Main Results: European PICUs had fewer beds (median, 11 vs 24; p < 0.001). European patients were younger (median, 1 vs 6 yr; p < 0.001), had higher severity of illness (median Pediatric Index of Mortality-3, 5.0 vs 3.8; p = 0.02), and were more often admitted from the ward (37% vs 24%). Invasive mechanical ventilation, central venous access, and vasoactive infusions were used more frequently in European patients (85% vs 68%, p = 0.002; 91% vs 82%, p = 0.05; and 71% vs 50%; p < 0.001, respectively). Raw morbidity and mortality outcomes were worse for European compared with U.S. patients, but after adjusting for patient characteristics, there were no significant differences in mortality, multiple organ dysfunction, disability at discharge, length of stay, or ventilator/vasoactive-free days. Conclusions: Children with severe sepsis admitted to European PICUs have higher severity of illness, are more likely to be admitted from hospital wards, and receive more intensive care therapies than in the United States. The lack of significant differences in morbidity and mortality after adjusting for patient characteristics suggests that the approach to care between regions, perhaps related to PICU bed availability, needs to be considered in the design of future international clinical trials in pediatric severe sepsis.
- Published
- 2016
15. Comparison of Pediatric Severe Sepsis Managed in US and European ICUs
- Author
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Giuliano, J.S., Markovitz, B.P., Brierley, J., Levin, R., Williams, G., Lum, L.C.S., Dorofaeff, T., Cruces, P., Bush, J.L., Keele, L., Nadkarni, V.M., Thomas, N.J., Fitzgerald, J.C., Weiss, S.L., Fontela, P., Tucci, M., Dumistrascu, M., Skippen, P., Krahn, G., Bezares, E., Puig, G., Puig-Ramos, A., Garcia, R., Villar, M., Bigham, M., Polanski, T., Latifi, S., Giebner, D., Anthony, H., Hume, J., Galster, A., Linnerud, L., Sanders, R., Hefley, G., Madden, K., Thompson, A., Shein, S., Gertz, S., Han, Y., Williams, T., Hughes-Schalk, A., Chandler, H., Orioles, A., Zielinski, E., Doucette, A., Zebuhr, C., Wilson, T., Dimitriades, C., Ascani, J., Layburn, S., Valley, S., Markowitz, B., Terry, J., Morzov, R., McInnes, A., McArthur, J., Woods, K., Murkowski, K., Spaeder, M., Sharron, M., Wheeler, D., Beckman, E., Frank, E., Howard, K., Carroll, C., Nett, S., Jarvis, D., Patel, V., Higgerson, R., Christie, L., Typpo, K., Deschenes, J., Kirby, A., Uhl, T., Rehder, K., Cheifetz, I., Wrenn, S., Kypuros, K., Ackerman, K., Maffei, F., Bloomquist, G., Rizkalla, N., Kimura, D., Shah, S., Tigges, C., Su, F., Barlow, C., Michelson, K., Wolfe, K., Goodman, D., Campbell, L., Sorce, L., Bysani, K., Monjure, T., Evans, M., Totapally, B., Chegondi, M., Rodriguez, C., Frazier, J., Steele, L., Viteri, S., Costarino, A., Spear, D., Hirshberg, E., Lilley, J., Rowan, C., Rider, C., Kane, J., Zimmerman, J., Greeley, C., Lin, J., Jacobs, R., Parker, M., Culver, K., Loftis, L., Jaimon, N., Goldsworthy, M., Fitzgerald, J., Nadkarni, V., Bush, J., Diliberto, M., Alen, C., Gessouroun, M., Sapru, A., Lang, T., Alkhouli, M., Kamath, S., Friel, D., Daufeldt, J., Hsing, D., Carlo, C., Pon, S., Scimeme, J., Shaheen, A., Hassinger, A., Qiao, H., Giuliano, J., Tala, J., Vinciguerra, D., Fernandez, A., Carrero, R., Hoyos, P., Jaramillo, J., Posada, A., Izquiierdo, L., Piñeres Olave, B.E., Donado, J., Dalmazzo, R., Rendich, S., Palma, L., Lapadula, M., Acuna, C., Clement De Clety, S., Dujardin, M., Berghe, C., Renard, S., Zurek, J., Steinherr, H., Mougkou, K., Critselis, E., Di Nardo, M., Picardo, S., Tortora, F., Rossetti, E., Fragasso, T., Cogo, P., Netto, R., Dagys, A., Gurskis, V., Kevalas, R., Neeleman, C., Lemson, J., Luijten, C., Wojciech, K., Pagowska-Klimek, I., Szczepanska, M., Karpe, J., Nunes, P., Almeida, H., Rios, J., Vieira, M., Revilla, P., Urbano, J., Lopez-Herce, J., Bustinza, A., Cuesta, A., Hofheinz, S., Rodriguez-Nunez, A., Sanagustin, S., Gonzalez, E., Riaza, M., Piaya, R., Soler, P., Esteban-Torne E, Laraudogoitia, J., Monge, C., Herrera, V., Granados, J., Gonzalez, C., Koroglu, T., Ozcelik, E., Baines, P., Plunkett, A., Davis, P., George, S., Tibby, S., Harris, J., Agbeko, R., Lampitt, R., Peters, M., Jones, A., Dominguez, T., Thiruchelvam, T., Deep, A., Ridley, L., Bowen, W., Macleod, I., Gray, M., Hemat, N., Alexander, J., Ali, S., Pappachan, J., McCorkell, J., Fortune, P., MacDonald, M., Hudnott, P., Suyun, Q., Singhi, S., Nallasamy, K., Lodha, R., Shime, N., Tabata, Y., Saito, O., Ikeyama, T., Kawasaki, T., Lum, L., Abidin, A., Kee, S., Tang, S., Jalil, R., Guan, Y., Yao, L., Lin, K., Ong, J., Salloo, A., Doedens, L., Mathivha, L., Reubenson, G., Moaisi, S., Pentz, A., Green, R., Schibler, A., Erickson, S., McEneiry, J., Long, D., Coulthard, M., Millar, J., Delzoppo, C., Morritt, M., Watts, N., Beca, J., Sherring, C., and Bushell, T.
- Published
- 2016
16. ETHNIC IDENTITY AND PROPENSITY FOR PRACTICE AMONG AFRICAN-DESCENDED MSW STUDENTS
- Author
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Walter J. Pierce, Sharron M. Singleton, and Rhonda E. Hudson
- Subjects
Social work ,media_common.quotation_subject ,Significant difference ,Immigration ,Ethnic group ,Self-concept ,Additional research ,First generation ,Education ,Social work education ,Psychology ,Social psychology ,Social Sciences (miscellaneous) ,media_common - Abstract
This article explores the difference between ethnic identity scores for Africandescended MSW students who are native to this country, who are first generation born of immigrant parents, and who are foreign-born Black immigrants. The research further explores whether ethnic identity is associated with the students' commitment to work with their own ethnic groups. Results indicate that all three groups of students demonstrate high ethnic identity, and variability in group means was not statistically significant. However, statistically significant difference existed among the 3 groups on 1 of the measures of propensity for practice. Also determined was a significant relationship between ethnic identity and the propensity for practice items. Implications for social work education and additional research are highlighted.
- Published
- 2011
17. Exploring Queer Consciousness Among Social Workers
- Author
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Paulina Martinez, Sharron M. Singleton, and Allan Barsky
- Subjects
Value (ethics) ,Sociology and Political Science ,Social work ,media_common.quotation_subject ,Redress ,Gender studies ,Gender Studies ,Queer ,Lesbian ,Consciousness ,Prejudice ,Psychology ,Social psychology ,media_common ,Diversity (politics) - Abstract
The purpose of this study is to examine the attitudes of MSW practitioners toward lesbians and gay men using a recently developed instrument. Whereas prior research focused on blatantly homophobic or heterosexist attitudes, this research uses a measurement tool based on the concept of queer consciousness (QC) and measures subtle forms of prejudice, including both positive and negative attitudes along four dimensions: Value gay and lesbian progress/diversity, resist traditional sex and gender roles, positive beliefs about lesbians, and positive beliefs about gay men. Research findings indicate negative attitudes toward lesbians and gay men in three out of the four dimensions for the sample of social work practitioners. This article concludes with suggestions for social work educators who want to redress areas of subtle prejudice and promote higher levels of QC.
- Published
- 2011
18. Student Cheating Habits: A Predictor Of Workplace Deviance
- Author
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Sharron M. Graves
- Subjects
Academic integrity ,Workplace deviance ,Cheating ,Psychology ,Social psychology ,Deviance (sociology) ,Retail sector ,Management ,Business environment - Abstract
Unethical behavior seems to be increasing exponentially in every facet of today’s business environment. Property and production deviance are just two of the unethical behaviors exhibited by employees. According to a study conducted by S. Nonis and C. Swift (2001), students who engage in dishonest acts in college classes are more likely to engage in dishonest acts in the workplace. Research conducted during the three year period 2002 - 2005 by Don McCabe in conjunction with The Center for Academic Integrity at Duke University reveals that 70 percent of the 50,000 undergraduate students surveyed admit to some cheating (McCabe 2005). This article reports the results of a student survey documenting the self-reported cheating habits of business and non-business majors and their reported involvement in deviant activities in the workplace. The research indicates that a higher percentage of non-business majors report cheating on tests and homework than business majors and students who cheat in high school and/or college are more likely to engage in certain deviant behaviors in the workplace. In addition, the article also compares the percentage of students engaging in property and production deviance with the results of an earlier study by R. C. Hollinger and J. P. Clark examining workplace deviance among employees in the retail sector.
- Published
- 2008
19. Acute kidney injury in pediatric severe sepsis : An independent risk factor for death and new disability
- Author
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Fitzgerald, Julie C., Basu, Rajit K., Akcan-Arikan, Ayse, Izquierdo, Ledys M., Piñeres Olave, Byron E., Hassinger, Amanda B., Szczepanska, Maria, Deep, Akash, Williams, Duane, Sapru, Anil, Roy, Jason A., Nadkarni, Vinay M., Thomas, Neal J., Weiss, Scott L., Furth, Susan, Fontela, P., Tucci, M., Dumistrascu, M., Skippen, P., Krahn, G., Bezares, E., Puig, G., Puig-Ramos, A., Garcia, R., Villar, M., Bigham, M., Polanski, T., Latifi, S., Giebne, D., Anthony, H., Hume, J., Galster, A., Linnerud, L., Sanders, R., Hefley, G., Madden, K., Thompson, A., Shein, S., Gertz, S., Han, Y., Hughes-Schalk, A., Chandler, H., Orioles, A., Zielinski, E., Doucette, A., Zebuhr, C., Wilson, T., Dimitriades, C., Ascani, J., Layburn, S., Valley, S., Markowitz, B., Terry, J., Morzov, R., Mcinnes, A., McArthur, J., Woods, K., Murkowski, K., Spaeder, M., Sharron, M., Wheeler, D., Beckman, E., Frank, E., Howard, K., Carroll, C., Nett, S., Jarvis, D., Patel, V., Higgerson, R., Christie, L., Typpo, K., Deschenes, J., Kirby, A., Uhl, T., Rehder, K., Cheifetz, I., Wrenn, S., Kypuros, K., Ackerman, K., Maffei, F., Bloomquist, G., Rizkalla, N., Kimura, D., Shah, S., Tigges, C., Su, F., Barlow, C., Michelson, K., Wolfe, K., Goodman, D., Campbell, L., Sorce, L., Bysani, K., Monjure, T., Evans, M., Totapally, B., Chegondi, M., Rodriguez, C., Frazier, J., Steele, L., Viteri, S., Costarino, A., Spear, D., Hirshberg, E., Lilley, J., Rowan, C., Rider, C., Kane, J., Zimmerman, J., Greeley, C., Lin, J., Jacobs, R., Parker, M., Culver, K., Loftis, L., Jaimon, N., Goldsworthy, M., Bush, J., Diliberto, M., Allen, C., Gessouroun, M., Lang, T., Alkhouli, M., Kamath, S., Friel, D., Daufeldt, J., Hsing, D., Carlo, C., Pon, S., Scimeme, J., Shaheen, A., Qiao, H., Giuliano, J., Tala, J., Vinciguerra, D., Fernandez, A., Carrero, R., Hoyos, P., Jaramillo, J., Posada, A., Izquiierdo, L., Donado, J., Dalmazzo, R., Rendich, S., Palma, L., Lapadula, M., Acuna, C., Cruces, P., Clement De Clety, S., Dujardin, M., Berghe, C., Renard, S., Zurek, J., Steinherr, H., Mougkou, K., Critselis, E., Di Nardo, M., Picardo, S., Tortora, F., Rossetti, E., Fragasso, T., Cogo, P., Netto, R., Dagys, A., Gurskis, V., Kevalas, R., Neeleman, C., Lemson, J., Luijten, C., Wojciech, K., Pagowska-Klimek, I., Karpe, J., Nunes, P., Almeida, H., Rios, J., Vieira, M., Garcia Iniguez, JP, Revilla, P., Urbano, J., Lopez-Herce, J., Bustinza, A., Palacios, A., Hofheinz, S., Rodriguez-Nunez, A., Sanagustin, S., Gonzalez, E., Riaza, M., Piaya, R., Soler, P., Esteban, E., Laraudogoitia, J., Monge, C., Herrera, V., Granados, J., Gonzalez, C., Koroglu, T., Ozcelik, E., Baines, P., Plunkett, A., Davis, P., George, S., Tibby, S., Harris, J., Agbeko, R., Lampitt, R., Brierley, J., Peters, M., Jones, A., Dominguez, T., Thiruchelvam, T., Ridley, L., Bowen, W., Levin, R., Macleod, I., Gray, M., Hemat, N., Alexander, J., Ali, S., Pappachan, J., McCorkell, J., Fortune, P., MacDonald, M., Hudnott, P., Suyun, Q., Singhi, S., Nallasamy, K., Lodha, R., Shime, N., Tabata, Y., Saito, O., Ikeyama, T., Kawasaki, T., Lum, L., Abidin, A., Kee, S., Tang, S., Jalil, R., Guan, Y., Yao, L., Lin, K., Ong, J., Salloo, A., Doedens, L., Mathivha, L., Reubenson, G., Moaisi, S., Pentz, A., Green, R., Schibler, A., Long, D., Fitzgerald, Julie C., Basu, Rajit K., Akcan-Arikan, Ayse, Izquierdo, Ledys M., Piñeres Olave, Byron E., Hassinger, Amanda B., Szczepanska, Maria, Deep, Akash, Williams, Duane, Sapru, Anil, Roy, Jason A., Nadkarni, Vinay M., Thomas, Neal J., Weiss, Scott L., Furth, Susan, Fontela, P., Tucci, M., Dumistrascu, M., Skippen, P., Krahn, G., Bezares, E., Puig, G., Puig-Ramos, A., Garcia, R., Villar, M., Bigham, M., Polanski, T., Latifi, S., Giebne, D., Anthony, H., Hume, J., Galster, A., Linnerud, L., Sanders, R., Hefley, G., Madden, K., Thompson, A., Shein, S., Gertz, S., Han, Y., Hughes-Schalk, A., Chandler, H., Orioles, A., Zielinski, E., Doucette, A., Zebuhr, C., Wilson, T., Dimitriades, C., Ascani, J., Layburn, S., Valley, S., Markowitz, B., Terry, J., Morzov, R., Mcinnes, A., McArthur, J., Woods, K., Murkowski, K., Spaeder, M., Sharron, M., Wheeler, D., Beckman, E., Frank, E., Howard, K., Carroll, C., Nett, S., Jarvis, D., Patel, V., Higgerson, R., Christie, L., Typpo, K., Deschenes, J., Kirby, A., Uhl, T., Rehder, K., Cheifetz, I., Wrenn, S., Kypuros, K., Ackerman, K., Maffei, F., Bloomquist, G., Rizkalla, N., Kimura, D., Shah, S., Tigges, C., Su, F., Barlow, C., Michelson, K., Wolfe, K., Goodman, D., Campbell, L., Sorce, L., Bysani, K., Monjure, T., Evans, M., Totapally, B., Chegondi, M., Rodriguez, C., Frazier, J., Steele, L., Viteri, S., Costarino, A., Spear, D., Hirshberg, E., Lilley, J., Rowan, C., Rider, C., Kane, J., Zimmerman, J., Greeley, C., Lin, J., Jacobs, R., Parker, M., Culver, K., Loftis, L., Jaimon, N., Goldsworthy, M., Bush, J., Diliberto, M., Allen, C., Gessouroun, M., Lang, T., Alkhouli, M., Kamath, S., Friel, D., Daufeldt, J., Hsing, D., Carlo, C., Pon, S., Scimeme, J., Shaheen, A., Qiao, H., Giuliano, J., Tala, J., Vinciguerra, D., Fernandez, A., Carrero, R., Hoyos, P., Jaramillo, J., Posada, A., Izquiierdo, L., Donado, J., Dalmazzo, R., Rendich, S., Palma, L., Lapadula, M., Acuna, C., Cruces, P., Clement De Clety, S., Dujardin, M., Berghe, C., Renard, S., Zurek, J., Steinherr, H., Mougkou, K., Critselis, E., Di Nardo, M., Picardo, S., Tortora, F., Rossetti, E., Fragasso, T., Cogo, P., Netto, R., Dagys, A., Gurskis, V., Kevalas, R., Neeleman, C., Lemson, J., Luijten, C., Wojciech, K., Pagowska-Klimek, I., Karpe, J., Nunes, P., Almeida, H., Rios, J., Vieira, M., Garcia Iniguez, JP, Revilla, P., Urbano, J., Lopez-Herce, J., Bustinza, A., Palacios, A., Hofheinz, S., Rodriguez-Nunez, A., Sanagustin, S., Gonzalez, E., Riaza, M., Piaya, R., Soler, P., Esteban, E., Laraudogoitia, J., Monge, C., Herrera, V., Granados, J., Gonzalez, C., Koroglu, T., Ozcelik, E., Baines, P., Plunkett, A., Davis, P., George, S., Tibby, S., Harris, J., Agbeko, R., Lampitt, R., Brierley, J., Peters, M., Jones, A., Dominguez, T., Thiruchelvam, T., Ridley, L., Bowen, W., Levin, R., Macleod, I., Gray, M., Hemat, N., Alexander, J., Ali, S., Pappachan, J., McCorkell, J., Fortune, P., MacDonald, M., Hudnott, P., Suyun, Q., Singhi, S., Nallasamy, K., Lodha, R., Shime, N., Tabata, Y., Saito, O., Ikeyama, T., Kawasaki, T., Lum, L., Abidin, A., Kee, S., Tang, S., Jalil, R., Guan, Y., Yao, L., Lin, K., Ong, J., Salloo, A., Doedens, L., Mathivha, L., Reubenson, G., Moaisi, S., Pentz, A., Green, R., Schibler, A., and Long, D.
- Abstract
Objectives: The prevalence of septic acute kidney injury and impact on functional status of PICU survivors are unknown. We used data from an international prospective severe sepsis study to elucidate functional outcomes of children suffering septic acute kidney injury. Design: Secondary analysis of patients in the Sepsis PRevalence, OUtcomes, and Therapies point prevalence study: acute kidney injury was defined on the study day using Kidney Disease Improving Global Outcomes definitions. Patients with no acute kidney injury or stage 1 acute kidney injury ("no/mild acute kidney injury") were compared with those with stage 2 or 3 acute kidney injury ("severe acute kidney injury"). The primary outcome was a composite of death or new moderate disability at discharge defined as a Pediatric Overall Performance Category score of 3 or higher and increased by 1 from baseline. Setting: One hundred twenty-eight PICUs in 26 countries. Patients: Children with severe sepsis in the Sepsis PRevalence, OUtcomes, and Therapies study. Interventions: None. Measurements and Main Results: One hundred two (21%) of 493 patients had severe acute kidney injury. More than twice as many patients with severe acute kidney injury died or developed new moderate disability compared with those with no/mild acute kidney injury (64% vs 30%; p < 0.001). Severe acute kidney injury was independently associated with death or new moderate disability (adjusted odds ratio, 2.5; 95% CI, 1.5-4.2; p = 0.001) after adjustment for age, region, baseline disability, malignancy, invasive mechanical ventilation, albumin administration, and the pediatric logistic organ dysfunction score. Conclusions: In a multinational cohort of critically ill children with severe sepsis and high mortality rates, septic acute kidney injury is independently associated with further increased death or new disability.
- Published
- 2016
20. Comparison of pediatric severe sepsis managed in U.S. and European ICUs
- Author
-
Giuliano, John S., Markovitz, Barry P., Brierley, Joe, Levin, Richard, Williams, Gary, Lum, Lucy Chai See, Dorofaeff, Tavey, Cruces, Pablo, Bush, Jenny L., Keele, Luke, Nadkarni, V., Thomas, Neal J., Fitzgerald, Julie C., Weiss, Scott L., Fontela, P., Tucci, M., Dumistrascu, M., Skippen, P., Krahn, G., Bezares, E., Puig, G., Puig-Ramos, A., Garcia, R., Villar, M., Bigham, M., Polanski, T., Latifi, S., Giebner, D., Anthony, H., Hume, J., Galster, A., Linnerud, L., Sanders, R., Hefley, G., Madden, K., Thompson, A., Shein, S., Gertz, S., Han, Y., Williams, T., Hughes-Schalk, A., Chandler, H., Orioles, A., Zielinski, E., Doucette, A., Zebuhr, C., Wilson, T., Dimitriades, C., Ascani, J., Layburn, S., Valley, S., Terry, J., Morzov, R., McInnes, A., McArthur, J., Woods, K., Murkowski, K., Spaeder, M., Sharron, M., Wheeler, D., Beckman, E., Frank, E., Howard, K., Carroll, C., Nett, S., Jarvis, D., Patel, V., Higgerson, R., Christie, L., Typpo, K., Deschenes, J., Kirby, A., Uhl, T., Rehder, K., Cheifetz, I., Wrenn, S., Kypuros, K., Ackerman, K., Maffei, F., Bloomquist, G., Rizkalla, N., Kimura, D., Shah, S., Tigges, C., Su, F., Barlow, C., Michelson, K., Wolfe, K., Goodman, D., Campbell, L., Sorce, L., Bysani, K., Monjure, T., Evans, M., Totapally, B., Chegondi, M., Rodriguez, C., Frazier, J., Steele, L., Viteri, S., Costarino, A., Spear, D., Hirshberg, E., Lilley, J., Rowan, C., Rider, C., Kane, J., Zimmerman, J., Greeley, C., Lin, J., Jacobs, R., Parker, M., Culver, K., Loftis, L., Jaimon, N., Goldsworthy, M., Diliberto, M., Alen, C., Gessouroun, M., Sapru, A., Lang, T., Alkhouli, M., Kamath, S., Friel, D., Daufeldt, J., Hsing, D., Carlo, C., Pon, S., Scimeme, J., Shaheen, A., Hassinger, A., Qiao, H., Tala, J., Vinciguerra, D., Fernandez, A., Carrero, R., Hoyos, P., Jaramillo, J., Posada, A., Izquiierdo, L., Piñeres Olave, B. E., Donado, J., Dalmazzo, R., Rendich, S., Palma, L., Lapadula, M., Acuna, C., Clement De Clety, S., Dujardin, M., Berghe, C., Renard, S., Zurek, J., Steinherr, H., Mougkou, K., Critselis, E., Di Nardo, M., Picardo, S., Tortora, F., Rossetti, E., Fragasso, T., Cogo, P., Netto, R., Dagys, A., Gurskis, V., Kevalas, R., Neeleman, C., Lemson, J., Luijten, C., Wojciech, K., Pagowska-Klimek, I., Szczepanska, M., Karpe, J., Nunes, P., Almeida, H., Rios, J., Vieira, M., Revilla, P., Urbano, J., Lopez-Herce, J., Bustinza, A., Cuesta, A., Hofheinz, S., Rodriguez-Nunez, A., Sanagustin, S., Gonzalez, E., Riaza, M., Piaya, R., Soler, P., Esteban, E., Laraudogoitia, J., Monge, C., Herrera, V., Granados, J., Gonzalez, C., Koroglu, T., Ozcelik, E., Baines, P., Plunkett, A., Davis, P., George, S., Tibby, S., Harris, J., Agbeko, R., Lampitt, R., Peters, M., Jones, A., Dominguez, T., Thiruchelvam, T., Deep, A., Ridley, L., Bowen, W., Macleod, I., Gray, M., Hemat, N., Alexander, J., Ali, S., Pappachan, J., McCorkell, J., Fortune, P., MacDonald, M., Hudnott, P., Suyun, Q., Singhi, S., Nallasamy, K., Lodha, R., Shime, N., Tabata, Y., Saito, O., Ikeyama, T., Kawasaki, T., Abidin, A., Kee, S., Tang, S., Jalil, R., Guan, Y., Yao, L., Lin, K., Ong, J., Salloo, A., Doedens, L., Mathivha, L., Reubenson, G., Moaisi, S., Pentz, A., Green, R., Giuliano, John S., Markovitz, Barry P., Brierley, Joe, Levin, Richard, Williams, Gary, Lum, Lucy Chai See, Dorofaeff, Tavey, Cruces, Pablo, Bush, Jenny L., Keele, Luke, Nadkarni, V., Thomas, Neal J., Fitzgerald, Julie C., Weiss, Scott L., Fontela, P., Tucci, M., Dumistrascu, M., Skippen, P., Krahn, G., Bezares, E., Puig, G., Puig-Ramos, A., Garcia, R., Villar, M., Bigham, M., Polanski, T., Latifi, S., Giebner, D., Anthony, H., Hume, J., Galster, A., Linnerud, L., Sanders, R., Hefley, G., Madden, K., Thompson, A., Shein, S., Gertz, S., Han, Y., Williams, T., Hughes-Schalk, A., Chandler, H., Orioles, A., Zielinski, E., Doucette, A., Zebuhr, C., Wilson, T., Dimitriades, C., Ascani, J., Layburn, S., Valley, S., Terry, J., Morzov, R., McInnes, A., McArthur, J., Woods, K., Murkowski, K., Spaeder, M., Sharron, M., Wheeler, D., Beckman, E., Frank, E., Howard, K., Carroll, C., Nett, S., Jarvis, D., Patel, V., Higgerson, R., Christie, L., Typpo, K., Deschenes, J., Kirby, A., Uhl, T., Rehder, K., Cheifetz, I., Wrenn, S., Kypuros, K., Ackerman, K., Maffei, F., Bloomquist, G., Rizkalla, N., Kimura, D., Shah, S., Tigges, C., Su, F., Barlow, C., Michelson, K., Wolfe, K., Goodman, D., Campbell, L., Sorce, L., Bysani, K., Monjure, T., Evans, M., Totapally, B., Chegondi, M., Rodriguez, C., Frazier, J., Steele, L., Viteri, S., Costarino, A., Spear, D., Hirshberg, E., Lilley, J., Rowan, C., Rider, C., Kane, J., Zimmerman, J., Greeley, C., Lin, J., Jacobs, R., Parker, M., Culver, K., Loftis, L., Jaimon, N., Goldsworthy, M., Diliberto, M., Alen, C., Gessouroun, M., Sapru, A., Lang, T., Alkhouli, M., Kamath, S., Friel, D., Daufeldt, J., Hsing, D., Carlo, C., Pon, S., Scimeme, J., Shaheen, A., Hassinger, A., Qiao, H., Tala, J., Vinciguerra, D., Fernandez, A., Carrero, R., Hoyos, P., Jaramillo, J., Posada, A., Izquiierdo, L., Piñeres Olave, B. E., Donado, J., Dalmazzo, R., Rendich, S., Palma, L., Lapadula, M., Acuna, C., Clement De Clety, S., Dujardin, M., Berghe, C., Renard, S., Zurek, J., Steinherr, H., Mougkou, K., Critselis, E., Di Nardo, M., Picardo, S., Tortora, F., Rossetti, E., Fragasso, T., Cogo, P., Netto, R., Dagys, A., Gurskis, V., Kevalas, R., Neeleman, C., Lemson, J., Luijten, C., Wojciech, K., Pagowska-Klimek, I., Szczepanska, M., Karpe, J., Nunes, P., Almeida, H., Rios, J., Vieira, M., Revilla, P., Urbano, J., Lopez-Herce, J., Bustinza, A., Cuesta, A., Hofheinz, S., Rodriguez-Nunez, A., Sanagustin, S., Gonzalez, E., Riaza, M., Piaya, R., Soler, P., Esteban, E., Laraudogoitia, J., Monge, C., Herrera, V., Granados, J., Gonzalez, C., Koroglu, T., Ozcelik, E., Baines, P., Plunkett, A., Davis, P., George, S., Tibby, S., Harris, J., Agbeko, R., Lampitt, R., Peters, M., Jones, A., Dominguez, T., Thiruchelvam, T., Deep, A., Ridley, L., Bowen, W., Macleod, I., Gray, M., Hemat, N., Alexander, J., Ali, S., Pappachan, J., McCorkell, J., Fortune, P., MacDonald, M., Hudnott, P., Suyun, Q., Singhi, S., Nallasamy, K., Lodha, R., Shime, N., Tabata, Y., Saito, O., Ikeyama, T., Kawasaki, T., Abidin, A., Kee, S., Tang, S., Jalil, R., Guan, Y., Yao, L., Lin, K., Ong, J., Salloo, A., Doedens, L., Mathivha, L., Reubenson, G., Moaisi, S., Pentz, A., and Green, R.
- Abstract
Objectives: Pediatric severe sepsis remains a significant global health problem without new therapies despite many multicenter clinical trials. We compared children managed with severe sepsis in European and U.S. PICUs to identify geographic variation, which may improve the design of future international studies. Design: We conducted a secondary analysis of the Sepsis PRevalence, OUtcomes, and Therapies study. Data about PICU characteristics, patient demographics, therapies, and outcomes were compared. Multivariable regression models were used to determine adjusted differences in morbidity and mortality. Setting: European and U.S. PICUs. Patients: Children with severe sepsis managed in European and U.S. PICUs enrolled in the Sepsis PRevalence, OUtcomes, and Therapies study. Interventions: None. Measurements and Main Results: European PICUs had fewer beds (median, 11 vs 24; p < 0.001). European patients were younger (median, 1 vs 6 yr; p < 0.001), had higher severity of illness (median Pediatric Index of Mortality-3, 5.0 vs 3.8; p = 0.02), and were more often admitted from the ward (37% vs 24%). Invasive mechanical ventilation, central venous access, and vasoactive infusions were used more frequently in European patients (85% vs 68%, p = 0.002; 91% vs 82%, p = 0.05; and 71% vs 50%; p < 0.001, respectively). Raw morbidity and mortality outcomes were worse for European compared with U.S. patients, but after adjusting for patient characteristics, there were no significant differences in mortality, multiple organ dysfunction, disability at discharge, length of stay, or ventilator/vasoactive-free days. Conclusions: Children with severe sepsis admitted to European PICUs have higher severity of illness, are more likely to be admitted from hospital wards, and receive more intensive care therapies than in the United States. The lack of significant differences in morbidity and mortality after
- Published
- 2016
21. Comparison of Pediatric Severe Sepsis Managed in U.S. and European ICUs
- Author
-
Giuliano, J., Markovitz, B., Brierley, J., Levin, R., Williams, G., Lum, L., Dorofaeff, T., Cruces, P., Bush, J., Keele, L., Nadkarni, V., Thomas, N., Fitzgerald, J., Weiss, S., Fontela, P., Tucci, M., Dumistrascu, M., Skippen, P., Krahn, G., Bezares, E., Puig, G., Puig-Ramos, A., Garcia, R., Villar, M., Bigham, M., Polanski, T., Latifi, S., Giebner, D., Anthony, H., Hume, J., Galster, A., Linnerud, L., Sanders, R., Hefley, G., Madden, K., Thompson, A., Shein, S., Gertz, S., Han, Y., Williams, Teresa, Hughes-Schalk, A., Chandler, H., Orioles, A., Zielinski, E., Doucette, A., Zebuhr, C., Wilson, T., Dimitriades, C., Ascani, J., Layburn, S., Valley, S., Markowitz, B., Terry, J., Morzov, R., McInnes, A., McArthur, J., Woods, K., Murkowski, K., Spaeder, M., Sharron, M., Wheeler, D., Beckman, E., Frank, E., Howard, K., Carroll, C., Nett, S., Jarvis, D., Patel, V., Higgerson, R., Christie, L., Typpo, K., Deschenes, J., Kirby, A., Uhl, T., Rehder, K., Cheifetz, I., Wrenn, S., Kypuros, K., Ackerman, K., Maffei, F., Bloomquist, G., Rizkalla, N., Kimura, D., Shah, S., Tigges, C., Su, F., Barlow, C., Michelson, K., Wolfe, K., Goodman, D., Campbell, L., Sorce, L., Bysani, K., Monjure, T., Evans, M., Totapally, B., Chegondi, M., Giuliano, J., Markovitz, B., Brierley, J., Levin, R., Williams, G., Lum, L., Dorofaeff, T., Cruces, P., Bush, J., Keele, L., Nadkarni, V., Thomas, N., Fitzgerald, J., Weiss, S., Fontela, P., Tucci, M., Dumistrascu, M., Skippen, P., Krahn, G., Bezares, E., Puig, G., Puig-Ramos, A., Garcia, R., Villar, M., Bigham, M., Polanski, T., Latifi, S., Giebner, D., Anthony, H., Hume, J., Galster, A., Linnerud, L., Sanders, R., Hefley, G., Madden, K., Thompson, A., Shein, S., Gertz, S., Han, Y., Williams, Teresa, Hughes-Schalk, A., Chandler, H., Orioles, A., Zielinski, E., Doucette, A., Zebuhr, C., Wilson, T., Dimitriades, C., Ascani, J., Layburn, S., Valley, S., Markowitz, B., Terry, J., Morzov, R., McInnes, A., McArthur, J., Woods, K., Murkowski, K., Spaeder, M., Sharron, M., Wheeler, D., Beckman, E., Frank, E., Howard, K., Carroll, C., Nett, S., Jarvis, D., Patel, V., Higgerson, R., Christie, L., Typpo, K., Deschenes, J., Kirby, A., Uhl, T., Rehder, K., Cheifetz, I., Wrenn, S., Kypuros, K., Ackerman, K., Maffei, F., Bloomquist, G., Rizkalla, N., Kimura, D., Shah, S., Tigges, C., Su, F., Barlow, C., Michelson, K., Wolfe, K., Goodman, D., Campbell, L., Sorce, L., Bysani, K., Monjure, T., Evans, M., Totapally, B., and Chegondi, M.
- Abstract
Copyright © 2016 by the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies.Objectives: Pediatric severe sepsis remains a significant global health problem without new therapies despite many multicenter clinical trials. We compared children managed with severe sepsis in European and U.S. PICUs to identify geographic variation, which may improve the design of future international studies. Design: We conducted a secondary analysis of the Sepsis PRevalence, OUtcomes, and Therapies study. Data about PICU characteristics, patient demographics, therapies, and outcomes were compared. Multivariable regression models were used to determine adjusted differences in morbidity and mortality. Setting: European and U.S. PICUs. Patients: Children with severe sepsis managed in European and U.S. PICUs enrolled in the Sepsis PRevalence, OUtcomes, and Therapies study. Interventions: None. Measurements and Main Results: European PICUs had fewer beds (median, 11 vs 24; p < 0.001). European patients were younger (median, 1 vs 6 yr; p < 0.001), had higher severity of illness (median Pediatric Index of Mortality-3, 5.0 vs 3.8; p = 0.02), and were more often admitted from the ward (37% vs 24%). Invasive mechanical ventilation, central venous access, and vasoactive infusions were used more frequently in European patients (85% vs 68%, p = 0.002; 91% vs 82%, p = 0.05; and 71% vs 50%; p < 0.001, respectively). Raw morbidity and mortality outcomes were worse for European compared with U.S. patients, but after adjusting for patient characteristics, there were no significant differences in mortality, multiple organ dysfunction, disability at discharge, length of stay, or ventilator/vasoactive-free days. Conclusions: Children with severe sepsis admitted to European PICUs have higher severity of illness, are more likely to be admitted from hospital wards, and receive more intensive care therapies than in the United States. The lack of
- Published
- 2016
22. Ministers' Perceptions of Foster Care, Adoptions, and the Role of the Black Church
- Author
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Fay Roseman and Sharron M. Singleton
- Subjects
African american ,Gerontology ,Economic growth ,Resource (biology) ,Sociology and Political Science ,Black church ,media_common.quotation_subject ,education ,Survey research ,humanities ,Additional research ,Foster care ,Work (electrical) ,Political science ,Perception ,Law ,Demography ,media_common - Abstract
Results from survey research of 51 Black ministers indicate that the Black church is potentially an untapped resource for the placement of African American children in permanent homes. The study population indicated knowledge of the need for African American foster care and adoptive families but did not include this need as part of the focus of work for their respective churches. Implications for additional research are highlighted.
- Published
- 2004
23. Multiple nonfunctional alleles of CCR5 are frequent in various human populations
- Author
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Blanpain, C., Benhur Lee, Tackoen, M., Puffer, B., Boom, A., Libert, F., Sharron, M., Wittamer, V., Vassart, G., Doms, R. W., and Parmentier, M.
- Subjects
Receptors, CCR5 ,Recombinant Fusion Proteins ,Molecular Sequence Data ,Immunology ,Gene Expression ,Receptors, Cell Surface ,CHO Cells ,HIV Envelope Protein gp120 ,Binding, Competitive ,Biochemistry ,Cell Line ,Iodine Radioisotopes ,Radioligand Assay ,Cricetinae ,Animals ,Humans ,Amino Acid Sequence ,Chemokine CCL4 ,Luciferases ,Alleles ,Chemokine CCL3 ,Dose-Response Relationship, Drug ,Cell Biology ,Hematology ,Macrophage Inflammatory Proteins ,Mutation ,HIV-1 ,Cytokines ,Protein Binding - Abstract
CCR5 is the major coreceptor for macrophage-tropic strains of the human immunodeficiency virus type I (HIV-1). Homozygotes for a 32-base pair (bp) deletion in the coding sequence of the receptor (CCR5Delta32) were found to be highly resistant to viral infection, and CCR5 became, therefore, one of the paradigms illustrating the influence of genetic variability onto individual susceptibility to infectious and other diseases. We investigated the functional consequences of 16 other natural CCR5 mutations described in various human populations. We found that 10 of these variants are efficiently expressed at the cell surface, bind [(125)I]-MIP-1beta with affinities similar to wtCCR5, respond functionally to chemokines, and act as HIV-1 coreceptors. In addition to Delta32, six mutations were characterized by major alterations in their functional response to chemokines, as a consequence of intracellular trapping and poor expression at the cell surface (C101X, FS299), general or specific alteration of ligand binding affinities (C20S, C178R, A29S), or relative inability to mediate receptor activation (L55Q). A29S displayed an unusual pharmacological profile, binding and responding to MCP-2 similarly to wtCCR5, but exhibiting severely impaired binding and functional responses to MIP-1alpha, MIP-1beta, and RANTES. In addition to Delta32, only C101X was totally unable to mediate entry of HIV-1. The fact that nonfunctional CCR5 alleles are relatively frequent in various human populations reinforces the hypothesis of a selective pressure favoring these alleles. (Blood. 2000;96:1638-1645)
- Published
- 2000
24. Discordant identification of pediatric severe sepsis by research and clinical definitions in the SPROUT international point prevalence study
- Author
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Weiss, S., Fitzgerald, J., Maffei, F., Kane, J., Rodriguez-Nunez, A., Hsing, D., Franzon, D., Kee, S., Bush, J., Roy, J., Thomas, N., Nadkarni, V., Fontela, P., Tucci, M., Dumistrascu, M., Skippen, P., Krahn, G., Bezares, E., Puig, G., Puig-Ramos, A., Garcia, R., Villar, M., Bigham, M., Polanski, T., Latifi, S., Giebner, D., Anthony, H., Hume, J., Galster, A., Linnerud, L., Sanders, R., Hefley, G., Madden, K., Thompson, A., Shein, S., Gertz, S., Han, Y., Williams, Teresa, Hughes-Schalk, A., Chandler, H., Orioles, A., Zielinski, E., Doucette, A., Zebuhr, C., Wilson, T., Dimitriades, C., Ascani, J., Layburn, S., Valley, S., Markowitz, B., Terry, J., Morzov, R., McInnes, A., McArthur, J., Woods, K., Murkowski, K., Spaeder, M., Sharron, M., Wheeler, D., Beckman, E., Frank, E., Howard, K., Carroll, C., Nett, S., Jarvis, D., Patel, V., Higgerson, R., Christie, L., Typpo, K., Deschenes, J., Kirby, A., Uhl, T., Rehder, K., Cheifetz, I., Wrenn, S., Kypuros, K., Ackerman, K., Bloomquist, G., Rizkalla, N., Kimura, D., Shah, S., Tigges, C., Su, F., Barlow, C., Michelson, K., Wolfe, K., Goodman, D., Campbel, L., Sorce, L., Bysani, K., Monjure, T., Evans, M., Totapally, B., Chegondi, M., Rodriguez, C., Frazier, J., Weiss, S., Fitzgerald, J., Maffei, F., Kane, J., Rodriguez-Nunez, A., Hsing, D., Franzon, D., Kee, S., Bush, J., Roy, J., Thomas, N., Nadkarni, V., Fontela, P., Tucci, M., Dumistrascu, M., Skippen, P., Krahn, G., Bezares, E., Puig, G., Puig-Ramos, A., Garcia, R., Villar, M., Bigham, M., Polanski, T., Latifi, S., Giebner, D., Anthony, H., Hume, J., Galster, A., Linnerud, L., Sanders, R., Hefley, G., Madden, K., Thompson, A., Shein, S., Gertz, S., Han, Y., Williams, Teresa, Hughes-Schalk, A., Chandler, H., Orioles, A., Zielinski, E., Doucette, A., Zebuhr, C., Wilson, T., Dimitriades, C., Ascani, J., Layburn, S., Valley, S., Markowitz, B., Terry, J., Morzov, R., McInnes, A., McArthur, J., Woods, K., Murkowski, K., Spaeder, M., Sharron, M., Wheeler, D., Beckman, E., Frank, E., Howard, K., Carroll, C., Nett, S., Jarvis, D., Patel, V., Higgerson, R., Christie, L., Typpo, K., Deschenes, J., Kirby, A., Uhl, T., Rehder, K., Cheifetz, I., Wrenn, S., Kypuros, K., Ackerman, K., Bloomquist, G., Rizkalla, N., Kimura, D., Shah, S., Tigges, C., Su, F., Barlow, C., Michelson, K., Wolfe, K., Goodman, D., Campbel, L., Sorce, L., Bysani, K., Monjure, T., Evans, M., Totapally, B., Chegondi, M., Rodriguez, C., and Frazier, J.
- Abstract
Introduction: Consensus criteria for pediatric severe sepsis have standardized enrollment for research studies. However, the extent to which critically ill children identified by consensus criteria reflect physician diagnosis of severe sepsis, which underlies external validity for pediatric sepsis research, is not known. We sought to determine the agreement between physician diagnosis and consensus criteria to identify pediatric patients with severe sepsis across a network of international pediatric intensive care units (PICUs). Methods: We conducted a point prevalence study involving 128 PICUs in 26 countries across 6 continents. Over the course of 5 study days, 6925 PICU patients <18 years of age were screened, and 706 with severe sepsis defined either by physician diagnosis or on the basis of 2005 International Pediatric Sepsis Consensus Conference consensus criteria were enrolled. The primary endpoint was agreement of pediatric severe sepsis between physician diagnosis and consensus criteria as measured using Cohen's ?. Secondary endpoints included characteristics and clinical outcomes for patients identified using physician diagnosis versus consensus criteria. Results: Of the 706 patients, 301 (42.6 %) met both definitions. The inter-rater agreement (? ± SE) between physician diagnosis and consensus criteria was 0.57 ± 0.02. Of the 438 patients with a physician's diagnosis of severe sepsis, only 69 % (301 of 438) would have been eligible to participate in a clinical trial of pediatric severe sepsis that enrolled patients based on consensus criteria. Patients with physician-diagnosed severe sepsis who did not meet consensus criteria were younger and had lower severity of illness and lower PICU mortality than those meeting consensus criteria or both definitions. After controlling for age, severity of illness, number of comorbid conditions, and treatment in developed versus resource-limited regions, patients identified with severe sepsis by physician diagnosis
- Published
- 2015
25. Contributors
- Author
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Beverley Ann Alderton, Jonathan W. Ball, Alberto Rodriguez Barbon, Margaret Batchelder, Hugues Beaufrère, Michelle Bingley, Michael C. Blanco, Teresa Bradley Bays, Cynthia J. Brown, Anne Burgdorf-Moisuk, Michael V. Campagna, Michelle L. Campbell-Ward, Brendan Carmel, Cathy T.T. Chan, Jaime Chin, John Chitty, Deborah Cottrell, David A. Crum, Julie DeCubellis, Stephen J. Divers, Thomas M. Donnelly, Michael Dutton, Will Easson, David Eshar, Brian A. Evans, Peter G. Fischer, James G. Fox, Amy J. Funk, Alexis García, Jennifer Graham, Caroline Hahn, Katleen Hermans, Candace Hersey-Benner, Gretta Howard, Gwendolyn R. Jankowski, Emma Keeble, Dominique L. Keller, Peter Kerr, Sharron M. Kirchain, Megan Kirchgessner, La'Toya Latney, John Henry Lewington, Brad A. Lock, Rebecca L. Malakoff, Caralee Manley, Christoph Mans, Robert P. Marini, Jorge Martínez, Jörg Mayer, Anna Meredith, Huynh Minh, Mark A. Mitchell, Holly S. Mullen, Jason Norman, Brian S. Palmeiro, Jean A. Paré, Mary M. Patterson, David Perpiñán, Carrie A. Phelps, Charly Pignon, Anthony A. Pilny, Chantale L. Pinard, Romain Pizzi, Christal Pollock, Lauren V. Powers, Aidan Raftery, Viviane Silva Raymundo, Drury R. Reavill, Virgina C.G. Richardson, Cecilia Robat, Helen E. Roberts, William Rosenblad, David Sanchez-Migallon Guzman, Richard A. Saunders, Shannon N. Shaw, James L. (Jay) Shelton, Alana Shrubsole-Cockwill, Nico J. Schoemaker, Jeffrey Smith, Scott J. Stahl, Simon R. Starkey, W. Michael Taylor, Thomas N. Tully, Molly Varga, David Vella, Wolf von Bomhard, Narelle Walter, James F.X. Wellehan, Cameron J.G. Whittaker, Katherine E. Whitwell, Bruce H. Williams, Kimberlee B. Wojick, Kevin M. Wright, Nicole R. Wyre, and Trevor T. Zachariah
- Published
- 2013
26. Improvisation as a Concept for Understanding and Treating Violent Behavior among African American Youth
- Author
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Walter J. Pierce and Sharron M. Singleton
- Subjects
Improvisation ,Minority group ,media_common.quotation_subject ,05 social sciences ,Behavioural sciences ,Poison control ,050109 social psychology ,Empathy ,Racism ,0501 psychology and cognitive sciences ,Social organization ,Sociocultural evolution ,Psychology ,Social psychology ,Social Sciences (miscellaneous) ,050104 developmental & child psychology ,media_common - Abstract
VioLit summary: OBJECTIVE: This paper by Pierce and Singleton introduced the concept of improvisation to better understand and treat violence among African-American youth. METHODOLOGY: The authors employed a non-experimental critical review of the literature. FINDINGS/DISCUSSION: The authors argued that African-American youth employ a strategy of improvisation to achieve their goals. They defined improvisation as "the means of making do with what one has, using the resources immediately available" (p. 445). According to the authors, African-Americans were forced, due to limited resources, to use the strategy of improvisation throughout their history in the United States. First, African-Americans in the days of slavery employed several improvisational strategies. Slaves developed their own language to preserve their cultural heritage. They performed the role of the 'happy slave.' They also used spiritual gatherings as a mechanism to develop and maintain some sort of social support network. During and after Reconstruction, the environment remained hostile for African-Americans in the United States. Again, their access to the means of achievement was limited. The improvisational strategies commonly employed in this time were to script or plan interactions with whites and to develop and maintain their own social support networks. The authors argued that throughout their history in the U.S., African-Americans learned that the future was unpredictable and learned to focus on short term goals to survive, i.e., they learned to become oriented to the present rather than the future. According to the authors, both of these lessons contribute to the violence common among African-Americans. However, the authors acknowledged current lessons that also contribute to the prevalence of violence. First, it was argued that African-Americans deny their feelings and experiences, hence, losing some of their empathic ability. Second, it was argued that African-American youth learn to mimic conventional behavior just to get by. Third, the authors contended that games such as 'dozens' are improvisational techniques that enables the youth to practice defending themselves in unpredictable situations. According to the authors, each of these improvisational strategies helped many in this community cope with the limited opportunities available to African-Americans in the U.S. AUTHORS' RECOMMENDATIONS: The authors suggested that the concept of improvisation could not only help shed light on violence committed by African-American youth but could serve as a guide to construct meaningful and cost efficient intervention strategies. In general, the authors suggested that role playing exercises, accompanied by analyses of performance, could help young people come to grips with their fears in certain everyday violence-provoking situations. Moreover, they suggested alternative, non-violent improvisational strategies could be identified and practiced. The authors argued that such role playing could also help develop empathy by having individuals play victims. (CSPV Abstract - Copyright © 1992-2007 by the Center for the Study and Prevention of Violence, Institute of Behavioral Science, Regents of the University of Colorado) Juvenile Offender Juvenile Treatment Juvenile Violence Violence Treatment African American Violence African American Offender African American Juvenile Minority Group Violence Intervention Violence Causes Violence Treatment Literature Review Social Organization Sociocultural Factors Socioeconomic Factors Environmental Factors History of Crime-Violence Racism Racial Factors 10-03
- Published
- 1995
27. Faculty Personal Comfort and the Teahing of Content on Racial Oppression
- Author
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Sharron M. Singleton
- Subjects
Oppression ,Health (social science) ,Social work ,Higher education ,business.industry ,media_common.quotation_subject ,Professional development ,Racism ,Grounded theory ,Education ,Consciousness raising ,Pedagogy ,Sociology ,business ,Content (Freudian dream analysis) ,media_common - Abstract
In-depth interviews were conducted with faculty from four East Coast schools of social work. Personal comfort in the teaching of oppression content was analyzed using grounded theory methodology. Findings about the origins, nature, consequences and management of discomfort are presented.
- Published
- 1994
28. An Exploratory Study of Physical Phenotype, Biomarkers and Psychosocial Health Parameters in Boys with Klinefelter Syndrome
- Author
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Close, Sharron M.
- Subjects
Endocrinology ,FOS: Biological sciences ,Genetics ,Nursing ,FOS: Health sciences - Abstract
Klinefelter Syndrome (KS) is a genetic condition that occurs only in males. In adult men, KS is associated with reproductive, cardiometabolic, bone and psychosocial health problems that are believed to emerge during peri-puberty. In children, the condition is under-diagnosed and not well understood due to the wide-ranging spectrum of physical features. Although pediatric studies are rare, androgen deficiency is believed to underlie many of the KS-related abnormalities in both physical and emotional well-being. The purpose of this dissertation was to systematically describe the physical and psychosocial health of peri-pubertal boys with KS. Aim I of the study was to explore associations between physical and psychosocial health while Aim II explored body composition and bone mineral density. For Aim I, a cross-sectional exploratory study examining the associations between physical phenotype, reproductive hormones, cardiometabolic risk factors, and psychosocial health was conducted in a sample of 43 boys with KS between the ages of 8 and 18 years. Physical examination, laboratory and self-administered psychosocial health data were analyzed using descriptive statistics and univariate and multivariate linear regression techniques. For Aim II, a retrospective chart review examining body composition and bone mineral density (BMD) was conducted of 20 KS patients ages 8-18 years who attended a pediatric endocrine practice at a Columbia University-affiliated hospital. Aim I participants demonstrated a range of physical phenotype features. On average, boys showed at least 5 KS physical traits. Gonadotropins were elevated without androgen deficiency in most boys. Adverse cardiovascular risk factors were observed in about a third of the boys with higher frequency in pubertal boys. Quality of life and self-esteem scores were low compared to reference standards; average scores for self-concept and depression were within the normal range. Physical phenotype was inversely associated with quality of life, but not with the other measures of psychosocial health. Low testosterone was associated with interpersonal problem subscale of the Children's Depression Inventory, but not for other psychosocial measures. Serum testosterone was not associated with cardiometabolic biomarkers. For Aim II, boys with KS demonstrated a higher mean body fat by Dual Energy Xray Aborptiometry (DEXA) compared to a healthy reference group and overall mean normal lumbar spine BMD. Four of the oldest boys demonstrated lower BMD than expected for age. Findings from this study suggest that in peri-pubertal boys with KS, phenotype may adversely influence quality of life especially with respect to school and physical function. The adverse psychosocial health of boys with KS may not be related to androgen deficiency. Biomarkers of cardiometabolic risk were most evident in pubertal boys. Testosterone does not appear to be a main mediating factor in cardiometabolic risk in this age group. KS boys may have increased fat as measured by DEXA and normal BMD. The onset of bone loss present in KS men may begin in late adolescence. The implications from this study include recommendations that primary care providers and developmental specialists become more familiar with the clinical pattern of KS as represented by physical, hormonal as well as behavioral signs and symptoms. In primary care, it is recommended that complete genital examination including testicular volume measurement be conducted during well-child visits and that karyotype be ordered on boys who show a high index of suspicion for this diagnosis. A multidisciplinary team-approach for management KS-related symptoms needs to be created for each child and family affected by KS with integration of services between pediatrician, endocrinologist, developmental, psychological and school specialists. It is also recommended that boys with KS be referred for baseline bone mineral assessment during adolescence.
- Published
- 2011
- Full Text
- View/download PDF
29. Discordant identification of pediatric severe sepsis by research and clinical definitions in the SPROUT international point prevalence study
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Weiss, Scott L, Fitzgerald, Julie C., Maffei, Frank A., Kane, Jason M., Rodriguez Nunez, Antonio, Hsing, Deyin D., Franzon, Deborah, Kee, Sze Ying, Bush, Jenny L., Roy, Jason A., Thomas, Neal J., Nadkarni, Vinay M., Fontela, P., Tucci, M., Dumistrascu, M., Skippen, P., Krahn, G., Bezares, E., Puig, G., Puig Ramos, A., Garcia, R., Villar, M., Bigham, M., Polanski, T., Latifi, S., Giebner, D., Anthony, H., Hume, J., Galster, A., Linnerud, L., Sanders, R., Hefley, G., Madden, K., Thompson, A., Shein, S., Gertz, S., Han, Y., Williams, T., Hughes Schalk, A., Chandler, H., Orioles, A., Zielinski, E., Doucette, A., Zebuhr, C., Wilson, T., Dimitriades, C., Ascani, J., Layburn, S., Valley, S., Markowitz, B., Terry, J., Morzov, R., Mcinnes, A., Mcarthur, J., Woods, K., Murkowski, K., Spaeder, M., Sharron, M., Wheeler, D., Beckman, E., Frank, E., Howard, K., Carroll, C., Nett, S., Jarvis, D., Patel, V., Higgerson, R., Christie, L., Typpo, K., Deschenes, J., Kirby, A., Uhl, T., Rehder, K., Cheifetz, I., Wrenn, S., Kypuros, K., Ackerman, K., Maffei, F., Bloomquist, G., Rizkalla, N., Kimura, D., Shah, S., Tigges, C., Su, F., Barlow, C., Michelson, K., Wolfe, K., Goodman, D., Campbel, L., Sorce, L., Bysani, K., Monjure, T., Evans, M., Totapally, B., Chegondi, M., Rodriguez, C., Frazier, J., Steele, L., Viteri, S., Costarino, A., Thomas, N., Spear, D., Hirshberg, E., Lilley, J., Rowan, C., Rider, C., Kane, J., Zimmerman, J., Greeley, C., Lin, J., Jacobs, R., Parker, M., Culver, K., Loftis, L., Jaimon, N., Goldsworthy, M., Fitzgerald, J., Weiss, S., Nadkarni, V., Bush, J., Diliberto, M., Alen, C., Gessouroun, M., Sapru, A., Lang, T., Alkhouli, M., Kamath, S., Friel, D., Daufeldt, J., Hsing, D., Carlo, C., Pon, S., Scimeme, J., Shaheen, A., Hassinger, A., Qiao, H., Giuliano, J., Tala, J., Vinciguerra, D., Fernandez, A., Carrero, R., Hoyos, P., Jaramillo, J., Posada, A., Izquiierdo, L., Piñeres Olave, B. E., Donado, J., Dalmazzo, R., Rendich, S., Palma, L., Lapadula, M., Acuna, C., Cruces, P., Clement De Clety, S., Dujardin, M., Berghe, C., Renard, S., Zurek, J., Steinherr, H., Mougkou, K., Critselis, E., Di Nardo, M., Picardo, S., Tortora, F., Rossetti, E., Fragasso, T., Cogo, Paola, Netto, R., Dagys, A., Gurskis, V., Kevalas, R., Neeleman, C., Lemson, J., Luijten, C., Wojciech, K., Pagowska Klimek, I., Szczepanska, M., Karpe, J., Nunes, P., Almeida, H., Rios, J., Vieira, M., Revilla, P., Urbano, J., Lopez Herce, J., Bustinza, A., Cuesta, A., Hofheinz, S., Rodriguez Nunez, A., Sanagustin, S., Gonzalez, E., Riaza, M., Piaya, R., Soler, P., Esteban, E., Laraudogoitia, J., Monge, C., Herrera, V., Granados, J., Gonzalez, C., Koroglu, T., Ozcelik, E., Baines, P., Plunkett, A., Davis, P., George, S., Tibby, S., Harris, J., Agbeko, R., Lampitt, R., Bierley, J., Peters, M., Jones, A., Dominguez, T., Thiruchelvam, T., Deep, A., Ridley, L., Bowen, W., Levin, R., Macleod, I., Gray, M., Hemat, N., Alexander, J., Ali, S., Pappachan, J., Mccorkell, J., Schibler, A., Fortune, P., Macdonald, M., Hudnott, P., Erickson, S., Millar, J., Delzoppo, C., Williams, G., Morritt, M., Mceneiry, J., Long, D., Dorofaeff, T., Coulthard, M., Watts, N., Suyun, Q., Singhi, S., Nallasamy, K., Lodha, R., Shime, N., Tabata, Y., Saito, O., Ikeyama, T., Kawasaki, T., Lum, L., Abidin, A., Kee, S., Tang, S., Jalil, R., Beca, J., Sherring, C., Bushell, T., Guan, Y., Yao, L., Lin, K., Ong, J., Salloo, A., Doedens, L., Mathivha, L., Reubenson, G., Moaisi, S., Pentz, A., and Green, R.
- Subjects
Male ,medicine.medical_specialty ,Biomedical Research ,Adolescent ,lnfectious Diseases and Global Health Radboud Institute for Molecular Life Sciences [Radboudumc 4] ,Practice Patterns ,macromolecular substances ,Critical Care and Intensive Care Medicine ,Sepsis ,Intensive care ,Epidemiology ,Severity of illness ,Clinical endpoint ,Prevalence ,Medicine ,Humans ,Practice Patterns, Physicians' ,Preschool ,Intensive care medicine ,Child ,Pediatric intensive care unit ,Observer Variation ,Physicians' ,business.industry ,Research ,Organ dysfunction ,Infant, Newborn ,Infant ,Child, Preschool ,Female ,Treatment Outcome ,Newborn ,medicine.disease ,3. Good health ,Clinical trial ,medicine.symptom ,business - Abstract
Introduction Consensus criteria for pediatric severe sepsis have standardized enrollment for research studies. However, the extent to which critically ill children identified by consensus criteria reflect physician diagnosis of severe sepsis, which underlies external validity for pediatric sepsis research, is not known. We sought to determine the agreement between physician diagnosis and consensus criteria to identify pediatric patients with severe sepsis across a network of international pediatric intensive care units (PICUs). Methods We conducted a point prevalence study involving 128 PICUs in 26 countries across 6 continents. Over the course of 5 study days, 6925 PICU patients Results Of the 706 patients, 301 (42.6 %) met both definitions. The inter-rater agreement (κ ± SE) between physician diagnosis and consensus criteria was 0.57 ± 0.02. Of the 438 patients with a physician’s diagnosis of severe sepsis, only 69 % (301 of 438) would have been eligible to participate in a clinical trial of pediatric severe sepsis that enrolled patients based on consensus criteria. Patients with physician-diagnosed severe sepsis who did not meet consensus criteria were younger and had lower severity of illness and lower PICU mortality than those meeting consensus criteria or both definitions. After controlling for age, severity of illness, number of comorbid conditions, and treatment in developed versus resource-limited regions, patients identified with severe sepsis by physician diagnosis alone or by consensus criteria alone did not have PICU mortality significantly different from that of patients identified by both physician diagnosis and consensus criteria. Conclusions Physician diagnosis of pediatric severe sepsis achieved only moderate agreement with consensus criteria, with physicians diagnosing severe sepsis more broadly. Consequently, the results of a research study based on consensus criteria may have limited generalizability to nearly one-third of PICU patients diagnosed with severe sepsis.
- Published
- 2015
30. Dating violence prevention in middle school and high school youth
- Author
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Sharron M. Close
- Subjects
Counseling ,Pediatrics ,medicine.medical_specialty ,Health Knowledge, Attitudes, Practice ,Adolescent ,Psychology, Adolescent ,Poison control ,Violence ,Suicide prevention ,Occupational safety and health ,Developmental psychology ,Sex Factors ,Risk Factors ,Intervention (counseling) ,Injury prevention ,Health care ,Prevalence ,Medicine ,Humans ,Mass Screening ,Dating violence ,Child Abuse ,Longitudinal Studies ,Child ,business.industry ,Incidence ,Courtship ,Human factors and ergonomics ,General Medicine ,United States ,Primary Prevention ,Psychiatry and Mental health ,Cross-Sectional Studies ,Adolescent Behavior ,Research Design ,Female ,New York City ,Public Health ,Pshychiatric Mental Health ,Power, Psychological ,business ,Attitude to Health - Abstract
hen young adolescents hurt each other withinthe contexts of attraction and dating, questions emergeconcerning the etiology and prevention of such actions.The subject of dating violence among teens has beenstudied in the literature since 1981 (Makepeace, 1981).The purpose of this work is to present a case reportregarding relationship abuse and to review the litera-ture on the subject of dating violence prevention inmiddle school and high school youth. The case reportwas generated from a health care maintenance visitconducted at a hospital-based middle school cliniclocated in the Bronx, New York. The review will examinethe problem of relational abuse among young datingadolescents, risk factors, gender differences, and currentprogram strategies for intervention. This paper willalso discuss additional strategies to assist teens in theacquisition and carry-over of newly-learned relation-ship skills as they apply to the development of inti-mate relationships.
- Published
- 2005
31. Further validation of the Qualitative Scoring System for the modified bender-gestalt test
- Author
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G. Terrence Ryan, Sharron M. Aabye, Leslie A. Baker, and Gary G. Brannigan
- Subjects
Scoring system ,School age child ,Validation test ,business.industry ,Test validity ,computer.software_genre ,Bender-Gestalt Test ,Education ,Cognitive test ,Developmental psychology ,Developmental and Educational Psychology ,Achievement test ,Artificial intelligence ,business ,Psychology ,computer ,Natural language processing - Published
- 1995
32. Homing defect of cultured human hematopoietic cells in the NOD/SCID mouse is mediated by Fas/CD95
- Author
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Bianling Liu, Ian D. Lewis, John E. Wagner, Johannes C.M. Van der Loo, Anne I. Goldman, and Sharron M Buckley
- Subjects
Cancer Research ,CD34 ,Mice, SCID ,Biology ,Mice ,Cell Movement ,Mice, Inbred NOD ,Genetics ,medicine ,Cell Adhesion ,Animals ,Humans ,fas Receptor ,Lymphocyte homing receptor ,Molecular Biology ,Cells, Cultured ,Cell adhesion molecule ,Cell Differentiation ,Cell Biology ,Hematology ,Fas receptor ,Hematopoietic Stem Cells ,Molecular biology ,Transplantation ,Haematopoiesis ,medicine.anatomical_structure ,Immunology ,Bone marrow ,Homing (hematopoietic) ,Stem Cell Transplantation - Abstract
Objective. To determine the bone marrow homing efficiency (20 hours) of cultured compared to noncultured umbilical cord blood (UCB)-derived human hematopoietic cells in the nonobese diabetic/severe combined immunodeficient (NOD/SCID) mouse, and to explain the difference in homing between these populations. Methods. Human UCB CD34 + cells were cultured for up to 5 days, reselected, and used for transplantation, phenotype analysis, and functional studies, including adhesion and trans-endothelial migration assays. Seeding of CD34 + cells was measured after labeling of cells with 111-Indium, while homing of colony-forming cells (CFC) and SCID-repopulating (SRC) cells was determined using functional assays. Results. Short-term culture was associated with a decrease in the 20-hour homing of CD34 + cells, CFC, and SRC to the BM. Although cultured compared to noncultured cells showed increased expression and function (adhesion/migration) of several cell adhesion molecules described to play a role in homing and engraftment, culture also induced expression of Fas/CD95 and rendered cells more susceptible to apoptosis. Finally, we demonstrate that the level of Fas/CD95 on cultured cells was inversely related to the ability of CFC to home to the BM, and that the homing of cultured CFC could be restored by incubating cells prior to transplantation with Fas/CD95-blocking mAb ZB4. Conclusion. These data implicate Fas/CD95 in the homing defect of cultured human hematopoietic cells in the NOD/SCID transplant model and suggest that prevention of apoptosis may be an important strategy to improve engraftment of ex vivo–manipulated HSC in a clinical setting.
- Published
- 2003
33. The effect of mental health practitioners' racial sensitivity on African Americans' perceptions of service
- Author
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Sharron M. Singleton-Bowie
- Subjects
Gerontology ,Service (business) ,medicine.medical_specialty ,Sociology and Political Science ,Higher education ,business.industry ,media_common.quotation_subject ,Mental health ,Quality of life (healthcare) ,Perception ,Medicine ,business ,Psychiatry ,media_common - Published
- 1995
34. Sepsis Alters the Megakaryocyte-Platelet Transcriptional Axis Resulting in Platelet Lymphotoxicity.
- Author
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Freishtat, RJ, primary, Sharron, M, additional, Benton, AS, additional, Wiles, AA, additional, Sabzevheri, N, additional, and Hoffman, EP, additional
- Published
- 2009
- Full Text
- View/download PDF
35. Interventions Following Mass Violence and Disasters: Strategies for Mental Health Practice
- Author
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Singleton, Sharron M.
- Subjects
Interventions Following Mass Violence and Disasters: Strategies for Mental Health Practice (Book) -- Book reviews ,Books -- Book reviews ,Family and marriage ,Sociology and social work - Published
- 2007
36. Student Cheating Habits: A Predictor Of Workplace Deviance
- Author
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Graves, Sharron M., primary
- Published
- 2008
- Full Text
- View/download PDF
37. Multiple nonfunctional alleles of CCR5 are frequent in various human populations.
- Author
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Blanpain, Cédric, Lee, B., Tackoen, Marie, Puffer, B, Boom, Alain, Libert, Frédérick, Sharron, M, Wittamer, Valérie, Vassart, Gilbert, Doms, Robert W., Parmentier, Marc, Blanpain, Cédric, Lee, B., Tackoen, Marie, Puffer, B, Boom, Alain, Libert, Frédérick, Sharron, M, Wittamer, Valérie, Vassart, Gilbert, Doms, Robert W., and Parmentier, Marc
- Abstract
CCR5 is the major coreceptor for macrophage-tropic strains of the human immunodeficiency virus type I (HIV-1). Homozygotes for a 32-base pair (bp) deletion in the coding sequence of the receptor (CCR5Delta32) were found to be highly resistant to viral infection, and CCR5 became, therefore, one of the paradigms illustrating the influence of genetic variability onto individual susceptibility to infectious and other diseases. We investigated the functional consequences of 16 other natural CCR5 mutations described in various human populations. We found that 10 of these variants are efficiently expressed at the cell surface, bind [(125)I]-MIP-1beta with affinities similar to wtCCR5, respond functionally to chemokines, and act as HIV-1 coreceptors. In addition to Delta32, six mutations were characterized by major alterations in their functional response to chemokines, as a consequence of intracellular trapping and poor expression at the cell surface (C101X, FS299), general or specific alteration of ligand binding affinities (C20S, C178R, A29S), or relative inability to mediate receptor activation (L55Q). A29S displayed an unusual pharmacological profile, binding and responding to MCP-2 similarly to wtCCR5, but exhibiting severely impaired binding and functional responses to MIP-1alpha, MIP-1beta, and RANTES. In addition to Delta32, only C101X was totally unable to mediate entry of HIV-1. The fact that nonfunctional CCR5 alleles are relatively frequent in various human populations reinforces the hypothesis of a selective pressure favoring these alleles. (Blood. 2000;96:1638-1645), Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S., info:eu-repo/semantics/published
- Published
- 2000
38. Epitope mapping of CCR5 reveals multiple conformational states and distinct but overlapping structures involved in chemokine and coreceptor function.
- Author
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Lee, B., Sharron, M, Blanpain, Cédric, Doranz, Benjamin J., Vakili, Jalal, Setoh, P, Berg, E, Liu, GUO-LI, Guy, H R, Durell, S R, Parmentier, Marc, Chang, C N, Price, K, Tsang, M, Doms, Robert W., Lee, B., Sharron, M, Blanpain, Cédric, Doranz, Benjamin J., Vakili, Jalal, Setoh, P, Berg, E, Liu, GUO-LI, Guy, H R, Durell, S R, Parmentier, Marc, Chang, C N, Price, K, Tsang, M, and Doms, Robert W.
- Abstract
The chemokine receptor CCR5 is the major coreceptor for R5 human immunodeficiency virus type-1 strains. We mapped the epitope specificities of 18 CCR5 monoclonal antibodies (mAbs) to identify domains of CCR5 required for chemokine binding, gp120 binding, and for inducing conformational changes in Env that lead to membrane fusion. We identified mAbs that bound to N-terminal epitopes, extracellular loop 2 (ECL2) epitopes, and multidomain (MD) epitopes composed of more than one single extracellular domain. N-terminal mAbs recognized specific residues that span the first 13 amino acids of CCR5, while nearly all ECL2 mAbs recognized residues Tyr-184 to Phe-189. In addition, all MD epitopes involved ECL2, including at least residues Lys-171 and Glu-172. We found that ECL2-specific mAbs were more efficient than NH2- or MD-antibodies in blocking RANTES or MIP-1beta binding. By contrast, N-terminal mAbs blocked gp120-CCR5 binding more effectively than ECL2 mAbs. Surprisingly, ECL2 mAbs were more potent inhibitors of viral infection than N-terminal mAbs. Thus, the ability to block virus infection did not correlate with the ability to block gp120 binding. Together, these results imply that chemokines and Env bind to distinct but overlapping sites in CCR5, and suggest that the N-terminal domain of CCR5 is more important for gp120 binding while the extracellular loops are more important for inducing conformational changes in Env that lead to membrane fusion and virus infection. Measurements of individual antibody affinities coupled with kinetic analysis of equilibrium binding states also suggested that there are multiple conformational states of CCR5. A previously described mAb, 2D7, was unique in its ability to effectively block both chemokine and Env binding as well as coreceptor activity. 2D7 bound to a unique antigenic determinant in the first half of ECL2 and recognized a far greater proportion of cell surface CCR5 molecules than the other mAbs examined. Thus, the epitope r, Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S., info:eu-repo/semantics/published
- Published
- 1999
39. Extracellular cysteines of CCR5 are required for chemokine binding, but dispensable for HIV-1 coreceptor activity.
- Author
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Blanpain, Cédric, Lee, B., Vakili, Jalal, Doranz, Benjamin J., Govaerts, Cédric, Migeotte, Isabelle, Sharron, M, Dupriez, Vincent, Vassart, Gilbert, Doms, Robert W., Parmentier, Marc, Blanpain, Cédric, Lee, B., Vakili, Jalal, Doranz, Benjamin J., Govaerts, Cédric, Migeotte, Isabelle, Sharron, M, Dupriez, Vincent, Vassart, Gilbert, Doms, Robert W., and Parmentier, Marc
- Abstract
CCR5 is the major coreceptor for macrophage-tropic human immunodeficiency virus type I (HIV-1). For most G-protein-coupled receptors that have been tested so far, the disulfide bonds linking together the extracellular loops (ECL) are required for maintaining the structural integrity necessary for ligand binding and receptor activation. A natural mutation affecting Cys20, which is thought to form a disulfide bond with Cys269, has been described in various human populations, although the consequences of this mutation for CCR5 function are not known. Using site-directed mutagenesis, we mutated the four extracellular cysteines of CCR5 singly or in combination to investigate their role in maintaining the structural conformation of the receptor, its ligand binding and signal transduction properties, and its ability to function as a viral coreceptor. Alanine substitution of any single Cys residue reduced surface expression levels by 40-70%. However, mutation of Cys101 or Cys178, predicted to link ECL1 and ECL2 of the receptor, abolished recognition of CCR5 by a panel of conformation sensitive anti-CCR5 antibodies. The effects of the mutations on receptor expression and conformation were partially temperature-sensitive, with partial restoration of receptor expression and conformation achieved by incubating cells at 32 degrees C. All cysteine mutants were unable to bind detectable levels of MIP-1beta, and did not respond functionally to CCR5 agonists. Surprisingly, all cysteine mutants did support infection by R5 strains of HIV, though at reduced levels. These results indicate that both disulfide bonds of CCR5 are necessary for maintaining the structural integrity of the receptor necessary for ligand binding and signaling. Env binding and the mechanisms of HIV entry appear much less sensitive to alterations of CCR5 conformation., Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S., info:eu-repo/semantics/published
- Published
- 1999
40. Ministers' Perceptions of Foster Care, Adoptions, and the Role of the Black Church
- Author
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Singleton, Sharron M., primary and Roseman, Fay, additional
- Published
- 2004
- Full Text
- View/download PDF
41. ChemR23, a putative chemoattractant receptor, is expressed in monocyte-derived dendritic cells and macrophages and is a coreceptor for SIV and some primary HIV-1 strains.
- Author
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Samson, M, Edinger, A L, Stordeur, P, Rucker, J, Verhasselt, Valérie, Sharron, M, Govaerts, Cédric, Mollereau, Catherine, Vassart, Gilbert, Doms, Robert W., Parmentier, Marc, Samson, M, Edinger, A L, Stordeur, P, Rucker, J, Verhasselt, Valérie, Sharron, M, Govaerts, Cédric, Mollereau, Catherine, Vassart, Gilbert, Doms, Robert W., and Parmentier, Marc
- Abstract
Leukocyte chemoattractants act through a rapidly growing subfamily of G protein-coupled receptors. We report the cloning of a novel human gene encoding an orphan receptor (ChemR23) related to the C3a, C5a and formyl Met-Leu-Phe receptors, and more distantly to the subfamilies of chemokine receptors. ChemR23 transcripts were found to be abundant in monocyte-derived dendritic cells and macrophages, treated or not with LPS. Low expression could also be detected by reverse transcription-PCR in CD4+ T lymphocytes. The gene encoding ChemR23 was assigned by radiation hybrid mapping to the q21.2-21.3 region of human chromosome 12, outside the gene clusters identified so far for chemoattractant receptors. Given the increasing number of chemoattractant receptors used by HIV-1, HIV-2 and SIV as coreceptors, ChemR23 was tested in fusion assays for potential coreceptor activity by a range of viral strains. None of the tested HIV-2 strains made use of ChemR23 as a coreceptor, but several SIV strains (SIVmac316, SIVmac239, SIVmacl7E-Fr and SIVsm62A), as well as a primary HIV-1 strain (92UG024-2) used it efficiently. ChemR23 therefore appears as a coreceptor for immunodeficiency viruses that does not belong to the chemokine receptor family. It is also a putative chemoattractant receptor relatively specific for antigen-presenting cells, and it could play an important role in the recruitment or trafficking of these cell populations. Future work will be required to identify the ligand(s) of this new G protein-coupled receptor and to define its precise role in the physiology of dendritic cells and macrophages., Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S., FLWIN, info:eu-repo/semantics/published
- Published
- 1998
42. Homing defect of cultured human hematopoietic cells in the NOD/SCID mouse is mediated by Fas/CD95
- Author
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Liu, Bianling, primary, Buckley, Sharron M, additional, Lewis, Ian D, additional, Goldman, Anne I, additional, Wagner, John E, additional, and van der Loo, Johannes C.M, additional
- Published
- 2003
- Full Text
- View/download PDF
43. Utilization of chemokine receptors, orphan receptors, and herpesvirus-encoded receptors by diverse human and simian immunodeficiency viruses.
- Author
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Rucker, J, Edinger, A L, Sharron, M, Samson, M, Lee, B., Berson, J F, Yi, Y, Margulies, B, Collman, R G, Doranz, Benjamin J., Parmentier, Marc, Doms, Robert W., Rucker, J, Edinger, A L, Sharron, M, Samson, M, Lee, B., Berson, J F, Yi, Y, Margulies, B, Collman, R G, Doranz, Benjamin J., Parmentier, Marc, and Doms, Robert W.
- Abstract
Human immunodeficiency virus type 1 (HIV-1) requires both CD4 and a coreceptor to infect cells. Macrophage-tropic (M-tropic) HIV-1 strains utilize the chemokine receptor CCR5 in conjunction with CD4 to infect cells, while T-cell-tropic (T-tropic) strains generally utilize CXCR4 as a coreceptor. Some viruses can use both CCR5 and CXCR4 for virus entry (i.e. are dual-tropic), while other chemokine receptors can be used by a subset of virus strains. Due to the genetic diversity of HIV-1, HIV-2, and simian immunodeficiency virus (SIV) and the potential for chemokine receptors other than CCR5 or CXCR4 to influence viral pathogenesis, we tested a panel of 28 HIV-1, HIV-2, and SIV envelope (Env) proteins for the ability to utilize chemokine receptors, orphan receptors, and herpesvirus-encoded chemokine receptor homologs by membrane fusion and virus infection assays. While all Env proteins used either CCR5 or CXCR4 or both, several also used CCR3. Use of CCR3 was strongly dependent on its surface expression levels, with a larger number of viral Env proteins being able to utilize this coreceptor at the higher levels of surface expression. ChemR1, an orphan receptor recently shown to bind the CC chemokine I309 (and therefore renamed CCR8), was expressed in monocyte and lymphocyte cell populations and functioned as a coreceptor for diverse HIV-1, HIV-2, and SIV Env proteins. Use of ChemR1/CCR8 by SIV strains was dependent in part on V3 loop sequences. The orphan receptor V28 supported Env-mediated cell-cell fusion by four T- or dual-tropic HIV-1 and HIV-2 strains. Three additional orphan receptors failed to function for any of the 28 Env proteins tested. Likewise, five of six seven-transmembrane-domain receptors encoded by herpesviruses did not support Env-mediated membrane fusion. However, the chemokine receptor US28, encoded by cytomegalovirus, did support inefficient infection by two HIV-1 strains. These findings indicate that additional chemokine receptors can function as, Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S., info:eu-repo/semantics/published
- Published
- 1997
44. Differential utilization of CCR5 by macrophage and T cell tropic simian immunodeficiency virus strains.
- Author
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Edinger, A L, Amedee, A, Miller, Kirk, Doranz, Benjamin J., Endres, M, Sharron, M, Samson, M, Lu, Z H, Clements, J E, Murphey-Corb, M, Peiper, S C, Parmentier, Marc, Broder, C C, Doms, Robert W., Edinger, A L, Amedee, A, Miller, Kirk, Doranz, Benjamin J., Endres, M, Sharron, M, Samson, M, Lu, Z H, Clements, J E, Murphey-Corb, M, Peiper, S C, Parmentier, Marc, Broder, C C, and Doms, Robert W.
- Abstract
Certain chemokine receptors serve as cofactors for HIV type 1 envelope (env)-mediated cell-cell fusion and virus infection of CD4-positive cells. Macrophage tropic (M-tropic) HIV-1 isolates use CCR5, and T cell tropic (T-tropic) strains use CXCR4. To investigate the cofactors used by simian immunodeficiency viruses (SIV), we tested four T-tropic and two M-tropic SIV env proteins for their ability to mediate cell-cell fusion with cells expressing CD4 and either human or nonhuman primate chemokine receptors. Unlike HIV-1, both M- and T-tropic SIV envs used CCR5 but not CXCR4 or the other chemokine receptors tested. However, by testing a panel of CCR5/CCR2b chimeras, we found that the structural requirements for CCR5 utilization by M-tropic and T-tropic SIV strains were different. T-tropic SIV strains required the second extracellular loop of CCR5 whereas a closely related M-tropic SIV strain could, like M-tropic HIV-1 strains, use the amino-terminal domain of CCR5. As few as two amino acid changes in the SIV env V3 domain affected the regions of CCR5 that were critical for fusogenic activity. Receptor signaling was not required for either fusion or infection. Our results suggest that viral tropism may be influenced not only by the coreceptors used by a given virus strain but also by how a given coreceptor is used., Journal Article, Research Support, U.S. Gov't, P.H.S., info:eu-repo/semantics/published
- Published
- 1997
45. Expression of multiple functional chemokine receptors and monocyte chemoattractant protein-1 in human neurons
- Author
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Coughlan, C.M, primary, McManus, C.M, additional, Sharron, M, additional, Gao, Z.-Y, additional, Murphy, D, additional, Jaffer, S, additional, Choe, W, additional, Chen, W, additional, Hesselgesser, J, additional, Gaylord, H, additional, Kalyuzhny, A, additional, Lee, V.M.-Y, additional, Wolf, B, additional, Doms, R.W, additional, and Kolson, D.L, additional
- Published
- 2000
- Full Text
- View/download PDF
46. Utilization of chemokine receptors, orphan receptors, and herpesvirus-encoded receptors by diverse human and simian immunodeficiency viruses
- Author
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Rucker, J, primary, Edinger, A L, additional, Sharron, M, additional, Samson, M, additional, Lee, B, additional, Berson, J F, additional, Yi, Y, additional, Margulies, B, additional, Collman, R G, additional, Doranz, B J, additional, Parmentier, M, additional, and Doms, R W, additional
- Published
- 1997
- Full Text
- View/download PDF
47. Two distinct CCR5 domains can mediate coreceptor usage by human immunodeficiency virus type 1
- Author
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Doranz, B J, primary, Lu, Z H, additional, Rucker, J, additional, Zhang, T Y, additional, Sharron, M, additional, Cen, Y H, additional, Wang, Z X, additional, Guo, H H, additional, Du, J G, additional, Accavitti, M A, additional, Doms, R W, additional, and Peiper, S C, additional
- Published
- 1997
- Full Text
- View/download PDF
48. Further validation of the Qualitative Scoring System for the modified bender-gestalt test
- Author
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Brannigan, Gary G., primary, Aabye, Sharron M., additional, Baker, Leslie A., additional, and Ryan, G. Terrence, additional
- Published
- 1995
- Full Text
- View/download PDF
49. Sepsis alters the megakaryocyte-platelet transcriptional axis resulting in granzyme B-mediated lymphotoxicity.
- Author
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Freishtat RJ, Natale J, Benton AS, Cohen J, Sharron M, Wiles AA, Ngor WM, Mojgani B, Bradbury M, Degnan A, Sachdeva R, Debiase LM, Ghimbovschi S, Chow M, Bunag C, Kristosturyan E, Hoffman EP, Freishtat, Robert J, Natale, Joanne, and Benton, Angela S
- Abstract
Rationale: Sepsis-related mortality results in part from immunodeficiency secondary to profound lymphoid apoptosis. The biological mechanisms responsible are not understood.Objectives: Because recent evidence shows that platelets are involved in microvascular inflammation and that they accumulate in lymphoid microvasculature in sepsis, we hypothesized a direct role for platelets in sepsis-related lymphoid apoptosis.Methods: We studied megakaryocytes and platelets from a murine-induced sepsis model, with validation in septic children, which showed induction of the cytotoxic serine protease granzyme B.Measurements and Main Results: Platelets from septic mice induced marked apoptosis of healthy splenocytes ex vivo. Platelets from septic granzyme B null (-/-) mice showed no lymphotoxicity.Conclusions: Our findings establish a conceptual advance in sepsis: Septic megakaryocytes produce platelets with acutely altered mRNA profiles, and these platelets mediate lymphotoxicity via granzyme B. Given the contribution of lymphoid apoptosis to sepsis-related mortality, modulation of platelet granzyme B becomes an important new target for investigation and therapy. [ABSTRACT FROM AUTHOR]- Published
- 2009
- Full Text
- View/download PDF
50. Evaluating Internal Controls.
- Author
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Graves, Sharron M., Longenecker, Bill, Marsh, Treba L., and Milstead, Heidi
- Subjects
- *
INTERNAL auditing , *GOVERNMENT accounting , *AUDITING , *ACCOUNTING - Abstract
Highlights the implementation of control self-assessment (CSA) in governments in the U.S. to enhance internal auditing control. Definition of CSA; Background on the development of CSA; Benefits of self-assessment; Approaches to CSA; Extent of CSA usage. INSET: A CASE STUDY IN CONTROL SELF-ASSESSMENT.
- Published
- 2003
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