Zobrazeno 1 - 10
of 27
pro vyhledávání: '"James D Acton"'
Publikováno v:
Clinical pediatrics. 60(11-12)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7948fca6f7b1315eb6f39d1cfaa5ecc3
https://pubmed.ncbi.nlm.nih.gov/34528464
https://pubmed.ncbi.nlm.nih.gov/34528464
Publikováno v:
The Clinical Respiratory Journal. 12:2397-2403
Introduction FEV1 is considered the gold standard spirometric measure for the assessment and management of cystic fibrosis lung disease. Recent evidence suggests that tests at lower lung volumes may be more sensitive. Objectives To assess how many ot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b7b6991fbb9300ff0f450b076fa7179
https://doi.org/10.1111/crj.12920
https://doi.org/10.1111/crj.12920
Publikováno v:
The clinical respiratory journal. 12(8)
FEVTo assess how many other spirometric tests are abnormal in the presence of a normal FEVThis was a retrospective analysis of 3169 spirometry tests on 184 patients with cystic fibrosis aged 6-57 years. Tests were acceptable if they met ATS criteria.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4352c7d56b9a3e106464973d552d1f2c
https://pubmed.ncbi.nlm.nih.gov/29920961
https://pubmed.ncbi.nlm.nih.gov/29920961
Autor:
Andrea J. Hoberman, Raouf S. Amin, J. Denise Wetzel, James D Acton, Barbara A. Chini, Amitra K Chima, Christopher Siracusa, Gary L. McPhail, Jeanne Weiland
Publikováno v:
BMJ Quality & Safety. 23:i56-i63
Background In 2001, Cincinnati Children9s Hospital embarked on a journey to improve healthcare delivery to patients with cystic fibrosis (CF). Data from the Cystic Fibrosis Foundation National Patient Registry revealed our below-average clinical outc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10b3b05c5c8aa0585d5efd172a2916de
https://doi.org/10.1136/bmjqs-2013-002361
https://doi.org/10.1136/bmjqs-2013-002361
Autor:
Philip M. Farrell, James D. Acton, Margaret Rosenfeld, Peter J. Mogayzel, Carol Conrad, Peter Hiatt, Lyndia C. Brumback, Margaret Kloster, Robert G. Castile, Thuy L. Vu, Andrew A. Colin, Gwendolyn S. Kerby, Meeghan A. Hart, Jonathan O. Swanson, Stephanie D. Davis, Robin Johnson
Publikováno v:
European Respiratory Journal. 42:1545-1552
The optimal strategy for monitoring cystic fibrosis lung disease in infancy remains unclear. Our objective was to describe longitudinal associations between infant pulmonary function tests, chest radiograph scores and other characteristics. Cystic fi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9153fae49bd4d566ea910f9ff2c0c091
https://doi.org/10.1183/09031936.00138412
https://doi.org/10.1183/09031936.00138412
Autor:
James D. Acton, Ronald E. Bokulic, Thomas H. Inge, Gail H. Deutsch, Claire Langston, Alan S. Brody, Lisa R. Young
Publikováno v:
Chest. 139:1060-1071
Background The diagnostic gold standard for neuroendocrine cell hyperplasia of infancy (NEHI) is demonstration of increased numbers of neuroendocrine cells (NECs) amid otherwise near-normal lung histology. Typical clinical and radiographic features o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49391caf04131777bfed0b35170c1bd0
https://doi.org/10.1378/chest.10-1304
https://doi.org/10.1378/chest.10-1304
Autor:
Lyndia C. Brumback, Robert G. Castile, Margaret Kloster, Meeghan A. Hart, Margaret Rosenfeld, Peter J. Mogayzel, Gwendolyn S. Kerby, Carol Conrad, Andrew A. Colin, Stephanie L. Wilcox, Robin Johnson, James D. Acton, Peter Hiatt, Stephanie D. Davis
Publikováno v:
American Journal of Respiratory and Critical Care Medicine. 182:1387-1397
The conducting of clinical trials in infants with cystic fibrosis (CF) has been hindered by lack of sensitive outcome measures.To evaluate safety, feasibility, and ability to detect abnormalities in lung function of serial pulmonary function tests (P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2cdf5f171768c978211c011b6faf912
https://doi.org/10.1164/rccm.200908-1236oc
https://doi.org/10.1164/rccm.200908-1236oc
Publikováno v:
Pediatric Pulmonology. 46:153-159
Background Although studies have assessed symptoms of depression and anxiety in individuals with cystic fibrosis (CF), few have been conducted since the advent of new medical treatments (e.g., nebulized antibiotics, ThAIRpy Vest). Study objectives we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16cc58e8ba9effd0658623c73250124e
https://doi.org/10.1002/ppul.21334
https://doi.org/10.1002/ppul.21334
Autor:
Randall L. Rosenblatt, Daniel Rosenbluth, Marcia Katz, Henry L. Dorkin, Patrick A. Flume, Moira L. Aitken, Michelle S. Howenstine, Manu Jain, David C. McGiffin, Joseph M. Pilewski, Ahmet Uluer, Craig W. Lillehei, Beryl J. Rosenstein, Hector H. Gutierrez, Terry B. White, James D. Acton, Randall K. Young, Thomas M. Egan, Kathryn A. Sabadosa, Steven Strausbaugh, Mary K Lester, Sally E. Mitchell, Douglas S. Holsclaw, Bruce C. Marshall, Mike Mulligan, David M. Orenstein, Donna Beth Willey-Courand, Peter J. Mogayzel, Susanna A. McColley, Souheil Saddekni, Melissa Chin, Lynne M. Quittell, Paul Mohabir, Christopher M. Oermann, James R. Yankaskas, Michael P. Boyle, Robert J. Kuhn, R. Duane Davis, Jill Fleige, Michael J. Rock, Elizabeth Tullis, Anne M Downs, James L. Cunningham, Peter J Murphy, John L. Colombo, Linda L. Wolfenden, Thomas W. Ferkol, Patricia M. Joseph, Jeffrey S. Wagener, George Z. Retsch-Bogart, Christopher H. Goss, Karen A. Robinson, Carlos Milla, Felix Ratjen, Michael S. Schechter, Patricia E. Burrows, Aruna Sannuti, Charles B. Huddleston, Robert L. Vender, Leslie Hazle, Mark J. Sands, Charles T. Burke, Wickii T. Vigneswaran, Ronald C. Rubenstein, Guillermo A. doPico, Jerry A. Nick, Wyn Hoover, Mark H. Wholey
Publikováno v:
American Journal of Respiratory and Critical Care Medicine. 182:298-306
Cystic fibrosis (CF) is a recessive genetic disease characterized by dehydration of the airway surface liquid and impaired mucociliary clearance. As a result, individuals with the disease have difficulty clearing pathogens from the lung and experienc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee82205e6b63ce9b3731b135f84a4850
https://doi.org/10.1164/rccm.201002-0157oc
https://doi.org/10.1164/rccm.201002-0157oc
Publikováno v:
The Journal of Pediatrics. 153:752-757
Objective To compare lung function and nutritional outcomes in cystic fibrosis (CF) for 2 birth cohorts in our CF center. Study design Patients with CF born between 1985 and 2000 treated in our CF center before age 5 years were included. The patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c27e6c43f58285e0e4dc7ba4f9eed11
https://doi.org/10.1016/j.jpeds.2008.07.011
https://doi.org/10.1016/j.jpeds.2008.07.011