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Accessed 12 October 2014.",{},{"id":24,"text":1077,"url":24,"identifiers":1078},"10.1086\u002F341940",{"doi":1077},{"id":24,"text":1080,"url":24,"identifiers":1081},"10.1016\u002FS0934-8840(11)80342-7",{"doi":1080},{"id":24,"text":1083,"url":24,"identifiers":1084},"10.1001\u002Fjama.2012.264",{"doi":1083},{"id":1086,"createTime":1087,"updateTime":1087,"relativeEntities":1088,"slug":1089,"properties":1090,"entityType":141,"verifyStatus":142,"verifyTime":1087,"verifyNote":143,"syncStatus":23,"languages":1104,"translateLanguages":24,"viewCount":25,"primaryUrl":1105,"fullTextUrl":24,"authors":1106,"publicationType":398,"publisherRelationship":1229,"citationCount":508,"citationInfo":1260,"publishDate":438,"publishYear":439,"citationAnalyzeStatus":23,"lastCitationAnalyze":24,"indexDatabases":24,"openAccess":24,"references":1262,"isForceReanalyzing":462},"5870f052-f405-4f12-98af-2068728f8911","2024-08-30T13:20:00.340+00:00",[],"Pediatric-Sporotrichosis-in-Jilin-Province-of-China-2010-2016-a-Retrospective-Study-of-704-Cases",{"mag":1091,"keywords":1093,"openalex":1094,"abstract":1096,"title":1098,"pm":1100,"doi":1102},{"VOID":1092},"2964668976",{},{"VOID":1095},"W2964668976",{"EN":1097},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\n               \u003Cjats:sec>\n                  \u003Cjats:title>Background\u003C\u002Fjats:title>\n                  \u003Cjats:p>Pediatric patients make a substantial contribution to the epidemiologic profile of sporotrichosis in Jilin Province, a region of China in which the disease is strongly endemic. However, the exact epidemiologic and clinical manifestations of childhood sporotrichosis in China are unclear.\u003C\u002Fjats:p>\n               \u003C\u002Fjats:sec>\n               \u003Cjats:sec>\n                  \u003Cjats:title>Methods\u003C\u002Fjats:title>\n                  \u003Cjats:p>The medical records of 704 pediatric patients aged &amp;lt;15 years with sporotrichosis diagnosed by fungus culture at the Department of Dermatology at the First Hospital of Jilin University in a 7-year period (January 2010 to December 2016) were reviewed retrospectively. The patients were from rural areas of Jilin Province, located in northeast China.\u003C\u002Fjats:p>\n               \u003C\u002Fjats:sec>\n               \u003Cjats:sec>\n                  \u003Cjats:title>Results\u003C\u002Fjats:title>\n                  \u003Cjats:p>Among the 704 pediatric patients, the male\u002Ffemale ratio was 1.41:1, and the highest incidence of sporotrichosis (63%) occurred in those aged 0 to 6 years; 561 patients (80%) contracted sporotrichosis in a colder month. Overall, 655 (93%) patients had lesions in the facial region, whereas 602 (86%) patients had fixed cutaneous sporotrichosis. The incidence of the fixed cutaneous form in the 0- to 6-year age group was significantly higher than that in the 7- to 14-year age group (P = .009). Patients were treated with 10% potassium iodide solution, itraconazole, or terbinafine.\u003C\u002Fjats:p>\n               \u003C\u002Fjats:sec>\n               \u003Cjats:sec>\n                  \u003Cjats:title>Conclusions\u003C\u002Fjats:title>\n                  \u003Cjats:p>The characteristics of pediatric sporotrichosis in Jilin Provence include the following: (1) a more frequent occurrence in the colder months; (2) the facial region is affected predominantly, in most cases manifesting in the fixed cutaneous form; and (3) significantly more cases occur in younger children than in older ones. Decaying cornstalks used as fire materials might be the source of infection in this population; however, additional research is needed to explore the exact mechanism of infection.\u003C\u002Fjats:p>\n               \u003C\u002Fjats:sec>",{"EN":1099},"Pediatric Sporotrichosis in Jilin Province of China (2010–2016): a Retrospective Study of 704 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Physicians in China reported what is believed to be the first adult case of a SARS-CoV-2 infection associated with acute Guillain-Barré syndrome (GBS), followed by 5 adult Italian patients and another case in the United States. In the current report, we present one of the first descriptions of an association of GBS and SARS-CoV-2 infection in a child. In our facility, an 11-year-old boy presented with typical features of GBS and, after 5 days, a morbilliform skin rash over the palms of both hands. Three weeks before the start of the neurological symptoms, the boy had experienced an episode of mild febrile illness with mild respiratory manifestations and a persistent cough. The diagnosis of SARS-CoV-2 infection was confirmed by oropharyngeal swab on reverse-transcription polymerase chain reaction assay. The disease course of our patient strongly suggests a possible relationship between the development of GBS and SARS-CoV-2 infection. 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patients and carriers of chronic granulomatous disease, J Pediatr, 134, 780, 10.1016\u002FS0022-3476(99)70299-4",{"doi":2336},"10.1016\u002FS0022-3476(99)70299-4",{"id":24,"text":2338,"url":24,"identifiers":2339},"Sillevis Smitt, 1990, Discoid lupus erythematosus-like lesions in carriers of X-linked chronic granulomatous disease, Br J Dermatol, 122, 643, 10.1111\u002Fj.1365-2133.1990.tb07286.x",{"doi":2340},"10.1111\u002Fj.1365-2133.1990.tb07286.x",{"id":24,"text":2342,"url":24,"identifiers":2343},"Brandrup, 1981, Discoid lupus erythematosus-like lesions and stomatitis in female carriers of X-linked chronic granulomatous disease, Br J Dermatol, 104, 495, 10.1111\u002Fj.1365-2133.1981.tb08163.x",{"doi":2344},"10.1111\u002Fj.1365-2133.1981.tb08163.x",{"id":24,"text":2346,"url":24,"identifiers":2347},"Kragballe, 1981, Relation of monocyte and neutrophil oxidative metabolism to skin and oral lesions in carriers of chronic granulomatous disease, Clin Exp Immunol, 43, 390",{},{"id":24,"text":2349,"url":24,"identifiers":2350},"Cale, 2007, Cutaneous and other lupus-like symptoms in carriers of X-linked chronic granulomatous disease: incidence and autoimmune serology, Clin Exp Immunol, 148, 79, 10.1111\u002Fj.1365-2249.2007.03321.x",{"doi":2351},"10.1111\u002Fj.1365-2249.2007.03321.x",{"id":24,"text":2353,"url":24,"identifiers":2354},"Moltyaner, 2003, Underlying chronic granulomatous disease in a patient with bronchocentric granulomatosis, Thorax, 58, 1096, 10.1136\u002Fthorax.58.12.1096",{"doi":2355},"10.1136\u002Fthorax.58.12.1096",{"id":24,"text":2357,"url":24,"identifiers":2358},"Foti, 2004, Lupus erythematosus-like lesions in a carrier of X-linked chronic granulomatous disease: a case report and personal considerations, Int J Dermatol, 43, 840, 10.1111\u002Fj.1365-4632.2004.01950.x",{"doi":2359},"10.1111\u002Fj.1365-4632.2004.01950.x",{"id":24,"text":2361,"url":24,"identifiers":2362},"Lekstrom-Himes, 2005, Inhibition of human neutrophil IL-8 production by hydrogen peroxide and dysregulation in chronic granulomatous disease, J Immunol, 174, 411, 10.4049\u002Fjimmunol.174.1.411",{"doi":2363},"10.4049\u002Fjimmunol.174.1.411",{"id":24,"text":2365,"url":24,"identifiers":2366},"van de Veerdonk, 2010, Reactive oxygen species-independent activation of the IL-1beta inflammasome in cells from patients with chronic granulomatous disease, Proc Natl Acad Sci U S A, 107, 3030, 10.1073\u002Fpnas.0914795107",{"doi":2367},"10.1073\u002Fpnas.0914795107",{"id":24,"text":2369,"url":24,"identifiers":2370},"de Luca, 2014, IL-1 receptor blockade restores autophagy and reduces inflammation in chronic granulomatous disease in mice and in humans, Proc Natl Acad Sci U S A, 111, 3526, 10.1073\u002Fpnas.1322831111",{"doi":2371},"10.1073\u002Fpnas.1322831111",{"id":24,"text":2373,"url":24,"identifiers":2374},"Kasahara, 1997, Involvement of reactive oxygen intermediates in spontaneous and CD95 (Fas\u002FAPO-1)-mediated apoptosis of neutrophils, Blood, 89, 1748, 10.1182\u002Fblood.V89.5.1748",{"doi":2375},"10.1182\u002Fblood.V89.5.1748",{"id":24,"text":2377,"url":24,"identifiers":2378},"Rieber, 2012, Current concepts of hyperinflammation in chronic granulomatous disease, Clin Dev Immunol, 2012, 252460, 10.1155\u002F2012\u002F252460",{"doi":2379},"10.1155\u002F2012\u002F252460",{"id":24,"text":2381,"url":24,"identifiers":2382},"Brown, 2003, Diminished production of anti-inflammatory mediators during neutrophil apoptosis and macrophage phagocytosis in chronic granulomatous disease (CGD), J Leukoc Biol, 73, 591, 10.1189\u002Fjlb.1202599",{"doi":2383},"10.1189\u002Fjlb.1202599",{"id":24,"text":2385,"url":24,"identifiers":2386},"Sanford, 2006, Abnormal apoptosis in chronic granulomatous disease and autoantibody production characteristic of lupus, Rheumatology (Oxford), 45, 178, 10.1093\u002Frheumatology\u002Fkei135",{"doi":2387},"10.1093\u002Frheumatology\u002Fkei135",{"id":24,"text":2389,"url":24,"identifiers":2390},"Singel, 2016, NOX2-dependent regulation of inflammation, Clin Sci (Lond), 130, 479, 10.1042\u002FCS20150660",{"doi":2391},"10.1042\u002FCS20150660",{"id":24,"text":2393,"url":24,"identifiers":2394},"Harbort, 2015, Neutrophil oxidative burst activates ATM to regulate cytokine production and apoptosis, Blood, 126, 2842, 10.1182\u002Fblood-2015-05-645424",{"doi":2395},"10.1182\u002Fblood-2015-05-645424",{"id":24,"text":2397,"url":24,"identifiers":2398},"Sanmun, 2009, Involvement of a functional NADPH oxidase in neutrophils and macrophages during programmed cell clearance: implications for chronic granulomatous disease, Am J Physiol Cell Physiol, 297, C621, 10.1152\u002Fajpcell.00651.2008",{"doi":2399},"10.1152\u002Fajpcell.00651.2008",{"id":24,"text":2401,"url":24,"identifiers":2402},"Fernandez-Boyanapalli, 2015, Impaired efferocytosis in human chronic granulomatous disease is reversed by pioglitazone treatment, J Allergy Clin Immunol, 136, 1399, 10.1016\u002Fj.jaci.2015.07.034",{"doi":2403},"10.1016\u002Fj.jaci.2015.07.034",{"id":24,"text":2405,"url":24,"identifiers":2406},"Foster, 1998, Host defense molecule polymorphisms influence the risk for immune-mediated complications in chronic granulomatous disease, J Clin Invest, 102, 2146, 10.1172\u002FJCI5084",{"doi":2407},"10.1172\u002FJCI5084",{"id":24,"text":2409,"url":24,"identifiers":2410},"Sibley, 2014, Assessment of atherosclerosis in chronic granulomatous disease, Circulation, 130, 2031, 10.1161\u002FCIRCULATIONAHA.113.006824",{"doi":2411},"10.1161\u002FCIRCULATIONAHA.113.006824",{"id":24,"text":2413,"url":24,"identifiers":2414},"Jaggi, 2012, Utility of screening for chronic granulomatous disease in patients with inflammatory bowel disease, J Clin Immunol, 32, 78, 10.1007\u002Fs10875-011-9608-5",{"doi":2415},"10.1007\u002Fs10875-011-9608-5",{"id":24,"text":2417,"url":24,"identifiers":2418},"Sullivan, 2014, USIDNET: a strategy to build a community of clinical immunologists, J Clin Immunol, 34, 428, 10.1007\u002Fs10875-014-0028-1",{"doi":2419},"10.1007\u002Fs10875-014-0028-1",{"id":2421,"createTime":2422,"updateTime":2422,"relativeEntities":2423,"slug":2424,"properties":2425,"entityType":141,"verifyStatus":142,"verifyTime":2422,"verifyNote":143,"syncStatus":23,"languages":2437,"translateLanguages":24,"viewCount":25,"primaryUrl":2438,"fullTextUrl":24,"authors":2439,"publicationType":398,"publisherRelationship":3302,"citationCount":3335,"citationInfo":3336,"publishDate":3338,"publishYear":3339,"citationAnalyzeStatus":23,"lastCitationAnalyze":24,"indexDatabases":24,"openAccess":24,"references":3340,"isForceReanalyzing":462},"55a5bb46-7c6b-47aa-ab3d-e5d4e36b4145","2024-10-11T05:52:20.562+00:00",[],"Multicenter-Interim-Guidance-on-Use-of-Antivirals-for-Children-With-Coronavirus-Disease-2019-Severe-Acute-Respiratory-Syndrome-Coronavirus-2",{"keywords":2426,"openalex":2427,"abstract":2429,"title":2431,"pm":2433,"doi":2435},{},{"VOID":2428},"W4206405674",{"EN":2430},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\u003Cjats:sec>\u003Cjats:title>Background\u003C\u002Fjats:title>\u003Cjats:p>Although coronavirus disease 2019 (COVID-19) is a mild infection in most children, a small proportion develop severe or critical illness. Data describing agents with potential antiviral activity continue to expand such that updated guidance is needed regarding use of these agents in children.\u003C\u002Fjats:p>\u003C\u002Fjats:sec>\u003Cjats:sec>\u003Cjats:title>Methods\u003C\u002Fjats:title>\u003Cjats:p>A panel of pediatric infectious diseases physicians and pharmacists from 20 geographically diverse North American institutions was convened. Through a series of teleconferences and web-based surveys, a set of guidance statements was developed and refined based on review of the best available evidence and expert opinion.\u003C\u002Fjats:p>\u003C\u002Fjats:sec>\u003Cjats:sec>\u003Cjats:title>Results\u003C\u002Fjats:title>\u003Cjats:p>Given the typically mild course of COVID-19 in children, supportive care alone is suggested for most cases. For children with severe illness, defined as a supplemental oxygen requirement without need for noninvasive or invasive mechanical ventilation or extracorporeal membrane oxygenation (ECMO), remdesivir is suggested, preferably as part of a clinical trial if available. Remdesivir should also be considered for critically ill children requiring invasive or noninvasive mechanical ventilation or ECMO. A duration of 5 days is appropriate for most patients. The panel recommends against the use of hydroxychloroquine or lopinavir-ritonavir (or other protease inhibitors) for COVID-19 in children.\u003C\u002Fjats:p>\u003C\u002Fjats:sec>\u003Cjats:sec>\u003Cjats:title>Conclusions\u003C\u002Fjats:title>\u003Cjats:p>Antiviral therapy for COVID-19 is not necessary for the great majority of pediatric patients. For children with severe or critical disease, this guidance offers an approach for decision-making regarding use of remdesivir.\u003C\u002Fjats:p>\u003C\u002Fjats:sec>",{"EN":2432},"Multicenter Interim Guidance on Use of Antivirals for Children With Coronavirus Disease 2019\u002FSevere Acute Respiratory Syndrome Coronavirus 2",{"VOID":2434},"32918548",{"VOID":2436},"10.1093\u002Fjpids\u002Fpiaa115",[145],"https:\u002F\u002Facademic.oup.com\u002Fjpids\u002Farticle\u002F10\u002F1\u002F34\u002F5904884",[2440,2472,2494,2516,2537,2558,2596,2617,2639,2658,2683,2706,2729,2751,2773,2788,2807,2829,2851,2868,2891,2923,2940,2957,2975,2996,3017,3046,3067,3089,3110,3133,3151,3168,3188,3204,3226,3247,3262,3284],{"id":2441,"sortIndex":2442,"researcher":24,"roles":2443,"affiliations":2444,"properties":2465},"ae929333-b075-4d83-8ea7-5d8e18a62d76",39,[],[2445,2455],{"id":2446,"sortIndex":166,"affiliation":2447,"properties":24},"4f950855-0384-4f91-ac53-59b3c1821b52",{"id":2448,"createTime":2449,"updateTime":2449,"relativeEntities":2450,"slug":2451,"properties":2452,"entityType":61,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},"28665114-bf6f-4144-a458-c8cd01ccfb94","2024-10-11T05:52:20.739+00:00",[],"Division-of-Infectious-Diseases-Department-of-Pediatrics-Boston-Children-s-Hospital-Boston-Massachusetts-USA",{"title":2453},{"EN":2454},"Division of Infectious Diseases, Department of Pediatrics, Boston Children's Hospital, Boston, Massachusetts, USA",{"id":2456,"sortIndex":25,"affiliation":2457,"properties":24},"3ada12f6-0386-48fc-9d49-a943bded578a",{"id":2458,"createTime":2459,"updateTime":2459,"relativeEntities":2460,"slug":2461,"properties":2462,"entityType":61,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},"784ef4a6-7cf1-45d0-88e5-07979bfa163a","2024-10-11T05:52:20.668+00:00",[],"Antimicrobial-Stewardship-Program-Boston-Children-s-Hospital-Boston-Massachusetts-USA",{"title":2463},{"EN":2464},"Antimicrobial Stewardship Program, Boston Children's Hospital, Boston, Massachusetts, USA",{"openalex":2466,"orcid":2468,"title":2470},{"VOID":2467},"A5020385033",{"VOID":2469},"https:\u002F\u002Forcid.org\u002F0000-0002-8191-0027",{"EN":2471},"Mari Nakamura",{"id":2473,"sortIndex":2474,"researcher":24,"roles":2475,"affiliations":2476,"properties":2487},"b5b8c29f-d87a-4d0e-a6c5-3e7bb2e5a2f3",17,[],[2477],{"id":2478,"sortIndex":25,"affiliation":2479,"properties":24},"c89adb36-d359-41b3-8e3c-e58a892f469c",{"id":2480,"createTime":2481,"updateTime":2481,"relativeEntities":2482,"slug":2483,"properties":2484,"entityType":61,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},"fae68371-baf8-4bd2-ac90-7893d8377414","2024-10-11T05:52:20.640+00:00",[],"Department-of-Pharmacy-Lucile-Packard-Children-s-Hospital-Stanford-Palo-Alto-California-USA",{"title":2485},{"EN":2486},"Department of Pharmacy, Lucile Packard Children's Hospital Stanford, Palo Alto, California, USA",{"openalex":2488,"orcid":2490,"title":2492},{"VOID":2489},"A5088752736",{"VOID":2491},"https:\u002F\u002Forcid.org\u002F0000-0001-9520-6420",{"EN":2493},"Laura L. Bio",{"id":2495,"sortIndex":2496,"researcher":24,"roles":2497,"affiliations":2498,"properties":2509},"c4f5bbfc-aaa7-43d9-96c6-940b535432e8",24,[],[2499],{"id":2500,"sortIndex":25,"affiliation":2501,"properties":24},"9cbe1f4a-5e53-4d96-a658-f8fbcc7f1c5f",{"id":2502,"createTime":2503,"updateTime":2503,"relativeEntities":2504,"slug":2505,"properties":2506,"entityType":61,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},"6bc64dbe-ab65-4b1c-ba24-ce03ca1bc1f0","2024-10-11T05:52:20.691+00:00",[],"Division-of-Infectious-Diseases-Department-of-Pediatrics-Washington-University-and-St-Louis-Children-s-Hospital-St-Louis-Missouri-USA",{"title":2507},{"EN":2508},"Division of Infectious Diseases, Department of Pediatrics, Washington University and St. Louis Children's Hospital, St. Louis, Missouri, USA",{"openalex":2510,"orcid":2512,"title":2514},{"VOID":2511},"A5017147084",{"VOID":2513},"https:\u002F\u002Forcid.org\u002F0000-0003-3865-2728",{"EN":2515},"Rachel C. Orscheln",{"id":2517,"sortIndex":435,"researcher":24,"roles":2518,"affiliations":2519,"properties":2530},"4d53360d-9022-4c2d-aa0c-066400753977",[],[2520],{"id":2521,"sortIndex":25,"affiliation":2522,"properties":24},"46102776-7338-4768-bf8c-f3044471c833",{"id":2523,"createTime":2524,"updateTime":2524,"relativeEntities":2525,"slug":2526,"properties":2527,"entityType":61,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},"486a15fd-7022-405c-b289-b3a436c128ac","2024-10-11T05:52:20.611+00:00",[],"Division-of-Infectious-Diseases-Department-of-Pediatrics-Vanderbilt-University-and-Monroe-Carell-Jr-Children-s-Hospital-Nashville-Tennessee-USA",{"title":2528},{"EN":2529},"Division of Infectious Diseases, Department of Pediatrics, Vanderbilt University and Monroe Carell Jr. Children's Hospital, Nashville, Tennessee, USA",{"openalex":2531,"orcid":2533,"title":2535},{"VOID":2532},"A5081978275",{"VOID":2534},"https:\u002F\u002Forcid.org\u002F0000-0003-2655-0900",{"EN":2536},"Mark R. Denison",{"id":2538,"sortIndex":209,"researcher":24,"roles":2539,"affiliations":2540,"properties":2551},"9fceb29e-73f9-4171-b9d8-a7dbeb75043e",[],[2541],{"id":2542,"sortIndex":25,"affiliation":2543,"properties":24},"d257f216-aaeb-400a-8161-708b26274665",{"id":2544,"createTime":2545,"updateTime":2545,"relativeEntities":2546,"slug":2547,"properties":2548,"entityType":61,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},"6943df44-86a7-4953-97d2-1876ea7a6704","2024-10-11T05:52:20.575+00:00",[],"Division-of-Pediatric-Infectious-Diseases-Department-of-Pediatrics-University-of-Alabama-at-Birmingham-Birmingham-Alabama-USA",{"title":2549},{"EN":2550},"Division of Pediatric Infectious Diseases, Department of Pediatrics, University of Alabama at Birmingham, Birmingham, Alabama, USA",{"openalex":2552,"orcid":2554,"title":2556},{"VOID":2553},"A5037870463",{"VOID":2555},"https:\u002F\u002Forcid.org\u002F0000-0001-9038-9109",{"EN":2557},"David W. 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10.1093\u002Fjac\u002Fdkaa253",{"doi":3817},"10.1093\u002Fjac\u002Fdkaa253",{"id":24,"text":3819,"url":24,"identifiers":3820},"Choi, 2020, Clinical characteristics and disease progression in early-stage COVID-19 patients in South Korea, J Clin Med, 9, 1959, 10.3390\u002Fjcm9061959",{"doi":3821},"10.3390\u002Fjcm9061959",{"id":24,"text":3823,"url":24,"identifiers":3824},"Qiu, 2020, Clinical and epidemiological features of 36 children with coronavirus disease 2019 (COVID-19) in Zhejiang, China: an observational cohort study, Lancet Infect Dis, 20, 689, 10.1016\u002FS1473-3099(20)30198-5",{"doi":3825},"10.1016\u002FS1473-3099(20)30198-5",{"id":3827,"createTime":3828,"updateTime":3828,"relativeEntities":3829,"slug":3830,"properties":3831,"entityType":141,"verifyStatus":142,"verifyTime":3828,"verifyNote":143,"syncStatus":23,"languages":3847,"translateLanguages":24,"viewCount":25,"primaryUrl":3848,"fullTextUrl":24,"authors":3849,"publicationType":398,"publisherRelationship":4188,"citationCount":4220,"citationInfo":4221,"publishDate":4223,"publishYear":439,"citationAnalyzeStatus":23,"lastCitationAnalyze":24,"indexDatabases":24,"openAccess":24,"references":4224,"isForceReanalyzing":462},"9413bd3f-1a51-446f-8421-8e61a5db2eee","2024-10-11T05:52:15.324+00:00",[],"Multidisciplinary-Guidance-Regarding-the-Use-of-Immunomodulatory-Therapies-for-Acute-Coronavirus-Disease-2019-in-Pediatric-Patients",{"mag":3832,"keywords":3834,"pmc":3835,"openalex":3837,"abstract":3839,"title":3841,"pm":3843,"doi":3845},{"VOID":3833},"3049581053",{},{"VOID":3836},"7454742",{"VOID":3838},"W3049581053",{"EN":3840},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\u003Cjats:sec>\u003Cjats:title>Background\u003C\u002Fjats:title>\u003Cjats:p>Immune-mediated lung injury and systemic hyperinflammation are characteristic of severe and critical coronavirus disease 2019 (COVID-19) in adults. Although the majority of severe acute respiratory syndrome coronavirus 2 infections in pediatric populations result in minimal or mild COVID-19 in the acute phase of infection, a small subset of children develop severe and even critical disease in this phase with concomitant inflammation that may benefit from immunomodulation. Therefore, guidance is needed regarding immunomodulatory therapies in the setting of acute pediatric COVID-19. This document does not provide guidance regarding the recently emergent multisystem inflammatory syndrome in children (MIS-C).\u003C\u002Fjats:p>\u003C\u002Fjats:sec>\u003Cjats:sec>\u003Cjats:title>Methods\u003C\u002Fjats:title>\u003Cjats:p>A multidisciplinary panel of pediatric subspecialty physicians and pharmacists with expertise in infectious diseases, rheumatology, hematology\u002Foncology, and critical care medicine was convened. Guidance statements were developed based on best available evidence and expert opinion.\u003C\u002Fjats:p>\u003C\u002Fjats:sec>\u003Cjats:sec>\u003Cjats:title>Results\u003C\u002Fjats:title>\u003Cjats:p>The panel devised a framework for considering the use of immunomodulatory therapy based on an assessment of clinical disease severity and degree of multiorgan involvement combined with evidence of hyperinflammation. Additionally, the known rationale for consideration of each immunomodulatory approach and the associated risks and benefits was summarized.\u003C\u002Fjats:p>\u003C\u002Fjats:sec>\u003Cjats:sec>\u003Cjats:title>Conclusions\u003C\u002Fjats:title>\u003Cjats:p>Immunomodulatory therapy is not recommended for the majority of pediatric patients, who typically develop mild or moderate COVID-19. For children with severe or critical illness, the use of immunomodulatory agents may be beneficial. The risks and benefits of such therapies are variable and should be evaluated on a case-by-case basis with input from appropriate specialty services. When available, the panel strongly favors immunomodulatory agent use within the context of clinical trials. 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10.1093\u002Fofid\u002Fofy325",{"doi":5067},"10.1093\u002Fofid\u002Fofy325",{"id":24,"text":5069,"url":24,"identifiers":5070},"Lippi, 2020, Thrombocytopenia is associated with severe coronavirus disease 2019 (COVID-19) infections: a meta-analysis, Clin Chim Acta, 506, 145, 10.1016\u002Fj.cca.2020.03.022",{"doi":5071},"10.1016\u002Fj.cca.2020.03.022",{"id":24,"text":5073,"url":24,"identifiers":5074},"Sen, 2016, Macrophage activation syndrome, Indian J Pediatr, 83, 248, 10.1007\u002Fs12098-015-1877-1",{"doi":5075},"10.1007\u002Fs12098-015-1877-1",{"id":24,"text":5077,"url":24,"identifiers":5078},"Cao, 2020, High-dose intravenous immunoglobulin as a therapeutic option for deteriorating patients with coronavirus disease 2019, Open Forum Infect Dis, 7, ofaa102, 10.1093\u002Fofid\u002Fofaa102",{"doi":5079},"10.1093\u002Fofid\u002Fofaa102",{"id":24,"text":5081,"url":24,"identifiers":5082},"McNab, 2015, Type I interferons in infectious disease, Nat Rev Immunol, 15, 87, 10.1038\u002Fnri3787",{"doi":5083},"10.1038\u002Fnri3787",{"id":24,"text":5085,"url":24,"identifiers":5086},"Ye, 2019, Interferon-λ orchestrates innate and adaptive mucosal immune responses, Nat Rev Immunol, 19, 614, 10.1038\u002Fs41577-019-0182-z",{"doi":5087},"10.1038\u002Fs41577-019-0182-z",{"id":24,"text":5089,"url":24,"identifiers":5090},"Prokunina-Olsson, 2020, COVID-19 and emerging viral infections: the case for interferon lambda, J Exp Med, 217, e20200653, 10.1084\u002Fjem.20200653",{"doi":5091},"10.1084\u002Fjem.20200653",{"id":24,"text":5093,"url":24,"identifiers":5094},"Muir, 2014, A randomized phase 2b study of peginterferon lambda-1a for the treatment of chronic HCV infection, J Hepatol, 61, 1238, 10.1016\u002Fj.jhep.2014.07.022",{"doi":5095},"10.1016\u002Fj.jhep.2014.07.022",{"id":24,"text":5097,"url":24,"identifiers":5098},"Agarwal, 2018, 96 weeks treatment of tenofovir alafenamide vs. tenofovir disoproxil fumarate for hepatitis B virus infection, J Hepatol, 68, 672, 10.1016\u002Fj.jhep.2017.11.039",{"doi":5099},"10.1016\u002Fj.jhep.2017.11.039",{"id":24,"text":5101,"url":24,"identifiers":5102},"Korean Association for the Study of the Liver., 2019, KASL clinical practice guidelines for management of chronic hepatitis B, Clin Mol Hepatol, 25, 93, 10.3350\u002Fcmh.2019.1002",{"doi":5103},"10.3350\u002Fcmh.2019.1002",{"id":24,"text":5105,"url":24,"identifiers":5106},"Chu, 2020, Comparative replication and immune activation profiles of SARS-CoV-2 and SARS-CoV in human lungs: an ex vivo study with implications for the pathogenesis of COVID-19 [manuscript published online ahead of print April 9, 2020], Clin Infect Dis, 10.1093\u002Fcid\u002Fciaa410",{"doi":5107},"10.1093\u002Fcid\u002Fciaa410",{"id":24,"text":5109,"url":24,"identifiers":5110},"O’Brien, 2020, Weak induction of interferon expression by SARS-CoV-2 supports clinical trials of interferon lambda to treat early COVID-19 [manuscript published online ahead of print April 17, 2020], Clin Infect Dis, 10.1093\u002Fcid\u002Fciaa453",{"doi":5111},"10.1093\u002Fcid\u002Fciaa453",{"id":24,"text":5113,"url":24,"identifiers":5114},"Hung, 2020, Triple combination of interferon beta-1b, lopinavir-ritonavir, and ribavirin in the treatment of patients admitted to hospital with COVID-19: an open-label, randomised, phase 2 trial, Lancet, 395, 1695, 10.1016\u002FS0140-6736(20)31042-4",{"doi":5115},"10.1016\u002FS0140-6736(20)31042-4",{"id":24,"text":5117,"url":24,"identifiers":5118},"Gaeta, 2002, Premature discontinuation of interferon plus ribavirin for adverse effects: a multicentre survey in ‘real world’ patients with chronic hepatitis C, Aliment Pharmacol Ther, 16, 1633, 10.1046\u002Fj.1365-2036.2002.01331.x",{"doi":5119},"10.1046\u002Fj.1365-2036.2002.01331.x",{"id":24,"text":5121,"url":24,"identifiers":5122},"Raison, 2005, Neuropsychiatric adverse effects of interferon-alpha: recognition and management, CNS Drugs, 19, 105, 10.2165\u002F00023210-200519020-00002",{"doi":5123},"10.2165\u002F00023210-200519020-00002",{"id":24,"text":5125,"url":24,"identifiers":5126},"Planet, 2016, Lambda interferon restructures the nasal microbiome and increases susceptibility to Staphylococcus aureus superinfection, mBio, 7, e01939, 10.1128\u002FmBio.01939-15",{"doi":5127},"10.1128\u002FmBio.01939-15",{"id":24,"text":5129,"url":24,"identifiers":5130},"Davidson, 2015, Disease-promoting effects of type I interferons in viral, bacterial, and coinfections, J Interferon Cytokine Res, 35, 252, 10.1089\u002Fjir.2014.0227",{"doi":5131},"10.1089\u002Fjir.2014.0227",{"id":24,"text":5133,"url":24,"identifiers":5134},"Locatelli, 2020, Emapalumab in children with primary hemophagocytic lymphohistiocytosis, N Engl J Med, 382, 1811, 10.1056\u002FNEJMoa1911326",{"doi":5135},"10.1056\u002FNEJMoa1911326",{"id":5137,"createTime":5138,"updateTime":5138,"relativeEntities":5139,"slug":5140,"properties":5141,"entityType":141,"verifyStatus":142,"verifyTime":5138,"verifyNote":143,"syncStatus":23,"languages":5157,"translateLanguages":24,"viewCount":25,"primaryUrl":5158,"fullTextUrl":24,"authors":5159,"publicationType":398,"publisherRelationship":5445,"citationCount":3069,"citationInfo":5477,"publishDate":5479,"publishYear":5480,"citationAnalyzeStatus":23,"lastCitationAnalyze":24,"indexDatabases":24,"openAccess":24,"references":5481,"isForceReanalyzing":462},"2a333fe2-fa03-45f8-a06b-485b13d4197c","2025-02-06T04:24:40.170+00:00",[],"A-Multicenter-Consortium-to-Define-the-Epidemiology-and-Outcomes-of-Pediatric-Solid-Organ-Transplant-Recipients-With-Inpatient-Respiratory-Virus-Infection",{"mag":5142,"keywords":5144,"pmc":5145,"openalex":5147,"abstract":5149,"title":5151,"pm":5153,"doi":5155},{"VOID":5143},"2789425479",{},{"VOID":5146},"7107524",{"VOID":5148},"W2789425479",{"EN":5150},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\n               \u003Cjats:sec>\n                  \u003Cjats:title>Background\u003C\u002Fjats:title>\n                  \u003Cjats:p>Respiratory virus infection (RVI) in pediatric solid organ transplant (SOT) recipients poses a significant risk; however, the epidemiology and effects of an RVI after pediatric SOT in the era of current molecular diagnostic assays are unclear.\u003C\u002Fjats:p>\n               \u003C\u002Fjats:sec>\n               \u003Cjats:sec>\n                  \u003Cjats:title>Methods\u003C\u002Fjats:title>\n                  \u003Cjats:p>A retrospective observational cohort of pediatric SOT recipients (January 2010 to June 2013) was assembled from 9 US pediatric transplant centers. Charts were reviewed for RVI events associated with hospitalization within 1 year after the transplant. An RVI diagnosis required respiratory symptoms and detection of a virus (ie, human rhinovirus\u002Fenterovirus, human metapneumovirus, influenza virus, parainfluenza virus, coronavirus, and\u002For respiratory syncytial virus). The incidence of RVI was calculated, and the association of baseline SOT factors with subsequent pulmonary complications and death was assessed.\u003C\u002Fjats:p>\n               \u003C\u002Fjats:sec>\n               \u003Cjats:sec>\n                  \u003Cjats:title>Results\u003C\u002Fjats:title>\n                  \u003Cjats:p>Of 1096 pediatric SOT recipients (448 liver, 289 kidney, 251 heart, 66 lung, 42 intestine\u002Fmultivisceral), 159 (14.5%) developed RVI associated with hospitalization within 12 months after their transplant. RVI occurred at the highest rates in intestine\u002Fabdominal multivisceral (38%), thoracic (heart\u002Flung) (18.6%), and liver (15.6%) transplant recipients and a lower rate in kidney (5.5%) transplant recipients. RVI was associated with younger median age at transplant (1.72 vs 7.89 years; P &lt; .001) and among liver or kidney transplant recipients with the receipt of a deceased-donor graft compared to a living donor (P = .01). The all-cause and attributable case-fatality rates within 3 months of RVI onset were 4% and 0%, respectively. Multivariable logistic regression models revealed that age was independently associated with increased risk for a pulmonary complication (odds ratio, 1.24 [95% confidence interval, 1.02–1.51]) and that receipt of an intestine\u002Fmultivisceral transplant was associated with increased risk of all-cause death (odds ratio, 24.54 [95% confidence interval, 1.69–327.96]).\u003C\u002Fjats:p>\n               \u003C\u002Fjats:sec>\n               \u003Cjats:sec>\n                  \u003Cjats:title>Conclusions\u003C\u002Fjats:title>\n                  \u003Cjats:p>In this study, hospital-associated RVI was common in the first year after pediatric SOT and associated with younger age at transplant. All-cause death after RVI was rare, and no definitive attributable death occurred.\u003C\u002Fjats:p>\n               \u003C\u002Fjats:sec>",{"EN":5152},"A Multicenter Consortium to Define the Epidemiology and Outcomes of Pediatric Solid Organ Transplant Recipients With Inpatient Respiratory Virus Infection",{"VOID":5154},"29538674",{"VOID":5156},"10.1093\u002Fjpids\u002Fpiy024",[145],"https:\u002F\u002Facademic.oup.com\u002Fjpids\u002Farticle\u002F8\u002F3\u002F197\u002F4925905",[5160,5179,5198,5219,5236,5257,5279,5296,5338,5355,5376,5397,5411,5428],{"id":5161,"sortIndex":62,"researcher":24,"roles":5162,"affiliations":5163,"properties":5174},"219da50a-4d4a-4b57-a1af-d778b820733d",[],[5164],{"id":5165,"sortIndex":25,"affiliation":5166,"properties":24},"516670ba-88fa-472f-87f0-53e977db93a7",{"id":5167,"createTime":5168,"updateTime":5168,"relativeEntities":5169,"slug":5170,"properties":5171,"entityType":61,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},"e0872d5f-b5ed-415c-87bc-8a217a40ccb2","2025-02-06T04:24:40.223+00:00",[],"Department-of-Pediatrics-Section-of-Infectious-Diseases-Texas-Children-s-Hospital-Baylor-College-of-Medicine-Houston",{"title":5172},{"EN":5173},"Department of Pediatrics, Section of Infectious Diseases, Texas Children's Hospital, Baylor College of Medicine, Houston",{"openalex":5175,"title":5177},{"VOID":5176},"A5110309252",{"EN":5178},"Leigh R. Sweet",{"id":5180,"sortIndex":150,"researcher":24,"roles":5181,"affiliations":5182,"properties":5193},"09539b9b-2482-429f-8ffd-e0b2343a7638",[],[5183],{"id":5184,"sortIndex":25,"affiliation":5185,"properties":24},"d4e9c274-8635-491f-8c7f-d774d781b381",{"id":5186,"createTime":5187,"updateTime":5187,"relativeEntities":5188,"slug":5189,"properties":5190,"entityType":61,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},"bd86ad53-8aeb-4b67-99a9-1f84d6b3c691","2025-02-06T04:24:40.184+00:00",[],"Seattle-Children-s-Research-Institute-Seattle-Children-s-Hospital-and-University-of-Washington",{"title":5191},{"EN":5192},"Seattle Children's Research Institute, Seattle Children's Hospital, and University of Washington",{"openalex":5194,"title":5196},{"VOID":5195},"A5036747735",{"EN":5197},"Alastair Murray",{"id":5199,"sortIndex":166,"researcher":24,"roles":5200,"affiliations":5201,"properties":5212},"208ac3dc-31db-4856-904a-6d8d102cf9a9",[],[5202],{"id":5203,"sortIndex":25,"affiliation":5204,"properties":24},"d62adc7a-b532-40b0-8edd-21e0daa0d0f3",{"id":5205,"createTime":5206,"updateTime":5206,"relativeEntities":5207,"slug":5208,"properties":5209,"entityType":61,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},"b46879f5-0cbe-4d02-b9ad-4b67d2f9d230","2025-02-06T04:24:40.212+00:00",[],"Departments-of-Pediatrics-and-Molecular-Genetics-and-Microbiology-Duke-University-Durham-North-Carolina",{"title":5210},{"EN":5211},"Departments of Pediatrics and Molecular Genetics and Microbiology, Duke University, Durham, North Carolina",{"openalex":5213,"orcid":5215,"title":5217},{"VOID":5214},"A5056810823",{"VOID":5216},"https:\u002F\u002Forcid.org\u002F0000-0002-5446-1094",{"EN":5218},"William J. Steinbach",{"id":5220,"sortIndex":233,"researcher":24,"roles":5221,"affiliations":5222,"properties":5229},"af466be4-ad2c-4e18-b637-e9d698e814a3",[],[5223],{"id":5224,"sortIndex":25,"affiliation":5225,"properties":24},"5b86a4a7-4e91-4470-947e-ebdeacff85bc",{"id":5167,"createTime":5168,"updateTime":5168,"relativeEntities":5226,"slug":5170,"properties":5227,"entityType":61,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},[],{"title":5228},{"EN":5173},{"openalex":5230,"orcid":5232,"title":5234},{"VOID":5231},"A5024481017",{"VOID":5233},"https:\u002F\u002Forcid.org\u002F0000-0002-0457-7689",{"EN":5235},"Flor M. 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Michaels",{"id":5258,"sortIndex":706,"researcher":24,"roles":5259,"affiliations":5260,"properties":5272},"97d7ada0-4c63-4d3f-93f6-da7014cb1820",[],[5261],{"id":5262,"sortIndex":25,"affiliation":5263,"properties":24},"8f5632d0-68cd-4b0f-b9b3-353823be540c",{"id":5264,"createTime":5265,"updateTime":5266,"relativeEntities":5267,"slug":5268,"properties":5269,"entityType":61,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},"53212041-b06c-4980-b8d4-ccedb7df7c23","2024-10-12T21:58:42.069+00:00","2025-02-06T04:24:40.233+00:00",[],"Department-of-Pediatrics-Albert-Einstein-College-of-Medicine-and-Children-s-Hospital-at-Montefiore-Bronx-New-York-",{"title":5270},{"EN":5271},"Department of Pediatrics, Albert Einstein College of Medicine and Children's Hospital at Montefiore, Bronx, New York.",{"openalex":5273,"orcid":5275,"title":5277},{"VOID":5274},"A5025731778",{"VOID":5276},"https:\u002F\u002Forcid.org\u002F0000-0001-9974-0786",{"EN":5278},"Betsy C. 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