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2 irect effectiveness (surveillance study) was febrile acute respiratory illness in an unvaccinated hou
3 nfirmed influenza in a vaccinated child with febrile acute respiratory illness, analysed in the modif
8 disability with delayed speech, a history of febrile and/or non-febrile seizures, and a wide-based, s
10 including aphthae, gastrointestinal disease, febrile attacks, and small-vessel vasculitis characteris
13 nalyze changes by month to the proportion of febrile cases prescribed a blood culture compared with t
16 investigated autoantibody (AAb) profiles in febrile children (<= 5 years) admitted to a hospital in
17 l 2018, data were prospectively collected on febrile children aged 0-18 years presenting to 12 EDs in
19 ) to decide on antibiotic prescription among febrile children at risk of pneumonia has not been teste
21 cterize dengue virus (DENV) infections among febrile children enrolled in a pediatric cohort study wh
22 was conducted to estimate the proportion of febrile children hospitalized at the study hospitals.
24 the e-POCT tool was non-inferior to that of febrile children managed by a validated electronic algor
25 to determine whether the clinical outcome of febrile children managed by the e-POCT tool was non-infe
28 prescription rate of antibiotics is high for febrile children visiting the emergency department (ED),
29 arried out with plasma samples obtained from febrile children with confirmed bacterial infection (n =
32 inguishing bacterial from viral infection in febrile children, to facilitate effective clinical manag
38 (CHIKV), a mosquito-borne alphavirus, causes febrile disease, muscle and joint pain, which can become
42 st 12 weeks of therapy significantly reduced febrile episodes and deaths compared with placebo withou
43 ity and age, altering the risk of developing febrile episodes and suggesting that host immunity plays
45 levated temperature conditions that simulate febrile episodes, especially at the beginning of the par
46 rations of HRP2 were substantially higher in febrile HRP2-positive patients than in afebrile HRP2-pos
48 y hospitalizations with acute respiratory or febrile illness (ARFI) and clinician-ordered real-time r
49 lizations for acute respiratory infection or febrile illness (ARFI) and influenza-associated ARFI amo
50 ies: healthy control, nonfebrile DENV, other febrile illness (OFI), and apparent DENV using multivari
52 tober 2017 met study criteria for confirmed (febrile illness and culture positivity or >=four-fold ri
53 V) is a mosquito-borne RNA virus that causes febrile illness and debilitating arthralgia in humans.
54 ungo virus infection presented with an acute febrile illness and died rapidly from massive hemorrhage
55 determinants of healthcare seeking for acute febrile illness and enteric fever risk in these communit
57 riates were explored as risk factors for RSV febrile illness and RSV pneumonia or hospitalization.
58 help improve interpretation of the burden of febrile illness and shape policy on fever case managemen
59 >=four-fold rise in SAT titre) or probable (febrile illness and single SAT titre >=160) brucellosis.
64 havirus that causes explosive epidemics of a febrile illness characterized by debilitating arthralgia
65 dardised surveillance of blood culture-based febrile illness in 13 African sentinel sites with previo
66 an genotype ZIKAV caused an outbreak of mild febrile illness in 2007 in Yap State, Federated States o
68 s (CCHFV) is a tick-borne pathogen causing a febrile illness in humans, which can progress to hemorrh
71 ion, we estimate incidence of RSV-associated febrile illness in the first 6 months of life and identi
72 sease are major causes of invasive bacterial febrile illness in the sampled locations, most commonly
73 7 plasma samples collected 2-12 months after febrile illness in Western and coastal Kenya (1993-2016)
74 ciated with infectious mononucleosis (IM), a febrile illness in which patients have high circulating
75 rizing healthcare-seeking patterns for acute febrile illness is critical for generating population-ba
77 management of children with undifferentiated febrile illness outside of malaria are not well understo
80 kungunya fever (CHIKF), a self-limited acute febrile illness that can progress to chronic arthralgic
81 ever is often self-limiting, presenting as a febrile illness that can result in atypical pneumonia.
82 hi A, frequently presents as a nonlocalizing febrile illness that is difficult to distinguish from ot
83 causes human monocytic ehrlichiosis (HME): a febrile illness that may progress to fatal sepsis with m
85 k, and surgical sites who had a diagnosis of febrile illness that was either suspected or blood cultu
86 ldren aged 2-59 months presenting with acute febrile illness to 9 outpatient clinics in Dar es Salaam
87 ic illness ranges from a mild, self-limiting febrile illness to one manifested by plasma leakage that
88 the PERFORM (Personalised Risk assessment in Febrile illness to Optimise Real-life Management across
90 -Congo haemorrhagic fever (CCHF) is a severe febrile illness transmitted by Hyalomma ticks in endemic
91 Plasmodium falciparum infections lead to febrile illness unless the host has sufficient immunity,
96 ease following VEEV infection manifests as a febrile illness with flu-like symptoms, which can progre
98 Among 1524 patients hospitalized with acute febrile illness, 133 isolates were found among 115 patie
99 ptomatic dengue patients experience an acute febrile illness, 5-20% progress to severe infection asso
103 supportive treatment to dengue patients with febrile illness, which is difficult to diagnose clinical
104 15, for occurrence of acute undifferentiated febrile illness, with clinical and laboratory data avail
105 and Southeast Asia and a rare cause of acute febrile illness, Zika virus (ZIKAV) arose from obscurity
106 nfants and children who suffered episodes of febrile illness-induced neurodegeneration or cardiac fai
122 0.85; 95% CI, 0.81 to 0.90), and nonmalarial febrile illnesses (1122 vs. 1424 episodes; incidence rat
123 matology can be easily confounded with other febrile illnesses (e.g., dengue fever and leptospirosis)
125 milar adjustments may be indicated for other febrile illnesses for which QT-interval-prolonging medic
130 mprove the clinical outcome of children with febrile illnesses while reducing antibiotic use through
131 for the diagnosis of acute undifferentiated febrile illnesses with presently available tests, which
133 suspected enteric fever, controls with other febrile illnesses, and healthy controls in Dhaka, Bangla
134 gue and other pathogens that can cause acute febrile illnesses, the search for secondary pathogens wi
136 TREM-1 at clinical presentation can identify febrile individuals at risk of all-cause febrile mortali
137 the course of medical care of 0- to 3-mo-old febrile infants (n = 913) and subsequently archived at -
138 mmonly used or optimal thresholds identified febrile infants 60 days or younger with IBIs with high a
141 eported successful treatment of a child with febrile infection-related epilepsy syndrome (FIRES), a s
144 l presentation and management of a cohort of febrile Kenyan children at five hospital/clinic sites fr
146 cMSP33D7 had a significantly reduced risk of febrile malaria (adjusted hazard ratio, 0.36 [95% confid
148 itemia was associated with a reduced risk of febrile malaria in older children (> 3 years), while in
149 ally distinct from those of individuals with febrile malaria in the transmission season, coinciding w
150 es previously shown to be protective against febrile malaria in this same cohort were significantly a
160 25 [51%]), anaemia (25 [47%] and 24 [49%]), febrile neutropaenia (17 [32%] and 21 [43%]), and pneumo
163 , were neutropenia (340 [15%] vs 328 [15%]), febrile neutropenia (112 [5%] vs 142 [6%]), and leucopen
164 rade 3 or worse were neutropenia (20 [30%]), febrile neutropenia (12 [18%]), and thrombocytopenia (si
165 sed neutrophil count (31 [12%] vs 27 [11%]), febrile neutropenia (14 [6%] vs 16 [6%]), diarrhoea (12
167 of 37 patients), neutropenia (15 [41%]), and febrile neutropenia (15 [41%]) in the pazopanib group, a
168 thrombocytopenia (30%), hypertension (15%), febrile neutropenia (15%), and lung infection (11%).
169 common grade 3 or 4 adverse events included febrile neutropenia (16 [41%] of 39), neutropenia (12 [3
171 reatment-related serious adverse events were febrile neutropenia (18 patients [7%]), sepsis or septic
172 he most common grade 3-4 adverse events were febrile neutropenia (22 [66%]), bloodstream infections (
173 gher with ramucirumab than with placebo were febrile neutropenia (24 [9%] of 258 patients in the ramu
174 ll 285 serious adverse events recorded, were febrile neutropenia (27 [17%] of 155 serious adverse eve
176 adverse events (>=10% in either group) were febrile neutropenia (31 [42%] vs 28 [39%]), decreased wh
177 grade 3/4 toxicities were neutropenia (62%), febrile neutropenia (35%), and peripheral sensory neurop
178 ing infection (16.9% v 10.7%, respectively), febrile neutropenia (35.0% v 17.7%, respectively), mucos
179 onhematologic toxicities with regimen M were febrile neutropenia (39.2%) and infections (21.6%).
180 events, including incidence and severity of febrile neutropenia (41 [18%] patients in the A+CHP grou
181 ommon grade 3 or greater adverse events were febrile neutropenia (42%), thrombocytopenia (38%), and W
182 neutropenia (124 [60%] of 207 patients) and febrile neutropenia (48 [23%]), whereas in the placebo g
184 group), neutropenia (47 [15%] vs 92 [30%]), febrile neutropenia (57 [18%] vs 34 [11%]), leucopenia (
185 e 3/4 neutropenia (45.8% v 21.5%; P < .001), febrile neutropenia (6.3% v 3.7%; P = .019), and diarrhe
186 s irrespective of relation to treatment were febrile neutropenia (97 [39%] of 252), anaemia (61 [24%]
187 nts occurring in 5% or more of patients were febrile neutropenia (98 [39%] of 252; five related to tr
189 ea (five [2%]) in the quizartinib group, and febrile neutropenia (five [5%]), sepsis or septic shock
190 r more patients) were pneumonia (five [6%]), febrile neutropenia (five [6%]), pulmonary embolism (thr
191 nt (IEAT) in oncohematological patients with febrile neutropenia (FN) and its impact on mortality.
192 y group compared with pneumonia (four [4%]), febrile neutropenia (four [4%]), anaemia (three [3%]), a
193 vs 28 [6%]; grade 4, 98 [20%] vs 77 [15%]), febrile neutropenia (grade 3, 52 [10%] vs 31 [6%]; grade
195 naemia (11 [25%]), leukopenia (seven [16%]), febrile neutropenia (seven [16%]), and pneumonia (seven
196 openia (eight [16%]), anaemia (seven [14%]), febrile neutropenia (six [12%]), and leucopenia (six [12
199 neutropenia (three [9%] of 35 patients) and febrile neutropenia (three [9%]) in the control group.
204 An antibiotic cycling-based strategy for febrile neutropenia effectively reduced carbapenem use,
206 ed after paclitaxel only if patients had had febrile neutropenia in a prior cycle or at investigator
208 he most common grade 3-4 adverse events were febrile neutropenia in seven (14%) patients, decreased n
210 ignancy unit: monthly antibiotic cycling for febrile neutropenia that included cefepime (+/- metronid
213 11 (10%) patients, of which neutropenia and febrile neutropenia were the most common (five [5%] pati
214 11%] events), and anaemia and neutropenia or febrile neutropenia were the most frequent grade 3 or wo
215 event in the subcutaneous daratumumab group (febrile neutropenia) and four in the intravenous group (
217 f 270 patients; nine [3%] vs no patients had febrile neutropenia), infections (86 [31%] vs 48 [18%]),
219 imumab plus platinum-etoposide group (death, febrile neutropenia, and pulmonary embolism [n=2 each];
220 0%) included nausea, diarrhea, constipation, febrile neutropenia, fatigue, hypokalemia, decreased app
222 vents included one (3%) patient with grade 3 febrile neutropenia, one (3%) patient with grade 4 hyper
224 most common noninfectious reactions include febrile nonhemolytic transfusion reactions, allergic tra
226 safely reduces unnecessary antibiotic use in febrile, nonseverely neutropenic pediatric patients with
227 s (>30 min); or with clusters of two or more febrile or afebrile seizures within a 24-h period were a
228 urrent prolonged (>10 min) febrile seizures; febrile or afebrile status epilepticus (>30 min); or wit
232 n southeast Asia, antibiotic prescription in febrile patients attending primary care is common, and a
234 and identify risk factors for brucellosis in febrile patients from a pastoralist community of Tanzani
235 re defined by positive RDT and controls were febrile patients from the same clinic with a negative RD
236 In this case-control study, we enrolled febrile patients presenting to outpatient departments at
238 Surveillance for arboviral diseases among febrile patients was performed at an emergency health un
247 had been cultivated in MHB experienced short febrile periods (median, 3.2 days), limited weight loss
248 ad been cultivated in BHI experienced longer febrile periods (median, 5.5 days) and greater weight lo
252 ere judged to be related to vaccination (one febrile reaction and one anaphylaxis) and one possibly r
254 inate between anaphylaxis and cardiovascular/febrile reactions, ROC curve analysis revealed a reasona
261 ines and attenuated systemic circulatory and febrile responses, likely reflecting decreased systemic
263 tinct acute encephalopathy syndromes, simple febrile seizures (14), other seizures (16), acute ataxia
264 pilepsy was lower in patients with prolonged febrile seizures (14.3%, 6.3-29.4) and survivors of acut
265 ts from an epilepsy GWAS meta-analysis and a febrile seizures (FS) GWAS are significantly more enrich
266 a subset of children experiencing prolonged febrile seizures (FSs), the most common type of childhoo
267 was raised in individuals with a history of febrile seizures (hazard ratio [HR] 1.12, 95% CI 1.08-1.
268 tinct acute encephalopathy syndromes, simple febrile seizures (n = 14), other seizures (n = 16), acut
269 ased with a growing number of admissions for febrile seizures (p<0.0001) and with later onset of chil
270 were categorised according to occurrence of febrile seizures and epilepsy, before entering the follo
271 g of KCC2, found previously in patients with febrile seizures and epilepsy, has been demonstrated to
272 articipant (2.9%, 0.5-14.5) in the prolonged febrile seizures group developed temporal lobe epilepsy
274 included associations of SCN1A with "complex febrile seizures" (HP: 0011172; p = 2.1 x 10(-5)) and "f
276 ayed speech, a history of febrile and/or non-febrile seizures, and a wide-based, spastic, and/or stif
277 ry clinical discharge diagnoses (eg, sepsis, febrile seizures, dehydration, or other non-respiratory
278 drawal, age at onset of epilepsy, history of febrile seizures, number of seizures before remission, a
281 resenting with recurrent prolonged (>10 min) febrile seizures; febrile or afebrile status epilepticus
283 n patient from New Caledonia presenting with febrile splenomegaly,weight loss, life-threatening autoi
284 o three months apart and are under long-term febrile surveillance to detect dengue by serotype-specif
285 b) Mass Screen and Treat (MSAT) classifed by febrile, symptomatic infections, and (c) Mass Test and T
286 opheles mosquitoes and presents with generic febrile symptoms that are challenging to diagnose clinic
287 with arthritogenic alphaviruses results in a febrile syndrome characterized by debilitating musculosk
290 Vs) since TRPV1/TRPV4 antagonism blocked the febrile Th2 switch, while TRPV1 agonists mediated a Th2
291 patient recuperation starting from the early febrile to the defervescence and convalescent stages of
294 ations of atypical and recurrent episodes of febrile UTI should focus on urinary tract abnormalities,
300 reatment after a neutropenic patient becomes febrile, whether and how to modify the initial treatment