ライフサイエンスコーパス: ill

1 and not pregnant, breastfeeding, or severely ill).

2 laria parasites in their blood without being ill.

3 om surrogates for the chronically critically ill.

4 d with increased mortality in the critically ill.

5 posite outcome was death or delisting as too ill.

6 None of their 57 contacts were subsequently ill.

7 ew ground in understanding why people become ill.

8 n CMV-seropositive adults who are critically ill.

9 medication use practices for the critically ill.

10 Among acutely ill adult patients requiring Intensive Care Unit admissi

11 his was a prospective study in 10 critically ill adult patients who received CVVH from April 2014 to

12 Frailty is common in critically ill adults aged 18 years and older and is independently

13 optimal nutritional strategy for critically ill adults at high nutritional risk is unclear.

14 ic candidiasis in immunocompetent critically ill adults did not reduce mortality and may have decreas

15 r decisions related to liberating critically ill adults from mechanical ventilation.

16 phalographic recordings from 4772 critically ill adults in 3 academic medical centers from February 2

17 been shown to improve outcomes in critically ill adults or children after cardiac surgery.

18 Critically ill adults requiring continuous renal replacement therap

19 , double-blind trial, we assigned critically ill adults to receive either the freshest available, com

20 Forty critically ill adults with fever (core temperature, >/= 38.3 degree

21 As, was developed to discriminate critically ill adults with infection-positive versus infection-nega

22 sociations of free light chain in critically ill adults with sepsis have not been previously reported

23 uid most commonly administered to critically ill adults, but it may be associated with acute kidney i

24 o, no protocol, or usual care) in critically ill adults.

25 the impact of bowel protocols in critically ill adults.

26 on from mechanical ventilation in critically ill adults.

27 ociated with delirium and coma in critically ill adults.

28 not affect 90-day mortality among critically ill adults.

29 mortality after transfusion among critically ill adults.

30 act patient-important outcomes in critically ill adults.

31 on from mechanical ventilation in critically ill adults.

32 e detected in the myocardium of both acutely ill and convalescent NHPs.

33 after pneumococcal infection in both acutely ill and convalescent NHPs.

34 V genomic DNA is frequently detected in both ill and healthy children.

35 nfections, particularly affecting critically ill and immunocompromised patients.

36 f advanced age (mean, 68 years), chronically ill, and had severe disease.

37 nd consequences of delirium among critically ill Arabic speaking patients.

38 bidities, and were less likely to be acutely ill as measured by organ failures.

39 choice of empiric antibiotics in critically ill burn patients.

40 ction among NUTrition Risk in the Critically Ill category, mortality, and protein and energy intake,

41 ction among NUTrition Risk in the Critically Ill category, time to discharge alive, and protein and e

42 some detail, the maturation complexes remain ill characterized.

43 ational cohort study included all critically ill children 21 years or younger admitted to a 20-bed, m

44 mode of mechanical ventilation in critically ill children admitted to PICU in an unplanned fashion ma

45 Delirium occurs frequently in critically ill children and is independently associated with mortal

46 sion of the SOFA score (pSOFA) in critically ill children and to evaluate the Sepsis-3 definitions in

47 from central venous catheters in critically ill children and to examine the effect of the guideline

48 luding increased mortality, among critically ill children and young adults.

49 not to disclose poor prognosis to seriously ill children can be challenging, especially when the req

50 ntions on clinical outcomes among critically ill children in a United Kingdom study.

51 rescribing micronutrient-fortified SQ-LNS to ill children presenting for primary care in rural Gambia

52 Studies involving critically ill children who have not undergone cardiac surgery are

53 enter trial, we randomly assigned critically ill children with confirmed hyperglycemia (excluding pat

54 Critically ill children with hyperglycemia did not benefit from tig

55 ribe the frequency of delirium in critically ill children, its duration, associated risk factors, and

56 Delirium is prevalent among critically ill children, yet associated outcomes and modifiable ris

57 iatrogenic withdrawal syndrome in critically ill children.

58 e, of the Sepsis-3 definitions in critically ill children.

59 logical advancements involved in the care of ill children.

60 nd fight our way out of the egg to break the ill-conceived illusion of nanomedicine.

61 ee energy (MFE) predictions are known to be "ill conditioned" in that small changes to the thermodyna

62 MFE accuracy, the presence of both well- and ill-conditioned sequences indicates the continued need f

63 fine quantitative thresholds for well versus ill conditioning.

64 tal power radiated through this mechanism is ill constrained, as the lower limit of the electron ener

65 d the role of the intestine, however, remain ill defined.

66 catheters in this patient population remains ill defined.

67 this ecosystem and to clinical outcomes are ill defined.

68 decisions during placenta development remain ill defined.

69 pathways that regulate their development are ill defined.

70 from specific NADPH oxidase isoforms remains ill defined.

71 elopment and progression, but mechanisms are ill defined.

72 ition play in the pathophysiology of FXS are ill defined.

73 stage, but their functional capacity remains ill defined.

74 emic brain, their exact contribution remains ill defined.

75 in and immune cells from the bovine host are ill defined.

76 f injury development following insult remain ill-defined and there are no FDA approved pharmaceutical

77 K3alpha and GSK3beta, whose functions remain ill-defined because of a lack of inhibitors that can dis

78 CALMs with jagged or ill-defined borders of the coast of Maine subtype tend t

79 us and noisy Hoxa5 expression, as well as an ill-defined boundary phenotype in Dicer mutants.

80 Early studies employing ill-defined catalysts showed evidence for retention of t

81 uropathic corneal pain (NCP) is currently an ill-defined disease.

82 ntiation and large vacuoles, or in small and ill-defined glands.

83 Quiescent CNV appeared as an ill-defined hyperfluorescent lesion without leakage or p

84 R-Chk1 DNA damage response (DDR) pathway via ill-defined mechanisms.

85 stic value, it harbours shortcomings such as ill-defined parameters for subtypes and grading criteria

86 is include: involvement of the lumbar spine, ill-defined paraspinal abnormal contrast enhancement, di

87 -type band at approximately 500 nm and broad ill-defined Q-type band(s) in the region 600-950 nm, whi

88 itional heterogeneity of the films and their ill-defined surfaces.

89 intricately linked to the varying (and still ill-defined) physiological functions and cellular expres

90 ugh the causes of these Abs remain broad and ill-defined, a genetic deficiency in C1 complex (C1qC1r2

91 the pathogenesis of human breast cancer are ill-defined, but our analysis of publically available ar

92 d progenitor cell (HSPC) fate choices remain ill-defined.

93 ll maintenance, but the ligands involved are ill-defined.

94 nderpinning coronary artery formation remain ill-defined.

95 underlie breast epithelial hierarchy remain ill-defined.

96 y fatal but the mechanisms of disease remain ill-defined.

97 mal traffic affects T cell signaling remains ill-defined.

98 1 in mitochondrial fusion and energetics are ill-defined.

99 iated neurocognitive disorder (HAND) remains ill-defined.

100 regulatory effects on chromatin that remain ill-defined.

101 e diverse features of these disorders remain ill-defined.

102 phy-induced PIF phosphorylation has remained ill-defined.

103 consequences of takotsubo cardiomyopathy are ill-defined.

104 cell subsets in cancer immunotherapy remains ill-defined.

105 e cross-talk between M2 and NK cells remains ill-defined.

106 g-associated immunosuppression in humans are ill-defined.

107 which the role of neuroinflammation remains ill-defined.

108 airway remodelling and inflammation remains ill-defined.

109 bution of these variants to tumorigenesis is ill-defined.

110 ion to riverbed sediment geochemistry remain ill-defined.

111 chanisms underlying their progression remain ill-defined.

112 estinal barrier, it is possible that similar ill effects could be seen in humans consuming contaminat

113 shing diets of feedlot cattle to counter the ill-effects of feeding diets with rapidly digestible car

114 The high mortality rate in critically ill elderly patients has led to questioning of the benef

115 Among critically ill elderly patients in France, a program to promote sys

116 n for systematic ICU admission in critically ill elderly patients reduces 6-month mortality compared

117 show that standard polytomous regression is ill equipped to detect outcome heterogeneity and will ge

118 which existing electronic health records are ill equipped to manage.

119 Traditional in vitro methods are ill-equipped to study these critical events in the conte

120 Instead, ill fishers shifted their fishing methods.

121 Ill fishers were also less likely to fish using legal me

122 When ill, fishers were more likely to use methods that were i

123 Using a minimal model of ill-fitting, sticky particles, we demonstrate robust fib

124 Results Patients who reported a terminally ill health status had worse QOL (unstandardized coeffici

125 01) among patients who reported a terminally ill health status.

126 hree), strong for sexual risk taking, mental ill health, and problematic alcohol use (ORs of more tha

127 Study that increased with age, obesity, and ill health.

128 mportant contributor to the global burden of ill-health and health inequality.

129 f noninfectious sepsis given that critically ill humans never exist in a germ-free state.

130 Critically ill immunocompromised patients with hypoxemic acute resp

131 o patients at visits), patients feeling "too ill" in 8 (16.7%), patient refusal in 8 (16.7%), and int

132 that focuses on single epidemics and acutely ill individuals, the subtle dynamical influence of chron

133 dical management among a group of critically ill infants who were suspected to have genetic disorders

134 o exome, a rapid genomic assay for seriously ill infants.

135 e of clinical exome sequencing in critically ill infants.

136 taken from a prospective study of critically ill intensive care unit (ICU) patients meeting two of fo

137 tured interviews with chronically critically ill long-term acute care hospital patients or surrogates

138 Chronically ill, medicated SZ patients and matched controls (n=25 SZ

139 Immunoneutralizing glucagon in critically ill mice only transiently affected glucose and lipid met

140 Human AML cells from terminally ill mice treated with chemotherapy (chemoAML) had higher

141 In critically ill mice, infusion of amino acids increased glucagon and

142 a from 16 mechanically ventilated critically ill obese patients were analyzed.

143 Atelectasis develops in critically ill obese patients when undergoing mechanical ventilatio

144 ival for nonadmitted patients considered too ill/old than for ICU-admitted patients and nonadmitted p

145 for ICU refusal in patients considered "too ill/old" were advanced age and low functional status.

146 nonadmitted patients who were considered too ill/old, indicating a benefit of ICU admission.

147 d 32.7% and 11.5% in patients considered too ill/old, respectively.

148 ing facilities who fall may not be seriously ill or injured, but policies often require immediate tra

149 search study (eg, known dementia, terminally ill, or recently bereaved).

150 hole blood glucose measurement in critically ill patient care settings.

151 biota." Under this framework, the critically ill patient is viewed as a host colonized by pathobiota

152 system was acceptable for use in critically ill patient settings when compared to the central labora

153 rmance of blood glucose meters in critically ill patient settings.

154 A critically ill patient with multiple postoperative infections repea

155 We enrolled critically ill patients (>/=18 years) needing mechanical ventilatio

156 ntration-time data from 214 adult critically-ill patients (creatinine clearance 0-236mL/min; 29 recei

157 until day 5 of the ICU stay in 30 critically ill patients (median [interquartile range] age 63 [57-67

158 Critically ill patients 6 months to 5 years old.

159 Critically ill patients admitted between July 2000 and October 2008

160 a prospective cohort study of 350 critically ill patients admitted to intensive care units at an acad

161 adjusted 90-day mortality risk in critically ill patients admitted with sepsis.

162 udies that randomly assigned 2607 critically ill patients after trauma to an ESA or placebo (or no ES

163 ies of 36 mechanically ventilated critically ill patients and compared with those isolated from biops

164 elayed gastric emptying occurs in critically ill patients and impairs the delivery, digestion, and ab

165 Focus on critically ill patients and included evaluations in other patient c

166 bes the experience of chronically critically ill patients and surrogates in an long-term acute care h

167 healthcare costs associated with critically ill patients as it has been shown that, despite almost c

168 Surgical and critically ill patients at a tertiary medical center between 2011 a

169 m randomized controlled trials in critically ill patients by assessing the incidence of eligibility f

170 fusion poses significant risks to critically ill patients by increasing their susceptibility to acute

171 Diaphragm muscle fibers from critically ill patients displayed significant atrophy and contracti

172 Critically ill patients have manifest diaphragm muscle fiber atroph

173 ervational studies, but trials in critically ill patients have not shown benefit.

174 Chronically critically ill patients have recurrent infections, organ dysfunctio

175 reliability of codes relevant to critically ill patients in administrative data.

176 mize the support of the family of critically ill patients in the ICU.

177 stating that the use of meters in critically ill patients is "off-label" and constitutes "high comple

178 ess of diaphragm muscle fibers in critically ill patients is accompanied by impaired mitochondrial fu

179 Delirium in critically ill patients is associated with poor clinical outcomes.

180 ificance of diaphragm weakness in critically ill patients is evident: it prolongs ventilator dependen

181 ectroencephalography (EEG) use in critically ill patients is expanding.

182 In sepsis, the disease course of critically ill patients is often complicated by muscle failure lead

183 associated with AKI and death in critically ill patients is unknown.

184 antibiotic and steroid therapy in critically ill patients not fitting into established disease entiti

185 We enrolled 136 critically ill patients on mechanical ventilation and/or vasopresso

186 ing by surrogates for chronically critically ill patients on mechanical ventilation.

187 nt for this source of calories in critically ill patients receiving nutrition on CVVH may result in o

188 vance the study and management of critically ill patients requiring mechanical ventilation.

189 rve how surrogates of chronically critically ill patients respond to information about prognosis from

190 Less severely ill patients seem to benefit less in terms of olanzapine

191 A large portion of former critically ill patients show small fiber deficits which seem to be

192 antibiotic-associated colitis in critically ill patients signified by microbiota depletion, and rees

193 ate diagnosis for Arabic speaking critically ill patients suffering from delirium is limited by the n

194 on for pediatricians who care for critically ill patients to encounter families who object to discont

195 ations to be self-administered by terminally ill patients to hasten their death.

196 The diverse responses of critically ill patients to infection with multi-drug resistant (MDR

197 Critically ill patients transported within the hospital by critical

198 em model to estimate seizure risk in acutely ill patients undergoing continuous EEG.

199 in predicting 6-month outcomes of critically ill patients varied depending on the outcome being predi

200 nflammatory markers compared with critically ill patients who do not develop ICU-acquired weakness.

201 Critically ill patients who have a high risk of bleeding but requir

202 surements were performed on 1,698 critically ill patients with 257 different clinical conditions and

203 Among critically ill patients with acute kidney injury, exposure to posit

204 rsus Delayed Initiation of RRT in Critically Ill Patients with AKI (ELAIN) Trial from 90 days to 1 ye

205 ther earlier initiation of RRT in critically ill patients with AKI can improve outcomes remains debat

206 early initiation of RRT in these critically ill patients with AKI significantly reduced the occurren

207 ailable technique for identifying critically ill patients with intracranial hypertension.

208 We studied 16,968 critically ill patients with Kidney Disease Improving Global Outcom

209 for the use of corticosteroids in critically ill patients with sepsis and septic shock, acute respira

210 Among 20750 critically ill patients with sepsis in 107 hospitals with PCT avail

211 respiratory distress syndrome in critically ill patients with sepsis.

212 rease duration of antibiotics for critically ill patients with sepsis.

213 d not affect overall mortality in critically ill patients with sepsis.

214 A total of 1,080 critically ill patients with sepsis.

215 on, outcome, and host response in critically ill patients with sepsis.

216 trial fibrillation in a cohort of critically ill patients with sepsis.

217 PATIENTS/Twenty-six critically ill patients with Sequential Organ Failure Assessment sc

218 ication patterns, and outcomes of critically ill patients with severe acute respiratory infection fro

219 e should limit the PaO2 levels of critically ill patients within a safe range, as we do with other ph

220 ith placebo or no intervention in critically ill patients without neutropenia, but the quality of the

221 f an invasive fungal infection in critically ill patients without neutropenia?

222 rolonged hemodialysis sessions in critically ill patients without the need to systemically monitor io

223 s Target Enteral Feeding in Adult Critically Ill Patients) trial.

224 ng 51 intrahospital transports of critically ill patients, 80% of whom were mechanically ventilated.

225 tion, labor-intensive support for critically ill patients, and effective chronic disease management.

226 ic treatment, glucose targets for critically ill patients, and treatment of hospitalized patients.

227 nt for treatment of infections in critically ill patients, are lacking.

228 Chronically critically ill patients, defined by tracheotomy for prolonged mecha

229 hrelin in control subjects and in critically ill patients, during feeding and fasting, and to search

230 Among critically ill patients, exposure to positive or negative fluid bal

231 Among hospitalized medically ill patients, extended-duration betrixaban significantly

232 Newly admitted critically ill patients, greater than or equal to 48 hours on mecha

233 In critically ill patients, infusing glucose with insulin did not lowe

234 e evolution of a new phenotype of critically ill patients, its potential underlying mechanism, and it

235 or physicians to provide care for critically ill patients, particularly at institutions with worse cl

236 In critically ill patients, plasma concentration of ghrelin significan

237 ed small nerve fiber pathology in critically ill patients, which may contribute to chronic pain state

238 mes influence decision making for critically ill patients, yet little is known regarding their accura

239 used to assess immune function in critically ill patients.

240 reased morbidity and mortality in critically ill patients.

241 ience the same side-effects as more severely ill patients.

242 th, and other adverse outcomes in critically ill patients.

243 tile weakness of the diaphragm in critically ill patients.

244 italized and immunocompromised or critically ill patients.

245 chanically ventilated and sedated critically ill patients.

246 holding proton pump inhibitors in critically ill patients.

247 isting poor outcomes for infected critically ill patients.

248 fill resource gaps in caring for critically ill patients.

249 llow-up analysis from a cohort of critically ill patients.

250 ion practices that is specific to critically ill patients.

251 ut possibly increase morbidity in critically ill patients.

252 ents are difficult to complete in critically ill patients.

253 and preventing pressure injuries in acutely ill patients.

254 duration for seizure detection in critically ill patients.

255 ess of intrahospital transport of critically ill patients.

256 n the unexplained anemias seen in critically ill patients.

257 lood glucose monitoring system in critically ill patients.

258 get ventilation (OTV) delivery in critically-ill patients.

259 sociated with risk of seizures in critically ill patients.

260 ofound pathologies encountered in critically ill patients.

261 sician diversity reflects that of critically ill patients.

262 associated with poor outcomes in critically ill patients.

263 duration of delirium and coma in critically ill patients.

264 essure, and heart rate in febrile critically ill patients.

265 dgment of the risk of seizures in critically ill patients.

266 r cause of respiratory failure in critically ill patients.

267 ng to questions over their use in critically ill patients.

268 individual organ dysfunctions in critically ill patients.

269 weaning difficulty in ventilated critically ill patients.

270 observed in this large cohort of critically ill patients.

271 pitalized patients (including the critically ill), patients undergoing stress echocardiography, and p

272 e performance of Septicyte Lab in critically ill pediatric patients.

273 By this logic, ill people reduce the time and effort that they put into

274 a can still be challenging and represents an ill-posed problem which is generally approached with ad

275 luding explicit rate constants results in an ill-posed problem with a vast number of potential soluti

276 However, this is in most cases an ill-posed problem, as the affiliation of a node to a sin

277 Many men are physically and psychologically ill-prepared and suffer from lack of information and sup

278 subfields were found in the more chronic and ill schizophrenia patients of Data set 2.

279 Based on the Nutrition Risk in Critically Ill score, 378 of 894 (42.3%) patients were categorized

280 ated by the NUTrition Risk in the Critically Ill score.

281 There may be excess morbidity in critically ill selective serotonin reuptake inhibitor/serotonin-nor

282 deduction, reasoning in well-structured and ill-structured problem spaces, novel strategy generation

283 Hospitalized acutely medically ill subjects (n=7513) were randomized in a double-dummy

284 Ill subjects recorded symptoms and provided blood and na

285 parative methods of evolutionary biology are ill suited to explain unique events.

286 al dynamics during specified tasks, they are ill-suited for tracking single-unit activity over longer

287 th cellulitis were found to be less severely ill than patients with necrotizing fasciitis.

288 tion variability would expose the critically ill to both piperacillin under and overdosing.

289 Here we show that clinically ill transgenic mice overexpressing hamster prion protein

290 ration of the ESA epoetin alfa to critically ill trauma patients has been associated with a reduction

291 esis-stimulating agents (ESAs) in critically ill trauma patients.

292 owever, how one code relates to the other is ill understood.

293 ork provides a mechanism for this previously ill-understood effect and illuminates the complex influe

294 Prominent examples are ill-understood metallic states in d- and f-band compound

295 CCC DNA is converted, in a multistep and ill-understood process, from a relaxed circular (RC) DNA

296 CCC DNA is converted, in a multistep and ill-understood process, from relaxed circular (RC) DNA.

297 ults worldwide, but its pathogenesis remains ill-understood.

298 pective APEX trial substudy (Acute Medically Ill Venous Thromboembolism Prevention With Extended Dura

299 r outcomes among patients who are critically ill with suspected infection.

300 Ball pythons fell ill within 2 months of infection and displayed signs of