ライフサイエンスコーパス: oximetry

1 ially detectable through screening via pulse oximetry.

2 rophysiological activity, pulse and cerebral oximetry.

3 or clinical acquisition of images in retinal oximetry.

4 n measurements using dual-wavelength retinal oximetry.

5 iloxanes as pO(2)-reporters for PISTOL-based oximetry.

6 eremia with magnetic resonance imaging-based oximetry.

7 linical application of multiwavelength pulse oximetry.

8 heter) and correlated with microdialysis and oximetry.

9 measured by electron paramagnetic resonance oximetry.

10 e analysis of cellular respiration using EPR oximetry.

11 ion to quantify related parameters using EPR oximetry.

12 bor to either "open" or "masked" fetal pulse oximetry.

13 monitored by electron paramagnetic resonance oximetry.

14 roscopy and of O2 consumption by fiber-optic oximetry.

15 ls and their mutants was investigated by EPR oximetry.

16 ith transcranial doppler and overnight pulse oximetry.

17 obin plus reduced hemoglobin) measured by co-oximetry.

18 , arterial blood gas measurements, and pulse oximetry.

19 Test if a novel panel consisting of pulse oximetry, 12-lead electrocardiography, and serum troponi

20 anial pressure, 3) jugular venous continuous oximetry, 4) regional saturation of oxygen using near-in

21 The most frequent interventions-pulse oximetry (66.5%), other monitoring (59.6%), and suppleme

22 .9; p<0.001), as was use of continuous pulse oximetry (78% vs. 58%, respectively; p=0.001).

23 nd favourable cost-effectiveness makes pulse oximetry a promising candidate for improving the prognos

24 Pulse oximetry, a relatively inexpensive technology, has the p

25 emain major challenges to implementing pulse oximetry-a cheap, decades old technology-into routine ca

26 ff from 14 Kenyan hospitals to examine pulse oximetry adoption.

27 nea using questionnaire plus nocturnal pulse oximetry against using polysomnography to identify patie

28 One-third of pulse oximetry alarm notifications were for clinically relevan

29 Provision of more reliable oximetry allows caregivers to act in a more efficient an

30 Cerebral oximetry allows real-time, noninvasive cerebral oxygenat

31 oxygen system compared to introducing pulse oximetry alone.

32 If we avoided oximetry altogether, then symptoms together with body ma

33 In-depth oximetry analysis demonstrated that functions of mitocho

34 e in vivo by electron paramagnetic resonance oximetry and (19)fluorine-MRI relaxometry.

35 itude underwent echocardiography, finger-tip oximetry and blood measurements of cardiac troponin I (c

36 Jugular oximetry and brain tissue oxygen pressure monitoring are

37 Cardiac monitoring, pulse oximetry and capnography are used, often without strong

38 (SaO(2)) and superior vena caval (SvO(2)) co-oximetry and cerebral oxygen saturation (ScO(2)) measure

39 tal admission, particularly the use of pulse oximetry and chest radiography.

40 inpatient records to explore roles of pulse oximetry and clinical guidelines on hospital attendance

41 rt and respiratory rate) and WristOx2 (pulse-oximetry and derived pulse rate) sensors.

42 ith the medium-throughput plate reader-based oximetry and EPR spin trapping as confirmatory assays, i

43 dissolved in hexafluorobenzene, for in vivo oximetry and imaging of oxygen concentration in tissues

44 y publications addressing knowledge of pulse oximetry and those warning against the use of transmissi

45 p apnea symptom questionnaire, and underwent oximetry and two-night polysomnography.

46 pected of bacterial pneumonia, bedside pulse oximetry and urinary antigen testing for Streptococcus p

47 or interaction between SpO2 threshold (pulse oximetry) and clinical guidelines, clustering by child,

48 electrocardiogram), oxygen saturation (pulse oximetry), and brachial artery blood flow and shear rate

49 and standard vital signs (heart rate, pulse oximetry, and body temperature) were monitored at regula

50 s the oxygen saturation as measured by pulse oximetry, and DLCO is the diffusing capacity for carbon

51 ery pressure, central venous pressure, pulse oximetry, and end-tidal CO(2) were continuously monitore

52 lower Glasgow Coma Scale score, lower pulse oximetry, and nursing home residence during out-of-hospi

53 UV-visible spectroscopy, electrode oximetry, and pH stat were used to study Fe(II) oxidatio

54 Blood pressure, electrocardiography, oximetry, and symptoms were monitored by a nurse with ex

55 Blood pressure, ECG, oximetry, and symptoms were monitored.

56 s (somatosensory-evoked potentials, cerebral oximetry, and transcranial Doppler ultrasound) were used

57 n arterial blood pressure, heart rate, pulse oximetry, and transcutaneous oxygen and carbon dioxide t

58 Simultaneous blood gas, pulse oximetry, and ventilator settings were collected.

59 Nadir oxygen saturation as measured by pulse oximetry, apnea-hypopnea index, and the fraction of even

60 sensors offer great potential for future EPR oximetry applications in preclinical research.

61 on to assess the impact of introducing pulse oximetry as a prognostic tool to distinguish severe from

62 We assessed the performance of pulse oximetry as a screening method for the detection of crit

63 The concept of using pulse oximetry as a screening method to detect undiagnosed cri

64 prospectively assessed the accuracy of pulse oximetry as a screening test for congenital heart defect

65 ncluding the introduction of universal pulse oximetry at a hospital in Chisinau, Moldova, where only

66 safety checklist and the provision of pulse oximetry at a referral hospital in Moldova, a lower-midd

67 on control of breathing, inaccuracy of pulse oximetry at low oxygen saturations, and temperature-indu

68 e of 0.79 (95% CI, 0.67-0.93) for peripheral oximetry at the instant the vital sign first crossed thr

69 Determination of pulse co-oximetry-based hemoglobin in patients presenting with se

70 ing to the development of new types of pulse oximetry-based monitoring techniques.

71 estation >34 weeks) were screened with pulse oximetry before discharge.

72 We also sought risk factors for pulse oximetry below 90%.

73 recent years to expand the utility of pulse oximetry beyond the simple measurement of arterial oxyge

74 s can discern clinically relevant peripheral oximetry, blood pressure, and respiratory rate alerts fr

75 Oximetry by near infrared spectroscopy reflects the bala

76 that include prompts, the promotion of pulse oximetry by senior doctors, and monitoring and feedback

77 Tissue oximetry can assist in diagnosis and prognosis of many d

78 Pulse oximetry can be used reliably to estimate the arterial o

79 Pulse oximetry can significantly increase the incidence of cor

80 acity of the lung for carbon monoxide, pulse oximetry, chest radiograph, and high-resolution thoracic

81 arrest while undergoing continuous cerebral oximetry, clearly demonstrated the ability of the INVOS

82 mination of the pulmonary circulation, pulse oximetry, complete blood count, and serum chemistries an

83 th two oximeters, one employing conventional oximetry (conventional pulse oximeter, CPO) and one usin

84 Pulse oximetry correlates well with cooximeter-measured satura

85 Our findings suggest that pulse oximetry could be beneficial in supplementing clinical s

86 data, reproducing the shapes of experimental oximetry curves with high accuracy.

87 des the available normal polysomnography and oximetry data for reference and documents the structural

88 Pulse oximetry data from 54 countries suggested that around 77

89 ate and meaningful model to evaluate the EPR oximetry data on cellular respiration to quantify relate

90 onsumption calculated using combined CMR and oximetry data was 173 mL/min per m(2), higher than the a

91 lasting 2 minutes or longer per 100 hours of oximetry decreased from 11.5 to 6.4 (P < 0.002).

92 EPR oximetry demonstrated that the ischemic wound tissue had

93 sought to quantitatively define the error in oximetry-derived flow parameters using phase-contrast ca

94 epatopulmonary syndrome underwent home pulse-oximetry during sleep.

95 ly-phenols were demonstrated by differential oximetry during the inhibited autoxidation of model subs

96 ater likelihood of a patient receiving pulse oximetry during the post-intervention period compared wi

97 erial hemoglobin oxygen saturation (by pulse oximetry), end-tidal PCO2, and carotid artery blood flow

98 ir readiness and reported that all had pulse oximetry equipment onsite and 74.4% had access to same-d

99 ithm using questionnaire and nocturnal pulse oximetry excluded few patients from sleep studies, but i

100 ndex, oxygen saturation as measured by pulse oximetry/Fi(O(2)) had a greater weight than respiratory

101 io of oxygen saturation as measured by pulse oximetry/Fi(O(2)) to respiratory rate) for determining H

102 us body mass index for everyone, followed by oximetry for a subset; and (5) oximetry for all.

103 , followed by oximetry for a subset; and (5) oximetry for all.

104 The overall sensitivity of pulse oximetry for detection of critical congenital heart defe

105 was the sensitivity and specificity of pulse oximetry for detection of critical congenital heart defe

106 essed the screening characteristics of pulse oximetry for HPS.

107 studies that assessed the accuracy of pulse oximetry for the detection of critical congenital heart

108 llow-up group to 6.8 events per 100 hours of oximetry for the long-term follow-up group; P = .10).

109 o decrease (from 8.1 events per 100 hours of oximetry for the short-term follow-up group to 6.8 event

110 x conditions was combined with multispectral oximetry for two-dimensional oxygen saturation mapping.

111 tiveness of intermittent vs continuous pulse oximetry found similar length of hospital stay and safet

112 his effort include the extension of cerebral oximetry from the operating room into the critical care

113 y group and 15 of 105 (14.3%) in the altered oximetry group (difference, 7% [95% CI, -0.3% to 0.2%];

114 medical visits for bronchiolitis in the true oximetry group and 15 of 105 (14.3%) in the altered oxim

115 Forty-four of 108 patients (41%) in the true oximetry group and 26 of 105 (25%) in the altered oximet

116 try group and 26 of 105 (25%) in the altered oximetry group were hospitalized within 72 hours (differ

117 nadir oxygen saturation as measured by pulse oximetry >82.5%) + (Fhypopneas >58.3%).

118 Routine use of pulse oximetry has been associated with changes in bronchiolit

119 Reliance on pulse oximetry has been associated with increased hospitalizat

120 Tissue oximetry has been suggested as a noninvasive tool to con

121 ssuming access to supplemental oxygen, pulse oximetry has the potential to avert up to 148,000 deaths

122 OCT capillary oximetry has the potential to provide new insights into

123 erimental sensors based on reflectance pulse oximetry have been developed for use in internal sites s

124 ission tomography (15O PET) and brain tissue oximetry have demonstrated increased oxygen diffusion gr

125 Recent advances in pulse oximetry have made it possible to noninvasively measure

126 Pulse oximetry identified fatal pneumonia episodes at HCs in M

127 from the green channel of a dual wavelength oximetry image.

128 al vessel calibre measurements obtained from oximetry images are in good agreement to those obtained

129 ses suggested that the introduction of pulse oximetry improved oxygen practices prior to implementati

130 s for universal CCHD screening through pulse oximetry in birth hospitals.

131 vo by darkfield microscopy and multispectral oximetry in experimental murine models of ALI induced by

132 , which, as determined by magnetic resonance oximetry in live mice, was accompanied by a correspondin

133 ng clinical guidelines with or without pulse oximetry in Malawi.

134 ured by a clinical severity score, and pulse oximetry in room air was done.

135 luate the use of noninvasive cerebral tissue oximetry in the care of children with severe anemia.

136 To assess the accuracy of pulse oximetry in the diagnosis of hypoxemia in SCD, we compar

137 using electron paramagnetic resonance (EPR) oximetry in the forebrain of rats under isoflurane, keta

138 gh the increased cost of bronchodilators and oximetry in these patients may serve as target areas for

139 diabetic ketoacidosis and, along with pulse oximetry, in lung-function laboratories to estimate bloo

140 lls showed reduced mitochondrial function by oximetry, including a reduction in maximal respiratory c

141 re reactivity index (PRx and wPRx), cerebral oximetry index (COx and wCOx), and hemoglobin volume ind

142 terial blood pressure at the lowest cerebral oximetry index (nadir index) for each 24-hour period of

143 the lower limit of autoregulation, cerebral oximetry index approaches 1, because cerebral blood flow

144 Monitoring cerebral oximetry index may provide a novel method for precisely

145 Global cerebral oximetry index was associated with functional outcomes a

146 The cerebral oximetry index was continuously monitored with near-infr

147 me group, lateral displacement, and cerebral oximetry index were assessed using multivariate linear r

148 Cerebral oximetry index, derived from near-infrared spectroscopy

149 py signals to generate the variable cerebral oximetry index.

150 The integration of cerebral oximetry into cardiac arrest resuscitation provides a no

151 aseline period (enabling evaluation of pulse oximetry introduction) and evaluated mortality and pract

152 study periods: baseline (usual care), pulse oximetry introduction, and stepped introduction of a mul

153 Auto-scored positional oximetry is a clinically viable alternative to an auto-s

154 Cerebral oximetry is a complimentary monitoring modality during s

155 Magnetic resonance imaging-based oximetry is a new calibration-free technique taking adva

156 Measurement of the SMV %HbO2 with MR oximetry is a promising test for diagnosis of chronic me

157 Pulse oximetry is a safe, feasible test that adds value to exi

158 Pulse oximetry is a ubiquitous non-invasive medical sensing me

159 Routine screening for CCHD using pulse oximetry is being increasingly supported and was added t

160 Electron paramagnetic resonance (EPR) oximetry is being widely used to measure the oxygen cons

161 INTERPRETATION: Pulse oximetry is highly specific for detection of critical co

162 Given pulse oximetry is increasingly substituting for arterial blood

163 Conclusion: Pulse oximetry is not sufficiently sensitive to screen for HPS

164 r hepatopulmonary syndrome (HPS) using pulse oximetry is recommended in liver transplant (LT) candida

165 Pulse oximetry is ubiquitous but detailed understanding of the

166 ement of total hemoglobin, based on pulse co-oximetry, is a continuous and noninvasive method that ha

167 Along with pulse oximetry, it has reduced anesthesia-related morbidity an

168 Vital signs, pulse oximetry, laser Doppler flowmetry, and toe temperature w

169 The only independent predictors of pulse oximetry less than 90% were baseline pulse oximetry (odd

170 Where some oxygen is available, pulse oximetry may improve oxygen usage and clinical outcomes

171 re- and postprandial magnetic resonance (MR) oximetry measurements of the SMV %HbO2, with flow-indepe

172 EPR oximetry measurements show ketamine increases cortical P

173 Here we extend oximetry measurements to capillaries and investigate all

174 mittent pulse oximetry monitoring (ie, pulse oximetry measurements were obtained along with a schedul

175 Pulse oximetry measurements with true saturation values displa

176 spin trapping with DEPMPO together with EPR oximetry methods can be used to provide sensitive and sp

177 to undergo continuous or intermittent pulse oximetry monitoring (ie, pulse oximetry measurements wer

178 Our results suggest that intermittent pulse oximetry monitoring can be routinely considered in the m

179 lines discourage the use of continuous pulse oximetry monitoring in hospitalized children with bronch

180 Continuous pulse oximetry monitoring is recommended to improve safety dur

181 Intermittent pulse oximetry monitoring of nonhypoxemic patients with bronch

182 length of stay did not differ based on pulse oximetry monitoring strategy (48.9 hours [95% CI, 41.3-5

183 Comparison with brain tissue oximetry monitoring suggested that the threshold for inc

184 The overall continuous pulse oximetry monitoring use percentage in these patients, no

185 orted routine use of blood pressure or pulse oximetry monitoring, and 75% reported daily rounds were

186 Side effects were monitored by pulse oximetry, nasal end-tidal capnography, and serial blood

187 ression model was used to estimate the pulse oximetry need for countries that did not provide data.

188 aturation measurements using dual-wavelength oximetry, noncontact tonometry, and manual sphygmomanome

189 tient clinics lack capacity to conduct pulse oximetry, nutritional assessment, or HIV testing, then w

190 e oximetry less than 90% were baseline pulse oximetry (odds ratio, 0.71; 95% CI, 0.64-0.79; p < 0.001

191 ansplantation underwent endobronchial tissue oximetry of native and donor bronchi at 0, 3, and 30 day

192 systemic hypoxia (85 % O2 saturation; pulse oximetry of the earlobe).

193 We and others previously achieved oximetry on major retinal vessels and measured the total

194 were no differences in laser Doppler, pulse oximetry, or toe temperature measurements during or afte

195 ty [10.4%], and 10 133 White [41.4%]), pulse oximetry overestimated SaO2 for Black (adjusted mean dif

196 Oximetry overestimated systemic blood flow (Qs) by an av

197 ore, respiratory rate, heart rate, and pulse oximetry oxygen saturation values were recorded at basel

198 II severity score (p = 0.03), baseline pulse oximetry (p < 0.001), baseline PaO2/FIO2 ratio (p = 0.02

199 , metered dose inhalers (p = .01), and pulse oximetry (p = .02).

200 arterial blood gas monitoring, chemistry, co-oximetry panels, parathyroid hormone assays, and coagula

201 Cerebral microdialysis, brain tissue oximetry (PbO2), and oxygen-15 positron emission tomogra

202 d the full oxygen system period to the pulse oximetry period and evaluated odds of death for children

203 Compared to the pulse oximetry period, the full oxygen system had no associati

204 H(2)O(2) as oxidant was studied by electrode oximetry, pH-stat, UV-visible spectrophotometry, and ele

205 Electrode oximetry/pH stat was used to study iron oxidation and hy

206 agnosis (biomarkers and intraoperative renal oximetry), prevention (statin therapy, acetylsalicylic a

207 ong with the use of a biocompatible charcoal oximetry-probe suspension, enabled 3D spatial imaging of

208 ls show great potential as intracellular EPR oximetry probes and imaging agents.

209 ylmethyl (TAM) radicals are commonly used as oximetry probes for electron paramagnetic resonance imag

210 Cerebral oximetry provided real-time information regarding the qu

211 ses were done on all babies for whom a pulse oximetry reading was obtained.

212 s, those with an artificially elevated pulse oximetry reading were less likely to be hospitalized wit

213 obtaining intermittent or "spot check" pulse oximetry readings for those who show clinical improvemen

214 flow showed no perfusion in the infarct, and oximetry readings were between 60 and 65.

215 In the second case, oximetry readings were obtained in a patient with a righ

216 more than 6 hours than those with unaltered oximetry readings.

217 ta (heart rate, respiratory rate, peripheral oximetry) recorded on all admissions at 1/20 Hz, and non

218 of 100 Hz we decomposed the raw signal in an oximetry recording (<1 Hz) and LFP recording (>1 Hz), de

219 ta collected included all preoperative pulse oximetry recordings, all values from preoperative arteri

220 weak areas in ICU monitoring, such as pulse oximetry reliability.

221 ults: Of 128 children included in the study, oximetry results in 8 cases were excluded owing to motio

222 Results of pulse co-oximetry revealed that the mean carboxyhemoglobin level

223 spectrometry, UV spectrometry, and electrode oximetry revealed that the mineral core forms by at leas

224 (3) usually, an associated decline in pulse oximetry saturation.

225 access to postdischarge newborn care, pulse oximetry screening for congenital heart disease, and cir

226 Pulse oximetry screening for cyanotic congenital heart disease

227 f clinicians felt the case for routine pulse oximetry screening had not been proven.

228 Pulse oximetry screening is a highly specific, moderately sens

229 Pulse oximetry screening should be routine and performed at th

230 reporting the test accuracy of routine pulse oximetry screening, and involving over 150 ,000 babies,

231 Reflectance oximetry sensors are distinct and their application rath

232 s the development of novel reflectance pulse oximetry sensors for the esophagus and bowel, and presen

233 The use of novel reflectance pulse oximetry sensors has been successfully demonstrated.

234 Furthermore, electron paramagnetic resonance oximetry showed a gradual but significant reduction in c

235 Measurements using spin label oximetry showed a substantial difference in the level of

236 Cerebral oximetry showed fast rise in regional oxygen saturation

237 Pulse oximetry showed oxygen desaturations below 90% in 101 (3

238 Pulse oximetry significantly underestimates true arterial satu

239 Pulse oximetry slightly overestimated oxyhemoglobin percentage

240 hieve oxygen saturation as measured by pulse oximetry (Sp(O(2))) that decreased from 95% to 86%.

241 zed assessment of oxygen saturation by pulse oximetry (SpO(2) ), arterial blood gas, spirometry, and

242 t for oxygen saturation as measured by pulse oximetry (Spo(2)) was 90%.

243 aturation of hemoglobin as measured by pulse oximetry (Spo(2)) were monitored continuously throughout

244 rcise oxygen saturation as measured by pulse oximetry [Spo(2)] = 86.5 +/- 2.9%) participated.

245 m Hg; oxygen saturation as measured by pulse oximetry [Spo(2)], 88 to 92%) or liberal oxygen therapy

246 m score, multi-slice CT, perfusion CT, pulse oximetry (SpO2%), and hemoglobin concentration (Hb).

247 s study, blood oxygen saturation using pulse oximetry (SpO2) and pulse rate were measured daily on a

248 when oxygen saturation as measured by pulse oximetry (SpO2) dropped to less than 84%, or after 60 mi

249 arget oxygen saturation as measured by pulse oximetry (SpO2) of 88-92% (n = 52) or a liberal oxygenat

250 ration (arterial [SaO2] or measured by pulse oximetry [SpO2]) </= 90%.

251 xyhemoglobin saturation as measured by pulse oximetry [Spo2], 89 to 93%).

252 ratory rate [RR], oxygen saturation by pulse oximetry [Spo2], mean arterial pressure [MAP]) was devel

253 gies including continuous superior vena cava oximetry (SvO2), phenoxybenzamine (POB), strategies to m

254 EPR (ESR) is a suitable noninvasive oximetry technique.

255 act on clinical care of improved, innovative oximetry technology.

256 itoring, advances in intrapartum fetal pulse oximetry, thresholds of acidosis associated with fetal i

257 ity, and positive predictive value of tissue oximetry to detect systemic hypoperfusion, multisite NIR

258 mating cardiac output; b) the standard pulse oximetry to screen for pulmonary problems; c) transcutan

259 s to titrate arterial O(2) saturation (pulse oximetry) to 80%, while remaining normocapnic via a rebr

260 llary tests (such as chest imaging and pulse oximetry) to improve pneumonia identification; second, t

261 Jugular venous bulb oximetry, transcranial Doppler ultrasonography, electroe

262 The cardiac index, pulse oximetry, transcutaneous oxygen tension, transcutaneous

263 trospective analysis of three clinical tumor oximetry trials involving two oxygen sensors (charcoal p

264 Oximetry underestimated CMR-measured pulmonary blood flo

265 stics, guideline-discordant continuous pulse oximetry use decreased from 53% (95% CI, 49%-57%) to 23%

266 The mortality impact of pulse oximetry use during infant and childhood pneumonia manag

267 Measure continuous pulse oximetry use in children with bronchiolitis.

268 Continuous pulse oximetry use percentages were risk standardized using th

269 Hospital-level unadjusted continuous pulse oximetry use ranged from 2% to 92%.

270 Minimal pulse oximetry value during endotracheal intubation was the pr

271 independently associated with minimal pulse oximetry value were the Simplified Acute Physiology Scor

272 ons between preoxygenation devices and pulse oximetry values during endotracheal intubation.

273 in from sublingual mucosa correlated with co-oximetry values of blood withdrawn from a central venous

274 and routinely assessed in patients by pulse oximetry, variability at the single-cell level has not b

275 With the exception of pulse oximetry vital sign days, the readings in most vital sig

276 arterial blood pressure, cerebral perfusion/oximetry, VT characteristics, and ablation outcomes.

277 Sensitivity of pulse oximetry was 75.00% (95% CI 53.29-90.23) for critical ca

278 congenital heart disease (CCHD) using pulse oximetry was added to the recommended uniform screening

279 ects was particularly low when newborn pulse oximetry was done after 24 h from birth than when it was

280 nistration, monitoring with continuous pulse oximetry was frequent and varied widely among hospitals.

281 Neuromonitoring using cerebral oximetry was performed to evaluate a cerebral desaturati

282 Co-oximetry was used to measure MetHb (%) and other hemoglo

283 label electron paramagnetic resonance (EPR) oximetry was used to measure the oxygen consumption from

284 caval (SsvcO2), and pulmonary venous (SpvO2) oximetry was used to test whether SaO2 accurately predic

285 not be done with reasonable accuracy unless oximetry was used.

286 inhibition.Oxyhaemoglobin saturation (pulse oximetry) was decreased (P<0.001) with hypoxia (63 +/- 2

287 The mean hemoglobin concentration, by co-oximetry, was 5.014 mmol x L(-1), coefficient of variati

288 primary outcome, receipt of continuous pulse oximetry, was measured using direct observation.

289 Using electron paramagnetic resonance oximetry, we have observed an initial fast decrease of p

290 To estimate availability of pulse oximetry, we sent surveys to anaesthesia providers in 72

291 least 30% of the recording time on nocturnal oximetry were assigned, in a 1:1 ratio, to receive eithe

292 oxygen extraction fraction, and brain tissue oximetry were measured in patients during [18F]FMISO and

293 e Louise AMS score, and Sao2 level (by pulse oximetry) were measured.

294 This strategy was comparable in accuracy to oximetry, which had a negative likelihood ratio of 0.12,

295 res and quantified the availability of pulse oximetry, which is an essential monitoring device during

296 Oxygen saturation was monitored by pulse oximetry, which recorded the number of times saturation

297 ygen saturation (SaO2) was measured by pulse oximetry while children were awake and asleep.

298 se contrast angiography and pre-ductal pulse oximetry, while regional cerebral oxygen saturation was

299 developments and applications of reflectance oximetry with an emphasis on the potential clinical and

300 We also found that the combination of pulse oximetry with integrated management of childhood illness