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1  and clinical application of multiwavelength pulse oximetry.
2 rly labor to either "open" or "masked" fetal pulse oximetry.
3 oke, with transcranial doppler and overnight pulse oximetry.
4 its impact on PPG based applications such as pulse oximetry.
5 ed on arterial blood gas but not detected by pulse oximetry.
6 of consolidation by imaging and hypoxemia by pulse oximetry.
7 were similar with intermittent vs continuous pulse oximetry.
8 ors respiratory status as assessed by reflex pulse oximetry.
9 e-/sex-matched controls undergoing overnight pulse oximetry.
10 maging, arterial blood gas measurements, and pulse oximetry.
11 potentially detectable through screening via pulse oximetry.
12          Test if a novel panel consisting of pulse oximetry, 12-lead electrocardiography, and serum t
13              The most frequent interventions-pulse oximetry (66.5%), other monitoring (59.6%), and su
14  +/- 1.9; p<0.001), as was use of continuous pulse oximetry (78% vs. 58%, respectively; p=0.001).
15 0 mm Hg; or oxygen saturation as measured by pulse oximetry, 91-94%) or high-oxygenation (Pa(O(2)), 1
16 0 mm Hg; or oxygen saturation as measured by pulse oximetry, 96-100%) target until ICU discharge or 2
17 tion and favourable cost-effectiveness makes pulse oximetry a promising candidate for improving the p
18                                              Pulse oximetry, a relatively inexpensive technology, has
19 here remain major challenges to implementing pulse oximetry-a cheap, decades old technology-into rout
20                                   Rationale: Pulse oximetry accuracy varies across races, underscorin
21 udy suggest that racial and ethnic biases in pulse oximetry accuracy were associated with greater occ
22  peripheral oxygen saturation as measured by pulse oximetry (adjusted MD at 5 minutes, 15.3 percentag
23 nd staff from 14 Kenyan hospitals to examine pulse oximetry adoption.
24 eep apnea using questionnaire plus nocturnal pulse oximetry against using polysomnography to identify
25                                 One-third of pulse oximetry alarm notifications were for clinically r
26 aceted oxygen system compared to introducing pulse oximetry alone.
27 he accuracy of oxygen saturation measured by pulse oximetry among Black and White pediatric patients.
28  Documents also agreed on the routine use of pulse oximetry and blood pressure monitoring during endo
29                          Cardiac monitoring, pulse oximetry and capnography are used, often without s
30  hospital admission, particularly the use of pulse oximetry and chest radiography.
31 spital inpatient records to explore roles of pulse oximetry and clinical guidelines on hospital atten
32 y survey and retrospective clinical audit of pulse oximetry and medical oxygen availability and use i
33 We aimed to evaluate availability and use of pulse oximetry and medical oxygen in seven LMICs in Asia
34                                              Pulse oximetry and oxygen are complementary cost-effecti
35        We found that availability and use of pulse oximetry and oxygen in these seven LMICS (which ha
36 trategies and programmes, and integration of pulse oximetry and oxygen into clinical guidelines, serv
37 act, cost, and cost-effectiveness of routine pulse oximetry and oxygen on ALRI outcomes at scale rema
38  impact and cost-effectiveness of scaling up pulse oximetry and oxygen on childhood ALRI outcomes in
39 ated by publications addressing knowledge of pulse oximetry and those warning against the use of tran
40 ts suspected of bacterial pneumonia, bedside pulse oximetry and urinary antigen testing for Streptoco
41 ed heart and respiratory rate) and WristOx2 (pulse-oximetry and derived pulse rate) sensors.
42 ount for interaction between SpO2 threshold (pulse oximetry) and clinical guidelines, clustering by c
43 rate (electrocardiogram), oxygen saturation (pulse oximetry), and brachial artery blood flow and shea
44 t-level and hospital-level use of continuous pulse oximetry, and (2) real-time 1:1 feedback to clinic
45 ected, and standard vital signs (heart rate, pulse oximetry, and body temperature) were monitored at
46 O(2) is the oxygen saturation as measured by pulse oximetry, and DLCO is the diffusing capacity for c
47 ry artery pressure, central venous pressure, pulse oximetry, and end-tidal CO(2) were continuously mo
48 hild was monitored with electrocardiography, pulse oximetry, and invasive blood pressure via femoral
49  rate, lower Glasgow Coma Scale score, lower pulse oximetry, and nursing home residence during out-of
50 x, mean arterial blood pressure, heart rate, pulse oximetry, and transcutaneous oxygen and carbon dio
51                      Simultaneous blood gas, pulse oximetry, and ventilator settings were collected.
52       Nadir oxygen saturation as measured by pulse oximetry, apnea-hypopnea index, and the fraction o
53 naccuracies in oxygen saturation measured by pulse oximetry are present in patients with COVID-19 and
54 gression to assess the impact of introducing pulse oximetry as a prognostic tool to distinguish sever
55               We assessed the performance of pulse oximetry as a screening method for the detection o
56                         The concept of using pulse oximetry as a screening method to detect undiagnos
57    We prospectively assessed the accuracy of pulse oximetry as a screening test for congenital heart
58 stringent BPD definition based on systematic pulse oximetry assessment at 36 weeks' postmenstrual age
59 ist, including the introduction of universal pulse oximetry at a hospital in Chisinau, Moldova, where
60 rgical safety checklist and the provision of pulse oximetry at a referral hospital in Moldova, a lowe
61 The proportion of neonates and children with pulse oximetry at admission increased from 2365 (23.7%)
62 d age on control of breathing, inaccuracy of pulse oximetry at low oxygen saturations, and temperatur
63 h leading to the development of new types of pulse oximetry-based monitoring techniques.
64             Methods: PWADs were derived from pulse oximetry-based photoplethysmography signals in thr
65 ies (gestation >34 weeks) were screened with pulse oximetry before discharge.
66              We also sought risk factors for pulse oximetry below 90%.
67 rch in recent years to expand the utility of pulse oximetry beyond the simple measurement of arterial
68 cords that include prompts, the promotion of pulse oximetry by senior doctors, and monitoring and fee
69                                              Pulse oximetry can be used reliably to estimate the arte
70                                              Pulse oximetry can significantly increase the incidence
71 ng capacity of the lung for carbon monoxide, pulse oximetry, chest radiograph, and high-resolution th
72 ed examination of the pulmonary circulation, pulse oximetry, complete blood count, and serum chemistr
73 were similar for intermittent and continuous pulse oximetry considering societal and health care pers
74                                              Pulse oximetry correlates well with cooximeter-measured
75                    Our findings suggest that pulse oximetry could be beneficial in supplementing clin
76                                    Expanding pulse oximetry coverage to all facilities reduced travel
77 s on day 1 of health-facility admission (ie, pulse oximetry coverage).
78                                              Pulse oximetry data from 54 countries suggested that aro
79 h hypoxemia were quantified using continuous pulse oximetry data that had been sampled every 10 secon
80 ed greater likelihood of a patient receiving pulse oximetry during the post-intervention period compa
81 with hepatopulmonary syndrome underwent home pulse-oximetry during sleep.
82 P, arterial hemoglobin oxygen saturation (by pulse oximetry), end-tidal PCO2, and carotid artery bloo
83 ed their readiness and reported that all had pulse oximetry equipment onsite and 74.4% had access to
84 lighted critical limitations in conventional pulse oximetry, especially in diverse populations.
85  gas-derived oxygen saturation < 88% despite pulse oximetry-estimated oxygen saturation >= 92%), and
86                                              Pulse oximetry-estimated oxygen saturation on average ov
87 ight-thousand two-hundred eighty-five paired pulse oximetry-estimated oxygen saturation-arterial bloo
88 E)), end-tidal carbon dioxide ( PETCO2 ) and pulse oximetry estimation of oxygen saturation ( SpO2 ),
89  algorithm using questionnaire and nocturnal pulse oximetry excluded few patients from sleep studies,
90 .99), lower oxygen saturation as measured by pulse oximetry/Fi(O(2)) before induction (OR, 0.998; 95%
91  the index, oxygen saturation as measured by pulse oximetry/Fi(O(2)) had a greater weight than respir
92 he ratio of oxygen saturation as measured by pulse oximetry/Fi(O(2)) to respiratory rate) for determi
93 tcome was the sensitivity and specificity of pulse oximetry for detection of critical congenital hear
94                   The overall sensitivity of pulse oximetry for detection of critical congenital hear
95 We assessed the screening characteristics of pulse oximetry for HPS.
96 lected studies that assessed the accuracy of pulse oximetry for the detection of critical congenital
97  effectiveness of intermittent vs continuous pulse oximetry found similar length of hospital stay and
98  as reduced oxygen saturation as measured by pulse oximetry/fraction of inspired oxygen (FiO(2)) and
99 r) + (nadir oxygen saturation as measured by pulse oximetry &gt;82.5%) + (Fhypopneas >58.3%).
100                                              Pulse oximetry guides clinical decisions, yet does not u
101                                              Pulse oximetry guides triage and therapy decisions for C
102                               Routine use of pulse oximetry has been associated with changes in bronc
103                                  Reliance on pulse oximetry has been associated with increased hospit
104 hat, assuming access to supplemental oxygen, pulse oximetry has the potential to avert up to 148,000
105    Experimental sensors based on reflectance pulse oximetry have been developed for use in internal s
106                           Recent advances in pulse oximetry have made it possible to noninvasively me
107                                              Pulse oximetry identified fatal pneumonia episodes at HC
108  analyses suggested that the introduction of pulse oximetry improved oxygen practices prior to implem
109 e home-based monitoring using spirometry and pulse oximetry in adults with asthma, bronchiectasis/cys
110 s for future research of home spirometry and pulse oximetry in asthma, bronchiectasis/cystic fibrosis
111 rements for universal CCHD screening through pulse oximetry in birth hospitals.
112 ebite, oxygen administration, and the use of pulse oximetry in first aid, with the inclusion of pedia
113 ed using clinical guidelines with or without pulse oximetry in Malawi.
114 ow nasal oxygen, the expansion of the use of pulse oximetry in place of arterial blood gases, the use
115 e measured by a clinical severity score, and pulse oximetry in room air was done.
116 ngs support the standard use of intermittent pulse oximetry in stable infants hospitalized with bronc
117                    To assess the accuracy of pulse oximetry in the diagnosis of hypoxemia in SCD, we
118 et standard targets for oxygen saturation by pulse oximetry in the first 10 minutes or for clinical n
119 s with diabetic ketoacidosis and, along with pulse oximetry, in lung-function laboratories to estimat
120 upport front-line health-care workers to use pulse oximetry, including rethinking traditional binary
121  be effective, including the introduction of pulse oximetry into routine hospital care and clinical a
122  the baseline period (enabling evaluation of pulse oximetry introduction) and evaluated mortality and
123  three study periods: baseline (usual care), pulse oximetry introduction, and stepped introduction of
124 2)) 315 (if oxygen saturation as measured by pulse oximetry is 97%) to identify hypoxemia; 3) retain
125                                              Pulse oximetry is a noninvasive technology that is integ
126                                              Pulse oximetry is a safe, feasible test that adds value
127                                              Pulse oximetry is a ubiquitous non-invasive medical sens
128             Routine screening for CCHD using pulse oximetry is being increasingly supported and was a
129                              INTERPRETATION: Pulse oximetry is highly specific for detection of criti
130                                        Given pulse oximetry is increasingly substituting for arterial
131                                  Conclusion: Pulse oximetry is not sufficiently sensitive to screen f
132 ing for hepatopulmonary syndrome (HPS) using pulse oximetry is recommended in liver transplant (LT) c
133                                              Pulse oximetry is ubiquitous but detailed understanding
134                                   Along with pulse oximetry, it has reduced anesthesia-related morbid
135                                 Vital signs, pulse oximetry, laser Doppler flowmetry, and toe tempera
136 tudy, overestimation of oxygen saturation by pulse oximetry led to delayed delivery of COVID-19 thera
137           The only independent predictors of pulse oximetry less than 90% were baseline pulse oximetr
138 oxemia with oxygen saturation as measured by pulse oximetry &lt;80% was the major physiologic predictor
139 tomic Fontan obstruction, clinical cyanosis (pulse oximetry &lt;90%), polycythemia, portal variceal dise
140 oxemia with oxygen saturation as measured by pulse oximetry &lt;90%.
141 Hg, pulse >=110 bpm, or peripheral cutaneous pulse oximetry &lt;=92%), prediagnosis anticoagulant use, o
142              Where some oxygen is available, pulse oximetry may improve oxygen usage and clinical out
143 cility and ward levels, including documented pulse oximetry measurement on admission, documented oxyg
144                                              Pulse oximetry measurements on admission were documented
145  intermittent pulse oximetry monitoring (ie, pulse oximetry measurements were obtained along with a s
146                                              Pulse oximetry measurements with true saturation values
147 signed to undergo continuous or intermittent pulse oximetry monitoring (ie, pulse oximetry measuremen
148        Our results suggest that intermittent pulse oximetry monitoring can be routinely considered in
149  guidelines discourage the use of continuous pulse oximetry monitoring in hospitalized children with
150                                   Continuous pulse oximetry monitoring is recommended to improve safe
151                                 Intermittent pulse oximetry monitoring of nonhypoxemic patients with
152  mean length of stay did not differ based on pulse oximetry monitoring strategy (48.9 hours [95% CI,
153                       The overall continuous pulse oximetry monitoring use percentage in these patien
154 0% reported routine use of blood pressure or pulse oximetry monitoring, and 75% reported daily rounds
155               Side effects were monitored by pulse oximetry, nasal end-tidal capnography, and serial
156 ve regression model was used to estimate the pulse oximetry need for countries that did not provide d
157  outpatient clinics lack capacity to conduct pulse oximetry, nutritional assessment, or HIV testing,
158 f pulse oximetry less than 90% were baseline pulse oximetry (odds ratio, 0.71; 95% CI, 0.64-0.79; p <
159 e, with a blood pressure of 160/72 mm Hg and pulse oximetry of 93% on 6 L/min oxygen therapy through
160 e, with a blood pressure of 160/72 mm Hg and pulse oximetry of 93% on 6 L/min oxygen therapy through
161 d mild systemic hypoxia (85 % O2 saturation; pulse oximetry of the earlobe).
162        We model 15 scenarios ranging from no pulse oximetry or oxygen (null scenario) to high coverag
163  There were no differences in laser Doppler, pulse oximetry, or toe temperature measurements during o
164  air oxygen saturation of 85% as measured by pulse oximetry, or use of mechanical ventilation).
165 thnicity [10.4%], and 10 133 White [41.4%]), pulse oximetry overestimated SaO2 for Black (adjusted me
166 ge requiring supplemental oxygen to maintain pulse oximetry oxygen saturation of 95% or higher.
167 ion of admitted neonates and children with a pulse oximetry oxygen saturation reading documented in t
168 hma Score, respiratory rate, heart rate, and pulse oximetry oxygen saturation values were recorded at
169 Score II severity score (p = 0.03), baseline pulse oximetry (p < 0.001), baseline PaO2/FIO2 ratio (p
170  .001), metered dose inhalers (p = .01), and pulse oximetry (p = .02).
171 ompared the full oxygen system period to the pulse oximetry period and evaluated odds of death for ch
172                              Compared to the pulse oximetry period, the full oxygen system had no ass
173 OM), wearable photoplethysmography (WD), and pulse oximetry (PO) during baseline, ischemia, and reper
174 ment Surfactant Positive Airway Pressure and Pulse Oximetry Randomized Trial Neuroimaging and Neurode
175  Analyses were done on all babies for whom a pulse oximetry reading was obtained.
176 iolitis, those with an artificially elevated pulse oximetry reading were less likely to be hospitaliz
177  only obtaining intermittent or "spot check" pulse oximetry readings for those who show clinical impr
178 cal signs and symptoms, admission diagnoses, pulse oximetry readings, oxygen therapy details, and fin
179     Data collected included all preoperative pulse oximetry recordings, all values from preoperative
180 cially weak areas in ICU monitoring, such as pulse oximetry reliability.
181 o; and (3) usually, an associated decline in pulse oximetry saturation.
182 f the 188 high-risk cases, 94 (50.0%) passed pulse oximetry screening and 36 (19.1%) were initially d
183 nates: access to postdischarge newborn care, pulse oximetry screening for congenital heart disease, a
184                                              Pulse oximetry screening for cyanotic congenital heart d
185 rity of clinicians felt the case for routine pulse oximetry screening had not been proven.
186                                              Pulse oximetry screening is a highly specific, moderatel
187                                              Pulse oximetry screening should be routine and performed
188 udies reporting the test accuracy of routine pulse oximetry screening, and involving over 150 ,000 ba
189 reviews the development of novel reflectance pulse oximetry sensors for the esophagus and bowel, and
190                 The use of novel reflectance pulse oximetry sensors has been successfully demonstrate
191                                              Pulse oximetry showed oxygen desaturations below 90% in
192                                              Pulse oximetry significantly underestimates true arteria
193                                              Pulse oximetry slightly overestimated oxyhemoglobin perc
194 00 mm Hg or oxygen saturation as measured by pulse oximetry Sp(O(2)):Fi(O(2)) 315 (if oxygen saturati
195 according to peripheral oxygen saturation by pulse oximetry (Sp o2 )/F io2 ratio compared with Pa o2
196  to achieve oxygen saturation as measured by pulse oximetry (Sp(O(2))) that decreased from 95% to 86%
197 tocolized assessment of oxygen saturation by pulse oximetry (SpO(2) ), arterial blood gas, spirometry
198  target for oxygen saturation as measured by pulse oximetry (Spo(2)) (90%; goal range, 88 to 92%), an
199 oxygen saturation (SaO(2)) of <88% despite a pulse oximetry (SpO(2)) reading of >=92%), and whether r
200 r limit for oxygen saturation as measured by pulse oximetry (Spo(2)) was 90%.
201 ygen saturation of hemoglobin as measured by pulse oximetry (Spo(2)) were monitored continuously thro
202  readings of arterial blood gas (SaO(2)) and pulse oximetry (SpO(2)) were obtained, black patients ha
203 %; exercise oxygen saturation as measured by pulse oximetry [Spo(2)] = 86.5 +/- 2.9%) participated.
204 o 70 mm Hg; oxygen saturation as measured by pulse oximetry [Spo(2)], 88 to 92%) or liberal oxygen th
205 ion levels in arterial blood, SaO(2), and by pulse oximetry, SpO(2)).
206 symptom score, multi-slice CT, perfusion CT, pulse oximetry (SpO2%), and hemoglobin concentration (Hb
207 In this study, blood oxygen saturation using pulse oximetry (SpO2) and pulse rate were measured daily
208 quest, when oxygen saturation as measured by pulse oximetry (SpO2) dropped to less than 84%, or after
209                                              Pulse oximetry (SpO2) is routinely used for transcutaneo
210 the time to oxygen saturation as measured by pulse oximetry (Spo2) less than 80% (event) during 35 mi
211 with target oxygen saturation as measured by pulse oximetry (SpO2) of 88-92% (n = 52) or a liberal ox
212  hemoglobin oxygen saturation as measured by pulse oximetry (SpO2) to fraction of inspired oxygen (Fi
213 ation levels in arterial blood (SaO2) and by pulse oximetry (SpO2).
214 n saturation (arterial [SaO2] or measured by pulse oximetry [SpO2]) </= 90%.
215 ion (oxyhemoglobin saturation as measured by pulse oximetry [Spo2], 89 to 93%).
216  respiratory rate [RR], oxygen saturation by pulse oximetry [Spo2], mean arterial pressure [MAP]) was
217 rt monitoring, advances in intrapartum fetal pulse oximetry, thresholds of acidosis associated with f
218 t-effective strategy is the full scale-up of pulse oximetry to 90% usage rate and oxygen to 80% avail
219 r estimating cardiac output; b) the standard pulse oximetry to screen for pulmonary problems; c) tran
220 xic gas to titrate arterial O(2) saturation (pulse oximetry) to 80%, while remaining normocapnic via
221 h ancillary tests (such as chest imaging and pulse oximetry) to improve pneumonia identification; sec
222                           The cardiac index, pulse oximetry, transcutaneous oxygen tension, transcuta
223 oxygen (null scenario) to high coverage (90% pulse oximetry usage and 80% oxygen availability) across
224 rategies for guideline-discordant continuous pulse oximetry use among hospitalized children with bron
225 acteristics, guideline-discordant continuous pulse oximetry use decreased from 53% (95% CI, 49%-57%)
226                      The mortality impact of pulse oximetry use during infant and childhood pneumonia
227 onal guidelines recommend against continuous pulse oximetry use for hospitalized children with bronch
228 ite) during a 3.5-month period of continuous pulse oximetry use in children with bronchiolitis not re
229                           Measure continuous pulse oximetry use in children with bronchiolitis.
230              Guideline-discordant continuous pulse oximetry use in hospitalized children was measured
231                                   Continuous pulse oximetry use percentages were risk standardized us
232         Hospital-level unadjusted continuous pulse oximetry use ranged from 2% to 92%.
233 nicians when guideline-discordant continuous pulse oximetry use was discovered during in-person data
234   Intermittent (every 4 hours) vs continuous pulse oximetry using an oxygen saturation target of 90%
235 ry 4 hours, n = 114) or continuous (n = 115) pulse oximetry, using an oxygen saturation target of 90%
236                                      Minimal pulse oximetry value during endotracheal intubation was
237 actors independently associated with minimal pulse oximetry value were the Simplified Acute Physiolog
238 ociations between preoxygenation devices and pulse oximetry values during endotracheal intubation.
239 ients were significantly more likely to have pulse oximetry values that masked an indication for COVI
240 rstood and routinely assessed in patients by pulse oximetry, variability at the single-cell level has
241 Is) were recorded, and relationships between pulse oximetry variables and survival were analyzed.
242                        With the exception of pulse oximetry vital sign days, the readings in most vit
243                               Sensitivity of pulse oximetry was 75.00% (95% CI 53.29-90.23) for criti
244 itical congenital heart disease (CCHD) using pulse oximetry was added to the recommended uniform scre
245 rt defects was particularly low when newborn pulse oximetry was done after 24 h from birth than when
246 n administration, monitoring with continuous pulse oximetry was frequent and varied widely among hosp
247 thetic inhibition.Oxyhaemoglobin saturation (pulse oximetry) was decreased (P<0.001) with hypoxia (63
248   The primary outcome, receipt of continuous pulse oximetry, was measured using direct observation.
249                  To estimate availability of pulse oximetry, we sent surveys to anaesthesia providers
250            Electrocardiography telemetry and pulse oximetry were monitored continuously, and live con
251 ), Lake Louise AMS score, and Sao2 level (by pulse oximetry) were measured.
252  theatres and quantified the availability of pulse oximetry, which is an essential monitoring device
253           Oxygen saturation was monitored by pulse oximetry, which recorded the number of times satur
254     Oxygen saturation (SaO2) was measured by pulse oximetry while children were awake and asleep.
255 ng phase contrast angiography and pre-ductal pulse oximetry, while regional cerebral oxygen saturatio
256                 It is imperative to validate pulse oximetry with expanded racial inclusion.
257        We also found that the combination of pulse oximetry with integrated management of childhood i

 
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