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1 PROM identified KO phenotypes with accuracies as high as
2 PROM introduces probabilities to represent gene states a
3 PROM rate was 4%.
4 PROMs uptake and awareness is increasing in reconstructi
6 blications illustrate the need to administer PROMs at a postoperative interval relevant to the antici
8 ically significant findings were limited and PROMs' intervention effect sizes were predominantly smal
9 key terms: ["chronic" AND "*sinusitis"] AND [PROM OR patient reported outcome measure* OR quality of
10 g pentoxifylline demonstrated improved AROM, PROM, and muscle strength and decreased limb edema and p
12 management of chronic rhinosinusitis (CRS), PROMs will play an essential role in informing and tailo
14 ative risks and 95% confidence intervals for PROM per each interquartile-range increase in pollutants
15 ith impaired AROM and 19 of 22 with impaired PROM improved; 11 of 19 patients with muscle weakness sh
17 tiple patient-reported outcomes measurement (PROM) tools is recommended to capture long-term degree o
19 ic use of patient-reported outcome measures (PROMs) has been advocated as an effective way to standar
20 terest in patient-reported outcome measures (PROMs) to inform improvements in health care delivery.
26 (defined as prelabour rupture of membranes [PROM], preterm <37 weeks PROM, and prolonged ROM) had a
29 lled probabilistic regulation of metabolism (PROM) that achieves this synthesis and enables straightf
30 mortality (STS Predicted Risk of Mortality [PROM]) of 7% to 6% and transcatheter aortic valve replac
31 This review examined whether inclusion of PROM in routine clinical practice is associated with imp
32 de were associated with an increased risk of PROM (for carbon monoxide, relative risk (RR) = 1.09, 95
37 defect predictions compared to the original PROM MTB model, and it can successfully predict growth d
41 on can potentially have an impact on preterm PROM, there is no available evidence on such an impact.
43 ase-control analyses to estimate the preterm PROM risk associated with 1 interquartile-range increase
44 crom and PM2.5 light absorption with preterm PROM and gestational age at the rupture of membranes (RO
45 % and transcatheter aortic valve replacement PROM (TVT PROM) of 4% to 3% (both p < 0.0001) from 2012
46 st provided the highest quality CRS-specific PROMs, whereas the EQ-5D provided the highest quality ge
47 al access (HR, 1.37; 95% CI, 1.27-1.48), STS PROM score greater than 15% vs less than 8% (HR, 1.82; 9
49 tion, 383 (202 TAVR and 181 SAVR) had an STS PROM of 7% or less (median [interquartile range]: TAVR,
52 tratified patients by the overall median STS PROM score (7%) and analyzed clinical outcomes and quali
53 s <3.3 g/dl, falls in the past 6 months, STS PROM score >7%, and severe (>/=5) Charlson comorbidity s
54 ic Surgeons Predicted Risk of Mortality (STS PROM) alone is sufficient to define decreased risk, the
55 gh mean STS predicted risk of mortality (STS PROM) for surgical valve replacement (8.34%), were highl
56 ic Surgeons Predicted Risk of Mortality (STS PROM) has trended downward in US TAVR trials and the STS
58 ic Surgeons Predicted Risk of Mortality (STS PROM), and subjective criteria to assess patients' eligi
60 bly with SAVR in high-risk patients with STS PROM scores traditionally considered intermediate risk.
61 ic Surgeons Predicted Risk of Mortality (STS-PROM) (<4% versus >/=4%), there was no statistically sig
64 models contain many fewer interactions than PROM and yet produce significantly more accurate growth
65 ry Influence Network (EGRIN) models with the PROM framework to create enhanced metabolic-regulatory n
68 scatheter aortic valve replacement PROM (TVT PROM) of 4% to 3% (both p < 0.0001) from 2012 to 2015.
72 pture of membranes [PROM], preterm <37 weeks PROM, and prolonged ROM) had a 2.3 (95% CI 1.0-5.4) time
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