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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
5                                A total of 15 PROMs validated for use in adult patients with CRS were
6 blications illustrate the need to administer PROMs at a postoperative interval relevant to the antici
7 active and passive range of motion (AROM and PROM), muscle strength, limb edema, and pain.
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
11                                   Future CRS PROMs will need to incorporate clinical domains that ass
12  management of chronic rhinosinusitis (CRS), PROMs will play an essential role in informing and tailo
13                          The quality of each PROM was assessed and reported using standardized criter
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
16                                 Importantly, PROM represents the successful integration of a top-down
17 tiple patient-reported outcomes measurement (PROM) tools is recommended to capture long-term degree o
18           Patient-reported outcome measures (PROMs) are now recognised as the most appropriate instru
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.
21 n-related quality of life outcomes measures (PROMs).
22 ASER) causes premature rupture of membranes (PROM) in 10% to 20% of pregnancies.
23              Premature rupture of membranes (PROM) is a major factor that predisposes women to preter
24      Preterm premature rupture of membranes (PROM) is the leading identifiable predisposing factor fo
25 or (PTL), or premature rupture of membranes (PROM).
26  (defined as prelabour rupture of membranes [PROM], preterm <37 weeks PROM, and prolonged ROM) had a
27  the Probabilistic Regulation of Metabolism (PROM) framework.
28      Probabilistic Regulation Of Metabolism (PROM) provides a partial solution, but it does not incor
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
33         Ozone exposure increased the risk of PROM on the day of delivery (RR = 1.06, 95% CI: 1.02, 1.
34 ew was to identify and assess the quality of PROMs being used for adults with CRS.
35 fy recent publications describing the use of PROMs following reconstructive urological surgery.
36                           The routine use of PROMs increases the frequency of discussion of patient o
37  defect predictions compared to the original PROM MTB model, and it can successfully predict growth d
38             IDREAM consistently outperformed PROM using any of three popular yeast metabolic models a
39              We found an increase in preterm PROM risk of up to 50% (95% confidence interval: 4, 116)
40  = 1.15, 95% CI: 1.06, 1.25) but not preterm PROM.
41 on can potentially have an impact on preterm PROM, there is no available evidence on such an impact.
42 ht as a consequence of either PTL or preterm PROM.
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
48 -ring procedures were high risk, with an STS PROM for mitral valve replacement of 11%.
49 tion, 383 (202 TAVR and 181 SAVR) had an STS PROM of 7% or less (median [interquartile range]: TAVR,
50 nderwent an attempted implant and had an STS PROM of 7% or less.
51 opathy Questionnaire in patients with an STS PROM score of 7% or less.
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
57 S Predicted Risk of Operative Mortality (STS PROM) score of 7.1%.
58 ic Surgeons Predicted Risk of Mortality (STS PROM), and subjective criteria to assess patients' eligi
59 t increased surgical risk based on their STS PROM score and other risk factors.
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
62                             In some studies, PROMs are associated with improved symptom control, incr
63         More research is required to support PROM cost-benefit in terms of patient safety, clinician
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
66                                  Most of the PROMs were developed for research purposes such as deter
67 exposures merit further study in relation to PROM.
68 scatheter aortic valve replacement PROM (TVT PROM) of 4% to 3% (both p < 0.0001) from 2012 to 2015.
69       After validating the approach, we used PROM to build a genome-scale integrated metabolic-regula
70                                     By using PROM, we constructed an integrated regulatory-metabolic
71       Overall, the highest quality validated PROMs for adults with CRS were (1) the 22-item Sinonasal
72 pture of membranes [PROM], preterm <37 weeks PROM, and prolonged ROM) had a 2.3 (95% CI 1.0-5.4) time
73                 Yet, the question of whether PROMs can lead to actual improvements in the quality of
74 m birth, but evidence of a relationship with PROM is sparse.

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