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1 1.96; p = 0.02) each independently conferred mortality risk.
2 mall but statistically significant increased mortality risk.
3 exposures were all associated with increased mortality risk.
4 hylloquinone with incident CVD and all-cause mortality risk.
5 elp identify coinfected patients with higher mortality risk.
6 n linked to cardiovascular disease (CVD) and mortality risk.
7 tized for interventions and policy to reduce mortality risk.
8 erm follow-up is needed to better assess the mortality risk.
9 CVI) is associated with increased stroke and mortality risk.
10 e to the optimal dose) further increased the mortality risk.
11 ow changes in these factors alter individual mortality risk.
12 ture, altered gut microbiota and have a high mortality risk.
13 ack generalizable, cross-scale indicators of mortality risk.
14 e matrix through which animals disperse with mortality risk.
15 sugar intake is associated with an increased mortality risk.
16 g hemoglobinopathy patients did not increase mortality risk.
17 ansitions across multimorbidity patterns and mortality risk.
18 ial distribution of greenspace in cities and mortality risk.
19 ent air pollution and cardiovascular disease mortality risk.
20 ext] exposure contributes to cardiopulmonary mortality risk.
21 ted with blood culture positivity and 28-day mortality risk.
22 Cox regression was used to assess mortality risk.
23 ays (1.8; 1.1-2.9) increased post-transplant mortality risk.
24 ompeting risks regression to assess waitlist mortality risk.
25 take, intake of different sugar sources, and mortality risk.
26 r meat intake were associated with increased mortality risk.
27 on between urban greenspace distribution and mortality risk.
28 igher SRH was strongly associated with lower mortality risk.
29 han BMI, should be considered in relation to mortality risk.
30 Septic shock carries a high mortality risk.
31 ithin the first week independently increased mortality risk.
32 are associated with increased morbidity and mortality risk.
33 mprove our ability to monitor and anticipate mortality risk.
34 ral atherosclerosis, and with cardiovascular mortality risk.
35 s is associated with reductions in all-cause mortality risk.
36 Repeated HFHs further increased mortality risk.
37 grip strength (GS) is associated with lower mortality risk.
38 rail recipients may be a marker of increased mortality risk.
39 rmed HLA DSA is associated with an increased mortality risk.
40 actors such as pathogen burden and extrinsic mortality risk.
41 City cohort, elderly patients are at highest mortality risk.
42 ore age 40 years, yields large reductions in mortality risk.
43 nically ventilated patients face the highest mortality risk.
44 th pure AR, AR + MR + TR exhibit the largest mortality risk.
45 may contribute to a higher epigenetic-based mortality risk.
46 , but there was no significant difference in mortality risk.
47 ss attenuation of CAV progression and higher mortality risk.
48 sociated with disease progression and higher mortality risk.
49 a modest but persistent increased long-term mortality risk.
50 hydrate reserves and an unrealistically high mortality risk.
51 s increased over time, as has its associated mortality risk.
52 It may also be related to an increased mortality risk.
53 itting increasing cardiovascular disease and mortality risk.
54 2.07-6.62, p < 0.0001), but did not increase mortality risk.
55 nd IT does not confer additional in-hospital mortality risk.
56 surveillance studies estimating RSV-related mortality risk.
57 urgery significantly increases morbidity and mortality risks.
58 should consider the urban-rural disparity in mortality risks.
59 for whom anaemia can increase morbidity and mortality risks.
60 g an emergency operation realize the average mortality risk?
61 ars of delivery in both England and Canada-a mortality risk 11-12 times higher than for control mothe
63 lume surgeons and hospitals had the greatest mortality risk (5.0%), except in the case of older-sick
64 mortality (2635 vs 6881 90-day deaths; crude mortality risk, 5.49% vs 1.22%; adjusted absolute risk d
65 haracteristics, absolute reductions in total mortality risk (6.4 percentage points, 95% CI 0.1-12.7)
66 This group had a 4.54 times higher all-cause mortality risk (95% CI 4.07-5.06) than that of children
67 ness and an ATE of 25.6% reduction in 30-day mortality risk (95% CI, 18.9-32.3; P < .0001) estimated
68 confidence intervals (CI) of overall cancer mortality risk, according to quartiles (q) of the index.
71 who accepted DCD50 offers had 49% decreased mortality risk (adjusted hazard ratio [aHR] (0.46) 0.51(
73 m/s, patients with Vmax >/=5 m/s had greater mortality risk (adjusted hazard ratio=1.86 [1.55-2.54];
74 t benzodiazepine prescription also increased mortality risk after consideration of duration of OAT (a
78 (6.4 percentage points, 95% CI 0.1-12.7) and mortality risk after transition (5.7 percentage points,
80 R, 0.80; 95% CI, 0.65-0.97) but had a higher mortality risk (aHR, 2.00; 95% CI, 1.59-2.55) afterward;
82 ]: 2.493.494.89, P < 0.001), but a 62% lower mortality risk (aHR: 0.310.380.46, P < 0.001) beyond thi
83 s who accepted an SDL had a 7.88-fold higher mortality risk (aHR: 4.807.8812.93, P < 0.001) in the fi
85 aHR]:2.493.494.89, p<0.001), but a 62% lower mortality risk (aHR:0.310.380.46, p<0.001) beyond this.
86 s who accepted an SDL had a 7.88-fold higher mortality risk (aHR:4.807.8812.93, p<0.001) in the first
87 in widespread areas (i.e. it projected a low mortality risk), although the model highlighted critical
89 the United States have reported an increased mortality risk among individuals with NAFLD, but the pop
90 the United States have reported an increased mortality risk among individuals with NAFLD; therefore,
91 Sitting is associated with all-cause and CVD mortality risk among the least physically active adults;
93 idea using the specific factor of extrinsic mortality risk, an important factor in evolutionary theo
95 gs suggest short sedentary bouts still carry mortality risk and are not a healthful alternative to pr
96 pecies-driven by an interaction between nest mortality risk and brood size-and predicted the age of f
97 iduals within populations vary enormously in mortality risk and longevity, but the causes of this var
99 was associated with incremental increases in mortality risk and medical costs and reductions in life
101 ess, coinfected patients still have a higher mortality risk and more severe hepatocellular carcinoma
103 ine and Gray method to account for competing mortality risk, and Andersen-Gill modeling to analyze to
104 interval (CI): 2.82, 3.05) higher all-cause mortality risk, and participants who increased their CPD
105 sis of hazard ratios (HRs) was performed for mortality risk, and pooled odds ratios (PORs) were calcu
107 rventions for men and older women at highest mortality risk are needed to improve HIV treatment outco
109 association between chili pepper intake and mortality risk are scarce, with a lack of studies from M
113 ers: (1) diagnosis, (2) patient morbidity or mortality risk assessment, (3) disease outbreak predicti
116 nsorship and used Cox regression to estimate mortality risk associated with IRD kidney acceptance ver
117 Significantly elevated respiratory disease mortality risk associated with long-term O(3) exposure w
123 ealth, there are few studies quantifying the mortality risk associated with their co-occurrence in th
124 years, incident HFH was associated with high mortality risk at 1 year, declining but remaining elevat
125 ere stratified and analyzed by categories of mortality risk at ICU admission.Measurements and Main Re
126 shaped association with BMI, with the lowest mortality risks at 22.5 kg/m(2) for both men and women.
127 To quantify and compare 9-year all-cause mortality risk attributable to modifiable risk factors a
128 splantation (HTx) recipients experience high mortality risk attributed to increased nonadherence to i
129 ed to NHW patients, NHB patients had a lower mortality risk before 24 months (aHR, 0.80; 95% CI, 0.65
130 Further studies are warranted to assess the mortality risk beyond the first month after RSV illness
132 sease, sTNFR1 predicted short-to-medium term mortality risk but not risk of progressive renal functio
133 s >20E% were associated with a 30% increased mortality risk, but increased risks were also found at i
134 ensive care treatment have a high short-term mortality risk, but this alters favorably with increasin
136 the role of matrix on movement behaviour and mortality risk, can incorporate species distribution to
137 llected data from the Swedish Apolipoprotein Mortality Risk cohort on persons 35 to 79 years old who
138 M) has been associated with a higher 10-year mortality risk compared to patients with single primary
139 s who were 30-day survivors of first stroke, mortality risk compared with the general population rema
140 migrants had comparable or lower injury and mortality risks compared to respondents remaining in Ban
141 a 38% (95% CI, 6% to 80%) increased relative mortality risk, corresponding to 4.6% absolute increase,
143 as not associated with a change in operative mortality (risk difference, -0.69%; 95% CI, -2.7% to 1.3
146 lem that implicates inequities and extrinsic mortality risk - documenting more future-oriented thinki
147 te HIV- and tuberculosis-associated COVID-19 mortality risks due to residual confounding, both HIV an
148 low high gradient SAS displayed considerable mortality risk during follow up compared with normal flo
151 tilation was associated with lower all-cause mortality risk, even among persistent clean fuel users (
152 ed to elevated cardiometabolic and all-cause mortality risk, extending our understanding about the ro
156 nic risk scores (PRS) for 13 diseases and 12 mortality risk factors into sex-specific composite PRS (
157 y attenuated after adjusting for non-genetic mortality risk factors measured at study entry (i.e., mi
160 gnificantly associated with several clinical mortality risk factors: high-sensitivity C-reactive prot
161 nt knowledge of ARDS trends in incidence and mortality, risk factors, and recently described endotype
162 os (SMRs) to compare cause-specific relative mortality risk following cHL to that expected in the gen
163 r analyses have attempted to quantify excess mortality risk for astronauts exposed to space radiation
165 There was a beneficial association with mortality risk for replacing total sedentary time with b
168 PAD are at lower risk for MACE and all-cause mortality, risk for limb events was similar between sexe
169 Higher nut intake was associated with lower mortality risk from both cardiovascular and noncardiovas
172 e combined proxy indicators of morbidity and mortality risk from the most recent Demographic and Heal
173 ients continue to face increased nonlymphoma mortality risks from multiple, potentially preventable c
174 Norway using survey data in three cities and mortality risks from the Emerging Risk Factor Collaborat
175 e previously-derived Emergency Heart failure Mortality Risk Grade for 7-day (EHMRG7) and 30-day (EHMR
178 e, was independently associated with greater mortality risk (hazard ratio =1.13 per +1 SD [95% CI, 1.
181 entinoids was also associated with increased mortality risk; however, for z-drugs there was no eviden
183 nonpreferred recipients had a 41% increased mortality risk (HR: 1.171.411.70, p<0.001) and 39% incre
184 nonpreferred recipients had a 41% increased mortality risk (HR: 1.171.411.70; P < 0.001) and 39% inc
185 .5 and < 12.5 were associated with increased mortality risk (HR: 3.33, 95% CI 1.23-8.99, p = 0.018 an
188 D3] at diagnosis are associated with a lower mortality risk in colorectal cancer (CRC) patients.
191 stic value, although its capacity to predict mortality risk in HIV-HCV-coinfected patients has never
192 evaluate how use of these treatments altered mortality risk in HIV-positive adults with multidrug-res
195 n (CrAg) titers are strongly associated with mortality risk in individuals with HIV-associated crypto
196 dialysis vintage is associated with a higher mortality risk in KTR, and this association might be exp
198 lucidate the findings of increased all-cause mortality risk in patients receiving basal insulin, espe
199 BS) is commonly used as a predictor of early mortality risk in patients with bloodstream infections (
200 cancer is associated with a higher all-cause mortality risk in patients with NSCLC, which is partly m
201 tic enrichment strategy to estimate baseline mortality risk in pediatric septic shock.Objectives: To
203 thromboembolism is associated with increased mortality risk in some populations, but how frequently i
204 d patients with a 46.4% (95% CI 37.8%-55.2%) mortality risk in the high-risk group compared to 12.5%
205 to power in predicting short and medium-term mortality risk in the overall cohort: AUROCS for liver r
208 y or myomectomy is associated with increased mortality risk in women with occult uterine cancer.
209 ower morcellation was associated with higher mortality risk in women with occult uterine sarcoma, esp
217 tangling the roles of movement behaviour and mortality risk is fundamental to accurately interpreting
218 The association between urban greenspace and mortality risk is well known, but less is known about ho
219 e had increased all-cause and cardiovascular mortality risks (log rank P=0.004 and P=0.003, respectiv
220 e measured to assign a PERSEVERE-II baseline mortality risk.Measurements and Main Results: Among 379
223 ally significant associations with increased mortality risk: multivariable-adjusted HR (95% CI) in th
224 eyed physicians for their estimates of 7-day mortality risk, obtained for each patient before knowled
227 ed with expected population survival, excess mortality risks of pure AR, AR + OMR, and AR + FMR were
228 , p = 0.049) to be independent predictors of mortality risk on admission in severe COVID-19 patients.
230 ity groupings improved the stratification of mortality risk, particularly when applied 6 h after PARD
233 ld, 3.1% among children 1-5 months old, 4.4% mortality risk post-discharge, and 13.5% mortality reduc
236 sting that hypochloremia may account for the mortality risk previously attributed to hyponatremia.
238 ths (HR 1.7; CI 1.0-2.8) increased wait-list mortality risk; pulmonary exacerbation time 15-28 days (
239 s associated with physiologic impairment and mortality risk.PurposeTo determine whether participant-l
241 (mosquitoes observed, n = 7380): cumulative mortality (risk ratio 0.99, 95% confidence interval [CI]
242 tion was not associated with a difference in mortality (risk ratio, 0.90; 95% CI, 0.74-1.10; p = 0.31
244 ood health at baseline (for example, 10-year mortality risk ratio, 1.62 [CI, 1.37 to 1.90]) but not a
246 erranean diet reduced cardiovascular disease mortality risk related to long-term exposure to air poll
254 and cessation of solid fuel use cuts excess mortality risks swiftly and substantially within 5 years
256 trast, Hispanic patients had a lower overall mortality risk than NHW patients (aHR, 0.61; 95% CI, 0.5
257 , obese women with WL < 5% had a lower 60-mo mortality risk than normal-weight women with WL < 5% (ad
258 ese women with WL >= 5% did not have a lower mortality risk than normal-weight women with WL < 5%.
260 uppression (IS) is associated with decreased mortality risk that is not fully explained by attenuatio
261 water relations, as a potential indicator of mortality risk that is physiologically relevant and inte
262 additionally used other tobacco products had mortality risks that were as high and sometimes higher t
265 virus (HIV) increases cardiovascular disease mortality risks to a greater degree among women than men
266 time required for adjusted rehospitalization/mortality risks to decline 50% from maximum values after
274 When compared with controls, the overall mortality risk was greatest in the first year after diag
275 k group with a four-fold increase in suicide mortality risk was identified based on the out-of-sample
277 g status, and inotrope requirement, waitlist mortality risk was lower at Adult Congenital Heart Assoc
283 e adjacent position on the kidney match-run, mortality risk was significantly higher for next-sequent
287 ving further from childbirth facilities, but mortality risks were not lower despite this increased se
289 is often related to severity of illness and mortality risk, whereas overtreatment or undertreatment
290 V remodeling conferred a >2-fold increase in mortality risk, which remained significant (p < 0.01) wh
292 .44 additional points to equalize children's mortality risk with the age-standardized mortality rate
293 rately rank children and equalize children's mortality risk with the age-standardized mortality rate
295 weak evidence for elevated CVD and all-cause mortality risks with more sitting among those meeting th
296 was associated with a reduction in all-cause mortality risk within 1 year (hazard ratio, 0.73 [95% CI
300 een religious service attendance and reduced mortality risk, yet research identifying mediators remai