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1 ontrolled trials) or Newcastle-Ottawa Scale (observational studies).
2 in randomized trials) and selection bias (in observational studies).
3 th system were included in this prospective, observational study.
4 the trial design was altered to a single-arm observational study.
5 This was a cross-sectional observational study.
6 Longitudinal, population-based observational study.
7 This was an ongoing, prospective observational study.
8 erobacteriaceae, a prospective, multicenter, observational study.
9 cutively enrolled in an ongoing longitudinal observational study.
10 as from confounding, a central aspect of any observational study.
11 ations will improve the quality of EHR-based observational studies.
12 Blood Institute quality assessment tool for observational studies.
13 h decreased risk for SARS-CoV-1 infection in observational studies.
14 gy guidelines for reporting meta-analyses of observational studies.
15 nd circulating cholesterol concentrations in observational studies.
16 esearch and reporting principles relevant to observational studies.
17 nalysis of randomized controlled studies and observational studies.
18 rable to those from intervention and genetic observational studies.
19 ded-10 RCTs, 4 non-RCT interventions, and 23 observational studies.
20 We performed an umbrella review of observational studies.
21 esults of common statistical methods used in observational studies.
22 ed for confounding adjustment in analysis of observational studies.
23 nconsistently associated with cancer risk in observational studies.
24 d more underlying diseases than those in the observational studies.
25 ormed a meta-analysis of available data from observational studies.
26 comes should be corroborated in future large observational studies.
27 plemented by a systematic review of relevant observational studies.
28 nd control for confounding was inadequate in observational studies.
29 ials, meta-analyses, systematic reviews, and observational studies.
30 ng these systems has been based primarily on observational studies.
31 idence interval (CI): RCTs, 1.70, 1.33-2.16; observational studies, 1.32, 1.13-1.54] were consistentl
33 titutional review board-approved prospective observational study (2006-2013), study participants with
35 dies (18 randomized controlled trials and 21 observational studies; 33 867 participants) were include
36 ts who initiated FTY in a 2-year multicentre observational study, 36 were classified as 'Active' or '
37 s with AH who were enrolled in a multicenter observational study, 36 with alcohol use disorder (AUD),
39 ed confounding, which is commonly present in observational studies, a key limitation is that many sev
40 r disease from the Women's Health Initiative Observational Study, a weighted linear regression analys
41 ndings from randomized controlled trials and observational studies, additional studies are needed to
42 0 982 women in the Women's Health Initiative Observational Study, aged 50 to 79 years, who were witho
43 In this 4 year multicentre retrospective observational study, all clinical samples referred for 1
47 in inadvertently during MDA campaigns in the observational studies and 397 pregnant women (399 pregna
50 rom systematic reviews with meta-analyses of observational studies and physical health outcomes assoc
51 patient datasets obtained from retrospective observational studies and prospective clinical trials.
52 nciling differences between experimental and observational studies and providing evidence for the sha
53 ains unsettled with discordant findings from observational studies and randomized clinical trials.
56 ssessed using the Newcastle-Ottawa Scale for observational studies and the Cochrane Risk of Bias Tool
58 nducted a quasiexperimental before-and-after observational study and analyzed 3 groups with different
61 impact disease, we performed a retrospective observational study and found that history of macular de
62 .8% vs 2.3% without statin use; P < .001) in observational studies, and should be considered preopera
64 3) How much information obtained from, e.g., observational studies, animal models, and genetic studie
66 r, there are currently no reliable data from observational studies, as the high variability in the fl
75 oration (TERAVOLT) registry is a multicentre observational study composed of a cross-sectional compon
79 TTING, AND PARTICIPANTS: US population-based observational study conducted between March 9, 2020, and
87 is a prospective, multicentre, longitudinal, observational study done in 56 neurosurgical centres acr
88 6 patients were recruited into a prospective observational study (DRKS00005335) upon admission into o
90 Hypertension (IDH) study, a community-based observational study, enrolled 408 participants who had O
91 ; n = 40 647), and Women's Health Initiative Observational Study (enrollment 1993-1998; follow-up 199
92 EXPECT) pregnancy registry was a prospective observational study established in 2006 to evaluate peri
93 lenge of obtaining fresh tissues.METHODSThis observational study evaluated 6 individuals with HIV (n
95 Randomized controlled trials and prospective observational studies evaluating pre and post-procedure
97 is an open-label, multinational, prospective observational study evaluating the long-term safety and
99 r existing comorbidities, this retrospective observational study finds no evidence for an effect of p
100 ecent meta-analyses of randomized trials and observational studies found no beneficial effects of red
101 high- or moderate-risk health care settings, observational studies found that risk for infection with
111 se etiologies, especially severe sepsis, and observational studies have linked CMV reactivation with
117 cy, is prevalent; this is of concern because observational studies have shown negative associations w
122 a and cost estimates in 2016 US dollars from observational studies, health facility costings and publ
123 timates were obtained from data collected in observational studies, health-facility costings, and fro
126 Materials and Methods In this retrospective observational study, hospitalized patients aged 18 years
127 of 16 participant centers, this multicenter observational study identified validation patients, who
128 ion to June 3, 2019, for clinical trials and observational studies in adult patients with non-Hodgkin
129 conducted according to the Meta-analysis Of Observational Studies in Epidemiology (MOOSE) guidelines
130 ed a study according to the Meta-analysis of Observational Studies in Epidemiology guidelines for rep
133 supported by experimental animal models and observational studies in humans, findings from intervent
138 e performed this prospective cross-sectional observational study in a multi-site London hospital.
140 cators Research Tracking in Hospitals was an observational study in five hospitals in Bangladesh, Nep
142 cialist hospital, we conducted a prospective observational study in its Medicine and Surgery wards, r
151 evere influenza.Methods: This retrospective, observational study included critically ill patients wit
156 ed for confirmatory endomyocardial biopsies; observational studies indicate that the diagnosis of ATT
159 articipated in the Women's Health Initiative Observational Study, investigating the relations of GI,
163 A challenge of meta-analyzing results from observational studies is that summary measures of risk d
166 rent synergistic effect reported in previous observational studies may also underestimate independent
171 s assessments, in particular, for reviews of observational studies of environmental exposures, and we
172 ory syndrome coronavirus 2 (SARS-CoV-2), and observational studies of mask use and coronavirus infect
178 ust 2017 was conducted, selecting controlled observational studies of the association of prenatal ant
184 diction and a propensity score (PS) matching observational study of 26,779 individuals from a COVID-1
185 his was a prospective, multicenter (n = 14), observational study of 265 hospitalized adults with MRSA
187 rformed a single-institution, retrospective, observational study of 488 consecutive patients with pri
193 ecruited to a UK hospital-based, multicentre observational study of adults with imaging confirmed spo
195 COPD.Methods: This was a post hoc long-term observational study of an historical cohort of 201 patie
196 hed her seminal paper on the methods for the observational study of behaviour, automated detection an
197 prospective, international, cross-sectional observational study of children with PARDS from 100 cent
198 erformed secondary analysis of a prospective observational study of children with septic shock in who
212 eta-analysis of either published or preprint observational studies or randomized control trials (RCT)
217 luded one randomised controlled trial and 25 observational studies, provided results for 5,143 adult
219 of individual participant data from eligible observational studies published between Jan 1, 1980, and
220 ed controlled trials (RCTs), and comparative observational studies published from 2007 through 2019.
221 nd prospective and retrospective comparative observational studies published from 2008 through 2019.
222 h was performed to identify English-language observational studies published from inception to Septem
226 This systematic review and meta-analysis of observational studies reporting adjusted risk estimates
227 iews and Meta-Analyses guidelines, including observational studies reporting long-term sequelae, HRQo
229 conducted a systematic electronic search for observational studies reporting the outcomes associated
230 a decreased risk of myocardial infarction in observational studies (SE: 0.79, 95% CI: 0.75-0.84) were
234 vanted trivalent influenza vaccine (TIV) and observational studies suggest aTIV better prevents hospi
237 lysis, and a large international multicenter observational study suggest that extracorporeal life sup
239 ded in the short-term to critically evaluate observational studies suggesting risks associated with m
241 mized clinical trials (RCTs) and comparative observational studies that enrolled adults with COPD wit
242 among clinicians on how to critically review observational studies that have incorporated these analy
244 for randomised controlled trials (RCTs) and observational studies that reported adverse events in pr
249 consistent findings of randomized trials and observational studies; that animal products skew the die
250 c analysis of data collected for prospective observational studies, the authors studied 293 study par
252 -analyses, randomized controlled trials, and observational studies to develop 14 best practices.
253 predator-prey interactions, the capacity for observational studies to identify mechanistic drivers of
260 s of randomized controlled trials (RCTs) and observational studies was conducted to assess the associ
271 aim of the present 7-year follow-up clinical observational study was to assess the survival of dental
277 his prospective, multicenter, international, observational study, we enrolled women with a clinical d
290 Data from this multicountry, facility-based, observational study were collected on 15 neonatal care p
291 ty-one studies (2'930 patients, five RCT, 16 observational studies) were retained for the analysis.
293 ing women from the Women's Health Initiative-Observational Study (WHI-OS, n = 926), the WHI-Hormone T
294 tudies, which support biotic resistance, and observational studies, which find that native and non-na
295 n the endTB (expand new drug markets for TB) Observational Study, which enrolled a large, heterogeneo
299 effusions were prospectively recruited to an observational study with biological samples stored at pr
300 es) in the WHI-OS (Women's Health Initiative Observational Study), with replication in an independent