ライフサイエンスコーパス: life table

1 using the World Health Organization standard life table.

2 s were examined using the age-stage, two-sex life table.

3 nd analyzed them using an age-stage, two-sex life table.

4 rformed using the Kaplan-Meier estimator and life table.

5 opulation and death rates from the Minnesota life tables.

6 ditions at the age of 20 was estimated using life tables.

7 relative survival by SES utilizing Hong Kong life tables.

8 nd 10-14 years, inclusive) using appropriate life tables.

9 using both the race-adjusted and -unadjusted life tables.

10 outh Korea and with mathematical analysis of life tables.

11 fe lost was calculated according to Canadian life tables.

12 d Centers for Disease Control and Prevention life tables.

13 on comparisons of survival models with U.S. life tables.

14 ected with hazard-based modifications to the life tables.

15 d on age and sex alone, was calculated using life tables.

16 pulations at risk with census counts and NIH life tables.

17 mortality was estimated from United Kingdom life tables.

18 and 1996 by means of Kaplan-Meier actuarial life-tables.

19 d-generated expected mortality rates from BC life-tables.

20 s lifetime risks (ELR) were calculated using life tables accounting for all-cause mortality.

21 The life table-adjusted cumulative risk of loss after gestat

22 sease, stage at diagnosis, and survival), US life tables (all cause mortality), and the medical liter

23 We also did intention-to-treat Kaplan-Meier life table analyses and followed up women who did not us

24 Life table analyses showed that intrinsic rate of increa

25 In life-table analyses (log-rank test), incidence of the me

26 Life-table analyses revealed no fitness loads affecting

27 Life-table analyses showed that joint replacement was pe

28 Life-table analyses were used to compare 2-year overall

29 st 2 consecutive study visits) determined by life-table analyses, and at least 10 letter (>/=2 line)

30 urvival and success rates were calculated by life-table analyses.

31 Life-tables analyses were used to estimate gains in life

32 Kaplan-Meier life table analysis showed similar survival rates at 1,

33 Here, we used age two-sex life table analysis to examine demographic parameters on

34 he 1, 2, and 5-year survival estimates using life table analysis were 72, 48, and 23%.

35 By life table analysis, the probability of detecting dyspla

36 By life table analysis, we found that losartan and doxycycl

37 Results up to 4 years were evaluated by life table analysis.

38 l outcomes were evaluated using Kaplan-Meier life table analysis.

39 inical recurrence rates (intent to treat) by life-table analysis at 24 months were 50% (95% confidenc

40 and success rate (SR) were calculated using life-table analysis for both M and R short implants.

41 A Kaplan-Meier life-table analysis revealed that the incidence of zoste

42 ion of OPMD caused marked debility, although life-table analysis showed no decrease in life expectanc

43 Life-table analysis showed that in patients who survived

44 Life-table analysis showed that the cumulative proportio

45 The life-table analysis showed that the group 1 patients had

46 Life-table analysis showed the mean times to a diagnosis

47 Life-table analysis shows the ipsilateral stroke-free ra

48 We used life-table analysis to estimate gains in life expectancy

49 udy enrollment, 1661 patients died (15.9% by life-table analysis).

50 On life-table analysis, 90-day recurrence rates with mean S

51 st, Wilcoxon matched-pairs signed-rank test, life-table analysis, Kaplan-Meier method, and log-rank t

52 With use of life-table analysis, overall primary and secondary 1-yea

53 By life-table analysis, the likelihood of remission during

54 By life-table analysis, the rate of stroke was 2.2% (95% co

55 By life-table analysis, women were significantly less likel

56 Transitions are estimated using life-table analysis.

57 Durability of PFSS was determined with life-table analysis.

58 were analyzed statistically and by means of life-table analysis.

59 Statistical analysis was conducted using a life-table analysis.

60 r within 30 days), and 5-year survival, from life-table analysis.

61 Well-known methods to do this, such as the life table and age adjustment, exist for binary nonrecur

62 lobal Burden of Disease Study 2021 reference life table and forecasts of cause-specific mortality und

63 e and comprehensive actuarial foundation for life table and mortality analysis, it suggests new possi

64 Life table and multivariate analysis also demonstrated t

65 re compared by means of chi-square tests and life table and random effects model analyses.

66 e, 6-12), determined by comorbidity-adjusted life tables and 43% were randomized to VKAs.

67 llivan method, which was applied to Eurostat life tables and age-specific prevalence of activity limi

68 We aimed to estimate life tables and annual numbers of deaths for 187 countri

69 anges in mortality over time by constructing life tables and conducting survival analysis of age-at-d

70 lity weights were derived from the actuarial life tables and Global Burden of Disease study, respecti

71 er-pregnant female donors was analyzed using life tables and time-varying Cox proportional hazards mo

72 nt-level microsimulation model based on U.S. life-tables and in-trial results was used to estimate li

73 rn between 1878 (earliest year with complete life tables) and 1914 (last birth cohort for which male

74 by the time of expected patient death (1990 life tables) and whose Gleason score was less than 4 in

75 e, diabetes, and cancers were modelled using life tables, and changes in greenhouse gas emissions ass

76 fetime horizon using regression modeling, US life tables, and external data where needed.

77 tified by sex, was calculated using a period life table approach from age- and sex-specific mortality

78 PANTS: This decision analytical model used a life-table approach and was conducted between December 2

79 Using a life-table approach, the authors quantified the degree t

80 e 20th century (for which benchmark national life tables are available), mortality is consistently lo

81 pecific disease incidence rates and abridged life tables are examples of binned data.

82 Sex- and age-specific life tables are needed to compute various cancer surviva

83 oss-sectional study involved a simulation of life tables based on national death and population count

84 We present sex- and age-specific life tables based on socioeconomic status at the census

85 We incorporated these estimates in the life table by the Sullivan method to produce HALE estima

86 es at birth by quintiles of deprivation, and life tables by census tract and province.

87 We merged these data with estimated life tables by race and ethnicity, sex, age, location (c

88 For example, the construction of life tables, calculating the percentage mortality of pre

89 For life table calculations, we used prevalence, incidence r

90 et of Alzheimer's disease was derived from a life table constructed by using age-of-onset distributio

91 In this study, we collected life table data for the sweetpotato weevil, Cylas formic

92 er were calculated using incidence rates and life table data obtained from the Surveillance, Epidemio

93 Analysis excluded 2019 because life table data were not available for many peer countri

94 e, Epidemiology, and End Results program and life table data.

95 the US cancer population using registry and life-table data.

96 calculated from Berkeley Mortality Database life tables derived from population matched by gender an

97 ach we describe augments existing methods of life table design and analysis, and contributes to the d

98 A life table estimate of transmission at 6 to 8 weeks was

99 gery demonstrated less strabismus (29 of 50; life-table estimate, 58.0%) than the older cohort (>/= 4

100 ths of follow-up in 38 pseudophakic infants (life-table estimate, 66.7%) and 42 infants (life-table e

101 (life-table estimate, 66.7%) and 42 infants (life-table estimate, 74.5%) treated with contact lenses

102 han the older cohort (>/= 49 days; 51 of 64; life-table estimate, 80.0%; P<0.01).

103 Kaplan-Meier life-table estimates for continuous complete remission (

104 Kaplan-Meier life-table estimates indicated that 25% of RA patients w

105 Life-table estimates of event-free survival and survival

106 mity of genomic alterations, correlates with life-table estimates of the probability of overall survi

107 of pregnancies/100 person-years of use) and life-table estimates of the probability of pregnancy wer

108 Life-table estimates were used to determine disease-free

109 According to life-table estimates, the rate of successful discontinua

110 second relapse (FF2R) were determined using life-table estimates.

111 ), and survival (S) were determined by using life-table estimates.

112 l (DDFS), and survival were determined using life-table estimates.

113 At 1 year using Kaplan-Meier life-table estimation, the transcarotid approach was ass

114 in time-dependent models using Kaplan-Meier life-table estimation.

115 Selfing and life-table experiments were performed for two such Daphn

116 nomas was compared among the groups with the life-table extension of the Mantel-Haenszel test.

117 ze goals of care for geriatric patients, but life tables fail to account for the great variability in

118 The results provide the first estimate of a life table for a population of ant colonies and the firs

119 tudy, we constructed the first comprehensive life table for CMBS to characterize its biological param

120 evalence of the health measure to a standard life table for the same period.

121 2)=0.78) of Ne/N in an empirical data set of life tables for 63 animal and plant species with diverse

122 Finally, we constructed abridged life tables for each America, year, and sex, and extract

123 County-level death rates and national life tables for each year were obtained from the U.S. Ce

124 lculated using 2019 single year sex-specific life tables for England and Wales.

125 Life tables for single year of age, sex, calendar year,

126 County, Minnesota, and mortality rates from life tables for the general population, we estimated the

127 is study utilised VetCompass data to develop life tables for the UK companion dog population and brok

128 Life-tables for contralateral breast cancers, which cons

129 This paper describes the major life table formulae and mortality models used to analyze

130 Using global supply data and 1,879 life tables from 103 countries, we test for these effect

131 We constructed abridged life tables from age-specific mortality rates and life e

132 pectancy in 2020 was estimated by simulating life tables from estimated age specific mortality rates

133 d to 2006-2019 race-adjusted and -unadjusted life tables from the Centers for Disease Control and Pre

134 of sustaining injury, as identified from US Life Tables from the National Vital Statistics Reports 2

135 f premature death (PPD) were conducted using life tables from the UN World Population Prospects 2024.

136 Life tables generated by the current study allow a deepe

137 nic Black Americans when using race-adjusted life tables hides racialized health disparity and perpet

138 ortality was extracted from country-specific life tables in the Human Mortality Database.

139 , while they are closer to those in national life tables in The Netherlands.

140 nosed in 111 patients (9.3% +/- 0.9%, 3-year life-table incidence).

141 A life table is a tabulated expression of life expectancy

142 fer and 100% IDDM by 32 days post-transfer), life-table (log-rank) analyses revealed that IDDM can be

143 groups was compared by means of Kaplan-Meier life-tables, log-rank test, and multivariate proportiona

144 a multiple cohort, proportional multistate, life table (Markov) model to estimate the health gains a

145 ent levels of lifestyle factors by using the life table method.

146 d using conditional probability based on the life table method.

147 se and cardiac survival was estimated by the life-table method and compared by the log-rank test.

148 -square analysis; rates were computed by the life-table method and compared using Mantel-Cox log-rank

149 months of follow-up was calculated using the life-table method and was compared across treatment grou

150 at the population level using the synthetic life-table method for DHS surveys.

151 of cardiac death or AMI was estimated by the life-table method.

152 Long-term survival was estimated by the life-table method.

153 culated for the study cohort by the standard life-table method.

154 ll in-hospital deaths) were estimated by the life-table method.

155 Cumulative POF risk was estimated using the life-table method.

156 ive treatments employed before intervention; life-table methodology on an intent-to-treat basis with

157 Using life table methods and accounting for competing risks, t

158 We used multistate life table methods and transition rates estimated from p

159 bserved survival was calculated by actuarial life table methods for three new node-positive subgroups

160 -specific mortality rates is calculated with life table methods that are among the oldest and most fu

161 We used life table methods to calculate life expectancy at birth

162 We used life table methods to calculate the primary outcome, the

163 this cohort study, mortality estimates using life table methods were calculated with the National Can

164 We calculated HALE with life table methods, incorporating estimates of average h

165 tion was not significant when analyzed using life table methods.

166 rtality rates for all causes of death, using life table methods.

167 er competing causes of death, using standard life table methods.

168 obability of dying before age 70 years, with life table methods.

169 ) and overall survival (OS) were analyzed by life-table methods according to clinical and biologic fe

170 We used multistate life-table methods and microsimulation to estimate life

171 Four UK centres have used life-table methods to analyse the long-term results of c

172 Application of standard life-table methods to calculate life expectancy by year,

173 We used life-table methods to calculate the burden of cancer mor

174 Outcome analysis used standard life-table methods.

175 oronary heart disease) by multiple-decrement life-table methods.

176 Outcome analyses used standard life-table methods.

177 life year" (PALY), we constructed a dynamic life table model for the Australian working-age populati

178 ARTICIPANTS: This economic evaluation used a life table model in combination with a Markov model to c

179 d a multiple-cohort, proportional multistate life table model to estimate the effect of a 20% tax on

180 We used a proportional multi-state life table model to estimate the health impact of prohib

181 We adopt a microsimulation-based multistate life table model to provide estimates of HEs across four

182 a multiple cohort, proportional, multistate, life table model to simulate the effect of mandating eit

183 To measure re-screening by age 45, a life table model was developed.

184 expectancy were assessed using the IOMLIFET life table model.

185 A life-table model, projecting age-specific prostate cance

186 We also used life table modelling to estimate years-of-life lost attr

187 We used life table modelling to translate the mortality rate rat

188 Multistate life table models were used to estimate sex-specific hea

189 Multistate life table models with covariates age, gender, occupatio

190 For this purpose, an age-stage, two-sex life table of the predator was constructed at four const

191 Life tables of female baboons (Papio hamadryas) in two w

192 n be elucidated via several stage-structured life tables of plant populations manipulated by herbivor

193 idated via several methods: stage-structured life tables of plant populations manipulated by herbivor

194 parison, expected survival was obtained from life tables of the population of British Columbia, Canad

195 om the National Center for Health Statistics life tables on the white population in Minnesota, using

196 age- and gender-matched group obtained from life tables (p < 0.0001).

197 contrast, heterozygotes had their fertility life table parameters significantly reduced on Cry1Ac/Cr

198 Hosts and conditions similarly affect life table performance.

199 ectancy and mortality data were derived from life tables, previous studies, and national databases.

200 pregnancy in these women, we used cumulative life-table probabilities and proportional-hazards analys

201 tment-free survival rates were determined by life-table product limit estimates.

202 Survival probabilities from the U.S. life tables providing the most similar survival experien

203 With the use of clinically determined life tables, reductions in radiation-attributable lung c

204 Life table regression models were used to identify basel

205 CD2 expression level (> 75% positivity), the life table relative event rate (RER) was 1.22 for patien

206 Transient life table response experiment (LTRE) analysis showed th

207 ed bird to quantify transients, and we use a life table response experiment (LTRE) to measure the con

208 Using life table response experiment analyses, we compared pop

209 Retrospective life table response experiment analysis revealed that th

210 However, retrospective life table response experiment analysis showed that rapi

211 and undisturbed conditions were evaluated as Life Table Response Experiment and showed that C. microp

212 Life table response experiments (LTREs) decompose differ

213 raphic theory, we develop a set of transient life table response experiments (LTREs) for decomposing

214 -term population growth rate using transient life table response experiments (LTREs).

215 We applied a transient Life-Table Response Experiment ('transient-LTRE') to dem

216 Life-table response experiments with the crustacean Ceri

217 Life tables revealed no statistical difference between t

218 Life table statistics and factors affecting population g

219 Life-table stroke-free rates at 1, 5, and 8 years were s

220 Life tables summarise a population's mortality experienc

221 1981-1984 and followed to age 10 years, via life table survival and Cox multivariate analyses.

222 Life-table survival analysis was performed, and proporti

223 ts as input parameters in a relational model life table system.

224 sex, and length of follow-up using modified life table technique and surveillance epidemiology end r

225 Life table techniques and the Mlwin 3.05 module for the

226 scipline of classical demography that brings life table techniques, mortality models, experimental sy

227 ops the "Life-Event Table," an analog of the life table that can analyze occurrence of diverse types

228 We developed a multistate life table to calculate life expectancy for individuals

229 mparing the age at death to the GBD standard life table to calculate remaining life expectancy.

230 int models and used Kaplan-Meier methods and life tables to calculate median survival and age at deat

231 relative survival, constructing 252 complete life tables to control for background mortality by age,

232 We used the Chiang method of abridged life tables to estimate life expectancy at age 20 years

233 We developed synthetic cohort life tables to estimate the cumulative prevalence of con

234 pursue three aims: first, we created period life tables to examine longevity trends in Washington D.

235 d Centers for Disease Control and Prevention Life Tables to project age- and cause-specific mortality

236 "baseline" age-specific hazards in the local life tables to reflect the life expectancy associated wi

237 on weekly death counts by cause, as well as life tables, to quantify excess mortality and life years

238 e expectancy were estimated using multistate life tables under a discrete-time Markov process assumpt

239 cancer than with the census-derived national life tables used by the SEER Program.

240 ctancy at birth by sex and subcity unit with life tables using age-specific mortality rates estimated

241 Life tables varied widely between breeds.

242 However, race-adjusted life tables vastly underestimated total YLL and YLL per

243 ive survivors and the expected survival from life tables was not statistically significant.

244 appropriate race-specific and state-specific life tables was up to 2% lower for breast cancer and up

245 Furthermore, the life tables we produced are needed to estimate cancer sp

246 nal Health and Career Path Survey and French life tables, we quantified the impact of 4 major work-re

247 Abridged cohort life tables were constructed to calculate life expectanc

248 In-trial results and US life tables were used to develop a Markov cohort model t

249 obability of death was calculated from these life tables with 1-year age-specific mortality rates.

250 opulations overall and by sex using abridged life tables with 5-year age intervals.

251 as well as moderate hypothermia (p < .01 by life table), without a significant difference between mi