ライフサイエンスコーパス: blood draw

1 f contamination among the different sites of blood draw.

2 who had fasted for more than 10 hours before blood draw.

3 age, time since initial screen, and year of blood draw.

4 ccording to age, smoking status, and time of blood draw.

5 valent cardiovascular disease, and timing of blood draw.

6 ontrol subjects by age, smoking, and time of blood draw.

7 -period since initial screening, and date of blood draw.

8 r age, smoking, fasting status, and month of blood draw.

9 e and matched by age, sex, race, and date of blood draw.

10 and nondiabetics with an overnight fast for blood draw.

11 detect tuberculosis infection using a single blood draw.

12 patient samples processed immediately after blood draw.

13 stage and outcome measures from the date of blood draw.

14 mass spectrometry and adjusted for season of blood draw.

15 volumes commonly available from fingerstick blood draw.

16 to each case by age, race, sex, and month of blood draw.

17 able to cooperate with fingerstick or venous blood draw.

18 eminating tumor cell population via a simple blood draw.

19 .6% other), hysterectomy status, and date of blood draw.

20 rial biopsies and a pre-operative peripheral blood draw.

21 xome sequencing coverage than DNA from fresh blood draw.

22 time of blood draw, and hours fasting before blood draw.

23 the reduction began as early as 7 hours post-blood draw.

24 ot vary by adult BMI or menopausal status at blood draw.

25 ge, race, duration of follow-up, and time of blood draw.

26 zed with respect to their volume and site of blood draw.

27 s, who underwent standardized interviews and blood draws.

28 le out AMI in 58% of patients without serial blood draws.

29 mprehensive follow-up schedule with frequent blood draws.

30 and interleukin-6 were assayed from baseline blood draws.

31 were matched to the cases by age and date of blood drawing.

32 or age, smoking, fasting status, and date of blood drawing.

33 8 and were free of cardiovascular disease at blood drawing.

34 rmally and without sophisticated reagents or blood drawing.

35 aw (n = 175), and PTSD that persisted beyond blood draw 1 (chronic PTSD; n = 174).

36 ma at either blood draw (n = 175), trauma at blood draw 1 but no PTSD at either draw (n = 175), and P

37 not using exogenous hormones at the time of blood draw (1989-1990).

38 2 patients became PCR negative on a repeated blood draw 5 months after initial detection of C pneumon

39 atment and the other isolate (R712) was from blood drawn after treatment with daptomycin.

40 50 cases and 314 controls matched on date of blood draw, age at blood draw, and region was used to de

41 .88) but not among women aged >/=40 years at blood draw (all Pheterogeneity </= 0.05).

42 c or psychiatric history completed a fasting blood draw and a brief neuropsychological test battery.

43 d 377 cases of breast cancer diagnosed after blood draw and before June 2000; two controls were match

44 st for cases with shortest lag times between blood draw and diagnosis (<3 years).

45 atched per case on age, menopausal status at blood draw and diagnosis, fasting status, and time of da

46 by postmenopausal hormone use, years between blood draw and diagnosis, or after adjustment for estrad

47 rtion who would permit being enrolled in the blood draw and lumbar puncture studies, respectively, we

48 udies that included either a blood draw or a blood draw and lumbar puncture to explore older persons'

49 f 969 cases of breast cancer diagnosed after blood draw and prior to June 1, 1998, were individually

50 red from each bronchoscopy and corresponding blood draw and subjected to polychromatic flow cytometry

51 n models were further adjusted for season of blood draw and when analyses were restricted to the firs

52 the predictive ability of models requiring a blood draw and/or a voiding cystourethrogram.

53 Recommended procedures for blood drawing and for processing samples are described.

54 e influence of factors such as the volume of blood drawn and the site of blood draw on the rates of b

55 rom the area under the curve (AUC) of serial blood draws and cumulative urinary excretion during a 24

56 f 35 patients with T1D (<6 mo after onset at blood draw) and 41 age-matched controls were assayed by

57 The difference between day 0 (<13 hours post-blood draw) and day 1 (24-37 hours) measurements was ana

58 ing, prepregnancy weight, gestational age at blood draw, and child sex) with mean IQ were assessed by

59 cipants underwent cognitive testing, fasting blood draw, and FDG-PET at baseline.

60 by age, ethnicity, clinical center, time of blood draw, and follow-up duration.

61 by age, ethnicity, clinical center, time of blood draw, and follow-up time.

62 by cohort, age, sex, race/ethnicity, date of blood draw, and follow-up time.

63 r Los Angeles), birth year, date and time of blood draw, and hours fasting before blood draw.

64 by age, ethnicity, clinical center, time of blood draw, and length of follow-up.

65 sion, adjusting for maternal race, season of blood draw, and other potential confounders.

66 ntrols matched on date of blood draw, age at blood draw, and region was used to determine concentrati

67 cted in a 2:1 ratio matched for age, date of blood draw, and smoking status (n = 532).

68 g based on simultaneous intravenous sensing, blood draws, and intraarterial sensing, we found that in

69 in a phase II MV trial during the period of blood draws, and were selected for this study in a blind

70 nts had clinical evaluations, brain MRI, and blood draws annually.

71 Carboxyhemoglobin was measured in whole blood drawn around 13 weeks' gestation.

72 2,075 indicated active HT use at the time of blood draw at study initiation and 15,661 did not.

73 elling antecubital venous cannula placed for blood drawn at baseline, 60, 120, and 180 minutes after

74 the Wallach Memory Recognition Test and had blood drawn at half-hour intervals over the course of an

75 violation by having missed blood samples or blood drawn at unscheduled times (group 2).

76 sk of type 1 diabetes in a birth cohort with blood draws at ages 9, 15, and 24 months and yearly ther

77 r ex vivo stimulation with LPS compared with blood drawn before the start of the infusion, and (b) 17

78 atal bacteremia; one isolate (S613) was from blood drawn before treatment and the other isolate (R712

79 CTCs from 7.5 mL of whole blood drawn before treatment initiation (baseline) and m

80 ising 6 study periods, during which they had blood draws before and after medication administration.

81 After adjustment for month of blood draw, breast cancer status, colorectal cancer stat

82 l number did not change within 24 hours post-blood draw, but CD4 expression decreased 2.0+/-2.8% (P<0

83 ing method is less invasive than "classical" blood drawing, can be performed conveniently at home, an

84 l participants underwent 3 lumbar punctures, blood draw, clinical assessment of strength, motor funct

85 genes in 100% of parental exomes from fresh blood draw, compared with only 82% of autopsy-sourced SD

86 absence of a contact system inhibitor during blood draw, contact activation of FXI can mistakenly app

87 ched to cases by cohort, age, sex, race, and blood draw date.

88 A lower vitamin D was associated with the blood draw during fall/winter months (P < .001), older a

89 ; subjects who selected plasma testing had a blood draw during the office visit.

90 cid composition were determined from fasting blood drawn during the final 4 d of each 3-wk diet perio

91 106 (with smokers in the satiated state) and blood draws during PET scanning to determine TSPO affini

92 Following the baseline blood draw, each subject was randomized to receive eithe

93 n of systemic corticosteroids at the time of blood draw for microarray analysis were classified in th

94 e change in BMI between 2002 and the time of blood draw for TCDD measurement (adjusted OR, 2.37; 95%

95 All blood drawn for culture from adult inpatients and emerge

96 and lifestyle, were examined physically, had blood drawn for DNA extraction, were tested for presence

97 male) underwent clinical assessment and had blood drawn for genotyping and methylation analysis.

98 rual cycle (primary outcome measure) and had blood drawn for gonadal hormone and neurosteroid levels

99 itizens responded to a questionnaire and had blood drawn for HIV testing in the absence of documentat

100 ldren 18 months to 19.9 years of age who had blood drawn for medical indications during an outpatient

101 These subjects also had fasting blood drawn for serum cholesterol, glucose, and a number

102 Blood draws for the detection of insulin autoantibody, g

103 protein 3 in 6,520 women aged 32-70 years at blood draw from the Nurses' Health Study (1990-2006) and

104 ons to be expanded up to 500-fold in a 60-mL blood draw from the same donor.

105 PCR test results for HIV DNA on venous blood drawn from children ages 0-2 days and 3-5 months w

106 In experiments with fresh blood drawn from filaria-infected patients, we found no

107 on in human disease, the assay was tested on blood drawn from macaques infected with F. tularensis Sc

108 preparation was obtained from 10 ml of whole blood drawn from one age-matched donor rat.

109 ients with MS were significantly elevated in blood drawn from the internal jugular vein and a periphe

110 ates were body mass index, winter and spring blood draw, history of diabetes, sedentary behavior, smo

111 metriosis risk among women aged <40 years at blood draw (IGF-1: IRR = 1.60, 95% CI: 0.86, 2.98; IGFBP

112 in 1,095 women who were free of diabetes at blood draw in 1989-1990 and participated in two case-con

113 cancer, and diabetes mellitus at the time of blood drawing in 1990.

114 CD64 indices were performed with peripheral blood drawn in tandem with blood cultures from 109 patie

115 and neurotrophins was observed in peripheral blood drawn in the first days of life.

116 re was complete concordance between 60 ml of blood drawn in the first two sets of 30 ml and three 20-

117 asting endothelial function measurements and blood draws in the morning after PSG.

118 Conclusion Blood pressure readings, blood draws, injections, and number or duration of fligh

119 measurement, patients reported the number of blood draws, injections, blood pressure measurements, tr

120 is increases risk of lymphedema, ipsilateral blood draws, injections, blood pressure readings, and ai

121 ssessment survey that reported the number of blood draws, injections, blood pressure readings, trauma

122 y was to investigate the association between blood draws, injections, blood pressure readings, trauma

123 sting age, smoking, fasting status, month of blood draw, lipids, body mass index, and other cardiovas

124 d the baseline questionnaire, interview, and blood draw (lipopolysaccharide-stimulated production of

125 s and 1,066 age-, sex-, race-, and season-of blood draw-matched controls from 8 prospective cohort st

126 terviews) was defined as no trauma at either blood draw (n = 175), trauma at blood draw 1 but no PTSD

127 ex, clinic, year of enrollment, and month of blood draw (n=405).

128 Nine biomarkers were assayed from blood draws obtained on ED presentation.

129 as the volume of blood drawn and the site of blood draw on the rates of blood culture contamination.

130 Plasma was prepared from whole blood drawn on ICU admission in patients with influenza

131 mer's disease studies that included either a blood draw or a blood draw and lumbar puncture to explor

132 l model (environmental risk factors only, no blood draw or assays required) were created.

133 Viral load information was obtained via blood draw or medical record abstraction.

134 y 1994, 780 had confirmed type 2 diabetes at blood drawing or during follow-up to 1998 and were free

135 or level was associated within 6 years after blood draw (OR (</= 3 years), 95% CI, 1.4, 1.1-1.9, P =

136 d change increase and undergoing one or more blood draws (P = .62), injections (P = .77), number of f

137 use, physical activity, alcohol intake, and blood draw parameters.

138 year 2006 were analyzed for their volume of blood drawn, patient's weight, site of blood draw used,

139 RNA was measured by quantitative RT-PCR from blood drawn perioperatively in patients undergoing thyro

140 Even with optimal blood drawing, plasma TGF-beta1 was lower in mice render

141 blood draw study, and nearly half (48%) to a blood draw plus lumbar puncture study.

142 81% for the blood draw study and 70% for the blood draw plus lumbar puncture study.

143 PRP was prepared from whole blood drawn prior to surgery and applied to root surface

144 during follow-up of more than 10 years after blood draw (quintile 5 vs. quintile 1: odds ratio = 2.55

145 After adjustment for age and date of blood draw, race, and body mass index, androgens were fo

146 0) diagnosed at least 5 years after baseline blood draw (range, 5-12 years; median 9 years) and frequ

147 s exposed to chemotherapy, with older age at blood draw (recurrent OC odds ratio [OR], 17.24; 95% CI,

148 also had TMA-positive results from the same blood draw; six were positive on repeat testing.

149 Blood-draw specimens (108) obtained at the same time fro

150 eway over their advance consent: 81% for the blood draw study and 70% for the blood draw plus lumbar

151 ) were willing to grant advance consent to a blood draw study, and nearly half (48%) to a blood draw

152 On day 1 after a fasting blood draw, subjects consumed 300 g yellow maize porridg

153 We derived serum from blood draws taken from 76 young and elderly subjects imm

154 er, ethnicity, and body mass index underwent blood draw the next morning for soluble CD40 ligand, asy

155 -hydroxyvitamin D concentration and month of blood draw, the highest values being during the summer m

156 ritically ill surgical patients, cultures of blood drawn through a catheter are less specific than th

157 Positive predictive value of cultures of blood drawn through a catheter is low and, when obtained

158 Culture of blood drawn through an indwelling central venous cathete

159 o a General Clinical Research Center and had blood drawn through an intravenous line for determinatio

160 zed hematology-oncology patients, culture of blood drawn through either the central catheter or perip

161 . brumae grew from a quantitative culture of blood drawn through the catheter.

162 f follow-up) were matched by age and date of blood draw to 400 controls who were alive and free of ca

163 The median time from second blood draw to cancer diagnosis was 16 years; median foll

164 ched by age, race, sex, and calendar date of blood draw (to control for seasonal variation).

165 ong those diagnosed 10 years or longer after blood draw (upper tertile OR, 0.60; CI, 0.40-0.90), but

166 me of blood drawn, patient's weight, site of blood draw used, and blood culture results.

167 ation, ethnicity, body mass index, season of blood draw, vascular risk, and apolipoprotein E4 genotyp

168 relates of 25(OH)D included male sex, summer blood draw, vigorous physical activity, vitamin D intake

169 CO exposure during the month of blood draw was estimated using a regression model contai

170 A single blood draw was the only procedure categorized as minimal

171 of endocarditis-related bacteria from all 6 blood draws was 23%, 33%, and 60% for the toothbrushing,

172 Among 115 patients who underwent sequential blood draws, we evaluated the relationship between chang

173 f contamination among the different sites of blood draw were as follows: peripheral venipuncture, 36%

174 amin D or calcium supplements, and season of blood draw were considered as confounders.

175 and controls with matching age and month of blood draw were studied.

176 PET/CT, whole-body probe counts, and blood drawing were performed over 8 d to assess pharmaco

177 Plasma was collected from infants if venous blood draws were ordered by pediatricians.

178 Photoacoustic tomography and blood draws were performed at day 10 and then 24 h after

179 PET imaging, whole-body probe counts, and blood draws were performed to assess pharmacokinetics, b

180 s, among whom electrocardiograms and fasting blood draws were repeated at 3-year intervals from 1993

181 control for chemotherapy exposure and age at blood draw when testing the association of somatic mosai

182 en were instructed to visit the clinic for a blood draw when the monitor indicated an LH surge.

183 od collection, race/ethnicity, and timing of blood draw within the menstrual cycle.