ライフサイエンスコーパス: urine collection

1 y of, day prior, and 2- to 5-d lags prior to urine collection).

2 s suggesting frequent incompliance with 24-h urine collection.

3 animals for 48 hours in metabolic cages for urine collection.

4 ected over urine clearance as it requires no urine collection.

5 on) at participants' homes the year prior to urine collection.

6 tes (RHiNO) cohort, underwent spirometry and urine collection.

7 erent occasions, using both spot and 24-hour urine collection.

8 w studies assessing sodium intake using 24-h urine collection.

9 generally greater with PCP use within 6 h of urine collection.

10 randomly selected to participate in the 24-h urine collection.

11 ng; external counting; and blood, fecal, and urine collection.

12 cretion rate should be measured from a timed urine collection.

13 is most precisely ascertained by using timed urine collection.

14 ernal source (W:T variance) with single 24-h urine collection.

15 nction in animal studies that do not involve urine collection.

16 residence at cohort enrollment, and date of urine collection.

17 external probe and calibrated using complete urine collections.

18 ing, plasma clearance measurements and timed urine collections.

19 markers of dietary protein in their 24-hour urine collections.

20 esis period) and 18-h (post-diuretic period) urine collections.

21 lipid peroxidation, was measured in 24 hour urine collections.

22 ations, but few large-scale studies use 24-h urine collections.

23 akes estimated from 24-h dietary recalls and urine collections.

24 from four 24-h dietary recalls and two 24-h urine collections.

25 iltration rate, and proteinuria from 24-hour urine collections.

26 um excretion was measured in 2 baseline 24-h urine collections.

27 ulation-based study including data from 24-h urine collections.

28 d four 24-h dietary recalls and 2 timed 24-h urine collections.

29 um excretion was measured daily in the 24-hr urine collections.

30 ith coronary artery disease provided 24-hour urine collections.

31 24-hour dietary recalls and 2 timed 24-hour urine collections.

32 tion and metabolism were assessed using 24-h urine collections.

33 d adolescents, using UIE measurement in 24-h urine collections.

34 CEHC and alpha-CMBHC excretions in three 8-h urine collections (0-24 h) and plasma alpha-tocopherol,

35 efore and during 24 hours post-sugars with 3 urine collections: 0-2, 2-8, and 8-24 hours.

36 as highest from exposure to rotavirus during urine collection (~10(-1)) and struvite production (~10(

37 -2)), though risks from Shigella spp. during urine collection (~10(-3)) and struvite production (~10(

38 in a diverse urban population by using 24-h urine collections, 2) corroborate potassium excretion by

39 ng employed consistent doses and duration of urine collection (3 h).

40 Two overnight urine collections (48 h apart) from 170 uterine fibroid

41 212 persons [75% of those selected for 24-h urine collection; 53% (equal to 71% x 75% of those selec

42 s, an oral glucose tolerance test, overnight urine collection, a 12-lead resting electrocardiogram, m

43 Among those with a complete 24-h urine collection, a random one-half were asked to collec

44 importance of estimating, from repeated 24-h urine collections, a population's habitual salt intake a

45 dardized 24-hour dietary recalls and 24-hour urine collections administered over 3 years of follow-up

46 ribution was assumed in the body organs with urine collection after the study.

47 diagnosed with incident breast cancer after urine collection and before June 1, 2007.

48 By simplifying and standardizing urine collection and by expanding access beyond traditio

49 g status, menopausal status, or time between urine collection and diagnosis (all Pinteraction values

50 t cancer among women with </=5 years between urine collection and diagnosis was 0.74 (Q4 vs. Q1; 95%

51 aminants might leach from materials used for urine collection and influence statistical analysis of m

52 ne albumin and creatinine in an untimed spot urine collection and reporting albumin-to-creatinine rat

53 re to rotavirus and Shigella spp. during CBS urine collection and subsequent struvite fertilizer prod

54 Protocolized blood and urine collection and transrectal ultrasound-guided syste

55 of renal dysfunction over the 72 hours after urine collection and with hospital mortality.

56 man in both seasons, we obtained two 24-hour urine collections and 2 spot urine samples, as well as s

57 Twenty-four-hour urine collections and 24-h ambulatory blood pressure ass

58 NO metabolites (NOx) were assayed in 24-hour urine collections and exhaled NO (FE(NO)) determined at

59 At the end of each period, 24-h urine collections and fasting blood samples were obtaine

60 Serial blood samples, 24-hr urine collections and nuclear images were collected unti

61 Serial blood samples, 24-hr urine collections and nuclear images were collected up t

62 ult equation, creatinine clearance from 24-h urine collection, and a new regression equation derived

63 o rejection episode noted within 30 d before urine collection, and a urine decoy cell analysis was co

64 h low education, heaving smoking, old age at urine collection, and abdominal obesity.

65 Baseline fasting blood, overnight urine collection, and clinical measurements were perform

66 Renal function was assessed by 24-h urine collection, and CRI was defined as measured creati

67 one matched (age, menopausal status, date of urine collection, and day of laboratory assay) to popula

68 a medical history and physical examination, urine collection, and phlebotomy.

69 Data included blood and urine collections, and the organ uptake value was measur

70 Nighttime urine collections are a potential alternative, as they p

71 Sodium and potassium measured in 24-h urine collections are often used as reference measuremen

72 ssessed the feasibility of implementing 24-h urine collections as part of a nationally representative

73 living kidney donor candidates with 24-hour urine collections assessed as accurate by comparing meas

74 ne protein creatinine ratio based on 24-hour urine collection at weeks 24 and 36, respectively, in th

75 Sodium excretion was measured in two 24-hour urine collections at baseline.

76 Potassium was measured in 24-h urine collections at baseline.

77 hout proteinuria (20 mg protein in a 24-hour urine collection) at 30(6)/(7) weeks of gestation.

78 atio to baseline in UPCR sampled from a 24-h urine collection) at 6 months.

79 rea excretion was measured in repeated 24-hr urine collections between 6 and 18 months after transpla

80 sirable in the areas of anesthesia, ureteral urine collections, blood collections, volume replacement

81 ly, these have been quantified using a 24-hr urine collection, but spot urine measurements (albumin-c

82 erage sodium excretion from multiple 24-hour urine collections, but such an approach is impractical.

83 A single 24-h urine collection cannot predict sodium, potassium, or ch

84 lytes is difficult and usually predicated on urine collections, commonly for 24 h, which are consider

85 intigraphy was 58.3 +/- 4.7 h (n = 20), with urine collection confirming the loss of between 2.2% and

86 bset of 10 PCPs that were used within 6 h of urine collection contributed to at least 70% of the weig

87 creatinine/urea clearance based on 24 hours urine collection could be explained.

88 This suggests that fasting blood and urine collections could be used to estimate polyphenol b

89 Phase HPV Urine Test combines a proprietary urine collection device with a novel large-volume DNA ex

90 ations in 285 patients) underwent supervised urine collections entailing an immediate pre-diuretic sp

91 ard for estimating sodium intake is the 24-h urine collection, few studies have used this biomarker t

92 ntion trials can be determined with a single urine collection for albuminuria assessment per study vi

93 ded a fasting blood sample and a single 24-h urine collection for stone risk analysis.

94 ation of all cases, the utility of a 24-hour urine collection for uric acid, and even the difficulty

95 stimation supports the continued use of 24-h urine collections for assessing population and individua

96 ial donors performed one to three outpatient urine collections for Ccr measurement.

97 low-burden, low-cost alternative to 24-hour urine collections for estimation of population sodium in

98 ) and remained significantly elevated in all urine collections for the 8-h period of the study (analy

99 on of its levels as a biomarker, by repeated urine collection from a group of volunteers over 4 weeks

100 However, urine collection from newborn infants presents a potenti

101 Contamination most likely occurs during urine collection from surrounding vaginal, perineal, and

102 he hypertension cohort, containing 1757 24-h urine collections from 1090 individuals, divided into da

103 They obtained 24-hour urine collections from 121 consecutive clinic patients w

104 e electrophoresis of a sample from a 24-hour urine collection (grade A).

105 explicit instructions, started and ended the urine collection in a urine study mobile examination cen

106 We were able to test the value of 24-h urine collections in a unique, ultra-long-term balance s

107 ars with complete blood pressure and 24-hour urine collections in the 2014 National Health and Nutrit

108 xamined differences in 2-h compared with 1-h urine collections in the lactulose rhamnose (LR) dual su

109 loop diuretic followed by a supervised timed urine collection including spot urine samples at 1 and 2

110 ) years after gadolinium exposure, a 24-hour urine collection indicated that the gadolinium level rem

111 In this paper, a novel approach for urine collection is proposed, which circumvents many of

112 n a crossover design, with serial plasma and urine collection <=24 h and 48 h, respectively.

113 nalyses that excluded potentially incomplete urine collections [Mage's equation mean difference: -109

114 One-hour urine collection may be insufficient to reflect small bo

115 gliflozin: n = 15) provided accurate 24-hour urine collections (mean age 59 +/- 14 years; left ventri

116 as to identify and recommend the appropriate urine collection method for the study of bacterial commu

117 nary metabolites of F2-isoprostanes in timed urine collections offers an advantage over measuring unm

118 s determined from isotope enrichment in spot urine collections on days 3-7.

119 for deaths from cardiometabolic diseases) at urine collection or perhaps among those who had higher e

120 ood packaging use 24 h before and during the urine collection period was collected at 5 time points f

121 en were exposed to all phthalates during the urine collection periods.

122 Proteinuria was determined from a 24-hour urine collection prior to imaging on GD18.

123 d water protocol (energy biomarker), 24-hour urine collection (protein biomarker), and self-reports o

124 insurmountable, logistic challenges of 24-h urine collection remain a barrier for research on the re

125 by a radionuclide method not dependent upon urine collection (rGFR).

126 was documented (780 mg protein in a 24-hour urine collection), schistocytes were detected in the per

127 r regression models were adjusted for age at urine collection, sex, self-reported race/ethnicity, and

128 creatinine ratio in this population, a 24-hr urine collection should be considered before making majo

129 nd demonstrated that their use within 6 h of urine collection strongly predicted MEP and paraben urin

130 ma and PTSD, was used to select a subset for urine collection studies conducted in a sleep laboratory

131 l voiding patterns, acute urinary retention, urine collection techniques, diagnosis in young infants,

132 Notably, risk of infection was higher during urine collection than during struvite production due to

133 subset of participants who completed a 24-h urine collection, the risk for kidney stones was directl

134 TS immunoglobulin (Ig)G, followed by an 18-h urine collection to quantitate the excretion of albumin

135 which takes an average of 1.5 to 2 days from urine collection to results, delaying optimal therapy.

136 report Bland-Altman analyses on the value of urine collections to estimate intake.

137 Eight-hour urine collections to measure creatinine clearance were c

138 nts using meticulously obtained timed 6-hour urine collections to quantify loop diuretic-induced cumu

139 creatinine/urea clearance based on 24 hours urine collection values.

140 ght fast; no other foods were ingested until urine collection was complete.

141 creatinine/urea clearance based on 24 hours urine collection was developed using stepwise linear reg

142 Timing of urine collection was not important for these parameters.

143 A 24-hr urine collection was obtained for determination of [15N]

144 A 24-h urine collection was obtained simultaneously.

145 A 24-hour urine collection was performed on days 17 and 29 postinj

146 tions, and an aliquot of the preceding 6 hrs urine collection was sent for magnesium and potassium de

147 . 1.73 m(-2) The mean +/- SD number of 24-h urine collections was 3.5 +/- 0.8/participant, and the m

148 ted seafood consumption within 2 days before urine collection were excluded from the analyses.

149 ls (0-6 and 7-24 h), and aliquots from these urine collections were analyzed using high performance l

150 Baseline urine aliquots and 24-hr urine collections were collected on days 3, 7, and 11 du

151 um concentration, 3-d food records, and 24-h urine collections were completed at baseline and 4 wk.

152 Twenty-four-hour urine collections were completed every 4 wk to determine

153 spite different treatment goals; ( 2 ) timed urine collections were completed in only a minority of p

154 response rate and 75% completion rate, 24-h urine collections were deemed feasible and implemented i

155 Twenty-four-hour urine collections were included from three clinical stud

156 taining known amounts of MeIQx and PhIP, and urine collections were made 0-12 and 12-24 h after a mea

157 od pressure monitoring was done and complete urine collections were made for the next 36 h.

158 Two consecutive 24-h urine collections were obtained after a baseline period

159 In 2013, 24-hour urine collections were obtained from 554 participants in

160 mated to metabolism cages, and baseline 24-h urine collections were obtained.

161 Plasma sampling and urine collections were performed on both days 1 and 5 of

162 Plasma sampling and urine collections were performed to characterize the pha

163 daily blood samples were obtained and 24-hr urine collections were performed.

164 , 1-d household salt disappearance, and 24-h urine collections were repeated in a subset of 40 partic

165 bumin (0.25 MBq), multiple blood samples and urine collections were taken between 0 and 4 h.

166 Ten-hour overnight urine collections were taken for measurement of urinary

167 inary albumin-to-creatinine ratio (ACR; spot urine collection) were measured in 5042 participants in

168 s compared with estimates from multiple 24-h urine collections, which were statistically corrected fo

169 creatinine/urea clearance based on 24 hours urine collection with superior performance than currentl

170 Urine collection within 15 mins of intensive care unit a