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1 that observed with serum samples obtained by venipuncture.
2 ation, during pregnancy, and after stressful venipuncture.
3 y diverting a 1-ml sample (DS) from the same venipuncture.
4 od films prepared using samples collected by venipuncture.
5 mice and they rapidly stopped bleeding after venipuncture.
6 ng salivary cortisol levels before and after venipuncture.
7 l venous or arterial catheter and peripheral venipuncture.
8 e, statistically less than from a peripheral venipuncture.
9 ecific than those obtained from a peripheral venipuncture.
10 theters and culture of blood from peripheral venipuncture.
11 relation to these surface landmarks for IJV venipuncture.
12 lex Prep Kit II for skin disinfection before venipuncture.
13 theters and culture of blood from peripheral venipuncture.
14 ugh a central venous catheter and peripheral venipuncture.
15 alue, apparently less than from a peripheral venipuncture.
16 es of blood draw were as follows: peripheral venipuncture, 36%; arterial, 10%; and central venous acc
18 ety of anticoagulants and serum collected by venipuncture and capillary blood collection protocols.
19 avoid the costs and concerns associated with venipuncture and spotted serum samples can be stored at
21 rning bacteremia, including the technique of venipuncture and urine antigen testing, were of interest
24 tter during invasive procedures (injections, venipuncture, and surgery) than during noninvasive proce
25 red to 99mTc-red cells include: (a) only one venipuncture, (b) little exposure to patient's blood, (c
28 ting in fingerstick blood followed by NAT in venipuncture blood yields relatively lower viremia sensi
30 ed that diversion of the first milliliter of venipuncture blood-the initial specimen diversion techni
32 We therefore assessed CMV DNA load in paired venipuncture-collected plasma samples and finger-stick D
33 mall-molecule profiles of the capillary- and venipuncture-collected samples revealed 23 statistically
37 years, undergoing diagnostic interviews and venipuncture for measurement of two inflammatory biomark
40 addition, 2 mL venous blood was collected by venipuncture from all participants to determine serum le
43 e during routine invasive procedures such as venipuncture, intravenous cannulation, urethral catheter
44 can be of particular advantage in cases when venipuncture is difficult to perform-for example, with n
48 We conclude that our hypothesis is valid: venipuncture needles soil blood culture specimens with u
51 499 observations, 426 were catheter-negative/venipuncture-negative, 19 were catheter-positive/venipun
52 d cultures, 469 (85%) were catheter-negative/venipuncture-negative, 32 (6%) were catheter-positive/ve
54 g for 20% of non-completers, and not wanting venipuncture (OR, 0.43 [0.22-0.85], 95% CI), p = 0.015,
55 mechanical complications of percutaneous IJV venipuncture, particularly when the anterior or posterio
56 ure-negative, 32 (6%) were catheter-positive/venipuncture-positive, 17 (3%) were catheter-negative/ve
57 puncture-negative, 19 were catheter-positive/venipuncture-positive, 18 were catheter-negative/venipun
58 ure-positive, 17 (3%) were catheter-negative/venipuncture-positive, and 33 (6%) were catheter-positiv
59 puncture-positive, 18 were catheter-negative/venipuncture-positive, and 36 were catheter-positive/ven
60 obtained from indwelling catheters or direct venipuncture preoperatively, during surgery, and daily u
62 For catheter draws compared with peripheral venipuncture, sensitivity was 78% (confidence interval [
63 For catheter draw compared with peripheral venipuncture, sensitivity was 89% (95% CI, 79% to 98%) a
65 eter specimens were compared with peripheral venipuncture, the difference between positive predictive
68 r skin antisepsis prior to all blood culture venipunctures, which were obtained by nurses or clinical
69 he Cepheid GeneXpert Ebola assay on clinical venipuncture whole blood (WB) and buccal swab (BS) speci
70 with our control culture (C) definition: one venipuncture with two sequentially obtained specimens, 1
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