ライフサイエンスコーパス: vascular catheter

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1 on through the transient placement of a 5-Fr vascular catheter.

2 lly wrapped around the proximal segment of a vascular catheter.

3 ally prepared under general anaesthesia with vascular catheters.

4 y justifying the continued use of multilumen vascular catheters.

5 -Dawley rats weighing 275-425 g with chronic vascular catheters.

6 ts were instrumented with a tracheostomy and vascular catheters.

7 zed and instrumented with a tracheostomy and vascular catheters.

8 es were continuously monitored by indwelling vascular catheters.

9 zed and instrumented with a tracheostomy and vascular catheters.

10 ed on 42-h-fasted conscious dogs fitted with vascular catheters.

11 nal age) were instrumented with amniotic and vascular catheters, an electrocardiogram (ECG) electrode

12 on (term ca 145 days) were instrumented with vascular catheters and a femoral artery Transonic flow p

13 n (dGA; term is approximately 145 days) with vascular catheters and a Transonic flow probe around a f

14 ally prepared under general anaesthesia with vascular catheters and a Transonic flow probe positioned

15 d between 117 and 120 days of gestation with vascular catheters and an umbilical flow probe.

16 Rats were instrumented chronically with vascular catheters and bilateral guide cannulae directed

17 their singleton fetus were instrumented with vascular catheters and flow probes around an umbilical a

18 groups of conscious dogs fitted with chronic vascular catheters and intracerebroventricular (i.c.v.)

19 ion under general halothane anaesthesia with vascular catheters and transit-time ultrasonic flow prob

20 heep at 0.8 gestation were instrumented with vascular catheters and Transonic flow probes around an u

21 tion (term is ca 145 days) with amniotic and vascular catheters and with a transit-time flow probe ar

22 tion (term is ca 145 days) with amniotic and vascular catheters and with a transit-time flow probe ar

23 und the umbilical cord, amniotic and femoral vascular catheters and with transit-time flow probes aro

24 Candida cells adhere to a surface, such as a vascular catheter, and become encased in an extracellula

25 Many central vascular catheters (CVCs) are removed unnecessarily beca

26 dida albicans biofilms, including those from vascular catheter, denture, and urinary catheter models

27 Silicone vascular catheters have a greater risk of infection and

28 ed in the parasagittal parietal cortices and vascular catheters in the sagittal sinus and brachioceph

29 sor-masked randomized trial in patients with vascular catheters inserted for an expected duration of

30 e of culturing a single segment of a central vascular catheter is inadequate and needs to be reexamin

31 infection were nasal carriage, presence of a vascular catheter, low CD4 count, and neutropenia.

32 hetized and mechanically ventilated, and had vascular catheters placed.

33 er complement activation in vitro than other vascular catheter polymer materials.

34 le drapes was measured, and surveillance for vascular catheter-related infection was performed.

35 on termed the dorsal vagal complex (DVC) and vascular catheters to enable direct DVC infusion and blo

36 orsal margin of the CeA in male Wistar rats; vascular catheters were also placed at this time.

37 Patients with indwelling vascular catheters were excluded.

38 Crown-rump length-measuring devices and vascular catheters were implanted in 12 sheep fetuses at

39 Under general anaesthesia, vascular catheters were inserted and a Transonic flow pr

40 a history of multiple infections of central vascular catheters with other organisms, requiring cours

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