ライフサイエンスコーパス: regional perfusion

1 tests of interaction (including normothermic regional perfusion).

2 ic perfusion systems or in situ normothermic regional perfusion.

3 c machine perfusion, and one on normothermic regional perfusion.

4 and abdominal procurements, and normothermic regional perfusion.

5 belling identified no significant changes in regional perfusion.

6 est does not prevent successful normothermic regional perfusion.

7 an evolution in the pattern of reduction in regional perfusion.

8 The use of abdominal normothermic regional perfusion (A-NRP) during organ procurement is a

9 ecent studies have reported exercise-induced regional perfusion abnormalities on single-photon positr

10 Extent of regional perfusion abnormalities was estimated.

11 In a subgroup analysis of patients without regional perfusion abnormalities, TID-positive patients'

12 ad ECG is a marker of a prior MI, defined by regional perfusion abnormalities, which has a substantia

13 t a wide range was observed in those without regional perfusion abnormalities.

14 d the images for extent of visually apparent regional perfusion abnormalities.

15 perfusion images demonstrated no evidence of regional perfusion abnormalities.

16 ed perfusion techniques such as normothermic regional perfusion and ex-situ perfusion (normothermic o

17 In addition to clinical measures of regional perfusion and function, an experimentally valid

18 livers recovered using in situ normothermic regional perfusion and highest in alteplase-treated live

19 atients with renal insufficiency with normal regional perfusion and LV function, mostly because of el

20 hypothesized that the combined assessment of regional perfusion and oxygenation with CMR could clarif

21 comes of controlled DCD LT with normothermic regional perfusion and subsequent ex situ machine perfus

22 tion following thoracoabdominal normothermic regional perfusion and suggests that 10 degrees C may of

23 than 70 y were evaluated during normothermic regional perfusion and then randomly assigned to dual hy

24 ACs) were subsequently analyzed to determine regional perfusion and volume, glomerular filtration rat

25 expanding DCDD through in situ normothermic regional perfusion, and expanding DCDD through ex situ m

26 urate automatic scores for the assessment of regional perfusion, and overcomes the low-specificity li

27 Abdominal normothermic regional perfusion (aNRP) for donation after circulatory

28 can be salvaged with abdominal normothermic regional perfusion (aNRP).

29 -COR-NMP), or in situ abdominal normothermic regional perfusion (aNRP).

30 diated to dose d, and Rd is the reduction in regional perfusion anticipated at dose d.

31 recovery as well as postmortem normothermic regional perfusion are described, as are the use of adju

32 ention of CsA-induced hypoxia independent of regional perfusion (blood oxygen level-dependent magneti

33 In protocol 2, changes in regional perfusion caused by partial left anterior desce

34 des first evidence that machine perfusion at regional perfusion centers may be a safe and economical

35 Regional perfusion defect was greater during stress and

36 lar tree, as opposed to changes in the worst regional perfusion defect, have not been described durin

37 Age-adjusted multivariate analysis confirmed regional perfusion defects (relative hazard, 2.51; 95% c

38 defects; (ii) size and severity of localized regional perfusion defects caused by flow-limiting steno

39 In patients without regional perfusion defects on clinical read and no known

40 Regional perfusion defects were created by means of coro

41 At follow-up PET, new regional perfusion defects were seen in 40% of patients.

42 ing is used in clinical practice to quantify regional perfusion defects.

43 ndently of, and around significant localized regional perfusion defects; (ii) size and severity of lo

44 e and during the WLST and after normothermic regional perfusion/extracorporeal membrane oxygenation.

45 ination of death, or the use of normothermic regional perfusion for the in situ preservation of organ

46 ponse model based on RT-induced reduction in regional perfusion (function) was used to predict region

47 mma-variate curve-fitting was performed, and regional perfusion, glomerular filtration rate, and rena

48 he putamina, which normally have the highest regional perfusion, had cerebral blood flow values 24% b

49 Normothermic regional perfusion has been reported to improve outcomes

50 Normothermic regional perfusion has shown to be critical to achieve o

51 er circulatory death (DCD) with normothermic regional perfusion has the potential to increase the don

52 Notably, the use of normothermic regional perfusion improved primary nonfunction rates in

53 ice following thoracoabdominal normothermic regional perfusion in donation after circulatory death h

54 t best semiquantitative in nature, assessing regional perfusion in relative terms.

55 these approaches can be divided into in situ regional perfusion in the donor and ex situ machine perf

56 preservation include the use of normothermic regional perfusion in the donor and ex vivo organ preser

57 Ex situ machine perfusion and in situ regional perfusion in the donor are emerging as potentia

58 han men in estimates of global perfusion and regional perfusion in the midcingulate/corpus callosum,

59 Microspheres were injected to provide regional perfusion information.

60 at the relationship between the systemic and regional perfusion is dependent on the underlying cause

61 The sum of predicted RT-induced changes in regional perfusion is related to RT-induced changes in p

62 tion (P = 0.001) and in subjects with normal regional perfusion (n = 178; P = 0.036), whereas stress

63 machine perfusion (n = 8), and normothermic regional perfusion (n = 2).

64 whether the limbic system undergoes dynamic regional perfusion network alterations during seizures.

65 The adoption of normothermic regional perfusion (NRP) after donation after circulator

66 er circulatory death (DCD) with normothermic regional perfusion (NRP) allowed assessment of liver qua

67 Normothermic regional perfusion (NRP) allows in situ assessment of DC

68 ical tenets of thoracoabdominal normothermic regional perfusion (NRP) and abdominal NRP; (2) provide

69 rage (SCS), or thoracoabdominal normothermic regional perfusion (NRP) and donor hearts recovered from

70 rovides a unique bench test for normothermic regional perfusion (NRP) and dual hypothermic oxygenated

71 Normothermic regional perfusion (NRP) and ex situ machine perfusion (

72 Normothermic regional perfusion (NRP) and normothermic machine perfus

73 Normothermic regional perfusion (NRP) and normothermic machine perfus

74 a protocol based on the use of normothermic regional perfusion (NRP) before organ procurement.

75 n yield and associated costs of normothermic regional perfusion (NRP) compared to super-rapid recover

76 Normothermic regional perfusion (NRP) has emerged as a vital techniqu

77 Normothermic regional perfusion (NRP) has recently been used to augme

78 Normothermic regional perfusion (NRP) has the potential to increase t

79 u machine perfusion (es-MP) and normothermic regional perfusion (NRP) have been introduced in the Uni

80 Normothermic regional perfusion (NRP) improves recipient outcomes and

81 al effect of clamping following normothermic regional perfusion (NRP) in donation after circulatory d

82 ch vessel (AAV) clamping during normothermic regional perfusion (NRP) in donation after circulatory d

83 The benefits of normothermic regional perfusion (NRP) in posttransplant outcomes afte

84 A period of normothermic regional perfusion (NRP) in the donor may reverse these

85 Thoracoabdominal normothermic regional perfusion (NRP) is a new method for in situ rep

86 Normothermic regional perfusion (NRP) is a surgical technique that ca

87 mic machine perfusion (NMP) and normothermic regional perfusion (NRP) may enhance the preservation of

88 The availability of in situ normothermic regional perfusion (NRP) or ex situ normothermic machine

89 In situ normothermic regional perfusion (NRP) or restarting the heart in the

90 cDCD liver transplant (LT) with normothermic regional perfusion (NRP) preservation.

91 egal considerations surrounding normothermic regional perfusion (NRP) procurement.

92 tion utilizing thoracoabdominal normothermic regional perfusion (NRP) protocols (cDCDD-NRP), provides

93 In situ normothermic regional perfusion (NRP) restores a blood supply to the

94 Use of normothermic regional perfusion (NRP) to enable organ reconditioning

95 We evaluated whether the use of normothermic regional perfusion (NRP) was associated with increased o

96 ed a novel protocol for in situ normothermic regional perfusion (NRP) which complied with these requi

97 HOPE) and compare the effect of normothermic regional perfusion (NRP) with that of direct procurement

98 eath (cDCD) program, which uses normothermic regional perfusion (NRP), and involves short cold ischem

99 them recovered with the use of normothermic regional perfusion (NRP), and recipients of donation aft

100 Normothermic regional perfusion (NRP), based on the use of extracorpo

101 on and 35.0% were classified as normothermic regional perfusion (NRP).

102 erioperative strategies such as normothermic regional perfusion (NRP).

103 cDCD livers are recovered using normothermic regional perfusion (NRP).

104 ling [ISC]) or 33-36 degrees C (normothermic regional perfusion [NRP]).

105 blood flow to study the impact of global and regional perfusion on PIB retention.

106 s the need for thoracoabdominal normothermic regional perfusion or ex situ perfusion systems.

107 The rapid initiation of normothermic regional perfusion or extracorporeal membrane oxygenatio

108 , oxygen consumption, arterial lactate), and regional perfusion parameters (gastric mucosal Pco2, ski

109 sceptibility have a greater heterogeneity in regional perfusion parameters than emphysema-free smoker

110 Central and regional perfusion parameters were obtained at baseline,

111 Quantitative image analysis determined regional perfusion parameters, pulmonary blood flow (PBF

112 ed and accepted for LT based on normothermic regional perfusion parameters.

113 a our center's thoracoabdominal normothermic regional perfusion pathway.

114 pattern indicates disturbed autoregulation, regional perfusion pressure gradients, or redistribution

115 ease (COPD), information is limited on early regional perfusion (Q(r)) alterations.

116 antation using thoracoabdominal normothermic regional perfusion recovery with a donation from a circu

117 To determine the role of HPV in the regional perfusion redistribution in bronchoconstricted

118 n of a retention index describing global and regional perfusion reserve are feasible using a solid-st

119 In the patients, the regional perfusion reserve matched the coronary flow res

120 infarction, KR31173 retention, corrected for regional perfusion, revealed AT1R up-regulation in the i

121 h hemodialysis, a renal transplant, abnormal regional perfusion (summed stress score > 4), or reduced

122 The novel approach of thoracic normothermic regional perfusion (TA-NRP) for in-situ preservation of

123 Thoracoabdominal normothermic regional perfusion (TA-NRP) has been increasingly used f

124 ently, in situ thoracoabdominal normothermic regional perfusion (TA-NRP) has emerged as a novel techn

125 Thoracoabdominal normothermic regional perfusion (TA-NRP) has emerged as a powerful te

126 approach using thoracoabdominal normothermic regional perfusion (TA-NRP) shows promise for better rec

127 Thoracoabdominal normothermic regional perfusion (TA-NRP) would likely expand the quan

128 ticularly with thoracoabdominal normothermic regional perfusion (TA-NRP), on the use of DCD lungs.

129 onor, known as thoracoabdominal normothermic regional perfusion (taNRP) or outside of the donor, know

130 ial aspects of thoracoabdominal normothermic regional perfusion, this method of heart recovery offers

131 In addition, the use of normothermic regional perfusion to resuscitate abdominal organs of do

132 perfusion (US$6489-12 686), and normothermic regional perfusion (US$9287; single study).

133 Normothermic regional perfusion used during DCD abdominal organ retri

134 ured adult with glutaric aciduria type 1 had regional perfusion values within the normal range, but t

135 amic shock (T1) simultaneously decreased all regional perfusion variables in both models.

136 he endotoxemic model, however, the different regional perfusion variables were only normalized at T3

137 coronary flow, 2) in an in-vivo model during regional perfusion variations, and 3) in humans during p

138 Regional perfusion was assessed in the sublingual, intes

139 Regional perfusion was estimated from the double product

140 Regional perfusion was estimated using a previously desc

141 Regional perfusion was measured using arterial spin labe

142 of regional volumes and relative measures of regional perfusion were calculated.

143 mothermic machine perfusion, or normothermic regional perfusion were included.

144 Significant alterations in regional perfusion were not observed.

145 ical considerations surrounding normothermic regional perfusion with DCD.

146 Regional perfusion with Tf-CRM107 produces tumor respons