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1 plantation) and temperatures (hypo-, sub, or normothermic).
2 or 48 hrs and then were rewarmed or remained normothermic.
3 likely to develop an SSI than those who were normothermic.
4 imb was then attached to a custom-made, near-normothermic (30-33 degrees C) ex situ perfusion system
5 phorylated at 5 and 24 h after stroke in the normothermic (37 degrees C) brain; hypothermia augmented
6 rees C with 1 hour of circulatory arrest) or normothermic (37 degrees C) CPB for 2 hours.
7 olution during a 30-minute period of global, normothermic (37 degrees C) ischemia followed by 30 minu
8 on underwent ex situ viability testing using normothermic (37 degrees C) machine perfusion (NMP) afte
9                                        After normothermic (37 degreesC) ischaemia/reperfusion, signif
10 d to either hypothermic (32-34 degrees C) or normothermic (37-39 degrees C) conditions, and received
11 (over 400 recorded hours) were normal in all normothermic and hyperthermic control rats, and none of
12                    Conversely, a minority of normothermic and hyperthermic controls had (brief) seizu
13 normal and elevated pressures and under both normothermic and hypothermic conditions.
14 aseline cerebral blood flow is similar after normothermic and hypothermic CPB, beta-adrenergic respon
15 ma patients and is a durable measure in both normothermic and hypothermic patient groups.
16 rease and increase CVC, respectively, during normothermic and whole-body heating conditions in restin
17  minute periods of data were examined during normothermic and whole-body heating conditions.
18                                           In normothermic animals and to a greater degree in hyperthe
19                                    Ten of 12 normothermic animals failed to survive the reperfusion p
20                                              Normothermic animals were maintained at 37 +/- 0.2 degre
21                                              Normothermic animals were maintained at 37+/-0.2 degrees
22 kt activity measured in an in vitro assay in normothermic animals.
23 d decreased blood flow were observed only in normothermic animals.
24 ardiac arrest characterized by 12 minutes of normothermic asystole and a high cardiopulmonary resusci
25                           Patients receiving normothermic blood had less postoperative right ventricu
26 ediately upon reperfusion and 1 h later; all normothermic brains showed space immunoreactivity at 4 h
27                                At the end of normothermic bypass diameter of cerebrocortical microves
28 parietal cerebral cortex underwent 10-minute normothermic bypass, 40-minute cooling on cardiopulmonar
29 HODS AND Mice were subjected to 8 minutes of normothermic CA and resuscitated with chest compression
30 ing (CABG) (n = 6; low SOE), hypothermic and normothermic CABG (n = 3; moderate to low SOE), or CABG
31 y-cerebral resuscitation following 9 mins of normothermic cardiac arrest in male vs. female dogs.
32 brain, heart, and organism (within 5 mins of normothermic cardiac arrest no-flow), which increases th
33                                        After normothermic cardiac arrest of 11 mins in dogs, mild res
34  to complete recovery after 10 to 15 mins of normothermic cardiac arrest without blood flow.
35 angendorff-perfused and exposed to 40-minute normothermic, cardioplegic global ischemia and 30 minute
36 ocrit supporting cerebral oxygenation during normothermic cardiopulmonary bypass (CPB) in dogs.
37             Previous studies have found that normothermic cardiopulmonary bypass (CPB) is associated
38     When epinephrine was administered during normothermic cardiopulmonary resuscitation, postresuscit
39        Epinephrine, when administered during normothermic cardiopulmonary resuscitation, significantl
40 the lungs with preservation of the abdominal normothermic circulation throughout the thoracic procure
41                                        Under normothermic conditions (34 degrees C) and at 39 degrees
42 igher during passive leg heating compared to normothermic conditions (FVC at highest dose of respecti
43 reases in FVC during leg heating compared to normothermic conditions (maximal decreases in FVC during
44 ypothermic animals (n = 12) were returned to normothermic conditions 120 minutes after clamp removal.
45 m 0 to 1000 mug/mL under subnormothermic and normothermic conditions in PS.
46 he hypothermic animals that were returned to normothermic conditions survived.
47               Under halothane anesthesia and normothermic conditions, 72 DNX inbred mice were subject
48 R is unclear, especially after the return to normothermic conditions.
49 h the addition of oxygen carriers; and under normothermic conditions.
50  dose of respective drugs during heating vs. normothermic conditions: PE: 3.7 +/- 0.4 vs. 2.0 +/- 0.3
51 ics, PS sustained bacterial growth under sub(normothermic) conditions, whereas growth was absent in c
52 gia for 5 minutes, followed by 60 minutes of normothermic continuous cardioplegic administration with
53 dioplegic arrest and rewarming compared with normothermic control (37 +/- 3 vs 69 +/- 3 microns/s, P
54 nd prolonged external cooling (21+/-14%) vs. normothermic control (61+/-32%) and brief external cooli
55 prolonged external cooling (18+/-9 secs) vs. normothermic control (74+/-17 secs) and brief external c
56 nd prolonged external cooling (score, 0) vs. normothermic control (score, 20) and brief external cool
57                             Except for three normothermic control animals, all animals were resuscita
58                                   A historic normothermic control group was matched (one-to-one) by m
59 ere cooled to 30 degrees C for 1 hour; and a normothermic control group, in which mice were kept at 3
60 was severely impaired when compared with the normothermic control group.
61 myocyte velocity of shortening compared with normothermic control values (33+/-2 versus 66+/-2 microm
62  assigned to the following treatment groups: normothermic control, incubation in cell culture media f
63                    Rats were randomized to a normothermic control, neurotensin-induced hypothermia, b
64 ytes were randomly assigned to 3 groups: (1) normothermic control: 37 degrees C x 2 hours (n = 116);
65 of spontaneous circulation compared to 9% in normothermic controls (*p < .01 vs. normothermia).
66 %*, and 0%, respectively, compared to 2% for normothermic controls (*p < .05 vs. normothermia).
67 te myocyte shortening velocity compared with normothermic controls (22.0 +/- 1.6 versus 57.2 +/- 2.6
68 , and 14%, respectively, compared to 17% for normothermic controls and survival with good neurologic
69 fluid and in homogenized lungs compared with normothermic controls but was associated with reduced ba
70 in rats treated with hypothermia compared to normothermic controls in both injury groups (P < 0.05).
71 ted (hyperthermic controls), as well as with normothermic controls.
72                       Five animals served as normothermic controls.
73 spinal neurons (127% increase) compared with normothermic controls.
74 m uninstrumented controls (91+/-2%) or after normothermic CPB (84+/-4%).
75  79 men, mean age 63 (40 to 77) years)] with normothermic CPB and cardioplegic arrest of the heart or
76                  Pigs (n = 6) were placed on normothermic CPB and hearts were arrested for 1 hour wit
77                       Pigs were subjected to normothermic CPB for 90 minutes, followed by post-CPB pe
78 -dependent) was between 0.09 and 0.14 during normothermic CPB in dogs.
79 d by 8-bromo-cAMP was markedly reduced after normothermic CPB, and this change was directly related t
80 s are unchanged in the skeletal muscle after normothermic CPB.
81 A desensitizes alpha-adrenoceptors more than normothermic CPB.
82  arterial blood pressure (MAP) on CBF during normothermic CPB.
83 16) of change in MAP on change in CBF during normothermic CPB.
84                                        While normothermic, CVP was 6.3 +/- 0.2 mmHg and PCWP was 9.5
85 roup I and group II patients were maintained normothermic during OLT); and group III (n=5), had uncon
86  Seven subjects underwent 30 mmHg LBNP while normothermic, during passive heat stress (increased inte
87  negative pressure (LBNP) while subjects are normothermic, during skin-surface cooling, and during wh
88 f four groups: normothermic placebo control; normothermic epinephrine; hypothermic placebo control; a
89  C flush; target temperature, 15 degrees C); normothermic EPR (N-EPR; 38 degrees C flush); and contro
90 r lung reconditioning in a model of extended normothermic EVLP.
91                                 A program of normothermic ex situ liver perfusion (NESLiP) was develo
92                                              Normothermic ex situ liver perfusion enabled assessment
93                                              Normothermic ex situ liver perfusion has the potential t
94                                              Normothermic ex situ liver perfusion was performed using
95 rafts appeared viable after 24 hours of near-normothermic ex situ perfusion.
96 ith a novel technique of pressure-controlled normothermic ex vivo kidney perfusion (NEVKP) in heart-b
97   We compared continuous pressure-controlled normothermic ex vivo kidney perfusion (NEVKP) with stati
98                                              Normothermic ex vivo kidney perfusion might help to decr
99                                              Normothermic extracorporeal liver perfusion (NELP) has b
100 animals were resuscitated and submitted to a normothermic follow-up (control group) or to 3 hours of
101  rats were subjected to either 7 or 8 min of normothermic forebrain ischemia (bilateral carotid occlu
102 ental hearts were subjected to 30 minutes of normothermic global ischemia followed by 2 hours of repe
103  The hearts were then subjected to 20 min of normothermic global ischemia followed by 25 min of reper
104  minutes before being subjected to zero-flow normothermic global ischemia for 35 minutes and reperfus
105 mic group (35.4+/-0.1 degrees C) than in the normothermic group (36.7+/-0.1 degrees C) (P<.001) and r
106 posite Score versus 20.0% of patients in the normothermic group (p = 0.317).
107 test, compared with 55.5% of patients in the normothermic group (p = 0.865).
108 mic episode, glutamate concentrations in the normothermic group peaked at levels approximately three
109 rdiac events occurred less frequently in the normothermic group than in the hypothermic group (1.4% v
110 ycardia also occurred less frequently in the normothermic group than in the hypothermic group (2.4% v
111 r in the hypothermia group compared with the normothermic group.
112 bral organ damage were assessed at 96 hrs.In normothermic groups 1 and 4, all 12 dogs achieved sponta
113   Myocardial damage scores were worse in the normothermic groups compared with both hypothermic group
114 te Examination scores in the hypothermic and normothermic groups were 27.4 +/- 3.8 and 26.8 +/- 4.5,
115 idence of impairment between hypothermic and normothermic groups.
116  unused human kidneys in a series of ex-vivo normothermic haemo-reperfusion models.
117  unused human kidneys in a series of ex vivo normothermic hemoreperfusion models.
118 a nonhibernating mammal and that recovery of normothermic homeostasis ensues upon rewarming.
119 an 'area' control site has been described in normothermic humans.
120 ls were randomized into 4 groups (n=6 each): normothermic, hypothermic-2 hours, hypothermic-5 hours,
121  Langendorff method and subjected to global, normothermic I/R (20/40 minutes), with or without prior
122 tected the human donor proximal tubules from normothermic-induced cell swelling.
123                                        After normothermic infusions of dopamine at different doses (4
124 liver for 1 hour after a 15-minute period of normothermic intestinal ischemia.
125 el, 45 hearts underwent 30 minutes of global normothermic ischemia after infusion of 50 mL of cardiop
126 been shown to confer protection in models of normothermic ischemia and reperfusion injury and to init
127 icant sparing of CA1 neurons relative to the normothermic ischemia group was observed.
128 lmonary bypass, a 45-minute period of global normothermic ischemia was followed by 60 minutes of inte
129 d mechanism of effect have been primarily of normothermic ischemia where adenosine was given pre-isch
130 abbit hearts were subjected to 45 minutes of normothermic ischemia with cardioplegic arrest.
131                                 After global normothermic ischemia, significant decreases in cardiac
132  shown to enhance myocardial tolerance after normothermic ischemia-reperfusion.
133 istar rats were subjected to 30 or 60 min of normothermic ischemia.
134 groups before and after a 6-minute period of normothermic ischemia.
135 erformance deficits relative to shams in the normothermic ischemic group, with the postischemic hypot
136  hypothermic), after rewarming (hypotensive, normothermic) just before discontinuation of cardiopulmo
137                          ASO when applied in normothermic kidney machine perfusion reduced renal miR-
138 urement of urinary biomarkers during ex vivo normothermic kidney perfusion (EVKP) may aid in the asse
139                     We conclude that ex vivo normothermic kidney perfusion with a plasma-free red cel
140                                        While normothermic,LBNP reduced blood volume in all regions (t
141  stress + clamp successfully restored to the normothermic level (P = 0.99) and increased MCA V(mean)
142 ive heat stress with P(ETCO2) clamped at the normothermic level (using a computer-controlled sequenti
143 pidly (n = 6) or slowly (n = 5) increased to normothermic levels.
144 uent volume loading returned those values to normothermic levels.
145 ontaneous circulation, they underwent either normothermic life support (control group, n = 12) or hyp
146 sion, rabbits underwent either oxygen (Gas), normothermic liquid (Liquid Warm), or cold liquid (Liqui
147                                      Ex situ normothermic machine perfusion (NMP) can be performed af
148 sent the first patients transplanted using a normothermic machine perfusion (NMP) device that transpo
149 xperimentation, outcomes of a first clinical normothermic machine perfusion (NMP) liver trial in the
150 les, potentially administered during ex vivo normothermic machine perfusion of human organs, could be
151                                              Normothermic machine perfusion of the liver (NMP-L) is a
152 ted livers following viability assessment by normothermic machine perfusion of the liver (NMP-L).
153 tatic cold storage, the liver was subject to normothermic machine perfusion with a plasma-free red ce
154 d, preserved, and implanted under continuous normothermic machine perfusion.
155 ro (approximately 0.2 Hz) and in most intact normothermic mammals.
156                                    Following normothermic MCA occlusion, spectrin immunoreactivity wa
157 ed from 5 to >10 mins the previously longest normothermic no-flow time that could be reversed to comp
158 nesthetized, instrumented, and randomized to normothermic (Nor) or hypothermic (Hy) conditions.
159 is study included five treatment groups: (1) normothermic (Normo)-brain temperature was maintained at
160 e of the liver to ischemia-reperfusion under normothermic or hypothermic conditions.
161 re not modulated by arterial baroreflexes in normothermic or moderately heated individuals.
162  artery (MCA) occlusion and were either kept normothermic or rendered mildly hypothermic shortly afte
163 grees C throughout ischemia and reperfusion (Normothermic), or given 1 h of hypothermic conditions (2
164 se cefazolin be used for prophylaxis in (sub)normothermic organ preservation with PS.
165 olated working rat hearts were arrested with normothermic oxygenated potassium cardioplegia for 5 min
166       Intubated, anesthetized rats underwent normothermic parasagittal fluid-percussion brain injury
167 wer admission Glasgow Coma Scale scores than normothermic patients (p = .04) and tended to have highe
168 ermic patients were 3 times more likely than normothermic patients to develop MODS (21% vs. 9%, P = 0
169 try were performed every 6 hrs for 24 hrs in normothermic patients who were at rest for at least 30 m
170  were increased over time in hypothermic vs. normothermic patients.
171 nation for mortality in both hypothermic and normothermic patients.
172 ion, the 55-year-old female recipient of the normothermic perfused kidney had slow graft function but
173                    A short period of ex vivo normothermic perfusion (EVNP) immediately before transpl
174                                      Ex vivo normothermic perfusion (EVNP) is a novel method of prese
175                                      Ex vivo normothermic perfusion (EVNP) prior to transplantation m
176 after perfusion and assessment using ex vivo normothermic perfusion (EVNP).
177 aastricht category III donors with abdominal normothermic perfusion and concomitant cold lung flushin
178                                              Normothermic perfusion failed to resuscitate porcine liv
179                                        After normothermic perfusion for 15 minutes and separation fro
180 WI group) were placed in an EVLP circuit for normothermic perfusion for 3 hours.
181 also reviews pulsatile machine perfusion and normothermic perfusion for pancreas preservation techniq
182                                              Normothermic perfusion has been shown to resuscitate and
183                                              Normothermic perfusion is an alternative but little stud
184      The authors report a case of preimplant normothermic perfusion of a suboptimal liver from a 57-y
185                            We report ex vivo normothermic perfusion of human pancreases procured but
186                           Preimplant ex situ normothermic perfusion of the liver appears to be a prom
187                                              Normothermic perfusion was continued for 2 hr before in
188                           After 132 minutes, normothermic perfusion was stopped and implantation begu
189 x vivo viability assessment using postmortem normothermic perfusion, and overall macroscopic appraisa
190 rfusion (26 degrees C) interspersed by 3 min normothermic perfusion.
191 alternative preservation techniques, such as normothermic perfusion.
192 ipient outcomes were documented after 4 h of normothermic perfusion.
193                                              Normothermic, physiologically regulated male Sprague-Daw
194 it of autoregulation compared to postarrest, normothermic piglets.
195 hen randomly assigned to one of four groups: normothermic placebo control; normothermic epinephrine;
196 he effective antibiotic prophylaxis for (sub)normothermic preservation by investigating whether Staph
197 f Wisconsin solution for 4 hours followed by normothermic preservation for 20 hours (total preservati
198 gned to the following groups: group W (n=5), normothermic preservation for 24 hours; and group C (n=4
199 f short duration of cold preservation before normothermic preservation on the function of porcine NHB
200 postischemic hypothermia (30 degrees C); (c) normothermic procedures combined with delayed injections
201       To establish the role of P-selectin in normothermic pulmonary ischemia, mice were subjected to
202                                           In normothermic pups, Fos immunoreactivity peaked at early
203 ntusion volume was larger in hypothermic vs. normothermic rats (44.3 +/- 4.2 vs. 28.6 +/- 4.0 mm, p <
204                                    Conscious normothermic rats (n=12 per group) were also given RSR13
205 e (MK-801) was then constructed in conscious normothermic rats subjected to 75 min of MCAO.
206               Groups 1, 3 and 5 consisted of normothermic rats that underwent either 6 (for CBF measu
207       Corresponding to GSK 3beta activity in normothermic rats, beta-catenin phosphorylation transien
208 - and pCREB-immunoreactive cells compared to normothermic rats.
209 obal brain ischemia (12.5 min) in ventilated normothermic rats.
210 ced contusion volumes, compared with hypoxic normothermic rats.
211 fect on body temperature when given alone to normothermic rats.
212 opil and only selective neuronal necrosis in normothermic rats.
213 t the end of hypothermia in hypothermic (vs. normothermic) rats (p <.05), indicating that hypothermia
214 ncentrations were higher in hypothermic (vs. normothermic) rats at the end of both hypothermia and re
215                                  A period of normothermic regional perfusion (NRP) in the donor may r
216    We developed a novel protocol for in situ normothermic regional perfusion (NRP) which complied wit
217                                              Normothermic regional perfusion has been reported to imp
218 recovery and preservation include the use of normothermic regional perfusion in the donor and ex vivo
219                                              Normothermic regional perfusion used during DCD abdomina
220 rculatory arrest does not prevent successful normothermic regional perfusion.
221      Peroxynitrite anions may play a role in normothermic renal ischemia and reperfusion.
222  Herein, we report the first case of ex vivo normothermic renal transplant perfusion in man.
223  in the hippocampus were elevated at 16 h of normothermic reperfusion versus 48 h with BC reperfusion
224 hermia for 30 minutes followed by 2 hours of normothermic reperfusion.
225  University of Wisconsin solution after 1 hr normothermic reperfusion.
226  C) CP (St Thomas II) followed by 30 minutes normothermic reperfusion.
227 q/L K+, 4 degrees C) for 2 hours followed by normothermic reperfusion; and (3) preconditioning/cardio
228 tly better than delayed post-ROSC cooling or normothermic resuscitation.
229 protein level of beta-catenin degraded after normothermic stroke.
230  vs. 42%, p < .001), spent more percent time normothermic (T < or =37.2 degrees C, 59% vs. 3%, p < .0
231 72F) mutation regulates p53 stability at the normothermic temperature, but it is the increased recrui
232 with organ preservation steering toward (sub)normothermic temperatures, bacterial contamination may b
233           Compared with adults who were kept normothermic, those who underwent therapeutic hypothermi
234 cant difference between the hyperthermic and normothermic tissue; there was a large increase in sodiu
235 markedly greater when compared to LBNP while normothermic (torso: 73 +/- 2%; heart: 72 +/- 3%; spleen
236 thermic group and eight patients were in the normothermic treatment group.
237 ons, but did not change CVC in either of the normothermic trials.
238 lowing cardiopulmonary bypass (normotensive, normothermic) using mixed-model analysis of variance.
239 tility after PCO cardioplegia was similar to normothermic values in control (57+/-2 microm/s) and CHF
240 e 34 degrees C; and in group 4 (n = 5), with normothermic venovenous shunt.
241           Hearts were subjected to 30 min of normothermic, zero-flow ischemia followed by 30-min repe

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