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1 ct to treatment assignment (OPCAB or CABG on cardiopulmonary bypass).
2 nction in patients after cardiac surgery and cardiopulmonary bypass.
3 verse events after cardiac surgery requiring cardiopulmonary bypass.
4 h risk of morbidity and mortality undergoing cardiopulmonary bypass.
5 rdiopulmonary physiology and the sequelae of cardiopulmonary bypass.
6 rombocytopenic and have cardiac surgery with cardiopulmonary bypass.
7 f methylprednisolone for patients undergoing cardiopulmonary bypass.
8 corporeal membrane oxygenation compared with cardiopulmonary bypass.
9 r major morbidity after cardiac surgery with cardiopulmonary bypass.
10 h risk of morbidity and mortality undergoing cardiopulmonary bypass.
11 frequently occur after cardiac surgery with cardiopulmonary bypass.
12 were hemodynamically stable with no need for cardiopulmonary bypass.
13 in patients undergoing cardiac surgery with cardiopulmonary bypass.
14 d lower in the sepsis group during and after cardiopulmonary bypass.
15 lving inflammatory response during and after cardiopulmonary bypass.
16 mean arterial blood pressure targets during cardiopulmonary bypass.
17 extraction, early after cardiac surgery with cardiopulmonary bypass.
18 infants undergoing surgery with and without cardiopulmonary bypass.
19 ngenital heart disease both with and without cardiopulmonary bypass.
20 similar rates after surgery with or without cardiopulmonary bypass.
21 ily on methods of vital organ support during cardiopulmonary bypass.
22 to 36 months of age, undergoing surgery with cardiopulmonary bypass.
23 al circulatory arrest or continuous low-flow cardiopulmonary bypass.
24 e elective, and almost all patients required cardiopulmonary bypass.
25 al management strategies for separation from cardiopulmonary bypass.
26 in in group B was 104 +/- 160 at 4 hrs after cardiopulmonary bypass.
27 from cardiopulmonary bypass or use to avoid cardiopulmonary bypass.
28 ed management of cerebral oxygenation during cardiopulmonary bypass.
29 rSo(2) during the 60-minute period following cardiopulmonary bypass.
30 evels decrease in infants and children after cardiopulmonary bypass.
31 25 at 4, 24, and 48 hrs, respectively, after cardiopulmonary bypass.
32 s to achieve separation from or avoidance of cardiopulmonary bypass.
33 d no acute conversion to surgery or need for cardiopulmonary bypass.
34 an 2 years old undergoing heart surgery with cardiopulmonary bypass.
35 with group B before and 24 and 48 hrs after cardiopulmonary bypass.
36 deep hypothermic circulatory arrest or even cardiopulmonary bypass.
37 an their racial counterparts who had CABG on cardiopulmonary bypass.
38 al echocardiography, cardiac surgery, and/or cardiopulmonary bypass.
39 ms obtained during initiation and weaning of cardiopulmonary bypass.
40 ll with cardiac arrest and longer periods of cardiopulmonary bypass.
41 yocardial arrest and reperfusion achieved by cardiopulmonary bypass.
42 ine after CABG is not specific to the use of cardiopulmonary bypass.
43 preservation, followed by resuscitation with cardiopulmonary bypass.
44 after the induction of anesthesia and before cardiopulmonary bypass.
45 heart valve interventions without the use of cardiopulmonary bypass.
46 o attenuate the coagulopathy associated with cardiopulmonary bypass.
47 ollowed by 20 mins of EPR using miniaturized cardiopulmonary bypass.
48 ary revascularization without utilization of cardiopulmonary bypass.
49 for each ordered dose within 24 hours after cardiopulmonary bypass.
50 e onset of immunoparalysis in the setting of cardiopulmonary bypass.
51 hile patient is hemodynamically supported on cardiopulmonary bypass.
52 e undergoing cardiac surgery with the use of cardiopulmonary bypass.
53 ples before and after the ischemic insult of cardiopulmonary bypass.
54 drome in 31.3%, and 95.2% of procedures used cardiopulmonary bypass.
55 e undergoing cardiac surgery with the use of cardiopulmonary bypass.
56 patients who underwent cardiac surgery with cardiopulmonary bypass.
57 hours, and 18-24 hours after separation from cardiopulmonary bypass.
59 The overall rate of LOF was 4.3% (return to cardiopulmonary bypass, 2.6%; intraaortic balloon pumps,
60 3) and during the 60-minute period following cardiopulmonary bypass (65+/-11% versus 75+/-10%, P=0.00
61 rSo(2) from postinduction to 60 minutes post cardiopulmonary bypass (71+/-10% versus 78+/-6%, P=0.01)
62 ion harvesting (98.9%, 66.0%, and 68.1%) and cardiopulmonary bypass (83.4%, 45%, and 36.9%) were less
63 Right atrial biopsies were collected before cardiopulmonary bypass and 10 minutes after aortic cross
65 pg/mL) for all patients was 21 +/- 63 before cardiopulmonary bypass and 80 +/- 145, 43 +/- 79, and 19
69 opolysaccharide group but only at the end of cardiopulmonary bypass and beginning of postbypass (p <
70 ize the morbidity associated with the use of cardiopulmonary bypass and circulatory arrest in patient
71 Cardiac surgery, especially when employing cardiopulmonary bypass and deep hypothermic circulatory
72 ficant difference was found between low-flow cardiopulmonary bypass and deep hypothermic circulatory
73 th ischemia and reperfusion injury following cardiopulmonary bypass and deep hypothermic circulatory
74 inotropes, and RBC transfusion starting from cardiopulmonary bypass and ending 8 hours after arrival
75 ed for nonemergent cardiac surgery requiring cardiopulmonary bypass and had recognized risk factors f
76 xcellent, this technique requires the use of cardiopulmonary bypass and is associated with protracted
79 in-induced thrombocytopenia in patients post cardiopulmonary bypass and on extracorporeal membrane ox
80 uggested that CABG techniques that eliminate cardiopulmonary bypass and reduce aortic manipulation ma
81 ssue obtained from patients before and after cardiopulmonary bypass and reperfusion and left ventricu
83 ry to attenuate the inflammatory response to cardiopulmonary bypass and surgical trauma; however, evi
84 ney injury) in high-risk patients undergoing cardiopulmonary bypass and that the protective effect is
85 ified in the lipopolysaccharide group during cardiopulmonary bypass and the postbypass period (p < 0.
86 Levels of plasma hemoglobin increased during cardiopulmonary bypass and were associated (p < 0.01) wi
88 line (in a subset), the beginning and end of cardiopulmonary bypass, and 2 hours and 24 hours after c
89 uits of heater-cooler units connected to the cardiopulmonary bypass, and air samples collected when t
90 have been introduced to minimize exposure to cardiopulmonary bypass, and improve outcomes for these h
91 ure, avoidance of the detrimental effects of cardiopulmonary bypass, and larger effective orifice are
93 of coronary artery disease, prolonged use of cardiopulmonary bypass, and severe primary graft dysfunc
96 and repair on an arrested heart, but require cardiopulmonary bypass, aortic cross-clamping, sternotom
98 igations were pursued: (1) identification of cardiopulmonary bypass-associated M. chimaera infection
100 ive patients undergoing cardiac surgery with cardiopulmonary bypass at 12 hospitals from October 6, 2
101 Neonates undergoing cardiac surgery with cardiopulmonary bypass at 2 centers were enrolled in a d
102 ars or older undergoing cardiac surgery with cardiopulmonary bypass at 8 cardiac surgical centers in
103 n, the hepatic resection was performed under cardiopulmonary bypass because of extended vena cava thr
104 nd cooled to 16 degrees C to 18 degrees C on cardiopulmonary bypass before instituting deep hypotherm
105 ronary artery bypass graft-only surgery with cardiopulmonary bypass between August 2001 and May 2005.
106 04) rSo(2) during the 60-minute period after cardiopulmonary bypass but not with other perfusion phas
107 l concentration occurred during surgery with cardiopulmonary bypass but was no longer present after c
108 es cardiac output after cardiac surgery with cardiopulmonary bypass, but a detailed analysis of its e
109 oronary artery bypass grafting surgery using cardiopulmonary bypass by 32 surgeons at 8 centers in no
111 thods of oxygenation and ventilation such as cardiopulmonary bypass can be used successfully to treat
112 ented with arterial and venous catheters and cardiopulmonary bypass cannulae) were randomized to conv
116 oplegic arrest followed by reperfusion after cardiopulmonary bypass causes microvascular dysfunction
117 ventive surgical strategies (PSS: peripheral cardiopulmonary bypass, circulatory arrest, and non-medi
118 the extracorporeal membrane oxygenation and cardiopulmonary bypass cohorts was 45.4 (+/- 15.6) and 6
119 e coronary syndrome (ACS) patients requiring cardiopulmonary bypass (coronary artery bypass graft sur
121 cal dysfunction following reperfusion or the cardiopulmonary bypass-coronary artery bypass graft-indu
123 tive, cardiac surgery using cardioplegia and cardiopulmonary bypass (CP/CPB) subjects myocardium to h
124 vs 28 (27-30) points; P = 0.021], length of cardiopulmonary bypass (CPB) [CPB; 133 (112-163) vs 119
126 nt inhibitor of complement activation during cardiopulmonary bypass (CPB) has been shown to significa
131 ciated with cerebral hypoxia-ischemia during cardiopulmonary bypass (CPB) remains limited, largely du
133 ecognized immune response to protamine after cardiopulmonary bypass (CPB) surgery with potential impo
137 nic artificial surfaces, for example, during cardiopulmonary bypass (CPB), induces a highly procoagul
138 reased in performing CABG without the use of cardiopulmonary bypass (CPB), to reduce postoperative co
152 average mean arterial blood pressure during cardiopulmonary bypass did not differ, the mean arterial
153 y bypass and were associated (p < 0.01) with cardiopulmonary bypass duration (R = 0.22), depletion of
154 te analysis, baseline cholesterol levels and cardiopulmonary bypass duration were significant and ind
155 lve mean pressure gradient <40 mm Hg, longer cardiopulmonary bypass duration, and prosthesis-patient
156 ndergoing primary isolated CABG surgery with cardiopulmonary bypass during calendar year 2008 at 798
157 rposition approach to liver transplantation, cardiopulmonary bypass during liver transplantation in t
158 seline), at cardiopulmonary bypass start, at cardiopulmonary bypass end, and 3 and 24 hours after car
159 h-risk patients undergoing CABG surgery with cardiopulmonary bypass enrolled between October 2006 and
160 cal approach, and in providing a timely post-cardiopulmonary bypass evaluation of the procedure, ther
161 ficant bleeding and hypofibrinogenemia after cardiopulmonary bypass, fibrinogen concentrate is noninf
162 ading dose of study drug was administered on cardiopulmonary bypass followed by a continuous infusion
163 R or N-EPR, resuscitation was initiated with cardiopulmonary bypass for 60 mins and mechanical ventil
164 tween ages 1 month to 18 years who underwent cardiopulmonary bypass for cardiac surgery and survived
166 pulmonary bypass and 4, 24, and 48 hrs after cardiopulmonary bypass for measurement of plasma arginin
168 ents undergoing CABG surgery with or without cardiopulmonary bypass from February 1, 2002, through Ma
169 ts having coronary bypass graft surgery with cardiopulmonary bypass from November 1996 to June 2000 a
170 acic surgery and a possible association with cardiopulmonary bypass heater-cooler units following ale
171 of reducing the inflammatory response after cardiopulmonary bypass; however, the value of this appro
174 l improvements, including the development of cardiopulmonary bypass in the 1950s, large-scale repair
175 ronary-artery bypass grafting (CABG) without cardiopulmonary bypass in the elderly are still undeterm
176 among patients undergoing CABG surgery with cardiopulmonary bypass in US hospitals in an adult cardi
177 Changes in LV function at the conclusion of cardiopulmonary bypass included decreased stroke area (f
178 an effort to prevent deleterious effects of cardiopulmonary bypass, including the associated inflamm
179 tension or recipients who required prolonged cardiopulmonary bypass increased the risk for mortality.
180 ng coronary artery bypass graft surgery with cardiopulmonary bypass, increased atrial matrix metallop
181 indicates that immature WM is vulnerable to cardiopulmonary bypass-induced injury but has an intrins
182 eration was observed within a few days after cardiopulmonary bypass-induced ischemia-reperfusion inju
183 n this model, WM injury was identified after cardiopulmonary bypass-induced ischemia-reperfusion inju
184 ic arrest (CP) followed by reperfusion after cardiopulmonary bypass induces coronary microvascular dy
185 ardiogram, pulmonary artery catheterization, cardiopulmonary bypass, inhaled nitric oxide, and inhale
187 ry bypass grafting performed with the use of cardiopulmonary bypass is a well-validated treatment for
190 ng coronary artery bypass graft surgery with cardiopulmonary bypass, it reduced cardiac matrix metall
191 ergoing coronary artery bypass grafting with cardiopulmonary bypass, levosimendan compared with place
194 levels before elective cardiac surgery with cardiopulmonary bypass may be a simple biomarker for the
196 % CI, 5.1-68.4; p = 0.001) with earlier post-cardiopulmonary bypass measures of uncertain utility.
197 extensive surgical procedures, avoidance of cardiopulmonary bypass, minimizing injury from radiocont
199 of myocardial blood flow and separation from cardiopulmonary bypass, MMP interstitial activity increa
202 lower quartile (< 9.2 pg/mL) at 4 hrs after cardiopulmonary bypass (n = 29), labeled group A, were e
204 less than 18 years old, procedures requiring cardiopulmonary bypass, no preexisting renal dysfunction
205 imary outcome when measured 18-24 hours post-cardiopulmonary bypass (odds ratio, 18.6; 95% CI, 5.1-68
206 C transfusion during surgery and duration of cardiopulmonary bypass (odds ratio, 2.98; 95% CI, 1.96-4
209 CABG to undergo the procedure either without cardiopulmonary bypass (off-pump CABG) or with it (on-pu
210 e effect of MR reduction without surgery and cardiopulmonary bypass on left ventricular (LV) dimensio
211 (CABG) surgery may be performed either with cardiopulmonary bypass (on pump) or without cardiopulmon
212 technique (off-pump CABG), as compared with cardiopulmonary bypass (on-pump CABG), are not clearly e
216 ement of patients requiring procedures using cardiopulmonary bypass or interventions in the catheteri
217 olytic drugs for use in cardiac surgery with cardiopulmonary bypass or organ transplantations to redu
218 olytic drugs for use in cardiac surgery with cardiopulmonary bypass or organ transplantations to redu
219 e use in the context of failure to wean from cardiopulmonary bypass or use to avoid cardiopulmonary b
220 (OR, 2; 95% CI, 1.2-3.3; P = 0.008); use of cardiopulmonary bypass (OR, 3.4; 95% CI, 2.2-5.3; P < 0.
223 ts who underwent elective cardiac surgery on cardiopulmonary bypass, paired samples of the right atri
225 atically increased arginase-1 levels in post-cardiopulmonary bypass peripheral blood mononuclear cell
226 f myeloid-derived suppressor cells from post-cardiopulmonary bypass peripheral blood mononuclear cell
229 near horizon is the combination of advanced cardiopulmonary bypass plus a cocktail of multiple agent
230 WMI was also associated with the duration of cardiopulmonary bypass, postoperative lactate level, bra
231 corporeal cardiopulmonary resuscitation with cardiopulmonary bypass potentially provides cerebral rep
232 cardiac surgery, since it is recognized that cardiopulmonary bypass presents many precipitating risk
233 -associated lipocalin measured 3 hours after cardiopulmonary bypass provided excellent early risk str
234 a cardiovascular surgeon, perfusionist, and cardiopulmonary bypass pump facilitates lifesaving repai
235 ion of haptoglobin at end and 24 hours after cardiopulmonary bypass (R = 0.12 and 0.15, respectively)
236 tively), lactate dehydrogenase levels at end cardiopulmonary bypass (R = 0.27), and change in creatin
237 T1 correlated with RV T1 (r=0.45, P<0.001), cardiopulmonary bypass (r=0.30, P=0.007), and aortic cro
239 tively low at baseline and remains low after cardiopulmonary bypass regardless of hemodynamic stabili
243 tive therapies such as cricothyroidotomy and cardiopulmonary bypass should be available if first-line
244 s before anesthesia induction (baseline), at cardiopulmonary bypass start, at cardiopulmonary bypass
245 in was 4.9 +/- 2.6 in group A at 4 hrs after cardiopulmonary bypass, statistically unchanged from its
248 tinal bleeding is common following pediatric cardiopulmonary bypass surgery for congenital heart dise
250 led trial on infants 2.5 to 12 kg undergoing cardiopulmonary bypass surgery, aimed at (1) demonstrati
251 a, such as that induced by cardiac arrest or cardiopulmonary bypass surgery, causes cell death in vul
252 levant condition of systemic sterile stress, cardiopulmonary bypass surgery, we confirmed the initial
258 ts with congenital heart disease who undergo cardiopulmonary bypass, those who receive extracorporeal
260 = 2.4), hemodynamic instability (OR = 2.8), cardiopulmonary bypass time >120 minutes (OR = 6.2), per
261 ergency status (P=0.006), rupture (P=0.004), cardiopulmonary bypass time >120 minutes (P<0.04), and p
262 e 139.8] versus 412.8 [132] min, P < 0.001), cardiopulmonary bypass time (220 [63] versus 176 [73] mi
263 ood operation (HR, 2.3; P=0.001), and longer cardiopulmonary bypass time (HR, 1.1 per 10 minutes; P=0
267 prised 72% of procedures and had a mean (SD) cardiopulmonary bypass time of 200 minutes (83) minutes.
271 analysis, age more than 65 years, prolonged cardiopulmonary bypass time, and severe pulmonary hypert
272 r resistance index, graft ischemic time, and cardiopulmonary bypass time, donor low-dose dopamine was
273 included pre-operative diuretic use, longer cardiopulmonary bypass time, operation prior to 1991, at
275 ve coronary artery bypass graft surgery with cardiopulmonary bypass to determine whether doxycycline
277 s undergoing cardiac surgery with the use of cardiopulmonary bypass to receive either methylprednisol
279 duled for elective cardiac surgery requiring cardiopulmonary bypass under total anesthesia with intra
280 justing for pretransplantation lung disease, cardiopulmonary bypass use, and population stratificatio
283 patients had a moderate or large injury, and cardiopulmonary bypass was required in 13 patients with
286 a in extracorporeal membrane oxygenation and cardiopulmonary bypass were 6.4% (19/298) and 0.6% (18/2
287 ral blood mononuclear cells before and after cardiopulmonary bypass were analyzed for the expression
288 lack of mitral annuloplasty, and duration of cardiopulmonary bypass were associated with increased ri
289 ombined coronary artery bypass grafting with cardiopulmonary bypass were enrolled from June 2013 unti
292 ient >20 mm Hg) and prolonged intraoperative cardiopulmonary bypass were significant risk factors for
293 chemical pleurodesis procedure and prolonged cardiopulmonary bypass were significantly associated wit
294 autoregulation threshold (mm Hg x min/hr of cardiopulmonary bypass) were both higher in patients wit
295 ystemic inflammatory response to surgery and cardiopulmonary bypass, which in turn may mediate prolon
296 531 patients undergoing cardiac surgery with cardiopulmonary bypass who had a moderate-to-high risk o
297 cases of aortic aneurysm repair, 7 involving cardiopulmonary bypass with deep hypothermic circulatory
298 ing antegrade cerebral perfusion, the use of cardiopulmonary bypass with mild hypothermia, and the in
299 cheduled for routine cardiac procedures with cardiopulmonary bypass without documented dementia were
300 c subgroups of pediatric patients undergoing cardiopulmonary bypass would benefit from potential trea