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1 olonged ventilation, renal insufficiency and primary graft dysfunction.
2  risk is directly related to the severity of primary graft dysfunction.
3 mong subjects who died by 30 days, 43.6% had primary graft dysfunction.
4 ts at our program and graded the severity of primary graft dysfunction according to the International
5 emia-reperfusion injury is the main cause of primary graft dysfunction after lung transplantation and
6 reperfusion injury is a major determinant of primary graft dysfunction after lung transplantation, an
7 y be a novel therapeutic strategy to prevent primary graft dysfunction after lung transplantation.
8    However, there was no association between primary graft dysfunction and acute rejection or lymphoc
9 etion may help to predict the development of primary graft dysfunction and avoid the need for retrans
10 ence of major complications including severe primary graft dysfunction and early mortality rates were
11 d a significantly higher incidence of severe primary graft dysfunction and higher short- and long-ter
12     Postoperatively, the incidence of severe primary graft dysfunction and the incidence of acute ren
13                                              Primary graft dysfunction contributes to nearly half of
14    Among the 334 recipients, 65 did not have primary graft dysfunction (grade 0), 130 had grade 1, 69
15 nts surviving at least 1 year, those who had primary graft dysfunction had significantly worse surviv
16                                 Survivors of primary graft dysfunction have increased risk of death e
17          Long-term outcomes of subjects with primary graft dysfunction have not been studied.
18 the lung for ischemia reperfusion injury and primary graft dysfunction in the recipient.
19 ed use of cardiopulmonary bypass, and severe primary graft dysfunction increased the risk for death i
20                                              Primary graft dysfunction is a common complication after
21                                              Primary graft dysfunction is a severe acute lung injury
22                                              Primary graft dysfunction is associated with an increase
23  which are now discarded because the risk of primary graft dysfunction is considered too great.
24                   We evaluated the impact of primary graft dysfunction on acute rejection, lymphocyti
25                    We examined the impact of primary graft dysfunction on bronchiolitis obliterans sy
26 evels are associated with the development of primary graft dysfunction (PGD) after lung transplantati
27 1) levels in plasma would be associated with primary graft dysfunction (PGD) after lung transplantati
28                                              Primary graft dysfunction (PGD) is a major complication
29                                              Primary graft dysfunction (PGD) is a significant cause o
30                                              Primary graft dysfunction (PGD) is a significant contrib
31                                              Primary graft dysfunction (PGD) is the main cause of ear
32                                              Primary graft dysfunction (PGD) is the most important ca
33           Twenty-three patients with Grade 3 primary graft dysfunction (PGD) were frequency matched w
34 l allografts may be at an increased risk for primary graft dysfunction (PGD), the leading cause of ea
35  demographics may influence the incidence of primary graft dysfunction (PGD).
36 antation with good early outcome [absence of primary graft dysfunction- (PGD) grade 3]; (II) PGD3: bi
37 intensive care unit stay (P = 0.74), highest primary graft dysfunction score (P = 0.67) and hospital
38 e care unit stay, hospital stay, and highest primary graft dysfunction score within 72 hours) and lon
39 Wisconsin solution in grafts with subsequent primary graft dysfunction, suggesting a slower recovery
40 All-cause mortality at 30 days was 42.1% for primary graft dysfunction versus 6.1% in patients withou
41                     The overall incidence of primary graft dysfunction was 10.2% (95% confidence inte
42 hiolitis obliterans syndrome associated with primary graft dysfunction was independent of acute rejec
43        In multivariable regression analysis, primary graft dysfunction was the predominant perioperat
44   In the univariable analysis, all grades of primary graft dysfunction were associated with a signifi
45        We sought to test the relationship of primary graft dysfunction with both short- and long-term

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