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1 ; P=0.002 for liver and HR, 2.42; P=0.01 for lung transplants).
2 dity and mortality among patients undergoing lung transplant.
3 ronchiolitis obliterans, and rejection after lung transplant.
4 biome changes with disease exacerbations and lung transplant.
5 ilitated by pseudomonas infection and single lung transplant.
6 is similar to findings in humans with acute lung transplant.
7 well as improved function of the allogeneic lung transplant.
8 d with higher odds of not being accepted for lung transplant.
9 ended intensive care including the option of lung transplant.
10 or clinical outcomes, particularly following lung transplant.
11 esource use during index hospitalization for lung transplant.
12 increased risk of delisting or death before lung transplant.
13 s seems to be an emerging pathogen mainly in lung transplants.
14 t; 58 (17.6%), heart transplant; 54 (16.4%), lung transplant; 34 (10.3%), liver transplant; and 6 (1.
16 years; heart transplant, 269,715 life-years; lung transplant, 64,575 life-years; pancreas-kidney tran
18 neumonia (aHR, 1.8; 95% CI, 1.3-2.3), single lung transplant (aHR, 1.3; 95% CI, 1.0-1.7), and idiopat
19 tistically significant in kidney, liver, and lung transplants, although liver and lung recipients had
20 cause of early morbidity and mortality after lung transplant and is characterized by severe hypoxemia
21 change in mean total hospital charges among lung transplant and other solid-organ transplant recipie
23 sociation between the center volume of adult lung transplants and 1-year recipient mortality that is
24 Recipients of multivisceral, redo, and lobar lung transplants and those who underwent pretransplant c
25 severity, and potential contraindications to lung transplant, and before or after use of the lung all
28 s demonstrate that the airways involved in a lung transplant are relatively hypoxic at baseline and t
32 plant Outcomes Group who underwent bilateral lung transplant at our institution between 2004 and 2014
34 tus of both donor and recipient may identify lung transplants at heightened risk for late-onset cytom
37 rvival were estimated among adults receiving lung transplants between June 2010 and June 2015 based o
41 V infection in donors and kidney, heart, and lung transplant candidates and recipients and recommend
42 ectrum of prior cardiothoracic procedures in lung transplant candidates and the impact of prior proce
45 We performed an ecologic study of 12 187 lung transplant candidates listed at 56 U.S. lung transp
46 ied from 1987 to 2013 to identify first-time lung transplant candidates who were tracked from wait li
50 s typically considered the primary metric of lung transplant center performance in the United States.
52 d to determine the association between adult lung transplant center volume and 1-year recipient morta
53 is an increasingly important determinant of lung transplant center volume and that policies that imp
58 hough case loads vary substantially among US lung transplant centers, the impact of center effects on
59 alveolar lavage (BAL), techniques central to lung transplant clinical practice, provide a unique oppo
60 inal organs by means of EVLP with a standard lung transplant cohort through a multicenter open trial.
65 R, 1.05; 95% CI, 0.91-1.21; P = .47) and for lung transplants during the day were 83.8% vs 82.6% duri
66 R, 1.05; 95% CI, 0.88-1.26; P = .59) and for lung transplants during the day were 92.7% vs 91.7% duri
67 idence interval, 0.83-1.32; P = .67) and for lung transplants during the day were 96.0% vs 95.5% duri
69 re is no evidence of inferior outcomes after lung transplant from brain-dead donors who have had a pe
71 ations, an intervention was necessary in the lung transplant group compared to 32% (n = 79/245) in th
73 on, recipients of a kidney, liver, heart, or lung transplant have an increased risk for diverse infec
75 with experience of performing more than 170 lung transplants in the first 5 years of the lung alloca
76 All recipients of kidney, liver, heart, and lung transplants in the United Kingdom between 1987 and
77 tween C57BL/6J and DBA/2J) (Haplotype H2b/d) lungs transplanted into DBA/2J (H2d) recipients were ide
82 miR-16 and miR-195 levels were also noted in lung transplant (LTx) patients with DSA compared with LT
83 ated hemoglobin [HbA1c]) and survival in all lung transplant (LTx) recipients and those with either p
84 humidified high flow nasal cannula (HFNC) in lung transplant (LTx) recipients readmitted to intensive
86 eae was performed in heart transplant (HTx), lung transplant (LTx), and mechanical circulatory suppor
87 e examined in vivo using an orthotopic mouse lung transplant model and in vitro using isolated bone m
88 conclusion, we have developed an orthotopic lung transplant model in the ferret with documented long
90 tibility complex-mismatched mouse orthotopic lung transplant model, we investigated a conditioning re
91 accelerates tissue damage and increases post-lung transplant mortality in cystic fibrosis patients.
92 s], 2 kidney transplants [n=164 patients], 3 lung transplants [n=110 patients], and 1 liver transplan
94 in FiO2; 95% CI, 1.0-1.2; P = 0.01); single lung transplant (OR, 2; 95% CI, 1.2-3.3; P = 0.008); use
95 efined as time to death, acute exacerbation, lung transplant, or decrease in forced vital capacity (F
96 nt and the composite rates for death, double-lung transplant, or restenosis at 36 months were 5% and
98 recipients from the multicenter, prospective Lung Transplant Outcomes Group cohort enrolled between J
102 etrospective cohort study of patients in the Lung Transplant Outcomes Group who underwent bilateral l
107 treatment phase viral kinetics (P = 0.005), lung transplant (P = 0.002), CMV donor (D)+/recipient (R
109 tection rates at 40 HAU (95% healthy and 97% lung transplant; P = 1.0) and at 160 HAU (24% healthy an
111 cted from patients with BOS (n = 10), stable lung transplant patients (n = 18), and healthy aged-matc
112 lected from patients with BOS (n=10), stable lung transplant patients (n=18) and healthy aged-matched
113 uggest that MMF is present in the airways of lung transplant patients and might affect the structural
114 itamin D deficiency is present in 47% of our lung transplant patients and seems independently associa
115 >/=2% is associated with poor outcome in our lung transplant patients as demonstrated by worse CLAD-f
116 ected in the bronchoalveolar lavage fluid of lung transplant patients diagnosed with IA that received
117 ec [FEV(1)] %predicted) were measured in 131 lung transplant patients during their yearly posttranspl
118 are elevated in bronchoalveolar lavage from lung transplant patients prior to diagnosis of bronchiol
119 e (AUC) for each biomarker in the BALF of 40 lung transplant patients who had at least four samples o
121 Thirty-six of 71 (51%) phase 1 cases were lung transplant patients with positive respiratory cultu
131 bsequent graft failure in kidney, heart, and lung transplants: patients without antibodies had superi
139 nt, voluntary, web-based survey of heart and lung transplant providers to assess current practice pat
141 e of 6 h and of 73 min, respectively) on rat lung transplants receiving aspiration of gastric fluid w
142 Longitudinal posttransplant monitoring of a lung transplant recipient (A2, CMV seropositive) who rec
144 omonas isolates and airway samples from a CF-lung transplant recipient during two years, and followed
146 thod to sequencing of cfDNA in the plasma of lung transplant recipients (40 samples, six patients).
147 ssociated with treatment among the colonized lung transplant recipients (8/12 [67%] vs 3/25 [12%] who
148 s not associated with increased mortality in lung transplant recipients (9/43 [20.9%] in infected die
150 n (CLAD) is the major outcome limitation for lung transplant recipients (LTR) after the first year, a
151 longitudinal study cohort of 63 consecutive lung transplant recipients (LTR) with a median follow-up
152 maintenance of CMV-specific T cell memory in lung transplant recipients (LTRs) is critical for host d
154 ACR) in the bronchoalveolar lavage (BAL) of lung transplant recipients (LTRs) to determine the assoc
160 retrospectively analyzed serum samples from lung transplant recipients (n = 108) for antibodies to s
161 in B lipid complex every 24 hr for 4 days in lung transplant recipients achieved amphotericin B conce
162 V) replication and disease commonly occur in lung transplant recipients after stopping anti-CMV proph
163 the single most important cause of death in lung transplant recipients after the first postoperative
164 sion of FoxP3 by flow cytometry in 14 stable lung transplant recipients and 6 lung transplant recipie
165 y artery disease has a high prevalence among lung transplant recipients and has historically been a c
166 ains a serious postoperative complication in lung transplant recipients and is associated with signif
167 rflow obstruction that affects a majority of lung transplant recipients and limits long-term posttran
168 cer-specific survival were noted between non-lung transplant recipients and nontransplant patients.
171 The incidence of PML among heart and/or lung transplant recipients at 1 institution was 1.24 per
173 ral blood mononuclear cell specimens from 39 lung transplant recipients at the time of transplantatio
174 ssessed in sequential cohorts composed of 82 lung transplant recipients before and 83 patients after
176 specimens from symptomatic and asymptomatic lung transplant recipients both by culture (using a clin
177 d in bronchoalveolar lavage (BAL) fluid from lung transplant recipients by enzyme-linked immunosorben
178 usly monitors for rejection and infection in lung transplant recipients by sequencing of cell-free DN
179 and posttransplant CLAD and survival in 191 lung transplant recipients consecutively transplanted.
181 alysis of transbronchial biopsies from human lung transplant recipients demonstrated an association b
184 Respiratory tract microbial communities in lung transplant recipients differ in structure and compo
187 of M. hominis infections were identified in lung transplant recipients from the same thoracic intens
188 ) was increased in bronchoalveolar lavage of lung transplant recipients growing P. aeruginosa (11.5 [
191 ncreased total hospital charges occurred for lung transplant recipients in 2005, corresponding to LAS
192 the primary site of coccidioidal infection, lung transplant recipients in endemic areas remain parti
193 polymorphisms that have been investigated in lung transplant recipients in relation to the devlopment
194 etrospective cohort study of adult heart and lung transplant recipients in the United Network for Org
201 their initial LT hospitalization, bilateral lung transplant recipients received 7 to 10 days of mica
203 efits of voriconazole use when prescribed to lung transplant recipients should be carefully weighed v
205 We sought to identify genetic variants in lung transplant recipients that are responsible for incr
207 e investigated a single-center cohort of 340 lung transplant recipients undergoing transplant during
209 After genetic data quality control, 680 lung transplant recipients were included in the analysis
214 ngitudinally in bronchoalveolar lavages from lung transplant recipients who developed bronchiolitis o
215 n 14 stable lung transplant recipients and 6 lung transplant recipients who eventually developed BOS.
218 from 30 healthy subjects and 8 kidney and 9 lung transplant recipients who received influenza vaccin
219 eviewed the medical files of 224 consecutive lung transplant recipients who underwent surgery over a
220 tein expression are significantly reduced in lung transplant recipients with BOS compared to BOS-free
221 protein (CCSP), a marker for Clara cells, in lung transplant recipients with BOS, BOS-free patients a
225 3, and -4 in bronchoalveolar lavage (BAL) of lung transplant recipients with good outcome and BOS usi
226 se (PRM(PD)) were compared between bilateral lung transplant recipients with irreversible spirometric
231 pients, 190 liver transplant recipients, 102 lung transplant recipients, 79 heart transplant recipien
232 ore commonly than early-onset CMV disease in lung transplant recipients, and is associated with an in
233 elopment of squamous cell carcinoma (SCC) in lung transplant recipients, by attempting to account for
234 factors for common fungal infections seen in lung transplant recipients, evaluates the clinical effic
238 In bronchoalveolar lavage fluid from human lung transplant recipients, NETs were more abundant in p
239 es from healthy subjects, HIV+ subjects, and lung transplant recipients, providing a gradient of incr
240 Posttransplant complications for pediatric lung transplant recipients, similar to complications for
242 ntially bronchiolitis obliterans syndrome in lung transplant recipients, with a greater propensity fo
274 three patients (86%) with NTM infection were lung transplant recipients; 18 of 43 (41.8%) were treate
279 assess the likelihood of transitioning from lung transplant (state 1) to BOS (state 2), from transpl
280 There is an unmet clinical need to increase lung transplant successes, patient satisfaction and to i
282 rding to the International Society for Heart Lung Transplant system for cellular rejection with immun
283 The primary outcome was the proportion of lung transplants that developed cytomegalovirus infectio
286 ion between frailty and disability using the Lung Transplant Valued Life Activities disability scale.
287 ty-five centers were classified according to lung transplant volume in 2005-2010, with 8,228 adults (
288 nited Kingdom, there are 216 patients on the lung transplant waiting list and 17 on heart and lung tr
289 cohort study of 13,346 adults placed on the lung transplant waiting list in the United States betwee
290 iation was present for heart transplant, and lung transplant was associated with higher mortality.
291 An adverse effect of ECMO at the time of lung transplant was evident in low-volume centers but ab
292 at Medicaid recipients were not accepted for lung transplant were 1.56-fold higher (95% confidence in
293 d for with propensity score analysis, double-lung transplants were associated with better graft survi
296 lants, one islet transplant and three double lung transplants were performed with primary function.
298 f cytomegalovirus prophylaxis in all at-risk lung transplants; whether cytomegalovirus serostatus can
300 , it remains an important complication after lung transplant with potentially preventable risk factor
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