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1 ge, 13-17 years; 24 girls; 18 with palliated single ventricle).
2 mproved patient outcomes for patients with a single ventricle.
3 eloped for the palliation of children with a single ventricle.
4 m and extends along the entire length of the single ventricle.
5 erm advantage for patients with a functional single ventricle.
6 cal management of patients with a functional single ventricle.
7 intensive care management of patients with a single ventricle.
8 procedures were performed in patients with a single ventricle.
9 <0.001) but not in children with a palliated single ventricle.
10 g HT evaluation in children with a palliated single ventricle.
11 the first years of life among patients with single ventricle.
12 cases of hypoplastic left heart syndrome and single ventricle.
13 tive palliation for patients with functional single ventricles.
14 erformance in young patients with functional single ventricles.
15 s performed in 35 patients with a functional single ventricle (1 week to 12 years old) at various sta
16 T burden was highest in complex CHD, such as single ventricle (22.8%) and d-transposition of the grea
18 .0% (95% confidence interval, 32.6 to 43.5); single ventricle, 56.1% (95% confidence interval, 49.9 t
19 ast decade, as the majority of patients with single ventricle anatomy who have undergone the Fontan o
20 0 feet) were analyzed for patients born with single-ventricle anatomy who would now be of adult age.
22 t highest risk are infants with a functional single ventricle and patients with suprasystemic pulmona
25 ties are commonly present in patients with a single ventricle, and detection of these lesions increas
26 ultivariate analysis, weight <4 kg, having a single ventricle, and emergency status were significantl
27 pulmonary atresia intact ventricular septum, single ventricle, and tricuspid atresia born in 1996 to
28 ence of a large ventricular septal defect, a single-ventricle approach to repair should be considered
29 and performance changes occur in functional single ventricles as they progress through staged Fontan
30 d randomized clinical trials in infants with single ventricle CHD and 270 controls from The Cancer Ge
32 lack of information, gaps in clinical care, single ventricle complications, and heart failure in the
34 ticles regarding management of newborns with single-ventricle defects have been published during the
35 rience in newborns undergoing palliation for single-ventricle defects, in particular, hypoplastic lef
38 n coarctation of the aorta, late outcomes in single-ventricle disease, cognitive and psychiatric issu
43 enic CNVs seem to contribute to the cause of single ventricle forms of CHD in >/=10% of cases and are
44 gement strategy for patients with functional single ventricle has evolved to include staging bidirect
47 ; P<0.001) but not in those with a palliated single ventricle (hazard ratio, 1.3; 95% confidence inte
48 ing patient, who had borderline functionally single ventricle heart disease (unbalanced atrioventricu
51 ported to improve outcomes for patients with single-ventricle heart disease during the period between
53 cedure for the palliation of patients with a single-ventricle heart, there have been very few reports
56 This review suggests that the diagnosis of single ventricle, initiation of ECMO in the operating ro
57 factors: age, ventricular morphology (right single ventricle, left single ventricle [RV/LV]), fenest
58 (MBT) shunt, the first palliative stage for single-ventricle lesions with systemic outflow obstructi
62 n young pediatric patients with a functional single ventricle, matrix-array 3DE measurements of mass
63 entricular septal defect (n=3), functionally single ventricle (n=3) and ventricular septal defect wit
71 urgical management consisted of a functional single-ventricle palliation in 38 patients (83%) and biv
73 nd of a spectrum of LV hypoplasia, mandating single-ventricle palliation or cardiac transplantation.
74 nital heart surgery, especially after failed single-ventricle palliation, is presenting new obstacles
77 articular interest, conduit reoperations and single ventricle pathway modifications are still an art
79 ary collateral (SPC) flow occurs commonly in single ventricle patients after superior cavo-pulmonary
82 tment with phosphodiesterase-5 inhibitors in single ventricle patients with heart failure, including
83 on is routinely used as a diagnostic tool in single ventricle patients with superior cavopulmonary co
84 rends toward worse outcomes were observed in single ventricle patients, biventricular patients with l
85 ion of VADs in complex circulations, such as single ventricle patients, remains infrequent and is ass
87 edback mechanisms, 12 intubated, ventilated, single-ventricle patients in SCPC physiology (age 2.2+/-
88 the total cavopulmonary connection (TCPC) in single-ventricle patients undergoing Fontan can be calcu
94 T FINDINGS: Infants following palliation for single ventricle physiology have persistent growth failu
95 livery of adequate nutrition in infants with single ventricle physiology is essential to improve outc
96 ents undergoing cavopulmonary palliation for single ventricle physiology may be impacted by living at
97 e whether pathogenic CNVs among infants with single ventricle physiology were associated with inferio
98 with transposition of the great arteries and single ventricle physiology were included in this analys
99 atrial septal defects, tetralogy of Fallot, single ventricle physiology, and following cardiac trans
100 heart malformations are those with so-called single ventricle physiology, in which there is only one
101 ndergoing Fontan procedures as palliation of single ventricle physiology, the addition of a fenestrat
105 espiratory support; 4) expanding research of single ventricle physiology; 5) advances in the treatmen
107 (hazard ratio, 3.66; 95% CI, 2.26-5.92) and single-ventricle physiology (hazard ratio, 1.98; 95% CI,
108 erformance in children and young adults with single-ventricle physiology after the Fontan operation.
110 odynamically detrimental in circumstances of single-ventricle physiology and should be used with caut
111 zation is standard practice in patients with single-ventricle physiology before bidirectional Glenn a
118 Administration of enalapril to infants with single-ventricle physiology in the first year of life di
120 ouble-blind trial involving 230 infants with single-ventricle physiology randomized to receive enalap
124 volumes and mass in pediatric patients with single-ventricle physiology would aid clinical managemen
125 lnerability indicators, renal insufficiency, single-ventricle physiology, and coagulation disorder.
126 ly fatal disorder occurring in children with single-ventricle physiology, and other diseases, as well
127 rdization: patient age, renal insufficiency, single-ventricle physiology, procedure-type risk group,
128 osition of the great arteries and 12 who had single-ventricle physiology--with the use of magnetic re
134 is a successful palliation for children with single-ventricle physiology; however, many will eventual
140 e physiologic requirements for success after single ventricle reconstruction has resulted in dramatic
143 Examining the available data in light of the Single Ventricle Reconstruction trial is insightful as f
145 and Blood Institute Pediatric Heart Network Single Ventricle Reconstruction Trial public data set wa
147 multi-institutional Pediatric Heart Network Single-Ventricle Reconstruction Trial, interstage mortal
148 epair (closure of septal defects) instead of single-ventricle repair (Norwood palliation and Fontan o
150 lar morphology (right single ventricle, left single ventricle [RV/LV]), fenestration open (FO) or clo
152 ations for surgical palliation of functional single ventricle since the initial report by Fontan and
154 dies in zebrafish, a lower vertebrate with a single ventricle, that latent TGF-beta binding protein 3
155 monary artery shunt alone in patients with a single ventricle to facilitate ventricular volume unload
156 e 5-year survival in infants with functional single ventricle, to define factors associated with surv
157 nts (median age, 7 months) with a functional single ventricle undergoing CMR under general anesthesia
158 ional echocardiography (3DE) measurements of single-ventricle volumes, mass, and ejection fraction wi
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