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排序方式: 共有209条查询结果,搜索用时 15 毫秒
61.
62.
Bronchopulmonary dysplasia and very low birthweight: Lung function at 11 years of age 总被引:2,自引:0,他引:2
LW DOYLE GW FORD A. OLINSKY AML KNOCHES C. CALLANAN 《Journal of paediatrics and child health》1996,32(4):339-343
Objective : To determine the relationship between lung function at 11 years of age and bronchopulmonary dysplasia (BPD) in very low birthweight (VLBW) children.
Methodology : This study comprised 154 consecutive surviving VLBW children, divided into three groups with respect to their neonatal respiratory morbidity: group I developed BPD; group II required assisted ventilation but did not develop BPD; and group III required no assisted ventilation. Lung function tests were measured on 120/154 (77.9%) children at 11 years of age. The relationship between various lung function variables and neonatal lung disease was analysed by multiple linear regression.
Results : Several lung function variables reflecting airflow were significantly diminished in the BPD group ( n = 15), and residual volume was significantly higher. Despite poorer lung function overall, few children in the BPD group had lung function abnormalities in the clinically significant range ( n = 2 [13.3%] with a forced expired volume in 1 s <75% predicted; n = 2 [13.3%] with a forced vital capacity <75% predicted; n = 1 [6.7%] with a residual volume/total lung capacity >35%). There were no significant differences in lung function variables between group II ( n = 41) and group III ( n = 64). Changes in lung function tests between 8 and 11 years did not vary significantly between the three groups.
Conclusions : VLBW children with BPD in the newborn period have poorer lung function at 11 years of age than other surviving VLBW children without BPD, although few have lung function abnormalities in the clinically significant range. 相似文献
Methodology : This study comprised 154 consecutive surviving VLBW children, divided into three groups with respect to their neonatal respiratory morbidity: group I developed BPD; group II required assisted ventilation but did not develop BPD; and group III required no assisted ventilation. Lung function tests were measured on 120/154 (77.9%) children at 11 years of age. The relationship between various lung function variables and neonatal lung disease was analysed by multiple linear regression.
Results : Several lung function variables reflecting airflow were significantly diminished in the BPD group ( n = 15), and residual volume was significantly higher. Despite poorer lung function overall, few children in the BPD group had lung function abnormalities in the clinically significant range ( n = 2 [13.3%] with a forced expired volume in 1 s <75% predicted; n = 2 [13.3%] with a forced vital capacity <75% predicted; n = 1 [6.7%] with a residual volume/total lung capacity >35%). There were no significant differences in lung function variables between group II ( n = 41) and group III ( n = 64). Changes in lung function tests between 8 and 11 years did not vary significantly between the three groups.
Conclusions : VLBW children with BPD in the newborn period have poorer lung function at 11 years of age than other surviving VLBW children without BPD, although few have lung function abnormalities in the clinically significant range. 相似文献
63.
Genotypes of glutathione transferase M1 and P1 and their significance for lung DNA adduct levels and cancer risk 总被引:21,自引:16,他引:21
Ryberg D; Skaug V; Hewer A; Phillips DH; Harries LW; Wolf CR; Ogreid D; Ulvik A; Vu P; Haugen A 《Carcinogenesis》1997,18(7):1285-1289
The A-G polymorphism at codon 104 in the glutathione S-transferase P1
(GSTP1) gene was examined in 138 male lung cancer patients and 297 healthy
controls. The patients had significantly higher frequency of the GG
genotype (15.9%) and a lower frequency of AA (38.4%) than the controls
(9.1% and 51.5%, respectively). The level of hydrophobic DNA- adducts were
determined in lung tissue from 70 current smokers. Patients with the GG
genotype had a significantly higher adduct level than patients with AA
(15.5 +/- 10.2 vs 7.9 +/- 5.1 per 10(8) nucleotides, P = 0.006). We also
analyzed the deletion polymorphism in the GSTM1 gene in 135 male patients
and 342 controls. The patients were stratified according to histology,
smoking dose, age, adduct level and mutational types found in the tumors
(Ki-ras and p53 genes). The results consistently indicated that the GSTM1
null genotype was associated with a slightly increased lung cancer risk.
When the combined GST M1 and P1 genotypes were examined, patients with the
combination null and AG or GG had significantly higher adduct levels than
all other genotype combinations (P = 0.011). The distribution of combined
genotypes was also significantly different in cases and controls, mainly
due to increased frequency of the combination GSTM1 null and GSTP1 AG or GG
among patients.
相似文献
64.
Follistatin and activin A in extra-embryonic coelomic and amniotic fluids and maternal serum in early pregnancy 总被引:2,自引:0,他引:2
Riley SC; Balfour C; Wathen NC; Chard T; Evans LW; Groome NP; Wallace EM 《Human reproduction (Oxford, England)》1998,13(9):2624-2628
Follistatin is a specific binding protein which controls bioavailability of
activins and inhibins which have an important role in fetal development. In
the first trimester of pregnancy bioactive dimeric inhibins are found at
high concentrations in the extra- embryonic coelomic fluid, but the
distribution of follistatin and activins is not known. We have used
recently developed immunoassays for follistatin, activin A and activin AB
to determine their presence in the intrauterine compartments during early
pregnancy. Follistatin was present in highest concentrations in the
extra-embryonic coelomic fluid (11.72 +/- 1.70 ng/ml; median +/- SEM), with
less in maternal serum (6.35 +/- 4.58) and lowest amounts in amniotic fluid
(0.97 +/- 0.52). Follistatin concentrations in extra-embryonic coelomic
fluid were highly correlated with both dimeric inhibin isoforms. Activin A
was present in only barely detectable amounts in some samples of extra-
embryonic coelomic fluid (41% of samples) and maternal serum (26%) and was
undetectable in all amniotic fluid samples. Activin AB was undetectable in
all compartments. The presence of follistatin in the amniotic and
extra-embryonic coelomic fluids may regulate the availability of bioactive
activins and inhibins which are released into the intrauterine compartments
during the development of the fetus and placenta in early pregnancy.
相似文献
65.
Jentina Wind Marloes Faut Tim C van Smaalen Ernest LW van Heurn 《Critical care (London, England)》2013,17(5):R217
Introduction
Organ donation after circulatory death (DCD) has become an accepted strategy to reduce the shortage of organs for transplantation in many European countries. The use and number of DCD donors varies between countries. The purpose of this study was to evaluate the available protocols for DCD in Europe.Methods
We contacted national transplant societies and responsible transplant co-ordinators in the countries that perform DCD to obtain DCD protocols. We compared information on the protocols and additional data including: inclusion and exclusion criteria for donation, legislation, determination of death and preservation methods.Results
In ten European countries DCD is performed, eight of which describe the methods in protocols. There are large differences in used DCD categories, legislation and the way death is determined. Protocols differ in the detail in which DCD procedures are described and the way methods are supported by additional consensus statements and ethical frameworks.Conclusions
Although DCD is an established strategy to enlarge the donor pool and to contribute to the reduction of the waiting list for transplantation, its potential has not been fully utilized yet. To further promote DCD transplantation, it is important to share expertise and obtain consensus, so that this can be translated into more uniform and solid protocols supported by the competent authorities, transplant and intensive care professionals, which may eventually result in a further promotion of DCD transplantation in Europe. 相似文献66.
Dominguez R; Young LW; Ledesma-Medina J; Cienfuegos J; Gartner JC; Bron KM; Starzl TE 《Radiology》1985,157(2):339-344
The postoperative diagnostic imaging examinations of 44 children who underwent 59 orthotopic liver transplantations were reviewed. The imaging modalities used for the evaluation of suspected complications include plain roentgenography, ultrasonography (US), computed tomography (CT), nuclear scintigraphy, arteriography, percutaneous and operative cholangiography, and endoscopic retrograde cholangiopancreatography. The main postoperative complications included ischemia, thrombosis (hepatic artery and portal vein), infarction, obstruction or leakage of the biliary anastomosis, hepatic and perihepatic infection, and allograft rejection. US, the most frequently used abdominal imaging modality, was best suited for detection of biliary duct dilatation, fluid collections in or around the transplanted liver, and hepatic arterial, inferior vena caval, and portal vein thrombosis. CT was especially helpful in corroborating findings of infection and in locating abscesses. Technetium 99m sulfur colloid (early- and late-phase imaging) provided a sensitive, although nonspecific, means of assessing allograft vascularization and morphology. Angiography showed vascularity most clearly, and cholangiography was the most useful in the assessment of bile duct patency. A diagnostic imaging algorithm is proposed for evaluation of suspected complications. 相似文献
67.
Short rib-polydactyly syndrome type 3 总被引:3,自引:0,他引:3
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