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1.
Arch Gynecol Obstet ; 288(1): 57-64, 2013 Jul.
Article de Anglais | MEDLINE | ID: mdl-23400353

RÉSUMÉ

PURPOSE: Very premature delivery is a major cause of infant morbidity and mortality. Obesity, diabetes and pregnancy hypertension are known risk factors for pregnancy complications. The study aimed to scrutinize differences of pregnancy complications in a cohort of very premature deliveries compared to a national group. METHODS: In a multicenter study performed between January 2009 and December 2010 including 1,577 very low birth weight (VLBW) infants, we compared parental reported pregnancy problems of VLBW infants with a national cohort (KIGGS). We compared reported pregnancy complications to reasons for premature delivery and neonatal outcome within the group of VLBW infants. RESULTS: While parents of the national cohort reported pregnancy-induced hypertension in 8 %, parents of VLBW infants reported this complication more frequently (27 %). Mothers of the national cohort were significantly younger (1 year), suffered less from obesity, anaemia, diabetes. Regression analysis showed that hypertension (OR = 5.11) and advanced maternal age (OR = 1.03) increased the risk for premature birth. Women with hypertension were likely to experience a clinically indicated premature delivery, had more VLBW infants with a moderate growth restriction, but less multiples and their infants had less intraventricular haemorrhages grade 3 or 4. Otherwise, neonatal outcome was correlated with gestational age but not with the pregnancy complications diabetes, hypertension or obesity. CONCLUSION: Premature birth seems to be correlated to gestational hypertension and associated problems in about » of VLBW infants. Further studies should focus on preventing and treating gestational hypertension to avoid premature delivery and associated neonatal morbidity.


Sujet(s)
Diabète/épidémiologie , Hypertension artérielle/épidémiologie , Nourrisson très faible poids naissance , Obésité/épidémiologie , Naissance prématurée/épidémiologie , Études cas-témoins , Femelle , Allemagne/épidémiologie , Âge gestationnel , Humains , Nouveau-né , Odds ratio , Grossesse , Analyse de régression , Facteurs de risque
2.
Acta Paediatr ; 91(11): 1174-8, 2002.
Article de Anglais | MEDLINE | ID: mdl-12463314

RÉSUMÉ

AIM: Pneumonia in childhood may be associated with surfactant dysfunction and severe acute respiratory distress syndrome (ARDS). The aim of this study was to investigate the effects of surfactant treatment on oxygenation in 8 infants (age range: 1 mo to 13 y) with severe respiratory failure owing to viral, bacterial or Pneumocystis Carinii pneumonia. METHODS AND RESULTS: Instillation of a modified porcine surfactant (Curosurf) improved gas exchange immediately. Median paO2/FiO2 increased from 66 to 140 mmHg (8.8-18.7 kPa; p < 0.01) within 1 h of surfactant treatment. Seven of the 8 patients received multiple surfactant doses. Four patients (50%) died 3-62 d after surfactant treatment. However, 6 patients (75%) were immunodeficient, so that the observed mortality rate was mainly due to the underlying disease. CONCLUSION: Surfactant dysfunction probably plays a role in the pathophysiology of severe paediatric ARDS triggered by pneumonia, as it was found that surfactant instillation rapidly improved gas exchange in the majority of the affected infants in our study. Larger randomized controlled studies are necessary to evaluate the effects of surfactant treatment on morbidity and mortality.


Sujet(s)
Produits biologiques , Phospholipides , Échanges gazeux pulmonaires , Surfactants pulmonaires/usage thérapeutique , Syndrome de détresse respiratoire du nouveau-né/traitement médicamenteux , Syndrome de détresse respiratoire du nouveau-né/physiopathologie , /traitement médicamenteux , /physiopathologie , Adolescent , Enfant , Enfant d'âge préscolaire , Femelle , Humains , Nourrisson , Nouveau-né , Mâle
3.
Ther Drug Monit ; 19(6): 628-31, 1997 Dec.
Article de Anglais | MEDLINE | ID: mdl-9421102

RÉSUMÉ

Tacrolimus (FK 506) is a new, potent immunosuppressive drug for primary and rescue therapy in liver and kidney transplantation. Therapeutic drug monitoring is essential for this drug because of its narrow therapeutic window. Blood levels are monitored routinely by enzyme linked immunoassay (ELISA) or by microparticle enzyme immunoassay (MEIA). In a 13-year-old recipient of a liver transplant who had poor hepatic function during the first postoperative week, the authors observed unusually high tacrolimus blood concentrations using either the ELISA (26.6 to 49.0 microg/l) or MEIA (58.5 to 64.5 microg/l). Parent drug levels measured in the same blood samples by high-performance liquid chromatography/mass spectrometry (HPLC/MS) were up to 10-fold lower (5.1 to 9.0 microg/l). The discrepancies between the immunoassay and HPLC/MS results could not be attributed to any of the known metabolites of tacrolimus.


Sujet(s)
Surveillance des médicaments/méthodes , Immunosuppresseurs/pharmacocinétique , Tacrolimus/pharmacocinétique , Adolescent , Chromatographie en phase liquide à haute performance , Test ELISA , Femelle , Humains , Immunosuppresseurs/sang , Immunosuppresseurs/métabolisme , Transplantation hépatique , Spectrométrie de masse , Tacrolimus/sang , Tacrolimus/métabolisme
4.
Monatsschr Kinderheilkd ; 140(9): 633-8, 1992 Sep.
Article de Allemand | MEDLINE | ID: mdl-1435816

RÉSUMÉ

BACKGROUND: An increasing incidence of systemic candidiasis has been reported in low birth weight infants requiring intensive care. We have retrospectively analyzed mucocutaneous Candida-colonization and infection rate in 422 preterm infants with a birthweight < 1,500 g. METHODS: All infants were treated at the NICU, University of Göttingen, from 1/1985-5/1991. 359 neonates (85%) were on mechanical ventilation, no prophylactic antimycotic regimen was applied. Mucocutaneous swabs and cultures from various anatomic sites were regularly obtained from all infants. RESULTS: 37/422 preterm infants (8.8%) had mucocutaneous colonization with candida, none of our patients developed systemic candidiasis. In 7 mechanically ventilated patients (1.9%) Candida albicans or Candida tropicalis was repeatedly detected in the bronchial secretions; 1 patient who had invasive Candida-pneumonia was effectively treated with 5-Fluocytosin and Fluconazol. 4/352 (1.1%) central silastic catheters were colonized with Candida albicans; none of these patients required specific treatment. CONCLUSION: The low rate of mucocutaneous Candida-colonization and invasive infection found in our patients may be explained--at least in part--by epidemiological and obstetrical factor as well as by the procedures of the neonatal management.


Sujet(s)
Candidose mucocutanée chronique/épidémiologie , Infection croisée/épidémiologie , Fongémie/épidémiologie , Nourrisson à faible poids de naissance , Maladies du prématuré/épidémiologie , Candidose mucocutanée chronique/traitement médicamenteux , Césarienne , Infection croisée/traitement médicamenteux , Études transversales , Association de médicaments , Fluconazole/usage thérapeutique , Flucytosine/usage thérapeutique , Fongémie/traitement médicamenteux , Allemagne/épidémiologie , Humains , Incidence , Nouveau-né , Maladies du prématuré/traitement médicamenteux , Unités de soins intensifs néonatals , Mycoses pulmonaires/traitement médicamenteux , Mycoses pulmonaires/épidémiologie , Facteurs de risque
5.
Monatsschr Kinderheilkd ; 140(1): 27-33, 1992 Jan.
Article de Allemand | MEDLINE | ID: mdl-1565105

RÉSUMÉ

IIAC is a rare cardiovascular disease characterized by calcification of the membrana elastica interna and intimal proliferation in smaller and bigger arteries. This report describes a premature infant of 36 week gestational age with IIAC, which developed a hypertrophic-obstructive cardiomyopathia, acute renal failure and renovascular hypertension due to complete occlusion of both renal arteries, and eventually died at an age of 85 days. To date 86 cases of IIAC have been published. In 42 patients whose case records have been reported since 1960, cardiac failure and myocardial ischemia or infarction were the most commun clinical signs. In 54% of cases the electrocardiogramm showed myocardial ischemia. Characteristically neonates or young infants were affected by this disease, the mean onset of symptoms was 2 months, the mean time of survival was 4.2 month of age. Coronary arteries were calcified in 85% of cases; in addition, typical morphological changes were found in the arteries of lung, kidney, extremities, mesenterium, spleen, brain and the aorta. Extravascular calcification (kidney, soft tissue) could be demonstrated in 37% of the patients. The etiology of this rare disease is unknown.


Sujet(s)
Artériopathies oblitérantes/congénital , Calcinose/congénital , Angiographie , Artériopathies oblitérantes/imagerie diagnostique , Artériopathies oblitérantes/anatomopathologie , Membrane basale/anatomopathologie , Calcinose/imagerie diagnostique , Calcinose/anatomopathologie , Humains , Nouveau-né , Mâle , Muscles lisses vasculaires/anatomopathologie , Thrombose/congénital , Thrombose/imagerie diagnostique , Thrombose/anatomopathologie , Tomodensitométrie
6.
Monatsschr Kinderheilkd ; 139(2): 102-4, 1991 Feb.
Article de Allemand | MEDLINE | ID: mdl-2038346

RÉSUMÉ

Tracheal agenesis is a rare congenital anomaly which presents immediately after birth an absolute respiratory insufficency. This report describes a new-born infant with a tracheal agenesis Typ II which was combined with an esophageal atresia and distal esophagotracheal fistula. In addition, costal synostosis was found. These malformations can be added to the VATER-association. Resuscitation of our patient (orotracheal and esophageal intubation, emergency coniotomy) was unsuccessful. However, in most cases of tracheal agenesis with esophagotracheal communication primary resuscitation is possible by esophageal intubation and by application of continuous positive pressure ventilation. Diagnosis must be confirmed by immediate contrast roentgenography or endoscopy. The results of surgery are disappointing until now.


Sujet(s)
Syndrome de détresse respiratoire du nouveau-né/anatomopathologie , Trachée/malformations , Malformations multiples/anatomopathologie , Atrésie de l'oesophage/anatomopathologie , Oesophage/anatomopathologie , Humains , Nouveau-né , Trachée/anatomopathologie , Fistule trachéo-oesophagienne/congénital , Fistule trachéo-oesophagienne/anatomopathologie
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