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1.
Klin Padiatr ; 227(2): 61-5, 2015 Mar.
Article in English | MEDLINE | ID: mdl-25751679

ABSTRACT

BACKGROUND: Only sparse data exist about children with septic shock in Europe. The present study aimed to evaluate demographics, treatment, outcome and risk factors for mortality in Western Germany. PATIENTS: Children with septic shock aged 2 months to 17 years. METHODS: In a multi-center retrospective study of 20 children's hospitals data were obtained and analyzed by chart review. Risk factors for mortality were identified and assessed by multivariate regression analysis. RESULTS: Overall mortality in 83 cases with septic shock was 25% (21 patients). Significant risk factors were high PRISM III score, low pH, low arterial systolic blood pressure, presence of disseminated intravascular coagulation and extent of multi-organ failure, but not lactate (p=0.05) and base excess (p=0.065). Mortality in hospitals which treated 10 or more patients (category 1) was 17% and increased to 22% in hospitals which treated 3-6 patients (category 2). In hospitals with only 1 or 2 patients (category 3) mortality rate was 61% (p<0.01 when compared to category 1 or 2). A stepwise increase was also seen in the severely sick patients according to PRISM III (>19): category 1: 23%, category 2: 40%, category 3: 62.5% (p<0.05 for comparison of category 1 and 3). Multivariate analysis of significant risk factors revealed low number of treated patients as the only individual risk factor for mortality. CONCLUSION: Mortality from pediatric septic shock in an urban area in Western Germany is high. Disease severity and treatment in a department with few cases were associated with increased mortality.


Subject(s)
Bacterial Infections/epidemiology , Shock, Septic/epidemiology , Urban Population/statistics & numerical data , Virus Diseases/epidemiology , Adolescent , Bacterial Infections/mortality , Bacterial Infections/therapy , Child , Child, Preschool , Combined Modality Therapy , Cross-Sectional Studies , Female , Germany , Hospital Mortality , Hospitals, Pediatric/statistics & numerical data , Hospitals, University/statistics & numerical data , Humans , Infant , Injury Severity Score , Intensive Care Units, Pediatric/statistics & numerical data , Male , Opportunistic Infections/epidemiology , Opportunistic Infections/mortality , Opportunistic Infections/therapy , Prospective Studies , Risk Factors , Shock, Septic/mortality , Shock, Septic/therapy , Treatment Outcome , Virus Diseases/mortality , Virus Diseases/therapy
2.
Z Geburtshilfe Neonatol ; 217(6): 215-9, 2013 Dec.
Article in English | MEDLINE | ID: mdl-24363249

ABSTRACT

BACKGROUND: Nicotine and alcohol consumption have been associated with premature delivery and adverse neonatal outcome. We wanted to analyze the influence of self-reported nicotine and alcohol consumption on outcome of VLBW infants. MATERIAL AND METHODS: In an ongoing multicenter study 2475 parents of former very low birth weight (VLBW) infants born between January 2009 and December 2011 answered questionnaires about maternal smoking habits and alcohol consumption during pregnancy. 2463 (99.5%) completed questions on alcohol consumption and 2462 (99.5%) on smoking habits. These infants were stratified to reported maternal smoking and alcohol consumption during pregnancy. We compared the reasons for premature delivery, neonatal outcome and parental reports on bronchitis during the first year of life, as well as growth and development at age 2 years to pregnancy exposure. RESULTS: In nicotine exposed infants intrauterine growth restriction (31 vs. 21%, p<0.01), a birth weight below the 10th percentile (26 vs. 17%, p<0.01) and placenta abruption (9.2 vs. 5.8%, p<0.05) was seen more often. Premature rupture of membranes (24 vs. 30%, p<0.05) or HELLP syndrome (6 vs. 11%, p<0.01) was less frequent. A birth weight below the 3rd percentile was seen more frequently in mothers with reported alcohol consumption (13 vs. 6%, p<0.05). We noted an increased rate of BPD and ROP if mothers reported smoking during pregnancy (p<0.05). Growth parameters and scores on Bayley Sscales of infant development at age 2 years did not differ. CONCLUSION: Smoking during pregnancy results in a high rate of growth restricted VLBW infants. Prenatal exposition to nicotine seems to increase postnatal complications such as BPD und ROP.


Subject(s)
Alcohol Drinking/epidemiology , Bronchitis/epidemiology , Bronchopulmonary Dysplasia/epidemiology , Fetal Growth Retardation/epidemiology , Infant, Very Low Birth Weight , Prenatal Exposure Delayed Effects/epidemiology , Smoking/epidemiology , Causality , Child, Preschool , Female , Germany/epidemiology , Humans , Infant , Infant, Newborn , Pregnancy , Prevalence , Retinopathy of Prematurity/epidemiology , Risk Factors
3.
Klin Padiatr ; 224(4): 276-81, 2012 Jul.
Article in English | MEDLINE | ID: mdl-22441803

ABSTRACT

The German Neonatal Network (GNN) is a prospective cohort study with the focus on long term development of very-low-birth-weight infants. It was the aim of this study to determine detailed information on causes of mortality in the GNN birth cohort 2010.Major contributors to hospital mortality were recorded by the attending neonatologists for the cohort of very-low-birth-weight (VLBW) infants born in centres of the German Neonatal Network (GNN) in 2010. The data quality was approved by on-site monitoring.2 221 VLBW infants were born in GNN centres in 2010, and death occurred in 221 infants. Male infants carried a higher risk than females (58.8% males among non-survivors vs. 51.7% among survivors, p=0.047). In 11 infants, the major contributor to death was not determined by the attending neonatologist. In 25 infants born at the limit of viability, comfort palliative care was primarily initiated and 14 infants had lethal malformations. The majority of non-survivors suffered from inflammatory diseases including sepsis- or necrotizing enterocolitis (NEC)-associated death (n=56). Respiratory pathology was a major contributor to death in 65 infants including 11 infants who died from pulmonary haemorrhage.Potentially preventable complications of preterm birth such as sepsis, NEC and pulmonary haemorrhage predominate the major contributors to mortality in the GNN 2010 cohort. In order to decrease the rate of these associated deaths, future trials should focus on prophylaxis and therapy optimization strategies for these outcomes.


Subject(s)
Cause of Death , Hospital Mortality , Infant, Premature, Diseases/mortality , Infant, Very Low Birth Weight , Cohort Studies , Enterocolitis, Necrotizing/mortality , Female , Germany , Hemorrhage/mortality , Humans , Infant, Newborn , Lung Diseases/mortality , Male , Prospective Studies , Respiratory Distress Syndrome, Newborn/mortality , Risk Factors , Sepsis/mortality , Sex Factors
4.
Klin Padiatr ; 223(5): 267-70, 2011 Sep.
Article in English | MEDLINE | ID: mdl-21913143

ABSTRACT

6 cases of clinical influenza A/H1N1(2009) infections were reported within the multi-center German Neonatal Network (GNN) during the primary hospital stay in the pandemic season 2009/2010 and 2010/2011. Clinical symptoms varied from transient hyperthermia to apnea and severe respiratory distress. 1 fatal course with systemic inflammatory response after perinatal transmission of A/H1N1(2009) was observed. Oseltamivir treatment in 3/6 infants was without side effects. The reported cases have major implications for the management of VLBW infants: i) fatal courses after perinatal transmission are possible, ii) postnatal A/H1N1(2009) infection may result in life threatening events at a time when the infant is otherwise stable, iii) vaccination should be recommended for parents and medical staff to avoid nosocomial transmission, iv) more data are needed on the benefit and harm of antiviral drugs in preterm infants, v) neonatologists should suspect A/H1N1(2009) infection when unexplained sepsis-like or respiratory symptoms occur in VLBW infants.


Subject(s)
Cross Infection/diagnosis , Infant, Extremely Low Birth Weight , Infant, Premature, Diseases/diagnosis , Infant, Very Low Birth Weight , Influenza A Virus, H1N1 Subtype , Influenza, Human/diagnosis , Antiviral Agents/therapeutic use , Cause of Death , Cross Infection/etiology , Cross Infection/mortality , Cross Infection/transmission , Diagnosis, Differential , Female , Germany , Gestational Age , Humans , Infant, Newborn , Infant, Premature, Diseases/drug therapy , Infant, Premature, Diseases/mortality , Influenza, Human/etiology , Influenza, Human/mortality , Influenza, Human/transmission , Male , Oseltamivir/therapeutic use , Pneumonia, Viral/diagnosis , Pneumonia, Viral/drug therapy , Pneumonia, Viral/mortality , Pneumonia, Viral/transmission , Respiratory Distress Syndrome, Newborn/diagnosis , Respiratory Distress Syndrome, Newborn/drug therapy , Respiratory Distress Syndrome, Newborn/mortality , Risk Factors , Sepsis/diagnosis , Sepsis/drug therapy , Sepsis/mortality , Survival Rate
5.
Neuropediatrics ; 33(3): 113-7, 2002 Jun.
Article in English | MEDLINE | ID: mdl-12200739

ABSTRACT

Aromatic L-amino acid decarboxylase (AADC) is a vitamin B 6 requiring enzyme involved in the biosynthesis of the neurotransmitters dopamine (DA) and serotonin. Lack of AADC leads to a combined deficiency of the catecholamines DA, norepinephrine (NE), epinephrine (E) as well as of serotonin. Here we describe premature twins who presented with severe seizures, myoclonus, rotatory eye movements and sudden clonic contractions. The patients showed an improvement of the clonic contractions under vitamin B 6 supplementation but died in the third week of life. In CSF and urine a biochemical pattern indicative of AADC deficiency was revealed. Concentrations of homovanillic acid (HVA), 5-hydroxyindoleacetic acid (5-HIAA) and 3-methoxy-4-hydroxyphenylglycol (MHPG) were decreased, in association with increased concentrations of 3-ortho-methyldopa (3-OMD) in CSF and significantly increased vanillactic acid in urine. The AADC enzyme substrates L-dopa and 5-hydroxytryptophan (5-HTP) were elevated in CSF. Elevated concentrations of threonine as well as of an unidentified compound in CSF rounded off the biochemical pattern. AADC activity was found to be increased in plasma and deficient in the liver. Molecular studies effectively ruled out a genetic defect in the AADC gene. The basis for the epileptic encephalopathy in the twins may be located in the metabolism of vitamin B 6 and remains to be defined.


Subject(s)
Aromatic-L-Amino-Acid Decarboxylases/blood , Aromatic-L-Amino-Acid Decarboxylases/deficiency , Brain Damage, Chronic/blood , Brain Damage, Chronic/genetics , Epilepsy/blood , Epilepsy/genetics , Twins , Aromatic-L-Amino-Acid Decarboxylases/genetics , Brain Damage, Chronic/cerebrospinal fluid , Diagnosis, Differential , Epilepsy/cerebrospinal fluid , Fatal Outcome , Humans , Infant, Newborn
6.
Pediatrics ; 102(5): 1153-60, 1998 Nov.
Article in English | MEDLINE | ID: mdl-9794948

ABSTRACT

OBJECTIVE: To investigate whether early (<1 hour after birth) surfactant administration would be superior to late treatment (2-6 hours after birth) in preterm infants. STUDY DESIGN: Randomized controlled multicenter clinical trial. PATIENTS AND METHODS: Prenatal randomization of all infants of 27 to 32 weeks' gestational age stratified by center after parental informed consent. Early treatment: 100 mg/kg body weight bovine surfactant (SF-RI1, Alveofact; Dr K. Thomae, Biberach, Germany) to infants requiring intubation after birth. Late treatment: identical dosage to infants requiring intubation up to 6 hours of age with the fraction of inspired oxygen >0.4 at 2 to 6 hours after birth. Primary endpoint: the time on mechanical ventilation. Main secondary endpoints: mortality, bronchopulmonary dysplasia, intraventricular hemorrhage >/=grade III, and periventricular leukomalacia. Sample size calculation: at least 280 infants to prove superiority of either approach (alpha = 0.05; beta = 0.90). RESULTS: Enrollment of 317 infants, 154 randomized to early surfactant treatment, 163 to late surfactant treatment. Study infants (all following data intent-to-treat groups: early versus late surfactant) were similar with respect to: gestational age, 29.5 +/- 1.6 weeks versus 29.7 +/- 1.6 weeks; birth weight, 1227 +/- 367 g versus 1269 +/- 334 g; and the rate of prenatal corticosteroids, 79.9% versus 72.8%. Duration of mechanical ventilation: 3 days (0-8) versus 2 days (0-6) (median, interquartile); further outcome variables: death or bronchopulmonary dysplasia (day 28) 25.9% versus 23.9%, mortality 3.2% versus 1.8%, intraventricular hemorrhage >/=grade III 6.5% versus 3.7%, and periventricular leukomalacia 5.2% versus 5.5% not differing statistically. CONCLUSION: In preterm infants with a high rate of prenatal glucocorticoids, early surfactant administration was not found to be superior to late treatment in terms of relevant outcome variables.


Subject(s)
Lipids/administration & dosage , Phospholipids , Pulmonary Surfactants/administration & dosage , Respiratory Distress Syndrome, Newborn/drug therapy , Drug Administration Schedule , Gestational Age , Humans , Infant, Newborn , Infant, Premature , Prenatal Care , Pulmonary Gas Exchange , Respiration, Artificial , Respiratory Distress Syndrome, Newborn/mortality , Respiratory Distress Syndrome, Newborn/therapy , Time Factors
7.
Z Geburtshilfe Perinatol ; 192(4): 181-3, 1988.
Article in German | MEDLINE | ID: mdl-3188602

ABSTRACT

A report is presented on a newborn with congenital malformations of the respiratory and gastrointestinal tract associated with total laryngo-tracheo-oesophageal cleft (type III). The history, the clinical course with respiratory distress after birth, the intra vitam diagnostic procedures with x-ray and laryngoscopy and the autopsy are reported. Additionally a situs inversus totalis, an aplasia of the right diaphragm and a hypoplasia of the lung on the right side were found. To the best of our knowledge this type of association has not been previously reported.


Subject(s)
Diaphragm/abnormalities , Esophagus/abnormalities , Larynx/abnormalities , Lung/abnormalities , Situs Inversus/pathology , Trachea/abnormalities , Diaphragm/pathology , Esophagus/pathology , Humans , Infant, Newborn , Larynx/pathology , Lung/pathology , Male , Trachea/pathology
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