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1.
Pediatr Pulmonol ; 57(11): 2763-2773, 2022 Nov.
Article in English | MEDLINE | ID: mdl-35931924

ABSTRACT

BACKGROUND: The long-term follow-up of lung function (LF) in extremely preterm (EP) infants with bronchopulmonary dysplasia (BPD) has shown a worldwide increase in small airway obstructions (SAO). OBJECTIVES: We investigated the relationships between intrauterine Ureplasma infection in EP infants and bubbly/cystic lung, BPD, and SAO at school age. METHODS: Placental pathology, placental Ureaplasma DNA (pU-DNA), and cord blood immunoglobulin M (IgM) (C-IgM) were investigated in 360 EP infants born from 1981 to 2004. Maternal amniotic inflammatory response (M-AIR) scores and hemosiderin deposition (HD) were estimated in the chorioamnion. The study subjects were divided into groups based on their M-AIR scores. Their LF at school age was compared with those of 33 healthy siblings. FINDINGS: pU-DNA and C-IgM were significantly related to SAO at school age (p < 0.012). M-AIR score 3 and pU-DNA >1000 units had an odds ratio (OR) of 35 (95% confidence interval: 10-172) and 18 (5.6-67) for bubbly/cystic lung, and 11 (3.1 - 43) and 31 (4.5-349) for severe BPD, and 5.3 (2.1-11) and 12 (2.4-74) for SAO, respectively. The ORs of surfactant treatment, BPD grade III, O2 at 40 weeks, HD, and C-IgM >30 mg/dl for SAO were 0.21 (0.075-0.58), 5.3 (2.1-15), 2.5 (1.4-4.6), 3.6 (1.5-9.1) and 2.5 (1.0-5.2). 84% (90/107) SAO infants showed no or mild BPD in infancy, and 61% of infants had no severe CAM. CONCLUSION: Our long-term cohort study of LF in EP infants revealed that intrauterine Ureaplasma was associated with bubbly/cystic lung, severe BPD, and SAO at school age.


Subject(s)
Airway Obstruction , Bronchopulmonary Dysplasia , Bronchopulmonary Dysplasia/complications , Cohort Studies , Female , Gestational Age , Hemosiderin , Humans , Immunoglobulin M , Infant , Infant, Extremely Premature , Infant, Newborn , Placenta , Pregnancy , Surface-Active Agents , Ureaplasma
2.
Am J Med Genet A ; 173(2): 360-367, 2017 Feb.
Article in English | MEDLINE | ID: mdl-28102591

ABSTRACT

Beckwith-Wiedemann syndrome (BWS) is a congenital overgrowth syndrome that is occasionally associated with hyperinsulinemic hypoglycemia (HH) in the neonatal period. Sotos syndrome (SS) and Kabuki syndrome (KS) are other malformation syndromes that may be complicated with HH, however, the detailed clinical characteristics of HH accompanied with these syndromes remain unclear. We herein conducted a nationwide questionnaire survey in Japan. We sent a primary questionnaire concerning the clinical experience for these syndromes to 347 perinatal care institutions. As a result, 222 departments or hospitals returned the questionnaires and the total numbers of BWS, SS, and KS patients were 113, 88, and 51, respectively. We sent a secondary questionnaire to 31 institutions where patients with these syndromes presented with HH during infancy. The secondary questionnaires were returned from the institutions and the numbers of patients were 16 for BWS, 9 for SS, and 3 for KS, respectively. Then, we compared the clinical characteristics of infants suffering from transient HH with and without these dysmorphic syndromes. As a result, BWS, SS, and KS patients showed significantly larger body size, lower Apgar scores, higher insulin levels at HH, and shorter durations of HH than non-dysmorphic infants with transient HH. We propose that a careful observation for the signs of HH, even if not specific to the syndromes, is important for the diagnosis of patients with BWS, SS, and KS in the postnatal period. © 2016 Wiley Periodicals, Inc.


Subject(s)
Abnormalities, Multiple/blood , Beckwith-Wiedemann Syndrome/blood , Face/abnormalities , Hematologic Diseases/blood , Hyperinsulinism/blood , Hypoglycemia/blood , Sotos Syndrome/blood , Vestibular Diseases/blood , Abnormalities, Multiple/diagnosis , Abnormalities, Multiple/epidemiology , Apgar Score , Beckwith-Wiedemann Syndrome/diagnosis , Beckwith-Wiedemann Syndrome/epidemiology , Female , Genetic Testing , Hematologic Diseases/diagnosis , Hematologic Diseases/epidemiology , Hematologic Tests , Humans , Infant, Newborn , Japan/epidemiology , Male , Phenotype , Population Surveillance , Pregnancy , Pregnancy Complications/epidemiology , Sotos Syndrome/diagnosis , Sotos Syndrome/epidemiology , Surveys and Questionnaires , Vestibular Diseases/diagnosis , Vestibular Diseases/epidemiology
3.
AJP Rep ; 6(1): e104-7, 2016 Mar.
Article in English | MEDLINE | ID: mdl-26929860

ABSTRACT

Acute osteomyelitis is uncommon in full-term neonates and occurs most frequently in those with critical illnesses, often following episodes of sepsis, skin infection, umbilical catheterization, urinary tract anomalies, or a complicated delivery. Here, we report a very rare case of acute rib osteomyelitis due to Staphylococcus aureus in a 13-day-old full-term male neonate. Ultrasonography (US) enabled diagnosis and revealed a coexisting costochondral junction rib fracture, which was not detected on routine chest radiography. Following a 29-day course of intensive parenteral antibiotic therapy, the patient was discharged in good health at 42 days of age without any scar formation. Due to its accessibility and safety, US can be a promising modality for detecting acute osteomyelitis in neonates with clinically highly suspected conditions in the neonatal intensive care unit setting, particularly those involving thin and mobile bones subject to respiratory motion. However, further studies are required to assess the utility of US in these cases and negative results. In low-risk neonates with osteomyelitis, an accompanying fracture should be considered.

4.
Arch Dis Child Fetal Neonatal Ed ; 100(4): F314-9, 2015 Jul.
Article in English | MEDLINE | ID: mdl-25783193

ABSTRACT

OBJECTIVE: To assess lung function at 8 years old in extremely low birthweight (ELBW) survivors and to identify perinatal determinants associated with impaired lung function. DESIGN: Retrospective cohort study. SETTING: Level III neonatal intensive care unit. PATIENTS: ELBW survivors born in 1990-2004 with available spirometry at 8 years old were studied. Children were excluded if they had a Wechsler Intelligence Scale for Children Third Edition full IQ <70. MAIN OUTCOME MEASURES: Multivariate logistic regression analysis was used to identify perinatal determinants associated with airway obstruction (forced expiratory volume in 1 s (FEV1)/forced vital capacity (FVC) ratio <80%) at school age and the predictive power of potential determinants. Potential risk factors and predictors assessed in this study were gestational age, birth weight, small for gestational age, sex, chorioamnionitis, premature rupture of membranes, antenatal steroids, surfactant administration, respiratory distress syndrome, postnatal steroids, severe bronchopulmonary dysplasia and bubbly/cystic appearances of the lungs by X-ray during the neonatal period. RESULTS: Of 656 ELBW survivors, 301 (45.9%) had attended a school-age follow-up at 8 years old. A total of 201 eligible children completed the lung function test. Bubbly/cystic appearance of the lungs (OR 4.84, 95% CI 1.26 to 18.70) was associated with a low FEV1/FVC ratio. Children with bubbly/cystic appearance had characteristics of immaturity and intrauterine inflammation. CONCLUSIONS: Within a cohort of ELBW infants, a bubbly/cystic appearance of the lungs in the neonatal period was the strongest determinant of a low FEV1/FVC ratio at school age.


Subject(s)
Bronchopulmonary Dysplasia , Fetal Diseases , Forced Expiratory Volume , Infant, Extremely Low Birth Weight , Lung/physiopathology , Respiratory Distress Syndrome, Newborn , Bronchopulmonary Dysplasia/complications , Bronchopulmonary Dysplasia/physiopathology , Child , Cohort Studies , Female , Fetal Diseases/physiopathology , Humans , Infant, Extremely Low Birth Weight/growth & development , Infant, Extremely Low Birth Weight/physiology , Infant, Newborn , Infant, Premature , Japan , Male , Respiratory Distress Syndrome, Newborn/complications , Respiratory Distress Syndrome, Newborn/physiopathology , Respiratory Function Tests/methods , Retrospective Studies , Risk Factors , Survivors/statistics & numerical data
5.
J Clin Microbiol ; 47(5): 1605-6, 2009 May.
Article in English | MEDLINE | ID: mdl-19261789

ABSTRACT

Rothia aeria, a gram-positive coccoid- to rod-shaped bacterium with irregular morphology, is an extremely rare causative organism of infections in humans. We report the first case of R. aeria sepsis clinically manifested in a female neonate soon after birth.


Subject(s)
Gram-Positive Bacterial Infections/diagnosis , Micrococcaceae/isolation & purification , Sepsis/microbiology , Adult , Anti-Bacterial Agents/therapeutic use , Bacterial Typing Techniques , Female , Gram-Positive Bacterial Infections/drug therapy , Gram-Positive Bacterial Infections/microbiology , Gram-Positive Bacterial Infections/pathology , Humans , Infant, Newborn , Microbial Sensitivity Tests , Sepsis/drug therapy , Sepsis/pathology
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