Neonatal acute respiratory distress syndrome (ARDS) is a clinical condition characterized by acute respiratory failure with refractory hypoxemia triggered by local or systemic etiologies during the neonatal period. Diagnosis primarily relies on the Montreux criteria. Oxygen index is recommended for grading index and lung ultrasound scoring is recommended for auxiliary diagnosis and treatment index. Current therapeutic strategies include high-frequency oscillatory ventilation, high-dose pulmonary surfactant administration, inhaled nitric oxide, intratracheal instillation of budesonide combined with surfactant, prone positioning, extracorporeal membrane oxygenation. Despite these interventions, targeted therapies remain limited. In particular, neonates with moderate or severe neonatal ARDS generally carry a poor prognosis, with mortality escalating in severe cases or those with systemic etiologies.

Objective To compare the efficacy and the effects on cardiac function of heated humidified high-flow nasal cannula(HHHFNC)and nasal continuous positive airway pressure(NCPAP)as initial treatment for preterm infants with neonatal respiratory dis-tress syndrome(NRDS).Methods The preterm infants with NRDS,gestational age＜35 weeks and requiring noninvasive ventilation ad-mitted to Xuzhou Central Hospital from January 2021 to November 2023 were enrolled for a prospective study and were randomly divided into the HHHFNC group and NCPAP group.The initial treatment was performed using HHHFNC and NCPAP respectively.The efficacy,safety and effects on cardiac function were compared.Results 55 cases were enrolled in HHHFNC group,and 53 cases were enrolled in NCPAP group.There were no statistically significant difference between the two groups in the number and total dose of the use of pulmona-ry surfactant,the number of apneas within 24hours of enrollment,the duration of noninvasive ventilation,the cases of noninvasive ventila-tion failure,the age achieving total enteral nutrition,the length and costs of hospitalization(P＞0.05).The incidence of nasal injury in the HHHFNC group was significantly lower than that in the NCPAP group(0 vs 11.3％,P=0.032).There were no statistically signifi-cant difference between the two groups in the pneumothorax,stage Ⅱ-Ⅲ necrotizing enterocolitis,hemodynamically significant patent ductus arteriosus,grade Ⅱ-Ⅳ intraventricular hemorrhage,bronchopulmonary dysplasia,and retinopathy of prematurity requiring treat-ment at the first screening(P＞0.05).There were no statistically significant difference between the two groups in fraction of inspired oxy-gen and arterial partial pressure of carbon dioxide,Plasma B-type natriuretic peptide(183.9±48.5ng/L vs 187.8±51.4ng/L,189.4±50.9ng/L vs 180.2±45.1ng/L)and Tei index of right ventricle(0.38±0.05 vs 0.40±0.06,0.38±0.06 vs 0.39±0.06)at 24±6h and 48±6h after noninvasive ventilation(P＞0.05).Conclusion In the initial treatment for preterm infants(gestational age＜35 weeks)with NRDS who need noninvasive ventilation,the efficacy of HHHFNC was similar to that of NCPAP,and the rate of nasal injury was lower.Other safety indexes and the effects on cardiac function were similar.

Objective To compare the efficacy and the effects on cardiac function of heated humidified high-flow nasal cannula(HHHFNC)and nasal continuous positive airway pressure(NCPAP)as initial treatment for preterm infants with neonatal respiratory dis-tress syndrome(NRDS).Methods The preterm infants with NRDS,gestational age＜35 weeks and requiring noninvasive ventilation ad-mitted to Xuzhou Central Hospital from January 2021 to November 2023 were enrolled for a prospective study and were randomly divided into the HHHFNC group and NCPAP group.The initial treatment was performed using HHHFNC and NCPAP respectively.The efficacy,safety and effects on cardiac function were compared.Results 55 cases were enrolled in HHHFNC group,and 53 cases were enrolled in NCPAP group.There were no statistically significant difference between the two groups in the number and total dose of the use of pulmona-ry surfactant,the number of apneas within 24hours of enrollment,the duration of noninvasive ventilation,the cases of noninvasive ventila-tion failure,the age achieving total enteral nutrition,the length and costs of hospitalization(P＞0.05).The incidence of nasal injury in the HHHFNC group was significantly lower than that in the NCPAP group(0 vs 11.3％,P=0.032).There were no statistically signifi-cant difference between the two groups in the pneumothorax,stage Ⅱ-Ⅲ necrotizing enterocolitis,hemodynamically significant patent ductus arteriosus,grade Ⅱ-Ⅳ intraventricular hemorrhage,bronchopulmonary dysplasia,and retinopathy of prematurity requiring treat-ment at the first screening(P＞0.05).There were no statistically significant difference between the two groups in fraction of inspired oxy-gen and arterial partial pressure of carbon dioxide,Plasma B-type natriuretic peptide(183.9±48.5ng/L vs 187.8±51.4ng/L,189.4±50.9ng/L vs 180.2±45.1ng/L)and Tei index of right ventricle(0.38±0.05 vs 0.40±0.06,0.38±0.06 vs 0.39±0.06)at 24±6h and 48±6h after noninvasive ventilation(P＞0.05).Conclusion In the initial treatment for preterm infants(gestational age＜35 weeks)with NRDS who need noninvasive ventilation,the efficacy of HHHFNC was similar to that of NCPAP,and the rate of nasal injury was lower.Other safety indexes and the effects on cardiac function were similar.

Neonatal acute respiratory distress syndrome (ARDS) is a clinical condition characterized by acute respiratory failure with refractory hypoxemia triggered by local or systemic etiologies during the neonatal period. Diagnosis primarily relies on the Montreux criteria. Oxygen index is recommended for grading index and lung ultrasound scoring is recommended for auxiliary diagnosis and treatment index. Current therapeutic strategies include high-frequency oscillatory ventilation, high-dose pulmonary surfactant administration, inhaled nitric oxide, intratracheal instillation of budesonide combined with surfactant, prone positioning, extracorporeal membrane oxygenation. Despite these interventions, targeted therapies remain limited. In particular, neonates with moderate or severe neonatal ARDS generally carry a poor prognosis, with mortality escalating in severe cases or those with systemic etiologies.

Objective:To study the risk factors, diagnosis and treatment of transient hyperinsulinemic hypoglycemia (HH) in newborns.Methods:From January 2016 to December 2020, newborns with transient HH (HH group) admitted to our hospital were enrolled in this retrospective nested case-control study. Newborns with similar gestational age (GA) (differences of GA<2 w) without HH were matched with 1∶2 ratio as the non-HH group. Clinical characteristics of the two groups were compared and the risk factors and therapeutic results of HH in newborns were analyzed using SPSS 20.0 statistical software.Results:A total of 39 cases were included in the HH group and 75 cases were matched in the non-HH group. The proportion of small for gestational age (SGA) [51.3%(20/39) vs. 32.0%(24/75)], the amount of amino acids (AA) in intravenous infusion[1.0(0.0,1.0) g/(kg·d) vs. 0.0(0.0,1.0) g/(kg·d)], the incidence of hypoglycemia [(4.3±1.9) times vs. (3.6±1.3) times] and the maximum glucose infusion rate (GIR)[(8.3±2.5) mg/(kg·min) vs. (7.4±1.1) mg/(kg·min)] in the HH group were higher than the non-HH group (all P<0.05). The platelet count in the HH group were lower than the non-HH group [(186.9±60.9)×10 9/L vs. (215.3±61.7)×10 9/L, P<0.05]. SGA ( OR=2.535, 95% CI 1.077~5.971), the amount of intravenous AA ( OR=2.180, 95% CI 1.029~4.619) and the maximum GIR ( OR=1.405, 95% CI 1.088~1.815) were independent risk factors for transient HH. In the HH group, 28/39 cases were treated with Diazoxide or Octreotide and the therapeutic effects were good with few adverse drug reactions (ADR). 37/39 cases were recovered within 28 d of birth and the other 2 cases were recovered at 2.5 m and 3.5 m, respectively. Conclusions:SGA, the amount of intravenous AA and higher GIR are risk factors for transient HH in newborns. Diazoxide or Octreotide are effective with few ADR in the treatment of transient HH. Most patients will recover from transient HH in 2 w to 3 m.

Objective:To study the clinical value of bladder stimulation technique (BST) for clean-catch urine collection in late newborns.Methods:From November 2020 to March 2022, relatively stable late newborns hospitalized in the Department of Neonatology of our hospital were enrolled in the prospective randomized controlled trial. The newborns were assigned into BST group and control group. In BST group, urine was collected using BST (suprapubic tapping alternating with lumbosacral massage for 5 min) 20~30 min after feeding and specimen were collected using urine bag before and after BST. In the control group, urine was collected using urine bag method. The urine collection was considered successful if >1 ml of urine not contaminated by faeces were collected within 60 min. The t-test and χ 2 test were used for data analysis. Results:A total of 231 late newborns were included with 117 cases in BST group and 114 in control group. The rate of successful urine collection in BST group was higher than control group (65.8% vs. 39.4%).The time needed for successful urine collection [(30.2±8.5) min vs. (40.7±12.9) min], the incidences of faeces contamination (2.5% vs. 21.1%) and urine contamination (11.7% vs. 26.7%) in BST group were all significantly lower than control group(all P<0.05). Male and female newborns in BST group had similar success rates of urine collection (65.6% vs. 66.0%). Male newborns in BST group had similar urine contamination rate with control group (9.5% vs. 11.5%) and female newborns in BST group had significantly lower urine contamination rate than control group (14.3% vs. 47.4%, P<0.05). Urine was successfully collected in 71 newborns in BST group with median duration of BST for 81 (61,132) s. No adverse effects were observed except for transient consolable crying. Conclusions:Compared with urine bag collection method, BST improves successful urine collection rates and reduces the time needed for urine collection and urine contamination rates (especially for females).

Objective:To study the efficacy and safety of oral acetaminophen or high-dose ibuprofen as rescue treatment after failure of conservative management in very preterm infants (VPIs) with haemodynamically significant patent ductus arteriosus (hsPDA).Methods:From May 2020 to November 2022, VPIs with hsPDA (gestational age<32 weeks and age 4~6 d) admitted to NICU of our hospital were prospectively enrolled. The rescue treatment was initiated if hsPDA still exist after 3~4 d of conservative management. The infants were randomly assigned into acetaminophen group (oral acetaminophen 15 mg/kg, once every 6 h for 3 d) and high-dose ibuprofen group (oral ibuprofen 20 mg/kg for the first dose, 10 mg/kg each dose after 24 h and 48 h). Before and after rescue treatment, the following were recorded: echocardiography, complete blood count, biochemistry, B-type natriuretic peptide (BNP), fecal occult blood test (FOBT) and transcranial Doppler ultrasound. Urine output and complications were also examined. SPSS 20.0 was used for statistical analysis.Results:A total of 36 cases were in the acetaminophen group and 37 in the high-dose ibuprofen group. The two groups showed similar efficacy as rescue treatment [80.6% (29/36) vs. 78.4% (29/37), P>0.05]. No significant differences existed in the incidences of upper gastrointestinal bleeding, positive FOBT, oliguria, stage Ⅱ-Ⅲ necrotizing enterocolitis and stage Ⅲ-Ⅳ intraventricular hemorrhage between the two groups ( P>0.05). After rescue treatment, the serum cystatin C in high-dose ibuprofen group was higher [(1.72±0.29) mg/L vs. (1.58±0.26) mg/L] and 24-hours urine output was lower [(3.1±1.0) ml/(kg·h) vs. (3.7±0.7) ml/(kg·h)] than the acetaminophen group (all P<0.05). No significant differences existed in serum creatinine, platelet count, BNP, alanine aminotransferase and total serum bilirubin between the two groups ( P>0.05). Conclusions:After failure of early conservative management in VPIs with hsPDA, when initiated within 7-10 d after birth, rescue treatment with oral acetaminophen or high-dose ibuprofen has a similar efficacy of 80%, and both drugs are safe. Oral high-dose ibuprofen may have a greater effect on renal function than acetaminophen.

This paper is to provide a basis for the establishment of an early diagnostic system for hypoxic-ischemic encephalopathy (HIE) by performing segmentation and feature extraction of lesions on the MR images of neonatal babies with HIE. The segmentation on MR images of HIE based on the genetic algorithm (GA) combined with a pulse-coupled neural network (PCNN) were carried out. There were better segmentation results by using PCNN segmentation based on GA than PCNN segmentation with fixed parameters. The data suggested that a PCNN based on GA could provide effective assistance for diagnosis and research.
Algorithms ; Female ; Humans ; Hypoxia-Ischemia, Brain ; diagnosis ; physiopathology ; Image Processing, Computer-Assisted ; Infant, Newborn ; Magnetic Resonance Imaging ; methods ; Male ; Neural Networks (Computer)

This paper is aimed to study a method and feasibility of early diagnostic system using hypoxic ischemic encephalopathy (HIE) in the newborns. Fifteen non-invasive indicators with high sensitivity and specificity were selected for the early diagnosis of HIE on the basis of related researches from the literature and the researches in our laboratory. The diagnostic test was done with 140 cases with the HIE, using the fussy BP neural network experiment system. The initial results showed that the accuracy rate was 100% for the training set and 95% for the testing set, and the error rate was 5%. The data suggested that the fuzzy back-propagation neural networks, with the clinical comprehensive indicators, exhibited a high accuracy for the early diagnosis of HIE. This method provides an objective and convenient new way for the early clinical diagnosis of the HIE.
Algorithms ; Diagnosis, Computer-Assisted ; methods ; Early Diagnosis ; Female ; Fuzzy Logic ; Humans ; Hypoxia-Ischemia, Brain ; diagnosis ; Infant, Newborn ; Male ; Neural Networks (Computer) ; Pattern Recognition, Automated ; methods ; Reproducibility of Results ; Sensitivity and Specificity

The aim of this experiment is to find a feasible impersonal index for analyzing the physiological mental fatigue level. Three characteristic parameters, relative power in different rhythm, barycenter frequency and power spectral entropy, are extracted from two channels' electroencephalogram (EEG) under two physiological mental fatigue states. Then relationships between such three parameters and physiological mental fatigue are analyzed to explore whether they can be of use for detecting (or monitoring) the mental fatigue level. The experiment results show that the relative power, barycenter frequency and power spectral entropy of EEG exhibit strong correlation with physiological mental fatigue level. While physiological mental fatigue level increases, the relative power in theta, alpha and beta rhythms, barycenter frequency and power spectral entropy of EEG decrease, but the relative power in delta rhythm of EEG increases. The relative power in four rhythms, barycenter frequency and power spectral entropy of EEG reflect the change of physiological mental fatigue level sensitively, and may hopefully be used as indexes for detecting physiological mental fatigue level.
Adult ; Electroencephalography ; Entropy ; Humans ; Male ; Mental Fatigue ; physiopathology ; Signal Processing, Computer-Assisted ; Young Adult