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1.
Journal of Medical Informatics ; (12): 53-58,68, 2017.
Article in Chinese | WPRIM | ID: wpr-669156

ABSTRACT

The paper begins with the ontology construction requirements based on ontology reuse and transformation of existing resources,combines the current situations of study on technical progress and tools for ontology construction at home and abroad,and conducts code development of tools for ontology construction and function realization based on WebProtege class library.In the process of realization,pay attention to the interactive mode of combination of automatic tool processing and manual review,and collect specific sample data to verify the feasibility and usability of applying the developed tools for ontology construction.

2.
Chinese Journal of Contemporary Pediatrics ; (12): 1068-1073, 2013.
Article in Chinese | WPRIM | ID: wpr-345646

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the clinical effect of combination therapy with high-frequency oscillation ventilation (HFOV), pulmonary surfactant (PS) and inhaled nitric oxide (iNO) in the treatment of neonatal hypoxemic respiratory failure (HRF).</p><p><b>METHODS</b>A total of 116 neonates with HRF were studied, and they were randomly divided into two groups: triple therapy (n=58) and dual therapy (n=58). The triple therapy group received HFOV, PS, and iNO, while the dual therapy group received HFOV and iNO. Blood gas values, PaO2/FiO2 (P/F), oxygenation index (OI), and pulmonary arterial pressure (PA) were determined before treatment and after 24 and 48 hours of treatment. Among the neonates with different P/F ratios and OI values and with or without persistent pulmonary hypertension of the newborn (PPHN), the treatment outcomes of two groups were compared.</p><p><b>RESULTS</b>The durations of mechanical ventilation and iNO therapy in the triple therapy group were significantly shorter than in the dual therapy group (P<0.01). After 24 and 48 hours of treatment, the triple therapy group had significantly improve PaO2 and PaCO2 compared with the dual therapy group (P<0.01). After 24 and 48 hours of treatment, the neonates with PPHN in the triple therapy group had significantly decreased PA compared with the dual therapy group (P<0.01). In the cases with a P/F ratio of ≤50, the triple group had a significantly higher cure rate than the dual therapy group (P<0.05). In both groups, the P/F ratios of the neonates who died were significantly lower than those of survivors (P<0.01). In the cases with an OI of ≥40, the triple group had a significantly higher cure rate than the dual therapy group (P<0.05). In both groups, the OI values of the neonates who died were significantly higher than those of survivors (P<0.01). In neonates with PPHN, the triple group had a significantly higher cure rate than the dual therapy group (P<0.05). The triple therapy group had a significantly shorter length of hospital stay (P<0.01) and a significantly higher cure rate (P<0.05) compared with the dual therapy group. There were no significant differences in complications between the two groups (P>0.05). No severe side effect was found during the treatment in either group.</p><p><b>CONCLUSIONS</b>Triple therapy with HFOV, PS and iNO is a more effective treatment for neonatal HRF compared with the dual therapy with HFOV and iNO. The triple therapy can significantly improve oxygenation and survival rate, providing a new treatment for the neonates with HRF, especially the critical cases who suffer severe lung disease with PPHN and have a P/F ratio of ≤50 or an OI of ≥40.</p>


Subject(s)
Female , Humans , Infant, Newborn , Male , Administration, Inhalation , High-Frequency Ventilation , Hypoxia , Length of Stay , Nitric Oxide , Oxygen , Blood , Prognosis , Pulmonary Surfactants , Therapeutic Uses , Respiratory Insufficiency , Therapeutics
3.
Chinese Journal of Contemporary Pediatrics ; (12): 502-505, 2012.
Article in Chinese | WPRIM | ID: wpr-320609

ABSTRACT

<p><b>OBJECTIVE</b>To study therapeutic effect and safety of early administration of oral ibuprofen in very low birth weight infants (VLBWIs) with patent ductus arteriosus (PDA).</p><p><b>METHODS</b>A total of 64 symptomatic VLBWIs (within 24 hours after birth) with PDA confirmed by bedside Color Doppler ultrasound were randomly divided into two groups: treatment and control (n=32 each). The treatment group was orally administered ibuprofen within 24 hours after birth at 10 mg/kg, followed 24 hours later by a second dose of 5 mg/kg and 48 hours later by a third dose of 5 mg/kg. The control group was treated with placebo (normal saline) at 1 mL/kg, followed 24 hours later by a second dose of 0.5 mL/kg and 48 hours later by a third dose of 0.5 mL/kg. The therapeutic efficacies and adverse effects in both groups were observed.</p><p><b>RESULTS</b>The treatment group showed a significantly higher closure rate of ductus arterious than the control group after one course of treatment (84% vs 41%; P<0.01). The incidence rates of periventricular leukomalacia and bronchopulmonary dysplasia were significantly lower in the treatment group than in the control group (P<0.05). The duration of mechanical ventilation and mean hospitalization time were significantly shorter in the treatment group than in the control group (P<0.05). There were no significant differences in the incidence rates of intraventricular hemorrhage, early pulmonary hemorrhage and necrotizing enterocolitis between the two groups (P>0.05). No obvious adverse effects were observed in both groups.</p><p><b>CONCLUSIONS</b>Early administration of oral ibuprofen for treatment of PDA in VLBWIs can decrease the incidence rates of some early complications and shorten hospitalization time, but causes no significant adverse effects.</p>


Subject(s)
Female , Humans , Infant, Newborn , Male , Administration, Oral , Anti-Inflammatory Agents, Non-Steroidal , Ductus Arteriosus, Patent , Drug Therapy , Ibuprofen , Infant, Very Low Birth Weight , Length of Stay
4.
Chinese Journal of Contemporary Pediatrics ; (12): 783-786, 2011.
Article in Chinese | WPRIM | ID: wpr-339532

ABSTRACT

<p><b>OBJECTIVE</b>To compare the efficacy of nasal synchronized intermittent positive pressure ventilation (NSIPPV) and nasal continuous positive airway pressure ventilation (NCPAP) for the treatment of apnea in preterm infants.</p><p><b>METHODS</b>Eighty preterm infants with apnea from August 2010 to January 2011 were randomly administered with NSIPPV and NCPAP (n=40 each).The blood gas results before and 2 hrs after ventilation, time of using ventilator, therapeutic efficacy and complications were compared between the two groups.</p><p><b>RESULTS</b>There were no significant differences in the blood gas results between the two groups before ventilation. The blood gas results (pH, PO2, PCO2) in the NSIPPV group were better than those in the NCPAP group 2 hrs after ventilation. The time of using ventilator in the NSIPPV group was shorter than that in the NCPAP group (50±9 h vs 91±11 h; P<0.01). There were no significant differences in the total effective rate between the NSIPPV and the NCPAP groups (95% vs 85%; P>0.05). The proportion of ventilator weaning within 3 days in the NSIPPV group (23/40) was higher than that in the NCPAP group (14/40) (P<0.05). The incidence of complications in the NSIPPV group was not different from that in the NCPAP group (22% vs 25%).</p><p><b>CONCLUSIONS</b>NSIPPV appears to be superior to NCPAP for the treatment of apnea in preterm infants.</p>


Subject(s)
Humans , Infant, Newborn , Apnea , Therapeutics , Blood Gas Analysis , Continuous Positive Airway Pressure , Infant, Premature , Intermittent Positive-Pressure Ventilation , Methods
5.
Chinese Journal of Contemporary Pediatrics ; (12): 195-197, 2010.
Article in Chinese | WPRIM | ID: wpr-270390

ABSTRACT

<p><b>OBJECTIVE</b>To study the efficacy of endotracheal lavage in neonatal ventilator-associated pneumonia (VAP).</p><p><b>METHODS</b>Fifty-eight neonates with VAP between January 2002 and December 2008 were randomly assigned to two groups: lavage and control (n=29 each). After withdrawal from ventilator, both groups received sensitive antibiotics therapy according to sputum culture results as well as supportive treatment. The lavage group was additionally treated with endotracheal lavage (2-3 times daily). The therapeutic effects were compared between the two groups.</p><p><b>RESULTS</b>There were no significant differences in the average time of mechanical ventilation between the lavage and the control groups. The effective rate in the lavage group (93%) was significantly higher than that in the control group (69%; p<0.05). Three percent of patients in the lavage group required twice or more mechanical ventilation compared with 24% in the control group (p<0.05). Blood gas analysis results were obviously improved in the lavage group 2 hrs after treatment (p<0.01).</p><p><b>CONCLUSIONS</b>Endotracheal lavage can decrease the number in mechanical ventilation and improve therapeutic effects in neonates with VAP.</p>


Subject(s)
Female , Humans , Infant, Newborn , Male , Incidence , Pneumonia, Ventilator-Associated , Epidemiology , Therapeutics , Respiration, Artificial , Therapeutic Irrigation , Methods , Trachea
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