Neurally adjusted ventilatory assist (NAVA) in preterm newborn infants with respiratory distress syndrome-a randomized controlled trial

被引:55
作者
Kallio, Merja [1 ,2 ]
Koskela, Ulla [1 ,2 ]
Peltoniemi, Outi [1 ,2 ]
Kontiokari, Tero [1 ]
Pokka, Tytti [1 ,2 ]
Suo-Palosaari, Maria [3 ,4 ,5 ]
Saarela, Timo [1 ,2 ]
机构
[1] Univ Oulu, PEDEGO Res Unit, Med Res Ctr Oulu, Oulu, Finland
[2] Oulu Univ Hosp, Dept Children & Adolescents, BOX 5000, FIN-90014 Oulu, Finland
[3] Univ Oulu, Med Res Ctr Oulu, Oulu, Finland
[4] Oulu Univ Hosp, Dept Diagnost Radiol, Oulu, Finland
[5] Univ Oulu, Oulu, Finland
关键词
Edi signal; Invasive ventilation; NAVA; Neonate; Preterm infant; Respiratory distress; PERSISTENT PULMONARY-HYPERTENSION; BRONCHOPULMONARY DYSPLASIA; MECHANICAL VENTILATION; CARE; DIAGNOSIS; CROSSOVER; PRESSURE; FAILURE; BIRTH; GRAMS;
D O I
10.1007/s00431-016-2758-y
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Neurally adjusted ventilatory assist (NAVA) improves patient-ventilator synchrony during invasive ventilation and leads to lower peak inspiratory pressures (PIP) and oxygen requirements. The aim of this trial was to compare NAVA with current standard ventilation in preterm infants in terms of the duration of invasive ventilation. Sixty infants born between 28 + 0 and 36 + 6 weeks of gestation and requiring invasive ventilation due to neonatal respiratory distress syndrome (RDS) were randomized to conventional ventilation or NAVA. The median durations of invasive ventilation were 34.7 h (quartiles 22.8-67.9 h) and 25.8 h (15.6-52.1 h) in the NAVA and control groups, respectively (P = 0.21). Lower PIPs were achieved with NAVA (P = 0.02), and the rapid reduction in PIP after changing the ventilation mode to NAVA made following the predetermined extubation criteria challenging. The other ventilatory and vital parameters did not differ between the groups. Frequent apneas and persistent pulmonary hypertension were conditions that limited the use of NAVA in 17 % of the patients randomized to the NAVA group. Similar cumulative doses of opiates were used in both groups (P = 0.71). Conclusions: NAVA was a safe and feasible ventilation mode for the majority of preterm infants suffering from RDS, but the traditional extubation criteria were not clinically applicable during NAVA.
引用
收藏
页码:1175 / 1183
页数:9
相关论文
共 30 条
[1]   Current trends in paediatric and neonatal ventilatory care - a nationwide survey [J].
Alander, Merja ;
Peltoniemi, Outi ;
Saarela, Timo ;
Anttila, Eija ;
Pokka, Tytti ;
Kontiokari, Tero .
ACTA PAEDIATRICA, 2013, 102 (02) :123-128
[2]   Comparison of pressure-, flow-, and NAVA-Triggering in pediatric and neonatal ventilatory care [J].
Alander, Merja ;
Peltoniemi, Outi ;
Pokka, Tytti ;
Kontiokari, Tero .
PEDIATRIC PULMONOLOGY, 2012, 47 (01) :76-83
[3]   Diagnosis and management of persistent pulmonary hypertension of the newborn [J].
Bendapudi, Perraju ;
Rao, Gopinath Gangadhara ;
Greenough, Anne .
PAEDIATRIC RESPIRATORY REVIEWS, 2015, 16 (03) :157-161
[4]  
Brown H., 2015, Applied mixed models in medicine
[5]   Mechanical Ventilation of the Premature Neonate [J].
Brown, Melissa K. ;
DiBlasi, Robert M. .
RESPIRATORY CARE, 2011, 56 (09) :1298-1311
[6]   RESPIRATORY-DISTRESS SYNDROME TREATED WITH HUMAN SURFACTANT - RADIOGRAPHIC FINDINGS [J].
EDWARDS, DK ;
HILTON, SV ;
MERRITT, TA ;
HALLMAN, M ;
MANNINO, F ;
BOYNTON, BR .
RADIOLOGY, 1985, 157 (02) :329-334
[7]   Characterisation of the Hering-Breuer deflation reflex in the human neonate [J].
Hannam, S ;
Ingram, DM ;
Rabe-Hesketh, S ;
Milner, AD .
RESPIRATION PHYSIOLOGY, 2000, 124 (01) :51-64
[8]   Intravenous Paracetamol Decreases Requirements of Morphine in Very Preterm Infants [J].
Harma, Antti ;
Aikio, Outi ;
Hallman, Mikko ;
Saarela, Timo .
JOURNAL OF PEDIATRICS, 2016, 168 :36-40
[9]   Persistent pulmonary hypertension of the newborn: Advances in diagnosis and treatment [J].
Jain, Amish ;
McNamara, Patrick J. .
SEMINARS IN FETAL & NEONATAL MEDICINE, 2015, 20 (04) :262-271
[10]   Epidemiology of Bronchopulmonary Dysplasia [J].
Jensen, Erik A. ;
Schmidt, Barbara .
BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY, 2014, 100 (03) :145-157