Noninvasive ventilation in immunocompromised pediatric patients: Eight years of experience in a pediatric oncology intensive care unit

被引:57
作者
Pancera, Christiane Finardi [1 ]
Hayashi, Massami
Fregnani, Jose Humberto [4 ,5 ]
Negri, Elnara M. [2 ]
Deheinzelin, Daniel [2 ]
de Camargo, Beatriz [3 ]
机构
[1] Hosp Canc AC Camargo, Ctr Tratamento & Pesquisa, Dept Pediat, Pediat Intens Care Unit, Sao Paulo, Brazil
[2] Hosp Canc AC Camargo, Adult Intens Care Unit, Sao Paulo, Brazil
[3] Hosp Canc AC Camargo, Ctr Tratamento & Pesquisa, Dept Pediat Oncol, Sao Paulo, Brazil
[4] Dept Morphol, Sao Paulo, Brazil
[5] Dept Stat, Sao Paulo, Brazil
关键词
cancer; children; noninvasive ventilation; intensive care unit;
D O I
10.1097/MPH.0b013e3181754198
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: The experience of noninvasive positive pressure ventilation (NPPV) in the pediatric setting is limited. The aim of the present study is to retrospectively evaluate the effectiveness of NPPV in pediatric immunocompromised patient admitted in our PICU (Pediatric Intensive Care Unit) for acute respiratory failure. Design/Setting: Retrospective cohort study of children admitted to the PICU of Hospital do Cancer between June 1997 and May 2005 requiring ventilatory support. Results: A total of 239 admissions were included. The first mechanical ventilation (MV) technique used was NPPV in 120 (50.2%) patients [noninvasive ventilation (NIV) group] and conventional MV in 119 (49.8%) [invasive ventilation (IV) group]; 25.8% of the patients from the NIV group subsequently required intubation. Patients in the IV group were more likely to be in a severe clinical status. Characteristics associated with severe clinical status were median value for therapeutic intervention scoring system score (37.5 points IV vs. 29 points NIV, P < 0.0001), presence of > 2 organs failure (63.6% TV vs. 36.4% NIV, P < 0.0001), cardiac failure (62.5% IV vs. 37.5% NIV, P < 0.000 1), and septic shock (63.9% IV vs. 36. 1 % NIV, P < 0.0001). Documented severe pulmonary disease was significantly higher (67.6%) in IV group, P = 0.02. Baseline values of arterial pCO(2), hypoxemia, arterial pH, and respiratory rate did not differ between the groups. Multivariate analysis showed that independent predictive factors for intubation were solid tumors (P = 0.012), cardiovascular dysfunction (P < 0.0001), and therapeutic intervention scoring system score ! 40 points (P = 0.018). Conclusions: Our results encourage the use of NPPV as a first-line treatment in children with malignancies who develops acute respiratory failure, except in those with severe hemodynamic status.
引用
收藏
页码:533 / 538
页数:6
相关论文
共 29 条
[21]   Non-invasive pressure support ventilation in acute hypoxemic respiratory failure: common strategy for different pathologies? [J].
Nava, S ;
Carlucci, A .
INTENSIVE CARE MEDICINE, 2002, 28 (09) :1205-1207
[22]   USE OF BIPAP(R) BY NASAL MASK IN THE TREATMENT OF RESPIRATORY INSUFFICIENCY IN PEDIATRIC-PATIENTS - PRELIMINARY INVESTIGATION [J].
PADMAN, R ;
LAWLESS, S ;
VONNESSEN, S .
PEDIATRIC PULMONOLOGY, 1994, 17 (02) :119-123
[23]   Noninvasive ventilation via bilevel positive airway pressure support in pediatric practice [J].
Padman, R ;
Lawless, ST ;
Kettrick, RG .
CRITICAL CARE MEDICINE, 1998, 26 (01) :169-173
[24]   Treatment of acute respiratory failure by helmet-delivered non-invasive pressure support ventilation in children with acute leukemia: a pilot study [J].
Piastra, M ;
Antonelli, M ;
Chiaretti, A ;
Polidori, G ;
Polidori, L ;
Conti, G .
INTENSIVE CARE MEDICINE, 2004, 30 (03) :472-476
[25]  
Prado F, 2005, REV MED CHILE, V133, P525
[26]   Noninvasive continuous positive airway pressure delivered by helmet in hematological malignancy patients with hypoxemic acute respiratory failure [J].
Principi, T ;
Pantanetti, S ;
Catani, F ;
Elisei, D ;
Gabbanelli, V ;
Pelaia, P ;
Leoni, P .
INTENSIVE CARE MEDICINE, 2004, 30 (01) :147-150
[27]  
SHAH PS, 2005, COCHRANE DATA BASE S, V20
[28]  
Teague W Gerald, 2005, Paediatr Respir Rev, V6, P52
[29]  
Thill Peter J, 2004, Pediatr Crit Care Med, V5, P337, DOI 10.1097/01.PCC.0000128670.36435.83