-
Je něco špatně v tomto záznamu ?
High-frequency jet ventilation improves gas exchange in extremely immature infants with evolving chronic lung disease
R Plavka, M Dokoupilova, L Pazderova, P Kopecky, V Sebron, M Zapadlo, M Keszler
Jazyk angličtina Země Spojené státy americké
Typ dokumentu klinické zkoušky, práce podpořená grantem
Grantová podpora
NR8360
MZ0
CEP - Centrální evidence projektů
PubMed
17094040
DOI
10.1055/s-2006-954821
Knihovny.cz E-zdroje
- MeSH
- chronická nemoc MeSH
- klinické křížové studie MeSH
- lidé MeSH
- nemoci nedonošenců * terapie MeSH
- novorozenec s extrémně nízkou porodní hmotností MeSH
- novorozenec MeSH
- pilotní projekty MeSH
- plicní nemoci * terapie MeSH
- plicní ventilace MeSH
- progrese nemoci MeSH
- spotřeba kyslíku MeSH
- vysokofrekvenční proudová ventilace * metody MeSH
- Check Tag
- lidé MeSH
- novorozenec MeSH
- Publikační typ
- klinické zkoušky MeSH
- práce podpořená grantem MeSH
Extremely preterm infants often develop chronic lung disease (CLD) characterized by heterogeneous aeration; poorly supported, floppy airways; and air trapping. High-frequency jet ventilation (HFJV) with high end-expiratory pressure (optimal lung volume strategy [OLVS]) may improve airway patency, lead to better gas distribution, improve gas exchange, and facilitate extubation. In a pilot trial, this study sought to explore the effect of HFJV on oxygenation, ventilation, and ease of extubation in preterm infants with evolving CLD and refractory respiratory failure (RRF). From September 2002 to October 2004, 12 episodes of RRF developed in 10 ventilated extremely immature infants with evolving CLD (10 on conventional and two on high-frequency oscillation). Chorioamnionitis was confirmed in all infants, patent ductus arteriosus was ligated in five patients, and UREAPLASMA UREALYTICUM was cultured from trachea in four patients. HFJV with OLVS was initiated when oxygenation index (OI) > 10 or exhaled tidal volume (V TE) >or= 7 mL/kg were required to maintain partial pressure of carbon dioxide, arterial (Pa CO2) < 60 mm Hg. Inspiratory time (0.02/s) and frequency (310 to 420/min) were set initially with adjustment of pressure amplitude to keep Pa CO2 between 45 and 55 mm Hg. Ventilatory stabilization and weaning from mechanical ventilation with extubation to nasal continuous positive airway pressure (CPAP) were the goals of this approach. Gas exchange data were analyzed by Analysis of variance for repeated measures. Ten patients on 11 occasions of RRF were extubated to nasal CPAP successfully in a median of 15.5 days. Nine of 10 patients survived (one died of pentalogy of Cantrell), all required supplemental O2 at 36 weeks. Pa CO2 decreased within 1 hour after the initiation of HFJV, and OI decreased by 24 hours. Both remained significantly lower until successful extubation ( P < 0.02). Compared with conventional ventilation or high-frequency oscillatory ventilation, HFJV used with OLVS appears to improve gas exchange and may facilitate weaning from mechanical ventilation (MV) in extremely immature infants with evolving CLD. These encouraging pilot data need to be confirmed in a larger clinical trial.
Citace poskytuje Crossref.org
Literatura
- 000
- 00000naa a2200000 a 4500
- 001
- bmc13030775
- 003
- CZ-PrNML
- 005
- 20130926092933.0
- 007
- ta
- 008
- 130926s2006 xxua f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1055/s-2006-954821 $2 doi
- 035 __
- $a (PubMed)17094040
- 040 __
- $a ABA008 $d ABA008 $e AACR2 $b cze
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Plavka, Richard, $d 1957- $7 xx0084863 $u Division of Neonatology, Department of Obstetrics and Gynecology, 1st Medical Faculty, Charles University, Prague, Czech Republic
- 245 10
- $a High-frequency jet ventilation improves gas exchange in extremely immature infants with evolving chronic lung disease / $c R Plavka, M Dokoupilova, L Pazderova, P Kopecky, V Sebron, M Zapadlo, M Keszler
- 504 __
- $a Literatura
- 520 9_
- $a Extremely preterm infants often develop chronic lung disease (CLD) characterized by heterogeneous aeration; poorly supported, floppy airways; and air trapping. High-frequency jet ventilation (HFJV) with high end-expiratory pressure (optimal lung volume strategy [OLVS]) may improve airway patency, lead to better gas distribution, improve gas exchange, and facilitate extubation. In a pilot trial, this study sought to explore the effect of HFJV on oxygenation, ventilation, and ease of extubation in preterm infants with evolving CLD and refractory respiratory failure (RRF). From September 2002 to October 2004, 12 episodes of RRF developed in 10 ventilated extremely immature infants with evolving CLD (10 on conventional and two on high-frequency oscillation). Chorioamnionitis was confirmed in all infants, patent ductus arteriosus was ligated in five patients, and UREAPLASMA UREALYTICUM was cultured from trachea in four patients. HFJV with OLVS was initiated when oxygenation index (OI) > 10 or exhaled tidal volume (V TE) >or= 7 mL/kg were required to maintain partial pressure of carbon dioxide, arterial (Pa CO2) < 60 mm Hg. Inspiratory time (0.02/s) and frequency (310 to 420/min) were set initially with adjustment of pressure amplitude to keep Pa CO2 between 45 and 55 mm Hg. Ventilatory stabilization and weaning from mechanical ventilation with extubation to nasal continuous positive airway pressure (CPAP) were the goals of this approach. Gas exchange data were analyzed by Analysis of variance for repeated measures. Ten patients on 11 occasions of RRF were extubated to nasal CPAP successfully in a median of 15.5 days. Nine of 10 patients survived (one died of pentalogy of Cantrell), all required supplemental O2 at 36 weeks. Pa CO2 decreased within 1 hour after the initiation of HFJV, and OI decreased by 24 hours. Both remained significantly lower until successful extubation ( P < 0.02). Compared with conventional ventilation or high-frequency oscillatory ventilation, HFJV used with OLVS appears to improve gas exchange and may facilitate weaning from mechanical ventilation (MV) in extremely immature infants with evolving CLD. These encouraging pilot data need to be confirmed in a larger clinical trial.
- 590 __
- $a bohemika - dle Pubmed
- 650 02
- $a chronická nemoc $7 D002908
- 650 02
- $a klinické křížové studie $7 D018592
- 650 02
- $a progrese nemoci $7 D018450
- 650 12
- $a vysokofrekvenční proudová ventilace $x metody $7 D006611
- 650 02
- $a lidé $7 D006801
- 650 02
- $a novorozenec s extrémně nízkou porodní hmotností $7 D052577
- 650 02
- $a novorozenec $7 D007231
- 650 12
- $a nemoci nedonošenců $x terapie $7 D007235
- 650 12
- $a plicní nemoci $x terapie $7 D008171
- 650 02
- $a spotřeba kyslíku $7 D010101
- 650 02
- $a pilotní projekty $7 D010865
- 650 02
- $a plicní ventilace $7 D012123
- 655 _2
- $a klinické zkoušky $7 D016430
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Dokoupilová, Milena $7 jx20070511013 $u Division of Neonatology, Department of Obstetrics and Gynecology, 1st Medical Faculty, Charles University, Prague, Czech Republic
- 700 1_
- $a Pazderová, Libuše $7 xx0084873 $u Division of Neonatology, Department of Obstetrics and Gynecology, 1st Medical Faculty, Charles University, Prague, Czech Republic
- 700 1_
- $a Kopecký, Pavel, $7 xx0129616 $u Division of Neonatology, Department of Obstetrics and Gynecology, 1st Medical Faculty, Charles University, Prague, Czech Republic $d 1962-
- 700 1_
- $a Sebroň, Václav, $7 xx0084601 $u Division of Neonatology, Department of Obstetrics and Gynecology, 1st Medical Faculty, Charles University, Prague, Czech Republic $d 1959-
- 700 1_
- $a Zapadlo, Miloš $7 xx0084619 $u Division of Neonatology, Department of Obstetrics and Gynecology, 1st Medical Faculty, Charles University, Prague, Czech Republic
- 700 1_
- $a Keszler, Martin $7 xx0084621 $u Georgetown University, Washington, Columbia
- 773 0_
- $t American Journal of Perinatology $x 0735-1631 $g Roč. 23, č. 8 (2006), s. 467-472 $p Am J Perinatol $w MED00000279
- 773 0_
- $p Am J Perinatol $g 23(8):467-72, 2006 Nov $x 0735-1631
- 910 __
- $a ABA008 $y 3 $z 0
- 990 __
- $a 20130926083255 $b ABA008
- 991 __
- $a 20130926093445 $b ABA008
- 999 __
- $a ok $b bmc $g 994890 $s 829219
- BAS __
- $a 3
- BMC __
- $a 2006 $b 23 $c 8 $d 467-472 $i 0735-1631 $m American journal of perinatology $x MED00000279 $n Am J Perinatol
- GRA __
- $a NR8360 $p MZ0
- LZP __
- $a 2013-09/išbo