Respiratory transition in infants delivered by cesarean section

被引:135
作者
Jain, Lucky [1 ]
Dudell, Golde G. [1 ]
机构
[1] Emory Univ, Sch Med, Atlanta, GA 30322 USA
关键词
cesarean delivery; term infant; fetal lung fluid clearance; respiratory distress syndrome; transient tachypnea of the newborn; epithelial sodium channel;
D O I
10.1053/j.semperi.2006.07.011
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
One of the biggest challenges a newborn faces after birth is the task of making a smooth transition to air breathing. This task is complicated by the fact that fetal lungs are full of fluid which must be cleared rapidly to allow for gas exchange. Respiratory morbidity as a result of failure to clear fetal lung fluid is not uncommon, and can be particularly problematic in some infants delivered by elective cesarean delivery (ECS). Given the high rates of cesarean deliveries in the USA and worldwide, the public health and economic impact of morbidity in this subgroup is considerable. Whereas the occurrence of birth asphyxia, trauma, and meconium aspiration is reduced by elective Cesarean delivery, the risk of respiratory distress secondary to transient tachypnea of the newborn, surfactant deficiency, and pulmonary hypertension is increased. It is clear that physiologic events in the last few weeks of pregnancy coupled with the onset of spontaneous labor are accompanied by changes in the hormonal milieu of the fetus and its mother, resulting in preparation of the fetus for neonatal transition. Rapid clearance of fetal lung fluid is a key part of these changes, and is mediated in large part by transepithelial Na reabsorption through amiloride-sensitive Na channels in the alveolar epithelial cells, with only a limited contribution from mechanical factors and Starling forces. This chapter discusses the physiologic mechanisms underlying fetal lung fluid absorption and explores potential strategies for facilitating neonatal transition when infants are delivered by ECS before the onset of spontaneous labor. © 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:296 / 304
页数:9
相关论文
共 112 条
[51]  
HUMPHREYS PW, 1967, J PHYSIOL-LONDON, V193, P1, DOI 10.1113/jphysiol.1967.sp008340
[52]   Alveolar fluid transport: a changing paradigm [J].
Jain, L ;
Eaton, DC .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2006, 290 (04) :L646-L648
[53]   Physiology of fetal lung fluid clearance and the effect of Labor [J].
Jain, L ;
Eaton, DC .
SEMINARS IN PERINATOLOGY, 2006, 30 (01) :34-43
[54]   Alveolar fluid clearance in developing lungs and its role in neonatal transition [J].
Jain, L .
CLINICS IN PERINATOLOGY, 1999, 26 (03) :585-+
[55]   Expression of highly selective sodium channels in alveolar type II cells is determined by culture conditions [J].
Jain, L ;
Chen, XJ ;
Ramosevac, S ;
Brown, LA ;
Eaton, DC .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2001, 280 (04) :L646-L658
[56]   Antisense oligonucleotides against the α-subunit of ENaC decrease lung epithelial cation-channel activity [J].
Jain, L ;
Chen, XJ ;
Malik, B ;
Al-Khalili, O ;
Eaton, DC .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 1999, 276 (06) :L1046-L1051
[57]   Nitric oxide inhibits lung sodium transport through a cGMP-mediated inhibition of epithelial cation channels [J].
Jain, L ;
Chen, XJ ;
Brown, LA ;
Eaton, DC .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 1998, 274 (04) :L475-L484
[58]  
Jobe AH, 1997, BIOL NEONATE, V72, P305
[59]   Glucocorticoids in perinatal medicine: Misguided rockets? [J].
Jobe, AH .
JOURNAL OF PEDIATRICS, 2000, 137 (01) :1-3
[60]   Functional ion channels in pulmonary alveolar type I cells support a role for type I cells in lung ion transport [J].
Johnson, MD ;
Bao, HF ;
Helms, MN ;
Chen, XJ ;
Tigue, Z ;
Jain, L ;
Dobbs, LG ;
Eaton, DC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (13) :4964-4969