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支气管肺发育不良的小婴儿的正常肺血管阻力和左心室肥厚:一项超声心动图和病理学研究。

Normal pulmonary vascular resistance and left ventricular hypertrophy in young infants with bronchopulmonary dysplasia: an echocardiographic and pathologic study.

作者信息

Malnick G, Pickoff A S, Ferrer P L, Peyser J, Bancalari E, Gelband H

出版信息

Pediatrics. 1980 Oct;66(4):589-96.

PMID:6448973
Abstract

To evaluate the cardiac anatomy and functional hemodynamics in young infants with chronic lung disease, nine patients, aged 2 to 7 months, with a clinical diagnosis of bronchopulmonary dysplasia (BPD) underwent echocardiographic examination. All infants required supplemental O2 (mean FIO2 35%) to maintain adequate systemic oxygenation (Pao2 greater than 50 mm Hg). None of the infants had evidence of a patent ductus arteriosus at the time of examination. Echocardiographic measurements of left and right ventricular systolic time intervals revealed normal systolic time interval ratios suggesting pulmonary vascular resistances. However, echocardiographic evidence of left ventricular hypertrophy was found in eight of the nine infants, while right ventricular anterior wall thickness and right ventricular diastolic dimensions were not increased. Two infants died; marked left ventricular hypertrophy was noted at the time of postmortem examination while the right ventricular wall thickness was normal. The findings of left ventricular hypertrophy led to a retrospective review of autopsy material of seven patients who died with BPD over the past year. In six of seven cases examined, left ventricular posterior wall thickening was noted (range 7 to 11 mm); while the right ventricular wall thickness was normal (range 2 to 5 mm). These data suggest that (1) as assessed by echocardiography, the pulmonary vascular resistance is not significantly elevated in young infants with BPD, and (2) a hypertrophic left ventricle evolves which may assume importance in the pathogenesis of pulmonary edema in BPD, though the precise etiology remains undetermined.

摘要

为评估患有慢性肺病的幼儿的心脏解剖结构和功能性血流动力学,对9名年龄在2至7个月、临床诊断为支气管肺发育不良(BPD)的患儿进行了超声心动图检查。所有婴儿均需补充氧气(平均吸入氧分数35%)以维持足够的全身氧合(动脉血氧分压大于50 mmHg)。检查时,所有婴儿均无动脉导管未闭的迹象。超声心动图测量左、右心室收缩时间间期显示收缩时间间期比值正常,提示肺血管阻力正常。然而,9名婴儿中有8名发现有左心室肥厚的超声心动图证据,而右心室前壁厚度和右心室舒张内径未增加。2名婴儿死亡;尸检时发现有明显的左心室肥厚,而右心室壁厚度正常。左心室肥厚的发现促使对过去一年中7名死于BPD的患者的尸检材料进行回顾性研究。在检查的7例病例中有6例发现左心室后壁增厚(范围为7至11 mm);而右心室壁厚度正常(范围为2至5 mm)。这些数据表明:(1)通过超声心动图评估,患有BPD的幼儿肺血管阻力未显著升高;(2)会出现肥厚性左心室,这可能在BPD肺水肿的发病机制中具有重要意义,尽管确切病因仍未确定。

相似文献

1
Normal pulmonary vascular resistance and left ventricular hypertrophy in young infants with bronchopulmonary dysplasia: an echocardiographic and pathologic study.支气管肺发育不良的小婴儿的正常肺血管阻力和左心室肥厚:一项超声心动图和病理学研究。
Pediatrics. 1980 Oct;66(4):589-96.
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G Ital Cardiol. 1983;13(1):51-7.

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Atrial septal defect closure is associated with improved clinical status in patients ≤ 10 kg with bronchopulmonary dysplasia.房间隔缺损封堵术与体重≤10千克的支气管肺发育不良患者临床状况改善相关。
Pulm Circ. 2023 Oct 20;13(4):e12299. doi: 10.1002/pul2.12299. eCollection 2023 Oct.
2
ACE inhibition for severe bronchopulmonary dysplasia - an approach based on physiology.血管紧张素转换酶抑制剂治疗重度支气管肺发育不良——一种基于生理学的方法。
Physiol Rep. 2018 Sep;6(17):e13821. doi: 10.14814/phy2.13821.
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A new look at bronchopulmonary dysplasia: postcapillary pathophysiology and cardiac dysfunction.
支气管肺发育不良的新视角:毛细血管后病理生理学与心脏功能障碍
Pulm Circ. 2016 Dec;6(4):508-515. doi: 10.1086/688641.
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Left ventricular diastolic dysfunction in bronchopulmonary dysplasia.支气管肺发育不良中的左心室舒张功能障碍
J Pediatr. 2008 Feb;152(2):291-3. doi: 10.1016/j.jpeds.2007.11.006.
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Long term sequelae of bronchopulmonary dysplasia (chronic lung disease of infancy).支气管肺发育不良(婴儿慢性肺病)的长期后遗症。
Thorax. 2001 Apr;56(4):317-23. doi: 10.1136/thorax.56.4.317.
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Changes in pulmonary arterial pressure in preterm infants with chronic lung disease.患有慢性肺病的早产儿肺动脉压力的变化
Arch Dis Child Fetal Neonatal Ed. 2000 May;82(3):F243-7. doi: 10.1136/fn.82.3.f243.
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Cardiac effects of short course dexamethasone in preterm infants.短期地塞米松对早产儿心脏的影响。
Arch Dis Child Fetal Neonatal Ed. 1998 Mar;78(2):F133-7. doi: 10.1136/fn.78.2.f133.
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Bronchopulmonary dysplasia: then and now.支气管肺发育不良:过去与现在。
Arch Dis Child. 1990 Oct;65(10 Spec No):1076-81. doi: 10.1136/adc.65.10_spec_no.1076.