scholarly journals Localized Pulmonary Interstitial Emphysema Which Occurred After Non-invasive Mechanical Ventilatory Support

Author(s):  
Esra Türe ◽  
Hakan Ildır ◽  
Abdullah Yazar ◽  
Fatih Akın ◽  
Sevgi Pekcan
2021 ◽  
Author(s):  
Tamao Shinohara ◽  
Yohei Hasebe ◽  
Daisuke Watanabe ◽  
Fuminori Numano ◽  
Tomohiro Saito ◽  
...  

Abstract Background: Acquired cystic lung disease is a serious respiratory complication of bronchopulmonary dysplasia in premature infants. Most cases of acquired cystic lung disease underlying bronchopulmonary dysplasia involve pulmonary interstitial emphysema. Although this is a reversible condition, there are a few instances where surgery might be necessary. An accurate diagnosis is important to decide the therapeutic strategy for acquired cystic lung disease. Here, we report a rare case of a giant pulmonary bulla in an infant treated with bullectomy. Case presentation: A male infant born at 23 weeks of gestation with a birth weight of 524 g was initially diagnosed with respiratory distress syndrome. During mechanical ventilatory support, he presented with recurrent pneumothorax and a gradually expanding pulmonary cyst in the right lung. Chest CT at 5 months of age revealed a large cyst located in the subpleural area adjacent to the multiple cystic air spaces. These findings are consistent with the diagnosis of giant pulmonary bulla with pulmonary interstitial emphysema underlying bronchopulmonary dysplasia . At 9 months of age, the giant pulmonary bulla expanded further due to acute bronchitis for which he developed respiratory failure and obstructive shock. This warranted a bullectomy for the giant pulmonary bulla. After the operation, the unresected pulmonary interstitial emphysema lesion did not expand further. He is currently three years old and has no respiratory problems. Conclusions: This case demonstrated that chest CT is useful for providing valuable anatomical information necessary in deciding the treatment strategy for acquired cystic lung disease in infants.


2020 ◽  
Vol 2020 (8) ◽  
Author(s):  
María D P Martínez ◽  
Francisco G Alvarez ◽  
Jorge M Mallea ◽  
Sadia Z Shah ◽  
Si M Pham ◽  
...  

ABSTRACT Recent years have witnessed evolution of lung allocation strategies to prioritize sicker recipients. In the pre-transplant period, this has translated into increased utilization of invasive extracorporeal or mechanical ventilatory support as a bridge to lung transplantation. The morbidity associated with these strategies warrants consideration to less invasive respiratory support modalities. Herein, we present a case highlighting successful bridge to lung transplantation with a relatively non-invasive negative pressure ventilator.


2020 ◽  
Vol 23 (81) ◽  
pp. 8-11
Author(s):  
Jelena Vojnović ◽  
Sanja Hromiš

Non-invasive ventilation is a form of mechanical ventilatory support that doesn't require endotracheal intubation of the patient. The interface (mask) is a connection between the device and the patient that allows the set pressure gradient supplied by the ventilator to be transmitted to the airways. Today, there are different types of interfaces, which differ in shape, size, mechanical properties, and comfort. Despite the wide of different mask, common reasons for poor patient adaptation to NIV are related to side effects of the interface such as air loss, skin damage, and mask discomfort. We can prevent these side effects with a basic knowledge of the principles of handling and selecting the optimal interface.


CHEST Journal ◽  
1993 ◽  
Vol 104 (2) ◽  
pp. 647-648 ◽  
Author(s):  
Tai-Shion Lee ◽  
Kuo-Tong Liao

2006 ◽  
Vol 100 (1) ◽  
pp. 56-65 ◽  
Author(s):  
Marieke L. Duiverman ◽  
Gerrie Bladder ◽  
Aafke F. Meinesz ◽  
Peter J. Wijkstra

The Lancet ◽  
1993 ◽  
Vol 341 (8860) ◽  
pp. 1603 ◽  
Author(s):  
E.L. Abrahamson ◽  
M. Viswanath ◽  
I.Z. Kovar ◽  
S. Al Jawad

PEDIATRICS ◽  
1977 ◽  
Vol 60 (3) ◽  
pp. 273-281
Author(s):  
John L. Watts ◽  
Ronald L. Ariagno ◽  
June P. Brady

To determine pulmonary function abnormalities in patients with neonatal bronchopulmonary dysplasia (BPD), we measured distribution of ventilation by nitrogen washout, minute and tidal volume, and arterial and alveolar gases in three groups of ten preterm infants with similar birth weights (mean = 1,340 g) and gestational ages (mean = 30.3 weeks). Infants in group A were never artificially ventilated, those in group B were ventilated but had no subsequent BPD, and those in group C were ventilated and developed BPD. Infants with BPD had severe maldistribution of ventilation (pulmonary clearance delay 223% versus 47% and 60% for groups A and B). They had decreased tidal volumes (5.3 ml versus 7.0 and 6.2 ml) and higher respiratory rates (60/min versus 47 and 48) but similar minute volumes. They also had increased Paco2 (53.6 torr versus 41.9 and 43.4 torr) and increased arterial-alveolar carbon dioxide gradients (6.8 torr versus 3.1 and 1.8 torr). There was no statistically significant difference between groups B and C for the time spent in fractional inspired oxygen > 0.40 and > 0.60, or the time ventilated or intubated, or the incidence of patent ductus arteriosus. Early pulmonary interstitial emphysema was much more common in the infants who subsequently developed BPD (eight of ten versus two of ten, P < .01).


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