bronchomalacia/éidéime

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AiltTrialacha cliniciúlaPaitinní

Roghnaigh cineál sórtála

6 torthaí

Postobstructive Pulmonary Edema following Tonsillectomy/Adenoidectomy in a 2-Year-Old with Poland-Moebius Syndrome.

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Logáil Isteach / Cláraigh

A 2-year-old male with Poland-Moebius syndrome was transferred from a local hospital to the Pediatric ICU at Children's Hospital of Georgia for suspected postobstructive pulmonary edema (POPE) after tonsillectomy/adenoidectomy (T&A). The patient's respiratory status ultimately declined and he

A Case of the TOF with APV Complicated with Polyhydramnios and Severe Bronchomalacia.

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Logáil Isteach / Cláraigh

Absent pulmonary valve syndrome (APVS) is a rare congenital heart disease with severe pulmonary insufficiency, characterized with aneurysmal dilation in the pulmonary artery and one or both of its branches. We presented a rare case with APVS and literature review in this letter. Prenatal USG

Synchronous airway lesions and outcomes in infants with severe laryngomalacia requiring supraglottoplasty.

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Logáil Isteach / Cláraigh

OBJECTIVE To quantify the prevalence and the impact of synchronous airway lesions identified by endoscopy in infants undergoing supraglottoplasty for severe laryngomalacia (LM). METHODS Retrospective study. METHODS Tertiary care pediatric hospital. METHODS Sixty patients who underwent

Radiological findings of complications after lung transplantation.

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Logáil Isteach / Cláraigh

Complications following lung transplantation may impede allograft function and threaten patient survival. The five main complications after lung transplantation are primary graft dysfunction, post-surgical complications, alloimmune responses, infections, and malignancy. Primary graft dysfunction, a

Bronchoscopy in neonates with severe bronchopulmonary dysplasia in the NICU.

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Logáil Isteach / Cláraigh

To describe the findings, resulting changes in management, and safety profile of flexible bronchoscopy in the neonates with severe bronchopulmonary dysplasia.This was a retrospective case series of twenty-seven neonates with severe bronchopulmonary

Vascular tracheobronchial compression syndromes-- experience in surgical treatment and literature review.

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Logáil Isteach / Cláraigh

Between January 1988 and December 1997 a total of 22 patients (age: 8 days-46 years) were operated for vascular airway compression syndromes with respiratory insufficiency. Vascular anomalies in tracheal compression were double aortic arch in 7 patients, (2 previously operated elsewhere), right

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Herbal & Natural Medicine

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