Lobar atelectasis in cystic fibrosis and treatment with recombinant human DNase I

Shah, Pallav L.; Scott, Sandra; Hodson, Margaret E.

doi:10.1016/0954-6111(94)90063-9

Cited by 26 publications

(11 citation statements)

References 5 publications

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“…MR can detect atelectasis as on CT. This is a highly relevant observation, seeing that atelectasis is associated with poor outcome and requires aggressive medical treatment (53–55). MRI was used to evaluate treatment effectiveness in one patient and showed complete resolution of the atelectasis (Fig.…”

Section: Discussionmentioning

confidence: 99%

Lung morphology assessment using MRI: A robust ultra‐short TR/TE 2D steady state free precession sequence used in cystic fibrosis patients

Failo

Wielopolski

Tiddens

et al. 2009

Magnetic Resonance in Med

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To evaluate feasibility and diagnostic quality of ultra-short TR/TE two-dimensional (2D) steady state free precession (SSFP) MRI for cystic fibrosis (CF) patients. We performed lung MRI at 1.5 Tesla in 20 CF-patients (6 -17 years, 12 males). Axial, coronal, and sagittal sections were acquired in inspiration and expiration with maximum breath-hold time 10 s. MR and CT images were scored using a modified Brody scoring system to assess bronchiectasis, mucous plugging, atelectasis/consolidations, and air trapping.

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Section: Discussionmentioning

confidence: 99%

Lung morphology assessment using MRI: A robust ultra‐short TR/TE 2D steady state free precession sequence used in cystic fibrosis patients

Failo

Wielopolski

Tiddens

et al. 2009

Magnetic Resonance in Med

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“…(3) increased cough; (4) fever (38°C); (5) increased wheezing; (6) decreased exercise tolerance, malaise, fatigue, or lethargy; (7) FEVX or FVC decreased 10% from a previously recorded value; (8) radiographic changes indicative of a new pulmonary process; or (9) changes in chest sounds. A non-PDE (NPDE) was noted when a patient had fewer than four of the above abnormalities.…”

Section: Methodsmentioning

confidence: 99%

Treatment of Idiopathic Bronchiectasis With Aerosolized Recombinant Human DNase I

O’Donnell

Barker

Ilowite

et al. 1998

Chest

391

239

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“…Surfactant administration was reported to improve ventilation by re-aeration of atelectatic regions and help wean children from mechanical ventilation [161]. Similarly, bronchoscopically administered recombinant human DNase has been used in cystic fibrosis patients [162], non-cystic fibrosis patients [163], and premature neonates [164], with variable success.…”

Section: Atelectasis Treatmentmentioning

confidence: 99%

ERS statement: interventional bronchoscopy in children

et al. 2017

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Paediatric airway endoscopy is accepted as a diagnostic and therapeutic procedure, with an expanding number of indications and applications in children. The aim of this European Respiratory Society task force was to produce a statement on interventional bronchoscopy in children, describing the evidence available at present and current clinical practice, and identifying areas deserving further investigation. The multidisciplinary task force panel performed a systematic review of the literature, focusing on whole lung lavage, transbronchial and endobronchial biopsy, transbronchial needle aspiration with endobronchial ultrasound, foreign body extraction, balloon dilation and occlusion, laser-assisted procedures, usage of airway stents, microdebriders, cryotherapy, endoscopic intubation, application of drugs and other liquids, and caregiver perspectives. There is a scarcity of published evidence in this field, and in many cases the task force had to resort to the collective clinical experience of the committee to develop this statement. The highlighted gaps in knowledge underline the need for further research and serve as a call to paediatric bronchoscopists to work together in multicentre collaborations, for the benefit of children with airway disorders.

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Lobar atelectasis in cystic fibrosis and treatment with recombinant human DNase I

Cited by 26 publications

References 5 publications

Lung morphology assessment using MRI: A robust ultra‐short TR/TE 2D steady state free precession sequence used in cystic fibrosis patients

Lung morphology assessment using MRI: A robust ultra‐short TR/TE 2D steady state free precession sequence used in cystic fibrosis patients

Treatment of Idiopathic Bronchiectasis With Aerosolized Recombinant Human DNase I

ERS statement: interventional bronchoscopy in children

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