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Since this was a retrospective study, we did not perform respiratory function tests that would have provided information about the patient's functional status.
Primary endpoints were changes in respiratory function tests and a modified NIH clinical score.
Safety and adverse events were assessed by reported signs and symptoms, physical examinations, blood tests, cardiac and respiratory function tests.
Clinical diagnosis was made by a group of medical experts after examining the responses to a standardized clinical interview, respiratory function tests, and allergy tests.
Chest X-ray imaging, electrocardiography, and respiratory function tests were normal.
Respiratory function tests were performed with a Vitalograph® Compact spirometer (Buckingham, UK).
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Each patient also underwent the following functional and biological investigations: respiratory function test, measurement of exhaled nitric oxide (eNO), collection of exhaled breath condensate (EBC), and nasal wash.
His respiratory function test was within the normal range.
Both corrected and uncorrected parameters were correlated with age, height, weight, plasma creatinine and respiratory function test parameters using a Pearson correlation matrix.
Despite repeated aspiration pneumonia, preoperative chest radiography showed no consolidation, and the results of a respiratory function test showed 1.9 L of forced expiratory capacity (FEV1.0) and 79.6% of vital capacity (%VC).
Parents were usually present during the respiratory function testing.
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