Rheological and transport properties of airway secretions in cystic fibrosis‐relationships with the degree of infection and severity of the disease

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Abstract
It has recently been suggested that in cystic fibrosis (CF), there is no rheological abnormality of airway secretions other than that associated with purulence, and that the apparent inhibition in the mucociliary transport rate might be partly due to a ciliary inhibitor present in these secretions. In order to ascertain this assumption, expectorated airway secretions were collected without salivary contamination in twenty‐four CF patients and the rheological properties were measured. Using a photometric method, the effects of CF sputum samples were analysed on the ciliary beat frequency (Fm) of the frog palate, and we measured their mucociliary transport rate (TR). In all but one CF sputum, TR and Fm were lower than that of the control frog mucus (median TR: 18±7 and 11±6 mm min‐1; median Fm: 12±3 and 11±3 Hz, respectively). In the eighteen patients in whom the rheological properties were outside the range for optimal mucociliary transport, the clinical Shwachman score was significantly (P0) was significantly higher (P0: 24±4 Pa. s) and TR, expressed as a percentage of the reference value, was significantly lower (PTr: 54±5%) in comparison with the values obtained for the thirteen non‐superinfected CF patients (median ±0, 15 Pa. s and median TR: 66% respectively). The CF patients with markedly hypervis‐cous sputum (±0 higher than 30 Pa. s) exhibited a low Shwachman score.