Implementation of pediatric home spirometry: potential height bias

Patients with cystic fibrosis and other respiratory conditions have their lung function frequently monitored for routine care. Although the use of patient-initiated home spirometry was reported as early as 1982, its utilization has not been generalized [1]. Lack of low-cost, accurate devices, and lack of reimbursement for coaching, and data review hindered the generalization of its use.
Source: Journal of Cystic Fibrosis - Category: Respiratory Medicine Authors: Tags: Letter to the Editor Source Type: research