The saccharin test measures nasal mucociliary clearance. It is simple to perform, inexpensive, reproducible and is a screening test for the diagnosis of primary ciliary dyskinesia. Study objective - To establish the normal range of the ST in a group of presumed normal Brazilian children, and compare the results with those from the literature. Setting - The study was conducted in 2 schools in São Paulo, Brazil. Participants - Two hundred and thirty eight schoolchildren, 134 boys and 104 girls, age range 10.8-16.8 years, were studied. Information on respiratory diseases and smoking habits of parents were obtained from a questionnaire completed by the parents. Results - The questionnaires were analyzed and the children were then divided into 5 groups.The mean ST value in the group of normal children was 7.5 ± 2.8 minutes, comparable to the literature. The mean ST value in children with parental smoking, upper respiratory tract infection (URTI) within the preceding week, or allergy and URTI was not significantly different from the normal group. However, there was a significant difference between the normal group and those with allergy. As the standard deviation was greater in the groups with URTI, the population was reorganized into 2 groups, the criteria being the presence or not of URTI within the preceding week. Again, the mean ST values were not significantly different, but the variability was significantly different in the group with URTI. In 99% of the children studied the test took less than 30 minutes. Conclusions - Saccharin test values over 30 minutes should be considered abnormal and retested. We recommend that the test should not be performed during or within one month following an URTI.

Keywords: Saccharin test. Nasal mucociliary clearance.

Pneumatoceles usually have a benign presentation. The authors describe an uncommon case of a 3-month-old boy who had a first episode of pneumonia and left pleural effusion. At the age of 2, he had another episode of pneumonia with pneumatoceles formation. He progressed with wheezing and enlargement of the pneumatoceles, chickenpox, urinary infection, liver abscess and toxocariasis. When he was 3 years old, the patient was admitted to hospital with pneumonia, giant bilateral pneumatoceles, status asthmaticus and possible immunodeficiency. Due to a restrictive pulmonary disorder, a chest tube was placed in one of the pneumatoceles, but there was no improvement in his respiratory status. He progressed to sepsis and respiratory failure, needing mechanical ventilation. The patient was submitted to bilateral bullectomy with expansion of the collapsed lung. However, he died soon after the surgery. This was an uncommon case with pneumatoceles that evolved to respiratory failure requiring surgical intervention.

Keywords: Pneumatoceles. Bullous lung disease. Cysts. Staphyloccocal pneumonia. Ventilatory insufficiency. Bullectomy.

Objective: To analyze the effects of Pilates mat exercises in patients with cystic fibrosis (CF). Methods: This was a clinical trial involving 19 CF patients recruited from either the CF Outpatient Clinic of the State University at Campinas Hospital de Clínicas or the Children's Institute of the University of São Paulo School of Medicine Hospital das Clínicas. All of the patients performed Pilates mat exercises for four months (one 60-min session per week). The variables studied (before and after the intervention) were respiratory muscle strength, MIP, MEP, FVC, and FEV1. Results: After the intervention, MIP was significantly higher in the male patients (p = 0.017), as were MIP and MEP in the female patients (p = 0.005 and p = 0.007, respectively). There were no significant differences between the pre- and post-intervention values of FVC or FEV1, neither in the sample as a whole nor among the patients of either gender. Conclusions: Our results show that Pilates mat exercises have beneficial effects on respiratory muscle strength in CF patients. (Brazilian Registry of Clinical Trials - ReBEC; identification number RBR-86vp8x [http://www.ensaiosclinicos.gov.br])

Keywords: Cystic fibrosis; Muscle strength; Exercise movement techniques; Respiratory function tests.