CFDB - Cystic Fibrosis DataBase

Other Reviews - Other Review

ALPINE2: Efficacy and safety of 14-day vs 28-day inhaled aztreonam for Pa eradication in children with cystic fibrosis.

Study design (if review, criteria of inclusion for studies)

Studies in English; RCT; subjects diagnosed as having CF; children or adolescents aged 6–18 years; exercise training intervention lasting at least 2 weeks. A control group had to be present.

List of included studies (4)

Schneiderman-Walker 2000; Selvadurai 2002; Klijn 2004; Orenstein 2004

Participants

4 RCT: Schneiderman-Walker et al. (control=36; aerobic=36); Selvadurai et al. (control=21; aerobic=21, resistance=22); Klijn et al. (control=9; anaerobic=11); Orenstein et al. (control=26; stregth=30)

Interventions

exercise intervention

Outcome measures

pulmonary function (FEV1; FVC) and fitness outcomes (VO2; leg strength; peak power)

Main results

gth in one or more intervention group (p≤0.03); improvements lasted up to 12 months (one RCT). Findings for aerobic fitness were inconsistent (four RCTs). Exercise training was associated with significant improvement from baseline in one intervention group of one short-term RCT (p<0.01) and with significant deterioration from baseline in one intervention group of one long-term RCT (p<0.01). Anaerobic fitness was significantly improved in the intervention group compared to controls (p<0.0001) in the only RCT that reported this outcome (short term).

Authors' conclusions

The review concluded that both aerobic exercise and strength training may benefit pulmonary function, aerobic fitness and strength among children with cystic fibrosis. Factors that limited the review included the small amount of evidence available and inconsistencies between studies. Therefore, the author's conclusions may require cautious interpretation. Both aerobic exercise and strength training may benefit pulmonary function, aerobic fitness and strength among children with cystic fibrosis. - The author stated that children with mild to severe cystic fibrosis may benefit from exercise training, especially in an in-patient setting. Both short-term and long-term strength programmes were effective, even in prepubertal children. - The author stated that research was needed into the most effective exercise programme for children with cystic fibrosis. Research needed to include which exercise modalities (or combinations) and what intensity, duration and dose of exercise were most effective. The author recommended research (RCTs included) of home-delivered exercise, strength training and anaerobic exercise that reported outcomes such as quality of life, need for chest physiotherapy, recurrent infection rate, nutritional status and physiological end points.

Keywords: Adolescent; Child; exercise; Infant; non pharmacological intervention - devices OR physiotherapy; strength training;