CFDB - Cystic Fibrosis DataBase

primary studies published RCT

Pilot safety study of liposomal prostaglandin (PGE1) in respiratory exacerbations in cystic fibrosis.

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

RCT

Participants

8 pediatric CF patients with stable CF who required tube feeding.

Interventions

isotopic infusion of [1-(13)C]valine and [(15)N(2)]urea. 3 randomly allocated isocaloric diets with normal (NP), intermediate (IP), and high (HP) amounts of protein (1.5, 3, and 5 g . kg(-1) . d(-1), respectively) by continuous drip feeding during a 4-d period at 6-wk intervals. Each patient acted as his or her own control.

Outcome measures

On the fourth day of feeding, whole-body protein synthesis and breakdown were measured.

Main results

Protein synthesis was significantly higher in the HP group (x +/- SEM. 1.78 +/- 0.07 micromol . kg(-1) . min(-1)) than in the IP (1.57 +/- 0.08 micromol . kg(-1) . min(-1); P=0.001) and NP (1.37 +/- 0.07 micromol . kg(-1) . min(-1); P < 0.001) groups. There were no significant differences in protein breakdown. Net retention of nitrogen was significantly higher in the HP group (12.93 +/- 1.42 micromol . kg(-1) . min(-1)) than in the IP (7.61 +/- 1.40 micromol . kg(-1) . min(-1); P=0.01) and HP (2.48 +/- 0.20 micromol . kg(-1) . min(-1); P < 0.001) groups.

Authors' conclusions

In stunted children with CF requiring tube feeding, the highest stimulation of whole-body protein synthesis was achieved with a short-term dietary protein intake of 5 g . kg(-1) . d(-1).

Keywords: Child; non pharmacological intervention - diet; Proteins; Supplementation; Continuous;