CRP and cystic fibrosis: CF patients enrolled at the end of an inpatient admission at The Prince Charles Hospital, BrisbaneDischarge determined by self-reported improvement in patient's symptoms and objective evidence of a reduction in CRP and an improvement in lung parametersPA post-discharge measured by SenseWear armband for 5–7 daysTo monitor time to next pulmonary exacerbation (days), all participants were followed-up for 12 months