RESUMEN
Background: Liver disease in patients with cystic fibrosis (CF) is an understudied and increasingly common concern. The prevalence of cystic fibrosis liver disease (CFLD) in Canada has not been clearly established, although it is now the third leading cause of death among patients with CF. The current literature identifies a range in prevalence from 4% to 65%, which implies the need for further research. This study aimed to determine the prevalence of CFLD among adult patients with CF in Newfoundland and Labrador. Methods: Charts of patients with CF from the St. John's, Newfoundland, CF clinics were reviewed retrospectively for the presence of elevated liver enzymes, imaging or biopsy of the liver, and other etiologies of liver disease. Prevalence was determined for patients meeting the criteria for CFLD in the population as a whole and for those who had undergone all pertinent investigations. Results: The diagnostic guidelines for CFLD were met in 14 of 57 cases (24.6% prevalence). Severe CFLD was present in 9 patients (15.8%). Among all patients with CF, 33 (57.9%) had isolated liver enzyme elevation. Eleven patients had not had the requisite imaging performed for accurate diagnosis. Among the subset who had undergone imaging, the prevalence of CFLD was 30%. Conclusions: This study attempted to fill the gap in Canadian CFLD prevalence data by examining the population with CF in Newfoundland and Labrador. The prevalence of CFLD was found to be between 25% and 30%. More accurate determination of prevalence could be done with future cross-sectional or prospective studies.
RESUMEN
BACKGROUND: Patients with chronic obstructive pulmonary disease (COPD) are often nonadherent with medications and have poor inhaler technique. Community pharmacists can help to improve health-related quality of life and overall outcomes in patients with COPD. We aim to measure the effectiveness of a systematic, pharmacist-driven intervention on patients with diagnosed COPD. METHODS/DESIGN: This pragmatic, parallel-group, cluster randomized controlled trial is designed to determine the effectiveness of a multifactorial, pharmacist-led intervention on medication adherence, inhaler technique, health-related quality of life, health care resource utilization including COPD exacerbations, and use of medications. Participating pharmacies in Newfoundland and Labrador (NL), Canada will be randomly assigned to either the intervention or the control group. The intervention group will deliver an enhanced form of care that emphasizes COPD management. The control group will provide usual care and a COPD education pamphlet. Included patients will be aged 40 years or older, have a physician-confirmed diagnosis of COPD, and be able to answer questionnaires in English. The primary outcomes are the between-group difference in the change from baseline to 6 months in medication adherence using the Medication Possession Ratio (MPR) and the Morisky Medication Adherence Scale (MMAS-8). The secondary outcomes are also measured from baseline to 6 months, and include the proportion of patients with a clinically significant change in adherence, the proportion of patients defined as having "good adherence," the mean MPR between groups, quality of life as measured by the St. George's Respiratory Questionnaire, medication inhalation technique using a pharmacist-scored checklist, health care resource utilization and antibiotic and orally administered corticosteroid use for COPD exacerbations. Differences between groups will be analyzed at the individual patient level while controlling for clustering effect. DISCUSSION: A pharmacist-led COPD intervention has the potential to improve patient medication adherence, thus increasing quality of life, possibly decreasing pulmonary exacerbations and reducing utilization of acute health care resources. Methods and results taken from this study could be used to enhance the delivery of COPD care by community pharmacists in a real-world setting. This would serve to enhance COPD population health and quality of life. TRIAL REGISTRATION: International Standard Randomized Controlled Trial Number (ISRCTN) ISRCTN78138190 , registered on 3 February 2016.