Literature DB >> 28018152

Evaluation of Medication-related Self-care Skills in Patients With Cystic Fibrosis.

Kelsey Lackey Lewis1, Barnabas John2, Michelle Condren3, Sandra M Carter4.   

Abstract

BACKGROUND: As the life expectancy of patients with cystic fibrosis (CF) increases, the focus on ensuring success with medication therapies is increasingly important. The ability of patients to autonomously manage medications and related therapies is poorly described in the literature.
OBJECTIVE: The goal of this project was to assess the level of medication-related knowledge and self-care skills in patients with CF.
METHODS: This project took place in a Cystic Fibrosis Foundation accredited affiliate center. Eighty-nine patients between the ages of 6 and 60 were eligible to participate based on inclusion and exclusion criteria. Pharmacists administered a 16-item questionnaire and detailed medication history during clinic visits from January through May 2014.
RESULTS: Forty-five patients 6 to 41 years old participated in the study. The skills most often performed independently were preparing nebulizer treatments (85%) and telling someone if they feel their medicines are causing a problem (89%). Skills least often performed were carrying a medication list (82%) and bringing a medication list to appointments (76%). In respondents 21 years of age and older, less than 75% of respondents were involved with obtaining financial resources, maintaining equipment, carrying a medication list, or rinsing their mouth after using inhaled medicines. Participants were able to provide drug name, dose, and frequency of use for pancreatic enzymes and azithromycin 37% and 24% of the time, respectively.
CONCLUSIONS: In the population surveyed, many medication-related skills had not been acquired by early adulthood. Assessing and providing education for medication-related self-care skills at all ages are needed.

Entities:  

Keywords:  cystic fibrosis; patient advocacy; quality improvement; self efficacy; self-care

Year:  2016        PMID: 28018152      PMCID: PMC5178812          DOI: 10.5863/1551-6776-21.6.502

Source DB:  PubMed          Journal:  J Pediatr Pharmacol Ther        ISSN: 1551-6776


  10 in total

Review 1.  Cystic fibrosis adult care: consensus conference report.

Authors:  James R Yankaskas; Bruce C Marshall; Beth Sufian; Richard H Simon; David Rodman
Journal:  Chest       Date:  2004-01       Impact factor: 9.410

2.  A clinical tool to measure the components of health-care transition from pediatric care to adult care: the UNC TR(x)ANSITION scale.

Authors:  Maria E Ferris; Donna H Harward; Kristi Bickford; J Bradley Layton; M Ted Ferris; Susan L Hogan; Debbie S Gipson; Lynn P McCoy; Stephen R Hooper
Journal:  Ren Fail       Date:  2012-05-14       Impact factor: 2.606

3.  Measuring the transition readiness of youth with special healthcare needs: validation of the TRAQ--Transition Readiness Assessment Questionnaire.

Authors:  Gregory S Sawicki; Katryne Lukens-Bull; Xiaoping Yin; Nathan Demars; I-Chan Huang; William Livingood; John Reiss; David Wood
Journal:  J Pediatr Psychol       Date:  2009-12-29

4.  Improving transition from pediatric to adult cystic fibrosis care: lessons from a national survey of current practices.

Authors:  Suzanne Elizabeth McLaughlin; Marie Diener-West; Alka Indurkhya; Haya Rubin; Rebekah Heckmann; Michael Patrick Boyle
Journal:  Pediatrics       Date:  2008-05       Impact factor: 7.124

5.  Health care autonomy in children with chronic conditions: implications for self-care and family management.

Authors:  Barbara L Beacham; Janet A Deatrick
Journal:  Nurs Clin North Am       Date:  2013-02-22       Impact factor: 1.208

Review 6.  Measures of readiness to transition to adult health care for youth with chronic physical health conditions: a systematic review and recommendations for measurement testing and development.

Authors:  Lisa A Schwartz; Lauren C Daniel; Lauren D Brumley; Lamia P Barakat; Kimberly M Wesley; Lisa K Tuchman
Journal:  J Pediatr Psychol       Date:  2014-06-01

7.  Supporting the health care transition from adolescence to adulthood in the medical home.

Authors:  W Carl Cooley; Paul J Sagerman
Journal:  Pediatrics       Date:  2011-06-27       Impact factor: 7.124

8.  Motivating adherence among adolescents with cystic fibrosis: youth and parent perspectives.

Authors:  Gregory S Sawicki; Karen S Heller; Nathan Demars; Walter M Robinson
Journal:  Pediatr Pulmonol       Date:  2014-03-10

9.  High treatment burden in adults with cystic fibrosis: challenges to disease self-management.

Authors:  Gregory S Sawicki; Deborah E Sellers; Walter M Robinson
Journal:  J Cyst Fibros       Date:  2008-10-26       Impact factor: 5.482

10.  Measuring self-care independence in children with cystic fibrosis: the Self-Care Independence Scale (SCIS).

Authors:  Susana R Patton; Julie L Graham; Laurie Varlotta; Douglas Holsclaw
Journal:  Pediatr Pulmonol       Date:  2003-08
  10 in total
  2 in total

1.  Virtual medication tours with a pharmacist as part of a cystic fibrosis telehealth visit.

Authors:  Nicole Warda; Shannon M Rotolo
Journal:  J Am Pharm Assoc (2003)       Date:  2021-04-20

2.  Decreased Wait Time and Increased Satisfaction With Bedside Pancreatic Enzyme Dosing for the Inpatient Adolescent With Cystic Fibrosis: A Quality Improvement Project Comparing Enzyme Self-Administration to Nurse Administration.

Authors:  Brandi Middour-Oxler; Margaret Gettis; Betsy Dye
Journal:  J Patient Exp       Date:  2021-01-12
  2 in total

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