An summary of the data collection instruments for outcome management in the Chronic Heart Failure project.
Written in 2008; 1,437 words; 8 sources; APA; $ 47.95
Paper Summary:
This paper summarizes the various date collection methods present for the outcome management in the Chronic Heart Failure (CHF) project. The author addresses the assessment method for each data collection instrument and describes the questions asked in each questionnaire.
Outline:
Minnesota Living with Heart Failure Questionnaire
Chronic Heart Failure Questionnaire
Kansas City Cardiomyopathy Questionnaire
Short Form 36
Short Form 12
Duke Health Profile
Primary Care Assessment Survey
From the Paper:
"The questionnaire asks about frequent physical and psychological symptoms experienced by the CHF patient such as peripheral edema, insomnia, dyspnea, easy fatigability, depression and anxiety. Inquiries on the patient's social and physical functional capacities are also asked and rated by the patient. These include the patient's ability to walk at a certain distance, do household chores, effects of CHF on the patient's cognitive skills and travel habits. The patient is also asked to rate how his disease has affected his family. Pharmacologic and non-pharmacologic treatments are also considered."
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