Measurement of Symptoms and Quality of Life in Patients with Heart FailureValidation of a three-factor measurement model of dyspnea in hospitalized adults with heart failure
Section snippets
Design and Setting
The study used a prospective, longitudinal correlational design. Participants were adults admitted for treatment of new-onset or decompensated HF to an urban academic medical center or a Department of Veterans Affairs medical center in the southwestern United States. The ethical review bodies of both institutions approved the study, and signed informed consent was obtained from all participants.
Eligibility
Participants were at least 18 years of age, able to speak and understand English, and of sufficient
Results
The median and modal hospital day on study day 1 was hospital day 1 (25th to 75th percentile: hospital day 1–2; range: hospital day 1–5). Cumulatively, 24% of the sample (n = 29) were enrolled on the day of admission, 72% (n = 86) by hospital day 1, 87% by hospital day 2 (n = 104), and 96% (n = 114) by hospital day 3. Only 5 participants (4%) were enrolled after hospital day 3 (4 on hospital day 4 and 1 on hospital day 5). All descriptors were endorsed by at least 60% of participants for day 0 (
Discussion
Overall, the same 3-factor/7-indicator measurement model fit the study day 1 and day 0 data and the COPD data satisfactorily and substantially better than any alternative model. All 3 factors had strong internal consistency reliability regardless of diagnosis or study day. To our knowledge, this is the first time that a specific measurement model of dyspnea sensory quality has been validated in an independent sample using CFA methods (which supports the internal validity of the 3-factor
Conclusions
This study demonstrates that intensity ratings for 3 sensory quality factors can be measured consistently and reproducibly with only a few descriptors both across diagnoses and across time points within a diagnosis. Although a single-item rating of intensity or distress has demonstrated responsiveness to clinical change in acute HF syndromes,31, 39, 40 using a single item assumes that differences in sensory quality are irrelevant to feeling better or worse. As far as we are aware, such an
Acknowledgments
The authors thank all the patients who participated or were willing to consider participating in the study, as well as the members of the inpatient cardiology services and the nursing staff of the participating hospitals. The authors thank Jessica Benton, RN, MSN, ACNP-C, Rebecca Mayo, PhD, RN, FNP-C, Eleanor Miranda, RN, MSN, FNP-C, Susie Stokely, RN, MSN, ACNP-C, Julia Silva, RN, BSN, and Vivian Yarmola, RN, MSN, for assistance. The authors thank Anne Mattarella of the UNM College of Nursing
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2019, Parkinsonism and Related DisordersCitation Excerpt :Furthermore, the diagnosis of dyspnea was based on a question used in routine clinical care by pulmonologists specializing in dyspnea. As dyspnea is a subjective perception of breathing discomfort [28], the assignment of a patient to the symptomatic group depended on his personal experience spontaneously reported. Indeed, there is no threshold or no validated questionnaire to consider if someone is dyspneic or not dyspneic.
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Conflict of Interest: none
Funded by a grant from the National Institute of Nursing Research (1 R15 NR008883). The opinions expressed in this article are solely those of the authors.