Functional Assessment of Chronic Illness Therapy-Fatigue Scale is valid in patients with psoriatic arthritis

Chandran, Vinod; Bhella, Sita; Schentag, Catherine T.; Gladman, Dafna D.

doi:10.1136/ard.2006.065763

Cited by 180 publications

(168 citation statements)

References 23 publications

Supporting

Mentioning

157

Contrasting

Unclassified

Order By: Relevance

“…In patients with cancer and rheumatoid arthritis, the FACIT fatigue scale has shown excellent reliability and strong association with the vitality scales of the SF-36. [26][27][28][29] While most fatigue instruments measure the overall experience of fatigue over a period of time ranging from weeks to months, dialysis patients also experience day-to-day and diurnal variation in fatigue. Fatigue assessments using traditional instruments may fail to capture this variability due to recall bias.…”

Section: Measurement Of Fatiguementioning

confidence: 99%

Fatigue in Patients Receiving Maintenance Dialysis: A Review of Definitions, Measures, and Contributing Factors

Jhamb

Weisbord

Steel

et al. 2008

American Journal of Kidney Diseases

284

300

View full text Add to dashboard Cite

Fatigue is a debilitating symptom or side effect experienced by many patients on long-term dialysis. Fatigue has a considerable effect on patients' health-related quality of life and is viewed as being more important than survival by some patients. There are many challenges renal providers face when attempting to reduce fatigue in dialysis patients. The lack of a reliable, valid, and sensitive fatigue scale complicates the accurate identification of this symptom. Symptoms of daytime sleepiness and depression overlap with fatigue, making it difficult to target specific therapies. Moreover, many chronic health conditions common in the long-term dialysis population may lead to the development of fatigue and contribute to the day-to-day and diurnal variation of fatigue in patients. Key to improving the assessment and treatment of fatigue is improving our understanding of potential mediators, as well as potential therapies. Cytokines have emerged as an important mediator of fatigue and have been studied extensively in cancer related fatigue. In addition, although erythropoietin stimulating agents (ESA) have been shown to mitigate fatigue, the recent controversy regarding ESA dosing in chronic kidney disease (CKD) suggests that ESA therapy may not serve as the sole therapy to improve fatigue in this population. In conclusion, fatigue is an important and often underrecognized symptom in the dialysis population. Possible interventions for minimizing fatigue in patients on long-term dialysis should be aimed at improving health care provider awareness, developing improved methods of measurement, better understanding of the pathogenesis, as well as management of known contributing factors.

show abstract

Section: Measurement Of Fatiguementioning

confidence: 99%

Fatigue in Patients Receiving Maintenance Dialysis: A Review of Definitions, Measures, and Contributing Factors

Jhamb

Weisbord

Steel

et al. 2008

American Journal of Kidney Diseases

284

300

View full text Add to dashboard Cite

show abstract

“…Construct validity was demonstrated by distinguishing between groups known to differ on stage of disease, performance status, and need for emotional support (Lyons et al 2009). The FACIT-F was found to have high internal validity (Cronbach's alpha = 0.96) (Chandran et al 2007). Further, FACIT-F is a brief, valid measure for monitoring this important symptom and has demonstrated reliability and sensitivity to change in clients with a variety of chronic health conditions (Cella et al 2005;Tennant et al 2012).…”

Section: Methodsmentioning

confidence: 99%

Health Related Quality of Life and Care Dependency among Elderly Hospital Patients: An International Comparison

Dijkstra

Hakverdioğlu

Muszalik

et al. 2015

Tohoku J. Exp. Med.

View full text Add to dashboard Cite

Many countries in Europe and the world have to cope with an aging population. Although health policy in many countries aims at increasing disability-free life expectancy, elderly patients represent a significant proportion of all patients admitted to different hospital departments. The aim of the research was to investigate the relationship between health-related quality of life (HRQOL) and the care dependency status among elderly hospital patients. In 2012, a descriptive survey was administered to a convenience sample of 325 elderly hospital patients (> 60 years) from The Netherlands (N = 125), from Poland (N = 100), and from Turkey (N = 100). We employed the Functional Assessment of Chronic Illness Therapy (FACIT) Measurement System and the Care Dependency Scale. FACIT is a collection of HRQOL questionnaires that assess multidimensional health status in people with various chronic illnesses. From demographic variables, gender (female) (r = −0.13, p < 0.05), age and informal care given by family members (r = −0.27 to 0.27, p < 0.01) were significantly correlated with the care dependency status for the whole samples. All HRQOL variables, hearing aid and duration of illness correlated with care dependency status (r = −0.20 to 0.50, p < 0.01). Moreover, the FACIT sum score (Poland and Turkey) and functional wellbeing (The Netherlands) are significantly associated with the decrease in care dependency status. Thus, the FACIT variables are the most powerful indicators for care dependency. The study provides healthcare professionals insight into improvement of quality of care in all three countries.

show abstract

“…Some of the PRO instruments used in PsA clinical trials were initially created for other diseases 14,15,16,17 ; other generic PRO instruments are also used in PsA trials with the goal of characterizing overall population health, including the Medical Outcomes Study 36-Item Short Form Survey (SF-36) 18 . PRO instruments such as Psoriatic Arthritis Quality of Life questionnaire (PsAQoL), the Psoriasis Symptom Inventory, and the Psoriatic Arthritis Impact of Disease questionnaire (PsAID) have all made strides to incorporate patient feedback in the disease-specific measurement of PRO in PsA 19,20,21,22 .…”

Section: Rheumatologymentioning

confidence: 99%

Evaluation of Self-reported Patient Experiences: Insights from Digital Patient Communities in Psoriatic Arthritis

Sunkureddi

Doogan²,

Heid³

et al. 2018

J Rheumatol

View full text Add to dashboard Cite

Objective.To evaluate the types of experiences and treatment access challenges of patients with psoriatic arthritis (PsA) using self-reported online narratives.Methods.English-language patient narratives reported between January 2010 and May 2016 were collected from 31 online sources (general health social networking sites, disease-focused patient forums, treatment reviews, general health forums, mainstream social media sites) for analysis of functional impairment and 40 online sources for assessment of barriers to treatment. Using natural language processing and manual curation, patient-reported experiences were categorized into 6 high-level concepts of functional impairment [social, physical, emotional, cognitive, role activity (SPEC-R), and general] and 6 categories to determine barriers to treatment access (coverage ineligibility, out-of-pocket cost, issues with assistance programs, clinical ineligibility, formulary placement/sequence, doctor guidance). The SPEC-R categorization was also applied to 3 validated PsA patient-reported outcome (PRO) instruments to evaluate their capacity to collect lower-level subconcepts extracted from patient narratives.Results.Of 15,390 narratives collected from 3139 patients with PsA for exploratory analysis, physical concepts were the most common (81.5%), followed by emotional (50.7%), cognitive (20.0%), role activity (8.1%), and social (5.6%) concepts. Cognitive impairments and disease burden on family and parenting were not recorded by PsA PRO instruments. The most commonly cited barriers to treatment were coverage ineligibility (51.6%) and high out-of-pocket expenses (31.7%).Conclusion.Patients often discussed physical and emotional implications of PsA in online platforms; some commonly used PRO instruments in PsA may not identify cognitive issues or parenting/family burden. Nearly one-third of patients with PsA reported access barriers to treatment.

show abstract

Functional Assessment of Chronic Illness Therapy-Fatigue Scale is valid in patients with psoriatic arthritis

Cited by 180 publications

References 23 publications

Fatigue in Patients Receiving Maintenance Dialysis: A Review of Definitions, Measures, and Contributing Factors

Fatigue in Patients Receiving Maintenance Dialysis: A Review of Definitions, Measures, and Contributing Factors

Health Related Quality of Life and Care Dependency among Elderly Hospital Patients: An International Comparison

Evaluation of Self-reported Patient Experiences: Insights from Digital Patient Communities in Psoriatic Arthritis

Contact Info

Product

Resources

About