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The impact of fibromyalgia on health status according to the types, demographic background and pain index
B. Ghavidel-Parsa1, A. Bidari2, A.A. Maafi3, A. Hassankhani4, A. Hajiabbasi5, A. Montazeri6, O. Sanaei7, B. Ghalehbaghi8
- Rheumatology Research Center, Razi Hospital, School of Medicine, Guilan University of Medical Sciences, Rasht, Iran.
- Department of Rheumatology, Iran University of Medical Sciences, Tehran, Iran. bidari.a@iums.ac.ir
- Student Research Center, Guilan University of Medical Sciences, Rasht, Iran.
- Student Research Center, Guilan University of Medical Sciences, Rasht, Iran.
- Rheumatology Research Center, Razi Hospital, School of Medicine, Guilan University of Medical Sciences, Rasht, Iran.
- Mental Health Research Group, Health Metrics Research Center, Iranian Institute for Health Sciences Research, Academic Center for Education, Culture & Research, Tehran, Iran.
- Golestan Research Center of Gastroenterology and Hepatology, Golestan University of Medical Sciences, Gorgan, Iran.
- Otolaryngology and Head and Neck Surgery Research Center, Iran University of Medical Sciences, Tehran, Iran.
CER9280
2016 Vol.34, N°2 ,Suppl.96
PI 0134, PF 0139
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PMID: 27157398 [PubMed]
Received: 22/01/2016
Accepted : 19/04/2016
In Press: 02/05/2016
Published: 06/05/2016
Abstract
OBJECTIVES:
To compare fibromyalgia (FM) core symptoms, FM impact severity and health status between the recently defined type A and type B of fibromyalgia. To compare disease impact and health status between FM patients and non-FM chronic pain control group. Finally, to compare health related quality of life and disease symptom severity by demographic background and widespread pain index (WPI).
METHODS:
A total of 284 consecutive FM patients and 96 non-FM control patients were enrolled. The information of four questionnaires including the Fibromyalgia Survey Questionnaire (FSQ), the Fibromyalgia Impact Questionnaire (FIQ), the 12-item Short Form Health Survey (SF-12) and questionnaires regarding demographic features were collected from a local FM registry.
RESULTS:
Of all FM patients, 102 (94%) and 7 (6%) were type A and B, respectively. We found statistically significant differences in symptomatology, the FIQ scores and the SF-12 subscales across two type and control groups (p<0.001). However, when we compared these scores pairwise, except WPI there were no significant differences in other scores between type A and B. Also, there were no significant differences in FIQ and SF-12 scores across different age or educational status groups. Interestingly, patients with higher WPI had significantly higher FIQ (overall, symptom, and total) scores, worse PCS-12 and MCS-12 scores, and vice versa.
CONCLUSIONS:
Type B constitutes a minor but important component of FM that probably has a marked impact on the patient’s perceived illness severity and quality of life. Further, WPI probably is the most important single indicator of disease severity and quality of life in FM.