Pain Coping Strategies and Quality of Life in Women with Fibromyalgia: Does Age Make a Difference? Journal of Musculoskeletal Pain, Vol. 9(2) 2001, pp. 5-18 Carol S. Burckhardt, PhD, RN; Sharon R. Clark, PhD., RN and Robert M. Bennett, MD, FRCP Carol S. Burckhardt. PhD, RN, is Professor of Nursing and Assistant Professor of Medicine [Research], Sharon R. Clark, PhD, RN, is Associate Professor of Nursing and Assistant Professor of Medicine [Research], and Robert M. Bennett, MD, FRCP, is Professor of Medicine, all in the Division of Arthritis and Rheumatic Diseases, Department of Medicine, School of Medicine, Oregon Health Sciences University, Portland. Oregon. Address correspondence to: Carol S. Burckhardt, PhD. PMHNP. School of Nursing, SN-5N, Oregon Health Sciences University, 3181 SW Sam Jackson Park Road, Portland. OR 97201 [E--mail: mailto:burckhac@ohsu.edu ]. Submitted: June 29, 2000 Accepted without revisions: September 19, 2000 ABSTRACT. Objectives: To characterize and compare the demographics, symptom profiles, pain coping strategies, and quality of life in three age groups of women with fibromyalgia [FMS] . Methods: Self-report questionnaires. including the Fibromyalgia Impact Questionnaire [FIQ], Beck Depression Inventory, Coping Strategies Questionnaire, and Quality of Life Scale, were filled out by 343 consecutive women who were participating in FMS treatment programs. Patients were divided into three age groups for purposes of data analysis. Results: The youngest age group had their symptoms for a significantly shorter period of time than the middle age and older age groups. Tender point pain score, the FIQ physical functioning and well-being items, and perceived ability to decrease pain were significantly worse for the youngest age group when compared to the other two groups. The youngest group had significantly higher catastrophizing scores and lower quality of life than the oldest age group. Discriminant function analysis between the youngest and oldest groups revealed that a combination of six variables: length of symptoms, quality of life, tender point pain score, morning tiredness, behavioral activity strategies, and a pain control/rational thinking factor were 84% accurate in classifying these patients into their original groups. When length of symptoms was excluded, the remaining five variables were 79%, accurate in classifying the patients. Conclusions: Young women with FMS perceive the severity of FMS to be higher and respond with more distress than older women with FMS. This finding is largely independent of symptom length. KEYWORDS. Fibromyalgia, women, fibromyalgia impact questionnaire, coping strategies questionnaire, quality of life scale Introduction: Coping with chronic illness is a life-long task that cuts across developmental stages. For women with fibromyalgia [FMS], these stages may range from childhood to old age. Fibromyalgia is known to affect children and adolescents as well as adults (1,2); however, the average age at onset is about 45-48 years (3). Thus, much of the research to date has focused on women in midlife. Nevertheless, many women in their 20's and 30's are diagnosed with FMS at the same time that they are taking on the roles and responsibilities of work, marriage, and parenthood. Most younger as well as middle-aged women with FMS worry that their symptoms will become worse as they grow older. The general belief among many clinicians is that symptom severity is enduring and less amenable to treatment the longer symptoms have been present. To date, this belief has not been subjected to scientific scrutiny in FMS clinical groups. Although symptoms tend to remain persistent for many patients with FMS (4-6), two studies have found that a majority of women with FMS rate their symptoms as decreased in intensity from when they were first diagnosed (7,8). Another report, which compared elderly women with FMS to younger FMS patients, found that symptoms of anxiety as well as symptom aggravation by weather, mental stress, and poor sleep were significantly less common among the elderly women (9). Additionally, a 4.5 year follow-up study of FMS patients given a 14 week course of treatment found that increasing age predicted lower levels of pain and lack of energy (10). Whether these findings represent changes in the symptoms themselves, changes in coping with symptoms, adaptation to life circumstances, or simply faulty memory is largely unknown. In any case, one thing is clear, longitudinal studies to date have failed to confirm any pattern of worsening with age. The possibility exists that FMS may be at its highest intensity in the early years after diagnosis. Getting through the period of uncertainty, learning about the illness and its treatment, coming to terms with having a chronic problem, and establishing new patterns of living are stressful tasks to accomplish at any time in life (I I-13). When these tasks are coupled with the heavily task-oriented work of young adulthood, one might expect that symptom severity and distress would be unusually high and that satisfaction with one's quality of life might be lower (14). If this is the case, more attention should be paid to developing strategies that assist young women with FMS to better cope with symptoms and decrease them to manageable levels so that they can concentrate more fully on the developmental tasks of young adulthood. Earlier we reported the use of coping strategies by a group of women who entered and a subsample that completed an FMS treatment program. The use of positive coping strategies was found to be associated with positive outcomes. Depression and negative beliefs, such as catastrophizing, were significantly related to more symptoms and decreased quality of life (15). In this paper we extend the work to a larger cohort of patients from two sites. Specifically, we report the results of analyses designed to answer the question of whether a set of demographic and role variables, FMS symptoms, depression, perceived control, coping strategies, and quality of life assessment could distinguish younger from older patients with FMS. © 2001 by The Haworth Press, Inc. All rights reserved.