#2239 Association between chronic pain, quality of life and perceived social support among patients on maintenance hemodialysis
Abstract Background and Aims Chronic pain is a common health problem among maintenance hemodialysis (HD) patients. Its multifactorial origin may be related to underlying renal disease, comorbidities, or dialysis treatment itself. Nevertheless, there is a lack of consistent data quantifying the burden of chronic pain in this population and its association with quality of life (QoL). This study aimed to examine the prevalence and characteristics of chronic pain in patients treated with chronic HD, and assess its relationship with QoL and perceived social support. Method This cross-sectional study involved 120 maintenance HD patients. General demographic, clinical and laboratory data were collected from the patient's medical records. The Brief Pain Inventory was used to evaluate determinants of chronic pain: prevalence, pain severity and pain interference with daily activities. Pain chronicity was specified by persisting or recurring pain for at least 3 months. Quality of life (QoL) was assessed with a 36-item Short-Form Health Survey (SF36), yielding two summary measures: the Physical Component Summary (PCS), defined by dimensions of physical functioning, physical role, bodily pain and general health; and the Mental Component Summary (MCS), which includes dimensions of vitality, social functioning, role emotional and mental health. Higher scores indicated better QoL. The Multidimensional Scale of Perceived Social Support (MPSS) was used to measure individual perception of support. Results were analyzed with adequate descriptive statistics, T-test for parametric data and Hi-square or Fisher's exact test for frequencies. Results The study population included 71 (59%) males, mean age 62.9 ± 11.01 years, dialysis vintage 4–283 months (Med 54), body mass index 24.6 ± 4.5. Diabetes, secondary hyperparathyroidism and hypertension were present in 37%, 23.3% and 87.5% of cases respectively. Charlson's Comorbidity Index was 6.13 ± 2.23. Only 12.5% of patients lived alone, whereas others resided with spouses, children, or both (31.7%, 21.7% and 34.2% respectively). Two-thirds of patients (80; 66.7%) suffered from chronic pain. Pain severity was reported as mild, moderate or severe by 57.5%, 27.5% and 15.0% of subjects respectively. The patients rated pain interference with daily activity as none, mild, moderate and strong in 17.5%, 15.0%, 36.3% and 31.3% of cases respectively. The majority reported one (41.3%) or two (25.0%) areas affected with pain, most commonly the knees (26.%) and lumbosacral region (19%). Half of the patients (50.5%) used pain medications, while 74.4% practised alternative methods for pain relief. Only 8.9% reported successful pain management. The majority of patients perceived high social support (85.8%) Patients with chronic pain had significantly lower PCS (41.0 ± 19.7 vs 60.0 ± 19.4; P < 0.001), MCS (54.4 ± 22.9 vs 68.0 ± 22.5; P = 0.003), and total SF36 score (47.7 ± 19.8 vs 64.0 ± 19.4; P < 0.001), indicating significantly worse QoL compared to patients without pain. Patients with perceived lower social support also had significantly lower PCS (37.5 ± 20.1 vs 49.0 ± 21.4; P = 0.04), MCS (43.1 ± 19.3 vs 61.5 ± 23.3; P = 0.003), and total SF36 score (40.3 ± 19.0 vs 55.3 ± 20.7; P = 0.06). There was no significant difference in pain severity (4.9 ± 2.9 vs 3.8 ± 1.9, P = 0.095) and pain interference (4.3 ± 2.8 vs 4.0 ± 2.8, P = 0.688) between patients with moderate and high social support respectively. Patients with moderate support reported significantly less painful spots (2.5 ± 2.2 vs 4.0 ± 3.7, P = 0.048). Conclusion Maintenance HD patients are commonly affected by chronic pain which significantly impacts their QoL. Patients mostly perceived high social support, which was associated with better QoL. Pain is generally undermanaged in HD population and strategies are needed to address this matter systematically.
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