ArticleBMC health services research2013
Patients with unexplained physical symptoms have poorer quality of life and higher costs than other patient groups: a cross-sectional study on burden.
Article in BMC health services research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 3 of them syntheses that pooled it.
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Who cites it
45 citing papers in PubMed, 3 syntheses or guidelines pooled it.
- Pooled it
- Tests for central sensitization in general practice: a Delphi study.BMC family practice · 2021Pooled it
- Cost-effectiveness of interventions for medically unexplained symptoms: A systematic review.PloS one · 2018Pooled it
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- Predictors for use of psychosocial services in patients with metastatic colorectal cancer receiving first line systemic treatment.BMC cancer · 2019Trial
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- Patient-reported symptoms in predicting the subsequent progression of chronic health conditions among childhood cancer survivors.Communications medicine · 2026Article
- Symptom burden in middle-aged women, the role of immigrant status.BMC public health · 2025Article
- Early Symptom Warnings and Long-Term Health Conditions in Childhood Cancer Survivors: Insights from the Childhood Cancer Survivor Study and St. Jude Lifetime Cohort Study.Research square · 2025Article
- Outcome measurement in functional neurological disorder: A qualitative study on the views of patients, caregivers and healthcare professionals.Journal of neurology · 2025Article
- Global research status and trends of somatic symptom disorder: A bibliometric study.World journal of psychiatry · 2025Article
- Alexithymia mediates the pathway from negative life events to somatic symptoms: a cross-sectional study in a psychosomatic outpatient sample.Frontiers in psychiatry · 2025Article
- Health symptoms and post-COVID-19: Comparing symptomatic groups based on self-reported and primary care data.PloS one · 2025Article
- Explaining persistent physical symptoms to patients in general practice: can tests to measure central sensitisation add value? A mixed-methods study.BMC primary care · 2024Article
- Article
- The role of fatigue in patients with complex regional pain syndrome.Journal of neurology · 2024Article
- Optimism, Resilience, and General Self-Efficacy Predict Lower Somatic Burden during the COVID-19 Pandemic.Healthcare (Basel, Switzerland) · 2024Article
- The burden of persistent symptom diagnoses in primary care patients: a cross-sectional study.Scandinavian journal of primary health care · 2024Article
- Somatic symptoms in schizophrenia: Association with socio-demographic and clinical characteristics, disability and quality of life.Indian journal of psychiatry · 2023Article
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Abstract
backgroundTo determine whether healthcare resources are allocated fairly, it is helpful to have information on the quality of life (QoL) of patients with Unexplained Physical Symptoms (UPS) and on the costs associated with them, and on how these relate to corresponding data in other patient groups. As studies to date have been limited to specific patient populations with UPS, the objective of this study was to assess QoL and costs in a general sample of patients with UPS using generic measures.
methodsIn a cross-sectional study, 162 patients with UPS reported on their QoL, use of healthcare resources and lost productivity in paid and unpaid work. To assess QoL, the generic SF-36 questionnaire was used, from which multidimensional quality-of-life scores and a one-dimensional score (utility) using the SF-6D scorings algorithm were derived. To assess costs, the TiC-P questionnaire was used.
resultsPatients with UPS reported a poor QoL. Their QoL was mostly decreased by limitations in functioning due to physical health, and the least by limitations in functioning due to emotional problems. The median of utilities was 0.57, and the mean was 0.58 (SD = .09).The cost for the use of healthcare services was estimated to be €3,123 (SD = €2,952) per patient per year. This cost was enlarged by work-related costs: absence from work (absenteeism), lower on-the-job productivity (presenteeism), and paid substitution of domestic tasks. The resulting mean total cost was estimated to be €6,815 per patient per year.
conclusionsThese findings suggest that patients with UPS have a high burden of disease and use a considerable amount of healthcare resources. In comparison with other patient groups, the QoL values of patients with UPS were among the poorest and their costs were among the highest of all patient groups. The burden for both patients and society helps to justify the allocation of sufficient resources to effective treatment for patients with UPS.
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