The DOI matches its Crossref record; 32 of the 32 references it cites were found in a registry or an index.
The prognosis of functional limb weakness: a 14-year case-control study
Open accessAbstract
Reliable data on the prognosis of functional motor disorder are scarce, as existing studies of the prognosis of functional motor disorder are nearly all retrospective, small and uncontrolled. In this study we used a prospectively recruited, controlled cohort design to assess misdiagnosis, mortality and symptomatic and health outcome in patients with functional limb weakness compared to neurological disease and healthy control subjects. We also carried out an exploratory analysis for baseline factors predicting outcome. One hundred and seven patients with functional limb weakness, 46 neurological and 38 healthy control subjects from our previously studied prospective cohort were traced for follow-up after an average of 14 years. Misdiagnosis was determined in a consensus meeting using information from records, patients and their GPs. Numbers and causes of death were collected via death certificates. Outcome of limb weakness, physical and psychiatric symptoms, disability/quality of life and illness perception were recorded with self-rated questionnaires. Outcome measures were compared within and between groups. Seventy-six patients (71%) with functional limb weakness, 31 (67%) neurological and 23 (61%) healthy controls were included in follow-up. Misdiagnosis was found in one patient in the functional limb weakness group (1%) and in one neurological control (2%). Eleven patients with functional limb weakness, eight neurological control subjects and one healthy control subject had died. Weakness had completely remitted in 20% of patients in the functional limb weakness group and in 18% of the neurological controls (P = 0.785) and improved in a larger proportion of functional limb weakness patients (P = 0.011). Outcomes were comparable between patient groups, and worse than the healthy control group. No baseline factors were independent predictors of outcome, although somatization disorder, general health, pain and total symptoms at baseline were univariably correlated to outcome. This study is the largest and longest follow-up study of functional limb weakness. Misdiagnosis in functional limb weakness is rare after long-term follow-up. The disorder is associated with a higher mortality rate than expected, and symptoms are persistent and disabling. It appears difficult to predict outcome based on common baseline variables. These data should help inform clinicians to provide a more realistic outlook of the outcome and emphasize the importance of active and targeted therapy.
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“In a 14-year prospective case–control study of 89 patients with functional limb weakness published in 2019, the only person who had a diagnosis at follow-up which in hindsight may have been a better explanation for their symptoms had been diagnosed with MS. This patient had comorbid FND and MS [18].”
From Functional neurological disorder and multiple sclerosis: a systematic review of misdiagnosis and clinical overlap (2022) · cites this paper as [18]
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“This patient had comorbid FND and MS [18].”
From Functional neurological disorder and multiple sclerosis: a systematic review of misdiagnosis and clinical overlap (2022) · cites this paper as [18]
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“Clinical practice suggests that FND diagnoses do generally remain stable [7, 17, 18]”
From Functional neurological disorder and multiple sclerosis: a systematic review of misdiagnosis and clinical overlap (2022) · cites this paper as [18]
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Citations
Cites
Handbook of Clinical Neurology
Drake, M. J. (2015) · Handbook of clinical neurology · Cited by 592
The prognosis of functional (psychogenic) motor symptoms: a systematic review
Gelauff, J., Stone, J., Edwards, M., & Carson, A. (2014) · Journal of Neurology, Neurosurgery & Psychiatry · doi:10.1136/jnnp-2013-305321 · Cited by 368 · cited 4×
“As duration of symptoms has been found to be a negative prognostic factor (Gelauff et al., 2014), prognosis may be better in patients presenting to primary care or emergency settings.”
BackgroundMethodInfluentialSelf-citationSystematic review of misdiagnosis of conversion symptoms and “hysteria”
Stone, J., Smyth, R., Carson, A., Lewis, S., Prescott, R., Warlow, C., & Sharpe, M. (2005) · BMJ · doi:10.1136/bmj.38628.466898.55 · Cited by 358 · cited 1×
“Rates of diagnostic revision have been 4% since 1970 (Stone et al., 2005).”
BackgroundSelf-citationStone, J., Carson, A., Duncan, R., Coleman, R., Roberts, R., Warlow, C., Hibberd, C., Murray, G., Cull, R., Pelosi, A., et al. (2009) · Brain · doi:10.1093/brain/awp220 · Cited by 356 · cited 4×
“Not all diagnostic revision represents a ‘misdiagnosis’ and we categorized patients according to the classification of Stone et al. (2009).”
BackgroundMethodInfluentialSelf-citationSlater revisited: 6 year follow up study of patients with medically unexplained motor symptoms
Crimlisk, H. L., Bhatia, K., Cope, H., David, A., Marsden, C. D., & Ron, M. A. (1998) · BMJ · doi:10.1136/bmj.316.7131.582 · Cited by 328 · cited 5×
“The two studies that have investigated this have found no correlation between somatoform disorders and outcome (Crimlisk et al., 1998; Ibrahim et al., 2009).”
BackgroundInfluentialPsychogenic movement disorders: frequency, clinical profile, and characteristics.
Factor, S. A., Podskalny, G. D., & Molho, E. (1995) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.59.4.406 · Cited by 313 · cited 1×
“Factors that have most consistently correlated with positive outcome in the literature included an early diagnosis and short duration of symptoms at baseline (Knutsson and Mårtensson, 1985; Couprie et al., 1995; Factor et al., 1995; Mace and Trimble, 1996; Crimlisk et al., 1998; Feinstein et al., 2001; Thomas et al.,…”
BackgroundDiagnostic and pathophysiological aspects of psychogenic tremors
Deuschl, G., Köster, B., Lücking, C. H., & Scheidt, C. E. (1998) · Movement Disorders · doi:10.1002/mds.870130216 · Cited by 283 · cited 2×
“functional motor symptoms the limited available data do not provide a meaningful answer (Crimlisk et al., 1998; Deuschl et al., 1998; Feinstein et al., 2001; Stone et al., 2003).”
BackgroundThe symptom of functional weakness: a controlled study of 107 patients
Stone, J., Warlow, C. P., & Sharpe, M. (2010) · Brain · doi:10.1093/brain/awq068 · Cited by 273 · cited 2×
“Most of these factors were based on standardized questionnaires (Stone et al., 2010).”
BackgroundSelf-citationCarson, A. J., Stone, J., Hibberd, C., Murray, G. D., Duncan, R., Coleman, R. J., Warlow, C., ROBERTS, R. C., Pelosi, A. J., Cavanagh, J., et al. (2011) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.2010.220640 · Cited by 273 · cited 2×
“Our own large epidemiological study of patients presenting to neurologists with symptoms lacking a pathophysiological explanation, a wider phenotype than functional motor symptoms (Carson et al., 2011), found a much lower frequency of that diagnostic revision and highlighted that actual diagnostic error was rare (4 ou…”
BackgroundResultSelf-citationPsychiatric outcome in patients with a psychogenic movement disorder: a prospective study.
Feinstein, A., Stergiopoulos, V., Fine, J., & Lang, A. E. (2001) · PubMed · Cited by 195
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Symptom Duration and Treatment Timing as Prognostic Factors in Pediatric Functional Motor Disorders
Všianská, P., Esposito, D., Innocenti, A., Všianský, V., Špilárová, Z., Geroin, C., Tinazzi, M., Danhofer, P., & Baglioni, V. (2026) · Pediatric Neurology · doi:10.1016/j.pediatrneurol.2026.09.022
Sloan, M. A., Leschziner, G. D., Arunasalam, A., D’Cruz, D. P., Calderwood, L., Harwood, R., Kaul, A., Bosley, M., Pitkänen, M., Gnanapavan, S., et al. (2026) · Rheumatology International · doi:10.1007/s00296-026-06296-w
Metadata
- Authors
- Gelauff, J. M., Carson, A., Ludwig, L., Tijssen, M. A. J., & Stone, J.
- Affiliations
- University Medical Center Groningen (NL)
- University of Edinburgh (GB)
- Corresponding author
- Gelauff, Jeannette M
- Venue
- Brain
- Publisher
- Oxford University Press (OUP)
- Published
- 2019-06-05
- Volume
- 142
- Issue
- 7
- Pages
- 2137-2148
- ISSN
- 0006-8950 (ISSN-L)
- 1460-2156
- OpenAlex
- W2948558558
- Cited by
- 102
- References
- 32
- Citations by year
- 2026: 13 · 2025: 11 · 2024: 14 · 2023: 17 · 2022: 18 · 2021: 7 · 2020: 17 · 2019: 5
- FWCI
- 9.36
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Brain (publishedVersion, cc-by-nc)
- PubMed (publishedVersion)
- University of Groningen research database (University of Groningen / Centre for Information Technology) (publishedVersion, other-oa)
- Edinburgh Research Explorer (University of Edinburgh) (submittedVersion, cc-by-nc)
- University of Groningen research database (University of Groningen / Centre for Information Technology) (submittedVersion, other-oa)
- Funders
- NHS Research Scotland Career Fellowship
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Psychosomatic Disorders and Their Treatments
- Health Sciences › Medicine › Psychiatry and Mental health › Fibromyalgia and Chronic Fatigue Syndrome Research
- Health Sciences › Health Professions › Physical Therapy, Sports Therapy and Rehabilitation › Musculoskeletal pain and rehabilitation
- Keywords
- prognosis, misdiagnosis, mortality, disability, quality of life, illness perception, somatization disorder, long-term follow-up, prognostic factors
- MeSH terms
- Cause of Death, Diagnostic Errors, Disability Evaluation, Female, Follow-Up Studies, Humans, Male, Middle Aged, Nervous System Diseases, Prognosis, Prospective Studies, Quality of Life, Remission Induction, Time Factors, Case-Control Studies, Muscle Weakness
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