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Abstract and Figures

Functional somatic syndrome (FSS) occurs in as many as 30% of patients in general medical practice, but it is infrequently a topic of formal instruction. Many physicians feel uncomfortable with medically unexplained symptoms and are unfamiliar with how to assess or manage them. Traditional medical approaches can be ineffective and can contribute to iatrogenic or adverse physiologic effects in patients. Physicians treating patients with FSS should not only consider standard medical tests, but they should also try to gain a deeper behavioral understanding of the mind-body connections that underlie the presenting symptoms. Osteopathic physicians, with their emphasis on holistic patient care, are in a key position to treat patients with FSS. This review provides a brief recapitulation of the literature and illustrates key factors in the assessment and management of FSS.
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Functional Somatic Syndrome: Assessment and
Management
Christopher J. Graver, PhD
Financial Disclosures:
None reported.
Support: None reported.
Disclaimer: The views
expressed herein are those of
the authors and do not
necessarily reect the ofcial
policy or position of the
Department of the Army,
Department of Defense, or the
US Government.
Address correspondence to
Christopher J. Graver, PhD,
Neuropsychology, MCHJ-
CLU-CP, 9040 Jackson Ave,
Tacoma, WA 98431-1100.
E-mail:
christopher.j.graver.civ@
mail.mil
Submitted
March 02, 2017;
revision received
May 12, 2017;
accepted
June 14, 2017.
Functional somatic syndrome (FSS) occurs in as many as 30% of patients in
general medical practice, but it is infrequently a topic of formal instruction.
Many physicians feel uncomfortable with medically unexplained symptoms
and are unfamiliar with how to assess or manage them. Traditional medical
approaches can be ineffective and can contribute to iatrogenic or adverse
physiologic effects in patients. Physicians treating patients with FSS should
not only consider standard medical tests, but they should also try to gain a
deeper behavioral understanding of the mind-body connections that underlie
the presenting symptoms. Osteopathic physicians, with their emphasis on
holistic patient care, are in a key position to treat patients with FSS. This
review provides a brief recapitulation of the literature and illustrates key
factors in the assessment and management of FSS.
J Am Osteopath Assoc. 2017;117(8):511-519
doi:10.7556/jaoa.2017.101
Keywords: functional somatic syndrome, medical unexplained symptoms, somatic symptoms
Functional somatic syndrome (FSS) has been around for thousands of years.
1
Various terminology has been used to describe FSS throughout the years, includ-
ing hysteria,somatoform disorders,medically unexplained symptoms, and fash-
ionable illnesses.
1
Current terminology in the Diagnostic and Statistical Manual of
Mental Disorders, fth edition,
2
includes somatic symptom disorder,conversion dis-
order, and illness anxiety disorder. However, for the purposes of the present review, the
term functional somatic syndrome will be used to describe a combination of symptoms
that cannot be fully explained by pathologic conditions or diseases and that cause func-
tional impairment or disruption of everyday activities, without evidence of the patient
intentionally feigning their symptoms. Functional somatic syndrome is a term that
patients nd minimally offensive when describing their condition, but it is not suggested
as formal diagnostic terminology.
2
The aim of this review is to impart a framework for
successful assessment and treatment of patients with FSS.
Functional somatic syndrome is commonly encountered in the general and specialty
health care settings.
3
A review on the prevalence of somatoform disorders and medically
unexplained symptoms in primary care found that at least 1 medically unexplained
symptom was observed in 40% to 49% of all primary care patients.
4
In a neurologic prac-
tice, approximately one-third of new patients were found to have symptoms not fully
explained by neurologic causes.
5
Nevertheless, physicians fail to consider FSS in the dif-
ferential diagnosis as much as 90% of the time when presented with nonspecic symp-
toms that are unexplained by medical tests or known diseases.
6
Additionally, physicians
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The Journal of the American Osteopathic Association August 2017 |Vol 117 |No. 8 511
are more likely to seek to medically explain symptoms
regardless of the available evidence.
7
In the present
article, I review the literature on FSS and describe
assessment and management techniques for this
condition.
Assessment and Diagnosis
Appropriate diagnosis of FSS is just as important as
that of medically explained illnesses, and the rate of
misdiagnosis in patients presenting with FSS is only
about 4%.
8
Failing to consider FSS can result in detri-
mental outcomes from both the clinical and economic
perspective. Patients with FSS present with nonspecic
symptoms that typically include myalgia, joint pain,
back pain, headache, fatigue, feeling faint or dizzy,
chest pain, heart palpitations, trembling, diarrhea and
constipation, insomnia, and cognitive issues (eg, lack
of attention, loss of memory). These symptoms are
often within the realm of normal human experience.
9
Clusters of nonspecic symptoms have been labeled as
chronic fatigue syndrome, Lyme disease, bromyalgia,
irritable bowel syndrome, and atypical chest pain.
10
Henningsen et al
11
described nearly 30 different labels
for conditions in which patients present with FSS.
Nevertheless, several studies have found that symptoms
do not cluster into easily dened, distinct syndromes
and should not be presumed to be independent.
12,13
When symptoms are clustered into groups, managing
subsets of those symptoms as unique conditions can
lead to misdiagnosis, ineffective treatment, and failure
to recognize and manage the underlying cause of the
individual symptoms.
Patients with FSS have been shown to have more
than twice the use and costs of health care services
than a patient with a medically-conrmed illnesses.
14,15
For example, Sicras-Mainar et al
16
found that compared
with a reference population, patients with bromyalgia
had 5010 more in health care costs, had more
comorbidities, had an average of 6 more outpatient
visits annually, missed more days of work, and used
more pain-relieving medication. Also, patients with
bromyalgia were more likely to undergo surgical pro-
cedures compared with patients with a rheumatic dis-
order.
16
From a clinical perspective, as many as 55%
of patients with FSS whose symptoms are managed
with standard medical approaches will experience
adverse effects because the underlying cause of the
symptoms is not addressed.
17
Functional somatic syndrome has a strong correlation
to psychological conditions, such as depression and
anxiety, as well as a history of trauma or abuse.
Depressive episodes, negative life events, the number
of medically unexplained symptoms at baseline, attri-
butional style, autonomic sensations, and catastrophic
cognitions should be considered when a patient pre-
sents with FSS.
18
Studies found that 80% of people
with FSS had a history of an anxiety or depressive dis-
order, per standard diagnostic criteria,
15
and people
with a history of anxiety or depressive disorders were
nearly 3 times more likely to have FSS.
19
In another
study,
18
investigators examined a sample of patients in
Health Maintenance Organization plans and found that
half of the patients in the top 10% of ambulatory care
users had anxiety, depression, or somatization.
Functional somatic syndrome has also been asso-
ciated with a history of childhood abuse or neglect.
20
Bonvanie et al
21
discovered that stressful life events in
adolescence were associated with FSS, even when
adjusting for levels of functional somatic symptoms,
anxiety and depression symptoms, and socioeconomic
status before the stressful life event. In an epidemiolo-
gic study of more than 1200 women, Walker et al
22
concluded that the number of symptoms without clear
medical explanation that a patient presented with dir-
ectly correlated to the number of reported adverse
childhood experiences. In addition, FSS can develop
as a result of natural life stressors. For example, after
the San Francisco Bay Area earthquake of 1989, a
sample of residents reported signicantly greater
numbers and frequency of dissociative symptoms,
including derealization and depersonalization; distor-
tions of time; and alterations in cognition, memory,
and somatic sensations up to 4 months after the
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512 The Journal of the American Osteopathic Association August 2017 |Vol 117 |No. 8
earthquake compared with their baseline symptoms 1
week before the earthquake.
23
These nonspecic cogni-
tive and somatic symptoms represent a subjective index
of affective distress with low correlations to objective
testing.
24,25
Although patients with FSS report more symptoms
and higher degrees of disability than those with trad-
itionally dened medical or psychological conditions,
physicians may perceive symptom severity and disabil-
ity as less severe when the symptoms are not medically
supported.
7
Apex clinical care is always a goal, but
many physicians are not trained in how to assess or
manage symptoms of FSS. A survey of medical stu-
dents in the United Kingdom showed that no specic
course covered the topic of FSS, and, if the topic was
covered, it was inconsistent and disparate across
medical schools.
26
In my experience, this lack of train-
ing regarding FSS and discrete medical proles can
lead to physicians feeling mild discomfort or anxiety
and resentment when patients present with FSS. These
feelings can also stem from limited exposure and train-
ing in enhanced care, which includes a treatment model
that draws on explanations for symptoms in broad biop-
sychosocial terms, in general practice settings.
27
Osteopathic physicians, with their holistic approach to
patient care, are in a unique and advantageous position
to offer enhanced care to patients with FSS.
Unreported stressors may be the most damaging to
physical and mental health, whereas disclosure of stres-
sors can result in improved measures of cellular
immune system function and fewer health care visits.
28
Stressors may go unreported because it may be more
comfortable for patients with FSS to focus on physical
symptoms rather than exploring mental stressors.
29
It
is critical to investigate FSS symptoms in the context
of ongoing stress, but patients may experience this
assessment as hostile and adversarial. If an adversarial
mindset dominates the encounter, then exploring psy-
chosocial factors becomes difcult. Page and Wessely
7
proposed that such encounters can be viewed by
patients as rejecting, colluding, or empowering.
Patients who feel rejected will continue to seek other
opinions and resources (eg, outpatient visits, emer-
gency department visits, medical tests and procedures,
medication).
7
Physicians who collude with patients
can encourage iatrogenic illness and overuse of
medical tests, often with adverse effects.
7
Collaborating with patients and empowering them to
be a part of controlling their symptoms is the most
benecial approach for the patient, the physician, the
patients family, and the health care system because
these patients are less likely to feel rejected, can work
with the physician on proposed treatments, and are
less likely to seek unnecessary resources.
7
Patients with FSS must be approached differently
than other patients. The physician must keep in mind
that, despite research
28,29
showing a strong association
with psychological factors, patients with FSS
often present with only physical symptoms.
30
Well-documented stressors, medical history, and behav-
ioral health conditions are imperfectly recalled and
make the prospect of illusory mental health likely to
be unintentional.
31
For example, as many as 40% of
people who had documented abuse in childhood fail to
report it, even if they are directly questioned about it.
32
Patients with FSS also tend be biased in their recall of
symptoms before an onset marker (the start of the rst
symptoms identied by the patient to cause a change
in their health) and may minimize past symptoms.
33
Furthermore, they are more likely to incorrectly report
previous medical diagnoses or test ndings and over-
pathologize their medical history than patients with a
conrmed disease.
34
On the one hand, directly con-
fronting the lack of evidence for a conrmed medical
cause of a patients symptoms is likely to put them on
the defensive and leave them feeling rejected. On the
other hand, accepting subjective reports without skepti-
cism or objective evidence can lead to collusion.
Contrary to many patients, those with FSS become
more anxious when more tests are run, even if the
results are negative.
17
These patients tend to catastro-
phize their illness as being rare and serious if it cannot
be detected by standard tests and even minor or
irrelevant abnormalities in the results become
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The Journal of the American Osteopathic Association August 2017 |Vol 117 |No. 8 513
hypothesis-generating, which then increases their
anxiety.
7
The Figure illustrates this cycle.
Physicians can take certain actions to aid in a posi-
tive patient-physician relationship, including listening
openly, documenting a detailed medical history, and
documenting the exhaustive list of symptoms.
35
This
approach includes asking about the onset and course
of the symptoms and, specically, how patients are
functionally limited by the symptoms. Part of this
initial encounter includes gently probing for life stres-
sors, particularly in a manner that allows the patient to
begin to externalize the source of stress.
35
It is also
helpful to ask similar questions in multiple different
ways to ensure consistency and limit corroboration.
Often, the particular end-state behavioral manifestation
of FSS relates to modeling, which highlights the
importance of asking whether the patient knows
anyone with a similar condition.
35
If patients have
been evaluated or treated for FSS before, it is important
to ask about their previous experiences to ensure that
negative experiences are not repeated and expectations
can be accurately managed. Then, a routine physical
examination and basic tests (eg, complete blood cell
count, comprehensive metabolic panel, thyroid-
stimulating hormone test) can be ordered, per the physi-
cians judgment. Once an organic cause has been
excluded, further examination and investigation should
only be initiated if new symptoms develop.
7
Given the
complex nature of the symptoms and history presented
by patients with FSS, it can be benecial to both the
patient and the physician to develop visual aids, as sug-
gested by Stone et al,
35
that document patientssymp-
toms, stress level, and duration of symptoms.
Stone et al
36
reported that more than 90% of patients
with FSS found it offensive to be told that their symp-
toms were all in the mind, and as many as 50% of
patients with FSS considered it offensive to be told
their condition was psychosomatic or medically unex-
plained.
36
Fewer patients with FSS (<15%) took
offensetoatermlikefunctional somatic to describe
their symptoms. Patients with FSS respond in a more
positive way when they are offered reassurance (eg, I
have looked carefully, and there seems to be nothing
of serious or life-threatening concern) and a functional
approach to management (eg, Your body is not
working as well as it should,”“Perhaps your body is
trying to tell you something,”“Everyone copes with
stress in different ways) than being told overtly there
is no medical explanation for their symptoms or trying
to convince them of an isolated psychological cause.
37
Because psychological symptoms frequently remain
unrecognized or untreated in patients with FSS, these
patients will often express dismay, trepidation, or even
rejection of suggestions to see a behavioral health
Figure.
The presentation and assessment cycle of a patient with functional somatic syndrome.
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514 The Journal of the American Osteopathic Association August 2017 |Vol 117 |No. 8
professional.
38
They may feel as though the physician
is rejecting their claim to legitimate medical symptoms
and abandoning them. Physicians can have more
success with patients by standing with them and
helping them to understand the results of medical tests
completed in terms of a broad umbrella of factors
inuencing their condition.
Management
There are 3 common ways that patients with FSS react
to their symptoms.
39
Patients who sought to understand
the psychological and physical interplays of their symp-
toms had better success in life; patients who sought
symptom relief and legitimization from physicians
were less able to carry out independent activities of
dailylivingandfeltentitledtobeexcusedfrom
normal social obligations; and patients who expressed
worry about missed diagnoses sought excessive
medical help, protested when their demands for investi-
gations or treatments were resisted, and were not reas-
sured by negative test results or their physicians
benign assessment.
39
Although patients with FSS can have positive medical
test results that indicate an underlying physiological
issue, the resulting symptoms and disabilities are not
entirely explained by or are more severe than expected
by the organic syndrome alone.
40
An FSS can have
physiologic examination ndings associated with it,
because it is causing real symptoms, but one must be
cognizant that it is also signicantly overrepresented in
terms of comorbid psychological conditions.
27
Functional somatic syndrome with physiologic examin-
ation ndings associated with them share more similar-
ities than differences with other symptoms of FSS in
terms of management; thus, behavioral health treatment
remains an integral part of optimal management.
41,42
Positive functional restoration outcomes (the ability to
engage in independent activities of daily living) are more
likely when physicians take a collaborative approach with
patients.
43
Collaborating with patients includes changing
their attitudes about their symptoms, helping them to
understand that their symptoms are not life-threatening
or disabling, and alleviating dysfunctional thoughts that
create anxiety regarding their health.
37
A qualitative
review of different ways to manage symptoms of FSS
suggests that a combination of the following 3 factors is
most effective: (1) create a nonthreatening, therapeutic
environment; (2) provide interventions that do not
require specialized training in behavioral health (eg,
motivational interviewing, tangible explanations, reassur-
ance, regularly scheduled appointments); and (3) recom-
mend specic interventions with behavioral health
specialists and psychotropic medication.
44
Researchers
have suggested different approaches to the treatment of
patients with FSS: an organ-oriented approach (ie, symp-
tomatic treatment), acognitive interpersonal approach (ie,
cognitive processing of health-related anxiety), or a con-
textual approach (cultural beliefs, workplace character-
istics, incentives).
11
Regarding the latter approach, the
family system should be kept in mind as well. An associ-
ation has been found between FSS behaviors and
attention-seeking or withdrawal behaviors of signicant
others.
45
It has also been found that dependency on a sig-
nicant other predicted greater long-term health care use
(>90 days), and yet, a literature search revealed no studies
of families of patients with FSS.
45
Patient-physician
visits that include a brief physical examination instead
of ordering tests based on subjective reports of symptoms
translates to decreased health care use and better physical
functioning in patients with FSS, even though this
approach may run counter to most medical training.
46
The most consistent nding in randomized controlled
trials (RCTs) has been the benet of cognitive behavioral
therapy in patients with FSS. A study
44
concluded that
cognitive behavioral therapy is an evidence-based treat-
ment for FSS. Several reviews also found evidence sup-
porting the use of cognitive behavioral therapy in the
management of FSS.
41,42
In a review of RCTs, 85% of
the included studies showed that the use of cognitive
behavioral therapy signicantly beneted patients with
FSS.
47
In a meta-analysis of 27 studies, cognitive behav-
ioral therapy had a small to moderate positive effect in
patients with FSS.
48
A study that examined patients in
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The Journal of the American Osteopathic Association August 2017 |Vol 117 |No. 8 515
secondary care clinics with chronic fatigue syndrome
showed that 3 to 14 sessions of cognitive behavioral
therapy resulted in reduced fatigue and increased phys-
ical function.
49
In another study, patients with FSS who
completed an average of 7 cognitive behavioral therapy
sessions reported fewer days spent in the hospital and
fewer visits to the emergency department, suggesting
that the sessions helped patients avoid catastrophizing
physiologic experiences that can lead to emergent,
costly care.
50
In a small pilot study examining the use
of cognitive behavioral therapy in a primary care
setting, a 1-hour initial session and three 20-minute ses-
sions had an effect size of 0.5 for physical symptom
reduction, and 72% of patients with FSS reported that
the intervention helped them to effectively cope with
their symptoms.
51
In a meta-analysis of 13 RCTs exam-
ining mindfulness-based stress reduction and cognitive
therapies, a small to moderate positive effect was found
on pain, symptom severity, depression, anxiety, and
quality of life in patients with FSS that underwent these
therapy sessions.
In addition to positive patient outcomes, cognitive
behavioral therapy is also a cost-effective way to manage
FSS.
52
When comparing the effect of mindfulness
therapy with medical care from a specialist, Fjorback
et al
53
showed that after 15 months of treatment, about
half as many patients in the mindfulness therapy group
were receiving disability, and their total direct health
care costs were an average of $1754 less, including the
cost of therapy, than those in the specialist care group.
A Cochrane review that analyzed the use of medica-
tion to manage symptoms in patients with FSS found
that there was no evidence supporting the efcacy of tri-
cyclic antidepressants over a placebo, and there was low-
quality evidence of benet from new-generation antide-
pressants and natural products, such as St. Johns
wort.
54
Data have shown that escitalopram is more
effective than placebo in managing FSS at 6 and 12
weeks, but long-term term follow-up information is not
available.
55
The benet of antidepressants is conicting,
though, as a study found that symptoms in patients with
FSS in the otolaryngologic region could be successfully
managed with selective serotonin reuptake inhibitors.
56
Systematic reviews examining FSS have indicated that
antidepressants can be benecial even if overt evidence
of depression is not present,
57
but Stone et al
37
sug-
gested that patients should be informed that their symp-
toms can improve without medication, and this option
is merely to explore all avenues of treatment.
Physical treatments (ie, exercise, autogenic training,
progressive muscle relaxation) for patients with FSS
have shown promise in a number of studies. A
Cochrane review showed that exercise has positive
effects on sleep habits, fatigue, physical functioning,
and self-perceived health in patients with FSS,
similar to the effects of cognitive behavioral therapy,
with no documented adverse effects.
58
Graded exer-
cise therapy is the most frequent physical treatment
recommended, with programs emphasizing the role
of physiologic dysregulation to manage fatigue. An
RCT that compared the effects of graded exercise
therapy with that of conventional medical care in
patients with chronic fatigue syndrome showed that
the exercise group had greater improvement in symp-
toms and less fatigue than the standard medical care
group.
59
In another study examining patients with
chronic fatigue syndrome, 69% attained adequate
physical functioning on the SF-36 physical function-
ing subscale
60
after participating in a graded exercise
therapy program vs 6% of control patients.
61
In add-
ition, cognitive behavioral therapy combined with
graded exercise therapy has led to clinically signi-
cant benet for multiple conditions, including
chronic fatigue syndrome and bromyalgia.
62,63
Additionally, a 10-week RCT
64
was conducted to
compare psychophysiologic management strategies
(eg, stress education, heart rate variability training,
progressive muscle relaxation with electromyography
feedback, autogenic training) with visits with a psychi-
atric physician for care while waiting for psychophysio-
logic treatment. The psychophysiologic treatmentonly
group showed a decrease in depressive and physical
symptoms and an increase in functional abilities by the
end of the treatment.
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516 The Journal of the American Osteopathic Association August 2017 |Vol 117 |No. 8
Many other options have been suggested for the man-
agement of symptoms of FSS, including standard
medical treatments (eg, medication, surgical procedures),
reattribution therapy, psychodynamic therapy, hypnosis,
and herbal remedies, but these either do not have support
in the empirical literature or the support they have is based
on anecdotal evidence, case studies, or small case series
without appropriate comparison groups, including sham
or placebo procedures, and without appropriate blinding
to the treatment groups, raising their risk of bias.
Conclusion
Patients with FSS present a unique challenge to physi-
cians, as these patients do not have conrmatory
medical ndings to explain their symptoms, and trad-
itional approaches to management of symptoms, such
as medication, are unlikely to be benecial in isolation.
Although they can be complex, perplexing, and enig-
matic, the symptoms of FSS are no less real or debilitat-
ing than those caused by medically explained illnesses,
and these patients are no less deserving of medical
attention. Symptoms of FSS can be successfully
managed if physicians take a collaborative and inclusive
approach to care. Positive outcomes do not depend on
convincing patients of the psychological nature of their
symptoms. Instead, physicians can best care for these
patients by helping them recognize the multitude of
factors that may be affecting their lives and working to
restore them to healthy functioning. Osteopathic
physicians are in a prime position to provide this
comprehensive biopsychosocial approach to care that
can lead to optimal outcomes in patients with FSS.
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© 2017 American Osteopathic Association
Whats on Your Mind?
The Journal of the American Osteopathic Association invites readers to submit personal
reections, essays stories, poetry, and perspectives to its humanities section, In Your Words.
For submission requirements, visit http://jaoa.org/ss/authors.aspx.
REVIEW
The Journal of the American Osteopathic Association August 2017 |Vol 117 |No. 8 519
... Functional somatic syndromes (FSS) are a group of persistent chronic pain syndromes where symptoms cannot be explained by physical or structural bodily defects or somatic disease [1]. Many terms have been used to describe FSS including hysteria, somatoform disorders, medically unexplained symptoms, and fashionable illnesses with somatic symptom disorder (SSD), conversion disorder, and illness anxiety disorder described in the Diagnostic and Statistical Manual of Mental Disorders, 5th edition [2]. FSS are considered as dysautonomia [3], i.e., a medical issue arising from the autonomic nervous system. ...
... Treatment options for FSS patients remain under question, with exercise, diet, cognitive behavioural therapy (CBT), and sleep recommended for preventing an FSS flare-up. CBT appears most beneficial in the treatment of FSS [2]. Regular exercise improves sleep, fatigue, and physical function in FSS patients having similar benefits to CBT. ...
... Studies reporting the efficacy of antidepressant drug therapy for the treatment of FSS are lacking. Indeed, some studies report a lack of efficacy of antidepressant therapy in FSS patients [2]. Typically, non-steroidal anti-inflammatory therapeutics are ineffective in FSS. ...
Article
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Functional somatic syndromes are increasingly diagnosed in chronically ill patients presenting with an array of symptoms not attributed to physical ailments. Conditions such as chronic fatigue syndrome, fibromyalgia syndrome, or irritable bowel syndrome are common disorders that belong in this broad category. Such syndromes are characterised by the presence of one or multiple chronic symptoms including widespread musculoskeletal pain, fatigue, sleep disorders, and abdominal pain, amongst other issues. Symptoms are believed to relate to a complex interaction of biological and psychosocial factors, where a definite aetiology has not been established. Theories suggest causative pathways between the immune and nervous systems of affected individuals with several risk factors identified in patients presenting with one or more functional syndromes. Risk factors including stress and childhood trauma are now recognised as important contributors to chronic pain conditions. Emotional, physical, and sexual abuse during childhood is considered a severe stressor having a high prevalence in functional somatic syndrome suffers. Such trauma permanently alters the biological stress response of the suffers leading to neuroexcitatory and other nerve issues associated with chronic pain in adults. Traumatic and chronic stress results in epigenetic changes in stress response genes, which ultimately leads to dysregulation of the hypothalamic-pituitary axis, the autonomic nervous system, and the immune system manifesting in a broad array of symptoms. Importantly, these systems are known to be dysregulated in patients suffering from functional somatic syndrome. Functional somatic syndromes are also highly prevalent co-morbidities of psychiatric conditions, mood disorders, and anxiety. Consequently, this review aims to provide insight into the role of the nervous system and immune system in chronic pain disorders associated with the musculoskeletal system, and central and peripheral nervous systems.
... Persistent chronic pain conditions like fibromyalgia, myalgic encephalomyelitis (ME)/chronic fatigue syndrome (CFS), IBS and TMJ are defined as functional somatic syndromes where symptoms cannot be explained by physical damage or disease and a psychological explanation is proposed (42,43). Our study found that the majority of hEDS/HSD and fibromyalgia patients self-reported subluxations, dislocations (hEDS) and other joint issues like TMJ. ...
Article
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Background Joint pain is a common symptom in patients with hypermobile Ehlers-Danlos Syndrome (hEDS), hypermobility spectrum disorders (HSD) and fibromyalgia. The goal of this study was to determine whether symptoms and comorbidities overlap in patients diagnosed with hEDS/HSD and/or fibromyalgia. Methods We retrospectively examined self-reported data from an EDS Clinic intake questionnaire in patients diagnosed with hEDS/HSD, fibromyalgia, or both vs. controls with an emphasis on joint issues. Results From 733 patients seen at the EDS Clinic, 56.5% (n = 414) were diagnosed with hEDS/HSD and fibromyalgia (Fibro), 23.8% (n = 167) hEDS/HSD, 13.3% (n = 98) fibromyalgia, or 7.4% (n = 54) none of these diagnoses. More patients were diagnosed with HSD (76.6%) than hEDS (23.4%). Patients were primarily White (95%) and female (90%) with a median age in their 30s (controls 36.7 [18.0, 70.0], fibromyalgia 39.7 [18.0, 75.0], hEDS/HSD 35.0 [18.0, 71.0], hEDS/HSD&Fibro 31.0 [18.0, 63.0]). There was high overlap in all 40 symptoms/comorbidities that we examined in patients diagnosed with fibromyalgia only or hEDS/HSD&Fibro, regardless of whether they had hEDS or HSD. Patients that only had hEDS/HSD without fibromyalgia had far fewer symptoms/comorbidities than patients with hEDS/HSD&Fibro. The top self-reported issues in patients that only had fibromyalgia were joint pain, hand pain when writing or typing, brain fog, joint pain keeping from daily activities, allergy/atopy and headache. Five issues that significantly and uniquely characterized patients diagnosed with hEDS/HSD&Fibro were subluxations (dislocations in hEDS patients), joint issues like sprains, the need to stop sports due to injuries, poor wound healing, and migraine. Conclusion The majority of patients seen at the EDS Clinic had a diagnosis of hEDS/HSD plus fibromyalgia that was associated with more severe disease. Our findings indicate that fibromyalgia should be routinely assessed in patients with hEDS/HSD and vis-a-versa to improve patient care.
... Some individuals with mental distress may only present with physical symptoms, while they deny any mental symptoms [12]. These individuals are typically referred to non-psychiatric wards and may be diagnosed with conditions, such as medically unexplained symptoms and functional somatic syndromes, or conditions with unknown origins, as conventional medical tests and examinations do not explain their subjective symptoms [13,14]. However, these patients often respond positively to treatments with antidepressants and anxiolytics, indicating that the etiopathology of mental distress may be associated with chronic stress-induced dysfunctions of brain activity [15][16][17]. ...
Article
Full-text available
Identifying mental distress is a complex task, particularly when individuals experience physical symptoms. Traditional self-report questionnaires that detect psychiatric symptoms using emotional words may not work for these individuals. Consequently, there is a need for a screening tool that can identify both the physical and mental symptoms of mental distress in individuals without a clinical diagnosis. Our study aimed to develop and validate a scale that measures mental distress by measuring the extent of brain overwork, which can be extrapolated as the burden of mental distress. In this population-based cross-sectional study, we recruited a total of 739 adults aged 16–65 years from 64 sampling centers of a cohort in Mongolia to validate a 10-item self-report questionnaire. Internal consistency was measured using McDonald’s ω coefficient. Test–retest reliability was analyzed using intraclass correlation coefficients. Construct and convergent validities were examined using principal component analysis (PCA) and confirmatory factor analysis (CFA). The Hospital Anxiety and Depression Scale (HADS) and the abbreviated version of World Health Organization Quality of Life (WHOQOL-BREF) were used to evaluate criterion validity. Among the participants, 70.9% were women, 22% held a bachelor’s degree or higher, 38.8% were employed, and 66% were married. The overall McDonald’s ω coefficient was 0.861, demonstrating evidence of excellent internal consistency. The total intraclass correlation coefficient of the test–retest analysis was 0.75, indicating moderate external reliability. PCA and CFA established a three-domain structure that provided an excellent fit to the data (RMSEA = 0.033, TLI = 0.984, CFI = 0.989, χ2 = 58, p = 0.003). This 10-item scale, the Brain Overwork Scale (BOS-10), determines mental distress in three dimensions: excessive thinking, hypersensitivity, and restless behavior. All the items had higher item-total correlations with their corresponding domain than they did with the other domains, and correlations between the domain scores had a range of 0.547–0.615. BOS-10 correlated with HADS, whereas it was inversely correlated with WHOQOL-BREF. In conclusion, the results suggest that BOS-10 is a valid and reliable instrument for assessing mental distress in the general population. The scale screens for mental distress that is characterized by subjective symptoms such as excessive thinking, hypersensitivity, and restless behavior. The current findings also demonstrate that the BOS-10 is quantitative, simple, and applicable for large group testing. This scale may be useful for identifying at-risk individuals who may require further evaluation and treatment for mental distress.
... However, the symptoms can be successfully managed when practitioners take a collaborative and inclusive approach to care by helping patients recognize the multitude of factors that may be affecting their lives and working with them to restore healthy functioning. According to Graver [42], osteopathic practitioners are in an ideal position to provide this type of comprehensive biopsychosocial approach to care for optimal outcomes in patients with MUS. ...
Article
Full-text available
Historical osteopathic principles and practices (OPP)—considering the patient as a dynamic interaction of the body, mind, and spirit and incorporating the body’s self-healing ability into care—are inherited from traditional/complementary and alternative (CAM) principles. Both concepts are familiar to contemporary osteopathic practitioners, but their incorporation into healthcare for evidence-informed, patient-centered care (PCC) remains unclear. Further, a polarity exists in the osteopathic profession between a ‘traditional-minded’ group following historical OPP despite evidence against those models and an ‘evidence-minded’ group following the current available evidence for common patient complaints. By shifting professional practices towards evidence-based practices for manual therapy in line with the Western dominant biomedical paradigm, the latter group is challenging the osteopathic professional identity. To alleviate this polarity, we would like to refocus on patient values and expectations, highlighting cultural diversity from an anthropological perspective. Increasing an awareness of diverse sociocultural health assumptions may foster culturally sensitive PCC, especially when including non-Western sociocultural belief systems of health into that person-centered care. Therefore, the current medical anthropological perspective on the legacy of traditional/CAM principles in historical OPP is offered to advance the osteopathic profession by promoting ethical, culturally sensitive, and evidence-informed PCC in a Western secular environment. Such inclusive approaches are likely to meet patients’ values and expectations, whether informed by Western or non-Western sociocultural beliefs, and improve their satisfaction and clinical outcomes.
... 41 FSS are characterized by a combination of symptoms that cannot be fully explained by pathologic conditions or diseases and cause a gradual impairment to everyday life. 42 Apart from fibromyalgia, other common syndromes that belong to this group are irritable bowel syndrome (IBS), chronic fatigue syndrome (CFS), and functional dyspepsia (FD). 41 The association between OAB and these syndromes has been discussed before. ...
Article
Full-text available
Background Overactive bladder is a common syndrome that significantly affects the quality of life. Fibromyalgia is characterized by widespread pain, impacting patients' lives. The exact mechanisms of the two syndromes remain unknown, but there is an overlap between the suspected pathophysiologies. Objective To present an overview of the current research on the association between overactive bladder (OAB) and fibromyalgia. Search strategy A systematic search of four electronic databases was conducted. Search strategy Studies examining the correlation between OAB and fibromyalgia with female patients aged over 18 years were included. Data collection and analysis Two reviewers screened the studies for eligibility. Eligible studies were screened for quality. A meta‐analysis was performed for eligible studies. Main results Seven studies were included in the final review, of which six presented a positive association between the syndromes. The studies demonstrated a positive association between fibromyalgia and the severity of OAB and an adverse effect on the quality of life related to OAB. A mean effect size of 1.96 (95% confidence interval 0.85–3.06) was calculated. Conclusion OAB and fibromyalgia are both complex and multifactorial syndromes. The study presents an association between them, but additional studies on the topic should be conducted for a more precise conclusion.
Article
Full-text available
In Mongolia, there is limited data on the prevalence and correlates of common mental health conditions. This study addresses this data gap by exploring anxiety, depression, and brain overwork. The aim of this study was to determine normative data on these conditions in the general population of Mongolia. This nationwide, population-based, cross-sectional study was conducted in 48 sampling centers across Mongolia in 2020. A total of 613 participants (190 men and 423 women) with a mean age of 41.8 ± 12.4 years were recruited. The participants completed the Hospital Anxiety and Depression Scale (HADS) and the Brain Overwork Scale (BOS-10). Vital signs, body measurements, and lifestyle determinants were also assessed. The prevalence of anxiety was 9.9%, depression was 4.9%, and brain overwork was 18.3% among the participants. Anxiety and depression were correlated with brain overwork symptoms. Brain overwork was associated with young age, unemployment, low income, and alcohol use. These findings suggest that anxiety, depression, and brain overwork are a significant problem in the general population of Mongolia. Further research is needed to develop effective interventions to reduce the prevalence and risk factors of anxiety, depression, and brain overwork.
Article
Study Design Systematic Review Objective To perform a systematic review assessing the relationship between functional somatic syndromes (FSSs) and clinical outcomes after spine surgery. Methods A systematic review of online databases (PubMed and Web of Science) through December 2021 was conducted via PRISMA guidelines to identify all studies investigating the impact of at least one FSS (fibromyalgia, irritable bowel syndrome (IBS), chronic headaches/migraines, interstitial cystitis, chronic fatigue syndrome, multiple chemical sensitivity) on outcomes after spine surgery. Outcomes of interest included patient reported outcome measures (PROMs), postoperative opioid use, cost of care, complications, and readmission rates. Results A total of 207 records were identified. Seven studies (n = 40,011 patients) met inclusion criteria with a mean MINORS score of 16.6 out of 24. Four studies (n = 21,086) reported postoperative opioid use; fibromyalgia was a strong risk factor for long-term opioid use after surgery whereas the association with chronic migraines remains unclear. Two studies (n = 233) reported postoperative patient reported outcome measures (PROMs) with mixed results suggesting a possible association between fibromyalgia and less favorable PROMs. One study (n = 18,692) reported higher postoperative complications in patients with fibromyalgia. Conclusion Patients with fibromyalgia and possibly migraines are at higher risk for prolonged postoperative opioid use and less favorable PROMs after spine surgery. There is limited research on the relationship between other Functional somatic syndromes (FSSs) and outcomes following spine surgery. Growing evidence suggests the variation in outcomes after spine procedures may be attributed to non-identifiable organic patient factors such as FSSs.
Article
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In this proof-of-concept study, we used a systems perspective to conceptualize and investigate treatment-related dynamics (temporal and cross-sectional associations) of symptoms and elements related to the manifestation of a common functional somatic syndrome (FSS), Globus Sensations (GS). We analyzed data from 100 patients (M = 47.1 years, SD = 14.4 years; 64% female) with GS who received eight sessions of group psychotherapy in the context of a randomized controlled trial (RCT). Symptoms and elements were assessed after each treatment session. We applied a multilevel graphical vector-autoregression (ml GVAR) model approach resulting in three separate, complementary networks (temporal, contemporaneous, and between-subject) for an affective, cognitive, and behavioral dimension, respectively. GS were not temporally associated with any affective, cognitive, and behavioral elements. Temporally, catastrophizing cognitions predicted bodily weakness (r = 0.14, p < 0.01, 95% confidence interval (CI) [0.04–0.23]) and GS predicted somatic distress (r = 0.18, p < 0.05, 95% CI [0.04–0.33]). Potential causal pathways between catastrophizing cognitions and bodily weakness as well as GS and somatic distress may reflect treatment-related temporal change processes in patients with GS. Our study illustrates how dynamic NA can be used in the context of outcome research.
Article
Purpose: To perform a systematic review assessing the relationship between functional somatic syndromes (FSSs) and patient-reported outcome measures (PROMs), post-operative opioid consumption, and hospitalization costs after shoulder and elbow surgery. Methods: A systematic review of the PubMed and Web of Science databases was conducted according to PRISMA guidelines to identify all studies evaluating the effect of having at least 1 FSS (fibromyalgia, irritable bowel syndrome, chronic headaches, chronic low back pain) on outcomes after shoulder and elbow surgeries. Outcomes of interest included postoperative analgesic use, patient reported outcome measures (PROMs), and hospitalization costs. Results: The review identified a total of 320 studies, of which 8 studies met the inclusion criteria. The total number of participants in our 8 included studies was 57,389. Three studies (n=620) reported PROMs. These studies demonstrated that the presence of at least one FSS is predictive of significantly higher pain scores and lower quality of recovery, DASH, ASES, and SANE scores postoperatively. Although scores were inferior in among patients with FSS, two of the three studies showed improvement in PROMs in this group of patients. Seven studies (n= 56,909) reported postoperative opioid use. Of these, 5 reported that a diagnosis of at least one FSS was a strong risk factor for long-term opioid use after surgery. One study (n= 480) found that time-driven activity-based costs were significantly higher in patients with FSSs. Conclusions: Patients with functional somatic syndromes have less favorable PROMs postoperatively, consume more opioids postoperatively, and have higher healthcare costs after elective shoulder and elbow procedures. While PROMs among patients with FSSs are inferior compared to those without FSSs, PROMs still improve compared to baseline. Level of evidence: Level III, systematic review of Level II-III studies.
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Individuals presenting with atypical, medically unexplained symptoms can present a challenge for clinicians in determining the source of such symptoms, as well as their accuracy. Neuropsychologists are in a unique position to consider the accuracy of symptom presentation and cognitive performance through the use of symptom and performance validity tests (SVTs and PVTs, respectively). In a forensic or disability setting, where external incentives are present and evidence of response bias exists, the clinician may report findings to a third party with no responsibility to or relationship with the individual examined. However, in clinical settings, the clinician has a treating relationship that entails broader responsibilities and collaboration, necessitating management and integration of response bias into the explanation of examination results, subsequent treatment recommendations, and overall clinical care. For these reasons, it is pertinent that clinicians understand diagnostic criteria, prevalence, and clinical features of conditions that accompany medically unexplained symptoms, including how individuals with these clinical conditions might perform on neuropsychological testing.
Article
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Because of the recurrent nature of depression, there is a need for a rapid means of screening for history of depression that is either valid in itself or an efficient means of identifying respondents needing further assessment. This study examined the validity and efficiency of assessment of lifetime history of depression by self-report screening questions in comparison with the results of a structured interview assessment conducted a year earlier. Self-reported lifetime 2-week mood disturbance was unrelated to the results of the earlier interview. Self-report of treated episodes of mood disturbance were related to interview-assessed history of depression, but too modestly for practical applications. Self-report of past depression was more strongly related to concurrent distress than to the earlier interview assessment of history of depression. Implications of these findings for screening and assessment of history of depression are discussed.
Article
Full-text available
The purpose of this study was to investigate the effect of negative life events on functional somatic symptoms (FSSs) in adolescents, based on data from 957 participants of the population cohort TRacking Adolescents' Individual Lives Survey. Life events experienced between age 16 and age 19 were assessed with the Kendler's Life Stress interview. FSSs at age 19 and age 16 were measured with the Youth and Adult Self-Report. The hypotheses were tested by the use of a latent change model. Life events predicted FSSs, even when adjusted for pre-event levels of FSSs, symptoms of anxiety and depression, and socio-economic status (B = 0.006, 95% CI [0.003, 0.008], β = .32). Whereas illness-related life events did not predict FSSs independently (B = -0.003, 95% CI [-0.005, 0.09], β = .05), non-illness-related life events did (B = 0.007, 95% CI [0.004, 0.010], β = .31). A past-year diagnosis of anxiety and/or depression had a significant influence on the association between life events and FSSs (B = 0.37, 95% CI [0.30, 0.46], β = .71), while female sex, exposure to childhood adversities, and family malfunctioning had not. In conclusion, our findings show that FSSs are associated with negative life events in older adolescents. We did not find evidence for stronger effects of illness-related events.
Article
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The literature contains variable figures on the prevalence of somatoform disorders and medically unexplained symptoms in primary care. The pertinent literature up to July 2014 was retrieved by a systematic search in the PubMed/MEDLINE, PsychInfo, Scopus, and Cochrane databases. The methodological quality and heterogeneity (I2) of the retrieved trials were analyzed. The prevalence rates of medically unexplained symptoms, somatoform disorders, and their subcategories were estimated, along with corresponding 95% confidence intervals (CI), with the aid of random-effects modeling. From a total of 992 identified publications, 32 studies from 24 countries involving a total of 70 085 patients (age range, 15-95 years) were selected for further analysis. All had been carried out between 1990 and 2012. The primary studies were more heterogeneous overall; point prevalences for the strict diagnosis of a somatization disorder ranged from 0.8% (95% CI 0.3-1.4%, I2 = 86%) to 5.9% (95% CI 2.4-9.4%, I2 = 96%), with higher estimated prevalences in studies that applied less restrictive diagnostic criteria. At least one type of somatoform disorder was diagnosable by DSM-IV and/or ICD-10 criteria in a fraction of primary-care patients that ranged from 26.2% (95% CI 19.1-33.3%, I2 = 98%) to 34.8% (95% CI 26.6-44.6%; I2 = 92%). The percentage of patients complaining of at least one medically unexplained symptom ranged from 40.2% (95% CI 0.9-79.4%; I2 = 98%) to 49% (95% CI 18-79.8%, I2 = 98%). The quality of the studies, in general, was only moderate. No relationship was found between study quality and prevalence estimates. The statistical heterogeneity of the included studies is very high. Somatoform disorders and medically unexplained symptoms are more common than generally assumed. The found prevalences highlight the importance of these conditions in primary care.
Article
Objective Patients with functional somatic syndromes (FSS) such as fibromyalgia and chronic fatigue syndrome have a poor outcome and can incur high healthcare and societal costs. We aimed to compare the medium-term (16 months) cost-effectiveness and the long-term (40 months) economic outcomes of a bespoke cognitive-behavioural group treatment (STreSS) with that of enhanced usual care (EUC). Methods We obtained complete data on healthcare and indirect costs (i.e. labour-marked-related and health-related benefits) from public registries for 120 participants from a randomised controlled trial. Costs were calculated as per capita public expenses in 2010 €. QALYs gained were estimated from the SF-6D. We conducted a medium-term cost-effectiveness analysis and a long-term cost-minimization analysis from both a healthcare (i.e. direct cost) and a societal (i.e. total cost) perspective. Results In the medium term, the probability that STreSS was cost-effective at thresholds of 25,000 to 35,000 € per QALY was 93 - 95 % from a healthcare perspective, but only 50 - 55 % from a societal perspective. In the long term, however, STreSS was associated with increasing savings in indirect costs, mainly due to a greater number of patients self-supporting. When combined with stable long-term reductions in healthcare expenditures, there were total cost savings of 7,184 € (95 % CI 2,271 to 12,096, p=0.004) during the third year after treatment. Conclusion STreSS treatment costs an average of 1545 €. This cost was more than offset by subsequent savings in direct and indirect costs. Implementation could both improve patient outcomes and reduce costs.
Article
Background: Reliable longitudinal data of patients with functional somatic symptoms in general practice are lacking. Aims: To identify distinctive features in patients with chronic functional somatic symptoms, and to determine whether these symptoms support the hypothesis of the existence of specific somatic syndromes. Design of Study: Observational study, with a comparison control group. Setting: Four primary care practices affiliated with the university of Nijmegen in the Netherlands. Method: One hundred and eighty-two patients diagnosed between 1998 and 2002 as having chronic functional somatic symptoms and 182 controls matched by age, sex, socioeconomic status were included. Data on comorbidity referrals, diagnostic tests, and hospital admissions over a period of 10 years prior to the diagnosis were collected. Medication use and number of visits to the general practitioner (GP) were extracted from the moment computerised registration was started. Results: In the 10 years before the diagnosis of chronic functional somatic symptoms, significantly more patients than controls presented functional somatic symptoms in at least two body systems, and used more somatic and psychotropic drugs. They visited the GP twice as much, statistically had significantly more psychiatric morbidity, and were referred more often to mental health workers and somatic symptoms than for controls, but hospital admissions rates were equal. Conclusion: Patients with chronic functional somatic symptoms have a great diversity of functional somatic symptoms. They use more somatic and psychotropic drugs than controls in the years before diagnosis. Moreover, they show high rates of referrals and psychiatric morbidity. The diversity of symptoms of patients with chronic functional somatic symptoms supports the concept that symptoms do not cluster in well defined distinct syndromes. Therefore, patients and chronic functional somatic symptoms should preferably not be classified into medical subspecialty syndromes.