Efns guideline on the treatment of tensiontype headache report of an efns task force
European Journal of Neurology 2010, 17: 1318–1325
E F N S G U I D E L I N E S / C M E A R T I C L E
EFNS guideline on the treatment of tension-type headache –Report of an EFNS task force
L. Bendtsena, S. Eversb, M. Lindec, D. D. Mitsikostasd, G. Sandrinie and J. SchoenenfaDepartment of Neurology, Danish Headache Centre, Glostrup Hospital, University of Copenhagen, Copenhagen, Denmark; bDepartment of
Neurology, University of Mu¨nster, Mu¨nster, Germany; cInstitute of Neuroscience and Physiology, The Sahlgrenska Academy, University of
Gothenburg, Sweden and Norwegian National Headache Centre, St. Olavs Hospital, Trondheim Norway and Department of Neuroscience,
Norwegian University of Science and Technology, Trondheim, Norway; dDepartment of Neurology, Headache Clinic, Athens Naval Hospital,
Athens, Greece; eUniversity Centre for Adaptive Disorders and Headache, IRCCS C. Mondino Institute of Neurology Foundation, University
of Pavia, Pavia Italy; and fDepartment of Neurology, Headache Research Unit, University of Lie`ge, Lie`ge, Belgium
Background: Tension-type headache (TTH) is the most prevalent headache type and
is causing a high degree of disability. Treatment of frequent TTH is often difficult.
Objectives: To give evidence-based or expert recommendations for the different treat-
ment procedures in TTH based on a literature search and the consensus of an expert panel. Methods: All available medical reference systems were screened for the range of
clinical studies on TTH. The findings in these studies were evaluated according to the
recommendations of the EFNS resulting in level A, B or C recommendations andgood practice points. Recommendations: Non-drug management should always be considered although thescientific basis is limited. Information, reassurance and identification of trigger factorsmay be rewarding. Electromyography (EMG) biofeedback has a documented effect inTTH, whilst cognitive-behavioural therapy and relaxation training most likely areeffective. Physical therapy and acupuncture may be valuable options for patients withfrequent TTH, but there is no robust scientific evidence for efficacy. Simple analgesicsand non-steroidal anti-inflammatory drugs are recommended for the treatment ofepisodic TTH. Combination analgesics containing caffeine are drugs of second choice. Triptans, muscle relaxants and opioids should not be used. It is crucial to avoidfrequent and excessive use of analgesics to prevent the development of medication-overuse headache. The tricyclic antidepressant amitriptyline is drug of first choice forthe prophylactic treatment of chronic TTH. Mirtazapine and venlafaxine are drugs ofsecond choice. The efficacy of the prophylactic drugs is often limited, and treatmentmay be hampered by side effects.
meta-analyses, whilst the vast amount of uncontrolled
reports of non-drug treatment will not be considered.
These guidelines aim to give evidence-based recom-
A brief clinical description of the headache disorders is
mendations for the acute and prophylactic drug treat-
included. The definitions follow the diagnostic criteria
ment of TTH. In addition, the guidelines aim to provide
of the International Headache Society (IHS) [1].
a short overview on non-drug treatment of TTH basedon the best performed controlled trials, reviews and
Tension-type headache is classified into three subtypes
Correspondence: L. Bendtsen, Chairperson, Department of
according to headache frequency: infrequent episodic
Neurology, Danish Headache Centre, Glostrup Hospital, Universityof Copenhagen, DK-2600 Glostrup, Copenhagen, Denmark
TTH (<1 day of headache per month), frequent epi-
(tel.: +45 432 32062; fax +45 4323 3839; e-mail: larben01@glo.
sodic TTH (1–14 days of headache per month) and
chronic TTH (‡15 days per month) [1] (Table 1). This
This is a Continuing Medical Education article, and can be found with
division may seem artificial but has proved to be highly
corresponding questions on the Internet at http://www.efns.org/EFNS
relevant for several reasons. First impact on quality of
Continuing-Medical-Education-online.301.0.html. Certificates forcorrectly answering the questions will be issued by the EFNS.
life differs considerably between the subtypes. A person
European Journal of Neurology Ó 2010 EFNS
Guideline for treatment of tension-type headache
Table 1 Diagnostic criteria of tension-type headache of the IHS
class III evidence, whilst a level C rating (possibly
effective, ineffective or harmful) requires at least twoconvincing class III studies [4].
2.1 Infrequent episodic tension-type headache
A. At least 10 episodes occurring on <1 day per month on average
In general, non-pharmacological management should
(<12 days per year) and fulfilling criteria B–D
always be considered in TTH [5]. When it comes to
B. Headache lasting from 30 min to 7 days
pharmacological management, the general rule is that
C. Headache has at least two of the following characteristics:
patients with episodic TTH [1] are treated with symp-
tomatic (acute) drugs, whilst prophylactic drugs should
2. Pressing/tightening (non-pulsating) quality3. Mild or moderate pain intensity
be considered in patients with very frequent episodic
4. Not aggravated by routine physical activity such as walking or
TTH and in patients with chronic TTH [1]. Analgesics
are often ineffective in patients with chronic TTH.
Furthermore, their frequent use produces risk of tox-
1. No nausea or vomiting (anorexia may occur)
icity (e.g. kidney and liver problems) as well as of
2. No more than one of photophobia or phonophobia
2.2 Frequent episodic tension-type headache
A. At least 10 episodes occurring on ‡1 but <15 days per month
for at least 3 months (‡12 and <180 days per year) and fulfilling
A literature search was performed using the reference
databases MedLine, Science Citation Index and the
Cochrane Library; the key word used were Ôtension-type
A. Headache occurring on ‡15 days per month on average
headacheÕ (last search October 2009). In addition, a
for >3 months (‡180 days per year) and fulfilling criteria B–D
review book [7] and treatment recommendations from
B. Headache lasts hours or may be continuous
the British Association for the Study of Headache [8]
1. No more than one of photophobia, phonophobia or mild
were considered. Trials published in English and con-
ducted amongst adult patients (aged 18 and older) with
2. Neither moderate or severe nausea or vomiting
reasonable criteria designed to distinguish TTH frommigraine were considered. For drug treatments, ran-
having headache every day from the time of waking,
domized placebo-controlled trials and trials comparing
persisting until bedtime, month in and month out, is
different treatments were considered. For non-drug
disabled. At the other extreme, a mild headache once
treatments, controlled trials were considered.
every other month has very little impact on health orfunctional ability and needs little if any medical atten-
tion. Second, the pathophysiological mechanisms maydiffer significantly between the subtypes; peripheral
All authors performed an independent literature search.
mechanisms are probably more important in episodic
The first draft of the manuscript was written by the
TTH, whereas central pain mechanisms are pivotal in
chairman of the task force. All other members of the
chronic TTH [2]. Third, treatment differs between the
task force read the first draft and discussed changes by
subtypes, with symptomatic and prophylactic treat-
email. Three more drafts were then written by the
ments being more appropriate for episodic and chronic
chairman and each time discussed by email. All recom-
TTH, respectively. Therefore, a precise diagnosis is
mendations had to be agreed to by all members of the
mandatory and should be established by means of a
task force unanimously. The background of the research
headache diary [3] completed for at least 4 weeks.
strategy and of reaching consensus and the definitions
The recommendations in this article are based on the
of the recommendation levels used in this article have
scientific evidence from clinical trials and on the expert
been described in the EFNS recommendations [4].
consensus by the respective task force of the EFNS. Thelegal aspects of drug prescription and drug availability
in the different European countries will not be consid-ered. The definitions of the recommendation levels
The lifetime prevalence of TTH was as high as 78% in a
follow the EFNS criteria [4]. Briefly, a level A rating
population-based study in Denmark, but the majority had
(established as effective, ineffective or harmful) requires
episodic infrequent TTH (1 day a month or less) without
at least one convincing class I study or at least two
specific need of medical attention [9]. Nevertheless, 24–
consistent convincing class II studies. A level B rating
37% had TTH several times a month, 10% had it weekly
(probably effective, ineffective or harmful) requires at
and 2–3% of the population had chronic TTH usually
least one convincing class II study or overwhelming
lasting for the greater part of a lifetime [9,10].
Ó 2010 The Author(s)European Journal of Neurology Ó 2010 EFNS European Journal of Neurology 17, 1318–1325
The female:male ratio of TTH is 5:4 indicating that,
secondary headache is suspected (e.g. the headache
unlike migraine, women are only slightly more affected
characteristics are untypical), if the course of headache
than men [11,12]. The average age of onset of TTH is
attacks changes or if persistent neurological or psycho-
higher than that in migraine, namely 25–30 years in
pathological abnormalities are present. Significant
cross-sectional epidemiological studies [10]. The preva-
co-morbidity, e.g. anxiety or depression, should be
lence peaks between the age of 30 to 39 and decreases
identified and treated concomitantly. Poor compliance
slightly with age. Poor self-rated health, inability to
with prophylactic treatment may be a problem in chronic
relax after work and sleeping few hours per night have
TTH as it is in migraine [18]. It should be explained to the
been reported as risk factors for developing TTH [13].
patient that frequent TTH only seldom can be cured, but
A recent review of the global prevalence and burden
that a meaningful improvement often can be obtained
of headaches [11] showed that the disability of TTH as a
with the combination of drug and non-drug treatments.
burden of society was greater than that of migraine,which indicates that the overall cost of TTH is greater
than that of migraine. Two Danish studies have shownthat the number of workdays missed in the population
Acute drug therapy refers to the treatment of individual
was three times higher for TTH than for migraine
attacks of headache in patients with episodic and
[10,14], and a US study has also found that absenteeism
chronic TTH. Most headaches in patients with episodic
because of TTH is considerable [15]. The burden is
TTH are mild to moderate, and the patients often can
particularly high for the minority who have substantial
self-manage using simple analgesics (paracetamol or
and complicating co-morbidities [16].
aspirin) or non-steroidal anti-inflammatory drugs(NSAIDs). The efficacy of the simple analgesics tends todecrease with increasing frequency of the headaches. In
patients with chronic TTH, the headaches are often
TTH is characterized by a bilateral, pressing tightening
associated with stress, anxiety and depression, and
pain of mild to moderate intensity, occurring either in
simple analgesics are usually ineffective and should be
short episodes of variable duration (episodic forms) or
used with caution because of the risk of medication-
continuously (chronic form). The headache is not
overuse headache at a regular intake of simple analge-
associated with the typical migraine features as vomit-
sics above 14 days a month or triptans or combination
ing, severe photophobia and phonophobia. In the
analgesics above 9 days a month [19]. Other interven-
chronic form, only one of the latter two accompanying
tions such as non-drug treatments and prophylactic
symptoms or mild nausea is accepted [1] (Table 1).
pharmacotherapy should be considered.
Because of lack of accompanying symptoms and the
The effect of acute drugs in TTH has been examined
relatively milder pain intensity, patients are rarely
in many studies, and these have used many different
severely incapacitated by their pain. TTH is the most
methods for the measurement of efficacy. The guide-
featureless of the primary headaches, and because many
lines for drug trials in TTH from the International
secondary headaches may mimic TTH, a diagnosis of
Headache Society recommend pain-free after 2 h as the
TTH requires exclusion of other organic disorders.
primary efficacy measure [20]. This has been used insome studies whilst many studies have used other effi-cacy measures such as pain intensity difference, time to
meaningful relief. This makes comparison of results
The diagnosis of TTH is based on the typical patientÕs
A correct diagnosis should be assured by means of a
headache diary [3] recorded over at least 4 weeks. Thediagnostic problem most often encountered is to dis-
Paracetamol 1000 mg was significantly more effective
criminate between TTH and mild migraine. If the
than placebo in most [21–27] but not all [28,29] trials,
headache is strictly unilateral, the debated entity cervi-
whilst three trials found no significant effect of paraceta-
cogenic headache should be considered [17]. The diary
mol 500 mg to 650 mg compared with placebo [21,28,30].
may also reveal triggers and medication overuse, and
Aspirin has consistently been reported more effective than
it will establish the baseline against which to measure
placebo in doses of 1000 mg [21,31,32], 500 mg to 650 mg
the efficacy of treatments. Identification of a high intake
[21,32–34] and 250 mg [32]. One study found no difference
of analgesics is essential because medication overuse
in efficacy between solid and effervescent aspirin [34].
requires specific treatment [6]. Paraclinical investi-
Ibuprofen 800 mg [33], 400 mg [24,25,33,35,36] and
gations, in particular brain imaging, is necessary if
200 mg [37] are more effective than placebo, as are
European Journal of Neurology Ó 2010 EFNS European Journal of Neurology 17, 1318–1325
Guideline for treatment of tension-type headache
ketoprofen 50 mg [28,37], 25 mg [27,29,37] and 12.5 mg
between paracetamol and NSAIDs or between these
[29]. One study could not demonstrate a significant
drugs and placebo [41]. However, it is well known that
effect of ketoprofen 25 mg possibly because of a low
NSAIDs have more gastro-intestinal side effects than
number of patients [28]. Diclofenac 25 mg and 12.5 mg
paracetamol, whilst the use of large amounts of par-
have been reported effective [35], whilst there are no
acetamol may cause liver injury. Amongst the NSAIDs,
trials of the higher doses of 50–100 mg proved effective
ibuprofen seems to have the most favourable side effect
in migraine. Naproxen 375 mg [26] and 550 mg [30,38]
and metamizole 500 and 1000 mg [31] have also beendemonstrated effective. The latter drug is not available
in many countries, because it carries a minimal (if at all)risk of causing agranulocytosis. Treatment with intra-
The efficacy of simple analgesics and NSAIDs is
muscular injection of ketorolac 60 mg in an emergency
increased by combination with caffeine 64–200 mg
department has been reported effective [39].
[22,23,42–45]. There are no comparative studies exam-ining the efficacy of combination with codeine. It is
clinically well known that caffeine withdrawal can cause
There are only few studies investigating the ideal dose for
headache and chronic daily headache has been reported
drugs used for the acute treatment of TTH. One study
to be associated with use of over-the-counter caffeine
demonstrated a significant dose–response relationship of
combination products [46]. Therefore, it is probable
aspirin with 1000 mg being superior to 500 and 500 mg
that combinations of simple analgesics or NSAIDs with
being superior to 250 mg [32]. Ketoprofen 25 mg tended
caffeine are more likely to induce MOH than simple
to be more effective than 12.5 mg [29], whilst another
analgesics or NSAIDs alone. Until otherwise proven,
study found very similar effects of ketoprofen 25 and
we therefore recommend that simple analgesics or
50 mg [37]. Paracetamol 1000 mg seems to be superior to
NSAIDs are drugs of first choice and that combinations
500 mg, as only the former dose has been demonstrated
of one of these drugs with caffeine are drugs of second
effective. In lack of evidence, the most effective dose of a
choice for the acute treatment of TTH. Combinations
drug well tolerated by a patient should be chosen. Sug-
of simple analgesics with codeine or barbiturates should
gested doses are presented in Table 2.
not be used, because use of the latter drugs increases therisk of developing medication-overuse headache [46].
Comparison of simple analgesicsFive studies reported NSAIDs to be significantly more
effective than paracetamol [24,25,28–30], whilst threestudies could not demonstrate a difference [21,26,27].
Triptans have been reported effective for the treatment
Five studies have compared efficacy of different
of interval headaches [47], which were most likely mild
NSAIDs, and it has not be possible to clearly demon-
migraines [48], in patients with migraine. Triptans most
likely do not have a clinically relevant effect in patients
with TTH [49,50] and cannot be recommended. Musclerelaxants have not been demonstrated effective in epi-
sodic TTH [51]. Use of opioids increases the risk of
A thorough review of the acute drug treatment of TTH
developing medication-overuse headache [46]. Opioids
could not detect any difference in adverse events
are not recommended for the treatment of TTH.
Table 2 Recommended drugs for acute therapy of tension-type headache
Gastrointestinal side effects, risk of bleeding
Side effects as for ibuprofen, only doses of 12.5–25 mg tested in TTH
Less risk of gastrointestinal side effects compared with NSAIDs
The level of recommendation considers side effects and consistency of the studies. There is sparse evidence for optimal doses. The most effectivedose of a drug well tolerated by a patient should be chosen; NSAID, non-steroidal anti-inflammatory drugs; TTH, tension-type headache;aCombination with caffeine 65–200 mg increases the efficacy of ibuprofen [43] and paracetamol [23,42], but possibly also the risk for developingmedication-overuse headache [46,53]. Level of recommendation of combination drugs containing caffeine is therefore B.
Ó 2010 The Author(s)European Journal of Neurology Ó 2010 EFNS European Journal of Neurology 17, 1318–1325
curve (AUC) to be used as primary efficacy measure [20].
These parameters have been used in some studies, whilst
Simple analgesics and NSAIDs are the mainstays in the
other studies have used other efficacy measures such as
acute therapy of TTH (Table 2). Paracetamol 1000 mg is
pain reduction from baseline, headache intensity. This
probably less effective than the NSAIDs but has a better
makes comparison of results between studies difficult.
gastric side effect profile [52]. Ibuprofen 400 mg may berecommended as drug of choice amongst the NSAIDs
because of a favourable gastrointestinal side effect pro-file compared with other NSAIDs [52]. Combination
Lance and Curran [54] reported amitriptyline 10–25 mg
analgesics containing caffeine are more effective than
three times daily to be effective, whilst Diamond and
simple analgesics or NSAIDs alone but are regarded by
Baltes [55] found amitriptyline 10 mg/day but not 60 mg/
some experts [53] to more likely induce medication-
day to be effective. Amitriptyline 75 mg/day was reported
overuse headache. Physicians should be aware of the risk
to reduce headache duration in the last week of a 6-week
of developing medication-overuse headache as a result of
study [56], whilst no difference in effect size between ami-
frequent and excessive use of all types of analgesics in
triptyline 50–75 mg/day or amitriptylinoxide 60–90 mg/
acute therapy [6]. Triptans, muscle relaxants and opioids
day and placebo was found in one study [57]. However,
do not play a role in the treatment of TTH.
also the frequencies of side effects were similar on ami-
Although simple analgesics and NSAIDs are effective
triptyline and placebo in the latter study. The inability to
in episodic TTH, the degree of efficacy has to be put in
detect the well-known side effects of amitriptyline suggests
perspective. For example, the proportion of patients that
insensitivity of the trial for reasons which remain obscure.
were pain-free 2 h after treatment with paracetamol
Bendtsen et al. [58] found that amitriptyline 75 mg daily
1000 mg, naproxen 375 mg and placebo were 37%, 32%
reduced the area-under-the-headache curve (calculated as
and 26%, respectively [26]. The corresponding rates for
headache duration times headache intensity) by 30%
paracetamol 1000 mg, ketoprofen 25 mg and placebo
compared with placebo, which was highly significant.
were 22%, 28% and 16% in another study with 61%,
Holroyd and colleagues [59] treated patients with antide-
70% and 36% of subjects reporting worthwhile effect,
pressants (83% took amitriptyline median dose 75 mg
respectively [27]. Thus, efficacy is modest, and there is
daily and 17% took nortriptyline median dose 50 mg
clearly room for better acute treatment of episodic TTH.
daily) and compared this with stress management therapyand with a combination of stress management and anti-depressant treatment. After 6 months, all three treatments
reduced headache index with approximately 30% more
Simple analgesics and non-steroidal anti-inflammatory
than placebo, which was highly significant.
drugs are recommended for the treatment of episodicTTH. Combination analgesics containing caffeine are
drugs of second choice. It is crucial to avoid frequentand excessive use of analgesics to prevent the develop-
The tricyclic antidepressant clomipramine 75–150 mg
ment of medication-overuse headache.
daily [60] and the tetracyclic antidepressants maprotiline75 mg daily [61] and mianserin 30–60 mg daily [60] havebeen reported more effective than placebo. Interestingly,
some of the newer more selective antidepressants with
Prophylactic pharmacotherapy should be considered in
action on serotonin and noradrenaline seem to be as
patients with chronic TTH, and it can be considered in
effective as amitriptyline with the advantage that they
patients with very frequent episodic TTH. Co-morbid
are tolerated in doses needed for the treatment of a
disorders, e.g. overweight or depression, should be taken
concomitant depression. Thus, the noradrenergic and
into account. For many years, the tricyclic anti-
specific serotonergic antidepressant mirtazapine 30 mg/
depressant amitriptyline has been used. More lately
day reduced headache index by 34% more than placebo
other antidepressants, NSAIDs, muscle relaxants,
in difficult to treat patients without depression including
anticonvulsants and botulinum toxin have been tested in
patients who had not responded to amitriptyline [62].
chronic TTH. The effect of prophylactic drugs in TTH
The efficacy of mirtazapine was comparable to that of
has been examined in surprisingly few placebo-con-
amitriptyline reported by the same group [58]. A sys-
trolled studies, which have used different methods for
tematic review concluded that the two treatments may be
the measurement of efficacy. The guidelines for drug
equally effective for the treatment of chronic TTH [63].
trials in TTH from the International Headache Society
The serotonin and noradrenaline reuptake inhibitor
recommend days with TTH or area-under-the-headache
venlafaxine 150 mg/day [64] reduced headache days
European Journal of Neurology Ó 2010 EFNS European Journal of Neurology 17, 1318–1325
Guideline for treatment of tension-type headache
from 15 to 12 per month in a mixed group of patients
Table 3 Recommended drugs for prophylactic therapy of tension-type
with either frequent episodic or chronic TTH. Low-dose
mirtazapine 4.5 mg/day alone or in combination with
ibuprofen 400 mg/day was not effective in chronic TTH.
The selective serotonin reuptake inhibitors (SSRIs),
citalopram [58] and sertraline [65], have not been found
more effective than placebo. SSRIÕs have been compared
with other antidepressants in six studies. These studies
were reviewed in a Cochrane analysis that concluded
that SSRIÕs are less efficacious than tricyclic antide-
pressants for the treatment of chronic TTH [66].
The level of recommendation considers side effects and number andquality of the studies.
There have been conflicting results for treatment withthe muscle relaxant tizanidine [61,67], whilst theNMDA-antagonist memantine was not effective [68].
dose [58]. Therefore, it is advisable to change to other
Botulinum toxin has been extensively studied [69–79]. It
prophylactic therapy, if the patient does not respond
was concluded in a systematic review that botulinum
after 4 weeks on maintenance dose. The side effects of
toxin is likely to be ineffective or harmful for the
amitriptyline include dry mouth, drowsiness, dizziness,
treatment of chronic TTH [63]. The prophylactic effect
obstipation and weight gain. Mirtazapine, of which the
of daily intake of simple analgesics has not been studied
major side effects are drowsiness and weight gain, or
in trials that had this as the primary efficacy parameter,
venlafaxine, of which the major side effects are vomiting,
but explanatory analyses indicated that ibuprofen
nausea, dizziness and loss of libido, should be considered
400 mg/day was not effective in one study [80]. On the
if amitriptyline is not effective or not tolerated. Dis-
contrary, ibuprofen increased headache compared with
continuation should be attempted every 6–12 months.
placebo indicating a possible early onset of medication-
The physician should keep in mind that the efficacy of
overuse headache [80]. Topiramate [81] and buspirone
preventive drug therapy in TTH is often modest and that
[82] have been reported effective in open-label studies.
the efficacy should outweigh the side effects.
Amitriptyline has a clinically relevant prophylactic
Amitriptyline is drug of first choice for the prophylactic
effect in patients with chronic TTH and should be drug
treatment of chronic TTH. Mirtazapine and venlafax-
of first choice (Table 3). Mirtazapine or venlafaxine are
probably effective, whilst the older tricyclic and tetra-cyclic antidepressants, clomipramine, maprotiline and
mianserin, may be effective. A recent systematic review[63] concluded that amitriptyline and mirtazapine are
Information, reassurance and identification of trigger
the only forms of treatment that can be considered
proven beneficial for the treatment of chronic TTH. However, the last search was performed in 2007 before
Non-drug management should be considered for all
publication of the study on venlafaxine [64].
patients with TTH and is widely used. However, the
Amitriptyline should be started at low dosages
scientific evidence for efficacy of most treatment
(10–25 mg/day) and titrated by 10–25 mg weekly until
modalities is sparse [83–86]. The very fact that the
the patient has either good therapeutic effect or side
physician takes the problem serious may have a thera-
effects are encountered. It is important that patients are
peutic effect, particularly if the patient is concerned
informed that this is an antidepressant agent but has an
about serious disease, e.g. brain tumour, and can be
independent action on pain. The maintenance dose is
reassured by thorough examination. Identification of
usually 30–75 mg daily administered 1–2 h before bed-
trigger factors should be performed, as coping with
time to help to circumvent any sedative adverse effects.
triggers may be of value [87]. The most frequently
The effect is not related to the presence of depression
reported triggers for TTH are stress (mental or physi-
[58]. A significant effect of amitriptyline may be
cal), irregular or inappropriate meals, high intake or
observed already in the first week on the therapeutic
withdrawal of coffee and other caffeine containing
Ó 2010 The Author(s)European Journal of Neurology Ó 2010 EFNS European Journal of Neurology 17, 1318–1325
Table 4 Non-pharmacological treatments for tension of tension-type
cause of low power there is conflicting evidence to
support or refute the effectiveness of EMG biofeedbackcompared with placebo or any other treatments [85].
However, a recent extensive and thorough meta-anal-
ysis including 53 studies concluded that biofeedback
has a medium-to-large effect. The effect was found to be
long lasting and enhanced by combination with relax-
ation therapy [97]. The majority of the studies included
employed EMG biofeedback. It was not possible todraw reliable conclusions as to whether the effect dif-
The level of recommendation considers number and quality of thestudies.
fered between patients with episodic and chronic TTH.
drinks, dehydration, sleep disorders, too much or too
The aim of cognitive-behavioural therapy is to teach the
little sleep, reduced or inappropriate physical exercise,
patient to identify thoughts and beliefs that generate
psycho-behavioural problems as well as variations
stress and aggravate headaches. These thoughts are then
during the female menstrual cycle and hormonal sub-
challenged, and alternative adaptive coping self-
stitution [88–90]. It has been demonstrated that stress
instructions are considered. A variety of exercises may be
induces more headache in patients with chronic TTH
used to challenge thoughts and beliefs, including exper-
than in healthy controls probably through hyperalgesic
imenting with adoption of another personÕs view of the
effects on already sensitized pain pathways [91].
situation, actively generating other possible views of a
Information about the nature of the disease is
situation and devising a behavioural experiment to test
important. It can be explained that muscle pain can lead
the validity of a particular belief [96]. One study found
to a disturbance of the brainÕs pain-modulating mech-
cognitive-behavioural therapy, treatment with tricyclic
anisms [2,92,93], so that normally innocuous stimuli are
antidepressants and a combination of the two treatments
perceived as painful, with secondary perpetuation of
better than placebo with no significant difference
muscle pain and risk of anxiety and depression. The
between treatments [59], whilst another study reported
prognosis in the longer run was found to be favourable
no difference between cognitive-behavioural therapy and
in a population-based 12-year epidemiological follow-
amitriptyline [98]. Cognitive-behavioural therapy may
up study, because approximately half of all individuals
be effective but there is no convincing evidence [63,85].
with frequent or chronic TTH had remission of theirheadaches [13]. It is not known whether the same is true
for individuals who seek medical consultation.
The goal of relaxation training is to help the patient torecognize and control tension as it arises in the courseof daily activities. Relaxation training involves a range
of affective, cognitive and behavioural techniques, such
A large number of psycho-behavioural treatment strat-
as breathing exercises and meditation. Relaxation
egies have been used to treat chronic TTH. EMG bio-
training has been compared with no treatment or
feedback, cognitive-behavioural therapy and relaxation
waiting list control [99–103] and with other interven-
training have been investigated the most. However, only
tions [104–107]. A recent review concluded that there is
few trials have been performed controlled with sufficient
conflicting evidence that relaxation is better than no
power and clear outcome measures [85]. Hypnotherapy
treatment, waiting list or placebo [85].
has been reported effective [94], but there is not con-vincing evidence for its effect in TTH [85,95].
ConclusionsEMG biofeedback has an effect in TTH, whilst cogni-
tive-behavioural therapy and relaxation training may
The aim of EMG biofeedback is to help the patient to
have an effect in TTH, but at this moment, there is no
recognize and control muscle tension by providing
convincing evidence to support this [63,85]. These
continuous feedback about muscle activity. Sessions
treatments are relatively time-consuming, but unfortu-
typically include an adaptation phase, baseline phase,
nately, there are no documented guidelines for which
training phase where feedback is provided and a self-
psycho-behavioural treatment(s) to choose for the
control phase where the patient practices controlling
individual patient. Therefore, until scientific evidence is
muscle tension without the aid of feedback [96]. A
provided, common sense must be used. Thus, it is likely
recent review including 11 studies concluded that be-
that cognitive-behavioural therapy will be most bene-
European Journal of Neurology Ó 2010 EFNS European Journal of Neurology 17, 1318–1325
Guideline for treatment of tension-type headache
ficial for the patient where psycho-behavioural prob-
[110,113,127], relaxation [113] or a combination of
lems or affective distress play a major role [96], whilst
massage and relaxation [128]. Collectively, these trials
biofeedback or relaxation training may be preferable
suggest slightly better results for some outcomes with the
latter therapies according to the recent Cochrane anal-ysis [86]. Together, the available evidence suggests thatacupuncture could be a valuable option for patients
suffering from frequent TTH, but more research is nee-
Physical therapy is widely used for the treatment of
ded before final conclusions can be made.
TTH and includes the improvement of posture, mas-
A recent study reported no effect of greater occipital
sage, spinal manipulation, oromandibular treatment,
nerve block in patients with chronic TTH [129].
exercise programs, hot and cold packs, ultrasound andelectrical stimulation, but the majority of these modal-
ities have not been properly evaluated [108]. Activetreatment strategies are generally recommended [108].
Non-drug management should always be considered
A recent review concluded that exercise may have a
although the scientific basis is limited (Table 4). Infor-
value for TTH [109]. Carlson et al. [110] reported better
mation, reassurance and identification of trigger factors
effect of physiotherapy than acupuncture. A controlled
may be rewarding. EMG biofeedback has a docu-
study [111] combined various techniques such as mas-
mented effect in TTH, whilst cognitive-behavioural
sage, relaxation and home-based exercises and found a
therapy and relaxation training most likely are effective,
modest effect. It was reported that adding craniocervi-
but there is no convincing evidence. Physical therapy
cal training to classical physiotherapy was better than
and acupuncture may be valuable options for patients
physiotherapy alone [112]. A recent study found no
with frequent TTH, but there is no robust scientific
significant long-lasting differences in efficacy amongst
relaxation training, physical training and acupuncture[113]. Spinal manipulation has no effect in episodic
TTH [114] and no convincing effect in chronic TTH[115,116]. Oromandibular treatment with occlusal
These recommendations should be updated within
splints is often recommended but has not yet been tes-
ted in trials of reasonable quality and cannot be rec-ommended in general [117]. There is no firm evidence
for efficacy of therapeutic touch, cranial electrotherapyor transcutaneous electrical nerve stimulation [84].
The present guidelines were developed without external
It can be concluded that there is a huge contrast
financial support. The authors report the following
between the widespread use of physical therapies and
financial supports: Lars Bendtsen: Salary by Glostrup
the lack of robust scientific evidence for efficacy of these
University Hospital. Honoraria in 2009 from MSD and
therapies and that further studies of improved quality
Pfizer; Stefan Evers: Salary by the University of Mu¨n-
are necessary to either support or refute the effective-
ster. Honoraria or grants by Addex Pharma, AGA
ness of physical modalities in TTH [84,108,118,119].
Medical Corporation, Allergan, AstraZeneca, BerlinChemie, Boehringer Ingelheim, CoLucid, Desitin, Eisai,GlaxoSmithKline, Ipsen, Janssen-Cilag, Merz, MSD,
Novartis, Pfizer, Reckitt-Benckiser and UCB; Mattias
The prophylactic effect of acupuncture has been inves-
Linde: Salary from the Cephalea Headache Centre and
tigated in several trials in patients with frequent episodic
Gothenburg University, Sweden. Honoraria or grants
or chronic TTH. A review [63] and a meta-analysis [120]
in 2009 from Allergan, AstraZeneca, MSD and The
concluded that there is no evidence for efficacy of acu-
Swedish Migraine Association; Dimos D. Mitsikostas:
puncture in TTH. Two trials reported better effect of
Salary by Athens Naval Hospital. Honoraria or grants
acupuncture than basic care or waiting list but no better
for 2009 by Bayer-Schering, Janssen-Cilag, Lilly, Merk-
effect of Chinese acupuncture when compared to sham
Serono, Novartis, MSD and UCB; Giorgio Sandrini:
acupuncture [121,122], whilst a recent Cochrane analysis
Salary from University of Pavia. Honoraria in 2009
[86] concluded that there was overall a slightly better
from Allergan, Solvay Pharma and Newrons Alpha and
effect from acupuncture than from sham acupuncture
Jean Schoenen: Salary from the University of Lie`ge.
based on the results from five trials [122–126]. Four
Honoraria or grants in 2009 from Janssen-Cilag, GSK,
Ó 2010 The Author(s)European Journal of Neurology Ó 2010 EFNS European Journal of Neurology 17, 1318–1325
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