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ben_uk
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Excellent CH article in The Lancet
« on: Sep 8th, 2005, 7:38pm » |
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Cluster headache: pathogenesis, diagnosis, and management
The Lancet 2005; 366:843-855 DOI:10.1016/S0140-6736(05)67217-0
http://www.thelancet.com/journals/lancet/article/PIIS0140673605672170/fu lltext
http://download.thelancet.com/pdfs/journals/0140-6736/PIIS01406736056721 70.pdf
Here is a small sample from the article:-
“Cluster headache is a stereotyped primary pain syndrome characterised by strictly unilateral severe pain, localised in or around the eye and accompanied by ipsilateral autonomic features. The syndrome is characterised by the circadian rhythmicity of the short-lived attacks, and the regular recurrence of headache bouts, which are interspersed by periods of complete remission in most individuals. Headaches often start about 1–2 h after falling asleep or in the early morning, and show seasonal variation, suggesting that the hypothalamus has a role in the illness. Consequently, the vascular theory has been superseded by recognition that neurovascular factors are more important. The increased familial risk suggests that cluster headache has a genetic component in some families. Neuroimaging has broadened our pathophysiological view and has led to successful treatment by deep brain stimulation of the hypothalamus. Although most patients can be treated effectively, some do not respond to therapy. Fortunately, time to diagnosis of cluster headache has improved. This is probably the result of a better understanding of the pathophysiology in combination with efficient treatment strategies, leading to a broader acceptance of the syndrome by doctors……
Why do cluster headache attacks start and, more importantly, why do they stop after a fairly defined period of time? What exactly causes the switch from inactive to active periods, and vice versa? The role of the human clock system implicates the suprachiasmatic nucleus and, consequently, photoperiod changes have been thought to be a crucial external factor. However, this theory implies that light therapy should work, whereas in my experience it does not. Moreover, melatonin has no effect, and in most patients the circadian rhythm is indeed stereotyped (highly homogeneous), whereas the annual rhythm is highly individual.
The relevance of the high proportion of smokers among patients with cluster headache is not known. In the active period, cluster headache is reliably triggered by alcohol, histamine, and nitrates,8 but the mechanism whereby these factors induce an attack is not understood. One common feature of histamine, alcohol, and nitrates is their vasodilating effect. Nitroglycerin is a pro-drug for nitric oxide, which can activate the trigeminal vascular system. However, recent data indicate that neither the vessels nor the peripheral part of the trigeminal system are needed in development of a full-blown attack.
The mechanism of the effectiveness of oxygen in treating cluster headache is not understood. Reductions in cerebral blood flow, cerebral vasoconstriction, activation of descending inhibitory neurons from the brainstem, and an abnormal chemoreceptor sensitivity in cluster headache have been suggested. Notably, none of the preventive medicines used in cluster headache are given on the basis of proven theoretical background their use is based on purely empirical evidence.
Deep brain stimulation of the hypothalamus is highly specific and successful in patients with intractable cluster headache. However, it is still highly experimental. How stimulation of an area that is thought to act as a pacemaker for acute cluster attacks can prevent these attacks is not known.The past decade has seen remarkable progress toward unravelling the mystery of primary headache disorders. Because cluster headache and trigeminal autonomic headaches are much less common than migraine, most funding for headache research goes into migraine. Consequently, we have excellent quality-of-life data and a fairly accurate neurobiological model for migraine, with substantial knowledge of the genetic basis and thorough data on peripheral and central pain modulation. This information has led to a highly specific acute treatment designed just for migraine, notably the triptans, which, incidentally, also work in cluster headache but not, for example, in tension type headache. Understanding the fascinating basis of a relapsing-remitting headache syndrome on the basis of a precise circadian and circannual mechanism will not only benefit patients, but will also help to unravel the physiological interaction between the internal biological clock and pain perception and control. Bearing in mind that the excruciating pain in cluster headache has led to it being coined a “suicide headache”, we need to accept the challenge.”
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vig
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Re: Excellent CH article in The Lancet
« Reply #1 on: Sep 8th, 2005, 7:55pm » |
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cool stuff Ben
thanks!
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Chillrmn1
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Re: Excellent CH article in The Lancet
« Reply #2 on: Sep 8th, 2005, 8:01pm » |
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Quite interesting indeed.
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lindysmom
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Re: Excellent CH article in The Lancet
« Reply #3 on: Sep 14th, 2005, 4:56pm » |
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having just done an ER stint 2 night s ago with blood under my finger nails from trying to rip the beast out of the inside of my head I can fully relate to the "suicide headache" phrase. Not one I had heard before can can definatly relate to...sad to say.
Very, very cool article though. The talk about deep brain stimulation is wild to me....my dad just had it one month ago tomorrow for Parkinson's. He gets everything turned on tomorrow and for him it is nothing short of a miracle. So maybe there is more hope for us than we realize in the progress department.
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Jeepgun
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Re: Excellent CH article in The Lancet
« Reply #4 on: Sep 14th, 2005, 5:39pm » |
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Outstanding article!! Way to go!!
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Her: ..... "WHAT is the MATTER with you!?"
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clusterkat
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Re: Excellent CH article in The Lancet
« Reply #5 on: Sep 15th, 2005, 10:10am » |
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i wish to convey a heartfelt thanx.
understanding our chronic conditions,
is the key to treatment.
this is a excellant article about ch.
*smiles warmly*
^kat
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"top of the pain chain!"
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aceserve
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Re: Excellent CH article in The Lancet
« Reply #6 on: Sep 15th, 2005, 11:43am » |
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Hi,
Care to share your Lancet userame and password? I registered with The Lancet online to read the whole article, but was told it is only for paying customers.
Yours,
Ace
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Ahhh, what a relief to be pain free. Hang in there. Good times are comin'.
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rextangle
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Re: Excellent CH article in The Lancet
« Reply #7 on: Sep 15th, 2005, 9:26pm » |
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Thank you very much for that post! 
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ben_uk
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Re: Excellent CH article in The Lancet
« Reply #8 on: Sep 18th, 2005, 7:54am » |
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Cluster headache: pathogenesis, diagnosis, and management
Arne May
Summary
Cluster headache is a stereotyped primary pain syndrome characterised by strictly unilateral severe pain, localised in or around the eye and accompanied by ipsilateral autonomic features. The syndrome is characterised by the circadian rhythmicity of the short-lived attacks, and the regular recurrence of headache bouts, which are interspersed by periods of complete remission in most individuals. Headaches often start about 1–2 h after falling asleep or in the early morning, and show seasonal variation, suggesting that the hypothalamus has a role in the illness. Consequently, the vascular theory has been superseded by recognition that neurovascular factors are more important. The increased familial risk suggests that cluster headache has a genetic component in some families. Neuroimaging has broadened our pathophysiological view and has led to successful treatment by deep brain stimulation of the hypothalamus. Although most patients can be treated effectively, some do not respond to therapy. Fortunately, time to diagnosis of cluster headache has improved. This is probably the result of a better understanding of the pathophysiology in combination with efficient treatment strategies, leading to a broader acceptance of the syndrome by doctors.
Clinical features
“Imagine, your eye is pushed out of its socket and your right eyelid is beginning to swell shut. You start squinting and your eye is tearing, you are convinced there was blood pouring out. A red-hot knife is crushed into your head, excruciating, horrible, horrible pain. Your only saving grace is to pace from room to room, crying, flinging yourself to the floor, until eventually the pain drains from you. Waiting for the next attack to happen is a terrible, scary feeling. I sometimes think that I will go mad. I'm exhausted but then the next one hits.”
This is an example of how a cluster headache patient might describe his pain in an outpatient setting. Cluster headache, one of the most severe pain syndromes—female patients describe each attack as being worse than childbirth—is still underdiagnosed and suboptimally managed in primary care.1 Results of a recent health-related quality-of-life study in 56 patients suggest that cluster headache has substantial effects on patients' ability to function, even when appropriate treatments are used.2 Typically, attacks can strike up to eight times a day, are relatively short-lived, and are characterised by strictly unilateral severe head pain accompanied by autonomic symptoms.3 A side shift is mentioned in only about 15% of cases.4 Unlike individuals with migraine, patients with cluster headache are restless and prefer to pace about or sit and rock back and forth. Some patients will exert pressure on the painful area with a hand over the affected eye and temple. Many will isolate themselves during the headache or leave the house to get into cold or fresh air, and tend to become aggressive during an attack.
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ben_uk
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Re: Excellent CH article in The Lancet
« Reply #9 on: Sep 18th, 2005, 7:54am » |
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The unilateral autonomic symptoms such as ptosis, miosis, lacrimation, conjunctival injection, rhinorrhoea, and nasal congestion occur only during the pain attack and are ipsilateral to the pain, indicating parasympathetic hyperactivity and sympathetic impairment (figure 1). In some patients, the signs of sympathetic paralysis (miosis and ptosis) persist indefinitely,5 but intensify during attacks. Sweating and bloodflow to the skin also increase on the painful side, particularly in areas of sympathetic deficit.6 About 3% of patients have no autonomic symptoms,7 and in rare cases sympathetic disturbances persist on the previously affected side of the face in patients in whom cluster headaches have switched sides.
Another clinical feature of the syndrome is the circadian rhythmicity of the painful attacks, which are relatively short (15–180 min). In the episodic form, headaches occur daily for some weeks followed by a period of remission. On average, a cluster period lasts 6–12 weeks, and remissions can last up to 12 months. In the chronic form, attacks occur without substantial periods of remission. When chronic cluster headache is unresponsive to medical treatments, it becomes a serious problem and surgical options may have to be considered.
Epidemiology and genetics
Compared with migraine, cluster headache is uncommon.9–11 The disorder has a prevalence of less than 1%,12 and mostly affects men.13,14 The episodic form is most common, affecting 80–90% of cluster headache patients. It is characterised by periods of headaches (clusters or bouts) and periods of remission. During a bout, patients may experience one to eight attacks per day, and bouts can last from 7 days to 12 months.3 While in remission, patients are usually asymptomatic. The chronic form of cluster headache lacks remissions, and is diagnosed after a year without remission or if remission has lasted less than 30 days. A chronic cluster may arise de novo (primary chronic cluster headache) or evolve from the episodic type (secondary chronic cluster headache).
One of the most urgent questions patients put to their doctors is whether, as in migraine, the cluster attacks decline with age. Longitudinal data for cluster headache are anecdotal and only recently have data from larger epidemiological studies become available;13,15 overall, the authors of these reports assume that within the natural course of the condition, the symptoms remit with age.
The largest epidemiological study to date reports data for about 550 patients with episodic and chronic cluster headache over an observation period of more than 30 years (1963–97).16 In this study, there was a trend towards a decreasing male preponderance; the male-to-female ratio was substantially higher among patients with onset before 1970 than in those with onset after 1970, whereas the proportion of episodic to chronic form did not change during the study period. According to prospective studies, the syndrome occurs about three times more often in men than in women, and is clinically identical in both sexes.13 Mechanisms associated with sex hormone regulation, and environmental factors related to lifestyle, have been suggested to account for the increase in numbers of women diagnosed with cluster headache since 1970.16 The nature of the sex-related and age-related pattern of cluster headache onset is unclear. However, the increase in the diagnosis in women might also be the result of increased awareness and acceptance of the disorder by doctors, due to improved understanding of cluster headache pathophysiology.17–22
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ben_uk
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Re: Excellent CH article in The Lancet
« Reply #10 on: Sep 18th, 2005, 7:55am » |
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The medical history often reveals a high incidence of head trauma with brain concussion,23–25 but it is hard to prove a cause-and-effect relation. Interestingly, up to 85% of patients with chronic headache are also chronic cigarette smokers.23 Quitting smoking has no effect on the disease. The question arises whether chronic nicotine consumption is needed as a trigger to initiate the syndrome, possibly on the basis of some genetic background.
Before 1990, cluster headache was not generally thought to be an inherited disorder.26,27 However, reports of cluster headache in monozygotic twins28 and familial occurrence of cluster headache in 7% of families, resulting in a 14-fold increase in risk of cluster headache in first-degree relatives and a two-fold increased risk for second-degree relatives,29 show that genetic factors should be considered. In a study of 186 index patients and 624 first-degree relatives, investigators showed a positive family history of cluster headache in 11% of the index patients. They concluded that no precise mode of inheritance could be ascertained.30 A complex segregation analysis of cluster headache has suggested that an autosomal dominant gene has a role in some families,31 although some evidence exists for autosomal recessive or multifactorial inheritance in others.12 However, future studies should take into account that since cluster headache can start between the ages of 7 years32 and 83 years,33 the distinction between affected and unaffected individuals is clearly provisional. To date, the increased familial risk strongly supports the hypothesis that cluster headache has a genetic component, at least in some families.21 However, no clear molecular genetic clues have yet been identified. In view of the paroxysmal character and circadian and circannual rhythmicity of the disease, future studies need to focus on ion channel genes and clock genes.
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ben_uk
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Re: Excellent CH article in The Lancet
« Reply #11 on: Sep 18th, 2005, 7:56am » |
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Pathophysiology
Although the syndrome is well defined from a clinical point of view3 and has been recognised for more than two centuries,34 its pathophysiology is still poorly understood. However, the past decade has seen remarkable progress toward solving the pathophysiological puzzle.22 Any pathophysiological model needs to explain the three major features of cluster headache: trigeminal distribution of the pain, ipsilateral cranial autonomic features, and (circadian) episodic pattern of attacks. The vascular theory, which is based on an inflammation of the walls of the cavernous sinus (the only peripheral anatomical location where a single pathology could involve trigeminal C-fibres and sympathetic fibres),35 has been superseded by recognition that neurovascular events and some central impulse generator or oscillator seem to be more important. The severe unilateral pain is likely to be mediated by activation of the first (ophthalmic) division of the trigeminal nerve, whereas the autonomic symptoms such as lacrimation are due to activation of the cranial parasympathetic outflow from the seventh cranial nerve.36
Autonomic features
The sympathetic paralysis (miosis and ptosis) is due to a neuropraxic injury of postganglionic fibres in most patients.37 Currently, at least three possible sources of the autonomic symptoms are discussed: (1) the autonomic dysregulation might originate centrally in association with a hypothalamic disturbance;19,38 (2) a vasodilation or perivascular oedema (due to trigeminal-parasympathetic overactivity during attacks) compromises the carotid canal and consequently the traversing sympathetic fibres;39 and (3) the autonomic symptoms are secondary to trigeminal discharge.40,41
The possibility that parasympathetic hyperactivity is solely responsible for ocular sympathetic deficit has been discussed.42 About 3% of patients have no autonomic symptoms,7 and patients with and without autonomic symptoms have been described in the same families.43,44 In rare cases pain and autonomic symptoms may fully dissociate.45 However, a typical cluster attack will be strictly one-sided and will have prominent ipsilateral autonomic symptoms.3
The relapsing-remitting course,46 its seasonal variation,46 and the clockwise regularity47 of single episodes are characteristic, and suggest that the biological clock—namely the hypothalamus—is involved in the origin of the illness.48–50 Substantially lowered concentrations of testosterone in the plasma of men with cluster headache provided the first evidence of such a role.51 This evidence is further supported by a reduced response to thyrotropin-releasing hormone52 and a range of other circadian irregularities that have been reported in patients with cluster headache.50,53,54 Melatonin, in particular, is a marker of the circadian system; a blunted nocturnal peak in melatonin and complete loss of circadian rhythm have been reported in cluster headache.53,55 The endogenous circadian rhythm is controlled by an oscillator in the suprachiasmatic nuclei in the ventral hypothalamus, and is entrained to temporal environmental cues by light conditions via a retino-hypothalamic pathway.56 Clinical observations thus suggest the hypothalamus or a closely related structure as a candidate trigger for the acute attacks of cluster headache.
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ben_uk
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Re: Excellent CH article in The Lancet
« Reply #12 on: Sep 18th, 2005, 7:56am » |
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Functional imaging
Functional imaging work with PET has confirmed a highly specific activation of the hypothalamic grey matter in nitroglycerin-triggered and spontaneous cluster headaches,57,58 suggesting involvement in the pain process in a permissive or triggering manner rather than simply a response to first division nociception per se.17 Although the headache syndromes that form the group known as trigemino-autonomic cephalgias (cluster headache, paroxysmal hemicrania, and short-lasting neuralgiform headache with conjunctival injection and tearing [SUNCT]) share typical clinical features,59 in most cases a subclassification is possible and reasonable, as therapeutic regimens and responses differ. Since many of the basic features of SUNCT are shared by cluster headache and paroxysmal hemicrania, investigators have questioned whether there is a shared pathophysiological basis that might be expressed in similar cerebral activation patterns.
Neuroimaging in related syndromes
Using blood-oxygen-dependent functional MRI, three independent case reports investigating four patients with spontaneous SUNCT episodes uniformly found an activation next to the hypothalamic spot that was activated in cluster headache.60–62 The same prominent activation in the hypothalamic grey matter was found in a patient suffering from excruciating trigemino-autonomic headaches, in whom frequency and duration of attacks and therapeutic response allowed no clear-cut classification.63 These findings suggest that the underlying cause of trigemino-autonomic cephalagias might indeed be similar, and the variation in duration and frequency might be generally dependent on a different disorder of the hypothalamic neurons, perhaps a modulation of neuronal activity or a different involvement of the trigeminovascular system. These case studies underline the conceptual value of the term trigemino-autonomic cephalgias for the group of headaches focused around the trigeminal-autonomic reflex. Moreover, these findings emphasise the importance of the hypothalamus as a key region in the pathophysiological process of such headaches.
Another unilateral headache that is accompanied by trigeminal autonomic features is hemicrania continua. It is a strictly unilateral, continuous headache of moderate intensity, with superimposed exacerbations of severe intensity that are then accompanied by autonomic features and migrainous symptoms.64 The syndrome is exquisitely responsive to indometacin. Although, for theoretical reasons, it is not included among the trigeminal-autonomic headaches,3 a substantial activation of the contralateral posterior hypothalamus and ipsilateral dorsal rostral pons has been described in seven patients with hemicrania continua.65 Additionally, there was activation of the ipsilateral ventrolateral midbrain, which extended over the red nucleus and the substantia nigra, and bilateral pontomedullary junction. This study showed that the neuroimaging markers of both the trigeminal autonomic cephalgias (hypothalamus)22 and migraine (brainstem)66,67 are noted in hemicrania continua, mirroring the clinical phenotype that, in fact, shows some overlap with trigeminal autonomic headaches and migraine.65 Taken together, just as in the case of an atypical trigemino-autonomic headache,63 the functional imaging data in hemicrania continua65 emphasise that primary headache syndromes can be distinguished on a functional neuroanatomical basis by areas of activation specific to the clinical presentation. However, in view of the consistency of the PET findings with the clinical presentation, the question remains whether the brain of such patients is indeed structurally normal.
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ben_uk
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Re: Excellent CH article in The Lancet
« Reply #13 on: Sep 18th, 2005, 7:57am » |
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Hypothalamic deep brain stimulation
Recently, voxel-based morphometry has shown a structural difference in grey matter density—a lesion coinciding with the inferior posterior hypothalamus—in patients with cluster headache68 (but not those with migraine)69 compared with healthy volunteers. In terms of the stereotactic coordinates, the lesion occurs in about the same area in which activation during an acute cluster headache attack is noted in PET (figure 2).57 This work has even led to the successful introduction of a therapeutic target using deep brain stimulation of the posterior hypothalamic grey matter.70 So far, successful operations have been reported in 20 patients with intractable chronic cluster headache,70–72 some with a follow-up of more then 4 years.
Attacks reappear when the stimulator is switched off, and disappear when it is turned on again. Notably, it takes several days or even weeks between turning the unipolar stimulator on or off and change of the clinical picture.73 The method is reversible and the procedure is well tolerated in most patients, with no substantial side-effects. However, one patient had an intracerebral hemorrhage during the operation.72 This event led to the development of strict criteria and technical prerequisites for the selection of patients who should have operations.74 From a clinical point of view, it is interesting that trigeminal hypaesthesia and anaesthesia did not occur in any of the patients who received hypothalamic deep brain stimulation, and that hypothalamic stimulation does not affect anaesthesia dolorosa.71 This observation strengthens the hypothesis that the pain of cluster headache does not arise from a primary dysfunction of the trigeminal nerve itself, but is generated directly from the brain.23 In this context, it is noteworthy that electrical stimulation of the superior sagittal sinus, a trigeminally innervated structure, activates the supraoptic nucleus and posterior hypothalamic area,75 and a monosynaptic pathway connecting the hypothalamus and trigeminal nucleus has been documented.76 The posterior hypothalamus is able to both decrease or enhance nociceptive responses in the trigeminal nucleus caudalis.77 Little is known about the circuits and mechanisms underlying the effect of deep brain stimulation; however, activation of thalamo-cortical pathways and changes in cortical activity are probably involved.78 Further research in this field is urgently needed and the recently developed possibility of combining deep brain stimulation with PET will certainly help to unravel the brain circuitry implicated in stimulation-produced analgesia.
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ben_uk
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Re: Excellent CH article in The Lancet
« Reply #14 on: Sep 18th, 2005, 7:57am » |
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In summary, the pathogenesis of cluster headache is complex and remains incompletely understood. It is probably better to regard the condition as a hypothalamic syndrome rather than as a simple headache. In doing so, the contributions of both peripheral and central structures are considered, and this description takes into account the hypothalamic symptoms such as aggressiveness, sleep disturbance, restlessness, and endocrine and vegetative symptoms typically encountered in many patients. Whether it is primary to the disease or only an epiphenomenon, the peripheral nervous system's role in episodic cluster headache is beyond dispute. Interestingly, the peripheral part of the trigeminal nerve is not necessarily needed for some chronic forms of the disease,19 which means that the syndrome may be progressive. Whether inflammation of the walls of the cavernous sinus occurs, a process that has been thought to obliterate venous outflow and thus injure the traversing sympathetic fibres of the intracranial internal carotid artery and its branches, is controversial.35,79,80 That the hypothalamus is involved, at least in primary cluster headache, seems indisputable. At a minimum, primary cluster headache is characterised by hypothalamic activation with secondary activation of the trigemino-facial reflex, probably via a trigemino-hypothalamic pathway (figure 3).76 In long-standing chronic cluster headache, the autonomic symptoms and headache may be generated entirely through central mechanisms, as activation of the trigemino-facial reflex is no longer necessary to display the full clinical picture.19
Pain afferents from the trigeminovascular system synapse on the trigeminocervical complex (TNC), and then project to the thalamus and lead to activation in cortical areas known to be involved in pain transmission. Either a direct effect of the hypothalamus or a reflex activation of the parasympathetic outflow from the superior salivatory nucleus (SSN) predominantly through the pterygopalatine (sphenopalatine) ganglion, leads to the parasympathetic symptoms ipsilateral to the pain. A third-order sympathetic nerve lesion, thought to be caused by vascular changes in the cavernous sinus loggia with subsequent irritation of the local plexus of nerve fibres, results in a partial Horner's syndrome. The key site in the CNS for triggering the pain and controlling the cycling aspects is in the posterior hypothalamic grey matter region, modulated by phase-shifting in the suprachiasmatic nuclei.
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ben_uk
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Re: Excellent CH article in The Lancet
« Reply #15 on: Sep 18th, 2005, 7:58am » |
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Diagnosis
The diagnosis of cluster headaches is exclusively clinical. The International Classification of Headache Disorders3 uses explicit diagnostic criteria (panel), which are “unambiguous, precise and with as little room for interpretation as possible”. That at least 14 synonyms for cluster headache have been used in the past shows the an earlier lack of understanding of aetiology, and the importance of operational, explicit diagnostic criteria for research and clinical practice. Cluster headache, in its typical form, is unmistakable. However, no single instrumental examination can define, ensure, or differentiate idiopathic headache syndromes.81 Nevertheless, in the clinical setting, the use of neuroimaging (cranial CT, MRI, MR angiography, etc) in patients with headache varies widely. Electrophysiological and laboratory examinations, including examination of the CSF, are not helpful. For the initial diagnosis and in the case of an abnormal neurological examination, a cranial CT scan and cranial MRI should be considered, to exclude abnormalities of the brain. Mass lesions or malformations in the midline have been described in patients with symptomatic cluster headache, especially older patients
International classification of headache disorders3
Criteria
(A) At least five headache attacks fulfilling criteria B-D
(B) Severe or very severe unilateral orbital, supraorbital, and/or temporal headache attacks, which last untreated for 15–180 min. During part (but less than half) of the time course of the cluster headache, attacks may be less severe, less frequent, or of shorter or longer duration
(C) The headache is accompanied by at least one of the following symptoms ipsilateral to the pain:
(1) Conjunctival injection or lacrimation
(2) Nasal congestion and/or rhinorrhoea
(3) Eyelid oedema
(4) Forehead and facial sweating
(5) Miosis and/or ptosis
(6) A sense of restlessness and agitation
(D) The attacks have a frequency from one every other day to eight per day
(E) History and physical and neurological examination do not suggest any other disorder, or they are ruled out by appropriate investigations
Episodic cluster headache
At least two cluster periods lasting 7 days to 1 year separated by pain-free periods lasting >1 month
Chronic cluster headache
Attacks occur for more than 1 year without remission or with remission <1 month.
Probable cluster headache
Attacks fulfilling all but one of the criteria for cluster headache
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ben_uk
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Re: Excellent CH article in The Lancet
« Reply #16 on: Sep 18th, 2005, 7:58am » |
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Differential diagnosis
The trigemino-autonomic cephalgias are outlined in the revised version of the classification of the International Headache Society.3 All these syndromes have two features in common: short-lasting, unilateral, severe headache attacks accompanied by typical autonomic symptoms. The syndromes differ in duration, frequency, and rhythmicity of the attacks,59 in the intensity of pain and autonomic symptoms, and in treatment options (table).55,84 There are reports of aura in cluster headache85 and even a “hemiplegic cluster”.86 There seem to be some cases of cluster headache without headache,44 as well as the opposite: cluster headache without autonomic symptoms,7,87 and even bilateral cases.8 In a series of case reports presenting three atypical cluster headaches, it has been suggested that as more cluster patients are seen by headache specialists, new forms of this well-defined primary headache syndrome will be identified.88 However, the concept of trigemino-autonomic syndromes is certainly useful for clinicians seeking a pathophysiological understanding of the primary neurovascular headaches, and allows us to put the various treatment and prevention strategies in context.
Management
The guidelines of the International Headache Society3 represent a compromise between scientific rigour and practicality. However, because the syndrome is quite rare, it is still essential to collect and publish large case series regarding clinical manifestations, differences between the sexes, and treatment options in cluster headache. Case reports are also important as it becomes clearer that chronic headache is part of a larger spectrum of primary headache syndromes59 and that overlap with other trigemino-autonomic headache syndromes may occur.89,90
The treatment of cluster headache is based on empirical data rather than on a pathophysiological concept.89,91 Although the headaches are usually extremely painful, drug treatment in cluster headache shows a placebo rate similar to that observed in treatment of migraine92—about 30%. In general, cluster headache treatment can be divided into acute therapy for stopping individual attacks and prophylactic therapy for preventing recurrent attacks during the cluster period.64,78,93 Non-drug treatment is ineffective in nearly all patients.
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ben_uk
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Re: Excellent CH article in The Lancet
« Reply #17 on: Sep 18th, 2005, 7:59am » |
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Acute treatment
Inhalation of pure oxygen via a non-rebreathing facial mask, with a flow rate of at least 7 L/min (sometimes >10 L/min), is effective at stopping cluster headache attacks.94,95 The inhalation should be for 20 min in a sitting, upright position. No contra-indications are known for the use of oxygen; it is safe and has no side-effects. In some patients, oxygen is effective even when the pain is most intense, whereas in others the attack is delayed for minutes to hours, rather than completely aborted. In the latter case, oxygen intake must be restricted; otherwise, the frequency of attacks may increase. About 60% of all patients with cluster headache respond to this treatment with a substantial reduction in pain within 20–30 min.96,97 A disadvantage of oxygen is that patients must have continuous access to the oxygen supply (usually an oxygen tank and regulator), which may be impractical. Although hyperbaric oxygen has been much discussed as a therapeutic option, a placebo-controlled, double-blind trial has confirmed unambiguously that it is ineffective in preventing cluster headache attacks.98
In double-blind, placebo-controlled trials, the 5-HT1B/D agonist sumatriptan injected subcutaneously was effective in about 75% of all cluster headache patients (ie, pain-free within 20 min).99–101 It is safe, with no evidence of tachyphylaxis or rebound in most patients, even after frequent use.102–104 Contraindications are cardiovascular and cerebrovascular disorders and untreated arterial hypertension. The most uncomfortable side-effects are chest pain and distal paresthesia.105 In open and double-blind, placebo-controlled trials, sumatriptan nasal spray 20 mg106,107 and oral zolmitriptan 10 mg108 were also effective within 30 min. I have found 5 mg zolmitriptan nasal spray to be highly effective (unpublished data). The pre-emptive use of 5-HT1B/D agonists (triptans) in cluster headache remains controversial. 100 mg oral sumatriptan given three times a day was not effective in preventing cluster headache attacks in a placebo-controlled trial.109 In open trials, 40 mg eletriptan per day110 or 2•5–5•0 mg naratriptan per day111 reduced the number of cluster headache attacks.
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ben_uk
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Re: Excellent CH article in The Lancet
« Reply #18 on: Sep 18th, 2005, 8:00am » |
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Oral ergotamine has been used in the treatment of cluster headache attacks for more than 50 years46,112 and is effective when given very early in the attack. It has been recommended as an aerosol spray for the treatment of acute cluster headache.113 However, modern trials are scarce. The intranasal application of dihydroergotamine in cluster headache attacks was no better than placebo in a single trial.114 Recently, the intravenous application of 1 mg dihydroergotamine over 3 days has been shown to be effective in stopping severe cluster attacks in an open retrospective trial.115 Use of ergotamine for short-term prophylaxis has also been studied. Ergotamine suppositories need a long time until the onset of effectiveness; a dose of 2 mg in the evening has been proposed to prevent cluster headache attacks during the night.89,112
The nasal application of lidocaine (1 mL with a concentration of 4–10%, ipsilateral to the pain; the head should be reclined by 45° and rotated to the affected side by 30° to 40°) is effective in at least a third of patients.116–118 The drug is thought to block the sphenopalatine fossa region. The use of lidocaine evolved from investigations to determine whether the observed clinical usefulness of cocaine in aborting acute cluster headache attacks119 was due to the drug's anaesthetic or euphoric properties.
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ben_uk
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Re: Excellent CH article in The Lancet
« Reply #19 on: Sep 18th, 2005, 8:00am » |
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Prioritisation of acute therapy
Because of the rapid onset and short time to peak intensity of cluster headache pain, subcutaneous sumatriptan is the treatment of choice. The absorption and pharmacological actions of oral medications are usually too slow. Oxygen is the other standard treatment. Topical application of lidocaine is comparatively less efficient and has inconsistent effects. However, one could argue that every patient should try it at least once, since if it works, it is easy to administer and has no systemic side-effects, which is important since patients can sometimes have as many as eight attacks a day.
Preventive pharmacotherapy
The importance of an effective preventive regimen cannot be overstated. Since many patients have between one and eight attacks a day, repeated attempts at abortive therapy may result in overmedication or toxicity. The primary goal of preventive therapy is to suppress attacks and to maintain this suppression over the expected duration of the cluster period. To achieve this goal, an individual treatment regimen must be formulated with the patient. In episodic cluster headache, medication should be withdrawn when the expected cluster period is over. In chronic cluster headache, medication should be gradually reduced once every other month, to assess whether it is still necessary.
The cornerstone of maintenance prophylaxis is verapamil. A daily dose of 240–320 mg verapamil is the established treatment of choice in the prophylaxis of episodic and chronic cluster headache,64,91 although few sufficient double-blind, placebo-controlled trials are available. Results of placebo-controlled trials showed efficacy of both verapamil and lithium, with verapamil acting more rapidly than lithium.120,121 In some cases, a daily dose of more than 720 mg verapamil may be necessary.64,122 Because of this apparent dose-response relation, a total daily dose of 480–720 mg is recommended before the treatment is regarded as unsuccessful. Regular ECG monitoring is required. Side-effects of verapamil are bradycardia, oedema, gastrointestinal discomfort, constipation, and dull headache.123 However, the drug is generally well tolerated and can be used safely in conjunction with sumatriptan, ergotamine, corticosteroids, and other preventive agents. No evidence is available for an optimal dosage for verapamil. An increase of 80 mg every 3 days is recommended. The full effect of verapamil can be expected within 2–3 weeks. Both the regular and extended-release preparations have been shown to be useful, but no direct comparative trials are available. Since verapamil is usually well tolerated, it is also the drug of choice for continuous treatment in chronic cluster headache. In the first 2 weeks of verapamil administration, steroids may also be given (30–100 mg prednisone or 2×4 mg dexamethasone per day). In two small open studies, nimodipine was also effective.124,125
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ben_uk
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Re: Excellent CH article in The Lancet
« Reply #20 on: Sep 18th, 2005, 8:01am » |
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Lithium has been studied in cluster headache prophylaxis in a daily dose of 600–1500 mg in more than 20 open trials.126 The proportion of patiends that had an improvement in chronic cluster headache was reported to be as high as 78% (63% in episodic cluster headache). A placebo-controlled trial, however, did not reproduce the beneficial effect in episodic cluster headache.127 However, in a comparative, double-blind crossover study, lithium and verapamil showed similar efficacy (with a more rapid improvement with verapamil) and tolerability was better with verapamil.128 The concentration of the drug in the plasma should be monitored and kept between 0•6 mmol/L and 1•2 mmol/L.129 Regular monitoring of liver, renal, and thyroid function and of electrolytes is needed. Major side-effects are hyperthyroidism, tremor, and renal dysfunction. As lithium in general has a narrow therapeutic window, it is particularly recommended for chronic cluster headache when other drugs are ineffective or contraindicated.
Methysergide has been recommended for episodic cluster headache,16,130–133 but no placebo-controlled, double-blind studies are available. In open studies, the number of patients who benefited from methysergide ranged from 20% to 73%; the drug was more effective in episodic cluster headache.134 The doses given in the open studies varied from 4 mg to 16 mg. Usually, methysergide is administered at a daily dose of 4–8 mg and can be increased up to 12 mg (starting with 1 mg per day). Methysergide is metabolised to an active metabolite, methylergometrine,135 and should be used with caution when patients are receiving other ergotamine derivatives or triptans. The short-term side-effects include nausea, muscle cramps, abdominal pain, and pedal oedema. Since a high incidence of pulmonary and retroperitoneal fibrosis is seen with long-term use, the continuous use of methysergide is limited to 3–4 months.136,137
No adequate randomised, placebo-controlled trials are available for the use of corticosteroids in cluster headache. Several open studies and case series have been published and reviewed.16,130 All the open studies confirmed the clinically well-known efficacy of steroids given in different regimens (>30 mg prednisone per day; 2×4 mg dexamethasone per day). These drugs are a very effective option for initial prophylaxis, rapidly suppressing attacks during the time needed for the longer-acting preventive agents to take effect. However, some patients are attack-free only with steroids, and continuous administration of steroids is necessary. As with verapamil, no evidence for the best regimen of steroid administration is available. For the beginning of steroid treatment, 60–100 mg of prednisone given once a day for at least 5 days is recommended, then decreasing the dose by 10 mg every day. About 70–80% of all cluster headache patients respond to steroids. Intravenous and oral application of steroids can also be successfully combined.138
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Re: Excellent CH article in The Lancet
« Reply #21 on: Sep 18th, 2005, 8:01am » |
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Refractory patients
In 10–20% of patients, the above medications are not effective or the cluster periods develop resistance. Intolerance or contra-indications may further limit standard treatments. The following medications have some importance as third-line therapy, mostly based on small, open studies.
The antiserotonergic drug pizotifen (3 mg per day) has been shown to be effective in cluster headache prophylaxis in a single-blind, placebo-controlled trial.139 However, a review of seven small studies,140 suggests that pizotifen has only a modest effect. Side-effects such as tiredness and weight gain further limit this drug's use. Valproic acid has been studied in three open trials, with inconsistent results.141–143 These trials suggest that valproic acid can be tried as a drug of third choice in a daily dose of 5–20 mg per kg bodyweight. Likewise, some open studies suggest that topiramate is effective in the prophylaxis of cluster headache.144–147 The recommended dose is at least 100 mg per day, with a starting dose of 25 mg. The main side-effects are cognitive disturbances, paraesthesias, and weight loss. The drug is contra-indicated in patients with nephrolithiasis.
For the ipsilateral intranasal application of capsaicin, two open trials148,149 and one double-blind, placebo-controlled trial150 have been published, showing efficacy in about two-thirds of patients after repeated application. Intranasal application of civamide showed a modest efficacy in a double-blind, placebo-controlled study.151
10 mg of oral melatonin was effective in a double-blind, placebo-controlled study.152 In otherwise refractory cluster headache, however, melatonin did not produce any additional efficacy.153 There is meagre evidence from a small open study for the efficacy of baclofen (15–30 mg),154 and there is no sufficient evidence for the efficacy of botulinum toxin155 or transdermal clonidine156 in the prophylactic treatment of cluster headache.
Although there is no valid evidence that combinations of various prophylactic drugs work better in cluster headache, some patients may do better with a combination than with extensive high doses of a single drug. In clinical practice, a combination of drugs is often needed, generally using a moderate dose of verapamil (240–480 mg) as the standard medication and any of the above prophylactic drugs as add-on therapy. On the basis of a consensus obtained at the 9th International Headache research seminar, some combinations of drugs have been recommended in patients otherwise refractory to single preventive treatment.157
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ben_uk
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Re: Excellent CH article in The Lancet
« Reply #22 on: Sep 18th, 2005, 8:02am » |
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Surgical treatment
If all drugs are ineffective and a secondary cluster headache has been excluded, surgical treatment can be discussed with the patient. Surgical procedures should be considered with great caution because no reliable long-term observational data are available and because they can induce trigeminal neuralgia or anaesthesia dolorosa. Different methods have been suggested to prevent cluster headache: application of glycerol or local anaesthetics into the cisterna trigeminalis of the Gasserian ganglion;158 radiofrequency rhizotomy of the Gasserian ganglion159 or of the trigeminal nerve;160 microvascular decompression;161 and resection or blockade of the greater superficial petrosal nerve162 or of the ganglion sphenopalatinum.163 However, there are also case reports of the complete inefficacy of surgical treatment in cluster headache and related syndromes.19,164–166 In some cases, blockade of the greater occipital nerve was effective, and this approach may be tried before any other surgical procedure.167,168 In general, any surgical procedure on peripheral trigeminal structures in episodic cluster headache must be judged with great caution, as the nature of the disorder is to remit. On the other hand, in chronic cluster headache, there is strong evidence that even a complete trigeminal denervation is not effective.19 Deep brain stimulation of the posterior inferior hypothalamus has been shown to be effective in most of a sample of patients with intractable cluster headache.70–73 Recommendations for the selection of patients for this procedure have been published.74
Prioritisation of preventive therapy
Patients with chronic and long-lasting active periods of episodic cluster headache should be principally treated with verapamil. Because of the relatively long time required for increasing the dosages of verapamil until it takes effect, corticosteroids, ergotamine, or even triptans with a long half-life can be used as an effective initial prophylactic option. Methysergide or corticosteroids are the medication of choice in short-lasting active cluster periods (less than 2 months). Lithium and valproic acid are thought to be helpful, but only as second-line, therapy. When patients cannot tolerate standard medications, or these are contraindicated, combinations of other drugs should be explored. Corticosteroids should, if at all possible, be used only for short-term prophylaxis. Surgical procedures should be viewed with great caution; despite excellent results, even hypothalamic deep brain stimulation must be regarded as highly experimental.
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ben_uk
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Re: Excellent CH article in The Lancet
« Reply #23 on: Sep 18th, 2005, 8:03am » |
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Unresolved issues and the future
Why do cluster headache attacks start and, more importantly, why do they stop after a fairly defined period of time? What exactly causes the switch from inactive to active periods, and vice versa? The role of the human clock system implicates the suprachiasmatic nucleus and, consequently, photoperiod changes have been thought to be a crucial external factor. However, this theory implies that light therapy should work, whereas in my experience it does not. Moreover, melatonin has no effect, and in most patients the circadian rhythm is indeed stereotyped (highly homogeneous), whereas the annual rhythm is highly individual.
The relevance of the high proportion of smokers among patients with cluster headache is not known. In the active period, cluster headache is reliably triggered by alcohol, histamine, and nitrates,8 but the mechanism whereby these factors induce an attack is not understood. One common feature of histamine, alcohol, and nitrates is their vasodilating effect. Nitroglycerin is a pro-drug for nitric oxide, which can activate the trigeminal vascular system. However, recent data indicate that neither the vessels nor the peripheral part of the trigeminal system are needed in development of a full-blown attack.
The mechanism of the effectiveness of oxygen in treating cluster headache is not understood. Reductions in cerebral blood flow, cerebral vasoconstriction, activation of descending inhibitory neurons from the brainstem, and an abnormal chemoreceptor sensitivity in cluster headache have been suggested. Notably, none of the preventive medicines used in cluster headache are given on the basis of proven theoretical background their use is based on purely empirical evidence.
Deep brain stimulation of the hypothalamus is highly specific and successful in patients with intractable cluster headache. However, it is still highly experimental. How stimulation of an area that is thought to act as a pacemaker for acute cluster attacks can prevent these attacks is not known.
The past decade has seen remarkable progress toward unravelling the mystery of primary headache disorders. Because cluster headache and trigeminal autonomic headaches are much less common than migraine, most funding for headache research goes into migraine. Consequently, we have excellent quality-of-life data and a fairly accurate neurobiological model for migraine, with substantial knowledge of the genetic basis and thorough data on peripheral and central pain modulation. This information has led to a highly specific acute treatment designed just for migraine, notably the triptans, which, incidentally, also work in cluster headache but not, for example, in tension type headache. Understanding the fascinating basis of a relapsing-remitting headache syndrome on the basis of a precise circadian and circannual mechanism will not only benefit patients, but will also help to unravel the physiological interaction between the internal biological clock and pain perception and control. Bearing in mind that the excruciating pain in cluster headache has led to it being coined a “suicide headache”, we need to accept the challenge.
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ben_uk
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Re: Excellent CH article in The Lancet
« Reply #24 on: Sep 18th, 2005, 8:19am » |
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There is more:- PET Imaging, photos, diagrams, charts
Buy the Mag:-
The Lancet - Vol. 366, Issue 9488, 3 September 2005, Pages 843-855
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