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=Vasovagal syncope=
=Triggers for Vasovagal Syncope=
Vasovagal syncope can occur after exposure of a lot of different triggers. Recognised triggers for vasovagal syncope are prolonged orthostatic stress, blood drawing, medical instrumentation and psychological stressors.
Vasovagal syncope can occur after exposure of a lot of different triggers. Recognised triggers for vasovagal syncope are prolonged orthostatic stress, blood drawing, medical instrumentation and psychological stressors.


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Foremost, the diagnostic workup of all patients presenting with exercise-related syncope is aimed at '''excluding dangerous [[Cardiac syncope|cardiac conditions]]''' and includes echocardiography and exercise testing <cite>Krediet04b</cite>. Risk factors for a cardial problem are fainting while sitting or supine and suddenly fainting ''during'' exercise without presyncope.
Foremost, the diagnostic workup of all patients presenting with exercise-related syncope is aimed at '''excluding dangerous [[Cardiac syncope|cardiac conditions]]''' and includes echocardiography and exercise testing <cite>Krediet04b</cite>. Risk factors for a cardial problem are fainting while sitting or supine and suddenly fainting ''during'' exercise without presyncope.
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Characteristically, syncope may occur while the individual is '''standing motionless''' during the first five to ten minutes after exercise <cite>Bjurstedt</cite>. Especially athletes in the (ultra) endurance sports are at risk for post exercise vasovagal syncope e.g. after marathon swimming (Finlay et al., 1995) or marathon running (Tsutsumi & Hara, 1979;Holtzhausen & Noakes, 1995;Holtzhausen & Noakes, 1997).
Characteristically, syncope may occur while the individual is '''standing motionless''' during the first five to ten minutes after exercise <cite>Bjurstedt</cite>. Especially athletes in the (ultra) endurance sports are at risk for post exercise vasovagal syncope e.g. after marathon swimming <cite>Finlay</cite> or marathon running <cite>Tsutsumi</cite><cite>Holtzhausen95</cite><cite>Holtzhausen97</cite>.
Vasovagal syncope after routine treadmill testing is rare (estimated 0,2% (Schlesinger, 1973)). However, when treadmill testing is immediately followed by passive head-up tilt testing, this percentage can increase up to 50-70% (Bjurstedt et al., 1983).  
Vasovagal syncope after routine treadmill testing is rare (estimated 0,2% <cite>Schlesinger</cite>). However, when treadmill testing is immediately followed by passive head-up tilt testing, this percentage can increase up to 50-70% <cite>Bjurstedt</cite>.  
Vasovagal syncope after exercise is considered to be a benign occurrence (Krediet et al., 2004b).
Vasovagal syncope after exercise is considered to be a benign occurrence <cite>Krediet04b</cite>.


===Muscle pump===
===Muscle pump===
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==Vasovagal syncope in airliners==
==Vasovagal syncope in airliners==
Vasovagal episodes are the most common in-flight medical events, and may affect patients of all ages (Gendreau & DeJohn, 2002). In addition to prolonged motionless sitting, the use of alcohol, anxiety  and mild hypoxia during air travel all may predispose to vasovagal faints (Sutton, 1999). Cabin pressure in commercial aircraft is usually adjusted to the equivalent of an altitude of 1500 to 2500 m above sea level. It appears that hypoxic syncope results from the super-imposed vasodilator effects of hypoxia on the cardiovascular system (Halliwill & Minson, 2005).  
Vasovagal episodes are the most common in-flight medical events, and may affect patients of all ages <cite>Gendreau</cite>.  
The following may all predispose vasovagal faints during air travel <cite>Sutton</cite>:<br>
* Prolonged motionless sitting
* The use of alcohol
* Anxiety
* Mild hypoxia during air travel
Cabin pressure in commercial aircraft is usually adjusted to the equivalent of an altitude of 1500 to 2500 m above sea level. It appears that hypoxic syncope results from the super-imposed vasodilator effects of hypoxia on the cardiovascular system <cite>Halliwill</cite>.  


===Treatment===
===Treatment===
Patients, who otherwise never experienced a (severe) vasovagal episode may suffer from convulsive syncope during air travel (Wieling et al., 2006). These patients should be advised to have a high salt intake in the days prior to travelling by plane, reducing anti-hypertensive medication –if feasible- and drinking non-alcoholic beverages galore during the trip. Especially during long flights (> 2 hours) they should perform in-chair muscle tensing and relaxing exercise and have a regular walk through the isle. In recurrent cases midodrine prior to flying or supportive stockings can be considered.
Patients, who otherwise never experienced a (severe) vasovagal episode may suffer from convulsive syncope during air travel <cite>Wieling06</cite>. These patients should be advised to have:
* A high salt intake in the days prior to travelling by plane
* Reduce anti-hypertensive medication –if feasible-  
* And drink non-alcoholic beverages galore during the trip.  
Especially during long flights (> 2 hours) they should perform in-chair [[Physical counterpressure manoeuvers|muscle tensing and relaxing exercise]] and have a regular walk through the isle. In recurrent cases '''midodrine''' prior to flying or '''supportive stockings''' can be considered.


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==Sleep vasovagal syncope==
==Sleep vasovagal syncope==
Sleep vasovagal syncope is defined as loss of consciousness in a non-intoxicated adult occurring during the night (e. g. 10:00 pm to 7:00 am), in which the patient wakes up with pre-syncopal and abdominal symptoms (i.e. an urge to defecate) and losses consciousness in bed or immediately upon standing. There is no tongue biting or post-ictal confusion. There is usually a history of daytime vasovagal syncope and there seems to be a more pronounced fear of blood and medical procedures than in other syncope patients (Jardine et al., 2006b). Physical examination, ECG and EEG are within normal limits. The vasovagal reaction is thought to start while asleep (Krediet et al., 2004a;Jardine et al., 2006a), and continuing after waking up, hence the name. During syncope there may be a profound sinus-bradycardia (Krediet et al., 2004a). Vasovagal sleep syncope occurs at all ages.
Sleep vasovagal syncope is defined as loss of consciousness in a non-intoxicated adult occurring during the night (e. g. 10:00 pm to 7:00 am), in which the patient wakes up with pre-syncopal and abdominal symptoms (i.e. an urge to defecate) and losses consciousness in bed or immediately upon standing.  
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There is no tongue biting or post-ictal confusion. There is usually a history of daytime vasovagal syncope and there seems to be a more pronounced fear of blood and medical procedures than in other syncope patients <cite>Jardine06b</cite>. Physical examination, ECG and EEG are within normal limits. The vasovagal reaction is thought to start while asleep <cite>Krediet04a</cite><cite>Jardine06a</cite>, and continuing after waking up, hence the name. During syncope there may be a profound sinus-bradycardia <cite>Krediet04a</cite>. Vasovagal sleep syncope occurs at all ages.


===Differential Diagnosis===
===Differential Diagnosis===
Sleep vasovagal syncope is diagnosed by excluding beyond reasonable doubt the hereafter mentioned disorders (Jardine et al., 2006a).
Sleep vasovagal syncope is diagnosed by excluding beyond reasonable doubt the hereafter mentioned disorders <cite>Jardine06a</cite>.
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Epilepsy is the foremost alternative diagnosis to consider, but can often easily be ruled out on clinical grounds. Complex partial, generalized tonic-clonic and myoclonic epilepsy may occur during sleep and can imitate syncope when causing cause sinus-bradycardia (Tinuper et al., 2001).  
Epilepsy is the foremost alternative diagnosis to consider, but can often easily be ruled out on clinical grounds. Complex partial, generalized tonic-clonic and myoclonic epilepsy may occur during sleep and can imitate syncope when causing cause sinus-bradycardia <cite>Tinuper</cite>.  
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There are a number of related conditions, including “'''abdominal epilepsy'''” and '''Panayiotopoulos syndrome''' (typically with vomiting) (Covanis, 2006), in which the associated clinical features are abdominal pain and confusion.  
There are a number of related conditions, including “'''abdominal epilepsy'''” and '''Panayiotopoulos syndrome''' (typically with vomiting) <cite>Covanis</cite>, in which the associated clinical features are abdominal pain and confusion.  
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Sleep paralysis and hypnogogic hallucinations occur in '''narcolepsy''' but also as isolated phenomena, mostly with other characteristic features in the history (e. g., daytime somnolence, in contrast to syncope there’s no amnesia.) and abnormal polysomnography, which can also be used to diagnose sleep apnoea and night terrors.  
Sleep paralysis and hypnogogic hallucinations occur in '''narcolepsy''' but also as isolated phenomena, mostly with other characteristic features in the history (e. g., daytime somnolence, in contrast to syncope there’s no amnesia.) and abnormal polysomnography, which can also be used to diagnose sleep apnoea and night terrors.  
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Occasionally cardiac disorders may cause cardiac arrhythmias during sleep. Most of these are unlikely if the 12-lead ECG is normal, and in some patients long-term ambulatory ECG monitoring is required (Brierley et al., 2001).
Occasionally cardiac disorders may cause cardiac arrhythmias during sleep. Most of these are unlikely if the 12-lead ECG is normal, and in some patients long-term ambulatory ECG monitoring is required <cite>Brierley</cite>.
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Some patients with a diagnosis of defaecation syncope (see below) described abdominal and pre-syncopal symptoms that started simultaneously during sleep (Pathy, 1978;Fisher, 1979); there may be some overlap between this condition and sleep syncope (Jardine et al., 2006a).
Some patients with a diagnosis of defaecation syncope (see below) described abdominal and pre-syncopal symptoms that started simultaneously during sleep <cite>Pathy</cite><cite>Fisher</cite> there may be some overlap between this condition and sleep syncope <cite>Jardine06a</cite>.


==References==
==References==
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#Krediet04b pmid=15480927
#Krediet04b pmid=15480927
#Bjurstedt pmid=6650203
#Bjurstedt pmid=6650203
 
#Finlay pmid=8531620
#Tsutsumi pmid=52682
#Holtzhausen95 pmid=8614313
#Holtzhausen97 pmid=9397327
#Schlesinger pmid=4800477
#Gendreau pmid=11932475
#Sutton pmid=11543489
#Halliwill pmid=15531565
#Wieling06 pmid=16836688
#Jardine06b Jardine DL, Krediet CT, Cortelli P, & Wieling W (2006b). Sleep syncope: clinical features and autonomic profiles. Clin Auton Res 16, 321-322.
#Krediet04a pmid=15084573
#Tinuper pmid=11701591
#Covanis pmid=16950946
#Brierley pmid=11445105
#Pathy pmid=83099
#Fisher pmid=264159
</biblio>
</biblio>


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# Secondly, if feasible, modification of antihypertensive drugs should be considered.  
# Secondly, if feasible, modification of antihypertensive drugs should be considered.  
Surgical or pharmacological destruction of (the oesophageal branches of) the vagus nerve has shown not to be successful. Based on predominantly positive therapeutic response in over a dozen cases, the treatment of choice of oesophageal syncope is insertion of a cardiac demand pacemaker (Basker & Cooper, 2000). Management of persisting neuralgia is symptomatic.
Surgical or pharmacological destruction of (the oesophageal branches of) the vagus nerve has shown not to be successful. Based on predominantly positive therapeutic response in over a dozen cases, the treatment of choice of oesophageal syncope is insertion of a cardiac demand pacemaker (Basker & Cooper, 2000). Management of persisting neuralgia is symptomatic.
=Arterial system=
The arterial system consists of three major groups of arteries.
These are:
*Elastic arteries
*Muscular arteries
*Arterioles
== Elastic arteries ==
Elastic arteries are the '''aorta''' and the '''major branches of it''' close to the heart. The vessel walls contain the most elastin of all vessels and elastin is found in all the vessels layers. Elastic arteries also contain smooth muscle cells, but these are mostly inactive in vasoconstriction. By elastically dilating when [[Blood pressure|blood pressure]] increases (right after a heartbeat) and contracting when [[Blood pressure|pressure]] drops they maintain [[Blood flow|blood flow]] in between heartbeats. The elasticity also gives a more constant [[Blood pressure|BP]] throughout the rest of the vascular system. The diameter of elastic arteries ranges from ''2.5 to 1 cm''.
== Muscular arteries ==
Muscular arteries have a diameter of 1 to 0.3 cm and derive from elastic arteries. Muscular arteries regulate the [[Blood flow|blood flow]] to specific organs. They are active during vasoconstriction and contain relatively the most smooth muscle cells in the tunica media. They contain less elastin than elastic arteries and are thus less distensible.
== Arterioles ==
The smallest arteries are called arterioles. The tunica media of the arterioles mostly contain smooth muscle cells. Their diameter ranges from 0.3 cm to 10 µm, and the smallest arterioles lead into '''capillary beds'''. [[Blood flow]] into capillary beds is regulated by these arterioles. The arterioles change in diameter due to '''neural, hormonal and local chemical influences'''. These changes in diameter lead to the changes in [[Blood flow|blood flow]] in the capillary beds. When arterioles constrict, the capillary beds that lay behind the constricting arterioles is bypassed. When they dilate, [[Blood flow|blood flow]] in the capillary beds increases dramatically. 
== Capillaries ==
[[File:Capillary_Bed_aangepast.jpg|frame|Capillary bed]]
Capillaries are no arteries. They are the smallest of all blood vessels and their function is to exchange materials with every cell in the body. The average capillary diameter is 8 to 10 µm, so that red blood cells can just pass through them.
A capillary bed consists of a network of interweaving capillaries. These capillary beds connect arterioles, and venules, the smallest vessels of the [[Venous system|venous system]]. In most of the capillary beds, two types of vessels are found:
*a vascular shunt
*and true capillaries
A '''vascular shunt''' connects connects an arteriole with a [[Venous system|venule]] directly. These vessels do not exchange materials with the surrounding fluid. True capillaries exchange materials. The arteriole that directly connects with the capillaries is called a terminal arteriole and this arteriole feeds directly into the metarteriole. This metarteriole feeds into the thoroughfare channel and then the [[Venous system|postcapillary venule]]. These vessels together make the vascular shunt.
'''True capillaries''' normally branch off the metarteriole and empty in the [[Venous system|postcapillary venule]]. The root of the true capillaries is surrounded by smooth muscle cells. This is called a precapillary sphincter. It acts as a valve that regulates [[Blood flow|blood flow]] through the capillary bed. If the sphincters are contracted, the blood will pass through the vascular shunt, and no exchange of materials will take place. If the valves are relaxed, blood will flow through the capillaries and exchange with the surrounding cells occurs.
=Postural Tachycardia Syndrome (POTS)=
POTS is a hetergeneous group of disorders with similar cinlical manifestations. POTS is characterized by a combination of an abnormally high heart frequency (tachycardia) while standing (postural) and symptoms of palpitations, light-headedness, and other sensations that occur due to cerebral hypoperfusion (see [[Symptoms and signs of presyncope|symptoms and signs of presyncope]])
</div>
An abnormal heart rate respons is defined as:
* Sustained heart rate increment of > 30 bpm within 10 minutes of standing or head-up tilt
* Patients aged 12-19 years require an increment of > 40 bpm
* '''Or''' a heart rate that exceeds 120 bpm
* The heart rate increment cannot be associated conditions as prolonged bed rest, or medications that diminish vascular or autonomic tone
* Symptoms of cerebral hypoperfusion and autonomic overactivity
==Pathophysiology==
The etiology and pathophysiology of POTS are unknown, but are likely to be heterogeneous. The syndrome is associated with deconditioning, recent viral illness, chronic fatigue syndrome and a limited or restricted autonomic  neuropathy.  The differential diagnosis includes conditions that cause tachycardia, such as thyrotoxicosis, inappropriate sinus tachycardia and other cardiac rhythm abnormalities, pheochromocytoma, hypoadrenalism, anxiety, dehydration, and medications (e.g., vasodilators, diuretics, and b-agonists). Many patients report that their symptoms started after a febrile illness, pregnancy, surgery, trauma or sepsis. The present thought on the pathophysiology of POTS after such an event is that POTS is an autoimmune disorder.
==Epidemiology==
The prevalence of POTS is not known, but estimates suggest at least 500.000 people are affected by POTS in the United States alone<cite>Grubb</cite>. The syndrome is more common in women.
==Clinical presentation==
The orthostatic symptoms of POTS consists of light-headedness, visual blurring or tunnel vision, palpitations, tremulousness, and weakness (especially in the legs). Other symptoms include fatigue, exercise intolerance, hyperventilation, shortness of breath, anxiety, chest pain, nausea, acral coldness or pain, and concentration difficulaties and headaches. On clinical examination, in addition to the heart rate increment, pulse pressure may be reduced and acral coldness may be present. Continued standing may lead to venous prominence, cyanosis and foot swelling. A hyperadrenergic state is present in some patients who have a resting tachycardia, sweating, and tremulousness.
==References==
<biblio>
#Grubb pmid=18506020
</biblio>
===test===
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