Cardiology

May 2014

FocusCardiology

Dizziness: if not vertigo could it be cardiac disease?

Volume 43, No.5, May 2014 Pages 264-269

Maja Susanto

Background

Dizziness is a common presentation in general practice. However, the symptom of dizziness represents a spectrum of pathology from benign to serious.

Objective/s

This review provides an evaluation of a patient presenting with presyncope/syncope.

Discussion

Dizziness can be a symptom of one of four conditions: vertigo, presyncope, disequilibrium or light-headedness. It is often unclear what patients mean by dizziness as they use this term loosely. Hence, clinicians must be vigilant in evaluating patients presenting with dizziness and be mindful of red flags that may indicate serious pathology. This review begins with a case study describing the wide range of causes of dizziness. Careful history taking and physical examination are pivotal in evaluating patients presenting with dizziness.

Case study

A woman aged 75 years presented to the emergency department with recurrent dizziness and fainting episodes.

Dizziness is a common presentation that accounts for about 5% of primary care visits.1 When a patient describes dizziness, it can reflect one of four conditions (Table 1).1,2 Unfortunately, patients tend to use the term dizziness loosely. In the case study described in this article, the patient presented with dizziness followed by fainting episodes, indicating presyncope rather than vertigo.

Table 1. Four categories causing a sensation of dizziness1,2
CategoriesPathophysiologyAetiology
Vertigo
= spinning sensation
Vestibular pathology Vestibular neuritis
Labyrinthitis
Meniere’s disease
Presyncope
= fainting sensation
Reduced cerebral perfusion Volume depletion
Neurocardiogenic syncope
Dysequilibrium
= imbalance sensation
Gait disorder Myelopathy
Peripheral neuropathy
Parkinson’s disease
Light-headedness
= sensation of disconnection from the environment
Psychological disorder Anxiety
Depression

She had a history of hypertension, stable familial haemochromatosis, gastroesophageal reflux disease and hypothyroidism, which was treated with thyroxine but treatment was ceased due to euthyroid status. She is a lifelong non-smoker and drinks three glasses of wine each day with dinner. Her medications include lercanidipine 20 mg daily, irbesartan 150 mg daily and omeprazole 20 mg daily.

The additional information produces a list of differential diagnoses. Chronic hypertension may cause left ventricular diastolic dysfunction, leading to low cardiac output, which may lead to cardiac arrhythmias.3 Haemachromatosis can contribute to the development of cardiomyopathy.4–6 The accumulation of iron in the myocardium can lead to severe left ventricular diastolic dysfunction that ultimately leads to heart failure and cardiac arrhythmias.5,6 Similarly, over-replacement of thyroxine can lead to a hyperthyroid state, which, in turn, can lead to atrial tachyarrythmias presenting with palpitations and dizziness. On the other hand, hypothyroidism may cause hypotension and bradycardia, which also lead to dizziness. However, in this case, the patient’s euthyroid status rules out these possibilities. A history of gastroesophageal reflux raises the possibility of peptic ulcer development, which may cause anaemia or volume depletion, contributing to her dizziness.3 Lastly, the combination of a calcium channel blocker and an angiotensin receptor blocker may cause postural hypotension.

Eight months before her current presentation to the emergency department, while sitting and having lunch, she had two episodes of sudden dizziness followed by syncope lasting for 1–2 minutes. She described a prodrome of hot sensation and diaphoresis prior to loss of consciousness. She immediately presented to her GP and her antihypertensive medication was adjusted. An ECG revealed normal sinus rhythm at 80 beats per minute (Figure 1). No further investigation was done at that stage but she was advised to go to hospital if the dizziness recurred.

Figure 1. ECG of patient X

Figure 1. ECG of patient X

She had been well over the next 8 months but 18 hours before her current presentation to the emergency department, she experienced five separate but similar episodes of dizziness while lying in bed. These episodes were also followed by syncopal episodes lasting between a few seconds to 2 minutes. Again, there was no precipitant or sudden change in posture or emotion prior to the dizziness. This time she was referred to hospital for further assessment.

The additional information above confirms that the dizziness was not associated with head movement and was not postural in nature. There was no history of bleeding or volume depletion. It is worrisome that the dizziness was always followed by syncopal episodes that increased in frequency over a period of 24 hours. It is unlikely that the dizziness is due to vestibular dysfunction and is more likely to be due to a cardiac arrhythmia such as bradyarrythmia.

On examination her blood pressure was 155/85 mmHg when lying down and 175/90mmHg when standing, and heart rate was 73 beats per minute. Her temperature was 36.3°C, oxygen saturation was 97% at room air and her random blood sugar was 6.2 mmol/L. Her Glasgow coma scale was 15/15 and she was alert and orientated. Cardiovascular examination revealed dual heart sounds with ejection systolic murmur at the aortic region radiating to the carotids. Jugular venous pressure was not elevated and there was no pedal oedema or calf tenderness. Lung auscultation was clear and respiratory rate was 20 respirations per minute. Abdominal and neurological examinations were normal. A blood test showed haemoglobin 143 g/L, white cell count 9.7 x 109/L, sodium 137 mmol/L, potassium 4.2 mmol/L, magnesium 0.8 mmol/L, free T4 12.5 pmol/L, thyroid stimulating hormone 0.16 mU/L, iron 24 umol/L, transferrin 26 umol/L, transferrin saturation 46% and ferritin 38 µg/L.

Blood pressure was slightly elevated but there was no postural decrease on standing, which suggests safe dosage of the antihypertensive combination and excludes volume depletion. Her heart rate was within normal limits and glucose level was normal, which excludes hypoglycaemia. Her oxygen saturation was maintained in room air, which makes a diagnosis of pulmonary embolism unlikely. Neurological examination was normal, excluding a neurological disorder. The ejection systolic murmur may account for aortic stenosis and requires further investigation with echocardiography. The blood tests are reassuring.

The patient was admitted for cardiac monitoring. A similar episode recurred the next morning, coinciding with 14 seconds of ventricular standstill on telemetry (Figure 2). An echocardiogram showed normal left ventricular size, hyperdynamic systolic function, an ejection fraction of 75% and normal valvular structure. A carotid ultrasound showed no haemodynamically significant carotid artery disease.

Figure 2. Telemetry of patient X

Figure 2. Telemetry of patient X

On the basis of the telemetry result, the patient’s prodrome of dizziness and syncopal episode is due to an arrhythmia. The normal echocardiogram excludes structural heart disease. The ejection systolic murmur heard in the examination may represent systolic flow murmur.

The patient received a dual-chamber pacemaker with a lower rate limit of 50 beats per minute.

Discussion

Patients often describe presyncope as a feeling of fainting or dizziness. It is caused by global cerebral hypoperfusion and is usually associated with compensatory activation of the sympathetic nervous system, which manifests as symptoms of diaphoresis and tachycardia.2 Presyncope episode is often followed by syncope, a transient loss of consciousness followed by complete and spontaneous recovery.7 This phenomenon was seen in the case above.

There are multiple causes of presyncope/syncope, which can affect people of any age. In general, it can be classified into three broad categories: neurally mediated syncope, orthostatic hypotension and cardiac syncope8 (Table 2). Rarer causes include syncope secondary to neurological, metabolic and psychogenic disorder.

Table 2. Etiology of presyncope/syncope8
Neurally mediated syncope Vasovagal syncope Provoked by
  • pain
  • fear, emotion
  • venesection
Situational syncope Provoked by
  • coughing
  • micturition
  • defaecation
Orthostatic hypotension Primary autonomic failure Lewy body disease
Multiple system atrophy
Secondary autonomic failure Diabetes
HIV neuropathy
Postprandial hypotension  
Drug-induced Anti-hypertensives, diuretics, antidepressants
Volume loss  
Cardiac syncope Arrhythmias Sinus node dysfunction
Atrioventricular dysfunction
Supraventricular tachycardia
Ventricular tachycardias
Atrial fibrillation
Structural cardiac disease Valvular heart disease
Ischaemic heart disease
Cardiomyopathy
Pericardial disease

Generally, the three categories of presyncope/syncope are associated with three different age groups. Neurally mediated syncope, such as vasovagal or situational syncope, often affect children and young adults.9 A study by Kang et al in children aged 3–18 years showed that syncope may be related to prolonged standing (30%), movement (13%) or a change in body position (9%).9 It may also be situational (ie. provoked by micturition, defecating or coughing).9 Syncope in this age group is usually considered low risk.

In middle-aged people (40–70 years), 10–20% of syncopal episodes have a cardiac aetiology.10 Adult athletes often experience exercise-induced syncope, which may be associated with underlying structural heart disease (ie. hypertrophic obstructive cardiomyopathy and Wolff-Parkinson-White syndrome).11 Often, a family history of sudden death is an important clue. In adults who have multimorbidities and risk factors, the incidence of coronary atherosclerosis is high. As this is a modifiable disease requiring secondary prevention, careful investigation and early intervention are vital. People in this age group (40–70 years) are also at risk of syncope related to arrhythmias.12 Initial investigation should include 12-lead ECG, 24-hour Holter monitoring or 7-day event loop recorder.12 Electrolyte imbalance may predispose to arrhythmias and, therefore, routine blood tests to measure levels of electrolytes and magnesium are important. If these investigations are negative, an electrophysiological study may be considered.12 If an underlying structural heart disease is suspected, transthoracic echocardiography should be considered. If a cardiac ischaemic event is suspected, troponin and cardiac stress test should be requested. Misdiagnosing cardiac syncope can be fatal and in this age group it is usually considered high risk and further investigation is warranted until all differential diagnoses have been explored.

In elderly people (>70 years), syncope is often associated with orthostatic hypotension secondary to autonomic failure, volume loss or medications. Age-related physiological changes, such as blunting of baroreflex sensitivity, reduced intravascular blood volume, greater susceptibility to infection, reduced myocardial elasticity and increased afterload, play a significant part in syncope in this age group.13 Medication review is crucial especially for medications that reduce blood pressure (eg. antihypertensive drugs, anti-parkinsonian drugs), affect cardiac output (eg. beta blockers, antiarrhythmics), prolong QT interval (eg. tricyclic antidepressants, amiodarone), cause drowsiness (ie. sedatives, cocaine) or affect electrolytes (ie. diuretics).14 Syncope in this age group requires careful assessment of their medication, comorbidities and fluid status.

Neurological disorders that cause syncope include seizures, migraine, transient ischaemic attacks and stroke.11 Electroencephalography should be requested if seizures are suspected.11 A computed tomography (CT) scan of the head is useful to rule out acute intracranial haemorrhage; however, routine head scans are not recommended for patients with low suspicion of neurological disease as diagnostic yield is low.11 In transient ischaemic attacks or stroke, syncope often results from disturbances in vertebrobasilar circulation presenting as vertigo and nystagmus.11 In such cases, magnetic resonance imaging (MRI) of the head is superior to imaging of the posterior circulation.11 Metabolic causes include hypoxia, hypo-/hyperglycaemia, anaemia and dehydration.11 This can be easily assessed by clinical examination and baseline blood tests. Intoxication with alcohol or illicit drug use is common in the younger age group. Lastly, psychogenic disorders should be considered when other aetiologies have been excluded. Social psychiatric histories are important in such cases and referral to a psychiatrist may be helpful.

The severity of syncope ranges from benign to fatal and distinguishing between different aetiologies can be challenging, as described above. Evaluation of patients presenting with syncope is outlined in Figure 3. Quinn et al have devised a syncope risk-stratification tool known as the San Francisco Syncope Rule.15 This tool is used to classify patients as high risk for fatality if they have any element of ‘CHESS’: congestive cardiac failure, haematocrit <30%, electrocardiogram abnormality, shortness of breath or systolic blood pressure <90 mmHg.15 A validation study in 2006 showed a 98% sensitivity and 56% specificity for predicting serious outcome.15 This risk-stratification tool together with with the red-flags described in Table 3 can be used to help general practitioners to ascertain safety discharge.

Figure 3: Evaluation of patients with pre-syncope/syncope in GP practice

Figure 3: Evaluation of patients with pre-syncope/syncope in GP practice16

Table 3. Cardiac red flags 8,11
Symptoms Chest pain Coronary artery disease
Worsening shortness of breath on exertion Heart failure
Palpitation or ‘skipped beats’ Arrhythmias
Signs Fluid overload Heart failure
Murmurs Valvular heart disease
Carotid bruits Carotid artery stenosis
Past history Ventricular arrhythmias, coronary vascular disease
Family history Sudden death
ECG findings Ischemic changes ST and T wave ischaemic changes
Prolonged QTc QTc >500 msec
Atrial fibrillation New atrial fibrillation
Persistent sinus bradycardia/tachycardia HR <40 or >120
Non-sustained ventricular tachycardia 4 or more VT beat
Brugada pattern J-point ST elevation V1–V3 and right bundle branch block
Wolf-Parkinson-White syndrome or supraventricular tachycardia Short PR interval and delta wave
Atrioventricular block Prolonged PR interval and bundle branch block
Right ventricular dysplasia Right bundle branch block with QRS >110 ms in V1, an epsilon wave in V1–V2 and T-wave inversion in right precordial leads

Conclusion

Dizziness is a common clinical presentation. The biggest challenge for doctors is to formulate a diagnosis and to be able to identify patients with high-risk features that will require further investigation and urgent management to avoid fatality. Careful history taking and physical examination are pivotal in this case.

Competing interest: None.
Provenance and peer review: Commissioned; externally peer reviewed.

Acknowledgements

I wish to acknowledge the help provided by Dr Karam Kostner MD, PhD, FRACP, Consultant Cardiologist and Lipidologist at Mater Hospital for his assistance in the completion of this article.

References

  1. Post R, Dickerson L. Dizziness: A diagnostic approach. Am Fam Physician 2010;82:361–68.
  2. Samuels M, Pomerantz B, Sadow P. Case 14-2010: A 54-year-old woman with dizziness and falls. N Engl J Med. 2010;362:1815–23.
  3. Thibault GE. Diagnostic strategy – the shotgun versus the arrow. N Engl J Med 1995;332:321–25.
  4. Powell LW. Hemochromatosis. In: Longo DL, et al, eds. Harrison’s Principles of Internal Medicine 18th ed. New York: McGraw-Hill; 2012; vol 2:3162–67
  5. McCarthy GM, McCarthy CJ, Kenny D, Crowe J, Eustace S. Hereditary hemochromatosis: a common, often unrecognized, genetic disease. CCJM 2002;69:224–37.
  6. Kremastinos D, Farmakis D. Iron overload cardiomyopathy in clinical practice. Circulation 2011;124:2253–63.
  7. Kapoor W. Syncope. N Engl J Med 2000;343:1856–62.
  8. Freeman R. Syncope. New York: Harrisons’s Principles of Internal Medicine, 2011.
  9. Kang MH, Xu Y, Wang C, et al. Causes of unexplained syncope in children. CJCP 2012;14:771–74.
  10. Lipsitz LA, Wei JY, Rowe JW. Syncope in an elderly, institutionalized population: prevalence, incidence, and associated risk. Q J Med 1985;55:45–54.
  11. Tadros GM, Oren JW, Costello JM. Syncope in young patients I: an approach to the patient with syncope. Hospital Physician 2002;38:47–54.
  12. Farwell DJ, Sulke AN. Does the use of a syncope diagnostic protocol improve the investigation and management of syncope? Heart 2004;90:52–58.
  13. Dreger N, Denson K, Manzi G, Wessel B. Cardiac causes of syncope in geriatric patients. F Fast Fact #202012. Available at www.mcw.edu/Geriactric-Fast-Facts/Index/gff020.htm [Accessed 8 January 2014].
  14. Morag R. Syncope. Available at emedicine.medscape.com/article/811669-overview [Accessed 8 January 2014].
  15. Quinn J, McDermott D, Stiell I, Kohn M, Wells G. Prospective validation of the San Francisco syncope rule to predict patients with serious outcomes. Ann Emerg Med 2006;47:448–54.
  16. Shribman J. Arrhythmia from a GP perspective. Available at www.heartrhythm-congress.com/files/file/ Presentations_Tuesday/J_Shribman_ Arrhythmia_from_a_primary_care_perspective.pdf [Accessed 23 September 2013].

Correspondence afp@racgp.org.au

Yes     No

Declaration of competing interests *

Yes No

Additional Author (remove)

Yes No

    

 

 

 

 

Competing Interests: 

Your comment is being submitted, please wait

 

Download citation in RIS format (EndNote, Zotero, RefMan, RefWorks)

Download citation in BIBTEX format (RefMan)

Download citation in REFER format (EndNote, Zotero, RefMan, RefWorks)

For more information see Wikipedia: Comparison of reference management software
Advertisement loading...

Advertisement

Type

Focus

2014