Cyanosis – Causes, Symptoms, Diagnosis, Treatment

Cyanosis – Causes, Symptoms, Diagnosis, Treatment

Cyanosis /Cyan means ‘blue’ and the abnormal bluish discoloration of the skin and mucous membranes is referred to as “cyanosis”. It is a pathologic sign, and not a disease by itself. Underlying diseases that increase the deoxygenated hemoglobin to 5.0 g/dl or more leads to cyanosis. Cyanosis can be best appreciated in areas with rich superficial vasculature and thin overlying dermis. These include lips, nose, earlobes, oral cavity, extremities, and tips of fingers and toes. Cyanosis usually becomes evident in hypoxemia, that is, abnormally low concentration of oxygenation (<80-85%) in arterial blood. However, it is not sensitive or a specific indicator of hypoxemia. Since cyanosis is a clinical sign, a proper evaluation is important to determine the etiology of cyanosis.

Acrocyanosis is due to a decrease in the amount of oxygen delivered to the tissues of the extremities. Several mechanisms for primary acrocyanosis have been proposed, but the precise mechanism remains elusive. Potential pathophysiological disturbances include abnormal arteriolar tone, alteration of microvascular responsiveness with capillary and venular dilation and stasis, and abnormal sympathetic nervous system activity.

Types of Cyanosis

Cyanosis is further classified as central, peripheral, and differential.

  • Central cyanosis – is a generalized bluish discoloration of the body and the visible mucous membranes, which occurs due to inadequate oxygenation secondary to conditions that lead to an increase in deoxygenated hemoglobin or the presence of abnormal hemoglobin.
  • Peripheral cyanosis – is the bluish discoloration of the distal extremities (hands, fingertips, toes), and can sometimes involve circumoral and periorbital areas. Mucous membranes are generally not involved. Peripheral cyanosis is rarely a life-threatening medical emergency. However, it is essential to determine the underlying cause and its timely management to prevent potential complications.
  • Differential cyanosis – is the asymmetrical bluish discoloration between the upper and lower extremities. It usually indicates serious underlying cardiopulmonary conditions.

The bluish discoloration despite adequate oxygenation is sometimes seen due to the ingestion of drugs, toxins, or metals. This is called ‘Pseudocyanosis.’

Pathophysiology

Cyanosis is due to inadequate oxygenation of blood. It results when the deoxyhemoglobin exceeds 5.0 g/dL. The bright red color of the blood is due to an adequate content of oxygen in the blood, which changes to a darker red with a reduced level of oxygen reflecting more blue light making the skin appear to have a blue tint. However, the blue tint is more apparent with high hemoglobin count.

The pathophysiology of cyanosis is as follows:

Hypoxic Hypoxia – Due to decreased oxygen tension and content in arterial and venous blood, the oxygen diffusion to the tissues is decreased.

  • Inspired air is low in oxygen content: Sea level, high altitude
  • Decreased ventilation: Emphysema, respiratory center depression
  • Decreased diffusion through the alveolar-capillary membrane: fibrosis, interstitial edema
  • Right to left shunting of blood in the heart: patent ductus arteriosus (PDA), interventricular or interatrial defects

Stagnant Hypoxia – In this oxygen tension and content in the arterial blood is normal, but the hypoxia is due to reduced or uneven blood flow to the tissues. As a result of the increased extraction of the available oxygen at the tissue level, the oxygen tension, and content in the venous blood decrease.

  • Generalized reduced blood flow: Congestive heart failure.
  • Localized reduced blood flow: Peripheral vascular diseases such as Raynaud which can lead to peripheral vessel spasm (the lack of blood flow leads to the white coloration of fingers, followed by bluish discoloration when the veins dilate to keep the blood flow going, finally returning to red color on the restoration of blood flow)

Asphyxia – In this, there is both hypoxia as well as increased levels of carbon dioxide (hypercapnia)

Peripheral cyanosis occurs due to the inability of the body to deliver oxygen-rich blood to the peripheral tissues. Congestive peripheral cyanosis can be caused due to the slowing of blood flow. Ischemic peripheral cyanosis occurs when vasoconstriction leads to diminished peripheral blood flow. In peripheral cyanosis, there is normal arterial oxygen saturation but increased oxygen extraction by the peripheral tissue in the capillary bed in the setting of peripheral vasoconstriction and decreased peripheral blood flow. This results in a significant difference in the saturation between the arterial and venous blood, with increased deoxygenated blood on the venous side of the capillary beds.

Reduced cardiac output in heart failure and shock can lead to peripheral cyanosis, if severe. Lack of pressure prevents an adequate supply of oxygen-rich blood to the extremities. Also, hypotension produces reflex cutaneous vasoconstriction to shunt blood from extremities to the internal organs. This redistribution of blood flow from extremities causes cyanosis of extremities.

Exposure to cold increases the transit time through capillary beds. This results in cyanosis due to increased unloading of oxygen from the blood to the tissues.

Benign vasomotor changes can cause acrocyanosis, a form of peripheral cyanosis. It can be a normal finding in babies which resolves within the first few days of life. Additionally, it can also be seen in infancy when babies cry, vomit, regurgitate, cough, hold their breath. It is not considered pathologic unless there is significantly low cardiac output leading to cutaneous vasoconstriction.

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In the Raynaud phenomenon, abnormal vasospasm occurs with exposure to change in temperature and emotional events. The diminished blood flow causes a blue discoloration of the fingers and toes.

About 98% of oxygen is normally bound to hemoglobin, with the remaining 2% dissolved in plasma.

Causes of Cyanosis

Central cyanosis may be due to the following causes
  • Hypoventilation due to conditions affecting the central nervous system, such as intracranial hemorrhage, tonic-clonic seizures, and heroin overdose.
  • Pulmonary causes leading to ventilation-perfusion mismatch and impaired alveolar-arterial diffusion, for instance, bronchospasm (asthma), pulmonary embolism, pneumonia, bronchiolitis, pulmonary hypertension, hypoventilation, and COPD
  • Cardiovascular causes include heart failure, congenital heart diseases (right to left shunting), and valvular heart diseases.
  • Hemoglobinopathies including methemoglobinemia, sulfhemoglobinemia
  • Polycythemia
  • High altitude
  • Hypothermia
  • Obstructive sleep apnea
  • Pulmonary
  • Impaired gas exchange secondary to pneumonia
  • Embolism and ventilation-perfusion mismatch
  • Impaired gas diffusion via the alveoli
  • High altitude
  • Anatomic shunts
  • Right to left shunt in congenital heart disease
  • Arteriovenous malformation
  • Intrapulmonary shunt

1. Central nervous system (impairing normal ventilation)

  • Intracranial hemorrhage
  • Drug overdose (e.g. heroin)
  • Tonic–clonic seizure (e.g. grand mal seizure)

2. Respiratory system

  • Pneumonia
  • Bronchiolitis
  • Bronchospasm (e.g. asthma)
  • Pulmonary hypertension
  • Pulmonary embolism
  • Hypoventilation
  • Chronic obstructive pulmonary disease, or COPD (emphysema)

3. Cardiovascular diseases

  • Congenital heart disease (e.g. Tetralogy of Fallot, right to left shunts in heart or great vessels)
  • Heart failure
  • Valvular heart disease
  • Myocardial infarction

4. Blood

  • Methemoglobinemia * Note this causes “spurious” cyanosis, in that, since methemoglobin appears blue,[7] the patient can appear cyanosed even in the presence of a normal arterial oxygen level.
  • Polycythaemia
  • Congenital cyanosis (HbM Boston) arises from a mutation in the α-codon which results in a change of primary sequence, H → Y. Tyrosine stabilises the Fe(III) form (oxyhaemoglobin) creating a permanent T-state of Hb.

5. Others

  • High altitude, cyanosis may develop in ascents to altitudes >2400 m.
  • Hypothermia
  • Obstructive sleep apnea
Peripheral cyanosis

Peripheral cyanosis is the blue tint in fingers or extremities, due to an inadequate or obstructed circulation.[8] The blood reaching the extremities is not oxygen-rich and when viewed through the skin a combination of factors can lead to the appearance of a blue color. All factors contributing to central cyanosis can also cause peripheral symptoms to appear but peripheral cyanosis can be observed in the absence of heart or lung failures. Small blood vessels may be restricted and can be treated by increasing the normal oxygenation level of the blood.

Peripheral cyanosis may be due to the following causes:

  • All common causes of central cyanosis
  • Reduced cardiac output (e.g. heart failure or hypovolaemia)
  • Cold exposure
  • Chronic obstructive pulmonary disease (COPD)
  • Arterial obstruction (e.g. peripheral vascular disease, Raynaud phenomenon)
  • Venous obstruction (e.g. deep vein thrombosis)
Differential cyanosis

Differential cyanosis is the bluish coloration of the lower but not the upper extremity and the head. This is seen in patients with a patent ductus arteriosus.

  • Patients with a large ductus develop progressive pulmonary vascular disease, and pressure overload of the right ventricle occurs.
  • As soon as pulmonary pressure exceeds aortic pressure, shunt reversal (right-to-left shunt) occurs. The upper extremity remains pink because the brachiocephalic trunk, left common carotid trunk and the left subclavian trunk is given off proximal to the PDA.

Symptoms of Cyanosis

Acrocyanosis is characterized by peripheral cyanosis: persistent cyanosis of the hands, feet, or face.[rx] The extremities often are cold and clammy and may exhibit some swelling (especially in the warmer weather).[rx][rx] The palms and soles exhibit a wide range of sweating from moderately moist to profuse, but all peripheral pulses should have normal rate, rhythm, and quality.[rx][rx] Exposure to cold temperatures worsens the cyanosis, while it often improves on warming.[rx] Aside from the color changes, patients normally are asymptomatic and therefore there is usually no associated pain. The most common sign, discoloration, usually is what prompts patients to seek medical care.[rx][rx]

1. Age-related and the nature of Cyanosis onset

  • Cyanosis caused by congenital heart disease, which in turn causes anatomical right-to-left shunts, that may have been prevalent from birth or the early years of life.
  • Acute onset ofCyanosis, which could be caused by conditions like pulmonary emboli, cardiac failure, pneumonia or asthma.
  • People suffering from COPD (Chronic Obstructive Pulmonary Disease) may develop Cyanosis over time and an associated condition called polycythaemia may exacerbate the intensity of Cyanosis.

2. Previous history:

  • Cyanosis may also be caused by any lung disease of sufficient intensity.

3. Drug history: there are a set of drugs that may result in methemoglobinemia (e.g. nitrates, dapsone) or sulfhemoglobinemia (e.g. metoclopramide).

4. Associated symptoms:

  • Pain in the chest: Cyanosis that is associated with pleuritic chest pains could be caused by pulmonary embolism or pneumonia. Pulmonary oedema could cause dull, painful chest tightness.
  • Dyspnoea: this is a condition that may suddenly occur in conjunction with pulmonary emboli, pulmonary oedema or asthma.
  • Gasping for or shortness of breathing difficulties
  • Fever
  • Headache
  • Profuse sweating profusely
  • Pain or numbness in the arms, legs, hands, fingers, or toes
  • Paling or whitening of the arms, legs, hands, fingers, or toes
  • Dizziness or fainting.
  • Temperature: conditions like pneumonia and pulmonary emboli that could be with pyrexia.
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The patient will also exhibit symptoms like

  • Central Cyanosis – this condition produces a bluish discolouration, specially noticed on the mucous membranes of the lips, tongue, fingers and toes.
  • Peripheral Cyanosis – this condition affects the fingers, toes and skin surrounding the lips, is not noticed around mucous membranes.
  • A combination of clubbing and Cyanosis is frequent observed in congenital heart disease; it may be prevalent in pulmonary diseases, like lung abscess, bronchiectasis, cystic fibrosis; as also in pulmonary arteriovenous shunts.
  • Pressure in the jugular venous system increases with congestive cardiac failure.

After a respiratory examination:

  • Poor chest expansion is a condition that is noticed in patients with chronic bronchitis, and asthma. Reduced chest expansion may be noticed with conditions like lobar pneumonia.
  • Dullness to percussion is sometimes noticed in an area of consolidation.
  • Crepitation that is localised may sometimes be heard in conditions like lobar pneumonia. Crepitation is often more likely in conditions like bronchopneumonia and pulmonary oedema. Entry of air may be low with conditions like COPD or asthma. Bronchial breathing may be affected and wheezing sounds may sometimes be heard, in conditions like asthma.

Abnormal heart sounds that are sometimes heard, may suggest origins in the cardiac area. Features that are localised may indicate aetiology of Peripheral Cyanosis. These could cover oedema in venous insufficiency or absence of Peripheral pulses and an ischaemic condition in arterial occlusion

Peripheral cyanosis is characterized by the following:

  • Localized cyanosis affecting only extremities
  • Pink tongue as mucous membranes are almost never involved
  • Cold extremities as compared to warm extremities in central cyanosis
  • Clubbing is absent
  • Pulse volume usually low
  • Capillary refill time more than 2 sec
  • Disappears with massage and warming
  • Dyspnea usually absent

In children, the most common etiologies for life-threatening central cyanosis are congenital heart disorders and polycythemia. The common causes of peripheral cyanosis in this age group are cold exposure and acrocyanosis.

Diagnosis of Cyanosis

History and Physical

The detailed history and physical examination are vital in determining the underlying cause of cyanosis. The provider should inquire about the onset, duration, intake, or exposure to poisonous substances, exposure to the cold, site where cyanosis can be appreciated, and associated symptoms.

Physical examination should be carried out in an adequate light for the correct assessment of cyanosis. Poor light exposure, the thickness of the skin, and pigmentation of the skin can affect the accuracy of physical assessment. Cheeks, nose, ears, and oral mucosa are the best areas to assess cyanosis as the skin in these areas is thin, and blood supply is good. This can help determine if the cyanosis is generalized, limited to extremities, or if there is a difference in the bluish discoloration in different extremities.

  • Painless blue fingers, hands, nose, lips, toes, or feet
  • Digits may often feel cool.
  • Symptoms worsen with cooler temperatures.
  • Onset typically in 2nd or 3rd decade
  • Symptoms are long-standing but not generally progressive.
  • Can be associated with hyperhidrosis of hands (“sweaty palms”)
Physical Exam
  • Cyanosis of affected areas, usually distal hands and feet
  • Bilateral involvement
  • Peripheral pulses are strong.
  • No trophic changes (no loss of hair) nor ulcerations
Differential Diagnosis
  • RP
  • Staining of skin (Consider wiping the skin with an alcohol swab.)
  • Chilblains
  • Livedo reticularis
  • Peripheral neuropathy affecting vascular flow
  • Complex regional pain syndrome (previously reflex sympathetic dystrophy or causalgia)
  • Occlusive arterial disease (usually affects only one limb and is progressively painful)
Initial Tests (lab, imaging)
  • All tests are typically normal with acrocyanosis, but it is a diagnosis of exclusion and usually needs further evaluation to rule out secondary cause of acrocyanosis.
  • Capillary oximetry
  • Complete blood count (CBC)
  • If concerned about connective tissue diseases, CBC, antinuclear antibody (ANA), erythrocyte sedimentation rate (ESR), and C-reactive protein (CRP) to screen
  • If concerned about hypercoagulable state: anticardiolipin antibodies, prothrombin gene mutation, proteins C and S, factor V Leiden, antithrombin III, and others
  • CMP and/or metabolic screening
  • CT, MRI, NCV, and so forth

The inspection – also includes looking for any thoracic cage deformity, accessory muscle use for respiration (nasal flaring, grunting, intrathoracic/supraclavicular retractions), asymmetry of chest expansion, discomfort in breathing, audible breath sounds, clubbing, posture, etc. These are helpful in narrowing down the underlying causes, especially if the cause is cardiac or pulmonary. It is helpful to carry out the palpation of brachial and femoral pulses, tactile and vocal fremitus, assessment of ventilation, and measurement of blood pressure in all four extremities.

Evaluation
  • Co-oximetry and simple oximetry – are spectrophotometry methods to measure arterial blood oxygenation. Pulse oximetry is a non-invasive method as compared to co-oximetry, which requires a sample of arterial blood.
  • To begin with, pulse oximetry –  a non-invasive and easily available test, should be done to rule out life-threatening hypoxemia as a cause. It is used to assess oxygenation; however, it may falsely indicate hypoxemia in peripheral cyanosis and dyshemoglobinemias. For instance, the value may be low if measured on an affected limb in both central and peripheral cyanosis.
  • Co-oximetry – in addition to measuring oxygen saturation, can be used for arterial blood gas analysis. Arterial blood gas analysis shows normal arterial oxygenation in peripheral cyanosis, i.e., 85-100%. Contrary to this, the arterial oxygen saturation is low in central cyanosis. This test also determines the value of hemoglobin derivatives such as oxygenated hemoglobin, deoxygenated hemoglobin, and dyshemoglobins (methemoglobin, carboxyhemoglobin, sulfhemoglobin, etc.). It, therefore, only indicates low oxygen levels in hypoxemia due to central cyanosis. In pseudocyesis, both pulse oximetry and co-oximetry reveal normal oxygen levels.
  • Peripheral blood film – hemoglobin concentration, blood glucose, and sepsis workup should be considered depending on the clinical scenario to evaluate the causes of cyanosis.
  • ECG, and CT scan – can be done to evaluate the cardiopulmonary cause. Echocardiogram and invasive cardiac evaluation may be necessary in some cases.
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Treatment of Cyanosis

The following treatment may be considered at primary stage

  • Antidepressants
  • Antihypertensive drugs
  • Erectile dysfunction drugs
  • Nitroglycerin
  • Anti asthmatic drugs
  • Carbonail iron, folic acid, vitamin b complex, vitamin c

You may also need to avoid certain medications that constrict blood vessels as a side effect. These include types of

  • beta-blockers
  • migraine medications
  • birth control pills
  • pseudoephedrine-based cold and allergy medicines
  • Treatment with vasoactive drugs is not recommended but traditionally is mentioned as optional. However, there is little, if any, empirical evidence that vasoactive drugs (α-adrenergic blocking agents or calcium channel blockers) are effective.[rx][rx]

There is no standard medical or surgical treatment for acrocyanosis, and treatment, other than reassurance and avoidance of cold, is usually unnecessary. The patient is reassured that no serious illness is present. 

The treatment of central cyanosis, which is a clinical sign, is focused on the management of underlying conditions.

  • Initial stabilization with oxygen support through regular/high flow nasal cannula is required for pulmonary oxygen diffusion impairment. In some conditions, assisted ventilation may be necessary.
  • Metabolic abnormalities such as hypoglycemia and hypocalcemia should be corrected, if present. Metabolic abnormalities can occur as a result of the inability to feed secondary to cyanotic heart diseases in children.
  • For cyanotic heart diseases, initial stabilization and airway management should be the priority. Cardiology referral for assessment and intervention is necessary for cyanotic congenital heart diseases such as tricuspid atresia, tetralogy of Fallot, etc. For congenital heart disease correction, surgical intervention is required. Drugs such as prostaglandin E1 infusion are used for ductal dependent conditions for pulmonary blood flow.
  • Drugs such as diuretics, ACE inhibitors, inotropic drugs are considered for heart failure.
  • Antibiotic prophylaxis in cyanotic heart disease patients to prevent bacterial endocarditis.
  • Methylene blue is used for treating methemoglobinemia-induced cyanosis.
  • The best therapy to manage blue discoloration due to exposure to gold and silver salts is the removal of offending agents.

The goal of the management of peripheral cyanosis is to identify and treat the underlying cause of vasoconstriction and the limited supply of oxygen-rich blood to the extremities. Peripheral cyanosis is usually reversible with restoration of the oxygenated blood flow to the extremities. It can rarely pose a life-threatening emergency. However, timely management is important to improve the outcome and prevent any potential complications.

  • Gentle warming and massage of the affected parts provide symptomatic relief and reversal of peripheral cyanosis caused by exposure to cold and Raynaud phenomenon.
  • In addition, longer-term lifestyle changes may be required in some conditions, such as Raynaud phenomenon. Limiting the intake of caffeine and nicotine/smoking, both of which can cause blood vessel narrowing is beneficial.
  • Drugs that cause blood vessel relaxation may be used in peripheral cyanosis. These include antihypertensive drugs, antidepressants, and erectile dysfunction medications. In addition, drugs that constrict blood vessels such as beta-blockers, pseudoephedrine containing medications, birth control pills, and migraine drugs, should be avoided.
  • When peripheral cyanosis is seen in sick looking children with signs of shock, rapid treatment should be done. Airway and breathing management with further evaluation of the cause of shock is warranted. The therapy is based upon the type of shock. Serious conditions, such as heart failure, must be treated in a hospital as an emergency.
  • All causes of central cyanosis can also cause extremity cyanosis. Correcting the underlying cause is the key to managing such cases.

An interprofessional approach involving various subspecialties is warranted to diagnose and manage the underlying cause of cyanosis.

References

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