In obtaining the history of a patient with suspected Raynaud phenomenon, clinicians should address the age of onset, the location of affected areas, the presence of symmetry, the presence of digital ulcerations, and severity of the attacks. The presence of other systemic symptoms should be elicited to rule out secondary Raynaud phenomena. Provoking factors should be identified once confirmed to be Raynaud phenomenon. Provoking factors may include exposure to cold temperatures or sympathetic nervous system stimulation from emotional stress or being startled. Certain factors increase the likelihood for increased frequency of attacks, increased severity with worse pain. These include the presence of stress, female gender, low temperature, and the presence of a concurrent connective tissue disease. The later the onset of Raynaud phenomenon, particularly in the 30s and 40s age range, the higher the risk of the development of a connective tissue disorder.

Raynaud phenomena typically affect fingers (distal areas). A Raynaud phenomenon attack is sudden with the development of cold digits and the demarcation of "white" areas also known as skin pallor or white attack. Instead of white attack, there may be cyanotic skin changes, otherwise known as a blue attack. The white or blue attack typically remains for approximately 20 minutes. After the Raynaud phenomenon flare, vascular reperfusion with subsequent rewarming occurs. This results in erythematous areas where the flare occurred. It is known as reactive hyperemia. 

A Raynaud phenomenon attack starts out with a single digit and then spreads to other digits symmetrically on both hands. The thumb is typically spared. If the thumb is affected, this may be a sign of secondary Raynaud phenomenon. It may also result in cutaneous vasospasm affecting facial areas, ears, knees, or nipples.

As a result of vasoconstriction, pin and needles sensation, numbness or finger aches or pain are common complaints with Raynaud phenomenon attacks. If the Raynaud phenomenon attack is severe, typically with secondary Raynaud phenomenon, digital ulceration of the tips of fingers and toes may occur due to prolonged vasoconstriction with subsequent tissue ischemia. Eventual gangrene or loss of digits may occur in severe forms of Raynaud phenomenon attacks. In general, Raynaud phenomenon attacks are less severe in primary Raynaud phenomenon compared to secondary Raynaud phenomenon. 

Another skin finding seen during a Raynaud phenomenon attack is livedo reticularis. This results in purplish mottling or reticular pattern over the skin due to small blood vessel clots. This finding is reversible with rewarming but is irreversible with secondary causes, such as antiphospholipid syndrome, vasculitis, cold agglutinin disease, or peripheral vascular disease.

Nailfold capillary microscopy is utilized as a diagnostic method to differentiate primary Raynaud phenomena from secondary Raynaud phenomenon. It analyzes microvascular and morphologic changes in peripheral vessels seen with CTD, such as changes in architecture, capillary size, capillary density, the presence of hemorrhage, and avascular areas without capillary loops. This is done using a dermatoscope or ophthalmoscope. Nailfold videocapillaroscopy can also be used. Abnormal nail-fold microscopy is correlated with an increased likelihood of the development of CTD. The changes were seen are capillary loops appear enlarged or there is a loss of capillary loops. If there are mega-capillaries with a decreased capillary density, then these changes are indicative of scleroderma. [9][10][11]

Treatment of Raynaud phenomenon aims at decreasing the frequency and severity of the attacks with prevention of tissue ischemia. Treatment response is measured by the Raynaud Condition Score (RCS). This scoring system looks at the quality of life, frequency and severity of attacks, and the effect of Raynaud phenomenon on an individual.  [6][12][13]

Conservative medical management to prevent Raynaud phenomenon attacks is a lifestyle change. This includes avoiding exposure to cold, staying warm, avoiding stimulants, avoiding anxiety or emotional stress, and smoking cessation.

If the patient fails to respond to only conservative therapy, then pharmacologic therapy with a vasodilating mechanism of action is used. Dihydropyridine calcium channel blockers (DHP CCBs) are the first-line pharmacologic treatment for Raynaud phenomenon. DHP CCBs include amlodipine and nifedipine. When starting CCBs, the medication is started at the lowest dose and gradually titrated every 4 weeks depending on the patient's response. Monitoring blood pressure response is important, particularly if the patient has baseline blood pressures that are low.

  1. Amlodipine dosage: Minimum 5 mg to maximum 20 mg daily

  2. Nifedipine dosage: Minimum 30 mg to maximum 180 mg daily

The medication may be administered as either slow-release form, rapid or short-acting form, or long-acting form. Typically, the slow-release or long-acting forms of CCBs are used. An urgent situation prompts the use of a rapid, short-acting form of CCB, which is used more frequently in patients with severe form of Raynaud phenomenon.

Adverse effects of DHP CCB includes dose-related peripheral edema, palpitations, reflex tachycardia, dose-related dizziness, and headaches. 

Contraindications to DHP CCB are hypotension, peripheral edema, angina, myocardial infarction. It should also be avoided in patients with severe aortic stenosis, hypertrophic cardiomyopathy, and severe pulmonary hypertension.

CCBs should be avoided in pregnancy unless digit ischemia is present. 

If the patient fails to respond to DHP CCB therapy, a phosphodiesterase (PDE) inhibitor. It can be added to the current CCB therapy if partial treatment response is noted to the CCB. If there is no treatment response to the CCB, then the PDE inhibitor can be used as monotherapy. Sildenafil is started at a low dose, 20 mg daily, and then titrated depending on response over a period of 4 to 6 weeks with a maximum dose of 20 mg 3 times a day.

Alternative therapy to treatment failure using CCB and PDE inhibitor is topical nitrates, such as nitroglycerin, which is a direct vasodilator. Typically, 2% nitroglycerin ointment is used and applied to affected Raynaud phenomenon areas. Topical nitrates are absorbed systemically and may result in adverse systemic effects, such as hypotension, dizziness, and headache.

Other options, if the patient does not respond to the above therapies, include the following: losartan, fluoxetine, and prazosin.

If tissue ischemia is present in the digits and symptoms are severe, then intravenous infusion of prostaglandin is used. Different intravenous prostaglandins include iloprost, epoprostenol, treprostinil, and alprostadil. Prostaglandin functions as a strong vasodilator and also prevents platelet cell aggregation.

Bosentan blocks endothelin-1 vasoconstrictive effect. This is used in recurrent digit ulceration in CTD, such as systemic sclerosis. Surgery to remove the particular sympathetic nerves that cause vasoconstriction, also known as sympathectomy, can be used in severe, refractory cases.

In the setting of secondary Raynaud phenomenon and history of ischemic ulceration, low dose aspirin 81 mg should be used daily. If there is aspirin intolerance or contraindication, clopidogrel, or dipyridamole can be used instead.[14][15]

There are different conditions or disease that appear similar to Raynaud phenomenon. This includes the following external blood vessel compression, complex regional pain syndrome, erythromelalgia, acute idiopathic blue finger also known as paroxysmal finger hematoma, acrocyanosis, occlusive peripheral vascular disease, peripheral neuropathy, and excessive cold sensitivity.

With primary Raynaud phenomenon, spontaneous remission, whereby the patient has been free of Raynaud phenomenon attacks, may occur. Spontaneous remission is not seen with secondary Raynaud phenomenon. Pregnancy has been shown to improve Raynaud phenomenon since there is an improvement in peripheral blood flow and oxygenation due to increase in red blood cell mass and plasma volume.

Severe Raynaud phenomenon may result in tissue ischemia, leading to necrosis followed by amputation of the affected area.

Vascular surgery consult is needed for sympathectomy. A primary care physician can treat primary Raynaud phenomenon. Rheumatology should be consulted if there is secondary Raynaud phenomenon.

 an interprofessional approach to Raynaud phenomenon

Raynaud phenomenon is best managed with an interprofessional team of healthcare professionals. The key to improving the morbidity is education. Besides the physician, the nurse and the pharmacist are in a prime position to educate the patient about the hazards of smoking. In addition, patients have to be told to insulate their hands and fingers from the cold. The pharmacists must make sure that the patient is on no medication that can cause vasoconstriction of the blood vessels. When ulcers develop the patient should be told to seek medical help as soon as possible to avert gangrene. A wound care nurse should be consulted on educating the patient on the care of the wounds and the type of dressings to use. A dietary consult is recommended as there is some evidence that a diet rich in omega 3-fatty acids may be beneficial in preventing Raynaud phenomenon. [16][17][18](Level V)

Outcomes

The prognosis for patients with primary Raynaud phenomenon in young people is good with little morbidity or mortality. However, if the patient does not change lifestyle or smokes, then ischemia may affect the distal tips of the fingers and lead to necrosis. There are reports that in the elderly population with Raynaud phenomenon, the risk of adverse cardiac events may be increased compared to the general population. For patients with secondary Raynaud phenomenon, the prognosis depends on the underlying disorder. In general, the quality of life for these patients is poor as they need to adopt a rigid lifestyle. Plus, many other secondary causes often have no cures and relapses are common.[2][19][20] [Level 5]