Raynaud's phenomenon

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Raynaud's phenomenon
Classification & external resources
Hands with Raynaud's phenomenon
ICD-10 I73.0
ICD-9 443.0
DiseasesDB 25933
eMedicine med/1993 
MeSH D011928

Raynaud's phenomenon (RAY-noz), in medicine, is a vasospastic disorder causing discoloration of the fingers, toes, and occasionally other extremities, named for French physician Maurice Raynaud (1834 - 1881). The cause of the phenomenon is unknown, but emotional stress and cold are classically triggers, and the discoloration follows a characteristic pattern in time: white, blue and red. It comprises both Raynaud's disease (primary Raynaud's), where the phenomenon is idiopathic, and Raynaud's syndrome (secondary Raynaud's), where it is secondary to something else.

Contents

The phenomenon is more common in women than men, with the Framingham Study finding that 5.8% of men and 9.6% of women suffered from it.

There is a familial component to primary Raynaud's, and presentation is typically before 30. Smoking worsens frequency and intensity of attacks, and there is a hormonal component. Sufferers are more likely to have migraine and angina than controls.

Secondary Raynaud's has a number of associations:

It is important to realise that Raynaud's can herald these diseases by periods of more than 20 years in some cases, making it effectively their first presenting symptom. This can be the case in the CREST syndrome, of which Raynaud's is a part.

The condition causes painful, pale, cold extremities. This can often be distressing to those who are not diagnosed, and sometimes it can be obstructive. If someone with Raynaud's is placed in too cold a climate, it could potentially become dangerous.

Unilateral Raynaud's, or that which is present only in the hands or feet, is almost certainly secondary, as primary Raynaud's is a systemic condition. However, a patient's feet may be affected without him or her realizing it.

In pregnancy, this sign normally disappears due to increased surface blood flow.

A careful history will often reveal whether the condition is primary or secondary. Once this has been established, investigations are largely to identify or exclude possible secondary causes.

Treatment options are dependent on the type of Raynaud's present. Raynaud's syndrome is treated primarily by addressing the underlying cause, but includes all options for Raynaud's disease as well. Treatment of primary Raynaud's focuses on avoiding triggers:

  • Avoidance of any environmental triggers, e.g. cold, drilling, etc. (although emotional stress is a recognised trigger, it tends to be impossible to consciously avoid).
  • Warm clothing for the extremities such as mittens or HeatBands
  • Hormone regulation and assessment of the type of hormonal contraception used, if any. Contraception which is low in estrogen is preferable, and the progesterone only pill is often prescribed.
  • Smoking cessation.

  • Drug treatment is normally with a calcium channel blocker, frequently nifedipine to prevent arterioconstriction.[1][2] It has the usual uncommon side effects of headache, flushing, and ankle edema; but normally result in needing to to stop the drug.[3]
  • There is some evidence that Angiotensin II receptor antagonists (often Losartan) reduce frequency and severity of attacks,[4] and possibly better than nifedipine.[5]
  • Alpha-1 adrenergic blockers such as prazosin can be used to control Raynaud's vasospasms under supervision of a health care provider.[6]
  • In a study published in the November 8, 2005 issue of Circulation, sildenafil (Viagra) improved both microcirculation and symptoms in patients with secondary Raynaud's phenomenon resistant to vasodilatory therapy. The authors, led by Dr Roland Fries (Gotthard-Schettler-Klinik, Bad Schönborn, Germany), report: "In the present study, capillary blood flow was severely impaired and sometimes hardly detectable in patients with Raynaud's phenomenon. Sildenafil led to a more than 400% increase of flow velocity."[7]

  • The extract of the Ginkgo biloba leaves (Egb 761, 80mg) may reduce frequency of attacks.[8]
  • Two separate gels combined on the fingertip (somewhat like two-part epoxy, they cannot be combined before use because they will react) increased blood flow in the fingertips by about three times. One gel contained 5% sodium nitrite and the other contained 5% ascorbic acid. The milliliter of combined gel covered an area of ~3 cm². The gel was wiped off after a few seconds.[9]

  1. ^ Kahan A, Weber S, Amor B, Saporta L, Hodara M, Degeorges M (1981). "Nifedipine and Raynaud's phenomenon". Ann. Intern. Med. 94 (4 pt 1): 546. PMID 7212523. 
  2. ^ Kahan A, Weber S, Amor B, Saporta L, Hodara M, Degeorges M (1982). "[Controlled study of nifedipine in the treatment of Raynaud's phenomenon]" (in French). Rev Rhum Mal Osteoartic 49 (5): 337–43. PMID 6285445. 
  3. ^ Smith CR, Rodeheffer RJ (1985). "Raynaud's phenomenon: pathophysiologic features and treatment with calcium-channel blockers". Am. J. Cardiol. 55 (3): 154B–157B. PMID 3881908. 
  4. ^ Pancera P, Sansone S, Secchi S, Covi G, Lechi A (1997). "The effects of thromboxane A2 inhibition (picotamide) and angiotensin II receptor blockade (losartan) in primary Raynaud's phenomenon". J. Intern. Med. 242 (5): 373–6. PMID 9408065. 
  5. ^ Dziadzio M, Denton CP, Smith R, et al (1999). "Losartan therapy for Raynaud's phenomenon and scleroderma: clinical and biochemical findings in a fifteen-week, randomized, parallel-group, controlled trial" (PDF). Arthritis Rheum. 42 (12): 2646–55. doi:<2646::AID-ANR21>3.0.CO;2-T 10.1002/1529-0131(199912)42:12<2646::AID-ANR21>3.0.CO;2-T. PMID 10616013. 
  6. ^ Waldo R (1979). "Prazosin relieves Raynaud's vasospasm". JAMA 241 (10): 1037. PMID 762741. 
  7. ^ Fries R, Shariat K, von Wilmowsky H, Böhm M (2005). "Sildenafil in the treatment of Raynaud's phenomenon resistant to vasodilatory therapy". Circulation 112 (19): 2980–5. doi:10.1161/CIRCULATIONAHA.104.523324. PMID 16275885. 
  8. ^ Muir AH, Robb R, McLaren M, Daly F, Belch JJ (2002). "The use of Ginkgo biloba in Raynaud's disease: a double-blind placebo-controlled trial". Vasc Med 7 (4): 265–7. PMID 12710841. 
  9. ^ Tucker AT, Pearson RM, Cooke ED, Benjamin N (Nov 13 1999). "Effect of nitric-oxide-generating system on microcirculatory blood flow in skin of patients with severe Raynaud's syndrome: a randomised trial". Lancet 354 (9191): 1670–5. PMID 10568568. 

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