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Raynaud's Syndrome.jpg|
Raynaud's phenomenon
ICD-10 I730
ICD-9 443.0
OMIM [1]
DiseasesDB 25933
MedlinePlus [2]
eMedicine med/1993
MeSH {{{MeshNumber}}}

Raynaud's phenomenon (pronounced /reɪˈnoʊz/) (rāy-NŌZ), in medicine, is a vasospastic disorder causing discoloration of the fingers, toes, and occasionally other extremities. This condition can also cause nails to become brittle with longitudinal ridges. Named for French physician Maurice Raynaud (1834 - 1881), the cause of the phenomenon is believed to be the result of vasospasms that decrease blood supply to the respective regions. Emotional stress and cold are classic triggers of the phenomenon, 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,[1] and Raynaud's syndrome (secondary Raynaud's), where it is caused by some other instigating factor. Measurement of hand-temperature gradients is one tool used to distinguish between the primary and secondary forms.[2]

It is possible for the primary form to progress to the secondary form.[3]

PrevalenceEdit

The phenomenon is more common in women than men, with the Framingham Study finding that 5% of men and 8% of women suffer from it.[verification needed]

EpidemiologyEdit

There is a familial component to primary Raynaud's, and presentation is typically before two. Smoking worsens frequency and intensity of attacks, and there is a hormonal component. Caffeine also worsens the attacks. 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.

SymptomsEdit

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 primary, and will probably not progress to a secondary condition. In pregnancy, this sign normally disappears due to increased surface blood flow. Raynaud's has also occurred in breastfeeding mothers, causing nipples to turn white and be extremely painful. Nifedipine, a calcium channel blocker and vasodilator was recommended to increase blood flow to the extremities and noticeably relieved pain to the breast, in a extremely small study group.[5]

Investigations Edit

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.

PathophysiologyEdit

Primary Raynaud phenomenon, stemming from Raynaud disease, is an exaggeration of vasomotor responses to cold or emotional stress. More specifically, it is a hyperactivation of the sympathetic system causing extreme vasoconstriction of the peripheral blood vessels, leading to tissue hypoxia. Chronic, recurrent cases of Raynaud phenomenon can result in atrophy of the skin, subcutaneous tissues, and muscle. It can also rarely cause ulceration and ischemic gangrene.[6]

TreatmentEdit

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:

General measuresEdit

  • Avoidance of any environmental triggers, e.g. cold, vibration, etc. (although emotional stress is a recognized 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.

Emergency measuresEdit

  • If white finger (Raynaud's) occurs unexpectedly and a source of warm water is available allow tepid to slightly warm water to run over the affected digits while gently massaging the area. Continue this process until the white area turns pink or a normal healthy color.
  • If triggered by exposure in a cold environment, and no warm water is available, place the affected digits in a warm body cavity - arm pit, crotch, or even in the mouth. Keep the affected area warm at least until the whiteness returns to pink or a healthy color, avoid continued exposure to the cold.

Drug therapyEdit

  • Drug treatment is normally with a calcium channel blocker, frequently nifedipine to prevent arterioconstriction.[7][8] It has the usual common side effects of headache, flushing, and ankle edema; but normally result in not needing to stop the drug.[9]
  • There is some evidence that Angiotensin II receptor antagonists (often Losartan) reduce frequency and severity of attacks,[10] and possibly better than nifedipine.[11]
  • Alpha-1 adrenergic blockers such as prazosin can be used to control Raynaud's vasospasms under supervision of a health care provider.[12]
  • 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."[13]

Surgical interventionEdit

Alternative and research approachesEdit

  • The extract of the Ginkgo biloba leaves (Egb 761, 80 mg) may reduce frequency of attacks.[15]
  • 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.[16]

See alsoEdit

ReferencesEdit

  1. Template:DorlandsDict
  2. Anderson ME, Moore TL, Lunt M, Herrick AL (2007). The 'distal-dorsal difference': a thermographic parameter by which to differentiate between primary and secondary Raynaud's phenomenon. Rheumatology (Oxford) 46 (3): 533–8.
  3. Hirschl M, Hirschl K, Lenz M, Katzenschlager R, Hutter HP, Kundi M (2006). Transition from primary Raynaud's phenomenon to secondary Raynaud's phenomenon identified by diagnosis of an associated disease: results of ten years of prospective surveillance. Arthritis Rheum. 54 (6): 1974–81.
  4. Gayraud M (2007). Raynaud's phenomenon. Joint Bone Spine 74 (1): e1–8.
  5. Barclay, Laurie Raynaud's Phenomenon of the Nipple May Cause Painful Breastfeeding. Medscape. medscape.com. URL accessed on 2009-03-21.
  6. Kumar, Vinay; Nelso Fausto, Abul Abbas (2004). Robbins & Cotran Pathologic Basis of Desease, 542, Saunders.
  7. 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.
  8. Kahan A, Weber S, Amor B, Saporta L, Hodara M, Degeorges M (1982). [Controlled study of nifedipine in the treatment of Raynaud's phenomenon]. Rev Rhum Mal Osteoartic 49 (5): 337–43.
  9. Smith CR, Rodeheffer RJ (1985). Raynaud's phenomenon: pathophysiologic features and treatment with calcium-channel blockers. Am. J. Cardiol. 55 (3): 154B–157B.
  10. 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.
  11. 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. Arthritis Rheum. 42 (12): 2646–55.
  12. Waldo R (1979). Prazosin relieves Raynaud's vasospasm. JAMA 241 (10): 1037.
  13. 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.
  14. Wang WH, Lai CS, Chang KP, et al (2006). Peripheral sympathectomy for Raynaud's phenomenon: a salvage procedure. Kaohsiung J. Med. Sci. 22 (10): 491–9.
  15. 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.
  16. 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.

External linksEdit

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