eMedicine Specialties > Dermatology > Allergy & Immunology

Urticaria, Dermographism: Treatment & Medication

Author: Simone Laube, MD, MRCP, Consulting Staff, Department of Dermatology, Aberdeen Royal Infirmary, UK
Contributor Information and Disclosures

Updated: Feb 26, 2009

Treatment

Medical Care

Patients with simple dermographism are asymptomatic and require no therapy.
Recognition of the problem, avoidance of precipitating physical stimuli, reduction of stress and anxiety are important factors in medical care. Also, scratching because of dry skin can be reduced with good skin care and emollients.

H1 antihistamines are the drugs of choice. In some patients, several antihistamines or a combination of two may be required. Sedating antihistamines such as hydroxyzine can be helpful. Regular treatment may need to be continued for several months.

The addition of H2-receptor antagonists appears to result in little symptomatic benefit, although some studies have shown a further small reduction in the whealing response.10

Physical urticarias are usually unresponsive to systemic corticosteroids.

Narrowband UV-B phototherapy and oral psoralen plus UV-A light therapy have both been used as treatments for symptomatic dermographism. Subjective relief of pruritus and whealing and objective reduction of wheals are apparent.11 However, improvement is short-lived, and most patients relapse within 2-3 months of completing phototherapy.

Medication

The goals of pharmacotherapy are to reduce morbidity and to prevent complications.

Antihistamines

Act by competitive inhibition of histamine at the H1 receptor, H2 receptor, or both. This mediates wheal and flare reactions, bronchial constriction, mucus secretion, smooth muscle contraction, edema, hypotension, CNS depression, and cardiac arrhythmias.


Cetirizine (Zyrtec, Zyrtec Chewable Tablets)

Forms complex with histamine for H1-receptor sites in blood vessels, GI tract, and respiratory tract.

Adult

10 mg PO qd

Pediatric

<2 years: Not recommended
2-6 years: 5 mg PO qd or 2.5 mg PO bid
>6 years: Administer as in adults

Increases toxicity of CNS depressants

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Sedation and antimuscarinic effects (low); caution in hepatic or renal dysfunction; doses >10 mg/d may cause drowsiness


Loratadine (Claritin)

Selectively inhibits peripheral histamine H1 receptors.

Adult

10 mg PO qd

Pediatric

<2 years: Not recommended
2-12 years and <30 kg: 5 mg PO qd
>30 kg: Administer as in adults

Ketoconazole, erythromycin, procarbazine, and alcohol may increase levels

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Initiate therapy at lower dose in liver impairment


Desloratadine (Clarinex)

Long-acting tricyclic histamine antagonist selective for H1 receptor. Relieves nasal congestion and systemic effects of seasonal allergy. Major metabolite of loratadine, which, after ingestion, is metabolized extensively to active metabolite 3-hydroxydesloratadine.

Adult

5 mg PO qd

Pediatric

<12 years: Not established
>12 years: Administer as in adults

Data are limited; erythromycin and ketoconazole increase desloratadine and 3-hydroxydesloratadine plasma concentrations, but no increase in clinically relevant adverse effects, including QTc, observed

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

Decrease dose in hepatic impairment; rarely causes pharyngitis or dry mouth


Acrivastine (Semprex)

Competes with histamine for H1 receptors on GI tract, blood vessels, and respiratory tract, reducing hypersensitivity reactions.

Adult

8 mg PO tid

Pediatric

Not established

Guanethidine, methyldopa, reserpine, or beta-blockers may decrease effects; CNS depressants, alcohol, and sympathomimetics increase toxicity

Documented hypersensitivity; within 14 d of initiating MAOI therapy; severe coronary disease; severe hypertension; elderly

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

Sedation and antimuscarinic effects may occur; caution in high blood pressure, diabetes, ischemic heart disease, GI or GU obstruction, thyroid disease, prostatic hypertrophy, and increased intraocular pressure


Fexofenadine (Allegra)

Competes with histamine for H1 receptors on GI tract, blood vessels, and respiratory tract, reducing hypersensitivity reactions. Does not sedate.

Adult

60 mg PO bid

Pediatric

<12 years: Not recommended
>12 years: Administer as in adults

Toxicity increases with coadministration of erythromycin and ketoconazole

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

No data available on use while breastfeeding; may cause dizziness


Hydroxyzine (Atarax, Vistaril, Vistazine)

Sedative antihistamine that is also anxiolytic. Antagonizes H1 receptors in periphery. May suppress histamine activity in subcortical region of CNS.

Adult

Pruritus: 25 mg PO hs initially; increase prn to 25 mg PO tid/qid
Anxiety: 50-100 mg PO qid

Pediatric

<6 months: Not recommended
6 months to 6 years: 5-15 mg/d PO; increase to 50 mg/d PO divided tid/qid
>6 years: 15-25 mg/d PO; increase to 50-100 mg/d PO divided tid/qid

May enhance response to alcohol, barbiturates, and other CNS depressants

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

Associated with clinical exacerbations of porphyria (may not be safe for porphyria patients); ECG abnormalities (alterations in T waves) may occur; may cause drowsiness

More on Urticaria, Dermographism

Overview: Urticaria, Dermographism
Differential Diagnoses & Workup: Urticaria, Dermographism
Treatment & Medication: Urticaria, Dermographism
Follow-up: Urticaria, Dermographism
References

References

  1. Dinc A, Karaayvaz M, Caliskaner AZ, Pay S, Erdem H, Turan M. Dermographism and atopy in patients with Behcet's disease. J Investig Allergol Clin Immunol. Nov-Dec 2000;10(6):368-71. [Medline].

  2. Martorell A, Sanz J, Ortiz M, Julve N, Cerda JC, Ferriols E. Prevalence of dermographism in children. J Investig Allergol Clin Immunol. May-Jun 2000;10(3):166-9. [Medline].

  3. Lambiris A, Greaves MW. Dyspareunia and vulvodynia: unrecognised manifestations of symptomatic dermographism. Lancet. Jan 4 1997;349(9044):28. [Medline].

  4. Matthews CN, Warin RP. Cold urticaria and cold precipitated dermographism. Br J Dermatol. Jan 1970;82:91. [Medline].

  5. Jedele KB, Michels VV. Familial dermographism. Am J Med Genet. May 1 1991;39(2):201-3. [Medline].

  6. Grimm V, Mempel M, Ring J, Abeck D. Congenital symptomatic dermographism as the first symptom of mastocytosis. Br J Dermatol. Nov 2000;143(5):1109. [Medline].

  7. Taskapan O, Harmanyeri Y. Evaluation of patients with symptomatic dermographism. J Eur Acad Dermatol Venereol. Jan 2006;20(1):58-62. [Medline].

  8. Wallengren J, Isaksson A. Urticarial Dermographism: Clinical features and response to psychosocial stress. Acta Derm Venereol. 2007;87:493-8. [Medline].

  9. Wu JJ, Huang DB, Murase JE, Weinstein GD. Dermographism secondary to trauma from a coral reef. J Eur Acad Dermatol Venereol. Nov 2006;20:1337-8. [Medline].

  10. Sharpe GR, Shuster S. In dermographic urticaria H2 receptor antagonists have a small but therapeutically irrelevant additional effect compared with H1 antagonists alone. Br J Dermatol. Nov 1993;129(5):575-9. [Medline].

  11. Borzova E, Rutherford A, Konstantinou GN, Leslie KS, Grattan CE. Narrowband ultraviolet B phototherapy is beneficial in antihistamine-resistant symptomatic dermographism: A pilot study. J Am Acad Dermatol. Sept 2008;59:752-7. [Medline].

  12. van der Valk PG, Moret G, Kiemeney LA. The natural history of chronic urticaria and angioedema in patients visiting a tertiary referral centre. Br J Dermatol. Jan 2002;146(1):110-3. [Medline].

  13. Casale TB, Sampson HA, Hanifin J, et al. Guide to physical urticarias. J Allergy Clin Immunol. Nov 1988;82(5 Pt 1):758-63. [Medline].

  14. Champion RH. Urticaria: then and now. Br J Dermatol. Oct 1988;119(4):427-36. [Medline].

  15. Giam YC, Rajan VS. An approach to urticaria. Ann Acad Med Singapore. Jan 1983;12(1):74-80. [Medline].

  16. Grattan CEH, Kobza Black A. Urticaria and mastocytosis. In: Burns DA, Breathnach SM, Cox N, Griffiths C, eds. Rook's Textbook of Dermatology. Vol 3. 7th ed. London, England: Blackwell Science; 2004:47.1-47.37.

  17. Jorizzo JL, Smith EB. The physical urticarias. An update and review. Arch Dermatol. Mar 1982;118(3):194-201. [Medline].

  18. Kirby JD, Matthews CN, James J, Duncan EH, Warin RP. The incidence and other aspects of factitious wealing (dermographism). Br J Dermatol. Oct 1971;85(4):331-5. [Medline].

  19. Kobza Black A. The physical urticarias. In: Champion RH, Greaves MW, Kobza Black A, Pye RJ, eds. The Urticarias. Edinburgh, Scotland: Churchill Livingstone; 1985:168-90.

  20. Nettis E, Pannofino A, D'Aprile C, Ferrannini A, Tursi A. Clinical and aetiological aspects in urticaria and angio-oedema. Br J Dermatol. Mar 2003;148(3):501-6. [Medline].

  21. Wong RC, Fairley JA, Ellis CN. Dermographism: a review. J Am Acad Dermatol. Oct 1984;11(4 Pt 1):643-52. [Medline].

Further Reading

Keywords

dermatographism, urticaria, urticarial dermographism, factitious urticaria, allergy, allergic reaction, anaphylaxis, anaphylactoid reaction, angioedema, triple response of Lewis, linear wheal, whealing, red dermatographism, red urticaria, skin scratch reactions, hives, itching

Contributor Information and Disclosures

Author

Simone Laube, MD, MRCP, Consulting Staff, Department of Dermatology, Aberdeen Royal Infirmary, UK
Simone Laube, MD, MRCP is a member of the following medical societies: British Association of Dermatologists
Disclosure: Nothing to disclose.

Medical Editor

Shyam Verma, MBBS, DVD, FAAD, Adjunct Clinical Assistant Professor, Department of Dermatology, University of Virginia, State University of New York at Stonybrook, Penn State University
Shyam Verma, MBBS, DVD, FAAD is a member of the following medical societies: American Academy of Dermatology
Disclosure: Nothing to disclose.

Pharmacy Editor

Richard P Vinson, MD, Assistant Clinical Professor, Department of Dermatology, Texas Tech University School of Medicine; Consulting Staff, Mountain View Dermatology, PA
Richard P Vinson, MD is a member of the following medical societies: American Academy of Dermatology, Association of Military Dermatologists, Texas Dermatological Society, and Texas Medical Association
Disclosure: Nothing to disclose.

Managing Editor

Paul Krusinski, MD, Director of Dermatology, Professor, Department of Internal Medicine, Fletcher Allen Health Care, University of Vermont
Paul Krusinski, MD is a member of the following medical societies: American Academy of Dermatology, American College of Physicians, and Society for Investigative Dermatology
Disclosure: Nothing to disclose.

CME Editor

Catherine Quirk, MD, Clinical Assistant Professor, Department of Dermatology, Brown University
Catherine Quirk, MD is a member of the following medical societies: Alpha Omega Alpha and American Academy of Dermatology
Disclosure: Nothing to disclose.

Chief Editor

William D James, MD, Paul R Gross Professor of Dermatology, University of Pennsylvania School of Medicine; Vice-Chair, Program Director, Department of Dermatology, University of Pennsylvania Health System
William D James, MD is a member of the following medical societies: American Academy of Dermatology and Society for Investigative Dermatology
Disclosure: elsevier Royalty Other; american college of physicians Honoraria Other

 
 
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