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Texte intégral de l'article
 
  Version imprimable

Treatment of scabies with ivermectin


European Journal of Dermatology. Volume 9, Numéro 2, 100-1, March 1999, Thérapeutique


Summary  

Auteur(s) : A. Offidani, A. Cellini, O. Simonetti, C. Fumelli, Clinica Dermatologica, Ospedale Umberto I, Piazza Cappelli 1, 60100 Ancona, Italy..

Illustrations

ARTICLE

Scabies, unfortunately, is still a problem in Italy. Mass tourism and immigration are the main causes of the diffusion of the parasite in our country. Current topical treatments are impractical, not very efficient and irritating. For such reasons, we considered the experimental use of ivermectin, the only oral therapy presently available for this disease.

Ivermectin is similar in structure to a macrolide antibiotic, but without antibiotic activity. It is extremely effective against nematodes and mites [1]. Moreover the 10-year history of the use of oral ivermectin to control endemic onchocerciasis indicates that it is an extremely safe drug. For the aforementioned reasons, in 1992, it was proposed for the treatment of human scabies [2-4].

Methods and results

Our study consisted of six patients, four males and two females, age range: 35-58 years, all suffering from severe scabies, of exotic origin, presenting nodular manifestations and secondary eczematisation. Most of the cases were initially misdiagnosed and therefore mistreated. None of the patients had received any topical antiscabietic treatment in the previous month. The diagnosis was made by scraping for microscopic evidence of mites, their eggs or their fecal pellets. Written consent was obtained from all patients after they has been informed about the nature and details of the study.

Each patient received 200 µg/kg of ivermectin (two tablets of 6 mg taken as single dose). The therapy was repeated after one week in the more serious cases. Patients were allowed to use only emollient local treatment, as necessary.

Patients were seen every week after the first dose of ivermectin.

The drug was extremely effective, especially regarding pruritus. Five patients out of six reported a significant reduction in pruritus and a return to a "good night's sleep" within 48 hours after treatment (the sixth patient's clinical history will be presented separately, with photo-documentation, showing the severity of the disease). Complete recovery occurred in four weeks. In particular a gradual improvement of the nodular manifestations was noticed during the follow-up visits. No side effects were seen in any patient.

Case 6 was the most serious and requires a more detailed presentation. C.G. is a 58-year-old male, who has been suffering from a psychologically debilitating pruritus for three months, despite undergoing systemic corticosteroid therapy for a total of 45 days (Fig. 1). He immediately underwent scraping for microscopic evidence of mites. Then he was asked to take 200 µg/kg of ivermectin in a single dose and to discontinue his current systemic corticosteroid therapy immediately.

He mentioned a reduction in his pruritus during his first follow-up interview, although he complained of worsening erythema, which was attributed to the suspension of the antinflammatory corticosteroid therapy. The patient was discharged with a prescription for emollient moisturizing cream, to be used as necessary and emollient soaks. He required a second dose one week after the first treatment. During the following weeks there was a progressive reduction in eczematization and an improvement of the nodular lesions. After 15 days of therapy the patient continued complaining about his insomnia, even though his pruritus was greatly reduced. An antihistamine and benzodiazepine were added for his problem. After four weeks, microscopic search for mites and their products was negative, so the patient was considered cured.

Discussion

Every year we observe a large number of new cases of scabies. Among these were mistreated cases, atypical features, unusual localisation, like the scalp, induced by prolonged corticosteroid therapy. The infestation can mimic: contact dermatitis, dermatitis herpetiformis, seborrhoeic dermatitis, drug induced eczema, bullous pemphigoid, etc. [5]. Often the diagnosis is not easy. Current topical treatments are irritating when used in patients with secondary eczematization and escoriations and are not effective in persistent irritable nodules. Ivermectin, taken in a single dose, represents an interesting choice with respect to local therapy, that has to be carefully applied to all the skin below the neck. In our experience ivermectin has been shown to be an effective treatment in scabies, especially regarding pruritus, without any side effects. Moreover no local therapy was needed in our patients, not even in those with nodular lesions.

The dose of ivermectin is 200 µg/kg taken in a single dose. The patients should be seen weekly and supervised for a period of a month, because the infestation could resolve within 4 weeks. In our study all members of the household were treated with a local scabiecide in order to avoid reinfestation. Disinfestation of clothing by high temperature laundering was required for all the patients. We excluded from the therapy elderly, children and subjects affected from any other illness because they did not meet the inclusion criteria. We think that ivermectin is an effective therapy even though further study is required to confirm our data.

REFERENCES

1. Goa KL, McTavish D, Glissold SP. Ivermectin: a review of its antifilarial activity, pharmacological properties and clinical efficacy in onchocerciasis. Drugs 1990; 42: 640-58.

2. Traitement de la gale par ivermectine. La sélection bibliographique du mois. Ann Dermatol Venereol 1996; 123: 697-700.

3. Meinking TL, Taplin D, Hermida JL, Pardo R, Kerdel FAFA. The treatment of scabies with ivermectin. N Engl J Med 1995; 333: 26-30.

4. Glaziou P, Cartel JL, Alzieu P, Briotel C, et al. Comparison of ivermectin and benzyl benzoate for treatment of scabies. Trop Med Parasitol 1933; 44: 331-2.

5. Pauluzzi P, Scarpa C. Atypical features of scabietic infestation. G Ital Dermatol Venereol 1995; 130: 307-10.


 

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