Literature DB >> 28513067

Interventions for cutaneous molluscum contagiosum.

Johannes C van der Wouden1, Renske van der Sande2, Emma J Kruithof1, Annet Sollie3, Lisette Wa van Suijlekom-Smit4, Sander Koning2.   

Abstract

BACKGROUND: Molluscum contagiosum is a common skin infection that is caused by a pox virus and occurs mainly in children. The infection usually resolves within months in people without immune deficiency, but treatment may be preferred for social and cosmetic reasons or to avoid spreading the infection. A clear evidence base supporting the various treatments is lacking.This is an update of a Cochrane Review first published in 2006, and updated previously in 2009.
OBJECTIVES: To assess the effects of specific treatments and management strategies, including waiting for natural resolution, for cutaneous, non-genital molluscum contagiosum in people without immune deficiency. SEARCH
METHODS: We updated our searches of the following databases to July 2016: the Cochrane Skin Group Specialised Register, CENTRAL, MEDLINE, Embase, and LILACS. We searched six trial registers and checked the reference lists of included studies and review articles for further references to relevant randomised controlled trials. We contacted pharmaceutical companies and experts in the field to identify further relevant randomised controlled trials. SELECTION CRITERIA: Randomised controlled trials of any treatment of molluscum contagiosum in people without immune deficiency. We excluded trials on sexually transmitted molluscum contagiosum and in people with immune deficiency (including those with HIV infection). DATA COLLECTION AND ANALYSIS: Two review authors independently selected studies, assessed methodological quality, and extracted data from selected studies. We obtained missing data from study authors where possible. MAIN
RESULTS: We found 11 new studies for this update, resulting in 22 included studies with a total of 1650 participants. The studies examined the effects of topical (20 studies) and systemic interventions (2 studies).Among the new included studies were the full trial reports of three large unpublished studies, brought to our attention by an expert in the field. They all provided moderate-quality evidence for a lack of effect of 5% imiquimod compared to vehicle (placebo) on short-term clinical cure (4 studies, 850 participants, 12 weeks after start of treatment, risk ratio (RR) 1.33, 95% confidence interval (CI) 0.92 to 1.93), medium-term clinical cure (2 studies, 702 participants, 18 weeks after start of treatment, RR 0.88, 95% CI 0.67 to 1.14), and long-term clinical cure (2 studies, 702 participants, 28 weeks after start of treatment, RR 0.97, 95% CI 0.79 to 1.17). We found similar but more certain results for short-term improvement (4 studies, 850 participants, 12 weeks after start of treatment, RR 1.14, 95% CI 0.89 to 1.47; high-quality evidence). For the outcome 'any adverse effect', we found high-quality evidence for little or no difference between topical 5% imiquimod and vehicle (3 studies, 827 participants, RR 0.97, 95% CI 0.88 to 1.07), but application site reactions were more frequent in the groups treated with imiquimod (moderate-quality evidence): any application site reaction (3 studies, 827 participants, RR 1.41, 95% CI 1.13 to 1.77, the number needed to treat for an additional harmful outcome (NNTH) was 11); severe application site reaction (3 studies, 827 participants, RR 4.33, 95% CI 1.16 to 16.19, NNTH over 40).For the following 11 comparisons, there was limited evidence to show which treatment was superior in achieving short-term clinical cure (low-quality evidence): 5% imiquimod less effective than cryospray (1 study, 74 participants, RR 0.60, 95% CI 0.46 to 0.78) and 10% potassium hydroxide (2 studies, 67 participants, RR 0.65, 95% CI 0.46 to 0.93); 10% Australian lemon myrtle oil more effective than olive oil (1 study, 31 participants, RR 17.88, 95% CI 1.13 to 282.72); 10% benzoyl peroxide cream more effective than 0.05% tretinoin (1 study, 30 participants, RR 2.20, 95% CI 1.01 to 4.79); 5% sodium nitrite co-applied with 5% salicylic acid more effective than 5% salicylic acid alone (1 study, 30 participants, RR 3.50, 95% CI 1.23 to 9.92); and iodine plus tea tree oil more effective than tea tree oil (1 study, 37 participants, RR 0.20, 95% CI 0.07 to 0.57) or iodine alone (1 study, 37 participants, RR 0.07, 95% CI 0.01 to 0.50). Although there is some uncertainty, 10% potassium hydroxide appears to be more effective than saline (1 study, 20 participants, RR 3.50, 95% CI 0.95 to 12.90); homeopathic calcarea carbonica appears to be more effective than placebo (1 study, 20 participants, RR 5.57, 95% CI 0.93 to 33.54); 2.5% appears to be less effective than 5% solution of potassium hydroxide (1 study, 25 participants, RR 0.35, 95% CI 0.12 to 1.01); and 10% povidone iodine solution plus 50% salicylic acid plaster appears to be more effective than salicylic acid plaster alone (1 study, 30 participants, RR 1.43, 95% CI 0.95 to 2.16).We found no statistically significant differences for other comparisons (most of which addressed two different topical treatments). We found no randomised controlled trial evidence for expressing lesions or topical hydrogen peroxide.Study limitations included no blinding, many dropouts, and no intention-to-treat analysis. Except for the severe application site reactions of imiquimod, none of the evaluated treatments described above were associated with serious adverse effects (low-quality evidence). Among the most common adverse events were pain during application, erythema, and itching. Included studies of the following comparisons did not report adverse effects: calcarea carbonica versus placebo, 10% povidone iodine plus 50% salicylic acid plaster versus salicylic acid plaster, and 10% benzoyl peroxide versus 0.05% tretinoin.We were unable to judge the risk of bias in most studies due to insufficient information, especially regarding concealment of allocation and possible selective reporting. We considered five studies to be at low risk of bias. AUTHORS'
CONCLUSIONS: No single intervention has been shown to be convincingly effective in the treatment of molluscum contagiosum. We found moderate-quality evidence that topical 5% imiquimod was no more effective than vehicle in terms of clinical cure, but led to more application site reactions, and high-quality evidence that there was no difference between the treatments in terms of short-term improvement. However, high-quality evidence showed a similar number of general side effects in both groups. As the evidence found did not favour any one treatment, the natural resolution of molluscum contagiosum remains a strong method for dealing with the condition.

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Year:  2017        PMID: 28513067      PMCID: PMC6481355          DOI: 10.1002/14651858.CD004767.pub4

Source DB:  PubMed          Journal:  Cochrane Database Syst Rev        ISSN: 1361-6137


  109 in total

1.  Topical cidofovir for molluscum contagiosum in children.

Authors:  E J Zabawski; C J Cockerell
Journal:  Pediatr Dermatol       Date:  1999 Sep-Oct       Impact factor: 1.588

2.  Insights into a novel treatment for molluscum.

Authors:  D S Lim; C A Egan
Journal:  Acta Paediatr       Date:  2003       Impact factor: 2.299

3.  Molluscum contagiosum in Dutch general practice.

Authors:  S Koning; M A Bruijnzeels; L W van Suijlekom-Smit; J C van der Wouden
Journal:  Br J Gen Pract       Date:  1994-09       Impact factor: 5.386

4.  Griseofulvin therapy in molluscum contagiosum.

Authors:  O P Singh; A Kanwar
Journal:  Arch Dermatol       Date:  1977-11

5.  Clinical trial of milkweed (Asclepius curussavica) in the treatment of warts.

Authors:  P N Behl; B K Bhatia
Journal:  Indian J Dermatol       Date:  1970-01       Impact factor: 1.494

6.  [Keratoconjunctivitis in molluscum contagiosum of the eyelids].

Authors:  C Haellmigk
Journal:  Klin Monbl Augenheilkd       Date:  1966       Impact factor: 0.700

7.  [Molluscum contagiosum: treatment with pulsed dye laser].

Authors:  S Hammes; B Greve; C Raulin
Journal:  Hautarzt       Date:  2001-01       Impact factor: 0.751

8.  An epidemiologic study of molluscum contagiosum in Anchorage, Alaska.

Authors:  T M Overfield; J A Brody
Journal:  J Pediatr       Date:  1966-10       Impact factor: 4.406

Review 9.  Molluscum contagiosum: recent advances in pathogenic mechanisms, and new therapies.

Authors:  Kathleen J Smith; Henry Skelton
Journal:  Am J Clin Dermatol       Date:  2002       Impact factor: 7.403

10.  Cutaneous manifestations of human immunodeficiency virus in Lusaka, Zambia.

Authors:  S K Hira; D Wadhawan; J Kamanga; D Kavindele; R Macuacua; P S Patil; M A Ansary; A M Macher; P L Perine
Journal:  J Am Acad Dermatol       Date:  1988-09       Impact factor: 11.527

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  6 in total

Review 1.  New Developing Treatments for Molluscum Contagiosum.

Authors:  Francesco Lacarrubba; Giuseppe Micali; Andrea Calogero Trecarichi; Enrica Quattrocchi; Giuseppe Monfrecola; Anna Elisa Verzì
Journal:  Dermatol Ther (Heidelb)       Date:  2022-10-14

Review 2.  Non-HPV Perianal and Anorectal Sexually Transmitted Viral Infections.

Authors:  Margarita Murphy; Gabriel Ryan Chedister; Virgilio George
Journal:  Clin Colon Rectal Surg       Date:  2019-09-06

3.  Molluscum Contagiosum on the Sole of the Foot in an Elderly Patient: A Case Report.

Authors:  Lee Firestone; Gene Mirkin; Xingpei Hao
Journal:  Am J Case Rep       Date:  2020-09-17

4.  Pooled Results of Two Randomized Phase III Trials Evaluating VP-102, a Drug-Device Combination Product Containing Cantharidin 0.7% (w/v) for the Treatment of Molluscum Contagiosum.

Authors:  Lawrence F Eichenfield; Elaine Siegfried; Pearl Kwong; Mark McBride; Jayson Rieger; David Glover; Cynthia Willson; Matthew Davidson; Patrick Burnett; Melissa Olivadoti
Journal:  Am J Clin Dermatol       Date:  2021-02-18       Impact factor: 7.403

5.  Topical adapalene for the treatment of follicular conjunctivitis due to periocular molluscum contagiosum in children.

Authors:  Jonathan S Yi; Kellie R Satterfield; Catherine S Choi; Markus D Boos; Michelle T Cabrera
Journal:  Am J Ophthalmol Case Rep       Date:  2022-01-22

6.  Safety and Efficacy of VP-102, a Proprietary, Drug-Device Combination Product Containing Cantharidin, 0.7% (w/v), in Children and Adults With Molluscum Contagiosum: Two Phase 3 Randomized Clinical Trials.

Authors:  Lawrence F Eichenfield; Wendy McFalda; Bradford Brabec; Elaine Siegfried; Pearl Kwong; Mark McBride; Jayson Rieger; Cynthia Willson; Matthew Davidson; Patrick Burnett
Journal:  JAMA Dermatol       Date:  2020-12-01       Impact factor: 10.282

  6 in total

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