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Diagnosis and Management of Infantile Hemangioma

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children in 8 studies), skin atrophy (0.95%-17% <strong>of</strong> children in five studies), hypopigmentation<br />

(1.4% to 16% <strong>of</strong> children in 6 studies), hypertension (0.11% to 5% <strong>of</strong> children in five studies),<br />

infection (2% to 15% <strong>of</strong> children in 5 studies), <strong>and</strong> behavioral changes (25% to 100% <strong>of</strong> children<br />

in four studies). Cushingoid appearance <strong>and</strong> growth retardation occurred regardless <strong>of</strong> dosage<br />

form (i.e., intralesional, oral).<br />

One study reported on several “ultrapotent” topical steroids (betamethasone dipropionate,<br />

clobetasol propionate, halobetasol propionate, 0.05%) in children with primarily superficial IH<br />

<strong>and</strong> noted that 2 <strong>of</strong> 34 children (agents received not specified) experienced hypopigmentation. 127<br />

Another reporting on several corticosteroids including oral prednisolone, clobetasol propionate,<br />

<strong>and</strong> intralesional triamcinolone plus betamethasone in 30 children with complicated IH reported<br />

adverse effects in the aggregate rather than by agent. 129 Most children received prednisolone, <strong>and</strong><br />

harms included decreased rate <strong>of</strong> linear growth (n=14), decreased weight gain (n=9), Cushingoid<br />

facies (n=7), increased weight gain (n=5), decreased head growth (n=4), hirsutism (n=4), delayed<br />

motor milestones (n=3), thrush (n=3), premature thelarche (n=2), increased rate <strong>of</strong> linear growth<br />

(n=1), sterid acne (n=1), gastritis (n=1), <strong>and</strong> varicella infection (n=1). 129 Three case series<br />

evaluating intralesional steroids reported that no adverse events occurred, 123,126,128 <strong>and</strong> none<br />

explicitly reported discontinuation <strong>of</strong> treatment due to adverse events.<br />

Table 9. Adverse effects in case series <strong>of</strong> steroids to treat IH<br />

Intervention<br />

Intralesional<br />

triamcinolone+betamethasone †<br />

Intralesional<br />

triamcinolone+dexamethasone<br />

Intralesional<br />

triamcinolone+prednisolone<br />

Harm/Adverse Event<br />

Number Of<br />

Studies<br />

(# Participants<br />

With Harm/Total<br />

Participants)<br />

Reported Rates<br />

Across Studies<br />

Cushingoid appearance 110,112 2 (5/100) 3%-10%<br />

Hypopigmentation 110 1 (2/70) 3%<br />

Periocular calcification 121 1 (1/34) 3%<br />

Abscess at injection site 111 1 (1/27) 4%<br />

Subcutaneous fat atrophy 111 1 (1/27) 4%<br />

Ulceration 120 1 (130/628) 21%<br />

Skin atrophy 120 1 (106/628) 17%<br />

Hypopigmentation 120 1 (101/628) 16%<br />

Infection 120 1 (91/628) 14%<br />

Cushingoid appearance 120 1 (37/628) 6%<br />

Growth retardation 120 1 (37/628) 6%<br />

Hypertension 120 1 (30/628) 5%<br />

Intralesional triamcinolone ** Ulceration 114,120 2 (150/1046) 4%-16%<br />

Infection 109,120 2 (105/991) 2%-12%<br />

Anaphylactic shock 115 1 (3/155) 2%<br />

Hypopigmentation 114,120 2 (93/1046) 1%-10%<br />

Peptic ulcer 114 1 (2/160) 1%<br />

* Skin atrophy 109,115,120 3 (106/1146) 0.95%-11%<br />

Entropion 114 1 (1/160) 0.63%<br />

Cushingoid appearance 115,120 2 (6/1041) 0.45%-1%<br />

Growth retardation 120 1 (4/886) 0.45%<br />

Hypertension 120 1 (1/886) 0.11%<br />

Intralesional<br />

betamethasone+dexamethasone<br />

Bruising at injection site 124 1 (NR/36) NR<br />

32

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