TY - JOUR T1 - Clinical Evaluation of Efficacy and Safety of Combined Topical Timolol and Oral Propranolol in Children with Infantile Hemangioma AU - Abdulhameed, Abdulameer Abdulbari AU - Al-hamdi, Kalil Esmail AU - Mathkoor, Muntaha Abdulhadi PY - 2018 DA - March DO - 10.5799/jcei.413049 JF - Journal of Clinical and Experimental Investigations JO - J Clin Exp Invest PB - Aydın ECE WT - DergiPark SN - 1309-8578 SP - 1 EP - 8 VL - 9 IS - 1 LA - en AB - Objective:To evaluate theefficacy and safety of combined topical timolol and oral propranolol intreatment of infantile hemangioma. Patientsand methods: Thisprospective study was conducted in Basra teaching hospital in Basra, Iraq,where a total of 23 infants with 34 lesions of different types of hemangiomawere included. All lesions were in proliferation phase. The infants’ ages wereless than one year. They were treated with topical timolol solution 0.5%combined with oral propranolol in a period of 12 weeks (8-16 weeks). Theresponse to treatment was evaluated clinically by using hemangioma score andVisual analogue scale. All infants followed 4-12 months after cessation ofdrugs. Results:By usinghemangioma score system; the combined therapy showed that, 28 (82.4%) lesionsshowed excellent response, two (5.9%) showed good response, four (11.8%) showedfair response and none of the lesions showed poor response at end of 16 weeks.At the end of 4 months superficial hemangioma showed 100% reduction in theirscore, while the ulcerative hemangioma showed 94.7% reduction in their scorewhile mixed hemangioma showed only 76.7% reduction in their scores. Completeresolution occurred in 50% of lesions after 4 months of treatment. Neitherincluded infants developed serious side effects nor, any of the regressedhemangioma recur during the follow up. Conclusion:Combinedtopical Timolol 0.5% solution and oral propranolol seems to be awell-tolerated, safe treatment option with a good to excellent responses. 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