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Published on: November 6, 2019
CO2 laser treatment for scars after cleft lip surgery: a systematic review and meta-analysis
Xuefei Pang1, Haoshu Chi1, Zongli Zhan1
1Department of Oral and Cranio-Maxillofacial Surgery, Shanghai Ninth People's Hospital, College of Stomatology, National Center for Stomatology, Shanghai Key Laboratory of Stomatology, Shanghai Jiao Tong University School of Medicine, Shanghai Jiao Tong University, National Clinical Research Center for Oral Diseases, Shanghai Research Institute of Stomatology, Shanghai, China.
Background:
Current studies are controversial on the optimal treatment of postoperative scar treatment by cleft lip. Our objective is to elucidate the therapeutic effect of CO2 laser on postoperative cleft lip scar treatment.
Methods:
A systematic review was performed and reported according to Preferred Reporting Items for Systematic Reviews and Meta-Analyses. We searched five electronic databases (EMBASE, PubMed, Web of Science, Cochrane Library and CNKI, from their inceptions until August 8, 2023) and independently assessed the methodological quality and bias risk of the included studies by two investigators using the Cochrane Handbook for Systematic Reviews. Quality assessment of the certainty of evidence was performed based on the Grading of Recommendations Assessment, Development, and Evaluation guidelines. Weighted mean difference of Vancouver Scar Scale were calculated to conduct meta-analysis by Stata statistical software version 14. We also estimated the pool sensitivity as well as testing the possibility of publication bias.
Results:
Five studies were included in this meta-analysis involving 255 subjects. Meta-analysis showed that compared with the control group, CO2 laser was more effective in treating post-cleft lip scars (WMD = 4.39, 95%CI = 0.54-8.23; Five studies with 255 participants; Low evidentiary certainty, I2 = 99.4%).
Conclusions:
Patients treated with CO2 laser therapy for postoperative cleft lip scar treatment tend to have a significant therapeutic effect especially in the early stages.
Trial Registration:
identifier CRD42023397042 (18/02/2023) [ https://www.crd.york.ac.uk/prospero/ ].
