Sanyrene (Sanyrene)

Effects of Moist Wound Healing Strategy on Healing Time of Burn Wound Donor Sites and Patients' Depression/Anxiety Symptoms.

Miao Xifei X, Wang Bao B, Chen Fang F, Liang Ziwei Z et al.

This study aimed to compare the effects of a Moist Wound Healing (MWH) strategy using Sanyrene liquid dressing versus Traditional Dry Care (TDC) with infrared lamp irradiation on donor site healing time and psychological symptoms in burn patients. A retrospective cohort of 173 patients undergoing split-thickness skin graft surgery was divided into TDC (n=92) and MWH (n=81) groups based on documented postoperative care. Healing time was assessed from postoperative day 7 until complete re-epithelialization. Pain was evaluated twice daily using the Numeric Rating Scale (NRS) during the 7-day intervention. Skin condition and scar quality were assessed via the Overall Dry Skin (ODS) score and Vancouver Scar Scale (VSS) at 1 and 3 months. Psychological symptoms were measured at 3 months using the Hospital Anxiety and Depression Scale (HADS). The MWH group exhibited a significantly shorter mean healing time (13.23 days vs 16.85 days, P<0.001) and a higher proportion of wounds healed within 7 days (35.8% vs 17.39%, P=0.006). From day 4 onward, MWH patients reported lower NRS pain scores (eg, 2.51 vs 2.98 on day 7, P<0.001). At follow-up, the MWH group had better ODS and VSS scores (all P<0.05) and lower HADS-Anxiety (P=0.005) and HADS-Depression scores (P=0.002). Multivariate analysis confirmed MWH as an independent protective factor against non-healing within 7 days (OR=0.624, P=0.002). MWH with Sanyrene dressing is associated with faster donor site healing, reduced pain, improved skin and scar outcomes, and better psychological well-being compared to TDC in burn patients.

A blinded-endpoint, randomized controlled trial of Sanyrene with natural active ingredient for prophylaxis of radiation dermatitis in patients receiving radiotherapy.

Long Xiaoli X, Guo Jing J, Yin Yutian Y, Cheng Ming M et al.

Randomized controlled study was conducted to evaluate the efficacy of Sanyrene® vs. control intervention (DaBao®, a complex of hyaluronic acid and Vitamin E) for acute radiation dermatitis in patients receiving radiotherapy. Patients with breast cancer or head and neck cancer undergoing radiotherapy (≥ 50 Gy) were eligible. Participants were randomly assigned to either Sanyrene arm or control intervention arm in a ratio of 1:1. The primary endpoint was incidence rate of ≥ grade 2 radiation induced dermatitis. (Trial Registration: ChiCTR2100050910, registration date: 9/7/2021) RESULTS: A total of 102 eligible patients were randomly assigned into the study. The rate of ≥ grade 2 radiation dermatitis was 22% in Sanyrene group, as compared with 67.3% in the control intervention group (P<0.001). The incidence of grade 3 radiation dermatitis was 20.4% and 8.0% in control intervention group and Sanyrene group, respectively (P = 0.076). Patients in Sanyrene group had a longer median time to reach ≥ grade 2 radiation dermatitis compared to these in control intervention group, with hazard ratio of 0.231 (95%CI:0.116-0.458, p < 0.001). Mean score of SD-16 were much higher in control intervention group than Sanyrene group at end of radiotherapy (25 vs.8.3), 2 weeks after radiotherapy (22.9 vs. 0.5) and 4 weeks after radiotherapy (4.2 vs.0), with significantly statistical difference between two groups. This trial suggests that Sanyrene is effective on preventing serious radiation dermatitis and improving skin related quality of life in patients with breast cancer or head and neck cancer receiving radiotherapy.

The Effect of Sanyrene Liquid Dressing in Preventing Radiation Dermatitis: A Systematic Review and Meta-analysis.

Li Siqing S, Chen Lanpeng L, Yang Zhaoxia Z, Luo Wenxin W et al.

To assess the efficacy of Sanyrene liquid dressing (Urgo Medical) in preventing radiation dermatitis (RD) among patients with cancer after radiotherapy. The authors searched the China National Knowledge Infrastructure, SinoMed, WanFang Data, PubMed, Web of Science, EMBASE, and the Cochrane Library databases for articles published from inception to January 2021. The preliminary search identified 146 studies. After removing duplicates, applying exclusion criteria, and screening titles and abstracts, 19 studies met the inclusion criteria. A standardized form was constructed to extract data from eligible studies. Two reviewers independently screened the literature, extracted data, and assessed the risk of bias of the included studies. The authors identified a total of 19 studies involving 1,508 patients that assessed the effectiveness of Sanyrene liquid dressing in preventing RD in patients with cancer after radiotherapy. The findings suggested that Sanyrene decreases the total incidence of RD (odds ratio [OR], 5.00; 95% CI, 2.77-9.03; P < .00001), as well as the incidence of RD grade 2 (OR, 0.55; 95% CI, 0.36-0.85; P = .007), grade 3 (OR, 0.22; 95% CI, 0.09-0.57; P = .002), and grade 4 (OR, 0.32; 95% CI, 0.13-0.78; P = .01). In addition, in comparison with controls, Sanyrene liquid dressing improves the cure rate (OR, 8.18; 95% CI, 4.03-16.60; P < .00001) and delays the occurrence of RD (mean difference, 3.69; 95% CI, 3.03-4.36; P < .00001). Sanyrene liquid dressing can decrease both the total incidence of RD and the incidence of RD above grade 2. It also improves the cure rate and delays the occurrence of RD. Thus, Sanyrene may be a superior option for preventing RD after radiotherapy. However, the findings were assessed as moderate- to low-quality evidence and more high-quality trials are needed to support this result.

[Effectiveness of Sanyrene in preventing decubiti, monitoring with transcutaneous oximetry].

Colin D D, Chomard D D, Bois C C, Saumet J L JL