Volume 42 Issue 4
Apr.  2026
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Zeng Y,Wang C,Lin HY,et al.Clinical efficacy of pressure therapy combined with narrow-band intense pulsed light for hypertrophic scars[J].Chin J Burns Wounds,2026,42(4):324-331.DOI: 10.3760/cma.j.cn501225-20251211-00518.
Citation: Zeng Y,Wang C,Lin HY,et al.Clinical efficacy of pressure therapy combined with narrow-band intense pulsed light for hypertrophic scars[J].Chin J Burns Wounds,2026,42(4):324-331.DOI: 10.3760/cma.j.cn501225-20251211-00518.

Clinical efficacy of pressure therapy combined with narrow-band intense pulsed light for hypertrophic scars

doi: 10.3760/cma.j.cn501225-20251211-00518
Funds:

Shanghai Plastic Surgery Research Center of Shanghai Priority Research Center 2023ZZ02023

Major and Key Cultivation Project of Shanghai Ninth People's Hospital of Shanghai Jiao Tong University School of Medicine JYZP010

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  •   Objective  To investigate the clinical efficacy of pressure therapy combined with narrow-band intense pulsed light (NB-IPL) for hypertrophic scars.  Methods  This study was a retrospective cohort study. From January 2023 to January 2025, 73 patients with hypertrophic scars who met the inclusion criteria were admitted to Shanghai Ninth People's Hospital of Shanghai Jiao Tong University School of Medicine. According to whether they underwent laser treatment, patients were divided into control group that received pressure therapy alone (35 cases, 14 males and 21 females, aged (32±9) years), and observation group that received NB-IPL in addition to pressure therapy (38 cases, 18 males and 20 females, aged (32±10) years). In the two groups of patients, pressure therapy was performed under body surface pressure monitoring to ensure effective pressure on the scar area. In combination therapy, NB-IPL treatment was administered once a month for 6 consecutive sessions. Before treatment and 9 months after treatment, the Vancouver scar scale (VSS) was used to evaluate scar appearance, and the visual analogue scale (VAS) was used to assess the pruritus severity and pain levels of scars. Nine months after treatment, patients' satisfaction with the scar improvement effect was evaluated using the Likert scale. During the treatment and 9 months after treatment, adverse reactions in patients, including skin contact dermatitis and pressure blisters, were observed and recorded, and the incidence of adverse reactions was compared between the two groups of patients.  Results  Nine months after treatment, the VSS scores of scar appearance of patients in control group and observation group were 7.4±1.4 and 6.1±1.7, respectively, which were significantly lower than the pretreatment scores of 11.5±1.8 and 11.2±1.9, respectively (with t values of -5.149 and -5.396, respectively, P<0.05); the VSS score of scar appearance of patients in observation group was significantly lower than that in control group (with mean difference (95% CI) of -1.2 (-1.8 to -0.6), t=-3.458, P<0.05). Nine months after treatment, the pruritus severity of scar in both control group and observation group of patients was significantly improved compared with that before treatment (with Z values of -4.815 and -5.407, respectively, P<0.05); the pruritus severity of scar in observation group of patients was significantly improved compared with that in control group (Z=-3.690, P<0.05). Nine months after treatment, the scar pain levels in both control group and observation group of patients were significantly improved compared with that before treatment (with Z values of -4.864 and -5.303, respectively, P<0.05); the scar pain level in observation group of patients was significantly improved compared with that in control group (Z=-1.994, P<0.05). Nine months after treatment, the score of patients' satisfaction with the scar improvement in observation group was significantly higher than that in control group (t=-2.964, P<0.05). During the treatment and 9 months after treatment, only 2 patients in control group experienced adverse reactions, while no obvious adverse reactions were observed in observation group of patients. There was no statistically significant difference in the incidence of adverse reactions between the two groups of patients (P>0.05).  Conclusions  The application of NB-IPL combined with pressure therapy significantly improves the appearance, pruritus severity and pain levels of hypertrophic scars without increasing treatment risks, and can enhance patient satisfaction. It is a safe and effective non-surgical combination treatment approach.

     

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