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Original Article
ARTICLE IN PRESS
doi:
10.25259/JCAS_59_2024

A comparative study of fractional carbon dioxide laser efficiency in the treatment of striae rubra and striae alba

Department of Dermatology, Venereology and Leprosy, Sri Venkateswaraa Medical College Hospital and Research Centre, Puducherry, India.

*Corresponding author: Karunanandhan Manobalan, Department of Dermatology, Venereology and Leprosy, Sri Venkateswaraa Medical College Hospital and Research Centre, Puducherry, India. manobalankaruna@gmail.com

Licence
This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, transform, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.

How to cite this article: Lakshmipathi L, Menon R, Singh Y, Jagdish N, Vishwanath K, Prasanna A, et al. A comparative study of fractional carbon dioxide laser efficiency in the treatment of striae rubra and striae alba. J Cutan Aesthet Surg. doi: 10.25259/JCAS_59_2024

Abstract

Objectives:

Striae distensae, commonly known as stretch marks, are prevalent skin lesions that cause significant cosmetic and psychological distress. They manifest as striae rubra, which are erythematous, or striae alba, which are hypopigmented. Current treatments often yield limited results, prompting interest in advanced modalities, such as fractional carbon dioxide (CO2) laser therapy. This study aims to evaluate and compare the efficacy of fractional CO2 laser therapy in treating striae rubra and striae alba, hypothesizing that early intervention can significantly improve the appearance of these lesions.

Material and Methods:

A longitudinal comparative study was conducted with 60 participants (30 with striae rubra and 30 with striae alba) at a tertiary care center. Patients received three fractional CO2 laser sessions at 4-week intervals. Primary outcomes were reductions in striae width and improvements in skin texture, assessed at baseline, 4 weeks, 8 weeks, and 20 weeks post-treatment. Patient satisfaction and adverse effects were secondary outcomes. Statistical analyses included McNemar’s test and Chi-square test for evaluating improvements and satisfaction scores.

Results:

Fractional CO2 laser therapy resulted in improvements in both types of striae. At 20 weeks, striae rubra showed slightly better improvement in width reduction, with 17% achieving over 75% reduction compared to 10% of striae alba. Patient satisfaction was high in both groups, with 23% reporting marked satisfaction in striae rubra compared to 17% in striae alba. Adverse effects were minimal and comparable across groups, with no significant differences in patient-reported outcomes.

Conclusions:

Fractional CO2 laser therapy is an effective and safe treatment for striae rubra and striae alba, with striae rubra showing slightly better outcomes. This therapy offers a non-invasive approach to improving skin texture and appearance, supporting its use as a standard treatment in dermatological practice. Further research with larger sample sizes and long-term follow-up is recommended to validate these findings and optimize treatment protocols.

Keywords

Carbon dioxide laser
Dermatology
Laser
Stretch marks
Striae distensae

INTRODUCTION

Striae distensae (SD), commonly known as stretch marks, are a prevalent dermatological condition characterized by linear atrophic dermal lesions that result from skin.1 These marks can manifest as striae rubra, which are erythematous and slightly raised, or as striae alba, which are hypopigmented and atrophic, reflecting a more chronic stage of skin damage.2,3 SD are not only a cosmetic concern but also contribute to significant psychological distress, particularly among women, who are disproportionately affected by this condition.4 The lesions frequently appear during periods of rapid skin stretching, such as puberty, pregnancy, or significant weight changes, and have been associated with conditions such as Cushing’s syndrome and Marfan syndrome.5 Furthermore, the use of corticosteroids, both topical and systemic, is a well-known precipitating factor. The pathogenesis of SD involves complex alterations in the dermal connective tissue framework, particularly affecting the extracellular matrix components such as collagen and elastin.6 Histologically, striae rubra exhibit increased vascularity and edema, whereas striae alba are marked by collagen reorganization and reduced vascularity.7 Despite their prevalence, there is no universally accepted standard treatment for SD. Traditional therapies, such as topical retinoids, hyaluronic acid, and microdermabrasion, offer limited efficacy and often require prolonged use to achieve modest improvements.8 Given the limitations of these conventional treatments, there is a growing interest in advanced therapeutic modalities that offer more substantial and lasting results.

Recently, laser therapy has emerged as a promising treatment option for SD, with fractional carbon dioxide (CO2) laser therapy at the forefront.9 This laser modality works by creating controlled microthermal injury zones in the skin, promoting collagen remodeling and neocollagenesis while sparing adjacent tissue.10 The fractional CO2 laser is particularly effective due to its ability to penetrate deeply into the dermis and stimulate fibroblast activity, resulting in improved skin texture and appearance.11 Previous studies have demonstrated the efficacy of fractional CO2 lasers in treating various dermatological conditions, including scars and photoaging, making them an attractive option for managing SD.12,13 Despite promising outcomes, there is a paucity of data directly comparing the effectiveness of fractional CO2 laser treatment on different types of striae, such as striae rubra and striae alba. Most existing studies focus on short-term improvements without comprehensively addressing long-term efficacy and patient satisfaction. In addition, there is a need for more rigorous clinical trials to establish standardized protocols regarding laser parameters, treatment intervals, and the number of sessions required to optimize outcomes.

The objective of this study is to evaluate the efficacy of fractional CO2 laser therapy in treating striae rubra versus striae alba. We hypothesize that early intervention with fractional CO2 lasers can lead to significant improvements in both the texture and appearance of these lesions, with variations in response depending on the type of striae. This study aims to provide robust clinical evidence to guide dermatologists in adopting laser therapy as a standard treatment for SD, ultimately improving patient outcomes and satisfaction. By addressing these research objectives, we hope to contribute valuable insights into the management of this common yet challenging dermatological condition.

MATERIAL AND METHODS

Study design

This study is a longitudinal, comparative study designed to evaluate the efficacy of fractional CO2 laser treatment in patients with striae rubra and striae alba. The study was conducted over a period of 18 months at the department of dermatology of a tertiary healthcare center, in India.

Ethics approval

Ethical approval was obtained from the institutional ethics committee and the study has adhered to the tenets outlined in the Declaration of Helsinki. Written informed consent was obtained from all participants prior to their inclusion in the study.

Setting

The study took place in a tertiary care teaching hospital equipped with the necessary facilities for dermatological research and laser treatment procedures. Patients were recruited from the outpatient department, ensuring a diverse and representative sample of individuals seeking treatment for SD.

Participants

Participants included patients aged 18 years and above who presented with a clinical diagnosis of either striae rubra or striae alba. Participants were recruited from the dermatology outpatient clinic. A total of 60 patients were enrolled in the study, with an equal number of 30 participants in each group. The recruitment process utilized a convenience sampling method, selecting participants who met the inclusion criteria and were willing to adhere to the study protocol.

Inclusion criteria

  • Age 18 years and above

  • Clinical diagnosis of striae rubra or striae alba

  • Ability and willingness to provide informed consent and comply with study procedures.

Exclusion criteria

  • Pregnancy or lactation

  • History of diabetes

  • Local skin infections

  • Contraindications to CO2 laser treatment, such as herpes simplex, lupus, xeroderma pigmentosum, or connective tissue disorders

  • Immunosuppression or history of malignancy or radiation therapy

  • Recent use of systemic corticosteroids or other treatments affecting skin healing.

Sample size

A sample size of 60 was determined based on a previous study indicating an 83.3% efficacy rate of fractional CO2 laser treatment. The calculation assumed a 95% confidence interval and a 5% margin of error, with 30 patients each for striae rubra and striae alba groups. Sample size is calculated using Openepi version 3.-

Study procedures

Each participant underwent fractional CO2 laser treatment using the SUDARFRAX fractional CO2 laser system. The treatment protocol involved three sessions for each patient spaced 4 weeks apart.

The laser parameters were carefully standardized: a spot size of 1 cm2, power of 12 watts, point energy of 40 mJ, and a pulse interval of 6 ms. The pulse duration was 1 ms in the first session, increased to 2 ms in the second, and further increased to 3 ms in the last session, while the pulse interval remained constant in all sessions. The change in pulse duration was based on the patient’s tolerability to the burning sensation, as an increase in pulse duration leads to deeper penetration, causing more thermal damage in the lesional tissue and surrounding areas due to increased heat diffusion. These settings were chosen based on previous studies and clinical guidelines to optimize efficacy while minimizing adverse effects. Before each laser session, a topical anesthetic cream containing 2.5% lidocaine and 2.5% prilocaine was applied to the affected areas for 45 min under occlusion to ensure patient comfort. All safety precautions were strictly followed, including the use of protective eyewear by both patients and medical staff throughout the procedure. Pre-treatment and post-treatment photographs were captured using a high-resolution 64-megapixel digital camera to document changes in the lesions. These images provided visual evidence of treatment efficacy and were used alongside clinical assessments to evaluate outcomes.

Outcome measures

The primary outcome measures were the reduction in striae width and improvement in skin texture, assessed at baseline, 4 weeks, 8 weeks, and 20 weeks post-treatment. Striae width was measured at its widest point, and improvement was graded on a scale of 0–4, with 0 indicating no improvement and 4 indicating excellent improvement (>75% reduction). Skin texture was evaluated using a similar grading system used by Sobhi et al. in their study to measure the skin texture improvement in striae, where 0 indicated no improvement and 4 indicated excellent improvement.13 These assessments were conducted by trained dermatologists to ensure consistency and accuracy. Secondary outcome measures included patient satisfaction, which was evaluated using a visual analog scale (VAS), ranging from 0 (no satisfaction) to 4 (marked satisfaction). Adverse effects were also recorded, including immediate and late reactions with immediate being more common than late. Among the immediate reactions, pain, burning and erythema were the most commonly observed, which resolved within a period of 7 days. The other immediate reactions include edema, dryness, pruritus, urticaria, petechiae, and reactivation of herpes simplex. Similarly, the common late reactions observed were persistent erythema beyond a week and post-inflammatory hyperpigmentation, which appeared later. The other late reactions were post-inflammatory hypopigmentation, milia, acne aggravation, and scarring.

Study variables and measurement

Data were collected using a structured pro forma that included demographic details, clinical history, and treatment outcomes. Measurements of striae width and texture were conducted using standardized techniques, and two trained dermatologists performed the assessment to minimize variability. To minimize bias, the study employed a consistent treatment protocol and standardized assessment methods. The main quantitative variables analyzed in this study included the percentage reduction in striae width and texture scores at various time points. Additional variables included patient satisfaction scores and the incidence of adverse effects.

Statistical methods

Statistical analysis was performed using the Statistical Package for the Social Sciences software version 23.0. Descriptive statistics, including means, medians, and standard deviations, were used to summarize baseline characteristics. McNemar’s test was employed to compare pre-and post-treatment improvements in striae width and skin texture. The Chi-square test was used to analyze differences in treatment outcomes between striae rubra and striae alba groups, as well as patient satisfaction scores. A P < 0.05 was considered statistically significant, indicating that the observed differences were unlikely to have occurred by chance.

RESULTS

The study included 60 participants, equally divided between the striae rubra (n = 30) and striae alba (n = 30) groups. The average age was similar in both groups, with the striae rubra group having a mean age of 28.2 years (standard deviation [SD] ± 7.9) and the striae alba group having a mean age of 27.2 years (SD ± 8.5), showing no statistically significant difference (P = 0.643). Gender distribution was also comparable, with 56.7% males and 43.3% females in the striae rubra group and 53.3% males and 46.7% females in the striae alba group (P = 0.793).

Fitzpatrick skin types were similarly distributed, with no significant differences (P = 0.903). Both groups showed similar mean body mass indexes (BMIs): 26.8 kg/m2 (SD ± 6.3) for striae rubra and 25.8 kg/m2 (SD ± 6.7) for striae alba (P = 0.615). Lesion sites were predominantly on the shoulder for both groups (40.0% for striae rubra and 43.3% for striae alba), with similar distributions for other body sites such as the abdomen, hips, and extremities, and no significant differences (P = 0.970). The baseline characteristics between the groups were well matched, allowing for a balanced comparison in subsequent analyses [Table 1].

Table 1: Baseline demographic and clinical characteristics of study participants (n=60).
Characteristic Striae rubra (n=30) Striae alba (n=30) Total (n=60) P-value
Mean age (years) 28.2±7.9 27.2±8.5 27.7±8.2 0.643
Gender (%)
  Male 17 (56.7) 16 (53.3) 33 (55.0) 0.793
  Female 13 (43.3) 14 (46.7) 27 (45.0)
Fitzpatrick skin type (%)
  III 6 (20.0) 7 (23.3) 13 (21.7) 0.903
  IV 11 (36.7) 11 (36.7) 22 (36.7)
  V 13 (43.3) 12 (40.0) 25 (41.7)
BMI (kg/m2) 26.8±6.3 25.8±6.7 26.3±6.5 0.615
Topical steroid use 5 (16.7) 5 (16.7) 10 (16.7) 1.000
Site of lesion (%)
  Shoulder 12 (40.0) 13 (43.3) 25 (41.7) 0.970
  Abdomen 7 (23.3) 7 (23.3) 14 (23.3)
  Hip 4 (13.3) 4 (13.3) 8 (13.3)
  Upper extremities 3 (10.0) 4 (13.3) 7 (11.7)
  Lower extremities 2 (6.7) 2 (6.7) 4 (6.7)
  Face and neck 1 (3.3) 0 (0.0) 1 (1.7)

BMI: Body mass index.

At the 4-week mark, most participants in both the striae rubra and striae alba groups showed no improvement in striae width and skin texture, with 90% of striae rubra and 97% of striae alba participants showing no change. By 8 weeks, the majority had <25% improvement in width (94% for striae rubra and 86% for striae alba) and similar percentages for skin texture, with no significant differences between groups (P > 0.5). At 20 weeks, the striae rubra group exhibited greater improvements [Figures 1 and 2], with 30% achieving 50–75% width reduction and 7% achieving over 75%, compared to 10% and 0% in the striae alba group [Figures 3 and 4], respectively [Table 2]. Skin texture also improved more in the striae rubra group, but overall differences between groups remained statistically non-significant at all-time points (P > 0.1).

Improvement of striae alba over the left shoulder at (a) baseline, (b) week 4, (c) week 8 and (d) week 20.
Figure 1:
Improvement of striae alba over the left shoulder at (a) baseline, (b) week 4, (c) week 8 and (d) week 20.
Improvement of striae alba over the right shoulder at (a) baseline, (b) week 4, (c) week 8 and (d) week 20.
Figure 2:
Improvement of striae alba over the right shoulder at (a) baseline, (b) week 4, (c) week 8 and (d) week 20.
Improvement of striae rubra over the left abdomen at (a) baseline, (b) week 4, (c) week 8 and (d) week 20.
Figure 3:
Improvement of striae rubra over the left abdomen at (a) baseline, (b) week 4, (c) week 8 and (d) week 20.
Improvement of striae rubra over the right abdomen at (a) baseline, (b) week 4, (c) week 8 and (d) week 20.
Figure 4:
Improvement of striae rubra over the right abdomen at (a) baseline, (b) week 4, (c) week 8 and (d) week 20.
Table 2: Comparison of improvement in striae width and skin texture at different time points between striae rubra and striae alba groups.
Time point Striae rubra (n=30) (%) Striae alba (n=30) (%) P-value
4 weeks
  Striae width
    No improvement 27 (90) 29 (97) 0.301
    <25% 3 (10) 1 (3)
  Skin texture
    No improvement 27 (90) 29 (97) 0.301
    <25% 3 (10) 1 (3)
8 weeks
  Striae width
    <25% 28 (94) 26 (86) 0.690
    25–50% 1 (3) 2 (7)
  Skin texture
    <25% 26 (87) 27 (90) 0.509
    25–50% 3 (10) 1 (3)
20 weeks
  Striae width
    <25% 4 (13) 8 (27) 0.144
    25–50% 13 (43) 16 (53)
    50–75% 9 (30) 3 (10)
    >75% 2 (7) 0 (0)
  Skin texture
    <25% 2 (7) 3 (10) 0.751
    25–50% 10 (33) 12 (40)
    50–75% 11 (36) 10 (33)
    >75% 5 (17) 2 (7)

At the 20-week follow-up, patient satisfaction levels were similar between the striae rubra and striae alba groups, with 23.3% of the striae rubra group and 16.7% of the striae alba group reporting marked satisfaction (VAS >75%). Moderate satisfaction was reported by 26.7% of the striae rubra group and 23.3% of the striae alba group. Mild satisfaction was higher in the striae alba group (26.7% vs. 16.7%), whereas poor satisfaction was identical in both groups at 33.3%. In terms of adverse effects, 20.0% of the striae rubra group experienced immediate adverse effects compared to 6.7% of the striae alba group (P = 0.495) with erythema and burning sensation being the most common immediate adverse effect in both groups. Late adverse effects were similar between groups, with 20.0% in the striae rubra group and 23.3% in the striae alba group with post-inflammatory hyperpigmentation being the most common [Table 3]. A majority of participants reported no adverse effects, with 60.0% in the striae rubra group and 70.0% in the striae alba group, indicating generally comparable outcomes between the two groups with no statistically significant differences (P > 0.1). Patients with Fitzpatrick skin types III and IV, low BMI, and no topical corticosteroid usage history showed good prognosis, whereas skin types V, high BMI, and corticosteroid usage history showed vice versa.

Table 3: Patient satisfaction and adverse effects at 20-week follow-up for striae rubra and striae alba groups.
Outcome measure Striae rubra (n=30) (%) Striae alba (n=30) (%) P-value
Satisfaction (VAS)
  Marked satisfaction (>75%) 7 (23.3) 5 (16.7) 0.745
  Moderate satisfaction (51–75%) 8 (26.7) 7 (23.3)
  Mild satisfaction (25–50%) 5 (16.7) 8 (26.7)
  Poor satisfaction (<25%) 10 (33.3) 10 (33.3)
Adverse effects (%)
  Immediate 6 (20.0) 2 (6.7) 0.495
  Late 6 (20.0) 7 (23.3)
  None 18 (60.0) 21 (70.0)

VAS: Visual analog scale.

DISCUSSION

Our study demonstrated that fractional CO2 laser treatment effectively improved both striae rubra and striae alba, with a slightly better outcome for striae rubra in terms of overall improvement and patient satisfaction. These results are consistent with the findings of Elmorsy et al. (2021), who reported significant clinical improvements in both types of striae with no significant differences between them.14 In our study, 17% of participants with striae rubra and 10% with striae alba achieved >75% overall improvement. This suggests that while fractional CO2 laser treatment is effective for both types, striae rubra, which are in a more active inflammatory stage, might respond more robustly due to their increased vascularity, which enhances the laser’s effects.15

Comparatively, Yang and Lee (2011) assessed the efficacy of nonablative fractional photothermolysis and ablative fractional CO2 laser resurfacing for treating SD and found both modalities to be effective and safe, particularly in Asian skin, but did not observe greater clinical improvement with either modality.11 In their study, the percentage of patients reporting “good” to “excellent” improvement was lower than in ours, possibly due to differences in skin type and the chronicity of the lesions treated. Kaewkes et al. (2022) evaluated the long-term efficacy of a fractional picosecond 1064-nm laser specifically for striae alba in individuals with darker skin and found moderate to marked improvement in 90% of subjects, with only a 10% incidence of transient post-inflammatory hyperpigmentation.16 These results are comparable to our findings for striae alba, suggesting that newer laser technologies may offer similar efficacy across different skin types. Lee et al. (2010) demonstrated a positive therapeutic effect using ablative fractional CO2 lasers for late-stage SD, reporting high participant satisfaction with 52% achieving 50–75% improvement, which aligns closely with our findings of high satisfaction levels and marked improvement in the striae rubra group.17 Malekzad et al. (2014) similarly showed significant improvements in striae alba with the Star Lux 500 laser, suggesting that fractional lasers, in general, provide substantial benefits in managing SD, regardless of the specific type or laser technology used.18

The biological differences between striae rubra and striae alba may account for the observed treatment outcomes in our study. Striae rubra, being in the inflammatory stage, have increased vascularity and cellular activity, which might enhance the fractional CO2 laser’s ability to promote collagen remodeling and skin renewal.19 The laser’s microthermal zones create controlled damage, stimulating the body’s natural wound-healing response and encouraging new collagen and elastin production. In contrast, striae alba, representing a more chronic phase, have reduced vascularity and dermal thinning, making it more challenging to achieve significant improvement.20 The limited blood supply and altered extracellular matrix in striae alba may hinder the laser’s effectiveness in stimulating substantial tissue regeneration.21 This difference in the biological environment likely contributes to the better outcomes observed in striae rubra, as the laser can leverage the active cellular processes to enhance skin repair and improve striae appearance. An increase in the pulse duration leads to deeper penetration causing more thermal damage in the lesional tissue and to the surrounding areas due to increased heat diffusion, in our study, the first session was started with 1 ms of pulse duration and increased 1 ms in each session with reaching 3 ms in the third session based on the tolerability of the patient to the burning sensation. The pulse interval was kept constant at 6 ms in all sessions.

The strengths of our study include a well-balanced design with equal numbers of participants in both striae rubra and striae alba groups, ensuring a fair comparison. The standardized treatment protocol and comprehensive follow-up assessments allowed for consistent and reliable outcome measurement. However, the study also has limitations, including the relatively small sample size and the subjective nature of patient satisfaction assessments. Furthermore, the lack of long-term follow-up limits our understanding of the sustained efficacy of fractional CO2 laser treatment. The inclusion of objective skin analysis technologies in future studies could enhance the precision of outcome evaluations.

Clinically, this study supports the use of fractional CO2 laser therapy as a viable treatment option for both striae rubra and striae alba, offering a non-invasive approach to improving skin texture and appearance. While striae rubra may respond more favorably, the treatment can still provide benefits for striae alba, making it a versatile option in dermatological practice. For future research, larger studies with extended follow-up periods are recommended to assess the long-term efficacy and safety of fractional CO2 lasers. In addition, exploring the combination of laser therapy with adjunctive treatments, such as topical agents or microneedling, may enhance outcomes further. This study contributes valuable insights into the management of SD, guiding clinicians in optimizing treatment strategies to improve patient outcomes and satisfaction.

CONCLUSION

The study demonstrates that fractional CO2 laser therapy effectively improves both striae rubra and striae alba, with slightly better outcomes for striae rubra due to its increased vascularity and active cellular processes. Fractional CO2 laser therapy is a safe, non-invasive treatment option that enhances skin texture and appearance in patients with SD, making it a versatile addition to dermatological practice.

Authors’ contributions:

LakshmiPrasad - Writing, investigation, data curation, Roshni Menon - Conceptualization, Yogindher Singh - Methodology, Supervision, Karunanandhan Manobalan - Formal analysis, validation Niharikaa, Kovalan, Aravind - Resources.

Ethical approval:

The research/study approved by the Institutional Review Board at Sri Venkateshwaraa Medical College, Hospital and Research Centre, number 122/SVMCH/IEC-Cert/February 24, dated 28th February, 2024.

Declaration of patient consent:

The authors certify that they have obtained all appropriate patient consent.

Conflicts of interest:

There are no conflicts of interest.

Use of artificial intelligence (AI)-assisted technology for manuscript preparation:

The authors confirm that there was no use of artificial intelligence (AI)-assisted technology for assisting in the writing or editing of the manuscript and no images were manipulated using AI.

Financial support and sponsorship: Nil.

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