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Study Summary
Study Summary
• This is a retrospective cohort with a total of 124
patients who underwent Vbeam Perfecta 595 nm
pulsed-dye laser (PDL) to treat port-wine stains
(PWS) at different body positions from March 2018 to
March 2023. Demographic data, lesions’ positions and
grading, as well as response rate were documented.
(Table 1)
• Photographs were taken before and after each
session, and the severity of the lesion was assessed
based on color and thickness, categorized into
four levels: 1 (pink-red), 2 (dark-red), 3 (purple-
dark), and 4 (purple-dark and/or nodular and
hypertrophic).
• Patients were treated with spot sizes 7 - 10 mm,
fluence 6 - 12 J/cm2
, and pulse duration 0.45 - 10 ms,
along with cryogen cooling. Topical anesthesia was
applied to the lesions 30 min before the treatment. The
treatment sessions occurred monthly, with a variable
number of sessions conducted (6-26 sessions).
• Clinical improvement scores of comparable
photographs were judged independently by two
dermatologists after the series of treatments using a
quartile grading (0: < 20% improvement; 1: 21-40%
improvement; 2: 41-60% improvement; 3: 61-80%
improvement; and 4: >80% improvement).
Vbeam®
Efficacy and safety of 595-nm pulsed dye laser treating port
wine stains in Vietnamese patients: analysis of 124 cases and
optimal treatment regimens
Author Name:
Hoang Thanh Tuan1
, Nguyen Xuan Tru2
, Luu Tuan Phong2
, Doan Vu Quoc Hanh2
, Nguyen Tien Manh2
, Pham Dieu Huong2
, Vu Thi
Da Thao2
Center Name:
1
Plastic and Reconstructive Aesthetic Surgery Center, Vietnam National Burn Hospital, Military Medical Institute, Hanoi, Vietnam;
2
Hoang Tuan Clinic, Hoang Quoc Viet, Hanoi, Vietnam
Publication Source: Tuan, H. T., Tru, N. X., Phong, L. T., Hanh, D. V. Q., Manh, N. T., Huong, P. D., & Da Thao, V. T. (2023).
Efficacy and safety of 595-nm pulsed dye laser treating port wine stains in Vietnamese patients: analysis of 124 cases and
optimal treatment regimens. Lasers in medical science, 38(1), 258. https://doi.org/10.1007/s10103-023-03926-8
Results
• The overall response rate across various lesion
grade was 73.4%. 49 cases (39.5%) had clinical
improvement grade 3 (61 – 80% improvement) while
42 patients (33.9%) had clinical improvement grade 4
(>80% improvement).
• All patients with lesion grade 1 (pink-red) reached
clinical improvement > 80% while >90% of patients
of lesion grade 2 (dark-red) could reach satisfactory
outcome.
Overall
response rate
was 73.4%
All patients
with lesion grade
1 reached clinical
improvement
> 80%
Study Summary
©2024 Candela Corporation. This material contains registered and unregistered trademarks, tradenames, service marks and brand names of Candela Corporation and its
affiliates. All other trademarks are the property of their respective owners. All rights reserved.CLI102751EN-AP
Disclaimer: The views and opinions expressed in this material are those of the authors and do not necessarily represent the official position of Candela Corporation or its
affiliates. All contents of this material are for informational purposes only and provided by Candela Asia-Pacific without warranties of any kind. Healthcare professionals are solely
responsible for making their own independent evaluation as to the suitability of any product for any particular purpose and in accordance with country specific regulations. The availability
of products and the indications mentioned in this material is subject to the regulatory requirements and product registration status in each country. Refer to the User Manual for country specific
indications. Products and technical specifications may change without notice. Please contact Candela Asia-Pacific for more details.
Conclusions
The study showed that Vietnamese patients with
Fitzpatrick skin classifications III to IV had an overall
response rate of 73.4% for PWS treatment with PDL,
where the outcomes were predominantly influenced by the
grade of the lesion, with lower-grade lesions achieving
better clearance and requiring fewer treatment
sessions.
Table 1. Demographic data and the overall response rates compared between groups
Clinical improvement grade (n, %) Response rate (%) (n)
Gender
Male (n = 17, 13.7%)
Female (n = 107, 86.3%)
Age
Young (11 - 39 years) (n = 96, 77.4%)
Old (≥ 40 years) (n = 28, 22.6%)
Lesion grade
1 (n = 5, 4%)
2 (n = 30, 24.2%)
3 (n = 52, 41.9%)
4 (n = 37, 29.8%)
Treatment session
6 - 10 (n = 22, 17.7%)
11 - 15 (n = 46, 37.1%)
≥ 16 (n = 56, 45.2%)
Total patients (n = 124)
Lesion position
Lateral face (n = 108, 83.7%)
Central face (n = 11, 8.5%)
Full face (n = 1, 0.8%)
Ear (n = 1, 0.8%)
Shoulder (n = 1, 0.8%)
Breast (n = 3, 2.3%)
Upper extremity (n = 2, 1.6%)
Lower extremity (n = 2, 1.6%)
Total lesions (n = 129)
0
1 (0.9%)
1 (1.0%)
1 (3.3%)
1 (2.2%)
1 (0.9%)
1 (9.1%)
1
4 (3.7%)
3 (3.1%)
1 (3.6%)
2 (3.3%)
2 (5.4%)
1 (4.5%)
2 (4.3%)
1 (1.8%)
3 (2.8%)
2 (18.2%)
2
4 (23.5%)
24 (22.4%)
22 (22.9%)
6 (21.4%)
2 (6.7%)
14 (26.9%)
12 (32.4%)
4 (18.2%)
13 (28.3%)
11 (19.6%)
25 (23.1%)
3 (27.3%)
1 (100%)
1 (50%)
3
10 (58.8%)
39 (36.4%)
37 (38.5%)
12 (42.9%)
9 (30.0%)
23 (44.2%)
17 (45.9%)
6 (27.3%)
16 (34.8%)
27 (48.2%)
44 (40.7%)
5 (45.5%)
1 (100%)
1 (33.3%)
1 (50%)
1 (50%)
4
3 (17.6%)
39 (36.4%)
33 (34.5%)
9 (32.1%)
5 (100%)
18 (60.0%)
13 (25.9%)
6 (16.2%)
11 (50.0%)
14 (30.4%)
17 (30.4%)
35 (32.4%)
1 (100%)
2 (66.7%)
1 (50%)
76.5% (13)
72.9% (78)
72.9% (70)
75% (21)
100% (5)
90.0% (27)
69.2% (36)
62.2% (23)
77.3% (17)
65.2% (30)
78.6% (44)
73.4% (71)
73.1% (79)
72.7% (8)
0% (1)
100% (1)
100% (1)
100% (3)
100% (2)
50% (1)
Discussion
• Gender and age did not significantly affect the
response rate.
• Although the response rate was not significantly
different across different positions, it could be
observed that the lateral face, ear, breast, and
upper extremity could reach better clinical
improvement than central facial sites or lower
extremity.
• Lesions grades 1 and 2 had a better response with
a shorter period of treatment (6 - 15 treatments). Lesion
grade 3 should be expected to have a response after a
longer duration of treatment. A regimen ≥ 16 treatments
should be expected for treating lesions grade 4.

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Dr. Hoang Tuan - CLI102751EN-AP_2024_APAC_Vbeam Study Summary PWS V_240227_094214.pdf

  • 1. Study Summary Study Summary • This is a retrospective cohort with a total of 124 patients who underwent Vbeam Perfecta 595 nm pulsed-dye laser (PDL) to treat port-wine stains (PWS) at different body positions from March 2018 to March 2023. Demographic data, lesions’ positions and grading, as well as response rate were documented. (Table 1) • Photographs were taken before and after each session, and the severity of the lesion was assessed based on color and thickness, categorized into four levels: 1 (pink-red), 2 (dark-red), 3 (purple- dark), and 4 (purple-dark and/or nodular and hypertrophic). • Patients were treated with spot sizes 7 - 10 mm, fluence 6 - 12 J/cm2 , and pulse duration 0.45 - 10 ms, along with cryogen cooling. Topical anesthesia was applied to the lesions 30 min before the treatment. The treatment sessions occurred monthly, with a variable number of sessions conducted (6-26 sessions). • Clinical improvement scores of comparable photographs were judged independently by two dermatologists after the series of treatments using a quartile grading (0: < 20% improvement; 1: 21-40% improvement; 2: 41-60% improvement; 3: 61-80% improvement; and 4: >80% improvement). Vbeam® Efficacy and safety of 595-nm pulsed dye laser treating port wine stains in Vietnamese patients: analysis of 124 cases and optimal treatment regimens Author Name: Hoang Thanh Tuan1 , Nguyen Xuan Tru2 , Luu Tuan Phong2 , Doan Vu Quoc Hanh2 , Nguyen Tien Manh2 , Pham Dieu Huong2 , Vu Thi Da Thao2 Center Name: 1 Plastic and Reconstructive Aesthetic Surgery Center, Vietnam National Burn Hospital, Military Medical Institute, Hanoi, Vietnam; 2 Hoang Tuan Clinic, Hoang Quoc Viet, Hanoi, Vietnam Publication Source: Tuan, H. T., Tru, N. X., Phong, L. T., Hanh, D. V. Q., Manh, N. T., Huong, P. D., & Da Thao, V. T. (2023). Efficacy and safety of 595-nm pulsed dye laser treating port wine stains in Vietnamese patients: analysis of 124 cases and optimal treatment regimens. Lasers in medical science, 38(1), 258. https://doi.org/10.1007/s10103-023-03926-8 Results • The overall response rate across various lesion grade was 73.4%. 49 cases (39.5%) had clinical improvement grade 3 (61 – 80% improvement) while 42 patients (33.9%) had clinical improvement grade 4 (>80% improvement). • All patients with lesion grade 1 (pink-red) reached clinical improvement > 80% while >90% of patients of lesion grade 2 (dark-red) could reach satisfactory outcome. Overall response rate was 73.4% All patients with lesion grade 1 reached clinical improvement > 80%
  • 2. Study Summary ©2024 Candela Corporation. This material contains registered and unregistered trademarks, tradenames, service marks and brand names of Candela Corporation and its affiliates. All other trademarks are the property of their respective owners. All rights reserved.CLI102751EN-AP Disclaimer: The views and opinions expressed in this material are those of the authors and do not necessarily represent the official position of Candela Corporation or its affiliates. All contents of this material are for informational purposes only and provided by Candela Asia-Pacific without warranties of any kind. Healthcare professionals are solely responsible for making their own independent evaluation as to the suitability of any product for any particular purpose and in accordance with country specific regulations. The availability of products and the indications mentioned in this material is subject to the regulatory requirements and product registration status in each country. Refer to the User Manual for country specific indications. Products and technical specifications may change without notice. Please contact Candela Asia-Pacific for more details. Conclusions The study showed that Vietnamese patients with Fitzpatrick skin classifications III to IV had an overall response rate of 73.4% for PWS treatment with PDL, where the outcomes were predominantly influenced by the grade of the lesion, with lower-grade lesions achieving better clearance and requiring fewer treatment sessions. Table 1. Demographic data and the overall response rates compared between groups Clinical improvement grade (n, %) Response rate (%) (n) Gender Male (n = 17, 13.7%) Female (n = 107, 86.3%) Age Young (11 - 39 years) (n = 96, 77.4%) Old (≥ 40 years) (n = 28, 22.6%) Lesion grade 1 (n = 5, 4%) 2 (n = 30, 24.2%) 3 (n = 52, 41.9%) 4 (n = 37, 29.8%) Treatment session 6 - 10 (n = 22, 17.7%) 11 - 15 (n = 46, 37.1%) ≥ 16 (n = 56, 45.2%) Total patients (n = 124) Lesion position Lateral face (n = 108, 83.7%) Central face (n = 11, 8.5%) Full face (n = 1, 0.8%) Ear (n = 1, 0.8%) Shoulder (n = 1, 0.8%) Breast (n = 3, 2.3%) Upper extremity (n = 2, 1.6%) Lower extremity (n = 2, 1.6%) Total lesions (n = 129) 0 1 (0.9%) 1 (1.0%) 1 (3.3%) 1 (2.2%) 1 (0.9%) 1 (9.1%) 1 4 (3.7%) 3 (3.1%) 1 (3.6%) 2 (3.3%) 2 (5.4%) 1 (4.5%) 2 (4.3%) 1 (1.8%) 3 (2.8%) 2 (18.2%) 2 4 (23.5%) 24 (22.4%) 22 (22.9%) 6 (21.4%) 2 (6.7%) 14 (26.9%) 12 (32.4%) 4 (18.2%) 13 (28.3%) 11 (19.6%) 25 (23.1%) 3 (27.3%) 1 (100%) 1 (50%) 3 10 (58.8%) 39 (36.4%) 37 (38.5%) 12 (42.9%) 9 (30.0%) 23 (44.2%) 17 (45.9%) 6 (27.3%) 16 (34.8%) 27 (48.2%) 44 (40.7%) 5 (45.5%) 1 (100%) 1 (33.3%) 1 (50%) 1 (50%) 4 3 (17.6%) 39 (36.4%) 33 (34.5%) 9 (32.1%) 5 (100%) 18 (60.0%) 13 (25.9%) 6 (16.2%) 11 (50.0%) 14 (30.4%) 17 (30.4%) 35 (32.4%) 1 (100%) 2 (66.7%) 1 (50%) 76.5% (13) 72.9% (78) 72.9% (70) 75% (21) 100% (5) 90.0% (27) 69.2% (36) 62.2% (23) 77.3% (17) 65.2% (30) 78.6% (44) 73.4% (71) 73.1% (79) 72.7% (8) 0% (1) 100% (1) 100% (1) 100% (3) 100% (2) 50% (1) Discussion • Gender and age did not significantly affect the response rate. • Although the response rate was not significantly different across different positions, it could be observed that the lateral face, ear, breast, and upper extremity could reach better clinical improvement than central facial sites or lower extremity. • Lesions grades 1 and 2 had a better response with a shorter period of treatment (6 - 15 treatments). Lesion grade 3 should be expected to have a response after a longer duration of treatment. A regimen ≥ 16 treatments should be expected for treating lesions grade 4.