SynthesisThe Cochrane database of systematic reviews2011
Lasers or light sources for treating port-wine stains.
Synthesis in The Cochrane database of systematic reviews, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 3 of them syntheses that pooled it.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
19 citing papers in PubMed, 3 syntheses or guidelines pooled it, 71 citations in OpenAlex.
- Laser and light-based treatments for port-wine birthmarks - a systematic review and network meta-analysis.Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG · 2025Pooled it
- Double pass 595-nm dye laser is not more effective than single pass: A systematic review and meta-analysis.Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging (ISSI) · 2023Pooled it
- Clinical outcome measures and scoring systems used in prospective studies of port wine stains: A systematic review.PloS one · 2020Pooled it
- Quantitative method for evaluation of aesthetic results after laser treatment for birthmarks.Lasers in medical science · 2013Trial
- Pathogenesis of Port-Wine Stains: Directions for Future Therapies.International journal of molecular sciences · 2022Review
- Willingness to Pay and Time Trade-off in Thai Patients with Port-Wine Stains.ClinicoEconomics and outcomes research : CEOR · 2022Article
- Improving imaging depth by dynamic laser speckle imaging and topical optical clearing for in vivo blood flow monitoring.Lasers in medical science · 2021Article
- Quality of Life and Psychological Effects of Port-Wine Stain: A Review of Literature.Clinical, cosmetic and investigational dermatology · 2021Review
- Striae distensae in adolescents: A mini review.Acta bio-medica : Atenei Parmensis · 2020Review
- The Evaluation of Laser Application in Surgery: A Review Article.Journal of lasers in medical sciences · 2019Review
- Histologic changes associated with talaporfin sodium-mediated photodynamic therapy in rat skin.Lasers in surgery and medicine · 2017Article
- Laser applications in surgery.Annals of translational medicine · 2016Review
- Transcutaneous laser treatment of leg veins.Lasers in medical science · 2014Review
- Extracranial vascular malformations (hemangiomas and vascular malformations) in children and adolescents - diagnosis, clinic, and therapy.GMS current topics in otorhinolaryngology, head and neck surgery · 2014Review
- Treatment of port wine stains with pulsed dye laser: a retrospective study of 848 cases in Shandong Province, People's Republic of China.Drug design, development and therapy · 2014Article
- Lasers for cutaneous congenital vascular lesions: a comprehensive overview and update.Lasers in medical science · 2013Review
- A seemingly insignificant lesion.Indian dermatology online journalArticle
- Treatment of capillary and venous cutaneous vascular malformations using long pulse 1,064-nm neodymium:yttrium-aluminum-garnet laser and intense pulsed light.Anais brasileiros de dermatologiaArticle
- What do Cochrane systematic reviews say about congenital vascular anomalies and hemangiomas? A narrative review.Sao Paulo medical journal = Revista paulista de medicinaReview
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors at 3 institutions in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundPort-wine stains are birthmarks caused by malformations of blood vessels in the skin. Port-wine stains manifest themselves in infancy as a flat, red mark and do not regress spontaneously but may, if untreated, become darker and thicker in adult life. The profusion of various lasers and light sources makes it difficult to decide which equipment is the best for treating port-wine stains.
objectivesTo study participant satisfaction, clinical efficacy, and adverse effects of the treatment of port-wine stains by lasers and light sources. SEARCH
methodsWe searched the following databases up to April 2010: the Cochrane Skin Group Specialised Register, the Cochrane Central Register of Controlled Trials (Clinical Trials) in The Cochrane Library, MEDLINE (from 2005), EMBASE (from 2007), LILACS (Latin American and Caribbean Health Science Information database, from 1982), and reference lists of articles. We also searched online trials registries for ongoing trials and contacted trial authors where appropriate. SELECTION CRITERIA: Randomised clinical trials (RCTs) of lasers or light sources for the treatment of port-wine stains. DATA COLLECTION AND ANALYSIS: Our outcomes of interest were participant satisfaction, reduction in redness of the port-wine stain as determined by clinical evaluation, and short- and long-term adverse effects of the treatments. Three authors independently extracted data and assessed trial quality. MAIN
resultsWe included 5 RCTs involving a total of 103 participants; all of the trials used a within-participant design. The interventions and outcomes were too varied to be combined statistically. All trials used the pulsed dye laser for comparisons.None of the studies focused on participant satisfaction, which was one of our primary outcomes, but participant preference was evaluated in three of five studies. Participants preferred the pulsed dye laser to intense pulsed light based on the clinical effect. They marginally preferred the Neodymium:YAG (yttrium-aluminium-garnet) (Nd:YAG) laser to the pulsed dye laser due to shorter lasting purpura, and pulsed dye laser in conjunction with cooling was preferred to treatment with pulsed dye laser alone.All trials examined short-term efficacy of less than six months after treatments with the pulsed dye laser, intense pulsed light, and Nd:YAG laser. The pulsed dye laser was evaluated in all five trials. Depending upon the setting of the pulsed dye laser, this resulted in more than 25% reduction in redness. This was after 1 to 3 treatments for up to 4 to 6 months postoperatively in 50% to 100% of the participants. There was only one study each of intense pulsed light and Nd:YAG laser.Two trials had no occurrence of long-term adverse effects, i.e. six months after treatment. Three trials reported pigmentary alterations in 3% to 24% of the participants, with the highest percentage occurring in Chinese participants with darker skin types. In one study one participant experienced scarring of the skin caused by a too-high dose of the laser used. Short-term side-effects included pain, crusting, and blistering in the first two weeks after treatment. AUTHORS'
conclusionsThe pulsed dye laser leads to clinically relevant clearance of port-wine stains. A limited number of RCTs evaluated the efficacy from intense pulsed light and other laser types. High-quality RCTs are needed to assess individual efficacy from different lasers and light sources, as well as participant satisfaction.
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What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.