| Literature DB >> 29805312 |
Tarcisio Vitor Augusto Lordani1, Celia Eliane de Lara1, Fabiana Borges Padilha Ferreira2, Mariana de Souza Terron Monich2, Claudinei Mesquita da Silva2, Claudia Regina Felicetti Lordani3, Fernanda Giacomini Bueno4, Jorge Juarez Vieira Teixeira5, Maria Valdrinez Campana Lonardoni5.
Abstract
The pharmaceutical industry has made great strides in providing drugs that are able to stimulate the healing process, but only 1-3% of all drugs that are listed in Western pharmacopoeias are intended for use on the skin or cutaneous wounds. Of these, at least one-third are obtained from plants. We sought to review the therapeutic effects of medicinal plants on human skin lesions. For this systematic review, we searched the PubMed, Scopus, and Web of Science databases to identify clinical trials that were published from 1997 to 2017. We reviewed studies that described the use of medicinal plants for the treatment of skin lesions in humans. Ten studies were selected, eight of which were published from 2007 to 2016, with a total of 503 patients. Among the plant species that were used for the treatment of human skin lesions, 12 belonged to 11 families and were included in the analysis. All of the plant species that were studied presented high therapeutic potential for the treatment of cutaneous lesions.Entities:
Mesh:
Year: 2018 PMID: 29805312 PMCID: PMC5901822 DOI: 10.1155/2018/7354250
Source DB: PubMed Journal: Mediators Inflamm ISSN: 0962-9351 Impact factor: 4.711
Figure 1Study flow chart (PRISMA).
Characteristics of included studies.
| Reference | Year | Study type | Sample | Scientific name (plant family) | Popular name in Brazil | Route of administration/treatment mode | Outcome |
|---|---|---|---|---|---|---|---|
| [ | 2010 | Case report | 1 |
| Babosa | The dressing was composed of sterile gauze for topical use, with an extract of | Treatment with the product ceased on August 22, for a total treatment duration of 2 months 11 days. The healing process was complete. |
| [ | 2010 | Clinical trial randomized | 90 |
| Sálvia | 20 ml intravenously every 12 h from the day of surgery until 3 days after surgery. | At 4 days after surgery, the women in the control group had significantly more ischemia and necrosis compared with group 2 ( |
| [ | 2011 | Clinical study | 101 |
| Jurema-preta | The test product tube was opened, and the product was applied drop by drop on the boundary of the wound such that the product formed a thin film over the entire wound surface. The wound was then covered with sterile cotton gauze to allow some air circulation. The wound was examined twice daily and cleaned if necessary, and fresh product was applied in an identical fashion. | The reduction of the mean wound surface area was much faster in the AS-21-treated group (reduction from 52.03 ± 36.66 cm2 on day 0 to 16.7 ± 20.5 cm2 [67.90%] on day 21 and 2.13 ± 3.86 cm2 [97.87%] on day 42). Complete healing was observed in 19 of 69 wounds (27.53%) after 4 weeks and in 41 of 69 wounds (59.4%) after 6 weeks. All of these results were statistically significant compared with the corresponding placebo values from day 14 onward ( |
|
| Pé de leão; alquemila | ||||||
| [ | 2012 | Clinical case studies | 4 |
| Angélica Chinesa | Sterile SBD.4 dressings were applied on lower-extremity chronic ulcers. | All wounds healed when the experimental SBD.4 dressing was applied. |
| [ | 2007 | Clinical trial | 40 |
| Jurema-preta | Treatment consisted of once-daily washings of the ulcerated area with clean boiled water and neutral soap followed by application of the hydrogel. The lesion was then covered with a simple dressing and compression bandage. | With this experimental treatment, 57.89% of the patients presented therapeutic efficacy at the end of week 4 of treatment, and nearly 100% presented therapeutic efficacy at the end of week 8. In the placebo group, only one patient presented therapeutic efficacy at week 6 ( |
| [ | 2011 | Clinical trial | 40 |
| Orégano | The study ointment was applied to the excision site by a medical assistant. The evaluating physicians were blinded to treatment. The excision site was then covered with a nonoclusive dressing. On day 0, the study ointment was provided to the patient in a concealed container, and the patients were instructed to apply the ointment twice daily to the site and cover it with a nonoclusive dressing. | The oregano ointment group had lower scar assessment scores (i.e., closer to normal skin) compared with the petrolatum group with regard to color, stiffness, thickness, and irregularity. The oregano ointment group presented statistically significant improvement in color compared with the petrolatum group on day 12 ( |
| [ | 2011 | Clinical trial | 120 |
| Rosmarinho | Controls and cases received povidone-iodine and essential lavender oil, respectively. A sitz bath using 5–7 drops of essential lavender oil in 4 l of water, twice daily for 10 days, was used in the case group. The control group received routine postnatal care using povidone-iodine. | A total of 25 subjects in the lavender group and 17 in the control group reported no pain at all, with no significant differences between groups. Thirty-one subjects (51.7%) in the lavender group and 13 subjects (21.7%) in the control group had no redness ( |
| [ | 2015 | Clinical trial | 16 |
| Astragalus | An NF3 powder that contained extract granules was formulated into sachets, and the subjects were instructed to take two sachets daily (5 g/sachet) for 6 months. | At the end of study, the wound areas decreased in six patients after NF3 treatment compared with only one patient in the placebo group. The mean wound area decreased by 47.8% and 14.1% in the NF3 and placebo groups, respectively ( |
|
| Rehmannia | ||||||
| [ | 2012 | Clinical trial | 34 |
| Bustamenta | The experimental group received treatment with a standardized (0.76% encecalin) | Ulcer size diminution was significantly higher ( |
| [ | 2016 | Clinical trial | 57 |
| Calêndula | Chronic venous leg ulcers were cleaned twice daily with 25 ml of sterile physiological saline solution immediately before applying an extract of | At the end of the 30-week study, 73.7% of the patients who were treated with the extract achieved complete epithelialization, with an average healing time of 13.3 ± 5.9 weeks. The proportion of completely healed patients in the control group was 31.6%, with an average healing time of 22.1 ± 5.9 weeks. The mean wound contraction in patients who were treated with the extract was 42.7 mm2/week, which was significantly greater ( |