| Literature DB >> 24605180 |
C Schulte-Uebbing1, S Schlett1, Id Craiut1, L Antal1, H Olah1.
Abstract
In a small praxis/ambulance study we evaluated data of 200 women with chronical recurrent cervical infections and with a cervix dysplasia (CIN 1, CIN 2). who got after the primary therapy a treatment with vitamin D vaginal suppositories (12.500 IU, 3 nights a week, for 6 weeks). We found that - when compared with the lactobacillus vaginal suppositories - the high dose vitamin D vaginal treatment might be more effective. Vitamin D showed very good anti-inflammatory effects. In the survey after six weeks therapy 79% of the women had "less vaginal problems," "less discharge" and "less problems with the sexual intercourse." Objectively after six weeks therapy only 7% of the patients still had bacterial and/or fungal vaginal infections that required a treatment. We found that vitamin D is reabsorbed by the vaginal mucosa, but the reabsorption may be individually very different. In the CIN 1 group we found six weeks after treatment good antidysplastic effects, in the CIN 2 group we often found no or only temporary antidysplastic effects. So this vaginal vitamin D treatment method might be an option for the therapy and prevention of chronical cervical infections and maybe of a cervic dysplasia CIN 1 (good antiinflammatory effects, antidysplastic effects). This small study is not representative. We need much bigger studies with much more dates and with a longer follow up. Caution: At the moment we do not know, if the vaginal vitamin D treatment with 12500 IE is possible in pregnancy. We have no experience. Therefore we recommend an effective contraception during the application.Entities:
Keywords: CIN 1; CIN 2; PAP III D; cervicitis; cervix cancer; cervix dysplasia; cholecalciferol; colpitis; conization; vaginal vitamin D treatment; vitamin D; vitamin D3
Year: 2014 PMID: 24605180 PMCID: PMC3940490 DOI: 10.4161/derm.27791
Source DB: PubMed Journal: Dermatoendocrinol ISSN: 1938-1972

Figure 1. Data of 200 “problem patients” evaluated. Percentage of bacterial and/or fungal infections before the treatment. Patients, suffering from G. vaginalis + E. coli + Coccus (E.coli, Streptococcus, Staphylococcus) 25.5% n = 51. Patients suffering from Streptococcus, Staphylococcus 22% n = 44. Patients suffering from G. vaginalis 8% n = 16. Patients suffering from C. albicans 19.5% n = 39. C. trachomatis (sometimes in combination coccus/candida) 22.5% n = 45. T. vaginalis 2.5% n = 5.