Efficacy and safety of treatment with the use of intraurethral alprostadil (Vitaros©) on demand in men with Spinal Cord Injury and Multiple Sclerosis. A prospective study.

Thomas C1, Kartsaklis P2, Konstantinidis C3

Research Type

Clinical

Abstract Category

Male Sexual Dysfunction

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Abstract 315
Transgender Health, Male Sexual Dysfunction, Urethra
Scientific Podium Short Oral Session 38
Friday 29th September 2023
16:45 - 16:52
Room 101
Male Multiple Sclerosis Sexual Dysfunction Spinal Cord Injury
1. General Hospital of Corinth, Greece,Urology Dept., 2. General Hospital of Patras, Greece, Urology Dept., 3. National Rehabilitation Center, Athens, Greece, Neurourology Dept.
Presenter
C

Charalampos Thomas

Links

Abstract

Hypothesis / aims of study
Till now the first line treatment of neurogenic erectile dysfunction is the use of PDE5 inhibitors. Our aim was to evaluate the efficacy and safety of  intraurethral alprostadil (Vitaros©)  on-demand in men with neurogenic ED due to SCI or MS as a viable alternative.
Study design, materials and methods
We prospectively collected data of 54 men suffering from SCI and 50 from MS who used Vitaros© for ED. The treatment protocol required a minimum administration of intraurethral alprostadil for at least twice a week, even without a subsequent sexual intercourse for a period of 6 weeks. Inclusion criteria included absence of ED prior the accident or the onset of the disease (IIEF-5 score >21, Erection Hardness Score-EHS ≥3, affirmatively answers to Sexual Encounter Profile Questions 2 and 3 -SEP2 & SEP3) and absence of moderate/severe cardiovascular disease, diabetes mellitus and metabolic syndrome. All men with SCI were performing intermittent catheterizations (ICs) and 75% of MS group (35 patients) respectively. Average age was 43.5 and 38.5 respectively, mean IIEF score prior the therapy 15 and 16 and EHS score 1.7 and 1.9.
Results
After 6 weeks, 6 patients dropped out from the group of SCI due to hypotension or urethral pain and 3 from MS group due to urethral pain. Vitaros© implied an improvement of 4.4 points for the IIEF-5 score and 1.1 for the EHS score in the SCI group, while the improvement for the MS group was 4.1 points and 1.3 points respectively. The subgroup of MS patients who did not perform ICs seems to have benefited the most in comparison with the other patients and none of them discontinued the treatment. At the end of the study, 23 SCI patients, and 27 MS patients selected Vitaros© to be added in their treatment agents of choice, as an alternative.
Interpretation of results
It seems that Vitaros© is an alternative treatment for neurogenic patients suffering from SCI and MS, less effective though in ICs users, and the most apparent reason of failure might be the alteration of urethral epithelium to squamous one, due to repetitive injuries as catheters pass through, making the agent less absorbable through it.
Concluding message
It seems that Vitaros© is an alternative treatment for neurogenic patients suffering from SCI and MS, less effective though in ICs users, and the most apparent reason of failure might be the alteration of urethral epithelium to squamous due to repetitive injuries as catheters pass through, making the agent less absorbable through it.
Figure 1
References
  1. Bodner DR, Haas CA, Krueger B, Seftel AD. Intraurethral alprostadil for treatment of erectile dysfunction in patients with spinal cord injury. Urology. 1999 Jan;53(1):199-202. doi: 10.1016/s0090-4295(98)00435-x. PMID: 9886612.
  2. Biering-Sørensen F, Sønksen J. Sexual function in spinal cord lesioned men. Spinal Cord. 2001 Sep;39(9):455-70. doi: 10.1038/sj.sc.3101198. PMID: 11571657.
  3. Thomas C, Konstantinidis C. Neurogenic Erectile Dysfunction. Where Do We Stand? Medicines (Basel). 2021 Jan 7;8(1):3. doi: 10.3390/medicines8010003. PMID: 33430218; PMCID: PMC7825654
Disclosures
Funding NONE Clinical Trial Yes Public Registry No RCT No Subjects Human Ethics not Req'd The proposed therapy is already approved by the European Urology Association, therefore it isn't under investigation Helsinki Yes Informed Consent Yes
Citation

Continence 7S1 (2023) 101032
DOI: 10.1016/j.cont.2023.101032

19/06/2024 23:27:34