- Information for physicians
- Titan OTR
- Testicular Implants
- Quallich SA, Ohl DA, Dunn RL. Evaluation of three penile prosthesis pump designs in a blinded survey of practitioners. Urologic Nurs. April 2008;28:101-108.
- Pescatori ES, Goldstein I. Intraluminal device pressures in 3-piece inflatable penile prostheses: the “pathophysiology” of mechanical malfunction. J Urol. February 1993;149(2):295-300.
- Data on file.
- Sadeghi-Nejad H. Penile prosthesis surgery: A review of prosthetic devices and associated complications. J Sex Med. 2007; Vol. 4: 296-309
- Wilson SK, Henry GD, Delk JR Jr, Cleves, MA. The Mentor Alpha I penile prosthesis with reservoir lock-out valve: effective prevention of auto-inﬂation with improved capability for ectopic reservoir placement. J Urol. improved capability for ectopic reservoir placement.
- John TT, Fairfax M, Dhabuwala C. Inﬂatable penile prosthesis components – an in vitro comparative study of antibacterial activity. Poster presentation at Sexual Medicine Society Conference. December 2007.
- Wolter CE, Hellstrom WJG. The hydrophilic-coated inflatable penile prosthesis: 1-year experience. J Sex Med. September 2004;1(2):221-224.
- Brinkman MJ, Henry GD, Wilson SK, et al. A survey of patients with inﬂatable penile prostheses for satisfaction. J Urol. July 2005;174(1):253-257.
Indications for use
The Titan Inﬂatable Penile Prosthesis is indicated for male patients suffering from erectile dysfunction (impotence) who are considered to be candidates for implantation of a penile prosthesis.
The Titan and Titan OTR Inﬂatable Penile Prosthesis is contraindicated in patients who have one or more of the following conditions:
- Patients with an active infection present anywhere in the body, especially urinary tract or genital infection.
- Patients with unresolved problems affecting urination, such as an elevated residual urine volume secondary to bladder outlet obstruction or neurogenic bladder.
- Patients unwilling to undergo any further surgery for device revision.
- Implantation of the device may make latent natural erections, as well as other interventional treatment options, impossible.
- Men with diabetes or spinal cord injuries, as well as immuno-compromised patients, may have an increased risk of infection associated with a prosthesis.
- Failure to evaluate and promptly treat erosion may result in a substantial worsening of the condition, leading to infection and loss of tissue.
- Implantation of a penile prosthesis may result in penile shortening, curvature or scarring.
- Pre-existing abdominal or penile scarring or contracture may make surgical implantation more complicated or impractical.
- This device contains solid silicone elastomer.
- Reuse of this single use product may create potential risk to user.
- Products containing iodine should be carefully rinsed to remove residual solutions from the prostheses and the implant site.
For additional information on indications, contraindications, warnings and precautions, please contact your Coloplast representative or call 1-800-533-0464.