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1.
Ann R Coll Surg Engl ; 89(4): 349-53, 2007 May.
Article in English | MEDLINE | ID: mdl-17535609

ABSTRACT

INTRODUCTION: Testicular prostheses produced from various materials have been in use since 1941. The absence of a testicle has been shown to be a psychologically traumatic experience for males of all ages. The indications for insertion of a prosthesis include absence or following orchidectomy from a number of causes such as malignancy, torsion and orchitis. The most common substance used around the world in the manufacture of these implants is silicone; however, in the US, this material is currently banned because of theoretical health risks. This has led to the development of saline-filled prostheses as an alternative. PATIENTS AND METHODS: A Medline search was carried out on all articles on testicular prosthesis between 1966 and 2006. CONCLUSIONS: This review highlights the controversies regarding prosthetic materials, the complications of insertion and the potential benefits of this commonly performed procedure.


Subject(s)
Prostheses and Implants/standards , Prosthesis Implantation/methods , Testis/surgery , Counseling , Forecasting , Genital Diseases, Male/surgery , Humans , Intraoperative Care/methods , Male , Prostheses and Implants/trends , Prosthesis Design , Prosthesis Implantation/trends , Testis/abnormalities , Time Factors
2.
Br J Neurosurg ; 20(6): 403-6, 2006 Dec.
Article in English | MEDLINE | ID: mdl-17439093

ABSTRACT

Phenytoin is often used to prevent postcraniotomy seizures, but is not always effective. We investigate changes in plasma phenytoin level ([phenytoin]) following craniotomy. The [phenytoin] in 28 patients who were receiving phenytoin (oral/ intravenous) and undergoing a craniotomy were prospectively measured 24 h preoperatively, immediately pre- and postcraniotomy, 24 and 48 h postoperatively. Factors examined included patients' age, sex, pathology, preoperative [phenytoin], operative duration and blood loss. Fifteen patients had [phenytoin] concentrations outside the therapeutic range. Twenty-five patients experienced a decrease in [phenytoin] immediately postcraniotomy: pre-, post- and 24 h postcraniotomy mean [phenytoin] were 13.4, 10.0 and 12.9 mg/l, respectively. Preoperative [phenytoin], operative duration and blood loss had significant correlation with the decrease in [phenytoin] (p < 0.05). In conclusion, < 50% of the patients had therapeutic preoperative [phenytoin]. In most patients, [phenytoin] decreases by 26% after craniotomy and returns to preoperative level within 24 h. These may contribute to early postoperative seizure development.


Subject(s)
Anticonvulsants/therapeutic use , Craniotomy , Phenytoin/therapeutic use , Seizures/prevention & control , Adult , Aged , Anticonvulsants/blood , Female , Humans , Infusions, Intravenous , Male , Middle Aged , Perioperative Care , Phenytoin/blood , Prospective Studies
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