The future of oral and maxillofacial surgery - retired viewpoint.

A reasoned argument as to why the status quo for oral and maxillofacial surgery training is not sustainable and an alternative is suggested. It is argued that the current financial burden, future pension provision and unacceptable work/life balance must be addressed immediately to ensure uptake of training posts for preservation of the specialty.

Oral health perceptions and client satisfaction among homeless adults attending a community-centred dental clinic.

Background: The homeless face significant barriers accessing dental care. Community-centred dental clinics might provide more accessible care to this group. This descriptive epidemiological study aimed to measure oral health perceptions and client satisfaction among homeless and similarly disadvantaged adults receiving community-centred dental care.

Pharmacokinetics and efficacy of low-dose ketoprofen in postoperative dental pain.

A double-blind, randomised trial was carried out to investigate the relationship between efficacy and various pharmacokinetic variables after single doses of racemic ketoprofen 12.5 and 25mg in patients with postoperative pain after third molar surgery over a 4-hour investigation period. Serial venous blood samples were obtained at 0, 0.

Analgesic efficacy of the cyclooxygenase-inhibiting nitric oxide donor AZD3582 in postoperative dental pain: Comparison with naproxen and rofecoxib in two randomized, double-blind, placebo-controlled studies.

Objective: This study assessed the analgesic efficacy of single doses of 4-(nitrooxy)butyl-(2S)-2-(6-methoxy-2-naphthyl) propanoate (AZD3582) in acute postoperative dental pain after the removal of an impacted mandibular third molar (ie, wisdom tooth).

Methods: Two randomized, placebo-controlled, double-blind studies were performed. In a dose-finding study, 242 patients were randomized to AZD3582 375, 750, 1500, or 2250 mg (n = 41, 37, 42, and 41, respectively); naproxen 500 mg (n = 39); or placebo (n = 42).

An investigation into the comparative efficacy of soluble aspirin and solid paracetamol in postoperative pain after third molar surgery.

Objective: To compare the efficacy of soluble aspirin 900 mg and paracetamol 1,000 mg in patients with postoperative pain after third molar surgery.

Design: A randomised, placebo controlled, double-blind study.

Setting: Day stay units of Oral and Maxillofacial Surgery at Cardiff Dental Hospital and Hexham General Hospital, Northumberland.