A.R. Mackenzie
Aberdeen Royal Infirmary
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Featured researches published by A.R. Mackenzie.
Journal of Infection | 1999
A.R. Mackenzie; R.B.S. Laing; S.J. Urbaniak; P.J. Molyneaux; J.G. Douglas; C.C. Smith
OBJECTIVE to assess the epidemiology of HIV infection in North-East Scotland. METHODS retrospective casenote review of all HIV-infected patients who have had contact with the Infection Unit in Aberdeen. RESULTS one hundred and forty-two HIV-infected patients were treated between April 1985 and December 1997. The risk behaviour related to the acquisition of the HIV infection was: 56 (39%) homosexually infected, 45 (32%) heterosexually-infected, 34 (24%) injecting drug users (IDUs), and seven (5%) blood products or not known. Sixteen of the 45 (36%) heterosexually-infected patients were native to Africa and 16 of the 34 (31%) IDUs were prisoners in Peterhead prison at the time of referral. Fifty-two (37%) of the cohort continue to attend the Infection Unit, 41 (29%) have relocated, 40 (28%) have died and nine (6%) have been lost to follow-up. The ratio of heterosexual:homosexual men:IDUs changed significantly between the first 7 years (12:21:25) and the second 6 years (33:35:9) of the review, with significantly more patients being infected through heterosexual contact and fewer infected by IDU in the second period-P<0.001. The median AIDS survival was 17 months. Survival was significantly longer in those patients who took anti-retroviral therapy (median = 20 months) than in the patients who opted not to take anti-retroviral therapy (median = 11 months)-P<0.01. CONCLUSIONS Although homosexual contact represents the commonest risk group for HIV infection in this region, the number of heterosexually-infected patients has increased significantly in the last 5 years. Temporary residents account for one-third of the HIV-infected population cared for in NE Scotland. Almost half of those lost to follow-up have returned to Africa or been released from prison. The introduction of anti-retroviral therapy has resulted in a dramatic improvement in AIDS survival in our cohort as it has done elsewhere.
The British Journal of Diabetes & Vascular Disease | 2013
Lukman Hakeem; R.B.S. Laing; Ivan Tonna; John G Douglas; A.R. Mackenzie
Staphylococcus aureus, the most virulent of the many staphylococcal species, has remained a major cause of morbidity and mortality despite the availability of numerous effective anti-staphylococcal antibiotics. S. aureus causes disease through both toxin-mediated and non-toxin-mediated mechanisms. This organism is responsible for both healthcare associated and community-based infections ranging from relatively minor skin and soft tissue infections to severe life threatening systemic infections. Patients with diabetes mellitus are at increased risk of invasive S. aureus infections. This article focuses on the spectrum of invasive S. aureus infections and discusses the clinical features, investigations and management of these infections in patients with diabetes mellitus.
International Journal of Antimicrobial Agents | 1999
R.B.S. Laing; A.R. Mackenzie; Helen Shaw; Ian M. Gould; J. Graham Douglas
A review of patients admitted to medical wards with respiratory infection was undertaken to look for differences in duration of intravenous (IV) therapy and length of patient stay based on the class of IV antimicrobial used in treatment. Data was analysed from 231 patients with community-acquired respiratory infection who were treated empirically for at least 24 h with either an IV cephalosporin (146 patients) or an IV penicillin or macrolide (85 patients). The severity of illness and indication for IV treatment was similar in each group. Those treated with a cephalosporin received IV therapy for a significantly longer period (mean = 4.44 days, SD = 2.6) than those given a penicillin or macrolide (mean = 3.3 days, SD = 1.8): P < 0.001. Patient stay was significantly longer in the cephalosporin group (mean = 11.6 days, SD = 10.4) than the penicillin/macrolide group (mean = 9.4 days, SD = 6.3): P = 0.04. These differences are most readily accounted for by the absence from the hospital formulary of a third generation oral cephalosporin, a drug that might be regarded as an obvious form of follow-on therapy in patients treated empirically with an injectable cephalosporin.
International Journal of Antimicrobial Agents | 2007
R.A. Seaton; Dilip Nathwani; P. Burton; C. McLaughlin; A.R. Mackenzie; S. Dundas; H. Ziglam; Y. Gourlay; K. Beard; E. Douglas
Journal of Infection | 2000
A.M. Cadwgan; W.A. Watson; R.B.S. Laing; A.R. Mackenzie; C.C. Smith; J.G. Douglas
International Journal of Antimicrobial Agents | 2003
A.R. Mackenzie; L. Robertson; B. Jappy; R.B.S. Laing; Ian M. Gould
South African Journal of Diabetes and Vascular Disease | 2014
Lukman Hakeem; R.B.S. Laing; Ivan Tonna; John G Douglas; A.R. Mackenzie
Journal of Infection | 2011
Umar Yousuf; Usman Ali Farooqui; Nargiza Persheyeva; Shi Foo; Claire McGoldrick; R.B.S. Laing; A.R. Mackenzie; Graham Douglas
/data/revues/01634453/v63i6/S0163445311002647/ | 2011
Umar Yousuf; Usman Ali Farooqui; Nargiza Persheyeva; Shi Foo; Claire McGoldrick; R.B.S. Laing; A.R. Mackenzie; Graham Douglas
Archive | 2009
Steven M. Donn; Sunil K. Sinha; Malcolm L. Chiswick; Hamish McKenzie; R.B.S. Laing; A.R. Mackenzie; Pamela Molyneaux; Abhijit M. Bal