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Dive into the research topics where Andrew Woodhouse is active.

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Featured researches published by Andrew Woodhouse.


Clinical Endocrinology | 2007

Bone mineral density remains stable in HAART‐treated HIV‐infected men over 2 years

Mark J Bolland; Andrew Grey; Anne Horne; Simon Briggs; Mark G. Thomas; Ellis-Pegler Rb; Andrew Woodhouse; Greg Gamble; Ian R. Reid

Objective  Recently we reported that human immunodeficiency virus (HIV)‐infected Caucasian men treated with highly active antiretroviral therapy (HAART) have normal weight‐adjusted bone mineral density (BMD), in contrast to most other cross‐sectional analyses, which have reported low BMD in HIV‐infected patients. We have now addressed the question of whether there is accelerated BMD loss over time in HIV‐infected men.


Clinical Endocrinology | 2006

Bone mineral density is not reduced in HIV‐infected Caucasian men treated with highly active antiretroviral therapy

Mark J Bolland; Andrew Grey; Anne Horne; Simon Briggs; Mark G. Thomas; Ellis-Pegler Rb; Andrew Woodhouse; Greg Gamble; Ian R. Reid

Objective   Recent studies have reported low bone mineral density (BMD) in patients infected with human immunodeficiency virus (HIV). Frequently these findings have been attributed to treatment with highly active antiretroviral therapy (HAART). We sought to determine whether BMD in HIV‐infected men treated with HAART for at least 3 months is different from that in healthy controls, and, if so, what HIV‐related factors might explain this finding.


Clinical Infectious Diseases | 2003

Three Days of Intravenous Benzyl Penicillin Treatment of Meningococcal Disease in Adults

Ellis-Pegler Rb; Lesley Galler; Sally Roberts; Mark G. Thomas; Andrew Woodhouse

New Zealand has experienced an epidemic of predominantly serogroup B meningococcal disease during the past decade. In a prospective study, we treated adults (age, >15 years) with meningococcal disease with intravenous benzyl penicillin (12 MU [7.2 g] per day) for 3 days. Sixty-one adults with suspected meningococcal disease were consecutively admitted during the 33-month period; 3 patients were excluded. The 58 patients had a mean age (+/- standard deviation [SD]) of 27.9+/-14.5 years (median, 21 years; range, 15-70 years). Forty-four patients had confirmed and 14 patients had probable meningococcal disease. Fifty-seven patients received 12 MU (7.2 g) and 1 received 8 MU (4.8 g) of benzyl penicillin per day. Thirteen patients received additional antibiotics within the first 24 h because of diagnostic uncertainties. Patients received a mean (+/-SD) of 3.0+/-0.5 days of treatment. No patients relapsed. Five patients died. All but 1 death occurred during benzyl penicillin treatment, and the only posttreatment death was not due to meningococcal disease. Three days of intravenous benzyl penicillin is sufficient treatment for adults with meningococcal disease. The usual recommendations for duration of treatment are excessive.


Scandinavian Journal of Infectious Diseases | 2009

Good outcome with trimethoprim 10 mg/kg/day-sulfamethoxazole 50 mg/kg/day for Pneumocystis jirovecii pneumonia in HIV infected patients

Mark G. Thomas; Priscilla Rupali; Andrew Woodhouse; Ellis-Pegler Rb

Pneumocystis jirovecii pneumonia (PCP) in human immunodeficiency virus (HIV)-infected patients is usually treated with trimethoprim (TMP)–sulfamethoxazole (SMX) 1920 mg 3 times daily (approximately equivalent to TMP 15 mg/kg/day–SMX 75 mg/kg/day) for 21 days. Pharmacokinetic data suggest that lower doses would be equally efficacious and might be associated with a lower incidence of adverse effects. We conducted a retrospective review of case notes for the first episode of laboratory-confirmed PCP in HIV-infected patients treated at Auckland City Hospital, from January 1991 through December 2007. Seventy-three of 84 (87%) patients were treated with TMP–SMX 960 mg 4 times daily or 3 times daily (approximately TMP 10 mg/kg/day–SMX 50 mg/kg/day). The overall mortality was 5/73 (7%). The mortality in patients with severe disease (transcutaneous oxygen saturation on admission ≤84%) was 3/16 (19%) and in patients admitted to the intensive care unit was 5/9 (56%). Fifteen of 73 (21%) patients required a change to an alternative treatment regimen because of adverse effects (rash in 10, rash plus fever in 3, neutropenia in 1, fever plus headache in 1). Treatment of PCP in adult HIV-infected patients with TMP–SMX 960 mg QID or TID appears to have comparable efficacy to treatment with higher doses and to be associated with a lower rate of treatment limiting adverse effects.


Journal of Clinical Microbiology | 2005

Involvement of Streptococcal Mitogenic Exotoxin Z in Streptococcal Toxic Shock Syndrome

Lily Yang; Mark G. Thomas; Andrew Woodhouse; Diana R. Martin; John D. Fraser; Thomas Proft

ABSTRACT We report a nonfatal case of streptococcal toxic shock syndrome (STSS) caused by a Streptococcus pyogenes emm118 strain encoding a novel variant of streptococcal mitogenic exotoxin Z (SMEZ-34). This variant was responsible for the major mitogenic activity in the cell culture supernatant. Patient sera showed seroconversion toward SMEZ, implying a role for this toxin in STSS.


Internal Medicine Journal | 2004

Short course intravenous benzylpenicillin treatment of adults with meningococcal disease

Simon Briggs; Ellis-Pegler Rb; Sally Roberts; Mark G. Thomas; Andrew Woodhouse

Abstract


Journal of Clinical Microbiology | 2009

Evolution of Central Nervous System Multidrug-Resistant Mycobacterium tuberculosis and Late Relapse of Cryptic Prosthetic Hip Joint Tuberculosis: Complications during Treatment of Disseminated Isoniazid-Resistant Tuberculosis in an Immunocompromised Host

Arlo Upton; Andrew Woodhouse; Vaughan R; Sandie Newton; Ellis-Pegler Rb

ABSTRACT We report a case of disseminated isoniazid-resistant tuberculosis in an immunocompromised patient with evolution of rifampin (rifampicin) resistance in the central nervous system. This was cured with intraventricular and oral treatment but was followed by a late relapse of the original infection in a prosthetic hip joint. We provide drug levels in cerebrospinal fluid and serum.


Internal Medicine Journal | 2007

Good outcome in HIV‐infected refugees after resettlement in New Zealand: population study

S. M. Nisbet; A. M. Reeve; Ellis-Pegler Rb; Andrew Woodhouse; R. J. H. Ingram; Sally Roberts; Susan McAllister; Mark G. Thomas

Background: The aims of this study were to determine the clinical characteristics on arrival and the subsequent clinical outcome of HIV‐infected UN quota refugees who settled in New Zealand during the last 11 years and to estimate their rate of HIV transmission.


The Journal of Clinical Endocrinology and Metabolism | 2007

Annual Zoledronate Increases Bone Density in Highly Active Antiretroviral Therapy-Treated Human Immunodeficiency Virus-Infected Men: A Randomized Controlled Trial

Mark J Bolland; Andrew Grey; Anne Horne; Simon Briggs; Mark G. Thomas; Ellis-Pegler Rb; Andrew Woodhouse; Greg Gamble; Ian R. Reid


Australian and New Zealand Journal of Medicine | 1995

Cytomegalovirus appendicitis in a patient with acquired immune deficiency syndrome (AIDS)

Andrew Woodhouse; Mark G. Thomas

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Mark G. Thomas

University College London

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Andrew Grey

University of Auckland

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Anne Horne

University of Auckland

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Greg Gamble

University of Auckland

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Ian R. Reid

University of Auckland

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