Tomaz Garcez
Central Manchester University Hospitals NHS Foundation Trust
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Publication
Featured researches published by Tomaz Garcez.
Clinical & Experimental Allergy | 2017
William Egner; T. M. Cook; Nigel Harper; Tomaz Garcez; Susana Marinho; Kl Kong; Shuaib Nasser; Mark G. Thomas; Amena Warner; John Hitchman; Katharina Floss
Guidelines for investigation of perioperative drug allergy exist, but the quality of services is unknown. Specialist perioperative anaphylaxis services were surveyed through the Royal College of Anaesthetists 6th National Audit Project.
Case Reports | 2016
Nicholas P. Jones; Tomaz Garcez; William G. Newman; David W. Denning
A 25-year-old woman presented with unilateral red eye and visual blur, and was found to have panuveitis with an inflammatory white mass at the macula, initially presumed to be Toxoplasma retinitis. After failure to respond, she underwent vitrectomy, which produced Candida albicans. Despite intraocular and systemic antifungal treatment, she lost all vision in that eye. Two years later, she developed unilateral hip osteomyelitis leading to total hip replacement and also revealing Candida infection. By clinical exome sequencing, she was then found to have caspase recruitment domain 9 (CARD9) deficiency, an autosomal recessive disorder that causes a specific susceptibility to candidal infections. She remains otherwise well but on lifelong fluconazole prophylaxis.
Clinical and Experimental Immunology | 2017
William Egner; Matthew Helbert; Ravishankar Sargur; Kirsty Swallow; Nigel Harper; Tomaz Garcez; Sinisa Savic; Louise Savic; E. Eren
We describe an observational survey of diagnostic pathways in 104 patients attending four specialist allergy clinics in the United Kingdom following perioperative hypersensitivity reactions to chlorhexidine reactions. The majority were life‐threatening. Men undergoing urological or cardiothoracic surgery predominated. Skin prick testing and specific immunoglobulin (sIg)E testing were the most common tests used for diagnosis. Fifty‐three per cent of diagnoses were made on the basis of a single positive test. Where multiple tests were performed the sensitivity of intradermal, basophil activation and skin prick testing was 68% (50–86%), 50% (10–90%) and 35% (17–55%), respectively. Seven per cent were negative on screening tests initially, and 12 cases were only positive for a single test despite multiple testing. Intradermal tests appeared most sensitive in this context. Additional sensitization to other substances used perioperatively, particularly neuromuscular blocking agents (NMBA), was found in 28 patients, emphasizing the need to test for possible allergy to all drugs to which the patient was exposed even where chlorhexidine is positive.
Clinical and Experimental Immunology | 2017
William Egner; Matthew Helbert; Ravishankar Sargur; Kirsty Swallow; Nigel Harper; Tomaz Garcez; Sinisa Savic; Louise Savic; Eren Effren
We describe an observational survey of diagnostic pathways in 104 patients attending four specialist allergy clinics in the United Kingdom following perioperative hypersensitivity reactions to chlorhexidine reactions. The majority were life‐threatening. Men undergoing urological or cardiothoracic surgery predominated. Skin prick testing and specific immunoglobulin (sIg)E testing were the most common tests used for diagnosis. Fifty‐three per cent of diagnoses were made on the basis of a single positive test. Where multiple tests were performed the sensitivity of intradermal, basophil activation and skin prick testing was 68% (50–86%), 50% (10–90%) and 35% (17–55%), respectively. Seven per cent were negative on screening tests initially, and 12 cases were only positive for a single test despite multiple testing. Intradermal tests appeared most sensitive in this context. Additional sensitization to other substances used perioperatively, particularly neuromuscular blocking agents (NMBA), was found in 28 patients, emphasizing the need to test for possible allergy to all drugs to which the patient was exposed even where chlorhexidine is positive.
Clinical and Experimental Immunology | 2018
Ben Shillitoe; Catherine Bangs; David Guzman; Andrew R. Gennery; Hj Longhurst; Mary Slatter; David Edgar; Moira Thomas; Austen Worth; Aarnoud Huissoon; Peter D. Arkwright; Stephen Jolles; Helen Bourne; Hana Alachkar; Sinisa Savic; Dinakantha Kumararatne; S Patel; Helen Baxendale; S. Noorani; Patrick Fk Yong; Catherine Waruiru; V. Pavaladurai; Peter Kelleher; Richard Herriot; Jolanta Bernatonienne; Malini V Bhole; C Steele; Grant Hayman; A. Richter; Mark Gompels
This is the second report of the United Kingdom Primary Immunodeficiency (UKPID) registry. The registry will be a decade old in 2018 and, as of August 2017, had recruited 4758 patients encompassing 97% of immunology centres within the United Kingdom. This represents a doubling of recruitment into the registry since we reported on 2229 patients included in our first report of 2013. Minimum PID prevalence in the United Kingdom is currently 5·90/100 000 and an average incidence of PID between 1980 and 2000 of 7·6 cases per 100 000 UK live births. Data are presented on the frequency of diseases recorded, disease prevalence, diagnostic delay and treatment modality, including haematopoietic stem cell transplantation (HSCT) and gene therapy. The registry provides valuable information to clinicians, researchers, service commissioners and industry alike on PID within the United Kingdom, which may not otherwise be available without the existence of a well‐established registry.
Clinical Medicine | 2018
Ben Shillitoe; Rob Hollingsworth; Mark Foster; Tomaz Garcez; David Guzman; J. David M. Edgar; Matthew Buckland
ABSTRACT Supply of immunoglobulin in the UK faces pressures due to increasing demand, cost and variable supply. This paper describes immunoglobulin replacement therapy (IGRT) in primary immunodeficiency (PID) and secondary immunodeficiency (SID) to assist in the ongoing planning of UK immunoglobulin provision. A retrospective analysis of the National Immunoglobulin Database and the UKPID registry was carried out. In total, 3,222 patients are registered as receiving IGRT for immunodeficiencies. Predominately antibody disorders made up the largest diagnostic category (61% of patients). The total cost of IGRT for immunodeficiency for 2015/16 was £40,673,350; an average annual cost of £1,099,254 per centre and £12,124 per PID patient. SCIg accounted for 43.8% and 50.1% of IGRT, with home therapy accounting for 42.7% and 57.5% of place of therapy in the National Immunoglobulin Database and UKPID registry respectively. In 2015/16 use of immunoglobulin in SID increased by 24% over the previous financial year. The overall trends of increasing demand in immunology are mirrored in other specialties, most notably neurology and haematology. These data are the first national overview of IGRT for immunodeficiencies, providing a valuable resource for clinicians and policy makers in the ongoing management of UK immunoglobulin supply.
/data/revues/00916749/unassign/S0091674914015164/ | 2014
Paul J. Turner; M. Hazel Gowland; Vibha Sharma; Despo Ierodiakonou; Nigel Harper; Tomaz Garcez; Richard Pumphrey; R. J. Boyle
BJA: British Journal of Anaesthesia | 2015
Louise Savic; Tomaz Garcez; P.M. Hopkins; Nigel Harper; Sinisa Savic
The Journal of Allergy and Clinical Immunology | 2014
Paul J. Turner; Vibha Sharma; Mimi L.K. Tang; M. Hazel Gowland; Nigel Harper; Tomaz Garcez; Richard Pumphrey; Robert J. Boyle
BJA: British Journal of Anaesthesia | 2013
Vibha Sharma; Nigel Harper; Tomaz Garcez; Peter D. Arkwright
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Central Manchester University Hospitals NHS Foundation Trust
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