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Dive into the research topics where Kate M. Mitchell is active.

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Featured researches published by Kate M. Mitchell.


The Lancet Global Health | 2014

Health benefits, costs, and cost-effectiveness of earlier eligibility for adult antiretroviral therapy and expanded treatment coverage: a combined analysis of 12 mathematical models.

Jeffrey W. Eaton; Nicolas A. Menzies; John Stover; Valentina Cambiano; Leonid Chindelevitch; Anne Cori; Jan A.C. Hontelez; Salal Humair; Cliff C. Kerr; Daniel J. Klein; Sharmistha Mishra; Kate M. Mitchell; Brooke E. Nichols; Peter Vickerman; Roel Bakker; Till Bärnighausen; Anna Bershteyn; David E. Bloom; Marie-Claude Boily; Stewart T. Chang; Ted Cohen; Peter J. Dodd; Christophe Fraser; Chaitra Gopalappa; Jens D. Lundgren; Natasha K. Martin; Evelinn Mikkelsen; Elisa Mountain; Quang D. Pham; Michael Pickles

BACKGROUND New WHO guidelines recommend initiation of antiretroviral therapy for HIV-positive adults with CD4 counts of 500 cells per μL or less, a higher threshold than was previously recommended. Country decision makers have to decide whether to further expand eligibility for antiretroviral therapy accordingly. We aimed to assess the potential health benefits, costs, and cost-effectiveness of various eligibility criteria for adult antiretroviral therapy and expanded treatment coverage. METHODS We used several independent mathematical models in four settings-South Africa (generalised epidemic, moderate antiretroviral therapy coverage), Zambia (generalised epidemic, high antiretroviral therapy coverage), India (concentrated epidemic, moderate antiretroviral therapy coverage), and Vietnam (concentrated epidemic, low antiretroviral therapy coverage)-to assess the potential health benefits, costs, and cost-effectiveness of various eligibility criteria for adult antiretroviral therapy under scenarios of existing and expanded treatment coverage, with results projected over 20 years. Analyses assessed the extension of eligibility to include individuals with CD4 counts of 500 cells per μL or less, or all HIV-positive adults, compared with the previous (2010) recommendation of initiation with CD4 counts of 350 cells per μL or less. We assessed costs from a health-system perspective, and calculated the incremental cost (in US


Proceedings of the Royal Society of London B: Biological Sciences | 2008

Persistence of the emerging pathogen Batrachochytrium dendrobatidis outside the amphibian host greatly increases the probability of host extinction.

Kate M. Mitchell; Thomas S. Churcher; Trenton W. J. Garner; Matthew C. Fisher

) per disability-adjusted life-year (DALY) averted to compare competing strategies. Strategies were regarded very cost effective if the cost per DALY averted was less than the countrys 2012 per-head gross domestic product (GDP; South Africa:


PLOS Neglected Tropical Diseases | 2011

Schistosoma haematobium treatment in 1-5 year old children: safety and efficacy of the antihelminthic drug praziquantel

Francisca Mutapi; Nadine Rujeni; Claire D. Bourke; Kate M. Mitchell; Laura J. Appleby; Norman Nausch; Nicholas Midzi; Takafira Mduluza

8040; Zambia:


PLOS ONE | 2011

Schistosome infection intensity is inversely related to auto-reactive antibody levels.

Francisca Mutapi; Natsuko Imai; Norman Nausch; Claire D. Bourke; Nadine Rujeni; Kate M. Mitchell; Nicholas Midzi; Mark E. J. Woolhouse; Rick M. Maizels; Takafira Mduluza

1425; India:


AIDS | 2013

Positive impact of a large-scale HIV prevention programme among female sex workers and clients in South India

Marie-Claude Boily; Michael Pickles; Catherine M Lowndes; B M Ramesh; Reynold Washington; Stephen Moses; Kathleen N. Deering; Kate M. Mitchell; Sushena Reza-Paul; James F. Blanchard; Anna Vassall; Michel Alary; Peter Vickerman

1489; Vietnam:


The Journal of Infectious Diseases | 2013

Integrated Analysis of Innate, Th1, Th2, Th17, and Regulatory Cytokines Identifies Changes in Immune Polarisation Following Treatment of Human Schistosomiasis

Claire D. Bourke; Norman Nausch; Nadine Rujeni; Laura J. Appleby; Kate M. Mitchell; Nicholas Midzi; Takafira Mduluza; Francisca Mutapi

1407) and cost effective if the cost per DALY averted was less than three times the per-head GDP. FINDINGS In South Africa, the cost per DALY averted of extending eligibility for antiretroviral therapy to adult patients with CD4 counts of 500 cells per μL or less ranged from


Proceedings of the National Academy of Sciences of the United States of America | 2012

Protective immunity to Schistosoma haematobium infection is primarily an anti-fecundity response stimulated by the death of adult worms

Kate M. Mitchell; Francisca Mutapi; Nicholas J. Savill; Mark E. J. Woolhouse

237 to


AIDS | 2015

Modelling the impact and cost-effectiveness of combination prevention amongst HIV serodiscordant couples in Nigeria.

Kate M. Mitchell; Aurélia Lépine; Fern Terris-Prestholt; Kwasi Torpey; Hadiza Khamofu; Morenike Oluwatoyin Folayan; Jonah Musa; James Anenih; Atiene S. Sagay; Emmanuel Alhassan; John Idoko; Peter Vickerman

1691 per DALY averted compared with 2010 guidelines. In Zambia, expansion of eligibility to adults with a CD4 count threshold of 500 cells per μL ranged from improving health outcomes while reducing costs (ie, dominating the previous guidelines) to


PLOS Computational Biology | 2011

Explaining Observed Infection and Antibody Age-Profiles in Populations with Urogenital Schistosomiasis

Kate M. Mitchell; Francisca Mutapi; Nicholas J. Savill; Mark E. J. Woolhouse

749 per DALY averted. In both countries results were similar for expansion of eligibility to all HIV-positive adults, and when substantially expanded treatment coverage was assumed. Expansion of treatment coverage in the general population was also cost effective. In India, the cost for extending eligibility to all HIV-positive adults ranged from


Parasite Immunology | 2008

The predicted impact of immunosuppression upon population age-intensity profiles for schistosomiasis

Kate M. Mitchell; Francisca Mutapi; Mark E. J. Woolhouse

131 to

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A Foss

University of London

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B M Ramesh

University of Manitoba

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Shajy Isac

University of Manitoba

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