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The children's FGM service is a dedicated monthly multidisciplinary clinic for girls under 18 years old who have had, are suspected to have had, or who may be at risk of having, FGM.
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This information is for patients receiving steroids for immunotherapy toxicity.
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This page is for patients receiving steroids for immunotherapy toxicity.
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Researchers at UCLH and UCL have completed the first and only randomised trial to explore a new approach to treating aggressive lung cancer.
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This booklet tells you about having a Vortex® Port-a-cath Insertion (implantable port) with the Interventional Radiology team.
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A number of tests are carried out by the routine haemostasis/haematology laboratories. These include full blood count, ESR, sickle cell and glandular fever screening, malaria antigen testing, blood films and acanthocytes, coagulation screens (INR/heparin monitoring), fibrinogen and D-dimers (DIC screening).
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UCLH is to lead an initiative to improve care for myeloma patients alongside Oxford University Hospitals NHS Foundation Trust (OUH) and University Hospital Southampton NHS Foundation Trust (UHS).
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Introduction This patient information leaflet is for patients who are doing a breath test at home. Please read it carefully before you start your test. Please complete your test within the next two…
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Introduction This patient information page is for patients who are doing a breath test at home. Please read it carefully before you start your test. Please complete your test within the next two…
File results
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FOI/2021/0643 - Bank and agency staffing vacancy rates and spending
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FOI/2021/0644 - Clinical guidelines on identification and management of maternity issues
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FOI/2021/0645 - Software suppliers for various applications
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FOI/2021/0649 - Physiotherapists/ occupational therapists staffing levels
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FOI/2021/0650 - Cyber Essentials Accreditation/ Certification
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FOI/2021/0657 - Patient list for Neuropsychiatry
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FOI/2021/0653 - Patient Quality Safety Committee in July 2021
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FOI/2021/0672 - Long Covid statistics
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FOI/2021/0691 - MHPS investigations
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FOI/2021/0700 - Treatment of rare diseases