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Key findings in the CQC Report: Staff were not following national regulation and guidance in relation to fire safety.
How long will my brother or sister stay in NNU?
If you are already in a bed on the ward, it may be necessary for you to move and be cared for in a bed in the corridor for a temporary period.
SLE Completed CQUIN in AKI and Home Dialysis successfully leading to publications and presentations in regional and national QI meetings Research: Principal
Consultant in Palliative Medicine
This resulted in 37 oncology patients of varying primary tumours and demographics.
In rare cases damage to the nerve can be permanent.
popularity in the UK.
Poster Download Background Offering patients the opportunity to participate in clinical trials is a priority in both the NHS 10 Year Plan and GHNHSFT
These wards would be linked to the main hospital wards in the Tower Block.
The Liver Specialist Team plays a vital role in the NHS, delivering comprehensive care to patients with liver diseases, and providing medical and emotional
the room you gave birth in until you’re ready to leave.
Minor change in confidence following equipment changes.
Chemical Pathology Notes Galactosaemia is an inherited metabolic disease caused by defects in galactose metabolism.
Ensure material is on labelled side of slide. 1g Rinse any residual material left in the syringe into the sample vial as in stage 2b below.
Department of Immunology Notes Skeletal muscle antibodies can be seen in patients with myasthenia gravis, particularly in those with thymoma.
Click on the guideline below for alternatives in non-stroke indications:
Our Respiratory medicine team specialise in the treatment of problems in regards to the the upper airway, the lungs, the chest wall and the ventilatory
Miss Coyle added: “Over the pandemic in certain specialities such as orthopaedics in particular we had to stop a lot of our operating.
The assay of primary hyperoxaluria (PH) metabolites may be indicated in cases of unexplained hyperoxaluria to help in identification of those in whom genetic
