Clinical outcomes are broadly agreed, measurable changes in health or quality of life that result from our care. Constant review of our clinical outcomes establishes standards against which to continuously improve all aspects of our practice.
At Great Ormond Street Hospital (GOSH), we have developed a pathway for children and young people having spinal surgery. Spinal surgery is a complex procedure, so we want you to understand the benefits and risks of the operation so you can make an informed decision about whether to go ahead. This page explains what will happen from your child’s initial clinic appointment through to discharge, which clinicians you may meet and what to expect.
When little Freya was born, her mum Sarah - a health professional - was delighted that her daughter appeared perfectly healthy. But at home a few days later, Sarah noticed a mark developing under Freya's chin.
NOTE: We review our guidelines regularly and this guideline is now past its review date. The content of the guideline below may not reflect the most recent evidence-based practice. Please use with caution.
Facilities for worship are provided within the hospital. A multifaith room on level 2 in the Southwood building is also available for prayer. Our patient advocates can provide information about other services and facilities that are available.
The purpose of this guideline is to provide guidance on the care and use of long term Central Venous Access Devices (CVAD) including advice on dealing with any problems encountered. For the purpose of this guideline, devices that are required to remain insitu greater than a month will be considered a long term CVAD.
Note: While this guideline refers to the 'child' throughout, all activities are applicable to young people
At 34 weeks pregnant, Charlotte was told her baby’s heart wasn’t developing properly. Consultants at Great Ormond Street Hospital (GOSH) diagnosed her baby, Joe, with Ebstein’s anomaly, a congenital heart defect affecting the flow of blood to the lungs. Here, Charlotte describes how Joe had emergency surgery twice at GOSH.
This guideline is intended to supplement the resources found in the 'When a Child Dies' (WACD) purple box located in every ward, which gives detailed information on the care of a child after death and, additionally, the ongoing care and attention that the child's family will require (Rationale 1).
Within 15 minutes of the birth of their baby daughter, Isobel, Abigail and Shaun knew that something was wrong. Here, Abigail shares her story of how Isobel was diagnosed with cystic fibrosis and her hopes for the future.