Information for patients and visitors
Nephrotic Syndrome
Children’s Services Women & Children’s Services
This leaflet has been designed to give you important information about your condition / procedure, and to answer some common queries that you may have.
Information for patients and visitors Introduction The aim of this leaflet is to provide you as carers or parents all the relevant information regarding Nephrotic Syndrome and answer some of the common concerns and queries.
What is Nephrotic Syndrome? Most people have two kidneys situated at the back of the abdomen. These act like a ‘filter’ by removing waste products and excess water from the blood to make urine. At the same time they prevent the loss of protein from the blood. Protein is essential to the body as it helps to balance the amount of water in the blood. Nephrotic Syndrome is a collection of symptoms which occur when the kidneys ‘filter’ does not work properly and allows large amounts of protein to be lost from the body in the urine. This is known as proteinuria.
How does this affect normal body function? Proteinuria results in an overload of fluid in the blood. This fluid can leak into the body tissue causing swelling or oedema. Oedema (swelling) is usually more noticeable in the legs but can occur all over, including around the stomach and may cause vomiting and diarrhoea.
Why does Nephrotic Syndrome occur? Although research continues, Nephrotic Syndrome is not common and the main causes are unknown. However, some rare causes may include kidney growths or the use of certain drugs
and therefore resolving these problems may improve the symptoms. It is suggested that Nephrotic Syndrome affects twice as many boys as girls and usually first occurs between the ages of 2-5 years.
How is Nephrotic Syndrome diagnosed? The condition is diagnosed by testing the blood and urine to determine the levels of protein. In rare cases or if there is a family history of nephrotic syndrome, a renal biopsy may be required (taking a small piece of kidney for examination).
Treatment Treatment usually involves the use of steroids. Steroids are a type of medication that may be used to reduce swelling in the body and help stop the loss of protein. Diuretics (water tablets) may also be used to treat symptoms of Nephrotic Syndrome. These are a type of medication used to help the body get rid of excess water. A type of protein may be given via a drip to replace the protein which has been lost in the urine. Diet is an important aspect of treatment and your child may be referred to a dietitian for information, advice and support.
Information for patients and visitors Benefits
Alternatives
Treatment aims to reduce the symptoms of Nephrotic Syndrome. Presently, there is no cure and children may have multiple episodes or relapses. However relapses may become less frequent and virtually all children will eventually grow out of the syndrome.
Steroid therapy remains the main treatment for Nephrotic Syndrome but where some children do not respond to this, other drugs are available.
Steroid treatment aims to reduce the swelling within 2 days to 4 weeks. The dose of steroids is usually given over a period of about 12 weeks in total and is gradually reduced before stopping.
What happens if the syndrome is left untreated?
Your child will be weighed regularly during treatment to measure how much of the excess fluid they have lost. An antibiotic may be prescribed to help fight infection that may occur as a result of swelling in the body. There may also be an increased risk of an infection due to low levels of protein in the body as protein is particularly important to the body’s immune system. Increasing protein content in the diet may help to replace protein lost in the urine. A no salt diet during a relapse is advised. Reducing or avoiding salt in the long term is also important to promote healthy kidneys as well as your family’s general health. It should be noted that many processed foods may have a high salt content.
Risks & Side Effects Side effects that may occur include increased appetite (which may lead to weight gain), swollen cheeks (sometimes termed ‘moonface’) and some behavioral changes such as aggressiveness.
These are usually considered for children who have needed a renal biopsy.
Without treatment kidney failure may occur. Infection may also occur as the result of swelling in the body.
Can my child lead a normal life? Yes. There is no need to restrict activity. However the condition does require careful monitoring and you will be asked to check your child’s urine on a daily basis using a simple dipstick test to determine the level of protein. You may be asked to record the levels. When taking steroid treatment your child should carry a steroid card which will provide essential information should your child become ill. It is advised that childhood immunisations should still be given but some may need rescheduling following any treatment for nephrotic syndrome.
Reference Section NLAG Guideline for the Treatment of Childhood Nephrotic Syndrome, Children’s Services May 2012.
Information for patients and visitors Contact Details for Further Information
and planning the NHS, training and educating staff, research etc.).
Family support is very valuable and relatives / family friends / carers will need to know which foods your child may have. Regular medical checkups will provide the opportunity to discuss any problems.
Everyone working for the NHS has a legal duty to keep information about you confidential. Information will only ever be shared with people who have a genuine need for it (e.g. your GP or other professionals from whom you have been receiving care) or if the law requires it, for example, to notify a birth.
Support can also be accessed from: The British Kidney Patient Association 3 The Windmills St Mary’s Close Turk Street Alton GU34 1EF Tele: 01420 541424 www.britishkidney-pa.co.uk
Concerns and Queries If you have any concerns / queries about any of the services offered by the Trust, in the first instance, please speak to the person providing your care. For Diana, Princess of Wales Hospital Alternatively you can contact the Patient Advice and Liaison Service (PALS) on (01472) 875403 or at the PALS office which is situated near the main entrance. For Scunthorpe General Hospital Alternatively you can contact the Patient Advice and Liaison Service (PALS) on (01724) 290132 or at the PALS office which situated on C Floor. Alternatively you can email:
[email protected]
Please be assured however that anyone who receives information from us is also under a legal duty to keep it confidential.
Zero Tolerance - Violent, Threatening and Abusive Behaviour The Trust and its staff are committed to providing high quality care to patients within the department. However, we wish to advise all patients / visitors that the following inappropriate behaviour will not be tolerated:
Swearing
Threatening / abusive behaviour
Verbal / physical abuse
The Trust reserves the right to withdraw from treating patients whom are threatening / abusive / violent and ensuring the removal of those persons from the premises. All acts of criminal violence and aggression will be notified to the Police immediately.
Risk Management Strategy
Confidentiality
The Trust welcomes comments and suggestions from patients and visitors that could help to reduce risk.
Information on NHS patients is collected in a variety of ways and for a variety of reasons (e.g. providing care and treatment, managing
Perhaps you have experienced something whilst in hospital, whilst attending as an outpatient or as a visitor and you felt at risk.
Information for patients and visitors Please tell a member of staff on the ward or in the department you are attending / visiting.
Moving & Handling The Trust operates a Minimal Lifting Policy, which in essence means patients are only ever lifted by nursing staff in an emergency situation. Patients are always encouraged to help themselves as much as possible when mobilising, and if unable to do so, equipment may be used to assist in their safe transfer. If you have any questions regarding moving and handling of patients within the Trust, please speak to a member of staff in the ward or department you are visiting. Northern Lincolnshire and Goole NHS Foundation Trust Diana Princess of Wales Hospital Scartho Road Grimsby 01472 874111 Scunthorpe General Hospital Cliff Gardens Scunthorpe 01724 282282 Goole & District Hospital Woodland Avenue Goole 01405 720720 www.nlg.nhs.uk Date of issue: November, 2015 Review Period: November, 2018 Author: Neurology/Diagnostic Unit IFP-418 v2.1 © NLGFT 2015
