Kidney biopsy

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Information about kidney biopsy

This page is for patients whose doctor has requested you have a kidney (renal) biopsy. We hope the following information will answer some of the questions you may have about this procedure. 

What is a kidney biopsy?

A kidney biopsy is a medical test, where a small sample of tissue is removed from your kidney with a needle. The sample is then sent to the pathology department where it is examined under a microscope.

Why do I need to have a kidney biopsy?

A kidney biopsy helps to assess and diagnose the problem, if any, in your kidney. Kidney biopsies are usually done for one of three reasons.

  1. To find out why a kidney is not functioning properly.
  2. To get a sample of a mass on a kidney.
  3. To assess a kidney before a kidney transplant.

The importance of a kidney biopsy is that it allows for the kidney cells to be assessed by a pathologist to help make a correct diagnosis and plan any necessary treatment.

Are there any alternatives to a kidney biopsy?

There is no other procedure that will give your doctor the same information as a kidney biopsy.

What are the risks associated with kidney biopsies?

A kidney biopsy is usually a safe procedure. Potential complications are uncommon and include:

  • Some people experience pain, which is usually not severe and can be controlled with simple painkillers.
  • Bleeding or bruising around the puncture site which should settle down by itself.
  • There is a small risk of minor internal bleeding after the biopsy. The risk is around 1 in 20 and will usually settle down by itself. The nurse will monitor your blood pressure and pulse during and after the procedure and you will stay in hospital for up to five hours after the procedure so that we can monitor you.
  • Some people pass blood in their urine after a biopsy. This will usually settle on its own within a few days. If you continue to pass blood for more than 1 week or if you pass a lot of blood, then contact the Imaging department to ask for assessment and advice. If you become unwell out of working hours, then attend A&E. The number for the Imaging department can be found on your appointment letter.
  • Occasionally people will have a significant bleed, in which case it may be necessary to do a further procedure to try to stop the bleeding. This will occur in approximately 1 in 50 people.
  • There is a very small risk of death. This risk is less than 1 in 1000.

What happens before the procedure?

You will need to have a blood test a few days before the procedure to check that you are not at increased risk of bleeding and that it will be safe to take the biopsy. This may be arranged to take place at your GP surgery. 

You can continue taking your normal medication. If you are on any medication that thins the blood we ask you to call the Imaging department using the number on your appointment letter. We may need to adjust your medication before undergoing this procedure. These may need to be stopped to keep the risk of bleeding to a minimum. This medication includes but is not limited to; aspirin, clopidogrel, warfarin, rivaroxaban, dabigatran and apixaban. 

Please arrange for someone to collect you from the hospital and take you home by car, as we advise you not to use public transport. You are not permitted to drive for 24 hours post-procedure and we would like someone to stay with you at home in the first 24 hours. Please inform the department if this is not possible, as we will need to identify alternative arrangements.

On the day of the procedure:

  • You should eat nothing for six hours before your appointment. You may drink water until the time of your appointment.
  • You will arrive at Gate 19 and be accompanied into our day case area.
  • You may take your normal medication unless instructed otherwise. It would be useful to bring a list of your usual medications.
  • Please inform us if you are allergic to anything. n You will be asked to change into a hospital gown and a small plastic tube (cannula) may be put into your arm.
  • A radiologist (x-ray doctor) will discuss the procedure with you. You will be given an opportunity to ask questions. If you want to go ahead with the procedure you will be asked to sign a consent form.
  • Once all the checks have been performed and consent signed, you will be taken to the procedure room on the trolley. There will be a nurse and a radiologist with you throughout the procedure.
  • The radiologist will use an ultrasound machine to look at your kidney to find the correct area to take the biopsy from.
  • Your skin will be cleaned with an antiseptic solution and covered with sterile drapes.
  • The radiologist will then inject a local anaesthetic into the area selected for biopsy, which will briefly sting and then go numb. Most people will feel a pushing sensation, but the biopsy is not usually painful. A special needle is used to remove a small piece of kidney tissue. Occasionally it is necessary to take more than one sample.
  • Once the radiologist has taken the sample, the needle will be removed, and the radiologist will apply a dressing.

What happens after the procedure?

  • You will be taken back to the day case area so that the nursing staff may monitor you closely.
  • If you are in pain tell the nursing staff so you can be given appropriate painkillers.
  • You will be required to stay flat for one hour and then sit up for a further two hours. Then walk around for half an hour.
  • You will be able to eat and drink as normal.
  • If everything is satisfactory, you will be free to go home. Please arrange for someone to collect you on discharge rather than drive yourself. n Have someone stay with you overnight.
  • You should rest for the remainder of that day and the following day, avoiding any strenuous activities for 36 hours.
  • Keep a regular check on the biopsy site. The dressing can be removed after 24 hours.
  • If you have any discomfort, take your usual pain relief as prescribed. But, if the pain is severe please contact the Imaging department using the number on your appointment letter.
  • Some people pass blood in their urine after a biopsy. This will usually settle on its own within a few days. If you continue to pass blood for more than 1 week or if you pass a lot of blood, then contact the Imaging department to ask for assessment and advice. If you become unwell out of working hours, then attend A&E.

What happens next?

The results of the biopsy will be sent to the consultant who referred you, who in turn will either contact you or write to your GP with the results. 

If you experience any symptoms you are concerned about, please contact the Imaging department directly on the number on your appointment letter or contact your GP or the emergency department. 

Finally, we hope this information is helpful. If you have any questions either before or after the procedure the staff in the Imaging department will be happy to answer them.

References

North Bristol NHS Trust (2022) “Ultrasound Guided Liver Biopsy” 

North Bristol NHS Trust (2022) “Kidney Biopsy Information for Patients” 

Halimi, J., Gatault, P., Louguet, H., Barbet, C., Bisson, A., Sautenet, B., Herbert, J., Buchler, M., Grammatico-Guillon, L. & Fauchier, L. Clinical Journal of the American Society of Nephrology (2020) “Major Bleeding and Risk of Death after Percutaneous Native Kidney Biopsies”

© North Bristol NHS Trust. This edition published June 2022. Review due June 2025. NBT003475

Fractional Exhaled Nitric Oxide (FeNO) Test

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What is a Fractional Exhaled Nitric Oxide (FeNO) test?

This is a quick and easy way to measure inflammation (irritation) in the lungs. 

The test may be done in the diagnosis of asthma, to evaluate a chronic cough, or to see how well treatment is working in a patient who has already been diagnosed with asthma. 

What does the test involve?

  • You should not smoke on the day of the test.
  • You should avoid eating nitrate rich foods (such as leafy green vegetables and beetroot) on the day of the test.
  • You will be asked to sit in a chair for testing
  • You will be asked to take a deep breath in as fully as possible and blow out at a steady pace for about ten seconds. 
  • The test takes about five minutes to complete. 

What happens after the test? 

The results will be sent to the healthcare professional that requested the test and they will discuss the results with you at your next appointment.

Reference 

ATS/ERS Recommendations for standardized procedures for the measurement of exhaled nitric oxide 2005 (Joint statement).

© North Bristol NHS Trust. This edition published June 2024. Review due June 2027. NBT002534.

Contact Respiratory Physiology

Exercise assessment

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Important information

  • Please avoid vigorous exercise on the day of your appointment.
  • Please take all medication as normal and please bring a list of all medication with you.
  • Please do not smoke, consume alcohol or eat a heavy meal within four hours of the test.
  • Please wear loose clothing and shoes suitable for exercise.
  • Do not wear lipstick or nail varnish/false nails.
  • Please do not wear any body lotion. 

Thank you for your co-operation. This will assist us in obtaining accurate information and enable us to provide you with the most appropriate treatment. 

What is an exercise assessment test?

An exercise assessment, also called cardiopulmonary exercise test, involves performing an increasing level of activity so that your heart and lungs can be monitored to assess your level of fitness.

Why do I need to have this test? 

These tests will help us understand what may be causing any limitation to the amount of activity you can do. This will help to give you the most appropriate treatment or advice.

Who will perform my test? 

The test will be performed by two respiratory physiologists. Respiratory physiologists are staff who have extensive training and knowledge in respiratory physiology and performing lung function tests.

What will happen during the test? 

Before the test begins the physiologist will explain the test to you in detail and answer any questions that you have. 

To begin with you will be asked to perform some breathing tests through a mouthpiece. You will then have some electrodes attached to your chest so we can monitor your heart and be fitted with a facemask so we can monitor your breathing. 

The exercise is usually done on a bicycle. Every minute the workload will increase until you feel you can no longer continue.

Frequently asked questions 

Will there be any discomfort or side effects of this test? 

This is a maximal test so you will feel short of breath and fatigued at the end but this will resolve once the test has ended. Your breathing and heart rhythm are monitored continuously during the test. At any time either you or the physiologist can stop the test.

Is there a different test I could have? 

There is no other test that would give us all this information about your exercise tolerance and limitations. 

When will I be told the results of my test? 

The results will be sent to the professional that requested the test. They will discuss the results with you at your next appointment. 

Further information

If you have any questions regarding your appointment please call us on 0117 414 9939.

© North Bristol NHS Trust. This edition published February 2025. Review due February 2028. NBT002876

Contact Respiratory Physiology

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Hypoxic challenge test

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Important information

  • Please continue to take all medications as normal.
  • Please do not wear nail varnish to your appointment.
  • You are advised not to book or pay for any flights until you have had the results of this test.
  • It is very dangerous to go on a flight if you have been advised against this or to travel without oxygen if you have been advised to use it. You could experience serious breathing difficulties.

Thank you for your co-operation. This will assist us in obtaining accurate information and enable us to provide you with the most appropriate treatment.

What is a hypoxic challenge test? 

A hypoxic challenge test is a procedure performed to give us information about what might happen to your blood oxygen levels if you travel in an aeroplane.

Why do I need to have this test? 

In an aircraft there is less oxygen available in the air. For people with a respiratory problem this can cause their oxygen levels to drop too low. This test will determine whether you need additional oxygen when you are in an aircraft. 

What happens during the test?

Before the test begins the Physiologist will explain the test to you in detail and will answer any questions that you may have. 

For the duration of the hypoxic challenge test you will be seated. A probe will be put on your finger. This will provide us with information about your blood oxygen levels. 

As part of the test it is also necessary to take several pinpricks of blood from your earlobe to provide further information about your blood oxygen levels. 

The test may take up to 90 minutes to complete. The length of the test may vary depending on your blood oxygen level. 

Frequently asked questions

Will I experience any discomfort or side effects?

The only discomfort you may experience is a slight scratch on your ear when a pinprick of blood is taken. There are no known side effects associated with this test.

Is there a different test I could have?

There is no other test that would give us this information about your blood oxygen levels in a flight environment.

When will I be told the results of my test?

The Physiologist will provide information about the outcome of the test at your appointment. The report will be sent to the professional requesting the test. If you require paperwork to be completed for the airline this will need to be completed either by your Consultant or GP. If you require oxygen it will be your responsibility to organise this with the airline that you are travelling with.

What should I wear when I attend for my test?

You should wear normal comfortable clothing.

Reference

British Thoracic Society Standards of Care Committee (2011) BTS Clinical Statement on air travel for passengers with respiratory disease. London: British Thoracic Society.

© North Bristol NHS Trust. This edition published February 2025. Review due February 2028. NBT002290.

Contact Respiratory Physiology

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Southmead Hospital Charity logo

See the impact we make across our hospitals and how you can be a part of it. 

Coronary angiogram and angioplasty/PCI

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Coronary angiogram 

This page is for patients whose doctor has requested that you have a coronary angiogram. The following information will answer some of the questions you may have about this procedure.

What is a coronary angiogram?

A coronary angiogram (sometimes called ‘cardiac catheterisation’) is an X-ray study which takes pictures of the blood flowing through the coronary arteries which supply the heart with blood. It can highlight narrowings or blockages in these arteries caused by fatty calcified deposits – coronary artery disease. 

Why do I need to have an angiogram?

The angiogram gives a detailed assessment of the arteries to give doctors extra information to help them decide on the appropriate treatment. If you have a narrowing coronary (heart) artery, that can be treated with ‘balloon coronary angioplasty and stent’ (PCI). This can be done in the same procedure or sometimes separately at a later date.  

What is an angioplasty/PCI?

Coronary angioplasty, often called PCI (Percutaneous Coronary Intervention), is a procedure where a balloon is used to open a blockage in a coronary artery. It is very similar to an angiogram procedure and is performed in the same room, under the same conditions, and the recovery is similar. The main difference is that an angiogram only collects information (pictures), whereas an angioplasty performs a treatment (inserting a stent). 

An angioplasty/PCI takes approximately 1-2 hours to perform. The length of time will vary from person to person depending on the complexity of the coronary artery disease. A balloon is used to stretch the artery and a stent (wire mesh tube) is then put in the narrowed artery and acts as internal scaffolding, keeping the artery open.

What are the risks?

Generally it is a very safe procedure. Potential complications are uncommon but include: 

Damage to the blood vessels in the leg or arm. Bleeding or haematoma (a lump/bruise under the skin) around the puncture site.

  • A small risk of stroke.
  • A small risk of heart attack.
  • A small risk of emergency cardiac surgery. 
  • A small risk of death.
  • Very rarely an allergic reaction to the injected substance.
  • X-ray is used in this procedure but with modern equipment the risk from the X-ray is very low.

What happens before the procedure? 

Pre-assessment

You will be invited to attend pre-assessment clinic/ telephone consultation, where we will explain the procedure to you and collect information. If you need an interpreter, please let us know as soon as possible. An ECG will be performed and you might be asked for a blood sample. 

You will need someone to take you to and from the procedure and who will stay with you at home overnight. If this is not possible, let us know in advance and we will arrange an overnight bed. They will not be able to stay with you on the day of the procedure.  

Please let us know if you might be pregnant. Also, let us know of any allergies, and bring a list of your current medication. 

Medication guidelines

  • If you take diuretics (water tablets), do not take them on the morning of your procedure as you may find it inconvenient.
  • If you are taking metformin (glucophage), ideally it should be stopped 48 hours prior and not re-started until 48 hours after your procedure. 
  • If you take warfarin, stop taking it 4 days prior to the procedure. 
  • If you take any other anticoagulant (blood thinner, e.g. rivabaxan, dabigatran, apixaban, edoxaban) stop taking it 2 days prior to the procedure.

It is now very common to have combined ‘angiogram and angioplasty (PCI)’ and it is very important that you take dual anti-platelet medication leading up to, and on, the morning of the procedure. This is usually a combination of aspirin and clopidogrel, or aspirin and ticagrelor. This will be discussed in pre-assessment, and prescribed if necessary. These medications are vital for the procedure to go ahead as they prevent blood clotting in the stent.

Preparation for the procedure checklist

  • Have nothing to eat after 6:30am if your procedure is in the morning.
  • Have nothing to eat after 10:30 am if your procedure is in the afternoon.  
  • You can drink water up until the procedure. 
  • Bring all your usual medication in with you on the day of the procedure.
  • Your wedding ring can be taped to your finger but please leave other valuables at home. Please remove all nail varnish.
  • Bring a newspaper or a book with you so that you will have something to do when the procedure is over.
  • Bring slippers and a dressing gown, but as few other possessions as possible. 
  • Take/stop taking medication as instructed. You should take your usual regular medication unless instructed otherwise.

On the day of the procedure 

When you arrive

You will arrive at the Imaging Department (Gate 19) and be accompanied into our day case area. A cardiologist will explain the procedure to you, and the benefits and potential risks. You will have an opportunity to ask questions. If you choose to go ahead with the procedure you will need to sign a consent form, which may be done during your pre-assessment visit. Please let us know of any allergies too. From there, you will be asked to change into a hospital gown and paper pants and a nurse will go through the procedure checklist and place a small plastic tube called a cannula, in a vein in your forearm to allow medications to be given if necessary during the procedure.

During the procedure

You will be taken to the Cardiac Catheterisation Laboratory (Cath Lab). You will be asked to lie down flat on the X-ray table with a pillow for the procedure. There will be a small team of nurses, doctors, cardiac physiologists and radiographers with you throughout. 

If you are feeling anxious, you will be offered sedation but will stay awake. The nurse will then cover you with a drape and clean the area at the top of your leg or wrist with antiseptic solution. Then the doctor will inject local anaesthetic into your wrist (if radial) or the area at the top of your leg (if femoral) which will briefly sting and then go numb. 

After this, you may just feel a pushing sensation when a small plastic tube (sheath) is inserted into your femoral or radial artery. A catheter is passed though the sheath and up inside the artery to the heart. Once the catheter reaches your coronary (heart) arteries, contrast liquid is injected into the bloodstream and X-ray images are taken.

The X-ray machine will move around you, but will not touch you. It is important that you stay still throughout to take the clearest pictures possible. Once the doctor has acquired enough images, the X-ray machine will be removed. 

If the doctor used the wrist artery (radial), a pressure device called a TR band will be placed on your wrist and inflated. This will be deflated gradually until it can be removed. Alternatively, if the doctor used the leg artery (femoral), a seal may be used to plug the artery or pressure will be applied either with a pressure device or manual pressure. 

What happens after the procedure?

You will be taken back to recovery/day case area initially, so that nursing staff can monitor your observations and the wound site very closely. Relax as much as you can and tell the nurse straight away if you experience any discomfort, notice any swelling or bleeding at the wound site, numbness in the leg/arm, or you feel unwell. You will be able to eat and drink as normal. Please make sure you drink plenty of fluids after this procedure which will help pass the contrast liquid out in the urine. 

How long will I have to stay in recovery?

Recovery time after an angiogram is usually around 3 hours, but can sometimes be longer. 

Recovery time after an angiogram is usually around 3 hours, but can sometimes be longer. If you have an angioplasty (PCI), your recovery time will be longer (about 6 hours) or you may require an overnight stay in hospital. This will be discussed in your pre-assessment appointment. 

If the doctor used the wrist radial artery:

  • The band around your wrist will be slowly deflated over 2-3 hours and then removed. This will be longer, usually 3-5 hours, for an angioplasty/PCI. 
  • The band will then be removed and replaced with a small dressing. 
  • Try not to move your wrist much while your artery is healing.
  • If the doctor used the leg femoral artery:

  • If a pressure device or manual pressure was used to stop the bleeding you will need to stay flat for 1 hour and bed rest for a total of 3 hours. 
  • If you have had a seal you can sit up straight away if there is no bleeding, and move around after 2 hours. This may be longer if bleeding occurs. require an overnight stay in hospital. This will be discussed in your pre-assessment appointment. 

What happens next? 

Before you are discharged

Before you are discharged, the doctor will discuss the results with you. If you have coronary artery disease that requires further treatment, the doctor will explain the options and there may be a meeting. This may be cardiac surgery (coronary artery bypass grafts – CABG), coronary angioplasty/PCI or drug therapy. You will then be given a discharge letter. 

Discharge advice

Do not do any heavy lifting or strenuous exercise, like weight lifting or cycling, for 4-5 days. Do not drive 48 hours after an angiogram and 1 week after an angioplasty/PCI (DVLA advice). Drink lots of water (2L) in the following 24 hours. If you were sedated, don’t sign any legal documentation for 48 hours.

Radial (wrist) puncture: 

  • Rest the arm for 2-3 days.
  • Avoid flexing/ bending the wrist, lifting and putting weight through the arm. 
  • Avoid bathing and washing up for 48 hours after. You may shower the following day, but avoid scrubbing the wound. If wet, replace the dressing with a plaster.

Femoral (groin) puncture: 

  • Avoid bending from the hip for 2-3 days or anything that strains stomach muscles. 
  • Avoid straining when going to the toilet. 
  • Apply light pressure over the puncture site, when coughing, sneezing, or laughing. 
  • Avoid bathing for 48 hours post procedure. You may shower the following day, but avoid scrubbing the wound, and pat dry thoroughly. 

Any problems

Complications are rare but can happen, particularly in the first 24 hours, so make sure you have a responsible adult with you. If the wound starts to bleed or swell suddenly, apply firm pressure to the puncture site for 10-20 minutes. If the wound is in the groin, lie flat while pressure is applied for you. If the bleeding stops, seek medical advice. If you are unable to stop the bleeding, call 999 immediately. 

A bruise around the site is common but should fade after 2-3 weeks. If it becomes swollen, or you develop persistent pain/ tenderness, contact your GP. If you get any chest discomfort after discharge that does not resolve 5-10 minutes after using your GTN spray, call 999.

© North Bristol NHS Trust.  This edition published June 2024. Review due June 2027. NBT002237.

Contact Cardiology

Cardiology Outpatient Bookings
Telephone: 0300 5550103

Cardiac Cath Lab Co-ordinator
Telephone: 0117 4149046

Cardiac Care Unit
Telephone: 0117 4140050

Acute Cardiology Ward
Telephone: 0117 4140050

Cardiac Catheter Laboratory
Telephone: 0117 4143500

Cardiac Testing
Telephone: 0117 4140800

Clevedon Hospital
Telephone: 01275 872212

Cardiac Rehabilitation
Telephone: 0117 4140040
Fax: 0117 4149468

Cardiology Secretaries
Fax: 0117 4149377

Eating less phosphate from additives

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Information for kidney patients who need to lower the phosphate levels in their blood.

Eating less phosphate from additives can help this.

Phosphate is often added to food by manufacturers as additives. This phosphate from additives gets into your blood stream more easily than the phosphate found naturally in foods. Phosphate additives can make your blood phosphate levels too high. 

This information explains which foods have these additives and how you can avoid them, and which foods you can eat that don’t have phosphate additives. 

Some foods are naturally high in phosphate (also known as phosphorous). You could eat less of these too. Ask your dietitian for advice about this.

How can I reduce phosphate additives?

To reduce the amount of phosphate additives you eat:

  • Eat freshly cooked, unprocessed food more often.
  • Check ingredient labels and limit foods with phosphate additives.
  • Swap to brands without phosphate additives.

Why do I need to reduce the phosphate level in my blood?

When the kidneys are not working properly, the level of phosphate in the blood often rises too high. The normal range for blood phosphate is between 0.8mmol/l and 1.5mmol/l. 

High levels of phosphate can cause:

  • Hardening of blood vessels.
  • Damage to your heart.
  • Weak bones.
  • Aching joints.
  • Itchy skin.

How do I eat less phosphate additives?

If a food contains phosphate additives, you will see the name or E number on the ingredient label. Additives with “phos” in their name contain phosphate. You may be able to swap to a different brand without phosphate additives. 

Check ingredient labels and try to avoid these additives:

E numberNameWhere found
E338 Phosphoric acidProcessed meats, sweets. cakes, chocolate, cola drinks.
E339Sodium phosphates Dried milk powder, canned soup, breaded chicken and fish, UHT products
E340Potassium phosphatesProcessed meats and cheeses, sports drinks, dried milk powder.
E341Calcium phosphatesShop-bought desserts and powder dessert mixes, instant pasta mixes.
E343Magnesium phosphatesBakery products, liquid egg, salt, substitutes.
E450DiphosphatesBakery products, processed meat and cheeses, soups and sauces.
E451TriphosphatesProcessed cheese, icing sugar, flavoured syrups.
E452PolyphosphatesProcessed potato products. 

To help you avoid phosphate additives, here are some examples of food labels. They show how phosphate additives are listed on the packaging.

Sausages

Sausages ingredient label with red circle around Polyphosphates

Cake

Cake ingredient label with red circle around Disodium Diphosphate

If food contains phosphate additives try checking similar options to find one without. 

What foods can I eat?

By choosing fresh, unprocessed foods where possible, you can reduce the phosphate additives you are eating. This will help to you lower your blood phosphate levels. 

Here are some suggestions for swaps:

Foods commonly containing phosphate additivesSuitable swaps - but always check labels
Ham. chicken, or turkey slices.Home cooked cold meat, chicken, or turkey. Or brands without phosphate additives.
Processed cheese spreads or dips.Flavoured or plain cream or cottage cheese.
Processed cheese slices, cheese triangles.Cheddar cheese or another hard cheese.
Naan bread, crumpets.Tortilla wraps, pitta bread, bread or English muffins.
Muffins, scones, sponge cakes.Fresh fruit, iced buns, fruit teacakes, hot cross buns, jam tarts, meringues, croissants, shortbread, digestive, and rich tea biscuits.
Cola drinks.Water, fruit squash, flavoured water, lemon or orangeade, non-alcoholic ginger beer.

It can be difficult to find processed meat without phosphate additives. Your dietitian can guide you on processed meats without additives available where you normally shop. 

Eating less red and processed meat is recommended for us all as they are linked with causing bowel cancer. They are also high in fat and salt. For healthier, lower phosphate options, see the NHS websites on the next page.

How can I eat more sustainably?

Many people want to eat food that is more environmentally friendly. These are good ideas for the planet and for you too:

  • Limit red and processed meats. Try some plant food sources of protein such as beans, lentils, soya mince, Quorn, and tofu instead.
  • Moderate the amount of dairy foods you eat and consider a plant-based milk.
  • Eat less processed food that is high in fat, sugar, and salt.

Summary

This page has shown you ways you can eat less phosphate from food additives by:

  • Eating freshly cooked, unprocessed food more often.
  • Checking labels for phosphate additives, and limiting foods with phosphate additives.
  • Swapping brands to avoid phosphate additives.

Useful webpages:

For guidance on healthy amounts of meat to help reduce your risk of bowel cancer:

Meat in your diet - NHS (www.nhs.uk)

Information on kidney disease and food written by the kidney dietitians at North Bristol NHS Trust:

Nutrition & Dietetics Patient Information (Kidney Disease) | North Bristol NHS Trust (nbt.nhs.uk)

Recipes to enable you to cook delicious kidney friendly meals from scratch:

Recipe Index | Kidney Care UK

Practical advice to help you reduce your weekly food shopping bill while maintaining a nutritious and kidney friendly diet:

Shop for a kidney friendly diet on a budget | Kidney Care UK

© North Bristol NHS Trust. This edition published May 2024. Review due May 2027. NBT003616.

New to Research

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Health research is about asking questions and finding new ways of improving patient care

Here at NBT, research is led by and carried out by clinical and non-clinical teams that include Nurses, Midwives, Doctors, Administrators, Clinical Trial Officers, Physiotherapists, Speech and Language Therapists, Clinical Librarians and more.

If you have an idea for research or would like to develop a career as an independent researcher, we can offer comprehensive support. This could include help with grant and training applications or navigating the research system.

We've spoken to people working in research carrying out many different roles. Read about or watch our My Role In Research colleagues.

People can become experts in their everyday surroundings, so they’re the ones best placed to solve problems or develop evidence through research. Whether you’re in a clinical or non-clinical role, we’re looking to increase the range of roles carrying out research at NBT. 

This webinar gives a good introduction to Research.

Contact research@nbt.nhs.uk for further help.

We're here to help! Here are some Frequently Asked Questions

How do I know if my study is research?

Research can be defined as the attempt to derive generalisable or transferable new knowledge to answer or refine relevant questions with scientifically sound methods. This excludes: audit; needs assessments; quality improvement and other local service evaluations. It also excludes routine banking of biological samples or data, except where this activity is integral to a self-contained research project designed to test a clear hypothesis.

If you are in any doubt, please contact the Research Development & Grants team – we can support your project or signpost you to a more appropriate team, if required. 

I am very busy in my current role, but I would like to get involved in research. Is there any way I can combine it with my day-to-day role?

Yes. There are lots of opportunities to get involved in research, including developing a project or grant application of your own, as part of your role. The R&D Department have funding available to cover your time to work in research. This would be discussed on a case-by-case basis with your department, so please get in touch with the Research Development & Grants team who can support you with conversations with your line manager and clinical division.

Do I need to have experience in research to write up a research proposal?

Research ideas and grant applications are welcome from everyone, no matter how much (or little) prior experience you have. The Research Development & Grants team can provide additional support to those that need it, especially if you are new to research.

Who should I contact to help me with costing my grant application and developing my project?

Please email the Research Development & Grants team: ResearchGrants@nbt.nhs.uk

What support can the Research Development & Grants team offer me?

The Research Development and Grants team can support you from early stages of developing a research idea. We can help to find suitable funding opportunities, calculate costs for an established proposal, and navigate systems for submitting your grant application, and much more.

When is it appropriate to reach out to the Research Development and Grants team?

Any time! From just having a brief idea for a research project, to needing final costings on a grant application. You can speak to the Research Development & Grants team at any stage of your research development. The sooner you contact us the better though, and the team will provide tailored support.

How long will it take to cost my research project for my grant application?

This is dependent on your project. But the Research Development and Grants team can support you with every aspect of your costing. The sooner you get in touch with us (i.e. as soon as you begin writing your grant application) the more support we can offer.

View Our Research

Doctor conducting research at NBT

Explore the ground-breaking research currently taking place at North Bristol NHS Trust.

About Research & Development

NBT Researcher

Find out more about our research and how we're working to improve patient care.

Contact Research

Research & Development
North Bristol NHS Trust
Level 3, Learning & Research building
Southmead Hospital
Westbury-on-Trym
Bristol, BS10 5NB

Telephone: 0117 4149330
Email: research@nbt.nhs.uk

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Preterm Birth Prevention Clinic

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Information for before your visit 

Why have I been referred?

Our Preterm Birth Prevention Clinics offer extra care for women who may be at higher risk for preterm (premature) birth. There are several reasons why women may be at higher risk, including if you have experienced any of the following:

  • Previous preterm birth.
  • Previous prelabour, premature rupture of membranes (water breaking early).
  • Previous miscarriage after 16 weeks gestation. 
  • Previous cervical surgery including caesarean sections at full cervical dilation.
  • Uterine anomalies.
  • Shortened cervix seen on ultrasound scan.

We offer the following assessments in the clinic:

  • An internal ultrasound scan to assess the length of your cervix.
  • A urine test and vaginal swab may be taken to screen for infection.

What will happen when I visit the clinic?

Please arrive 10 minutes before your appointment time so we can take your blood pressure and perform a urinalysis. These are routine tests offered at most antenatal appointments during your pregnancy.

You will see a doctor and a specialist preterm birth prevention midwife who will discuss your risks for preterm birth, including information regarding your current and previous pregnancies. All tests offered are safe for you and your baby.

You will be offered a transvaginal ultrasound scan to measure the length of your cervix. This scan involves a small ultrasound being inserted into the vagina - it requires an empty bladder.

What treatments do you offer?

Not everyone who attends the clinic will require treatment. Depending on the initial assessment you may be offered further monitoring and reassurance with repeat ultrasound scans.

If you are at higher risk of preterm birth, you may be offered vaginal hormone (progesterone) pessaries/tablets. More rarely a stitch around the cervix may be recommended to those at highest risk of preterm birth.

When to seek advice

Sometimes there are signs that you may be going into labour. Often the signs may not lead to preterm birth, but it’s important to seek urgent advice. These signs may include:

  • Period-like pains or cramps which come and go.
  • Constant back pain.
  • Fluid leaking from the vagina.
  • Bleeding from the vagina. 

If you think you may be in labour, do not wait for your next appointment. You should call the Central Delivery Suite at Southmead Hospital on the same day. The phone number is on the front of your yellow maternity notes. 

Should I still attend my antenatal appointments?

Yes, you should.

Lifestyle modifications

Many of the risks for preterm birth cannot be changed, however there are some lifestyle changes that can be made where possible.

  • Smoking has been associated with preterm birth, and therefore cutting down or stopping smoking is a positive step that can be taken to reduce the risk of your baby being born prematurely. You can speak with your midwife or with the doctor at the preterm birth prevention clinic for advice and ask for a referral for support with giving up smoking. 
  • Drinking alcohol during pregnancy has been associated with premature birth. Drinking no alcohol at all is safest. 
  • Tooth decay and gum disease has been associated with preterm birth, and therefore it is a good idea to see your dentist, especially if you think you may have tooth decay or toothache. You can organise free dental care with your maternity exemption card.

© North Bristol NHS Trust.  This edition published December 2024. Review due December 2027. NBT003698.

Contact Preterm Birth Prevention Clinic

Preterm Birth Prevention Clinic
Foetal Meicine Unit
Cotswold Outpatients,
Southmead Hospital
Westbury-on-trym
Bristol
BS10 5NB

0117 414 6928

Contact Severn Pathology

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Use of email

Our NBT email address has been accredited to the NHS Digital Accreditation Standard DCB1586 (The secure email standard - NHS Digital) so you can be assured when sending confidential information to us that this is as secure as NHS.net.

See individual department pages for telephone numbers and appropriate emails.

 

Address and location

Severn Pathology
Pathology Sciences Building
Southmead Hospital
Westbury-on-Trym
Bristol
BS10 5NB

Pathology Opening Hours

See specific departmental information for detailed contact information and availability.

A summary of opening hours are as follows:

For Blood Sciences departments (Chemistry, Haematology, Blood Transfusion and Specimen Reception) please see the following:

 

Microbiology: 8am–8pm weekdays out of these hours and Bank Holidays contact via NBT Switchboard.

Cellular Pathology: 9am-5pm out of these hours and Bank Holidays contact via NBT Switchboard.

Switchboard: 0117 9505050

Test Information

Community Acquired Pneumonia Research Priority Setting Project

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We are looking for people who have lived experience of Community Acquired Pneumonia. 

We would like you to join a group of health professionals to help us to see what research would make a difference to adults who have lived experience of community acquired pneumonia.

What is community acquired pneumonia? 

Community acquired pneumonia is the commonest reason that people are admitted to hospital in the UK. It is an infection of one or both lungs that is usually caused by bacteria and viruses. We call it community acquired because people who get it are living in the community as opposed to being in hospital at the time. 

What are we asking you to do? 

We are anticipating that the group will meet monthly for approximately 12 – 18 months. Most of the meetings will be held on-line (virtually) and will take no more than two hours per meeting. 

There may occasionally be face to face meetings which will be a little longer, to make good use of the opportunity to work together in this way. Travel expenses will be reimbursed, and you will also be compensated for your time with non-cash transferable vouchers as a way of saying thank you for your time. 

What do you need to do now? 

Who is funding the project? 

James Lind Alliance and Southmead Hospital Charity 

The James Lind Alliance is non-profit making initiative bringing patients, their families and carers, and clinicians together in a Priority Setting Partnership (PSP) to identify and prioritise uncertainties, or ‘unanswered questions’, about Community Acquired Pneumonia  that have not been answered by previous research, and are important to patients, their families and carers with lived experience, and professionals who look after them. 

Southmead Hospital Charity 

The Charity will be working closely with the Health Professionals and the James Lind Alliance to list  all the possible areas for research will then be discussed and the top 10 prioritised. This will ensure that researchers and those who fund research, focus on what really matters to both patients and clinicians. 

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