Pelvic floor exercises for men

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This page contains information for patients about pelvic floor exercises for men. 

Where are my pelvic floor muscles?

They are the layer of muscles that extend from your pubic bone at the front of your pelvis to your tail bone (coccyx) at the back of your pelvis. They are the the muscular support at base of your pelvis.

Illustration of male pelvic floor muscles

What are the functions of your pelvic floor?

  • Bladder control. 
  • Bowel control.
  • Sexual function.  
  • Stabilises the pelvis. 
  • Supports the pelvic organs.

Possible risk factors leading to pelvic floor weakness:

  • Prostate or pelvic surgery (e.g. prostatectomy).
  • Radiation to the pelvis.
  • Straining to poo due to chronic constipation.
  • Certain conditions such as MS, strokes, or uncontrolled diabetes.
  • Being overweight.
  • Chronic coughs.
  • Injury to the perineum. 

What are the symptoms of pelvic floor weakness in men?

Many men experience weakness of the pelvic floor. If this happens you may have a variety of symptoms including:

  • Leaking urine during activity, for example when you sneeze, cough or laugh (known as stress urinary incontinence).
  • A need to go to the toilet often during the day or night (known as frequency or nocturia, respectively).
  • An urgent need to visit the toilet and leaking before you get there (known as urgency incontinence).
  • You are unable to control the passing of wind or stool from your back passage.
  • Erectile dysfunction (the pelvic floor helps you maintain erections).
  • Post micturition dribble (leaking urine immediately after you have finished passing urine).

Why should I do pelvic floor exercises?

The pelvic floor muscles can be strengthened to increase the support of the pelvic organs. This can improve bladder and bowel control and can reduce/cure leakage of urine. It may also improve your ability to maintain an erection. 

Identifying the pelvic floor muscles

It’s important to know where the pelvic floor muscles are, so that you’re sure you’re exercising the correct muscles. To identify the pelvic floor muscles, tighten your back passage as if you’re trying to stop yourself passing wind; at the same time, imagine you’re trying to stop yourself passing urine.
You should have a sense of squeezing, pulling the back passage up and in. You may see the base of your penis retract slightly in your body and your testicles rise a little. Do not tighten your thighs or buttocks and do not hold your breath. After contracting it is important to feel the muscles relaxing and softening as you let go.  

How do I do pelvic floor exercises?

You can exercise your pelvic floor anywhere and anytime. They can be performed lying, sitting or standing  but to start with it may be easier to do the exercises sitting down. Make sure you’ve found the correct muscles and know how it should feel when you tighten them before trying these exercises.

There are two types of exercises, slow and fast, it is important you do both:

Exercise 1: slow pull-ups

  • Take a breath in. 
  • On the breath out, tighten the pelvic floor muscles. 
  • Return to normal breathing but continue to tighten for your length of hold, relax, and feel the muscle let go. 
  • Rest for 5 seconds. 
  • Repeat this 5 times.

As it gets easier, gradually increase length of hold and number of repetitions, aiming for 10 seconds.

Exercise 2: fast pull-ups 

  • Tighten the pelvic floor muscles quickly and then let go straight away. 
  • Repeat this 10 times – approximately 1 contraction per second.

You may find that the muscles are weak initially and that it takes a lot of concentration to exercise them, but this should improve with time

Do not practice stopping the flow of urine midstream as this may interfere with the normal process of emptying your bladder.

How often should I do my exercises?

Do exercises 1 and 2 during each session. As soon as you can, increase to 10 slow and 10 fast pull-ups. 

Aim to repeat these 3 times each day, so in total you will be doing 30 slow and 30 fast pull-ups a day. 

It will take up to 3-6 months of regular exercise to increase the strength in your pelvic floor muscles and hopefully reduce your symptoms.

As your muscles get stronger you may progress to doing the exercises standing up.

To help remind you to do your exercises daily try to combine them with an everyday activity, for example, when brushing your teeth, and after breakfast, lunch, and dinner. 

You can also download an app called Squeezy which is recommended by the NHS. It will send you reminders to do the exercises and you can personalise the programme to suit you.

How long should I continue with the exercises?

Once your symptoms have improved, continue with these exercises once daily for the rest of your life to keep these muscles fit and healthy (e.g., 10 slow and 10 fast pull-ups daily).

Additional tips

  • Being overweight can weaken the pelvic floor muscles so it is important to maintain a healthy BMI. 
  • You may want to try sitting in the correct toilet position to help with constipation like in the image below. (This is sat on a toilet with feet on a foot rest, knees higher than your hips, lean forward with your elbows onto your knees. Bulge out your abdomen and straighten your spine). 
  • You should try to drink 6-8 cups of fluid a day. 
  • Caffeinated drinks, alcohol, acidic drinks (fruit juices) and fizzy drink can irritate your bladder and cause urgency; we suggest avoiding these. 
  • Tighten the pelvic floor muscles before lifting anything heavy or if you are going to sneeze or cough. 
  • If you have urgency, contract your pelvic floor muscles when you have the desire to empty your bladder and only move when the desire has passed.
Diagram of correct position to sit on toilet

Image courtesty of Bladder and Bowel Community:
www.bladderandbowel.org/help-information/resources/toilet-positions/

© North Bristol NHS Trust.  This edition published May 2024. Review due May 2027. NBT002673.

Over 50s and alcohol use

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This information is for people over 50 years old, who are drinking  alcohol above low risk guidelines (14 units most weeks) and are worried about their drinking.

It may also be of use to carers, friends, or health professionals who are worried about an older person’s drinking.

What’s different about alcohol for older people?

Anyone at any age can drink too much. Sometimes health problems can be mistake for conditions related to ageing, rather than our drinking habits. People drink alcohol for many reasons:

  • It might be just a habit or routine; they have always drunk. 
  • Significant changes in life roles - retirement, no longer caring for dependent children, bereavement, separation/divorce - leading to more opportunity/time to drink.
  • Boredom, loss of social contacts, loss of hobbies/interests.
  • Change in social group, revolving around pubs/clubs.

As we get older, our bodies change; we, lose muscle, gain fat and break down alcohol more slowly.

This means that we can become more sensitive to the effects of alcohol. Other health problems can also make us more susceptible to the effects of alcohol.

We sometimes react more slowly and balance may deteriorate with age - even a small amount of alcohol can make us more unsteady and at risk of falls.

So, even if our alcohol routine hasn’t changed it can affect us more and can impact on our quality of life

Lower risk drinking

The Department of Health Guidelines state that there is no safe level of alcohol use. The more you drink, the more likely it is that alcohol will harm your health. Drinking 14 units a week or less, is considered low risk. However, the changes to our bodies as we age, mean that safe drinking levels for older people are probably less than this. 

It is important to know how much alcohol we drink. Drinks containing alcohol show the number of units they contain on the label. There are also unit calculators online e.g. Alcohol Concern UK. 

For example:

  • A pint of ordinary strength beer (4%) or a double whisky (50mls) both contain two units.
  • A 75cl bottle of wine contains 8 - 10 units and so a glass of wine might contain anything from 1 to 3 units depending on its size.

If you drink 10 units daily, you have alcohol in your body for 10 hours. Over time this puts strain on your liver, which is why alcohol free days are so important.

Lower risk drinking advice is:

  • Have two or three alcohol free days each week. 
  • It’s important to spread drinks evenly over a few days.
  • Binge drinking (six or more units) over a matter of hours increases risk of accidental injuries and these risks can increase with age.

Risk behaviours

Alcohol can impair your judgement and alter your behaviour. You can misread situations and react in ways that are out of character. Alcohol can increase your vulnerability to financial and sexual exploitation. Arguments can escalate into assault or fights. 

Delay making important decisions if you have been drinking; consider getting advice/support from trusted friends/family/healthcare professions.

Driving

Don’t drink and drive. On average it takes a healthy liver an hour to process one unit of alcohol. An evening drink can mean you still have alcohol in your system the next morning. The safest option is to avoid drinking alcohol altogether when driving.

 

Alcohol and medicine

Alcohol can enhance the effect of some medications, such as painkillers or sleeping tablets, and reduce the effect of others, such as medications to thin the blood (Rivaroxaban) and antidepressants.  

Check with your doctor if it is safe for you to drink with your particular health problems and/or medication. Ask your pharmacist and/or read the leaflet that comes with your prescription, over-the-counter or herbal medicines.

What are the risks of drinking too much?

Alcohol can damage nearly every part of the body:

  • The stomach lining - ulcers or bleeding.
  • The liver - fatty liver, cirrhosis and liver failure.
  • Heart muscle - heart failure produces a build-up of fluid in the lungs which results in shortness of breath.
  • Cancer - 6% of cancers world wide can be linked to alcohol. Mouth, stomach, liver and breast cancers have strong links with alcohol use.
  • Malnutrition - alcohol has lots of calories for energy, but none of the protein, fats, vitamins or minerals you need to keep the body in good repair. People who drink most days are recommended to take Thiamine and Sanatogen.
  • Sense of balance - falls and accidents (even when not intoxicated).
  • Blackouts, seizures or fits.
  • Stroke.
  • Poor sleep - broken sleep, early morning waking and daytime tiredness.
  • Menopause - increase in symptoms.

Not everyone who drinks too much will develop health problems, but the more you drink, the more likely you are to get such problems.

Alcohol and mental health

Anxiety

Alcohol can be a short term fix to relieve anxiety, but the  anxiety will return. It is not a long term solution. So the temptation is to drink again to feel better.

Depression

Alcohol is a depressant. Low mood and depression can lead to a loss of interest in things you used to enjoy. You can feel tired, but have difficulty sleeping. It becomes more difficult to take things in when reading or following a TV programme. Your appetite can be poor, and your body can become depleted of essential nutrition for normal brain function. In extreme cases you may feel life is not worth living.

Hearing voices

This is less common but can happen if you have been drinking heavily for a long time. It starts with vague noises, like leaves rustling, and gradually becomes distinct voices. These can be unpleasant and distracting.

Confusion

Alcohol use plus poor or absent diet can result in low  Thiamine and Magnesium. This can cause confusion and poor memory. If not treated this leads to Alcohol Related Brain Injury, including Korsakoff’s dementia.

Cut down your drinking

Keep a drink diary, this is a good starting point for change. Write down the date, what type of drinks you have, how many units, and add up the total number of units each day. Bottles/cans have information about number of units. 

Have an alcohol reduction plan 

  • Think about hobbies, interests, and social opportunities that don’t involve alcohol. This may be a brand new activity or something that you used to enjoy. 
  • Alcohol can fill a gap when you are bored so don’t leave space. Occupy yourself and get out of the routine/habits that revolve around alcohol.
  • Local Council websites/libraries will have information about volunteering opportunities, wellbeing groups and leisure activities in your local area.
  • Friends and family can support you to make changes.
  • Home measures are usually large ones. Use a measure or a smaller glass, and make sure you keep track. Don’t top-up your glass before it’s empty. Put the bottle away between drinks.
  • Make each drink last longer. Drink a soft drink or water with, or after, each alcoholic drink.
  • Eat something before you drink, this will help slow down the absorption of alcohol into your body.
  • Plan two or three alcohol-free days a week.
  • If you have a lapse or don’t manage to cut down as you had hoped, don’t give up! If it was an easy thing to do you would have done it already.
  • Have a plan and acknowledge your successes.

     

What support and treatments are available?

If you are drinking dependently, it could be unpleasant or even dangerous for you to stop drinking abruptly (cold turkey) as your body is accustomed to alcohol.

Talk to your GP or healthcare professional about alcohol. Each person is different, so speaking to a medical professional about your own circumstances is always a good starting point. Ask about a prescription of Thiamine and Sanatogen A-Z Complete. Your GP may be able to offer a medically supported detox (depending on your alcohol intake, your physical/mental health, and your support at home). You will need a robust plan about how to stay abstinent following detox.

Your GP can offer information about local community alcohol service. They can refer you or you can self-refer.

Community alcohol services, support you to make changes either by a safe/slow reduction or by medically supported detox.

If your goal is abstinence, but cravings for alcohol are a problem, there are medications that might be of use to you, to help reduce these cravings. Ask your GP or local alcohol service.

Discuss with your GP access to Wellbeing support/social prescribing/counselling services. If you are drinking to help manage anxiety, low mood or physical problem, a wellbeing service can help provide alternative strategies, not reliant on alcohol.

Support Groups: Mutual aid organisations AA (Alcoholics Anonymous) and SMART Recovery. These offer abstinence based recovery support. Look at their websites for up to date meeting details.

By making healthier choices about alcohol you can start to see the positive effects on your health and wellbeing.
 

Support organisations

Age UK
Bristol: 0117 929 7537
South Gloucestershire 0145 441 1707

Alcoholics Anonymous
Bristol helpline: 0117 926 5520
Email: help@aamail.org

SMART Recovery
Self-Help Addiction Recovery | UK Smart Recovery

Bristol ROADS/ Bristol DHI
0117 440 0540

BDP 50+ Crowd
0117 440 0540

South Gloucestershire DHI
0800 073 3011

North Somerset We Are With You
01934 427940

Drinkline
0300 123 1110

© North Bristol NHS Trust.  This edition published August 2023. Review due August 2026. NBT003101.

Southmead Hospital Charity Research Fund - Public Panel

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Interested in joining our Southmead Hospital Charity Research Public Panel? 

The Public Panel are members of the public who help us to review applications of potential research projects. Public members do not need any research experience. The panel provide feedback to shortlisted applicants and make a decision who will be awarded the money to carry out their proposed research project.

Discover some of the frequently asked questions below. 

For more information and to apply to be a member, please email researchgrants@nbt.nhs.uk.

SHC - Public Panel

What is Southmead Hospital Charity Research Fund?

  • A charitable fund established in 2006.
  • Applications are assessed in a two stage process
  • Supports research projects from all clinical areas, led by researchers of all levels of experience.
  • Supports high quality research projects with the potential for making a real impact within the NHS. 

Why do we have a public panel?

Benefits for research and healthcare:

  • Members of the public should help decide how donated public funds are spent 
  • Bring a unique perspective
  • Ensures that the process is focused on what is important to patients.
  • Ensure research has considered the participants point of view

Do I need any experience to take part in the public panel?

  • Everyone is welcome on the Public Panel, no previous experience needed. 
  • All perspectives are equally important 

When is the Public Panel taking place?

Two meetings will be held one around the end of July and the second at the end of September.

What is involved if I take part?

  • There will be a short introduction/training session about taking part- 1hr long
  • You will be expected to read and comment on Researchers applications for Funding before attending the meetings
    • The minimum you will need to read is a summary written in plain English of around one page long (500 words) per application
    • We expect there will be around 8-12 applications
    • We ask you to fill in a feedback form (4 questions) to get your comments on the researchers’ applications
    • We give you at least two weeks to read and comment on the applications
  • You will be expected to attend two panel meetings
    • The meetings are two hours long (with breaks) and will most likely be held online
    • In the meetings panel is split into smaller groups and discuss their opinions of the applications with one of our Facilitators
  • We ask two volunteers from our public panel to attend the awarding meeting to represent the views of the panel

Will I receive re-imbursement for my time?

  • You will receive payment for two hours of pre reading per meeting at £25 per hour and £5 for home working 
  • You will receive payment for attending the meetings at £25 per hour and £5 for home working

Microscopically controlled surgery (Mohs) Patient Information

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This page has information for patients who are having Microscopically controlled surgery (Mohs). 

Top tips for your surgery visit

  • Your surgery could take the whole day and usually at least half a day.
  • Please bring some lunch. Coffee and tea are available.
  • Please arrange for someone to collect you at the end of your procedure. It is not advisable to use public transport or to drive yourself. One family member may be able to stay with you during the day.
  • Please wear light, loose and easily removable clothes.
  • Make sure you arrive in good time for your appointment.

The Mohs micrographic surgery explained

Mohs micrographic surgery is a highly effective treatment for certain skin cancers. It can offer the best chance of cure whilst only taking the smallest amount of tissue necessary. The treatment allows the tumour to be removed completely bit by bit in one visit to the hospital, minimising the amount of normal skin removed and potentially reducing scarring.

Each time a piece of skin is removed, it is checked for cancer while you wait. This means you will sit in a recovery area near the operating theatre with a dressing on your wound between stages of the operation whilst the specimens are processed. If there is tumour left behind, further removal (another stage) is needed. Most patients need 1-3 stages before reconstruction. Each stage may take 1 hour or longer to be analysed. You may wait longer between stages as there will be several patients having treatments. 

Once the cancer is completely removed, we will usually reconstruct the wound on the same day. Occasionally it is better to wait a few more days for further tests or to see another surgeon. If this is necessary it will usually be discussed with you beforehand. Very occasionally it can become necessary to decide this on the day of surgery due to unforeseen circumstances.

Reconstruction of the wound may involve a skin graft or skin flap. This will be discussed with you.

Mohs micrographic surgery is usually carried out under local anaesthetic (i.e. you are awake). If a general anaesthetic is required for any part of your operation, this will be discussed with you.

Mohs micrographic surgery is most often used on basal cell carcinoma (BCC) when:

  • The tumour boundaries are difficult to see.
  • The tumour has regrown or some has been left behind after previous treatment.
  • The tumour is in an important area such as the nose, ear, lip, or eyelid where it is particularly useful to remove as little skin as possible.

A more detailed explanation and video demonstration of Mohs micrographic surgery is available online via: 

Dermatological surgery and laser unit - Overview | Guy's and St Thomas' NHS Foundation Trust (guysandstthomas.nhs.uk

What are the risks?

  • Bleeding: you may get some oozing from the wound after the operation. This is usually not serious but may lead to bruising. If this bleeding continues, it can usually be stopped by holding firm pressure on the wound constantly for 20 minutes. 
  • Scarring: every attempt is made to repair the wound in a way that will allow the scars to be hidden as much as possible. We will discuss repair options on the day. 
  • Incomplete removal and further treatment: we double check some results afterwards and very rarely find a tumour has been missed on the day. This can mean we recommend further treatment, but not always. 
  • Recurrence: the tumour rarely regrows years later.
  • Allergic reactions: this is extremely rare but you can get a reaction to rubber gloves, antiseptic solution, local anaesthetics, antibiotics and the dressing. Make sure to tell the doctor if you are allergic to any of these. 
  • Delayed repair: rarely if your tumour is complex, you may need to return a few days later for further surgery and repair. Occasionally, the wounds are large or complex and you may need another specialist surgeon, which we will discuss and arrange with you.

Before your operation

Things to be aware of: 

  • You will need to arrange time off from work or your usual responsibilities for at least 1 week after the surgery. The amount of time will depend on the complexity of surgery and the type of activities you normally do. You do not want to go on holiday within at least 2 weeks of surgery, which allows sufficient time for the wound to settle down and to have most problems dealt with before you go. Please discuss this with the doctor.
  • You may eat and drink normally before and after your operation, unless told otherwise.
  • If on Warfarin, please get a blood test (INR) five working days before surgery and find out the result. Please bring this result with you. The INR should be steady and between 2 to 2.5 ideally. If not please contact us straight away and ask your GP to alter your dose. If not we may have to cancel your surgery when you arrive.
  • We do not usually ask you to stop aspirin or other ‘blood thinning’ tablets unless you are taking more than one together. This should be discussed with you in clinic. These medicines include aspirin, dipyridamole (Persantin or Asasantin Retard), clopidogrel (Plavix), warfarin, dabigatran (Pradaxa), apixaban (Eliquis), rivaroxaban (Xarelto), edoxaban (Lixiana), and heparin. Usually, the reason for taking the medicine is more important than the minimal risk of a bad experience from some bleeding or bruising after surgery.
  • Take all other regular medications as normal.
  • Before you attend for surgery, please remove all make-up and jewellery from your face (i.e. earrings), not just from the area being treated.
  • If your surgery is in a hair-bearing area, we may clip the hairs nearby to improve access and ease of dressings. If you are shaving, please do so the night before surgery. There is some evidence that shaving just before surgery can increase the chances of wound infection.
  • Please tell the doctor well before your operation if you have any implanted devices - for example a pacemaker, defibrillator, deep brain stimulator etc. You may need a device check before the procedure if your usual check is overdue. If so, we will arrange that and let you know.
  • Smoking harms the healing process. You can improve your chances of good healing and a better scar by stopping smoking at least a few days before surgery, until at least a few days afterwards. This can be a good opportunity to kick start stopping altogether if you wish, which will help your general health too.
    For Stop Smoking advice phone: 
    0300 123 1044 
    or visit 
    Quit smoking - Better Health - NHS (www.nhs.uk)

What will happen on the day?

Please come to the Brunel building at Southmead Hospital. Report to the waiting area at Gate 24b. You will need to allow enough time to reach Gate 24b before your appointment. When you have arrived, a nurse will escort you to the theatre area, where you will be given a hospital gown to wear.

If you are late your operation may need to be cancelled. At times parking can be difficult so allow plenty of time. You can travel to the hospital by whatever means you wish, but you will not be fit to drive yourself home or use public transport after the operation.

The lesion may be photographed before and during the procedure with your consent. Local anaesthetic is injected to numb the area. You will be fully awake throughout the procedure. You may need repeated injections throughout the day to keep the area numbed. 

Occasionally if your wound is large or complex, another type of specialist surgeon may come to reconstruct your wound or might do this at your local hospital if you live far from Bristol. Sometimes you may need to go to the main operating theatres upstairs in the hospital for part of your operation or reconstruction. This will usually have been arranged in advance, and sometimes might involve a general anaesthetic.

Stitches

If you have stitches in your wound, we often ask you to come back the following week for them to be removed, or you may need to arrange to have them removed at your GP surgery.

If a change of dressing is needed, then either the practice nurse at your local GP surgery or district nurse could 
usually do this for you. We can help you arrange this on the day of surgery.

Will the area be painful afterwards?

  • After the local anaesthetic has worn off (approximately 2 hours), the area will often be somewhat painful and we advise you to take regular Paracetamol for the next couple of days (depending on your usual medications).
  • You may experience some bruising and swelling; this should settle down within a few days, but may last longer.
  • The surgeon may prescribe a course of antibiotics for you to take after the operation.

How will the wound be repaired/reconstructed?

There are several options depending on the size and position of the wound.

Healing naturally (secondary intention healing)

  • What does this mean? Healing naturally usually takes longer than if closed together (about one to two weeks per cm of wound diameter). It may be a good choice for a small wound that cannot easily be closed together or if you want a simpler, quicker operation to avoid a skin graft or skin flap, and reduce your visits to hospital.
  • How do I care for the wound? The wound will require a change of dressing two or three times per week until healed, but this is usually done by your GP practice or district nurse.
  • What will my scar look like? In the right area healing naturally usually ends up looking very good, but this can take many weeks.

Direct closure (sewing the edges together usually in a line)

  • When can this be done? Most Mohs surgery wounds are too complex to use this technique. Otherwise this usually gives the quickest healing, easiest aftercare, and best scar.

Skin graft (using a patch of skin from somewhere else)

  • Where does the skin graft come from? The “donor” site is usually where the skin is loose and thin and it is easy to stitch the edges together (e.g. above your collar bone, neck, or behind your ear).
  • How is the skin graft put on? The graft will usually be stitched in place. Often, a small wad of dressing material is stitched over to hold the graft firmly.
  • What will my skin graft look like? Usually some bruising and crusting in the first few weeks. It can take up to 18 months for a scar to ‘mature’, usually becoming pale, soft, flat and supple. Your doctor will do their best to match the skin graft to the skin removed so that it blends in as much as possible. Sometimes it is almost unnoticeable, but other times it is more difficult to hide and the differences to the surrounding skin are more obvious.

Local flap (moving nearby skin or muscle whilst still attached)

  • What will my local flap look like? The aim of using nearby skin is to provide a better match to the skin removed. Usually this is successful but the appearance varies similar to skin grafts.

 

Going home

Bleeding

When you go home you will have a bulky dressing covering your wound; this is essential for pressure to stop any bleeding. It is important to leave this on. If you experience bleeding from the wound, apply direct firm pressure to the wound for 20 minutes. This should stop the bleeding. If this does not help contact us on the numbers below, or your GP.

Infection

The usual signs of infection are pain, swelling, redness, increased temperature of the skin near the wound (or a fever), pus from the wound. Pain, swelling and redness are common in the first three days after surgery but should be improving. If not, the wound may be infected, and you may need antibiotics. If you see these signs seek medical advice from us or your GP.

Other tips

  • It is advisable to avoid alcohol for 48 hours after surgery to reduce the risk of bleeding.
  • If you are elderly or frail, we recommend having a relative or friend with you overnight after the surgery or at least contactable nearby.
  • Avoid bending over, straining, or exerting yourself, and sleep more upright than usual (i.e. with an extra pillow) for a few days to reduce swelling.
  • Once healed, care for any skin graft with daily moisturiser, and sunscreen when exposed. Grafts remain more sensitive long term.
  • Leave the dressing in place and dry for the first 48 hours, then remove it carefully or soak it off, unless you have been told otherwise (e.g. for skin grafts it is left     untouched for 7 days and removed by us in hospital).
  • Change a dressing if it gets wet or dirty. A wet dressing can lead to an infection. For skin grafts just change the outer dressing and do not disturb underneath, or contact us.
  • Keep the wound clean. Wash it daily after dressings have been removed, but avoid the direct force of the shower on the wound.
  • Apply petroleum jelly (e.g. Vaseline) from a new clean pot with a clean cotton bud several times a day.
  • You may have self absorbing stitches. These usually fall out within 3 weeks. Otherwise, stitches are usually removed after 7 days, in hospital or at your GP practice. 

Contact phone numbers

If you want to know more or have any questions or concerns, please contact us. 

If you have trouble with your wound in the days after surgery, the Dermatology nurses can be reached on  0117 414 8704 between about 9am - 5.30pm most weekdays, or call the secretaries on 0117 414 7621.

There is no Dermatology on-call service for wound problems out-of-hours, so there is a formal arrangement between Dermatology and Plastic Surgery to provide help instead.

  • Between 5 - 8pm on Monday to Friday, and between 8am - 8pm at weekends, please call the Plastic Surgery coordinator on 0117 414 8300
  • After 8pm, please call Southmead Hospital on 0117 950 5050 and ask to be put through to the Plastic Surgery SHO on call, quoting this leaflet.

Other options for problems out-of-hours include advice from your local out-of-hours GP service, walk-in centre, or the Emergency Department. If you must seek help show them this leaflet and please let us know what has happened as soon as possible afterwards.

Cancellation or rearrangement of an appointment

If you cannot attend or no longer need your appointment, please phone 0117 414 7416 and tell us.

Appointments are precious. Enable another patient to take your place. Please give us as much notice as possible.

© North Bristol NHS Trust.  This edition published December 2023. Review due December 2026. NBT002949

Cellular Pathology Key Contacts

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Contact our services using the key contacts below.

Contact Details

Job Title

Name

Contact Details

Lead PathologistDr Tim Bates

Tel: 0117 3427622

Email: timothy.bates@nbt.nhs.uk

Laboratory ManagerSaima Rasib

Tel: 0117 4149849

Email: saima.rasib@nbt.nhs.uk

Operations ManagerMark Orrell

Tel: 0117 4149875

Email: mark.orrell@nbt.nhs.uk

General Enquiries

Tel: 0117 4144890

Fax: 0117 4149390

Email: CellularPathologyCytologyEnquiries@nbt.nhs.uk /

 CellularPathologyHistologyEnquiries@nbt.nhs.uk

Address:

Severn Pathology

Cellular Pathology

Pathology Sciences Building

Southmead Hospital

Bristol

BS10 5NB

 

Test Information

Sample vials for testing

Includes details of sample types, volumes, special precautions, turnaround times & reference ranges.

Cellular Pathology Key Contacts

Declining a blood transfusion

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This page gives you information about your right to decline a blood transfusion or blood products as part of your treatment.

If you are a Jehovah’s Witness, you may have heard ‘blood products’ described as ‘fractions.’

Can anyone decline a blood transfusion?

Yes. North Bristol NHS Trust wants to be sure that we treat every patient in a way that recognises and respects their individual, cultural and religious beliefs.

As a Trust, we have a programme to conserve blood and minimise the number of transfusions given to patients. If you decline treatment with blood products we want to ensure that you make an informed decision; your doctor will discuss the possible risks and benefits of treatment with and without blood products.

  • It is your decision whether or not you are willing to accept the risks declining a blood transfusion and blood products. If you are a Jehovah’s Witness you may wish to discuss this with your ministers.
  • Please be aware that your doctor has the right to decide if they are unwilling to perform your surgery under these circumstances. 
  • If this is the case he or she will need to work with you to make a referral to a consultant who is known, in principle, to accept patients who request non-blood management. Your local Jehovah’s Witness Hospital Liaison Committee may be able to assist you or your doctors with this process.
  • This can be done using the Trust ‘Checklist’ and if you are a Jehovah’s Witness you may have an ‘Advance Decision to Refuse Specified Medical Treatment’ (this is provided by your local Ministers and is sometimes known as a ‘No Blood Form’). Show these documents to your medical team so that they can take copies and include them in your medical notes. 
  • You may have to go over the ‘Checklist’ more than once during your admission so that doctors directly involved in your care, who did not see you in Pre-Assessment Clinic, can confirm your wishes. This will definitely be required if more procedures are required than was originally expected.
  • At all times during your hospital admission, even if an emergency arises, we will respect your wishes.

What happens if I am admitted to hospital as an emergency?

If you are admitted to hospital as an emergency and we know your wishes, they will be respected. A team of medical professionals and the Jehovah’s Witnesses’ Bristol Hospital Liaison Committee have put together a plan of care for dealing with such situations and you can be confident that you will receive the best possible care and treatment during your hospital stay.

It is possible that in an emergency situation you may not be able to communicate your wishes. Therefore, it is essential that once you decide you do not wish to receive blood products you carry an ‘Advance Decision Form’ and may consider wearing a ‘No Blood Wristband’. 

I want to decline a blood transfusion and blood products

Once you have decided that you do not wish to receive a blood transfusion or blood products, there are several things you must do to help us respect your wishes:

  • Inform us in writing that you do not wish to receive blood transfusion or blood products. This can be done by completing the Trust ‘Checklist for Jehovah’s Witnesses and Other Patients who Decline Blood Transfusion’.
  • Carry an ‘Advance Decision Form’ with you at all times so that, if you are found unwell and cannot communicate, your wishes will be respected.
  • Before any operation sign a standard consent form, clearly indicating that you consent to the planned procedure but that you do not consent to a blood transfusion/ specified products.

What happens if I have a planned admission to hospital?

Before attending hospital for your surgery, you will be invited to a Pre-Assessment Clinic where you will see a doctor or nurse. At this appointment please make the nurse or doctor aware that you do not wish to receive a blood transfusion and any blood products you have specified as part of your treatment. 

If you can assist in this process by attending with a Trust ‘Checklist’ pre-prepared that will be helpful but, in any event, you should let the hospital team know your wishes as early as possible, so that they may plan your care. 

Please ensure that your wishes are specified in writing. 

What if I change my mind?

You have the right to change your mind about receiving a blood transfusion or blood products at any time. 

If you do change your mind, you must let your medical team know immediately so that your decision may be recorded in your medical records, and your treatment plan may be adapted according to your wishes.

I have further questions

If you have any further questions or concerns that are not covered by this leaflet, please discuss them with a member of your medical team. If they are unable to answer your questions they will find someone who can.

Further help for Jehovah’s Witnesses

Further help is available from:

Your local minister.

The Bristol Hospital Liaison Committee for Jehovah’s Witnesses. Contact details can be provided by a member of your medical team, or alternatively you can make contact by email: info@bristol-hlc.org.uk

© North Bristol NHS Trust. This edition published April 2023. Review due April 2026. NBT003190.

Advice following a blood tranfusion

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This page has information for patients who have had a blood transfusion. 

Most blood transfusions take place without problems but having a blood transfusion carries with it a very small risk of developing 
side effects. These may develop within several hours, or in some cases may happen days or weeks later.

These side effects are often mild, but it is still important to report any unusual or unexpected symptoms to a doctor or nurse (or midwife if your transfusion was related to pregnancy/childbirth).

Please contact the hospital for advice if you experience any of the following after having a blood transfusion:

  • A high temperature - feeling feverish, hot, and clammy.
  • Shivering or ‘cold chills’.
  • Breathing problems.
  • Extreme tiredness.
  • Passing blood in your urine.
  • Passing much less, or very dark, urine.
  • Itchy skin rash.
  • Pain in the lower back (loin pain).
  • Unexpected or unexplained bruising.
  • Jaundice (yellow colour of the white of your eyes or your skin).

When contacting the hospital for advice, please inform the hospital staff that you have recently had a blood transfusion.

On discharge the staff will explain to you how to obtain assistance in the event of a problem (both 'in hours' and 'out of hours'), and will give you a written copy of this information in a leaflet and:

  • The ward/departments daytime, and night time/weekend contact phone numbers.
  • The date and time of last transfusion.

If you are unable to make contact with the hospital where you had your transfusion, then please contact your GP as soon as possible.

In the rare event of an emergency (life threatening problems, for example difficulty with breathing), call 999 for an ambulance and bring your leaflet into hospital with you.

If you would like further information or advice about this, or other aspects of blood transfusion, please discuss this with your hospital doctor, nurse or midwife.

References 

Acknowledgements: The Leeds Teaching Hospitals NHS Trust, Taunton & Somerset Hospital NHS Trust)

Information contained in this leaflet has been produced in collaboration with the NHSBT Better Blood Transfusion Team.

© North Bristol NHS Trust. This edition published January 2024. Review due January 2027. NBT002585

Anti-synthetase syndrome

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Information for patients about anti-synthetase syndrome. 

Anti-synthetase syndrome is an autoimmune disease. This means that the condition and the symptoms associated with it, are caused by your immune system being over-active. Anti-synthetase syndrome presents with a set of symptoms, together with the identification of one of several specific antibodies against your own cells, known as anti-synthetase autoantibodies. These autoantibodies are immune system proteins that target specific proteins within your own body (the tRNA synthetase enzymes).

Eight anti-synthetase antibodies have been identified so far as being significant in this disease. By far the most common of these is anti-Jo-1. Others include PL-7 and PL-12. Five additional anti-synthetase antibodies have been identified so far, but these are much rarer.

What are the symptoms?

Not all patients with anti-synthetase syndrome are the same. It is a spectrum condition, where there can be a mixture of symptoms, or some symptoms are more prominent. Symptoms associated with anti-synthetase syndrome include the following:

Interstitial Lung Disease (ILD)

As many as 75% of those with anti-synthetase syndrome have ILD. This may be the first or only symptom of the condition. 

The ILDs are a group of lung diseases where there are varying degrees of lung inflammation or irreversible scarring (fibrosis) of the tissue around the air sacs (alveoli). In ILD it can be more difficult for the lungs to transfer oxygen into the bloodstream, and as a result, the body may not get the oxygen it needs to function properly. This can cause breathlessness and/or a cough from the irritation.  Patients may also complain of fatigue.  A ‘crackle’ sound is heard when listening to the chest with a stethoscope.

Muscle inflammation

Patients may experience muscle pain, fatigue and weakness. This typically affects the muscles across the shoulders and the pelvis/thighs.

Inflammatory arthritis

Patients may experience pain, stiffness, swelling, redness or warmth around joints. This typically affects small joints hands, feet but larger joints can be involved as well.

Fever

Some patients can present with a fever that is unrelated to infection or other causes. 

Raynaud’s phenomenon

This is when very small blood vessels can spasm or constrict leading to reduced blood flow, typically involving the fingers and toes. The nose and ears can also be affected. These episodes are usually triggered by cold or stress.  They can last several minutes to several hours and can cause the affected part to feel numb and cold and to turn white or blue.

Mechanic’s finger or hands

The skin on the sides of the fingers (usually just the thumb, index and middle fingers) becomes dry and cracked with characteristic thickening. It can be sore with broken areas. 

What tests will I have?

Your specialists will take a detailed medical history and perform a thorough physical examination. You may be asked to have the following investigations:

  • Chest X-ray.
  • Lung function tests – breathing tests which so how well your lungs are working. These are used later to monitor your lung disease and how it is progressing. You may also be asked to have a walk test where you will be asked to rate your degree of breathlessness and measure your walking distance and oxygen levels.
  • A CT scan of your chest shows a detailed picture of your lungs. There are characteristic features on the CT scan that can allow your specialist to identify either scarring or inflammation of lung tissue.
  • A series of blood tests including a screen for specific autoantibodies related to CTD-ILD.
  • Some people may also have a bronchoscopy, where a small flexible tube is passed down into your lungs, allowing collection of cells which may help with diagnosis.
  • If you have joint and muscle symptoms, additional tests will include joint X-rays, ultrasound scans, and muscle MRI scans.

What treatment is available?

Treatments may differ depending on the symptoms you have, and your specialist will discuss whether a particular treatment is right for you.

Medications

Steroids are produced naturally in the body by the adrenal gland. Additional steroids in the form of prednisolone can be given to attempt to reduce inflammation in some patients. They are usually given in tablet form but may be given intravenously. If you are prescribed steroid tablets on a long-term basis, you should not stop them abruptly. You will be given a ‘steroid emergency card’ which you should always carry with you.

The specialist may also assess the need for bone protection medication and anti-reflux treatment whilst on steroids.

Immunosuppressive medication

Cyclophosphamide, Mycophenolate mofetil and Azathioprine are medications that modulate the immune system to achieve disease control.

When used with a corticosteroid such as prednisolone, it can also allow the dose of the steroid to be reduced and in some cases, may allow the steroids to be withdrawn altogether. As a result, they are sometimes also called a ‘steroid-sparing agent’. You will require regular blood tests to monitor your response to treatment.

New treatments are becoming available, and your specialist will decide upon these treatments on an individual basis.

Other medications and therapies are used to relieve symptoms, such as cough, breathlessness, joint and muscle pain and Raynaud’s. Your specialist will discuss options with you on an individual basis.

Other treatments

Pulmonary rehabilitation is a supervised exercise and education programme that can help you to learn to manage your breathlessness and remain active. The programmes are multidisciplinary, meaning that the team includes respiratory physiotherapists, nurses, dieticians, doctors and others, and can help improve your energy, strength, and quality of life.

As fibrosis inhibits an adequate supply of oxygen into the bloodstream, some individuals may require supplemental oxygen therapy. Where the levels of oxygen are low, oxygen therapy may help with breathlessness and enable individuals to be more active. Corrected levels of oxygen in the blood are necessary for normal body functions and reducing additional health problems.

You should also discuss with your physician if there are any clinical trials in which you can participate. Clinical trials are voluntary research studies, conducted in people, which are designed to answer specific questions about the safety and/or effectiveness of medications.

A small minority of patients may require assessment for and be suitable for lung transplantation.

How can I help myself?

Have your seasonal vaccinations (COVID-19 and Flu) and the pneumonia vaccination (you only have this once).

You may be eligible for a variety of benefits such as Attendance Allowance or Personal Independence Payment if you need help with personal care or getting about.

Our specialist nurse runs a regular Pulmonary Fibrosis Support Group which is a space for discussion with other patients with ILD. Here we also aim to provide several presentations from a variety of guest speakers and charities.

Keep active and do what you enjoy!

Further information and resources

Action for pulmonary fibrosis: 
Home (actionpf.org)

British Lung Foundation: 
Asthma + Lung UK (asthmaandlung.org.uk)

Versus Arthritis UK: 
Versus Arthritis | A future free from arthritis

Myositis UK: 
Home - Myositis UK
 

How to contact us

For ILD related queries:

Bristol Interstitial Disease Service
Respiratory admin 0117 414 7762
ILD@nbt.nhs.uk

For CLD related queries (not related to lungs/breathing):

Rheumatology advice 0117 414 0600
rheumatologyadviceline@nbt.nhs.uk

© North Bristol NHS Trust.  This edition published May 2024. Review due May 2027. NBT003470.

Care of plaster casts

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Care of plaster casts

Your cast may be made out of plaster of Paris or a synthetic material. The following advice is for both types. You will also be given verbal advice.

It is important that you eat a healthy diet and drink plenty of fluids to help with bone and wound healing while you are in a cast. 

Please help us look after your plaster. It is an essential part of your treatment. We hope the following information will help you. 

Do

  • Exercise joints not held in the plaster as much as possible.
  • Elevate the limb, especially during the first 2 weeks. Don’t let your limb hang down unless being used.
  • Use sticks, crutches, or frames as instructed. Please return equipment when it is no longer needed after you are discharged.
  • Keep your plaster completely dry.
  • Wear the shoe provided if you are allowed to weight bear on the plaster.
  • Take advice before driving.
  • Take advice before flying or travelling. 

Do not

  • Interfere with your plaster in any way.
  • Poke anything down your plaster.
  • Write on your plaster of Paris for 48 hours after it’s been applied.
  • Write on your synthetic plaster for 2 hours after it’s been applied.
  • Leave your limb unsupported or stand for long periods.
  • Stand or put weight on your plastered limb unless instructed by the doctor, nurse, or physiotherapist.
  • Cut your plaster.
  • Get the plaster wet. It may disintegrate (fall apart) or cause skin problems.
  • Smoke. Do not smoke as this slows down bone healing.

Please ring us if your plaster:

  • Rubs.
  • Cracks.
  • Itches excessively.
  • Softens.
  • Becomes loose or uncomfortable.

Please ring us first, then return to the hospital immediately if the following happen (out of hours go to the Emergency Department): 

  • Your toes or fingers become blue, pale, or discoloured.
  • Sudden increase in swelling, numbness, or pins and needles.
  • Your limb becomes more painful.
  • You feel “pins and needles” or numbness.
  • You have a blister-like pain or rubbing under the plaster.
  • You have discharge, wetness, or smell under your cast.
  • You drop any object down inside your cast.

Deep Vein Thrombosis (DVT) and Pulmonary Embolism (PE)

What is a DVT? 

A DVT is a blood clot that forms in a vein. It is possible for a DVT to form in any vein but it most commonly happens in the leg.

What is a PE?

A PE is a blood clot in the lungs, caused when part of a DVT breaks off and travels in the bloodstream to the lungs. 

What can I do to reduce my risk of getting a DVT/PE? 

  • Stay as mobile as possible. If walking is difficult exercise your legs and feet by flexing your knees and ankles, rotating your feet, and wriggling your toes. Do this as often as you can.
  • Drink plenty of fluids as dehydration increases your risk of getting a DVT or PE. (Renal patients, please check your fluid allowance with your renal clinical team).
  • If you have been given stockings or injections to reduce the risk of DVT/PE, please use them as instructed.
  • Eat a healthy diet and maintain a healthy weight.
  • Don’t smoke.

How do I know if I have a DVT or PE?

Signs of a DVT include: 

  • Pain.
  • Swelling.
  • Discolouration of the skin (red, purple, or blue).

Signs of a PE: 

  • A cough - with or without blood stained phlegm.
  • Breathlessness - more than usual for you.
  • Chest pain.
  • Collapsing (this is an emergency - phone 999).

If you develop any of the symptoms or a DVT or PE please get medical advice the same day. Phone 111, your GP surgery, or go to the nearest Accident and Emergency Department.

Remember

If you have any problems or concerns about your plaster, don’t hesitate to contact the staff. 

Driving advice

We advise that you do not drive whilst in a cast, boot, or splint.

Any concerns please contact your car insurer or the DVLA.

Holiday insurance advice

If you plan to go on holiday and you have taken out holiday insurance, please inform your insurance company.

If you plan to go on holiday and have not taken out holiday insurance we advise that you do. If you develop any complications whilst away you may not be covered.

© North Bristol NHS Trust. This edition published October 2024. Review due October 2027. NBT002018

Support your local hospital charity

Southmead Hospital Charity logo

Find out about what we do and how you can support us. 

Contact Plaster Room

0117 414 8607 or 0117 414 8606

Monday to Thursday: 08:30 to 17:30

Friday: 08:30 to 16:30

Weekends and bank holidays: 09:00 to 13:30

Information on your brace

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Information on your brace

This page should be used as a general guide only.

  • Make sure you fasten the straps securely but not overly tight.
  • Wear the brace next to skin - not over clothes.
  • The brace should not hurt, but you may feel a little uncomfortable while you get used to it.
  • Remove the brace to check the skin at regular intervals.
  • If you have any rubs or red mars, contact the plaster room.
  • Most braces can be washed with soap and water and left to air dry.
  • Do not place on or near a heat source.
  • If you are having any problems with the brace contact the plaster room.
  • If you are concerned the brace is causing a sore, leave it off and contact the plaster room.

Deep Vein Thrombosis (DVT) and Pulmonary Embolism (PE)

What is a DVT? 

A DVT is a blood clot that forms in a vein. It is possible for a DVT to form in any vein but it most commonly happens in the leg.

What is a PE?

A PE is a blood clot in the lungs, caused when part of a DVT breaks off and travels in the bloodstream to the lungs. 

What can I do to reduce my risk of getting a DVT/PE? 

  • Stay as mobile as possible. If walking is difficult exercise your legs and feet by flexing your knees and ankles, rotating your feet, and wriggling your toes. Do this as often as you can.
  • Drink plenty of fluids as dehydration increases your risk of getting a DVT or PE. (Renal patients, please check your fluid allowance with your renal clinical team).
  • If you have been given stockings or injections to reduce the risk of DVT/PE, please use them as instructed.
  • Eat a healthy diet and maintain a healthy weight.
  • Don’t smoke.

How do I know if I have a DVT or PE?

Signs of a DVT include: 

  • Pain.
  • Swelling.
  • Discolouration of the skin (red, purple, or blue).

Signs of a PE: 

  • A cough - with or without blood stained phlegm.
  • Breathlessness - more than usual for you.
  • Chest pain.
  • Collapsing (this is an emergency - phone 999).

If you develop any of the symptoms or a DVT or PE please get medical advice the same day. Phone 111, your GP surgery, or go to the nearest Accident and Emergency Department.

© North Bristol NHS Trust. This edition published October 2024. Review due October 2027. NBT003231

Support your local hospital charity

Southmead Hospital Charity logo

Find out about what we do and how you can support us. 

Contact Plaster Room

0117 414 8607 or 0117 414 8606

Monday to Thursday: 08:30 to 17:30

Friday: 08:30 to 16:30

Weekends and bank holidays: 09:00 to 13:30