Cone biopsy

Making decisions about treatment 

Before you make a decision about treatment, it is important to understand the procedure, including benefits, risks and possible effects. Your colposcopist should explain these to you and give you the chance to ask any questions. You may also want to talk over your options with your family or friends.

It can help to write a list of questions and take it to your appointment. The form below suggests some questions you might like to ask and has space for you to write down any others you think of.

Questions you could ask 

• What types of treatment can I have?
• What does the treatment do?
• What could happen if I choose not to have treatment?
• How long will the treatment take?
• Do I need to bring anything to the appointment?
• Will I be able to get home by myself after treatment?
• What physical effects might I experience after treatment?
• What emotional effects might I experience after treatment? 

Preparing for cone biopsy

Your appointment will happen in a colposcopy clinic at a hospital. You may have a cone biopsy as an outpatient or an inpatient. This could mean you either:

• have the treatment and can go home the same day
• need to stay overnight in the hospital.

Read about colposcopy >

You usually have a general anaesthetic for a cone biopsy. This means you will be asleep during the surgery and won’t feel anything. 

The hospital wants to keep you and their staff protected from COVID-19 (coronavirus), so they will be following government guidance on social distancing and using appropriate personal protective equipment (PPE), including masks, gloves and aprons. You will also need to wear a face covering while in the hospital. 

If you take blood thinning medication or have a condition that affects your blood, it is important to tell your colposcopist before your appointment. You may have a higher risk of bleeding after the treatment.

 

What can and can’t I do after cone biopsy?

You may have some physical effects after cone biopsy. These usually last up to 4 weeks. Until these have stopped, it is best to avoid:

• tampons or menstrual cups – you can use a period pad instead
• penetrative vaginal sex – including fingers, tongues and other objects
• heavy exercise that causes you to sweat, such as running or a gym workout
• swimming
• long baths – you can continue to shower as normal.  

If you have any questions about what you can and can’t do after cone biopsy, speak with your colposcopist. 

Risks of cone biopsy

Cone biopsy is usually successful. The benefit of the treatment is that it can prevent potential cervical cancer from developing or remove cervical cancer which, in many cases, will outweigh the risks. However, like all treatments, cone biopsy has risks and you may have some physical or emotional effects because of the treatment. 

Talk to your colposcopist before treatment if you are worried about any risks. They can answer your questions and give you support. After treatment, your GP or a specialist doctor will be able to offer support.

Bleeding  

About 85 in 100 (85%) people experience bleeding after this type of treatment. About 15 in 100 (15%) people do not experience bleeding. Bleeding is expected after cone biopsy and can last between 2 days to up to 4 weeks. 

You may have bleeding because of the soft scab that forms on the cervix where the cells were removed. This may bleed while it heals. 

The bleeding is usually like a period, but may be slightly heavier than your normal period. About 10 days after treatment, the bleeding may get heavier. This is common and a sign that the scab is healing. Your first period after treatment may be slightly heavier or out-of-sync with your regular cycle. 

Important! If you are on blood thinning medication or you have a haematological condition, you must tell your colposcopist because you may have a higher risk of bleeding after cone biopsy. If the bleeding is soaking through a period pad every hour, call the contact number given by your colposcopy team or call 111 out of hours. This is sometimes called delayed haemorrhaging. The hospital team or 111 will be able to advise you and make sure you get the right care. 

Pain   

About 67 in 100 (67%) people experience pain after this type of treatment. About 33 in 100 (33%) people do not experience pain. 

Some pain is expected for between 2 days to up to 4 weeks after treatment. The pain varies from person to person, but should not be too severe. It is often described as a cramping pain, like a period. You can talk to your doctor about over-the-counter medication that should help.  

Important! Some people may experience pain for longer, but it usually goes away within 3 months. If you are in a lot of pain or find it is affecting your day-to-day life, talk to your GP. They can advise on pain medication, offer reassurance based on your medical history and, if needed, will be able to check you are healing properly.

Changes to vaginal discharge

About 65 in 100 (65%) people have changes to their vaginal discharge. About 35 in 100 (35%) people don’t have any changes to their vaginal discharge. 

Changes to vaginal discharge can last for about 4 weeks. Straight after treatment, you may have a watery, brown vaginal discharge. 

About 10 days after treatment, you may notice a coffee granule-like vaginal discharge. This is normal and a sign that the soft scab on your cervix is healing. 

Important! Between about 1 and 14 in 100 (0.8% to 14%) people get an infection after cone biopsy. Talk to your GP if your vaginal discharge smells bad, or is a yellow or green colour. If there is a chance you have an infection, you will be offered antibiotics.

Premature birth or late miscarriage

You should still be able to have children after a cone biopsy. It’s a smaller surgery, so you will still have:

• most of your cervix 
• your womb 
• your ovaries.

After a cone biopsy there is a slightly higher risk of miscarriage and premature birth, as well as complications if the baby is very premature. This can be very distressing to think about.

If you have had a cone biopsy, the risk of giving birth before 37 weeks is about 11 in 100 (11%). If you have not had treatment, this risk is about 7 out of 100 (7%).

If you get pregnant in future, it is important to tell your midwife that you have had a cone biopsy. They may offer to do an ultrasound scan of your cervix. If they think it is short and there is a risk you may have the baby a bit early, they may offer you a cervical stitch (cervical cerclage). This is an operation where a stitch is placed around the cervix. It is usually done between 12 and 24 weeks of pregnancy, although it may be done later.

Speak to your healthcare team to find out your individual risks and what can help. The charity Tommy’s also provides information about having a safe and healthy pregnancy.

Read about pregnancy on the Tommy’s website >

Other possible risks of treatment

Jo’s Cervical Cancer Trust has spoken with women and people with a cervix who have had treatment for cervical cell changes to understand their experiences. In most cases, they had LLETZ for high-grade cell changes – CIN2 or CIN3. The figures in this section are taken from that research to help you feel as prepared as possible.

It is important to remember that everyone heals at a different pace and will have a different experience after treatment.

Impact on your feelings 

You may have strong feelings about what treatment means for your physical wellbeing and future. These feelings could be positive, such as relief that you have had treatment, but you may also feel worried about how your body will recover. 

For the women and other people with a cervix that we spoke with:

• 86 in 100 (86%) had fears about cancer, while 14 in 100 (14%) did not
• 71 in 100 (71%) had anxiety after treatment, while 29 in 100 (29%) did not
• 45 in 100 (45%) had fears about their fertility, while 55 in 100 (55%) did not
• 24 in 100 (24%) experienced depression after treatment, while 76 in 100 (76%) did not.

All of your feelings and concerns, including any we don’t mention in this guide, are valid and it is important you get the right support to deal with them. Here are some of the ways you could get support.

Get support from loved ones

Some people find that a support network of friends and family helps their emotional recovery after treatment. There are lots of ways they can help, from talking your feelings through, to offering a distraction and positive presence. 

Talk to your GP or another trusted doctor

Before, during and after treatment, you will be in the care of professionals who want to make the experience as good as possible for you. If you are worried about anything, talk to them so they can give you the right support and ease any concerns. Or, if you have another doctor you know and trust, ask to talk with them about any worries.

Get support from Jo’s Cervical Cancer Trust and other charities

There are many charities and organisations who offer support services so you can feel listened to and work through your feelings. These services can also signpost to other places that may be able to help. 

Get support >

Ask for a referral to counselling

If you feel that expert support would help, you can self-refer or ask your GP to make a referral for NHS counselling. You can also make an appointment privately, for a cost.

Search for a private counsellor on the British Association for Counselling and Psychotherapy website >

Sex and relationships

You may experience sex and intimacy differently after treatment. This may also have an impact on your relationships. These differences may be because of physical changes, emotional changes, or both. 

In the women and other people with a cervix that we spoke with, about 46 in 100 (46%) had changes to how they feel, while 54 in 100 (56%) did not. These changes included feeling less attractive or confident, as well as worries about passing on HPV.

Pain during or after sex

About 33 in 100 (33%) people had pain during or after sex, while 67 in 100 (67%) did not. In most cases, this pain lasted for less than 3 months. In some cases, pain during or after sex lasted for:

• between 3 and 12 months in 5 in 100 (5%)
• between 1 and 3 years in 6 in 100 (6%) 
• between 3 and 5 years in 3 in 100 (3%) 
• more than 5 years in 5 in 100 (5%). 

Bleeding during or after sex

About 22 in 100 (22%) people had bleeding during or after sex, while 78 in 100 (78%) did not. In most cases, the bleeding lasted for less than 3 months. In some cases, the bleeding lasted for:

• between 3 and 12 months in 3 in 100 (3%)
• between 1 and 3 years in 3 in 100 (3%) 
• between 3 and 5 years in 1 in 100 (1%) 
• more than 5 years in 2 in 100 (2%).

Getting support

It is important to see your GP if you have any symptoms such as pain or bleeding. They can examine you and talk through ways to make it better, such as using more lubricant during sex to lessen any pain.

It may help to speak to a trusted person about any loss of confidence – whether that is a partner, family, friends, your GP, or other people who have had treatment. Talking through your worries might ease them or give you new ideas about how to handle them. 

If you and a partner are struggling to reconnect after treatment, you may want to consider couples counselling. An unbiased expert can help you start and explore conversations around sex and intimacy, so you can find solutions together. You can self-refer through local NHS services, speak with your GP, or search for a local counsellor yourself.