Pharyngoplasty is an operation to change the shape and function of the soft palate and the area around it called the pharynx. Some children whose cleft involves the palate develop a ‘nasal’ tone to their voice, because the soft palate is too short and air escapes through their nose when speaking.
A pharyngoplasty aims to reduce the space behind the palate so less air escapes during speech. Other children with nasal speech, not caused by a cleft palate, can also benefit from the pharyngoplasty operation.
Is there anything I should do before the operation?
Where possible, we advise you to keep your child away from children or adults who have colds, ‘flu’ or other infections in the weeks running up to the operation. This will reduce the chance that your child’s operation will have to be postponed because he or she is not well.
What happens before the operation?
You will receive basic information on coming into hospital with your admission letter.
You will need to bring your child to Dinosaur ward for a pre-admission appointment in the month leading up to the operation. The purpose of this appointment is to meet the ward team who will be looking after your child. The nurses will show you around the ward, explain about your stay and ask you some general questions. Your child will need to have a medical check up and maybe a blood test to make sure he or she is well. Some photos may be taken for medical records.
A doctor may also come to see you to explain the operation in more detail, discuss any worries you may have and ask you to give your permission for the operation by signing a consent form. If your child has any medical problems, such as allergies, please tell us. If your child is taking any medicines, please bring these with you. Another doctor (an anaesthetist) will visit you on the day of surgery to explain about the general anaesthetic.
What does the operation involve?
The operation is carried out by one of the specialist surgeons in the team. It involves shaping the tissue at the back of the throat to make it easier to block off air escaping through the nose. No tissue or material is taken from elsewhere. The surgeon uses an operating microscope to allow the small structures to be accurately shaped.
The operation usually takes from one to two hours, but expect your child to be away from the ward for two to three hours.
What anaesthetic is used?
Your child is given a general anaesthetic by an anaesthetist who specialises in giving anaesthetics to babies and children. One parent or carer may be able to go with your child to the anaesthetic room and stay until he or she is asleep.
This usually involves your child breathing some anaesthetic gas. Later, a tube is passed into the airway (trachea) to safeguard breathing. A cannula (thin, plastic tube) is put in a vein and usually left in place for a short time after the operation. Fluids are given through this tube during the operation and afterwards.
Are there any risks?
There is a small risk of infection following this or any operation, but your child will be given an antibiotic during the operation, and continue to take antibiotics afterwards in liquid or syrup. Every anaesthetic carries a risk of complications, but this is very small.
Your child’s mouth will be sore after the operations, but the nurses will give your child pain relief medicine.
If your child’s mouth swells a lot after the operation, he or she may have difficulty breathing for a while. This complication is rare. If this happens, the doctors will put a tube in your child’s nostril to make breathing easier while the swelling goes down.
It is likely that your child will snore to some extent immediately after the operation. Breathing through the nose will be reduced but some children overcome this by breathing through their mouth. This usually improves over a few weeks and rarely continues.
When can I see my child after the operation?
Your child will go to the recovery room after the operation and one parent or carer will be able to go there with a nurse as your child is waking up. During the operation, local anaesthetic is put in the wound and the anaesthetist gives intravenous pain relief to reduce postoperative discomfort. Nonetheless, your child may be distressed and hungry.
We expect there to be a little blood around the face from the nose or mouth, but this is entirely normal and nothing to be concerned about.
When will my child have something to eat and drink?
We are happy for your child to have something to eat and drink as soon as he or she is awake after the anaesthetic. The first few times may be difficult, partly because the lip is numb from the operation. We advise a soft diet for the first two weeks after the operation.
More information about food and drink is in the later section When you get home.
What happens afterwards?
At first there may be some bleeding from the mouth but this usually stops quickly. Only very rarely will any further measures be necessary to stop the bleeding. The corners of your child’s mouth may become sore after the operation but this will improve within a few days.
When your child has returned to the ward, fluid and puree food may be offered as soon as he or she is awake. If your child is reluctant to drink it may be necessary to give extra fluid through the drip. The drip will be removed once he or she is drinking well again. It is important to give your child some sterile water after eating and drinking to keep the wound clean.
Your child will have a sore mouth after the operation and so may not feel like eating or drinking much. Various medicines can be given at regular intervals to help ease the pain and make feeding more comfortable.
A course of antibiotics will be prescribed to reduce the risk of infection. You will need to continue giving this medicine for a few days after leaving hospital to complete the course.
When you get home
Feeding
By the time your child goes home, he or she should be getting back to a normal pattern of food and drink. We recommend a soft diet for two weeks after the operation. This could include cereal with warm milk, custard, tinned spaghetti, mashed potato, yoghurts and fruit. Your child should not have hard foods such as crisps, apples, toast, chips, bread or boiled sweets for the first two weeks or so. It is also important to make sure that your child is drinking enough.
Please encourage your child to rinse his or her mouth well with water after all food, drink and liquid medicines. This helps cleanse the palate and stops food collecting around the operation site, which could lead to infection or wound breakdown.
Your child’s swallow may feel different after the operation so please reassure him or her that it will improve and take time to adjust.
Medicines
Your child will need to take a course of antibiotics, which we will give you before you go home. It is important to finish the course as instructed on the bottle even if your child has recovered well. You can give pain relief medicines, such as paracetamol syrup or ibuprofen syrup, at home following the dosage instructions on the bottle.
Infection
Infection after cleft palate repair is rare, but signs of infection include:
- Swelling or redness of the palate
- Irritability
- Raised temperature
- Loss of appetite
If your child develops any of these signs, please call the ward or your family doctor (GP), as a repeat course of antibiotics may be needed.
Rest and recuperation
Try to keep your child away from people with coughs and colds for the first few weeks after the operation. You may want to keep your child away from school for about two weeks.
Follow up
The
Speech and Language Therapy department will send you a routine follow up appointment for around six months after the operation. Sometimes, the therapist will want to see your child three months after the operation but we will have explained this when the operation was planned.
If you have any questions, please call:
- Great Ormond Street, Children’s Hospital, Peter Pan Ward 020 7829 8825
- Clinical Nurse Specialist 020 7813 8439
- St Andrew’s Centre, Broomfield Hospital, Moonbeam Ward 01245 516 094 or 01245 516 095
- Clinical Nurse Specialist 01245 516 029
Last reviewed by Great Ormond Street Hospital: September 2009
Ref: 09F0797 © GOSH Trust September 2009
Compiled by the North Thames Cleft Centre at Great Ormond Street Hospital and St Andrew’s Centre, Broomfield Hospital in collaboration with the Child and Family Information Group at GOSH
This information does not constitute health or medical advice and will not necessarily reflect treatment at other hospitals. If you have any questions, please ask your doctor. No liability can be taken as a result of using this information.
