Breast Reconstruction Surgery – Possible Side Effects

 

  

Reconstructive breast surgery is now more common than it used to be, with techniques and implants improving all the time, and the risk of complications reducing. However, there are still some risks connected with any type of surgery and a few that are particularly connected with breast reconstruction using breast implants. If you are worried about any of these possible problems, please talk to your surgeon.

 

Side effects and complications specific to breast enhancement surgery are rare, but may include: implant rupture/deflation, capsular contracture, infection, necrosis, haematoma/seroma, inflammatory reaction, extrusion, wrinkling and folds, interference with standard mammography, pain, breast feeding complications, change in breast sensation, dissatisfaction with cosmetic results, rotation, ptosis, distortion, calcification, tissue atrophy/chest wall deformity, gel diffusion, adulterated fill, inadequate tissue flap, and deformation.

 

Rupture

 

If the outer shell of a silicone breast implant breaks (this is called implant rupture), the gel usually stays in the area around the implant, and on rare occasions very small amounts of silicone might move into other parts of the body. This migration of silicone is diminished with improved modern implants, and current research does not indicate any adverse effects from this ‘free’ silicone gel, except the presence of some local enlarged lymph nodes. In some cases rupture might be ‘silent’ and not cause any symptoms. However, most surgeons recommend that a ruptured implant is removed.

 

Gel leakage

 

In rare cases, minute quantities of silicone might diffuse through the shell of gel-filled implants. However with the advance of implant technology and shell design such as barrier coating, gel diffusion is drastically reduced. If gel did leak out, it would mostly be contained by tissue that the body forms around the implant which helps prevent the gel from seeping into surrounding tissues. Leakage of a small amount of silicone rarely causes problems and usually does not require any action. If there is a lot of leakage, your surgeon may recommend further surgery.

 

Deflation

 

This can occur with saline implants immediately or slowly over a period of time and is noticed by loss of size or shape of your breast. Causes of deflation include damage during surgery, capsular contracture, trauma or intense physical manipulation and unknown/ unexplained reasons. A deflated implant requires additional surgery to remove and to possibly replace the breast implant.

 

Rippling of the breast implant

 

Visible rippling may occur with implants.

 

Capsular Contracture

 

When any foreign body, such as a breast implant, is put into your body, your immune system responds by forming fibrous tissue (a capsule) around it. Within the natural healing process, this fibrous tissue might contract. This is known as capsular contracture. If this contraction is severe, you may have tightening, hardening, and changes in the shape of the reconstructed breast, which may be uncomfortable.

 

In many patients, contractures will never occur. In other patients contractures can occur weeks or years after implantation, as the body’s response to any foreign object varies greatly from person to person. How much the capsule will contract, if at all, is hard to predict. In some cases, correction of capsular contracture may require surgical intervention and it is possible for capsular contracture to reoccur. Nevertheless improvements in breast implant design, especially with textured implants, and surgical techniques have contributed to reduce the rates of capsular contracture.

 

Reoperation

 

Additional surgery to the breast and/or implant will likely be necessary over the course of their life. You may decide to change the size or type of implant, requiring a reoperation, or you may have a reoperation to improve or correct your initial surgical outcome.

 

Breast Implant Removal

 

Breast implants have a limited lifetime and the implant may have to be removed or replaced which may necessitate revision surgery. Various factors, including the type of implant inserted, the type of surgery, injury to the breast, and excessive repetitive compression of the implant, may impact the longevity of the implants.

 

Pain

 

As expected following any invasive surgical procedure, pain of varying intensity and duration may occur following breast implant surgery. Very occasionally, severe pain associated with arm movement has been reported. If you have any pain following surgery, you should contact your surgeon or doctor for prompt investigation.

 

Changes in the Nipple

 

It will not be possible to preserve the nipple if there is any possibility that it may contain cancer cells. Although it is possible to reconstruct the nipple, it is important to note that reconstructed nipples usually have no sensation; you can discuss this with your surgeon, who can advise you what your options are.

 

Infection

 

Infection is possible in any operation. If you develop an infection you will need to see your doctor as soon as possible and you may need to have a further operation to remove the implant or tissue expander until the infection has cleared and then replace your implant. Although most infections can be treated successfully, infections can cause serious problems and may result in increased scarring. In a small number of cases these infections may come back.

 

Dissatisfaction with Cosmetic Results

 

Scar deformity, hypertrophic scarring, capsular contracture, asymmetry, displacement, incorrect size, unanticipated contour, palpability, and sloshing (Natrelle 150 and saline-filled implants), may occur. In some cases, cosmetic concerns may also lead to medical concerns. Careful surgical planning and technique can minimise, but not preclude, the risk of such results. Pre-existing asymmetry may not be entirely correctable. Revision surgery may be indicated to maintain patient satisfaction but carries additional considerations and risks. If the patient is dissatisfied with the cosmetic result, revision surgery may be indicated; the device can be replaced with another device of different height, width, projection, volume, shape or filling, or may be placed in a different position in order to achieve a cosmetic result which is more pleasing to the patient.

 

Allergic reaction to anaesthetic

 

Nobody knows exactly how frequently anaesthetics cause allergic reactions. At the moment, the best estimate is that a life-threatening allergic reaction (anaphylaxis) happens during 1 in 10,000 to 1 in 20,000 anaesthetics. Your anaesthetist will choose the drugs for your anaesthetic by taking into account many different factors, in particular, the type of operation, your physical condition and whether you are allergic to anything.

 

Most people make a full recovery from anaphylaxis. It isn’t known how many anaphylactic reactions during anaesthesia lead to death or permanent disability. One review article suggests that 1 in 20 serious reactions can lead to death. This would mean that the chance of dying as a result of an anaphylactic reaction during anaesthesia is between 1 in 200,000 and 1 in 400,000 anaesthetics.

 

Nerve damage

 

It’s possible, but highly unlikely, that you could suffer nerve damage after a general anaesthetic. The size of the area may vary according to the nerves affected, from a very small patch of numbness, tingling or pain, to most of a limb. The pain can be a continuous, aching pain or a sharp, shooting pain. You may also get inappropriate warm or cold sensations. If motor nerves are damaged, there may be weakness or paralysis (loss of movement) of muscles in that area. The risk of a significant peripheral nerve injury lasting more than 3 months is estimated to be less than 1 in 2,000 patients having a general anaesthetic. Permanent damage, lasting more than a year, is estimated to occur in less than 1 case in 5,000.

 

Poor wound healing

 

Wound healing may take longer in cases of infection, bleeding, fluid accumulation, overly tight stitches, over-large implants, improper support during healing, and pressure against the scar tissue.

 

To avoid poor wound healing, your surgeon may recommend that you wear a sports bra for approximately 5 months after surgery. Your physician can direct you to specialised bras that are also available. Wound healing may also take longer in patients who have diabetes or who smoke.

 

Potential general effects on health

 

There has been some controversy about the use of silicone gel-filled implants and their possible influence on developing autoimmune diseases such as connective tissue diseases (CTDs). CTDs are chronic inflammatory autoimmune disorders which can affect all connective tissues, i.e. joints, skin, muscles, and blood vessels, and therefore have multiple effects on many different organs throughout the body.

 

Several large studies have failed to establish a link between breast implants and well-defined CTDs. Even though few studies have been carried out, current literature suggests that there is no association between breast implants and connective tissue disease-like syndromes (atypical connective tissue diseases). Moreover, it is difficult to define atypical connective tissue diseases. These diseases seem to occur at the same rate in women with or without breast implants, which makes it difficult to conclude whether breast implants play a role in the development of such diseases. If you have any concerns, you should speak to your surgeon.

 

Our breast implants are backed by a replacement policy. So for peace of mind, be sure to review our NatrellePLUS Warranty.

 
Getting Ready
Get the answers and information you need during your consultation.
Be Prepared
Be Prepared
Breast Augmentation Patient Information Leaflet
Download our Breast  Augmentation Patient Information Leaflet.
Download Now
Download Now
Note: This leaflet is provided in Adobe® Reader® format (PDF). In order to view PDF documents, you must have the free Adobe Reader software installed on your computer. If you do not have the Adobe Reader, download it from the Adobe Web site.
 

Locate a Surgeon

Find breast augmentation experts in your area that use Natrelle™ products.

Radius

www.natrelle.eu  For non-UK visitors, click here to find your Natrelle™ website

Why keep all of this information about Natrelle™ to yourself?
Fill in the fields below to share it with your friends.

*All fields are required
*Your Name
*Your E-mail
*Friend's Name
*Friend's E-mail

Natrelle Sign Up

Picture yourself with the breasts you’ve always dreamed of. Sign up to use the Natrelle modeller and see your vision come to life. Plus, you’ll receive updates on latest developments in breast enhancement.
If you are considering Breast implants please tell us what outcome you are most interested in so we can send you tailored information:



By submitting, you are indicating that you are over the age of 18 and agree to the
Terms and Conditions.

Terms of Use (Registration)

You will only be able to register as a member of the Natrelle Web site if you accept Allergan's Terms of Registration. Please read and review these Terms of Registration carefully to ensure that you understand them fully. If you accept the conditions, please mark the relevant box on the registration page.

Your registration with the Natrelle Web site will be governed by the following terms and conditions:

  • TERMS OF USE: The Terms of Use will be incorporated into the Terms of Registration and apply to your registration in full.
  • PRIVACY POLICY
    • When you register with the Natrelle Web site, your personal details will be held on a database within the EU or outside the EU administered by Allergan Limited, 1st Floor, Marlow International, Marlow, Bucks SL7 1YL. You agree to Allergan using your personal details for the following purposes:
      • Administration and maintenance relating to your use of and registration with the Natrelle Web site;
      • Provision of health and other medical information that Allergan identifies may be of interest to you based on your personal profile;
      • Research surveys;
      • Direct marketing, PROVIDED THAT you have provided your explicit consent;
    • SENSITIVE DATA: You understand that by registering with the Web site you will need to provide Allergan with certain information relating to your health, which is regarded as sensitive data under UK data protection legislation. By consenting to Allergan processing your personal data you also consent to Allergan processing your sensitive data for the purposes described in clause 2 above.
    • DIRECT MARKETING: You understand that you have the right to prevent Allergan from sending direct marketing material to you. Allergan will only send such materials to you and process your personal data for that purpose in the event that you positively agree to receive such materials. Such materials may be sent to you by Allergan on behalf of the third party users of the Web site referred to in clause 7 below.
    • SECURITY: Allergan takes the security of your personal details extremely seriously. It has implemented technology and security policies designed to protect the personal details under our control. Allergan also follows strict security procedures as required by the U.K. Data Protection Act 1998. These cover the storage and disclosure of any personal details you have provided, and the prevention of unauthorized access.
    • THIRD PARTIES: You understand that by registering with the Web site you will be able to communicate directly with certain healthcare professionals and health clinics, and that they will be able to communicate with you in return. You understand that it is your responsibility to ensure such healthcare professionals and health clinics process any personal and sensitive data you provide them with in compliance with data protection legislation.
    • HEALTHCARE DISCLAIMER: In providing you with contact details for health professionals and clinics, Allergan is not providing you with a medical referral, nor is it making any recommendation on a preferred healthcare provider. You understand that the final choice in these matters lies with you. Allergan does not accept any responsibility for your choice.
    • AMEND YOUR DETAILS or WITHDRAW CONSENT: At any time you can request that your personal details on the Natrelle database be amended, corrected or updated. You also may at any time withdraw any consent you have given to Allergan to process your personal and sensitive data and to receive direct marketing materials, as well as your acceptance of these Terms of Registration. Such withdrawal must be in writing. However, if you elect to so withdraw your consent or acceptance, Allergan may be required to terminate your participation in the Web site and the information and services offered by it. All correspondence should be addressed to the Data Protection Officer at Allergan Limited.