Surgical Breast Enlargement
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A risk list is not a prediction. It is the set of possibilities you should understand before consenting, together with how likely they are, how they are treated and who pays for further care.
Smoking, existing conditions, implant type, size and surgical technique can all affect risk. Ask your surgeon to explain what applies to you rather than quoting a general figure.
Most complications have a management pathway: antibiotics or drainage for infection, surgery for a large haematoma, capsule surgery for contracture, and removal or replacement for rupture. Ask who would manage each problem, where, and at what cost. A plan that describes only the operation but not the aftercare is incomplete.
Be careful with percentages: they depend on the study, the implant, how long people were followed and how a complication was defined. A single figure cannot describe your risk. Ask where the numbers come from, and ask what happens if the complication occurs.
You do not have to decide at the first consultation. A cooling-off period gives you time to check the surgeon, the facility and the implant. If a clinic discourages this, treat that as a warning sign.
A proper consent process means you receive written information, the surgeon explains benefits, risks and alternatives, you have time to reflect and ask questions, and you can say no at any point.
A clinic that welcomes tough questions about risk is a good sign. See the breast implant safety guide.
Before publication: qualified clinician review and current Indian regulatory verification, where relevant, are required. Sources: FDA: Risks and Complications of Breast Implants ยท CDSCO: Medical Devices Rules, 2017.
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Return to the full category guide.
Candidacy, risks and when to seek medical help.
Study findings, limitations and original publications.
The parent guide to rupture, contracture, ALCL and monitoring.
Infection, haematoma and seroma.