History of Breast Augmentation
Breast augmentation has become one of the most frequently performed
cosmetic plastic surgeries. In 2000 alone, over 200,000 U.S. women
had a breast augmentation for purely cosmetic purposes. The first
surgical breast augmentation procedure was introduced in 1890. This
breast augmentation, paraffin injections approach led to infections,
hardening of the breasts, and lump formations in the breast. By
1920 the paraffin injection breast augmentation technique was totally
abandoned.
Following the first attempt at surgical breast augmentation was
the introduction of fat transplants in the 1920s. Fatty tissue was
surgically removed from the abdomen and buttock area and transferred
into the breasts. This breast augmentation procedure was also unsuccessful
because the body would quickly reabsorb the fat, leaving the breasts
in a lumpy, asymmetrical condition. The prominent scar that resulted
at the removal site also made this breast augmentation approach
undesirable, and it was no longer performed by the 1940s.
|
The acceptance people have towards plastic
surgery and breast augmentation has shifted over the years
as more and more people describe desiring plastic surgery
procedures in order to feel young inside and outside
|
Japanese prostitutes began to use silicone shots during World War
II for breast augmentation to supposedly lure American servicemen.
By the early 1960s this breast augmentation procedure had become
popular amongst topless dancers in the Las Vegas and San Francisco
area. Soon after the surge of popularity with silicone shots came
reports of serious complications in the mid-1960s. The breast augmentation
complications included chronic inflammation, infections that can
necessitate mastectomy, organ damage due to silicone migration,
and tumor like lumps. Since this type of breast augmentation complications
surfaced the procedure has been eliminated from mainstream, though
it continues to be performed in underground circles.
In the 1950s, polyvinyl sponges began to be implanted into the
breasts for breast augmentation. Different types of synthetic sponges
were also available, but the initial satisfaction with this type
of breast augmentation was very temporary. The breast implants were
found to shrink and harden within a year, and the removal of the
sponges disfigured some women and was impossible for others. Infections,
inflamed tissue, and a link between this type of breast augmentation
surgery and cancer began to surface.
The first silicone breast implant was developed in 1961. In 1963
this breast augmentation surgery began to be marketed and continual
improvements were attempted for the thirty years that followed.
The complications with silicone breast implants included capsular
contracture and the solution to combat it was attempted by covering
the implant with polyurethane foam in 1982. A decade later, after
more than 100,000 U.S. women had gotten this type of breast augmentation,
the FDA released a report that showed polyurethane foam can break
down into the body and form a carcinogen. The manufacturer withdrew
the implant and by the late 1980s the gel was found to lead out
of the sac and into the body, raising safety concerns.
In 1995, Europe launched a trilucent breast implant, which was
filled with fat from soybean oil. This was seen as a natural approach
to breast augmentation, and about 9,000 women worldwide received
this procedure before the 1999 withdrawal. This breast augmentation
technique was found to contain filler that could become toxic in
the body as it breaks down. This type of breast augmentation surgery
was never approved in the U.S.
In 1988, Dow Corning, one of the silicone breast implants largest
manufacturer settled a class action lawsuit for $3.2 billion for
170,000 women. In 1999, the Institute of Medicine issued a 400-page
report that concluded the silicone breast implants do not cause
major illnesses, but the main concern with that type of breast augmentation
surgery was the tendency for the implant to leak or rupture, leading
to infections, hardening, and breast tissue scarring.
The FDA approved saline implants that had been on the market for
years but had not yet received approval. There was a warning issued
by the FDA regarding the alarmingly high rate the saline implants
break at, requiring additional breast augmentation surgeries. Most
recently, in 2001, the Brava Breast Enhancement and Shaping System
hit the market. This is a bra-like device with two hard plastic
domes ringed with silicone that sucks the air out of the domes and
creates a vacuum that is supposed to induce the breast tissue to
grow about one cup size. This new type of breast augmentation must
be worn for 10 hours a day for months.
To find out your breast augmentation options, click
here to find a board certified breast augmentation surgeon.
top of page
|