The Dalkon Shield was a contraceptive intrauterine device
(IUD) developed by the Dalkon Corporation and marketed by the A.H. Robins
Company. The Dalkon Shield was found to cause severe injury to a
a disproportionately large percentage of its users, which eventually led to
numerous lawsuits, in which juries awarded millions of dollars in compensatory
and punitive damages.
History
In 1970, the A.H. Robins Company acquired the Dalkon Shield
from the Dalkon Corporation, founded by Hugh J. Davis, M.D. The Dalkon
Corporation had only four shareholders: the inventors Davis and Irwin Lerner,
their attorney Robert Cohn, and Thad J. Earl, M.D., a medical practitioner in
Defiance, Ohio. In 1971, Dalkon Shield went into the market, beginning in the
United States and Puerto Rico, spearheaded by a large marketing campaign. At
its peak, about 2.8 million women used the Dalkon Shield in the U.S.
At the time of its introduction, the Dalkon Shield was
promoted as a safer alternative compared to birth control pills, which at the
time were the subject of many safety concerns.
Initial reports in the medical literature raised questions about whether
its efficacy in preventing pregnancy and expulsion rate was as good as those
claimed by the manufacturer, but failed to detect the tendency of the device to
cause septic abortion and other severe infections.
In June 1973, the Centers for Disease Control and Prevention
(CDC) conducted a survey of 34,544 physicians with practices in gynecology or
obstetrics regarding women who had been hospitalized or had died with
complications related to the use of an IUD in the previous 6 months. A total of
16,994 physicians responded, yielding 3,502 unique case reports of women
hospitalized in the first 6 months of 1973. Based on the survey response rate,
the CDC estimated that a total of 7,900 IUD related hospitalizations occurred
during this 6-month period. Based on an estimate of 3.2 million IUD users, the
CDC estimated an annual device-related hospitalization rate of 5 per 1000 IUD
users. The survey also provided 5 reports of device-related fatalities, with
four of these related to severe infection. One of the five was associated with
the Dalkon Shield. Based on these data, the CDC estimated an IUD-related
fatality rate of 3 per million users per year of use, which it compared
favorably to the mortality risks associated with pregnancy and other forms of
contraception. Importantly, the survey showed that the Dalkon Shield was
associated with an increased rate of pregnancy-associated complications leading
to hospitalization.
By 1974, approximately 2.5 million women had received the
Dalkon intrauterine device. In June of that year, the medical director of A.H.
Robins published a letter to the editor of the British Medical Journal stating
that the company was aware of an "apparent increase in the number of cases
of septic abortions" including 4 fatalities, but stating that "there
is no evidence of a direct cause-and-effect relationship between wearing of the
Dalkon Shield and the occurrence of septicemia". The letter recommended
precautions including pregnancy tests for women who missed their period and
immediate removal of the device in women who were found to be pregnant. In October 1974, a series of four case
reports of septic pregnancies were published in the journal Obstetrics and
Gynecology". In 1975, the CDC
published a study associating the Dalkon Shield with a higher risk of
spontaneous abortion-related death compared to other IUDs.
As many as 200,000 women made claims against the A.H. Robins
Company, mostly related to claims associated with pelvic inflammatory disease
and loss of fertility. The company eventually filed for bankruptcy. The
company's representatives argued that pelvic infections have a wide variety of
causes and that the Dalkon Shield was no more dangerous than other forms of
birth control. Lawyers for the plaintiffs argued that the women they
represented would be healthy and fertile today if not for the device.
Scientists from the CDC stated that both arguments have merit.
Aftermath
More than 300,000 lawsuits were filed against the A.H.
Robins Company – the largest tort liability case since asbestos. The federal
judge, Miles W. Lord, attracted public commentary for his judgments,
impositions of personal liability, and public rebukes of the company
heads. The cost of litigation and
settlements (estimated at billions of dollars) led the company to file for
Chapter 11 bankruptcy protection in 1985. As a result, Robins sold the company
to American Home Products (now Wyeth).
In 1976, the Medical Device Amendments to the Food, Drug,
and Cosmetic Act mandated the U. S. Food and Drug Administration, for the first
time, to require testing and approval of "medical devices", including
IUDs.
The Dalkon Shield became infamous for its serious design
flaw: a porous, multifilament string upon which bacteria could travel into the
the uterus of users, leading to sepsis, injury, miscarriage, and death. Modern
Intrauterine devices (IUDs) use monofilament strings, which do not pose this
grave risk to users.
In popular culture
The A.H. Robins Company and the Dalkon Shield were featured
in a February 2018 episode of Swindled, as well as a July 2018 episode of Crime
Junkies.
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