Cornell University: Permanent birth control methods for women have up to 6% failure rates

Hysteroscopic sterilization, a nonincisional procedure, was found to be as effective as minimally invasive laparoscopic sterilization in preventing pregnancy, but both methods had higher-than-expected failure rates, according to a new study led by an investigator at Weill Cornell Medicine.

The comparative study, published April 12 in Fertility and Sterility, found that both methods had failure rates of 5% to 6% percent at five years post-procedure. Dr. Aileen Gariepy conducted the investigation while at Yale School of Medicine; she is now director of complex family planning in the Department of Obstetrics and Gynecology at Weill Cornell Medicine. Co-investigators included Dr. Eleanor Bimla Schwarz from the University of California, San Francisco, and University of California, Davis, and Dr. Diana Zuckerman from the National Center for Health Research.

“The rate we found is five to six times higher than the sterilization failure rate of 1% that’s often cited by physicians when counseling patients,” Gariepy said. The 1% figure, she noted, is based on decades-old data from the U.S. Collaborative Review of Sterilization study.

With 219 million women and their partners relying on female sterilization, considered a permanent way to prevent pregnancy, it is the most commonly used contraceptive method worldwide. In the United States, sterilization is more commonly used by women insured by Medicaid than those with private health insurance, according to researchers.

The goal of the study was to compare the effectiveness of hysteroscopic and laparoscopic sterilization procedures. For laparoscopic sterilization, a surgeon makes a small incision near the belly button and can use an array of methods to cut or close off the fallopian tubes.

Hysteroscopic sterilization uses a medical device known by the trade name Essure to block the fallopian tubes. The implanted metal coils generate scar tissue over time, which prevents pregnancy.

The U.S. Food and Drug Administration (FDA) first approved Essure in 2002, with researchers reporting a cumulative pregnancy rate of zero from two studies that followed 197 women with Essure over two years.

Amid increasing scrutiny from the FDA and questions about the device’s effectiveness and safety, the manufacturer chose to pull Essure from the market in 2019, citing decreased sales. But questions remained for women who didn’t experience problems and hadn’t had the device removed.

“Women and doctors want to know: ‘Can I rely on this for pregnancy prevention?’” Gariepy said.

Noting that hysteroscopic sterilization had become increasingly common among Medicaid-insured women, Gariepy and her collaborators – including patient stakeholders; investigators from several academic institutions; and community partners across the country – looked at Medicaid claims for hysteroscopic and laparoscopic sterilizations performed in California between 2008 and 2014. They excluded postpartum sterilizations, which are conducted using a different approach.

“Previous studies had looked at sterilization in women with commercial insurance, and their health outcomes are often different from someone with Medicaid,” Gariepy said. “It was important to look at the experiences of people with Medicaid and their real-world outcomes.”

Using the Medicaid data, researchers identified 5,906 women who had undergone hysteroscopic and 23,965 who had undergone laparoscopic sterilization. The average age was 33.

“At five years post-procedure, the cumulative rate of pregnancy was over 6% regardless of whether women received hysteroscopic or laparoscopic sterilization,” the researchers wrote.

“Women need to know the real risk of failure,” Gariepy said, adding that the findings show a need for further study into whether particular surgical techniques, for example, have contributed to the higher-than-expected pregnancy rates.