It's that their hearts are in the right place, they mean well. It just feels like the right thing to do. That seems to be enough justification.
Federal Agency Faces Fallout From Controversial Study That Put Babies at Risk
Sharyl Attkisson / @SharylAttkisson
A federal agency has taken controversial new steps to marginalize its own ethics body, according to new information revealed by the watchdog group Public Citizen. That after the federal ethics body criticized a government study that resulted in the deaths of some premature babies.
The government-backed study in question was called “SUPPORT.” It was conducted from 2006 to 2009 on 1,316 extremely premature infants at 23 academic institutions under the National Institutes of Health, which is part of the Department of Health and Human Services.
Critics say HHS has pressured and marginalized its own ethics office, which made critical findings of the agency.Controversy surfaced in March 2013 when the government’s own ethics body, the Office of Human Research Protections, dropped a bombshell.
The ethics office found the federal study’s consent forms violated government rules designed to protect human research subjects. According to OHRP, the consent forms “failed to describe the reasonably foreseeable risks of blindness, neurological damage and death” to babies in the study.
Read More: Did Government’s Experiment on Preemies Hide Risks?
More than a year and a half later, the federal government has yet to take enforcement action or make changes to address the shortfalls. Instead, critics say it has pressured and marginalized the ethics office that made the critical findings.
Fallout over the study has impacted the federal government’s current review of the longstanding rules that govern research on human test subjects. Watchdogs say the effort has been co-opted by the powerful research community, which has used the opportunity to push for a loosening—rather than strengthening—of human research consent rules.
Now, as the rules are being revised, internal emails obtained by Public Citizen indicate federal officials have transferred major responsibilities from the ethics office and assigned them to the National Institutes of Health, the very agency that conducted the questioned study.
Dr. Michael Carome (Photo: Angela Bradbery/Public Citizen)
See Public Citizen’s Nov. 20 letter, including internal emails showing the transfer of key writing responsibilities from the ethics body to NIH
“This shift of authority from the regulator to the regulated is unacceptable,” writes Carome, who once served as an ethics expert in OHRP.
HHS has not respond to Public Citizen’s letter and did not answer our request for comment.
‘I didn’t have a clue': Sharrissa Cook, Dreshan’s mom, with her father. (Photo: Angela Bradbery/Public Citizen)
Parental outrage
A number of parents have come forward to say they were misled when they enrolled their extremely ill newborns into the SUPPORT study, which stands for “Surfactant, Positive Airway Pressure, and Pulse Oximetry Randomized Trial.”
Parents say they were told it was just an effort to help their baby or gather data such as height and weight. Among other risks, the consent forms failed to disclose that oxygen monitors used on the study babies were intentionally rigged to give false readings.
Sharrissa Cook, then a 26-year-old single mother, says she had no idea she was enrolling her 1-pound, 11-ounce son Dreshan in an experiment. Cook says medical personnel at the University of Alabama at Birmingham told her SUPPORT was “a support group who would pretty much hold my hand through the developmental process.”
Dreshan shortly after birth. (Photo: Sharrissa Cook)
When the study results were published in the New England Journal of Medicine in May 2010, it revealed that babies were more likely to have serious vision disorders or die depending on the random study group to which they were assigned. It sparked ethical questions, and companion studies being conducted in other countries were halted.
Read More: ‘Input’ Stalls Agency’s Ethics Probe in Baby Oxygen Trials
Dr. Waldemar Carlo, director of the neonatology division at the study’s lead site, the University of Alabama at Birmingham Hospital, denied wrongdoing on behalf of the institutions that took part. In a May 2013 letter to the New England Journal of Medicine, Carlo stated, “Our consent forms were conscientiously drafted according to the Code of Federal Regulations and were based on the best available evidence.”
Government’s role
Earlier this year, Public Citizen accused officials in the office of Burwell’s predecessor, HHS Secretary Kathleen Sebelius, of knowingly allowing senior officials at the National Institutes of Health to interfere with the ongoing ethics investigation into SUPPORT.
In a Nov. 20 letter to Health and Human Services Secretary Sylvia Mathews Burwell, Carome asked HHS to reverse the move. (Photo: UPI/Newscom)
The inspector general investigated the allegations. In September, it issued a report confirming that NIH officials “encouraged” the ethics body to reverse its finding of a violation in the SUPPORT study consent forms. The IG also agreed with critics that NIH officials “provided input” on a letter the ethics body wrote backing off enforcement action for the violations. But the IG concluded no laws or policies had been broken.
Read More: Parents Fault Medical Research Study for Putting Preemies in Harm’s Way
Dr. Alan Guttmacher at the National Institutes of Health has defended SUPPORT and his agency’s role in it. He says it added to the body of knowledge on the subject of how much oxygen is safest for preemies.
“We stand by this study as it was conducted and look for ways to do research even better, if there is a better way to do it, in the future,” Guttmacher said.
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