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New ACOG guidelines: Invasive prenatal testing should be offered to all pregnant women

December 15th, 2007

From Obstetrics & Gynecology, Volume 110, No. 6, December 2007, page 1459 (ACOG membership or $20 payment required for articles.)

Heralding a change in standard obstetric practice, the American College of Obstetricians and Gynecologists has recommended that pregnant women of all ages – not just women aged 35 and over — should be offered invasive prenatal diagnostic testing such as amniocentesis and chorionic villus sampling to detect possible genetic abnormalities in their fetuses.

The recommendation, published in a practice bulletin in the December issue of the organization’s journal Obstetrics & Gynecology, dramatically expands women’s access to prenatal diagnosis, effectively making all prenatal tests and screens available to all of the 6 million American women who get pregnant each year. It will establish a new standard of care, and change expectations for insurance coverage and legal liability involving pregnancy.

Until now, obstetricians have usually offered invasive testing just to women at or above age 35 at delivery. The age threshold was chosen because at that age the risk of miscarriage as a result of the testing was roughly equal to the risk of having a child with Down syndrome, the most common genetic abnormality occurring in live births. In addition, the medical community balanced the cost of offering the testing against their calculation of the cost savings associated with preventing the birth of an infant with Down syndrome.

This past January, ACOG expanded the scope of prenatal testing by recommending for the first time that all pregnant women regardless of age be offered prenatal screening, a process in which a woman’s blood is used to calculate the risk that her fetus has an abnormality.

The December ACOG bulletin will open prenatal testing access wider still. The current bulletin does not explain why the professional organization has now dramatically expanded access to prenatal testing twice within a year. Researchers have maintained that universal access to prenatal testing will allow women to make their own informed decisions regarding their pregnancies and minimize disparities in access to health care.

The changes come at a time when growing numbers of medical malpractice lawsuits are pushing insurance costs for obstetricians and gynecologists to record highs, resulting in a situation that ACOG has called a “medical liability crisis.”

In a statement posted on the group’s website last year, ACOG executive vice president Ralph W. Hale said the rising tide of lawsuits was caused not by a high rate of medical wrongdoing but by unreasonable public expectations. “Ob-gyns are vulnerable because they practice in a high-risk field, and all too often, doctors are held liable for less than perfect outcomes,” he said.

ACOG’s current recommendation seems to thrust the 49,000-member professional organization deeper into the cultural debate over public attitudes toward abortion, particularly about where to draw the line between preventing disability and accepting human diversity.

The National Down Syndrome Congress (NDSC) last January condemned ACOG’s recommendation for universally offered prenatal screening, saying it conveyed “tacit approval for terminating pregnancies where the fetus has Down syndrome.” Studies say that approximately 9 out of 10 pregnancies in the U.S. in which Down syndrome is diagnosed end in abortion.

The NDSC also cited research noting that many doctors are not adequately prepared to deliver a diagnosis of Down syndrome, and often use negative language and out-of-date information.

Down syndrome, which results when a person has three copies of the 21st chromosome instead of the usual pair, is longest known and most common genetic birth defect, as well as the most common cause of intellectual disability. Approximately 250,000-350,000 Americans have Down syndrome, which occurs once in every 733 to 1,000 births, according to the NDSC and the National Down Syndrome Society.

Advocacy groups and parents say gains in health care and education have brought about markedly improved outcomes for these individuals over the past two decades, with many people with Down syndrome now completing high school, holding jobs and living semi-independently. But parents say these gains have not been adequately documented and are poorly understood within the obstetrics community.

In an apparent nod to the NDSC’s criticism, ACOG included in its December practice bulletin for the first time the recommendation that prospective parents who receive a diagnosis of a fetal disorder should be provided with “detailed information, if known, about the natural history of individuals” with the disorder.

ACOG also noted that “it may be very helpful” to refer prospective parents to advocacy groups such as the NDSC or the NDSS.

The bulletin does not, however, offer any recommendations for collecting or distributing information to doctors about the lives of people with Down syndrome or other chromosomal abnormalities, nor for training its 49,000 members in delivering and interpreting prenatal test information. A study published in ACOG’s journal last year found that 45 percent of obstetricians rated their training about prenatal testing as “barely adequate or nonexistent.”

As a result of the new ACOG bulletin, each pregnant woman will now need to decide which is greater: her fear of a chromosomal abnormality, or her fear that invasive testing could harm her fetus. The ACOG bulletin estimates that the risk of miscarriage as a result of the invasive tests is “as low as” one in 300-500, and “may be even lower with experienced individuals or centers.” Other estimates say that approximately one in every 200 women who undergoes invasive testing will miscarry her pregnancy.

The risk of a fetus with a chromosomal abnormality varies with the mother’s age. According to ACOG data, the lowest recorded risk goes to 19-year-olds, with a risk of 1 in 555, and the highest goes to a 49-year-old, with a risk of 1 in 6.

The financial impact of the new ACOG bulletin is not known, but could extend above the billion-dollar mark. Amniocentesis and chorionic villus sampling (CVS), the invasive tests, are both more expensive and more accurate than the maternal blood test screens. The consumer cost of each amniocentesis is more than $1,000. Chorionic villus sampling costs between $600 and $1200. More invasive tests would also call for an increase in costs for training, facilities and equipment.

Amniocentesis and CVS each involve removing and examining material from inside the uterus during pregnancy with a long needle or plastic tube to check for chromosomal differences.

The maternal blood-test screens do not deliver definitive results but only report the odds that a particular fetus may have an abnormality. They also carry a significant risk of both false positives and false negatives.

In a tacit acknowledgment of the ongoing abortion debate, the bulletin notes that “Prenatal diagnosis is not performed solely for assistance in the decision of pregnancy termination. It can provide useful information for the physician and the patient.”

The practice bulletin listed the recommendation for offering invasive diagnostic testing to all pregnant women as a “Level C” recommendation, one that is “based primarily on consensus and expert opinion.” This is the lowest rank used in justifying ACOG recommendations.

Higher rankings that may be used for ACOG recommendations are “Level A” (”based on good and consistent scientific evidence”) and “Level B” (”based on limited or inconsistent scientific evidence.”)

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6 Responses to “New ACOG guidelines: Invasive prenatal testing should be offered to all pregnant women”

  1. vicki Says:

    You know this is not Nazi Germany, and Hitler is dead. All people should not be perfect. They should be born the way God intended us to be. You know what costs us more money than kids with Down Syndrome? Meth-crack addicts on public aid or the foreigners who come into this country and go on public aid. What about the homeless who use our emergency rooms for a place to sleep and get detoxed from drinking binges? Hospitals have to write off those charges and our insurance rates keep going up. Or the Iraq war … this country needs to focus on the real problems!! That is what costs more than a child born with Down Syndrome!!

  2. Qadoshyah Says:

    Man, this is crazy! The ACOG seems to have some agenda to eliminate the group of individuals with DS. This is so sick and sad! My brother who’s almost 3 years old has DS and he’s such a blessing. I couldn’t image life without him!

    Educating the uninformed is something that is more than needed as always, but especially in our day and age that is so pro-abortion!

    Qadoshyah

  3. Kathryn Soper Says:

    Knowledge is power, but a little knowledge is a dangerous thing — for doctors and for parents. This new protocol, without education to augment it, is dangerous indeed.

  4. luetzowa Says:

    Disability is not something that needs to be prevented. All humans deserve life, despite differences or “abnormalities.” The question of “where to draw the line between preventing disability and accepting human diversity” should be extremely evident. Offering out-of-date information and biased labels on amniocentesis does not constitute a valiant effort for acceptance of diversity.

    It is time to educate the uninformed, to embrace change, and to create an accepting environment for ALL of the world’s people. The sheer act of screening for “chromosomal abnormalities” carriers a negative connotation, automatically influencing the mother’s potential view of her child with such a condition. The attitude of the medical industry needs to change; why not welcome every human life with open arms?

  5. Nathanael Bonnell Says:

    It’s much easier to decide that a person with Down Syndrome shouldn’t be allowed to live before that person has really had a chance to live. Not too many people would say that an adult with Down’s should be killed for being defective or a burden. This relates to Peter Singer’s controversial idea that a person doesn’t become a person until they can form coherent thoughts and show an identity. And, apparently, it’s all right to kill non-persons.

    I can’t abide by this idea, because I can make a simple analogy to autism. Autistic people may show little sign of a personality, and may not be able to express thoughts to others. But, when some of them find a means to express themselves through Facilitated Communication, we find out that they have just as much a personality as any “normal” person. So is it right to kill autistic people, unless they show some sign of communication? It can’t be. Instead we should help them. By extension, I don’t think we can morally abort fetuses with potential disabilities; we should help them.

  6. jennifergg Says:

    Oh, ugh. I will do a post about it, too.

    As with last year’s ACOG changes, and perhaps even more, I’m wishing for adequate education and support for all pregnant women.

    As a rule, I’m a believer in the power of information. But this one is tricky for me, because of all of the subtexts. And until we can ensure that each family is aware of all the implications, and all the consequences, the new ACOG guidelines feel like a step backward to me.

    Editor’s note: View Jennifer’s blog at: http://jennifergrafgroneberg.wordpress.com/

    Her upcoming book is Road Map to Holland: How I Found My Way through My Son’s First Two Years with Down Syndrome — due out in the spring.

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