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Prenatal Screening for Birth Defects/Ultrasound

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See also:

Subsections on this page:



General




Detecting Genetic Disorders in the Unborn [4/3/13] - It is now possible to sequence the entire genome of an unborn baby with only a sample of the mother's blood.  Wow!  Hats off to these research scientists!!!

It's not commercially available yet, but we can hope it won't be long now!  Maybe, just maybe, this will become an option for the dreaded Newborn Screen.



Women who were better informed chose fewer prenatal genetic tests
[9/23/14] - Pregnant women who received interactive computerized guidance on prenatal testing were better informed, but less likely to choose invasive testing than women who received typical prenatal care.

Revolutionary Fetal Chromosomal Analysis from Maternal Serum

Verinata Health, Inc. is proud to offer the verifi™ prenatal test — a non-invasive prenatal test that detects multiple fetal chromosomal aneuploidies using a single maternal blood draw with near-diagnostic accuracy. If you have ever wanted safer, simpler test results or wished to screen at 10 weeks instead of waiting, now you can — order the verifi™ prenatal test.



 Noninvasive Prenatal DNA Test Okay for Low-Risk Pregnancies [2/27/14]

Early testing was done in high-risk women.  This newest research shows that the test is similarly accurate in low-risk women.



Chromosomal Hits and Misses of Noninvasive Prenatal Testing [Medscape, 2/10/14] - A review of prenatal genetic screening options in a population of pregnant women in California showed that noninvasive prenatal testing (NIPT) would detect 83% of chromosome abnormalities, but miss approximately 17%.


Noninvasive prenatal detection and selective analysis of cell-free DNA obtained from maternal blood: evaluation for trisomy 21 and trisomy 18.
Sparks AB, Struble CA, Wang ET, Song K, Oliphant A.
Am J Obstet Gynecol. 2012 Apr;206(4):319.e1-9. Epub 2012 Jan 26.

CONCLUSION: Digital analysis of selected regions and FORTE enable accurate, scalable noninvasive fetal aneuploidy detection.


Screening for Fetal Chromosomal Abnormalities Reviewed  - this Medscape article offers a fabulous overview of available testing as of January, 2009.


Pregnant Women In The Dark On Prenatal Screening - Soon-to-be mums admit they feel 'left in the dark' when it comes to being told about the possible implications of prenatal screening - tests which could lead them down a path where they have to make difficult decisions about their unborn child.



Preconceptual "Universal Genetic Testing": The New Standard for Obstetric Care? [Medscape 12/11/11] - The cystic fibrosis gene is 1 of over 100 that can be screened for with a single swab of the patient's cheek. The cost for testing for all of these genes is about 5 times more than for CF testing alone, but it includes other common genes, like those that cause spinal muscular atrophy and Tay Sachs disease.

NEW for 2007! - Down screening urged for all pregnant women - There's a big change coming for pregnant women: Down syndrome testing no longer hinges on age 35.  The newest method, topping ACOG's recommendation for everyone, is a first-trimester screening that combines blood tests with a simple ultrasound exam, called a "nuchal translucency test" to measure the thickness of the back of the fetal neck.



False-Positive Prenatal Screens May Augur Problem Pregnancy [Medscape, 2/5/14]

National Society of Genetic Counselors

Genetic counseling is the process of helping people understand and adapt to the medical, psychological and familial implications of genetic contributions to disease.

This process integrates:

    * Collection and interpretation of family and medical histories to assess the chance of disease occurrence or recurrence
    * Education about inheritance, testing, management, prevention, resources and research
    * Counseling to promote informed choices and adaptation to the risk or condition.


BabyCenter.com has a nice web page to help parents learn about genetic counseling and prenatal screening choices.  It contains some nice information about values clarification and why you might choose prenatal screening even if you wouldn't consider terminating a pregnancy.


Prenatal Diagnosis - a comprehensive overview from Web pages of Greggory R. DeVore, MD - Fetal Medicine
These Web pages include information about Genetic Ultrasound Services, i.e. the use of ultrasound to detect Down syndrome, and compares it to the use of the Triple Marker Screening.


Risk of prenatal CVS same as amniocentesis: study - "Both procedures carry a small risk of miscarriage, but the study found that the risk attributable to CVS is the same as the risk of 1 in 370 seen with amniocentesis when adjusting for the earlier gestational age of the CVS procedure."

Chorionic Villus Sampling Compared With Amniocentesis and the Difference in the Rate of Pregnancy Loss.
Caughey AB, Hopkins LM, Norton ME.
Obstet Gynecol. 2006 Sep;108(3):612-616.

CONCLUSION: The loss rates for both amniocentesis and CVS at our institution have decreased over time. Because the decrease in loss rate for CVS has been greater, there is no longer a statistically significant difference between the two. These results are informative in both patient counseling and establishing widespread prenatal diagnostic and screening programs. LEVEL OF EVIDENCE: II-2.


Fetal nuchal translucency scan and early prenatal diagnosis of chromosomal abnormalities by rapid aneuploidy screening: observational study.
Chitty LS, Kagan KO, Molina FS, Waters JJ, Nicolaides KH.
BMJ. 2006 Feb 25;332(7539):452-5.

CONCLUSIONS: In the diagnosis of chromosomal abnormalities after first trimester screening for trisomy 21, a policy of qf-PCR for all samples and karyotyping only if the fetal NT thickness is increased would reduce the economic costs, provide rapid delivery of results, and identify 99% of the clinically significant chromosomal abnormalities.


Nuchal Translucent Scan


Prenatal Testing from americanpregnancy.org


Test Detects Down Syndrome Early - Screen relies on fetal neck width at 11 weeks, plus maternal blood protein levels


1st Trimester Ultrasound Scanning and similar web pages


As of July, 2005, Quest Diagnostics offers:

 Maternal Serum Screen 5 is a new prenatal screen for neural tube defects, Down syndrome, and trisomy 18. The screen includes invasive trophoblast antigen (ITA), a hyperglycosylated form of hCG, and 4 other markers. Early studies indicate that addition of ITA improves the Down syndrome detection rate.

Maternal Serum Screen, 1st Trimester is a new prenatal screening test for Down syndrome and trisomy 18. The test includes PAPP-A, ITA, and nuchal translucency (NT).


Prospective first-trimester screening for trisomy 21 in 30,564 pregnancies.
Avgidou K, Papageorghiou A, Bindra R, Spencer K, Nicolaides KH.
Am J Obstet Gynecol. 2005 Jun;192(6):1761-7.

CONCLUSION: The most effective method of screening for chromosomal defects is by first-trimester fetal NT and maternal serum biochemistry.

"In summary, "the detection rate of trisomy 21 and other major chromosomal defects by this method was about 90 percent, for a false-positive rate of 5 percent," write Avgidou et al."


ACOG Supports First-Trimester Screening for Fetal Aneuploidy - First-trimester screening is a viable method of detecting fetal aneuploidy. Moreover, the approach offers several possible advantages over second-trimester screening, according to a position statement released by the American College of Obstetricians and Gynecologists (ACOG). [6/30/04]


OK - I'm sorry . . . I can't take the hypocrisy any longer.  Now that doctors are getting serious competition from "entertainment ultrasound boutiques", suddenly they're talking about how dangerous ultrasound is.  Is it only dangerous if the money's going to someone without an MD?  What about routine ultrasound, which has been shown NOT TO BE BENEFICIAL in the absence of complications that are obvious from a clinical point of view, i.e. too much or too little amniotic fluid, baby not growing well, ruling out multiples, postdates, etc.?

For an overview of this issues, see 4-D Ultrasounds Are Risky Entertainment from Dr. Mercola's site.


All those false positives from the MS-AFP or triple screen and the long wait for the results of the amniocentesis significantly increase a woman's anxiety level.  Here's how those can cause problems later on:

Anxiety in Pregnancy Ups Kids' Behavioral Problems [Fri Jul 16, 2004 02:16 PM ET By Alison McCook ]
"Women who are chronically stressed out during the middle of a pregnancy are more likely to give birth to children who develop behavioral problems later in life. . . . The investigators found that women who were very anxious between the 12th and 22nd weeks of their pregnancies were more likely to have children who were also anxious and showed symptoms of attention deficit/hyperactivity disorder (ADHD)."


Janet Robinson published an article around 1999 in BJM or Practicing Midwife from a study based on interviews w. women who had serum screen positive for Downs and went on to deliver a normal baby.  Some of these women described lingering concerns about their baby's well-being, including an assumption that their infant was more vulnerable.


Speaking the Language of Genetics: A Primer [Medscape registration is free]


Pre-natal Diagnosis - Making Difficult Decisions, by Sarah J. Buckley, MD, from Women of Spirit


This is a fabulous article from Mothering Magazine:

Prenatal Testing and Informed Consent: Base Your Choices on the Evidence
By Peggy O'Mara
Issue 120, September/October 2003


In consideration of prenatal screening it is important to keep in mind that there is NO BENEFIT to the baby, only the actual harm of the invasive tests such as ultrasound and amniocentesis, and the potential of harm if the results aren't what the parents are hoping for.  Prenatal screening is generally used as a means of finding out if the baby is good enough or perfect enough to be allowed to live.  This kind of "tentative pregnancy" has ill effects on all tested babies, even those who are deemed good enough to be allowed to live.  (For more information about how a tentative pregnancy affects a fetus "in utero" and later throughout life, familiarize yourself with the work of APPPAH.)

Becoming a parent is a very serious matter, and if you cannot live with any child who is less than perfect, well, then, maybe you want to give some thought to the commitment one makes in choosing to become a parent.  If you can't accept and love a baby born with developmental problems, what will you do if your child develops problems later in life?  What will you do if your child is autistic or develops juvenile diabetes or leukemia or is disabled in an accident?  If your children don't disappoint you before you are born, you can generally bet that they will at some time disappoint you after they are born.  It takes tremendous maturity and responsibility to accept that in choosing to become a parent, you are offering to satisfy humanity's drive to propagate the species, and that your role as a parent is to serve the child, not the other way around.

Still, raising a child with developmental problems is a great deal of responsibility to take, and I'm sure there are babies who are better often being "terminated" than being born into a family that cannot love them because of their perceived shortcomings.  If this is your situation, please at least have the decency not to say that you are doing genetic screening for the baby's sake.


Actually, I have to disagree that prenatal screening confers no benefit to the baby.  Research indicates that parents who know in advance that their baby may have problems are better prepared and thus better able to be the best possible parents to these babies.  "Women who have delivered a child with a chromosomal aneuploidy, such as trisomy 21, are more satisfied with the outcome of their pregnancy when they learn of their child's diagnosis before delivery."  [from Pregnancy Outcomes After Prenatal Diagnosis of Aneuploidy - Medscape registration is free]


I also disagree.  There are some very rare conditions which need immediate treatment at birth in order to save the child's life.


Yes, there may be some very rare conditions which might benefit from prenatal diagnosis, but we need to look at the risk/benefit ratio.  The Cochrane Collaboration has done separate reviews of routine early and late ultrasound and found that neither has a clear benefit to either mother or child.  A crystal ball would allow us to screen only the very rare cases where the benefits are greater than the risks.


Chorionic Villus Sampling and Amniocentesis: Recommendations for Prenatal Counseling from the CDC


Evidence based screening for Down's syndrome. We should be prepared to re-examine entrenched practices.  [Medline entry]
Raeburn S
BMJ 2000 Mar 4;320(7235):592-3

Medscape has a nice commentary:

Screening for Down's syndrome based on maternal age and routine ultrasound testing is considerably more effective than assumed, according to a report in the March 4th issue of the British Medical Journal.

The results call into question the widespread use of serum screening for Down's syndrome, according to the study's lead author. "If you asked most obstetricians about the evidence for serum screening, I am sure that they would tell you that the case for its use was unassailable," the study's lead author, Dr. David T. Howe, of the Princess Anne Hospital in Southampton, England, told Reuters Health. "In fact, there has never been a controlled study of its effectiveness anywhere in the world."


Sheila Kitzinger on Ultrasound - A very nice piece by Sheila Kitzinger, excerpted from Rediscovering Birth.


Information about the legal obligations of California practitioners regarding prenatal genetic screening.


SOFT provides support for families affected by Patau's syndrome (trisomy 13), Edwards' syndrome (trisomy 18), partial trisomy, mosaicism, rings, translocation, deletion, and related disorders.


Obstetric Ultrasound


Prenatal Screening - Interpretation of Results


Genetic Screening Methods from Creighton University School of Medicine


Screening in pregnancy - written for parents


New 'Integrated' Prenatal Screening Test Can Detect 90% of Down Syndrome Cases With 5% False-Positive Rate [Feb 09, 2004]

A new prenatal screening test that carries no risk to the fetus can detect 90% of Down syndrome cases, but the test has a 5% false-positive rate and pregnant women must wait until the second trimester of pregnancy to receive the results, according to a study presented on Thursday at the Society for Maternal-Fetal Medicine Conference in New Orleans, the Wall Street Journal reports. The "integrated screen" test -- which combines information from a first-trimester ultrasound and blood tests conducted in the first and second trimesters -- "is creating excitement and controversy," according to the Journal. Researchers conducted the integrated screen on 33,557 pregnant women at 15 centers nationwide. The test correctly identified 90% of Down syndrome pregnancies but falsely identified the condition in 5% of the women tested. If researchers defined a positive result slightly different, false alarms would have occurred in only 1.4% of the women, but the positive detection rate for Down syndrome cases would have fallen to 80%. Women who test positive are offered an amniocentesis, a procedure in which a doctor inserts a needle into the pregnant woman's uterus to obtain fluid from the amniotic sac. Although amnios are almost 100% effective in detecting Down syndrome cases, they carry a small risk of miscarriage. With the integrated test, many women can avoid the invasive tests. The test "seems to be the most efficient screen" and "is associated with a lower need for amnio" than other screening procedures, Mary D'Alton, a Columbia University scientist who served as principal investigator in the trial, said. The test has created controversy among some obstetricians because women are not informed of their test results until the second trimester, which is a late stage for women who decide to terminate the pregnancy, according to the Journal (Johannes, Wall Street Journal, 2/6/04).


Blood Test for Down's Syndrome in First Trimester

Maternal Blood Test Can Detect Down's Syndrome in Fetus [Medscape registration is free.]



Cell-Free Fetal DNA Testing




See also: Non-Invasive Prenatal Testing - Midwives share their experiences with insurance billing for NIPT

Sequenom's cell-free DNA testing can count the baby's chromosomes from blood drawn from the mother's arm.  It can be performed as early as 10 weeks’ gestation with results provided to your health care provider approximately 5 days from receipt of your sample in our laboratory.  [Ed: Let's all applaud the availability of this amazing technology!!!]

Here are the choices - If you select "10+ Weeks", it shows the three main tests, towards the left, and then there's a "Test Comparison" option.  All of these tests detect the baby's sex.

The MaterniT GENOME test can analyze every chromosome of your baby to identify extra or missing parts of chromosomes or whole chromosome changes.  This is the most comprehensive, but it might not be covered by insurance for low-risk women. (Women over 35 are considered high risk.)  This sample test result for the GENOME test shows the complete list of things that it tests for.

The MaterniT21 PLUS test reports positive or negative results for trisomy 21, 18, and 13 as well as some other chromosomal abnormalities. This test is covered by most insurance companies even for low-risk women. This sample test result for the MaterniT21 PLUS test shows the complete list of things that it tests for.

The VisibiliT
tests reports positive or negatives results for the most common chromosomal abnormalities, trisomy 21 (Down syndrome) and trisomy 18 (Edwards syndrome).

Here are lots of sample results.

You can use their cost estimator to compare costs for the three tests.

You can look for a blood draw location near you.

For moms who are Rh negative and want to know if their baby is Rh positive before receiving the human blood products contained in RhoGAM, you can order the SensiGene RhD test. (My Sequenom rep says you can just write "SensiGene RhD" in the comments section of the req form, but it has to be a separate form and a separate specimen collection kit!)  Sadly, no insurance companies are covering this as of August, 2016, so it's a cash pay option only of $399.  [Ed: I'm appalled that insurance companies don't think it's medically necessary to perform a test that will allow 30% of pregnant women to forego the prenatal RhoGAM shot around 28 weeks in order to protect their baby's health and that of future babies.]


ClariTest
from GenPath: Their Non-Invasive Prenatal Screening provides screening for common chromosomal aneuploidies as well as an optional panel for five microdeletions. As of May, 2018, I've heard that this test costs $150 out-of-pocket max, if not covered by insurance.


Wikipedia offers a nice overview of Cell-free fetal DNA


ACOG's statement on Noninvasive Prenatal Testing for Fetal Aneuploidy


Cell-free Fetal DNA testing from UCSF

Blood Test Trumps Accuracy of Standard Screening in Detecting Down Syndrome in Early Pregnancy By Suzanne Leigh on April 01, 2015
and their associated FAQ: Cell-Free Fetal DNA Testing


The Harmony Prenatal Test is a blood test for trisomies 21 (Down syndrome), 18, and 13 that delivers accurate results from as early as 10 weeks of pregnancy.


Quest offers a new test (as of April, 2015) called the QNatal Advanced™ - "The NIPS screens for fetal chromosomal abnormalities: trisomy 21, 18 and 13, as well as fetal sex. In addition, when a clear result is seen, will also report fetal sex aneuploidies and select microdeletions, including 22q (DiGeorge syndrome), 15q (Prader-Willi/Angelman syndromes), 11q (Jacobsen syndrome), 8q (Langer-Giedion syndrome), 5p (Cri-du-chat syndrome), 4p (Wolf-Hirschhorn syndrome), and 1p36 deletion syndrome as an additional finding."

It's not clear where it's available, so call your local test centers for more information.



Cystic Fibrosis



Update on Preconception and Prenatal Carrier Screening for Cystic Fibrosis [Medscape registration is free]



Common Worrisome Finding on Early Ultrasounds



See also: Placenta Previa/Placenta Location


The white spot on the heart is called echogenic intracardiac focus and usually means there's a calcification of one of the papillary muscles. It is found in about 7% of ultrasounds at 13-16 weeks and 3% at 20-22 weeks (the incidence can be as high as 30% in Asians).
Implications:
Noted to be present in 25% of Downs Syndrome fetuses and 5% of normal fetuses.  The risk of Downs Syndrome in a fetus with echogenic intracardiac focus in about 0.002%.
Follow-up:
Karyotyping is not warranted.  The risk of amnio far outweighs the risk of Downs in a low risk population.  They usually resolve spontaneously and babies are born normal.  Pt may choose to have triple marker screen.   Patients may be referred to genetics for counseling if exceptionally anxious about this finding.

Renal Pelviectasis/Pyelectasis:
Definition:
A mild dilation of the fetal renal pelvis.  It is found in approximately 2% of normal fetuses.  It has been defined as >4mm before 33 weeks and >7mm after 33 weeks.
Implications:
Can sometimes be associated with obstruction and can lead to hydronephrosis.  The severity of pyelectasis may predict the development of hydronephrosis and possible postnatal complications.  While not an independent predictor, pyelectasis has also been found to be present in 15-25% of fetuses with Downs.  Other reasons that lead to hydronephrosis are: physiologic, uretropelvic junction obstruction, vesicocoureteral reflux, multiplastic kidney, posterior urethral valves, and ureterocele/ectopic ureters.  *But usually it is physiologic (ie fetus needs to pee!).
Follow-up:
A follow-up ultrasound should be done in 6-8 weeks.  Most often it will have spontaneously resolved.  If it is still present but less than 6mm the baby will be followed with ultrasounds 48 hours after birth and 3 months and after if needed.  If greater than 6mm the baby will be put on prophylactic antibiotics and be followed by ultrasound at 48 hours. Depending on the result (if there is a pathological cause for this) the baby may need additional testing and continued antibiotics.  It usually resolves spontaneously by 3 months.



Down Syndrome



Standard Down's screen topped by early alternative

First-trimester or second-trimester screening, or both, for Down's syndrome.
Malone FD et al.
N Engl J Med. 2005 Nov 10;353(19):2001-11.

"Our results demonstrate that first-trimester screening for Down's syndrome is highly effective," state the authors of an article published in the November 10, 2005, issue of the New England Journal of Medicine. Accurate comparison of the performances of different screening tests conducted at different times during pregnancy remains complex owing to concern about spontaneous pregnancy losses that may occur between first- and second-trimester screenings. The article presents findings from the First- and Second-Trimester Evaluation of Risk (FASTER) Trial with the goal of providing direct comparative data on currently available screening approaches for Down syndrome from a large population followed prospectively.

The study was conducted at 15 centers from October 1999 to December 2002. Participants included adolescents and women ages 16 or older pregnant with a singleton fetus with a gestational age at study entry ranging from 10 weeks, 3 days through 13 weeks, 6 days. Following an initial screening and risk assessment (adjusted for maternal age) during the first trimester, participants returned at 15-18 weeks gestation for second-trimester screening and risk assessment. Performance characteristics of screening tests for Down syndrome were estimated with first-trimester markers measured at 11, 12, and 13 completed weeks of gestation and with second-trimester markers measured at 15 through 17 weeks completed weeks of gestation. The analysis compared first-trimester screening for Down syndrome with second-trimester screening (the current standard of care) and with screening in both trimesters.

Complete first- and second-trimester screening data were available for 33,459 unaffected pregnancies and 87 pregnancies affected by Down syndrome. At a 5% false positive rate, the rates of detection of Down syndrome were as follows:

* With first-trimester combined screening, 87% at 11 weeks, 85 % at 12 weeks, and 82% at 13 weeks.

* With second-trimester quadruple screening, 81%.

* With serum integrated screening (single serum marker in the first trimester and quadruple serum markers in the second trimester), 88%.

* With fully integrated screening, 96%.

"When there is appropriate quality control . . . first-trimester combined screening is a powerful tool for the detection of Down's syndrome," conclude the authors. They add that consideration of the advantages of earlier diagnosis, the costs associated with different strategies, and patient preferences will help guide the choice between approaches.

Malone FD, Canick JA, Ball RH, et al. 2005. First-trimester or second-trimester screening, or both, for Down's syndrome. New England Journal of Medicine 353(19):2001-2011. Abstract available at http://content.nejm.org/cgi/content/short/353/19/2001


Antenatal screening for Down's syndrome - Nuchal translucency plus biochemical tests has the lowest false positive rate Alfirevic Z, Neilson JP. BMJ. 2004 Oct 9;329(7470):811-2.


I have just finished reading the fabulous book Down Is Up for Aaron Eagle : A Mother's Spiritual Journey With Down Syndrome, written by Vicki Noble about her special son.  She reports that in many cultures, people with Down Syndrome are regarded as shamans, healers or other special people of value to their community.  She also highlights the observation that we might regard Down Syndrome as a positive mutation, as those with Down Syndrome are often more peaceful, amiable and generally likable human beings.

I was intrigued by her observations that Down Syndrome is in some ways a disease of elimination, and that special attention to facilitating elimination and maintaining overall good health can support an expanded potential.  Then the thought occurred to me that perhaps Down Syndrome is like phenylketonuria - a metabolic disorder that causes brain damage as a side effect of a primary metabolic problem.  What if we discovered that Down Syndrome is a treatable metabolic disorder like phenylketonuria?  What if a special maternal diet could prevent the brain damage that is typically seen in newborns with Down Syndrome?  What if we could somehow support this human mutation to be all that it could be . . . a more peaceful human being with extra abilities gifted from the extra chromosome?



Prenatal Surgery



Recent developments in fetal medicine. [full text]
Kumar S, O'Brien A.
BMJ. 2004 Apr 24;328(7446):1002-6.


Womb surgery rescues Womb surgery rescues severe CDH cases
Source: Ultrasound in Obstetrics and Gynecology 2004; 24: 121-6


Fetal surgery  [BMJ 2003;326:461-462 ( 1 March )]


Fetal medicine or surgery as alternatives to abortion - Even parents who are opposed to abortion may consider prenatal testing as a way of identifying situations where prenatal surgery might result in a healthy child.


UCSF's Fetal Treatment Center FAQ

Brief, non-technical articles by members of the Fetal Treatment Center team that highlight areas of development and research interest in fetal diagnosis and treatment.


Fetal Surgery Offers Hope - Operating in the womb for spina bifida



New Pap-like Genetic Testing



Early screening for Down, cystic fibrosis [July 17, 2003]

Researchers have created a prenatal test that detects Down syndrome and cystic fibrosis as early as five weeks after conception.  The new test is based around PAP smears of the type normally taken for cervical cancer screening, and it can yield results the same day.

Scientists have known for years that fetal cells can be found in the cervix. However, this is the first time such cells have been efficiently isolated from cervical smears.

According to the researchers, the cells are DNA fingerprinted to distinguish the mother's own cells from the fetal cells. Then they test the fetal cells for genetic abnormalities using single cell DNA detection, new technology that uses smaller cell samples than chorionic villus sampling (CVS) or amniocentesis.

"They can take a single cell and expand the DNA and analyze it, as opposed to the previous techniques, when multiple cells had to be cultured and grown [in a laboratory] before you could get enough DNA to do an accurate test."

The lead researcher is Ian Findlay, of the Australian Genome Research Facility.

This test could be generally available within 2 years.



Triple Screen / Quad Screen / Penta Screen




It's very hard to find the normal value for different markers in the MSAFP / Quad Screen.  Many of the state-run screening programs don't want people interpreting their own results.



[from ob-gyn-l]


Fetal Indications Termination of Pregnancy Program


ACOG Issues Educational Bulletin on Maternal Serum Screening


False Positive Rates

Year 2000 statistics from California Dept. of Health Services - Genetic Disease Branch - 510-540-2534  [Statistics from previous years]

Screen positive reates for inital test results:


I believe that ACOG recently replaced their "bulletin" about MSAFP with a triple screen bulletin. I feel that the cost differential is very worthwhile. But, what is a cost differential? Often these are artificial. In Iowa the state program is automatically the triple screen for about $70 which is less than many companies charge for afp alone. I think the same is true for the large California program where the cost of testing of abnormals (amnio, sono) is factored in. The differential in average detection will be 25% of Downs for AFP alone to about 60% for the triple screen.

For reasons above I personally consider triple screen to be standard of practice. Women over 35 (as with all patients) should discuss their options of invasive testing right off the bat (amnio or CVS), triple screen (understanding the number of missed cases, but also the high chance they will be down screen positive because age is factored in. I think about 25% of 35 year olds will be screen positive.), and ultrasound (also will miss many cases), etc. My experience is that patients are often steered to a particular course by a physician's preference but I think the patient deserves a pretty full explanation and then should make the decision herself.


If you screen all your patients (incl. < 35) with double/triple test your false positive rate must increase (the 60% pick-up rate applies only to maternal age > 35).


NOT TRUE!!

It is well documented that the Down syndrome prenatal detection rate of 60% for a false positive rate of 5% is a common finding when triple screening is offered to women of ALL ages, not just those over 35 (see Palomaki et al. in J Med Screening, 1996, 3: 12-17).

The false positive rate and the detection rate will vary, depending on the age distribution of the screened population. In women over 35, the detection rate is close to 90%, with a false positive rate of 25%. Therefore, 75% of patients over 35 will be informed that their risk is below the risk cut-off for consideration of amniocentesis (in North America, usually that of a 35.5 year old).

If triple screening is available to women of all ages, and if there is close attention to communicating the results of the screen to patients such that the patients understand their own risk (instead of a general population risk like "women over 35"), the amniocentesis rate will diminish. Why? Because the false positive rate of the triple screen is always lower than the percentage of pregnant women who are over 35.

Returning to the original question, is triple screening justified over MSAFP, the answer is "yes". In addition to the studies in the reference quoted above, we just reported our detection of Down syndrome in 10,540 screened women (median age 29.4 years) using a risk cut-off of 1:385 with a false positive rate of 8%. Of 21 cases at mid-trimester, maternal age detected 6 (29%), age+MSAFP detected 8 (38%), age+AFP+hCG (the "double" screen) detected 12 (57%) and age+AFP+uE3+hCG (the "triple" screen) detected 15 (71%). Approximately 11% of our population is over the age of 35 (possible 11% amniocentesis rate); however, the amniocentesis rate for ALL reasons was only 8%.



Amniocentesis



Amniocentesis


Amniocentesis - Search & Destroy by Dave Stewart of NAPSAC- link temporarily unavailable



Ultrasound Resources



PanoramaScan.com - The Ultimate Ob/Gyn, 2D, 3D/Live 4D Ultrasound Source Online - This web site is dedicated for eager-to-learn gynecologists, obstetricians, sonologists and sonographers who want to obtain a huge amount of information about gynecological and obstetric ultrasound (Ob/Gyn ultrasound) , whether a 2D scan or a 3D/4D real time scan. Browse the huge library of ultrasound images, videos, documents and presentations for any obstetric ultrasound, gynecological ultrasound, basic embryology (sonoembryology) and fetal therapy ultrasound subject.


A Comprehensive Guide to Obstetric Ultrasound by Joseph Woo


Preg.info - Ultrasound Scan Information - Information about the goals of ultrasounds at different points in pregnancy


Prenatal Ultrasound from The International Chiropractic Pediatric Association (ICPA)


What is Ultrasound? A Definition of its Use and Practice [from Mothering Magazine]
Elizabeth Bruce explains how ultrasound works and what the indications for its use are.



A Revised Formula Better Estimates Gestational Age From US Biometrics [2/12/16]  - A revision of a 30-year-old formula estimates gestational age more accurately from biometric data on ultrasound, new research suggests.

"The results show that we can be accurate with prediction of gestational age within seven days between 14 and 20 weeks, within 10 days between 21 and 28 weeks, and within 17 days between 29 and 40 weeks," Dr. Daniel W. Skupski, from New York-Presbyterian/Queens in Flushing, New York, told Reuters Health by email.


Misinformation Surrounding Fetal Weight Estimation and Due-Dates -- Enough to Make Anyone Grumpy.   Linda Johnson explains why...

I wonder what the docs and US techs think about Hadlock. He was the physician who figured out the measurements for fetal parts such as the biparietal diameter, femur length, etc. should be for the various gestational ages. His premise was that for an average size baby (7-7.5 lbs), these are the average measurements. There are actually 26 or more algorithms for determining fetal weight/size. A good link with really technical/statistical stuff is Estimation of Fetal Weight from emedicine.com or google fetal biometrics.

All of these measurements are based on averages of babies from the 10th-90th percentile for that gestational age, but whether it is ethnically and racially representative may be questionable. (Think the average Vietnamese vs. Swedes). If you have a baby that will have long legs and probably be tall as an adult, then the femur length will probably be in the 90th percentile and your baby will be predicted to be macrosomic. If you have babies with smaller heads (10th percentile) then the baby will probably be predicted to be IUGR.

Now if those measurements are used as the basis for determining the due date because the docs just don't believe the mom, a baby that is smaller will be assumed to not be as far along in the pregnancy because all babies will be 7-7.5# at birth (please note the sarcasm there). The opposite is true with a baby that will be long. It appears to be due sooner. None of that changes when conception occurred or when term occurs (37-42 weeks).

Changing the due date based on the US measurements shows a very basic misunderstanding of the limits of US, the statistical significance of the algorithms, and the expertise of the US tech.


Parameters for Ultrasound Exams in Pregnant Women [Medscape registration is free]


Placenta-Grading by Tara Herzberg, MD


Cochrane Collaboration Abstracts:

    * Ultrasound for fetal assessment in early pregnancy
    * Routine ultrasound in late pregnancy (after 24 weeks gestation)


OB-GYN Ultrasound Online - An Interactive Text and Journal


Ultrasound in Pregnancy, Infertility and Gynecology and General Ultrasound - a wealth of information, albeit somewhat overly enamored of technology.  This site has a large page called ultrasound in pregnancy web book


Obstetrical Ultrasound Measurements - nice tables of gestational age and typical measurements



Here are some gems from PanoramaScan.com - Ultrasound and Doppler Education in Obstetrics and Gynecology

Subject: Spina Bifida - Early Detection
Question:Earliest gestational age for detection?
Answer: The earliest gestational age for diagnosis is made on 22 weeks gestation after completion of the neural arches of the sacrum.
Detection is based on:
Indirect signs such as lemon sign, banana sign and effacement of the cisterna magna. Ventriculomegaly can be associated.
Direct signs best detected on axial planes are the 'C' or 'U' shape of the affected vertebrae, due to absence of the dorsal arches. Interruption of the cutaneous contour with/without a meningocele is commonly associated.
 
Subject: Down's syndrome (Trisomy 21)
Question:Is this image is sufficient to diagnose a case of down syndrome?
Answer: Diagnoses of Down's syndrome is never reached using a sonogram. Multiple investigations and a certain criteria should be followed. High risk pregnant ladies (of age above 35 years old, previous case of Down's syndrome or family history) should be investigated by the triple marker test (PAPP A, beta HCG and estradiol) first of all.
If high risk (a risk of 1:200) plus a Nuchal skin fold thickening (NTT) above 3mm (with certain standards performed while obtaining an accurate NTT) is an indication for inavisve procedure (amniocentesis) for genetic karyotyping using cytogenetics which we call genetic ultrasound.
Soft markers for Downs' Syndrome are:
1- Echogenic bowel instead of the normal stomach bubble seen in ultrasound.
2- Nasal Hypoplasia or Dysplasia.
3- Reversal of flow in Ductus Venosus (triphasic waveform instead of the normal biphasic one).
4- Low set ear.
5- Upper slanting of the palpebral fissures (eye brows).
6- Abnormal facial morphology (as seen in this sonogram) is also included as a softmarker.

Diagnosis of Down's syndrome is only attaind using genetic ultrasound (amniocenetesis) in high risk group.  

Subject: Embryonic Heart Activity
Question: what is the normal embryonic heart rate
Answer:
Embryonic Heart Rate
The cutoff CRL for detecting cardiac activity by transvaginal probe is 4 mm, and by transabdominal 9 mm.
Heart rate progressively increases to 120-160 beats/minute after 6 to 7 weeks.

.Embryonic heart rate demonstrates certain physiologic variability within its normal range of frequencies that is 150-190 beats/minute for embryos bigger than 10 mm at 8-12 weeks of gestation.
.An embryonic heart rate less than 100 beats per minute (bpm) 7 weeks is recognized as embryonic bradycardia.
. An embryonic heart rate less than 70 bpm has been reported to result in a fetal demise in 100% patients.
.Bradycardia or arrhythmia could be considered as predictors for heart action cessation.
In these cases, an early hemodynamic heart failure was noticed with consequential gestational sac enlargement, yolk sac enlargement (more than 6 mm) and initial generalized hydrops.  



Ultrasound - Risks and Benefits



WASHINGTON (AP) -- Exposure to ultrasound can affect fetal brain development, a new study suggests. But researchers say the findings, in mice, should not discourage pregnant women from having ultrasound scans for medical reasons.

Ultrasound scans can affect brain development from CNN Health

"Rakic's paper said that while the effects of ultrasound in human brain development are not yet known, there are disorders thought to be the result of misplacement of brain cells during their development.

"These disorders range from mental retardation and childhood epilepsy to developmental dyslexia, autism spectrum disorders and schizophrenia," the researchers said.

"Their report is in Tuesday's edition of Proceedings of the National Academy of Sciences.

"The study of 335 mice concluded that in those whose mothers were exposed to a total of 30 minutes or more, "a small but statistically significant number" of brain cells failed to grow into their proper position and remained scattered in incorrect parts of the brain. The number of affected cells increased with longer exposures."

Ultrasound affects mouse brains from Reuters [8/9/06]

"The corresponding neurons in the human brain would probably be formed in the 16th week and continue to migrate for at least 1-2 weeks," Caviness wrote.
 

Prenatal exposure to ultrasound waves impacts neuronal migration in mice.
Ang ES Jr, Gluncic V, Duque A, Schafer ME, Rakic P.
Proc Natl Acad Sci U S A. 2006 Aug 22;103(34):12903-10. Epub 2006 Aug 10.

"Neurons of the cerebral neocortex in mammals, including humans, are generated during fetal life in the proliferative zones and then migrate to their final destinations by following an inside-to-outside sequence. The present study examined the effect of ultrasound waves (USW) on neuronal position within the embryonic cerebral cortex in mice. We used a single BrdU injection to label neurons generated at embryonic day 16 and destined for the superficial cortical layers. Our analysis of over 335 animals reveals that, when exposed to USW for a total of 30 min or longer during the period of their migration, a small but statistically significant number of neurons fail to acquire their proper position and remain scattered within inappropriate cortical layers and/or in the subjacent white matter. The magnitude of dispersion of labeled neurons was variable but systematically increased with duration of exposure to USW. These results call for a further investigation in larger and slower-developing brains of non-human primates and continued scrutiny of unnecessarily long prenatal ultrasound exposure."


From the Medscape article, Unnecessary Testing in Obstetrics, Gynecology, and General Medicine: Causes and Consequences of the Unwarranted Use of Costly and Unscientific (Yet Profitable) Screening Modalities by Martin Donohoe, MD, FACP [4/30/07]:

"Other monitoring tests may be misused. One example of this is fetal ultrasonography. Although it is helpful in estimating gestational age, identifying twin pregnancies, and detecting genetic anomalies, the American College of Obstetrics and Gynecology (ACOG) position is that routine ultrasonographic screening during pregnancy is not mandatory."


Multiple Prenatal Ultrasound Examinations Do Not Hinder Child Development - Medscape analysis - [Medscape registration is free]

This study confirmed that multiple ultrasound scans cause a reduction in fetal growth that disappears statistically as the years pass.

For those who like to think critically, consider that "the control group" had a single ultrasound.  I would personally like to see a control group that is not exposed to any ultrasound at all!

Also, despite findings of an increase in left-handedness among children exposed to repeated ultrasounds, this study does not appear to address that issue.  And this isn't just about the inconvenience of being left-handed in a right-handed world; there was a study that claimed that right-handed people live, on average, nine years longer than left-handed people.  This study has since been controverted, but it did raise some solid questions about how being left-handed endangers people in a world with tools and machinery built for right-handed people.

Effects of repeated prenatal ultrasound examinations on childhood outcome up to 8 years of age: follow-up of a randomised controlled trial.
Newnham JP, Doherty DA, Kendall GE, Zubrick SR, Landau LL, Stanley FJ.
Lancet. 2004 Dec 4;364(9450):2038-44.

"FINDINGS: Examinations were done at 1, 2, 3, 5, and 8 years of age on children born without congenital abnormalities and from singleton pregnancies (intensive group n=1362, regular group n=1352). The follow-up rate at 1 year was 85% (2310/2714) and at 8 years was 75% (2042/2714). By 1 year of age and thereafter, physical sizes were similar in the two groups. There were no significant differences indicating deleterious effects of multiple ultrasound studies at any age as measured by standard tests of childhood speech, language, behaviour, and neurological development."



I really like this web page about diagnostic ultrasound use during pregnancy:

I also found this one, which says the effect on the baby might be as loud as a subway train only if it is pointed directly at the baby's ear. Fortunately, the ear is of little interest in obstetric ultrasound, so the energy is rarely focused there.

For those of you who remember this from physics class, the Doppler effect is the bunching up or spacing out of sound waves caused by an object moving towards or away from you. The example given is almost always that of a train coming into or leaving a station.
Well, the ultrasound used for listening to the baby's heart and measuring fetal blood flow (which is different from ultrasound for getting a picture) uses the Doppler effect to assess the movement of the baby's heart and blood flow. It does a nifty job of translating that movement into a sound so that we feel as if we are actually hearing the baby's heartbeat or the blood flow, but we're not really.

So when I heard the effect of ultrasound's being compared to a subway train coming into a station, I kind of assumed there was some confusion about the Doppler effect. In fact, it seems as if they really are talking about decibel levels. :-)

Anyway, you've probably noticed that when anyone uses ultrasound on your baby, either to listen to the heartbeat or assess the baby visually, they are mostly aiming the transducer at the baby's midsection, since that's where most of the areas of interest are.

Also, I think a baby's sense of hearing doesn't develop until midway through the pregnancy, and most visual ultrasounds are done before then. Dopplers used to listen to the baby's heartbeat in later pregnancy and in labor are generally pointed as directly at the baby's heart as we can manage, and that's a good way away from the baby's ear at term.

I don't think ultrasound should be used without good reason, but it's an amazingly helpful diagnostic technique that is remarkably noninvasive to both mother and baby.

However, babies do seem to react to the Doppler; moms report that the babies kick and squirm more. However, this is almost always accompanied by asking the mom to recline, and it could be the position change that's causing the baby to kick and squirm. Sometimes, when I'm trying to assess the baby's position with the mom in an upright position, I'll use the Doppler to locate the baby's heart (through the distinctive sound it makes). I don't recall a mom's ever reporting more baby kicking or squirming when the mom is in an upright position. This makes me think it's probably the position change more than the Doppler use that is causing the baby to move.

Anyway, I respect a mother's wishes to minimize her baby's exposure to ultrasound, but when I weigh the evidence, the benefits of judicious use of ultrasound far outweigh the risks.


Ultrasound Scans- Cause for Concern by Sarah Buckley, MD  [This is one of the free articles available from BirthLove - Leilah McCracken's site.  In general, this is a subscription site - well worth the $10 membership fee.]  [Ed: birthlove.com is not available at this time.]

or a similar article - Ultrasound - Reasons for Caution, by Sarah J. Buckley, MD, from the section on Medical tests and procedures at Women of Spirit


British Medical Ultrasound Society - Guidelines for the safe use of diagnostic ultrasound equipment


ECMUS Safety Committee Tutorial - Epidemiology of diagnostic ultrasound exposure during human pregnancy


Obstetric Ultrasound - The Safety References by Joseph Woo - Recent Studies purporting to the safety of prenatal exposure to diagnostic ultrasound


Read the FDA's response to a petition to have Doppler fetoscopes changed to an over-the-counter status, rather than a controlled medical device. "OTC purchase and use of Doppler fetoscopes by a lay user raises new issues of safety and effectiveness.  . . . These products introduce acoustic energy into the body.  The potential for adverse effects from long-term exposure to the fetus in early pregnancy are unknown.  For example, there are some studies that suggest exposure to diagnostic ultrasound during pregnancy can have an effect on human development.  (Keiler et al., Early Human Development 50:233-245 (1998); Keiler et al., Epidemiology 12:618-623 (2001).) You may also be aware of ultrasound bone healing devices that operate at frequencies and output levels similar to those of ultrasound Doppler monitors.  These devices have been shown to produce biological effects in humans when used for only 20 minutes daily. (Duarte, L.R., Arch. Orthop. and Trauma Surg., 101:153-159 (1983).)  The agency has concluded that unsupervised exposure to ultrasound may pose a risk to the health of the mother or a developing fetus. . . . FDA has seen no evidence that there are benefits that would outweigh these possible risks associated with OTC availability of fetal ultrasound devices.  The materials you have provided do not establish that OTC purchase and use of these products would result in any medical benefit to the fetus or the mother.  FDA cannot rely upon the absence of  specific adverse events as a basis to determine that repeated, prolonged, and unsupervised ultrasound is safe.  . . . While I agree that women want to hear their unborn babies, I do not believe that consumers would purchase devices enabling them to achieve that purpose if the device might potentially cause harm to the fetus through uncontrolled and unlimited use."


Ultrasound linked to brain damage - Risk is 'only a possibility' but the discovery warrants further study, researcher says.  "LONDON - Swedish scientists have uncovered evidence suggesting that ultrasound scans on pregnant women can cause brain damage in their unborn babies."  [Dec. 10, 2001 - research scientist Professor Juni Palmgren]

Sinistrality-a side-effect of prenatal sonography: A comparative study of young men.
Kieler H, Cnattingius S, Haglund B, Palmgren J, Axelsson O.
Epidemiology 2001 Nov;12(6):618-23

"Although ultrasound during pregnancy is used extensively, there is little published on adverse fetal effects. We undertook a cohort study including men born in Sweden from 1973 to 1978 who enrolled for military service. We estimated relative risks for being born left-handed according to ultrasound exposure in fetal life using logistic regression analysis. Eligible for the study were 6,858 men born at a hospital that included ultrasound scanning in standard antenatal care (exposed) and 172,537 men born in hospitals without ultrasound scanning programs (unexposed). During the introduction phase (1973 to 1975) there was no difference in left-handedness between ultrasound exposed and unexposed (odds ratio = 1.03, 95% confidence interval (CI) = 0.91 to 1.17). When ultrasonography was offered more widely (1976 to 1978), the risk of left-handedness was higher among those exposed to ultrasound compared with those unexposed (odds ratio = 1.32, 95% CI = 1.16 to 1.51). We conclude that ultrasound exposure in fetal life increases the risk of left-handedness in men, suggesting that prenatal ultrasound affects the fetal brain."

See Related Articles


Is it possible that ultrasound could cause the baby's head to harden, thus making birth more difficult?

Accelerated healing of distal radial fractures with the use of specific, low-intensity ultrasound. A multicenter, prospective, randomized, double-blind, placebo-controlled study.
Kristiansen TK, Ryaby JP, McCabe J, Frey JJ, Roe LR.
J Bone Joint Surg Am. 1997 Jul;79(7):961-73.

"We concluded that this specific ultrasound signal accelerates the healing of fractures of the distal radial metaphysis and decreases the loss of reduction during fracture-healing."

See Related Articles


Diagnostic Ultrasound Imaging in Pregnancy - [THIS DOCUMENT IS NO LONGER VIEWED BY NIH AS GUIDANCE FOR CURRENT MEDICAL PRACTICE.] - National Institutes of Health Consensus Development Conference Statement. February 6-8, 1984

This is an old study, but it does a good job of describing the potential problems associated with ultrasound.

"A number of biological effects have been observed following ultrasound exposure in various experimental systems. These include reduction in immune response, change in sister chromatid exchange frequencies, cell death, change in cell membrane functions, degradation of macromolecules, free radical formation, and reduced cell reproductive potential."


Consumer Dopplers

This REALLY scares me!! The fact that anyone can get and use a doppler on their developing fetus, at any point and for any length of time in unlimited exposures, just scares the heck out of me. I can understand the occasional use or need in labor, when the heart tones are evaluated by a skilled attendant. The thought of people just wandering around out there whipping out the doppler each morning so grandma or the neighbors or little siblings can hear and "bond" with baby via a doppler signal, without knowing the potential risk (and do we truly know the risk?) well.... that is just plain frightening. I am not convinced that dopplers are safe. I know there have been studies that have shown doppler ultrasound can alter cellular activity. So we do this routinely and repeatedly to developing fetuses? Excuse me?  And now we are going to make such devices available to anyone with $35? Am I the only one who is startled by this? So reminiscent of the old days when shoe stores had the foot xray machines! Before it was clear the damage xray could have on the body. Seemed harmless enough at the time, and oh so much fun!

This is not just an amplifier, these are ultrasound devices. I believe the use should be restricted and not supplied to the general public. Most women having home or waterbirth also have qualified attendants who are skilled at interpreting normal and abnormal changes in FHT. If Jane Q Public is interested in FHTs, a fetoscope is simple and easy to use. Perhaps not so sexy to those who love technology ... but as far as I am concerned, normal birth could use a lot less of that.


According to Anne Frye, midwife and author of "Understanding Lab Work  in the Childbearing Year" (4th Ed.)p. 405:

Doppler Devices:  Many women do not realize that doppler fetoscopes are ultrasound devices. (apparently, neither do many care providers.  Time after time, women are assured by doctors and even some nurse midwives that a doppler is not an ultrasound device.) . . . .

Not well publicized for obvious reasons, doppler devices expose the fetus to more powerful ultrasound than real time (imaging) ultrasound exams.  One minute of doppler exposure is equal to 35 minutes of real time ultrasound.  This is an important point for women to consider when deciding between an ultrasound exam and listening with a doppler to determine viability in early pregnancy. . . . .

If you have a doppler, put it aside and make a concerted effort to learn to listen yourself!  Save your doppler for those rare occasions when you cannot hear the heart rate late into pushing or to further investigate suspected fetal death.  " copyright l990, Anne Frye, B.H. Holistic Midwifery.

Personally, after 23 years of attending births, I would not permit a doppler in my house if I were pregnant.  You always know that something is ultrasound because there will be "jelly" involved.  If you want a cheap listening device for the baby's heart just save the core from a roll of toilet paper. Put one end on the lower belly and the other on hubby's ear.  If you want to know your baby is doing well, count the fetal movements in a day.  Starting at 9 a.m. count each time the baby kicks.  There should be l0 distinct movements by 3 p.m.


I have a friend who's a chiropractor/homeopath.  He uses kinesiology to evaluate well-being and select remedies.  He related a story of one of his clients, who came in for an appointment very early in her pregnancy and then a few weeks later, after the first prenatal appointment.  My friend said that his evaluation of the fetus at the first appointment was that it was very healthy, but it had been traumatized by the second appointment.  His best guess was that the ultrasound had been a very traumatic event for the baby.

This has given me some food for thought; after all, what do we really gain by routinely using hand-held Dopplers to listen to the baby's heartbeat?  If there's no question of dates, it doesn't give us any information that will help this mother and baby to have a healthier pregnancy.  Even later in pregnancy, if we're concerned about the baby's well-being, it's easy enough to listen with a fetoscope or even just with your ear!  I'm sure that's much less traumatic for the baby.


Weighing the Risks: What You Should Know About Ultrasound [from Mothering Magazine]
Examining the risks, benefits and implications of the practice, Sarah Buckley questions if routine ultrasounds should be a part of most pregnancies.


Ultrasound - weighing the propaganda against the facts



Web Links re: Dangers of Ultrasound




Prenatal Ultrasound Tied to Autism Severity in At-Risk Kids [9/21/16] by Megan Brooks


Ultrasound pointed at the fetal head directly vibrates the sensitive hearing structure of the fetus, creating high-intensity noise in the audible range.  from A Noisy Womb [Acoustical Society of America - 142nd Meeting Press Release]

The sounds the fetus hears in the uterus during ultrasound procedures.

Spectral characteristics of the sound generated by ultrasound imaging systems in the human body.


Here's some web links re the dangers of ultrasound.  Don't use a doppler without giving this informed consent info.

Good/bad site. has some research results in it. Bioeffects of ultrasound studies 1980-1990
Studies in the 1980s and 90s purporting to the safety of prenatal exposure to diagnostic ultrasound:

Dyslexia : "In the first, Stark et al examined 425 children aged 7-12 who had antenatal exposure to ultrasound and 381 matched children who had not. They looked at 16 outcomes, one of which was dyslexia as measured by a single reading test and concluded that there was a significant correlation (p less than 0.01)." Non-right handedness "TI-le same Norwegian study did find a correlation between ultrasound exposure and non-right-handedness. 19% of the exposed children were non-right handed as compared with 15% of the controls. Although this result has been reported as significant, the correlation is relatively poor and is now the subject of ongoing research by the same group." "The meta-analyses of randomised controlled trials of adverse effects show only that there is a just significant increased tendency to non-right handedness in the offspring of women who had scans; the complexity of the study makes the observation difficult to interpret. Nevertheless continual vigilance is necessary particularly in areas of concern such as the use of pulsed Doppler in the first trimester. "

Obstetric Ultrasound - The Safety References (essentially the same page as above)

Ultrasound: Weighing the Propaganda Against the Facts by Beverley Lawrence Beech - "Obstetricians in Michigan (Lorenz et al., 1990) studied fifty-seven women who were at risk of giving birth prematurely. Half were given a weekly ultrasound examination; the rest had pelvic examinations. Preterm labour was more than doubled in the ultrasound group–52 percent–compared with 25 percent in the controls. Although the numbers were small the difference was unlikely to have emerged by chance."

Ultrasound: More Harm than Good? by Marsden Wagner (this is a good site to look at benefits vs risks, including having scans for "first pictures")

http://text.nlm.nih.gov/nih/cdc/www/41.htmlhttp://text.nlm.nih.gov/nih/cdc/www/41txt.html#Head3

Excerpt from the National Institutes of Health Consensus Development Conference Statement -- [February 6-8, 1984] - "For all practical purposes, fetal dose cannot be quantitated precisely. For this reason, there are no data on the dose to either the mother or the fetus in the clinical setting."

"A number of biological effects have been observed following ultrasound exposure in various experimental systems. These include reduction in immune response, change in sister chromatid exchange frequencies, cell death, change in cell membrane functions, degradation of macromolecules, free radical formation, and reduced cell reproductive potential. It should be noted that (a) some of the studies employed energy levels greater than would be expected to exist in clinical use; (b) in vitro exposure conditions to ultrasound used in many of the experiments are hard to place in perspective for risk assessment; (c) some of the observations, for example, sister chromatid exchange frequency changes and induction of chromosomal abnormalities, have not been reproducible, tending to refute the original findings. Nevertheless, some of the reported effects cannot be ignored or overlooked and deserve further study as outlined in our answer to Question 5. The existence of these studies is one of the factors that contributed to our decision that routine ultrasound screening cannot be recommended at this time." http://text.nlm.nih.gov/nih/cdc/www/41txt.html#Head6 "Ultrasound examinations performed solely to satisfy the family's desire to know the fetal sex, to view the fetus, or to obtain a picture of the fetus should be discouraged. In addition, visualization of the fetus solely for educational or commercial demonstrations without medical benefit to the patient should not be performed."

March of Dimes says: "Ultrasound is considered safe for mother and baby."
(editorial) Considered safe.  That doesn't mean they _are_ safe.  Xrays were "considered safe" for years until problems with over-exposure started to come into public scrutiny.  We know that listening to a rock concert can cause permanent damage to one's hearing.  Ultrasounds are high frequency sound waves.  By the time they get to the baby - what is he hearing? There are frequencies that can kill.  There are other frequencies that can do other types of damage.   Are we sure ultrasounds are safe?(end editorial)

Ultrasound - weighing the propaganda against the facts "Low detection rates (either from poor equipment or unskilled operators) means all the babies get the ultrasound dose but few of them get the 'benefits' of accurate diagnosis. The skill of the operators will vary (everybody has to learn sometime) but even with the best machines and the best operators misdiagnoses occur."

Ultrasound Studies "The study of Liebeskind et al in 1979 also indicated that exposure to diagnostic levels of ultrasound insonation for 30 minutes caused increase in SCEs in human lymphocytes and in a human lymphoblast line."

Birth Trauma (this site should be added to your "birth trauma" section - risks and benefits) "The routine use of ultrasound has caused some concern expressed in the research.  In a NEJM paper, the use of ultrasound did not change the perinatal outcome in 15,151 low©risk pregnancies.  Ultrasound has been found to be associated with delayed speech and dyslexia in children."

ULTRASOUND IN OBSTETRICS: A QUESTION OF SAFETY "Millions of women and their unborn children are being exposed to diagnostic ultrasound during pregnancy and childbirth without the women being advised prior to exposure that there has been no well-controlled scientific investigation carried out to study the delayed, long-term effects of ultrasound on human development. Ova, embryos and fetuses are often exposed to prolonged sonography because the physician or technician lacks sufficient expertise to evaluate what he or she is seeing."

Risks of Ultrasound Screening "I do not agree with the statement that "a lot of embryos have been exposed to ultrasound over the last 25 years with no documented ill effects." Lieberskind's research indicated changes in cell structure that persisted over 10 generations and although researchers attempted to rubbish the research it was repeated by other researchers, and now we have research from Ireland that also shows affected cells." "...there is no evidence that infant outcomes have been improved by routine ultrasound examinations.  Researchers have enthusiastically focused on what ultrasound could find but have paid little or no attention to the potential adverse long-term effects. As a result, despite ultrasound being enthusiastically used over the last 30 years, there is no good research that addresses the anxieties that ultrasound may be responsible for dyslexia, learning difficulties and behavioural problems."

Ultrasound Scans May Harm Unborn Babies "It would certainly seem prudent to avoid all routine absolutely unnecessary ultrasound scans for fetal observation. There appears to be more than enough evidence to warrant this recommendation. Pregnancy complications are another issue and one would have to weigh all the factors individually when attempting to determine the benefit/risk ratio."

Ultrasound Safe? "Ultrasound waves are known to affect living tissues in at least two ways. First, the sonar beam heats the highlighted area by about 2°F. This is presumed to be insignificant, based on whole-body heating in pregnancy, which seems to be safe up to 5°F. The second effect is cavitation, where the small pockets of gas that exist within mammalian tissue vibrate and then collapse. "

FETAL ULTRASOUND Ultrasound examination of the fetus may not be entirely harmless, reports Dr. Doreen Liebeskind at the Albert Einstein College of Medicine. Human lymphocytes and a continuously growing lymphoblast line exposed to diagnostic levels of ultrasound demonstrated a significant increase in the number of sister chromatid exchanges. Investigators believe that these exchanges indicated damage to chromosomes. (Family Practice News, April 1, 1980, p. 17) also (for your breast feeding page)

BREAST-FED BABIES/DOCTOR VISITS Breast-fed babies visit the doctor less often during the first six months than do bottle-fed infants, according to Dr. Randolph Paine, a University of Iowa physician. By six months of age, the breast- fed infants in his study had averaged 1.65 visits to the doctor while bottle-fed infants averaged 2.8. Over 75% of the breast-fed infants in the study had never visited the doctor, other than for routine checkups or accidents. Twelve percent had only one visit, and ten percent had two to five visits by the age of one year. Only three percent of the bottle-fed babies had no visits, and some of the remaining had as many as sixteen visits. Infants who were exclusively breast-fed for more than three months had significantly fewer visits during the entire first year of life, and the longer the infant is breast-fed and fewer the number of illness-related visits. Dr. Paine states that there are five advantages to breast feeding: (1) Human milk contains high levels of fatty acids which researchers feel may be important in the growth of the baby's brain, (2) Breast milk immunizes the baby until he can build his own immunity, (3) Breast-fed babies have fewer allergies than do bottle-fed infants, (4) Mother-infant bonding is strengthened through breast feeding and (5) feeding the baby is much more convenient and less expensive. (American Family Physician 21:210, January 1980, p. 210)



Biophysical Profile - BPP



Practical Guidelines for Antepartum Fetal Surveillance from the AAFP - describes fetal movement counts, nonstress test, contraction stress test, biophysical profile, modified biophysical profile and vibroacoustic stimulation.


Fetal Breathing Movements Decrease Soon Before Labor Starts

I recently observed a bio-physical profile done at 42 weeks by a sonogram school in Dallas. This particular mom got an ok to wait on a normal delivery at the birth center where she was planning her birth. If I understood correctly, a scoring system is used (similar to APGAR) to determine the overall health of the fetus. The only thing this baby was marked down for was that there were no respiratory movements. However, we were told that this was found to be a common occurrence up to 72 hours prior to the normal onset of labor. Because of this, the lady doing the US was not concerned as long as labor began within 72 hours (otherwise another Bio-physical). Labor did start right at 72 hours. 

All "normal" fetuses "breathe". Or at least they exhibit motions of the thorax, diaphragm, and abdomen that appear like breathing motions, thus the name for them. Fluid is moving in and out of the lungs. This has been documented using Doppler sonography to measure and image the fluid motions (for color Doppler images of this, see Cartier MS, Fetal Doppler, in DuBose TJ (Editor); FETAL SONOGRAPHY, W. B. Saunders Co. 1996, pp. 301 & color plate 13-33). As far as what is actually happening, who knows? The current theory is that this is a maturing process for the lungs, and may have something to do with preparing them by moving the amniotic fluids in and out of the lungs along with the lecithin sphingomyelin.

I do know that it is a normal and expected process. However, I am NOT familiar with the absence of "breathing motions" being normal within 72 hours of delivery. Of course, most of my experience has been in outpatient labs and I have not done too may sonograms right before delivery.


A physiologist told me that the decrease in fetal breathing is a result of prostaglandin increase. Agree that there could be benefits. Hadn't thought about yours with reduction of fluid in the lungs. I went with the mec. aspiration. 



Fetal Growth Charts



Birth Weight for Gestational Age - Public Health Agency of Canada


The Gestation Network aims to highlight the importance of an individual approach in the assessment of fetal growth, based on maternal, fetal and pregnancy characteristics.   This site contains free software for calculating gestational age and customised fetal growth limits and birthweight centiles.



Ultrasound Errors



June 20, 1995 issue of The Wall Street Journal, "Doctors Who Perform Fetal Sonograms Often Lack Sufficient Training and Skill."



Routine Ultrasound



I am finding that I have some clients who are particularly anxious to have an ultrasound and others who would shun one unless circumstances were dire.

I tell clients that US appears to be a wonderful tool, and that, to date, we know of no short-term adverse effects related to its use. However, they need to know that we only order them for medical indications (and I list these if they are interested) , that their insurance will only pay if there is an indication. Many people are surprised to find out that we don't know if there are any long term consequences of this technology and that moreover, it can take many years to figure that out. I tell them that is because of this that I would rather stick to ordering US when the info gained is really important in clinical decision making. This is a sensitive issue in some ways for me because my backup physician recently got a US machine and will US just about any thing that moves, and I understand why but it makes me uneasy (not that I don't know that this behavior is pretty commonplace).

I also talk to couples about the other ways in which we can be attuned to whether a pregnancy is going well, and emphasize that no technology can guarantee a perfect outcome but that by being responsible about self care, they play the primary role in ensuring good health for their offspring.


U/s can rule out some placental defects, and show heartbeat, but Doppler can usually give a heart beat too. otherwise its just window dressing. this is the "speech" I use about u/s in general.

It is my understanding that the ultrasound waves used in a sonogram are pulsed where the ultrasound waves used in the Doppler are continuous. They have the potential of being more dangerous than a sonogram in this spectacle of unknowns for two reasons. If the most damage is done from long exposure, then a fetal monitor during labor has more potential for damage than the others, if damage is more likely during a certain stage of development then the doptone device is sure to hit it. And, though I can't remember reference to this, isn't it also possible that a continuous wave is more dangerous in itself?

It seems a contradiction to me to on the one hand recommend that a client avoid a scan and on (or in) the other hand use a Doppler at prenatals and during her birth. Ultimately, I assume, we all will give the clients what they want if we can and unless we are emphatically opposed but I hope they can make informed choices.


I agree with the above statement. However, the statements about danger from ultrasound is exaggerated, for continuous wave Doptone or pulsed sonography (imaging). The Doptone has been in very wide use for decades with no problems found. How long do we have to go through this before we acknowledge that sound waves at the levels we are talking about just are not dangerous. Think about it, this is ultrasound, therefore can not be heard by humans or any living thing at these frequencies. However, what other high frequencies are people around every day that we can't hear? How about high frequency sounds from auto engines, jet engines, electric motors and house hold appliances? The major risk is during the embryogenesis stages for heating. Blood flow and interstitial fluid motions dissipate the heat faster than it can accumulate. I am sure a mother will raise her core temperature more by lying in the sun than from any medical use of ultrasound.


Recommendation against routine third-trimester ultrasound examination of the fetus - prepared for the U.S. Preventive Services Task Force



Avoiding Ultrasound



Ultrasound - No Benefits

All the various reports of obstetric ultrasound really point to scans producing only one benefit - they turn some perinatal losses into abortions, by removing some lethal congenital abnormalities in the second trimester. Any other screening use of ultrasounds is not supported by published evidence! 

Mother Rails Against Ultrasound


Doptones use continuous ultrasound waves. Those of you who want to avoid ultrasound should avoid doptones, ultrasound scans, and external electronic fetal monitoring. Ultrasound waves do cause changes at the cellular level, including causing them to heat up, grow in weird ways - loss of contact inhibition (contact inhibition is what keeps cells from growing into each other in normal circumstances) - cells that become cancerous lose their contact inhibition.

Ultrasound does cause cell changes, and should be used only when medically necessary or medically indicated. Or in labor, perhaps when it is easier to check the heartbeat quickly, if necessary.


The information about 1 min of Doppler = 35 min of ultrasound is in Anne Frye's Holistic Midwifery and her Understanding Diagnostic Tests in the Childbearing Year. This is because the waves used in a Doppler are continuous while the ones from an imaging ultrasound are pulsed. Electronic fetal monitors are continuous Doppler. Occasionally there is a place for this technology but all the time ? --- NO !!

This is from A Guide to Effective Care in Pregnancy and Childbirth by Enkin, Keirse and Chalmers. For those that don't know, this book is a guide to a huge two-volume book in which the studies done on most everything done in obstetrics have been evaluated and conclusions drawn. This work is also the basis for The Oxford Database of Perinatal Trials.

I quote " There has been surprisingly little well-organized research to evaluate possible adverse effects of ultrasound exposure on human fetuses. " ....... " The place of ultrasound for specific indications in pregnancy has been clearly established. The place, if any, for routine ultrasound has not as yet been determined. In view of the fact that its safety has not been convincingly established, such routine use should for the present be considered experimental, and should not be implemented outside of the context of randomized controlled trials. "

You might also be interested to know that what you hear with a Doppler is not actually the babies heartbeat. It is a man made sound. A transducer interprets the reflected ultrasound waves and turns them into an audible sound.


List of Links


http://www.changesurfer.com/Hlth/EFM.html
Efficacy and safety of intrapartum electronic fetal monitoring: an update.

http://www.childbirth.org/articles/efmref.html
Fetal Monitoring FAQ

http://www.childbirth.org/articles/efmfaq.html
Routine Electronic Monitoring Of Fetuses Is

http://www.childbirth.org/articles/efm1.html
On the safety of prenatal ultrasound

http://www.alternamoms.com/ultrasound.html
Risks of Ultrasound Screening

http://www.midwiferytoday.com/enews/enews1n31.htm
Shadow of a Doubt
safety of ultrasound scans

http://www.newscientist.com/ns/19990612/newstory12.html
Ultrasound
Report on US from Internat'l. Chiropractic Pediatric Assoc.

http://www.compleatmother.com/ultrasound_danger.htm
Ultrasound: Weighing the Propaganda Against the Facts

http://www.midwiferytoday.com/articles/ultrasound.htm
What happens when you alter settings on your diagnostic ultrasound machine?

Safety considerations for ultrasound
>http://www.efsumb.org/tutpap1.htm



Discussion Regarding Link Between Ultrasound and IUGR



Ultrasound vs. Fundal Measurement to Detect IUGR: Lancet 342 (1993) pp 887-891) - gave one group of women several scans, and the other one scan. The only difference was that the intensively scanned group had a higher IUGR rate.


Ultrasound may change baby's cell growth [Brennan, Dublin, New Scientist, 1999]


Effects of frequent ultrasound during pregnancy: a randomised controlled trial.
Newnham JP, Evans SF, Michael CA, Stanley FJ, Landau LI
Lancet 1993 Oct 9;342(8876):887-91

A study of over 1400 women in Perth, Western Australia compared pregnant mothers who had ultrasound only once during gestation with mothers who had five monthly ultrasounds from 18 weeks to 38 weeks. They found significantly higher intrauterine growth restriction in the intensive ultrasound group. These mothers gave birth to lower weight babies.

The researchers concluded that prenatal ultrasound imaging and Doppler flow exams should be restricted to clinically necessary situations. This recommendation comes at a time when ultrasound during prenatal visits has become increasingly popular and serves as a kind of entertainment feature of office check-up visits.


OB/GYN News July 15, 1993, Volume 28 #14, which says basically that ultrasound screening of low-risk women provides no clinical benefits for mother or baby, and did not change the rate of adverse perinatal outcomes. It discusses placenta previa, but nothing about growth retardation. In another article (from the Journal of Nurse-Midwifery Vol 29 No. 4 from July/August 1994) "Preliminary data from the United Kingdon suggests a higher incidence of leukemia is found in children exposed to diagnostic ultrasound. This article also mentions that one of the indicated uses is for establishing gestational age when there is a 2-3 week discrepancy in dates, but also does not specifically discuss growth retardation, however, this second article has a list of 16 references at the end.


More Discussion Regarding Link Between Ultrasound and IUGR



Rumors of DNA Changes from Ultrasound



What studies of DNA changes?
I've never heard of one!
Where are they!?
I'm serious... I REALLY WANT TO KNOW!
If they are out there, then we NEED to see them.
Does anyone have anything concrete anywhere?!


Hopefully someone will post NEW stuff, but a couple of old things things came to hand, from the '70s & early '80s when I was semi- organized & actually got some things into the file:

A letter to the editor in Birth & the Family Journal (now called Birth) V4:3 refers to these studies with conflicting results re chromosome damage (other studies are cited on other aspects of u/s):
Galperin-Lemaitre & Kirsch-Volders
Ultrasound & Mammalian DNA
Lancet 2:662, 4Oct75

Fischman
Ultrasound & Marrow-Cell Chromosomes
Lancet 2:920, 20 Oct73

Macintosh & Davey
Chromosome Aberrations Induced by Ultrasonic Fetal Pulse Detector
Brit Med J 4:92, 1970

Mermut, et al.
The Effects of Ultrasound on Human Chromosomes In-Vitro
Obstet Gynec 41:4, 1973

Fetal Effects of Ultrasound: A Growing Controversy, D. Haire; J Nurse-
Midwifery V29N4 July/Aug84
summarizes the (then) unknowns & areas of concern, gives references, and includes a sample/proposed informed consent form for u/s exposure. (!!)

Research in Ultrasound Bioeffects: A Public Health View, M E Stratmeyer;
Birth Fam J 7:2 Summer 80
reviews human & lab studies, gives references to the studies.

The People's Doctor V7N11 is on u/s, contains such tidbits as: "On February 13, 1979, the FDA sent a letter to all physicians notifying them of the biological effects in test animals exposed to ultrasound at levels representative of ultrasound's current diagnostic use." "...Dr Liebeskind [asst. prof. of radiology, Albert Einstein College of Medicine] observed changes in cell appearance, motility, and DNA synthesis that were passed on in succeeding cell generations..." (I think it's her work that I saw a video or movie about, years ago; there's a reference to her on a tv news show in at least one of the other papers listed here.) Also mentioned in this issue are the Oxford Survey of Childhood Cancers (Britain) and the WHO 1982 publication on ultrasound.

Birth 13:1 accidentally published some uncorrected proofs of articles on u/s, the corrected ones were subsequently published as a 'special supplement' in Dec '86.

ICEA has published position papers on diagnostic u/s & EFM which are well referenced & might be of interest; does anyone have recent versions of these?



Nuchal Translucent Scan



Ultra-Screen® from NTD Laboratories is a First-trimester prenatal screening protocol designed to provide patient specific risk for Down Syndrome, trisomy 18 and other chromosomal abnormalities. Ultra-Screen® combines ultrasound measurement of the fluid accumulation behind the neck of the fetus (nuchal translucency) with maternal serum markers and is the earliest and most effective Down Syndrome screen available.


Half of Chromosomal Defects Seen With Nuchal Translucency Are Not Trisomy 21


A lady colleague of mine has heard of a procedure, to determine the health of an unborn child early in the pregnancy, could anyone explain the procedure in reasonable technical detail, how it works its advantages, disadvantage and exactly what can be determined.

Using ultrasound at ~10 weeks it's possible to measure the thickness of the soft tissue at the back of the neck/base of skull. There are data to suggest that ( subject to correction for gestational age and maternal age ) can be used to predict the risk of Down's syndrome and other trisomies in the fetus. This is achieved with detection rates comparable to maternal serum screening and has the advantage of allowing earlier suspicion and thereby earlier definitive testing to give reassurance or allow option of termination of pregnancy.

There are also other data to suggest that with extreme nuchal thicknesses, even with normal chromosomes the fetus may have other life- threatening anomalies or be at risk of second trimester loss.

Other workers have cast doubts on the effectiveness and value of this method as a population based screening tool. More work is in progress, as is work attempting to combine nuchal scanning with ( new ) maternal serum markers.



Significance of Hydronephrosis/Pyelectasis



These days a dilated ureter is noten on the chart only when it is VERY dilated. And it isn't seen as cause for concern unless there are other problems found.


In a day and age where 'global' fees for prenatal care don't even begin to cover the costs of doing business (like malpractice insurance), this finding is yet another portal of opportunity to 'medicalize' pregnancy and therefore increase reimbursements for what is an otherwise normal developmental finding. It is also a very effective tool for creating dependency on the system by sowing seeds of doubt and then reinforcing them with anxiety in the form of serial visits/testing. I think this particular one is getting worn out as people get wise to it....... That said, my parameters in absence of any suspicion for abnl chromes would be  4mm to 7 mm watch, >7mm (as in 'very'?) refer MFM for eval/man.


I think it usually means the baby needs to urinate!



Significance of Cord Coiling



Factors that provide optimal umbilical protection during gestation

Contemporary OB/GYN 42 (3) March 1997 Strong TH

excerpts:

5% of fetuses lack umbilical vascular coiling

...among neonates without umbilical coiling, one team noted a 10% stillbirth rate. As such, the straight umbilical cord may present a risk for intrauterine death that exceeds that with maternal diabetes or hypertensive disease.

Other reports have have documented significantly increased rates of intrapartum FHR decelerations, operative interventions for fetal distress, and meconium staining. Some have noted higher rates of fetal growth retardation, oligohydramnios, fetal anomalies, low APGAR scores, low umbilical arterial pH values, neonatal intensive care unit admissions, and preterm deliveries.

Recommendations from the article:

Nuchal Cord on Ultrasound



See also: Nuchal Cord - Somersault Maneuver


Prenatal ultrasonographic diagnosis of nuchal cord(s): disregard, inform, monitor or intervene?
Sherer DM, Manning FA
Ultrasound Obstet Gynecol 1999 Jul;14(1):1-8


Nuchal cords: timing of prenatal diagnosis and duration.
Collins JH, Collins CL, Weckwerth SR, De Angelis L
Am J Obstet Gynecol 1995 Sep;173(3 Pt 1):768

Nuchal cords can be diagnosed prenatally with ultrasonographic imaging. A prospective study determined the timing of nuchal cord formation and, in some cases, resolution before delivery.

What do you do when you find a nuchal cord X's 2 in a normal pregnancy at 38 weeks gestation ???


I try to decide, from the u/s, whether it seems to be a tight wrap or just a loose one. If it's loose, I generally don't actually DO anything but make a mental note and watch for it at delivery. If it's noticeably tight, I tell the parents, get the mother to do kick counts and stuff, watch the AF volume, and be very nervous... If I even think about it, I do NSTs, but they are almost bound to show small variables, at least, from the beginning. And finally, I don't let the lady labor at home. At the first inkling of contractions, she goes in to be monitored.


Excellent plan. I would do pretty much the same thing.


How do you tell from ultrasound whether a nuchal cord is tight or not?


Interesting question... The best answer I can give you is, how do you tell (without touching) whether a nuchal cord AT DELIVERY is tight or not? I just look... it seems fairly obvious to me when a cord is tight or loose and flapping in the breeze. Ultrasounds are VERY good these days, and I haven't really given that question much thought.


Color Doppler should provide some information neh?


Not to belabor this point but i do recall speaking with Dick Berkowitz about nuchal cords on ultrasound and he was most emphatic in his suggestion that this NOT be reported. perhaps this finding in a woman who offers that her fetus' movements have significantly decreased might have a different import; but barring this, we create the great potential to create more problems than we avoid.


Dr Hon had a very good maneuver he used. Press on the fundus and watch response of the FHR.


Not an issue. Cords are common -- what, maybe 20% of kids at  birth?       (and I think it's a great reason to avoid AROM). The  kiddo is really unlikely to get the cord tight enough to cause problems in  pregnancy -..    I would not be any more -- or any less -- watchful at this  birth than at any other births. We've all seen TONS of cords round necks -- once twice three  times, more -- only on the most rare occasion is a cord ever an issue.  Heck,  half the time we hear the rare FHTs which are associated with cord pressure, the  cord isn't around the neck anyway -- it's wrapped elsewhere.

A baby is designed to have a cord long enough to allow it to  get born without causing difficulties. The uterus itself descends during second  stage as the baby travels through the birth canal, giving an extra six inches  or so of slack.        cause ANY  problem in labor. For a cord to cause serious problems with fetal circulation it  has to get really tight -- and if it's THAT tight it will generally interfere  with position and/or descent. The only cord around the neck which I would worry  about is the one on a transverse or breech baby --- if the kid has enough cord  slack to be a normal vertex, then I wouldn't worry at all. I think it proves the  cord will not become a problem.


I had a VBAC client whose ultrasound tech suspected a triple wrapped cord.  Baby was born yesterday at home - heart tones perfect throughout labor, head born, one loose cord wrap and easy birth.  10-10 apgars.  I stressed when told about the "cord wraps" and what to tell the Mom.  As it wasn't possible to say it was definite, we told her there appeared to be a cord wrapped around the baby's neck, maybe more than one time and we'd watch for problems relating to it.  She completely let it go and didn't worry.


I consider cord wraps a variation of normal, as long as the baby is not in distress, neither am I.  Fortunately, we have a supportive hospital to transport to which is five minutes away - so I am comfortable with this.



Unusual Benign Ultrasound Findings



Obstetrical Sonography: The Best Way to Terrify a Pregnant Woman by Roy A. Filly, M.D.- an excllent discussion of abnormalities which are not really abnormalities: choroid plexus cysts (3-31), echogenic intracardiac foci (32-36), mild pyelectasis (37-41), and echogenic bowel (42-45) .



FAQ: Choroid Plexus Cysts from ucsfhealth.org.  It seems to have written before cell-free DNA testing was available to rule out trisomies without risking a miscarriage from amnio.


Should I Be Worried About a Cyst in My Baby's Brain? (Cranial Ultrasound) - don't worry about only one isolated choroid plexus cyst smaller than 10 mm.



Possible Alternative to Ultrasound For Sex Determination



Fetal DNA Test of Mother's Blood Reliable in Sex Detection

Baby Gender Mentor™ Home DNA Gender Testing Kit - [6/05] - With a few drops of your maternal blood you can find out your baby’s sex AS EARLY AS FIVE WEEKS after conception  - costs $275.

Reading Mother's Eyes to Determine Baby's Sex

There are two very reliable ways that I use other than my feeling about what the sex of the baby is and that is reading the eyes. It is called sclarology ( the whites of the eyes) If you are looking at the eyes look at them as if you are looking at a clock face. In the right eye between about 7-8 o'clock if there is a vein then it is a boy. If in the left eye between 4-5 o'clock it is a girl. This is the uterus part of the eye. Then together with that I watch which side the baby lies on the most and stays on at the end if the left girl and if right boy. I'm only about 85% correct when reading boy eyes and 95% for girls. I've used this for many years and it is pretty reliable. It makes it harder if the moms eyes are real blood shot or veiny. Just something to test out. 

Embryonic Heart Rates



SEX, HEART RATE, and AGE by Terry J. DuBose, updated July 26, 2011


I do notice tachycardia in getting heart tones with a dopp very early in pregnancies. Do you notice this? Or do you think this is WNL for early development?


Fetal heart rate is higher in early pregnancy than in later pregnancy. We can listen with a Doppler at 14 weeks but not likely with a stethoscope till closer to 20 weeks. I think this is a normal thing we should expect.


I have done a lot of research on the embryonic heart. Actually, it is quite interesting. It is partially correct that the EHR is higher early in pregnancy than later, however only partially correct. The EHR starts out as early as we can see it with sonography at about 78-85 B/M in the early 5th LMP week. It then accelerates in a linear fashion to approx. 165-190 B/M in one month (early 9th week). That is an acceleration rate of approximately 3.3 B/M per day, or 10 B/M increases every 3 days. Then abruptly at approximately 9.2 LMP weeks it begins a relatively quick deceleration until the about the 18th week when it starts to level out, but still a slow deceleration to about 144 B/M near term. In our population (3000+ cases), embryos (5 of 6) that fell below the acceleration curve by more than 7 days (EHR age - CRL age) ended in 1st trimester miscarriage.  [Ed. CRL  = crown-rump length]

I realize that you can't find the faint EHR as early as we can see it and measure it with M-mode, but it really is quite fascinating. The embryonic heart rate acceleration is very consistent with little beat-to-beat variability, unlike the variation we expect (is normal) during the 2nd & 3rd trimester. I published the first regression formula for predicting the embryonic age from the HR, which is valid before 9.2 LMP weeks:

Embryonic age in days after LMP = EHR(0.3)+6 Embryonic age in days after conception = EHR(0.3)-8

This is only valid during the first month of life, but is more accurate than the gestational sac diameter, but not quite as accurate as the Crown-Rump Length. For more information including large population graphs, more regressions, and discussion of the heart rate throughout gestation see: DuBose TJ; FETAL SONOGRAPHY; W. B. Saunders Co., 1996; Chapter 12, Heart Rate.



Late Abortion for Catastrophic Pregnancies



For those women who have discovered catastrophic problems with their pregnancies and have decided to terminate the pregnancy rather than risk death due their own medical condition or otherwise tragic result in carrying a pregnancy to term . . . there is some good information at the web pages of the Boulder Abortion Clinic.  "Our purpose is to provide the safest possible abortion care and termination of pregnancies for fetal anomalies or medical indications.  We provide this care for women in a confidential, humane, and dignified outpatient setting giving the maximum emotional and social support."

 

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