Disclaimer

Showing posts with label Developmental Disorders. Show all posts
Showing posts with label Developmental Disorders. Show all posts

Wednesday, March 2, 2016

Gastroschisis in Fetal Development and the Rising Rates of Prevalence

By: Jana Andersson

Gastroschisis (gas-troh-skee-sis) may not be a term you are familiar with until you or someone you know has been given this terrifying diagnosis. While the better news is that in most cases with access to modern care this otherwise lethal condition is highly treatable. But the alarm call to all is that the prevalence of gastroschisis is on the rise. The cause of the disease remains unknown as does the reason for its increase. The following provides an overview of this congenital birth defect and also serves to increase public awareness and concern.

What is gastroschisis?

Gastroschisis belongs in the category of  “ventral wall defects” (ventral meaning “front of abdomen”) and is the most common disease in this class. Due to a malformation of the abdominal wall just to the right of the umbilical insertion the fetal intestines extrudes into the amniotic fluid. The event is generally isolated with rare instances of accompanying birth defects and few instances of genetic or chromosomal abnormalities. However, the number of new cases of has been markedly increasing. Gastroschisis is fatal without access to modern treatment. With treatment the survival rate is 95%.


Image Courtesy of the Centers for Disease Control and Prevention, National Center on Birth Defects and Developmental Disabilities


How is gastroschisis diagnosed?

Gastroschisis may be diagnosed by pregnancy screenings in the 2nd trimester. Due to the abdominal wall defect Alpha-fetoprotein (AFP) from the fetus is released into the amniotic fluid and crosses the placenta. The elevated levels in maternal blood will register on a blood test in 77-100 % of cases. A follow up ultrasound may identify gastroschisis. Additionally, a routine 2nd trimester ultrasound may independently diagnose the condition if no blood-work was performed or if previous levels were undetectable. There are no other maternal signs or symptoms.

Fetal signs in utero

·       AFP released into amnion from fetal tissues.
·       Sections of bowel float free in the amniotic sac and may include other organs.
·       In early pregnancy the bowel is of normal size but later the diameter may increase leading to obstruction, perforation, and lack of blood-flow.
·       Due to exposure the bowel may become irritated causing it to shorten, twist, or swell.
·       Primary nutrient loss is from membrane and muscular dysfunction.
·       Growth restriction occurs in 38-77% of cases
·       48% of fetuses/births are small size
·       Shortened gestation period of 35-37 weeks (40 is normal)

Treatment begins immediately after birth

Actions include:

·       Placement of IV for antibiotics, pain relief, and nutrition
·       Access to ventilator
·       Insertion of nasogastric tube to decompress/draw out bowel contents which could otherwise be taken up into the lungs.
·       Maintaining a temperature controlled environment
·       Maintaining sterile conditions

If the the amount of exposed bowel is small the organ can be put back in and the hole sutured within a day of birth.

If the amount of exposed bowel is large it may be repaired in stages. In such cases the intestines are put into a sterile plastic cylindrical bag called a silo. Utilizing spring tension the base of the bag seats tightly around the abdominal opening and the top of the bag mounts to a hook and is suspended over the infant much like an IV drip. The intestinal feed works by gravity and every 48 hours physical pressure is applied to the bag with a twist from the top. Over the course of 7-10 days a once large and swollen herniation will eventually fit back inside the cavity. The surgeon will then remove the silo and close up the wound.

The next challenge is recovery. The intestines may delay in working. Furthermore infants may experience disinterest in feeding, reflux, serious infections, and areas of intestinal death. Ultimately babies go home when they are feeding entirely by mouth, gaining weight and intestinal function has returned. The best case scenario for hospitalization is about a month but this can extend up to four.

Many afflicted infants go on to lead normal lives but 40% will need additional treatment at some point. Gastroschisis is the leading cause of intestinal transplantation.

What causes gastroschisis and why is there a hole in the abdominal wall to the right of the cord insertion?

The cause for gastroschisis is unknown. In normal early development the primitive gut evolves from the yolk sac and becomes the midgut – basically a long narrow tube. Thereafter this tube elongates faster than the embryonic body which forces an embryonic loop into the amnion. Later, this loop recedes back into abdomen. Earlier but in a different area of development the right umbilical vein regresses and dissolves in order to make way for an improved vascular system required for expanding growth. In gastroschisis the vascular disruption theory suggests a premature withdrawal of this right side umbilical vein before 28-32 conceptual days may lead to ischemia (cell death due to lack of blood flow) thereby adversely affecting the early evolving tissues that ultimately give rise to the abdominal defect specific to that region. Similarly it is also thought that ischemic injury to the mesenteric artery gives rise to the high rates of intestinal artresia (intestinal death) associated with gastroschisis.

What is the risk of having a baby with this birth defect?

According to the CDC
Cases per Births: 1 in 2,229
Estimated Annual Cases: 1871

·       Since the 1980s, the number of babies born with gastroschisis has increased, especially among young mothers aged younger than 20 years.

·       Between 1995-2005 cases of gastroschisis nearly doubled.

·       The prevalence of gastroschisis increased from 1995 to 2012 among mothers in every age group and for each racial/ethnic group that was studied (non-Hispanic whites, non-Hispanic blacks, and Hispanics).

FIGURE. Trends in gastroschisis prevalence, by maternal age group — 14 states,* 1995–2012

Graph image: CDC, Morbidity Mortality Weekly Report Weekly / January 22, 2016 / 65(2);23–26


Can gastroschisis be prevented?

Because the cause is unknown prevention is difficult to identify. Risk lessens after maternal age 25. Furthermore use of vasoconstrictors such as aspirin, ibuprofen, nasal decongestants, alcohol, and cigarettes during the first trimester of pregnancy can be related to the vascular pathology of the disease. More research is needed to explore genetic and environmental influences.

References
  
Ali Nawaz Khan, Sunaira Macdonald, Duree Sabih. 2015 Sept 25. Gastroschisis. Available from http://emedicine.medscape.com/article/403800-overview#a1

Chabra, Shilpi, Gleeson, Christine A.. 2006. Gastroschisis: Embryology, Pathogenesis, Epidemiology. NeoReviews Vol 6 No 11. Retrieved from: http://pedsurg.com.pe/Gastroquisis%20embriologia %20patogenesis%20y%20epidemiologia.pdf

Debich-Spicer, Diane E., Gilbert-Barness, Enid. Embryo and Fetal Pathology. 2004 May 31. Retrieved from: https://books.google.com/books?id=os_NQOiTu_4C&pg=PA510&lpg=PA510&dq=embryo+involution+veins+arteries&source=bl&ots=BX5Mji-ayl&sig=U3tknYr_vRr-hDyHdYqXAi5P8fg&hl=en&sa=X&ved=0ahUKEwif-suajuzKAhVU72MKHbsjCPMQ6AEIKjAD#v=onepage&q=embryo%20involution%20veins%20arteries&f=false

Facts about gastroschisis 2015 Nov 12. Retrieved from: http://www.cdc.gov/ncbddd/birthdefects/gastroschisis.html

Feldkamp, M. L., Carey, J. C. and Sadler, T. W. (2007), Development of gastroschisis: Review of hypotheses, a novel hypothesis, and implications for research. Am. J. Med. Genet., 143A: 639– 652. doi: 10.1002/ajmg.a.31578 Retreived from: http://onlinelibrary.wiley.com/doi/10.1002/ajmg.a.31578/abstract
Glasser, James G.. 2015 April 28. Pediatric Omphalocele and Gastroschisis. Retrieved from: http://emedicine.medscape.com/article/975583-overview

Ionescu, S., Mocanu, M., Andrei, B., Bunea, B., Carstoveanu, C., Gurita, A., ... & Selleh, M. (2014). General Report. Chirurgia, 109, 7-14. http://www.revistachirurgia.ro/pdfs/2014-1-7.pdf

Jones AM, Isenburg J, Salemi JL, et al. Increasing Prevalence of Gastroschisis — 14 States, 1995–2012. MMWR Morb Mortal Wkly Rep 2016;65:23–26. DOI: http://dx.doi.org/10.15585/mmwr.mm6502a2.
Key findings: gastroschisis – a serious birth defect - continues to increase. 2016 Jan 21. Retrieved from: http://www.cdc.gov/ncbddd/birthdefects/features/keyfindings-gastroschisis-increase.html
Key Findings: Updated National Birth Prevalence Estimates for Selected Birth Defects in the United States, 2004-2006. Reviewed 2016 Jan 21. Retrieved from: http://www.cdc.gov/ncbddd/birthdefects/features/birthdefects-keyfindings.html

National Library of Medicine (US). Genetics Home Reference [Internet]. Bethesda (MD): The Library; 2016 Feb 08. Abdominal Wall Defect; [reviewed 2012 Aug]. Available from: http://ghr.nlm.nih.gov/condition/abdominal-wall-defect

The Children's Hospital of Philadelphia (Producer). (2011, July 01) Inside out: understanding abdominal wall defects (AWD) [Video transcript] http://www.chop.edu/video/inside-out-understanding-abdominal-wall-defects-awd#.Vr9tD-YYFKm

Thomas, Kayle. Gastroschisis. Retrieved from http://averysangels.org/gastroschisis/

Monday, February 15, 2016

ZIKA: Balancing Fear with Facts

By: OCR-Mama

You have heard about Zika virus. You have seen the heart-wrenching images of babies born with microcephaly or an abnormally small head. The World Health Organization is talking about it. The Centers for Disease Control and Prevention is talking about it. Your grandma is calling you to talk about it. Zika is spreading rapidly and can have dire health effects. Even as I write this new stories are popping up by the minute, but what are the facts about Zika? What is the real risk for you as a pregnant mom in the US? Before you finish your gestation in a DEET-filled cave, let’s look at what is known and unknown about Zika.

What is Zika virus and how do you get it?


Zika virus disease or ZIKV or Zika fever is caused by a mosquito-borne virus that was first identified in 1947 in a caged rhesus monkey in Africa. In humans the first cases were identified in 1952. In 2013 and 2014 French Polynesia had a ZIKV outbreak with an uptick in central nervous system malformations including microcephaly.

In 2015 a Zika virus outbreak swept through Brazil. 2016 has seen no end to the outbreak and Zika continues to spread through the Americas. So although this disease is not new, the areas of the world that have been impacted by the Zika virus are expanding and the effects on these naive populations are getting attention.

Mosquitos carry the virus and infect the human by acting as a vector for transmission. Mosquitos are excellent vectors because they break through the top layer of skin or epidermis and get into the dermis below. They do this because blood is their meal, but this also allows the virus to make it’s way into the host’s blood. The skin, like a suit of armor, protects against most dangers but a poisonous needle piercing through a chink can cause grave harm.

The cells of the dermis called dendritic cells and fibroblasts have receptors that allow Zika to enter the cell and replicate. The virus has other factors contributing to the rapid spread in areas with many mosquitos. A mosquito can pick up Zika from an infected person and then pass it along to another person. Meaning, a mosquito can become a carrier by biting someone who is sick.

Transmission is no longer thought to be limited to the work of mosquitos either. There is growing evidence that Zika virus disease can be transmitted sexually and remains in semen longer than it has cleared from the blood in an infected person. So if your partner has travelled to a region with Zika it is wise to use condoms or abstain until he has been cleared from the disease whether or not symptoms occur. This route of transmission, however, is much less likely than from a mosquito. So while unlikely to be an issue, better safe than sorry.

Not all mosquitoes carry the Zika virus. In fact, transmission is mainly by Aedes mosquitoes which are most commonly found in tropical environments. For US women concerns about contracting Zika are mainly around travel to area that have cases of Zika and sexual contact with partners that have experienced Zika virus disease. The CDC and WHO are actively tracking the disease and issuing travel guidelines for pregnant women or women who may become pregnant. Currently no locally-acquired cases of this disease have presented in the US, but travel-related cases have. Tracking of the disease and its spread are ongoing and if you have travel plans check with these sources for the latest recommendations.

What are the symptoms of Zika virus disease?

If Zika virus disease occurs symptoms are likely to begin around a couple days after exposure and symptoms are generally mild, lasting 2-7 days. These symptoms include fever, skin rash, discomfort, headache, joint and muscle pain, and eye redness. Most people infected with Zika virus will have no lasting harm from the disease. If a woman is pregnant when the Zika virus is contracted, however, the virus may cause severe brain damage to the unborn and is linked to a condition called microcephaly. The relationship between Zika virus and microcephaly is not fully understood by scientists.

How is Zika virus disease treated?

Symptoms of Zika virus can be eased with rest, drinking plenty of water, and taking pain relievers like ibuprofen. No antiviral medications are recommended at this time for Zika and no vaccination is available. If you are pregnant and suspect you have Zika virus talk to your doctor about what tests are available. Blood, urine, and saliva tests may be used to find viral RNA and the CDC has released an algorithm for testing. Ultrasound may be used to look for calcifications in the fetal skull and microcephaly. Recommended testing is still controversial and not widely available. The reality is that if you haven’t travelled to a region currently affected by Zika or live in that region then you aren’t considered to be at risk for Zika.

What is microcephaly and does Zika cause it?


Microcephaly is a condition that literally means small head. The head grows in a developing fetus because the brain is growing. In microcephaly the brain is not growing normally and this can be linked to a range of serious difficulties. Many causes of microcephaly are known such as infections like rubella, toxoplasmosis, and cytomegalovirus. Malnutrition or toxic exposures in development like alcohol can also cause microcephaly. ZIKV genetic material has been found in the brain tissue samples of a fetus with microcephaly whose mother was exposed to ZIKV during her pregnancy and experienced symptoms of ZIKA fever in her 13th week of pregnancy. ZIKV genetic material has also been found through amniocentesis. It is not proven that Zika causes microcephaly, but researchers think that the virus may target and replicate in the developing brain of a fetus. Zika doesn’t seem to cause lasting harm in other organs or tissues but stays and replicates in the brain stem.

The best prevention for ZIKV is to not get bit by a mosquito. Consider guidelines and consult with your doctor about travel plans. Look at the EPA’s recommendation for mosquito repellants and follow the directions carefully if you are expecting exposure. If you do they are safe to use during pregnancy. Wearing long pants and shirts can help as well. Standing water is prime breeding ground for mosquitos and can become a safety risk so care should be taken to prevent this. So the ZIKV media frenzy may be inducing worries in your pregnant mind, but fear is a beast that thrives on attention. Arm yourself with facts and be well.

References:

Akpan, Nsikan (January 29, 2016  updated February 1, 2016) How does Zika virus shrink a baby’s brain and other FAQs.  PBS NewsHour. Retreived from: http://www.pbs.org/newshour/updates/zika-virus-faqs-ultrasound-detection/

Centers for Disease Control and Prevention. (February 12, 2016).
Facts about Microcephaly (article). Retreived from: http://www.cdc.gov/ncbddd/birthdefects/microcephaly.html

Centers for Disease Control and Prevention. (January 29, 2016).
Possible Association Between Zika Virus Infection and Microcephaly — Brazil, 2015
(Morbidity and Mortality Weekly Report).   Retreived from: http://www.cdc.gov/mmwr/volumes/65/wr/mm6503e2.htm

Mlakar, J M.D., Korva, M Ph.D., Tul, N M.D., Ph.D., Popović, M M.D., Ph.D., Poljšak-Prijatelj,  M Ph.D., Mraz, J  M.Sc.,... Avšič Županc, T Ph.D. (February 10, 2016) Zika Virus Associated with Microcephaly.  The New England Journal of Medicine.  DOI: 10.1056/NEJMoa1600651

McNeiL, D.G. Jr., Saint Louis, C. & St. Fleur, N.  ( February 16, 2016).  Short Answers to Hard Questions about Zika Virus. The New York Times. Retreived at: http://www.nytimes.com/interactive/2016/health/what-is-zika-virus.html?_r=0

World Health Organization.  (February 2016).  Zika Virus (fact sheet). Retreived from: http://www.who.int/mediacentre/factsheets/zika/en/