Our Blessing Named Jesse

Jesse Quintin was born September 26, 2007, the much-loved fifth son of Kristan and Chad. He was diagnosed shortly after birth with AV Canal Heart Defect and Down Syndrome. Thursday, January 10th, Jesse had surgery to repair his heart defect. Friday morning he suddenly went into cardiac arrest. After 45 min. of CPR he was attached to life support. By God's healing hand his heart started to beat again and he came off life support on January 13. We created this blog to keep everyone updated.





Monday, January 28, 2008

Chylothorax continues

So, the reason why fluid is accumulating in Jesse's chest (pleural space around his lungs) is because of the continuing chylothorax. This has not resolved on its own, despite trying octreotide (a hormone) and a special formula (Portagen). The next step is for Jesse to be placed on TPN (Total Parenteral Nutrition) - meaning he will be off bottles all together and totally fed intraveneously. This will last for the minimum of a week and maybe a month or more.

Below I've pasted a very good article about chylothorax that I found on the internet at http://tchin.org/resource_room/c_art_15e.htm I hope it's helpful to all of us in understanding what's going on.

Kristan is going to try to get on tonight to update everyone more.

By the way, Jesse's oxygen has been turned down again & he is breathing well.

Thank you everyone for your continued prayers.

Aunt Kim

****

Chylothorax is the accumulation of chyle in the pleural (lung) space. Chyle is usually a milky fluid comprised of lymph drainage, which carries fat, protein and white blood cells (lymphocytes). It occurs after injury to or obstruction of the thoracic duct. Injury to the thoracic duct during cardiovascular surgery occurs because of its proximity to the great vessels (aorta and pulmonary artery) in the chest, where the duct crosses from right to left. Most cases of chylothorax after surgery for congenital heart disease have occurred after non-open heart procedures, mainly subclavian-pulmonary artery shunt procedures, resection of coarctation of the aorta, and ligation of patent ductus arteriosus.

Symptoms of chylothorax are related to the amount of fluid present and the rate at which it accumulates and may include fatigue, shortness of breath at rest or on exertion, heaviness, and discomfort on the affected side. An initial trial of conservative therapy is indicated, since spontaneous closure can occur. Removing chyle from the pleural space is best accomplished by chest tube placement for continuing draining. This allows full re-expansion of the lung, which closes the lymph connection (fistula) by the lung’s compression effects. In order to maintain adequate nutrition while reducing lymph flow, it is recommended that the diet be changed to limit the fat source to medium-chain triglycerides (fats that are directly absorbed from the gut into the blood stream without having to go through the lymph system). Alternatively, the patient may need to take nothing by mouth and receive total parenteral nutrition (TPN) by receiving all nutrition through an IV or central line for many weeks. Since flow of chyle is minimized only when the gastrointestinal tract is completely at rest, others prefer to stop oral feedings altogether. The drainage of chyle usually slows or stops within 7 days after tube drainage and with changing of the diet to reduce lymph flow. If this does not occur, more aggressive action such as surgery may be recommended.

4 comments:

  1. Dearest Chad and Kristan,

    I will be on my knees in prayer for Jesse and for you. I am so glad that we have a God that goes before us and then continues to walk with us in everything we have to face.
    Love, Suzanne

    ReplyDelete
  2. Dear Kristan and Chad,
    I am praying for strength for Jesse as he heals. God is holding you close in our hearts and prayers spoken and silent. I will continue to lift you up daily. Know I am thinking of you.

    Love,
    Your cousin
    Nancy in Johnstown CO

    ReplyDelete
  3. Dear Chad and Kristan

    I know that you don't know me, but I just want to send your family my prayers.
    I found your blog while doing a search for Chylothorax--one of the many challenges my daughter faced in her first year of life.
    Jade was born with a number of things wrong--all apart of something called VACTERL Association.
    She spent almost the first 4 months in the NICU and had 5 major(and a few minor) surgeries before coming home. She has since had 2 more.
    Although we still face medical challenges, she has made a lot of progress over the years and by most accounts is a happy, thriving 5 year-old.
    I have been where you are and want you to know that there is light at the end of the tunnel.

    Be blessed

    Nina in Portland, OR
    shaninajohnson@yahoo.com

    ReplyDelete
  4. Chad & Kristan-

    I found your blog searching for CHD babies. My daugher, born 11-2007 was diagnosed with a Coarc. After her repair she also had Chylothorax. THey put her on Monogen, and within a month's time it had cleared up on it's own. We kept her on the monogen for an additional month jsut to be safe and there has been no additional fluid build up on her lungs.

    I hope and pray that you little one will be able to fight and overcome these steps, just like my little one did!

    Ashley in San Antonio, TX

    ReplyDelete