For the Kukan family, Thanksgiving of 2005 was definitely a time to be grateful. It was the day they took their little “miracle baby” home against all odds.
A 20-week alpha fetoprotein test showed a “genetic defect” in the baby Christa Kukan was carrying. The specialist in her North Jersey home town gave the baby a zero percent chance of survival.
While further testing showed no signs of chromosomal or heart defects, the result of an ultrasound indicated that baby Laura had a left congenital diaphragmatic hernia, a hole in the diaphragm (the muscle that separates the chest cavity from the abdominal cavity), which allows some of the abdominal organs to move up into the chest cavity. CDH can be life-threatening, as it can lead to pulmonary hypoplasia — underdevelopment of the lungs.
The specialist then recommended Christa and husband, Michael, seek the opinion of The Children’s Hospital of Philadelphia.
Although the diagnostic evaluation showed a very severe congenital diaphragmatic hernia with liver herniation and small lungs, “the doctors there were a little more optimistic,” remembers Christa. “They gave Laura a 65 percent chance.”
Christa’s pregnancy was followed closely by Dr. N. Scott Adzick and the Fetal Surgery team at Children’s Hospital. She gave birth at the Hospital of the University of Pennsylvania on September 12.
“The first positive sign was that she (Laura) didn’t need ECMO,” says Christa. ECMO, Extracorporeal Membrane Oxygenation, is a temporary heart/lung bypass machine that some babies with CDH need to help them survive the first few days or weeks following birth. “But she was put on a ventilator to help her breathe.”
Within 12 days, Laura was stable enough to have surgery to repair the hole. After the surgery, she remained on the ventilator, as well as medication for pulmonary hypertension.
Then came a minor setback. Laura, like many babies with CDH, suffered from gastroesophageal reflux (GERD), which allows acid and fluids from the stomach to move up into the esophagus and can cause heartburn, vomiting, feeding problems, or lung problems due to aspiration.
On November 11, she underwent a Nissen fundoplication, surgery that wraps the upper part of the stomach around the esophagus and sews it in place to help prevent food from refluxing up.
Later that month — on Thanksgiving Day — Laura went home on just two medications and a feeding tube.
“She still has the G-tube (feeding tube) because she isn’t taking any food by mouth yet,” says Christa, who learned how to insert and care for the tube along with her husband while still at Children’s Hospital.
For Christa and Michael, the business of caring for the tube was a bit intimidating at first. But for big sister, Michelle, 2 ½ , the feeding tube is business as usual.
“Michelle feeds her dolly with a stomach tube,” explains Christa. “And when we clean the site (of Laura’s tube), Michelle goes and gets her dolly to clean the dolly’s site.”
Both Michael and Christa credit The Children’s Hospital of Philadelphia with saving their baby’s life, and with helping them to cope with the every day stress of having a baby with CDH. She is followed in the multidisciplinary Pulmonary Hypoplasia Program at the Hospital, which brings the expertise of pediatric medical specialists to Laura in one setting.
“From the time we started being followed prenatally until the day we left, we were treated like family, not patients,” says Christa, adding that the couple is particularly grateful to the Newborn/Infant Center nurses who, “take such special care of your child.”
If she could tell other moms-to-be one thing about carrying a baby with CDH, Laura says she would tell them: “Don’t give up hope. Our little miracle baby defeated the odds, yours can, too.”
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