Giant Omphalocele Repair, Groff Family | The Children's Hospital of Philadelphia

Center for Fetal Diagnosis and Treatment

1 in 10,000: Charlotte’s Giant Omphalocele Repair

Lindsay Groff first heard of giant omphalocele at a routine 20-week ultrasound during her first pregnancy, when her unborn daughter Charlotte was diagnosed with the abdominal wall defect. Seen in approximately 1 in 10,000 births, giant omphalocele causes abdominal organs to protrude into the base of the umbilical Charlottecord.

Just over the river in New Jersey, Lindsay quickly made an appointment to get a second opinion at The Children’s Hospital of Philadelphia. It was there, at the Center for Fetal Diagnosis and Treatment, that she learned the extent of the diagnosis and what it would mean for her baby.

An omphalocele can vary drastically in size, containing anywhere from a portion of the small intestine to most of the abdominal organs. In the case of giant omphalocele, the majority of the liver protrudes into the umbilical cord, often resulting in underdeveloped lungs and a small abdomen, two factors that frequently cause complications after birth. Babies with omphalocele are also at an increased risk for other birth defects, such as cardiac or neural tube defects, and intestinal and urological anomalies.

Finding omphalocele experts

Learning that Charlotte’s condition would require many delicate surgeries and time in the Newborn/Infant Intensive Care Unit (N/IICU), Lindsay knew that she wanted the best. And being able to deliver on site in CHOP’s Special Delivery Unit (SDU), the world’s first birth facility specifically designed for mothers carrying babies with known birth defects, was an important element of the care available. Not only would Charlotte have immediate access to a specialized team of experts with more experience than any other doctors in repairing giant omphalocele, but both mom and baby would be cared for in the same location before and after delivery.

“It comforted me to know that the team that would be caring for us offered more experience than any other program in the world with repairing giant omphalocele,” says Lindsay. “I was under great care at a hospital in New Jersey, but at CHOP we would be surrounded by doctors who specialize in treating the sickest children.”

Groff underwent a comprehensive evaluation at the Center, which included a detailed level II ultrasound, a fetal echocardiogram (a specialized ultrasound of the fetal heart) and an ultrafast fetal MRI. She then met with the multidisciplinary team that would be treating her and her baby, including surgeons, maternal-fetal medicine specialists, and neonatologists, to go over treatment options and what to expect throughout the pregnancy.

Right from the start, Lindsay knew she had made the right choice. “Everyone I encountered, from scheduling and filling out paperwork to my appointments, was so caring and thoughtful.”

Welcoming Charlotte to the world

Charlotte was born by C-section on May 18, 2010 in the SDU, where she was immediately evaluated and stabilized by the extensive team at her bedside. Babies with giant omphalocele often require a C-section delivery to avoid rupture of the omphalocele sac and liver trauma.

“She was surprisingly big, born with a full head of hair,” remembers Lindsay. “The hardest part was not being able to hold her. They wheeled her to me before taking her to the N/IICU, which was a great surprise, a special 10 minutes that I will cherish forever.”

In the N/IICU, Charlotte’s exposed organs were covered with a protective wrap. In some omphalocele cases, the organs gradually return to the abdominal cavity with the aid of gravity, but giant omphalocele sometimes requires several surgeries to repair the defect.

On her second day of life, Charlotte underwent her first surgery right in the N/IICU under the care of an expert neonatal surgical team, a unique approach to care developed at CHOP that brings together an attending pediatric surgeon, an attending neonatologist and advanced practice nurses all specializing in the care of newborn surgical patients. Charlotte’s surgery was performed by CHOP surgeon-in-chief N. Scott Adzick, M.D., and over the next three months, she had a total of 7 surgeries to put her abdominal organs back inside her body. The final surgical procedure closed her abdominal wall and gave her a belly button.

Charlotte stayed in the N/IICU for 14 weeks. After six weeks, she was off the ventilator and allowed to eat by mouth. But she struggled with exhaustion and many other complications that prevented adequate weight gain, so her feedings continued to be supplemented with a naso-gastric (NG) tube.

“I spent every waking hour in the N/IICU,” says Lindsay. “The only reason I could go home and sleep in my own bed was that I knew my child was 100 percent cared for. She was in the best hands in the world, and I felt like a lot of the N/IICU nurses and doctors cared for her as if she was their own.”

Mom’s greatest gift

During that time, Lindsay’s overwhelming memory is of feeling powerless. But there was one important thing she could do. Before Charlotte was born, Lindsay had met with Diane Spatz, Ph.D., from CHOP’s Breastfeeding and Lactation Program, to discuss the importance of breastfeeding. Despite Charlotte’s struggles to eat by mouth, Lindsay could still contribute to her healing by pumping and freezing her breastmilk to be used in Charlotte’s NG feeds.

“I Charlotte and momlearned that my milk was a critical part of Charlotte’s care, not just food, but a powerful medicine that only I could give to her,” she says. “It helped me focus on something I could do to help my sick baby. When everything seemed out of control, it was the one thing I could do for her.”

Once Charlotte was strong enough to be held, Lindsay practiced kangaroo care (promoting skin to skin contact), slowly and carefully bringing Charlotte steps closer to breastfeeding under the guidance of the nurses and certified lactation consultants.

“They were giving high fives in the N/IICU when she breastfed,” remembers Lindsay.

Life after giant omphalocele

Today Charlotte is a rambunctious 2-year-old with a mind of her own. She has been eating without an NG tube for over a year, and continues to receive close follow-up care through the Pulmonary Hypoplasia Program, which addresses the issues of lung development that often accompany abdominal wall defects. The program brings together specialists in pediatric surgery, neonatology, gastroenterology, pulmonology, cardiology and nutrition in one setting for optimal long-term care.

“She’s thriving and amazing,” says Lindsay. “To look at her now, you would never know that she was so very sick. The support that I received allowed me to provide Charlotte with the best gift a mother can give her child. I have no doubt that my milk played a large role in her healing, complementing the unparalleled medical care that she received.”

November 2012

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