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Mia Vogel

Tetralogy of Fallot

Mia Vogel

When Mia Vogel landed at Pittsburgh International Airport with her adoptive parents Mary and Matt on Jan. 2, 2011, she was a very lucky, but very sick little girl. Not quite 4 years old, Mia had already embarked on a big adventure—traveling overseas from an orphanage in Xi’an, China, to begin a new year and a new life in a new country. But she was about to have an even bigger adventure that would take place at the Heart Institute at Children’s Hospital of Pittsburgh of UPMC.

Throughout the overseas flight, Mia had been vomiting, having trouble breathing, and her skin looked blue. Not sure whether her reaction was exacerbated by confusion or worry about her new surroundings, or something more serious, her new parents immediately took her to their pediatrician. Found to be very dehydrated, Mia was referred to Children’s Hospital of Pittsburgh of UPMC, where she was diagnosed with one of the most severe forms of the congenital heart defect known as tetralogy of Fallot, a condition characterized by low oxygen levels in the blood. Her disorder was causing cyanosis, or a bluish-purple color to the skin, and pulmonary atresia, a blockage of blood flow to the lungs.

When Mia arrived at Children’s, her condition was grave: Doctors initially thought that her condition was inoperable. But before sending her home with no hope, her lead physician, Vivek Allada, MD, assembled the team of Heart Institute physicians to review the results of her electrocardiograms, chest x-rays, echocardiograms, CT angiogram, and heart catheterization. The team designed a complex multi-stage treatment plan, which included a series of cardiac catheterizations and surgeries to repair and improve the blood flow to Mia’s lungs.

After four days in the hospital, Mia was sent home with her parents on aspirin and Lasix therapy to allow her to build some strength before her first surgery. Mia was placed on oxygen at home because her blood-oxygen saturation level was only 64 percent, and her skin was blue all of the time.

In March 2011, Victor Morell, MD, performed the first surgery to increase the blood flow to Mia’s lungs, installing a 12 mm Gore-Tex® shunt from her right ventricle to her pulmonary artery. “She was pink right out of surgery,” Mary recalls. Although Mia had been very scared during the experience, mainly because of her still-limited English, she weathered the surgery well and had a quick recovery, leaving the hospital after only four days. “She was a real trouper,” says Mary.

In December 2011, Mia had another surgery—this time, a more complex open heart surgery in which Dr. Morell installed a bigger shunt and performed a unifocalization procedure to move misdirected vessels to the pulmonary artery to restore blood flow to Mia’s lungs. This surgery was rougher for Mia, Mary recalls. “Mia remembered her last surgery and understood what was going on,” she says. “In addition, her lungs had been showing a reperfusion injury (because they were not used to getting blood flow), so she was given a paralytic drug and placed on a ventilator for three days to allow her lungs to heal without her trying to struggle against the breathing tube.” After a nine-day inpatient stay, Mia was discharged and went home to her family in New Wilmington.

Mia Vogel with her older brothers

Although she must have regular visits with Dr. Allada, periodic heart catheterizations to monitor her condition, and may have a few more medical hurdles in the future, Mia is in every way a very active, normal 5 year old. She swims like a fish, plays with Polly Pockets and her doll house, loves to color, is an eager student, and enjoys her older brothers Jacob, 12, and Logan, 10.

“Our goal from the beginning was to enable Mia to be a happy, healthy young girl with all the opportunities that every child has,” says Dr. Allada. “Before, she was only able to walk a few feet before tiring out and turning blue; now she has nearly normal oxygen levels and runs and plays like other kids. While there is more work to do, Mia has a great future ahead of her – she and her family are amazing!”

With her language skills developing appropriately for her age despite English being her second language, and hitting her other milestones, Mia is about to embark on another big adventure in the fall: Kindergarten! 

Last Update
August 22, 2012
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Last Update
August 22, 2012
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