Baby' s life saved with groundbreaking 3D printed device ..
from University
of Michigan that restored his breathing
Bioresorbable
splint used for first time, successfully stopped life-threatening
tracheobronchomalacia, case featured in New England Journal of Medicine
Ann Arbor, Mich. – Every day, their baby stopped breathing, his collapsed
bronchus blocking the crucial flow of air to his lungs. April and Bryan
Gionfriddo watched helplessly, just praying that somehow the dire predictions
weren’t true. “Quite a few doctors said he had a good chance of not leaving the
hospital alive,” says April Gionfriddo, about her now 20-month-old son, Kaiba.
“At that point, we were desperate. Anything that would work, we would take it
and run with it.” They found hope at the University of Michigan, where a new,
bioresorbable device that could help Kaiba was under development. Kaiba’s
doctors contacted Glenn Green, M.D., associate professor of pediatric
otolaryngology at the University of Michigan.
Green
and his colleague, Scott Hollister, Ph.D., professor of biomedical engineering
and mechanical engineering and associate professor of surgery at U-M, went
right into action, obtaining emergency clearance from the Food and Drug Administration
to create and implant a tracheal splint for Kaiba made from a biopolymer called
polycaprolactone. On February 9, 2012, the specially-designed splint was placed
in Kaiba at C.S. Mott Children’s Hospital. The splint was sewn around Kaiba’s
airway to expand the bronchus and give it a skeleton to aid proper growth. Over
about three years, the splint will be reabsorbed by the body. The case is
featured today in the New England Journal of Medicine. “It was amazing. As soon
as the splint was put in, the lungs started going up and down for the first
time and we knew he was going to be OK,” says Green. Green and Hollister were
able to make the custom-designed, custom-fabricated device using
high-resolution imaging and computer-aided design. The device was created
directly from a CT scan of Kaiba's trachea/bronchus, integrating an image-based
computer model with laser-based 3D printing to produce the splint. “Our vision
at the University of Michigan Health System is to create the future of health
care through discovery. This collaboration between faculty in our Medical
School and College of Engineering is an incredible demonstration of how we
achieve that vision, translating research into treatments for our patients,”
says Ora Hirsch Pescovitz, M.D., U-M executive vice president for medical
affairs and CEO of the U-M Health System. “Groundbreaking discoveries that save
lives of individuals across the nation and world are happening right here in
Ann Arbor. I continue to be inspired and proud of the extraordinary people and
the amazing work happening across the Health System.” Kaiba was off ventilator
support 21 days after the procedure, and has not had breathing trouble since
then. “The material we used is a nice choice for this. It takes about two to
three years for the trachea to remodel and grow into a healthy state, and
that’s about how long this material will take to dissolve into the body,” says
Hollister. “Kaiba’s case is definitely the highlight of my career so far. To
actually build something that a surgeon can use to save a person’s life? It’s a
tremendous feeling.” The image-based design and 3D biomaterial printing process
can be adapted to build and reconstruct a number of tissue structures.
Green and Hollister have already utilized the process to build and test patient
specific ear and nose structures in pre-clinical models. In addition, the
method has been used by Hollister with collaborators to rebuild bone structures
(spine, craniofacial and long bone) in pre-clinical models. Severe tracheobronchomalacia
is rare. About 1 in 2,200 babies are born with tracheomalacia and most children
grow out of it by age 2 or 3, although it often is misdiagnosed as asthma that
doesn’t respond to treatment. Severe cases, like Kaiba’s, are about 10 percent
of that number. And they are frightening, says Green. A normal cold can cause a
baby to stop breathing. In Kaiba’s case, the family was out at a restaurant
when he was six weeks old and he turned blue. “Severe tracheobronchomalacia has
been a condition that has bothered me for years,” says Green. “I’ve seen
children die from it. To see this device work, it’s a major accomplishment and
offers hope for these children.” Before the device was placed, Kaiba continued
to stop breathing on a regular basis and required resuscitation daily. “Even
with the best treatments available, he continued to have these episodes. He was
imminently going to die. The physician treating him in Ohio knew there was no
other option, other than our device in development here,” Green says. Kaiba is
doing well and he and his family, including an older brother and sister, live
in Ohio. “He has not had another episode of turning blue,” says April. “We are
so thankful that something could be done for him. It means the world to us.”
http://www.uofmhealth.org/news/archive/201305/baby%E2%80%99s-life-saved-groundbreaking-3d-printed-device
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