From: LifeNews.com
by Steven Ertelt
Doctors at the University of Michigan have saved a baby’s life using
the marvels of modern technology to “print” the child a new airway using
a goundbreaking 3-D printer to restore his breathing.
From the University of Michigan:
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.”
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