Caring for a child who has a tracheostomy requires experience that only a pediatric team of experts can provide. At Children's Hospital of Wisconsin, we care for children who require a tracheostomy and also children who require a tracheostomy with a home ventilator. Our multidisciplinary approach and commitment to the highest quality of care makes our program the premier tracheostomy/home ventilator program in the region. The Tracheostomy and Home Ventilator Program is part of the Division of Pediatric Pulmonary and Sleep medicine, which has been named among the nation’s best in the U.S. News & World Report Best Children’s Hospital report.
In this section
Meet our team
Meet the nationally-rated health care providers who make up our Tracheostomy and Home Ventilator Program.
- Provide care for children with tracheostomies or tracheostomy with a home ventilator across the spectrum of care. We pride ourselves on developing relationships with children and their families before tracheostomy placement.
- Provide multidisciplinary support both inpatient and outpatient
- Early involvement in decision making process with families and care teams in plan of care
- Educate and prepare parents and caregivers of respiratory technology dependent children to successfully care for their child
- Work closely with community resources (such as home care companies, home nursing, medical providers, school staff) to safely integrate back to their home community
Video: Caring for a child with a tracheostomy
Our physicians are among the best
Our program’s multidisciplinary approach and commitment to the highest quality of care makes our program the premier tracheostomy/home ventilator program in the region. Your child will receive care from multiple expertly trained physicians including pediatric pulmonologists, pediatric otolaryngologists, neonatologists, pediatric critical care specialists, and pediatric anesthesiologists. Our doctors are among the best in the nation and rank among The Best Doctors in America.
- We have treated over 800 children with tracheostomies since the inception of our program in 1984
- Our program was one of the first in the country to discharge children to home on a ventilator
- We currently care for over 200 children living in the Midwest
- The Tracheostomy/Home Ventilator Program is part of the Division of Pediatric Pulmonary and Sleep Medicine, which was named among the nation's best in U.S. News & World Report's 2014-15 Best Children's Hospitals report
- Our program developed an educational booklet and teaching video for parents and caregivers who care for a child with a tracheostomy
- Our interdisciplinary team offers a Pediatric Ventilator Certification Course to home care nurses monthly
The family experience
- We believe that trust, education and open communication are the key components to building strong relationships with children and their families, especially when a tracheostomy is first being discussed.
- We have a multidisciplinary team that works closely with each child and his or her family. Team members include a pulmonary physician, otolaryngologist, respiratory care practitioner, social worker, speech therapist and case manager.
- An advanced practice nurse or nurse clinician is assigned to work with the family to manage and coordinate both inpatient and outpatient care.
- All families and caregivers participate in a training program to prepare them to care for their child with a tracheostomy at home.
- Home care nurses receive ventilator training certification by our respiratory and nursing staff as required by the state of Wisconsin to care for a child on a home ventilator.
- We work closely with school nurses and educators to facilitate the child's transition back to school.
- Our speech therapists educate and share information with local community speech therapists to promote effective therapy plans to care for a child with a tracheostomy.
- We contact local EMS services and energy companies alerting them that a child is on a ventilator in their area.
Neonatal and pediatric trained specialists
As children grow their airway and lungs grow and change. It is important that their tracheostomy and home ventilator care is managed by neonatal and pediatric trained specialists. Our multidisciplinary team consists of providers who are neonatal and pediatric experts in their fields.
Quality and outcomes
- Our program sees approximately 30 to 40 new children every year who require a tracheostomy. Approximately half of the children require only a tracheostomy and the other half require a tracheostomy with a home ventilator.
- The number of children who are ready for decannulation, which means the child is off the ventilator and ready to have their tracheostomy removed, varies per year. Readiness to decannulate depends on the child's underlying condition, ability to breathe without a ventilator, and the ability to maintain an open airway.
- We have reviewed outcomes for 46 children who had a tracheostomy and were on a home ventilator that were successfully liberated from their home ventilator and decannulated between July 1999 and December 2011.
- The median age these children discontinued using a home ventilator was 25.5 months.
- The median age these children decannulated was 40.5 months.
- The majority of these children did not require home oxygen after decannulation.